3-Phenoxy-4-Pyridazinol Derivative and Herbicide Composition Containing The Same

专利摘要:
The present invention relates to a compound represented by the following formula (I), a salt thereof, an ester derivative thereof and a pesticide containing the same as an active ingredient, and a herbicidal composition containing the compound and the second herbicidal active compound as an active ingredient. <Formula I> In formula, R <1> is a hydrogen atom, a halogen atom, an alkyl group, etc., R 2 is a hydrogen atom, a halogen atom, an alkyl group, or the like, R 3 , R 4 , R 5 , R 6 and R 7 are independently of each other a hydrogen atom, a halogen atom, a substituted alkyl group, a substituted alkenyl group, an alkynyl group, a substituted cycloalkyl group, or the like, or R 3 , R 4 , R 5 , R 6 and R 7 may form a ring in which two adjacent groups may be substituted together with the carbon atom to which each is bonded, and m and n are each independently 0 or 1.
公开号:KR20040050061A
申请号:KR10-2004-7002273
申请日:2002-08-14
公开日:2004-06-14
发明作者:요시히사 쓰까모또；히로유끼 고마이；쥰지 가도따니；기요시 고이；시게루 미오；히데오 다께시바
申请人:상꾜 아그로 가부시키가이샤；
IPC主号:

专利说明:

3-phenoxy-4-pyridazinol derivatives and herbicide compositions containing them {3-Phenoxy-4-Pyridazinol Derivative and Herbicide Composition Containing The Same}
[2] Chemical Pharmaceutical Bulletin, 1972, Volume 20, Volume 10, pages 2191-2203 describes 3- (2-allylphenoxy) -6-chloro-4-methoxypyridazine, but 4 of pyridazine The 3-phenoxy-4-pyridazinol compound having a hydroxyl group at the position is not described, and there is no description regarding the herbicide.
[3] The Journal of the Chemical Society: Perkin Transaction I, 1975, 6, pages 534-538, discloses 3- (2-hydroxyphenoxy) -4-methoxypyridazine and 6-chloro-3- (2 -Hydroxyphenoxy) -4-methoxypyridazine is described, but the 3-phenoxy-4-pyridazinol compound having a hydroxyl group at the 4 position of pyridazine is not described, and the description of the herbicide is also described. none.
[4] U.S. Pat.No.5559080 discloses 3- (substituted phenoxy) pyridazine compounds having a haloalkylphenoxy group at the 4 position of pyridazine, but 3-phenoxy- having a hydroxyl group at the 4 position of pyridazine. 4-pyridazinol compounds are not described. In addition, the 3- (substituted phenoxy) pyridazine compound having a haloalkylphenoxy group at the 4-position of pyridazine has an oxygen atom bonded to the 4-position of pyridazine, blocked by a benzene ring, and its herbicidal activity is insufficient. Was.
[5] In addition, a large number of herbicides have been put into practical use as paddy herbicides and are widely used as a single agent and a mixed agent. However, paddy weeds are multi-type and also the germination and growth timing of each weed is not the same, in particular, the occurrence of perennial weeds is long term. Therefore, it is very difficult to control all the weeds by one herbicide spread. Therefore, as a herbicide, it is possible to cure many kinds of weeds, including annual weeds and perennial weeds, that is, it is effective in growing weed ranges and growing weeds, and maintains the weeding effect for a certain period of time, and is stable to rice fields. The emergence of this high drug is the most desired.
[6] In addition, although many herbicides are currently on the market and used as field-farming herbicides, many weeds to be controlled are more herbicidal effects and have broader herbicidal ranges because of their long development and long-term development. Herbicides that do not cause the problem of weakness are desired.
[7] 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-5-pyrazolyl-p-toluenesulfonate (hereinafter referred to as one of the active ingredients of the herbicidal composition of the present invention hereinafter referred to as the second herbicidal active compound) , Compound A, generic name pyrazolate), 2- [4- (2,4-dichlorobenzoyl) -1,3-dimethylpyrazol-5-yloxy] acetophenone (hereinafter referred to as compound B, Common names pyrazoxifen), 2- [4- (2,4-dichloro-m-toluoyl) -1,3-dimethylpyrazol-5-yloxy] -4'-methylacetophenone (hereinafter compound C, common name benzophenaf), 5-cyclopropyl-1,2-oxazol-4-yl α, α, α-trifluoro-2-mesyl-p-tolyl ketone (hereinafter compound D) , Generic name isoxaplutol), 2- (2-chloro-4-mesylbenzoyl) cyclohexane-1,3-dione (hereinafter referred to as compound E, generic name sulfotion), 2- (4- Mesyl-2-nitrobenzoyl) cyclohexane-1,3-dione (hereinafter referred to as compound F, generic name mesotrione) and 4-chloro-2- (methylsulfonyl) phenyl 5-cyclopropyl-4- Oxoxazolyl ketones (hereinafter referred to as compound G, generic name isoxacrorutol) are all known herbicidal compounds and are described in The Pesticide Manual 11th Edition pages 1049 to 1050, pages 1054 to 1055, pages 111 to 111, respectively. 112, The Pesticide Manual 12th Edition, page 563, page 848, page 602) and EP 470 856 (1990). These compounds have a high effect on annual broadleaf weeds and some perennial weeds, but the effects are not necessarily sufficient for rice weeds and some perennial weeds.
[1] The present invention relates to a 3-phenoxy-4-pyridazinol compound, a salt thereof, an ester derivative thereof and a pesticide containing the same as an active ingredient, and a 3-phenoxy-4-pyridazinol compound and a second herbicidal active compound. It relates to a herbicidal composition to contain as.
[8] The present inventors have intensively studied pyridazine derivatives having a phenoxy group at the 3 position, and as a result, the compound having a hydroxyl group at the 4 position of the pyridazine ring shows little damage to rice, and is widely used in a wide range of weed species. Finally, the inventors have discovered that the herbicidal activity is excellent in low doses and completed the present invention. In addition, the ester derivative, such as a bond between the oxygen atom and the acyl group at the 4-position of the pyridazine ring in the soil or in the plant is broken, and converted into a compound having a hydrogen atom bonded to the oxygen atom, has the same herbicidal activity. It was found that the present invention was completed.
[9] In addition, the present inventors completely control various weeds in one scattering and further improve the above problems of conventional herbicides such as the second herbicidally active compounds A, B, C, D, E, F and G. As a result of continuously searching for safe herbicides having high safety against rice and field crops and having very low toxicity to humans or livestock, the 3-phenoxy-4-pyridazinol derivative and the second herbicidal active compound are used as active ingredients. The present invention has been completed by discovering that it is possible to control the critical weeds with a smaller amount of the active ingredient by synergistic action, while expanding the range of the herbicide.
[10] The present invention
[11]
[12] [Wherein, R ¹ represents a hydrogen atom, a halogen atom, a C1 to C6 alkyl group, a C1 to C6 haloalkyl group, a C3 to C6 cycloalkyl group, a C2 to C6 alkenyl group, a cyano group, a C2 to C7 alkylcarbonyl group, di (C1 to C6) Alkyl) carbamoyl group, a phenyl group which may be substituted (this substituent is a substituent selected from Substituent Group A), a 5- or 6-membered heterocyclic group (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring) May also contain 1 to 2 nitrogen atoms), a C1 to C6 alkoxy group, a phenoxy group which may be substituted (this substituent is a substituent selected from Substituent Group A below) or 5 which may be substituted 6-membered heterocyclic oxy groups (this heterocycle contains one nitrogen atom, oxygen atom or sulfur atom in the ring and may also contain 1 to 2 nitrogen atoms, which substituents may be substituted with benzoyl groups ( This substituent is And it may be substituted) by a moiety selected from the group consisting of the substituent) and a C1 to C6 alkyl group is selected from the ventilation group A,
[13] R ² is a hydrogen atom, a halogen atom, a C1 to C6 alkyl group, a (C1 to C6 alkoxy) C1 to C6 alkyl group, a benzoyl group which may be substituted (this substituent is a substituent selected from substituent group A below), C2 to C7 alkoxy A carbonyl group, a phenoxy group which may be substituted (this substituent is a substituent selected from substituent group A below), a phenylthio group which may be substituted (this substituent is a substituent selected from substituent group A below) or a tree (C1 to C6) Alkyl) silicon group,
[14] R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ may each independently be substituted with a hydrogen atom, a halogen atom, a C 1 to C 6 alkyl group which may be substituted (the substituent being a substituent selected from Substituent Group B below), C2 to C6 alkenyl group (this substituent is a cyano group or nitro group), C2 to C6 alkynyl group, C3 to C6 cycloalkyl group which may be substituted (this substituent is a substituent selected from substituent group C below), C4 to C10 Bicycloalkyl group, cyano group, formyl group, C2 to C7 alkylcarbonyl group, benzoyl group which may be substituted (this substituent is a substituent selected from Substituent Group A), carboxyl group, C2 to C7 alkoxycarbonyl group, carbamoyl group, di (C1 to C6 alkyl) carbamoyl group, a phenyl group which may be substituted (this substituent is a substituent selected from Substituent Group A below), a 3 to 6 membered heterocyclic group which may be substituted (this heterocycle is 1 nitrogen in a ring atom, It may contain an oxygen atom or a sulfur atom, may also contain 1 to 2 nitrogen atoms, may be condensed with a benzene ring, and this substituent is a substituent selected from the following substituent group E), an amino group which may be substituted The substituent is a substituent selected from the following substituent group D), nitro group, hydroxyl group, C1 to C6 alkoxy group, C1 to C6 haloalkoxy group, (C1 to C6 alkoxy) C1 to C6 alkoxy group, phenoxy group which may be substituted ( This substituent is a pyridazinyloxy group substituted by a hydroxyl group or a halogen atom and a C1 to C6 alkoxy group, and a 5- to 6-membered heterocyclic oxy group which may be substituted (this heterocycle has one nitrogen atom, oxygen atom in the ring) Or a sulfur atom, and may also contain 1 to 2 nitrogen atoms, which substituent is a substituent selected from the following substituent group E, a phenylsulfonyloxy group which may be substituted Or a C1 to C6 alkylthio group, a C1 to C6 alkylsulfinyl group, a C1 to C6 alkylsulfonyl group or a tri (C1 to C6 alkyl) silicon group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ each represent a 3 to 6 membered cyclic hydrocarbon group which may be substituted together with the carbon atoms to which it is bonded, each of which is selected from the group consisting of nitrogen atom, oxygen atom and sulfur atom Interrupted by the same or different 1 to 2 heteroatoms, which substituents are halogen atoms, C1 to C6 alkyl groups, hydroxy C1 to C6 alkyl groups, C1 to C6 alkoxy groups, oxo groups, hydroxyimino groups or C1 to A C6 alkoxyimino group and substituted with a C1 to C6 alkyl group, it may be combined with a different C1 to C6 alkyl group or a cyclic carbon atom to form a new three-membered ring),
[15] m and n represent 0 or 1 independently of each other,
[16] Substituent group A is a group consisting of a halogen atom, a C1 to C6 alkyl group, a C1 to C6 haloalkyl group, a C3 to C6 cycloalkyl group, a cyano group, and a tri (C1 to C6 alkyl) silicon group,
[17] Substituent group B is a halogen atom, C3 to C6 cycloalkyl group, cyano group, C2 to C7 alkylcarbonyl group, C2 to C7 alkoxycarbonyl group, phenyl group, C1 to C6 alkoxy group, C1 to C6 alkylthio group, C1 to C6 alkylsulfinyl group, C1 to C6 alkylsulfonyl group, C1 to C4 alkylenedioxy group, hydroxyimino group and C1 to C6 alkoxyimino group,
[18] Substituent group C is a halogen atom, a C1 to C6 alkyl group which may be substituted (the substituent is a substituent selected from the substituent group B), a C3 to C6 cycloalkyl group, a C2 to C6 alkenyl group, a cyano group, a C2 to C7 alkylcarbonyl group , Benzoyl group, carboxyl group, C2 to C7 alkoxycarbonyl group, carbamoyl group, di (C1 to C6 alkyl) carbamoyl group, phenyl group which may be substituted (this substituent is a substituent selected from Substituent Group A), 5 or 6 Circle heterocyclic group (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain 1 to 2 nitrogen atoms), an amino group which may be substituted (this substituent is the following substituent group) Substituents selected from D), nitro groups, hydroxyl groups, C1 to C6 alkoxy groups, C1 to C6 haloalkoxy groups, phenoxy groups, C1 to C6 alkylthio groups, phenylthio groups, C1 to C6 alkylsulfinyl groups and C1 to C6 It is a group which consists of an alkylsulfonyl group,
[19] Substituent group D is a group consisting of a C1 to C6 alkyl group, a C2 to C7 alkylcarbonyl group, a C2 to C7 alkoxycarbonyl group, a di (C1 to C6 alkyl) carbamoyl group, and a C1 to C6 alkylsulfonyl group,
[20] Substituent group E is a halogen atom, a C1 to C6 alkyl group, a C1 to C6 haloalkyl group, a hydroxyl group, a phenylsulfonyl group which may be substituted (this substituent is a substituent selected from Substituent Group A) and di (C1 to C6 alkyl) Group consisting of a pamoyl group], salts thereof or ester derivatives thereof,
[21] Pesticides containing these as active ingredients, and
[22] One or two or more 3-phenoxy-4-pyridazinol derivatives selected from the group consisting of the compounds, salts and ester derivatives thereof, and
[23] 4- (2,4-Dichlorobenzoyl) -1,3-dimethyl-5-pyrazolyl-p-toluenesulfonate, 2- [4- (2,4-dichlorobenzoyl) -1,3-dimethylpyrazole- 5-yloxy] acetophenone, 2- [4- (2,4-dichloro-m-toluoyl) -1,3-dimethylpyrazol-5-yloxy] -4'-methylacetophenone, 5-cyclo Propyl-1,2-oxazol-4-yl α, α, α-trifluoro-2-mesyl-p-tolyl ketone, 2- (2-chloro-4-mesylbenzoyl) cyclohexane-1,3- In the group consisting of dione, 2- (4-mesyl-2-nitrobenzoyl) cyclohexane-1,3-dione and 4-chloro-2- (methylsulfonyl) phenyl 5-cyclopropyl-4-isooxazolyl ketone A herbicidal composition containing, as an active ingredient, one or two or more selected second herbicidal active compounds.
[24] In the present invention, the "halogen atom" is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom, preferably a fluorine atom, a chlorine atom or a bromine atom, more preferably a chlorine atom or a bromine atom, even more preferably Is a chlorine atom.
[25] In the present invention, the "C1 to C6 alkyl group" is a straight or branched chain alkyl group having 1 to 6 carbon atoms, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl , Isopentyl, 2-methylbutyl, neopentyl, 1-ethylpropyl, hexyl, 4-methylpentyl, 3-methylpentyl, 2-methylpentyl, 1-methylpentyl, 3,3-dimethylbutyl, 2,2- It may be a dimethylbutyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,3-dimethylbutyl or 2-ethylbutyl group, preferably straight or branched carbon having 1 to 4 carbon atoms It is a chain alkyl group (C1 to C4 alkyl group), More preferably, it is a C1-C3 linear or branched alkyl group (C1 to C3 alkyl group), More preferably, it is a C1-C2 alkyl group (C1 to C2 alkyl group), Especially preferably, it is a methyl group.
[26] In the present invention, the "C1 to C6 haloalkyl group" is the "C1 to C6 alkyl group" substituted with 1 to 5 "halogen atoms", which are the same or different, and for example, chloromethyl, dichloromethyl, trichloromethyl, 1-chloroethyl, 2-chloroethyl, 2,2,2-trichloroethyl, 1-chloropropyl, 3-chloropropyl, 1-chlorobutyl, 4-chlorobutyl, fluoromethyl, difluoromethyl, tri Fluoromethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, fluorochloromethyl, bromomethyl, 1-bromoethyl, 2-bro It may be a moethyl or iodomethyl group, preferably the same or different 1 to 3 substituents selected from the group consisting of a fluorine atom, a chlorine atom and a bromine atom is a substituted C1 to C3 alkyl group, more preferably the same 1 to 3 Fluorine or chlorine atoms It is a substituted C1 to C2 alkyl group, More preferably, it is a fluoromethyl, difluoromethyl, trifluoromethyl, or 2,2,2- trichloroethyl group, Especially preferably, it is a trifluoromethyl group.
[27] In the present invention, the "C3 to C6 cycloalkyl group" is a cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl group, Preferably it is a cyclopropyl or cyclobutyl group, More preferably, it is a cyclopropyl group.
[28] In the present invention, the "C2 to C6 alkenyl group" is a straight or branched chain alkenyl group having 2 to 6 carbon atoms, for example, vinyl, 1-methylvinyl, 1-propenyl, 1-methyl-1-propenyl, 2-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-ethyl-2-propenyl, 2-butenyl, 1-methyl-2-butenyl, 2-methyl- 2-butenyl, 1-ethyl-2-butenyl, 3-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 1-ethyl-3-butenyl, 2-pentenyl , 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 4-pentenyl, 1-methyl 4-pentenyl, 2-methyl-4-pentenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, or 5-hexenyl group, preferably a straight or branched chain having 2 to 4 carbon atoms Alkenyl group (C2 to C4 alkenyl group), more preferably a vinyl, 1-methylvinyl, 2-propenyl or 1-methyl-2-propenyl group.
[29] In the present invention, the "C2 to C7 alkylcarbonyl group" is a carbonyl group to which the "C1 to C6 alkyl group" is bonded, for example, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivalo It may be a hexanoyl or heptanoyl group, preferably a carbonyl group (C2 to C5 alkylcarbonyl group) to which a straight or branched chain alkyl group having 1 to 4 carbon atoms is bonded, and more preferably a straight or branched chain having 1 to 3 carbon atoms It is a carbonyl group (C2 to C4 alkylcarbonyl group) to which an alkyl group is bonded, particularly preferably an acetyl, propionyl, valeryl or pivaloyl group, and most preferably an acetyl group.
[30] In the present invention, the "di (C1 to C6 alkyl) carbamoyl group" is a carbamoyl group in which the same or different two "C1 to C6 alkyl groups" are bonded to a nitrogen atom, for example, dimethylcarbamoyl and methylethyl. Carbamoyl, diethylcarbamoyl, dipropylcarbamoyl, dibutylcarbamoyl, or dihexylcarbamoyl groups, preferably having the same two C 1 -C 3 straight or branched chain alkyl groups bonded together. Carbamoyl group (di (C1 to C3 alkyl) carbamoyl group), more preferably dimethylcarbamoyl group or diethylcarbamoyl group, still more preferably dimethylcarbamoyl group.
[31] In the present invention, the "tri (C1 to C6 alkyl) silicon group" is a silicon atom to which the same or different three "C1 to C6 alkyl groups" are bonded, for example, trimethylsilyl, triethylsilyl, triisopropylsilyl , A dimethylisopropylsilyl, t-butyldimethylsilyl or trihexylsilyl group, preferably a silicon atom (tri (C1 to C3 alkyl) bonded to three or three straight or branched chain alkyl groups having the same or different carbon atoms; Silicon group), more preferably trimethylsilyl or dimethylisopropylsilyl group, still more preferably trimethylsilyl group.
[32] In the present invention, the "substituted phenyl group (this substituent is a substituent selected from substituent group A)" is the "halogen atom", the "C1 to C6 alkyl group", the "C1 to C6 haloalkyl group", and The same or different 1-5 substituents selected from the group consisting of a "C3 to C6 cycloalkyl group", a cyano group and said "tri (C1 to C6 alkyl) silicon group" are phenyl groups which may be substituted, for example, phenyl, Fluorophenyl, difluorophenyl, trifluorophenyl, chlorophenyl, dichlorophenyl, trichlorophenyl, fluorochlorophenyl, methylphenyl, dimethylphenyl, trimethylphenyl, tetramethylphenyl, pentamethylphenyl, ethylphenyl, fluoro (methyl ) Phenyl, chloro (methyl) phenyl, bromo (methyl) phenyl, cyclopropylphenyl, cyclopropyl (fluoro) phenyl, chloro (cyclopropyl) phenyl, cyclopropyl (methyl) phenyl, (t Fluoromethyl) phenyl or fluoro (trifluoromethyl) phenyl group, preferably a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, the same selected from the group consisting of fluorine atom, chlorine atom and bromine atom Or a C1 to C3 alkyl group substituted with 1 to 3 different substituents ", a C3 to C4 cycloalkyl group, a cyano group and a tri (C1 to C3 alkyl) silicon group. Phenyl group, more preferably a phenyl, chlorophenyl, methylphenyl, trifluorophenyl or cyanophenyl group.
[33] In the present invention, "a 5 or 6 membered heterocyclic group (this heterocycle may contain 1 nitrogen atom, oxygen atom or sulfur atom in the ring and may also contain 1 to 2 nitrogen atoms)" is a hetero atom. It is a 5-6 membered heterocyclic group which contains 1 nitrogen atom, oxygen atom or sulfur atom and may also contain 1 to 2 nitrogen atoms, for example furyl, thienyl, pyrrolyl, pyrazolyl, It may be a dazolyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, triazolyl, pyranyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl or triazinyl group, preferably a 5-membered heterocyclic group (This heterocycle contains one nitrogen atom, oxygen atom or sulfur atom in the ring), and more preferably is a furyl or thienyl group.
[34] In the present invention, the "C1 to C6 alkoxy group" is a C1-C6 linear or branched alkoxy group, for example, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, s- Butoxy, t-butoxy, pentoxy, isopentoxy, 2-methylbutoxy, neopentoxy, 1-ethylpropoxy, hexyloxy, 4-methylpentoxy, 3-methylpentoxy, 2-methyl Pentoxy, 1-methylpentoxy, 3,3-dimethylbutoxy, 2,2-dimethylbutoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2 , 3-dimethylbutoxy or 2-ethylbutoxy group, preferably a straight or branched chain alkoxy group having 1 to 3 carbon atoms (C1 to C3 alkoxy group), more preferably a methoxy or ethoxy group, More preferably, it is a methoxy group.
[35] In the present invention, "substituted phenoxy group (this substituent is a substituent selected from substituent group A)" is the "halogen atom", the "C1 to C6 alkyl group", the "C1 to C6 haloalkyl group", The same or different 1 to 5 substituents selected from the group consisting of the "C3 to C6 cycloalkyl group", the cyano group and the "tri (C1 to C6 alkyl) silicon group" can be substituted, for example Phenoxy, fluorophenoxy, difluorophenoxy, trifluorophenoxy, chlorophenoxy, dichlorophenoxy, trichlorophenoxy, fluorochlorophenoxy, methylphenoxy, dimethylphenoxy, trimethylphenoxy , Tetramethylphenoxy, pentamethylphenoxy, ethylphenoxy, fluoro (methyl) phenoxy, chloro (methyl) phenoxy, bromo (methyl) phenoxy, cyclopropylphenoxy, cyclopropyl (fluoro) phenoxy City, Chloro Ropropyl) phenoxy, cyclopropyl (methyl) phenoxy, (trifluoromethyl) phenoxy or fluoro (trifluoromethyl) phenoxy group, preferably fluorine atom, chlorine atom, bromine atom, C1 To C3 alkyl group, "C1 to C3 alkyl group substituted with the same or different 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom", C3 to C4 cycloalkyl group, cyano group and tri (C1 to C3 alkyl) The same or different 1-3 substituents selected from the group consisting of silicon groups may be substituted, more preferably phenoxy, chlorophenoxy, methylphenoxy, trifluorophenoxy or cyanophenoxy group. .
[36] In the present invention, the "substituted benzoyl group (this substituent is a substituent selected from substituent group A)" means the "halogen atom", the "C1 to C6 alkyl group", the "C1 to C6 haloalkyl group", The same or different 1-5 substituents selected from the group consisting of said "C3 to C6 cycloalkyl group", cyano group and said "tri (C1 to C6 alkyl) silicon group" are benzoyl groups which may be substituted, for example Benzoyl, fluorobenzoyl, difluorobenzoyl, trifluorobenzoyl, chlorobenzoyl, dichlorobenzoyl, trichlorobenzoyl, fluorochlorobenzoyl, methylbenzoyl, dimethylbenzoyl, trimethylbenzoyl, tetramethylbenzoyl, pentamethylbenzoyl, ethylbenzoyl , Fluoro (methyl) benzoyl, chloro (methyl) benzoyl, bromo (methyl) benzoyl, cyclopropylbenzoyl, cyclopropyl (fluoro) benzoyl, chloro (shi Ropropyl) benzoyl, cyclopropyl (methyl) benzoyl, (trifluoromethyl) benzoyl or fluoro (trifluoromethyl) benzoyl group, preferably a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group , "C1 to C3 alkyl group substituted with the same or different 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom", C3 to C4 cycloalkyl group, cyano group and tri (C1 to C3 alkyl) silicon group The same or different 1-3 substituents selected from the group are benzoyl groups which may be substituted, more preferably benzoyl, chlorobenzoyl, dichlorobenzoyl, methylbenzoyl, trifluorobenzoyl or cyanobenzoyl group.
[37] In the present invention, "substituted 5- or 6-membered heterocyclic oxy group (this heterocycle may contain one nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain 1-2 nitrogen atoms) Wherein the substituent may be substituted with a benzoyl group which can be substituted (the substituent is a substituent selected from substituent group A) and a substituent selected from the group consisting of C1 to C6 alkyl groups. Benzoyl group (the substituent is a substituent selected from substituent group A) &quot; and &quot; as a complex atom that can be substituted by 1 to 3 substituents selected from the group consisting of the above &quot; C1 to C6 alkyl groups &quot; 5 to 6 membered heterocyclic oxy group which contains nitrogen atoms, oxygen atoms or sulfur atoms and may contain 1 to 2 nitrogen atoms, and preferably a fluorine atom, Chlorine atom, bromine atom, C1 to C3 alkyl group, "C1 to C3 alkyl group substituted with the same or different 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom", C3 to C4 cycloalkyl group, cyano group and One nitrogen atom as a complex atom substituted with a benzoyl group and the same two C1 to C3 alkyl groups which may be substituted by the same or different one to three substituents selected from the group consisting of tri (C1 to C3 alkyl) silicon groups, 5-membered heterocyclic oxy group which contains an oxygen atom or a sulfur atom and may further contain one nitrogen atom, and more preferably one benzoyl group and two C1 to C2 substituted by two chlorine atoms; It is a pyrazolyloxy group substituted by the alkyl group.
[38] In the present invention, "(C1 to C6 alkoxy) C1 to C6 alkyl group" is said "C1 to C6 alkyl group" in which one of said "C1 to C6 alkoxy groups" is substituted, for example, methoxymethyl, ethoxymethyl , Propoxymethyl, butoxymethyl, s-butoxymethyl, t-butoxymethyl, pentyloxymethyl, hexyloxymethyl, methoxyethyl, ethoxyethyl, propoxyethyl, butoxyethyl, methoxypropyl, meth It may be a methoxybutyl, methoxypentyl or methoxyhexyl group, preferably a C1 to C6 alkyl group substituted with one C1 to C3 alkoxy group, more preferably a methoxyethyl, ethoxyethyl or ethoxymethyl group.
[39] In the present invention, the "C2 to C7 alkoxycarbonyl group" is a carbonyl group to which the "C1 to C6 alkoxy group" is bonded, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl , Butoxycarbonyl, isobutoxycarbonyl, s-butoxycarbonyl, t-butoxycarbonyl, pentoxycarbonyl, isopentoxycarbonyl, 2-methylbutoxycarbonyl, neopentoxycarbonyl, 1-ethylpropoxycarbonyl, hexyloxycarbonyl, 4-methylpentoxycarbonyl, 3-methylpentoxycarbonyl, 2-methylpentoxycarbonyl, 1-methylpentoxycarbonyl, 3,3- Dimethylbutoxycarbonyl, 2,2-dimethylbutoxycarbonyl, 1,1-dimethylbutoxycarbonyl, 1,2-dimethylbutoxycarbonyl, 1,3-dimethylbutoxycarbonyl, 2,3- It may be a dimethylbutoxycarbonyl or 2-ethylbutoxycarbonyl group, preferably a carbon to which a C1 to C3 alkoxy group is bonded Group (C2 to C4 alkoxycarbonyl group), and more preferably is a methoxycarbonyl or ethoxycarbonyl group in, and more preferably a methoxycarbonyl group.
[40] In the present invention, "substituted phenylthio group (this substituent is a substituent selected from substituent group A)" is the "halogen atom", the "C1 to C6 alkyl group", and the "C1 to C6 haloalkyl group" Is a phenylthio group in which the same or different 1 to 5 substituents selected from the group consisting of the "C3 to C6 cycloalkyl group", the cyano group and the "tri (C1 to C6 alkyl) silicon group" can be substituted, and examples For example, phenylthio, fluorophenylthio, difluorophenylthio, trifluorophenylthio, chlorophenylthio, dichlorophenylthio, trichlorophenylthio, fluorochlorophenylthio, methylphenylthio, dimethylphenylthio, trimethylphenyl Thio, tetramethylphenylthio, pentamethylphenylthio, ethylphenylthio, fluoro (methyl) phenylthio, chloro (methyl) phenylthio, bromo (methyl) phenylthio, cyclopropylphenylthi , Cyclopropyl (fluoro) phenylthio, chloro (cyclopropyl) phenylthio, cyclopropyl (methyl) phenylthio, (trifluoromethyl) phenylthio or fluoro (trifluoromethyl) phenylthio group, preferably Preferably a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a "C1 to C3 alkyl group substituted with the same or different one to three substituents selected from the group consisting of a fluorine atom, a chlorine atom and a bromine atom", and a C3 to C4 cyclo The same or different 1-3 substituents selected from the group consisting of an alkyl group, a cyano group and a tri (C1 to C3 alkyl) silicon group are phenylthio groups which may be substituted, more preferably phenylthio, chlorophenylthio, methylphenylthio And trifluorophenylthio or cyanophenylthio group.
[41] In the present invention, the "C1 to C6 alkylthio group" is a C1-C6 linear or branched alkylthio group, for example, methylthio, ethylthio, propylthio, isopropylthio, butylthio, isobutylthio , s-butylthio, t-butylthio, pentylthio, isopentylthio, 2-methylbutylthio, neopentylthio, 1-ethylpropylthio, hexylthio, 4-methylpentylthio, 3-methylpentylthio, 2 -Methylpentylthio, 1-methylpentylthio, 3,3-dimethylbutylthio, 2,2-dimethylbutylthio, 1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio , 2,3-dimethylbutylthio or 2-ethylbutylthio group, preferably a straight or branched chain alkylthio group having 1 to 3 carbon atoms (C1 to C3 alkylthio group), more preferably methylthio or It is an ethylthio group, More preferably, it is a methylthio group.
[42] In the present invention, the "C1 to C6 alkylsulfinyl group" is a straight or branched chain alkylsulfinyl group having 1 to 6 carbon atoms, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, butylsulfur Finyl, isobutylsulfinyl, s-butylsulfinyl, t-butylsulfinyl, pentylsulfinyl, isopentylsulfinyl, 2-methylbutylsulfinyl, neopentylsulfinyl, 1-ethylpropylsulfinyl, hexylsulfinyl , 4-methylpentylsulfinyl, 3-methylpentylsulfinyl, 2-methylpentylsulfinyl, 1-methylpentylsulfinyl, 3,3-dimethylbutylsulfinyl, 2,2-dimethylbutylsulfinyl, 1,1 -Dimethylbutylsulfinyl, 1,2-dimethylbutylsulfinyl, 1,3-dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl or 2-ethylbutylsulfinyl group, preferably having 1 to 3 carbon atoms Linear or branched alkylsulfinyl groups (C1 to C3 alkylsulfinyl groups), more preferably methylsulfinyl or ethylsulfinyl groups, still more preferably It is a methyl sulfinyl group.
[43] In the present invention, the "C1 to C6 alkylsulfonyl group" is a C1-C6 linear or branched alkylsulfonyl group, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, butylsulfonyl Ponyl, Isobutylsulfonyl, s-butylsulfonyl, t-butylsulfonyl, pentylsulfonyl, isopentylsulfonyl, 2-methylbutylsulfonyl, neopentylsulfonyl, 1-ethylpropylsulfonyl, hexylsulfonyl , 4-methylpentylsulfonyl, 3-methylpentylsulfonyl, 2-methylpentylsulfonyl, 1-methylpentylsulfonyl, 3,3-dimethylbutylsulfonyl, 2,2-dimethylbutylsulfonyl, 1,1 -Dimethylbutylsulfonyl, 1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl or 2-ethylbutylsulfonyl group, preferably 1 to 3 carbon atoms Linear or branched alkylsulfonyl groups (C1 to C3 alkylsulfonyl groups), more preferably methylsulfonyl or ethylsulfonyl groups, still more preferably It is the methyl sulfonyl group.
[44] In the present invention, the "C1 to C4 alkylenedioxy group" is a straight or branched chain alkylenedioxy group having 1 to 4 carbon atoms, for example, methylenedioxy, ethylenedioxy, propylenedioxy, trimethylenedioxy or It may be a tetramethylenedioxy group, Preferably it is a C1-C2 alkylenedioxy group, More preferably, it is a 1, 2- ethylenedioxy group.
[45] In the present invention, the "C1 to C6 alkoxyimino group" is a linear or branched alkoxyimino group having 1 to 6 carbon atoms, for example, methoxyimino, ethoxyimino, propoxyimino, isopropoxyimino, butoxyyi Mino, isobutoxyimino, s-butoxyimino, t-butoxyimino, pentoxyimino, isopentoxyimino, 2-methylbutoxyimino, neopentoxyimino, 1-ethylpropoxyimino, hexyloxyimino, 4-methylpentoxyimino, 3-methylpentoxyimino, 2-methylpentoxyimino, 1-methylpentoxyimino, 3,3-dimethylbutoxyimino, 2,2-dimethylbutoxyimino, 1,1- Dimethylbutoxyimino, 1,2-dimethylbutoxyimino, 1,3-dimethylbutoxyimino, 2,3-dimethylbutoxyimino or 2-ethylbutoxyimino group, preferably having 1 to 3 carbon atoms Linear or branched alkoxyimino groups (C1 to C3 alkoxyimino groups), It is preferably methoxy or ethoxy toksiyi and the unexposed imino group, more preferably methoxy imino group.
[46] In the present invention, the "substituted C1 to C6 alkyl group (this substituent is a substituent selected from substituent group B)" means the "halogen atom", or the "C3 to C6 cycloalkyl group", cyano group, and " C2 to C7 alkylcarbonyl group ", said" C2 to C7 alkoxycarbonyl group ", phenyl group, said" C1 to C6 alkoxy group ", said" C1 to C6 alkylthio group ", said" C1 to C6 alkylsulfinyl group "," C1 To C6 alkylsulfonyl group ”, the“ C1 to C4 alkylenedioxy group ”, the hydroxyimino group or the“ C1 to C6 alkoxyimino group ”, and the“ C1 to C6 alkyl group ”, for example. Fluoromethyl, difluoromethyl, trifluoromethyl, 2,2,2-trichloroethyl, cyclopropylmethyl, cyanomethyl, acetylmethyl, acetylethyl, methoxycarbonylmethyl, methoxycarbonylethyl, Ethoxycarbonyl Methyl, ethoxycarbonylethyl, benzyl, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, methylthiomethyl, methylthioethyl, ethylthiomethyl, ethylthioethyl, methylsulfinylmethyl, methylsulfonyl It may be a methyl, 2- (1,3-dioxolanyl), hydroxyiminomethyl or methoxyiminomethyl group, preferably the same or different one to three substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom Substituted C1 to C3 alkyl group, or C3 to C4 cycloalkyl group, cyano group, C2 to C4 alkylcarbonyl group, C2 to C4 alkoxycarbonyl group, phenyl group, C1 to C3 alkoxy group, C1 to C3 alkylthio group, C1 to C3 alkylsulphi A C1 to C3 alkyl group in which a silyl group, a C1 to C3 alkylsulfonyl group, a C1 to C2 alkylenedioxy group, a hydroxyimino group or a C1 to C3 alkoxyimino group may be substituted, and more preferably the same 1 to C3 alkyl group. C1 to C2 alkyl or cyclopropyl group substituted with three fluorine atoms or chlorine atoms, cyano group, C2 to C3 alkylcarbonyl group, C2 to C3 alkoxycarbonyl group, phenyl group, C1 to C2 alkoxy group, C1 to C2 alkylthio group, C1 to Or a C1 to C2 alkyl group in which a C2 alkylsulfinyl group, a C1 to C2 alkylsulfonyl group, an ethylenedioxy group, a hydroxyimino group or a C1 to C2 alkoxyimino group can be substituted.
[47] In the present invention, "substituted C2 to C6 alkenyl group (this substituent is a cyano group or nitro group)" is the "C2 to C6 alkenyl group" substituted with a cyano group or nitro group, and preferably a cyano group or nitro group Substituted C2 to C3 alkenyl group, more preferably cyanovinyl or nitrovinyl group.
[48] In the present invention, the "C2 to C6 alkynyl group" is a C2-C6 linear or branched alkynyl group, for example, ethynyl, 2-propynyl, 1-methyl-2-propynyl, 1-ethyl-2 Propynyl, 2-butynyl, 1-methyl-2-butynyl, 1-ethyl-2-butynyl, 3-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 1-ethyl-3-butynyl, 2-pentynyl, 1-methyl-2-pentynyl, 1-ethyl-2-pentynyl, 3-pentynyl, 1-methyl-3-pentynyl, 2-methyl- 3-pentynyl, 4-pentynyl, 1-methyl-4-pentynyl, 2-methyl-4-pentynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl or 5-hexynyl, Preferably it is a C3-C4 alkynyl group (C3-C4 alkynyl group), More preferably, it is an ethynyl, 1-propynyl, or 2-propynyl group.
[49] In the present invention, the "substituted amino group (this substituent is a substituent selected from substituent group D)" is the "C1 to C6 alkyl group", the "C2 to C7 alkylcarbonyl group", and the "C2 to C7 alkoxycarbonyl group" , "Di (C1 to C6 alkyl) carbamoyl group" and "C1 to C6 alkylsulfonyl group" are amino groups which may be substituted by the same or different 1 to 2 substituents selected from the group consisting of For example amino, methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, s-butylamino, t-butylamino, pentylamino, isopentylamino, (2-methylbutyl) amino, neopentyl Amino, (1-ethylpropyl) amino, hexylamino, (4-methylpentyl) amino, (3-methylpentyl) amino, (2-methylpentyl) amino, (1-methylpentyl) amino, (3,3- Dimethylbutyl) amino, (2,2-dimethylpart Tyl) amino, (1,1-dimethylbutyl) amino, (1,2-dimethylbutyl) amino, (1,3-dimethylbutyl) amino, (2,3-dimethylbutyl) amino, (2-ethylbutyl) Amino, dimethylamino, (methyl) (ethyl) amino, diethylamino, dipropylamino, (methyl) (isopropyl) amino, diisopropylamino, dibutylamino, diisobutylamino, dis-butylamino, Dit-butylamino, dipentylamino, diisopentylamino, di (2-methylbutyl) amino, dinepentylamino, di (1-ethylpropyl) amino, dihexylamino, di (4-methylpentyl) amino , Di (3-methylpentyl) amino, di (2-methylpentyl) amino, di (1-methylpentyl) amino, di (3,3-dimethylbutyl) amino, di (2,2-dimethylbutyl) amino, Di (1,1-dimethylbutyl) amino, di (1,2-dimethylbutyl) amino, di (1,3-dimethylbutyl) amino, di (2,3-dimethylbutyl) amino, di (2-ethylbutyl ) Amino, acetylamino, propionylamino, butanoylamino, ( 2-methylpropanoyl) amino, pentanoylamino, (2,2-dimethylpropanoyl) amino, (2,2-dimethylpentanoyl) amino, (2-methylbutanoyl) amino, (3-methylbutayl Noyl) amino, hexanoylamino, heptanoylamino, (3,3-dimethylbutanoyl) amino, methoxycarbonylamino, ethoxycarbonylamino, propoxycarbonylamino, isopropoxycarbonylamino, butoxy Carbonylamino, isobutoxycarbonylamino, s-butoxycarbonylamino, t-butoxycarbonylamino, pentoxycarbonylamino, isopentoxycarbonylamino, (2-methylbutoxycarbonyl) amino, Neopentoxycarbonylamino, (1-ethylpropoxycarbonyl) amino, hexyloxycarbonylamino, (4-methylpentoxycarbonyl) amino, (3-methylpentoxycarbonyl) amino, (2- Methylpentoxycarbonyl) amino, (1-methylpentoxycarbonyl) amino, (3,3-dimethylbutoxycarbonyl) Mino, (2,2-dimethylbutoxycarbonyl) amino, (1,1-dimethylbutoxycarbonyl) amino, (1,2-dimethylbutoxycarbonyl) amino, (1,3-dimethylbutoxycarbon Carbonyl) amino, (2,3-dimethylbutoxycarbonyl) amino, (2-ethylbutoxycarbonyl) amino, dimethylcarbamoylamino, (methylethylcarbamoyl) amino, diethylcarbamoylamino, Dipropylcarbamoylamino, dibutylcarbamoylamino, dihexylcarbamoylamino, methylsulfonylamino, ethylsulfonylamino, propylsulfonylamino, isopropylsulfonylamino, butylsulfonylamino, t-butyl It may be sulfonylamino or hexylsulfonylamino, and preferably 1 to 2 C1 to C3 alkyl groups, or C2 to C4 alkylcarbonyl groups, C2 to C4 alkoxycarbonyl groups, di (C1 to C3 alkyl) carbamoyl groups, which are the same or different Or may be substituted by a C1 to C3 alkylsulfonyl group. Amino group, more preferably methylamino, ethylamino, dimethylamino, diethylamino, acetylamino, propionylamino, (2-methylpropanoyl) amino, (2,2-dimethylpropanoyl) amino, Methoxycarbonylamino, ethoxycarbonylamino, dimethylcarbamoylamino, diethylcarbamoylamino, methylsulfonylamino or ethylsulfonylamino group.
[50] In the present invention, the "C1 to C6 haloalkoxy group" is the "C1 to C6 alkoxy group" in which 1 to 5 "halogen atoms", which are identical or different, are substituted, for example, chloromethoxy, dichloromethoxy, Trichloromethoxy, 1-chloroethoxy, 2-chloroethoxy, 2,2,2-trichloroethoxy, 1-chloropropoxy, 3-chloropropoxy, 1-chlorobutoxy, 4-chlorobutoxy , Fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2,2-trifluoroethoxy, pentafluoroethoxy, fluorochloro Methoxy, bromomethoxy, 1-bromoethoxy, 2-bromoethoxy or iodinemethoxy group, preferably 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom Substituted C1 to C3 alkoxy group, more preferably The crab is a C1 to C2 alkoxy group substituted with the same 1 to 3 fluorine atoms or chlorine atoms, more preferably fluoromethoxy, difluoromethoxy, trifluoromethoxy or 2,2,2-trichloroethoxy group And particularly preferably trifluoromethoxy group.
[51] In the present invention, the "substituted C3 to C6 cycloalkyl group (this substituent is a substituent selected from substituent group C)" is the "halogen atom", said "substituted C1 to C6 alkyl group (this substituent is a substituent group Substituents selected from B) "," C3 to C6 cycloalkyl group "," C2 to C6 alkenyl group ", cyano group," C2 to C7 alkylcarbonyl group ", benzoyl group, carboxyl group, and" C2 to C7 alkoxy " Carbonyl group ", carbamoyl group, said" di (C1 to C6 alkyl) carbamoyl group ", said" substituted phenyl group (this substituent is a substituent selected from Substituent Group A) ", said" 5 or 6-membered complex Ventilation (this heterocycle contains one nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain one to two nitrogen atoms), '' the amino group which may be substituted (this substituent is a substituent groupA substituent selected from D) ", a nitro group, a hydroxyl group, said" C1 to C6 alkoxy group ", said" C1 to C6 haloalkoxy group ", a phenoxy group, said" C1 to C6 alkylthio group ", a phenylthio group, It is said "C3-C6 cycloalkyl group" substituted by the same or different 1-5 substituents chosen from the group which consists of said "C1-C6 alkylsulfinyl group" and said "C1-C6 alkylsulfonyl group", For example Fluorocyclopropyl, difluorocyclopropyl, chlorocyclopropyl, dichlorocyclopropyl, bromocyclopropyl, dibromocyclopropyl, iodocyclopropyl, methylcyclopropyl, ethylcyclopropyl, propylcyclopropyl, isopropylcyclo Propyl, butylcyclopropyl, t-butylcyclopropyl, hexylcyclopropyl, cyclopropylcyclopropyl, cyclobutylcyclopropyl, cyclopentyl Clopropyl, (fluoromethyl) cyclopropyl, (chloromethyl) cyclopropyl, (bromomethyl) cyclopropyl, (difluoromethyl) cyclopropyl, (trifluoromethyl) cyclopropyl, (trichloromethyl) cyclo Propyl, (2,2,2-trifluoroethyl) cyclopropyl, (2,2,2-trichloroethyl) cyclopropyl, vinylcyclopropyl, (methoxymethyl) cyclopropyl, (ethoxymethyl) cyclopropyl , (Isopropoxymethyl) cyclopropyl, (methylthiomethyl) cyclopropyl, (ethylthiomethyl) cyclopropyl, (isopropylthiomethyl) cyclopropyl, (methylsulfinylmethyl) cyclopropyl, (ethylsulfinylmethyl) Cyclopropyl, (methylsulfonylmethyl) cyclopropyl, (ethylsulfonylmethyl) cyclopropyl, cyanocyclopropyl, (1-methoxyiminoethyl) cyclopropyl, acetylcyclopropyl, propionylcyclopropyl, benzoylcyclopropyl, Carboxysis Ropropyl, methoxycarbonylcyclopropyl, ethoxycarbonylcyclopropyl, carbamoylcyclopropyl, (dimethylcarbamoyl) cyclopropyl, (diethylcarbamoyl) cyclopropyl, phenylcyclopropyl, (fluorophenyl ) Cyclopropyl, (chlorophenyl) cyclopropyl, tolylcyclopropyl, furylcyclopropyl, thienylcyclopropyl, pyridylcyclopropyl, aminocyclopropyl, (methylamino) cyclopropyl, (dimethylamino) cyclopropyl, (acetylamino ) Cyclopropyl, (methoxycarbonylamino) cyclopropyl, (3,3-dimethylureido) cyclopropyl, (methylsulfonylamino) cyclopropyl, nitrocyclopropyl, hydroxycyclopropyl, methoxycyclopropyl, to Methoxycyclopropyl, (trifluoromethoxy) cyclopropyl, phenoxycyclopropyl, methylthiocyclopropyl, ethylthiocyclopropyl, phenyl thi Cyclopropyl, methylsulfinylcyclopropyl, ethylsulfinylcyclopropyl, methylsulfonylcyclopropyl, ethylsulfonylcyclopropyl, dimethylcyclopropyl, methyl (ethyl) cyclopropyl, diethylcyclopropyl, biscyanocyclopropyl, trimethyl Cyclopropyl, tetramethylcyclopropyl, pentamethylcyclopropyl, methylcyclobutyl, vinylcyclobutyl, cyanocyclobutyl, carboxycyclobutyl, acetylcyclobutyl, methoxycarbonylcyclobutyl or aminocyclobutyl group, may be preferred. Preferably the same or different 1 to 5 substituents selected from the group consisting of a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C3 to C4 cycloalkyl group and a cyano group, or a "fluorine atom, a chlorine atom and a bromine atom C1 to substituted with the same or different 1-3 substituents selected from the group C3 alkyl group or C3 to C4 cycloalkyl group, cyano group, C2 to C4 alkylcarbonyl group, C2 to C4 alkoxycarbonyl group, phenyl group, C1 to C3 alkoxy group, C1 to C3 alkylthio group, C1 to C3 alkylsulfinyl group, C1 to C3 C1 to C3 alkyl group substituted with alkylsulfonyl group, C1 to C2 alkylenedioxy group, imino group or C1 to C3 alkoxyimino group '', C2 to C4 alkenyl group, C2 to C4 alkylcarbonyl group, benzoyl group, carboxyl group, C2 to C4 1 or the same or different one selected from the group consisting of alkoxycarbonyl group, carbamoyl group, di (C1-C3 alkyl) carbamoyl group, "fluorine atom, chlorine atom, bromine atom, C1-C3 alkyl group," fluorine atom, chlorine atom and bromine atom C1 to C3 alkyl group substituted with 3 to 3 substituents ", C3 to C4 cycloalkyl group, cyano group and tri (C1 to C3 alkyl) silicon group Is a phenyl group which may be substituted with different 1-3 substituents ", a 5-membered heterocyclic group (this heterocycle contains one nitrogen atom, oxygen atom or sulfur atom in the ring)," the same or different 1 to 2 C1 groups; Amino group which may be substituted by C3 to C3 alkyl group, or C2 to C4 alkylcarbonyl group, C2 to C4 alkoxycarbonyl group, di (C1 to C3 alkyl) carbamoyl group or C1 to C3 alkylsulfonyl group ”, nitro group, hydroxyl group, C1 to C3 alkyl group C3 to C4 cycloalkyl group substituted by a C3 alkoxy group, a C1 to C3 haloalkoxy group, a phenoxy group, a C1 to C3 alkylthio group, a phenylthio group, a C1 to C3 alkylsulfinyl group or a C1 to C3 alkylsulfonyl group, and Preferably the same or different 1 to 3 substituents selected from the group consisting of chlorine atom, bromine atom, C1 to C2 alkyl group, cyclopropyl group and cyano group, or "chlorine atom and C1 to C2 alkyl group substituted with the same 1-3 substituents selected from the group consisting of rom atoms, or cyclopropyl group, cyano group, C2 to C3 alkylcarbonyl group, C2 to C3 alkoxycarbonyl group, phenyl group, C1 to C2 alkoxy group, C1 to C2 C2 to C2 alkylthio group, C1 to C2 alkylsulfinyl group, C1 to C2 alkylsulfonyl group, 1,2-ethylenedioxy group, imino group or C1 to C2 alkyl group substituted with C1 to C2 alkoxyimino group ", C2 to C3 alkenyl group , C2 to C3 alkylcarbonyl group, benzoyl group, carboxyl group, C2 to C3 alkoxycarbonyl group, carbamoyl group, di (C1 to C2 alkyl) carbamoyl group, "chlorine atom, bromine atom, C1 to C2 alkyl group," same 1 to 3 Or a fluorine atom or a chlorine atom substituted with a C1 to C2 alkyl group ", a cyclopropyl group, a cyano group and a tri (C1 to C2 alkyl) silicon group A phenyl group in which one or two substituents may be substituted '', a furyl group, a thienyl group, "the same one or two C1 to C2 alkyl groups or C2 to C3 alkylcarbonyl groups, C2 to C3 alkoxycarbonyl groups, di (C1 to C2 alkyl) Amino group which may be substituted by carbamoyl group or C1 to C2 alkylsulfonyl group '', nitro group, hydroxyl group, C1 to C2 alkoxy group, C1 to C2 haloalkoxy group, phenoxy group, C1 to C2 alkylthio group, phenylthio group , A cyclopropyl group substituted with a C1 to C2 alkylsulfinyl group or a C1 to C2 alkylsulfonyl group.
[52] In the present invention, the "C4 to C10 bicycloalkyl group" is a C4-C10 bicyclic hydrocarbon, for example, bicyclobutyl, bicyclopentyl, bicyclohexyl, bicycloheptyl, bicyclooctyl, bicyclononyl Or a bicyclodecyl group, preferably a bicyclohexyl or bicycloheptyl group, more preferably a bicyclo [3.1.0] hexyl or bicyclo [4.1.0] heptyl group, more preferably Bicyclo [3.1.0] hexane-6-yl group.
[53] In the present invention, the "substituted phenylsulfonyl group (this substituent is a substituent selected from substituent group A)" means the "halogen atom", the "C1 to C6 alkyl group", and the "C1 to C6 haloalkyl group" , A phenylsulfonyl group wherein the same or different 1 to 5 substituents selected from the group consisting of the "C3 to C6 cycloalkyl group", the cyano group and the "tri (C1 to C6 alkyl) silicon group" can be substituted, For example, phenylsulfonyl, fluorophenylsulfonyl, difluorophenylsulfonyl, trifluorophenylsulfonyl, chlorophenylsulfonyl, dichlorophenylsulfonyl, trichlorophenylsulfonyl, fluorochlorophenylsulfonyl, Methylphenylsulfonyl, dimethylphenylsulfonyl, trimethylphenylsulfonyl, tetramethylphenylsulfonyl, pentamethylphenylsulfonyl, ethylphenylsulfonyl, fluoro (methyl) phenylsulfonyl, chloro (methyl) phenylsulfonyl, bro Parent (methyl) phenylsulfonyl, cyclopropylphenylsulfonyl, cyclopropyl (fluoro) phenylsulfonyl, chloro (cyclopropyl) phenylsulfonyl, cyclopropyl (methyl) phenylsulfonyl, (trifluoromethyl) phenylsul Phenyl or fluoro (trifluoromethyl) phenylsulfonyl group, preferably the same or different selected from the group consisting of fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group, "fluorine atom, chlorine atom and bromine atom The same or different 1 to 3 substituents selected from the group consisting of C1 to C3 alkyl groups substituted with 1 to 3 substituents, C3 to C4 cycloalkyl groups, cyano groups and tri (C1 to C3 alkyl) silicon groups may be substituted. It is a phenylsulfonyl group, More preferably, it is a phenylsulfonyl, chlorophenylsulfonyl, methylphenylsulfonyl, trifluorophenylsulfonyl, or cyanophenylsulfonyl group.
[54] In the present invention, the "di (C1 to C6 alkyl) sulfamoyl group" is a sulfamoyl group in which the same or different two "C1 to C6 alkyl groups" are bonded to a nitrogen atom, for example, dimethyl sulfamoyl and methyl ethyl sulfa. Moyl, diethylsulfamoyl, dipropylsulfamoyl, dibutylsulfamoyl or dihexylsulfamoyl, preferably a sulfamoyl group bound by two C1 to C3 alkyl groups, identical or different, more preferably dimethyl It is a sulfamoyl or diethyl sulfamoyl group, and also or preferably a dimethyl sulfamoyl group.
[55] In the present invention, the "substituted 3 to 6 membered heterocyclic group (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain 1 to 2 nitrogen atoms, Can be condensed with a benzene ring. This substituent is a substituent selected from the substituent group E. &quot; &quot; &quot; is selected from the group consisting of the &quot; halogen atom &quot;, the &quot; C1 to C6 alkyl group &quot; The same or different 1 to 3 substituents or hydroxyl groups, the "substituted phenylsulfonyl group (this substituent is a substituent selected from substituent group A)" or "di (C1 to C6 alkyl) sulfamoyl group" 3- to 6-membered complex which may be substituted by a benzene ring and which may be condensed with a benzene ring, which may contain 1 nitrogen atom, oxygen atom or sulfur atom and may also contain 1 to 2 nitrogen atoms Ventilation ", preferably a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group and a" C1 to C3 alkyl group substituted with the same or different one to three substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom " The same or different 1 to 2 substituents selected from the group consisting of, or hydroxyl groups, "fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group," the same or different 1 selected from the group consisting of fluorine atom, chlorine atom and bromine atom C1 to C3 alkyl group substituted with 3 to 3 substituents ", C3 to C4 cycloalkyl group, cyano group and tri (C1 to C3 alkyl) silicon group may be substituted with the same or different 1 to 3 substituents selected from the group consisting of Sulfonyl group "or" sulfamoyl group having the same or different two C1 to C3 alkyl groups bonded together " "A 3 to 6 membered heterocyclic group which contains one nitrogen atom, an oxygen atom or a sulfur atom and can also contain one nitrogen atom, which can be condensed with a benzene ring", more preferably chlorine Aziridine, in which the same 1 to 2 substituents selected from the group consisting of an atom, a bromine atom, a methyl group, an ethyl group and a trifluoromethyl group, or a hydroxyl group, a phenylsulfonyl group, a tolylsulfonyl group or a dimethylsulfamoyl group can be substituted, Oxiranyl, oxetanyl, pyrrolyl, furyl, thienyl, pyrazolyl, thiazolyl, pyridyl, benzimidazolyl or benzothiazolyl, more preferably the same consisting of a chlorine atom, a methyl group and a trifluoromethyl group Or a thienyl, pyrazolyl, thiazolyl group in which one or two different substituents may be substituted.
[56] In the present invention, "(C1-C6 alkoxy) C1-C6 alkoxy group" is a C1-C6 alkoxy group bonded to a C1-C6 alkoxy group, for example, methoxymethoxy, ethoxymethoxy, Propoxymethoxy, butoxymethoxy, s-butoxymethoxy, t-butoxymethoxy, pentyloxymethoxy, hexyloxymethoxy, methoxyethoxy, ethoxyethoxy, propoxyethoxy, butane It may be a methoxyethoxy, methoxypropoxy, methoxybutoxy, methoxypentyloxy or methoxyhexyloxy group, Preferably it is a C1-C3 alkoxy group substituted with the C1-C3 alkoxy group, More Preferably it is a methoxyethoxy, ethoxyethoxy or an ethoxymethoxy group.
[57] In the present invention, "the phenoxy group which may be substituted (this substituent is a pyridazinyloxy group substituted by a hydroxyl group or a halogen atom and a C1 to C6 alkoxy group)" means a phenoxy group wherein one hydroxyl group may be substituted, or It is a phenoxy group in which the pyridazinyloxy group substituted by the same or different 1-3 substituents selected from the group which consists of said "halogen atom" and said "C1-C6 alkoxy group", Preferably it is a hydroxyphenoxy group, Or a phenoxy group substituted with a pyridazinyloxy group substituted with one or two substituents selected from the group consisting of a fluorine atom, a chlorine atom, a bromine atom and a C1 to C3 alkoxy group, more preferably a chlorine atom, and A phenoxy group in which a pyridazinyloxy group in which a methoxy or ethoxy group is substituted one by one is substituted.
[58] In the present invention, the "substituted 5- to 6-membered heterocyclic oxy group (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain 1 to 2 nitrogen atoms) The substituent is a substituent selected from the substituent group E), said "halogen atom", said "C1 to C6 alkyl group", said "C1 to C6 haloalkyl group", hydroxyl group, said "substituted phenylsulfonyl group Substituent is a substituent selected from Substituent Group A) "and" di (C1 to C6 alkyl) sulfamoyl group "as the" complex atom which may be substituted by 1 to 2 substituents selected from the group consisting of , A 5 to 6 membered heterocyclic oxy group containing one nitrogen atom, an oxygen atom or a sulfur atom or containing 1 to 2 nitrogen atoms, and preferably a fluorine atom, a chlorine atom or bromine Atom, C1 to C3 alkyl group, "C1 to C3 alkyl group substituted with the same or different 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom", hydroxyl group, "fluorine atom, chlorine atom, bromine atom, C1 To C3 alkyl group, "C1 to C3 alkyl group substituted with the same or different 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom", C3 to C4 cycloalkyl group, cyano group and tri (C1 to C3 alkyl) A phenylsulfonyl group which may be substituted with the same or different 1 to 3 substituents selected from the group consisting of silicon groups '' and the same or selected from the group consisting of a sulfamoyl group having the same or different two C1 to C3 alkyl groups bonded thereto; "As a complex atom, one nitrogen atom, oxygen atom or sulfur atom may be substituted by And a 5-6 membered heterocyclic oxy group which may further contain one nitrogen atom, more preferably a chlorine atom, bromine atom, methyl group, ethyl group, trifluoromethyl group, hydroxyl group, phenylsulfonyl group, Pyridyloxy, pyrrolyloxy, furyloxy, thienyloxy, pyrazolyloxy, thiazolyloxy, pyri which may be substituted with one or two different substituents selected from the group consisting of a tolylsulfonyl group and a dimethylsulfamoyl group Midyloxy, pyrazinyloxy or pyridazinyloxy groups, more preferably pyridazinyloxy groups in which chlorine atoms and hydroxyl groups can be substituted.
[59] In the present invention, the "substituted phenylsulfonyloxy group (this substituent is a substituent selected from substituent group A)" means the "halogen atom", the "C1 to C6 alkyl group", and the "C1 to C6 haloalkyl group" Phenylsulfonyloxy group wherein the same or different 1 to 5 substituents selected from the group consisting of “C3 to C6 cycloalkyl group”, cyano group and “tri (C1 to C6 alkyl) silicon group” can be substituted. For example, phenylsulfonyloxy, fluorophenylsulfonyloxy, difluorophenylsulfonyloxy, trifluorophenylsulfonyloxy, chlorophenylsulfonyloxy, dichlorophenylsulfonyloxy, trichlorophenylsulfonyloxy , Fluorochlorophenylsulfonyloxy, methylphenylsulfonyloxy, dimethylphenylsulfonyloxy, trimethylphenylsulfonyloxy, tetramethylphenylsulfonyloxy, pentamethylphenylsulfonyloxy, ethylphen Sulfonyloxy, fluoro (methyl) phenylsulfonyloxy, chloro (methyl) phenylsulfonyloxy, bromo (methyl) phenylsulfonyloxy, cyclopropylphenylsulfonyloxy, cyclopropyl (fluoro) phenylsulfonyloxy , Chloro (cyclopropyl) phenylsulfonyloxy, cyclopropyl (methyl) phenylsulfonyloxy, (trifluoromethyl) phenylsulfonyloxy or fluoro (trifluoromethyl) phenylsulfonyloxy group, preferably Is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, "a C1 to C3 alkyl group substituted with the same or different one to three substituents selected from the group consisting of a fluorine atom, a chlorine atom and a bromine atom", and a C3 to C4 cycloalkyl group , Phenylsulfonyloxy, wherein the same or different 1-3 substituents selected from the group consisting of a cyano group and a tri (C1 to C3 alkyl) silicon group may be substituted, more preferably Phenylsulfonyloxy, chlorophenylsulfonyloxy, methylphenylsulfonyloxy, trifluorophenylsulfonyloxy or cyanophenylsulfonyloxy group.
[60] In the invention of the R ^3, R ^4, R ^5, R ⁶ and R ^7, "two (2) adjacent and 3 to 6 members which may, be substituted in to form together with the carbon atom to which they bind, respectively, cyclic hydrocarbon group ( This cyclic hydrocarbon may be interrupted by the same or different one or two complex atoms selected from the group consisting of nitrogen atoms, oxygen atoms and sulfur atoms, which substituents are halogen atoms, C1 to C6 alkyl groups, hydroxy C1 to C6 alkyl groups , C1 to C6 alkoxy group, oxo group, hydroxyimino group or C1 to C6 alkoxyimino group, and when C1 to C6 alkyl group is substituted, it is combined with different C1 to C6 alkyl group or cyclic carbon atom to form a new three-membered ring Can be added to the "halogen atom", the "C1 to C6 alkyl group", the "C1 to C6 alkyl group" substituted with 1 to 2 hydroxyl groups, the "C1 to C6 alkoxy group", an oxo group, Same or different selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, in which the same or different 1 to 4 substituents selected from the group consisting of a hydroxyimino group and the "C1 to C6 alkoxyimino group" can be substituted It is a saturated or unsaturated 3-6 membered cyclic hydrocarbon group, which may be interrupted by 1 to 2 heteroatoms, and may also form a cyclopropane ring cyclically, preferably -CH _2- , -CH ₂ CH ₂ -, -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -CH ₂ CH (CH ₃ ) CH _2- , -C (CH ₃ ) ₂ CH ₂ CH _2- , -CH ₂ C (CH ₃ ) ₂ CH _2- , -CH (OCH ₃ ) CH ₂ CH _2- , -C (OCH ₃ ) ₂ CH ₂ CH _2- , -CH ₂ C (OCH ₃ ) ₂ CH ₂ -,- C (= O) CH ₂ CH _2- , -CH ₂ C (= O) CH _2- , -C (= NOCH ₃ ) CH ₂ CH _2- , -CH ₂ CH ₂ CH ₂ CH _2- , -CH ( CH ₃ ) CH ₂ CH ₂ CH _2- , -C (CH ₃ ) ₂ CH ₂ CH ₂ CH _2- , -CH (OCH ₃ ) CH ₂ CH ₂ CH _2- , -CH = CH-CH = CH-, -OCH ₂ CH _2- , -OCH (CH ₃ ) CH _2- , -OCH ₂ CH (CH ₃ )-, -OC (CH ₃ ) ₂ CH ₂ -,- OCH = CH-, -OC (CH ₃ ) = CH-, -OCH = C (CH ₃ )-, -SCH = CH-, -N = CH-CH = CH-, -OCH ₂ O-, -OCH ( _{CH 3) O-, -OC (CH} 3) 2 O-, -OCF 2 O-, -OCH 2 CH 2 O-, -OCH = N-, -OC (CH 3) = N-,
[61]
[62] More preferably -CH ₂ CH _2- , -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -CH ₂ CH ₂ CH ₂ CH ₂ -,- CH = CH-CH = CH-, -OCH ₂ CH _2- , -OCH = CH-, -OCH = C (CH ₃ )-,-SCH = CH-, -N = CH-CH = CH-, -OCH ₂ O-, -OCH ₂ CH ₂ O-,
[63]
[64] More preferably -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -OCH ₂ CH _2- , -OCH = CH- or
[65]
[66] It is group represented by.
[67] Compound I of the present invention can be used as a salt used in conventional pesticides, for example, alkali metal salts, alkaline earth metal salts or ammonium salts, and when there are basic moieties in the molecule, for example, sulfates and hydrochlorides. And salts such as nitrates and phosphates. These salts are included in the present invention as long as they can be used as herbicides for agricultural horticulture.
[68] In the present invention, the "alkali metal salt" may be, for example, sodium salt, potassium salt or lithium salt, and preferably sodium salt or potassium salt.
[69] In the present invention, the "alkaline earth metal salt" may be, for example, a calcium salt or a magnesium salt, preferably a calcium salt.
[70] Solvates of the compounds of the present invention are also included in the present invention.
[71] Among the compounds of the present invention, there are also compounds having asymmetric carbon, in which case the present invention also includes mixtures of any ratio of one kind of optically active substance and several kinds of optically active substance.
[72] In the present invention, the "ester derivative" is a compound in which an acyl group is bonded to an oxygen atom of a hydroxyl group bonded to the 4-position of the pyridazine ring, and for example, a C2 to C15 alkylcarbonyl group which can be substituted (this substituent is a halogen atom, C1 to C6 alkoxy group, C2 to C7 alkoxycarbonyl group, C2 to C6 alkenyloxycarbonyl group which may be substituted (This substituent is C3 to C6 cycloalkyl group, cyano group and benzoyl group which may be substituted (This substituent is a halogen atom, C1 To C6 alkyl group, C1 to C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, same or different one to three substituents selected from the group consisting of C1 to C3 alkylsulfonyl group) 1 to 3 substituents, a C3 to C6 cycloalkenyloxycarbonyl group which may be substituted (this substituent is an oxo group and a substituent Benzoyl groups (wherein the substituents are the same or different from one to three selected from the group consisting of halogen atoms, C1 to C6 alkyl groups, C1 to C3 haloalkyl groups, C2 to C7 alkoxycarbonyl groups, nitro groups and C1 to C3 alkylsulfonyl groups) The same or different 1 to 2 substituents selected from the group consisting of substituents), and a 5- or 6-membered heterocyclic oxycarbonyl group which may be substituted (the heterocyclic ring contains one nitrogen atom, oxygen atom or sulfur atom in the ring). And may also contain 1 to 2 nitrogen atoms, which substituents are halogen atoms, C1 to C6 alkyl groups, phenoxy groups which may be substituted (the substituents are halogen atoms, C1 to C6 alkyl groups, C1 to C3 haloalkyl groups , Same or different 1 to 3 substituents selected from the group consisting of C3 to C6 cycloalkyl group and C2 to C7 alkoxycarbonyl group), 2,3-di A dro-1H-indenyloxy group and a benzoyl group which may be substituted (the group consisting of a halogen atom, a C1 to C6 alkyl group, a C1 to C3 haloalkyl group, a C2 to C7 alkoxycarbonyl group, a nitro group and a C1 to C3 alkylsulfonyl group The same or different 1 to 3 substituents selected from the group consisting of) or the same or different 1 to 3 substituents selected from the group), a phenyl group which may be substituted (the substituent is a halogen atom, C1 to C6 alkyl group, C1 to C3) The same or different 1-3 substituents selected from the group consisting of haloalkyl groups and C2 to C7 alkoxycarbonyl groups), the same or different 1-3 substituents selected from the group consisting of phenoxy groups and C1 to C6 alkylthio groups), C4 to C7 cycloalkylcarbonyl group, adamantylcarbonyl group, C3 to C7 alkenylcarbonyl group which may be substituted (this substituent is The same or different 1 to 2 substituents selected from the group consisting of a halogen atom and a phenyl group), a C3 to C7 alkynylcarbonyl group, a benzoyl group which may be substituted (the substituent being a halogen atom, a C1 to C6 alkyl group which may be substituted) These substituents are the same or different 1 to 3 substituents selected from the group consisting of a halogen atom and a phenyl group), a cyano group, a C2 to C7 alkylcarbonyl group, a C2 to C7 alkoxycarbonyl group, a C3 to C7 alkenyloxycarbonyl group which may be substituted (This substituent is a C3 to C6 cycloalkyl group, a cyano group and a benzoyl group which may be substituted. (This substituent is a halogen atom, C1 to C6 alkyl group, C1 to C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, nitro group and C1 to C3 alkyl. The same or different from 1 to 3 substituents selected from the group consisting of sulfonyl groups) Are the same or different from 1 to 3 substituents, C4 to C7 cycloalkenyloxycarbonyl group which may be substituted (this substituent is an oxo group and a benzoyl group which may be substituted (this substituent is a halogen atom, C1 to C6 alkyl group, C1 To C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, nitro group and C1 to C3 alkylsulfonyl group) or the same or different 1 to 2 substituents selected from the group consisting of Phenyl group, nitro group, C1 to C6 alkoxy group which may be substituted (this substituent is the same or different from 1 to 3 substituents selected from the group consisting of halogen atom and phenyl group), phenoxy group, 5 which may be substituted Or a six-membered heterocyclic oxycarbonyl group (this heterocycle contains one nitrogen atom, oxygen atom, or sulfur atom in the ring, and further includes 1-2) It may contain a nitrogen atom of, which substituent is a halogen atom, a C1 to C6 alkyl group, a phenoxy group which may be substituted (this substituent is a halogen atom, C1 to C6 alkyl group, C1 to C3 haloalkyl group, C3 to C6 cycloalkyl group and The same or different 1 to 3 substituents selected from the group consisting of C2 to C7 alkoxycarbonyl groups, 2,3-dihydro-1H-indenyloxy group and benzoyl group which may be substituted (the substituents are halogen atoms, C1 to The same or different 1 selected from the group consisting of C6 alkyl group, C1 to C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, nitro group and C1 to C3 alkylsulfonyl group) To 3 substituents) and a 5- or 6-membered heterocyclic oxysulfonyl group which may be substituted (this heterocycle has 1 nitrogen atom, oxygen atom or sulfur in the ring Atoms, and may also contain 1 to 2 nitrogen atoms, which substituents are halogen atoms, C1 to C6 alkyl groups, phenoxy groups which may be substituted (the substituents are halogen atoms, C1 to C6 alkyl groups, C1 to C3 The same or different 1 to 3 substituents selected from the group consisting of a haloalkyl group, a C3 to C6 cycloalkyl group and a C2 to C7 alkoxycarbonyl group), 2,3-dihydro-1H-indenyloxy group and a benzoyl group which may be substituted (This substituent is the same or different 1 to 3 substituents selected from the group consisting of halogen atom, C1 to C6 alkyl group, C1 to C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, nitro group and C1 to C3 alkylsulfonyl group) The same or different 1 to 3 substituents selected from the group consisting of the same or different 1 to 3 substituents selected from the group consisting of Protoyl group, a 3-6 membered heterocyclic carbonyl group which may be substituted (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain 1 to 2 nitrogen atoms, and heterocycle It may also form a 5-6 membered spiro ring containing 1 to 2 oxygen atoms on any carbon atom in the substituent, which substituent is a halogen atom, a C1 to C6 alkyl group which may be substituted (this substituent is a halogen atom and a phenyl group). The same or different 1 to 3 substituents selected from the group consisting of), a C2 to C7 alkylcarbonyl group, a C2 to C7 alkoxycarbonyl group, a phenyl group which may be substituted (the substituent is the same or different from 1 to 3 halogen atoms), nitro Group, hydroxyl group, C1 to C6 alkoxy group, phenoxy group, C1 to C6 alkylthio group, C2 to C6 alkenylthio group and phenylthio group The same or different 1 to 3 substituents, a 7 to 14 membered condensed 2 or tricyclic heterocyclic carbonyl group which can be substituted (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and May contain 1 to 2 nitrogen atoms or oxygen atoms, which substituents are the same or different 1 to 3 substituents selected from the group consisting of halogen atoms and C1 to C6 alkyl groups), 5 or 6 membered heterocyclic carbonyl A carbonyl group (this heterocycle contains one nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain one to two nitrogen atoms), a C2 to C7 alkoxycarbonyl group which may be substituted (this substituent is a halogen The same or different 1 to 3 substituents selected from the group consisting of atoms, C1 to C6 alkoxy groups and phenyl groups), C3 to C7 alkenyloxycarbonyl groups, Phenoxycarbonyl groups which may be substituted (the substituent being the same or different 1 selected from the group consisting of halogen atoms, C1 to C6 alkyl groups, cyano groups, C2 to C7 alkylcarbonyl groups, C2 to C7 alkoxycarbonyl groups, nitro groups and C1 to C6 alkoxy groups) To 3 substituents), a condensed polycyclic hydrocarbon oxycarbonyl group, a 5- or 6-membered heterocyclic oxycarbonyl group which may be substituted (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and also 1 to It may contain two nitrogen atoms, which substituent is a halogen atom, a C1 to C6 alkyl group, a phenoxy group which may be substituted (this substituent is a halogen atom, a C1 to C6 alkyl group, a C1 to C3 haloalkyl group, a C3 to C6 cycloalkyl group And the same or different 1 to 3 substituents selected from the group consisting of C2 to C7 alkoxycarbonyl groups), 2,3-dihydro-1H- Denyloxy group and benzoyl group which may be substituted (the substituent being the same selected from the group consisting of halogen atom, C1 to C6 alkyl group, C1 to C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, nitro group and C1 to C3 alkylsulfonyl group) Or the same or different 1 to 3 substituents selected from the group consisting of different 1 to 3 substituents), a carbamoyl group which may be substituted (this substituent is a C1 to C6 alkyl group which may be substituted (the substituent is a halogen) The same or different 1 to 3 substituents selected from the group consisting of atoms, C2 to C7 alkoxycarbonyl groups, cyano groups, phenyl groups and C1 to C6 alkoxy groups), C3 to C6 alkenyl groups, phenyl groups, C2 to C7 alkylcarbonyl groups, C2 to The same or different 1 to 3 substituents selected from the group consisting of C7 alkoxycarbonyl group and C1 to C6 alkoxy group, (C1 to C6 alkylthio) carbonyl group, (phenylthio) carbonyl group, C1 to C8 alkylsulfonyl group which may be substituted (the substituent being the same or different from 1 to 3 halogen atoms), phenylsulfonyl group which may be substituted (this The substituent is a halogen atom, C1 to C6 alkyl group, cyano group, C2 to C7 alkylcarbonyl group, C2 to C7 alkoxycarbonyl group, nitro group, C1 to C6 alkoxy group, C2 to C6 alkenyloxysulfonyl group which may be substituted (this substituent is C3 to C6 cycloalkyl group, cyano group and benzoyl group which may be substituted (the substituent consists of a halogen atom, C1 to C6 alkyl group, C1 to C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, nitro group and C1 to C3 alkylsulfonyl group The same or different 1 to 3 substituents selected from the group), or the same or different 1 to 3 substituents selected from the group), C3 to C6 cycloalkenyloxysulfonyl group (this substituent is an oxo group and a benzoyl group which may be substituted (this substituent is a halogen atom, C1 to C6 alkyl group, C1 to C3 haloalkyl group, C2 to C7 alkoxycarbonyl group, nitro group and C1) To the same or different 1 to 2 substituents selected from the group consisting of to C3 alkylsulfonyl group) and 5 or 6-membered heterocyclic oxysul which may be substituted) Ponyl groups (this heterocycle contains one nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain one to two nitrogen atoms, which substituents may be halogen atoms, C1 to C6 alkyl groups, to be substituted Phenoxy groups (this substituent consists of a halogen atom, a C1 to C6 alkyl group, a C1 to C3 haloalkyl group, a C3 to C6 cycloalkyl group and a C2 to C7 alkoxycarbonyl group Are the same or different 1 to 3 substituents selected from the group), 2,3-dihydro-1H-indenyloxy group and benzoyl group which may be substituted (the substituents are halogen atom, C1 to C6 alkyl group, C1 to C3) The same or different 1 to 3 substituents selected from the group consisting of a haloalkyl group, a C2 to C7 alkoxycarbonyl group, a nitro group and a C1 to C3 alkylsulfonyl group) The same or different 1 to 3 substituents selected from the group consisting of: a 5 or 6 membered heterocyclic oxysulfonyl group which may be substituted (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring) And may also contain 1 to 2 nitrogen atoms, which substituent is a halogen atom, a C1 to C6 alkyl group, a phenoxy group which may be substituted (this substituent is a halogen atom, C1 To C6 alkyl group, C1 to C3 haloalkyl group, C3 to C6 cycloalkyl group and the same or different 1 to 3 substituents selected from the group consisting of C2 to C7 alkoxycarbonyl group), 2,3-dihydro-1H-indenyloxy group And a benzoyl group which may be substituted (the substituent being the same or different 1 selected from the group consisting of halogen atoms, C1 to C6 alkyl groups, C1 to C3 haloalkyl groups, C2 to C7 alkoxycarbonyl groups, nitro groups and C1 to C3 alkylsulfonyl groups) To 3 substituents), the same or different 1 to 3 substituents selected from the group consisting of: di (C1 to C6 alkyl) sulfamoyl group, C1 to C6 alkoxysulfonyl group, di (C1 to C6 alkyl) phospho It may be a compound having a aryl group, a tri (C1 to C6 alkyl) silicon group or a triphenylsilicon group, preferably a C2 to C10 alkylcarbonyl group, a benzoyl group which may be substituted ( The group consists of a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 alkoxy group or a 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yloxycarbonyl group Same or different 1 to 2 substituents selected from the group), pyrrolidinylcarbonyl group, azetidinylcarbonyl group, C2 to C5 alkoxycarbonyl group which may be substituted (the substituent is selected from the group consisting of fluorine atom, chlorine atom and bromine atom) The same or different from 1 to 3 substituents), di (C1 to C3 alkyl) carbamoyl group, (C1 to C3 alkyl) (C1 to C3 alkoxy) carbamoyl group, C1 to C3 alkylsulfonyl group ( This substituent is the same or different from 1 to 3 substituents selected from the group consisting of a fluorine atom, a chlorine atom and a bromine atom) or a phenylsulfonyl group which may be substituted (this substituent is a fluorine atom, a chlorine atom) , Bromine atom, C1 to C3 alkyl group, 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yloxysulfonyl group and the same or different 1 to 1 selected from the group consisting of Two substituents), more preferably a C2 to C4 alkylcarbonyl group, a benzoyl group which may be substituted (this substituent is a methyl group or 4- (2,4-dichlorobenzoyl) -1,3-dimethyl- 1H-pyrazol-5-yloxycarbonyl group), 1-azetidinylcarbonyl group, 4-morpholinylcarbonyl group, optionally substituted C2 to C3 alkoxycarbonyl group (this substituent is 1 to 3 chlorine atoms), dimethyl Carbamoyl groups, methoxy (methyl) carbamoyl groups, optionally substituted C1 to C3 alkylsulfonyl groups (where these substituents are 1 to 3 fluorine atoms) or optionally substituted phenylsulfonyl groups (which substituents are chlorine atoms, Methyl group, 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yljade Is a sulfonyl group or a nitro group).
[73] (a) In the present invention, R ¹ is preferably a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (this halogen atom is 1 to 3 fluorine atoms), Cyclopropyl group, C2 to C3 alkenyl group, cyano group, C2 to C4 alkylcarbonyl group, di (C1 to C3 alkyl) carbamoyl group, phenyl group which may be substituted (this substituent is a fluorine atom, a chlorine atom, a bromine atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is the same or different 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group, cyano group and tri (C1 to C3 alkyl ) Same or different 1 to 2 substituents selected from the group consisting of silicon groups), furyl groups, thienyl groups, C1 to C3 alkoxy groups, phenoxy groups which may be substituted (the substituents are fluorine atoms, chlorine Atom, bromine atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (this halogen atom is 1 to 3 fluorine atoms), cyclopropyl group, cyano group and tri (C1 to C3 alkyl) silicon group The same or different 1 to 2 substituents or substituted pyrazolyloxy groups (which are 1 benzoyl group and 2 C1 to C3 alkyl groups substituted by 2 chlorine atoms), more preferably chlorine atoms , A bromine atom, a trifluoromethyl group or a cyano group, more preferably a chlorine atom or a bromine atom, and particularly preferably a chlorine atom.
[74] (b) In the present invention, R ² is preferably hydrogen atom, fluorine atom, chlorine atom, bromine atom, iodine atom, C1 to C3 alkyl group, (C1 to C3 alkoxy) C1 to C3 alkyl group, benzo which may be substituted (This substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (this halogen atom is the same or different one to three halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom. Zim), the same or different 1 to 2 substituents selected from the group consisting of a cyclopropyl group, a cyano group and a tri (C1 to C3 alkyl) silicon group), a C2 to C4 alkoxycarbonyl group, a phenoxy group which may be substituted (this substituent) Is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (in the group consisting of a fluorine atom, a chlorine atom and a bromine atom The same or different 1 to 3 halogen atoms selected), the same or different 1 to 2 substituents selected from the group consisting of a cyclopropyl group, a cyano group and a tri (C1 to C3 alkyl) silicon group), a phenyl which may be substituted Thio (this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (the halogen atom is the same or different from one to three halogens selected from the group consisting of fluorine atom, chlorine atom and bromine atom) Atom), a cyclopropyl group, a cyano group, and the same or different 1 to 2 substituents selected from the group consisting of a tri (C1 to C3 alkyl) silicon group) or a tri (C1 to C3 alkyl) silicon group, more preferably Is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethoxycarbonyl group or a trimethylsilyl group, more preferably To a hydrogen atom.
[75] (c) In the present invention, R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are preferably independently of each other a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, and C1 to substitutable. C4 alkyl group (this substituent is the same or different 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom, or C3 to C4 cycloalkyl group, C1 to C3 alkylthio group or C1 to C3 alkoxyimino group) , C2 to C3 alkenyl group, C2 to C3 alkynyl group, C3 to C5 cycloalkyl group which may be substituted (the substituent is a fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group, C3 to C4 cycloalkyl group, cyano group, C1 To C3 alkoxy group and C1 to C3 alkylthio group, the same or different 1 to 3 substituents selected from the group consisting of: C6 to C7 bicycloalkyl group, cyano group, C2 to C4 alkylcarbonyl group, C2 to C4 An alkoxycarbonyl group, a phenyl group which may be substituted (this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group or a C1 to C3 haloalkyl group (the halogen atom is the same or selected from the group consisting of fluorine atom, chlorine atom and bromine atom Different 1 to 3 halogen atoms), which may be substituted with a 5 to 6 membered heterocyclic group, which contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and also 1 to 2 nitrogen atoms Which may contain a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group and a C1 to C3 haloalkyl group (the halogen atom being the same or different from 1 to 3 selected from the group consisting of fluorine atom, chlorine atom and bromine atom) The same or different 1 to 2 substituents selected from the group consisting of halogen atoms), nitro groups, C1 to C3 alkoxy Groups, C1 to C3 haloalkoxy groups (the halogen atoms are the same or different from 1 to 3 halogen atoms selected from the group consisting of fluorine atoms, chlorine atoms and bromine atoms), phenoxy groups which may be substituted (this substituent is a fluorine atom, Chlorine atom, bromine atom and pyridazinyloxy group substituted by C1 to C3 alkoxy group) or C1 to C3 alkylthio group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are two adjacent And -CH ₂ CH _2- , -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -CH ₂ CH ₂ CH ₂ CH _2- , -CH = CH-CH = CH-, -OCH ₂ CH _2- , -OCH = CH-, -OCH = C (CH ₃ )-, -SCH = CH-, -N = CH-CH = CH-, -OCH ₂ O -, -OCH ₂ CH ₂ O-,
[76]
[77] Is a group represented by
[78] More preferably independently of each other a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C4 alkyl group which may be substituted (this substituent is 1 to 3 fluorine atoms or 1 cyclopropyl group), to be substituted A C3 to C4 cycloalkyl group (this substituent is the same 1 to 2 substituents selected from the group consisting of fluorine atom, chlorine atom, bromine atom, C1 to C2 alkyl group, cyclopropyl group and C1 to C2 alkoxy group), cyano group , A C2 to C3 alkoxycarbonyl group, a nitro group, a C1 to C3 alkoxy group or a trifluoromethoxy group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each adjacent two carbon atoms to which they are bonded; Together -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -OCH ₂ CH _2- , -OCH = CH- or
[79]
[80] In which R ³ is not a hydrogen atom,
[81] More preferably, independently of each other, a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C3 alkyl group, a C3 to C4 cycloalkyl group which may be substituted (this substituent consists of a chlorine atom and a C1 to C2 alkyl group) The same 1 to 2 substituents selected from the group), a cyano group or a C1 to C2 alkoxy group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are two adjacent to each other, Together are —CH ₂ CH ₂ CH ₂ — or —OCH═CH—, provided that R ³ is not a hydrogen atom,
[82] Especially preferably, independently of one another, a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethyl group, an isopropyl group, a cyclopropyl group which may be substituted (this substituent is two chlorine atoms) or methoxide group, or is R ^3, R ^4, R ^5, R ⁶ and R ⁷ are -CH ₂ CH ₂ CH ₂ with a two (2) adjacent to, and burnt-party wishes to join, respectively - are shown in the odd, provided R ³ is Not a hydrogen atom,
[83] Most preferably, R ³ is a fluorine atom, chlorine atom, bromine atom, iodine atom, methyl group, ethyl group, isopropyl group, cyclopropyl group or methoxy group, and R ⁷ is hydrogen atom, fluorine atom, chlorine atom, bromine atom , An iodine atom, a methyl group, an ethyl group, an isopropyl group, a cyclopropyl group or a methoxy group, and R ⁴ , R ⁵ and R ⁶ are each independently a hydrogen atom or a methyl group.
[84] (d) In the present invention, m and n are preferably all zero.
[85] Compound 1 of the present invention preferably
[86] (1a) R ¹ is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (this halogen atom is 1 to 3 fluorine atoms), a cyclopropyl group, C2 to C3 alke Nyl group, cyano group, C2 to C4 alkylcarbonyl group, di (C1 to C3 alkyl) carbamoyl group, phenyl group which may be substituted (this substituent is a fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (The halogen atom is the same or different 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group, cyano group and tri (C1 to C3 alkyl) silicon group selected from the group Same or different 1 to 2 substituents), furyl group, thienyl group, C1 to C3 alkoxy group, phenoxy group which may be substituted (this substituent is fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl) , A C1 to C3 haloalkyl group (this halogen atom is 1 to 3 fluorine atoms), a cyclopropyl group, a cyano group and a tri (C1 to C3 alkyl) silicon group, the same or different 1 to 2 substituents selected from the group ) Or a substituted pyrazolyloxy group (this substituent is one benzoyl group and two C1 to C3 alkyl groups substituted by two chlorine atoms),
[87] (1b) R ² is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C3 alkyl group, a (C1 to C3 alkoxy) C1 to C3 alkyl group, a benzoyl group which may be substituted (this substituent is a fluorine atom, Chlorine atom, bromine atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is the same or different 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group, cyan The same or different 1 to 2 substituents selected from the group consisting of no groups and tri (C 1 to C 3 alkyl) silicon groups, C 2 to C 4 alkoxycarbonyl groups, phenoxy groups which may be substituted (the substituents being fluorine atoms, chlorine atoms, bromine Atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is the same or different from 1 to 3 selected from the group consisting of fluorine atom, chlorine atom and bromine atom) Halogen atoms), a cyclopropyl group, a cyano group, and the same or different 1 to 2 substituents selected from the group consisting of tri (C1 to C3 alkyl) silicon groups), a phenylthio group which may be substituted (this substituent is fluorine Atom, chlorine atom, bromine atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is the same or different 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group , The same or different 1 to 2 substituents selected from the group consisting of a cyano group and a tri (C1 to C3 alkyl) silicon group) or a tri (C1 to C3 alkyl) silicon group,
[88] (1c) R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C4 alkyl group which may be substituted (the substituent is a fluorine atom , Same or different 1 to 3 substituents selected from the group consisting of a chlorine atom and a bromine atom, or a C3 to C4 cycloalkyl group, a C1 to C3 alkylthio group or a C1 to C3 alkoxyimino group), C2 to C3 alkenyl group, C2 To C3 alkynyl group, a C3 to C5 cycloalkyl group which may be substituted (the substituent is a fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group, C3 to C4 cycloalkyl group, cyano group, C1 to C3 alkoxy group and C1 to C3 The same or different 1 to 3 substituents selected from the group consisting of alkylthio groups), C6 to C7 bicycloalkyl group, cyano group, C2 to C4 alkylcarbonyl group, C2 to C4 alkoxycarbonyl group, can be substituted Is a phenyl group (this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group or a C1 to C3 haloalkyl group (this halogen atom is the same or different from one to three halogens selected from the group consisting of fluorine atoms, chlorine atoms and bromine atoms) 5-6 membered heterocyclic group which may be substituted (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain 1 to 2 nitrogen atoms, This substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group and a C1 to C3 haloalkyl group (the halogen atom is the same or different 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom) The same or different 1 to 2 substituents selected from the group consisting of), nitro group, C1 to C3 alkoxy group, C1 to C3 haloalkoxy group (this Halogen atoms are the same or different from 1 to 3 halogen atoms selected from the group consisting of fluorine atoms, chlorine atoms and bromine atoms, phenoxy groups which may be substituted (the substituents being fluorine atoms, chlorine atoms, bromine atoms and C1 to C3 alkoxy) Is a pyridazinyloxy group substituted by a group) or a C1 to C3 alkylthio group, or two adjacent R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each -CH together with the carbon atom to which they are bonded. ₂ CH _2- , -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -CH ₂ CH ₂ CH ₂ CH _2- , -CH = CH-CH = CH-, -OCH ₂ CH _2- , -OCH = CH-, -OCH = C (CH ₃ )-, -SCH = CH-, -N = CH-CH = CH-, -OCH ₂ O-, -OCH ₂ CH ₂ O-,
[89]
[90] Is a group represented by
[91] (1d) m and n are both compounds of 0,
[92] More preferably,
[93] (2a) R ¹ is a chlorine atom, bromine atom, trifluoromethyl group or cyano group,
[94] (2b) R ² is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethoxycarbonyl group or a trimethylsilyl group,
[95] (2c) R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C4 alkyl group which may be substituted (the substituent is 1 to Three fluorine atoms, or one cyclopropyl group, a C3 to C4 cycloalkyl group which may be substituted (the substituent consists of a fluorine atom, a chlorine atom, a bromine atom, a C1 to C2 alkyl group, a cyclopropyl group and a C1 to C2 alkoxy group) The same 1 to 2 substituents selected from the group), a cyano group, a C2 to C3 alkoxycarbonyl group, a nitro group, a C1 to C3 alkoxy group or a trifluoromethoxy group, or R ³ , R ⁴ , R ⁵ , R ⁶ And two of R ⁷ adjacent to each other, together with a carbon atom to which each is bonded, -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -OCH ₂ CH _2- , -OCH = CH- or
[96]
[97] In which R ³ is not a hydrogen atom,
[98] (2d) m and n are together 0;
[99] More preferably,
[100] (3a) R ¹ is a chlorine atom or a bromine atom,
[101] (3b) R ² is a hydrogen atom,
[102] (3c) R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C3 alkyl group, a C3 to C4 cycloalkyl group which may be substituted (This substituent is the same 1 to 2 substituents selected from the group consisting of a chlorine atom and a C1 to C2 alkyl group), a cyano group or a C1 to C2 alkoxy group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ^7, the adjacent two are each, -CH ₂ CH with the carbon atoms to which each is bonded to ₂ CH ₂ - or being the odd represented by -OCH = CH-, only R ³ is not a hydrogen atom,
[103] (3d) m and n are both compounds of 0,
[104] Particularly preferably,
[105] (4a) R ¹ is a chlorine atom,
[106] (4b) R ² is a hydrogen atom,
[107] (4c) R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethyl group, an isopropyl group, a cyclopropyl which may be substituted The group (this substituent is two chlorine atoms) or a methoxy group, or two adjacent groups of R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ , together with the carbon atom to which each is bonded -CH ₂ CH ₂ CH _{Is a group} represented by ₂ -provided that R ³ is not a hydrogen atom,
[108] (4d) m and n are both 0.
[109] Representative compounds of the invention are shown in Table 1 below, but the invention is not limited to these compounds.
[110] In the following, R ³ to R ⁷ "H" is ^{R 3, R 4, R 5} , R 6 and R ⁷ that are both hydrogen atoms, R ³ to "2-Cl" in R ⁷ is a R ³ "Me" is methyl group, "Et" is ethyl group, "Pr" is propyl group, "iPr" is isopropyl group, "cPr" is cyclopropyl group, "Bu" is butyl group, iBu "isobutyl group," sBu "is s-butyl group," tBu "is tert-butyl group," cBu "is cyclobutyl group," Pen "is pentyl group," cPen "is cyclopentyl group," neoPen ""is a neopentyl group," Hx "is a cyclohexyl group a," cHx "is a cyclohexyl group, in R ³ to R ⁷ _{'2-CH 2 CH 2 CH 2} -3 ' is a R ³ and R ⁴ tree a methylene group and the a, "= N-OMe" are methoxy imino group to which they form a 5-membered ring together with the carbon atom to which they bond, "= O" is a carbonyl group with the carbon atoms to which they are attached, "SO ₂ ( Ph-4-Me) ”is p-tol Sulfonyl group, "cPr-1-F" is a group 1-fluoro-cyclopropyl, _{"cPr-cis-2- (CH 2} ) 3 -cis-3 " of the formula
[111]
[112] The group represented by "C (-CH ₂ CH ₂ -)-CH ₂ CH ₂ " is a chemical formula
[113]
[114] The group represented by "CH (CH ₂ ) CH-CH ₂ " is a chemical formula
[115]
[116] The group represented by "CH (OCH ₂ ) ₂ " is a chemical formula
[117]
[118] Where "Fur" is a furyl group, "Thi" is a thienyl group, "Pyr" is a pyridyl group, "Azr" is an aziridinyl group, "Pyrd" is a pyrrolidinyl group, and "Pyrr" Pyrrolyl group, "Pyza" is pyrazolyl group, "Thiz" is thiazolyl group, "Pyzn" is pyridazinyl group, "Np" is naphthyl group, "1-Ad" is 1-adamantyl group, "Ioxa" is isoxazolyl group, "Tdia" is 1,2,3-thiadiazolyl group, "Bfur" is 1-benzofuranyl group, "Bthi" is 1-benzothienyl group, "Bthia" is 1,3-benzothiazolyl group, "Boxaz" is 1,3-benzodioxylyl group, "Iqu" isoquinolyl group, "Azet" is azetidinyl group, "Ppri" is pipelinyl group, " 1-Ppri-4-OCH ₂ CH ₂ O-4 ″ is a chemical formula
[119]
[120] A group represented by "Ppra" is a piperazyl group, "Morp" is a morpholinyl group, "Tmor" is a thiomorpholinyl group, "Carb" is a carbazolyl group, "Pthia" is a phenothiazinyl group, Thpy "is tetrahydro -2H- pyranyl group," Q ¹ "is oxiranyl group," Q ² "are benzo-oxazolyl group," Q ³ "is a group benzothiazolyl," Q ⁴ "is a fluorenyl group , "Q ⁵ " is 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl group, "Q ⁶ " is 6-chloro-3- (2-methylphenoxy ) -4-pyridazinyl group, "Q ⁷ 'is 6-chloro-3- (2-isopropylphenoxy) -4-pyridazinyl group," Q ⁸ "is 6-chloro-3- (2- cyclopropylphenoxy) -4-pyridazinyl group, "Q ^9" is 6-chloro-3- (2,3-dihydro -1H- inden-4-yloxy) -4-pyridazinyl group, " Q ¹⁰ 'is a 6-chloro-3- (2,6-dimethylphenoxy) -4-pyridazinyl group, and "Q ¹¹ " is a 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyrida Carbonyl group, "Q ^12" is 4- [2-chloro-3- (methoxycarbonyl) -4- (methylsulfonyl) benzoyl] -1-ethyl -1H- pyrazol-5-diary, "Q ¹³ 'is a 4- (2,4-dichloro-3-methylbenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl group, and "Q ¹⁴ " is 2- [2-chloro-4- (methyl Sulfonyl) benzoyl] -3-oxo-1-cyclohexen-1-yl group, "Q ¹⁵ " is 2- [4- (methylsulfonyl) -2-nitrobenzoyl] -3-oxo-1-cyclohexene -1-yl group, "Q ¹⁶ " is 2-cyano-1-cyclopropyl-3- [2- (methylsulfonyl) -4- (trifluoromethyl) phenyl] -3-oxo-1-prop A phenyl group, "Q ¹⁷ " means a 3- [4-chloro-2- (methylsulfonyl) phenyl] -2-cyano-1-cyclopropyl-3-oxo-1-propenyl group, and "Q ¹⁸ " 3,4-dihydro-2 (1H) -isoquinolyl groups are shown, respectively.
[121]
[122]
[123]
[124]
[125]
[126]
[127]
[128]
[129]
[130]
[131]
[132]
[133]
[134]
[135]
[136]
[137]
[138]
[139]
[140]
[141]
[142]
[143]
[144]
[145]
[146]
[147]
[148]
[149]
[150]
[151]
[152]
[153]
[154]
[155]
[156]
[157]
[158]
[159]
[160]
[161]
[162] _
[163]
[164]
[165]
[166]
[167]
[168]
[169]
[170]
[171]
[172]
[173]
[174]
[175]
[176]
[177]
[178]
[179]
[180]
[181]
[182]
[183]
[184]
[185]
[186]
[187]
[188]
[189]
[190]
[191]
[192]
[193]
[194]
[195]
[196]
[197]
[198]
[199]
[200]
[201]
[202]
[203]
[204]
[205]
[206]
[207]
[208]
[209]
[210]
[211]
[212]
[213]
[214]
[215]
[216]
[217]
[218]
[219]
[220]
[221]
[222]
[223]
[224]
[225]
[226]
[227]
[228]
[229]
[230]
[231]
[232]
[233]
[234]
[235]
[236]
[237]
[238]
[239]
[240]
[241]
[242]
[243]
[244]
[245]
[246]
[247]
[248]
[249]
[250]
[251]
[252]
[253]
[254]
[255] Among the above exemplary compounds, preferred compounds are compound numbers 124, 125, 126, 127, 128, 130, 131, 132, 134, 136, 139, 140, 144, 145, 151, 163, 173, 202, 207, 217 , 226, 249, 264, 265, 266, 267, 269, 270, 271, 272, 273, 279, 280, 284, 287, 292, 300, 304, 305, 306, 307, 308, 309, 311, 330 , 334, 336, 339, 344, 359, 361, 362, 364, 365, 370, 377, 385, 386, 387, 390, 391, 400, 401, 403, 410, 412, 413, 417, 422, 426 , 437, 438, 441, 443, 446, 450, 456, 459, 472, 478, 498, 505, 506, 507, 514, 515, 516, 521, 527, 528, 529, 531, 532, 534, 535 , 539, 541, 544, 547, 557, 562, 566, 571, 614, 618, 621, 623, 629, 640, 642, 658, 659, 662, 663, 664, 667, 700, 701, 702, 704 , 707, 708, 710,711, 712, 716, 717, 719, 728, 732, 733, 734, 735, 736, 737, 738, 740, 756, 758, 759, 760, 761, 762, 775, 778, 780 , 781, 782, 801, 802, 803, 804, 805, 806, 827, 834, 844, 845, 846, 850, 890, 894, 896, 911, 914, 931, 964, 965, 979, 982, 987 , 998, 1000, 1007, 1009, 1013, 1016, 1020, 1023, 1027, 1040, 1050, 1052, 1053, 1055, 1058, 1060, 1061, 1063, 1064, 1066, 1069, 1073, 1083, 1086, 1088, 1089, 1091, 1096, 1099, 1100, 1102, 1109, 1115, 1118, 1119, 1120, 1122, 1123, 1124, 1125, 1126, 1128, 1129, 1133, 1140, 1151, 1160, 1172, 1178, 1184, 1207, 1251, 1260, 1266, 1286, 1298, 1334, 1340, 1358, 1364, 1382, 1387, 1391, 1417, 1441, 1446, 1448, 1456, 1459, 1461, 1481, 1509, 1522, 1531, 1537, 1543, 1549, 1553, 1554, 1566, 1575, 1593, 1599, 1603, 1616, 1620, 1625, 1631, 1643, 1649, 1658, 1706, 1710, 1757, 1770, 1789, 1811, 1840, 1877, 1879, 1891, 1898, 1911, 1920, 1924, 1937, 1946, 1952, 1958, 1981, 1985, 2010, 2034, 2038, 2040, 2042, 2051, 2060, 2066, 2072, 2081, 2106, 2136, 2147, 2151, 2176, 2198, 2199, 2200, 2212, 2220, 2221, 2222, 2224, 2225, 2263, 2265, 2287, 2289, 2300, 2309, 2315, 2321, 2327, 2333, 2411, 2431, 2453, 2519, 2529, 2540, 2542, 2547, 2548, 2551, 2555, 2556, 2565, 2568, 2570, 2571, 2572, 2574, 2576, 2577, 2585, 2587, 2589, 2592, 2596, 2597, 2599, 2600, 2601, 2603, 2605, 2606, 2607, 2608 , 2609, 2614, 2662, 2671, 2677, 2697, 2703, 2709, 2715, 2721, 2727, 2733, 2739, 2746, 2752, 2758, 2764, 2770, 2776, 2782, 2788, 2805, 2814, 2820, 2826 , 2827, 2838, 2850, 2856, 2862, 2868, 2874, 2880, 2900, 2906, 2918, 2924, 2930, 2961,2970, 2976, 2982, 2988, 2994, 3001, 3016, 3022, 3028, 3034, 3040 , 3046, 3052, 3058, 3064, 3070, 3076, 3082, 3088, 3094, 3100, 3106, 3112, 3129, 3138, 3144, 3150, 3156, 3162, 3168, 3185, 3194, 3200, 3217, 3226, 3243 , 3252, 3258, 3264, 3270, 3276, 3282, 3288, 3294, 3300, 3306, 3312, 3318, 3324, 3330, 3336, 3342, 3348, 3354, 3360, 3366, 3372, 3378, 3384, 3390, 3396 , 3402, 3408, 3414, 3420, 3426, 3432, 3438, 3444, 3450, 3456, 3462, 3468, 3474, 3480, 3486, 3492, 3498, 3504, 3510, 3516, 3522, 3528, 3534, 3540, 3546 , 3552, 3558, 3564, 3570, 3576, 3582, 3588, 3594, 3600, 3606, 3612, 3618, 3624, 3630, 3636, 3642, 3648, 3654, 3660, 3666, 3672, 3678, 3684, 3690, 3696 , Shoes of 3702, 3708, 3714, 3720, 3755, 3780, 3786, 3792, 3798, 3805, 3811, 3837, 3843 or 3849 Compound,
[256] More preferably, compound numbers 124, 125, 126, 127, 128, 130, 132, 136, 139, 140, 144, 145, 151, 163, 173, 202, 217, 249, 264, 265, 266, 267 , 269, 270, 271, 284, 287, 300, 304, 308, 309, 311, 334, 336, 339, 361, 362, 377, 385, 386, 387, 390, 391, 401, 437, 438, 459 , 472, 505, 506, 507, 515, 516, 521, 528, 529, 531, 532, 534, 539, 541, 544, 547, 571, 621, 658, 659, 662, 663, 664, 667, 700 , 701, 702, 704, 707, 708, 711, 712, 717, 719, 732, 733, 734, 735, 736, 737, 738, 740, 756, 758, 759, 760, 762, 775, 778, 780 , 781, 782, 801, 802, 803, 806, 827, 834, 845, 846, 850, 896, 914, 931, 964, 965, 998, 1013, 1016, 1023, 1040, 1050, 1052, 1053, 1055 , 1058, 1060, 1061, 1063, 1064, 1066, 1069, 1073, 1086, 1088, 1089, 1091, 1096, 1099, 1100, 1102, 1109,1115, 1118, 1119, 1120, 1123, 1124, 1125, 1126 , 1129, 1133, 1140, 1151, 1160, 1172, 1178, 1184, 1207, 1260, 1266, 1286, 1298, 1334, 1340, 1358, 1364, 1382, 1387, 1391, 1417, 1441, 1446, 1448, 1481 , 1522, 1531, 1537, 1543, 1549, 1566, 157 5, 1593, 1599, 1616, 1620, 1625, 1631, 1643, 1649, 1658, 1710, 1770, 1789, 1811, 1840, 1879, 1891, 1911, 1937, 1946, 1958, 1981, 1985, 2010, 2034, 2038, 2040, 2042, 2051, 2060, 2066, 2072, 2081, 2106, 2136, 2151, 2176, 2200, 2212, 2220, 2225, 2265, 2289, 2300, 2309, 2327, 2333, 2411, 2519, 2529, 2540, 2542, 2556, 2565, 2568, 2576, 2577, 2587, 2597, 2599, 2600, 2601, 2605, 2609, 2614, 2662, 2671, 2677, 2697, 2703, 2709, 2715, 2721, 2727, 2733, 2739, 2746, 2752, 2758, 2764, 2770, 2776, 2782, 2788, 2805, 2814, 2820, 2826, 2850, 2856, 2862, 2868, 2874, 2880, 2900, 2906, 2918, 2924, 2930, 2961, 2970, 2976, 2982, 2988, 2994, 3022, 3028, 3034, 3040, 3046, 3052, 3058, 3064, 3070, 3076, 3082, 3088, 3094, 3100, 3106, 3112, 3129, 3138, 3144, 3162, 3168, 3185, 3194, 3200, 3217, 3226, 3243, 3252, 3258, 3264, 3270, 3276, 3282, 3288, 3294, 3300, 3306, 3312, 3318, 3324, 3330, 3336, 3342, 3348, 3354, 3360, 3366, 3372, 3378, 3384, 3390, 3396, 3402, 3408, 3414, 3420, 3426, 3432, 3438, 3444, 3450, 3456, 3 462, 3468, 3474, 3480, 3486, 3492, 3498, 3504, 3510, 3516, 3528, 3534, 3540, 3546, 3552, 3558, 3564, 3570, 3576, 3582, 3588, 3594, 3600, 3606, 3612, 3618, 3624, 3630, 3636, 3642, 3648, 3654, 3660, 3666, 3672, 3678, 3684, 3690, 3696, 3702, 3708, 3714, 3720, 3755, 3780, 3786, 3792, 3798, 3805, 3811, Compound of 3837, 3843 or 3849,
[257] More preferably, compound numbers 125, 126, 127, 128, 130, 132, 139, 140, 144, 145, 151, 163, 217, 249, 264, 265, 266, 284, 304, 308, 387, 390 , 391, 459, 472, 506, 507, 515, 516, 531, 539, 541, 621, 658, 659, 662, 700, 701, 702, 704, 711, 717, 719, 733, 734, 735, 740 , 758, 759, 762, 775, 780, 781, 801, 802, 803, 806, 827, 834, 846, 850, 931, 964, 965, 1023, 1040, 1050, 1052, 1053, 1055, 1058, 1061 , 1064, 1066, 1069, 1073, 1088, 1089, 1091, 1096, 1099, 1100, 1102, 1109, 1119, 1124, 1125, 1126, 1129, 1133, 1151, 1160, 1172, 1178, 1184, 1207, 1260 , 1286, 1298, 1334, 1340, 1358, 1382, 1417, 1441, 1481, 1522, 1531, 1537, 1543, 1549, 1566, 1593, 1599, 1616, 1625, 1631, 1643, 1649, 1770, 1811, 1891 , 1958, 2034, 2051, 2060, 2072, 2136, 2176, 2212, 2265, 2309, 2327, 2333, 2519, 2556, 2577, 2587, 2597, 2599, 2600, 2601, 2609, 2614, 2662, 2677, 2697 , 2709, 2715, 2721, 2727, 2733, 2739, 2746, 2752, 2758, 2764, 2770, 2776, 2782, 2788, 2805, 2814, 2820, 2826, 2850, 2862, 2868, 2874, 2900, 2918, 2924, 2930, 2961, 2970, 2988, 2994, 3022, 3034, 3046, 3058, 3064, 3076, 3082, 3094, 3106, 3112, 3129, 3144, 3162, 3168, 3185, 3217, 3243,3252, 3264, 3282, 3288, 3294, 3306, 3324, 3330, 3336, 3354, 3378, 3390, 3396, 3402, 3408, 3414, 3420, 3426, 3432, 3438, 3450, 3462, 3468, 3474, 3486, 3492, 3510, 3516, 3546, 3552, 3564, 3582, 3588, 3594, 3600, 3606, 3612, 3618, 3624, 3642, 3654, 3660, 3678, 3690, 3696, 3702, 3780, 3786, 3798, 3805, 3811, Compound of 3837, 3843 or 3849,
[258] Especially preferably, compound numbers 127, 128, 132, 139, 144, 217, 265, 284, 304, 391, 472, 506, 507, 515, 516, 539, 541, 621, 658, 659, 662, 704 , 711, 717, 719, 733, 735, 740, 758, 759, 762, 780, 781, 801, 802, 803, 806, 827, 846, 850, 931, 964, 965, 1023, 1040, 1052, 1058 , 1061, 1088, 1089, 1091, 1096, 1099, 1100, 1102, 1109, 1124, 1125, 1151, 1160, 1172, 1184, 1207, 1286, 1298, 1334, 1358, 1417, 1441, 1481, 1522, 1531 , 1537, 1543, 1566, 1593, 1599, 1616, 1625, 1631, 1643, 1770, 1811, 1891, 1958, 2034, 2051, 2176, 2212, 2265, 2309, 2327, 2333, 2597, 2599, 2614, 2662 , 2677, 2727, 2733, 2739, 2746, 2752, 2805, 2814, 2850, 2900, 2918, 2961, 2994, 3022, 3046, 3064, 3094, 3129, 3144, 3168, 3185, 3217, 3243,3264, 3288 , 3402, 3408, 3426, 3432, 3450, 3462, 3546, 3552, 3564, 3582, 3588, 3594, 3600, 3606, 3612, 3618, 3624, 3642, 3654, 3660, 3678, 3690, 3696, 3702, 3805 Or 3811 compound,
[259] Most preferably, 6-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 128), 6-chloro-3- (2-isopropylphenoxy) -4-pyridazinol (Compound No. 132), 6-chloro-3- (2-cyclopropylphenoxy) -4-pyridazinol (Compound No. 139), 6-chloro-3- [2- (2,2-dichlorocyclopropyl) Phenoxy] -4-pyridazinol (Compound No. 265), 6-chloro-3- (2,3-dihydro-1H-inden-4-yloxy) -4-pyridazinol (Compound No. 506), 6-chloro-3- (2-cyclopropyl-5-methylphenoxy) -4-pyridazinol (Compound No. 662), 6-chloro-3- (2-fluoro-6-isopropylphenoxy)- 4-pyridazinol (Compound No. 717), 6-chloro-3- (2-chloro-6-cyclopropylphenoxy) -4-pyridazinol (Compound No. 740), 6-chloro-3- (2, 6-dimethylphenoxy) -4-pyridazinol (Compound No. 801), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol (Compound No. 806), 6- Chloro-3- [2- (2,2-dichlorocycloprop Lofil) -6-methylphenoxy] -4-pyridazinol (Compound No. 827), 6-chloro-3- (2-cyclopropyl-3,5-dimethylphenoxy) -4-pyridazinol (Compound No.) 1023), 6-chloro-3- (6-cyclopropyl-3-fluoro-2-methylphenoxy) -4-pyridazinol (Compound No. 1052), 6-chloro-3- (6-cyclopropyl- 2,3-dimethylphenoxy) -4-pyridazinol (Compound No. 1061), 6-chloro-3- (2,3,5,6-tetramethylphenoxy) -4-pyridazinol (Compound No. 1125 ), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl acetate (Compound No. 1151), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy ) -4-pyridazinyl propionate (Compound No. 1160), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methylpropanoate (Compound No. 1172 ), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl pivalate (Compound No. 1207), 6-chloro-3- (2-cyclopropyl-6-methyl Phenoxy) -4-pyridazinyl 3-methyl-2-butenoate (Compound No. 1358), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl benzoate (Compound No. 1417), 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1481), 6-chloro-3- (2- Cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methoxybenzoate (Compound No. 1522), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyrida Genyl 3-methylbenzoate (Compound No. 1531), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-bromobenzoate (Compound No. 1543), 6- Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methylbenzoate (Compound No. 1566), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy ) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl phthalate (Compound No. 1625), 6-chloro -3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl isophthalate (compound No. 1631), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl isobutylcarbonate (Compound No. 1770), 6-chloro-3- (2-cyclopropyl -6-Methylphenoxy) -4-pyridazinyl dimethylcarbamate (Compound No. 1891), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-propane Sulfonate (Compound No. 2051), 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl benzenesulfonate (Compound No. 2176), 6-chloro-3- (2- Cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-chlorobenzenesulfonate (Compound No. 2212), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyrida Genyl 4-methylbenzenesulfonate (Compound No. 2265), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyrida Neyl 4-methoxybenzenesulfonate (Compound No. 2309), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1 , 3-dimethyl-1H-pyrazoyl-5-yl 1,2-benzenedisulfonate (Compound No. 2327), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyrida Genyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl 1,3-benzenedisulfonate (Compound No. 2333), 6-chloro-3- (2-cyclo Propyl-6-methylphenoxy) -4-pyridazinyl 3,3-dimethylbutanoate (Compound No. 2662), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridine Dazinyl ethyl succinate (Compound No. 2727), bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] succinate (compound no. 2733), 6-chloro- 3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl pentangioate (compound Number 2739) , Bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] pentanesioate (Compound No. 2746), 6-chloro-3- (2-cyclopropyl-6 -Methylphenoxy) -4-pyridazinyl 2-bromobenzoate (Compound No. 2805), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-ethyl Benzoate (Compound No. 2961), 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,5-dimethylbenzoate (Compound No. 3129), 6-chloro-3 -(2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-fluoro-4-methylbenzoate (Compound No. 3185), 6-chloro-3- (2-cyclopropyl-6-methyl Phenoxy) -4-pyridazinyl 3,5-difluorobenzoate (Compound No. 3217), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3, 5-dimethylbenzoate (Compound No. 3243), 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methoxy (methyl) carba Yit (Compound No. 3564), 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl bis (2-methoxyethyl) carbamate (Compound No. 3600), 6- Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-azetidinecarboxylate (Compound No. 3612) or 6-chloro-3- (2-cyclopropyl-6-methyl Phenoxy) -4-pyridazinyl 4-morpholinecarboxylate (Compound No. 3690).
[260] The 3-phenoxy-4-pyridazinol compound and ester derivatives thereof of the present invention can be produced by the methods of Steps A to N described below.
[261] (Step A)
[262]
[263] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> and R <^7> represent the same meaning as the above, L represents a leaving group, For example, a halogen atom, C1-C6 alkylsulfonyl jade Or a phenylsulfonyloxy group (where the phenylsulfonyloxy group may be substituted by the same or different 1 to 5 halogen atoms or C1 to C6 alkyl groups),
[264] X represents a hydrogen atom or an acyl group,
[265] In addition to X, Y is other protecting group of a hydroxyl group, For example, it may be a methyl group, a methoxymethyl group, a methoxyethoxymethyl group, or a benzyl group.
[266] Step A is a compound in which the hydroxyl group represented by Formula Ia or Formula VII of the present invention is protected by reacting a pyridazine compound represented by the formula (II) with a phenol compound represented by the formula (III), followed by chlorination, and reaction of an oxygen nucleophile. Is a step of preparing the compound Ib of the present invention by removing the protecting group of the compound VII.
[267] (Step A-1)
[268] Step A-1 is a step of reacting compound II with or without compound III in the presence or absence of a solvent, if necessary, in the presence of a base to prepare a phenoxypyridazine compound represented by the formula (IV).
[269] There is no restriction | limiting in particular if the base used is a base which shows pH 8 or more normally, For example, Alkali metal hydroxides, such as sodium hydroxide and potassium hydroxide; Alkali metal carbonates such as sodium carbonate, potassium carbonate and cesium carbonate; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal hydrides such as sodium hydride and potassium hydride; Alkali metals such as sodium and potassium; Aliphatic tertiary amines such as triethylamine, tributylamine and diisopropylethylamine; Aliphatic cyclic tertiary amines such as 1,4-diazabicyclo [2.2.2] octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU); Pyridines such as pyridine, collidine and 4- (N, N-dimethylamino) pyridine; organometallic bases such as n-butyllithium, s-butyllithium, lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide, preferably alkali metal hydroxides, alkali metal carbonates , Metal alkoxide, alkali metal hydride or alkali metal, more preferably potassium carbonate, potassium t-butoxide, sodium hydride or sodium.
[270] The amount of base used is usually 0.5 to 5 mol, preferably 1 to 3 mol, per 1 mol of compound II.
[271] The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide and the like; Or a mixed solvent thereof, preferably nitriles, halogenated hydrocarbons, ethers, aromatic hydrocarbons, amides or sulfoxides, more preferably dioxane, toluene, dimethylformamide or dimethyl sulfoxide to be.
[272] Although reaction temperature changes with raw material compounds, a reaction reagent, a solvent, etc., it is usually -90 degreeC-200 degreeC, Preferably it is 0 degreeC-100 degreeC.
[273] The reaction time is mainly 5 minutes to 48 hours, preferably 15 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[274] <Step A-2>
[275] Step A-2 is a step of producing a compound in which compound IV is chlorinated by a chlorinating agent in the presence or absence of a solvent to introduce a chlorine atom at the 4 position of the pyridazine ring represented by the general formula (V).
[276] The chlorinating agent to be used is not particularly limited as long as it chlorinates the aromatic ring, and may be, for example, chlorine, chlorine-iron chloride, sulfyl chloride, copper chloride, N-chlorosuccinimide or phosphorus pentachloride, preferably It is chlorine.
[277] The amount of chlorinating agent used is usually 0.5 to 10 mol, preferably 1 to 2 mol, relative to 1 mol of compound IV.
[278] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, phosphorus oxychloride; water; Alcohols such as methanol, ethanol and t-butanol; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Aliphatic hydrocarbons such as hexane, cyclohexane, heptane; Or a mixed solvent thereof, preferably phosphorus oxychloride, water, halogenated hydrocarbons or ethers, and more preferably phosphorus oxychloride.
[279] Although reaction temperature changes with kinds of raw material compound, reaction reagent, and the solvent used, it is usually -90 degreeC-200 degreeC, Preferably it is 0 degreeC-50 degreeC.
[280] The reaction time is mainly 5 minutes to 24 hours, preferably 15 minutes to 6 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[281] (Step A-3)
[282] Step A-3 reacts Compound V with an oxygen nucleophile represented by Formula VI in the presence or absence of a solvent and, optionally, in the presence of a base to protect the hydroxyl group represented by Compound Ia or Formula VII of the present invention. Process for preparing the compound.
[283] The base to be used is not particularly limited as long as it is a base having a pH of usually 8 or higher, and examples thereof include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; Alkali metal carbonates such as sodium carbonate, potassium carbonate and cesium carbonate; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal salts of organic acids such as sodium acetate, potassium acetate, sodium formate, potassium formate; Alkali metal hydrides such as sodium hydride and potassium hydride; Alkali metals such as sodium and potassium; Aliphatic tertiary amines such as triethylamine, tributylamine and diisopropylethylamine; Aliphatic cyclic tertiary amines such as 1,4-diazabicyclo [2.2.2] octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU); Pyridines such as pyridine, collidine and 4- (N, N-dimethylamino) pyridine; Organometallic bases such as butyllithium, s-butyllithium, lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide, preferably alkali metal hydroxides, alkali metal carbonates, metals Alkoxides, alkali metal salts of organic acids, alkali metal hydrides or alkali metals, more preferably sodium hydroxide, potassium hydroxide, potassium carbonate, potassium t-butoxide, sodium acetate, sodium formate, sodium hydride or sodium.
[284] The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Or a mixed solvent thereof, preferably water, alcohols, nitriles, ethers, amides or sulfoxides, more preferably water, methanol, acetonitrile, tetrahydrofuran, dioxane, dimethyl Formamide or dimethyl sulfoxide.
[285] Although reaction temperature changes with kinds of a raw material compound, a reaction reagent, and the solvent used, it is usually -90 degreeC-200 degreeC, Preferably it is 0 degreeC-100 degreeC.
[286] The reaction time is mainly 5 minutes to 24 hours, preferably 15 minutes to 6 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[287] In addition, compound VI can be used for this process, after reacting with a base previously to make it a salt.
[288] (Step A-4)
[289] Step A-4 is a step of preparing the compound Ib of the present invention by removing the protecting group of the hydroxyl group of the compound VII.
[290] The protecting group used in this step can be selectively removed from the compound VII, and there is no particular limitation as long as it provides the compound Ib. For example, methyl group, methoxymethyl group, benzyloxymethyl group, methoxyethoxymethyl group, 2- (trimethyl Silyl) ethoxymethyl group, methylthiomethyl group, phenylthiomethyl group, 2,2-dichloro-1,1-difluoroethyl group, tetrahydropyranyl group, phenacyl group, p-bromophenacyl group, cyclopropylmethyl group, allyl group , Isopropyl group, cyclohexyl group, t-butyl group, benzyl group, 2,6-dimethylbenzyl group, 4-methoxybenzyl group, 2-nitrobenzyl group, 2,6-dichlorobenzyl group, 4- (dimethyl Aminocarbonyl) benzyl group, 9-anthrylmethyl group, 4-picoryl group, heptafluoro-p-tolyl group or tetrafluoro-4-pyridyl group, preferably methyl group, methoxymethyl group, methoxy Ethoxymethyl group, methylthiomethyl group, tetrahydropyranyl group, phenacyl group, allyl Or a benzyl group, more preferably a methyl group.
[291] The method of removing the protecting group used in this step is not particularly limited as long as it can selectively remove the protecting group of the hydroxyl group, and a known method for each protecting group (for example, (Protective Groups in Organic Synthesis, 13th Edition) , Theodora W. Greene and Peter GM Wuts, JOHN WILEY & SONS, INC)) or according to such a method. For example, when the protecting group is a methyl group, the removal of the methyl group is, for example, potassium or sodium salt of 2-hydroxypyridine in dimethyl sulfoxide, sodium salt of ethanethiol in dimethylformamide, or tribromide in methylene chloride. This can be done by acting on boron. For example, when a protecting group is a methoxymethyl group, removal of a methoxymethyl group can be performed, for example by making trifluoroacetic acid act. For example, when the protecting group is a methoxyethoxymethyl group, the methoxyethoxymethyl group can be removed by, for example, reacting trifluoroacetic acid. For example, when the protecting group is a benzyl group, the benzyl group can be removed by catalytic hydrogenation.
[292] (Step B)
[293]
[294] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , L, X, and Y show the same meaning as the above.
[295] Step B is obtained by oxidizing the pyridazine compound represented by the formula (II), followed by reacting the phenol compound represented by the formula (III), subsequently chlorination, and reacting the oxygen nucleophile to react the hydroxyl acid represented by the compound (Ia) or the formula (VII) of the present invention. It is a process for preparing a compound protected by group, and also a process for preparing compound Ib of the present invention by removing the protecting group of compound VII.
[296] (Step B-1)
[297] Step B-1 is a step of preparing N-oxidepyridazine represented by the formula (VIII) by oxidizing compound II with or without a solvent by an oxidizing agent.
[298] The oxidizing agent to be used is not particularly limited as long as it converts amines into N-oxides. Acids, dichloromaleic acid-hydrogen peroxide, peroxymaleic acid, maleic acid-hydrogen peroxide, t-butylhydroperoxide, t-butylhydroperoxide-vanadiumoxyacetylacetonate, t-butylhydroperoxide-molybdenum chloride, hydrogen peroxide, etc. Peroxides; ozone; Or oxygen, preferably m-chloroperbenzoic acid (mcpba), trifluoroacetic anhydride-hydrogen peroxide or dichloromaleic acid-hydrogen peroxide.
[299] The amount of oxidizing agent used in the reaction is usually 0.5 to 100 mol, preferably 1 to 2 mol, based on 1 mol of compound II.
[300] The solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Or a mixed solvent thereof, preferably halogenated hydrocarbons, more preferably methylene chloride.
[301] Although reaction temperature changes with raw material compounds, a reaction reagent, a solvent, etc., it is usually -90 degreeC-200 degreeC, Preferably it is 0 degreeC-100 degreeC.
[302] The reaction time is mainly 5 minutes to 24 hours, preferably 15 minutes to 6 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[303] Although the isomer by which another nitrogen atom was oxidized may be by-produced by this process, the target N-oxide pyridazine can be obtained by refine | purifying after completion | finish of this process, or carrying out a subsequent process with mixing, and refine | purifying after completion | finish of the process. have.
[304] (Step B-2)
[305] Step B-2 is a step of reacting compound VIII with compound III in the presence or absence of a solvent and optionally in the presence of a base to prepare a phenoxypyridazine compound represented by the formula (IX).
[306] This process can be performed according to process A-1.
[307] (Step B-3)
[308] Step B-3 is a step for preparing compound V by reacting compound IX with phosphorus oxychloride in the presence or absence of a solvent.
[309] The amount of phosphorus oxychloride used in this step is usually 0.5 to 100 mol, preferably 1 to 5 mol, based on 1 mol of compound IX.
[310] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, and examples thereof include ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Aliphatic hydrocarbons such as hexane and cyclohexane; Or a mixed solvent thereof, preferably halogenated hydrocarbons, more preferably methylene chloride or chloroform.
[311] Although reaction temperature changes with raw material compounds, a reaction reagent, a solvent, etc., it is usually -90 degreeC-200 degreeC, Preferably it is 0 degreeC-100 degreeC.
[312] The reaction time is mainly 5 minutes to 72 hours, preferably 30 minutes to 24 hours, depending on the reaction temperature, the raw material compound, the reaction reagent, and the kind of the solvent used.
[313] (Step B-4)
[314] Step B-4 reacts Compound V with an oxygen nucleophile represented by Formula VI in the presence or absence of a solvent and, optionally, in the presence of a base to protect the hydroxyl group represented by Compound Ia or Formula VII of the present invention. Process for preparing the compound.
[315] This process is the same as that of process A-3.
[316] (Step B-5)
[317] Step B-5 is a step of removing the protecting group of the hydroxyl group of compound VII to produce compound Ib of the present invention.
[318] This process is the same as that of process A-4.
[319] (Step C)
[320]
[321] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X and Y show the same meaning as the above.
[322] Step C is a step of preparing a compound in which the hydroxyl group represented by Compound Ia or Formula VII of the present invention is protected by oxidizing Compound IV, followed by chlorination, and then reacting with an oxygen nucleophile, and further removing the protecting group of Compound VII by It is a process of preparing compound Ib of this invention.
[323] (Step C-1)
[324] Step C-1 is a step of oxidizing Compound IV with an oxidizing agent in the presence or absence of a solvent to produce N-oxidepyridazine represented by the formula (IX).
[325] This process can be performed according to process B-1.
[326] (Step C-2)
[327] Step C-2 is a step for producing compound V by reacting compound IX with phosphorus oxychloride in the presence or absence of a solvent.
[328] This process is the same as that of process B-3.
[329] (Step C-3)
[330] Step C-3 reacts Compound V with an oxygen nucleophile represented by Formula VI in the presence or absence of a solvent and, optionally, in the presence of a base to protect the hydroxyl group represented by Compound Ia or Formula VII of the present invention. Process for preparing the compound.
[331] This process is the same as process A-3 or B-4.
[332] (Step C-4)
[333] Step C-4 is a step of preparing the compound Ib of the present invention by removing the protecting group of the hydroxyl group of the compound VII.
[334] This process is the same as process A-4 or B-5.
[335] (Step D)
[336]
[337] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , L, X, and Y show the same meaning as the above.
[338] Step D is a step of preparing a compound in which the hydroxyl group represented by Formula Ia or Formula VII of the present invention is protected by reacting a phenol represented by Formula III with a pyridazine compound previously substituted with an oxygen functional group represented by Formula X. The process for preparing compound Ib of the present invention by removing the protecting group of compound VII.
[339] (Step D-1)
[340] Step D-1 is a step of reacting compound X with compound III in the presence or absence of a solvent and, optionally, in the presence of a base, to prepare a compound protected by hydroxyl group represented by compound Ia or formula VII of the present invention. to be.
[341] This process can be performed according to process A-1 or B-2.
[342] (Step D-2)
[343] Step D-2 is a step of preparing the compound Ib of the present invention by removing the protecting group of the hydroxyl group of the compound VII.
[344] This process is the same as process A-4, B-5, or C-4.
[345] (Step E)
[346]
[347] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , L, X, and Y show the same meaning as the above,
[348] m 'and n' represent 0 or 1, provided that m 'and n' are not zero at the same time.
[349] Step E is a step of preparing a compound protected by the compound Ic or the hydroxyl group represented by the formula (XII) of the present invention by reacting the pyridazine compound substituted with the oxygen functional group represented by the formula (X) in advance and then reacting the phenol represented by the formula (III). And the protecting group of Compound XII to remove Compound Id of the present invention.
[350] (Step E-1)
[351] Step E-1 is a step of oxidizing compound X in the presence or absence of a solvent with an oxidizing agent to produce N-oxidepyridazine represented by the formula (XI).
[352] This process can be performed according to process B-1 or C-1 when m '= 0 or n' = 0, and when m '= n' = 1, the amount of oxidant is excessively more reactive. It can carry out by using more stringent conditions, such as oxidizing using a high oxidizing agent.
[353] (Step E-2)
[354] Step E-2 is a step of reacting compound XI with compound III in the presence or absence of a solvent and optionally in the presence of a base to prepare a compound protected by hydroxyl group represented by compound Ic of the present invention or formula XII. to be.
[355] This process can be performed according to process A-1, B-2, or D-1.
[356] (Step E-3)
[357] Step E-3 is a step of producing the compound Id of the present invention by removing the protecting group of the hydroxyl group of the compound XII.
[358] This step is the same as step A-4, B-5, C-4 or D-2.
[359] (Step F)
[360]
[361] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X, Y, m ', and n' show the same meaning as the above.
[362] Step F is a step of oxidizing a compound in which the hydroxyl group represented by the compound Ia or the formula VII of the present invention is protected to prepare a compound in which the hydroxyl group represented by the compound Ic or the formula XII of the present invention is protected, and also a protecting group of the compound XII. To remove the compound Id of the present invention.
[363] (Step F-1)
[364] Step F-1 is a process for preparing a compound in which the hydroxyl group represented by the compound Ic or the formula XII of the present invention is protected by oxidizing the compound Ia or the compound VII of the present invention in the presence or absence of a solvent with an oxidizing agent. to be.
[365] This process can be performed according to process E-1.
[366] (Step F-2)
[367] Step F-2 is a step of producing the compound Id of the present invention by removing the protecting group of the hydroxyl group of the compound XII.
[368] This step is the same as step A-4, B-5, C-4, D-2 or E-3.
[369] (Process G)
[370]
[371] In said formula, R <^1> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X and Y have the same meaning as the above, R <^2a> has the same meaning as R <^2> except having excluded a hydrogen atom. Indicates.
[372] Step G protects the compound of the present invention If or the hydroxyl group represented by the formula XIV by metallizing the 5-position of the pyridazine ring of the compound protected by the compound Ie of the present invention or the formula XIII and then reacting with a precursor. And a process for preparing the compound Ig of the present invention by removing the protecting group of the compound XIV.
[373] (Step G-1)
[374] Step G-1 is carried out by reacting the compound protected by the compound Ie of the present invention or the hydroxyl group represented by the formula (XIII) with the metalizing agent in the presence or absence of a solvent and subsequently with the electrons agent. It is the process of manufacturing the compound in which the hydroxyl group represented by XIV is protected.
[375] The metallizing agent to be used is not particularly limited as long as it can metallize the aromatic ring, and examples thereof include organic lithium compounds such as methyllithium, butyllithium, s-butyllithium, t-butyllithium and phenyllithium; Organic magnesium compounds such as methylmagnesium chloride, methylmagnesium bromide, ethylmagnesium bromide and phenylmagnesium bromide; Organometallic amides such as lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal hydrides such as sodium hydride and potassium hydride; Alkali metals such as lithium, sodium and potassium; It may be an alkaline earth metal such as magnesium, preferably an organolithium compound, and more preferably butyllithium.
[376] The amount of the metallizing agent used in the reaction is usually 0.5 to 10 mol, preferably 1 to 2 mol, based on 1 mol of the compound Ie or the compound XIII.
[377] The nucleophile used in the reaction is not particularly limited as long as it is a nucleophile that reacts with an organometallic compound. For example, trimethylsilyl chloride, triethylsilyl chloride, t-butyldimethylsilyl chloride, trimethylsilyltrifluoromethanesulfonate Silylating agents; Acylating agents such as acetyl chloride, benzoyl chloride, ethyl chlorocarbonate, methyl chlorocarbonate, N, N-dimethylformamide and methyl formate; Carbonyl compounds such as acetaldehyde, benzaldehyde, acetone, cyclohexanone; Alkylating agents such as methyl iodide, methyl bromide and benzyl bromide; Fluorine, chlorine, bromine, iodine, N-fluorobenzenesulfonamide, 1-fluoro-2,6-dichloropyridinium triflate, N-chlorosuccinimide (NCS), N-bromosuccinimide (NBS Halogenating agents such as; Or carbon dioxide, preferably a silylating agent, acylating agent, alkylating agent or halogenating agent, more preferably trimethylsilyl chloride, benzoyl chloride, ethyl chlorocarbonate or methyl iodide.
[378] The amount of the former agent used in the reaction is usually 0.5 to 10 mol, preferably 1 to 3 mol, based on 1 mol of the compound Ie or the compound XIII.
[379] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Aliphatic hydrocarbons such as hexane and cyclohexane; Or a mixed solvent thereof, preferably ethers, and more preferably tetrahydrofuran.
[380] Although reaction temperature changes with kinds of a raw material compound, a reaction reagent, and the solvent used, it is usually -90 degreeC-100 degreeC, Preferably it is -70 degreeC-30 degreeC.
[381] The reaction time is mainly 5 minutes to 24 hours, preferably 30 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[382] (Step G-2)
[383] Step G-2 is a step of producing the compound Ig of the present invention by removing the protecting group of the hydroxyl group of the compound XIV.
[384] This step is the same as step A-4, B-5, C-4, D-2, E-3 or F-2.
[385] (Step H)
[386]
[387] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> and R <^7> represent the same meaning as the above, X ^<a> shows the same meaning as X except the hydrogen atom.
[388] Step H is a step of converting the ester derivative of the present invention represented by the formula (Ih) to the hydroxy body of the present invention represented by the formula (Ib).
[389] (Step H-1)
[390] Step H-1 is a step of reacting compound Ih of the present invention with a nucleophilic agent in the presence or absence of a solvent to produce compound Ib of the present invention.
[391] The nucleophile to be used is not particularly limited as long as the nucleophilic attack of the ester derivative is possible, and the ester bond can be cleaved into the acid moiety and the alcohol moiety. Hydroxides of alkali metals such as lithium hydroxide, sodium hydroxide and potassium hydroxide; Hydroxides of alkaline earth metals such as magnesium hydroxide and calcium hydroxide; Metal alkoxides such as sodium methoxide, sodium ethoxide, 2-hydroxypyridine potassium salt and 2-hydroxypyridine sodium salt; Alkali metal salts of organic acids such as sodium acetate, potassium acetate, sodium formate, potassium formate; Fluorides such as tetrabutylammonium fluoride and potassium fluoride; Chlorides such as lithium chloride and sodium chloride; Bromide such as lithium bromide, sodium bromide; iodide such as sodium iodide, potassium iodide; Or metal salts of sulfur compounds such as methanethiol sodium salt, ethanethiol sodium salt, preferably water, alkali metal hydroxides, metal alkoxides or alkali metal salts of organic acids, more preferably water, sodium hydroxide, hydroxide Potassium or sodium acetate.
[392] The amount of nucleophile to be used is usually 1 to 10 mol, preferably 1 to 5 mol, based on 1 mol of compound Ih.
[393] The solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Or a mixed solvent thereof, preferably water, alcohols, nitriles, ethers, amides or sulfoxides, and more preferably water, methanol, ethanol, tetrahydrofuran, dioxane, dimethylform Amide or dimethyl sulfoxide.
[394] Although reaction temperature changes with raw material compounds, a reaction reagent, a solvent, etc., it is usually -90 degreeC-200 degreeC, Preferably it is 0 degreeC-100 degreeC.
[395] The reaction time is mainly 5 minutes to 48 hours, preferably 15 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of the solvent used.
[396] In addition, this process can use a well-known method as deprotection of a normal hydroxyl group.
[397] (Step I)
[398]
[399] In said formula, R <^1> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> and X ^<a> represent the same meaning as the above.
[400] Step I is a step of converting the hydroxy body of the present invention represented by the formula (Ib) to the ester derivative of the present invention represented by the formula (Ih).
[401] (Step I-1)
[402] Step I-1 is a step for producing compound Ih of the present invention by reacting compound Ib of the present invention with an esterifying agent in the presence or absence of a solvent.
[403] The esterification agent to be used is not particularly limited as long as it esterifies a hydroxyl group. For example, acetyl chloride, acetyl bromide, acetic anhydride, trifluoroacetic acid, benzoyl chloride, methyl chlorocarbonate, ethyl chlorocarbonate, N, N-dimethyl Acylating agents such as carbamoyl chloride, methylchlorothioformate; Or a sulfonylating agent such as methanesulfonyl chloride, propanesulfonyl chloride, p-toluenesulfonyl chloride, trifluoromethanesulfonic acid anhydride, N, N-dimethylsulfamoyl chloride, preferably acetyl chloride, acetic anhydride , Trifluoroacetic anhydride, benzoyl chloride, methyl chlorocarbonate, ethyl chlorocarbonate, methanesulfonyl chloride, propanesulfonyl chloride, p-toluenesulfonyl chloride or trifluoromethanesulfonic anhydride, more preferably benzoyl chloride, p-toluenesulfonylchloride or anhydrous trifluoromethanesulfonic acid.
[404] The amount of esterifying agent used in the reaction is usually 0.5 to 10 mol, preferably 1 to 3 mol, based on 1 mol of compound Ib.
[405] The reaction is preferably carried out in the presence of a base.
[406] The base to be used is not particularly limited as long as it is a base having a pH of usually 8 or more, and examples thereof include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; Alkali metal carbonates such as sodium carbonate, potassium carbonate and cesium carbonate; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal hydrides such as sodium hydride and potassium hydride; Aliphatic tertiary amines such as triethylamine, tributylamine and diisopropylethylamine; Aliphatic cyclic tertiary amines such as 1,4-diazabicyclo [2.2.2] octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU); Pyridines such as pyridine, collidine and 4- (N, N-dimethylamino) pyridine; Or organometallic bases such as n-butyllithium, s-butyllithium, lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide, preferably aliphatic tertiary amines, aliphatic Cyclic tertiary amines or pyridines, more preferably triethylamine, 1,4-diazabicyclo [2.2.2] octane (DABCO), pyridine or 4- (N, N-dimethylamino) pyridine.
[407] The amount of base used for the reaction is usually 0.5 to 20 mol, preferably 1 to 5 mol, based on 1 mol of compound Ib.
[408] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, and examples thereof include ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Aliphatic hydrocarbons such as hexane, cyclohexane; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Or a mixed solvent thereof, preferably nitriles, halogenated hydrocarbons or ethers, and more preferably acetonitrile or methylene chloride.
[409] The reaction temperature mainly depends on the reaction temperature, the raw material compound, the reaction reagent and the kind of the solvent used, but is usually -90 ° C to 200 ° C, and preferably 0 ° C to 100 ° C.
[410] The reaction time is mainly 5 minutes to 48 hours, preferably 15 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[411] Moreover, this process can also use a well-known method as protection of a normal hydroxyl group.
[412] (Step J)
[413]
[414] In said formula, R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X and Y have the same meaning as the above, R <^1a> has the same meaning as R <^1> except the hydrogen atom .
[415] Step J reduces and oxidizes the 6-chloropyridazine derivative represented by the formula (IVa) to metallize it, and then reacts with a precursor agent to introduce a substituent at the 6 position of the pyridazine ring, and to perform a substitution reaction with a chlorination and an oxygen nucleophile. This is a step of preparing a compound in which the hydroxyl group represented by the compound Ii or the general formula XVIII of the present invention is protected, and a step of producing the compound Ij of the present invention by removing the protecting group of the compound XVIII.
[416] (Step J-1)
[417] Step J-1 is a step of producing Compound IVb in which R ¹ is a hydrogen atom in Compound IV by reacting Compound IVa in which R ¹ is a chlorine atom in Compound IV with a reducing agent in the presence or absence of a solvent.
[418] The reducing agent used for the reaction is not particularly limited as long as it can reduce the aromatic ring chlorine atom. For example, the reducing agent may be a reducing agent used in a normal hydrogenation reaction, and is preferably a hydrogen-palladium catalyst.
[419] When the hydrogenation reaction is carried out in this step, the hydrogen pressure is usually 1 atm to 100 atm, preferably 1 to 3 atm.
[420] The amount of palladium used for the hydrogenation reaction is usually 0.001 to 10 mol, preferably 0.01 to 1 mol, based on 1 mol of compound IVa.
[421] The hydrogenation reaction is preferably carried out in the presence of a base.
[422] The base to be used is not particularly limited as long as it is a base having a pH of usually 8 or more, and examples thereof include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; Alkali metal carbonates such as sodium carbonate, potassium carbonate and cesium carbonate; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal hydrides such as sodium hydride and potassium hydride; ammonia; Aliphatic tertiary amines such as triethylamine, trin-butylamine and diisopropylethylamine; Aliphatic cyclic tertiary amines such as 1,4-diazabicyclo [2.2.2] octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU); Pyridines such as pyridine, collidine and 4- (N, N-dimethylamino) pyridine; Or an organometallic base such as butyllithium, s-butyllithium, lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide, etc., preferably ammonia water or aliphatic tertiary amines, More preferably, it is ammonia water or triethylamine.
[423] The amount of base used for the reaction is usually 0.1 to 100 mol, preferably 1 to 3 mol, based on 1 mol of compound IVa.
[424] The solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Aliphatic hydrocarbons such as hexane and cyclohexane; Or a mixed solvent thereof, preferably alcohols, and more preferably methanol or ethanol.
[425] The reaction temperature mainly depends on the reaction temperature, the raw material compound, the reaction reagent and the kind of the solvent used, but is usually -90 ° C to 200 ° C, and preferably 0 ° C to 100 ° C.
[426] The reaction time is mainly 5 minutes to 48 hours, preferably 15 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of the solvent used.
[427] (Step J-2)
[428] Step J-2 is a step of oxidizing compound IVb in the presence or absence of a solvent with an oxidizing agent to produce N-oxidepyridazine represented by the formula (XV).
[429] This process can be performed according to process B-1 or C-1.
[430] (Step J-3)
[431] Step J-3 is a step for producing compound XVI of the present invention by reacting compound XV with or without a metalizing agent in the presence or absence of a solvent, followed by reaction with a precursor agent.
[432] This process can be performed according to process G-1.
[433] (Step J-4)
[434] Step J-4 is a process for preparing compound XVII by reacting compound XVI with phosphorus oxychloride in the presence or absence of a solvent.
[435] This process is the same as process B-3 or C-2.
[436] (Step J-5)
[437] Step J-5 reacts Compound XVII with an oxygen nucleophile represented by Formula VI in the presence or absence of a solvent and, optionally, in the presence of a base to protect the hydroxyl group represented by Compound Ii or Formula XVIII of the present invention. Process for preparing the compound.
[438] This process is the same as process A-3, B-4 or C-3.
[439] (Step J-6)
[440] Step J-6 is a step of preparing the compound Ij of the present invention by removing the protecting group of the hydroxyl group of the compound XVIII.
[441] This process is the same as process A-4, B-5, C-4, D-2, E-3, F-2, or G-2.
[442] (Step K)
[443]
[444] In said formula, R <^1a> , R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X and Y show the same meaning as the above.
[445] Step K is carried out by oxidizing the 6-chloropyridazine derivative of the present invention represented by the formula (Ik) or the 6-chloropyridazine derivative protected by the hydroxyl group represented by the formula (XIX), followed by dechlorolation and subsequent metallization. A process for preparing a compound in which the hydroxyl group represented by the compound Ii or the general formula XVIII of the present invention is protected by introducing self-reduction and finally reducing, and also removing the protecting group of the compound XVIII to produce the compound Ij of the present invention.
[446] (Step K-1)
[447] Step K-1 is a step of oxidizing compound Ik or compound XIX with an oxidizing agent in the presence or absence of a solvent to produce an N-oxypyridazine compound represented by the formula Il or XX.
[448] This process can be performed according to process B-1, C-1, or J-2.
[449] (Step K-2)
[450] Step K-2 is an N-oxide compound in which the pyridazine ring 6 position is a hydrogen atom by reacting an N-oxide compound Il or XX in which the pyridazine ring 6 position is a chlorine atom with or without a solvent in the presence or absence of a solvent. It is a process for manufacturing Im or XXI.
[451] This process can be performed according to process J-1.
[452] (Step K-3)
[453] Step K-3 reacts compound Im or XXI with or without a metalizing agent in the presence or absence of a solvent and subsequently with a former agent to prepare a compound protected by the compound In of the present invention or a hydroxyl group represented by formula XXII. It is a process to do it.
[454] This process can be performed according to process G-1 or J-3.
[455] (Step K-4)
[456] Step K-4 protects the hydroxyl group represented by the compound Ii or the formula XVIII of the present invention by reacting the N-oxide derivative represented by the formula In or XXII with phosphorus trichloride or phosphorus tribromide in the presence or absence of a solvent. Process for preparing the compound.
[457] The amount of phosphorus trichloride or phosphorus tribromide used is usually 0.5 to 100 mol, preferably 1 to 20 mol, relative to 1 mol of the compound In or XXII.
[458] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Aliphatic hydrocarbons such as hexane, cyclohexane, heptane; Or a mixed solvent thereof, preferably halogenated hydrocarbons, more preferably chloroform.
[459] The reaction temperature mainly depends on the reaction temperature, the raw material compound, the reaction reagent and the kind of the solvent used, but is usually -90 ° C to 200 ° C, and preferably 0 ° C to 100 ° C.
[460] The reaction time is mainly 5 minutes to 24 hours, preferably 15 minutes to 6 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[461] (Step K-5)
[462] Step K-5 is a step of producing the compound Ij of the present invention by removing the protecting group of the hydroxyl group of the compound XVIII.
[463] This process is the same as process A-4, B-5, C-4, D-2, E-3, F-2, G-2, or J-6.
[464] (Process L)
[465]
[466] In said formula, R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X and Y have the same meaning as the above, R <^1b> is R <^1> , except for excluding a hydrogen atom and a halogen atom. The same meaning is indicated.
[467] Step L is a step of preparing a compound in which the hydroxyl group represented by Compound Io or Formula XXIII of the present invention is protected by reacting a 6-chloropyridazine derivative represented by Formula Ik or XIX with an organometallic compound, and also a protecting group of Compound XXIII. To remove Compound Ip of the present invention.
[468] (Step L-1)
[469] Step L-1 is a process for preparing a compound protected by the compound Io of the present invention or a hydroxyl group represented by the formula XXIII by reacting the compound Ik or XIX with an organometallic compound in the presence or absence of a solvent and in the presence of a metal catalyst. to be.
[470] The organometallic compound to be used is not particularly limited as long as it is used in a cross coupling reaction in which the R ^1b group is substituted with a chlorine atom, and for example, an organic magnesium compound such as methylmagnesium chloride, ethylmagnesium bromide, or phenylmagnesium chloride; Organic zinc compounds such as phenyl zinc chloride; Organoaluminum compounds such as (diisobutyl) (1-hexenyl) aluminum; Organic tin compounds such as (vinyl) trimethyltin, (1-ethoxyvinyl) tributyltin, (2-furyl) tributyltin, and (2-thienyl) tributyltin; Organic boron compounds such as phenylboronic acid; Organic silicate compounds such as trimethylvinylsilicon-tris (dimethylamino) sulfoniumdifluorotrimethylsilicate; It may be potassium cyanide, and also an acetylene compound such as trimethylsilylacetylene and phenylacetylene may be used in the reaction like the organometallic compound in the presence of an amine such as triethylamine, and is preferably an organic tin compound or an organic boron compound. .
[471] The amount of the organometallic compound used in the reaction is usually 0.5 to 10 mol, preferably 1 to 2 mol, based on 1 mol of compound Ik or XIX.
[472] There is no restriction | limiting in particular if the metal catalyst used for this process is used for a cross coupling reaction, For example, they are a nickel catalyst and a palladium catalyst.
[473] The amount of the metal catalyst used in the reaction is usually 0.0001 to 10 mol, preferably 0.01 to 0.5 mol, based on 1 mol of the compound Ik or XIX.
[474] The solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Aliphatic hydrocarbons such as hexane and cyclohexane; Organic amines such as triethylamine and pyridine; Or a mixed solvent thereof, preferably ethers, aromatic hydrocarbons or amides, more preferably ether, tetrahydrofuran, toluene or dimethylformamide.
[475] The reaction temperature mainly depends on the reaction temperature, the raw material compound, the reaction reagent and the kind of the solvent used, but is usually -90 ° C to 200 ° C, and preferably 0 ° C to 130 ° C.
[476] The reaction time is mainly 5 minutes to 48 hours, preferably 15 minutes to 24 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[477] (Step L-2)
[478] Step L-2 is a step of removing the protecting group of the hydroxyl group of compound XXIII to produce compound Ip of the present invention.
[479] This process is the same as process A-4, B-5, C-4, D-2, E-3, F-2, G-2, J-6 or K-5.
[480] (Step M)
[481]
[482] In said formula, R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X and Y show the same meaning as the above.
[483] Step M is a step of preparing a compound Iq of the present invention or a compound protected by a hydroxyl group represented by Formula XXIV by cyanolating a 6-position unsubstituted N-oxidepyridazine derivative represented by Formula Im or XXI, and also Compound XXIV. It is a process of manufacturing the compound Ir of this invention by removing the protecting group of.
[484] (Step M-1)
[485] Step M-1 is a step of preparing a compound in which the hydroxyl group represented by the compound Iq or the formula XXIV of the present invention is protected by reacting the compound Im or XXI with a cyanoating agent in the presence or absence of a solvent.
[486] This process can be carried out according to known Reissert-Henze reactions (JOC, 48, 1983, 1375-1377; Heterocycles, 15, 1981, 981-984; Synthesis, 1983, 316-319, etc.). have.
[487] (Step M-2)
[488] Step M-2 is a step of producing the compound Ir of the present invention by removing the protecting group of the hydroxyl group of the compound XXIV.
[489] This step is the same as step A-4, B-5, C-4, D-2, E-3, F-2, G-2, J-6, K-5 or L-2.
[490] (Step N)
[491]
[492] In said formula, R <^2> , R <^3> , R <^4> , R <^5> , R <^6> , R <^7> , X and Y show the same meaning as the above.
[493] Step N is a process for preparing a compound in which the hydroxyl group represented by the compound Is or the formula XXV of the present invention is protected by dechlorination of the 6-chloropyridazine derivative represented by the formula Ik or XIX, and also by removing the protecting group of the compound XXV. It is the process of manufacturing the compound It of this invention.
[494] (Step N-1)
[495] Step N-1 is a step of preparing a compound in which the hydroxyl group represented by the compound Is or the general formula XXV of the present invention is protected by reacting the compound Ik or XIX with or without a solvent in the presence or absence of a solvent.
[496] This process can be performed according to process J-1 or K-2.
[497] (Step N-2)
[498] Step N-2 is a step of producing the compound It of the present invention by removing the protecting group of the hydroxyl group of the compound XXV.
[499] This step is the same as step A-4, B-5, C-4, D-2, E-3, F-2, G-2, J-6, K-5, L-2 or M-2 .
[500] (Process O)
[501]
[502] In said formula, R <^1> , R <^2> , R <^4> , R <^5> , R <^6> and R <^7> represent the same meaning as the above.
[503] Step O is a step of preparing the compound Iu of the present invention by reacting a 3,4-dichloropyridazine derivative represented by the general formula (XXVI) with a catechol derivative represented by the general formula (XXVII), followed by hydrolysis.
[504] (Step O-1)
[505] Step O-1 is a step of reacting compound XXVI with compound XXVII in the presence or absence of a solvent and optionally in the presence of a base to prepare a condensation compound represented by the formula (XXVIII).
[506] This step can be carried out in accordance with step A-1, B-2, D-1 or E-2, and the amount of base used is usually 1 to 10 mol, preferably 2 to 6 mol, based on 1 mol of compound XXVI. to be.
[507] (Step O-2)
[508] Step O-2 is a step of producing compound Iu of the present invention by hydrolyzing compound XXVIII.
[509] This process can be performed according to the case where Y is a hydrogen atom in process A-3, B-4 or C-3, and reaction temperature becomes like this. Preferably it is 80 degreeC-100 degreeC.
[510] (Process P)
[511]
[512] In said formula, R <^2> , R <^3> , R <^4> , R <^5> , R <^6> and R <^7> represent the same meaning as the above.
[513] Step P selectively hydrolyzes the 6 position of the 4,6-dichloropyridazine derivative represented by the formula Va to form compound XXIX, and then bromines the 4 and 6 positions with phosphorus oxybromide, followed by selectively It is a process which manufactures the compound in which the compound Iv of this invention or the hydroxyl group represented by Formula (XXXI) was protected by making oxygen nucleating agent react, and also the compound Iw of this invention is manufactured by removing the protecting group of compound XXXI.
[514] (Step P-1)
[515] Step P-1 is a step of producing a compound represented by the formula (XXIX) by hydrolyzing the compound Va in the presence or absence of a solvent and in the presence of an acid to selectively convert a 6-position chlorine atom to a hydroxyl group.
[516] The acid to be used is not particularly limited as long as it is an acid having a pH of 6 or less, and examples thereof include organic acids such as formic acid, acetic acid, oxalic acid, propionic acid, succinic acid, maleic acid, fumaric acid and benzoic acid; Inorganic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid and phosphoric acid; Or Lewis acids such as aluminum chloride, iron chloride, titanium chloride, boron trifluoride and the like, and are preferably organic acids, more preferably formic acid or acetic acid.
[517] This step is preferably carried out in the presence of a metal salt of acid.
[518] Examples of the metal salt of the acid used include alkali metal salts of organic acids such as sodium formate, potassium formate, lithium acetate, sodium acetate, potassium acetate, cesium acetate and sodium benzoate; Alkaline earth metal salts of organic acids such as magnesium formate, calcium formate, magnesium acetate, calcium acetate and magnesium benzoate; Alkali metal salts or alkaline earth metal salts of carbonic acid such as sodium carbonate, potassium carbonate, calcium carbonate, sodium hydrogen carbonate and potassium hydrogen carbonate; Or sodium fluoride, potassium fluoride, sodium chloride, potassium chloride, sodium bromide, potassium bromide, sodium iodide, potassium iodide, sodium sulfate, sodium hydrogen sulfate, potassium sulfate, potassium hydrogen sulfate, magnesium sulfate, sodium phosphate, sodium hydrogen phosphate, sodium dihydrogen phosphate , Alkali metal salts or alkaline earth metal salts of inorganic acids such as potassium phosphate, dipotassium hydrogen phosphate and potassium dihydrogen phosphate, preferably alkali metal salts of organic acids, more preferably sodium formate, potassium formate, sodium acetate or potassium acetate to be.
[519] The solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Organic acids such as formic acid, acetic acid and propionic acid; Or a mixed solvent thereof, preferably water, nitriles, ethers, amides, sulfoxides or organic acids, more preferably water, acetonitrile, tetrahydrofuran, dioxane, dimethylformamide, Dimethylsulfoxide, formic acid or acetic acid.
[520] The reaction temperature is usually -90 ° C to 200 ° C, preferably 0 ° C to 150 ° C, depending on the type of the starting compound, the reaction reagent and the solvent used.
[521] The reaction time is mainly 5 minutes to 24 hours, preferably 15 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[522] (Step P-2)
[523] Step P-2 is a step of reacting compound XXIX with phosphorus oxybromide in the presence or absence of a solvent to produce compound XXX.
[524] The amount of phosphorus oxybromide used in this step is usually 0.5 to 100 mol, preferably 1 to 10 mol, based on 1 mol of compound XXIX.
[525] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, and examples thereof include ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Aliphatic hydrocarbons such as hexane and cyclohexane; Or a mixed solvent thereof, preferably halogenated hydrocarbons, and more preferably methylene chloride and chloroform.
[526] Although reaction temperature changes with raw material compounds, a reaction reagent, a solvent, etc., it is usually -90 degreeC-200 degreeC, Preferably it is 0 degreeC-100 degreeC.
[527] The reaction time is mainly 5 minutes to 72 hours, preferably 30 minutes to 24 hours, depending on the reaction temperature, the raw material compound, the reaction reagent, and the kind of the solvent used.
[528] (Step P-3)
[529] Step P-3 reacts compound XXX with or without a solvent and, if necessary, with an oxygen nucleophile represented by Formula VI in the presence of a base to protect the hydroxyl group represented by Compound Iv or Formula XXX of the present invention. It is a process for preparing a compound.
[530] This process is the same as process A-3, B-4, C-3, or J-5.
[531] (Step P-4)
[532] Step P-4 is a step of producing the compound Iw of the present invention by removing the protecting group of the hydroxyl group of the compound XXXI.
[533] This process is a process A-4, B-5, C-4, D-2, E-3, F-2, G-2, J-6, K-5, L-2, M-2 or N- Same as 2.
[534] (Step Q)
[535]
[536] In the above formula, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ have the same meanings as above, and the compound represented by the formula XXXII is an oxygen nucleophile, sulfur nucleophile, nitrogen nucleophile Z is a substituent excluding a proton from an oxygen nucleophile, a sulfur nucleophile, or a nitrogen nucleophile, and may be, for example, an alkoxy group, a thioalkoxy group, a dialkylamino group, or the like.
[537] Step Q is a step of converting the hydroxy body of the present invention represented by the formula (Ib) to the ester derivative of the present invention represented by the formula (Iy).
[538] (Step Q-1)
[539] Step Q-1 is a step of producing compound Ix of the present invention by reacting compound Ib of the present invention with phosgene in the presence or absence of a solvent.
[540] The amount of phosgene used in the reaction is usually 0.5 to 10 mol, preferably 1 to 3 mol, based on 1 mol of compound Ib.
[541] The reaction is preferably carried out in the presence of a base.
[542] The base to be used is not particularly limited as long as it is a base having a pH of usually 8 or more, and examples thereof include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; Alkali metal carbonates such as sodium carbonate, potassium carbonate and cesium carbonate; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal hydrides such as sodium hydride and potassium hydride; Aliphatic tertiary amines such as triethylamine, tributylamine and diisopropylethylamine; Aliphatic cyclic tertiary amines such as 1,4-diazabicyclo [2.2.2] octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU); Pyridines such as pyridine, collidine and 4- (N, N-dimethylamino) pyridine; Or organometallic bases such as n-butyllithium, s-butyllithium, lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide, preferably aliphatic tertiary amines, aliphatic Cyclic tertiary amines or pyridines, more preferably triethylamine, 1,4-diazabicyclo [2.2.2] octane (DABCO), pyridine or 4- (N, N-dimethylamino) pyridine.
[543] The amount of base used for the reaction is usually 0.5 to 20 mol, preferably 1 to 5 mol, based on 1 mol of compound Ib.
[544] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, and examples thereof include ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Aliphatic hydrocarbons such as hexane, cyclohexane; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Or a mixed solvent thereof, preferably nitriles, halogenated hydrocarbons or ethers, and more preferably acetonitrile or methylene chloride.
[545] The reaction temperature mainly depends on the reaction temperature, the raw material compound, the reaction reagent and the kind of the solvent used, but is usually -90 ° C to 200 ° C, and preferably 0 ° C to 100 ° C.
[546] The reaction time is mainly 5 minutes to 48 hours, preferably 15 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[547] (Step Q-2)
[548] Step Q-2 is a step for producing compound Iy of the present invention by reacting compound Ix of the present invention with a nucleophilic agent represented by the formula (XXXII) in the presence or absence of a solvent and optionally in the presence of a base.
[549] The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, and examples thereof include ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Aliphatic hydrocarbons such as hexane and cyclohexane; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide; Or a mixed solvent thereof, preferably nitriles, halogenated hydrocarbons or ethers, and more preferably acetonitrile or methylene chloride.
[550] The base to be used is not particularly limited as long as it is a base having a pH of usually 8 or more, and examples thereof include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; Alkali metal carbonates such as sodium carbonate, potassium carbonate and cesium carbonate; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal hydrides such as sodium hydride and potassium hydride; Aliphatic tertiary amines such as triethylamine, tributylamine and diisopropylethylamine; Aliphatic cyclic tertiary amines such as 1,4-diazabicyclo [2.2.2] octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU); Pyridines such as pyridine, collidine and 4- (N, N-dimethylamino) pyridine; Or organometallic bases such as n-butyllithium, s-butyllithium, lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide, preferably aliphatic tertiary amines, aliphatic Cyclic tertiary amines or pyridines, more preferably triethylamine, 1,4-diazabicyclo [2.2.2] octane (DABCO), pyridine or 4- (N, N-dimethylamino) pyridine.
[551] The amount of base used for the reaction is usually 0.5 to 20 mol, preferably 1 to 5 mol, based on 1 mol of compound Ix.
[552] The nucleophile XXXII used for the reaction is not particularly limited as long as it replaces the chlorine atom of chlorocarbonate ester Ix. Examples of the oxygen nucleating agent include alcohols such as methanol, ethanol and propanol; Or phenols such as phenol and 4-chlorophenol, and as the sulfur nucleating agent, for example, thiols such as methanethiol, ethanethiol, propanethiol; Or thiophenols such as thiophenols, and as the nitrogen nucleating agent, for example, methylamine, dimethylamine, diethylamine, methyl (t-butyl) amine, methyl (cyanomethyl) amine, methyl (ethoxy) Carbonylmethyl) amine, bis (cyanomethyl) amine, bis (2-cyanoethyl) amine, bis (ethoxycarbonylmethyl) amine, bis (2-methoxyethyl) amine, bis (2-ethoxy Aliphatic chain amines such as ethyl) amine, bis (2-chloroethyl) amine, N, O-dimethylhydroxyamine; Aromatic amines such as methyl (phenyl) amine and methyl (pyridyl) amine; Aziridine, azetidine, pyrrolidine, piperidine, morpholine, thiomorpholine, N-methylpiperazine, N-phenylpiperazine, 2-methoxycarbonylpyrrolidine, 3-hydroxypyrrolidine , 4-bromopiperidine, 4-methylpiperidine, 2,2,6,6-tetramethylpiperidine, 2-ethoxycarbonylpiperidine, 4-ethoxycarbonylpiperidine, 2 Aliphatic cyclic amines such as, 6-dimethylmorpholine and 1,2,3,4-tetrahydroisoquinoline; Aromatic cyclic amines such as carbazole, 2,5-dimethylpyrrole, preferably methanol, ethanol, methanethiol, ethanethiol, methylamine, dimethylamine, methyl (cyanomethyl) amine, methyl (ethoxycar Bonylmethyl) amine, bis (cyanomethyl) amine, bis (2-cyanoethyl) amine, bis (ethoxycarbonylmethyl) amine, bis (2-methoxyethyl) amine, bis (2-ethoxyethyl ) Amine, bis (2-chloroethyl) amine, N, O-dimethylhydroxylamine, methyl (pyridyl) amine, azetidine, pyrrolidine, piperidine, morpholine, thiomorpholine, N-methylpipepe Razine, 2-methoxycarbonylpyrrolidine, 3-hydroxypyrrolidine, 2-ethoxycarbonylpiperidine, 4-ethoxycarbonylpiperidine, 2,6-dimethylmorpholine, 2, 5-dimethylpyrrole, more preferably dimethylamine, methyl (cyanomethyl) amine, methyl (ethoxycarbonylmethyl) amine, bis (cyanomethyl) amine, bis (ethoxycarbonylmethyl) Min, bis (2-methoxyethyl) amine, bis (2-ethoxyethyl) amine, N, O-dimethylhydroxylamine, azetidine, morpholine, thiomorpholine, N-methylpiperazine, 2-meth Oxycarbonylpyrrolidine, 3-hydroxypyrrolidine, 2-ethoxycarbonylpiperidine, 4-ethoxycarbonylpiperidine, 2,6-dimethylmorpholine.
[553] The amount of nucleophile used in the reaction is usually 0.5 to 20 mol, preferably 1 to 5 mol, based on 1 mol of compound Ix.
[554] The reaction temperature mainly depends on the reaction temperature, the raw material compound, the reaction reagent, and the kind of the solvent used, but is usually -90 ° C to 200 ° C, and preferably 0 ° C to 100 ° C.
[555] The reaction time is mainly 5 minutes to 48 hours, preferably 15 minutes to 12 hours, depending on the reaction temperature, the raw material compound, the reaction reagent and the kind of solvent used.
[556] In addition, after the end of each reaction step, whereby prior to the subsequent process, the R ¹ to R ⁷ in the functional group of the target compound of each step is are within the scope of the definitions of R ¹ to R ^7, it is possible to convert a functional group according to a conventional method.
[557] In addition, in step A-1, B-2, D-1 and E-2, when at least one of R ¹ and R ² is a chlorine atom, the chlorine atom in R ¹ or R ² in the step depending on the reaction conditions group
[558]
[559] May be substituted with, and in processes A-3, B-4, C-3 and J-5, when at least one of R ¹ and R ² is a chlorine atom, R ¹ in the process depending on the reaction conditions Alternatively, the chlorine atom in R ² may be substituted by the group OY, and in step P-3, the bromine atom at the 6-position of pyridazine ring, or, when R ² is a chlorine atom, the chlorine atom of R ² by the group OY Can be substituted.
[560] Starting compounds II of steps A and B may be commercially available, or are described, for example, in Industrial Chemistry Magazine, 1971, Vol. 74, No. 7, pages 1490-1491; Tetrahedron, 1999, Vol. 55, No. 52 , Pages 15067 to 15070; The Journal of Organic Chemistry, 1963, Vol. 28, pages 218 to 221) may be used or prepared according to these methods.
[561] Starting compounds X of steps D and E are described, for example, in Helvetica Chimica Acta, 1956, 39, 1755-1764; Monatshefte fur Chemie, 1968, 99, 15-81) , The letter u in Monatshefte fur Chemie represents u-umlaut); The method described in German Patent No. 1,912,472, filed on Nov. 12, 1970 (filed Apr. 12, 1969) (Ger. Offen. 1,912,472, 12 Nov 1970, Appl. 12 Mar 1996) can be prepared using or according to these methods. have.
[562] The phenol compound III used in process A, B, D, and E can be manufactured using a commercial thing, a well-known method, or a well-known method.
[563] 2-isobutylphenol can be prepared, for example, by the method described in the Canadian Journal of Chemistry, 1956, Vol. 34, pages 851-854.
[564] 2-pentylphenol can be prepared, for example, by the method described in Tetrahedron Letters, 1989, Vol. 30, 35, pages 4741-4744.
[565] 2-hexylphenol is described, for example, in commercially available 1-methoxy-2-vinylbenzene, in the method described in the Journal of the Chemical Society: Parkin transaction I, 2000, vol. 7, 1109-1116. Conversion of a group to a hexyl group), and the method described in the Journal of Medicinal Chemistry, 1977, Vol. 20, No. 10, pages 1317-1323 (conversion of phenylmethyl ether to phenol, demethylation reaction). can do.
[566] 2-cyclopropylphenol can be prepared, for example, by the method described in Bioorganic & Medicinal Chemistry, 1997, Vol. 5, No. 10, pages 1959-1968.
[567] 2- (1-methylcyclopropyl) phenols are described, for example, from commercially available 1- (2-methoxyphenyl) ethanone, The Journal of Organic Chemistry, 1963, Vol. 28, p. 1128 or Synthetic Communications, 1985, Vol. 15, Issue 10, pages 855-864 (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Organic Reactions, 1973, Volume 20, pages 1-131, or Journal of the Methods described in the American Chemical Society, 1975, volume 97, page 3428, or Tetrahedron Letters, 1998, volume 39, pages 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology , and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) can be prepared in accordance with the method (conversion of phenylmethyl ether to phenol, demethylation reaction). have.
[568] 2- (1-ethylcyclopropyl) phenol is described, for example, from commercially available 1- (2-methoxyphenyl) -1-propanone, The Journal of Organic Chemistry, 1963, Vol. 28, page 1128, Or the method described in Synthetic Communications, 1985, Vol. 15, No. 10, pages 855-864 (conversion of carbonyl groups to olefins, Wittig reactions), and Organic Reactions, 1973, Vol. 20, pages 1-131, Or in the Journal of the American Chemical Society, 1975, 97, 3428, or Tetrahedron Letters, 1998, 39, 8621-8624 (building cyclopropyl groups, Simmons-Smith reactions), and literature. (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) It can manufacture according to this.
[569] 2- (1-cyclopropylcyclopropyl) phenol is, for example, available from the commercially available 2,3-dihydro-4H-chromen-4-one, as described in Journal of the Chemical Society: Parkin transaction I, 1990, From cyclopropyl (2-hydroxyphenyl) methanone, which may be prepared by the method described in pages 689-693, the method described in (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838) (phenyl of phenol) Conversion to methyl ether, methylation reaction), and methods described in The Journal of Organic Chemistry, 1963, Vol. 28, p. 1128 or Synthetic Communications, 1985, Vol. 15, No. 10, pp. 855-864 Conversion to olefins, Wittig reactions, and Organic Reactions, 1973, Volume 20, pages 1-131, or Journal of the American Chemical Society, 1975, 97, 3428 pages, or Tetrahedron Letters, 1998 , Volume 39, pages 8621-8624 (Construction of cyclopropyl groups, S immons-Smith reaction), and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (with phenol of phenylmethylether). Conversion and demethylation reaction).
[570] 1- (2-hydroxyphenyl) cyclopropanecarbonitrile is described, for example, in the method described in the Journal of the American Chemical Society, 2000, Vol. 122, No. 4, pages 712-713, -Methoxyphenyl) cyclopropanecarbonitrile was prepared and prepared according to the method described in (Organic Synthesis, Collective Volume, Vol. 5, pages 412-414) (conversion of phenylmethyl ether to phenol, demethylation reaction). can do.
[571] 2- (1-phenylcyclopropyl) phenol is, for example, commercially available from 1- (2-methoxyphenyl) (phenyl) methanone, The Journal of Organic Chemistry, 1963, Vol. 28, page 1128 or Synthetic Communications, 1985, Volume 15, Issue 10, pages 855-864 (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Organic Reactions, 1973, Volume 20, pages 1-131 or Journal of the American Chemical Society, 1975, 97, 3428 pages or Tetrahedron Letters, 1998, 39, 8621-8624 (the construction of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry, 1993, No. 57, No. 9, pages 1572-1574 or Japanese Patent Laid-Open No. 11-322755) can be prepared according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction). Can be.
[572] 2- (2-methylcyclopropyl) phenol is, for example, commercially available from 1- (chloromethyl) -2-methoxybenzene (Journal of the American Chemical Society, 1973, 95, No. 2, 581). -582) (the construction of cyclopropyl groups), and the literature (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755). It can manufacture according to the method described (conversion of phenylmethyl ether to phenol, demethylation reaction).
[573] 2- (2,2-dimethylcyclopropyl) phenol is, for example, commercially available from 1- (chloromethyl) -2-methoxybenzene, Journal of the American Chemical Society, 1973, Vol. 95, No. 2 , Pages 581-582 (construction of cyclopropyl groups), and literature (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 It can manufacture according to the method (Conversion of phenylmethyl ether to a phenol, demethylation reaction) described in ().
[574] 2-[(cis-2, cis-3-dimethyl) -ref-1-cyclopropyl] phenol is, for example, commercially available from 1- (chloromethyl) -2-methoxybenzene, as described in the Journal of the American Methods described in the Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (construction of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572-1574 It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) described in the page or Unexamined-Japanese-Patent No. 11-322755.
[575] 2-[(cis-2, trans-3-dimethyl) -ref-1-cyclopropyl] phenol is, for example, commercially available 1- (chloromethyl) -2-methoxybenzene from the Journal of the American Methods described in the Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (construction of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572-1574 It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) described in the page or Unexamined-Japanese-Patent No. 11-322755.
[576] 2-[(trans-2, trans-3-dimethyl) -ref-1-cyclopropyl] phenol is, for example, commercially available 1- (chloromethyl) -2-methoxybenzene from the Journal of the American Methods described in the Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (construction of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572-1574 It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) described in the page or Unexamined-Japanese-Patent No. 11-322755.
[577] 2-[(ref-1, cis-5, cis-6) -bicyclo [3.1.0] hexa-6-yl] phenol is, for example, commercially available 1- (chloromethyl) -2-methoxybenzene From the method described in the Journal of the American Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (building of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, 57 It can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) as described in the volume, 9, 1572-1574 page or Unexamined-Japanese-Patent No. 11-322755.
[578] 2-[(ref-1, cis-5, trans-6) -bicyclo [3.1.0] hexa-6-yl] phenol is, for example, commercially available 1- (chloromethyl) -2-methoxybenzene From the method described in the Journal of the American Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (building of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, 57 It can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) as described in the volume, 9, 1572-1574 page or Unexamined-Japanese-Patent No. 11-322755.
[579] 2-[(ref-1, cis-6, cis-7) -bicyclo [4.1.0] hept-7-yl] phenol is, for example, commercially available 1- (chloromethyl) -2-methoxybenzene From the method described in the Journal of the American Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (building of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, 57 It can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) as described in the volume, 9, 1572-1574 page or Unexamined-Japanese-Patent No. 11-322755.
[580] 2-[(ref-1, cis-6, trans-7) -bicyclo [4.1.0] hept-7-yl] phenol is, for example, commercially available 1- (chloromethyl) -2-methoxybenzene From the method described in the Journal of the American Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (building of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, 57 It can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) as described in the volume, 9, 1572-1574 page or Unexamined-Japanese-Patent No. 11-322755.
[581] 2-[(2,2, cis-3-trimethyl) -ref-1-cyclopropyl] phenol is, for example, commercially available from 1- (chloromethyl) -2-methoxybenzene, as described in the Journal of the American Methods described in the Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (construction of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572-1574 It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) described in the page or Unexamined-Japanese-Patent No. 11-322755.
[582] 2-[(2,2, trans-3-trimethyl) -ref-1-cyclopropyl] phenol is, for example, available from commercially available 1- (chloromethyl) -2-methoxybenzene, as described in the Journal of the American Methods described in the Chemical Society, 1973, Vol. 95, No. 2, pages 581-582 (construction of cyclopropyl groups), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572-1574 It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) described in the page or Unexamined-Japanese-Patent No. 11-322755.
[583] 2-cyclobutylphenol can be prepared, for example, by the method described in German patent DE-2825388.
[584] 1- (2-hydroxyphenyl) cyclobutanecarbonitrile can be prepared, for example, by the method described in the Pharmaceutical Chemistry Journal (English Translation), 1980, Vol. 14, No. 2, pages 114-118. .
[585] 1- (2-hydroxyphenyl) cyclobutanecarboxylic acid can be prepared, for example, by the method described in the Pharmaceutical Chemistry Journal (English Translation), 1980, Vol. 14, No. 2, pages 114-118. .
[586] 2- (1-propynyl) phenol can be prepared, for example, by the method described in Journal of the Chemical Society: Parkin transaction I, 1998, pages 477-484.
[587] 2- (cyclopropylmethyl) phenol is, for example, available from the commercially available 2,3-dihydro-4H-chromen-4-one, as described in Journal of the Chemical Society: Parkin transaction I, 1990, 689-693 From cyclopropyl (2-hydroxyphenyl) methanone which can be prepared by the method described in page), it can be prepared according to the method described in Organic Reactions (1941, Vol. 1, p. 155) (Clemmensen reduction). .
[588] 2- (methoxymethyl) phenol can be prepared, for example, by the method described in Tetrahedron Letters, 1999, Vol. 40, p. 6049.
[589] 2- (ethoxymethyl) phenol can be prepared, for example, by the method described in Tetrahedron Letters, 1999, Vol. 40, p. 6049.
[590] 2- (1,3-dioxolan-2-yl) phenol can be prepared, for example, by the method described in Tetrahedron Letters, 1989, Vol. 30, No. 13, pages 1609-1612.
[591] 1- (2-hydroxyphenyl) ethanone O-methyloxime is described, for example, from commercially available 1- (2-hydroxyphenyl) ethanone (Journal of the American Chemical Society, 1986, vol. 108, Page 6016-6023).
[592] 3 '-(trifluoromethyl) [1,1'-biphenyl] -2-ol is, for example, commercially available from 2-iodophenol and 3- (trifluoromethyl) phenylboronic acid. It can be manufactured according to the method (phenylation reaction, Suzuki-Miyaura coupling reaction) described in Chemical Reviews, 1995, 95, 2457-2483.
[593] 2- (1H-pyrrole-1-yl) phenol can be prepared, for example, by the method described in The Journal of Antibiotics, 1994, Vol. 47, No. 5, pages 602-605.
[594] 2- (2-thienyl) phenol can be prepared, for example, by the method described in the Journal of Heterocyclic Chemistry, 1985, Vol. 22, pages 1667-1669.
[595] 2- (3-thienyl) phenol can be prepared, for example, by the method described in Journal of Heterocyclic Chemistry, 1985, Vol. 22, pages 1667-1669.
[596] 2- (1H-pyrazol-1-yl) phenol can be prepared, for example, by the method described in the Canadian Journal of Chemistry, 1963, Vol. 41, pages 2086-2092.
[597] 2- (3,5-dimethyl-1H-pyrazol-1-yl) phenol can be prepared, for example, by the method described in Heterocycles, 1982, Vol. 19, No. 8, pages 1487-1495.
[598] 2- [3- (trifluoromethyl) -1H-pyrazol-1-yl] phenol is, for example, commercially available from 1- (2-methoxyphenyl) hydrazine hydrochloride, Journal of Fluorine Chemistry 1998 1, (2-methoxyphenyl) -3- (trifluoromethyl) -1H-pyrazole was prepared by the method described in (1992, p. 23), and (Organic Synthesis, Collective Volume, Volume 5, pages 412-414) can be produced according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction).
[599] 2- [4- (trifluoromethyl) -1H-pyrazol-1-yl] phenol is, for example, commercially available from 1- (2-methoxyphenyl) hydrazine hydrochloride, Tetrahedron Letters, 1996 , 37, 11, p. 1829, to prepare 1- (2-methoxyphenyl) -4- (trifluoromethyl) -1H-pyrazole, and (Organic Synthesis, Collective Volume). , Vol. 5, pp. 412-414), and the method (conversion of phenylmethyl ether to phenol, demethylation reaction).
[600] 2- [5- (trifluoromethyl) -1H-pyrazol-1-yl] phenol is, for example, commercially available from 1- (2-methoxyphenyl) hydrazine hydrochloride, as described in Journal of Fluorine Chemistry, 1- (2-methoxyphenyl) -5- (trifluoromethyl) -1H-pyrazole was prepared by the method described in 1998, vol. 92, p. 23, and described in Organic Synthesis, Collective Volume, Volume 5, pages 412-414) can be manufactured according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction).
[601] 5- (2-hydroxyphenyl) -N, N-dimethyl-1H-pyrazole-1-sulfonamide is for example from commercial 4-chloro-2- (1H-pyrazol-5-yl) phenol , 3- (5-chloro-2-hydroxyphenyl) -N, N-dimethyl, which may be prepared according to the method described in Journal of Medicinal Chemistry, 1998, Volume 41, No. 12, pages 2019-2028. From -1H-pyrazole-1-sulfonamide, it can manufacture according to the method (contact hydrogenation reaction) described in the literature (Experimental chemistry course 4th edition 26 volume 251-266 pages).
[602] 3- (2-hydroxyphenyl) -N, N-dimethyl-1H-pyrazole-1-sulfonamide is for example from commercial 4-chloro-2- (1H-pyrazol-5-yl) phenol , 3- (5-chloro-2-hydroxyphenyl) -N, N-dimethyl, which may be prepared according to the method described in Journal of Medicinal Chemistry, 1998, Volume 41, No. 12, pages 2019-2028. From -1H-pyrazole-1-sulfonamide, it can manufacture according to the method (contact hydrogenation reaction) described in the literature (Experimental chemistry course 4th edition 26 volume 251-266 pages).
[603] 2- (4-methyl-1,3-thiazol-2-yl) phenol is, for example, a method described in Japanese Patent Laid-Open No. 11-60552 (from cyano groups) from commercial 2-hydroxybenzonitrile. Thioamidation reaction) and Liebigs Annalen der Chemie, 1890, vol. 259, page 236.
[604] 2- (1,3-benzothiazol-2-yl) phenol can be prepared, for example, by the method described in The Journal of Organic Chemistry, 1970, Vol. 35, pages 3147-3149.
[605] 2- (dimethylamino) phenol can be prepared, for example, by the method described in Journal of Medicinal Chemistry, 1998, Vol. 41, pages 4800-4818.
[606] 2- (2-methoxyethoxy) phenol can be prepared, for example, from commercial pyrocatechol according to the method described in Journal of the Chemical Society: Parkin transaction I, 1980, pages 756-758. Can be.
[607] 2- (isopropylsulfanyl) phenol can be prepared, for example, by the method described in Tetrahedron, 1970, Vol. 26, pages 4449-4471.
[608] 3-cyclopropylphenol is, for example, from commercially available 1-bromo-3-methoxybenzene (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255) (the construction of cyclopropyl groups, Suzuki-Miyaura coupling reaction) and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, No. 9, page 1572-1574, or Japanese Patent Laid-Open (Hei) 11-322755) (phenylmethyl ether To phenol, demethylation reaction).
[609] 3- (2-furyl) phenol is a 2- (3-methoxyphenyl) furan by the method described, for example, in The Journal of Organic Chemistry, 1993, Vol. 58, No. 17, pages 4722-4726. And the process described in Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (conversion of phenylmethyl ether to phenol, Demethylation reaction).
[610] 4-cyclopropylphenol is, for example, from the commercially available 1-bromo-4-methoxybenzene (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255), the method described in the construction of the cyclopropyl group, Suzuki-Miyaura coupling reaction) and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, No. 9, page 1572-1574, or Japanese Patent Laid-Open (Hei) 11-322755) (phenylmethyl ether To phenol, demethylation reaction).
[611] 2-bromo-3-methylphenols are described, for example, from commercial 2-methoxy-6-methylaniline, in Organic Synthesis, Collective Volume, Vol. 3, pages 185-187; The Journal of Organic Chemistry, 1977, Vol. 42, pages 2426-2430 (Aniline Conversion to Bromobenzene, Sandmeyer Reaction, etc.), and Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572 It can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) described in -1574 page or Unexamined-Japanese-Patent No. 11-322755.
[612] 3-fluoro-2-methylphenol can be prepared according to the method described in commercial 3-fluoro-2-methylbenzaldehyde from the Journal of the Chemical Society: Parkin transaction I, 1974, page 1353. .
[613] 3-Chloro-2-methylphenol was prepared from commercially available 1-chloro-3-methoxy-2-methylbenzene by the method described in Organic Synthesis, Collective Volume, Vol. 5, pages 412-414 (phenylmethyl ether To phenol, demethylation reaction).
[614] 3-methoxy-2-methylphenol is prepared from commercial 2-methyl-1,3-benzenediol (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838) (phenyl phenyl ether of phenol). And conversion to methylation reaction).
[615] 2-cyclopropyl-3-methylphenols are described, for example, from commercial 2-methoxy-6-methylaniline, in Organic Synthesis, Collective Volume, Vol. 3, pages 185-187; The Journal of Organic Chemistry, 1977, Vol. 42, pages 2426-2430 (Aniline Conversion to Bromobenzene, Sandmeyer Reaction, etc.), and Tetrahedron Letters, 1979, Vol. 20, pages 4159-4162; Tetrahedron, 1997 , 53, 43, pages 14599-14614; or Bulletin of the Chemical Society of Japan, 1971, Vol. 44, pages 2237-2248 (conversion reaction of aromatic bromide with aromatic aldehydes), and literature (The Journal of Organic Chemistry, 1963, 28, 1128; Synthetic Communications, 1985, 15, 10, 855-864) (Conversion of Carbonyl Group to Olefin, Wittig Reaction), and Literature (Organic Reactions, 1973, Volume 20, pages 1-131 or Journal of the American Chemical Society, 1975, Volume 97, page 3428 or Tetrahedron Letters, 1998, Volume 39, pages 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry , 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755, and the method (conversion of phenylmethyl ether to phenol, demethylation reaction).
[616] 2-cyclopropyl-3-methoxyphenols are described, for example, from commercially available 2,6-dimethoxybenzaldehyde, in The Journal of Organic Chemistry, 1963, Vol. 28, page 1128 or Synthetic Communications, 1985, 15 Vol. 10, pages 855-864 (conversion of carbonyl groups to olefins, Wittig reaction), and Organic Reactions, 1973, Volume 20, pages 1-131 or Journal of the American Chemical Society, 1975 Year 97, page 3428 or Tetrahedron Letters, 1998, Volume 39, pages 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry, 1993 , No. 57, No. 9, pages 1572-1574 or Japanese Patent Application Laid-Open No. Hei 11-322755 can be prepared according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction).
[617] 4-indanol can be produced, for example, from commercial 4-hydroxy-1-indanone according to the method described in Organic Reactions (1941, Vol. 1, page 155) (Clemmensen reduction).
[618] 3-methyl-4-indanol can be prepared, for example, by the method described in the Journal of Applied Chemistry, 1959, Vol. 9, pp. 629, 637.
[619] 1-Methyl-4-indanol can be prepared, for example, by the method described in the Journal of the Chemical Society, 1961, pages 2773-2777.
[620] 2,2-dimethyl-4-indanol can be prepared, for example, by the method described in the Journal of Chemical Research Miniprint, 1985, Vol. 8, pages 2724-2747.
[621] Spiro [cyclopropane-1,3 '-(2', 3'-dihydro-1'H-indene-4'-ol)] is, for example, a commercial 2,3-dihydro-4H-chromen From 4-ols, the methods described in Bioorganic and Medicinal Chemistry, 1999, Vol. 7, 12, pages 2801-2810 (synthesis of 7-hydroxy-1-indanon), and Organic Synthesis, Collective Volume, Volume 4, pages 836-838 (Conversion of Phenols to Phenylmethylether, Methylation Reactions), and The Journal of Organic Chemistry, 1963, Vol. 28, 1128 or Synthetic Communications, 1985. , 15, 10, pages 855-864 (Conversion of Carbonyl Group to Olefin, Wittig Reaction), and Organic Reactions, 1973, 20, 1-131 or Journal of the American Chemical Society, 1975, Vol. 97, page 3428 or Tetrahedron Letters, 1998, Vol. 39, pages 8621-8624 (building cyclopropyl groups, Simmons-Smith reactions), and statements. Method described in second-hand (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) (conversion of phenylmethyl ether to phenol, demethylation reaction) It can manufacture according to this.
[622] 7-hydroxy-2,3-dihydro-1H-inden-1-one O-methyloxime is, for example, commercially available from 2,3-dihydro-4H-chromen-4-ol, see Bioorganic and Medicinal Chemistry, 1999, Vol. 7, 12, pages 2801-2810 (synthesis of 7-hydroxy-1-indanon), and Organic Synthesis, Collective Volume, Vol. 4, 836-838 The method described in pages (conversion of phenol to phenylmethyl ether, methylation reaction) and the method described in Chemical Pharmaceutical Bulletin, 1988, Vol. 36, No. 8, pages 3134-3137 (Conversion of Carbonyl Group to Oxime). ) And the method described in Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (Conversion of Phenylmethyl Ether to Phenol, Removal Methylation reaction).
[623] 2,3-dihydro-1-benzofuran-4-ol is, for example, 1-benzofuran-4-ol obtained by the method described in Helvetica Chimica Acta, 1933, Vol. 16, pages 121-129. From (Journal of the Chemical Society, 1948, p. 894) can be prepared by the method (reduction reaction of olefins).
[624] 3-methyl-2,3-dihydro-1-benzofuran-4-ol can be prepared, for example, by the method described in the Journal of the Chemical Society, 1951, pages 3229-3234. From -1-benzofuran-4-ol, it can manufacture according to the method (reduction reaction of an olefin) described in the Journal of the Chemical Society, 1948, page 894.
[625] 1-benzofuran-4-ol is obtained, for example, by the method described in Helvetica Chimica Acta, 1933, Vol. 16, pages 121-129.
[626] 3-methyl-1-benzofuran-4-ol can be prepared, for example, by the method described in the Journal of the Chemical Society, 1951, pages 3229-3234.
[627] 1-benzothiophen-4-ol can be prepared, for example, by the method described in the Journal of the American Chemical Society, 1935, Vol. 57, pages 1611-1615.
[628] 2-methyl-1,3-benzoxazol-4-ol can be prepared according to the method described, for example, in Journal of Medicinal Chemistry, 1987, Vol. 30, No. 1, pages 62-67. .
[629] 2,3-dihydro-1-benzofuran-7-ol is described in the Journal of the Chemical Society, 1948, page 894, for example, from commercially available 7-methoxy-1-benzofuran. (Hydrogenation reaction of benzofuran), and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, No. 9, 1572-1574 or Japanese Patent Laid-Open (Hai) 11-322755) (phenylmethyl ether To phenol, demethylation reaction).
[630] 1-benzofuran-7-ol can be obtained from, for example, commercially available 7-methoxy-1-benzofuran (Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 or Japan). It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) as described in patent publication (patent) 11-322755).
[631] 1,3-benzodioxol-4-ols are described, for example, from commercial 1,2,3-benzenetriols (Chemical Pharmaceutical Bulletin, 1981, Vol. 29, No. 10, pages 2893-2898). It may be prepared by the method described.
[632] 2,3-dihydro-1,4-benzodioxin-5-ols are described, for example, from commercial 1,2,3-benzenetriols, in the Journal of the Chemical Society: Parkin transaction I, 1988. , Pages 511 to 520).
[633] 2-methyl-1,3-benzoxazol-7-ol is described, for example, from commercial 3-nitro-1,2-benzenediol (Liebigs Annalen der Chemie, 1957, Vol. 608, p. 128). It can manufacture according to the method as described in (reduction reaction of a nitro group to an amino group), and the method as described in Journal of Medicinal Chemistry, 1987, Vol. 30, No. 1, pages 62-67.
[634] 2-bromo-4-tert-butylphenol can be prepared, for example, by the method described in Tetrahedron, 1999, Vol. 55, No. 28, pages 8377-8384.
[635] 2-ethyl-4-iodophenol can be prepared from commercial 2-ethylphenol by the method described in The Journal of Organic Chemistry, 1951, Vol. 16, pages 1117-1120.
[636] 4-Bromo-2-isopropylphenol can be prepared, for example, by the method described in Journal of Medicinal Chemistry, 1971, Vol. 14, No. 9, pages 789-792.
[637] 3-cyclopropyl-4-methylphenol is described, for example, in commercially available 2-bromo-1-methoxy-4-methylbenzene (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255). Method (Construction of Cyclopropyl Group, Suzuki-Miyaura Coupling Reaction) and Literature (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, No. 1572-1574 or Japanese Patent Laid-Open No. 11-322755) It can manufacture according to the method as described in (the conversion of phenylmethyl ether to a phenol, demethylation reaction).
[638] 5- (dimethylamino) -2-methylphenol can be prepared, for example, by the method described in the Journal of the Chemical Society, 1947, pages 182-191.
[639] 5-methoxy-2-methylphenol can be prepared, for example, by the method described in Chemical Abstracts, 1938, page 2519.
[640] 2-ethyl-5-methoxyphenol can be prepared, for example, by the method described in Chemical and Phamaceutical Bulletin, 1979, Vol. 27, No. 6, pages 1490-1494.
[641] 2,5-Diisopropylphenol can be prepared, for example, by the method described in The Journal of Organic Chemistry, 1980, Vol. 45, No. 22, pages 4326-4329.
[642] 2-cyclopropyl-5-fluorophenols are described, for example, by commercially available 2-bromo-5-fluorophenols (Helvetica Chimica Acta, 1992, Vol. 75, p. 457). Conversion to phenylmethoxymethyl ether, methoxymethylation reaction), and the method described in Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255 (Construction of cyclopropyl group, Suzuki-Miyaura coupling reaction) , And the method described in (Tetrahedron, 1998, Vol. 54, pages 15861-15869) (conversion of phenylmethoxymethyl ether to phenol, demethoxymethylation reaction).
[643] 5-chloro-2-cyclopropylphenol is described, for example, from commercial 4-chloro-2-methoxyphenol (The Journal of Organic Chemistry, 1997, Vol. 62, No. 2, pages 261-274). The method described (trifluoromethanesulfonylation of phenol), and the method described (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255) (construction of cyclopropyl groups, Suzuki-Miyaura coupling reaction), and Method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (Conversion of Phenylmethyl Ether to Phenol, Demethylation Reaction) It can manufacture according to this.
[644] 2-cyclopropyl-5-methylphenol is described, for example, from commercial 2-methoxy-4-methylphenol, in The Journal of Organic Chemistry, 1997, Vol. 62, No. 2, pages 261-274. The method described (trifluoromethanesulfonylation of phenol), and the method described (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255) (construction of cyclopropyl groups, Suzuki-Miyaura coupling reaction), and Method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (Conversion of Phenylmethyl Ether to Phenol, Demethylation Reaction) It can manufacture according to this.
[645] 2-cyclopropyl-5-ethylphenol is described, for example, from commercial 4-ethyl-2-methoxyphenol, The Journal of Organic Chemistry, 1997, Vol. 62, No. 2, pages 261-274. The method described (trifluoromethanesulfonylation of phenol), and the method described (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255) (construction of cyclopropyl groups, Suzuki-Miyaura coupling reaction), and Method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (Conversion of Phenylmethyl Ether to Phenol, Demethylation Reaction) It can manufacture according to this.
[646] 2-cyclopropyl-5-isopropylphenol is, for example, the method described in commercially available 3-isopropylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation reaction of phenol), and Methods described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (Conversion of Phenols to Phenylmethoxymethyl Ether, Methoxymethylation Reaction), and Tetrahedron Letters, 2000, 41, 4251-. The method described in the construction of a cyclopropyl group, the Suzuki-Miyaura coupling reaction, and the method described in the literature (Tetrahedron, 1998, Vol. 54, pages 15861-15869) with phenols of phenylmethoxymethylether Conversion and demethoxymethylation reaction).
[647] 4-cyclopropyl-3-hydroxybenzonitrile is described, for example, from commercial 4-hydroxy-3-methoxybenzonitrile, The Journal of Organic Chemistry, 1997, Vol. 62, No. 2, 261-. Page 274) (trifluoromethanesulfonylation of phenol), and the method described in the literature (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255) (Construction of cyclopropyl groups, Suzuki-Miyaura coupling) Reaction) and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (conversion of phenylmethyl ether to phenol, Demethylation reaction).
[648] 5-Fluoro-2-[(1E) -1-propenyl] phenol is described, for example, in the process described in the Journal of the Chemical Society: Parkin transaction I, 1994, pages 1823-1831. Rho-2-hydroxybenzaldehyde synthesis), and the methods described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenol to phenylmethyl ether, methylation reaction), and Synthetic Communications, 1985, Vol. 15, No. 10, pages 855-864 (conversion of carbonyl groups to olefins, Wittig reaction), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, It can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) as described in page 1572-1574 or Unexamined-Japanese-Patent No. 11-322755.
[649] 5-chloro-2-[(1E) -1-propenyl] phenol is described, for example, in the method described in The Journal of Organic Chemistry, 1964, Vol. 29, pages 2693-2698 (4-chloro-2). -Synthesis of hydroxybenzaldehyde), and the method described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenol to phenylmethyl ether, methylation reaction), Synthetic Communications, 1985 , 15, 10, pages 855-864 (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1157-1574 Or it can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) of Unexamined-Japanese-Patent No. 11-322755.
[650] 4- (dimethylamino) -2-hydroxybenzaldehyde can be produced, for example, by the method described in German patent DE 105103.
[651] 5-chloro-2-methoxyphenol is a method described in the literature (Organic Synthesis, Collective Volume, Vol. 2, pages 130-133), for example, from commercial 5-amino-2-methoxyphenol (aniline) To chlorobenzene, Sandmeyer reaction and the like).
[652] 5-bromo-2-methoxyphenols are described, for example, from commercial 5-amino-2-methoxyphenols (Organic Synthesis, Collective Volume, Vol. 3, pages 185-187; or The Journal of Organic). Chemistry, 1977, Vol. 42, pages 2426-2430), and can be manufactured according to the method (conversion of aniline to bromobenzene, Sandmeyer reaction, etc.).
[653] 3-hydroxy-4-methoxybenzonitrile can be prepared, for example, from commercially available methyl 3,4-dimethoxybenzoate by the method described in Synthesis, 1998, pages 329-332.
[654] 2,5-dimethoxyphenol can be prepared, for example, by the method described in The Journal of Organic Chemistry, 1987, Vol. 57, p. 4485.
[655] 2-Bromo-6-fluorophenol is, for example, from commercial 2-fluorophenols according to the method described in the literature (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation of phenol). It can manufacture.
[656] 2-Fluoro-6-propylphenol is described, for example, from commercial 2-fluorophenols, in the process described in Organic Reactions, 1949, Vol. 2, pages 1-48 (allylation of phenols, Claisen transitions). Reaction) and the method described in the Journal of the American Chemical Society, 1951, Vol. 73, pages 4152-4156 (conversion of allyl groups to propyl groups, hydrogenation reaction).
[657] 2-Fluoro-6-isopropylphenol is a method described in (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838), for example, from commercial 2-isopropyl-6-nitrophenol. Conversion to phenylmethyl ether, methylation reaction), the method described in Liebigs Annalen der Chemie (1975, 608, p. 128) (reduction reaction of nitro groups to amino groups), (Synthesis, 1989, 905) (Method of converting amino groups to fluorine atoms), and literature (Bioscience, Biotechnolory, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) It can manufacture according to the method (Conversion of phenylmethyl ether to a phenol, demethylation reaction) described in ().
[658] 2-cyclopropyl-6-fluorophenol is, for example, the method described in commercially available 2-fluorophenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation reaction of phenol), and Methods described in Helvetica Chemica Acta, 1992, Vol. 75, p. 457 (Conversion of Phenols to Phenylmethoxymethyl Ether, Methoxymethylation Reaction), and Tetrahedron Letters, 2000, 41, 4251- The method described in the construction of a cyclopropyl group, the Suzuki-Miyaura coupling reaction, and the method described in the literature (Tetrahedron, 1998, Vol. 54, pages 15861-15869) with phenols of phenylmethoxymethylether Conversion and demethoxymethylation reaction).
[659] 2-chloro-6-iodophenol can be prepared, for example, by the method described in The Journal of Organic Chemistry, 1988, Vol. 53, No. 22, pages 5281-5287.
[660] 2-Chloro-6-ethylphenol can be prepared, for example, by the method described in Journal of Chemical and Engineering Data, 1969, Vol. 14, page 392.
[661] 2-chloro-6-cyclopropylphenol is described, for example, from commercial 2-chlorophenols (Tetrahedron Letters, 1998, Vol. 39, p. 2947) described in the method (bromolation of phenol), and literature ( Helvetica Chimica Acta, 1992, Vol. 75, pages 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255 ) (Constitution of cyclopropyl groups, Suzuki-Miyaura coupling reaction), and the method (Tetrahedron, 1998, Vol. 54, pages 15861-15869) and the conversion of phenylmethoxymethylether to phenol And demethoxymethylation reaction).
[662] 2-chloro-6- (2-methyl-2-propenyl) phenol is described, for example, from commercial 2-chlorophenols, as described in Organic Reactions, 1949, Vol. 2, pages 1-48. Phenol allylation, Claisen transition reaction).
[663] 2-bromo-6-methylphenol can be prepared, for example, by the method described in Tetrahedron Letters, 1998, Vol. 39, p. 2947.
[664] 2-bromo-6-ethylphenol can be prepared, for example, from commercial 2-ethylphenol according to the method described in the literature (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation of phenol). Can be.
[665] 2-Bromo-6-cyclopropylphenol is, for example, the method described in the literature (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838) from commercially available 2,6-dibromophenol (of phenol Conversion to phenylmethyl ether, methylation reaction), and methods described in Tetrahedron Letters, 2000, 41, pages 4251-4255 (building of cyclopropyl groups, Suzuki-Miyaura coupling reactions), and literature ( In accordance with the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (conversion of phenylmethyl ether to phenol, demethylation reaction). It can manufacture.
[666] 3-Bromo-2-hydroxybenzonitrile is, for example, a method described in commercially available 2-hydroxybenzonitrile (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation reaction of phenol) It can manufacture according to this.
[667] 2-bromo-6-methoxyphenol can be prepared, for example, by the method described in Synthesis, 1999, Vol. 7, pp. 1127-1134.
[668] 2-iodo-6-methylphenol can be prepared, for example, by the method described in the Australian Journal of Chemistry, 1997, Vol. 50, No. 7, pp. 767-770.
[669] 2-ethyl-6-iodophenol is commercially available from 2-ethylphenol according to the method (iodization reaction of phenol) described in the Australian Journal of Chemistry, 1997, Vol. 50, No. 7, pp. 767-770. It can manufacture.
[670] 2-iodo-6-isopropylphenol is a commercially available 2-isopropylphenol, described in the Australian Journal of Chemistry, 1997, Vol. 50, No. 7, No. 767-770 (phenol iodide reaction). It can manufacture according to this.
[671] 2-isopropyl-6-methylphenol can be prepared, for example, by the method described in Bulletin de la Societe Chemique de France, 1962, pages 1700-1705.
[672] 2-s-butyl-6-methylphenol can be prepared, for example, by the method described in Angelwandte Chemie, 1957, Vol. 69, page 699, page 703. Also, for example, from commercial 2-methylphenols, the methods described in Organic Reactions (1949, Vol. 2, pages 1-48) (allylation of phenols, Claisen transition reactions), and the Journal of the It can also manufacture according to the method (Conversion of an allyl group to a propyl group, hydrogenation reaction) described in American Chemical Society, 1951, Vol. 73, pages 4152-4156.
[673] 2-cyclopropyl-6-methylphenol is, for example, commercially available 2-hydroxy-3-methylbenzaldehyde from the method described in (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838). Conversion to phenylmethyl ether, methylation reactions, and the methods described in The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, pages 855-864 Conversion of Carbonyl Groups to Olefins, Wittig Reactions, and Organic Reactions, 1973, 20, 1-131 or Journal of the American Chemical Society, 1975, 97, 3428 or Tetrahedron Letters, 1998, 39, pp. 8621-8624 (the construction of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Of the method described in Published (Pri) 11-322755 To phenol, and demethylation reaction).
[674] 2-methoxy-6-methylphenol is described, for example, in commercially available 1,2-dimethoxy-3-methylbenzene (Synthetic Communications, 1996, Vol. 26, No. 1, pages 49-62). It can manufacture by a method.
[675] 2,6-diethylphenol can be prepared, for example, by the method described in Journal of Medicinal Chemistry, 1960, Vol. 2, pages 201-212.
[676] 2-cyclopropyl-6-ethylphenol is, for example, commercially available 2-ethylphenol, described in the method (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation reaction of phenol), and literature ( Helvetica Chimica Acta, 1992, Vol. 75, pages 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255 ) (Constitution of cyclopropyl groups, Suzuki-Miyaura coupling reaction), and the method (Tetrahedron, 1998, Vol. 54, pages 15861-15869) and the conversion of phenylmethoxymethylether to phenol And demethoxymethylation reaction).
[677] 2,6-dipropylphenols are described, for example, in the methods described in Liebigs Annalen der Chemie, 1919, Vol. 418, pages 90-91 (synthesis of 2,6-diallylphenol), and in Bulletin de It can be produced by the method described in la Societe Chemique de France, 1937, Vol. 5, No. 4, pages 1080-1083 (conversion of allyl groups to propyl groups, hydrogenation reactions).
[678] 3-cyclopropyl-6-isopropylphenol is described, for example, in the process described in the Journal of the Chemical Society: Parkin transaction I, 1980, pages 1862-1865 (2-hydroxy-3-isopropylbenzaldehyde). Synthesis), and the methods described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenols to phenylmethyl ether, methylation reactions), and The Journal of Organic Chemistry, 1963, 28, page 1128 or Synthetic Communications, 1985, 15, 10, pages 855-864 (conversion of carbonyl groups to olefins, Wittig reactions), and Organic Reactions, 1973, 20, Pages 1-131 or Journal of the American Chemical Society, 1975, 97, 3428 or Tetrahedron Letters, 1998, 39, 8621-8624 (building cyclopropyl groups, Simmons-Smith reactions) , And Bioscience, Biotechnology, and Biochemistry, 1993 Can be prepared according to vol. 57, No. 9, pp. 1572-1574 or Japanese Provisional Patent Publication No. 11-322755), methods (transformation, demethylation reaction of phenylmethyl ether into phenol described).
[679] 3-tert-butyl-6-cyclopropylphenol is described, for example, in commercial 3-tert-butyl-2-hydroxybenzaldehyde, as described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838. Method (Conversion of Phenol to Phenylmethylether, Methylation Reaction), and the Journal of Organic Chemistry, 1963, Vol. 28, page 1128 or Synthetic Communications, 1985, Vol. 15, Issue 10, pages 855-864 Methods described in (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Organic Reactions, 1973, 20, pages 1-131 or Journal of the American Chemical Society, 1975, 97, 3428 or Tetrahedron Letters , 1998, 39, pages 8621-8624 (building of cyclopropyl groups, Simmons-Smith reaction), and Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 Page or the method described in Japanese Patent Laid-Open No. 11-322755 (to phenylmethyl It can be produced according to the conversion of ter to phenol, demethylation reaction.
[680] 2,6-dicyclopropylphenol is described, for example, in the method described in Tetrahedron Letters, 1997, Vol. 38, 17, pages 3111-3114 (synthesis of 2-hydroxyisophthalaldehyde), and literature ( Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (Conversion of Phenol to Phenylmethylether, Methylation Reaction), and The Journal of Organic Chemistry, 1963, Vol. 28, p. 1128 or Synthetic Communications, 1985, Volume 15, Issue 10, pages 855-864 (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Organic Reactions, 1973, Volume 20, pages 1-131 or Journal of the American Chemical Society, 1975, 97, 3428 pages or Tetrahedron Letters, 1998, 39, 8621-8624 (the construction of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 It can be produced according to Japanese Unexamined Patent Publication (Kokai) method described in 11-322755) (conversion of phenylmethyl ether into phenol, demethylation reaction).
[681] 2-cyclopropyl-6-methoxyphenol is described, for example, in commercially available 2-hydroxy-3-methoxybenzaldehyde (Helvetica Chimica Acta, 1992, Vol. 75, p. 457). Conversion to phenylmethoxymethyl ether, methoxymethylation reactions, and The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, 855-864 Methods described in (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Organic Reactions, 1973, 20, pages 1-131 or Journal of the American Chemical Society, 1975, 97, 3428 or Tetrahedron Letters , 1998, Vol. 39, pages 8621-8624 (the construction of cyclopropyl groups, Simmons-Smith reaction), and the method described in Tetrahedron, 1998, Vol. 54, pages 15861-15869 Conversion of oxymethyl ether to phenol, demethoxymethylation reaction) Can be prepared.
[682] 2-cyclopropyl-6-ethoxyphenol can be prepared by, for example, the method described in commercially available 3-ethoxy-2-hydroxybenzaldehyde (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838). Conversion of phenols to phenylmethyl ethers, methylation reactions, and the Journal of Organic Chemistry, 1963, Vol. 28, p. 1128 or Synthetic Communications, 1985, Vol. 15, No. 10, pp. 855-864 Methods (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Organic Reactions, 1973, Volume 20, pages 1-131 or Journal of the American Chemical Society, 1975, 97 pages 3428 or Tetrahedron Letters, 1998 (39), pages 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (phenyl methyl ether) The conversion of a phenol can be produced in accordance with the demethylation reaction).
[683] 2,6-di [(1E) -1-propenyl] phenol is described, for example, in the method described in Liebigs Annalen der Chemie, 1919, vol. 418, pages 90-91 (2,6-diallylphenol) Synthesis), and the method (isomerization reaction) described in the Journal of the American Chemical Society, 1956, Vol. 78, pages 1709-1713.
[684] 2,6-diallylphenol can be prepared, for example, by the method described in Liebigs Annalen der Chemie, 1919, Vol. 418, pages 90-91.
[685] 3,5-Diisopropylphenol can be prepared, for example, by the method described in US Pat. No. 27,90010.
[686] 2-Bromo-3,5-dimethylphenol was prepared from commercially available 3,5-dimethylphenol (Bulletin of the Chemical Society of Japan, 1993, Vol. 66, p. 1576) (the bromination reaction of phenol) Can be prepared according to
[687] 3,5-dimethyl-2-propylphenol can be prepared, for example, by the method described in Bulletin of the Chemical Society of Japan, 1968, Vol. 41, No. 3, pages 745-746.
[688] 2-cyclopropyl-3,5-dimethylphenol is a method described in the literature (Tetrahedron Letters, 1998, Vol. 39, p. 2947), for example, from commercial 3,5-dimethylphenol (bromolation of phenol) , And methods described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenols to phenylmethyl ether, methylation reactions), and Tetrahedron Letters, 1979, Vol. 20, 4159- 4162 pages; Tetrahedron, 1997, Vol. 53, No. 43, pages 14599-14614; or Bulletin of the Chemical Society of Japan, 1971, Vol. 44, pages 2237-2248 (aromatic aldehydes of aromatic bromide Conversion reaction), and the method described in The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, 855-864 (Conversion of Carbonyl Groups to Olefins). , Wittig Reactions, and Organic Reactions, 1973, 20, pp. 1-131 Or the method described in the Journal of the American Chemical Society, 1975, 97, 3428 or Tetrahedron Letters, 1998, 39, 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and literature ( In accordance with the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (conversion of phenylmethyl ether to phenol, demethylation reaction). It can manufacture.
[689] 3,5-dimethyl-2- (methylsulfanyl) phenol can be prepared, for example, by the method described in Tetrahedron Letters, 1999, Vol. 40, No. 35, pages 6357-6358.
[690] 2-bromo-3,6-dimethylphenol is described, for example, from commercially available 3,6-dimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation of phenol) It can manufacture according to this.
[691] 6-Bromo-3-fluoro-2-methylphenol is, for example, commercially available 3-fluoro-2-methylbenzaldehyde, from the Journal of the Chemical Society: Parkin transaction I, 1974, page 1353. From 3-fluoro-2-methylphenol that can be prepared according to the method described in (Tetrahedron Letters, 1998, Vol. 39, p. 2947), the method described in (bromolation reaction of phenol), and the literature (Organic Synthesis) , Collective Volume, Volume 4, pages 836-838 (conversion of phenols to phenylmethyl ether, methylation reactions) and methods described in Tetrahedron Letters, 2000, 41, pages 4251-4255 Construction of Cyclopropyl Group, Suzuki-Miyaura Coupling Reaction), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, page 1572-1574 or Japanese Patent Laid-Open No. 11-322755 According to the method described (conversion of phenylmethyl ether to phenol, demethylation reaction) It can manufacture.
[692] 6-Bromo-3-chloro-2-methylphenol is prepared from commercially available 1-chloro-3-methoxy-2-methylbenzene, described in Organic Synthesis, Collective Volume, Vol. 5, pages 412-414. From 3-chloro-2-methylphenol which can be produced according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction), the method described in (Tetrahedron Letters, 1998, 39, 2947 pages) Can be produced in accordance with the bromolation reaction of.
[693] 3-Chloro-6-cyclopropyl-2-methylphenol is described in commercial Synthesis, Collective Volume, Vol. 5, pages 412-414 from commercially available 1-chloro-3-methoxy-2-methylbenzene. From 3-chloro-2-methylphenol which can be produced according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction), the method described in (Tetrahedron Letters, 1998, 39, 2947 pages) Bromination reaction) and the method described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 2000 , 41, pages 4251-4255) (the construction of cyclopropyl groups, the Suzuki-Miyaura coupling reaction), and the methods described in the literature (Tetrahedron, 1998, Vol. 54, pages 15861-15869) Conversion of oxymethyl ether to phenol, demethoxymethylation reaction) There.
[694] 6-Bromo-2,3-dimethylphenol is a method described in, for example, commercially available 2,3-dimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation of phenol) It can manufacture according to this.
[695] 6-cyclopropyl-2,3-dimethylphenol is a method described in, for example, commercially available 2,3-dimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolysis of phenol) , And the method described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 2000, 41, 4251-4255) (method of constructing cyclopropyl group, Suzuki-Miyaura coupling reaction), and the method described in (Tetrahedron, 1998, Vol. 54, pages 15861-15869) of phenylmethoxymethylether To phenol, and demethoxymethylation reaction).
[696] 2-hydroxy-3,4-dimethylbenzaldehyde O-methyloxime is described, for example, from commercially available 2,3-dimethylphenol (Tetrahedron Letters, 1998, Volume 39, page 2947). Bromolation reaction), and the method described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 1979 , 20, 4159-4162; Tetrahedron, 1997, 53, 43, 14599-14614; or Bulletin of the Chemical Society of Japan, 1971, 44, 2237-2248 (aromatic) Conversion reaction of bromide to aromatic aldehyde), and the method described in Journal of the Chemical Society: Perkin transactions I, 1979, pages 643-645 (oxime reaction), and Tetrahedron, 1998, 54 Vol., Pp. 15861-15869) (The conversion of phenylmethoxymethyl ether to phenol According to, talme ethoxy methylation reaction) can be produced.
[697] 6-methoxy-2,3-dimethylphenol is a method described in, for example, commercially available 3,4-dimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (phenol bromination reaction) And Tetrahedron Letters, 1979, 20, 4159-4162; Tetrahedron, 1997, 53, 43, 14599-14614; or Bulletin of the Chemical Society of Japan, 1971, 44, 2237- 2248) (conversion reaction of aromatic bromide to aromatic aldehyde), and the method described in Journal of the Chemical Society: Parkin transaction I, 1974, page 1353.
[698] 6-Bromo-3-methoxy-2-methylphenol is prepared from commercial 2-methyl-1,3-benzenediol by the method described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838. From 3-methoxy-2-methylphenol which can be prepared according to the conversion of phenol to phenylmethyl ether, methylation reaction, the method described in Tetrahedron Letters, 1998, 39, page 2947 (bromine of phenol) Can be produced in accordance with the simulated reaction).
[699] 6-cyclopropyl-3-methoxy-2-methylphenol is prepared from commercially available 2-methyl-1,3-benzenediol, according to the method described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838. From 3-methoxy-2-methylphenol which can be prepared according to the conversion of phenol to phenylmethyl ether, methylation reaction, the method described in Tetrahedron Letters, 1998, 39, page 2947 (bromine of phenol) Modeling reactions) and the methods described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 2000, Volume 41, pages 4251-4255) (Construction of cyclopropyl groups, Suzuki-Miyaura coupling reaction), and the method described in literature (Tetrahedron, 1998, Vol. 54, pages 15861-15869) It can be produced according to the conversion of methyl ether to phenol, demethoxymethylation reaction).
[700] 2-cyclopropyl-3,6-dimethylphenol is described, for example, from commercially available 2,5-dimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (the bromination reaction of phenol) , And methods described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenols to phenylmethyl ether, methylation reactions), and Tetrahedron Letters, 1979, Vol. 20, 4159- 4162 or Tetrahedron, 1997, Vol. 53, No. 43, pages 14599-14614 or Bulletin of the Chemical Society of Japan, 1971, Vol. 44, pages 2237-2248 (of aromatic aldehydes of aromatic bromide Conversion reactions), and the methods described in The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, pages 855-864 (conversion of carbonyl groups to olefins, Wittig reaction), and Organic Reactions, 1973, 20, pp. 1-131 Or the method described in the Journal of the American Chemical Society, 1975, 97, 3428 or Tetrahedron Letters, 1998, 39, 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and literature. (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) It can manufacture according to this.
[701] 2-allyl-6-ethyl-3-methoxyphenol is, for example, 2-ethyl which may be prepared by the method described in Chemical and Phamaceutical Bulletin, 1979, Vol. 27, No. 6, pages 1490-1494. From -5-methoxyphenol, it can manufacture according to the method (Allylation reaction of a phenol, Claisen potential) described in the literature (Organic Reactions, 1949, Vol. 2, pages 1-48).
[702] 3,6-dimethyl-2-[(methylsulfanyl) methyl] phenol can be prepared by the method described, for example, in the Journal of the American Chemical Society, 1966, Vol. 88, No. 24, pages 5855-5864. Can be.
[703] 5-Bromo-4-indanol is described, for example, in commercially available 4-hydroxy-1-indanone (Journal of the American Chemical Society, 1946, Vol. 68, page 2487). Reduction of Bonyl Reaction can be prepared according to the Wolff-Kishner Reduction Reaction) and the method described in Tetrahedron Letters, 1998, 39, 2947 (phenol bromination reaction).
[704] 5-Methyl-4-indanol is described, for example, in commercially available 4-hydroxy-1-indanone (Journal of the American Chemical Society, 1946, vol. 68, page 2487). Reduction, Wolff-Kishner reduction), and methods described in Tetrahedron Letters, 1998, Vol. 39, p. 2947 (bromotylation of phenols), and Helvetica Chimica Acta, 1990, Vol. 75, p. 457 Method described in (Phenol Conversion to Phenylmethoxymethyl Ether, Methoxymethylation Reaction), and Method described in Helvetica Chimica Acta, 1990, Vol. 73, pp. 417-425 (Conversion of Bromo Group to Methyl Group) Reaction) and the method described in (Tetrahedron, 1998, Vol. 54, pages 15861-15869) (conversion of phenylmethoxymethyl ether to phenol, demethoxymethylation reaction).
[705] 5-ethyl-4-indanol is described, for example, in commercially available 4-hydroxy-1-indanone (Journal of the American Chemical Society, 1946, Vol. 68, page 2487). Reduction, Wolff-Kishner reduction), and the method described in Tetrahedron Letters (1998, Vol. 39, p. 2947) (bromolation reactions of phenols), and Helvetica Chimica Acta, 1992, Vol. 75, p. 457). Reaction (Conversion of Bromo Group to Ethyl Group) as described in the Methods described (Conversion of Phenols to Phenylmethoxymethyl Ether, Methoxymethylation Reaction) And the method described in (Tetrahedron, 1998, Vol. 54, pages 15861-15869) (conversion of phenylmethoxymethyl ether to phenol, demethoxymethylation reaction).
[706] 5-cyclopropyl-4-indanol is described, for example, in commercially available 4-hydroxy-1-indanone (Journal of the American Chemical Society, 1946, vol. 68, page 2487). Reduction of Bonyl Wolff-Kishner Reduction), and the process described in Tetrahedron Letters, 1998, 39, page 2947 (phenol bromination reaction) and in Organic Synthesis, Collective Volume, Vol. 4, 836 (Page 838) (conversion of phenol to phenylmethyl ether, methylation reaction), and the method described in (Tetrahedron Letters, 2000, Vol. 41, pages 4251-4255) (Construction of cyclopropyl groups, Suzuki- Miyaura coupling reaction) and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, No. 9, 1572-1574 or Japanese Patent Laid-Open (Hei) 11-322755) (phenol of phenylmethyl ether And conversion to demethylation).
[707] 6-Methyl-2,3-dihydro-1-benzofuran-7-ol is prepared by, for example, 2-methoxy-3, prepared by the method described in tetrahedron Letters, 1998, Vol. 39, p. 2947. From methylphenol, the method described in the Journal of the Chemical Society: Perkin transactions I, 1988, page 3029 (construction of the benzofuran ring), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, 9 6-methyl-1-benzofuran-7 which can be prepared according to the method described in Japanese Patent Application Publication No. 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (conversion of phenylmethyl ether to phenol and demethylation reaction). From -ol, it can manufacture according to the method (reduction reaction of an olefin) described in the Journal of the Chemical Society, 1948, page 894.
[708] 6-Bromo-1-benzofuran-7-ol is described, for example, from commercially available 7-methoxy-1-benzofuran (Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572). -1574 page (Japanese Patent Laid-Open No. 11-322755) (conversion of phenylmethyl ether to phenol, demethylation reaction), and the method described in Tetrahedron Letters, 1998, Vol. 39, p. 2947. It can manufacture according to (bromolation reaction of a phenol).
[709] 6-Methyl-1-benzofuran-7-ol is prepared from, for example, 2-methoxy-3-methylphenol prepared by the method described in Tetrahedron Letters, 1998, Volume 39, page 2947. Methods described in the Journal of the Chemical Society: Perkin transactions I, 1988, page 3029 (construction of benzofuran rings), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 or It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) described in Unexamined-Japanese-Patent No. 11-322755.
[710] 6-cyclopropyl-1-benzofuran-7-ol is available from, for example, commercially available 7-methoxy-1-benzofuran (Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572). -1574 page (Japanese Patent Laid-Open No. 11-322755) (conversion of phenylmethyl ether to phenol, demethylation reaction), and the method described in Tetrahedron Letters, 1998, Vol. 39, p. 2947. (Phenol bromination reaction), and the method described in Helvetica Chimica Acta (1992, Vol. 75, p. 457) (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters , 2000, 41, pages 4251-4255) (the construction of cyclopropyl groups, the Suzuki-Miyaura coupling reaction), and the methods described in Tetrahedron, 1998, 54, pages 15861-15869 It can manufacture according to (the conversion of phenyl methoxymethyl ether to a phenol, demethoxymethylation reaction). have.
[711] 2,4-dicyclopropyl-6-fluorophenols are described, for example, from commercial 2-fluorophenols (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (the bromination of phenols) ), And the method described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 2000, 41 , Pages 4251-4255 (building of cyclopropyl groups, Suzuki-Miyaura coupling reaction), and methods described in Tetrahedron (1998, Vol. 54, pages 15861-15869) (phenylmethoxymethylether To phenol, demethoxymethylation reaction).
[712] 2,4-Dibromo-3,6-dimethylphenol is a method described in, for example, commercially available 3,6-dimethylphenol (Tetrahedron Letters, 1998, 39, 2947). Can be produced in accordance with the simulated reaction).
[713] 2-bromo-4,6-dimethylphenol is described, for example, from commercially available 2,4-dimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation of phenol) It can manufacture according to this.
[714] 2-ethyl-4,6-diiodophenol is a commercially available 2-ethylphenol, which is described in the Australian Journal of Chemistry, 1997, Vol. 50, No. 7, pp. 767-770 (iodization reaction of phenol). Can be prepared according to
[715] 2-cyclopropyl-4,6-dimethylphenol is described, for example, from commercially available 2,4-dimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation of phenol) , And the method described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (conversion of phenol to phenylmethoxymethylether, methoxymethylation reaction), and Tetrahedron Letters, 2000, 41, 4251-4255) (method of constructing cyclopropyl group, Suzuki-Miyaura coupling reaction), and the method described in (Tetrahedron, 1998, Vol. 54, pages 15861-15869) of phenylmethoxymethylether To phenol, and demethoxymethylation reaction).
[716] 2-Bromo-3,5,6-trimethylphenol is described, for example, from commercially available 2,3,5-trimethylphenol (Tetrahedron Letters, 1998, Volume 39, page 2947). Bromolation reaction).
[717] 5,6-dimethyl-4-indanol is described, for example, from commercially available 7-methyl-2 H-chromen-2-one (Journal of Japan Chemical Society, 1974, pages 136-146 and Organic Reactions, 1941 It can be manufactured according to the method (Clemmensen reduction) as described in the year, volume 1, page 155).
[718] 1,2,3,5,6,7-hexahydro-s-indacene-4-ols are described, for example, from commercial indans, see Journal of the American Chemical Society, 1977, 99, 8007-. 8014 and Organic Reactions, 1941, Vol. 1, page 155), and the method described in Clemmensen Reduction, and the Journal of Organic Chemistry, 1977, Vol. 42, pages 3260-3264. have.
[719] 3- (1,3-dioxolan-2-yl) phenol is, for example, from 3-hydroxybenzaldehyde to the method described in Tetrahedron Letters, 1989, Vol. 30, No. 13, pages 1609-1612. It can manufacture according to this.
[720] 3 '-(trifluoromethyl) [1,1'-biphenyl] -3-ol is, for example, commercially available from 3-iodophenol and 3- (trifluoromethyl) phenylboronic acid; It can be manufactured according to the method (phenylation reaction, Suzuki-Miyaura coupling reaction) described in Chemical Reviews, 1995, 95, 2457-2483.
[721] 3-hydroxy-4-methylbenzonitrile can be prepared, for example, by the method described in Montshefte fur Chemie, 1957, Vol. 88, pp. 228, 230.
[722] Ethyl 3-hydroxy-4-methylbenzoate can be prepared, for example, by the method described in The Journal of Organic Chemistry, 1961, Vol. 26, pages 1732-1734.
[723] 3-hydroxy-4-methylbenzamide is, for example, from commercial 3-hydroxy-4-methylbenzoic acid according to the method described in Phosphorus and Sulfur, 1980, Vol. 9, pages 155-164. It can manufacture.
[724] 3,6-dimethyl-2-propylphenol can be produced by the method described, for example, in Journal of Polymer Science, 1948, Vol. 3, page 448, page 452.
[725] 2-hydroxy-3,4,6-trimethylbenzaldehyde can be prepared, for example, by the method described in Liebigs Annalen der Chemie, 1906, 347, page 379.
[726] 2-hydroxy-3,4,6-trimethylbenzaldehyde O-methyloxime is described, for example, in the method described in Liebigs Annalen der Chemie, 1906, vol. 347, page 379 (2-hydroxy-3,4). , 6-trimethylbenzaldehyde), and (Chmical Pharmaceutical Bulletin, 1988, Vol. 36, No. 8, pages 3134-3137).
[727] 2- [1- (methoxymethyl) cyclopropyl] phenol is, for example, 2-methoxy, which may be prepared by the method described in The Journal of Organic Chemistry, 1942, Vol. 7, pp. 444-456. From -1- (2-methoxyphenyl) ethanone, described in The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, 855-864 Methods (Conversion of Carbonyl Groups to Olefins, Wittig Reactions), and Organic Reactions, 1973, Volume 20, pages 1-131 or Journal of the American Chemical Society, 1975, 97 pages 3428 or Tetrahedron Letters, 1998 (39), pages 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (method of converting phenylmethyl ether to phenol and demethylation) Reaction).
[728] 2- (1-methoxycyclopropyl) phenol is, for example, 1-methoxy-2- which may be prepared by the method described in The Journal of Organic Chemistry, 1998, Vol. 63, pages 4632-4635. From (1-methoxyvinyl) benzene, Organic Reactions, 1973, 20, pages 1-131 or Journal of the American Chemical Society, 1975, 97, 3428 or Tetrahedron Letters, 1998, 39 , Pages 8621-8624 (building of cyclopropyl groups, Simmons-Smith reactions), and Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Publication ( It can be produced according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) described in (PH 11-322755).
[729] 2- (2-hydroxyphenyl) cyclopropanecarbonitrile can be prepared by the method described in, for example, the method described in Journal of Medicinal Chemistry, 1988, Vol. 31, No. 1, pages 37-54. From 2-methoxyphenyl) acrylonitrile, the method described in (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or JP 11-322755) (phenylmethyl Conversion of ethers to phenols, demethylation reactions, and methods described in Helvetica Chimica Acta, 1992, Vol. 75, p. 457 (conversion of phenols to phenylmethoxymethylether, methoxymethylation reactions), and Methods described in The Journal of Organic Chemistry, 1973, Vol. 38, pages 1793-1797 or The Journal of Organic Chemistry, 1970, Vol. 35, pages 374-379 (cyclopropaneation reactions), and Tetrahedron , 1998, Volume 54, pages 15861-15869) According to the conversion nolro, talme ethoxy methylation reaction) can be produced.
[730] 2- (2-ethoxycyclopropyl) phenol can be prepared by the method described in, for example, Heterocycles, 1998, Vol. 48, No. 7, pp. 1373-1394, [2- (methoxymethoxy) ) Phenyl] methanol, the method described in The Journal of Organic Chemistry, 1981, Vol. 46, pages 5143-5147 (conversion of benzyl alcohol to benzyl chloride), and Journal of the American Chemical Society, 1973 Year 95, No. 2, pages 581-582) (the construction of cyclopropyl groups), and the method described in the literature (Tetrahedron, 1998, Volume 54, pages 15861-15869) of phenylmethoxymethylether To phenol, and demethoxymethylation reaction).
[731] 2- (2,2-difluorocyclopropyl) phenol can be prepared by the method described in, for example, Bulletin de la Societe Chemique de France, 1995, pages 850-856. From 2-difluorovinyl) -2-methoxybenzene, The Journal of Organic Chemistry, 1973, Vol. 38, pages 1793-1797 or The Journal of Organic Chemistry, 1970, Vol. 35, pages 374-379. ) And the method described in (Organic Synthesis, Collective Volume, Vol. 5, pages 412-414) and the method (conversion of phenylmethyl ether to phenol, demethylation reaction). Can be.
[732] 2- (2,2-dichlorocyclopropyl) phenol can be prepared, for example, by 2- (methoxymethoxy) which can be prepared by the method described in Heterocycles, 1998, Vol. 48, No. 7, pp. 1373-1394. From benzaldehyde to the process described in The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, 855-864 (Conversion of Carbonyl to Olefin, Wittig) Reactions), and the methods described in Synthetic Communications, 1999, 29, 23, pages 4101-4112 (conversion of olefins to dichlorocyclopropane), and Tetrahedron, 1998, 54, 15861- Page 15869) (conversion of phenylmethoxymethyl ether to phenol, demethoxymethylation reaction).
[733] 2- (2,2-dibromocyclopropyl) phenol is, for example, commercially available from 1-methoxy-2-vinylbenzene (Synthetic Communications, 1999, Vol. 29, No. 23, pages 4101-4112). ), (Bromoform instead of chloroform, conversion of olefins to dibromocyclopropane), and the method described in (Organic Synthesis, Collective Volume, Vol. 5, pages 412-414) And ether conversion to phenol, demethylation reaction).
[734] 2-isopropenylphenols are described, for example, from commercially available 1- (2-methoxyphenyl) ethanone, The Journal of Organic Chemistry, 1963, Vol. 28, page 1128 or Synthetic Communications, 1985, 15 Vol. 10, pp. 855-864 (conversion of carbonyl groups to olefins, Wittig reaction), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 or Japan It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) as described in patent publication (patent) 11-322755).
[735] 3- (2-hydroxyphenyl) acrylonitrile can be prepared by the method described in, for example, the Journal of Medicinal Chemistry, 1988, Vol. 31, No. 1, pages 37-54. From -methoxyphenyl) acrylonitrile, the method described in (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) (phenylmethyl ether To phenol, demethylation reaction).
[736] 2-ethynylphenol can be prepared, for example, from commercially available 1-benzofuran by the method described in the Canadian Journal of Chemistry, 1997, Vol. 75, No. 9, pages 1256-1263.
[737] Bicyclo [4.2.0] octa-1,3,5-trien-2-ol is prepared, for example, by the method described in The Journal of Organic Chemistry, 1982, Vol. 47, pages 2393-2396. From 5-methoxybicyclo [4.2.0] octa-1,3,5-trien-7-one which can be described in the method described in Organic Reactions (1941, Vol. 1, p. 155) (Clemmensen reduction) , And (Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755 or Organic Synthesis, Collective Volume, Vol. 5, pages 412-414). It can manufacture according to the method as described in (the conversion of phenylmethyl ether to a phenol, demethylation reaction).
[738] 2-bromo-6-chlorophenol can be prepared, for example, from commercial 2-chlorophenols according to the method described in the literature (Tetrahedron Letters, 1998, Vol. 39, page 2947) (bromolation of phenol). Can be.
[739] 3-Bromo-2-hydroxybenzonitrile is, for example, a method described in commercially available 2-hydroxybenzonitrile (Tetrahedron Letters, 1998, Vol. 39, p. 2947) (bromolation reaction of phenol) It can manufacture according to this.
[740] 2- (2,2-dichlorocyclopropyl) -6-methylphenols are described, for example, from commercial 2-hydroxy-3-methylbenzaldehyde, in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838. ), The conversion of phenols to phenylmethyl ethers, methylation reactions, and The Journal of Organic Chemistry, 1963, Vol. 28, page 1128 or Synthetic Communications, 1985, Vol. 15, Issue 10, 855- Page 864) (conversion of carbonyl groups to olefins, Wittig reactions), and the process described in Synthetic Communications, 1999, Vol. 29, No. 23, pages 4101-4112 (conversion of olefins to dichlorocyclopropane). And the method described in (Organic Synthesls, Co1lective Volume, Vol. 5, pages 412-414) (conversion of phenylmethyl ether to phenol, demethylation reaction).
[741] 2-methyl-6-vinylphenol is described, for example, by the method described in commercial 2-hydroxy-3-methylbenzaldehyde (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838) (Phenylmethyl of phenol). Conversion to ethers, methylation reactions) and methods described in The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, 855-864 (olefins of carbonyl groups) Conversion, Wittig reaction) and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, 57, No. 9, page 1572-1574 or Japanese Patent Laid-Open No. 11-322755 Conversion and demethylation reaction).
[742] 6-cyclopropyl-3-fluoro-2-methylphenol is described, for example, in the commercially available 3-fluoro-2-methylbenzaldehyde (The Journal of Organic Chemistry, 1999, Vol. 64, pp. 7921-7928 or The method described in the Journal of the Chemical Society: Parkin transaction I, 1974, page 1353 (Baeyer-Villiger oxidation, conversion of aromatic aldehydes to phenols), and Tetrahedron Letters, 1998, 39, 2947. Method (Phenol Bromolation Reaction) and Methods (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838) (Conversion of Phenol to Phenylmethylether, Methylation Reaction) and Literature (Tetrahedron Letters, 2000 , 41, pages 4251-4255 (Construction of cyclopropyl groups, Suzuki-Miyaura coupling reaction) and Bioscience, Biotechno1ogy, and Blochemistry, 1993, 57, 9, pages 1572-1574 Or Japanese Patent Laid-Open No. 11-322755) Method can be prepared in accordance with (transformation, demethylation reaction of phenylmethyl ether into phenol).
[743] 5-methyl-1-benzofuran-4-ol can be prepared, for example, by methyl 4-hydroxy-1-benzofuran, which can be prepared by the process described in Tetrahedron, 1995, Vol. 51, pages 4009-4022. From -5-carboxylates, the method described in (0rganic Synthesis, Co1lective Volume, Vol. 4, pages 836-838) (conversion of phenol to phenylmethyl ether, methylation reaction) and the Journal of Organic Chemistry, The method described in 2001, 66, pages 4965-4972 (reduction of esters into alcohols) and the method described in Journal of Medicinal Chemistry, 1999, Vol. 42, No. 6, pages 1007-1017. To benzyl methanesulfonyl ester) and the method described in The Journal of Organic Chemistry, 1969, 34, 3923 or Synthetic Communications, 2001, 31, 9, 1373-1382 Reduction of compounds, tosylate, mesylate), and Bioscience, Biotechnology , and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) can be prepared in accordance with the method (conversion of phenylmethyl ether to phenol, demethylation reaction).
[744] 2- (2-chloro-2-fluorocyclopropyl) phenol can be prepared by the method described in, for example, Heterocycles, 1998, Vol. 48, No. 7, pp. 1373-1394. From oxymethoxy) benzaldehyde, to the process described in the Journal of Fluorine Chemistry, 1983, Vol. 23, pages 339-357 (conversion of carbonyl groups to chlorofluoroolefins), and to The Journal of Organic Chemistry, 1973. (38), pages 1793-1797 or The Journal of Organic Chemistry, 1970, 35, 374-379 (cyclopropaneation reaction), and Organic Synthesis, Collective Volume, Vol. 5, It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) described in pages 412-414).
[745] 3- (benzyloxy) phenol can be prepared, for example, by the method described in The Journal of Organic Chemistry, 1997, Vol. 62, No. 10, pages 3062-3075.
[746] 1-methyl-1H-indol-4-ol is, for example, commercially available from 4-methoxy-1-methyl-1H-indole, Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, It can manufacture according to the method (conversion of phenylmethyl ether to phenol, demethylation reaction) as described in page 1572-1574 or Unexamined-Japanese-Patent No. 11-322755.
[747] 1-Methyl-1H-indole-7-ol can be prepared, for example, by 7-methoxy-, which may be prepared by the method described in Journal of Medicinal Chemistry, 1992, Vol. 35, No. 1, pages 177-184. From 1-methyl-1H-indole, the method described in (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Laid-Open No. 11-322755) To phenol, and demethylation reaction).
[748] 1- (4-hydroxy-3-methylphenyl) ethanone O-methyloxime is, for example, available from the commercially available 1- (2-hydroxyphenyl) ethanone (Journal of the American Chemical Society, 1986, 108, pages 6016-6023).
[749] 2-isopropenyl-6-methylphenol is, for example, 1- (2-hydroxy-3-methylphenyl) eta, which may be prepared by the method described in Chemische Berichte, 1925, vol. 58, p. 41. From rice fields, the method described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenol to phenylmethyl ether, methylation reaction), and The Journal of Organic Chemistry, 1963, 28 Vol. 1, p. 1128 or Synthetic Communications, 1985, Vol. 15, No. 10, pages 855-864 (conversion of carbonyl groups to olefins, Wittig reaction), and Bioscience, Biotechnology, and Biochemistry, 1993, It can manufacture according to the method (conversion of phenylmethyl ether to a phenol, demethylation reaction) as described in 57, 9, 1572-1574 pages or Unexamined-Japanese-Patent No. 11-322755.
[750] 1,1-dimethyl-5-indanol can be prepared, for example, by the method described in Bulletin of the Chemical Society of Japan, 2000, Vol. 73, No. 12, pages 2779-2782. From oxy-1,1-dimethylindan, it can be produced according to the method described in (Organic Synthesis, Collective Volume, Vol. 5, pages 412-414) (conversion of phenylmethyl ether to phenol, demethylation reaction). .
[751] 3-Bromo-6-cyclopropyl-2-methylphenol is prepared from commercial 2-methyl-3-nitrophenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947). ), And the methods described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838, (Conversion of Phenols to Phenylmethylether, Methylation Reaction), and Organic Synthesis, Collective Volume, Vol. 1, Modifications of the method described in pages 445-447 (reduction of nitrophenol to aniline; 8.5 equivalents of zinc powder, 25 equivalents of ammonium chloride to nitrophenols, reaction at room temperature), and Tetrahedron Letters, 2000 , Vol. 41, pages 4251-4255 (Construction of cyclopropyl groups, Suzuki-Miyaura coupling reactions), and Organic Synthesis, Collective Volume, Vol. 3, pages 185-187 or The Journal of Organic Chemistry, 1977, Vol. 42, pages 2426-2430) (Conversion of aniline to bromobenzene, Sandmeyer reaction, etc.) and literature (Bioscience, Biotechnology, and Biochemistry, 1993, 57, 9, 1572-1574 or Japanese Patent Publication No. 11-322755). It can manufacture according to the method described (conversion of phenylmethyl ether to phenol, demethylation reaction).
[752] 6-Cyclopropyl-2-methyl-3-nitrophenol was prepared from commercial 2-methyl-3-nitrophenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947). , And the methods described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenols to phenylmethyl ether, methylation reactions), and Organic Synthesis, Collective Volume, Vol. 1, 445 A variation of the method described in page 447 (reduction of nitrophenol to aniline; 8.5 equivalents of zinc powder, 25 equivalents of ammonium chloride, based on nitrophenols at room temperature), and Tetrahedron Letters, 2000, 41, pages 4251-4255 (Construction of Cyclopropyl Group, Suzuki-Miyaura Coupling Reaction), and Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 Or the method described in JP 11-322755 A (phenylme Conversion of tilether to phenol, demethylation reaction) and the method described in (Tetrahedron, 1987, Vol. 43, No. 8, pages 1753-1758) (conversion of aniline derivatives to nitrobenzene). have.
[753] 5-Methyl-1,3-dihydro-2-benzofuran-4-ol is prepared according to the method described, for example, in the Journal of the American Chemical Society, 2000, Vol. 122, pages 11553-11554. can do.
[754] 2-Fluoro-3,5,6-trimethylphenol is, for example, 2,3,5-trimethyl-6- which may be prepared by the method described in Chemische Berichte, 1922, Vol. 55, p. 2384. From nitrophenols, the methods described in Organic Synthesis, Collective Volume, Vol. 4, pages 836-838 (conversion of phenols to phenylmethyl ether, methylation reactions), and Liebigs Annalen der Chemie, 1957, 608 Volume, page 128 or Organic Synthesis, Collective Volume, Vol. 5, pages 829-833 (reduction reaction of nitro groups to amino groups), and methods described in Synthesis, 1989, pages 905-908. (Conversion of aromatic amines to aromatic fluorides) and the method described in (Organic Synthesis, Collective Volume, Vol. 5, pages 412-414) (conversion of phenylmethyl ether to phenol, demethylation reaction). Can be.
[755] 2-chloro-3,5,6-trimethylphenol is a modification of the method described in, for example, commercially available 2,3,5-trimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947). Chlorination reaction of phenol; N-chlorosuccinimide can be used instead of N-bromosuccinimide.
[756] 2-iodo-3,5,6-trimethylphenol is a modification of the method described in, for example, commercially available 2,3,5-trimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947). It can manufacture according to (The iodide reaction of a phenol; N-iodosuccinimide is used instead of N-bromosuccinimide.).
[757] 2-ethyl-3,5,6-trimethylphenol can be prepared by the method described, for example, in Chemical Research in Toxicology, 1997, Vol. 10, No. 3, pages 335-343. From hydroxy-3,4,6-trimethylphenyl) ethanone (Journal of the American Chemical Society, 1946, vol. 68, page 2487) (reduction of carbonyl reaction Wolff-Kishner reduction reaction) It can synthesize | combine according to.
[758] 2-isopropenyl-3,5,6-trimethylphenol is, for example, 1- which can be prepared by the method described in Chemical Research in Toxicology, 1997, Vol. 10, No. 3, pages 335-343. From (2-hydroxy-3,4,6-trimethylphenyl) ethanone, the method described in (Organic Synthesis, Collective Volume, Vol. 4, pages 836-838) (conversion of phenol to phenylmethyl ether, methylation Reactions), and the methods described in The Journal of Organic Chemistry, 1963, 28, 1128 or Synthetic Communications, 1985, 15, 10, pages 855-864 (Conversion of Carbonyl Group to Olefin, Wittig Reaction) and the method described in Bioscience, Biotechnology, and Biochemistry, 1993, Vol. 57, No. 9, pages 1572-1574 or Japanese Patent Laid-Open No. 11-322755 (conversion of phenylmethyl ether to phenol, Demethylation reaction).
[759] 1- (2-hydroxy-3,4,6-trimethylphenyl) ethanone is prepared by the method described, for example, in Chemical Research in Toxicology, 1997, Vol. 10, No. 3, pages 335-343. can do.
[760] 2,3,5-trimethyl-6-nitrophenol can be prepared, for example, by the method described in Chemische Berichte, 1922, Vol. 55, p. 2384.
[761] 2,4-dichloro-3,5,6-trimethylphenol is a modification of the method described in, for example, commercially available 2,3,5-trimethylphenol (Tetrahedron Letters, 1998, Vol. 39, p. 2947). It can manufacture according to the method (chlorolation reaction of a phenol; N-chlorosuccinimide is used instead of N-bromosuccinimide).
[762] Pentamethylphenol can be prepared, for example, by the method described in the Journal of the Chemical Society, 1949, page 624.
[763] After completion of each reaction step, the target compound in each step can be collected from the reaction mixture according to a conventional method. For example, it is obtained by neutralizing the reaction mixture appropriately, and removing an insoluble matter by filtration, then adding an organic solvent that does not mix with water, and distilling off the solvent after washing with water. If desired, the obtained target compound can be further purified by a conventional method, for example, recrystallization, reprecipitation or chromatography.
[764] Compound I of the present invention may be a salt. These salts are included in the present invention as long as they can be used as herbicides for agricultural horticulture.
[765] Salts of the compound I of the present invention include, for example, alkali metal salts such as lithium, sodium, potassium and the like; Alkaline earth metal salts such as magnesium and calcium; Aluminum salts; Transition metal salts such as iron and copper; Amine salts such as ammonium, trimethylammonium, triethylammonium, tetramethylammonium and pyridinium; Inorganic inorganic acid salts such as hydrochloride, sulfate, and phosphate; Or organic acid salts such as formate, acetate, toluenesulfonate and oxalate.
[766] When the pyridazine derivative is an acid component of the salt, the salt can be prepared, for example, by mixing the pyridazine derivative and the base in the presence or absence of a solvent and distilling off the solvent.
[767] The base to be used is not particularly limited as long as it is a base having a pH of usually 8 or more, and examples thereof include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; Alkali metal carbonates such as sodium carbonate, potassium carbonate and cesium carbonate; Metal alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; Alkali metal salts of organic acids such as sodium acetate, potassium acetate, sodium formate, potassium formate; Alkali metal hydrides such as sodium hydride and potassium hydride; Alkali metals such as sodium and potassium; Aliphatic tertiary amines such as triethylamine, tributylamine and diisopropylethylamine; Aliphatic cyclic tertiary amines such as 1,4-diazabicyclo [2.2.2] octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU); Pyridines such as pyridine, collidine and 4- (N, N-dimethylamino) pyridine; Metal amides such as lithium amide and sodium amide; Or organometallic bases such as butyllithium, s-butyllithium, lithium diisopropylamide, sodium bis (trimethylsilyl) amide, lithium bis (trimethylsilyl) amide.
[768] The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide and the like; Or a mixed solvent thereof.
[769] When the pyridazine derivative becomes the base component of the salt, the salt can be prepared, for example, by mixing the pyridazine derivative and the acid in the presence or absence of a solvent and distilling off the solvent.
[770] The acid to be used is not particularly limited as long as it is an acid usually having a pH of 6 or less, and examples thereof include inorganic inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid and phosphoric acid; Or organic acids such as formic acid, acetic acid, toluenesulfonic acid, oxalic acid, benzo inorganic acid, and the like.
[771] The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, for example, water; Alcohols such as methanol, ethanol and t-butanol; Ketones such as acetone and methyl isobutyl ketone; Nitriles such as acetonitrile; Esters such as ethyl acetate; Halogenated hydrocarbons such as methylene chloride, chloroform and dichloroethane; Ethers such as diethyl ether, tetrahydrofuran and dioxane; Aromatic hydrocarbons such as toluene; Amides such as dimethylformamide and dimethylacetamide; Sulfoxides such as dimethyl sulfoxide and the like; Or a mixed solvent thereof.
[772] The composition of the present invention is a variety of weeds that are problematic in rice fields, for example, broadleaf weeds, such as turfgrass, paddygrass, bark flower, water star, back grass, moth buds, coot; Golden weeds and weeds, such as horsetail, tadpole, horseradish, beech, and water; And herbicidal activity against weeds and weeds such as snares, peels, and tacks, and no detrimental harm to rice.
[773] The composition of the present invention is a variety of weeds, such as purslane, chickweed, hyacinth, hair amaranth, wild grass, horseradish, mother-of-law, satin grass, tricolor violet, rake, honey grass Broad-leaf weeds, such as wild herbs, datura, crows, big fireballs, weasel; Chickweed and weeds such as chickweed; And herbicidal activity against weeds and weeds, such as true dongbang and hyangbuja, and also does not show problematic weakness for major crops such as corn, wheat, and soybean.
[774] The composition of the present invention can be used not only in fields and paddy fields, but also in orchards, mulberry fields and non-crop fields.
[775] The synergistic effect of the present invention is confirmed in a wide range of mixing ratios, and when the second herbicidal active compound is Compound A, B or C, the ratio of the second herbicidal active compound is usually 0.1 to 50 parts by weight based on 1 part by weight of the compound I. It is possible to prepare a useful herbicide by mixing with a mixture, the mixing ratio is preferably 0.2 to 20 parts by weight, more preferably 0.5 to 10 parts by weight, when the second herbicidal active compound is a compound D, E, F or G In general, a useful herbicide can be prepared by mixing the second herbicidal active compound in an amount of 0.01 to 100 parts by weight based on 1 part by weight of compound I, and the mixing ratio is preferably 0.02 to 50 parts by weight, more preferably 0.1 To 10 parts by weight. The herbicide of the present invention thus completed can obtain a high herbicidal effect by soil treatment or foliage treatment before and after germination of weeds.
[776] In the present invention, the 3-phenoxy-4-pyridazinol derivative and the second herbicidal active compound may be mixed and dispersed as one agent, or two active ingredients may be dispersed at the same time without mixing, and one effective The components may be spread first and other active ingredients later. In addition, the order of dispersion is arbitrary.
[777] The composition of the present invention may also disperse the original itself, and may be mixed with a carrier and other auxiliaries as necessary, and in the form of preparations commonly used as herbicides, for example powders, powders, granules, granules, hydrates, emulsions, It is prepared and used as an aqueous suspending agent, granulating hydrating agent, oil suspending agent, non-injection agent and the like.
[778] The compounds of the present invention may be mixed with a carrier and other auxiliaries (surfactants, etc.) as necessary and used in the form of formulations commonly used as herbicides, for example, powders, powders, granules, granules, hydrates, water-soluble agents, emulsions, solutions It is prepared and used as. Carrier as used herein means a synthetic or natural inorganic or organic substance that is mixed in herbicides to help the active ingredient compound reach plants or to facilitate storage, transport or handling of the active ingredient.
[779] Suitable solid carriers include clays represented by, for example, kaolinite group, montmorillonite group, attapulgite group and the like; Inorganic materials such as talc, mica, pyrophyllite, pumice, vermiculite, gypsum, dolomite, diatomaceous earth, magnesium lime, phosphorus lime, zeolite, silicic anhydride, synthetic calcium silicate, kaolin, bentonite and calcium carbonate matter; Vegetable organic substances such as soy flour, tobacco powder, hoe powder, flour, wood powder, starch, crystalline cellulose; Synthetic or natural high molecular compounds such as coumarone resin, petroleum resin, alkyd resin, polyvinyl chloride, polyalkylene glycol, ketone resin, ester gum, copal gum and dammar gum; Waxes such as carnauba wax, paraffin wax and beeswax; Or an element.
[780] Suitable liquid carriers include, for example, paraffinic or naphthenic hydrocarbons such as kerosine, mineral oil, spindle oil, white oil, etc .; Aromatic hydrocarbons such as benzene, toluene, xylene, ethylbenzene, cumene and methylnaphthalene; Chlorinated hydrocarbons such as carbon tetrachloride, chloroform, trichloroethylene, monochlorobenzene and chlorotoluene; Ethers such as dioxane and tetrahydrofuran; Ketones such as acetone, methyl ethyl ketone, diisobutyl ketone, cyclohexanone, acetophenone and isophorone; Esters such as ethyl acetate, amyl acetate, ethylene glycol acetate, diethylene glycol acetate, dibutyl maleate and diethyl succinate; Alcohols such as methanol, hexanol, ethylene glycol, diethylene glycol, cyclohexanol, benzyl alcohol; Ether alcohols such as ethylene glycol ethyl ether, ethylene glycol phenyl ether, diethylene glycol ethyl ether and diethylene glycol butyl ether; Polar solvents such as dimethylformamide and dimethyl sulfoxide; Or water.
[781] Surfactants used for the purpose of emulsification, dispersion, wetting, expansion, binding, disintegration control, active ingredient stabilization, fluidity improvement, rust prevention, promotion of absorption into plants, and the like may be ionic or nonionic.
[782] Examples of suitable nonionic surfactants include oxidation of alkylphenols such as ethylene polymerization adducts of higher aliphatic alcohols such as sucrose esters of fatty acids, lauryl alcohols, stearyl alcohols, and oleyl alcohols, isooctylphenols, and nonylphenols. Ethylene polymerization adducts of alkylnaphthols such as ethylene polymerization adducts, butylnaphthol and octylnaphthol, mono ethylene polymerization adducts of higher fatty acids such as palmitic acid, stearic acid and oleic acid, stearyl phosphoric acid, dilauryl phosphoric acid Or ethylene oxide adducts of dialkyl phosphoric acid, ethylene oxide adducts of higher aliphatic amines such as dodecylamine, stearic acid amide, higher fatty acid esters of polyhydric alcohols such as sorbitan, ethylene oxide adducts thereof and ethylene oxide And copolymers of propylene oxide and the like.
[783] Suitable anionic surfactants include, for example, alkyl sulfate ester salts such as sodium lauryl sulfate and oleyl alcohol sulfate esteramine salts, fatty acid salts such as sulfosuccinic acid dioctyl ester sodium, sodium oleate and sodium stearate, and isopropyl naphthalene sulfonic acid. Alkyl aryl sulfonates, such as sodium, the methylenebis naphthalene sulfonate, sodium lignin sulfonate, and sodium dodecylbenzene sulfonate, etc. are mentioned.
[784] Suitable cationic surfactants include higher aliphatic amines, quaternary ammonium salts, alkylpyridinium salts, and the like.
[785] In addition, the herbicide of the present invention includes other components, for example, gelatin, gum arabic, casein, albumin, glue, soda arginate, polyvinyl alcohol, carboxymetal cellulose, for the purpose of improving biological properties by improving the properties of the formulation. It may contain high molecular compounds such as methyl cellulose and hydroxymethyl cellulose, thixotropic agents such as sodium polyphosphate and bentonite and other auxiliary agents.
[786] Powders and coarse powders usually contain 0.1 to 25 parts by weight of the active ingredient, and the balance is a solid carrier.
[787] The hydrating agent and the granulating hydrating agent usually contain 1 to 90 parts by weight of the active ingredient, and the balance is a solid carrier and a dispersion wetting agent, and a protective colloid, a thixotropic agent and an antifoaming agent are added as necessary. Such formulations are suspended and dispersed in water when stirred in water.
[788] Granules and granules usually contain 0.1 to 35 parts by weight of the active ingredient, for example, and the remainder is mostly a solid carrier. The active ingredient compound is uniformly mixed with the solid carrier or uniformly fixed or adsorbed on the surface of the solid carrier, and the diameter of the particles is usually 0.2 to 1.5 mm.
[789] For example, the emulsion contains 1 to 70 parts by weight of the active ingredient compound, contains 5 to 20 parts by weight of an emulsifier, the remainder is a liquid carrier, and other auxiliaries such as rust preventive agents are added as necessary.
[790] An aqueous suspending agent or an oil suspending agent is obtained by suspending or emulsifying and dispersing the active ingredient in water or a high boiling organic solvent using a suitable surfactant, so as to maintain stability over time by adding a thickener or the like as necessary.
[791] The paddy feed agent is prepared by dividing the active ingredient into a suitable formulation such as powder, granules, tablets, emulsions, bulk tablets, etc., if necessary, and dividing them into water-soluble films or containers. Throw hundreds.
[792] In this way, when the compounds of the present invention prepared in various formulations are subjected to soil treatment before or after germination of weeds in paddy fields, for example, 1 g to 1000 g, preferably 10 g to 300 g per 10 ar, are used. Weeds can be effectively cured by processing.
[793] The treatment method of the compound of the present invention is usually formulated and can be subjected to soil treatment, foliage treatment or water reduction treatment before weeding or within about one month after germination. Soil treatment includes soil surface treatment and soil admixture treatment, and foliage treatment includes treatment at the upper side of the plant as well as extreme treatment to treat only weeds so as not to adhere to crops. Irrigation into the water;
[794] In order to broaden the herbicidal range with respect to the herbicide of this invention, another herbicide can be mix | blended.
[795] The herbicide of the present invention can be used, for example, by mixing with a plant growth regulator, fungicide, insecticide, acaricide, nematicide or fertilizer.
[796] Best Mode for Carrying Out the Invention
[797] Although the Example, preparation example, and test example of this invention are shown to the following, it demonstrates concretely, but this invention is not limited to these. In addition, in the following formulation example, "%" represents the weight%.
[798] Example 1 6-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 128)
[799] (1) 6-chloro-3- (2-methylphenoxy) pyridazine (Step A-1)
[800] A mixture of 278.7 g (1.87 mol) of 3,6-dichloropyridazine, 202.3 g (1.87 mol) of 2-methylphenol and 259 g (1.87 mol) of potassium carbonate was heated and stirred at 160 ° C. for 6 hours. The reaction mixture was cooled to 70 ° C. and 2 L of ethyl acetate was added. The mixture was washed sequentially with 1 mol / L aqueous sodium hydroxide solution (4 × 500 mL), water (4 × 500 mL) and saturated brine (50 mL) and dried over anhydrous magnesium sulfate. The solvent was distilled off and crystallized by adding isopropyl ether to the residue. The crystals were collected by filtration to give 234.2 g (1.06 mol, yield 56.7%) of 6-chloro-3- (2-methylphenoxy) pyridazine.
[801] (2) 4,6-dichloro-3- (2-methylphenoxy) pyridazine (Step A-2)
[802] 6-Chloro-3- (2-methylphenoxy) pyridazine (234.2 g, 1.06 mol) obtained in (1) was dissolved in phosphorus oxychloride (1.85 L), and 76.7 g (1.08 mol) of chlorine gas was added to the solution. ) Was blown for 4 hours. Nitrogen gas was blown into the reaction mixture to remove excess chlorine gas, and then phosphorus oxychloride was distilled off. The residue was dissolved in ethyl acetate (1.5 L), washed successively with water (4 x 500 mL) and saturated brine (200 mL), and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was washed with 500 mL of hexane to give 193.1 g of crude product. This crude product was recrystallized from a mixed solvent of hexane-ethyl acetate (400 mL-240 mL) to give 114.4 g (0.448 mol, 42.3%) of 4,6-dichloro-3- (2-methylphenoxy) pyridazine. Got it.
[803] (3) 6-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 128, step A-3)
[804] 100.0 g (0.392 mol) of 4,6-dichloro-3- (2-methylphenoxy) pyridazine obtained in (2) was dissolved in 1,4-dioxane (1 L), and sodium hydroxide ( An aqueous solution of purity 96%, 19.6 g, 0.470 mol) (400 mL of water) and 1.09 g (4.78 mmol) of tetrabutylammonium chloride were added and heated to reflux for 4 hours. The reaction mixture was concentrated under reduced pressure to a total amount of about 100 mL. An aqueous sodium hydroxide solution (13.1 g of sodium hydroxide dissolved in 1.4 L of water) and 500 mL of ethyl acetate were added to the residue. The aqueous layer was washed with ethyl acetate (3 × 200 mL) and adjusted to pH 5 by adding concentrated hydrochloric acid under ice-cooling. The precipitated solid was collected by suction filtration, washed with 1 L of water, and air dried. The obtained solid was recrystallized from acetonitrile to give 34.4 g (0.145 mol, yield 37.0%) of 6-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 128). Furthermore, after drying an organic layer with magnesium sulfate, the solvent was distilled off. The obtained residue was purified by silica gel column chromatography (YMC GEL, SIL 60, 350/250 mesh, hexane-ethyl acetate gradient) to give 6-chloro-3,4-bis (2-methylphenoxy) pyridazine 13.5 g (0.0414 mol, yield 10.5%) were obtained.
[805] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.35-7.08 (4H, m), 6.84 (1H, brs), 2.11 (3H, s).
[806] Melting point (° C): 211-213.
[807] Example 2 3- (2-methylphenoxy) -4-pyridazinol (Compound No. 5)
[808] (1) 6-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine (Step A-3)
[809] 3.00 g (11.8 mmol) of 4,6-dichloro-3- (2-methylphenoxy) pyridazine obtained in Example 1 (2) are dissolved in methanol (60 mL), and the solution is 95% sodium methoxide at room temperature. 1.00 g (17.6 mmol) of the seeds were added and stirred at 60 ° C for 4 hours. In addition, 1.00 g (17.6 mmol) of 95% sodium methoxide was added, the mixture was stirred at 60 ° C for 1 hour, and then allowed to stand at room temperature overnight. The reaction mixture was concentrated and ethyl acetate was added to the residue, and the mixture was washed sequentially with water and brine. After drying over anhydrous sodium sulfate, the residue obtained by distilling off the solvent was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 4: 1) to give 6-chloro-4-methoxy-3- (2 2.75 g (11.0 mmol, yield 93.2%) of -methylphenoxy) pyridazines were obtained.
[810] (2) 4-methoxy-3- (2-methylphenoxy) pyridazine (Step N-1)
[811] 2.00 g (7.98 mmol) of 6-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine obtained by (1) was dissolved in methanol (40 mL), and 5% palladium-carbon 0.20 in this solution. g was added and stirred for 4 hours in a hydrogen atmosphere (1 atmosphere). The reaction mixture was filtered through celite to concentrate the filtrate. The residue was purified by silica gel column chromatography (eluted with ethyl acetate followed by dichloromethane: methanol = 5: 1) to give 1.59 g (7.36) of 4-methoxy-3- (2-methylphenoxy) pyridazine. Mmol, yield 92.2%).
[812] (3) 3- (2-methylphenoxy) -4-pyridazinol (Compound No. 5, step N-2)
[813] 1.08 g (5.00 mmol) of 4-methoxy-3- (2-methylphenoxy) pyridazine obtained by (2), 0.24 g (6.0 mmol) of sodium hydroxide, water (5 mL) and 1,4-dioxane (5 mL) was stirred overnight. The reaction mixture was washed with ethyl acetate, the aqueous layer was made acidic with hydrochloric acid and extracted with ethyl acetate. The solvent was distilled off to obtain 0.21 g (10 mmol, yield 20%) of 3- (2-methylphenoxy) -4-pyridazinol (Compound No. 5).
[814] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 8.30 (1H, d, J = 7.2 Hz), 7.43-7.00 (5H, m), 6.43 (1H, d, J = 7.2 Hz), 2.18 (3H , s).
[815] Melting Point (° C): 169-171.
[816] Example 3 5-Chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 45)
[817] (1) 4,5-dichloro-3- (2-methylphenoxy) pyridazine
[818] 3- (2-methylphenoxy) pyridazine (can be prepared by the method described in Agricultural and Biological Chemistry, 1968, 32, 1376 and Agricultural and Biological Chemistry, 1969, 33, 96) } 16.4 g (88.2 mmol) and phosphorus oxychloride (200 mL) were mixed and the mixture was heated at 80 ° C. to introduce 8.5 g (120 mmol) of chlorine gas. Phosphorous oxychloride was distilled off from the reaction mixture, the residue was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Merck, 9385, hexane: ethyl acetate gradient) to give 4,5-dichloro-3- (2-methylphenoxy) pyridazine 6.61. g (25.9 mmol, yield 29.4%), 8.14 g (36.9 mmol, yield 41.8%) and 4-chloro-3- (2-methylphenoxy) for 5-chloro-3- (2-methylphenoxy) pyridazine 1.20 g (5.44 mmol, yield 6.17%) of pyridazine was obtained.
[819] (2) 5-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine (Step A-3)
[820] 5.10 g (20.0 mmol) of 4,5-dichloro-3- (2-methylphenoxy) pyridazine and methanol (70 mL) obtained by (1) were mixed, and 0.46 g of sodium (−8 ° C.) was added to this mixture. 20 mmol) was added and stirred for 8 minutes at -8 ° C for 8 hours and 30 minutes under ice-cooling. Ice-cold water was added to the reaction mixture, pH was adjusted to 3 with hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Merck, 9385, hexane: ethyl acetate gradient) to give 5-chloro-4-methoxy-3- (2-methylphenoxy) pyridine. 1.15 g (4.58 mmol, 22.9% yield) and 3.27 g (13.0 mmol, 65% yield) of 4-chloro-5-methoxy-3- (2-methylphenoxy) pyridazine were obtained.
[821] (3) 5-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 45, Step A-4, etc.)
[822] 5-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine 750 mg (2.99 mmol) obtained by (2), 156 mg (3.9 mmol) sodium hydroxide, 1,4-dioxane (5 mL) and water (10 mL) were mixed and the mixture was heated to reflux for 2 hours and 30 minutes with stirring. The reaction mixture was poured into ice-cold water and acidified with hydrochloric acid. The precipitated solid was collected by filtration and washed with water followed by hexane. 525 mg (2.22 mmol, Yield 74.2%) of 5-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 45) were obtained.
[823] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 8.68 (1H, s), 7.38-6.80 (4H, m), 5.32 (1H, brs), 2.13 (3H, s).
[824] Melting point (° C): 238-243.
[825] Example 4 5-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 66, Step I-1)
[826] 237 mg (1.00 mmol) and acetonitrile (8 mL) of 5-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 45) obtained by Example 3 were mixed and added to this mixture. Under stirring, 112 mg (1.00 mmol) of 1,4-diazabicyclo [2,2,2] octane were added, followed by 191 mg (1.00 mmol) of 4-methylbenzenesulfonylchloride, followed by 1 hour 30 minutes at room temperature. Stirred. Water was added to the reaction mixture, which was made acidic with hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (Wako gel C-100, hexane: ethyl acetate = 3: 1) to give 5-chloro-3- (2-methylphenoxy) -4 379 mg (0.969 mmol, yield 96.9%) of -pyridazinyl 4-methylbenzenesulfonate (Compound No. 66) was obtained.
[827] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.80 (1H, s), 7.77-6.75 (8H, m), 2.47 (3H, s), 1.98 (3H, s).
[828] Melting point (° C.): 140-143.
[829] Example 5 6-Chloro-3- (2-methylphenoxy) -4-pyridazinol 1-oxide (Compound No. 129, Step F-1)
[830] 135 mg (0.572 mmol) of 6-chloro-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 128) obtained by Example 1 and methylene chloride (6 mL) were mixed and added to this mixture. 247 mg (80% of purity, 1.14 mmol) of m-chloro perbenzoic acid were added, and it stirred for 16 hours under heating and reflux. After standing at room temperature for 2 days, the reaction mixture was poured into saturated aqueous sodium sulfite solution and washed with methylene chloride. The aqueous layer was made acidic with hydrochloric acid, extracted with methylene chloride, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was subjected to silica gel column chromatography (YMC GEL, SIL60, 350/250 mesh, Elution with ethyl acetate) gave 32.6 mg (0.129 mmol, yield 22.6%) of 6-chloro-3- (2-methylphenoxy) -4-pyridazinol 1-oxide (Compound No. 129). .
[831] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.34 (1H, s), 7.34-7.10 (4H, m), 2.20 (3H, s).
[832] Melting point (° C): 194-196.
[833] Example 6 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinol (Compound No. 139)
[834] (1) Mixture of 6-chloro-3- (2-cyclopropylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-cyclopropylphenoxy) pyridazine 1-oxide
[835] (Step B-2)
[836] 25.3 g (189 mmol) of 2-cyclopropylphenol, 1,4-dioxane (120 mL) and dimethylsulfoxide (120 mL) were mixed and, under ice-cooling, 23.2 g (207 mmol) of potassium tert-butoxide ) Was added and stirred for 10 minutes. 32.0 g (194 mmol) of 3,6-dichloropyridazine 1-oxide which is a known compound were added to this mixture, and it was left to stand at room temperature for 5 days. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 6-chloro-3- (2-cyclopropylphenoxy) pyridazine 1-oxide and 3-chloro- 43.3 g (165 mmol, yield 87.3%) of a mixture of 6- (2-cyclopropylphenoxy) pyridazine 1-oxide was obtained.
[837] (2) 4,6-dichloro-3- (2-cyclopropylphenoxy) pyridazine (Step B-3)
[838] A mixture of 6-chloro-3- (2-cyclopropylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-cyclopropylphenoxy) pyridazine 1-oxide obtained by (1) 43.3 g (165 mmol), chloroform (30 mL) and 18.0 mL (194 mmol) of phosphorus oxychloride were mixed and the mixture was heated to 60 ° C. to dissolve. It was concentrated by stirring at room temperature overnight. The residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 32.5 g (116 mmol, yield 70.3%) of 4,6-dichloro-3- (2-cyclopropylphenoxy) pyridazine.
[839] (3) 6-chloro-3- (2-cyclopropylphenoxy) -4-pyridazinol (Compound No. 139, step B-4)
[840] 32.5 g (116 mmol) of 4,6-dichloro-3- (2-cyclopropylphenoxy) pyridazine obtained in (2) were dissolved in dimethyl sulfoxide (500 mL), and 10% (W / V) sodium hydroxide 84 mL (210 mmol) aqueous solution was added and stirred overnight at room temperature. The reaction mixture was poured into ice-cold 1 mol / L aqueous sodium hydroxide solution and washed with ether. The aqueous layer was made acidic with hydrochloric acid, and the precipitated solid was collected by filtration and washed with water. Acetonitrile was added and heated to the obtained individual. After cooling overnight, the crystals were collected by filtration (14.04 g). The filtrate was concentrated and the residue was recrystallized from ethanol to give 2.64 g of crystals. These crystals were combined and 16.7 g (63.5 mmol, yield 54.7%) of 6-chloro-3- (2-cyclopropylphenoxy) -4-pyridazinol (Compound No. 139) were obtained.
[841] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.28-6.97 (4H, m), 6.82 (1H, s), 1.89-1.77 (1H, m), 0.87-0.73 (2H, m), 0.73- 0.58 (2H, m).
[842] Melting point (° C.): 229-231.
[843] Example 7 6-chloro-3- [2- (1-fluorocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 140)
[844] (1) 2- (methoxymethoxy) benzaldehyde
[845] 5.01 g (41.1 mmol) of commercially available salicyaldehyde was dissolved in N, N-dimethylformamide (20 mL), and ice-cold, 1.80 g (45.0 mmol) of 60% sodium hydride was added to the solution, and ice-cooled for 10 minutes. After stirring, 3.43 mL (45.2 mmol) of chloro (methoxy) methane was slowly added dropwise and stirred for 1 hour under ice cooling. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to give 6.54 g (39.4 mmol, yield 95.9%) of 2- (methoxymethoxy) benzaldehyde. )
[846] (2) 1- (methoxymethoxy) -2-vinylbenzene
[847] Under a nitrogen atmosphere, 877 mg (21.9 mmol) of 60% sodium hydride washed with hexane was suspended in dry dimethyl sulfoxide (10 mL), and the suspension was heated and stirred at 85 ° C. for 30 minutes, then returned to room temperature and further cooled under ice. A solution of 7.83 g (21.9 mmol) of dry dimethylsulfoxide (20 mL) in methyl (triphenyl) phosphonium bromide was slowly added dropwise. After stirring for 15 minutes at room temperature, 3.02 g (18.2 mmol) of a dry dimethylsulfoxide (9 mL) solution of 2- (methoxymethoxy) benzaldehyde obtained in (1) was added dropwise and stirred for 15 minutes at room temperature. The reaction mixture was poured into water and extracted with diethyl ether. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 2.54 g (15.5) of 1- (methoxymethoxy) -2-vinylbenzene. Mmol, yield 85.2%).
[848] (3) 1- (2-bromo-1-fluoroethyl) -2- (methoxymethoxy) benzene
[849] 1- (methoxymethoxy) -2- obtained by (2) in a solution of 1.47 g (9.13 mmol) of methylene chloride (10 mL) of N, N, N-triethylamine trifluoride (MEC-82) A solution of 1.00 g (6.09 mmol) of methylene chloride (5 mL) of vinylbenzene was added dropwise, and 1.19 g (6.70 mmol) of N-bromosuccinimide was added under ice cooling. After stirring for 2 hours under ice cooling, the temperature was raised to room temperature, followed by further stirring for 30 minutes. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution and extracted with methylene chloride. The organic layer was washed successively with dilute hydrochloric acid, water, and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was performed by preparative thin layer chromatography (developing as 1.05717 four pieces of MERCK company use ethyl acetate: hexane = 4: 1), and then preparative thin layer chromatography (1.057444 piece using MERCK company ethyl acetate: hexane = Purification by 10: 1) to obtain 1.24 g of crude product of 1- (2-bromo-1-fluoroethyl) -2- (methoxymethoxy) benzene.
[850] (4) 1- (1-fluorovinyl) -2- (methoxymethoxy) benzene
[851] 736.2 mg (11.15 mmol) of 85% potassium hydroxide was added to dry dimethyl sulfoxide (10 mL), followed by stirring at room temperature for 1 hour and 30 minutes, followed by 1- (2-bromo-1-fluoroethyl) obtained by (3). Crude product of 2- (methoxymethoxy) benzene 978.2 mg of dry dimethylsulfoxide (6 mL) solution was added dropwise and stirred for 2 hours, followed by heating and stirring at 60 ° C for 2 hours. The reaction mixture was poured into water and extracted with hexanes. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 632.7 mg of crude product of 1- (1-fluorovinyl) -2- (methoxymethoxy) benzene.
[852] (5) 1- (1-fluorocyclopropyl) -2- (methoxymethoxy) benzene
[853] In a nitrogen atmosphere, dry diethyl ether (5 mL) was added to a dry flask, and 1.97 mL (1.97 mmol) of diethyl zinc (1 M hexane solution) was added dropwise, followed by 1- (1-fluoro) obtained by (4). A crude purified product of rovinyl) -2- (methoxymethoxy) benzene 143.6 mg of a dry diethyl ether (3 mL) solution was added dropwise. After stirring for 10 minutes at room temperature, 0.19 mL (2.3 mmol) of diiodomethane was added dropwise, followed by heating to reflux for 4 hours 30 minutes. The reaction mixture was poured into a saturated aqueous ammonium chloride solution, then saturated aqueous sodium hydrogen carbonate solution was added thereto, stirred for a while, and then extracted with diethyl ether. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, and developed with ethyl acetate: hexane = 4: 1) to obtain 1- (1-fluorocyclopropyl). 80.5 mg of crude product of -2- (methoxymethoxy) benzene was obtained.
[854] (6) 2- (1-fluorocyclopropyl) phenol
[855] To the crude purified product of 1- (1-fluorocyclopropyl) -2- (methoxymethoxy) benzene obtained by (5) was added dropwise concentrated hydrochloric acid (0.3 mL) to 43.8 mg of methanol (6 mL) solution. It stirred by heating at 60 degreeC for 3 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to give 42.8 mg of crude product of 2- (1-fluorocyclopropyl) phenol.
[856] (7) 6-chloro-3- [2- (1-fluorocyclopropyl) phenoxy] pyridazine 1-oxide (step B-2)
[857] 42.8 mg of crude product of 2- (1-fluorocyclopropyl) phenol obtained by (6) was dissolved in a mixed solvent of 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL), and this solution To this was added 34.7 mg (0.310 mmol) of potassium tert-butoxide, followed by 46.4 mg (0.281 mmol) of 3,6-dichloropyridazine 1-oxide, followed by stirring at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 2 pieces, developed with ethyl acetate: hexane = 2: 1), and 6-chloro-3- [2- ( 28.0 mg (0.0996 mmol) of 1-fluorocyclopropyl) phenoxy] pyridazine 1-oxide were obtained.
[858] (8) 4,6-dichloro-3- [2- (1-fluorocyclopropyl) phenoxy] pyridazine (Step B-3)
[859] 28.0 mg (0.0996 mmol) of 6-chloro-3- [2- (1-fluorocyclopropyl) phenoxy] pyridazine 1-oxide obtained by (7) was dissolved in phosphorus oxychloride (1 mL), and The solution was stirred at rt overnight. Water and methylene chloride were added to the reaction mixture, stirred for 30 minutes, and extracted with methylene chloride. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 2 sheets, and developed with ethyl acetate: hexane = 2: 1) to obtain 4,6-dichloro-3- [2. 5.1 mg (0.017 mmol, yield 17%) of-(1-fluorocyclopropyl) phenoxy] pyridazine was obtained.
[860] (9) 6-chloro-3- [2- (1-fluorocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 140, step B-4)
[861] 5.1 mg (0.017 mmol) of 4,6-dichloro-3- [2- (1-fluorocyclopropyl) phenoxy] pyridazine obtained by (8) were added with 1,4-dioxane (2 mL) and dimethylsulfoxide. It was dissolved in a seed (2 mL) mixed solvent, 0.1 mL of 2 mol / L aqueous sodium hydroxide solution was added to the solution, and the mixture was stirred overnight at room temperature. The reaction mixture was poured into water, diluted hydrochloric acid was adjusted to pH 2, and then extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 1, developed with ethyl acetate) to give 6-chloro-3- [2- (1-fluorocyclopropyl). ) 4.0 mg (0.014 mmol, yield 82%) of phenoxy] -4-pyridazinol (Compound No. 140) was obtained.
[862] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.57-7.52 (1H, m), 7.39-7.31 (1H, m), 7.22-7.13 (1H, m), 7.00 (1H, d, J = 8.1 Hz ), 6.48 (1H, s), 1.32-1.22 (2H, m), 1.16-1.08 (2H, m).
[863] Melting point (° C): 152-157.
[864] Example 8 6-Chloro-3- {2- [1- (ethylsulfanyl) cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 207)
[865] (1) 1-methoxy-2-vinylbenzene
[866] Under nitrogen atmosphere, 1.92 g (48.0 mmol) of 60% sodium hydride washed with hexane was suspended in dry dimethyl sulfoxide (15 mL), and the suspension was heated and stirred at 85 ° C. for 30 minutes, and then returned to room temperature and further cooled with ice. , 17.2 g (48.2 mmol) of a dry dimethyl sulfoxide (35 mL) solution of methyl (triphenyl) phosphonium bromide was slowly added dropwise. After stirring for 20 minutes at room temperature, 4.83 mL (40.1 mmol) of commercial 2-methoxybenzaldehyde was added dropwise, stirred at room temperature for 1 hour, and then stirred at 65 ° C for 3 hours. The reaction mixture was poured into ice-cold water, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to give 3.29 g (24.5 mmol, yield 61.1) of 1-methoxy-2-vinylbenzene. %) Was obtained.
[867] (2) 1- (2-bromo-1-fluoroethyl) -2-methoxybenzene
[868] 2.01 g of 1-methoxy-2-vinylbenzene obtained by (1) in a solution of 3.60 g (22.4 mmol) of methylene chloride (20 mL) of N, N, N-triethylamine trifluoride (MEC-82) A (15.0 mmol) methylene chloride (6 mL) solution was added dropwise and 2.92 g (16.4 mmol) of N-bromosuccinimide were added under ice cooling. After stirring for 25 minutes under ice cooling, the temperature was raised to room temperature, followed by further stirring for 1 hour 30 minutes. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution and extracted with methylene chloride. The organic layer was washed sequentially with dilute hydrochloric acid, water, and saturated brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain 1- (2-bromo-1-fluoroethyl) -2-meth 1.39 g of crude product of oxybenzene was obtained.
[869] (3) 1- (1-fluorovinyl) -2-methoxybenzene
[870] 1.28 g (19.4 mmol) of 85% potassium hydroxide was added to dry dimethyl sulfoxide (10 mL), followed by stirring at room temperature for 30 minutes, followed by 1- (2-bromo-1-fluoroethyl) -2 obtained by (2). A solution of 1.50 g of a dry dimethylsulfoxide (10 mL) crude crude product of methoxybenzene was added dropwise and stirred overnight. The reaction mixture was poured into water and extracted with hexanes. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate gradient) to obtain crude purification of 1- (1-fluorovinyl) -2-methoxybenzene. 1.21 g of water were obtained.
[871] (4) 1- (1-fluorocyclopropyl) -2-methoxybenzene
[872] In a nitrogen atmosphere, dry diethyl ether (8 mL) was added to a dry flask, 19.88 mL (19.88 mmol) of diethyl zinc (1 mol / L hexane solution) was added dropwise, and 1- (1- obtained in (3). 1.21 g of a dry diethyl ether (8 mL) solution of crude purified product of fluorovinyl) -2-methoxybenzene was added dropwise. After stirring for 10 minutes at room temperature, 1.92 mL (23.86 mmol) of diiodomethane was added dropwise and heated to reflux for 6 hours. After standing at room temperature overnight, the reaction mixture was poured into a saturated aqueous ammonium chloride solution, then saturated aqueous sodium bicarbonate solution was added thereto, stirred for a while, and then extracted with diethyl ether. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate gradient) to obtain 1- (1-fluorocyclopropyl) -2-methoxybenzene. 1.06 g of purified product was obtained.
[873] (5) 2- [1- (ethylsulfanyl) cyclopropyl] phenol
[874] Under a nitrogen atmosphere, 765.3 mg (19.1 mmol) of 60% sodium hydride was suspended in dry N, N-dimethylformamide (8 mL), and 1.46 mL (19.8 mmol) of ethanethiol was slowly added dropwise to the suspension, followed by stirring for 15 minutes. And a dry N, N-dimethylformamide (5 mL) solution of 1.06 g of a crude purified product of 1- (1-fluorocyclopropyl) -2-methoxybenzene obtained by (4) was added dropwise thereto at 160 ° C. It stirred by heating for 5 hours. After cooling, 1 mol / L aqueous potassium hydroxide solution and diethyl ether were added to the reaction mixture. The aqueous layer was separated and washed with diethyl ether. Dilute hydrochloric acid was added thereto, the mixture was adjusted to pH 2 and extracted with diethyl ether. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain a crude product of 2- [1- (ethylsulfanyl) cyclopropyl] phenol. 0.26 g was obtained.
[875] (6) 6-chloro-3- {2- [1- (ethylsulfanyl) cyclopropyl] phenoxy} pyridazine 1-oxide (step B-2)
[876] 0.26 g of crude product of 2- [1- (ethylsulfanyl) cyclopropyl] phenol obtained by (5) was dissolved in a mixed solvent of 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL). To the solution was added 265.5 mg (2.37 mmol) of potassium tert-butoxide, followed by 390.3 mg (2.37 mmol) of 3,6-dichloropyridazine 1-oxide, followed by stirring at room temperature overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by Merck, 1.05744, 3 pieces, and developed as ethyl acetate: hexane = 2: 1), and 6-chloro-3- {2- [ 138.4 mg (0.428 mmol) of 1- (ethylsulfanyl) cyclopropyl] phenoxy} pyridazine 1-oxide were obtained.
[877] (7) 4,6-dichloro-3- {2- [1- (ethylsulfanyl) cyclopropyl] phenoxy} pyridazine (Step B-3)
[878] 138.4 mg (0.428 mmol) of 6-chloro-3- {2- [1- (ethylsulfanyl) cyclopropyl] phenoxy} pyridazine 1-oxide obtained by (6) was added to phosphorus oxychloride (1 mL). It melt | dissolved and this solution was stirred overnight at room temperature. Water and methylene chloride were added to the reaction mixture, which was stirred for 30 minutes and then extracted with methylene chloride. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by Merck, 1.05744 using 2 sheets, and developing as ethyl acetate: hexane = 4: 1), and it is 4,6-dichloro-3- {2-. 94.4 mg (0.277 mmol, yield 64.7%) of [1- (ethylsulfanyl) cyclopropyl] phenoxy} pyridazine were obtained.
[879] (8) 6-chloro-3- {2- [1- (ethylsulfanyl) cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 207, Step B-4)
[880] 94.4 mg (0.277 mmol) of 4,6-dichloro-3- {2- [1- (ethylsulfanyl) cyclopropyl] phenoxy} pyridazine obtained by (7) was added to 1,4-dioxane (1 mL). And it was dissolved in a mixed solvent of dimethyl sulfoxide (1 mL), 0.69 mL (1.38 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the solution, and the mixture was stirred at room temperature overnight. After adding water and ethyl acetate to the reaction solution, the aqueous layer was separated and washed with ethyl acetate. Dilute hydrochloric acid was added thereto, the pH was adjusted to 2 and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, used in two pieces, developed with ethyl acetate) to give 6-chloro-3- {2- [1- (ethylsulfanyl 47.5 mg (0.147 mmol, Yield 53.1%) of cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 207) were obtained.
[881] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.45-7.07 (4H, m), 6.69 (1H, s), 2.46 (2H, q, J = 7.3 Hz), 1.28-1.02 (9H, m).
[882] Melting point (° C): 88.
[883] Example 9 6-chloro-3- [2- (2,2-dichlorocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 265)
[884] (1) 1- (2,2-dichlorocyclopropyl) -2- (methoxymethoxy) benzene
[885] 305 mg (1.86 mmol) of 1- (methoxymethoxy) -2-vinylbenzene obtained in Example 7 (2) were dissolved in chloroform (12 mL), and 5 mL (63 mmol) of 50% aqueous sodium hydroxide solution was added thereto. ) Was added dropwise, and then 54.1 mg (0.237 mmol) of benzyl (triethyl) ammonium chloride were added and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with chloroform. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, and developed with ethyl acetate: hexane = 1: 2) to obtain 1- (2,2-dichlorocyclopropyl 387 mg (1.57 mmol, yield 84.4%) of () -2- (methoxymethoxy) benzene were obtained.
[886] (2) 2- (2,2-dichlorocyclopropyl) phenol
[887] 203 mg (0.822 mmol) of 1- (2,2-dichlorocyclopropyl) -2- (methoxymethoxy) benzene obtained in (1) were dissolved in methanol (5 mL), and 0.1 mL of concentrated hydrochloric acid was added to this solution. It stirred at 60 degreeC for 2 hours. After confirming the disappearance of the raw material by thin layer chromatography, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 194 mg of a crude product of 2- (2,2-dichlorocyclopropyl) phenol.
[888] (3) 6-chloro-3- [2- (2,2-dichlorocyclopropyl) phenoxy] pyridazine 1-oxide (step B-2)
[889] Crude purified 194 mg, 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL) of 2- (2,2-dichlorocyclopropyl) phenol obtained by (2) were mixed and added to this mixture. Under ice-cooling, 118 mg (1.05 mmol) of potassium tert-butoxide were added and stirred for 10 minutes. 157 mg (0.952 mmol) of 3, 6- dichloropyridazine 1-oxides were added here, and it stirred at room temperature overnight. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 sheets, and developed with ethyl acetate: hexane = 1: 2) to give 6-chloro-3- [2- (2 268 mg of crude product of, 2-dichlorocyclopropyl) phenoxy] pyridazine 1-oxide was obtained.
[890] (4) 4,6-dichloro-3- [2- (2,2-dichlorocyclopropyl) phenoxy] pyridazine (Step B-3)
[891] 268 mg of crude product of 6-chloro-3- [2- (2,2-dichlorocyclopropyl) phenoxy] pyridazine 1-oxide obtained by (3) and 3 mL of phosphorus oxychloride were mixed, The mixture was stirred at rt overnight. Water and dichloromethane were added to the reaction mixture, which was stirred for 30 minutes. The mixture was separated, the organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 sheets, and developed with ethyl acetate: hexane = 1: 2) to obtain 4,6-dichloro-3- [2-. 162 mg (0.463 mmol, 1- (2,2-dichlorocyclopropyl) -2- (methoxymethoxy) benzene in 3 steps yield, 56.3% (2,2-dichlorocyclopropyl) phenoxy] pyridazine )
[892] (5) 6-chloro-3- [2- (2,2-dichlorocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 265, step B-4)
[893] 162 mg (0.463 mmol), 1,4-dioxane (3 mL) and dimethyl 4,6-dichloro-3- [2- (2,2-dichlorocyclopropyl) phenoxy] pyridazine obtained by (4) Sulfoxide (3 mL) was mixed and 1.15 mL (2.30 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the mixture and stirred overnight at room temperature. The reaction mixture was poured into water and made acidic with diluted hydrochloric acid. This mixture was extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, developed with ethyl acetate) to give 6-chloro-3- [2- (2,2-dichlorocyclopropyl). 50.0 mg (0.151 mmol, yield 32.6%) of phenoxy] -4-pyridazinol (Compound No. 265) was obtained.
[894] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.55-7.15 (4H, m), 6.69 (1H, s), 2.90 (1H, dd, J = 10.6, 8.8 Hz), 2.07-1.89 (2H, m ).
[895] Melting point (° C): 158-163.
[896] Example 10 6-chloro-3- (2-hydroxyphenoxy) -4-pyridazinol (Compound No. 384)
[897] (1) 3-chloro [1,4] benzodioxino [2,3-c] pyridazine (Step O-1)
[898] 3.49 g (80.0 mmol) of 55% sodium hydride are suspended in 1,4-dioxane (30 mL), and in this suspension 4.40 g (40 mmol) of a solution of 1,4-dioxane (30 mL) of pyrocatechol, 3,4,6-trichloropyridazine (described in The Journal of Organic Chemistry, 1963, Vol. 28, pages 218-221), 7.30 g (39.9 mmol) of 1,4-dioxane ( 30 mL) was added and heated to reflux for 2 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with 1 mol / L sodium hydroxide and water, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was recrystallized from methyl isobutyl ketone to obtain 6.15 g (27.8 mmol, yield 69.7%) of 3-chloro [1,4] benzodioxino [2,3-c] pyridazine. .
[899] (2) 6-chloro-3- (2-hydroxyphenoxy) -4-pyridazinol (Compound No. 384, step O-2)
[900] 5.52 g (25.0 mmol) of 3-chloro [1,4] benzodioxino [2,3-c] pyridazine obtained by (1), 1.30 g (31.2 mmol) of 96% sodium hydroxide, dimethyl sulfoxide (55 mL) and water (15 mL) were stirred at 90 ° C for 1 h. The reaction mixture was poured into ice-cold water, acidified with hydrochloric acid, and extracted with ethyl acetate. The solvent was distilled off and the residue was washed with isopropyl ether to give 4.90 g (20.5 mmol, yield 82.0%) of 6-chloro-3- (2-hydroxyphenoxy) -4-pyridazinol (Compound No. 384). )
[901] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.25-6.40 (5H, m).
[902] Melting Point (° C): 216-219.
[903] Example 11 6-chloro-3- [2- (methylsulfinyl) phenoxy] -4-pyridazinol (Compound No. 404)
[904] (1) 6-chloro-3- [2- (methylsulfanyl) phenoxy] pyridazine 1-oxide (step B-2)
[905] 454 mg (3.24 mmol) of 2- (methylsulfanyl) phenol are dissolved in a mixed solvent of 1,4-dioxane (5 mL) and dimethylsulfoxide (5 mL) and 519 mg of potassium tert-butoxide in this solution 4.63 mmol) was added and stirred for 35 minutes. 424 mg (2.57 mmol) of 3,6-dichloropyridazine 1-oxide was added to the mixture, followed by stirring for 3 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (elution with Waco gel C-100, hexane: ethyl acetate = 3: 1) to give 6-chloro-3- [2- (methylsulfanyl). 391 mg (1.46 mmol, yield 56.8%) of phenoxy] pyridazine 1-oxides were obtained.
[906] (2) 4,6-dichloro-3- [2- (methylsulfanyl) phenoxy] pyridazine (Step B-3)
[907] 288 mg (1.07 mmol) of 6-chloro-3- [2- (methylsulfanyl) phenoxy] pyridazine 1-oxide obtained by (1) and 1.00 mL (10.8 mmol) of phosphorus oxychloride were mixed, and The mixture was stirred overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, developed as hexane / ethyl acetate = 3/1) to obtain 4,6-dichloro-3- [2- (methylsulphur). 118 mg (0.411 mmol, yield 38.4%) of panyl) phenoxy] pyridazine were obtained.
[908] (3) 4,6-dichloro-3- [2- (methylsulfinyl) phenoxy] pyridazine
[909] 118 mg (0.411 mmol) of 4,6-dichloro-3- [2- (methylsulfanyl) phenoxy] pyridazine obtained in (2) were dissolved in 1,2-dichloroethane (4 mL), and 96.3 mg (80% purity, 0.446 mmol) of m-chloro perbenzoic acid were added, and it stirred at room temperature for 5 hours. The reaction mixture was poured into 10% aqueous sodium sulfite solution, extracted with ethyl acetate, washed with saturated brine and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, hexane: ethyl acetate = 1: 1, followed by 3: 1, then developed 1: 1) to give 4,6- 21.1 mg (0.0696 mmol, yield 16.9%) of dichloro-3- [2- (methylsulfinyl) phenoxy] pyridazine were obtained.
[910] (4) 6-chloro-3- [2- (methylsulfinyl) phenoxy] -4-pyridazinol (Compound No. 404, step B-4)
[911] 21.1 mg (0.0696 mmol) of 4,6-dichloro-3- [2- (methylsulfinyl) phenoxy] pyridazine obtained in (3) were dissolved in 1,4-dioxane (0.5 mL), and 0.12 mL (0.36 mmol) of 3 mol / L aqueous sodium hydroxide solution was added thereto, followed by stirring for 45 minutes. Dimethyl sulfoxide (0.5 mL) was added to this mixture, which was then stirred for 3 hours, poured into 10% hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (Merck Co., 1.05744, chloroform: methanol = 10: 1) to give 6-chloro-3- [2- (methylsulfinyl) phenoxy]. 2.1 mg (0.0074 mmol, 11% yield) of 4-pyridazinol (Compound No. 404) were obtained.
[912] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.90-7.84 (1H, m), 7.60-7.42 (2H, m), 7.14 (1H, dd, J = 9.2, 1.1 Hz), 6.62 (1H, s ), 2.92 (3H, s).
[913] Physical property: Amorphous.
[914] Example 12 6-Chloro-3- [2- (methylsulfonyl) phenoxy] -4-pyridazinol (Compound No. 406)
[915] (1) 6-chloro-3- [2- (methylsulfonyl) phenoxy] pyridazine 1-oxide
[916] 208 mg (0.774 mmol) of 6-chloro-3- [2- (methylsulfanyl) phenoxy] pyridazine 1-oxide obtained by Example 11 (1) were added to 1,2-dichloroethane (5 mL). It melt | dissolved and 829 mg (3.84 mmol) of 80% m-chloro perbenzoic acid were added to this solution, and it stirred at room temperature for 4 hours. The reaction mixture was poured into 10% aqueous sodium sulfite solution and extracted with ethyl acetate. The combined organic layers were washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the obtained residue was purified by preparative thin layer chromatography (developed by Merk, 1.05744, developed as hexane: ethyl acetate = 1: 1) to give 6-chloro-3- [2-methylsulfonyl) phenoxy. 132 mg (0.439 mmol, yield 56.7%) of ci] pyridazine 1-oxides were obtained.
[917] (2) 4,6-dichloro-3- [2- (methylsulfonyl) phenoxy] pyridazine (Step B-3)
[918] 111 mg (0.369 mmol) of 6-chloro-3- [2- (methylsulfonyl) phenoxy] pyridazine 1-oxide obtained by (1) and 1.00 mL (10.8 mmol) of phosphorus oxychloride were mixed and mixed Was stirred overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with saturated sodium bicarbonate and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, developed as hexane: ethyl acetate = 1: 1) to give 4,6-dichloro-3- [2- (methylsulfonyl ) 70.8 mg (0.222 mmol, yield 60.2%) of phenoxy] pyridazine were obtained.
[919] (3) 6-chloro-3- [2- (methylsulfonyl) phenoxy] -4-pyridazinol (Compound No. 406, step B-4)
[920] 70.8 mg (0.222 mmol) of 4,6-dichloro-3- [2- (methylsulfonyl) phenoxy] pyridazine obtained in (2) were dissolved in 1,4-dioxane (2.0 mL), and 0.45 mL (1.4 mmol) of 3 mol / L aqueous sodium hydroxide solution was added thereto, followed by stirring for 30 minutes. Dimethyl sulfoxide (2.0 mL) was added to the mixture, the mixture was stirred overnight, poured into water, and washed with a hexane-ethyl acetate mixed solvent. 10% hydrochloric acid was added to the aqueous layer to make it acid, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, developed with chloroform: methanol = 10: 1) to give 6-chloro-3- [2- (methylsulfonyl) phenoxy. 18.0 mg (0.0599 mmol, yield 27.0%) were obtained.
[921] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.00 (1H, dd, J = 7.7, 1.8 Hz), 7.71 (1H, ddd, J = 7.7, 7.7, 1.8 Hz), 7.43 (1H, ddd, J = 7.7, 7.7, 1.1 Hz), 7.32 (1H, br.d, J = 7.7 Hz), 6.62 (1H, s), 3.36 (3H, s).
[922] Physical property: Amorphous.
[923] Example 13 6-Chloro-3- (2-cyclopropyl-3-methoxyphenoxy) -4-pyridazinol (Compound No. 478)
[924] (1) 6-chloro-3- (2-cyclopropyl-3-methoxyphenoxy) -4-methoxypyridazine (step D-1)
[925] 190 mg (1.16 mmol) of 2-cyclopropyl-3-methoxyphenol were dissolved in a mixed solvent of 1,4-dioxane (2.5 mL) and dimethylsulfoxide (2.5 mL), and potassium tert-butoxide 146 was dissolved in this solution. mg (1.30 mmol) was added and stirred for 10 minutes. 170 mg (0.950 mmol) of 3,6-dichloro-4-methoxypyridazine was added to the mixture and allowed to stand overnight. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to give 6-chloro-3- (2-cyclopropyl-3-methoxyphenoxy). 90.1 mg (0.293 mmol, yield 30.8%) of 4-methoxypyridazine and 114 mg (0.371) of 3-chloro-6- (2-cyclopropyl-3-methoxyphenoxy) -4-methoxypyridazine Mmol, yield 39.1%).
[926] (2) 6-chloro-3- (2-cyclopropyl-3-methoxyphenoxy) -4-pyridazinol (Compound No. 478, step D-2)
[927] 24 mg (0.60 mmol) of 60% sodium hydride is suspended in dry N, N-dimethylformamide (DMF, 2 mL), 0.05 mL (0.7 mmol) of ethanethiol is added dropwise to the suspension solution at room temperature under ice-cooling. Stir for 10 minutes. To this mixture, 60.0 mg (0.195 mmol) of dry N, N-dimethylformamide 6-chloro-3- (2-cyclopropyl-3-methoxyphenoxy) -4-methoxypyridazine obtained by (1) was obtained. (DMF, 1.5 mL) was added and heated to reflux for 2 hours. The reaction mixture was cooled, poured into ice-cold 1 mol / L aqueous sodium hydroxide solution, and washed with ethyl acetate. Ice-cold hydrochloric acid was added to the aqueous layer, the pH was adjusted to 4, and the mixture was extracted with ethyl acetate. The ethyl acetate extracts were combined, washed successively with water and brine, and dried over sodium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by Merck, 1.05744, 3 pieces, and developed as hexane: ethyl acetate = 1: 1), and 6-chloro-3- (2-cyclo 15.2 mg (0.0519 mmol, Yield 26.6%) of propyl-3-methoxyphenoxy) -4-pyridazinol (Compound No. 478) was obtained.
[928] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.19 (1H, dd, J = 8.1, 8.4 Hz), 6.76 (1H, d, J = 8.1 Hz), 6.69 (1H, d, J = 8.4 Hz), 6.60 (1H, s), 3.85 (3H, s), 1.55-1.35 (1H, m), 0.85-0.60 (4H, m).
[929] Melting point (° C): 184-185.
[930] Example 14 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-yloxy) -6-chloro-4-pyridazinol (Compound No. 515)
[931] (1) 7-hydroxy-1-indanon
[932] 37.0 g (278 mmol) of aluminum chloride was mixed with 3.70 g (61.3 mmol) of sodium chloride, and the mixture was heated to dissolve at 150 ° C. and heated (50 ° C.) to commercially available 2,3-dihydro-4H-chromen-4 6.40 g (43.2 mmol) of -temperature was added and stirred at 200 ° C for 20 minutes. The reaction mixture (black) was cooled, gradually added to ice-cold hydrochloric acid (100 ml of concentrated hydrochloric acid and ice to 200 ml), and stirred for 30 minutes. Methylene chloride was added to this mixture for separation. The aqueous layer was filtered and the filtrate was extracted with methylene chloride. The organic layers were combined, washed successively with water and brine, and dried over sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 4.82 g (32.6 mmol, 75.2% of 7-hydroxy-1-indanone). )
[933] (2) 7- (methoxymethoxy) -1-indanon
[934] 1.00 g (6.76 mmol) of 7-hydroxy-1-indanon obtained in (1) was dissolved in N, N-dimethylformamide (DMF, 33 mL), the solution was ice-cooled, and 0.330 g of 60% sodium hydride. (8.25 mmol) was added in 4 portions and stirred for 30 minutes. 0.80 mL (11 mmol) of chloromethoxymethane was added dropwise to this mixture, followed by stirring at room temperature for 2 hours. The reaction mixture was poured into ice-cold saturated aqueous ammonium chloride solution (100 mL) and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 1.04 g (5.42 mmol) of 7- (methoxymethoxy) -1-indanon. , Yield 80.2%).
[935] (3) 7- (methoxymethoxy) -1-indanol
[936] 1.04 g (5.42 mmol) of 7-methoxymethoxy-1-indanon obtained in (2) was dissolved in methanol (20 mL), the solution was ice-cooled, and 164 mg (4.34 mmol) of sodium borohydride were added to room temperature. Stirred for 4 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 1.05 g (5.42 mmol) of 7- (methoxymethoxy) -1-indanol. , Yield 100%) was obtained.
[937] (4) a mixture of 4- (methoxymethoxy) -1H-indene and 7- (methoxymethoxy) -1H-indene
[938] 500 mg (2.58 mmol) of 7- (methoxymethoxy) -1-indanol obtained in (3) was dissolved in methylene chloride (3 mL), the solution was ice-cooled, and 0.50 mL (3.7 mmol) triethylamine. And 0.25 mL (3.3 mmol) of methanesulfonyl chloride were added and stirred for 2 hours. 0.80 mL (5.7 mmol) of triethylamine was added thereto, stirred for 1 hour, poured into water, and extracted with methylene chloride. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was dissolved in pyridine (3 mL) and heated to reflux for 4 hours. After standing at room temperature overnight, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 4- (methoxymethoxy) -1H-indene and 7- (methoxymethoxy 280 mg (1.59 mmol, yield 61.6%) of a mixture of methoxy) -1H-indene were obtained.
[939] (5) (2- (methoxymethoxy) -1,1a, 6,6a-tetrahydrocyclopropa [a] indene and 5- (methoxymethoxy) -1,1a, 6,6a-tetrahydro A mixture of cyclopropa [a] indenes
[940] Dry diethyl ether (5 mL) was added to a 30 mL eggplant flask under nitrogen stream and ice-cooled. 6.3 mL (6.3 mmol) of diethyl zinc (1.0 mol / L hexane solution) and 0.70 mL (8.5 mmol) of diiodomethane were added dropwise thereto, followed by stirring for 10 minutes. To this mixture was added 250 mg (1.42 mmol) of an ether solution (9 mL) of a mixture of 4- (methoxymethoxy) -1H-indene and 7- (methoxymethoxy) -1H-indene obtained by (4). It was dripped slowly. This mixture was heated to reflux for 4 hours. The reaction mixture was cooled and poured into saturated aqueous ammonium chloride solution. The same volume of saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extraction with ether. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain 2- (methoxymethoxy) -1,1a, 6,6a-tetrahydro. 150 mg (0.789 mmol, yield 55.6%) of a mixture of cyclopropa [a] indene and 5- (methoxymethoxy) -1,1a, 6,6a-tetrahydrocyclopropa [a] indene were obtained.
[941] (6) a mixture of 1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-ol and 1,1a, 6,6a-tetrahydrocyclopropa [a] indene-5-ol
[942] 2- (methoxymethoxy) -1,1a, 6,6a-tetrahydrocyclopropa [a] indene and 5- (methoxymethoxy) -1,1a, 6,6a- obtained by (5) 150 mg (0.789 mmol) of a mixture of tetrahydrocyclopropa [a] indenes were dissolved in methanol (6 mL), 2 drops of concentrated hydrochloric acid was added to the solution, followed by stirring at room temperature for 1 hour, followed by heating and stirring at 60 ° C for 20 minutes. . The reaction mixture was cooled, poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (developed by Merck, 1.05744, hexane: ethyl acetate = 2: 1) to obtain 1,1a, 6,6a-tetrahydrocyclopropa [ 80.0 mg (0.548 mmol, yield 69.5%) of a mixture of a] inden-2-ol and 1,1a, 6,6a-tetrahydrocyclopropa [a] indene-5-ol were obtained.
[943] (7) 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-yloxy) -6-chloropyridazine 1-oxide and 3- (1,1a, 6,6a A mixture of tetrahydrocyclopropa [a] inden-5-yloxy) -6-chloropyridazine 1-oxide (step B-2)
[944] Of 1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-ol and 1,1a, 6,6a-tetrahydrocyclopropa [a] indene-5-ol obtained by (6) 80.0 mg (0.548 mmol) of the mixture was dissolved in a mixed solvent of 1,4-dioxane (2 mL) and dimethyl sulfoxide (2 mL), and 85 mg (0.76 mmol) of potassium tert-butoxide was added to the solution for 10 minutes. Stirred. 82 mg (0.50 mmol) of 3,6-dichloropyridazine 1-oxides were added thereto, and the mixture was stirred overnight at room temperature. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 4, developed as hexane: ethyl acetate = 2: 1), and 3- (1,1a, 6,6a). -Tetrahydrocyclopropa [a] inden-2-yloxy) -6-chloropyridazine 1-oxide and 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] indene-5- 75.0 mg (0.273 mmol, yield 49.8%) of a mixture of yloxy) -6-chloropyridazine 1-oxide were obtained.
[945] (8) 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-yloxy) -4,6-dichloropyridazine and 3- (1,1a, 6,6a-tetra Hydrocyclopropa [a] inden-5-yloxy) -4,6-dichloropyridazine (Step B-3)
[946] 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-yloxy) -6-chloropyridazine 1-oxide and 3- (1,1a, obtained by (7) 75.0 mg (0.273 mmol) of a mixture of 6,6a-tetrahydrocyclopropa [a] inden-5-yloxy) -6-chloropyridazine 1-oxide were mixed with 0.30 mL (3.2 mmol) of phosphorus oxychloride The mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure to distill the phosphorus oxychloride, and the residue was subjected to preparative thin layer chromatography (Merck Co., 1.05744, 3 pieces, repeated four times as hexane / ethyl acetate = 9/1). Purified by 21.4 mg (0.0730 mmol, Yield 26.7%) of 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-yloxy) -4,6-dichloropyridazine And 32.6 mg (0.111 mmol, yield 40.7%) of 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-5-yloxy) -4,6-dichloropyridazine.
[947] (9) (3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-yloxy) -6-chloro-4-pyridazinol (Compound No. 515, Step B-4)
[948] 21.4 mg (0.0730 mmol) of dimethylsulfoxide of 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-2-yloxy) -4,6-dichloropyridazine obtained by (8) 0.1 mL (0.2 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the (3 mL) solution, followed by stirring at room temperature for 3 hours. The reaction mixture was poured into ice-cold 1 mol / L aqueous sodium hydroxide solution, and washed with ethyl acetate. The aqueous layer was separated, adjusted to pH 4 by adding concentrated hydrochloric acid under ice-cooling, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over sodium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 1, developed with chloroform: methanol = 10: 1), and 3- (1,1a, 6,6a- 10.3 mg (0.0375 mmol, yield 51.4%) of tetrahydrocyclopropa [a] inden-2-yloxy) -6-chloro-4-pyridazinol (Compound No. 515) were obtained.
[949] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.08 (1H, t, J = 7.7 Hz), 6.98 (1H, d, J = 7.7 Hz), 6.84 (1H, d, J = 7.7 Hz), 6.59 (1H, s), 3.20 (1H, dd, J = 17.2, 6.2 Hz), 2.94 (1H, d, J = 17.2 Hz), 2.30-2.15 (1H, m), 1.90-1.75 (1H, m), 1.05-0.90 (1 H, m).
[950] Melting point (° C): 245-247.
[951] Example 15 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-5-yloxy) -6-chloro-4-pyridazinol (Compound No. 516, Step B-4 )
[952] 32.6 mg (0.111 mmol) of 3- (1,1a, 6,6a-tetrahydrocyclopropa [a] inden-5-yloxy) -4,6-dichloropyridazine obtained by Example 14 (8) It was dissolved in dimethyl sulfoxide (3 mL), 0.1 mL (0.2 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to this solution, and the mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into ice-cold 1 mol / L aqueous sodium hydroxide solution, and washed with ethyl acetate. The aqueous layer was separated, adjusted to pH 4 by adding concentrated hydrochloric acid under ice-cooling, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over sodium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 1, developed with chloroform: methanol = 10: 1), and 3- (1,1a, 6,6a- 13.4 mg (0.0487 mmol, yield 43.9%) of tetrahydrocyclopropa [a] inden-5-yloxy) -6-chloro-4-pyridazinol (Compound No. 516) were obtained.
[953] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.25-7.05 (2H, m), 6.83 (1H, dd, J = 6.6, 2.6 Hz), 6.67 (1H, s), 3.00 (1H, dd, J = 17.2, 6.6 Hz), 2.78 (1H, d, J = 17.2 Hz), 2.50-2.35 (1H, m), 2.00-1.80 (1H, m), 1.15-1.00 (1H, m), 0.10-0.00 ( 1H, m).
[954] Melting point (° C): 211-213.
[955] Example 16 6-Chloro-3- (2-methoxy-5-methylphenoxy) -4-pyridazinol (Compound No. 704)
[956] (1) 6-chloro-3- (2-methoxy-5-methylphenoxy) pyridazine 1-oxide (step B-2)
[957] 167.5 mg (1.21 mmol) of commercial 2-methoxy-5-methylphenol are dissolved in a mixed solvent of 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL), and potassium tert-butoxide 142.8 is dissolved in this solution. mg (1.27 mmol) was added, followed by 202.9 mg (1.23 mmol) of 3,6-dichloropyridazine 1-oxide, followed by stirring at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 sheets, and developed with ethyl acetate: hexane = 2: 1) to obtain 6-chloro-3- (2-meth). 226.5 mg (0.849 mmol, yield 70.2%) of oxy-5-methylphenoxy) pyridazine 1-oxides were obtained.
[958] (2) 4,6-dichloro-3- (2-methoxy-5-methylphenoxy) pyridazine (Step B-3)
[959] 226.5 mg (0.849 mmol) of 6-chloro-3- (2-methoxy-5-methylphenoxy) pyridazine 1-oxide obtained by (1) was dissolved in phosphorus oxychloride (1 mL) to prepare the solution. Stir overnight at room temperature. Water and methylene chloride were added to the reaction mixture, which was stirred for 30 minutes and then extracted with methylene chloride. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 sheets, and developed with ethyl acetate: hexane = 2: 1) to obtain 4,6-dichloro-3- (2 205.3 mg (0.720 mmol, yield 84.8%) of -methoxy-5-methylphenoxy) pyridazine was obtained.
[960] (3) 6-chloro-3- (2-methoxy-5-methylphenoxy) -4-pyridazinol (Compound No. 704, step B-4)
[961] 205.3 mg (0.720 mmol) of 4,6-dichloro-3- (2-methoxy-5-methylphenoxy) pyridazine obtained by (2) was added with 1,4-dioxane (5 mL) and dimethyl sulfoxide ( 5 mL) was dissolved in a mixed solvent, and 1.8 mL (3.6 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the solution, followed by stirring at room temperature overnight. Water was added to the reaction solution, diluted hydrochloric acid was added to adjust the pH to 2, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, developed with ethyl acetate) to give 6-chloro-3- (2-methoxy-5-methylphenoxy. 148.1 mg (0.555 mmol, yield 77.1%) of p. 4-pyridazinol (Compound No. 704) was obtained.
[962] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.04-6.91 (3H, m), 6.66 (1H, s), 3.70 (3H, s), 2.27 (3H, s).
[963] Melting point (° C): 126-134.
[964] Example 17 6-Chloro-3- {2- [1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} -4-pyridazinol (Compound No. 728)
[965] (1) 3-fluoro-2-methoxybenzaldehyde
[966] To a commercial solution of 3.01 g (21.5 mmol) of acetonitrile (50 mL) of commercial 3-fluoro-2-hydroxybenzaldehyde, 5.92 g (42.8 mmol) of potassium carbonate and 6.66 mL (107 mmol) of methyl iodide were added and the mixture was heated to 90 ° C. The mixture was heated and stirred for 3 hours. After standing at room temperature overnight, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain 3.22 g of a crude product of 3-fluoro-2-methoxybenzaldehyde. .
[967] (2) 1-fluoro-2-methoxy-3-vinylbenzene
[968] Under nitrogen atmosphere, 273.2 mg (6.83 mmol) of 60% sodium hydride washed with hexane was suspended in dry dimethyl sulfoxide (3 mL), and the suspension was heated and stirred at 85 ° C. for 30 minutes, and then returned to room temperature and further, iced. On cooling, a solution of 2.44 g (6.83 mmol) of dry dimethylsulfoxide (8 mL) of methyl (triphenyl) phosphonium bromide was slowly added dropwise. After stirring for 30 minutes at room temperature, 877.4 mg of a dry dimethyl sulfoxide (5 mL) solution of crude product of 3-fluoro-2-methoxybenzaldehyde obtained in (1) was added dropwise, and stirred at room temperature for 30 minutes. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate gradient) to obtain 0.38 g of 1-fluoro-2-methoxy-3-vinylbenzene ( 2.5 mmol).
[969] (3) 1-cyclopropyl-3-fluoro-2-methoxybenzene
[970] In a nitrogen atmosphere, dry diethyl ether (5 mL) was added to a dry flask, and 9.20 mL (9.20 mmol) of diethyl zinc (1 mol / L hexane solution) was added dropwise to obtain the 1-fluoro- obtained by (2). A solution of 0.56 g (3.7 mmol) of dry diethyl ether (10 mL) in 2-methoxy-3-vinylbenzene was added dropwise. After stirring for 5 minutes at room temperature, 1.48 mL (18.4 mmol) of diiodomethane was added dropwise, followed by heating to reflux for 5 hours. After cooling to room temperature, 9.20 mL (9.20 mmol) of diethylzinc (1 mol / L hexane solution) and 1.48 mL (18.4 mmol) of diiodomethane were added, and the mixture was further heated to reflux for 4 hours. After standing at room temperature overnight, the reaction mixture was poured into saturated aqueous ammonium chloride solution. Saturated aqueous sodium hydrogen carbonate solution was added thereto, stirred for 30 minutes, and then extracted with diethyl ether. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain crude purification of 1-cyclopropyl-3-fluoro-2-methoxybenzene. 0.82 g of water was obtained.
[971] (4) 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} pyridazine 1-oxide (step B-2)
[972] Under nitrogen atmosphere, 288.8 mg (7.22 mmol) of 60% sodium hydride was suspended in dry N, N-dimethylformamide (3 mL), and 0.55 mL (7.5 mmol) of ethanethiol was slowly added dropwise to the suspension. After stirring for 15 minutes, a dry N, N-dimethylformamide (6 mL) solution of 402.1 mg of a crude product of 1-cyclopropyl-3-fluoro-2-methoxybenzene obtained in (3) was added dropwise, It stirred by heating at 160 degreeC for 5 hours. After standing at room temperature overnight, 1 mol / L aqueous potassium hydroxide solution and diethyl ether were added to the reaction mixture. The aqueous layer was separated, washed with diethyl ether, and diluted to pH 2 with dilute hydrochloric acid. The mixture was extracted with diethyl ether, the ether extracts were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (developing as 1.05744 3 sheets of MERCK company use ethyl acetate: hexane = 4: 1), and the mixture obtained 299.9 mg.
[973] 152.7 mg of this mixture are dissolved in a mixed solvent of 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL), and 116.1 mg (1.03 mmol) of potassium tert-butoxide are added to the solution, followed by 3,6- 162.6 mg (0.988 mmol) of dichloropyridazine 1-oxide were added and stirred overnight at room temperature. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by Merck, 1.05744, 3 pieces, and developed as ethyl acetate: hexane = 2: 1), and 6-chloro-3- {2- [ 46.6 mg (0.144 mmol) of 1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} pyridazine 1-oxide were obtained.
[974] (5) 4,6-dichloro-3- {2- [1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} pyridazine (Step B-3)
[975] 46.6 mg (0.144 mmol) of phosphorus oxychloride of 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} pyridazine 1-oxide obtained by (4) 0.5 mL) was stirred at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by Merck, 1.05744, use of 1 sheet, and developed as ethyl acetate: hexane = 4: 1), and 4,6- dichloro-3- {2 9.8 mg (0.028 mmol, yield 19%) of-[1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} pyridazine was obtained.
[976] (6) 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} -4-pyridazinol (Compound No. 728, step B-4)
[977] 9.8 mg (0.028 mmol) of 4,6-dichloro-3- {2- [1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} pyridazine obtained by (5) were prepared using 1,4-dioxane. (1 mL) and dimethylsulfoxide (1 mL) were dissolved in a mixed solvent, and 0.07 mL (0.14 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the solution, which was stirred overnight at room temperature. The reaction mixture was poured into water, diluted hydrochloric acid was added to adjust pH to 2, and then extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, using 1 sheet, developed with ethyl acetate) to obtain 6-chloro-3- {2- [1- (ethylsulfanyl). 2.2 mg (0.0067 mmol, Yield 24%) of ethyl] -6-fluorophenoxy} -4-pyridazinol (Compound No. 728) was obtained.
[978] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.42 (1H, d, J = 8.1 Hz), 7.26-7.15 (1H, m), 7.07-6.97 (1H, m), 6.46 (1H, s), 4.33 (1H, q, J = 7.0 Hz), 2.42-2.20 (2H, m), 1.43 (3H, d, J = 7.0 Hz), 1.02 (3H, t, J = 7.0 Hz).
[979] Physical property: Amorphous.
[980] Example 18 6-Chloro-3- (2-chloro-6-isopropylphenoxy) -4-pyridazinol (Compound No. 738)
[981] (1) 1-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene
[982] 4.80 g (120 mmol) of 60% sodium hydride are suspended in dry tetrahydrofuran (60 mL) and in this suspension a solution of 13.6 g (100 mmol) of dry tetrahydrofuran (80 mL) of 2-isopropylphenol at 0 ° C. Was added dropwise. After stirring for 10 minutes at 0 ° C., a solution of 14.9 g (119 mmol) of dry tetrahydrofuran (80 mL) of 2-methoxyethoxymethylchloride was added dropwise. The reaction mixture was stirred for 2 hours under ice-cooling, poured into ice-cold water (250 mL), and extracted with ethyl acetate. The organic layers were combined, washed successively with 1 mol / L aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 50: 1) to give 1-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene 18.1 g (80.8 mmol, yield 80.8%) were obtained.
[983] (2) 1-chloro-3-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene
[984] 8.00 g (35.7 mmol) of 1-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene obtained in (1) were dissolved in dry ether (100 mL), and ice-cold in this solution. 34.4 mL (55.0 mmol) of butyllithium hexane solution (1.60 M) was added dropwise (reaction solution temperature 5-10 ° C), followed by stirring for 5 hours under ice-cooling. 2.51 g (35.4 mmol) of chlorine gas was blown in this, maintaining reaction liquid temperature at 5-10 degreeC. The reaction mixture was stirred for 1 hour under ice cooling, poured into 1 mol / L hydrochloric acid (300 mL), and extracted with ether. The organic layers were combined, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 100: 1) to give 1-chloro-3-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene. 4.38 g (16.9 mmol, yield 47.3%) were obtained.
[985] (3) 2-chloro-6-isopropylphenol
[986] 4.38 g (16.9 mmol) of 1-chloro-3-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene obtained by (2) were dissolved in dichloromethane (15 mL), 2.70 g (23.7 mmol) of fluoroacetic acid were added and stirred overnight at room temperature. The reaction mixture was poured into 1 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (eluted with hexane) to give 2.50 g (14.7 mmol, yield 87.0%) of 2-chloro-6-isopropylphenol.
[987] (4) 3-chloro-6- (2-chloro-6-isopropylphenoxy) pyridazine (Step A-1)
[988] 1.98 g (17.7 mmol) of potassium tert-butoxide, 1,4-dioxane (100 mL) and 2.50 g (14.7 mmol) of 2-chloro-6-isopropylphenol obtained from (3) were mixed and the mixture was Stir at room temperature for 20 minutes. To this was added 2.18 g (14.6 mmol) of 3,6-dichloropyridazine and heated to reflux for 4 hours. To the reaction mixture was added 0.50 g (4.5 mmol) of potassium tert-butoxide and heated to reflux for another 3 hours. The reaction mixture was allowed to cool, poured into 1 N hydrochloric acid (100 mL), and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to obtain 3.18 g (11.2) of 3-chloro-6- (2-chloro-6-isopropylphenoxy) pyridazine. Mmol, yield 76.2%).
[989] (5) 6-chloro-3- (2-chloro-6-isopropylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-chloro-6-isopropylphenoxy) pyridazine 1- Mixture of Oxides (Step C-1)
[990] 3.17 g (11.2 mmol) of 3-chloro-6- (2-chloro-6-isopropylphenoxy) pyridazine obtained by (4) are dissolved in dry dichloromethane (90 mL), and 80-85% in this solution 2.90 g (13.4-14.3 mmol) of m-chloroperbenzoic acid were added and heated to reflux for 13 hours. The reaction mixture was poured into 1N aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 6-chloro-3- (2-chloro-6-isopropylphenoxy) pyridazine 1-oxide and 2.82 g (9.43 mmol, yield 84.2%) of a mixture of 3-chloro-6- (2-chloro-6-isopropylphenoxy) pyridazine 1-oxide were obtained.
[991] (6) a mixture of 4,6-dichloro-3- (2-chloro-6-isopropylphenoxy) pyridazine and 3,4-dichloro-6- (2-chloro-6-isopropylphenoxy) pyridazine (Step C-2)
[992] 6-chloro-3- (2-chloro-6-isopropylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-chloro-6-isopropylphenoxy) pyridine obtained by (5) 2.80 g (9.36 mmol) of a mixture of chopped 1-oxide were mixed with 17.5 mL (189 mmol) of phosphorus oxychloride, and the mixture was heated to reflux for 2 hours 30 minutes. The reaction mixture was allowed to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate = 20: 1) to give 4,6-dichloro-3- (2-chloro-6-isopropylphenoxy) pyridazine. 0.850 g (2.67 mmol, melting point 90-91 ° C.), 4,6-dichloro-3- (2-chloro-6-isopropylphenoxy) pyridazine and 3,4-dichloro-6- (2-chloro- 1.78 g (5.60 mmol) of a mixture of 6-isopropylphenoxy) pyridazine was obtained.
[993] (7) 6-chloro-3- (2-chloro-6-isopropylphenoxy) -4-methoxypyridazine and 3-chloro-6- (2-chloro-6-isopropylphenoxy) -4- Methoxypyridazine (Step C-3)
[994] To methanol (10 mL) was added 0.080 g (3.5 mmol) of sodium and stirred at room temperature for 30 minutes. 0.830 g (2.61 mmol) of 4,6-dichloro-3- (2-chloro-6-isopropylphenoxy) pyridazine obtained in (6) was added thereto, followed by stirring at room temperature for 2 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, and the solvent was distilled off. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 10: 1), washed with hexane to crystallize, and then 6-chloro-3- (2-chloro-6-isopropylphenoxy) -4 0.720 g (2.30 mmol, yield 88.1%) of -methoxypyridazine was obtained. Meanwhile, a mixture of 4,6-dichloro-3- (2-chloro-6-isopropylphenoxy) pyridazine and 3,4-dichloro-6- (2-chloro-6-isopropylphenoxy) pyridazine 1.78 g (5.60 mmol) was reacted in the same manner to yield 1.25 g (3.99 mmol, 71.3% yield) of 6-chloro-3- (2-chloro-6-isopropylphenoxy) -4-methoxypyridazine, 3- 0.300 g (0.958 mmol, yield 17.1%) of chloro-6- (2-chloro-6-isopropylphenoxy) -4-methoxypyridazine was obtained.
[995] (8) 6-chloro-3- (2-chloro-6-isopropylphenoxy) -4-pyridazinol (Compound No. 738, Step C-4)
[996] 1.46 g (4.66 mmol) of 6-chloro-3- (2-chloro-6-isopropylphenoxy) -4-methoxypyridazine obtained by (6) was dissolved in dimethyl sulfoxide (13 mL), and this solution 3 mL (6.0 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the mixture, followed by stirring at 80 ° C for 3 hours. The reaction mixture was poured into water and made acidic with hydrochloric acid. The precipitated solid was collected by filtration, washed with water, and air dried. 1.33 g (4.45 mmol, yield 95.5%) of 6-chloro-3- (2-chloro-6-isopropylphenoxy) -4-pyridazinol (Compound No. 738) was obtained.
[997] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.40-7.05 (3H, m), 6.70 (1H, s), 2.98 (1H, septet, J = 6.2 Hz), 1.13 (6H, d, J = 6.2 Hz).
[998] Melting point (° C.): 218-233.
[999] Example 19 3- (2-Bromo-6-isopropylphenoxy) -6-chloro-4-pyridazinol (Compound No. 760)
[1000] (1) 1-bromo-3-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene
[1001] 5.18 g (23.1 mmol) of 1-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene obtained in Example 18 (1) was dissolved in dry ether (100 mL), and ice-cold in this solution. 22.3 mL (35.7 mmol) of n-butyllithium hexane solution (1.60M) was added dropwise (reaction solution temperature 5-10 ° C), followed by stirring for 5 hours under ice-cooling. 8.20 g (69.7 mmol) of 90% cyanide bromide was added thereto while maintaining the reaction liquid temperature at 5-10 ° C. The reaction mixture was stirred for 2 hours under ice-cooling, poured into ice-cold water (300 mL) and extracted with ether. The organic layers were combined, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 100: 1) to give 1-bromo-3-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene 3.40 g (11.2 mmol, yield 48.5%) were obtained.
[1002] (2) 2-bromo-6-isopropylphenol
[1003] 3.40 g (11.2 mmol) of 1-bromo-3-isopropyl-2-[(2-methoxyethoxy) methoxy] benzene obtained by (1) was dissolved in dichloromethane (10 mL), and 2.50 g (21.9 mmol) of trifluoroacetic acid were added and stirred overnight at room temperature. The reaction mixture was poured into 1 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (eluted with hexane) to give 2.27 g (10.6 mmol, yield 94.6%) of 2-bromo-6-isopropylphenol.
[1004] (3) 3- (2-bromo-6-isopropylphenoxy) -6-chloropyridazine (Step A-1)
[1005] 1.52 g (13.6 mmol) of potassium tert-butoxide, 1,4-dioxane (60 mL) and 2.27 g (10.6 mmol) of 2-bromo-6-isopropylphenol obtained by (2) were mixed and The mixture was stirred at rt for 20 min. To this was added 1.58 g (10.6 mmol) of 3,6-dichloropyridazine and heated to reflux for 7 hours 20 minutes. The reaction mixture was allowed to cool, poured into ice-cold water (110 mL), and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by recrystallization (isopropyl ether), followed by silica gel column chromatography (hexane: ethyl acetate gradient), to obtain 3- (2-bromo-6-isopropylphenoxy) -6. 2.68 g (8.17 mmol, yield 77.1%) of -chloropyridazine were obtained.
[1006] (4) 3- (2-bromo-6-isopropylphenoxy) -6-chloropyridazine 1-oxide and 6- (2-bromo-6-isopropylphenoxy) -3-chloropyridazine Mixture of 1-oxides (Step C-1)
[1007] 2.68 g (8.17 mmol) of 3- (2-bromo-6-isopropylphenoxy) -6-chloropyridazine obtained by (3) are dissolved in dry dichloromethane (35 mL), and 80-85 in this solution 2.12 g (9.80-10.4 mmol) of% m-chloroperbenzoic acid were added, followed by heating to reflux for 12 hours 30 minutes. The reaction mixture was poured into 1 mol / L aqueous sodium hydroxide solution and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate = 5: 1) to give 3- (2-bromo-6-isopropylphenoxy) -6-chloropyridazine 1 2.26 g (6.57 mmol, yield 80.4%) of a mixture of -oxide and 6- (2-bromo-6-isopropylphenoxy) -3-chloropyridazine 1-oxide were obtained.
[1008] (5) 3- (2-bromo-6-isopropylphenoxy) -4,6-dichloropyridazine and 6- (2-bromo-6-isopropylphenoxy) -3,4-dichloropyridazine Mixture of (Step C-2)
[1009] 3- (2-bromo-6-isopropylphenoxy) -6-chloropyridazine 1-oxide and 6- (2-bromo-6-isopropylphenoxy) -3- obtained by (4) -3- 2.14 g (6.22 mmol) of a mixture of chloropyridazine 1-oxide were mixed with 11.6 mL (125 mmol) of phosphorus oxychloride, and the mixture was heated to reflux for 3 hours. The reaction mixture was allowed to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with 1 mol / L aqueous sodium hydroxide solution, water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate = 20: 1) to give 3- (2-bromo-6-isopropylphenoxy) -4,6-dichloropyridine. 2.22 g (6.13 mmol, yield 98.6%) of a mixture of chopped and 6- (2-bromo-6-isopropylphenoxy) -3,4-dichloropyridazine were obtained.
[1010] (6) 3- (2-bromo-6-isopropylphenoxy) -6-chloro-4-methoxypyridazine (step C-3)
[1011] To methanol (20 mL) was added 0.180 g (7.8 mmol) of sodium and stirred at room temperature for 30 minutes. 3- (2-bromo-6-isopropylphenoxy) -4,6-dichloropyridazine and 6- (2-bromo-6-isopropylphenoxy) -3 obtained by (5) 2.22 g (6.13 mmol) of a mixture of 4-dichloropyridazine were added and stirred at room temperature for 4 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate = 15: 1), washed with hexane and crystallized to obtain 3- (2-bromo-6-isopropylphenoxy). 1.48 g (4.13 mmol, yield 67.4%) of -6-chloro-4-methoxypyridazine were obtained. Also, 0.21 g (0.59 mmol, yield 9.6%) of 6- (2-bromo-6-isopropylphenoxy) -3-chloro-4-methoxypyridazine was obtained simultaneously.
[1012] (7) 3- (2-bromo-6-isopropylphenoxy) -6-chloro-4-pyridazinol (Compound No. 760, step C-4)
[1013] 0.72 g (2.0 mmol) of 3- (2-bromo-6-isopropylphenoxy) -6-chloro-4-methoxypyridazine obtained by (6) was dissolved in dimethyl sulfoxide (10 mL), and An aqueous sodium hydroxide solution (manufactured by dissolving 100 mg of sodium hydroxide in 1.5 mL of water, 2.4 mmol) was added to the solution, followed by stirring at 80 ° C for 3 hours. The reaction mixture was poured into water and made acidic with hydrochloric acid. The precipitated solid was collected by filtration, washed with water and air dried. 0.56 g (1.6 mmol, 80% yield) of 3- (2-bromo-6-isopropylphenoxy) -6-chloro-4-pyridazinol (Compound No. 760) was obtained.
[1014] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.70-7.00 (3H, m), 6.89 (1H, s), 2.94 (1H, septet, J = 7.0 Hz), 1.16 (6H, d, J = 7.0 Hz).
[1015] Melting point (° C.): 232-253 (decomposition).
[1016] Example 20 3- (2-Bromo-6-tert-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 761)
[1017] (1) tert-butyl-2-[(2-methoxyethoxy) methoxy] benzene
[1018] 4.80 g (120 mmol) of 60% sodium hydride are suspended in dry tetrahydrofuran (25 mL), and in this suspension 15.0 g (100 mmol) of dry tetrahydrofuran (80 mL) at 0 ° C. The solution was added dropwise. After stirring for 10 minutes at 0 ° C., 14.9 g (119 mmol) of dry tetrahydrofuran (80 mL) solution of 2-methoxyethoxymethylchloride was added dropwise. The reaction mixture was stirred for 4 hours and 30 minutes under ice-cooling and left overnight at room temperature. To the reaction mixture, 1.20 g (30 mmol) of 60% sodium hydride and 3.8 g (30 mmol) of 2-methoxyethoxymethylchloride were added at 0 ° C, and the mixture was stirred at 0 ° C for 7 hours. The reaction mixture was poured into ice cold water (250 mL) and extracted with ethyl acetate. The organic layers were combined, washed with 2 N aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 20: 1) to give tert-butyl-2-[(2-methoxyethoxy) methoxy] benzene. 19.7 g (82.8 mmol, yield 82.8%) were obtained.
[1019] (2) 1-bromo-3-tert-butyl-2-[(2-methoxyethoxy) methoxy] benzene
[1020] 10.0 g (42.0 mmol) of tert-butyl-2-[(2-methoxyethoxy) methoxy] benzene obtained by (1) was dissolved in dry ether (120 mL), and ice-cold in this solution, n-butyl 42.1 mL (64.4 mmol) of a lithium hexane solution (1.53 M) was added dropwise, followed by stirring for 3 hours under ice-cooling. To this was added dropwise a solution of 14.8 g (126 mmol) of dry ether (20 mL) of 90% cyanide bromide. The reaction mixture was stirred for 3 hours under ice-cooling, poured into ice-cold water (300 mL) and extracted with ether. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 20: 1) to give 1-bromo-3-tert-butyl-2-[(2-methoxy 8.48 g (26.8 mmol, yield 63.8%) of ethoxy) methoxy] benzene were obtained.
[1021] (3) 2-bromo-6-tert-butylphenol
[1022] 8.38 g (26.4 mmol) of 1-bromo-3-tert-butyl-2-[(2-methoxyethoxy) methoxy] benzene obtained by (2) was dissolved in dichloromethane (30 mL), and this solution To this was added a solution of 9.03 g (79.2 mmol) of dichloromethane (20 mL) in trifluoroacetic acid, which was stirred overnight at room temperature. The reaction mixture was poured into ice-cold 1 mol / L hydrochloric acid, and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (eluted with hexane) to give 5.68 g (24.8 mmol, 93.9% yield) of 2-bromo-6-tert-butylphenol.
[1023] (4) 3- (2-bromo-6-tert-butylphenoxy) -6-fluoropyridazine (step A-1)
[1024] 4.84 g (21.1 mmol) of 2-bromo-6-tert-butylphenol obtained in (3) was dissolved in 1,4-dioxane (40 mL), and 3.55 g (31.7 mmol) of potassium tert-butoxide in this solution. ) And 1,4-dioxane (40 mL) were added and stirred at room temperature for 15 minutes. To this was added 2.45 g (21.1 mmol) of 3,6-difluoropyridazine and heated to reflux for 24 hours. The reaction mixture was allowed to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to obtain 3- (2-bromo-6-tert-butylphenoxy) -6-fluoropyridazine 1.70. g (5.23 mmol, yield 24.8%) was obtained.
[1025] (5) 6- (2-bromo-6-tert-butylphenoxy) -3-pyridazinol
[1026] 1.04 g (10.6 mmol) of potassium acetate in 1.70 g (5.23 mmol) of acetic acid (9 mL) of 3- (2-bromo-6-tert-butylphenoxy) -6-fluoropyridazine obtained by (4) Was added and stirred at 130-140 ° C. for 3 hours. The reaction mixture was allowed to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was washed with benzene, and 1.54 g (4.77 mmol, yield 91.2%, melting point 255-) of 6- (2-bromo-6-tert-butylphenoxy) -3-pyridazinol was obtained. 257 ° C.).
[1027] (6) 3- (2-bromo-6-tert-butylphenoxy) -6-chloropyridazine
[1028] 1.54 g (4.77 mmol) of 6- (2-bromo-6-tert-butylphenoxy) -3-pyridazinol obtained by (5) is mixed with 15 mL (162 mmol) of phosphorus oxychloride and this mixture Heated to reflux for 70 minutes. Phosphorus oxychloride was distilled off from the reaction mixture, poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 1.55 g (4.53 mmol, yield 95.0%) of 3- (2-bromo-6-tert-butylphenoxy) -6-chloropyridazine.
[1029] (7) 3- (2-bromo-6-tert-butylphenoxy) -6-chloropyridazine 1-oxide and 6- (2-bromo-6-tert-butylphenoxy) -3-chloro Mixture of pyridazine 1-oxides (step C-1)
[1030] 1.42 g (4.15 mmol) of 3- (2-bromo-6-tert-butylphenoxy) -6-chloropyridazine obtained by (6) are dissolved in dry dichloromethane (20 mL), and 80% in this solution. A solution of 1.08 g (4.99 mmol) of dry dichloromethane (10 mL) in m-chloroperbenzoic acid was added and heated to reflux for 20 hours. 0.275 g (1.27 mmol) of 80% m-chloroperbenzoic acid was added to the reaction mixture, and the mixture was heated to reflux for 3 hours 30 minutes, poured into 1 mol / L aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate = 10: 1) to give 3- (2-bromo-6-tert-butylphenoxy) -6-chloropyridazine 0.704 g (1.97 mmol, yield 47.5%) of a mixture of 1-oxide and 6- (2-bromo-6-tert-butylphenoxy) -3-chloropyridazine 1-oxide were obtained.
[1031] (8) 3- (2-bromo-6-tert-butylphenoxy) -4,6-dichloropyridazine and 6- (2-bromo-6-tert-butylphenoxy) -3,4-dichloro Pyridazine (Step C-2)
[1032] 3- (2-Bromo-6-tert-butylphenoxy) -6-chloropyridazine 1-oxide and 6- (2-bromo-6-tert-butylphenoxy)-obtained by (7) 0.704 g (1.97 mmol) of a mixture of 3-chloropyridazine 1-oxide were mixed with 5 mL (54 mmol) of phosphorus oxychloride, and the mixture was heated to reflux for 2 hours. The reaction mixture was allowed to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate = 20: 1) to give 3- (2-bromo-6-tert-butylphenoxy) -4,6-dichloro 0.474 g (1.26 mmol, yield 64.0%) of pyridazine, and 0.119 g (0.316 mmol, yield of 16.0%) of 6- (2-bromo-6-tert-butylphenoxy) -3,4-dichloropyridazine were obtained. .
[1033] (9) 3- (2-bromo-6-tert-butylphenoxy) -6-chloro-4-methoxypyridazine (step C-3)
[1034] 0.443 g (1.18 mmol) of 3- (2-bromo-6-tert-butylphenoxy) -4,6-dichloropyridazine obtained in (8) was dissolved in methanol (10 mL), and 28% in this solution. 0.545 g (2.83 mmol) of sodium methoxide-methanol solution and methanol (5 mL) were added and stirred at room temperature for 80 minutes. 0.10 g (0.52 mmol) of 28% sodium methoxide-methanol solution was added to the reaction mixture, stirred at room temperature for 2 hours, and then 0.15 g (0.78 mmol) of 28% sodium methoxide-methanol solution was added overnight at room temperature. Stirred. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 0.428 g (1.15 mmol, yield 97.5%) of 3- (2-bromo-6-tert-butylphenoxy) -6-chloro-4-methoxypyridazine.
[1035] (10) 3- (2-bromo-6-tert-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 761, step C-4)
[1036] 0.395 g (1.06 mmol) of 3- (2-bromo-6-tert-butylphenoxy) -6-chloro-4-methoxypyridazine obtained by (9) was dissolved in dimethyl sulfoxide (5 mL), An aqueous sodium hydroxide solution (manufactured by dissolving 50.8 mg of sodium hydroxide in 3 mL of water, 1.27 mmol) was added to the solution, followed by stirring at 80 ° C for 3 hours. An aqueous sodium hydroxide solution (42 mg of sodium hydroxide was dissolved in 3 mL of water, 1.1 mmol) and dimethyl sulfoxide (10 mL) were added, followed by further stirring at 80 ° C for 5 hours. After cooling, the reaction mixture was poured into ice-cold water and acidified with hydrochloric acid. The precipitated solid was collected by filtration, washed successively with water, hexane and isopropyl ether, and air dried. 0.309 g (0.863 mmol, Yield 81.4%) of 3- (2-bromo-6-tert-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 761) was obtained.
[1037] ¹ H-NMR (270 MHz, CDCl ₃ ) δ ppm: 9.55 (1H, brs), 7.47 (1H, dd, J = 8.1, 1.7 Hz), 7.41 (1H, dd, J = 8.1, 1.7 Hz), 7.08 (1H , t, J = 8.1 Hz), 6.58 (1H, brs), 1.34 (9H, s).
[1038] Melting Point (° C): 240-247.
[1039] Example 21 6-Chloro-3- (2,6-dimethylphenoxy) -4-pyridazinol (Compound No. 801)
[1040] (1) 6-chloro-3- (2,6-dimethylphenoxy) pyridazine 1-oxide (step B-2)
[1041] 268 mg (2.20 mmol), 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL) of 2,6-dimethylphenol were mixed and ice-cooled to 270 mg (2.41) of potassium tert-butoxide Mmol) was added and stirred for 10 minutes. 370 mg (2.24 mmol) of 3, 6- dichloropyridazine 1-oxides were added here, and it left to stand after stirring for 10 hours at room temperature. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 350 mg (1.39) of 6-chloro-3- (2,6-dimethylphenoxy) pyridazine 1-oxide. Mmol, yield 63.1%).
[1042] (2) 4,6-dichloro-3- (2,6-dimethylphenoxy) pyridazine (Step B-3)
[1043] 330 mg (1.31 mmol) of 6-chloro-3- (2,6-dimethylphenoxy) pyridazine 1-oxide obtained by (1) were diluted with dichloromethane (0.6 mL) and 0.60 mL (6.5 mmol) of phosphorus oxychloride. And the mixture was stirred for 1 hour, and further left for 5 days. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 322 mg (1.20 mmol) of 4,6-dichloro-3- (2,6-dimethylphenoxy) pyridazine. , Yield 91.6%).
[1044] (3) 6-chloro-3- (2,6-dimethylphenoxy) -4-pyridazinol (Compound No. 801, step B-4)
[1045] 300 mg (1.12 mmol) of 4,6-dichloro-3- (2,6-dimethylphenoxy) pyridazine obtained in (2) were dissolved in dimethyl sulfoxide (8 mL), and 10% (W / V) 0.80 mL (2.0 mmol) of aqueous sodium hydroxide solution was added and stirred overnight at room temperature. Furthermore, 0.80 mL (2.0 mmol) of 10% (W / V) sodium hydroxide aqueous solution was added, and after the raw material disappeared, the reaction mixture was poured into ice-cold water. After acidifying with hydrochloric acid, the mixture was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) and preparative thin layer chromatography (manufactured by Merck, 1.05744, developed with dichloromethane: methanol = 9: 1) to obtain 6- 128 mg (0.510 mmol, yield 45.5%) of chloro-3- (2,6-dimethylphenoxy) -4-pyridazinol (Compound No. 801) were obtained.
[1046] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.18-7.05 (3H, m), 6.83 (1H, s), 2.05 (6H, s),
[1047] Melting point (° C): 214-215.
[1048] Example 22 3- (2-tert-butyl-6-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 805)
[1049] (1) 3- (2-tert-butyl-6-methylphenoxy) -6-chloropyridazine (Step A-1)
[1050] 17.5 g (107 mmol) of 2-tert-butyl-6-methylphenol, 11.9 g (106 mmol) of potassium tert-butoxide and 1,4-dioxane (250 mL) are mixed and the mixture is stirred at room temperature for 30 minutes. Stirred. 15.0 g (101 mmol) of 2, 6- dichloropyridazines were added here, and it stirred at 100 degreeC for 3 hours and 15 minutes. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was crystallized from isopropyl ether to give 15.3 g (55.2 mmol, yield 54.6%) of 3- (2-tert-butyl-6-methylphenoxy) -6-chloropyridazine.
[1051] (2) 3- (2-tert-butyl-6-methylphenoxy) -6-chloropyridazine 1-oxide (step C-1)
[1052] 8.00 g (28.9 mmol) of 3- (2-tert-butyl-6-methylphenoxy) -6-chloropyridazine obtained by (1) were dried with dichloromethane (200 mL) and 8.50 g of 70% m-chloroperbenzoic acid. (34.4 mmol) and the mixture was stirred at room temperature for 4 days. The reaction mixture was poured into ice-cold saturated aqueous sodium sulfite solution and extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by crystallization or silica gel column chromatography from an ether-hexane mixed solvent to give 3- (2-tert-butyl-6-methylphenoxy) -6-chloropyridazine 1-jade Seed 7.04 g (24.0 mmol, yield 83.0%) was obtained.
[1053] (3) 3- (2-tert-butyl-6-methylphenoxy) -4,6-dichloropyridazine (step C-2)
[1054] 1.00 g (3.41 mmol) of 3- (2-tert-butyl-6-methylphenoxy) -6-chloropyridazine 1-oxide obtained by (2) was added to chloroform (10 mL) and 0.48 mL of phosphorus oxychloride ( 5.2 mmol) and the mixture was stirred under reflux for 24 hours and at room temperature for 2 days. The reaction mixture was poured into ice cold water and extracted with dichloromethane. The organic layers were combined, washed successively with saturated aqueous sodium hydrogen carbonate solution, water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was crystallized from an ether-hexane mixed solvent to obtain 0.767 g (2.47 mmol, yield 72.4% of 3- (2-tert-butyl-6-methylphenoxy) -4,6-dichloropyridazine. )
[1055] (4) 3- (2-tert-butyl-6-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 805, step C-3)
[1056] 354 mg (1.14 mmol) of 3- (2-tert-butyl-6-methylphenoxy) -4,6-dichloropyridazine obtained by (3) were added to dimethyl sulfoxide (10 mL) and 1 mol / L sodium hydroxide. It was mixed with 1.6 mL (1.6 mmol) of an aqueous solution, and the mixture was stirred at room temperature for 2 hours 30 minutes. The reaction mixture was poured into ice cold water and washed with ether. The aqueous layer was made acidic with hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was crystallized with an ether-hexane mixed solvent to afford 3- (2-tert-butyl-6-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 805). mg (0.587 mmol, yield 51.5%) were obtained.
[1057] ¹ H-NMR (90 MHz, CDCl ₃ ) δ ppm: 7.35-6.80 (3H, m), 6.50 (1H, s), 1.80 (3H, s), 1.18 (9H, s).
[1058] Melting point (° C.): 135-136.
[1059] Example 23 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol (Compound No. 806)
[1060] (1) 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-cyclopropyl-6-methylphenoxy) pyridazine 1- Oxide (Step B-2)
[1061] 221 mg (1.49 mmol) of 2-cyclopropyl-6-methylphenol are mixed with 1,4-dioxane (2 mL) and dimethylsulfoxide (2 mL), and on this mixture under ice-cooling, potassium tert-butoxide 184 mg (1.64 mmol) was added and stirred for 10 minutes. 258 mg (1.56 mmol) of 3,6-dichloropyridazine 1-oxides were added thereto, and the mixture was left for 3 days after stirring at room temperature for 10 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) pyridazine 1-oxide and 222 mg (0.801 mmol, yield 53.8%) of a mixture of 3-chloro-6- (2-cyclopropyl-6-methylphenoxy) pyridazine 1-oxide was obtained.
[1062] (2) 4,6-dichloro-3- (2-cyclopropyl-6-methylphenoxy) pyridazine (Step B-3)
[1063] 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-cyclopropyl-6-methylphenoxy) pyridine obtained by (1) 210 mg (0.758 mmol) of a mixture of chopped 1-oxide are dissolved in chloroform (1 mL), and 0.106 mL (1.14 mmol) of phosphorus oxychloride is added to the solution, and most of the chloroform is distilled off under a nitrogen stream, and then at room temperature. Stir for 2 days. In addition, chloroform (2 mL) and 0.150 mL (1.62 mmol) of phosphorus oxychloride were added, and most of the chloroform was distilled off under a nitrogen stream, followed by stirring for 3 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solution was distilled off and the residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 167 mg of 4,6-dichloro-3- (2-cyclopropyl-6-methylphenoxy) pyridazine. (0.566 mmol, Yield 74.7%) were obtained.
[1064] (3) 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol (Compound No. 806, step B-4)
[1065] 150 mg (0.508 mmol) of 4,6-dichloro-3- (2-cyclopropyl-6-methylphenoxy) pyridazine obtained in (2) were dissolved in dimethyl sulfoxide (3 mL), and 10% in this solution. 0.37 mL (0.925 mmol) of (W / V) sodium hydroxide aqueous solution was added, and it stirred at room temperature for 4 days. The reaction mixture was poured into ice-cold 5% aqueous sodium hydroxide solution and extracted with ether. The aqueous layer was made acidic with hydrochloric acid and extracted with ether. The organic layer was dried and concentrated. The residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, developed as dichloromethane: methanol = 20: 1) to give 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridine. 114 mg (0.412 mmol, yield 81.1%) of dazinol (Compound No. 806) were obtained.
[1066] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.13-7.03 (2H, m), 6.84-6.79 (2H, m), 2.06 (3H, s), 1.83-1.68 (1H, m), 0.82- 0.72 (2H, m), 0.64-0.51 (2H, m).
[1067] Melting point (° C): 201-202.
[1068] Example 24 6-Chloro-3- [2- (2,2-dichlorocyclopropyl) -6-methylphenoxy] -4-pyridazinol (Compound No. 827)
[1069] (1) 1- (2,2-dichlorocyclopropyl) -2-methoxy-3-methylbenzene
[1070] 304 mg (2.05 mmol) of 2-methoxy-1-methyl-3-vinylbenzene was dissolved in chloroform (12 mL), and 5 mL (63 mmol) of 50% aqueous sodium hydroxide solution was added dropwise to this solution, followed by benzyl (tri 59.9 mg (0.263 mmol) of ethyl) ammonium chloride were added and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with chloroform. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by Merck, 1.05744, 3 pieces, and developed as hexane: ethyl acetate = 4: 1), and 1- (2,2-dichlorocyclopropyl 390 mg (1.69 mmol, yield 82.4%) of 2-methoxy-3-methylbenzene were obtained.
[1071] (2) 2- (2,2-dichlorocyclopropyl) -6-methylphenol
[1072] 102 mg (0.442 mmol) of 1- (2,2-dichlorocyclopropyl) -2-methoxy-3-methylbenzene obtained in (1) were dissolved in dichloromethane (5 mL), and the solution was ice-cooled and stirred. Boron tribromide 0.045 mL (0.47 mmol) was added dropwise. The reaction mixture was stirred for 2 hours under ice-cooling, poured into water, and extracted with dichloromethane. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by Merck, 1.05744, 2 sheets, and developed as hexane: ethyl acetate = 2: 1), and 2- (2,2-dichlorocyclopropyl 76.9 mg (0.354 mmol, Yield 80.1%) of () -6-methylphenols were obtained.
[1073] (3) 6-chloro-3- [2- (2,2-dichlorocyclopropyl) -6-methylphenoxy] pyridazine 1-oxide (step B-2)
[1074] 198 mg (0.912 mmol) of 2- (2,2-dichlorocyclopropyl) -6-methylphenol obtained by (2) are mixed with 1,4-dioxane (3 mL) and dimethyl sulfoxide (3 mL) 113 mg (1.01 mmol) of potassium tert-butoxides were added to this mixture under ice cooling, and it stirred for 10 minutes. 151 mg (0.915 mmol) of 3,6-dichloropyridazine 1-oxides were added thereto, and the mixture was stirred overnight at room temperature. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, used three times, and developed three times with hexane: ethyl acetate = 2: 1). 6-chloro-3- [2- 257 mg of crude product of (2,2-dichlorocyclopropyl) -6-methylphenoxy] pyridazine 1-oxide was obtained.
[1075] (4) 4,6-dichloro-3- [2- (2,2-dichlorocyclopropyl) -6-methylphenoxy] pyridazine (Step B-3)
[1076] Crude 257 mg of 6-chloro-3- [2- (2,2-dichlorocyclopropyl) -6-methylphenoxy] pyridazine 1-oxide obtained by (3) was substituted with phosphorus oxychloride (3 mL ) And the mixture was stirred overnight at room temperature. Water and dichloromethane were added to the reaction mixture, which was stirred for 30 minutes. The mixture was separated, the organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 sheets, developed with hexane: ethyl acetate = 2: 1) to obtain 4,6-dichloro-3- [2-. 209 mg of (2,2-dichlorocyclopropyl) -6-methylphenoxy] pyridazine (0.574 mmol, yield of 2 steps from 2- (2,2-dichlorocyclopropyl) -6-methylphenol, 62.9%) Got it.
[1077] (5) 6-chloro-3- [2- (2,2-dichlorocyclopropyl) -6-methylphenoxy] -4-pyridazinol (Compound No. 827, step B-4)
[1078] 209 mg (0.574 mmol) of 4,6-dichloro-3- [2- (2,2-dichlorocyclopropyl) -6-methylphenoxy] pyridazine obtained by (4) was added to 1,4-dioxane (3 mL) and dimethyl sulfoxide (3 mL) were added, and 1.43 mL (2.86 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the mixture, which was stirred overnight at room temperature. The reaction mixture was poured into water and made acidic with diluted hydrochloric acid. This mixture was extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, developed with ethyl acetate) to give 6-chloro-3- [2- (2,2-dichlorocyclopropyl). 120 mg (0.349 mmol, Yield 60.8%) were obtained.)-6-Methylphenoxy] -4-pyridazinol (Compound No. 827).
[1079] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.25 (1H, br.d, J = 6.3 Hz), 7.16 (1H, t, J = 7.7 Hz), 6.98 (1H, d, J = 7.7 Hz) , 6.72 (1H, s), 2.85 (1H, doublet of doublets, J = 10.6, 8.8 Hz), 2.22 (3H, s), 2.05-1.86 (2H, m).
[1080] Melting point (° C): 213-215.
[1081] Example 25 6-Chloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] -4-pyridazinol (Compound No. 1109)
[1082] (1) 6,7-dihydro-1-benzofuran-4 (5H) -one
[1083] 11.2 g (0.100 mol) of 1,3-cyclohexanedione is dissolved in methanol (40 mL), and an aqueous solution (8 mL) of 6.60 g (0.100 mol) of 85% potassium hydroxide is added dropwise to the solution, followed by stirring at room temperature for 30 minutes. It was. The mixture was ice-cooled, and under stirring, 21.6 g (0.110 mol) of 40% aqueous chloroacetaldehyde solution was added, and the mixture was stirred overnight at room temperature. 2 mol / L aqueous hydrochloric acid solution was added dropwise to the reaction mixture, which was stirred at room temperature for 30 minutes and then extracted with ether. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to give 6,7-dihydro-1-benzofuran-4 (5H) -one. 8.63 g (0.0635 mol, yield 63.5%) were obtained.
[1084] (2) Methyl 4-oxo-4,5,6,7-tetrahydro-1-benzofuran-5-carboxylate
[1085] 3.00 g (22.1 mmol) of 6,7-dihydro-1-benzofuran-4 (5H) -one obtained by (1) was dissolved in dry tetrahydrofuran (10 mL), and in this solution under nitrogen stream,- At 78 ° C, 48.5 mL (48.5 mmol) of lithium bis (trimethylsilyl) amide (1.0 M tetrahydrofuran solution) was added dropwise. After stirring at -78 ° C for 30 minutes, 1.87 mL (24.1 mmol) of methyl chlorocarbonate was added dropwise, and the reaction mixture was returned to room temperature and stirred for 10 minutes. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain methyl 4-oxo-4,5,6,7-tetrahydro-1-. 3.93 g (20.3 mmol, yield 91.9%) of benzofuran-5-carboxylate was obtained.
[1086] (3) Methyl 4-hydroxy-1-benzofuran-5-carboxylate
[1087] 3.93 g (20.3 mmol) of methyl 4-oxo-4,5,6,7-tetrahydro-1-benzofuran-5-carboxylate obtained by (2) was added to 1,4-dioxane (100 mL). It dissolved, 5.51 g (24.3 mmol) of 2, 3- dichloro-5, 6-dicyano- 1, 4- benzoquinones was added, and it stirred at 120 degreeC for 3 hours. After the reaction mixture was allowed to cool, the insolubles were separated by filtration through celite, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (Wako Gel C-100, hexanes-ethyl acetate gradient) to give 2.04 g (10.6 mmol, yield of methyl 4-hydroxy-1-benzofuran-5-carboxylate 52.2%).
[1088] (4) Methyl 4-methoxy-1-benzofuran-5-carboxylate
[1089] To a solution of 2.04 g (10.6 mmol) of acetonitrile (60 mL) of methyl 4-hydroxy-1-benzofuran-5-carboxylate obtained by (3), 2.53 g (18.3 mmol) of potassium carbonate, followed by 2.85 methyl iodide mL (45.8 mmol) was added and heated to reflux for 3 h. After standing at room temperature overnight, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to give methyl 4-methoxy-1-benzofuran-5-carboxylate 2.01. g (9.76 mmol, yield 92.1%) was obtained.
[1090] (5) (4-methoxy-1-benzofuran-5-yl) methanol
[1091] 0.479 g of lithium aluminum hydride (12.6) under ice-cooling stirring in a dry tetrahydrofuran (20 mL) solution of 1.01 g (4.90 mmol) of methyl 4-methoxy-1-benzofuran-5-carboxylate obtained in (4). Mmol) was added little by little. The reaction mixture was stirred for 2 hours under ice cooling, and ethyl acetate was added little by little. Subsequently, water (0.5 mL), 3 N sodium hydroxide (0.5 mL), and water (1.5 mL) were added sequentially, followed by stirring for 30 minutes. The mixture was filtered through celite and the filtrate was concentrated to give 0.89 g of crude product of (4-methoxy-1-benzofuran-5-yl) methanol.
[1092] (6) 4-methoxy-5-methyl-1-benzofuran
[1093] 0.65 g of crude product of (4-methoxy-1-benzofuran-5-yl) methanol obtained by (5) was dissolved in dichloromethane (10 mL), and this solution was stirred with ice-cold 0.56 mL (4.03) under ice-cooling. Mmol), followed by dropwise addition of 0.31 mL (3.99 mmol) of methanesulfonyl chloride, followed by stirring for 1 hour under ice-cooling. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. Dry dimethyl sulfoxide (20 mL) was added to the residue obtained by distilling off the solvent, and 0.276 g (7.30 mmol) of sodium borohydride was added little by little. The mixture was stirred at room temperature for 1 hour, then poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (using MERCK Co., Ltd., 1.05717, use of 3 sheets, developed as hexane: ethyl acetate = 9: 1), and 4-methoxy-5-methyl-1- 0.284 g (1.75 mmol, yield 48.9% from methyl 4-methoxy-1-benzofuran-5-carboxylate) were obtained for benzofuran.
[1094] (7) 5-methyl-1-benzofuran-4-ol
[1095] 268 mg (6.71 mmol) of 60% sodium hydride are suspended in dry N, N-dimethylformamide (11 mL), and 0.51 mL (6.9 mmol) of ethanethiol is added dropwise to this suspension under a nitrogen gas stream, and the mixture is stirred at room temperature for 10 minutes. Stirred for a minute. To this was added a solution of 362 mg (2.23 mmol) of N, N-dimethylformamide (7 mL) of 4-methoxy-5-methyl-1-benzofuran obtained in (6), followed by heating to reflux for 1 hour 30 minutes. . The reaction mixture was allowed to cool, and 1 mol / L aqueous potassium hydroxide solution and diethyl ether were added thereto. The aqueous layer was washed with diethyl ether and adjusted to pH 2 by adding dilute hydrochloric acid. This was extracted with diethyl ether, and the obtained organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (developing with MERCK Co., Ltd. 1.05744 3 pieces use hexane: ethyl acetate = 2: 1), 5-methyl-1- benzofuran-4-ol 276 mg (1.86 mmol, yield 83.4%) were obtained.
[1096] (8) 6-chloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] pyridazine 1-oxide (step B-2)
[1097] 121 mg (0.818 mmol) of 5-methyl-1-benzofuran-4-ol obtained by (7) were mixed with 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL), and this mixture was added to this mixture. Under ice-cooling, 101 mg (0.902 mmol) of potassium tert-butoxide were added and stirred for 10 minutes. 134 mg (0.812 mmol) of 3,6-dichloropyridazine 1-oxides were added thereto, and the mixture was stirred overnight at room temperature. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by MERCK Co., Ltd., 1.05744, used three times, and developed three times with hexane: ethyl acetate = 2: 1), and 6-chloro-3-[(5 199 mg of a crude product of -methyl-1-benzofuran-4-yl) oxy] pyridazine 1-oxide was obtained.
[1098] (9) 4,6-dichloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] pyridazine (Step B-3)
[1099] 199 mg of a crude product of 6-chloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] pyridazine 1-oxide obtained in (8) and 3 mL of phosphorus oxychloride were mixed The mixture was stirred overnight at room temperature. Water and dichloromethane were added to the reaction mixture, which was stirred for 30 minutes. The mixture was separated, the organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was preparative thin layer chromatography (manufactured by MERCK, 1.05744, 3 sheets used, hexane: ethyl acetate = 2: 1 developed three times, and then MERCK, 1.05717, 2 sheets, hexane : Ethyl acetate = 2: 1 elution three times) to obtain 120 mg (0.407 mmol, 4,6-dichloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] pyridazine. Yield of 2 steps and 49.8%) were obtained from 4-hydroxy-5-methyl-1-benzofuran.
[1100] (10) 6-chloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] -4-pyridazinol (Compound No. 1109, step B-4)
[1101] 120 mg (0.407 mmol) of 4,6-dichloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] pyridazine obtained by (9) were added with 1,4-dioxane (3 mL). And dimethyl sulfoxide (3 mL), 1.01 mL (2.02 mmol) of 2 mol / L aqueous sodium hydroxide solution was added to the mixture, which was stirred overnight at room temperature. The reaction mixture was poured into water and made acidic with diluted hydrochloric acid. This mixture was extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by MERCK, 1.05744, use of 2 pieces, developed with ethyl acetate) to give 6-chloro-3-[(5-methyl-1-benzofuran- 70.0 mg (0.253 mmol, Yield 62.2%) of 4-yl) oxy] -4-pyridazinol (Compound No. 1109) was obtained.
[1102] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.65 (1H, d, J = 2.2 Hz), 7.32 (1H, d, J = 8.8 Hz), 7.18 (1H, d, J = 8.8 Hz), 6.73 (1H, s), 6.60 (1H, doublet of doublets, J = 2.2, 0.7 Hz), 2.23 (3H, s).
[1103] Melting point (° C): 222-225.
[1104] Example 26 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl trifluoromethanesulfonate (Compound No. 2081, Step I-1)
[1105] 50.3 mg (0.191 mmol) of 6-chloro-3- (2-cyclopropylphenoxy) -4-pyridazinol (Compound No. 139) obtained in Example 6 was dissolved in methylene chloride (2 mL), and 0.027 mL (0.19 mmol) of triethylamine was added dropwise, followed by dropwise 0.031 mL (0.19 mmol) of trifluoromethanesulfonic anhydride, followed by stirring at room temperature for 30 minutes. The reaction mixture was purified by preparative thin layer chromatography (manufactured by Merck Co., Ltd., 1.05744, use of 2 pieces, developed with ethyl acetate: hexane = 2: 1), and 6-chloro-3- (2-cyclopropylphenoxy)- 64.7 mg (0.164 mmol, yield 85.8%) of 4-pyridazinyl trifluoromethanesulfonate (Compound No. 2081) were obtained.
[1106] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.51 (1H, s), 7.26-7.19 (2H, m), 7.14-7.05 (2H, m), 1.89-1.81 (1H, m), 0.85-0.62 ( 4H, m).
[1107] Melting point (° C): 54-61.
[1108] Example 27 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2225, Step I-1)
[1109] 53.4 mg (0.203 mmol) of 6-chloro-3- (2-cyclopropylphenoxy) -4-pyridazinol (Compound No. 139) obtained in Example 6 was dissolved in acetonitrile (3 mL), and 23.1 mg (0.206 mmol) of 1,4-diazabicyclo [2,2,2] octane was added, followed by 39.2 mg (0.205 mmol) of 4-methylbenzenesulfonylchloride, followed by stirring at room temperature for 1 hour 30 minutes. The reaction mixture was poured into water, extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (developed by Merck, 1.05744, ethyl acetate: hexane = 2: 1) to give 6-chloro-3- (2-cyclopropylphenoxy). 68.8 mg (0.165 mmol, yield 81.3%) of 4-pyridazinyl 4-methylbenzenesulfonates (compound number 2225) were obtained.
[1110] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.87 (2H, d, J = 8.1 Hz), 7.58 (1H, s), 7.36 (2H, d, J = 8.1 Hz), 7.26-7.11 (2H, m ), 6.97-6.93 (1H, m), 6.74-6.70 (1H, m), 2.45 (3H, s), 1.67-1.59 (1H, m), 0.71-0.56 (4H, m).
[1111] Properties: Oily substance.
[1112] (Example 28) 2-[(6-chloro-4-{[(4-methylphenyl) sulfonyl] oxy} -3-pyridazinyl) oxy] phenyl 4-methylbenzenesulfonate (Compound No. 2233, Step I -One)
[1113] 0.60 g (2.5 mmol) of 6-chloro-3- (2-hydroxyphenoxy) -4-pyridazinol (Compound No. 384) obtained by Example 10, 1.06 g (5.5 mmol) of 4-methylbenzenesulfonylchloride ), 0.56 g (5.0 mmol) of 1,4-diazabicyclo [2.2.2] octane and acetonitrile (30 mL) were mixed, and the mixture was stirred for 3 hours at room temperature under reflux for 4 days. Acetonitrile was distilled off, water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was washed with a hexane-ethyl acetate (3: 1) mixed solvent to give 2-[(6-chloro-4-{[(4-methylphenyl) sulfonyl] oxy} -3-pyridine 1.0 g (1.8 mmol, yield 72%) of dazinyl) oxy] phenyl 4-methylbenzenesulfonate (Compound No. 2233) were obtained.
[1114] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.98-6.65 (13H, m), 2.40 (3H, s), 2.36 (3H, s).
[1115] Melting point (° C): 125.5-126.5.
[1116] Example 29 6-Chloro-5-methyl-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2372)
[1117] (1) 3-chloro-4-methyl-2,5-furandione and 3-chloro-4- (chloromethyl) -2,5-furandione
[1118] 224 g (2.00 mole) of 3-methyl-2,5-furandione and 11.2 g (0.415 mole) of iron (III) chloride hexahydrate were mixed, and the mixture was heated to 140 ° C. and 346 g (4.88 g) of chlorine gas was stirred. Mole) was blown for 7 hours 30 minutes. The mixture was then heated at 175 ° C. for 3 hours 30 minutes. The reaction mixture was distilled off under reduced pressure (5 mmHg) to collect an oil of 80 to 85 ° C. 223.5 g of crude product were obtained, including 3-chloro-4-methyl-2,5-furandione and 3-chloro-4- (chloromethyl) -2,5-furandione.
[1119] (2) 4-chloro-5-methyl-1,2-dihydro-3,6-pyridazinedione and 4-chloro-5- (chloromethyl) -1,2-dihydro-3,6-pyridazine Dion
[1120] 147 g (including 3-chloro-4-methyl-2,5-furandione and 3-chloro-4- (chloromethyl) -2,5-furandione) obtained by (1) were mixed with 400 mL of water. The mixture was mixed and heated to reflux to obtain a solution. An aqueous solution of 116 g (1.10 mol) of dihydrochloride hydrazine (dissolved in 400 mL of water) was added dropwise to this heated refluxed solution for 40 minutes. Then, the mixture was heated to reflux for 1 hour 30 minutes and allowed to cool. The precipitated crystals were collected by filtration, washed with hot water and then ethyl acetate to give 81.8 g of 4-chloro-5-methyl-1,2-dihydro-3,6-pyridazinedione (melting point 305-310 ° C). Got it. On the other hand, the filtrate was extracted with ethyl acetate, the organic layers were combined, washed with water, and dried over anhydrous sodium sulfate. 8.06 g of a mixture containing 4-chloro-5- (chloromethyl) -1,2-dihydro-3,6-pyridazinedione was obtained from the residue obtained by distilling off the solvent.
[1121] (3) 3,4,6-trichloro-5-methylpyridazine
[1122] 24.1 g (0.150 mol) of 4-chloro-5-methyl-1,2-dihydro-3,6-pyridazinedione obtained by (2) are mixed with 250 mL (2.76 mol) of phosphorus oxychloride and this mixture Heated to reflux for 1 h 40 min. Excess phosphorus oxychloride was distilled off from the reaction mixture, and the residue was mixed with ice-cold water. The crystals were collected by filtration and extracted with ethyl acetate. The organic layer was washed with water, and the solvent was distilled off. The obtained residue was distilled off under reduced pressure (0.7 mmHg) to collect an oil at 105 ° C to 110 ° C, and 25.1 g (0.127 mol, yield 84.7%, melting point 67.5-) of 3,4,6-trichloro-5-methylpyridazine 70 ° C.).
[1123] (4) 3,6-dichloro-4-methoxy-5-methylpyridazine
[1124] 7.90 g (40.1 mmol) of 3,4,6-trichloro-5-methylpyridazine obtained by (3) was mixed with methanol (100 mL), and ice-cold to 0.92 g (40 mmol) of sodium. Methanol solution (50 mL) was added dropwise, and the mixture was stirred for 1 hour under ice-cooling and 15 minutes under heating to reflux. 0.20 g (8.7 mmol) of sodium was added under ice cooling, and it was further heated to reflux for 15 minutes. The reaction solution was allowed to cool and methanol was distilled off. The residue was mixed with ice cold water and extracted with ethyl acetate. The organic layers were combined, washed with water, and the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (waco gel C-100, eluted with hexane: ethyl acetate = 5: 1) to give 5.1 g of crude product. This was distilled off under reduced pressure (0.07 mmHg) to collect an oil at 125 ° C to obtain 4.50 g (23.3 mmol, yield 58.1%) of 3,6-dichloro-4-methoxy-5-methylpyridazine.
[1125] (5) 3-chloro-5-methoxy-4-methyl-6- (2-methoxyphenoxy) pyridazine and 3-chloro-4-methoxy-5-methyl-6- (2-methoxyphenoxy A mixture of pyridazine (step D-1)
[1126] To 30.8 g (285 mmol) of 2-methylphenol, 1.66 g (38.0 mmol) of 55% sodium hydride was slowly added. After stirring at room temperature for 20 minutes, it overheated at 90 degreeC and lost the solid of sodium hydride. The mixture was cooled to 50 ° C, 3.69 g (19.1 mmol) of 3,6-dichloro-4-methoxy-5-methylpyridazine obtained in (4) was added, and the mixture was stirred at 110 ° C for 3 hours 30 minutes. The reaction mixture was allowed to cool, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with 20% aqueous sodium hydroxide solution, and the solvent was distilled off. The obtained residue was purified by silica gel column chromatography to obtain 3-chloro-5-methoxy-4-methyl-6- (2-methoxyphenoxy) pyridazine and 3-chloro-4-methoxy-5 1.38 g (5.21 mmol, yield 27.3%) of mixtures of -methyl-6- (2-methoxyphenoxy) pyridazine were obtained.
[1127] (6) 6-chloro-5-methyl-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2372, step D-2)
[1128] 3-chloro-5-methoxy-4-methyl-6- (2-methoxyphenoxy) pyridazine and 3-chloro-4-methoxy-5-methyl-6- (2- obtained by (5) 1.38 g (5.21 mmol) of a mixture of methoxyphenoxy) pyridazine are mixed with 1,4-dioxane (8 mL), to which an aqueous solution of 0.282 g (6.78 mmol) of 96% sodium hydroxide (13 mL of water is added). Used) and stirred at 110 ° C. for 4.5 hours. The reaction solution was poured into water, and extracted with ethyl acetate. The aqueous layer was made acidic with hydrochloric acid, and the precipitated crystals were collected by filtration to collect 0.249 g (0.992 mmol, 6-chloro-5-methyl-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2372), Yield 19.0%, melting | fusing point 209-213 degreeC).
[1129] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.50-6.95 (4H, m), 2.28 (3H, m), 2.11 (3H, m).
[1130] Melting point (° C): 209-213.
[1131] The crystals precipitated from the filtrate were collected by filtration to obtain 0.187 g (0.745 mmol, yield 14.3%) of 3-chloro-5-methyl-6- (2-methylphenoxy) -4-pyridazinol. On the other hand, after drying an organic layer with anhydrous sodium sulfate, the solvent was distilled off and 0.57g (yield 41%) of raw materials were collect | recovered.
[1132] Example 30 6-Chloro-5- (methoxymethyl) -3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2378)
[1133] (1) 3,4,6-trichloro-5- (chloromethyl) pyridazine
[1134] Phosphorus oxychloride was added to 7.8 g of the mixture containing 4-chloro-5- (chloromethyl) -1,2-dihydro-3,6-pyridazinedione obtained in Example 29, and the mixture was heated to reflux for 1 hour. It was. Excess phosphorus oxychloride was distilled off from the reaction mixture, and the residue was mixed with ice-cold water. The mixture was extracted with ethyl acetate, the organic layers were combined, washed with water, and dried over anhydrous sodium sulfate. The residue obtained by distilling a solvent off was refine | purified by the silica gel column chromatography (The Merck make, 9385, eluted with hexane: ethyl acetate = 10: 1), and 3,4,6-trichloro-5- (chloro 3.63 g (15.6 mmol, melting | fusing point 102-104 degreeC) of methyl) pyridazine were obtained.
[1135] (2) 3,6-dichloro-4-methoxy-5- (methoxymethyl) pyridazine
[1136] 2.32 g (10.0 mmol) of 3,4,6-trichloro-5- (chloromethyl) pyridazine obtained by (1) were dissolved in methanol (50 ml) by heating, and then cooled to -60 deg. Methanol solution (prepared from 0.23 g sodium and 5 mL methanol, 10.0 mmol) was added dropwise. The solution was stirred at −10 ° C. for 2 hours 30 minutes, and a methanol solution of sodium methoxide (prepared from 0.23 g of sodium and 5 mL of methanol, 10.0 mmol) was added dropwise. After stirring at −10 ° C. for 2 hours, the mixture was allowed to stand at room temperature overnight. The reaction mixture was concentrated and the residue was purified by silica gel column chromatography (Merck, 9385, eluted with hexane: ethyl acetate = 5: 1) to give 3,6-dichloro-4-methoxy-5- ( 1.85 g (8.30 mmol, yield 83.0%, melting | fusing point 28-32 degreeC) of methoxymethyl) pyridazine were obtained.
[1137] (3) 3-chloro-5-methoxy-4- (methoxymethyl) -6- (2-methylphenoxy) pyridazine (step D-1)
[1138] 432 mg (4.00 mmol) of 2-methylphenol, methanol (20 mL) and 92 mg (4.0 mmol) sodium were mixed and stirred at room temperature until sodium disappeared. Methanol of this mixture was distilled off, 50 mL of toluene was added to the residue, and it heated and refluxed. The mixture was ice-cooled, and 892 mg (4.00 mmol) of toluene solution (10 mL) of 3,6-dichloro-4-methoxy-5- (methoxymethyl) pyridazine obtained by (2) was added dropwise thereto to 3 hours. Heated to reflux. The reaction mixture was left at room temperature overnight, then washed with water followed by saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (first time; Merck, 9385, hexane: ethyl acetate = 5: 1; second time; Merck, 9385, hexane: ethyl acetate = 8). Purified by: 1), 0.487 g (1.65 mmol, yield 41.3%) of 3-chloro-5-methoxy-4- (methoxymethyl) -6- (2-methylphenoxy) pyridazine; 0.266 g (0.902 mmol, yield 22.6%) of 3-chloro-4-methoxy-5- (methoxymethyl) -6- (2-methylphenoxy) pyridazine was obtained.
[1139] (4) 6-chloro-5- (methoxymethyl) -3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2378, step D-2)
[1140] 0.354 g (1.20 mmol), 1,4-dioxane (2 mL) 3-chloro-5-methoxy-4- (methoxymethyl) -6- (2-methylphenoxy) pyridazine obtained by (3) ), 62 mg (1.49 mmol) of 96% sodium hydroxide and water (8 mL) were mixed, and the mixture was stirred at room temperature for 2 days and under reflux for 3 hours. Hydrochloric acid was added to the reaction mixture to pH 1, followed by extraction with ethyl acetate. The organic layers were combined, washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 0.336 g (1.20 mmol, yield 100%) of 6-chloro-5- (methoxymethyl) -3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2378). .
[1141] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 8.92 (1H, brs), 7.45-6.80 (4H, m), 4.39 (2H, s), 3.25 (3H, s), 2.25 (3H, s) .
[1142] Melting point (° C.): 123-126.
[1143] Example 31 Ethyl 6- (2-tert-butylphenoxy) -3-chloro-5-hydroxy-4-pyridazinecarboxylate (Compound No. 2386)
[1144] (1) 3- (2-tert-butylphenoxy) -6-chloro-4-methoxypyridazine
[1145] 5.87 g (39.1 mmol) of 2-tert-butylphenol, dimethyl sulfoxide (80 mL) and 4.38 g (39.0 mmol) of potassium t-butoxide were mixed and the mixture was stirred at room temperature for 20 minutes. 6.92 g (38.7 mmol) of dimethylsulfoxide solution (60 mL) of 3,6-dichloro-4-methoxypyridazine was added to the mixture, which was stirred for 40 minutes at room temperature and 45 minutes at 80 ° C. The reaction mixture was poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layers were combined, washed with water, then brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Merck, 9385, hexane: ethyl acetate gradient) to give 3- (2-tert-butylphenoxy) -6-chloro-4-meth 2.66 g (9.09 mmol, yield 23.5%) and 6- (2-tert- butylphenoxy) -3-chloro-4- methoxypyridazine were obtained 1.82 g (6.22 mmol, yield: 16.1%).
[1146] (2) ethyl 6- (2-tert-butylphenoxy) -3-chloro-5-methoxy-4-pyridazinecarboxylate (step G-1)
[1147] 783 mg (2.68 mmol) of 3- (2-tert-butylphenoxy) -6-chloro-4-methoxypyridazine obtained by (1) were dissolved in dry tetrahydrofuran (26 mL) to dissolve the solution. It cooled to 78 degreeC, 1.20 mL (2.80 mmol) of n-butyllithium hexane solutions (2.33 M) were added, and it stirred for 20 minutes. 0.330 mL (3.45 mmol) of ethyl chlorocarbonate was added here, and it stirred at the same temperature for 30 minutes. The reaction mixture was poured into saturated aqueous ammonium chloride solution and extracted with ether. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 5: 1) to give ethyl 6- (2-tert-butylphenoxy) -3-chloro-5-methoxy. 603 mg (1.65 mmol, yield 61.6%) of 4-pyridazinecarboxylate were obtained.
[1148] (3) ethyl 6- (2-tert-butylphenoxy) -3-chloro-5-hydroxy-4-pyridazinecarboxylate (Compound No. 2386, step G-2)
[1149] 419 mg (1.15 mmol) of ethyl 6- (2-tert-butylphenoxy) -3-chloro-5-methoxy-4-pyridazinecarboxylate obtained by (2), 1,4-dioxane, 1 An aqueous mol / L sodium hydroxide solution (2.0 mL, 2.0 mmol) and dimethylsulfoxide (2.0 mL) were mixed, and the mixture was stirred at room temperature for 2 hours 30 minutes and 80 ° C. for 4 hours 30 minutes. After cooling, the reaction solution was made acidic with hydrochloric acid and extracted with dichloromethane. The organic layers were combined, washed with brine and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography, ethyl 6- (2-tert-butylphenoxy) -3-chloro-5-hydroxy-4-pyridazinecarboxylate (Compound No. 2386) (337 mg (0.960 mmol, yield 83.5%)) was obtained.
[1150] Physical property: Amorphous.
[1151] Example 32 3,6-bis (2-methylphenoxy) -4-pyridazinol (Compound No. 2395)
[1152] (1) 3-chloro-5-methoxy-4,6-bis (2-methylphenoxy) pyridazine (Step D-1)
[1153] 5.32 g (49.3 mmol) of 2-methylphenol are dissolved in toluene (100 mL), and 1.13 g (49.1 mmol) of sodium is added to this solution, followed by 5.80 g (27.2) of 3,4,6-trichloro-5-methoxypyridazine. Mmol) was added and stirred under heating to reflux for 4 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) and recrystallization from isopropyl ether to give 3-chloro-5-methoxy-4,6-bis (2-methyl Phenoxy) pyridazine was obtained 3.0 g (8.4 mmol, yield 31%).
[1154] (2) 6-chloro-3,5-bis (2-methylphenoxy) -4-pyridazinol (Compound No. 2395, Step D-2)
[1155] 3-chloro-5-methoxy-4,6-bis (2) obtained by (1) in a mixture of 0.60 mL (4.7 mmol) of trimethylsilyl chloride, 0.60 g (4.0 mmol) of sodium iodide and acetonitrile (15 ml) 0.72 g (2.0 mmol) of methylphenoxy) pyridazine was added and stirred overnight. The reaction mixture was poured into ice-cold water and extracted with methylene chloride. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (chloroform: methanol gradient) to give 6-chloro-3,5- (2-methylphenoxy) -4-pyridazinol (Compound No. 2395 ) 0.45 g (1.3 mmol, yield 65%) were obtained.
[1156] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.32-7.05 (7H, m), 6.91 (1H, br.d, J = 7.3 Hz), 2.29 (3H, s), 2.19 (3H, s).
[1157] Melting Point (° C): 110-115.
[1158] Example 33 3- (2-tert-butylphenoxy) -6-chloro-5- (trimethylsilyl) -4-pyridazinol (Compound No. 2405)
[1159] (1) 3- (2-tert-butylphenoxy) -6-chloro-4-methoxy-5- (trimethylsilyl) pyridazine (step G-1)
[1160] 498 mg (1.70 mmol) of 3- (2-tert-butylphenoxy) -6-chloro-4-methoxypyridazine obtained in Example 31 (1) were dissolved in dry tetrahydrofuran (15 mL), and The solution was cooled to -78 ° C, 1.10 mL (1.87 mmol) of n-butyllithium hexane solution (1.70 M) was added and stirred for 20 minutes. 0.370 mL (2.91 mmol) of trimethylsilyl chloride was added thereto, followed by stirring for 10 minutes at the same temperature. The reaction mixture was poured into saturated aqueous ammonium chloride solution and extracted with ether. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography to obtain 596 mg of 3- (2-tert-butylphenoxy) -6-chloro-4-methoxy-5- (trimethylsilyl) pyridazine ( 1.63 mmol, yield 95.9%).
[1161] (2) 3- (2-tert-butylphenoxy) -6-chloro-5- (trimethylsilyl) -4-pyridazinol (Compound No. 2405, step G-2)
[1162] 0.17 g (1.1 mmol) sodium iodide, 0.14 mL (1.1 mmol) and acetonitrile (3.5 mL) were mixed and stirred in the mixture to 3- (2-tert-butylphenoxy obtained by (1). C) -6-chloro-4-methoxy-5- (trimethylsilyl) pyridazine 340 mg (0.932 mmol) was added and the mixture was stirred at room temperature for 1 hour 35 minutes. The reaction mixture was poured into saturated aqueous sodium sulfite solution and ice-cold diluted hydrochloric acid was added. The mixture was extracted with ethyl acetate, and the organic layers were combined and washed with saturated brine. The solvent was distilled off and the residue was purified by silica gel column chromatography to obtain 3- (2-tert-butylphenoxy) -6-chloro-5- (trimethylsilyl) -4-pyridazinol (Compound No. 2405). ) 275 mg (0.783 mmol, yield 84.0%).
[1163] ¹ H-NMR (90 MHz, CDCl ₃ ) δ ppm: 10.12 (1H, brs), 7.39-6.75 (4H, m), 1.24 (9H, s), 0.31 (9H, s).
[1164] Melting Point (° C): 160-163.
[1165] Example 34 6-Bromo-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2411)
[1166] (1) 5-chloro-6- (2-methylphenoxy) -3-pyridazinol (step P-1)
[1167] A mixture of 578 mg (2.27 mmol), acetic acid (10 mL) and 0.45 g (4.6 mmol) of potassium acetate, 4,6-dichloro-3- (2-methylphenoxy) pyridazine, obtained by Example 1 (2) It was heated to reflux for 5 hours. The reaction mixture was allowed to cool, 50 mL of water was added, and the mixture was extracted with ethyl acetate. The organic layers were combined and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was distilled off to obtain 461 mg (1.95 mmol, yield 85.9%) of 5-chloro-6- (2-methylphenoxy) -3-pyridazinol.
[1168] (2) 4,6-dibromo-3- (2-methylphenoxy) pyridazine (Step P-2)
[1169] 151 mg (0.637 mmol) of 5-chloro-6- (2-methylphenoxy) -3-pyridazinol obtained by (1), chloroform (3 mL) and 913 mg (3.18 mmol) of phosphorus oxybromide were mixed. The mixture was heated to reflux for 5 hours. The reaction mixture was allowed to cool, water and dichloromethane were added, and the mixture was stirred at room temperature for 1 hour. This mixture was extracted with dichloromethane. The organic layers were combined and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was distilled off. The obtained residue was purified by silica gel column chromatography to obtain 176 mg (0.512 mmol, yield 80.4%) of 4,6-dibromo-3- (2-methylphenoxy) pyridazine.
[1170] (3) 6-bromo-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2411, step P-3)
[1171] 114 mg (0.331 mmol) of 4,6-dibromo-3- (2-methylphenoxy) pyridazine obtained in (2) are dissolved in dimethyl sulfoxide (3 mL), and 2 mol / L hydroxide is dissolved in this solution. 0.80 mL (1.6 mmol) of aqueous sodium solution was added and the mixture was stirred at room temperature for 3 hours. Water was added to the reaction mixture, and the mixture was washed with ethyl acetate. The aqueous layer was made acidic with 4 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was washed with an ethyl acetate-ether mixed solvent to give 56.0 mg (0.199 mmol) of 6-bromo-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2411). , Yield 60.1%).
[1172] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.35-7.05 (4H, m), 6.82 (1H, brs), 2.10 (3H, s).
[1173] Melting Point (° C): 197-198.
[1174] Example 35 6-cyclopropyl-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2423)
[1175] (1) 6-cyclopropyl-4-methoxy-3- (2-methylphenoxy) pyridazine (Step L-1)
[1176] To 2.94 mL (1.47 mmol) of a tetrahydrofuran solution (0.5 mol / l) of 9-vorabicyclo [3.3.1] nonane was added 87.5 mg (0.735 mmol) of propargyl bromide and heated to reflux for 2 hours. The reaction mixture was cooled to room temperature, 0.74 mL (2.2 mmol) of 3 mol / L aqueous sodium hydroxide solution was added, and the mixture was stirred at room temperature for 70 minutes. Here, 168 mg (0.669 mmol) of 6-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine and 38.7 mg of tetrakis (triphenylphosphine) palladium obtained in Example 2 (1) 0.00334 mmol) was added sequentially and heated to reflux overnight. The reaction mixture was allowed to cool, water was added, and the mixture was extracted with ethyl acetate. The organic layers were combined and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was distilled off. The obtained residue was purified by silica gel column chromatography to obtain 121 mg (0.473 mmol, yield 70.1%) of 6-cyclopropyl-4-methoxy-3- (2-methylphenoxy) pyridazine.
[1177] (2) 6-cyclopropyl-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2423, step L-2)
[1178] 45.6 mg (0.479 mmol) of 2-hydroxypyridine was dissolved in dimethyl sulfoxide (2 mL), and 53.8 mg (0.480 mmol) of potassium tert-butoxide was added to the solution at room temperature, followed by stirring at room temperature for 10 minutes. To this was added 112 mg (0.438 mmol) of dimethylsulfoxide (1 mL) solution of 6-cyclopropyl-4-methoxy-3- (2-methylphenoxy) pyridazine obtained in (1) at 60 ° C. It stirred for 5 hours and 80 degreeC at 15 hours. Further, 45.6 mg (0.479 mmol) of 2-hydroxypyridine was added followed by 53.8 mg (0.480 mmol) of potassium tert-butoxide, followed by stirring at 80 ° C. for 4 hours 30 minutes. The reaction mixture was allowed to cool, water was added, and the mixture was washed with ethyl acetate. The aqueous layer was made acidic with 4 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was distilled off. The obtained residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, developed with ethyl acetate) to give 6-cyclopropyl-3- (2-methylphenoxy) -4-pyridazinol (Compound No. 2423). 28.6 mg (0.118 mmol, yield 26.9%) were obtained.
[1179] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.30-7.01 (4H, m), 6.19 (1H, s), 1.98-1.82 (1H, m), 1.23-1.12 (2H, m), 0.99-0.88 (2H, m).
[1180] Melting point (° C): 214-215.
[1181] Example 36 3- (2-methylphenoxy) -6-vinyl-4-pyridazinol (Compound No. 2436)
[1182] (1) 4-methoxy-3- (2-methylphenoxy) -6-vinylpyridazine (step L-1)
[1183] 123 mg (0.490 mmol) of 6-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine obtained in Example 2 (1) are dissolved in toluene (2 mL), and in this solution at room temperature 246 mg (0.776 mmol) of butyl (vinyl) tin was added followed by 119 mg (0.103 mmol) of tetrakis (triphenylphosphine) palladium followed by heating to reflux for 3 hours. The reaction mixture was left to cool, ethyl acetate (5 mL), water (3 mL) and sodium fluoride were added thereto, stirred for 30 minutes, and allowed to stand at room temperature overnight. The mixture was filtered through celite, ethyl acetate was added to the filtrate, and the organic layer was separated and washed with saturated brine. After drying over anhydrous sodium sulfate, the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 1: 2) to give 105 mg of 4-methoxy-3- (2-methylphenoxy) -6-vinylpyridazine ( 0.434 mmol, yield 88.6%).
[1184] (2) 3- (2-methylphenoxy) -6-vinyl-4-pyridazinol (Compound No. 2436, step L-2)
[1185] 33.7 mg (0.354 mmol) of 2-hydroxypyridine was dissolved in dimethyl sulfoxide (1 mL), and 39.7 mg (0.354 mmol) of potassium tert-butoxide was added to the solution at room temperature, followed by stirring at room temperature for 10 minutes. To this was added 85.8 mg (0.354 mmol) of dimethylsulfoxide (1 mL) solution of 4-methoxy-3- (2-methylphenoxy) -6-vinylpyridazine obtained in (1), and overnight at room temperature. It stirred at 50 degreeC for 4 hours and 30 minutes. The reaction mixture was allowed to cool, water was added, and the mixture was washed with ethyl acetate. The aqueous layer was made acidic with 4 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, and the solvent was distilled off. The obtained residue was purified by silica gel column chromatography (developed with hexane: ethyl acetate = 1: 4) to give 3- (2-methylphenoxy) -6-vinyl-4-pyridazinol (Compound No. 2436). 51.7 mg (0.227 mmol, yield 64.1%) were obtained.
[1186] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.35-7.03 (4H, m), 6.56-6.43 (2H, m), 6.16 (1H, d, J = 17.9 Hz), 6.16 (1H, d, J = 11.4 Hz), 2.11 (3H, s).
[1187] Melting Point (° C): 195-197.
[1188] Example 37 3- (2-methylphenoxy) -6- (1-propenyl) -4-pyridazinol (Compound No. 2442)
[1189] (1) 6-allyl-4-methoxy-3- (2-methylphenoxy) pyridazine (Step L-1)
[1190] 200 mg (0.797 mmol) of 6-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine obtained in Example 2 (1) are dissolved in toluene (4 mL), and this solution is allyl at room temperature. 305 mg (0.921 mmol) of (tributyl) tin was added followed by 96.8 mg (0.0838 mmol) of tetrakis (triphenylphosphine) palladium followed by heating to reflux for 3 hours 20 minutes. The reaction mixture was left at room temperature overnight, then ethyl acetate, water and sodium fluoride were added and stirred for 2 hours. The mixture was filtered through celite, ethyl acetate was added to the filtrate, and the organic layer was separated and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 62.1 mg (0.243 mmol, yield 30.5) of 6-allyl-4-methoxy-3- (2-methylphenoxy) pyridazine. %) Was obtained.
[1191] (2) 25.3 mg (0.267 mmol) of 2- (2-methylphenoxy) -6- (1-propenyl) -4-pyridazinol (Compound No. 2442, step L-2) 2-hydroxypyridine It was dissolved in sulfoxide (2 mL), and 29.9 mg (0.267 mmol) of potassium tert-butoxide was added to the solution at room temperature, followed by stirring for 10 minutes at room temperature. To this was added 62.1 mg (0.243 mmol) of dimethylsulfoxide (3 mL) solution of 6-allyl-4-methoxy-3- (2-methylphenoxy) pyridazine obtained in (1), followed by 8 at 100 ° C. It stirred for 5 hours and 30 minutes at hours and 130 degreeC. Further, 25.3 mg (0.267 mmol) of 2-hydroxypyridine was added followed by 29.9 mg (0.267 mmol) of potassium tert-butoxide, followed by stirring at 130 ° C. for 5 hours. The reaction mixture was allowed to cool, water was added, and the mixture was washed with ethyl acetate. The aqueous layer was made acidic with 4 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, and the solvent was distilled off. The obtained residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, developed with ethyl acetate), and 3- (2-methylphenoxy) -6- (1-propenyl) -4- 21.3 mg (0.0880 mmol, yield 36.2%) of pyridazinol (Compound No. 2442) were obtained.
[1192] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.32-7.03 (4H, m), 6.75-6.60 (1H, m), 6.44 (1H, s), 6.22-6.10 (1H, m), 2.10 ( 3H, s), 1.86 (3H, broad doublet, J = 6.6 Hz).
[1193] Melting point (° C.): 208-210.
[1194] Example 38 6- (2,6-dimethylphenoxy) -5-hydroxy-3-pyridazinecarbonitrile (Compound No. 2453)
[1195] (1) 6-chloro-3- (2,6-dimethylphenoxy) -4-methoxypyridazine 1-oxide (step K-1)
[1196] 3.42 g (12.9 mmol) of 6-chloro-3- (2,6-dimethylphenoxy) -4-methoxypyridazine, dichloromethane (110 mL) and 3.34 g (15.4 mmol) of 80% m-chloroperbenzoic acid The mixture was stirred for 16 days at room temperature. The reaction mixture was poured into ice-cold saturated aqueous sodium sulfite solution and extracted with dichloromethane. The organic layers were combined, washed successively with saturated aqueous sodium hydrogen carbonate solution, water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography to obtain 2.06 g (7.33 mmol) of 6-chloro-3- (2,6-dimethylphenoxy) -4-methoxypyridazine 1-oxide. , Yield 56.8%).
[1197] (2) 3- (2,6-dimethylphenoxy) -4-methoxypyridazine 1-oxide (step K-2)
[1198] 6.00 g (21.4 mmol) of 6-chloro-3- (2,6-dimethylphenoxy) -4-methoxypyridazine 1-oxide obtained by (1), methanol (200 mL), triethylamine 3.0 mL , Acetone (5 mL) and 0.5 g of 5% palladium carbon were mixed, and the mixture was shaken at 3.5 atmospheres of hydrogen pressure for 2 hours using a Parr reduction apparatus. The reaction mixture was filtered and the filtrate was concentrated. Water was added to the residue, followed by extraction with chloroform. The organic layers were combined, washed with brine and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was crystallized with an ether-dichloromethane mixed solvent to give 4.32 g (17.6 mmol, yield 82.2 of 3- (2,6-dimethylphenoxy) -4-methoxypyridazine 1-oxide. %) Was obtained.
[1199] (3) 6- (2,6-dimethylphenoxy) -5-methoxy-3-pyridazinecarbonitrile (step M-1)
[1200] 0.720 g (2.92 mmol) of 3- (2,6-dimethylphenoxy) -4-methoxypyridazine 1-oxide obtained by (2) was dissolved in dry N, N-dimethylformamide (15 mL), Trimethylsilyl cyanide 1.10 mL (8.25 mmol) and 2.00 mL (14.4 mmol) triethylamine were added to this solution, and it stirred at 90 degreeC for 1 hour and 30 minutes. The reaction mixture was poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography to give 0.675 g (2.65 mmol, yield 90.8) of 6- (2,6-dimethylphenoxy) -5-methoxy-3-pyridazinecarbonitrile. %) Was obtained.
[1201] (4) 6- (2,6-dimethylphenoxy) -5-hydroxy-3-pyridazinecarbonitrile (Compound No. 2453, step M-2)
[1202] 0.500 g (1.96 mmol) of 6- (2,6-dimethylphenoxy) -5-methoxy-3-pyridazinecarbonitrile obtained in (3) was dissolved in acetonitrile (5 mL), and trimethylsilyl in this solution. 0.300 mL (2.36 mmol) of chloride and 0.350 g (2.33 mmol) of sodium iodide were added and stirred at room temperature. 5 m of acetonitrile were added and stirred for 1 hour, followed by 3 mL of 1,4-dioxane, followed by stirring overnight. The reaction mixture was poured into an aqueous sodium sulfite solution and acidified by addition of 1 mol / L hydrochloric acid. Extracted with dichloromethane, washed with brine and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography to obtain 0.121 g (0.502) of 6- (2,6-dimethylphenoxy) -5-hydroxy-3-pyridazinecarbonitrile (Compound No. 2453). Mmol, yield 25.6%).
[1203] ¹ H-NMR (90 MHz, CDCl ₃ ) δ ppm: 11.3 (1H, brs), 7.09-6.99 (4H, m), 1.90 (6H, s).
[1204] Physical property: Amorphous.
[1205] Example 39 1- [5-hydroxy-6- (2-methylphenoxy) -3-pyridazinyl] ethanone (Compound No. 2455)
[1206] (1) 6- (1-ethoxyvinyl) -4-methoxy-3- (2-methylphenoxy) pyridazine (Step L-1)
[1207] 321 mg (1.28 mmol) of 6-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine obtained in Example 2 (1) were dissolved in toluene (6.5 mL), and the solution was stirred at room temperature ( 534 mg (1.48 mmol) of 1-ethoxyvinyl) (tributyl) tin was added followed by 155.3 mg (0.134 mmol) of tetrakis (triphenylphosphine) palladium followed by heating to reflux for 3 hours 20 minutes. The reaction mixture was left at room temperature overnight, then ethyl acetate, water and sodium fluoride were added and stirred for 2 hours. The mixture was filtered through celite, ethyl acetate was added to the filtrate, and the organic layer was separated and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give 51.8 mg of 6- (1-ethoxyvinyl) -4-methoxy-3- (2-methylphenoxy) pyridazine. (0.181 mmol, yield 14.1%) were obtained.
[1208] (2) 1- [5-hydroxy-6- (2-methylphenoxy) -3-pyridazinyl] ethanone (Compound No. 2455, step L-2)
[1209] 18.4 mg (0.194 mmol) of 2-hydroxypyridine was dissolved in dimethylsulfoxide (2 mL), 21.7 mg (0.194 mmol) of potassium tert-butoxide was added to this solution at room temperature, followed by stirring at room temperature for 10 minutes. Here, 50.4 mg (0.176 mmol) of dimethylsulfoxide (3 mL) solution of 6- (1-ethoxyvinyl) -4-methoxy-3- (2-methylphenoxy) pyridazine obtained by (1). Was added and stirred at 100 ° C. for 8 hours and 130 ° C. for 5 hours and 30 minutes. Further, 18.4 mg (0.194 mmol) of 2-hydroxypyridine was added followed by 21.7 mg (0.194 mmol) of potassium tert-butoxide, followed by stirring at 130 ° C. for 2 hours. The reaction mixture was allowed to cool, water was added, and the mixture was washed with ethyl acetate. The aqueous layer was made acidic with 4 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, and the solvent was distilled off. The obtained residue was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, developed with ethyl acetate) to obtain 1- [5-hydroxy-6- (2-methylphenoxy) -3-pyridine. 28.5 mg (0.117 mmol, yield 66.5%) of dazinyl] ethanone (Compound No. 2455) were obtained.
[1210] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.48-7.05 (5H, m), 2.58 (3H, s), 2.10 (3H, s).
[1211] Melting point (° C.): 182-185.
[1212] Example 40 3- (2-methylphenoxy) -6-phenyl-4-pyridazinol (Compound No. 2464)
[1213] (1) 4-methoxy-3- (2-methylphenoxy) -6-phenylpyridazine (Step L-1)
[1214] 210 mg (0.837 mmol) of 6-chloro-4-methoxy-3- (2-methylphenoxy) pyridazine obtained by Example 2 (1), toluene (4 mL) and water (0.5 mL) were mixed To this mixture, at room temperature, 161 mg (1.32 mmol) of phenylboronic acid, 365 mg (2.64 mmol) of potassium carbonate and 102 mg (0.0879 mmol) of tetrakis (triphenylphosphine) palladium were added sequentially, followed by heating under reflux for 2 hours 50 minutes. It was. After leaving the reaction mixture at room temperature overnight, the mixture was filtered through celite, and ethyl acetate and water were added to the filtrate. The organic layer was separated and washed with saturated brine. After drying over anhydrous sodium sulfate, the solvent was distilled off. The obtained residue was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 3: 1) to give 146 mg of 4-methoxy-3- (2-methylphenoxy) -6-phenylpyridazine ( 0.500 mmol, yield 59.7%) was obtained.
[1215] (2) 3- (2-methylphenoxy) -6-phenyl-4-pyridazinol (Compound No. 2464, step L-2)
[1216] 91.9 mg (0.966 mmol) of 2-hydroxypyridine was dissolved in dimethyl sulfoxide (1.5 mL), and 95.4 mg (0.850 mmol) of potassium tert-butoxide was added to the solution at room temperature, followed by stirring at room temperature for 10 minutes. To this was added a solution of 82.8 mg (0.283 mmol) of dimethyl sulfoxide (1 mL) of 4-methoxy-3- (2-methylphenoxy) -6-phenylpyridazine obtained in (1), at 60 ° C. Stir for 3 hours. The reaction mixture was allowed to cool, water was added, and the mixture was washed with ethyl acetate. The aqueous layer was made acidic with 4 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by distilling off a solvent was purified by preparative thin layer chromatography (manufactured by Merck, 1.05744, use of 3 pieces, developed with ethyl acetate) to obtain 3- (2-methylphenoxy) -6-phenyl-4- 70.8 mg (0.255 mmol, yield 90.1%) of pyridazinol (Compound No. 2464) was obtained.
[1217] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.78-7.66 (2H, m), 7.58-7.48 (3H, m), 7.35-7.08 (4H, m), 6.69 (1H, s), 2.15 ( 3H, s).
[1218] Melting Point (° C): 236-237.
[1219] Example 41 3,6-bis (2-fluorophenoxy) -4-pyridazinol (Compound No. 2485)
[1220] (1) 3,6-bis (2-fluorophenoxy) pyridazine
[1221] 2.69 g (24.0 mmol) of 2-fluorophenol were dissolved in dimethylsulfoxide (20 mL), and to the solution was added 2.69 g (24.0 mmol) of potassium tert-butoxide at room temperature. To this was added 1.49 g (10.0 mmol) of 2,6-dichloropyridazine, followed by stirring at 100 ° C for 3 hours. The reaction mixture was allowed to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with 1 mol / L aqueous sodium hydroxide solution, water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was washed with heated hexane and then heated isopropyl ether to obtain 1.71 g (5.70 mmol, yield 57.0%) of 3,6-bis (2-fluorophenoxy) pyridazine. .
[1222] (2) 3,6-bis (2-fluorophenoxy) pyridazine 1-oxide (step C-1)
[1223] 4.14 g (13.8 mmol) of 3,6-bis (2-fluorophenoxy) pyridazine obtained in (1) were dissolved in dry dichloromethane (40 mL), and 3.19 g (80% m-chloroperbenzoic acid in this solution) 14.8 mmol) was added and stirred for 7 days at room temperature. The reaction mixture was poured into ice-cold 1 mol / L aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 3: 1) to give 3,6-bis (2-fluorophenoxy) pyridazine 1-oxide. 2.24 g (7.09 mmol, yield 51.4%) were obtained.
[1224] (3) 4-chloro-3,6-bis (2-fluorophenoxy) pyridazine (Step C-2)
[1225] 2.20 g (6.96 mmol) of 3,6-bis (2-fluorophenoxy) pyridazine 1-oxide obtained by (2) and 50 mL of phosphorus oxychloride were mixed and the mixture was stirred at 90 ° C. for 1 hour. It was. The reaction mixture was allowed to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with 1 mol / L aqueous sodium hydroxide solution, water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (hexane: ethyl acetate = 10: 1) to obtain 1.95 g of 4-chloro-3,6-bis (2-fluorophenoxy) pyridazine. (5.82 mmol, yield 83.6%) were obtained.
[1226] (4) 3,6-bis (2-fluorophenoxy) -4-methoxypyridazine (Step C-3)
[1227] 1.44 g (4.30 mmol) of 4-chloro-3,6-bis (2-fluorophenoxy) pyridazine obtained by (3) were dissolved in methanol (20 mL), and 0.206 g (55% sodium hydride in this solution) 4.72 mmol) was added and stirred at 60 ° C for 1 hour. The reaction mixture was left to cool, poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (eluted with hexane: ethyl acetate = 10: 1) to give 3,6-bis (2-fluorophenoxy) -4-methoxypyridazine 1.03 g (3.12 mmol, yield 72.6%) was obtained.
[1228] (5) 3,6-bis (2-fluorophenoxy) -4-pyridazinol (Compound No. 2485, Step C-4)
[1229] 450 mg (1.36 mmol) of 3,6-bis (2-fluorophenoxy) -4-methoxypyridazine obtained by (4), 77 mg (1.85 mmol) of 96% sodium hydroxide, dimethyl sulfoxide (5 mL ) And water (1 mL) were mixed and the mixture was stirred at 90 ° C for 2 h. The reaction mixture was poured into ice-cold water and acidified with hydrochloric acid. This was extracted with ethyl acetate, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 0.380 g (1.20 mmol, yield 88.2%) of 3,6-bis (2-fluorophenoxy) -4-pyridazinol (Compound No. 2485).
[1230] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.60-7.08 (8H, m), 6.34 (1H, brs).
[1231] Melting point (° C.): 228.
[1232] Example 42 (2,4-dichlorophenyl) (5-{[5-hydroxy-6- (2-methylphenoxy) -3-pyridazinyl] oxy} -1,3-dimethyl-1H- Pyrazol-4-yl) methanone (Compound No. 2506)
[1233] (1) (5-{[5-chloro-6- (2-methylphenoxy) -3-pyridazinyl] oxy} -1,3-dimethyl-1H-pyrazol-4-yl) (2,4 -Dichlorophenyl) methanone
[1234] (2,4-dichlorophenyl) (5-hydroxy-1,3-dimethyl-1H-pyrazol-4-yl) methanone 109 mg (0.382 mmol), 4,6 obtained by Example 1 (2) 1.62 g (6.35 mmol) of dichloro-3- (2-methylphenoxy) pyridazine and 107 mg (0.775 mmol) of potassium carbonate were mixed and the mixture was stirred at 130 ° C. for 14 hours. The reaction mixture was cooled to room temperature and purified by silica gel column chromatography (hexane: ethyl acetate gradient) to give (5-{[5-chloro-6- (2-methylphenoxy) -3-pyridazinyl] 155 mg (0.308 mmol, yield 80.6%) of oxy} -1,3-dimethyl-1H-pyrazol-4-yl) (2,4-dichlorophenyl) methanone were obtained.
[1235] (2) (2,4-dichlorophenyl) (5-{[5-hydroxy-6- (2-methylphenoxy) -3-pyridazinyl] oxy} -1,3-dimethyl-1H-pyrazole -4-yl) methanone (Compound No. 2506, A-3 process)
[1236] (5-{[5-chloro-6- (2-methylphenoxy) -3-pyridazinyl] oxy} -1,3-dimethyl-1H-pyrazol-4-yl) obtained by (1) ( 12.3 mg (0.0244 mmol) 2,4-dichlorophenyl) methanone, 0.2 mL of dimethylsulfoxide and 0.012 mL of 10% (W / V) aqueous sodium hydroxide solution were mixed and stirred overnight at room temperature. The reaction mixture was poured into ice-cold water, made acidic with hydrochloric acid, and extracted with ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developed by Merck, 1.05744, dichloromethane: methanol = 10: 1) to obtain (2,4-dichlorophenyl) (5-{[5- 3.2 mg (0.00784 mmol) of hydroxy-6- (2-methylphenoxy) -3-pyridazinyl] oxy} -1,3-dimethyl-1H-pyrazol-4-yl) methanone (Compound No. 2506) , Yield 32%) and 4-[{[5-chloro-6- (2-methylphenoxy) -3-pyridazinyl] oxy} (2,4-dichlorophenyl) methylene] -2,5-dimethyl- 10.5 mg (0.0208 mmol, yield 85.4%) of 2,4-dihydro-3H-pyrazol-3-ones were obtained.
[1237] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.36-7.04 (7H, m), 6.20 (1H, brs), 3.64 (3H, s), 2.31 (3H, s), 2.20 (3H, s).
[1238] Physical property: Amorphous.
[1239] In addition, the following compounds were prepared by or in accordance with the methods of Examples 1 to 42 or Examples 622 to 646 described below.
[1240] Example 43 3-phenoxy-4-pyridazinol (Compound No. 1)
[1241] ¹ H-NMR (90 MHz, DMSO-d ₆ ) δ ppm: 12.66 (1H, brs), 8.21 (1H, d, J = 6.6 Hz), 7.09-7.54 (5H, m), 6.38 (1H, d, J = 6.6 Hz).
[1242] Melting Point (° C): 193.5.
[1243] Example 44 6-Chloro-3- {2- [1- (methoxymethyl) cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 163)
[1244] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.47-7.35 (1H, m), 7.32-7.02 (3H, m), 6.71 (1H, s), 3.47 (2H, s), 3.21 (3H, s ), 0.80-0.70 (4H, m).
[1245] Melting point (° C.): 187-190.
[1246] Example 45 3- (2-isopropylphenoxy) -4-pyridazinol (Compound No. 6)
[1247] ¹ H-NMR (90 MHz, DMSO-d ₆ ) δ ppm: 12.65 (1H, brs), 8.29 (2H, d, J = 6.6 Hz), 7.49-6.98 (4H, m), 6.36 (1H, d, J = 6.6 Hz), 3.20-2.89 (1H, m, J = 6.6 Hz), 1.16 (6H, d, J = 6.6 Hz).
[1248] Melting Point (° C): 181.5-182.
[1249] Example 46 6-Chloro-3- [2- (1-methoxycyclopropyl) phenoxy] -4-pyridazinol (Compound No. 202)
[1250] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.50-7.10 (4H, m), 6.67 (1H, s), 3.03 (3H, s), 1.00-0.85 (4H, m).
[1251] Melting point (° C): 157-165.
[1252] Example 47 2- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} cyclopropanecarbonitrile (Compound No. 226)
[1253] Transbody:
[1254] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.40-7.10 (4H, m), 6.75 (1H, s), 2.65-2.50 (1H, m), 1.65-1.45 (3H, m).
[1255] Melting point (° C.): 203-207.
[1256] Sheath:
[1257] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.40-7.15 (4H, m), 6.64 (1H, s), 2.59 (1H, q, J = 8.4 Hz), 2.05-1.90 (1H, m), 1.67-1.40 (2H, m).
[1258] Melting point (° C): 225-227.
[1259] Example 48 6-Chloro-3-phenoxy-4-pyridazinol (Compound No. 123)
[1260] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.60-7.00 (5H, m), 6.87 (1H, s).
[1261] Melting point (° C): 222-224.
[1262] Example 49 6-Chloro-3- (2-fluorophenoxy) -4-pyridazinol (Compound No. 124)
[1263] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.50-7.05 (4H, m), 6.70 (1H, s).
[1264] Melting Point (° C): 210-212.
[1265] Example 50 6-Chloro-3- (2-chlorophenoxy) -4-pyridazinol (Compound No. 125)
[1266] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.70-7.10 (4H, m), 6.95 (1H, s).
[1267] Melting Point (° C): 208-212.
[1268] Example 51 3- (2-Bromophenoxy) -6-chloro-4-pyridazinol (Compound No. 126)
[1269] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.68 (1H, dd, J = 7.5, 1.8 Hz), 7.53-7.10 (3H, m), 6.73 (1H, s).
[1270] Melting point (° C): 201-203.
[1271] Example 52 6-Chloro-3- (2-iodophenoxy) -4-pyridazinol (Compound No. 127)
[1272] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.89 (1H, dd, J = 7.7, 1.5 Hz), 7.45 (1H, td, J = 7.7, 1.5 Hz), 7.22 (1H, dd, J = 7.7 , 1.5 Hz), 7.04 (1H, td, J = 7.7, 1.5 Hz), 6.74 (1H, s).
[1273] Melting Point (° C): 216-217.
[1274] Example 53 6-Chloro-3- [2- (2-ethoxycyclopropyl) phenoxy] -4-pyridazinol (Compound No. 249)
[1275] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.26-7.05 (4H, m), 6.68 (1H, s), 3.46 (1H, q, J = 5.2 Hz), 3.30-3.15 (2H, m), 2.17-1.96 (1H, m), 1.10 (2H, doublet of doublets, J = 5.2 Hz, 8.5 Hz), 0.93 (3H, t, J = 7.0 Hz).
[1276] Melting point (° C.): 145-152.
[1277] Example 54 6-Chloro-3- [2- (2,2-difluorocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 264)
[1278] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.40-7.15 (4H, m), 6.72 (1H, s), 2.85-2.65 (1H, m), 1.90-1.65 (2H, s).
[1279] Melting Point (° C): 215-216.
[1280] Example 55 6-Chloro-3- (2-ethylphenoxy) -4-pyridazinol (Compound No. 130)
[1281] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.35-7.15 (3H, m), 7.10-7.02 (1H, m), 6.70 (1H, s), 2.56 (2H, q, J = 7.7 Hz), 1.17 (3H, t, J = 7.7 Hz).
[1282] Melting point (° C.): 217-218.
[1283] Example 56 6-Chloro-3- (2-propylphenoxy) -4-pyridazinol (Compound No. 131)
[1284] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.45-7.05 (4H, m), 6.90 (1H, s), 3.00-2.35 (2H, m), 1.95-1.26 (2H, m), 1.05- 0.68 (3 H, m).
[1285] Melting point (° C.): 170-172.
[1286] Example 57 6-Chloro-3- (2-isopropylphenoxy) -4-pyridazinol (Compound No. 132)
[1287] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.60-7.00 (4H, m), 6.92 (1H, s), 3.11 (1H, septet, J = 7.0 Hz), 1.18 (6H, d, J = 7.0 Hz).
[1288] Melting point (° C): 183.
[1289] Example 58 3- (2-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 133)
[1290] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 11.8 (1H, brs), 7.30-6.70 (4H, m), 6.53 (1H, s), 2.60-2.00 (2H, m), 1.80-0.60 (7H, m).
[1291] Melting point (° C): 149.5-150.
[1292] Example 59 6-Chloro-3- (2-isobutylphenoxy) -4-pyridazinol (Compound No. 134)
[1293] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 12.90 (1H, brs), 7.40-6.85 (4H, m), 6.50 (1H, s), 2.25 (2H, d, J = 10.0 Hz), 2.20-1.45 (1H, m, J = 10.0 Hz), 0.75 (6H, d, J = 10.0 Hz).
[1294] Melting Point (℃): 151.5-152.5.
[1295] Example 60 3- (2-s-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 135)
[1296] ¹ H-NMR (60 MHz, CDCl ₃ + DMF-d ₇ ) δ ppm: 7.35-6.80 (4H, m), 6.60 (1H, s), 3.05-2.50 (1H, m), 1.80-1.25 (2H, m) , 1.13 (3H, d, J = 6.2 Hz), 0.95-0.50 (3H, m).
[1297] Melting point (° C): 158-159.
[1298] Example 61 3- (2-tert-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 136)
[1299] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.55-6.85 (4H, m), 6.91 (1H, s), 5.32 (1H, brs), 1.35 (9H, s).
[1300] Melting Point (° C): 215-216.
[1301] Example 62 6-Chloro-3- (2-pentylphenoxy) -4-pyridazinol (Compound No. 137)
[1302] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 11.70 (1H, brs), 7.40-6.80 (4H, m), 6.50 (1H, s), 2.60-2.20 (2H, m), 1.80-0.60 (9H, m).
[1303] Melting Point (℃): 151.5-152.5.
[1304] Example 63 6-Chloro-3- (2-hexylphenoxy) -4-pyridazinol (Compound No. 138)
[1305] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.40-6.70 (4H, m), 6.53 (1H, s), 2.70-2.20 (2H, m), 2.00-0.60 (11H, m).
[1306] Melting Point (° C): 118-118.5.
[1307] Example 64 6-chloro-3- [2- (2,2-dichlorocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 265)
[1308] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.55-7.15 (4H, m), 6.69 (1H, s), 2.90 (1H, dd, J = 11.0, 10.8 Hz), 2.05-1.85 (2H, m ).
[1309] Melting point (° C): 158-163.
[1310] Example 65 6-Chloro-3- [2- (2,2-dibromocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 266)
[1311] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.41-7.36 (1H, m), 7.29-7.13 (3H, m), 6.71 (1H, s), 2.97-2.87 (1H, dd, J = 11.0, 8.4 Hz), 2.21-2.01 (2H, m).
[1312] Melting point (° C.): 208-210 (decomposition).
[1313] Example 66 6-Chloro-3- [2- (1-methylcyclopropyl) phenoxy] -4-pyridazinol (Compound No. 144)
[1314] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.40-7.35 (1H, m), 7.22-7.17 (2H, m), 6.99-6.94 (1H, m), 6.59 (1H, s), 1.25 (3H, s), 0.85-0.60 (2H, m), 0.60-0.45 (2H, m).
[1315] Melting Point (° C): 196-198.
[1316] Example 67 6-Chloro-3- [2- (1-ethylcyclopropyl) phenoxy] -4-pyridazinol (Compound No. 145)
[1317] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.35-7.10 (3H, m), 6.98 (1H, br.d, J = 7.3 Hz), 6.59 (1H, s), 1.50 (2H, q, J = 7.0 Hz), 1.26 (3H, t, J = 7.0 Hz), 0.67-0.50 (4H, m).
[1318] Melting point (° C): 162-165.
[1319] Example 68 6-Chloro-3- {2- [1- (cyclopropyl) cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 151)
[1320] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.35-7.29 (1H, m), 7.26-7.10 (2H m), 7.00-6.92 (1H, m), 6.58 (1H, s), 1.30-1.15 (1H m), 0.60-0.40 (4H, m), 0.27-0.15 (2H, m), 0.07-0.00 (2H, m).
[1321] Melting Point (° C): 180-182.
[1322] Example 69 1- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} cyclopropanecarbonitrile (Compound No. 173)
[1323] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.55-7.15 (5H, m), 1.65-1.20 (4H, m).
[1324] Melting Point (℃): 63-64.
[1325] Example 70 6-Chloro-3- [2- (1-phenylcyclopropyl) phenoxy] -4-pyridazinol (Compound No. 184)
[1326] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.65-7.55 (1H, m), 7.28-7.20 (2H, m), 7.17-6.95 (6H, m), 6.41 (1H, s), 1.19 (4H, s).
[1327] Melting Point (° C): 172-173.
[1328] Example 71 6-Chloro-3- (2-isopropenylphenoxy) -4-pyridazinol (Compound No. 304)
[1329] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.36-7.10 (4H, m), 6.66 (1H, s), 5.06 (1H, br.s), 5.02 (1H, br.s), 2.01 (3H , d, J = 1.5 Hz).
[1330] Melting point (° C.): 187-188.
[1331] Example 72 6-Chloro-3- [2- (2-methylcyclopropyl) phenoxy] -4-pyridazinol (Compound No. 217)
[1332] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.32-6.97 (4H, m), 6.82 (1H, brs), 1.89-1.78 (0.8H, m), 1.52-1.43 (0.2H, m), 1.05-0.60 (6H, m).
[1333] Melting point (° C): 192-208.
[1334] Example 73 6-Chloro-3- [2- (2-ethoxycyclopropyl) phenoxy] -4-pyridazinol (Compound No. 249)
[1335] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.30-7.05 (4H, m), 6.68 (1H, s), 3.51-3.15 (3H, m), 2.07-1.95 (1H, m), 1.13-1.06 (2H, m), 0.93 (3H, t, J = 7.1 Hz).
[1336] Melting point (° C.): 145-152.
[1337] Example 74 (2E) -3- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} acrylonitrile (Compound No. 306)
[1338] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.80-7.40 (3H, m), 7.35-7.15 (2H, m), 6.72 (1H, s), 6.30 (1H, d, J = 6.9 Hz).
[1339] Melting Point (° C): 190-192.
[1340] Example 75 6-Chloro-3- [2- (2,2-dimethylcyclopropyl) phenoxy] -4-pyridazinol (Compound No. 267)
[1341] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.30-7.10 (4H, m), 1.57 (1H, dd, J = 8.4, 6.2 Hz), 0.91-0.85 (1H, m), 0.85 (3H, s), 0.72-0.65 (1H, m), 0.65 (3H, s).
[1342] Melting point (° C.): 187-188.
[1343] Example 76 6-Chloro-3- {2-[(cis-2, cis-3-dimethyl) -ref-1-cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 269)
[1344] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.36-7.11 (4H, m), 6.68 (1H, s), 1.60 (1H, t, J = 8.4 Hz), 1.09-0.93 (8H, m).
[1345] Physical property: Amorphous.
[1346] Example 77 6-Chloro-3- {2-[(cis-2, trans-3-dimethyl) -ref-1-cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 270)
[1347] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.30-7.09 (4H, m), 6.80 (1H, brs), 1.56-1.50 (1H, m), 1.10-0.95 (1H, m), 1.03 ( 3H, s), 0.80-0.67 (1H, m), 0.71 (3H, s).
[1348] Melting Point (° C): 157-160.
[1349] Example 78 6-Chloro-3- {2-[(trans-2, trans-3-dimethyl) -ref-1-cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 271)
[1350] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.22-6.96 (4H, m), 6.70 (1H, s), 1.18-0.95 (9H, m).
[1351] Melting point (° C): 181-183.
[1352] Example 79 3- {2-[(ref-1, cis-5, cis-6) -bicyclo [3.1.0] hex-6-yl] phenoxy} -6-chloro-4-pyridage Gnoll (Compound No. 272)
[1353] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.40-7.05 (4H, m), 6.68 (1H, s), 2.05-1.60 (5H, m), 1.53 (2H, s), 1.35-1.20 (1H m), 0.25-0.05 (1H, m).
[1354] Melting point (° C): 215-240.
[1355] (Example 80) 3- {2-[(ref-1, cis-5, trans-6) -bicyclo [3.1.0] hex-6-yl] phenoxy} -6-chloro-4-pyridage Gnoll (Compound No. 273)
[1356] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.20-7.10 (2H, m), 7.10-6.90 (2H, m), 6.58 (1H, s), 1.80-1.40 (8H, m), 1.20-1.00 ( 1H, m).
[1357] Melting Point (° C): 137-139.
[1358] Example 81 3- {2-[(ref-l, cis-6, cis-7) -bicyclo [4.1.0] hept-7-yl] phenoxy} -6-chloro-4-pyridage Gnoll (Compound No. 274)
[1359] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.44 (1H, br.d, J = 6.3 Hz), 7.35-7.10 (3H, m), 6.66 (1H, s), 2.00-1.50 (5H, m ), 1.20-1.00 (4H, m), 0.90-0.65 (2H, m).
[1360] Melting point (° C):> 260.
[1361] Example 82 3- {2-[(ref-1, cis-6, trans-7) -bicyclo [4.1.0] hept-7-yl] phenoxy} -6-chloro-4-pyridage Gnoll (Compound No. 275)
[1362] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.20-7.10 (2H, m), 7.05-6.85 (2H, m), 6.58 (1H, s), 1.90-1.70 (2H, m), 1.60-1.40 ( 3H, m), 1.30-1.05 (6H, m).
[1363] Melting point (° C): 191-193.
[1364] Example 83 6-Chloro-3- {2-[(2,2, cis-3-trimethyl) -ref-1-cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 279)
[1365] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.30-7.00 (4H, m), 6.56 (1H, s), 1.42-1.22 (2H, m), 1.05-0.70 (9H, m).
[1366] Melting Point (° C): 118-120.
[1367] Example 84 6-Chloro-3- {2-[(2,2, trans-3-trimethyl) -ref-1-cyclopropyl] phenoxy} -4-pyridazinol (Compound No. 280)
[1368] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.26-7.06 (4H, m), 6.59 (1H, s), 1.70-1.50 (1H, m), 1.30-1.25 (1H, m), 1.09 (3H, s), 0.96 (3H, s), 0.75 (3H, s).
[1369] Melting point (° C): 160-162.
[1370] Example 85 6-Chloro-3- (2-cyclobutylphenoxy) -4-pyridazinol (Compound No. 284)
[1371] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.43-7.30 (1H, m), 7.30-7.18 (2H, m), 7.08-6.98 (1H, m), 6.69 (1H, s), 3.68-3.50 (1H, m), 2.25-1.70 (6H, m).
[1372] Melting Point (° C): 188-189.
[1373] Example 86 1- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} cyclobutanecarbonitrile (Compound No. 287)
[1374] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.50-7.20 (5H, m), 2.70-1.80 (6H, m).
[1375] Melting point (° C): 213-215.
[1376] Example 87 1- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} cyclobutanecarboxylic acid (Compound No. 288)
[1377] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.42-7.35 (1H, m), 7.35-7.20 (2H, m), 7.08-7.03 (1H, m), 6.66 (1H, s), 2.80-2.45 (4H, m), 2.22-1.95 (1H, m), 1.90-1.70 (1H, m).
[1378] Melting point (° C): 173-175.
[1379] Example 88 6-Chloro-3- (2-cyclopentylphenoxy) -4-pyridazinol (Compound No. 292)
[1380] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.41-7.35 (1H, m), 7.25-7.17 (2H, m), 7.08-7.02 (1H, m), 6.70 (1H, s), 3.14-3.06 (1H, m), 1.98-1.52 (8H, m).
[1381] Melting Point (° C): 178-180.
[1382] Example 89 6-Chloro-3- (2-cyclohexylphenoxy) -4-pyridazinol (Compound No. 293)
[1383] ¹ H-NMR (60 MHz, CDCl ₃ + DMF-d ₇ ) δ ppm: 7.40-6.70 (4H, m), 6.55 (1H s), 2.75 (1H, brs), 2.10-0.90 (10H, m).
[1384] Melting point (° C): 158-159.
[1385] Example 90 6-Chloro-3- [2- (trifluoromethyl) phenoxy] -4-pyridazinol (Compound No. 300)
[1386] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.76-7.27 (4H, m), 6.75 (1H, s), 5.47 (1H, s).
[1387] Melting Point (° C): 188.
[1388] Example 91 6-Chloro-3- [2- (1-propenyl) phenoxy} -4-pyridazinol (Compound No. 305)
[1389] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.70-6.90 (5H, m), 6.76 (1H, s), 6.50-6.20 (2H, m), 1.81 (3H, d, J = 5.0 Hz) .
[1390] Melting point (° C): 204-206.
[1391] Example 92 3- (2-allylphenoxy) -6-chloro-4-pyridazinol (Compound No. 307)
[1392] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.46-7.24 (4H, m), 6.96 (1H s), 6.20-5.60 (1H, m), 5.20-4.80 (2H, m), 3.46-3.26 (2H, m).
[1393] Melting Point (℃): 200-202.5.
[1394] Example 93 6-Chloro-3- [2- (1-propynyl) phenoxy] -4-pyridazinol (Compound No. 309)
[1395] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.43-7.32 (2H, m), 7.23-7.16 (2H, m), 6.73 (1H, s), 1.87 (3H, s).
[1396] Melting point (° C): 182-184.
[1397] Example 94 6-Chloro-3- [2- (cyclopropylmethyl) phenoxy] -4-pyridazinol (Compound No. 311)
[1398] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.45 (1H, dd, J = 7.3, 1.8 Hz), 7.31-7.17 (2H, m), 7.10 (1H, dd, J = 7.3, 1.8 Hz) , 2.38 (2H, d, J = 7.0 Hz), 1.00-0.88 (1H, m), 0.50-0.40 (2H, m), 0.22-0.11 (2H, m).
[1399] Melting point (° C): 165-168.
[1400] Example 95 3- (2-benzylphenoxy) -6-chloro-4-pyridazinol (Compound No. 315)
[1401] Melting point (° C.): 185-187.
[1402] Example 96 6-Chloro-3- [2- (methoxymethyl) phenoxy] -4-pyridazinol (Compound No. 324)
[1403] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.47 (1H, br.d, J = 7.7 Hz), 7.42-7.20 (2H, m), 7.15 (1H, br.d, J = 7.7 Hz) , 6.83 (1 H, brs), 4.35 (2 H, s), 3.23 (3 H, s).
[1404] Melting point (° C): 211-212.
[1405] Example 97 6-Chloro-3- [2- (ethoxymethyl) phenoxy] -4-pyridazinol (Compound No. 325)
[1406] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.47 (1H, br.d, J = 7.7 Hz), 7.42-7.20 (2H, m), 7.16 (1H, br.d, J = 7.7 Hz) , 6.82 (1H, br s), 4.38 (2H, s), 3.39 (2H, q, J = 7.0 Hz), 1.03 (3H, t, J = 7.0 Hz).
[1407] Melting point (° C.): 173-174.
[1408] Example 98 6-Chloro-3- [2- (1,3-dioxolan-2-yl) phenoxy] -4-pyridazinol (Compound No. 329)
[1409] Melting point (° C.): 143-145.
[1410] Example 99 1- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} ethanone O-methyl oxime (Compound No. 334)
[1411] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.47 (2H, t, J = 7.7 Hz), 7.31 (1H, d, J = 7.7 Hz), 7.24 (1H, d, J = 7.7 Hz), 6.85 (1 H, brs), 3.76 (2.8 H, s), 3.58 (0.2 H, s), 2.02 (2.8 H, s), 1.99 (0.2 H, s).
[1412] Melting point (° C): 165-167.
[1413] Example 100 Methyl 2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] benzoate (Compound No. 339)
[1414] ¹ H-NMR (60 MHz, CDCl ₃ + DMF-d ₇ ) δ ppm: 8.10-7.18 (4H, m), 6.80 (1H, s), 5.75 (1H, brs), 3.70 (3H, s).
[1415] Melting Point (° C): 188-191.
[1416] Example 101 3-([1,1'-biphenyl] -2-yloxy) -6-chloro-4-pyridazinol (Compound No. 344)
[1417] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.30-6.70 (10 H, m), 6.25 (1 H, s).
[1418] Melting Point (℃): 98-100.
[1419] (Example 102)
[1420] 6-chloro-3-{[3 '-(trifluoromethyl) [1,1'-biphenyl] -2-yl] oxy} -4-pyridazinol (Compound No. 348)
[1421] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.65-7.58 (2H, m), 7.51-7.26 (5H, m), 7.12-7.06 (1H, m), 6.41 (1H, brs).
[1422] Physical property: Paste form.
[1423] (Example 103)
[1424] 6-chloro-3-{[3 '-(trifluoromethyl) [1,1'-biphenyl] -2-yl] oxy} -4-pyridazinol (Compound No. 349)
[1425] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.71-7.64 (2H, m), 7.55-7.30 (5H, m), 7.20-7.13 (1H, m), 6.43 (1H, s).
[1426] Physical property: Paste form.
[1427] Example 104 6-Chloro-3- [2- (1-pyrrolidinyl) phenoxy] -4-pyridazinol (Compound No. 355)
[1428] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.19-6.73 (4H, m), 5.64 (1H, s), 3.32-3.25 (4H, m), 1.91-1.84 (4H, m).
[1429] Physical property: Amorphous.
[1430] Example 105 6-Chloro-3- [2- (1H-pyrrol-1-yl) phenoxy] -4-pyridazinol (Compound No. 356)
[1431] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.41-7.27 (4H, m), 6.95-6.93 (2H, m), 6.46 (1H, m), 6.10-6.08 (2H, m).
[1432] Physical property: Amorphous.
[1433] Example 106 6-Chloro-3- [2- (2-thienyl) phenoxy] -4-pyridazinol (Compound No. 359)
[1434] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.68-7.60 (1H, m), 7.45-7.05 (5H, m), 7.01-6.95 (1H, m), 6.52 (1H, s).
[1435] Physical property: Amorphous.
[1436] Example 107 6-Chloro-3- [2- (3-thienyl) phenoxy] -4-pyridazinol (Compound No. 361)
[1437] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.46-7.37 (3H, m), 7.30-7.15 (4H, m).
[1438] Melting Point (° C): 207-209.
[1439] Example 108 6-Chloro-3- [2- (1H-pyrazol-1-yl) phenoxy] -4-pyridazinol (Compound No. 362)
[1440] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.09 (1H, d, J = 2.2 Hz), 7.70 (1H, dd, J = 7.5, 2.4 Hz), 7.62 (1H, d, J = 2.2 Hz) , 7.50-7.27 (3H, m), 6.55 (1H, s), 6.39 (1H, t, J = 2.2 Hz).
[1441] Physical property: Amorphous.
[1442] (Example 109) 6-chloro-3- [2- (3,5-dimethyl-1H-pyrazol-1-yl) phenoxy] -4-pyridazinol (Compound No. 364)
[1443] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.60-7.32 (4H, m), 6.52 (1H, s), 5.86 (1H, s), 2.17 (3H, s), 2.10 (3H, s).
[1444] Physical property: Amorphous.
[1445] (Example 110)
[1446] 6-chloro-3- {2- [3- (trifluoromethyl) -1H-pyrazol-1-yl] phenoxy} -4-pyridazinol (Compound No. 365)
[1447] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.79 (1H, brs), 7.70-7.35 (5H, m), 7.06 (1H, brs), 6.68 (1H, s).
[1448] Physical property: Amorphous.
[1449] (Example 111)
[1450] 6-chloro-3- {2- [4- (trifluoromethyl) -1H-pyrazol-1-yl] phenoxy} -4-pyridazinol (Compound No. 366)
[1451] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 8.75 (1H, s), 8.11 (1H, s), 7.80-7.74 (1H, m), 7.58-7.38 (3H, m), 6.77 (1H, s).
[1452] Properties: Oily substance.
[1453] (Example 112)
[1454] 6-chloro-3- {2- [5- (trifluoromethyl) -1H-pyrazol-1-yl] phenoxy} -4-pyridazinol (Compound No. 367)
[1455] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 8.30 (1H, brs), 7.83-7.72 (1H, m), 7.60-7.40 (3H, m), 6.91 (1H, br.d, J = 2.6 Hz), 6.78 (1 H, s).
[1456] Physical property: Amorphous.
[1457] Example 113 5- {2-[(6-Chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} -N, N-dimethyl-1H-pyrazole-1-sulfonamide (Compound No. 369)
[1458] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.87 (1H, d, J = 2.6 Hz), 7.78 (1H, dd, J = 7.3, 1.8 Hz), 7.65-7.35 (3H, m), 7.20 (1H) , s), 7.03 (1H, d, J = 2.6 Hz), 2.86 (6H, s).
[1459] Melting point (° C): 151-152.
[1460] Example 114 3- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} -N, N-dimethyl-1H-pyrazole-1-sulfonamide (Compound No. 368)
[1461] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.19 (1H, d, J = 2.9 Hz), 8.12 (1H, s), 7.97 (1H, dd, J = 7.3, 2.2 Hz), 7.61 (1H, d , J = 1.5 Hz), 7.50-7.33 (2H, m), 6.98 (1H, d, J = 2.9 Hz), 2.83 (6H, s).
[1462] Melting Point (° C): 210-212.
[1463] Example 115 6-Chloro-3- [2- (4-methyl-1,3-thiazol-2-yl) phenoxy] -4-pyridazinol (Compound No. 370)
[1464] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.17 (1H, d, J = 7.7 Hz), 7.73 (1H, d, J = 7.7 Hz), 7.47 (1H, t, J = 7.7 Hz), 7.28 ( 1H, t, J = 7.7 Hz), 7.02 (1H, s), 6.98 (1H, s), 2.56 (3H, s).
[1465] Physical property: Amorphous.
[1466] Example 116 3- [2- (1,3-benzooxazol-2-yl) phenoxy] -6-chloro-4-pyridazinol (Compound No. 375)
[1467] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.31 (1H, dd, J = 7.9, 1.6 Hz), 7.73-7.30 (7H, m), 6.78 (1H, s).
[1468] Melting point (° C): 165-167.
[1469] Example 117 3- [2- (1,3-benzothiazol-2-yl) phenoxy] -6-chloro-4-pyridazinol (Compound No. 376)
[1470] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.12 (1H, d, J = 7.7 Hz), 8.00-7.84 (1H, m), 7.78 (1H, d, J = 7.7 Hz), 7.62-7.30 (5H m), 7.05 (1H, broad singlet).
[1471] Melting Point (° C): 215-217.
[1472] Example 118 6-chloro-3- [2- (dimethylamino) phenoxy] -4-pyridazinol (Compound No. 379)
[1473] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.17-6.96 (4H, m), 6.61 (1H, s), 2.75 (6H, s).
[1474] Physical property: Amorphous.
[1475] Example 119 6-Chloro-3- (2-nitrophenoxy) -4-pyridazinol (Compound No. 383)
[1476] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.16 (1H, d, J = 6.0 Hz), 7.90-7.33 (3H, m), 6.78 (1H, s).
[1477] Melting Point (℃): 99-100.
[1478] Example 120 6-Chloro-3- (2-ethynylphenoxy) -4-pyridazinol (Compound No. 308)
[1479] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.57-7.41 (2H, m), 7.30-7.20 (2H, m), 6.71 (1H, s), 3.60 (1H, s).
[1480] Melting point (° C): 189-191.
[1481] Example 121 6-Chloro-3- (2-methoxyphenoxy) -4-pyridazinol (Compound No. 385)
[1482] ¹ H-NMR (60 MHz, CDCl ₃ + DMF-d ₇ ) δ ppm: 7.30-6.80 (4H, m), 6.55 (1H, s), 3.69 (3H, s).
[1483] Melting point (° C): 191-194.
[1484] Example 122 6-Chloro-3- (2-ethoxyphenoxy) -4-pyridazinol (Compound No. 386)
[1485] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.26-7.02 (2H, m), 6.98-6.85 (2H, m), 6.57 (1H, s), 5.35 (1H, brs), 3.92 (2H, q, J = 7.0 Hz), 1.18 (t, 3H, J = 7.0 Hz).
[1486] Melting point (° C): 155-175.
[1487] Example 123 6-Chloro-3- (2-isopropoxyphenoxy) -4-pyridazinol (Compound No. 387)
[1488] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.28-7.10 (3H, m), 6.97 (1H, td, J = 7.3, 2.3 Hz), 6.83 (1H, brs), 4.52 (1H, septet, J = 6.2 Hz), 1.07 (6H, d, J = 6.2 Hz).
[1489] Melting Point (° C): 178-179.
[1490] Example 124 6-Chloro-3- [2- (difluoromethoxy) phenoxy] -4-pyridazinol (Compound No. 390)
[1491] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.40 (4H, s), 6.63 (1H, s), 6.53 (1H, t, J = 73.8 Hz).
[1492] Melting Point (° C): 210-212.
[1493] Example 125 6-Chloro-3- [2- (trifluoromethoxy) phenoxy] -4-pyridazinol (Compound No. 391)
[1494] ¹ H-NMR (200 MHz, CDCl ₃ + CD ₃ OD) δ ppm: 7.38-7.20 (4H, m), 6.60 (1H, s).
[1495] Melting point (° C): 215.
[1496] Example 126 6-chloro-3- [2- (2-methoxyethoxy) phenoxy] -4-pyridazinol (Compound No. 396)
[1497] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.26-6.93 (4H, m), 6.62 (1H, s), 4.78-4.03 (2H, m), 3.55-3.50 (2H, m), 3.24 (3H , s).
[1498] Physical property: Paste form.
[1499] Example 127 6-Chloro-3- [2- (2-hydroxyphenoxy) phenoxy] -4-pyridazinol (Compound No. 399)
[1500] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.27-6.75 (8H, m), 6.61 (1H, s).
[1501] Physical property: Amorphous.
[1502] Example 128 6-Chloro-3- {2- {2-[(6-chloro-4-ethoxy-3-pyridazinyl) oxy] phenoxy} phenoxy} -4-pyridazinol (Compound Number 400)
[1503] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.65-6.70 (8H, m), 6.63-6.59 (2H, m), 4.19 (2H, q, J = 7.0 Hz), 1.50 (3H, t, J = 7.0 Hz).
[1504] Physical property: Amorphous.
[1505] Example 129 6-chloro-3- [2- (methylsulfanyl) phenoxy] -4-pyridazinol (Compound No. 401)
[1506] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.43-7.11 (4H, m), 6.71 (1H, s), 2.40 (3H, s).
[1507] Melting point (° C): 174-175.
[1508] Example 130 6-Chloro-3- [2- (isopropylsulfanyl) phenoxy] -4-pyridazinol (Compound No. 403)
[1509] Melting Point (° C): 176-177.
[1510] Example 131 6-Chloro-3- (2-cyanophenoxy) -4-pyridazinol (Compound No. 330)
[1511] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.82-7.68 (2H, m), 7.46-7.34 (2H, m), 6.79 (1H, s).
[1512] Physical property: Amorphous.
[1513] Example 132 1- {2- [6-chloro-4-hydroxy-3-pyridazinyl] oxy} phenyl} ethanone (Compound No. 336)
[1514] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.88-7.85 (1H, m), 7.65-7.57 (1H, m), 7.43-7.26 (2H, m), 6.73 (1H, s), 2.50 (3H, br.s).
[1515] Melting point (° C): 186-189.
[1516] Example 133 6-Chloro-3- (3-chlorophenoxy) -4-pyridazinol (Compound No. 410)
[1517] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.45-7.10 (5H, m), 6.72 (1H, s).
[1518] Melting Point (° C): 217.
[1519] Example 134 6-Chloro-3- (3-iodophenoxy) -4-pyridazinol (Compound No. 412)
[1520] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.64-7.53 (2H, m), 7.28-6.70 (3H, m).
[1521] Melting point (° C): 202-203.
[1522] Example 135 6-Chloro-3- (3-methylphenoxy) -4-pyridazinol (Compound No. 413)
[1523] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.35-6.80 (4H, m), 6.95 (1H, s), 2.35 (3H, s).
[1524] Melting point (° C.): 205-208.
[1525] Example 136 6-Chloro-3- (3-isopropylphenoxy) -4-pyridazinol (Compound No. 415)
[1526] Melting Point (° C): 176-177.
[1527] Example 137 3- (3-tert-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 416)
[1528] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.40-6.65 (4H, m), 6.67 (1H, s), 1.27 (9H, s).
[1529] Melting point (° C.): 203-207.
[1530] Example 138 6-Chloro-3- (3-cyclopropylphenoxy) -4-pyridazinol (Compound No. 417)
[1531] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.35-7.20 (1H, m), 6.98-6.85 (3H, m), 6.78 (1H, brs), 2.00-1.88 (1H, m), 0.98- 0.87 (2H, m), 0.70-0.60 (2H, m).
[1532] Melting point (° C): 179-181.
[1533] Example 139 6-Chloro-3- [3- (trifluoromethyl) phenoxy] -4-pyridazinol (Compound No. 418)
[1534] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.70-7.40 (4H, m), 6.95 (1H, s).
[1535] Melting point (° C): 213-216.
[1536] Example 140 6-Chloro-3- [3- (2-furyl) phenoxy] -4-pyridazinol (Compound No. 419)
[1537] ¹ H-NMR (200 MHz, CDCl ₃ + CD ₃ OD) δ ppm: 7.55-7.35 (4H, m), 7.08-7.02 (1H, m), 6.67 (1H, d, J = 3.3 Hz), 6.59 (1H, brs), 6.48 (1H, doublet of doublets, J = 3.3, 1.8 Hz).
[1538] Melting Point (° C): 200-202.
[1539] Example 141 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] benzonitrile (Compound No. 420)
[1540] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.70-7.40 (4H, m), 6.75 (1H, s).
[1541] Melting point (° C.): 226-229.
[1542] Example 142 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] benzaldehyde (Compound No. 421)
[1543] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 9.96 (1H, s), 7.72-7.53 (3H, m), 7.46-7.41 (1H, m), 6.54 (1H, s).
[1544] Melting Point (° C): 188-192.
[1545] Example 143 1- {3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} ethanone (Compound No. 422)
[1546] Melting Point (° C): 195-198.
[1547] Example 144 Methyl 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] benzoate (Compound No. 423)
[1548] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 8.00-7.70 (2H, m), 7.70-7.30 (2H, m), 6.75 (1H, s), 3.30 (3H, s).
[1549] Melting point (° C.): 207.
[1550] Example 145 6-Chloro-3- (3-nitrophenoxy) -4-pyridazinol (Compound No. 424)
[1551] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 8.30-7.90 (2H, m), 7.90-7.70 (2H, m), 6.50 (1H, s), 5.80-5.15 (1H, brs).
[1552] Melting Point (° C): 217-219.
[1553] Example 146 6-Chloro-3- (3-methoxyphenoxy) -4-pyridazinol (Compound No. 425)
[1554] ¹ H-NMR (60 MHz, CDCl ₃ + DMF-d ₇ ) δ ppm: 7.50-7.10 (1H, m), 6.90-6.60 (3H, m), 6.70 (1H, s), 5.88 (1H, brs), 3.77 (3H, s).
[1555] Melting Point (° C): 199-203.
[1556] Example 147 6-Chloro-3- (4-chlorophenoxy) -4-pyridazinol (Compound No. 427)
[1557] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.45-7.38 (2H, m), 7.23-7.15 (2H, m), 6.70 (1H, s).
[1558] Melting point (° C.): 226-231.
[1559] Example 148 6-Chloro-3- (4-methylphenoxy) -4-pyridazinol (Compound No. 430)
[1560] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.25-6.83 (4H, m), 6.68 (1H, s), 2.25 (3H, s).
[1561] Melting point (° C): 261-263.
[1562] Example 149 6-Chloro-3- (4-isopropylphenoxy) -4-pyridazinol (Compound No. 432)
[1563] Melting point (° C): 233-235.
[1564] Example 150 3- (4-tert-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 433)
[1565] Melting point (° C.): 224-225.
[1566] Example 151 6-Chloro-3- (4-cyclopropylphenoxy) -4-pyridazinol (Compound No. 434)
[1567] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.15-7.02 (4H, m), 6.82 (1H, brs), 2.01-1.90 (1H, m), 0.99-0.90 (2H, m), 0.70- 0.62 (2H, m).
[1568] Melting point (° C): 221-227.
[1569] Example 152 6-chloro-3- (4-methoxyphenoxy) -4-pyridazinol (Compound No. 435)
[1570] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.26-6.85 (4H, m), 6.80 (1H, brs), 3.81 (3H, s).
[1571] Melting point (° C): 260-263.5.
[1572] Example 153 6-chloro-3- [4- (trimethylsilyl) phenoxy] -4-pyridazinol (Compound No. 436)
[1573] Melting Point (° C): 197-199.
[1574] Example 154 6-Chloro-3- (2,3-difluorophenoxy) -4-pyridazinol (Compound No. 437)
[1575] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.24-7.05 (3H, m), 6.73 (1H, s).
[1576] Melting Point (° C): 188-193.
[1577] Example 155 6-Chloro-3- (3-chloro-2-fluorophenoxy) -4-pyridazinol (Compound No. 438)
[1578] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.43-7.21 (3H, m), 6.75 (1H, s).
[1579] Melting Point (° C): 187-195.
[1580] Example 156 6-Chloro-3- [2-fluoro-3- (trifluoromethyl) phenoxy] -4-pyridazinol (Compound No. 441)
[1581] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.78-7.66 (2H, m), 7.48 (1H, t, J = 8.1 Hz), 6.83 (1H, s).
[1582] Melting Point (° C): 185-189.
[1583] Example 157 6-Chloro-3- (2,3-dichlorophenoxy) -4-pyridazinol (Compound No. 443)
[1584] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.62-7.57 (1H, m), 7.50-7.37 (2H, m), 6.89 (1H, s).
[1585] Melting point (° C): 233-238.
[1586] Example 158 6-chloro-3- [2-chloro-3- (trifluoromethyl) phenoxy] -4-pyridazinol (Compound No. 446)
[1587] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.74-7.55 (3H, m), 6.76 (1H, s).
[1588] Melting Point (℃): 170-200.
[1589] Example 159 3- (2-bromo-3-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 450)
[1590] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.35 (1H, t, J = 7.5 Hz), 7.27 (1H, dd, J = 7.5, 2.2 Hz), 7.16 (1H, dd, J = 7.5, 2.2 Hz), 6.87 (1 H, brs), 2.41 (3 H, s).
[1591] Melting Point (° C): 140-141.
[1592] Example 160 6-Chloro-3- (3-fluoro-2-methylphenoxy) -4-pyridazinol (Compound No. 453)
[1593] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.30-7.15 (1H, m), 7.08-6.85 (2H, m), 6.73 (1H, s), 2.09 (3H, d, J = 1.8 Hz).
[1594] Melting point (° C): 242-244.
[1595] Example 161 6-Chloro-3- (3-chloro-2-methylphenoxy) -4-pyridazinol (Compound No. 454)
[1596] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.39-7.12 (4H, m), 2.14 (3H, s).
[1597] Melting point (° C.): 250-252.
[1598] Example 162 6-Chloro-3- (2,3-dimethylphenoxy) -4-pyridazinol (Compound No. 456)
[1599] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.22-6.98 (3H, m), 6.77 (1H, s), 2.30 (3H, s), 2.02 (3H, s).
[1600] Melting Point (° C): 240-241.
[1601] Example 163 6-Chloro-3- (2-methyl-3-nitrophenoxy) -4-pyridazinol (Compound No. 458)
[1602] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.89-7.84 (1H, m), 7.58-7.47 (2H, m), 6.90 (1H, brs), 2.25 (3H, s).
[1603] Melting point (° C): 241-244.
[1604] Example 164 6-Chloro-3- (3-methoxy-2-methylphenoxy) -4-pyridazinol (Compound No. 459)
[1605] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.14 (1H, t, J = 8.4 Hz), 6.78 (1H, d, J = 8.4 Hz), 6.63 (1H, d, J = 8.4 Hz), 6.55 (1H, s), 3.83 (3H, s), 2.00 (3H, s).
[1606] Melting point (° C): 224-237.
[1607] Example 165 6-chloro-3- {3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -2-methylphenoxy} -4-pyridazinol (Compound No. 460 )
[1608] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.16 (1H, t, J = 8.4 Hz), 6.85 (2H, d, J = 8.4 Hz), 6.48 (2H, s), 2.15 (3H, s) .
[1609] Melting point (° C):> 290.
[1610] Example 166 6-Chloro-3- (2-cyclopropyl-3-methylphenoxy) -4-pyridazinol (Compound No. 472)
[1611] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.18 (1H, t, J = 7.7 Hz), 7.07 (1H, br.d, J = 7.7 Hz), 6.91 (1H, br.d, J = 7.7 Hz), 6.82 (1H, brs), 2.40 (3H, s), 1.43-1.28 (1H, m), 0.79-0.68 (2H, m), 0.59-0.48 (2H, m).
[1612] Melting Point (° C): 197-198.
[1613] Example 167 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl tetrahydro-2H-pyran-4-carboxylate (Compound No. 3856)
[1614] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.38 (1H, s), 7.15-7.04 (2H, m), 6.90-6.78 (1H, m), 4.10-3.95 (2H, m), 3.60-3.43 ( 2H, m), 3.03-2.86 (1H, m), 2.11 (3H, s), 2.06-1.90 (4H, m), 1.80-1.60 (1H, m), 0.80-0.50 (4H, m).
[1615] Properties: Caramel statue.
[1616] Example 168 Methyl 2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -6-fluorobenzoate (Compound No. 491)
[1617] ¹ H-NMR (270 MHz, CDCl ₃ ) δ ppm: 7.62 (1H, td, J = 8.4, 5.6 Hz), 7.23 (1H, t, J = 8.4 Hz), 7.02 (1H, d, J = 8.4 Hz), 3.83 (3 H, s).
[1618] Physical property: Amorphous.
[1619] Example 169 6-Chloro-3- (3-methyl-2-nitrophenoxy) -4-pyridazinol (Compound No. 498)
[1620] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.48 (1H, t, J = 8.1 Hz), 7.26 (1H, d, J = 8.1 Hz), 7.19 (1H, d, J = 8.1 Hz), 6.66 (1H, s), 2.37 (3H, s).
[1621] Melting point (° C): 191-200.
[1622] Example 170 6-Chloro-3- (2,3-dimethoxyphenoxy) -4-pyridazinol (Compound No. 503)
[1623] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.14-6.78 (4H, m), 3.84 (3H, s), 3.61 (3H, s).
[1624] Melting point (° C): 199-201.
[1625] Example 171 6-Chloro-3- (2,3-dihydro-1H-inden-4-yloxy) -4-pyridazinol (Compound No. 506)
[1626] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.20 (1H, t, J = 7.3 Hz), 7.14 (1H, d, J = 7.3 Hz), 6.92 (1H, d, J = 7.3 Hz), 6.83 (1H, brs), 2.92 (1H, t, J = 7.3 Hz), 2.64 (1H, t, J = 7.3 Hz), 2.00 (1H, quintet, J = 7.3 Hz).
[1627] Melting Point (℃): 230-232.
[1628] Example 172 6-chloro-3-[(3-methyl-2,3-dihydro-1H-inden-4-yl) oxy] -4-pyridazinol (Compound No. 507)
[1629] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.17 (1H, t, J = 7.7 Hz), 7.08 (1H, d, J = 7.7 Hz), 6.88 (1H, d, J = 7.7 Hz), 6.69 (1H, s), 3.35-3.15 (1H, m), 3.10-2.70 (2H, m), 2.40-2.15 (1H, m), 1.80-1.55 (1H, m), 1.15 (3H, d, J = 7.0 Hz).
[1630] Melting Point (℃): 232.
[1631] Example 173 6-Chloro-3-[(1-methyl-2,3-dihydro-1H-inden-4-yl) oxy] -4-pyridazinol (Compound No. 510)
[1632] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.21 (1H, dd, J = 8.1, 7.3 Hz), 7.09 (1H, d, J = 7.3 Hz), 6.91 (1H, d, J = 8.1 Hz) , 6.70 (1H, s), 3.30-3.05 (1H, m), 2.85-2.50 (2H, m), 2.40-2.20 (1H, m), 1.70-1.45 (1H, m), 1.29 (3H, d, J = 7.0 Hz).
[1633] Melting point (° C.): 228-230.
[1634] Example 174 6-chloro-3-[(2,2-dimethyl-2,3-dihydro-1H-inden-4-yl) oxy] -4-pyridazinol (Compound No. 513)
[1635] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.17 (1H, t, J = 7.7 Hz), 7.05 (1H, d, J = 7.7 Hz), 6.89 (1H, d, J = 7.7 Hz), 6.69 (1H, s), 2.76 (2H, s), 2.53 (2H, s), 1.13 (6H, s).
[1636] Melting point (° C): 220-223.
[1637] (Example 175) 6-chloro-3- {spiro [cyclopropane-1,3 '-(2', 3'-dihydro-1'H-indene)]-4'-yloxy} -4-pyri Dazinol (Compound No. 514)
[1638] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.15-6.95 (2H, m), 6.75 (1H, dd, J = 6.6, 2.6 Hz), 6.66 (1H, s), 3.02 (2H, dd, J = 7.7, 7.3 Hz), 2.15-1.95 (2H, m), 1.28-1.15 (2H, m), 0.80-0.70 (2H, m).
[1639] Physical property: Amorphous.
[1640] Example 176 6-Chloro-3- (4-fluorophenoxy) -4-pyridazinol (Compound No. 426)
[1641] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.26-7.05 (4H, m), 6.70 (1H, s).
[1642] Melting point (° C): 241-248.
[1643] Example 177 3- (bicyclo [4.2.0] octa-1,3,5-trien-2-yloxy) -6-chloro-4-pyridazinol (Compound No. 505)
[1644] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.22 (1H, dd, J = 8.2, 7.3 Hz), 6.96 (1H, d, J = 8.2 Hz), 6.91 (1H, d, J = 7.3 Hz) , 6.69 (1H, s), 3.19-3.11 (2H, m), 3.10-3.00 (2H, m).
[1645] Melting Point (° C): 145-155.
[1646] Example 178 7-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -2,3-dihydro-1H-inden-1-one O-methyloxime (Compound No. 520)
[1647] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.50-7.15 (2H, m), 7.07 (1H, dd, J = 8.1, 7.3 Hz), 6.55 (0.4H, s), 5.77 (0.6H, s ), 3.73 (1.8H, s), 3.67 (1.2H, s), 3.15-3.00 (2H, m), 2.90-2.73 (2H, m).
[1648] Melting point (° C):> 250.
[1649] Example 179 6-chloro-3- (5,6,7,8-tetrahydro-1-naphthalenyloxy) -4-pyridazinol (Compound No. 521)
[1650] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.14 (1H, t, J = 7.7 Hz), 6.98 (1H, d, J = 7.7 Hz), 6.89 (1H, d, J = 7.7 Hz), 6.82 (1H, brs), 2.80-2.70 (2H, m), 2.50-2.40 (2H, m), 1.85-1.70 (4H, m).
[1651] Melting Point (℃): 232-237.
[1652] Example 180 6-Chloro-3- (1-naphthyloxy) -4-pyridazinol (Compound No. 527)
[1653] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 8.10-7.20 (7H, m), 6.85 (1H, s), 6.20 (1H, brs).
[1654] Melting point (° C): 243-245.
[1655] Example 181 6-Chloro-3- (2,3-dihydro-1-benzofuran-4-yloxy) -4-pyridazinol (Compound No. 528)
[1656] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.11 (1H, t, J = 8.1 Hz), 6.65 (1H, s), 6.60 (1H, d, J = 8.1 Hz), 6.56 (1H d, J = 8.1 Hz), 4.53 (2H, t, J = 8.5 Hz), 2.97 (2H, t, J = 8.5 Hz).
[1657] Melting Point (° C): 219-221.
[1658] Example 182 6-chloro-3-[(3-methyl-2,3-dihydro-1-benzofuran-4-yl) oxy] -4-pyridazinol (Compound No. 529)
[1659] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.15 (1H, t, J = 8.1 Hz), 6.85 (1H, brs), 6.67 (1H, d, J = 8.1 Hz), 6.62 (1H, d , J = 8.1 Hz), 4.65 (1H, t, J = 8.8 Hz), 4.12-4.04 (1H, m), 3.50-3.39 (1H, m), 1.14 (3H, d, J = 7.0 Hz).
[1660] Melting point (° C): 238-245.
[1661] Example 183 3- (1-benzofuran-4-yloxy) -6-chloro-4-pyridazinol (Compound No. 531)
[1662] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.99 (1H, d, J = 2.0 Hz), 7.52 (1H, d, J = 7.8 Hz), 7.35 (1H, t, J = 7.8 Hz), 7.06 (1H, d, J = 7.8 Hz), 6.87 (1H, s), 6.81 (1H, d, J = 2.0 Hz).
[1663] Melting Point (° C): 220-225.
[1664] Example 184 6-Chloro-3-[(3-methyl-1-benzofuran-4-yl) oxy] -4-pyridazinol (Compound No. 532)
[1665] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.44 (1H, d, J = 1.5 Hz), 7.33-7.20 (2H, m), 6.91 (1H, dd, J = 7.0, 1.5 Hz), 6.61 ( 1H, s), 2.01 (3H, s).
[1666] Melting point (° C.): 218-225.
[1667] Example 185 3- (1-benzothien-4-yloxy) -6-chloro-4-pyridazinol (Compound No. 534)
[1668] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.75 (1H, d, J = 8.1 Hz), 7.53 (1H, d, J = 5.5 Hz), 7.35 (1H, dd, J = 8.1, 7.7 Hz) , 7.28 (1H, dd, J = 5.5, 0.7 Hz), 7.10 (1H, dd, J = 7.7, 0.7 Hz), 6.64 (1H, s).
[1669] Melting point (° C): 181-183.
[1670] Example 186 6-Chloro-3- (8-quinolinyloxy) -4-pyridazinol (Compound No. 535)
[1671] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 8.80 (1H, dd, J = 4.0, 1.5 Hz), 8.46 (1H, dd, J = 8.4, 1.5 Hz), 7.93-7.87 (1H, m) , 7.70-7.63 (2H, m), 7.57 (1H, doublet of doublets, J = 8.4, 4.0 Hz), 6.82 (1H, s).
[1672] Melting point (° C.):> 200 (decomposition).
[1673] Example 187 6-Chloro-3- (8-quinolinyloxy) -4-pyridazinol (Compound No. 536)
[1674] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 8.81 (1H, dd, J = 4.0, 1.5 Hz), 8.41 (1H, dd, J = 8.4, 1.5 Hz), 7.81 (1H, d, J = 7.0 Hz), 7.62-7.52 (2H, m), 7.41 (1H, d, J = 7.7 Hz), 6.63 (1H, s).
[1675] Melting point (° C.):> 180 (decomposition).
[1676] Example 188 6-Chloro-3-[(2-methyl-1,3-benzooxazol-4-yl) oxy] -4-pyridazinol (Compound No. 538)
[1677] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.55-7.32 (2H, m), 7.22-7.10 (1H, m), 6.73 (1H, s), 2.59 (3H, s).
[1678] Melting point (° C): 221-222.
[1679] Example 189 6-Chloro-3- (2,3-dihydro-1-benzofuran-7-yloxy) -4-pyridazinol (Compound No. 539)
[1680] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.13-7.08 (1H, m), 6.95 (1H, d, J = 7.3 Hz), 6.85 (1H, dd, J = 8.1, 7.3 Hz), 6.67 ( 1H, s), 4.54 (2H, t, J = 8.4 Hz), 3.30-3.20 (2H, m).
[1681] Physical property: Amorphous.
[1682] (Example 190)
[1683] 6-chloro-3-[(2,2-dimethyl-2,3-dihydro-1-benzofuran-7-yl) oxy] -4-pyridazinol (Compound No. 540)
[1684] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.08 (1H, d, J = 7.3 Hz), 6.96 (1H, d, J = 8.1 Hz), 6.87-6.79 (2H, m), 3.06 (2H , s), 1.37 (6H, s).
[1685] Melting point (° C.): 228-229.5.
[1686] Example 191 3- (1-Benzofuran-7-yloxy) -6-chloro-4-pyridazinol (Compound No. 541)
[1687] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.73 (1H, d, J = 2.2 Hz), 7.53 (1H, dd, J = 7.7, 1.4 Hz), 7.26 (1H, t, J = 7.7 Hz) , 7.15 (1H, doublet of doublets, J = 7.7, 1.4 Hz), 6.90 (1H, d, J = 2.2 Hz), 6.76 (1H, s).
[1688] Melting point (° C): 201-202.
[1689] Example 192 3- (1,3-benzodioxol-4-yloxy) -6-chloro-4-pyridazinol (Compound No. 544)
[1690] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 6.94-6.75 (4H, m), 6.01 (2H, s).
[1691] Melting point (° C): 206-211.
[1692] Example 193 6-Chloro-3- (2,3-dihydro-1,4-benzodioxin-5-yloxy) -4-pyridazinol (Compound No. 547)
[1693] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 6.90-6.72 (4H, m), 4.27-4.15 (4H, m).
[1694] Melting point (° C.): 218-223.5.
[1695] Example 194 6-Chloro-3-[(2-methyl-1,3-benzoxazol-7-yl) oxy] -4-pyridazinol (Compound No. 549)
[1696] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.52 (1H, dd, J = 8.1, 1.1 Hz), 7.37 (1H, t, J = 8.1 Hz), 7.21 (1H, dd, J = 8.1, 1.1 Hz), 6.76 (1 H, s), 2.65 (3 H, s).
[1697] Melting Point (° C): 197-202.
[1698] Example 195 6-Chloro-3- (2,4-dichlorophenoxy) -4-pyridazinol (Compound No. 552)
[1699] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.55 (1H, t, J = 1.8 Hz), 7.35 (2H, d, J = 1.8 Hz), 6.88 (1H, s).
[1700] Melting point (° C): 233-237.
[1701] Example 196 3- (2-Bromo-4-tert-butylphenoxy) -6-chloro-4-pyridazinol (Compound No. 556)
[1702] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.61 (1H, d, J = 2.0 Hz), 7.43 (1H, dd, J = 8.4, 2.0 Hz), 7.17 (1H, d, J = 8.4 Hz ), 6.73 (1 H, s), 1.32 (9 H, s).
[1703] Melting point (° C.):> 202 (decomposition).
[1704] Example 197 6-Chloro-3- (4-chloro-2-methylphenoxy) -4-pyridazinol (Compound No. 558)
[1705] ¹ H-NMR (60 MHz, DMSO-d ₆ + CDCl ₃ ) δ ppm: 7.40-7.10 (3H, m), 6.65 (1H, s), 2.18 (3H, s).
[1706] Melting point (° C): 235-235.5.
[1707] Example 198 6-Chloro-3- (2,4-dimethylphenoxy) -4-pyridazinol (Compound No. 559)
[1708] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.17-6.98 (3H, m), 6.85 (1H, s), 2.29 (3H, s), 2.07 (3H, s).
[1709] Melting point (° C.): 217.5.
[1710] Example 199 6-Chloro-3- (2-ethyl-4-iodophenoxy) -4-pyridazinol (Compound No. 562)
[1711] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.59 (1H, d, J = 2.2 Hz), 7.49 (1H, dd, J = 8.4, 2.2 Hz), 6.75 (1H, d, J = 8.4 Hz) , 6.48 (1H, s), 2.65-1.95 (2H, m), 1.16 (3H, t, J = 7.7 Hz).
[1712] Melting point (° C): 199-201.
[1713] Example 200 3- (4-Bromo-2-isopropylphenoxy) -6-chloro-4-pyridazinol (Compound No. 566)
[1714] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.44 (1H, brs), 7.37 (1H, dd, J = 8.0, 2.2 Hz), 7.00 (1H, d, J = 8.0 Hz), 6.73 (1H) , s), 3.01 (1H, septet, J = 6.8 Hz), 1.15 (6H, d, J = 6.8 Hz).
[1715] Melting point (° C): 215-225.
[1716] Example 201 3- (2-tert-butyl-4-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 567)
[1717] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.25 (1H, d, J = 2.0 Hz), 7.05 (1H, dd, J = 8.0, 2.0 Hz), 6.85 (1H, d, J = 8.0 Hz) , 6.70 (1H, s), 2.30 (3H, s), 1.35 (9H, s).
[1718] Melting Point (° C): 230-236.
[1719] Example 202 6-Chloro-3- (2-cyclopropyl-4-methylphenoxy) -4-pyridazinol (Compound No. 571)
[1720] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.05-6.95 (1H, m), 6.96 (1H, s), 6.81 (1H, s), 6.68 (1H, m), 2.30 (3H, s), 1.90-1.75 (1H, m), 0.90-0.70 (2H, m), 0.70-0.50 (2H, m).
[1721] Melting point (° C.): 239.
[1722] Example 203 6-Chloro-3- (2-chloro-5-methylphenoxy) -4-pyridazinol (Compound No. 614)
[1723] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.40 (1H, d, J = 8.5 Hz), 7.15 (1H, s), 7.10 (1H, d, J = 8.5 Hz), 6.70 (1H, s) , 2.35 (3H, s).
[1724] Melting point (° C): 170.
[1725] Example 204 6-Chloro-3- (5-chloro-2-methylphenoxy) -4-pyridazinol (Compound No. 618)
[1726] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.28 (1H, d, J = 8.8 Hz), 7.21-7.15 (1H, m), 7.16 (1H, s), 6.72 (1H, s), 2.15 ( 3H, s).
[1727] Melting point (° C): 174-180.
[1728] Example 205 6-Chloro-3- (2,5-dimethylphenoxy) -4-pyridazinol (Compound No. 621)
[1729] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.16 (1H, d, J = 9.0 Hz), 7.08 (1H, d, J = 9.0 Hz), 6.90 (1H, s), 6.70 (1H, s) , 2.30 (3H, s), 2.10 (3H, s).
[1730] Melting point (° C.): 80-83.
[1731] Example 206 6-Chloro-3- (5-isopropyl-2-methylphenoxy) -4-pyridazinol (Compound No. 623)
[1732] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.20 (1H, d, J = 7.5 Hz), 7.15-6.98 (1H, m), 6.95 (1H, s), 6.70 (1H, s), 2.88 ( 1H, septet, J = 7.5 Hz), 2.10 (3H, s), 1.23 (6H, d, J = 7.5 Hz).
[1733] Melting Point (° C): 168-169.
[1734] Example 207 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -4-methylbenzoic acid (Compound No. 626)
[1735] Melting point (° C): 238-240.
[1736] Example 208 3- (5-amino-2-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 627)
[1737] Melting point (° C.):> 310.
[1738] Example 209 6-Chloro-3- [5- (dimethylamino) -2-methylphenoxy] -4-pyridazinol (Compound No. 628)
[1739] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.08 (1H, d, J = 8.4 Hz), 6.68 (1H, s), 6.61 (1H, dd, J = 8.4, 2.6 Hz), 6.50 (1H, d, J = 2.6 Hz), 2.88 (6H, s), 2.02 (3H, s).
[1740] Melting point (° C): 181-182.
[1741] Example 210 6-Chloro-3- (5-methoxy-2-methylphenoxy) -4-pyridazinol (Compound No. 629)
[1742] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.16 (1H, d, J = 8.4 Hz), 6.78-6.67 (3H, m), 3.75 (3H, s), 2.07 (3H, s).
[1743] Melting point (° C.): 170-172.
[1744] Example 211 6-Chloro-3- (2-ethyl-5-methoxyphenoxy) -4-pyridazinol (Compound No. 635)
[1745] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.15 (1H, br.d, J = 8.0 Hz), 6.74 (1H, brs), 6.73 (1H, br.d, J = 8.0 Hz), 6.63 (1H, s), 3.73 (3H, s), 2.46 (2H, q, J = 7.0 Hz), 1.10 (3H, t, J = 7.0 Hz).
[1746] Melting point (° C): 124-126.
[1747] Example 212 6-Chloro-3- (2-isopropyl-5-methylphenoxy) -4-pyridazinol (Compound No. 640)
[1748] ¹ H-NMR (60 MHz, CDCl ₃ + DMF-d ₇ ) δ ppm: 7.50-6.70 (3H, m), 6.58 (1H, s), 3.30-2.60 (1H, m), 2.26 (3H, s), 1.13 (6H, d, J = 6.60 Hz).
[1749] Melting Point (° C): 193-195.
[1750] Example 213 6-Chloro-3- (3,5-diisopropylphenoxy) -4-pyridazinol (Compound No. 642)
[1751] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 7.25 (1H, d, J = 8.0 Hz), 7.11 (1H, d, J = 1.8 Hz), 6.92 (1H, dd, J = 8.0, 1.8 Hz ), 6.73 (1H, s), 2.84 (2H, septet, J = 7.0 Hz), 1.18 (6H, d, J = 7.0 Hz), 1.12 (6H, d, J = 7.0 Hz).
[1752] Melting point (° C): 231-235.
[1753] Example 214 3- (2-tert-butyl-5-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 650)
[1754] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.35 (1H, d, J = 8.0 Hz), 6.95 (1H, dd, J = 8.0, 1.5 Hz), 6.80 (1H, s), 6.70 (1H, s), 2.27 (3H, s), 1.35 (9H, s).
[1755] Melting point (° C.): 226.
[1756] Example 215 6-chloro-3- (2,5-ditert-butylphenoxy) -4-pyridazinol (Compound No. 653)
[1757] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.50-7.10 (3H, m), 6.94 (1H, s), 4.98 (1H brs), 1.37 (9H, s), 1.28 (9H, s).
[1758] Melting point (° C.): 249-258.
[1759] Example 216 6-Chloro-3- (2-cyclopropyl-5-fluorophenoxy) -4-pyridazinol (Compound No. 658)
[1760] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.10-6.85 (3H, m), 6.72 (1H, s), 1.92-1.75 (1H, m), 0.85-0.70 (2H, m), 0.70-0.54 (2H, m).
[1761] Melting point (° C.): 227-228.
[1762] Example 217 6-chloro-3- (5-chloro-2-cyclopropylphenoxy) -4-pyridazinol (Compound No. 659)
[1763] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.19 (1H, d, J = 7.7 Hz), 7.16 (1H, s), 7.01 (1H, d, J = 7.7 Hz), 6.72 (1H, s) , 1.94-1.79 (1H, m), 0.90-0.75 (2H, m), 0.75-0.58 (2H, m).
[1764] Melting Point (° C): 194-195.
[1765] Example 218 6-Chloro-3- (2-cyclopropyl-5-methylphenoxy) -4-pyridazinol (Compound No. 662)
[1766] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.96 (1H, d, J = 7.7 Hz), 6.89 (1H, s), 6.67 (1H, d, J = 7.7 Hz), 6.68 (1H, s) , 2.28 (3H, s), 1.87-1.73 (1H, m), 0.80-0.51 (4H, m).
[1767] Melting point (° C): 150-159.
[1768] Example 219 6-Chloro-3- (2-cyclopropyl-5-ethylphenoxy) -4-pyridazinol (Compound No. 663)
[1769] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.01 (1H, d, J = 8.0 Hz), 6.92 (1H, s), 6.92 (1H, d, J = 8.0 Hz), 6.69 (1H, s) , 2.61 (2H, t, J = 7.7 Hz), 1.88-1.72 (1H, m), 1.20 (3H, q, J = 7.7 Hz), 0.82-0.66 (2H, m), 0.65-0.52 (2H, m ).
[1770] Physical property: Amorphous.
[1771] Example 220 6-Chloro-3- (2-cyclopropyl-5-isopropylphenoxy) -4-pyridazinol (Compound No. 664)
[1772] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.05 (1H, dd, J = 7.7, 1.8 Hz), 7.00 (1H, brs), 6.93 (1H, d, J = 7.7 Hz), 6.70 (1H, s), 2.87 (1H, septet, J = 7.0 Hz), 1.90-1.72 (1H, m), 1.22 (6H, d, J = 7.0 Hz), 0.85-0.68 (2H, m), 0.68-0.52 (2H , m).
[1773] Melting point (° C): 211-212.
[1774] Example 221 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -4-cyclopropylbenzonitrile (Compound No. 667)
[1775] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.58-7.48 (2H, m), 7.15 (1H, d, J = 8.8 Hz), 6.74 (1H, s), 2.10-1.90 (1H, m), 1.05-0.93 (2H, m), 0.83-0.70 (2H, m).
[1776] Melting point (° C): 211-212.
[1777] Example 222 6-Chloro-3- [5-fluoro-2- (1-propenyl) phenoxy] -4-pyridazinol (Compound No. 679)
[1778] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.61-7.53 (1H, m), 7.03-6.90 (2H, m), 6.72 (1H, s), 6.44-6.19 (2H, m), 1.80 (3H , d, J = 5.5 Hz).
[1779] Melting Point (° C): 210-217.
[1780] Example 223 6-Chloro-3- [5-chloro-2- (1-propenyl) phenoxy] -4-pyridazinol (Compound No. 680)
[1781] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.55 (1H, d, J = 8.4 Hz), 7.24-7.17 (2H, m), 6.72 (1H, s), 6.46-6.30 (2H, m), 1.81 (3H, doublet, J = 5.1 Hz).
[1782] Melting point (° C): 221-224.
[1783] Example 224 2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -4- (dimethylamino) benzaldehyde (Compound No. 692)
[1784] ¹ H-NMR (90 MHz, DMSO-d ₆ ) δ ppm: 9.78 (1H, s), 7.69 (1H, d, J = 6.0 Hz), 6.81 (1H, s), 6.78-6.46 (2H, m), 3.05 (6H, s).
[1785] Melting point (° C): 124-127.
[1786] Example 225 3- (5-chloro-2-methoxyphenoxy) -6-chloro-4-pyridazinol (Compound No. 701)
[1787] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.23-7.18 (2H, m), 7.05 (1H, d, J = 8.8 Hz), 6.66 (1H, s), 3.73 (3H, s).
[1788] Melting point (° C): 143-155.
[1789] Example 226 3- (5-Bromo-2-methoxyphenoxy) -6-chloro-4-pyridazinol (Compound No. 702)
[1790] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.39-7.31 (2H, m), 7.02 (1H, d, J = 8.4 Hz), 6.67 (1H, s), 3.74 (3H, s).
[1791] Melting Point (° C): 135-137.
[1792] Example 227 6-Chloro-3- (4-fluoro-2-methylphenoxy) -4-pyridazinol (Compound No. 557)
[1793] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.14-6.88 (3H, m), 6.71 (1H, s), 2.16 (3H, s).
[1794] Melting point (° C.): 249-250.
[1795] Example 228 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -4-methoxybenzonitrile (Compound No. 707)
[1796] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.66 (1H, dd, J = 8.4, 2.2 Hz), 7.58 (1H, d, J = 2.2 Hz), 7.26 (1H, d, J = 8.4 Hz) , 6.71 (1 H, s), 3.85 (3 H, s).
[1797] Melting Point (° C): 187-192.
[1798] Example 229 6-Chloro-3- (2-methoxy-5-nitrophenoxy) -4-pyridazinol (Compound No. 708)
[1799] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.18 (1H, dd, J = 9.2, 2.6 Hz), 8.04 (1H, d, J = 2.6 Hz), 7.27 (1H, d, J = 9.2 Hz) , 6.59 (1 H, s), 3.89 (3 H, s).
[1800] Physical property: Amorphous.
[1801] Example 230 6-Chloro-3- (2,5-dimethoxyphenoxy) -4-pyridazinol (Compound No. 709)
[1802] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.04-6.99 (1H, m), 6.81-6.78 (2H, m), 6.68 (1H, s), 3.76 (3H, s), 3.70 (3H, s ).
[1803] Melting point (° C.): 150-152.
[1804] Example 231 6-chloro-3- (2,6-difluorophenoxy) -4-pyridazinol (Compound No. 710)
[1805] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.54-7.20 (3H, m), 6.88 (1H, s).
[1806] Melting point (° C): 209-213.
[1807] Example 232 6-Chloro-3- (2-chloro-6-fluorophenoxy) -4-pyridazinol (Compound No. 711)
[1808] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.35-7.13 (3H, m), 6.61 (1H, s).
[1809] Melting point (° C.): 235.
[1810] Example 233 3- (2-bromo-6-fluorophenoxy) -6-chloro-4-pyridazinol (Compound No. 712)
[1811] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.31-7.15 (3H, m), 6.65 (1H, s).
[1812] Physical property: Amorphous.
[1813] Example 234 6-Chloro-3- (2-fluoro-6-propylphenoxy) -4-pyridazinol (Compound No. 716)
[1814] Melting Point (° C): 134-137.
[1815] Example 235 6-Chloro-3- (2-fluoro-6-isopropylphenoxy) -4-pyridazinol (Compound No. 717)
[1816] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.35-7.15 (3H, m), 6.89 (1H, brs), 3.02 (1H, septet, J = 7.0 Hz), 1.14 (6H, J = 7.0 Hz ).
[1817] Melting point (° C.): 215-220.
[1818] Example 236 6-Chloro-3- (2-cyclopropyl-6-fluorophenoxy) -4-pyridazinol (Compound No. 719)
[1819] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.22-6.96 (2H, m), 6.81-6.71 (1H, m), 6.72 (1H, s), 2.03-1.89 (1H, m), 0.93-0.80 (2H, m), 0.69-0.62 (2H, m).
[1820] Melting point (° C.): 200-203.
[1821] Example 237 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -6-fluorophenoxy} -4-pyridazinol (Compound No. 728)
[1822] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.42 (1H, d, J = 8.1 Hz), 7.26-7.15 (1H, m), 7.07-6.97 (1H, m), 6.46 (1H, s), 4.33 (1H, q, J = 7.0 Hz), 2.42-2.20 (2H, m), 1.43 (3H, d, J = 7.0 Hz), 1.02 (3H, t, J = 7.0 Hz).
[1823] Physical property: Amorphous.
[1824] Example 238 6-Chloro-3- (2-fluoro-6-nitrophenoxy) -4-pyridazinol (Compound No. 731)
[1825] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.03-7.99 (1H, m), 7.78-7.53 (2H, m), 6.89 (1H, s).
[1826] Melting point (° C.): 210 (sublimation).
[1827] Example 239 6-Chloro-3- (2-fluoro-6-methoxyphenoxy) -4-pyridazinol (Compound No. 732)
[1828] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.26 (1H, dd, J = 15.0, 8.1 Hz), 7.02-6.91 (2H, m), 6.84 (1H, s), 3.75 (3H, s) .
[1829] Melting point (° C.): 190-194 (sublimation).
[1830] Example 240 6-Chloro-3- (2,6-dichlorophenoxy) -4-pyridazinol (Compound No. 733)
[1831] ¹ H-NMR (90 MHz, DMSO-d ₆ ) δ ppm: 7.70-7.10 (3H, m), 6.80 (1H, s).
[1832] Melting point (° C.): 265.
[1833] Example 241 6-chloro-3- (2-chloro-6-iodophenoxy) -4-pyridazinol (Compound No. 735)
[1834] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.90 (1H, d, J = 8.1 Hz), 7.64 (1H, d, J = 8.1 Hz), 7.12 (1H, t, J = 8.1 Hz), 7.02-6.80 (1 H, broad doublet).
[1835] Melting point (° C): 262-264.
[1836] Example 242 6-Chloro-3- (2-chloro-6-methylphenoxy) -4-pyridazinol (Compound No. 736)
[1837] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.50-7.00 (3H, m), 6.75 (1H, s), 2.22 (3H, s).
[1838] Melting point (° C.): 235.
[1839] Example 243 6-Chloro-3- (2-chloro-6-ethylphenoxy) -4-pyridazinol (Compound No. 737)
[1840] Melting Point (° C): 194-195.
[1841] Example 244 6-chloro-3- (5-fluoro-2-methoxyphenoxy) -4-pyridazinol (Compound No. 700)
[1842] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.13-6.94 (3H, m), 6.71 (1H, s), 3.74 (1H, s).
[1843] Melting point (° C): 187-191.
[1844] Example 245 6-Chloro-3- (2-chloro-6-cyclopropylphenoxy) -4-pyridazinol (Compound No. 740)
[1845] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.30 (1H, dd, J = 8.1, 1.5 Hz), 7.17 (1H, dd, J = 8.1, 7.7 Hz), 6.96 (1H, dd, J = 7.7 , 1.5 Hz), 6.76 (1H, s), 2.00-1.84 (1H, m), 0.95-0.80 (2H, m), 0.70-0.60 (2H, m).
[1846] Melting point (° C.): 224-225.
[1847] Example 246 6-Chloro-3- [2-chloro-6- (2-methyl-2-propenyl) phenoxy] -4-pyridazinol (Compound No. 746)
[1848] Melting Point (° C): 198-200.
[1849] Example 247 6-Chloro-3- (2-chloro-6-nitrophenoxy) -4-pyridazinol (Compound No. 754)
[1850] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.12 (1H, dd, J = 8.1, 1.5 Hz), 7.95 (1H, dd, J = 8.1, 1.5 Hz), 7.59 (1H, t, J = 8.1 Hz), 6.76 (1 H, s).
[1851] Physical property: Amorphous.
[1852] Example 248 6-Chloro-3- (2,6-dibromophenoxy) -4-pyridazinol (Compound No. 756)
[1853] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.65 (2H, d, J = 8.1 Hz), 7.11 (1H, t, J = 8.1 Hz), 6.74 (1H, brs).
[1854] Melting point (° C): 274-278.
[1855] Example 249 3- (2-bromo-6-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 758)
[1856] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.56 (1H, br.d, J = 7.7 Hz), 7.36 (1H, br.d, J = 7.7 Hz), 7.16 (1H, t, J = 7.7 Hz), 6.92 (1 H, brs), 2.14 (3 H, s).
[1857] Melting point (° C.): 242-243.
[1858] Example 250 3- (2-Bromo-6-ethylphenoxy) -6-chloro-4-pyridazinol (Compound No. 759)
[1859] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.49 (1H, dd, J = 7.9, 1.6 Hz), 7.32 (1H, dd, J = 7.9, 1.6 Hz), 7.14 (1H, t, J = 7.9 Hz), 6.75 (1H, s), 2.58 (2H, q, J = 7.5 Hz), 1.18 (3H, t, J = 7.5 Hz).
[1860] Melting Point (° C): 215-217.
[1861] Example 251 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -4-methoxybenzonitrile (Compound No. 707)
[1862] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.66 (1H, dd, J = 8.4, 2.2 Hz), 7.58 (1H, d, J = 2.2 Hz), 7.26 (1H, d, J = 8.4 Hz) , 6.71 (1 H, s), 3.85 (3 H, s).
[1863] Melting Point (° C): 187-192.
[1864] Example 252 3- (2-Bromo-6-chlorophenoxy) -6-chloro-4-pyridazinol (Compound No. 734)
[1865] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.64 (1H, dd, J = 1.5 Hz, 8.1 Hz), 7.52 (1H, dd, J = 1.5 Hz, 8.0 Hz), 7.21 (1H, t, J = 8.1 Hz), 6.76 (1 H, s).
[1866] Melting point (° C): 266-274.
[1867] Example 253 3- (2-Bromo-6-cyclopropylphenoxy) -6-chloro-4-pyridazinol (Compound No. 762)
[1868] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.51 (1H, d, J = 7.8 Hz), 7.14 (1H, t, J = 7.8 Hz), 7.02 (1H, d, J = 7.8 Hz), 6.89 (1H, s), 1,89-1.75 (1H, m), 0.88-0.75 (2H, m), 0.75-0.58 (2H, m).
[1869] Melting Point (℃): 230-232.
[1870] Example 254 3-Bromo-2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] benzonitrile (Compound No. 775)
[1871] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.00 (1H, dd, J = 8.1, 1.5 Hz), 7.82 (1H, dd, J = 8.1, 1.5 Hz), 7.37 (1H, t, J = 8.1 Hz), 6.75 (1 H, s).
[1872] Melting point (° C.): 188 (decomposition).
[1873] Example 255 3- (2-Bromo-6-methoxyphenoxy) -6-chloro-4-pyridazinol (Compound No. 778)
[1874] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.26-7.05 (3H, m), 6.70 (1H, s), 3.78 (3H, s).
[1875] Melting Point (° C): 220-221.
[1876] Example 256 6-Chloro-3- (2-iodo-6-methylphenoxy) -4-pyridazinol (Compound No. 780)
[1877] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.70 (1H, d, J = 7.7 Hz), 7.29 (1H, d, J = 8.1 Hz), 6.95 (1H, t, J = 7.7 Hz), 6.76 (1H, s), 2.20 (3H, s).
[1878] Melting point (° C.): 250-252.
[1879] Example 257 6-chloro-3- (2-ethyl-6-iodophenoxy) -4-pyridazinol (Compound No. 781)
[1880] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.72 (1H, dd, J = 7.7, 1.5 Hz), 7.33 (1H, dd, J = 7.7, 1.5 Hz), 7.00 (1H, t, J = 7.7 Hz), 6.76 (1H, s), 2.57 (2H, q, J = 7.7 Hz), 1.17 (3H, t, J = 7.7 Hz).
[1881] Melting point (° C): 242-244.
[1882] Example 258 6-Chloro-3- (2-iodo-6-isopropylphenoxy) -4-pyridazinol (Compound No. 782)
[1883] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.70 (1H, dd, J = 8.0, 1.5 Hz), 7.40 (1H, dd, J = 8.0, 1.5 Hz), 7.03 (1H, t, J = 8.0 Hz), 6.76 (1H, s), 3.01 (1H, septet, J = 7.0 Hz), 1.18 (6H, d, J = 7.0 Hz).
[1884] Melting Point (° C): 250-255.
[1885] Example 259 3-Bromo-2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] benzonitrile (Compound No. 775)
[1886] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.00 (1H, dd, J = 8.1, 1.5 Hz), 7.82 (1H, dd, J = 8.1, 1.5 Hz), 7.37 (1H, t, J = 8.1 Hz), 6.75 (1 H, s).
[1887] Melting point (° C.): 188 (decomposition).
[1888] Example 260 6-Chloro-3- (2-ethyl-6-methylphenoxy) -4-pyridazinol (Compound No. 802)
[1889] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.12-6.97 (3H, m), 6.52 (1H, s), 2.37 (2H, q, J = 7.6 Hz), 1.95 (3H, s), 1.04 (3H , t, J = 7.6 Hz).
[1890] Physical property: Amorphous.
[1891] Example 261 6-Chloro-3- (2-isopropyl-6-methylphenoxy) -4-pyridazinol (Compound No. 803)
[1892] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.23-7.06 (3H, m), 6.72 (1H, s), 2.96 (1H, septet, J = 7.0 Hz), 2.10 (3H, s), 1.16 ( 6H, d, J = 7.0 Hz).
[1893] Melting point (° C.): 215-220.
[1894] Example 262 3- (2-s-butyl-6-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 804)
[1895] Melting point (° C): 187-189.
[1896] Example 263 6-chloro-3- [2- (2,2-dichlorocyclopropyl) -6-methylphenoxy] -4-pyridazinol (Compound No. 827)
[1897] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.25 (1H, br.d, J = 6.2 Hz), 7.16 (1H, dd, J = 7.7, 7.3 Hz), 6.98 (1H, br.d, J = 7.7 Hz), 6.72 (1H, s), 2.85 (1H, dd, J = 11.0, 10.6 Hz), 2.22 (3H, s).
[1898] Melting point (° C): 213-215.
[1899] Example 264 6-Chloro-3- (2-methyl-6-vinylphenoxy) -4-pyridazinol (Compound No. 834)
[1900] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.46 (1H, dd, J = 6.6, 2.6 Hz), 7.25-7.05 (2H, m), 6.71 (1H, dd, J = 17.6, 11.4 Hz), 6.70 (1H, s), 5.74 (1H, dd, J = 17.6, 1.5 Hz), 5.21 (1H, dd, J = 11.4, 1.5 Hz), 2.11 (3H, s).
[1901] Physical property: Amorphous.
[1902] Example 265 6-Chloro-3- (6-cyclopropyl-3-fluoro-2-methylphenoxy) -4-pyridazinol (Compound No. 1052)
[1903] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.92-6.70 (3H, m), 2.06 (3H, d, J = 2.2 Hz), 1.85-1.70 (1H, m), 0.79-0.45 (4H, m ).
[1904] Melting point (° C): 230-231.
[1905] Example 266 6-Chloro-3- (2-methyl-6-nitrophenoxy) -4-pyridazinol (Compound No. 844)
[1906] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.95 (1H, d, J = 8.1 Hz), 7.76 (1H, d, J = 7.7 Hz), 7.45 (1H, dd, J = 8.1, 7.7 Hz ), 6.80 (1H, s), 2.20 (3H, s).
[1907] Physical property: Paste form.
[1908] Example 267 6-Chloro-3- (2-methoxy-6-methylphenoxy) -4-pyridazinol (Compound No. 845)
[1909] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.10-7.01 (1H, m), 6.79-6.72 (2H, m), 6.55 (1H, s), 3.64 (3H, s), 2.08 (3H, s) .
[1910] Physical property: Amorphous.
[1911] Example 268 6-Chloro-3- (2,6-diethylphenoxy) -4-pyridazinol (Compound No. 846)
[1912] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 10.21 (1H, brs), 7.02 (3H, brs), 6.47 (1H, s), 2.27 (4H, q, J = 7.6 Hz), 0.98 (6H, t , J = 7.6 Hz).
[1913] Melting point (° C): 181-185.
[1914] Example 269 6-Chloro-3- (2-cyclopropyl-6-ethylphenoxy) -4-pyridazinol (Compound No. 850)
[1915] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.11 (2H, d, J = 4.8 Hz), 6.85 (1H, t, J = 4.8 Hz), 6.71 (1H, s), 2.52 (2H, q, J = 7.5 Hz), 1.87-1.72 (1H, m), 1.16 (3H, t, J = 7.5 Hz), 0.80-0.65 (2H, m), 0.65-0.50 (2H, m).
[1916] Physical property: Amorphous.
[1917] Example 270 6-Chloro-3- (2,6-dipropylphenoxy) -4-pyridazinol (Compound No. 890)
[1918] Melting point (° C): 191-193.
[1919] Example 271 6-Chloro-3- (2,6-diisopropylphenoxy) -4-pyridazinol (Compound No. 894)
[1920] ¹ H-NMR (90 MHz, DMSO-d ₆ ) δ ppm: 7.28 (3H, s), 6.80 (1H, s), 2.88 (2H, septet, J = 7.0 Hz), 1.15 (12H, d, J = 7.0 Hz ).
[1921] Melting point (° C):> 285.
[1922] Example 272 6-Chloro-3- (2-cyclopropyl-6-isopropylphenoxy) -4-pyridazinol (Compound No. 896)
[1923] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.22-7.12 (2H, m), 6.83 (1H, brs), 6.82 (1H, dd, J = 6.6, 2.2 Hz), 2.91 (1H, septet, J = 7.0 Hz), 1.74-1.63 (1H, m), 1.11 (6H, d, J = 7.0 Hz), 0.75-0.71 (2H, m), 0.58-0.50 (2H, m).
[1924] Melting point (° C): 242-245.
[1925] Example 273 6-Chloro-3- (2-isopropyl-6-nitrophenoxy) -4-pyridazinol (Compound No. 911)
[1926] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 8.00 (1H, d, J = 7.7 Hz), 7.88 (1H, d, J = 7.7 Hz), 7.54 (1H, t, J = 7.7 Hz), 6.96 (1H, brs), 3.07 (1H, septet, J = 7.0 Hz), 1.16 (6H, d, J = 7.0 Hz).
[1927] Melting point (° C): 205-209.
[1928] Example 274 3- (2-tert-butyl-6-cyclopropylphenoxy) -6-chloro-4-pyridazinol (Compound No. 914)
[1929] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.28 (1H, br.d, J = 8.1 Hz), 7.10 (1H, dd, J = 8.1and 7.7 Hz), 6.90 (1H, d, J = 7.7 Hz), 6.70 (1H, s), 1.80-1.55 (1H, m), 1.34 (9H, s), 0.85-0.60 (2H, m), 0.50-0.20 (2H, m).
[1930] Melting point (° C): 230-231.
[1931] Example 275 6-Chloro-3- (2,6-dicyclopropylphenoxy) -4-pyridazinol (Compound No. 931)
[1932] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.08 (1H, t, J = 7.7 Hz), 6.81 (2H, d, J = 7.7 Hz), 6.71 (1H, s), 1.95-1.75 (2H, m), 0.85-0.70 (4H, m), 0.70-0.50 (4H, m).
[1933] Melting Point (° C): 232-234.
[1934] Example 276 6-Chloro-3- (2-cyclopropyl-6-methoxyphenoxy) -4-pyridazinol (Compound No. 964)
[1935] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.13 (1H, t, J = 8.1 Hz), 6.92 (1H, d, J = 8.1 Hz), 6.81 (1H, brs), 6.54 (1H, d , J = 8.1 Hz), 3.68 (3H, s), 1.87-1.78 (1H, m), 0.87-0.78 (2H, m), 0.64-0.56 (2H, m).
[1936] Melting point (° C): 194-199.
[1937] Example 277 6-Chloro-3- (2-cyclopropyl-6-ethoxyphenoxy) -4-pyridazinol (Compound No. 965)
[1938] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.07 (1H, t, J = 8.1 Hz), 6.84 (1H, dd, J = 8.4, 1.5 Hz), 6.71 (1H, s), 6.54 (1H, dd, J = 8.4, 1.5 Hz, 3.97 (2H, q, J = 7.0 Hz), 2.04-1.91 (1H, m), 1.18 (3H, t, J = 7.0 Hz), 0.89-0.79 (2H, m ), 0.66-0.60 (2H, m).
[1939] Melting point (° C): 174-179.
[1940] Example 278 6-chloro-3- {2,6-di [(1E) -1-propenyl] phenoxy} -4-pyridazinol (Compound No. 979)
[1941] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.40 (2H, d, J = 7.8 Hz), 7.15 (1H, t, J = 7.8 Hz), 6.72 (1H, s), 6.34 (2H, d, J = 16.4 Hz), 6.27 (2H, dd, J = 16.4, 4.9 Hz), 1.79 (6H, d, J = 4.9 Hz).
[1942] Melting point (° C): 163-164.
[1943] Example 279 6-Chloro-3- (2,6-diallylphenoxy) -4-pyridazinol (Compound No. 982)
[1944] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.20-7.15 (3H, m), 6.70 (1H, s), 5.95-5.75 (2H, m), 5.02-4.87 (4H, m), 3.26 (4H , d, J = 6.8 Hz).
[1945] Melting point (° C): 131-135.
[1946] Example 280 6-Chloro-3- (2,6-dimethoxyphenoxy) -4-pyridazinol (Compound No. 987)
[1947] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.19 (1H t, J = 8.3 Hz), 6.79-6.75 (3H m), 3.71 (6H, s).
[1948] Melting point (° C): 199-201.
[1949] Example 281 6-Chloro-3- (3,5-dimethylphenoxy) -4-pyridazinol (Compound No. 998)
[1950] ¹ H-NMR (60 MHz, DMSO-d ₆ ) δ ppm: 6.90-6.65 (4H, m), 2.27 (6H, s).
[1951] Melting Point (° C): 178-182.
[1952] Example 282 6-Chloro-3- (3-isopropyl-5-methylphenoxy) -4-pyridazinol (Compound No. 1000)
[1953] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.94 (1H, s), 6.84 (1H, s), 6.81 (1H, s), 6.69 (1H, s), 2.87 (1H, septet, J = 7.0 Hz), 2.32 (3H, s), 1.23 (6H, d, J = 7.0 Hz).
[1954] Melting point (° C): 204-206.
[1955] Example 283 6-Chloro-3- (3,5-diisopropylphenoxy) -4-pyridazinol (Compound No. 1007)
[1956] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.98 (1H, s), 6.87 (1H, s), 6.86 (1H, s), 6.68 (1H, s), 2.90 (2H, septet, J = 7.0 Hz), 1.24 (12H, d, J = 7.0 Hz).
[1957] Melting point (° C.): 249-253.
[1958] Example 284 3- [3,5-bis (trifluoromethyl) phenoxy] -6-chloro-4-pyridazinol (Compound No. 1009)
[1959] ¹ H-NMR (200 MHz, DMF-d ₇ ) δ ppm: 8.20-7.80 (3H, m), 6.94 (1H, s), 5.50-4.50 (1H, brs).
[1960] Melting point (° C): 237-242.
[1961] Example 285 3- (2-Bromo-3,5-dimethylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1013)
[1962] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.11 (1H, s), 7.00 (1H, s), 6.86 (1H, brs), 2.37 (3H, s), 2.27 (3H, s).
[1963] Melting point (° C): 240-244.
[1964] Example 286 6-Chloro-3- (2,3,5-trimethylphenoxy) -4-pyridazinol (Compound No. 1016)
[1965] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 6.90 (1H, s), 6.75 (1H, s), 6.70 (1H, s), 2.30 (6H, s), 2.02 (3H, s).
[1966] Melting point (° C.): 223-224.
[1967] Example 287 6-Chloro-3- (3,5-dimethyl-2-propylphenoxy) -4-pyridazinol (Compound No. 1020)
[1968] ¹ H-NMR (90 MHz, DMSO-d ₆ ) δ ppm: 6.90 (1H, s), 6.81 (1H, s), 6.77 (1H, s), 2.29 (3H, s), 2.21 (3H, s), 2.53 -2.19 (2H, m), 1.57-1.29 (2H, m), 0.86 (3H, t, J = 6.6 Hz).
[1969] Melting Point (° C): 154.5.
[1970] Example 288 6-Chloro-3- (2-cyclopropyl-3,5-dimethylphenoxy) -4-pyridazinol (Compound No. 1023)
[1971] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.89 (1H, s), 6.73 (1H, s), 6.69 (1H, s), 2.39 (3H, s), 2.26 (3H, s), 1.45- 1.28 (1 H, m), 0.78-0.67 (2 H, m), 0.65-0.51 (2 H, m).
[1972] Melting point (° C.): 200-203.
[1973] Example 289 6-Chloro-3- [3,5-dimethyl-2- (methylsulfanyl) phenoxy] -4-pyridazinol (Compound No. 1027)
[1974] Melting point (° C.): 213-214.
[1975] Example 290 3- (2-bromo-3,6-dimethylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1040)
[1976] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.16 (1H, d, J = 7.9 Hz), 7.10 (1H, d, J = 7.9 Hz), 6.72 (1H, s), 2.38 (3H, s) , 2.16 (3H, s).
[1977] Melting point (° C.): 255-257.
[1978] Example 291 3- (6-Bromo-3-fluoro-2-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1050)
[1979] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.51 (1H, dd, J = 8.8, 5.9 Hz), 7.00 (1H, t, J = 8.8 Hz), 6.96 (1H, s), 2.13 (3H, d, J = 2.2 Hz).
[1980] Physical property: Amorphous.
[1981] Example 292 3- (6-bromo-3-chloro-2-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1053)
[1982] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.47 (1H, d, J = 8.1 Hz), 7.23 (1H, d, J = 8.1 Hz), 6.64 (1H, s), 2.24 (3H, s) .
[1983] Melting point (° C): 254-260.
[1984] Example 293 6-Chloro-3- (3-chloro-6-cyclopropyl-2-methylphenoxy) -4-pyridazinol (Compound No. 1055)
[1985] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.18 (1H, d, J = 8.4 Hz), 6.81 (1H, d, J = 8.4 Hz), 6.64 (1H, s), 2.17 (3H, s) , 1.89-1.76 (1H, m), 0.80-0.71 (2H, m), 0.68-0.51 (2H, m).
[1986] Melting point (° C.): 233.
[1987] Example 294 3- (6-Bromo-2,3-dimethylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1058)
[1988] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.34 (1H, d, J = 8.1 Hz), 6.99 (1H, d, J = 8.1 Hz), 6.71 (1H, s), 2.28 (3H, s) , 2.12 (3H, s).
[1989] Melting point (° C): 263-268.
[1990] Example 295 6-Chloro-3- (2,3,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1060)
[1991] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.00 (2H, s), 6.73 (1H, s), 2.27 (3H, s), 2.07 (3H, s), 2.03 (3H, s).
[1992] Melting point (° C.): 228.
[1993] Example 296 6-Chloro-3- (6-cyclopropyl-2,3-dimethylphenoxy) -4-pyridazinol (Compound No. 1061)
[1994] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.96 (1H, d, J = 8.1 Hz), 6.72 (1H, d, J = 8.1 Hz), 6.69 (1H, s), 2.24 (3H, s) , 2.04 (3H, s), 1.85-1.70 (1H, m), 0.75-0.46 (4H, m).
[1995] Melting point (° C.): 229-234.
[1996] Example 297 2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -3,4-dimethylbenzaldehyde O-methyloxime (Compound No. 1063)
[1997] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.98 (1H, s), 7.50 (1H, d, J = 8.1 Hz), 7.11 (1H, d, J = 8.1 Hz), 6.69 (1H, s) , 3.81 (3H, s), 2.32 (3H, s), 2.06 (3H, s).
[1998] Physical property: Amorphous.
[1999] Example 298 6-Chloro-3- (6-methoxy-2,3-dimethylphenoxy) -4-pyridazinol (Compound No. 1064)
[2000] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.00 (1H, d, J = 8.4 Hz), 6.78 (1H, d, J = 8.4 Hz), 6.66 (1H, s), 3.69 (3H, s) , 2.23 (3H, s), 2.08 (3H, s).
[2001] Physical property: Amorphous.
[2002] Example 299 3- (6-Bromo-3-methoxy-2-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1066)
[2003] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.42 (1H, d, J = 9.2 Hz), 6.82 (1H, d, J = 9.2 Hz), 6.69 (1H, s), 3.86 (3H, s) , 2.05 (3H, s).
[2004] Melting point (° C): 246-253.
[2005] Example 300 6-Chloro-3- (6-cyclopropyl-3-methoxy-2-methylphenoxy) -4-pyridazinol (Compound No. 1069)
[2006] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.83 (1H, d, J = 8.8 Hz), 6.75 (1H, d, J = 8.8 Hz), 6.66 (1H, s), 3.81 (3H, s) , 1.99 (3H, s), 1.78-1.70 (1H, m), 0.69-0.63 (2H, m), 0.52-0.47 (2H, m).
[2007] Melting point (° C.): 250-253.
[2008] Example 301 6-Chloro-3- (2-cyclopropyl-3,6-dimethylphenoxy) -4-pyridazinol (Compound No. 1073)
[2009] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.20 (1H, d, J = 7.6 Hz), 6.95 (1H, d, J = 7.6 Hz), 6.68 (1H, s), 2.39 (3H, s) , 2.10 (3H, s), 1.50-1.25 (1H, m), 0.90-0.70 (2H, m), 0.70-0.50 (2H, m).
[2010] Melting point (° C): 171-175.
[2011] Example 302 3- (2-allyl-6-ethyl-3-methoxyphenoxy) -6-chloro-4-pyridazinol (Compound No. 1080)
[2012] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.11 (1H, d, J = 8.4 Hz), 6.85 (1H, s), 6.83 (1H, d, J = 8.4 Hz), 6.10-5.30 (1H , m), 5.00-4.60 (2H, m), 3.83 (3H, s), 3.30-3.10 (2H, m), 2.40 (2H, q, J = 7.6 Hz), 1.10 (3H, t, J = 7.6 Hz).
[2013] Melting point (° C.): 183-186.
[2014] Example 303 6-chloro-3- {3,6-dimethyl-2-[(methylsulfanyl) methyl] phenoxy} -4-pyridazinol (Compound No. 1083)
[2015] ¹ H-NMR (90 MHz, CD ₃ OD) δ ppm: 7.21-6.90 (2H, m), 6.71 (1H, s), 3.68 (2H, s), 2.38 (3H, s), 2.09 (3H, s), 2.00 (3H, s).
[2016] Physical property: Amorphous.
[2017] Example 304 3-[(5-bromo-2,3-dihydro-1H-inden-4-yl) oxy] -6-chloro-4-pyridazinol (Compound No. 1086)
[2018] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.39 (1H, d, J = 8.1 Hz), 7.05 (1H, d, J = 8.1 Hz), 6.71 (1H, s), 2.94 (2H, t, J = 7.3 Hz), 2.79 (2H, t, J = 7.3 Hz), 2.10-2.00 (2H, m).
[2019] Physical property: Amorphous.
[2020] Example 305 6-chloro-3-[(5-methyl-2,3-dihydro-1H-inden-4-yl) oxy] -4-pyridazinol (Compound No. 1088)
[2021] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.11-7.01 (2H, m), 6.83 (1H, brs), 2.88 (3H, t, J = 7.3 Hz), 2.59 (3H, t, J = 7.3 Hz), 2.06 (3H, s), 2.06-1.91 (2H, m).
[2022] Melting point (° C): 222-225.
[2023] Example 306 6-Chloro-3-[(5-ethyl-2,3-dihydro-1 H-inden-4-yl) oxy] -4-pyridazinol (Compound No. 1089)
[2024] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.06 (2H, s), 6.71 (1H, s), 2.91 (2H, t, J = 7.3 Hz), 2.67 (2H, t, J = 7.3 Hz) , 2.51 (2H, q, J = 7.7 Hz), 2.04 (2H, quintet, J = 7.3 Hz), 1.13 (3H, t, J = 7.7 Hz).
[2025] Melting Point (° C): 193-196.
[2026] Example 307 6-chloro-3-[(5-cyclopropyl-2,3-dihydro-1H-inden-4-yl) oxy] -4-pyridazinol (Compound No. 1091)
[2027] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.02 (1H, d, J = 7.7 Hz), 6.79 (1H, d, J = 7.7 Hz), 6.71 (1H, s), 2.90 (2H, t, J = 7.3 Hz), 2.72 (2H, t, J = 7.3 Hz), 2.18-1.98 (2H, m), 1.92-1.75 (1H, m), 0.82-0.70 (2H, m), 0.60-0.47 (2H , m).
[2028] Melting point (° C.): 218-220.
[2029] Example 308 6-chloro-3-[(6-methyl-2,3-dihydro-1-benzofuran-7-yl) oxy] -4-pyridazinol (Compound No. 1096)
[2030] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.99 (1H, d, J = 7.7 Hz), 6.72 (1H, d, J = 7.7 Hz), 6.70 (1H, s), 4.53 (2H, t, J = 8.8 Hz), 3.20 (2H, br.t, J = 8.8 Hz), 2.15 (3H, s).
[2031] Melting Point (° C): 217-219.
[2032] Example 309 3-[(6-bromo-1-benzofuran-7-yl) oxy] -6-chloro-4-pyridazinol (Compound No. 1099)
[2033] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.75 (1H, d, J = 2.2 Hz), 7.48 (1H, d, J = 8.4 Hz), 7.47 (1H, d, J = 8.4 Hz), 6.92 (1H, d, J = 2.2 Hz), 6.78 (1H, s).
[2034] Physical property: Amorphous.
[2035] Example 310 6-Chloro-3-[(6-methyl-1-benzofuran-7-yl) oxy] -4-pyridazinol (Compound No. 1100)
[2036] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.65 (1H, d, J = 2.2 Hz), 7.40 (1H, d, J = 8.1 Hz), 7.14 (1H, d, J = 8.1 Hz), 6.82 (1H, d, J = 2.2 Hz), 6.75 (1H, s), 2.31 (3H, s).
[2037] Properties: Oily substance.
[2038] Example 311 6-chloro-3-[(6-cyclopropyl-1-benzofuran-7-yl) oxy] -4-pyridazinol (Compound No. 1102)
[2039] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.65 (1H, d, J = 2.2 Hz), 7.40 (1H, d, J = 8.1 Hz), 6.87 (1H, d, J = 8.1 Hz), 6.81 (1H, d, J = 2.2 Hz), 6.75 (1H, s), 2.10-1.98 (1H, m), 0.98-0.80 (2H, m), 0.80-0.64 (2H, m).
[2040] Melting Point (° C): 175-180.
[2041] Example 312 6-chloro-3-[(5-methyl-1-benzofuran-4-yl) oxy] -4-pyridazinol (Compound No. 1109)
[2042] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.65 (1H, d, J = 2.2 Hz), 7.32 (1H, d, J = 8.4 Hz), 7.18 (1H, d, J = 8.4 Hz), 6.73 (1H, s), 6.60 (1H, d, J = 2.2 Hz), 2.23 (3H, s).
[2043] Melting point (° C): 222-225.
[2044] Example 313 6-Chloro-3- (2,4-dicyclopropyl-6-fluorophenoxy) -4-pyridazinol (Compound No. 1115)
[2045] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.71-6.65 (2H, m), 6.54 (1H, s), 2.02-1.81 (2H, m), 1.01-0.72 (4H, m), 0.68-0.60 (4H, m).
[2046] Physical property: Amorphous.
[2047] Example 314 6-chloro-3- (2,4-dibromo-3,6-dimethylphenoxy) -4-pyridazinol (Compound No. 1118)
[2048] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.54 (1H, s), 6..71 (1H, s), 2.56 (3H, s), 2.16 (3H, s).
[2049] Melting point (° C): 241-248.
[2050] Example 315 3- (2-bromo-4,6-dimethylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1119)
[2051] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.31 (1H, brs), 7.10 (1H, brs), 6.74 (1H, s), 2.31 (3H, s), 2.17 (3H, s).
[2052] Melting point (° C): 254-256.
[2053] Example 316 6-chloro-3- (2-ethyl-4,6-diiodophenoxy) -4-pyridazinol (Compound No. 1120)
[2054] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.03 (1H, d, J = 2.2 Hz), 7.66 (1H, d, J = 2.2 Hz), 6.74 (1H, s), 2.52 (2H, q, J = 7.7 Hz), 1.17 (3H, t, J = 7.7 Hz).
[2055] Melting point (° C): 142-144.
[2056] Example 317 6-Chloro-3- (2,4,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1122)
[2057] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.90 (2H, s), 6.71 (1H, s), 2.27 (3H, s), 2.07 (6H, s).
[2058] Melting point (° C): 235-239.
[2059] Example 318 6-Chloro-3- (2-cyclopropyl-4,6-dimethylphenoxy) -4-pyridazinol (Compound No. 1123)
[2060] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.88 (1H, brs), 6.69 (1H, s), 6.63 (1H, brs), 2.26 (3H, s), 2.09 (3H, s), 1.85- 1.70 (1H, m), 0.80-0.65 (2H, m), 0.65-0.50 (2H, m).
[2061] Melting Point (° C): 215-217.
[2062] Example 319 3- (2-bromo-3,5,6-trimethylphenoxy) -6-chloro-4-pyridazinol (Compound No. 1124)
[2063] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.13 (1H, s), 6.88 (1H, brs), 2.32 (3H, s), 2.23 (3H, s), 2.01 (3H, s).
[2064] Melting Point (° C): 280-290.
[2065] Example 320 6-Chloro-3- (2,3,5,6-tetramethylphenoxy) -4-pyridazinol (Compound No. 1125)
[2066] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.88 (1H, s), 6.69 (1H, s), 2.22 (6H, s), 1.98 (6H, s).
[2067] Melting point (° C.): 278-283.
[2068] Example 321 6-Chloro-3-[(5,6-dimethyl-2,3-dihydro-1 H-inden-4-yl) oxy] -4-pyridazinol (Compound No. 1129)
[2069] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.72 (1H, s), 6.68 (1H, s), 2.88 (2H, t, J = 7.4 Hz), 2.70 (2H, t, J = 7.4 Hz) , 2.24 (3H, s), 2.17 (3H, s), 2.05 (2H, quintet, J = 7.4 Hz).
[2070] Melting point (° C): 210-213.
[2071] Example 322 6-chloro-3- (1,2,3,5,6,7-hexahydro-s-indasen-4-yloxy) -4-pyridazinol (Compound No. 1133)
[2072] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.95 (1H, s), 6.65 (1H, s), 2.88 (4H, t, J = 7.3 Hz), 2.68 (4H, t, J = 7.3 Hz) , 2.20-1.90 (4H, m).
[2073] Physical property: Amorphous.
[2074] Example 323 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl acetate (Compound No. 1140)
[2075] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.40 (1H, s), 7.26-6.98 (4H, m), 2.40 (3H, s), 1.93-1.76 (1H, m), 0.85-0.59 (4H, m).
[2076] Physical property: Amorphous.
[2077] Example 324 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl acetate (Compound No. 1151)
[2078] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.39 (1H, s), 7.15-7.00 (2H, m), 6.90-6.75 (1H, m), 2.42 (3H, s), 2.12 (3H, s) , 1.90-1.67 (1 H, m), 0.85-0.50 (4 H, m).
[2079] Melting point (° C.): 98-101.
[2080] Example 325 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl pivalate (Compound No. 1207)
[2081] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.38 (1H, s), 7.15-7.05 (2H, m), 6.90-6.84 (1H, m), 2.13 (3H, s), 1.81-1.65 (1H, m), 1.41 (9H, s), 0.90-0.50 (4H, m).
[2082] Melting point (° C.): 84-87.
[2083] Example 326 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl decanoate (Compound No. 1251)
[2084] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.38 (1H, s), 7.15-7.05 (2H, m), 6.93-6.80 (1H, m), 2.67 (2H, t, J = 7.3 Hz), 2.12 (3H, s), 1.85-1.65 (3H, m), 1.55-1.10 (12H, m), 0.95-0.80 (3H, m), 0.80-0.65 (2H, m), 0.65-0.52 (2H, m) .
[2085] Properties: Oily substance.
[2086] Example 327 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl cyclopropanecarboxylate (Compound No. 1266)
[2087] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.43 (1H, s), 7.22-6.98 (4H, m), 2.00-1.75 (2H, m), 1.30-1.08 (4H, m), 0.86-0.51 ( 4H, m).
[2088] Melting point (° C.): 122-125.
[2089] Example 328 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl benzoate (Compound No. 1387)
[2090] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.23-8.18 (2H, m), 7.75-7.50 (3H, m), 7.60 (1H, s), 7.30-7.08 (4H, m), 2.18 (3H, s).
[2091] Properties: Oily substance.
[2092] Example 329 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl benzoate (Compound No. 1391)
[2093] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.20 (2H, d, J = 7.3 Hz), 7.74-7.50 (4H, m), 7.26-7.01 (3H, m), 6.98-6.97 (1H, m) , 1.91-1.80 (1H, m), 0.83-0.57 (4H, m).
[2094] Physical property: Amorphous.
[2095] Example 330 6-chloro-3- [4- (trimethylsilyl) phenoxy] -4-pyridazinyl benzoate (Compound No. 1396)
[2096] Melting point (° C.): 100-102.
[2097] Example 331 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl benzoate (Compound No. 1417)
[2098] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.24-8.20 (2H, m), 7.75-7.68 (2H, m), 7.67-7.52 (3H, m), 7.09-7.07 (2H, m), 6.87- 6.82 (1H, m), 2.16 (3H, s), 1.82-1.71 (1H, m), 0.75-0.71 (2H, m), 0.62-0.53 (2H, m).
[2099] Physical property: Amorphous.
[2100] Example 332 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1446)
[2101] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.35-8.08 (2H, m), 7.59 (1H, s), 7.68-7.00 (6H, m), 2.70 (3H, s), 2.21 (3H, s) .
[2102] Melting Point (° C): 91-93.
[2103] Example 333 6-Chloro-3- (2-isopropylphenoxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1448)
[2104] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.15-8.00 (2H, m), 7.58 (1H, s), 7.75-6.90 (6H, m), 3.40-2.85 (1H, m), 2.69 (3H, s), 1.15 (6H, d, J = 7.0 Hz).
[2105] Refractive Index: n _D ²² 1.5709.
[2106] Example 334 3- (2-s-butylphenoxy) -6-chloro-4-pyridazinyl 2-methylbenzoate (Compound No. 1450)
[2107] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.28-8.05 (1H, m), 7.60-7.05 (7H, m), 7.52 (1H, s), 3.05-2.60 (1H, m), 2.65 (3H, s), 1.70-1.00 (2H, m), 1.10 (3H, d, J = 7.0 Hz), 0.90-0.50 (3H, m).
[2108] Physical property: Paste form.
[2109] Example 335 6-Chloro-3- (2-cyclohexylphenoxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1455)
[2110] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.30-7.00 (8H, m), 7.54 (1H, s), 2.68 (1H, brs), 2.67 (3H, s), 2.00-1.00 (10H, m) .
[2111] Melting point (° C.): 89-91.
[2112] Example 336 3-([1,1'-biphenyl] -2-yloxy) -6-chloro-4-pyridazinyl 2-methylbenzoate (Compound No. 1456)
[2113] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.20-7.90 (1H, m), 7.60-7.10 (13H, m), 2.58 (3H, s).
[2114] Refractive Index: n _D ²⁸ 1.6055.
[2115] Example 337 3- (3-tert-butylphenoxy) -6-chloro-4-pyridazinyl 2-methylbenzoate (Compound No. 1457)
[2116] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.28-8.02 (1H, m), 7.55 (1H, s), 7.65-6.85 (7H, m), 2.64 (3H, s), 1.28 (9H, s) .
[2117] Melting Point (℃): 63-64.
[2118] Example 338 6-chloro-3- (3-methoxyphenoxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1458)
[2119] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.30-8.00 (1H, m), 7.70-7.10 (4H, m), 7.55 (1H, s), 6.90-6.60 (3H, m), 3.74 (3H, s), 2.64 (3H, s).
[2120] Melting point (° C): 66-67.
[2121] Example 339 6-Chloro-3- (2-isopropyl-5-methylphenoxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1459)
[2122] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.30-8.00 (1H, m), 7.54 (1H, s), 7.50-6.80 (6H, m), 3.30 -2.75 (1H, m), 2.65 (3H, s), 2.28 (3H, s), 1.15 (6H, d, J = 7.00 Hz).
[2123] Melting point (° C.): 95-97.
[2124] Example 340 6-Chloro-3- (1-naphthyloxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1461)
[2125] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.20-7.00 (12H, m), 2.65 (3H, s).
[2126] Melting Point (° C): 133-134.
[2127] Example 341 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 2-methoxybenzoate (Compound No. 1509)
[2128] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.11-7.89 (2H, m), 7.70-6.80 (6H, m), 7.50 (1H, s), 3.84 (3H, s), 2.10 (3H, s) .
[2129] Melting point (° C.): 114-116.
[2130] Example 342 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 4-methylbenzoate (Compound No. 1553)
[2131] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.07 (2H, d, J = 8.0 Hz), 7.58 (1H, s), 7.40-7.03 (4H, m), 7.36 (2H, d, J = 8.0 Hz ), 2.51 (3H, s), 2.23 (3H, s).
[2132] Melting point (° C.): 105-108.
[2133] Example 343 6-Chloro-3- (2-isopropylphenoxy) -4-pyridazinyl 4-methylbenzoate (Compound No. 1554)
[2134] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.28-7.82 (2H, m), 7.61 (1H, s), 7.51-6.90 (6H, m), 3.30-2.80 (1H, m), 2.46 (3H, s), 1.19 (6H, d, J = 7.0 Hz).
[2135] Refractive Index: n _D ²² 1.5731.
[2136] Example 344 6-chloro-3- (2-methylphenoxy) -4-pyridazinyl 2,4-dichlorobenzoate (Compound No. 1603)
[2137] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.04 (1H, d, J = 8.4 Hz), 7.58 (1H, s), 7.58-6.92 (6H, m), 2.20 (3H, s).
[2138] Melting Point (° C): 81-82.5.
[2139] Example 345 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl methyl carbonate (Compound No. 1658)
[2140] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.51 (1H, s), 7.23-6.98 (4H, m), 3.99 (3H, s), 1.91-1.82 (1H, m), 0.84-0.61 (4H, m).
[2141] Physical property: Amorphous.
[2142] Example 346 6-chloro-3- (2-methylphenoxy) -4-pyridazinyl ethyl carbonate (Compound No. 1706)
[2143] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.51 (1H, s), 7.38-7.00 (4H, m), 4.40 (2H, q, J = 7.0 Hz), 2.20 (3H, s), 1.40 (3H , t, J = 7.0 Hz).
[2144] Melting point (° C): 73-74.
[2145] Example 347 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl ethyl carbonate (Compound No. 1710)
[2146] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.51 (1H s), 7.26-6.98 (4H, m), 4.40 (2H, q, J = 7.0 Hz), 1.90-1.80 (1H, m), 1.41 ( 3H, t, J = 7.0 Hz), 0.84-0.60 (4H, m).
[2147] Physical property: Amorphous.
[2148] Example 348 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl isobutyl carbonate (Compound No. 1757)
[2149] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.45 (1H, s), 7.30-7.00 (4H, m), 4.08 (2H, d, J = 5.8 Hz), 2.16 (3H, s), 2.20-1.70 (1H, m), 0.96 (6H, d, J = 5.8 Hz).
[2150] Melting point (° C): 46-47.
[2151] Example 349 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 2,2,2-trichloroethyl carbonate (Compound No. 1789)
[2152] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.52 (1H, s), 7.28-7.03 (4H, m), 4.94 (2H, s), 2.18 (3H, s).
[2153] Physical property: Amorphous.
[2154] Example 350 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl phenyl carbonate (Compound No. 1840)
[2155] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.50-7.20 (5H, m), 7.20-7.05 (2H, m), 6.92-6.82 (1H, m), 2.16 (3H, s), 1.88-1.72 (1H, m), 0.80-0.55 (4H, m).
[2156] Properties: Oily substance.
[2157] Example 351 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl dimethylcarbamate (Compound No. 1877)
[2158] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.55 (1H, s), 7.40-6.92 (4H, m), 3.10 (3H, s), 3.01 (3H, s), 2.19 (3H, s).
[2159] Melting point (° C.): 107-109.
[2160] Example 352 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl dimethylcarbamate (Compound No. 1879)
[2161] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.22-6.98 (4H, m), 3.13 (3H, s), 3.04 (3H, s), 1.97-1.80 (1H, m) , 0.85-0.63 (4H, m).
[2162] Melting point (° C): 137-138.
[2163] Example 353 6-Chloro-3- [3- (trifluoromethyl) phenoxy] -4-pyridazinyl dimethylcarbamate (Compound No. 1881)
[2164] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.60 (1H, s), 7.65-7.22 (4H, m), 3.11 (3H s), 3.05 (3H s).
[2165] Melting Point (° C): 92-93.
[2166] Example 354 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl diethylcarbamate (Compound No. 1898)
[2167] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.55 (1H, s), 7.40-6.92 (4H, m), 3.41 (4H, q, J = 6.2 Hz), 2.20 (3H, s), 1.27 (6H , t, J = 6.2 Hz).
[2168] Melting point (° C): 74-75.5.
[2169] Example 355 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 1-pyrrolidinecarboxylate (Compound No. 1924)
[2170] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.42-7.02 (4H, m), 3.67-3.37 (4H, m), 2.19 (3H, s), 2.07-1.72 (4H, m).
[2171] Melting point (° C): 126-127.
[2172] Example 356 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl methanesulfonate (Compound No. 1981)
[2173] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.55 (1H, s), 7.33-7.06 (4H, m), 3.43 (3H, s), 2.20 (3H, s).
[2174] Properties: Oily substance.
[2175] Example 357 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl methanesulfonate (Compound No. 1985)
[2176] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.55 (1H, s), 7.26-7.23 (2H, m), 7.21-7.02 (2H, m), 3.44 (3H, s), 1.89-1.80 (1H, m), 0.86-0.61 (4H, m).
[2177] Melting point (° C): 162-172.
[2178] Example 358 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methanesulfonate (Compound No. 2010)
[2179] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56 (1H, s), 7.18-7.09 (2H, m), 6.91-6.86 (1H, m), 3.47 (3H, s), 2.16 (3H, s) , 1.82-1.68 (1H, m), 0.75-0.69 (2H, m), 0.67-0.55 (2H, m).
[2180] Physical property: Amorphous.
[2181] Example 359 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 1-propanesulfonate (Compound No. 2038)
[2182] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.34-7.05 (4H, m), 3.48 (2H, t, J = 7.7 Hz), 2.20 (3H, s), 2.10 (2H , sixtet, J = 7.7 Hz), 1.14 (3H, t, J = 7.7 Hz).
[2183] Melting Point (° C): 72-73.
[2184] Example 360 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl 1-propanesulfonate (Compound No. 2040)
[2185] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.28-7.15 (2H, m), 7.12-6.99 (2H, m), 3.52-3.45 (2H, m), 2.17-1.98 ( 2H, m), 1.92-1.78 (1H, m), 1.11 (3H, t, J = 7.3 Hz), 0.85-0.73 (2H, m), 0.69-0.60 (2H, m).
[2186] Physical property: Paste form.
[2187] Example 361 6-Chloro-3- (2,3-dihydro-1H-inden-4-yloxy) -4-pyridazinyl 1-propanesulfonate (Compound No. 2042)
[2188] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56 (1H, s), 7.26-7.14 (2H, m), 6.94 (1H, dd, J = 7.0, 1.8 Hz), 3.50-3.42 (2H, m) , 2.98 (2H, t, J = 7.3 Hz), 2.74 (2H, t, J = 7.3 Hz), 2.17-1.98 (4H, m), 1.12 (3H, t, J = 7.3 Hz).
[2189] Physical property: Paste form.
[2190] Example 362 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -5-iodo-4-pyridazinol (Compound No. 3849)
[2191] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.08-7.05 (2H, m), 6.84-6.80 (1H, m), 2.14 (3H, s), 1.86-1.75 (1H, m), 0.81-0.65 (2H, m), 0.60-0.52 (2H, m).
[2192] Physical property: Amorphous.
[2193] Example 363 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl trifluoromethanesulfonate (Compound No. 2106)
[2194] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.52 (1H, s), 7.19-7.09 (2H, m), 6.96-6.89 (1H, m), 2.15 (3H, s), 1.81-1.67 (1H, m), 0.73-0.58 (4H, m).
[2195] Melting point (° C.): 64-67.
[2196] Example 364 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl benzenesulfonate (Compound No. 2147)
[2197] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.10-7.83 (2H, m), 7.80-7.40 (3H, m), 7.59 (1H, s), 7.30-7.00 (3H, m), 6.90-6.60 ( 1H, m).
[2198] Melting point (° C.): 91.5-92.
[2199] Example 365 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl benzenesulfonate (Compound No. 2151)
[2200] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.02-7.98 (2H, m), 7.78-7.70 (1H, m), 7.62-7.54 (2H, m), 7.58 (1H, s), 7.26-7.09 ( 2H, m), 6.98-6.93 (1H, m), 6.78-6.69 (1H, m), 1.68-1.54 (1H, m), 0.74-0.52 (4H, m).
[2201] Properties: Oily substance.
[2202] Example 366 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl benzenesulfonate (Compound No. 2176)
[2203] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.07-8.01 (2H, m), 7.80-7.71 (1H, m), 7.65-7.56 (2H, m), 7.60 (1H, s), 7.11-6.99 ( 2H, m), 6.80 (1H, dd, J = 4.4, 2.4 Hz), 1.93 (3H, s), 1.61-1.45 (1H, m), 0.65-0.45 (4H, m).
[2204] Melting point (° C.): 105-106.
[2205] Example 367 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 4-chlorobenzenesulfonate (Compound No. 2198)
[2206] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.94 (2H, d, J = 8.4 Hz), 7.60 (1H, s), 7.59 (2H, d, J = 8.4 Hz), 7.23-7.09 (3H, m ), 6.90-6.60 (1H, m), 2.93 (3H, s).
[2207] Melting point (° C): 93-94.
[2208] Example 368 3- (2-isopropylphenoxy) -4-pyridazinyl 4-chlorobenzenesulfonate (Compound No. 2199)
[2209] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.91 (2H, d, J = 8.4 Hz), 7.62 (1H, s), 7.55 (2H, d, J = 8.4 Hz), 7.50-7.00 (3H, m ), 6.80-6.60 (1H, m), 3.20-2.50 (1H, m), 1.14 (6H, d, J = 7.0 Hz).
[2210] Refractive Index: n _D ²² 1.5315.
[2211] Example 369 3- (2-tert-butylphenoxy) -6-chloro-4-pyridazinyl 4-chlorobenzenesulfonate (Compound No. 2200)
[2212] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.05-7.05 (8H, m), 6.70-6.40 (1H, m), 1.26 (9H, s).
[2213] Melting Point (° C): 83.5-84.5.
[2214] Example 370 6-chloro-3- (2-methylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2220)
[2215] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.83 (2H, d, J = 8.4 Hz), 7.47 (2H, d, J = 8.4 Hz), 7.32-6.95 (4H, m), 6.85-6.55 (1H) m), 2.43 (3H, s), 1.98 (3H, s).
[2216] Melting point (° C.): 102-104.
[2217] Example 371 6-chloro-3- (2-ethylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2221)
[2218] Refractive Index: n _D ²⁸ 1.5847.
[2219] Example 372 6-Chloro-3- (2-isopropylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2222)
[2220] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.00-6.50 (8H, m), 7.55 (1H, s), 2.85 (1H, septet, J = 7.0 Hz), 2.42 (3H, s), 1.11 (6H , d, J = 7.0 Hz).
[2221] Melting Point (℃): 99-100.
[2222] Example 373 3- (2-s-butylphenoxy) -6-chloro-4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2223)
[2223] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.98-6.50 (8H, m), 7.52 (1H, s), 2.99-2.31 (1H, m), 2.41 (3H, s), 1.82-0.95 (2H, m), 1.08 (3H, d, J = 7.0 Hz), 0.90-0.35 (3H, m).
[2224] Melting Point (° C): 65-66.
[2225] Example 374 3- (2-tert-butylphenoxy) -6-chloro-4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2224)
[2226] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.98-7.00 (7H, m), 7.61 (1H s), 6.78-6.45 (1H, m), 2.40 (3H, s), 1.29 (9H, s).
[2227] Melting point (° C.): 98-99.
[2228] Example 375 5,6-dichloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol (Compound No. 3837)
[2229] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.08-7.06 (2H, m), 6.85-6.80 (1H, m), 2,14 (3H, s), 1.87-1.78 (1H, m), 0.81 -0.72 (2H, m), 0.64-0.52 (2H, m).
[2230] Physical property: Amorphous.
[2231] Example 376 6-chloro-3- (2-cyclohexylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2230)
[2232] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.00-6.50 (8H, m), 7.50 (1H, s), 2.50 (1H, brs), 2.40 (3H, s), 2.00-0.90 (10H, m) .
[2233] Melting point (° C): 120-121.
[2234] Example 377 3-([1,1'-biphenyl] -2-yloxy) -6-chloro-4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2231)
[2235] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.80-6.60 (14H, m), 2.42 (3H, s).
[2236] Melting point (° C.): 106-108.
[2237] Example 378 6-Chloro-3- (2-methoxyphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2232)
[2238] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.00-6.70 (8H, m), 7.56 (1H, s), 3.62 (3H, s), 2.44 (3H, s).
[2239] Melting point (° C.): 153-157.
[2240] Example 379 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl propionate (Compound No. 1160)
[2241] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.39 (1H, s), 7.14-7.05 (2H, m), 6.89-6.82 (1H, m), 2.72 (2H, q, J = 7.6 Hz), 2.12 (3H, s), 1.82-1.68 (1H, m), 1.31 (3H, t, J = 7.6 Hz), 0.77-0.53 (4H, m).
[2242] Melting Point (° C): 75-77.
[2243] Example 380 6-Chloro-3- (3-chlorophenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2234)
[2244] Refractive Index: n _D ²⁸ 1.5970.
[2245] Example 381 3- (3-tert-butylphenoxy) -6-chloro-4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2235)
[2246] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.73 (2H, d, J = 8.2 Hz), 7.49 (1H, s), 7.23 (2H, d, J = 8.2 Hz), 7.14 (1H, d, J = 4.0 Hz), 6.90-6.45 (3H, m), 2.38 (3H, s), 1.26 (9H, s).
[2247] Melting Point (° C): 56-57.
[2248] Example 382 6-chloro-3- [3- (trifluoromethyl) phenoxy] -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2236)
[2249] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.95-6.93 (9H, m), 2.40 (3H, s).
[2250] Refractive Index: n _D ^25.5 1.5556.
[2251] Example 383 6-Chloro-3- (3-cyanophenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2237)
[2252] ¹ H-NMR (90 MHz, CDCl ₃ ) δ ppm: 7.85 (2H, d, J = 8.0 Hz), 7.70-7.00 (7H, m), 2.49 (3H, s).
[2253] Physical property: Paste form.
[2254] Example 384 6-Chloro-3- (3-methoxyphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2238)
[2255] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.90-6.30 (8H, m), 7.47 (1H, s), 3.71 (3H, s), 2.40 (3H, s).
[2256] Melting point (° C.): 89-90.
[2257] Example 385 6-Chloro-3- (1-naphthyloxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2240)
[2258] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.90-6.80 (12H, m), 2.38 (3H, s).
[2259] Melting Point (° C): 92-94.
[2260] Example 386 3- (2-Bromo-4-tert-butylphenoxy) -6-chloro-4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2245)
[2261] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.89 (2H, d, J = 8.4 Hz), 7.63 (1H, s), 7.62-7.18 (3H, m), 6.84 (2H, d, J = 8.4 Hz ), 2.43 (3H, s), 1.29 (9H, s).
[2262] Melting point (° C.): 110-112.
[2263] Example 387 6-Chloro-3- (4-chloro-2-methylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2246)
[2264] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.95-7.75 (2H, m), 7.60-7.00 (5H, m), 6.80-6.60 (1H, m), 2.46 (3H, s), 2.00 (3H, s).
[2265] Melting Point (° C): 115-116.
[2266] Example 388 6-Chloro-3- (2,4-dimethylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2247)
[2267] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.94-7.78 (2H, m), 7.54 (1H, s), 7.41-7.23 (2H, m), 7.02-6.53 (3H, m), 2.46 (3H, s), 2.30 (3H, s), 1.96 (3H, s).
[2268] Melting point (° C.): 80-81.
[2269] Example 389 3- (4-bromo-2-isopropylphenoxy) -6-chloro-4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2248)
[2270] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.80 (2H, d, J = 8.4 Hz), 7.51 (1H, s), 7.45-7.10 (3H, m), 6.56 (2H, d, J = 8.4 Hz ), 2.85 (1H, septet, J = 6.8 Hz), 2.43 (3H, s), 1.10 (6H, d, J = 6.8 Hz).
[2271] Melting point (° C.): 119-122.
[2272] Example 390 6-Chloro-3- (2-isopropyl-5-methylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2249)
[2273] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.00-6.80 (6H, m), 7.56 (1H, s), 6.46 (1H, brs), 2.95-2.50 (1H, m), 2.44 (3H, s) , 2.25 (3H, s), 1.09 (6H, d, J = 7.0 Hz).
[2274] Melting point (° C.): 90-92.
[2275] Example 391 6-Chloro-3- (2,6-dimethylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2263)
[2276] Melting point (° C.): 89-90.
[2277] Example 392 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methylbenzenesulfonate (Compound No. 2265)
[2278] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.90 (2H, d, J = 8.1 Hz), 7.60 (1H, s), 7.38 (2H, d, J = 8.1 Hz), 7.11-7.01 (2H, m ), 6.80 (1H, dd, J = 6.6, 2.6 Hz), 2.47 (3H, s), 1.93 (3H, s), 1.59-1.46 (1H, m), 0.64-0.45 (4H, m).
[2279] Melting point (° C.): 85-87.
[2280] Example 393 6-Chloro-3- (2-methylphenoxy) -4-pyridazinyl 4-nitrobenzenesulfonate (Compound No. 2287)
[2281] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 8.41 (2H, d, J = 8.4 Hz), 8.33 (2H, d, J = 8.4 Hz), 7.61 (1H, s), 7.30-7.02 (3H, m ), 6.95-6.63 (1H, m), 2.03 (3H, s).
[2282] Melting point (° C): 166-169.
[2283] Example 394 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl 4-nitrobenzenesulfonate (Compound No. 2289)
[2284] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.39 (2H, d, J = 8.8 Hz), 8.23 (2H, d, J = 8.8 Hz), 7.59 (1H, s), 7.20-7.09 (2H, m ), 6.97-6.92 (1H, m), 6.77-6.73 (1H, m), 1.67-1.59 (1H, m), 0.78-0.54 (4H, m).
[2285] Melting point (° C): 158.
[2286] Example 395 6-Chloro-3- (2-cyclopropylphenoxy) -4-pyridazinyl dimethylsulfamate (Compound No. 2351)
[2287] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.60 (1H, s), 7.26-7.01 (4H, m), 3.09 (6H, s), 1.95-1.78 (1H, m), 0.85-0.63 (4H, m).
[2288] Properties: Oily substance.
[2289] Example 396 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methylpropanoate (Compound No. 1172)
[2290] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.38 (1H, s), 7.14-7.05 (2H, m), 6.90-6.83 (1H, m), 2.93 (1H, septet, J = 7.0 Hz), 2.13 (3H, s), 1.80-1.66 (1H, m), 1.36 (6H, d, J = 7.0 Hz), 0.78-0.56 (4H, m).
[2291] Melting point (° C.): 38-39.
[2292] Example 397 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl pentanoate (Compound No. 1178)
[2293] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.38 (1H, s), 7.13-7.00 (2H, m), 6.90-6.77 (1H, m), 2.68 (2H, t, J = 7.3 Hz), 2.12 (3H, s), 1.88-1.65 (3H, m), 1.60-1.35 (2H, m), 0.95 (3H, t, J = 7.3 Hz), 0.80-0.50 (4H, m).
[2294] Properties: Caramel statue.
[2295] Example 398 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-methylbutanoate (Compound No. 1184)
[2296] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.37 (1H, s), 7.14-7.07 (2H, m), 6.89-6.82 (1H, m), 2.55 (2H, d, J = 7.0 Hz), 2.27 (1H, br.septet, J = 6.8 Hz), 2.12 (3H, s), 1.80-1.67 (1H, m), 1.07 (6H, d, J = 6.6 Hz), 0.77-0.55 (4H, m).
[2297] Melting point (° C.): 71-74.
[2298] Example 399 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl pentadecanoate (Compound No. 1260)
[2299] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.37 (1H, s), 7.10-7.00 (2H, m), 6.87-6.77 (1H, m), 2.66 (2H, t, J = 6.4 Hz), 2.12 (3H, s), 1.85-1.65 (3H, m), 1.35-1.18 (22H, m), 0.95-0.82 (3H, m), 0.80-0.50 (4H, m).
[2300] Melting Point (° C): 35-37.
[2301] Example 400 6-Chloro-3-phenoxy-5- (trimethylsilyl) -4-pyridazinol (Compound No. 2402)
[2302] ¹ H-NMR (90 MHz, CDCl ₃ ) δ ppm: 12.0 (1H, brs), 7.30-6.81 (5H, m), 0.28 (9H, s).
[2303] Melting Point (° C): 119-120.
[2304] Example 401 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl cyclobutanecarboxylate (Compound No. 1286)
[2305] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.38 (1H, s), 7.14-7.05 (2H, m), 6.89-6.79 (1H, m), 3.58-3.40 (1H, m), 2.60-1.85 ( 6H, m), 2.13 (3H, s), 1.82-1.67 (1H, m), 0.80-0.67 (2H, m), 0.64-0.53 (2H, m).
[2306] Physical property: Paste form.
[2307] Example 402 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl cyclohexanecarboxylate (Compound No. 1298)
[2308] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.37 (1H, s), 7.15-7.05 (2H, m), 6.90-6.80 (1H, m), 2.78-2.60 (1H, m), 2.12 (3H, s), 1.90-1.20 (10H, m), 0.80-0.50 (4H, m).
[2309] Melting point (° C): oily substance.
[2310] Example 403 3- (2-isopropylphenoxy) -6-methyl-4-pyridazinol (Compound No. 2418)
[2311] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.40-7.35 (1H, m), 7.25-7.16 (2H, m), 7.04-6.98 (1H, m), 6.43 (1H, s), 3.06 (1H , septet, J = 7.0 Hz), 2.36 (3H, s), 1.18 (6H, d, J = 7.0 Hz).
[2312] Melting point (° C.): 259-260.
[2313] Example 404 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-bromobutanoate (Compound No. 1334)
[2314] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.44 (1H, s), 7.14-7.05 (2H, m), 6.90-6.83 (1H, m), 4.45 (1H, t, J = 7.6 Hz), 2.22 (1H, dq, J = 7.3, 7.6 Hz), 2.13 (3H, s), 1.81-1.69 (1H, m), 1.17 (3H, t, J = 7.3 Hz), 0.74-0.69 (2H, m), 0.58-0.56 (2H, m).
[2315] Physical property: Paste form.
[2316] Example 405 3- (2-isopropylphenoxy) -6- (trifluoromethyl) -4-pyridazinol (Compound No. 2431)
[2317] ¹ H-NMR (60 MHz, CDCl ₃ ) δ ppm: 7.60-6.70 (4H, m), 6.87 (1H, s), 2.97 (1H, septet, J = 7.0 Hz), 1.10 (6H, d, J = 7.0 Hz ).
[2318] Melting Point (° C): 126.5.
[2319] Example 406 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-chlorobutanoate (Compound No. 1340)
[2320] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.40 (1H, s), 7.14-7.05 (2H, m), 6.89-6.82 (1H, m), 3.68 (2H, t, J = 6.2 Hz), 2.91 (2H, t, J = 7.0 Hz), 2.31-2.18 (2H, m), 2.11 (3H, s), 1.79-1.65 (1H, m), 0.80-0.67 (2H, m), 0.63-0.53 (2H , m).
[2321] Physical property: Paste form.
[2322] Example 407 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-methyl-2-butenoate (Compound No. 1358)
[2323] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.44 (1H, s), 7.12-7.05 (2H, m), 6.88-6.80 (1H, m), 5.99-5.97 (1H, m), 2.26 (3H, d, J = 1.1 Hz), 2.13 (3H, s), 2.04 (3H, d, J = 1.1 Hz), 1.83-1.70 (1H, m), 0.77-0.64 (2H, m), 0.60-0.53 (2H , m).
[2324] Physical property: Paste form.
[2325] Example 408 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl (2E) -3-phenyl-2-propenoate (compound number 1364)
[2326] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.96 (1H, d, J = 16.0 Hz), 7.63-7.59 (2H, m), 7.53 (1H, s), 7.48-7.43 (3H, m), 7.09 -7.05 (2H, m), 6.86-6.81 (1H, m), 6.66 (1H, d, J = 16.0 Hz), 2.16 (3H, s), 1.83-1.75 (1H, m), 0.79-0.54 (4H , m).
[2327] Physical property: Amorphous.
[2328] Example 409 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methyl succinate (Compound No. 1382)
[2329] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.44 (1H, s), 7.08-7.02 (2H, m), 6.88-6.74 (1H, m), 3.69 (3H, s), 3.01 (2H, t, J = 7.3 Hz), 2.78 (2H, t, J = 7.3 Hz), 2.11 (3H, s), 1.85-1.65 (1H, m), 0.80-0.50 (4H, m).
[2330] Properties: Oily substance.
[2331] Example 410 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-chlorobenzoate (Compound No. 1441)
[2332] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.14 (1H, d, J = 8.8 Hz), 7.58 (1H, s), 7.59-7.39 (3H, m), 7.10-7.05 (2H, m), 6.88 -6.80 (1H, m), 2.16 (3H, s), 1.90-1.70 (1H, m), 0.85-0.50 (4H, m).
[2333] Properties: Oily substance.
[2334] Example 411 3- (2-methylphenoxy) -6- (2-thienyl) -4-pyridazinol (Compound No. 2478)
[2335] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56-7.48 (2H, m), 7.21-7.00 (4H, m), 6.97-6.90 (1H, m), 6.69 (1H, s), 2.11 (3H, s).
[2336] Melting point (° C): 86-87.
[2337] Example 412 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methylbenzoate (Compound No. 1481)
[2338] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.20 (1H, d, J = 7.0 Hz), 7.56 (1H, s), 7.52 (1H, d, J = 7.7 Hz), 7.40-7.28 (2H, m ), 7.10-7.00 (2H, m), 6.90-6.88 (1H, m), 2.69 (3H, s), 2.16 (3H, s), 1.90-1.70 (1H, m), 0.82-0.65 (2H, m) ), 0.65-0.50 (2H, m).
[2339] Properties: Oily substance.
[2340] Example 413 3,6-bis (2-methylphenoxy) -4-pyridazinol (Compound No. 2492)
[2341] ¹ H-NMR (60 MHz, DMF-d ₇ ) δ ppm: 7.40-6.90 (8H, m), 5.79 (1H, s), 2.19 (6H, brs).
[2342] Melting point (° C.): 247-250.
[2343] Example 414 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methoxybenzoate (Compound No. 1522)
[2344] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.09 (1H, dd, J = 7.9, 2.0 Hz), 7.68-7.57 (1H, m), 7.59 (1H, s), 7.15-7.03 (4H, m) , 6.90-6.82 (1H, m), 3.96 (3H, s), 2.17 (3H, s), 1.96-1.72 (1H, m), 0.78-0.65 (2H, m), 0.65-0.51 (2H, m) .
[2345] Physical property: gum phase.
[2346] Example 415 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-methylbenzoate (Compound No. 1531)
[2347] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.05-8.00 (2H, m), 7.58 (1H, s), 7.55-7.38 (2H, m), 7.10-7.05 (2H, m), 6.88-6.80 ( 1H, m), 2.46 (3H, s), 2.16 (3H, s), 1.90-1.68 (1H, m), 0.80-0.50 (4H, m).
[2348] Properties: Oily substance.
[2349] Example 416 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-chlorobenzoate (Compound No. 1537)
[2350] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.16 (2H, d, J = 8.8 Hz), 7.59 (1H, s), 7.54 (2H, d, J = 8.8 Hz), 7.14-7.07 (2H, m ), 6.88-6.83 (1H, m), 2.15 (3H, s), 1.84-1.69 (1H, m), 0.80-0.70 (2H, m), 0.62-0.55 (2H, m).
[2351] Physical property: Amorphous.
[2352] Example 417 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-bromobenzoate (Compound No. 1543)
[2353] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.07 (2H, d, J = 8.6 Hz), 7.70 (2H, d, J = 8.6 Hz), 7.59 (1H, s), 7.12-7.03 (2H, m ), 6.89-6.82 (1H, m), 2.15 (3H, s), 1.83-1.67 (1H, m), 0.78-0.50 (4H, m).
[2354] Physical property: Amorphous.
[2355] Example 418 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-iodobenzoate (Compound No. 1549)
[2356] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.94 (2H, s), 7.93 (1H, m), 7.62 (1H, s), 7.29 (1H, s), 7.12-7.09 (2H, m), 6.89 -6.87 (1H, m), 2.17 (3H, s), 1.84-1.73 (1H, m), 0.79-0.70 (2H, m), 0.62-0.55 (2H, m).
[2357] Physical property: Paste form.
[2358] Example 419 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methylbenzoate (Compound No. 1566)
[2359] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.10 (2H, d, J = 8.1 Hz), 7.60 (1H, s), 7.34 (2H, d, J = 8.1 Hz), 7.12-7.03 (2H, m ), 6.88-6.81 (1H, m), 2.46 (3H, s), 2.15 (3H, s), 1.85-1.71 (1H, m), 0.78-0.65 (2H, m), 0.62-0.52 (2H, m) ).
[2360] Melting point (° C.): 77.5-78.
[2361] Example 420 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-tert-butylbenzoate (Compound No. 1575)
[2362] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.15 (2H, d, J = 8.8 Hz), 7.59 (1H, s), 7.56 (2H, d, J = 8.8 Hz), 7.09-7.06 (2H, m ), 6.86-6.82 (1H, m), 2.15 (3H, s), 1.37 (9H, s), 1.82-1.73 (1H, m), 0.76-0.69 (2H, m), 0.60-0.56 (2H, m) ).
[2363] Melting point (° C): 139-142.
[2364] Example 421 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-nitrobenzoate (Compound No. 1593)
[2365] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.41 (4H, s), 7.61 (1H, s), 7.14-7.08 (2H, m), 6.89-6.83 (1H, m), 2.17 (3H, s) , 1.81-1.70 (1H, m), 0.80-0.71 (2H, m), 0.62-0.54 (2H, m).
[2366] Physical property: Amorphous.
[2367] Example 422 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methoxybenzoate (Compound No. 1599)
[2368] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.17 (2H, d, J = 8.8 Hz), 7.60 (1H, s), 7.12-7.04 (2H, m), 7.01 (2H, d, J = 8.8 Hz ), 6.88-6.82 (1H, m), 3.90 (1H, s), 2.16 (3H, s), 1.85-1.71 (1H, m), 0.78-0.69 (2H, m), 0.60-0.52 (2H, m) ).
[2369] Physical property: Amorphous.
[2370] Example 423 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,4-dichlorobenzoate (Compound No. 1616)
[2371] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.11 (1H, d, J = 8.4 Hz), 7.60-7.57 (2H, m), 7.42 (1H, dd, J = 8.4, 2.2 Hz), 7.14-7.08 (2H, m), 6.89-6.83 (1H, m), 2.15 (3H, s), 1.85-1.72 (1H, m), 0.78-0.67 (2H, m), 0.63-0.54 (2H, m).
[2372] Physical property: Amorphous.
[2373] Example 424 6-chloro-3- (2-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl phthalate (Compound No. 1620)
[2374] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.98-7.94 (1H, m), 7.88-7.84 (1H, m), 7.81-7.71 (2H, m), 7.57, (1H, s), 7.28-7.17 (6H, m), 7.08-7.03 (1H, m), 3.70 (3H, s), 2.26 (3H, s), 2.15 (3H, s).
[2375] Physical property: Amorphous.
[2376] Example 425 potassium 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinoate (compound number 3811)
[2377] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.05-6.95 (2H, m), 6.83-6.72 (1H, m), 6.47 (1H, s), 2.00-1.83 (1H, m), 0.80-0.64 (2H, m), 0.64-0.48 (2H, m).
[2378] Melting point (° C): 187-189.
[2379] Example 426 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazole -5-yl isophthalate (compound number 1631)
[2380] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.61 (1H, t, J = 1.5 Hz), 8.54-8.47 (1H, m), 8.22-8.16 (1H, m), 7.71 (1H, t, J = 8.1 Hz), 7.61 (1H, s), 7.15-6.96 (4H, m), 6.89-6.82 (1H, m), 3.67 (3H, s), 2.44 (3H, s), 2.17 (3H, s), 1.88-1.72 (1H, m), 0.83-0.71 (2H, m), 0.64-0.53 (2H, m).
[2381] Physical property: Amorphous.
[2382] Example 427 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-furoate (Compound No. 1643)
[2383] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.74-7.73 (1H, m), 7.56 (1H, s), 7.50 (1H, dd, J = 3.7, 0.7 Hz), 7.13-7.04 (2H, m) , 6.88-6.81 (1H, m), 6.65-6.63 (1H, m), 2.15 (3H, s), 1.85-1.71 (1H, m), 0.78-0.69 (2H, m), 0.62-0.52 (2H, m).
[2384] Physical property: Paste form.
[2385] Example 428 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-thiophenecarboxylate (Compound No. 1649)
[2386] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.07-8.05 (1H, m), 7.78-7.75 (1H, m), 7,58 (1H, s), 7.24-7.20 (1H, m), 7.13- 7.06 (2H, m), 6.89-6.83 (1H, m), 2.16 (3H, s), 1.83-1.71 (1H, m), 0.80-0.70 (2H, m), 0.65-0.55 (2H, m).
[2387] Physical property: Amorphous.
[2388] Example 429 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl isobutyl carbonate (Compound No. 1770)
[2389] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.49 (1H, s), 7.15-7.05 (2H, m), 6.89-6.82 (1H, m), 4.13 (2H, d, J = 6.6 Hz), 2.14 (3H, s), 2.09 (1H, br.septet, J = 7.0 Hz), 1.88-1.68 (1H, m), 1.01 (6H, d, J = 7.0 Hz), 0.78-0.52 (4H, m).
[2390] Melting Point (° C): 72-74.
[2391] Example 430 Allyl 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinylcarbonate (Compound No. 1811)
[2392] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.50 (1H, s), 7.15-7.06 (2H, m), 6.89-6.82 (1H, m), 6.10-5.90 (1H, m), 5.51-5.35 ( 2H, m), 4.84-4.80 (2H, m), 2.14 (3H, s), 1.85-1.70 (1H, m), 0.78-0.53 (4H, m).
[2393] Properties: Oily substance.
[2394] Example 431 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl dimethylcarbamate (Compound No. 1891)
[2395] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56 (1H, s), 7.13-7.05 (2H, m), 6.89-6.82 (1H, m), 3.16 (3H, s), 3.05 (3H, s) 2.15 (3H, s), 1.85-1.71 (1H, m), 0.78-0.54 (4H, m).
[2396] Melting point (° C.): 136-138.
[2397] Example 432 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl diethylcarbamate (Compound No. 1911)
[2398] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.10-7.07 (2H, m), 6.87-6.83 (1H, m), 3.48 (2H, q, J = 7.3 Hz), 3.41 (2H, q, J = 7.0 Hz), 2.15 (3H, s), 1.82-1.72 (1H, m), 1.29 (3H, t, J = 7.3 Hz), 1.23 (3H, t, J = 7.0 Hz) , 0.74-0.57 (4H, m).
[2399] Melting point (° C.): 119-121.
[2400] Example 433 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl diisopropylcarbamate (Compound No. 1920)
[2401] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.61 (1H, s), 7.10-7.00 (2H, m), 6.90-6.85 (1H, m), 4.20-3.90 (2H, m), 2.14 (3H, s), 1.87-1.67 (1H, m), 1.45-1.20 (12H, m), 0.80-0.50 (4H, m).
[2402] Melting point (° C.): 103-105.
[2403] Example 434 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-thiophenesulfonate (Compound No. 3792)
[2404] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.89-7.82 (2H, m), 7.58 (1H, s), 7.22-7.13 (1H, m), 7.13-7.02 (2H, m), 6.84-6.79 ( 1H, m), 1.99 (3H, s), 169-1.53 (1H, m), 0.70-0.48 (4H, m).
[2405] Physical property: Amorphous.
[2406] Example 435 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methyl (phenyl) carbamate (Compound No. 1946)
[2407] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.40-7.25 (6H, m), 7.11-7.08 (2H, m), 6.87-6.82 (1H, m), 3.42 (3H, br.s), 2.15 ( 3H, br.s), 1.82-1.68 (1H, m), 0.71-0.56 (4H, m).
[2408] Physical property: Amorphous.
[2409] Example 436 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl diphenylcarbamate (Compound No. 1952)
[2410] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.45-7.28 (11H, m), 7.16-7.09 (2H, m), 6.87-6.82 (1H, m), 2.11 (3H, s), 1.79-1.66 ( 1 H, m), 0.69-0.56 (4 H, m).
[2411] Physical property: Amorphous.
[2412] Example 437 O- [6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] S-methyl thiocarbonate (Compound No. 1958)
[2413] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.47 (1H, s), 7.13-7.06 (2H, m), 6.89-6.83 (1H, m), 2.49 (3H, s), 2.14 (3H, s) , 1.83-1.69 (1H, m), 0.78-0.65 (2H, m), 0.63-0.55 (2H, m).
[2414] Physical property: Paste form.
[2415] Example 438 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl ethanesulfonate (Compound No. 2034)
[2416] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.15-7.05 (2H, m), 6.92-6.82 (1H, m), 3.58 (2H, q, J = 7.4 Hz), 2.15 (3H, s), 1.82-1.68 (1H, m), 1.64 (3H, t, J = 7.4 Hz), 0.78-0.52 (4H, m).
[2417] Melting point (° C.): 96-97.
[2418] Example 439 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-propanesulfonate (Compound No. 2051)
[2419] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.18-7.05 (2H, m), 6.94-6.83 (1H, m), 3.53 (2H, t, J = 7.7 Hz), 2.20 -2.00 (2H, m), 2.15 (3H, s), 1.82-1.67 (1H, m), 1.15 (3H, t, J = 7.7 Hz), 0.80-0.50 (4H, m).
[2420] Melting Point (° C): 70.5-71.5.
[2421] Example 440 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-propanesulfonate (Compound No. 2060)
[2422] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.18-7.07 (2H, m), 6.93-6.82 (1H, m), 3.75 (1H, septet, 7.0 Hz), 2.15 (3H , S), 1.85-1.65 (1H, m), 1.65 (6H, d, J = 7.0 Hz), 0.78-0.50 (4H, m).
[2423] Properties: Oily substance.
[2424] Example 441 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-octanesulfonate (Compound No. 2066)
[2425] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.15-7.07 (2H, m), 6.89-6.85 (1H, s), 3.60-3.50 (2H, m), 2.15 (3H, s), 2.15-1.98 (2H, m), 1.83-1.67 (1H, m), 1.58-1.15 (10H, m), 0.95-0.83 (3H, m), 0.80-0.68 (2H, m), 0.65- 0.55 (2H, m).
[2426] Physical property: Paste form.
[2427] Example 442 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl chloromethanesulfonate (Compound No. 2072)
[2428] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.18-7.09 (2H, m), 6.92-6.85 (1H, m), 5.02 (2H, s), 2.16 (3H, s) , 1.83-1.68 (1H, m), 0.80-0.68 (2H, m), 0.65-0.55 (2H, m).
[2429] Physical property: Paste form.
[2430] Example 443 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,2,2-trifluoroethanesulfonate (Compound No. 2136)
[2431] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.55 (1H, s), 7.19-7.05 (2H, m), 6.90 (1H, dd, J = 6.6, 2.9 Hz), 4.39 (2H, q, J = 8.2 Hz), 2.15 (3H, s), 1.80-1.65 (1H, m), 0.80-0.50 (4H, m).
[2432] Physical property: Amorphous.
[2433] Example 444 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-chlorobenzenesulfonate (Compound No. 2212)
[2434] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.01-7.92 (2H, m), 7.62-7.53 (3H, m), 7.13-7.00 (2H, m), 6.85-6.77 (1H, m), 2.04 ( 3H, s), 1.58-1.45 (1H, m), 0.70-0.45 (4H, m).
[2435] Physical property: Flaw.
[2436] Example 445 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-nitrobenzenesulfonate (Compound No. 2300)
[2437] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.50-8.39 (2H, m), 8.33-8.20 (2H, m), 7.59 (1H, s), 7.15-7.00 (2H, m), 6.85-6.75 ( 1H, m), 1.94 (3H, s), 1.65-1.45 (1H, m), 0.75-0.45 (4H, m).
[2438] Physical property: Flaw.
[2439] Example 446 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methoxybenzenesulfonate (Compound No. 2309)
[2440] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.99-7.91 (2H, m), 7.61 (1H, s), 7.11-6.98 (4H, m), 6.80 (1H, dd, J = 2.6 Hz, 6.6 Hz ), 3.90 (3H, s), 1.95 (3H, s), 1.60-1.45 (1H, m), 0.70-0.45 (4H, m).
[2441] Properties: Caramel statue.
[2442] Example 447 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,4,6-trimethylbenzenesulfonate (Compound No. 2315)
[2443] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.13-6.98 (4H, m), 6.85-6.75 (1H, m), 2.70 (6H, s), 2.32 (3H, s) , 2.04 (3H, s), 1.65-1.45 (1H, m), 0.78-0.44 (4H, m).
[2444] Physical property: Amorphous.
[2445] Example 448 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,4,6-triisopropylbenzenesulfonate (Compound No. 2321)
[2446] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.52 (1H, s), 7.28-7.20 (2H, m), 7.10-6.98 (2H, m), 6.85-6.75 (1H, m), 4.16 (2H, septet, J = 6.6 Hz, 2.93 (1H, septet, J = 6.6 Hz), 1.93 (3H, s), 1.75-1.50 (1H, m), 1.35-1.20 (18H, m), 0.75-0.45 (4H , m).
[2447] Physical property: Amorphous.
[2448] (Example 449) 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazoyl -5-yl 1,2-benzenedisulfonate (Compound No. 2327)
[2449] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.52-8.40 (1H, m), 8.15-8.07 (1H, m), 8.00-7.82 (2H, m), 7.63 (1H, s), 7.18 (2H, s), 7.15-6.97 (3H, m), 6.79 (1H, dd, J = 7.0, 2.6 Hz), 3.84 (3H, s), 2.11 (3H, s), 1.99 (3H, s), 1.75-1.57 (1H, m), 0.74-0.45 (4H, m).
[2450] Properties: Caramel statue.
[2451] Example 450 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-chloro-3-nitrobenzenesulfonate (Compound No. 3786)
[2452] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.55 (1H, d, J = 2.2 Hz), 8.18 (1H, dd, J = 8.8, 2.2 Hz), 7.81 (1H, d, J = 8.8 Hz), 7.59 (1H, s), 7.13-7.06 (2H, m), 6.84-6.79 (1H, m), 1.98 (3H, s), 1.61-1.48 (1H, m), 0.68-0.52 (4H, m).
[2453] Physical property: Amorphous.
[2454] Example 451 6-chloro-3- [2- (2-chloro-2-fluorocyclopropyl) phenoxy] -4-pyridazinol (Compound No. 2519)
[2455] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.42-7.15 (4H, m), 6.70 (1H, s), 2.80-2.62 (1H, m), 2.18-1.65 (2H, m).
[2456] Melting Point (° C): 175-177.
[2457] Example 452 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,5-dichlorobenzenesulfonate (Compound No. 3780)
[2458] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.09-8.08 (1H, m), 7.61-7.52 (3H, m), 7.12-7.01 (2H, m), 6.81-6.76 (1H, m), 1.98 ( 3H, s), 1.67-1.49 (1H, m), 0.82-0.60 (2H, m), 0.58-0.48 (2H, m).
[2459] Physical property: Amorphous.
[2460] Example 453 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 10H-phenothiazine-10-carboxylate (Compound No. 3720)
[2461] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.76-7.67 (3H, m), 7.49-7.40 (3H, m), 7.40-7.23 (3H, m), 7.20-7.10 (2H, m), 6.95- 6.83 (1 H, m), 2.19 (3 H, s), 1.88-1.70 (1 H, m), 0.85-0.57 (4 H, m).
[2462] Physical property: Amorphous.
[2463] Example 454 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 9H-carbazole-9-carboxylate (Compound No. 3714)
[2464] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.40 (2H, d, J = 7.4 Hz), 8.02 (2H, d, J = 7.0 Hz), 7.99 (1H, s), 7.60-7.35 (4H, m ), 7.13-7.03 (2H, m), 6.92-6.80 (1H, m), 2.19 (3H, s), 1.90-1.73 (1H, m), 0.84-0.50 (4H, m).
[2465] Melting point (° C): 157-159.
[2466] Example 455 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,4-dihydro-2 (1H) -isoquinolinecarboxylate (Compound No. 3708 )
[2467] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.32-7.02 (6H, m), 6.90-6.78 (1H, m), 4.86 (1H, s), 4.72 (1H, s) , 3.92 (1H, t, J = 5.9 Hz), 3.81 (1H, t, J = 5.9 Hz), 3.05-2.95 (2H, m), 2.14 (3H, s), 1.86-1.67 (1H, m), 0.80-0.50 (4H, m).
[2468] Properties: Caramel statue.
[2469] Example 456 3- [3- (benzyloxy) phenoxy] -6-chloro-4-pyridazinol (Compound No. 2547)
[2470] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.48-7.25 (6H, m), 6.94-6.66 (4H, m), 5.07 (2H, s).
[2471] Melting point (° C): 184-185.
[2472] Example 457 3- [4- (benzyloxy) phenoxy] -6-chloro-4-pyridazinol (Compound No. 2548)
[2473] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.48-7.28 (5H, m), 7.12-6.96 (4H, m), 6.58 (1H, s), 5.07 (2H, s).
[2474] Melting Point (° C): 170-180.
[2475] Example 458 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-thiomorpholine carboxylate (Compound No. 3702)
[2476] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.53 (1H, s), 7.15-7.04 (2H, m), 6.92-6.80 (1H, m), 4.05-3.78 (4H, m), 2.75-2.64 ( 4H, m), 2.13 (3H, s), 1.85-1.65 (1H, m), 0.80-0.54 (4H, m).
[2477] Properties: Caramel statue.
[2478] Example 459 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,6-dimethyl-4-morpholinecarboxylate (Compound No. 3696)
[2479] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.54 (1H, s), 7.18-7.05 (2H, m), 6.94-6.80 (1H, m), 4.17-3.97 (2H, m), 3.78-3.55 ( 2H, m), 2.95-2.60 (2H, m), 2.14 (3H, s), 1.85-1.67 (1H, m), 1.35-1.15 (6H, m), 0.80-0.54 (4H, m).
[2480] Properties: Caramel statue.
[2481] Example 460 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-morpholinecarboxylate (Compound No. 3690)
[2482] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.13-7.06 (2H, m), 6.90-6.83 (1H, m), 3.70-3.55 (8H, m), 2.14 (3H, s), 1.83-1.68 (1H, m), 0.80-0.65 (2H, m), 0.65-0.53 (2H, m).
[2483] Melting point (° C): 102.5-103.5.
[2484] Example 461 6-Chloro-3-[(1-methyl-1H-indol-4-yl) oxy] -4-pyridazinol (Compound No. 2565)
[2485] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.29 (1H, d, J = 8.4 Hz), 7.17 (1H, t, J = 7.7 Hz), 7.13 (1H, d, J = 2.9 Hz), 6.85 (1H, d, J = 7.7 Hz), 6.72 (1H, s), 6.23 (1H, d, J = 2.9 Hz), 4.87 (3H, s).
[2486] Melting point (° C.): 203-206.
[2487] Example 462 6-Chloro-3-[(1-methyl-1H-indol-7-yl) oxy] -4-pyridazinol (Compound No. 2568)
[2488] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.42 (1H, d, J = 7.0 Hz), 7.07 (1H, d, J = 2.9 Hz), 6.99 (1H, t, J = 7.7 Hz), 6.86 (1H, d, J = 6,6 Hz), 6.74 (1H, s), 6.44 (1H, d, J = 2.9 Hz), 3.80 (3H, s).
[2489] Melting Point (° C): 219-221.
[2490] Example 463 1- {4-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -3-methylphenyl} ethanone (Compound No. 2570)
[2491] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.94-7.86 (2H, m), 7.21-7.16 (1H, m), 6.75 (1H, s), 2.60 (3H, s), 2.25 (3H, s ).
[2492] Melting point (° C): 182-184.
[2493] Example 464 {4-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -3-methylphenyl} ethanone O-methyloxime (Compound No. 2571)
[2494] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.59-7.51 (2H, m), 7.11-7.06 (1H, m), 6.71 (1H, s), 3.95 (3H, s), 2.20 (3H, s ).
[2495] Melting Point (° C): 189-192.
[2496] Example 465 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-phenyl-1-piperazinecarboxylate (Compound No. 3684)
[2497] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.60 (1H, s), 7.35-7.23 (2H, m), 7.13-7.04 (2H, m), 7.00-6.80 (4H, m), 3.95-3.84 ( 2H, m), 3.84-3.72 (2H, m), 3.31-3.18 (4H, m), 2.15 (3H, s), 1.86-1.66 (1H, m), 0.80-0.53 (4H, m).
[2498] Properties: Caramel statue.
[2499] Example 466 4-{[4- (benzoyloxy) -6-chloro-3-pyridazinyl] oxy} -3-methylphenyl benzoate (Compound No. 3850)
[2500] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.21-8.17 (4H, m), 7.72-7.48 (7H, m), 7.22-7.07 (3H, m), 2.21 (3H, s).
[2501] Melting Point (° C): 118-120.
[2502] Example 467 Methyl 3-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -4-methoxybenzoate (Compound No. 2574)
[2503] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.95 (1H, dd J = 8.6, 2.2 Hz), 7.78 (1H, d, J = 1.8 Hz), 7.19 (1H, d, J = 8.8 Hz), 6.71 (1H, s), 3.87 (3H, s), 3.84 (3H, s).
[2504] Melting Point (° C): 115-123.
[2505] Example 468 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methyl-1-piperazinecarboxylate (Compound No. 3678)
[2506] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.15-7.04 (2H, m), 6.90-6.80 (1H, m), 3.80-3.55 (4H, m), 2.54-2.40 ( 4H, m), 2.32 (3H, s), 2.14 (3H, s), 1.85-1.67 (1H, m), 0.80-0.52 (4H, m).
[2507] Properties: Caramel statue.
[2508] Example 469 6-Chloro-3- (2-isopropenyl-6-methylphenoxy) -4-pyridazinol (Compound No. 2577)
[2509] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.20-7.10 (3H, m), 6.66 (1H, s), 5.01 (1H, m), 4.95 (1H, m), 2.15 (3H, s), 1.99 (3H, s).
[2510] Melting point (° C.): 183-186.
[2511] Example 470 6-chloro-3-[(1,1-dimethyl-2,3-dihydro-1H-inden-5-yl) oxy-4-pyridazinol (Compound No. 2585)
[2512] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.15 (1H, d, J = 8.1 Hz), 6.95 (2H, br.d, J = 8.1 Hz), 6.68 (1H, s), 2.89 (2H, t, J = 7.3 Hz, 1.96 (2H, t, J = 7.3 Hz), 1.27 (6H, s).
[2513] Melting point (° C): 209-212.
[2514] Example 471 3- (3-Bromo-6-cyclopropyl-2-methylphenoxy) -6-chloro-4-pyridazinol (Compound No. 2587)
[2515] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.38 (1H, d, J = 8.4 Hz), 6.78 (1H, d, J = 8.4 Hz), 6.72 (1H, s), 2.22 (3H, s) , 1.85-1.72 (1H, m), 0.85-0.72 (2H, m), 0.65-0.50 (2H, m).
[2516] Melting point (° C.): 234-235.
[2517] Example 472 6-Chloro-3- (6-cyclopropyl-2-methyl-3-nitrophenoxy) -4-pyridazinol (Compound No. 2589)
[2518] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.80 (1H, d, J = 8.4 Hz), 7.02 (1H, d, J = 8.4 Hz), 6.77 (1H, s), 2.32 (3H, s) , 1.99-1.88 (1H, m), 0.95-0.88 (2H, m), 0.74-0.70 (2H, m).
[2519] Melting point (° C.): 140-143.
[2520] Example 473 6-Chloro-3-[(5-methyl-1,3-dihydro-2-benzofuran-4-yl) oxy] -4-pyridazinol (Compound No. 2592)
[2521] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.20 (1H, d, J = 7.7 Hz), 7.08 (1H, d, J = 7.7 Hz), 5.06 (2H, br.s), 4.88 (2H, br.s), 2.16 (3H, s).
[2522] Melting Point (° C): 188-200.
[2523] Example 474 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,2,6,6-tetramethyl-1-piperidinecarboxylate (compound Number 3672)
[2524] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7,53 (1H, s), 7.14-7.03 (2H, m), 6.90-6.78 (1H, m), 2.13 (3H, s), 1.90-1.62 ( 7H, m), 1.55 (12H, s), 0.80-0.52 (4H, m).
[2525] Properties: Caramel statue.
[2526] Example 475 6-Chloro-3- (2-fluoro-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 2597)
[2527] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.92 (1H, d, J = 7.0 Hz), 6.73 (1H, s), 2.24 (3H, s), 2.21 (3H, s), 2.06 (3H, s).
[2528] Melting point (° C.): 258-260.
[2529] Example 476 6-Chloro-3- (2-chloro-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 2599)
[2530] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 7.11 (1H, s), 6.86 (1H, br, s), 2.29 (3H, s), 2.24 (3H, s), 1.99 (3H, s) .
[2531] Melting point (° C): 298-300.
[2532] Example 477 6-chloro-3- (2-iodo-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 2600)
[2533] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.06 (1H, s), 6.75 (1H, s), 2.40 (3H, s), 2.26 (3H, s), 2.09 (3H, s).
[2534] Melting point (° C.): 235 (decomposition).
[2535] Example 478 6-chloro-3- (2-ethyl-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 2601)
[2536] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 6.95 (1H, s), 6.81 (1H, br.s), 2.32 (2H, q, J = 7.5 Hz), 2.24 (3H, s), 2.12 (3H, s), 1.94 (3H, s), 1.04 (3H, t, J = 7.5 Hz).
[2537] Melting Point (° C): 188-195.
[2538] Example 479 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1,4-dioxa-8-azaspiro [4.5] decane-8-carboxylate (Compound No. 3666)
[2539] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.15-7.04 (2H, m), 6.92-6.80 (1H, m), 3.99 (4H, s), 3.85-3.62 (4H, m), 2.14 (3H, s), 1.85-1.65 (5H, m), 0.80-0.50 (4H, m).
[2540] Properties: Caramel statue.
[2541] Example 480 6-Chloro-3- (2-isopropenyl-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 2605)
[2542] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.91 (1H, s), 6.58 (1H, s), 5.00-4.90 (2H, bm), 2.27 (3H, s), 2.20 (3H, s), 2.07 (3H, s), 1.96 (3H, s).
[2543] Physical property: Amorphous.
[2544] Example 481 1- [6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] 4-ethyl 1,4-piperidine dicarboxylate (Compound No. 3660)
[2545] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56 (1H, s), 7.13-7.04 (2H, m), 6.90-6.80 (1H, m), 4.30-4.00 (2H, m), 3.35-3.02 ( 2H, m), 2.65-2.45 (1H, m), 2.14 (3H, s), 2.10-1.93 (3H, m), 1.93-1.65 (4H, m), 1.25 (3H, t, J = 7.0 Hz) , 0.80-0.54 (4H, m).
[2546] Properties: Caramel statue.
[2547] Example 482 1- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -3,4,6-trimethylphenyl} ethanone (Compound No. 2607)
[2548] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.55 (1H, s), 6.72 (1H, s), 2.45 (3H, s), 2.36 (3H, s), 2.29 (3H, s), 2.11 ( 3H, s).
[2549] Physical property: Amorphous.
[2550] Example 483 6-Chloro-3- (2,3,5-trimethyl-6-nitrophenoxy) -4-pyridazinol (Compound No. 2608)
[2551] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.11 (1H, s), 6.65 (1H, s), 2.33 (3H, s), 2.28 (3H, s), 2.05 (3H, s).
[2552] Melting point (° C): 172-174.
[2553] Example 484 6-Chloro-3- (2,4-dichloro-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 2609)
[2554] ¹ H-NMR (200 MHz, DMSO-d ₆ ) δ ppm: 6.91 (1H, s), 2.46 (3H, s), 2.36 (3H, s), 2.10 (3H, s).
[2555] Example 485 6-Chloro-3- (2,3,4,5,6-pentamethylphenoxy) -4-pyridazinol (Compound No. 2614)
[2556] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.69 (1H, s), 2.23 (3H, s), 2.21 (6H, s), 2.02 (6H, s).
[2557] Melting point (° C.): 238-240 (decomposition).
[2558] Example 486 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,3-dimethylbutanoate (Compound No. 2662)
[2559] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.37 (1H, s), 7.13-7.05 (2H, s), 6.88-6.82 (1H, s), 2.55 (2H, s), 2.12 (3H, s) , 1.82-1.67 (1H, m), 1.15 (9H, s), 0.80-0.65 (2H, m), 0.63-0.52 (2H, m).
[2560] Melting Point (° C): 91-92.
[2561] Example 487 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-adamantanecarboxylate (Compound No. 2671)
[2562] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.37 (1H, s), 7.12-7.05 (2H, m), 6.92-6.80 (1H, m), 2.13 (3H, s), 2.08 (9H, s) , 1.76 (7 H, br.s), 0.85-0.45 (4 H, m).
[2563] Properties: Oily substance.
[2564] Example 488 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methylacrylate (Compound No. 2677)
[2565] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.48 (1H, s), 7.14-7.05 (2H, m), 6.89-6.83 (1H, m), 6.46 (1H, br.s), 5.91 (1H, br.s), 2.13 (3H, s), 2.09 (3H, s), 1.81-1.68 (1H, m), 0.78-0.53 (4H, m).
[2566] Melting Point (℃): 98-100.
[2567] Example 489 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-bromo-2-methylpropanoate (Compound No. 2697)
[2568] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.47 (1H, s), 7.11-7.08 (2H, m), 6.89-6.85 (1H, m), 2.13 (3H, s), 2.10 (6H, s) , 1.77-1.69 (1H, m), 0.74-0.58 (4H, m).
[2569] Melting point (° C.): 69-71.
[2570] Example 490 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-chloro-2,2-dimethylpropanoate (Compound No. 2703)
[2571] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.43 (1H, s), 7.13-7.05 (2H, m), 6.90-6.84 (1H, m), 3.76 (2H, s), 2.13 (3H, s) , 1.83-1.65 (1H, m), 1.50 (6H, s), 0.85-0.45 (4H, brs).
[2572] Melting point (° C.): 112-115.
[2573] Example 491 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-bromopentanoate (Compound No. 2709)
[2574] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.83 (1H, s), 7.11-7.05 (2H, m), 6.86-6.82 (1H, m), 3.43 (2H, d, J = 6.2 Hz), 2.73 (2H, d, J = 7.0 Hz), 2.12 (3H, s), 2.04-1.93 (4H, m), 1.77-1.69 (1H, m), 0.74-0.56 (4H, m).
[2575] Properties: Caramel statue.
[2576] Example 492 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl hydratroate (Compound No. 2715)
[2577] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.42-7.20 (5H, m), 7.32 (1H, s), 7.15-7.02 (2H, m), 6.86-6.75 (1H, m), 4.20-4.00 ( 1H, m), 2.04 (3H, s), 1.66 (3H, d, J = 7.0 Hz), 1.70-1.50 (1H, m), 0.70-0.42 (4H, m).
[2578] Properties: Oily substance.
[2579] Example 493 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl (4-methoxyphenyl) acetate (Compound No. 2721)
[2580] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.37 (1H, s), 7.27 (2H, d, J = 8.2 Hz), 7.13-7.05 (2H, m), 6.89-6.80 (3H, m), 3.91 (2H, s), 3.76 (3H, s), 2.07 (3H, s), 1.73-1.60 (1H, m), 0.75-0.50 (4H, m).
[2581] Physical property: Paste form.
[2582] Example 494 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl ethyl succinate (Compound No. 2727)
[2583] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.08-6.92 (2H, m), 6.85-6.68 (1H, m), 6.55 (1H, s), 4.14 (2H, br.q, J = 7.1 Hz) , 3.00 (1H, t, J = 7.0 Hz), 2.76 (1H, t, J = 7.0 Hz), 2.61 (2H, br, s), 1.98 (3H, s), 1.78-1.60 (1H, m), 1.25 (3H, t, J = 7.1 Hz), 0.75-0.40 (4H, m).
[2584] Physical property: Amorphous.
[2585] Example 495 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methyl-1-piperidinecarboxylate (Compound No. 3654)
[2586] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56 (1H, s), 7.14-7.04 (2H, m), 6.90-6.80 (1H, m), 4.35-4.10 (2H, m), 3.15-2.80 ( 2H, m), 2.14 (3H, s), 1.85-1.50 (4H, m), 1.35-1.06 (2H, m), 0.96 (3H, d, J = 6.2 Hz), 0.80-0.50 (4H, m) .
[2587] Properties: Caramel statue.
[2588] Example 496 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-bromo-1-piperidinecarboxylate (Compound No. 3648)
[2589] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.55 (1H, s), 7.15-7.04 (2H, m), 6.90-6.80 (1H, m), 4.54-4.38 (1H, m), 4.00-3.53 ( 4H, m), 2.30-1.90 (7H, m), 1.85-1.67 (1H, m), 0.80-0.50 (4H, m).
[2590] Properties: Caramel statue.
[2591] Example 497 Bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] succinate (Compound No. 2733)
[2592] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.32 (2H, s), 7.14-7.03 (4H, m), 6.88-6.81 (2H, m), 3.17 (4H, s), 2.10 (6H, s) , 1.80-1.65 (2H, m), 0.78-0.53 (8H, m).
[2593] Properties: Caramel statue.
[2594] Example 498 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methoxyacetate (Compound No. 2752)
[2595] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.43 (1H, s), 7.15-7.04 (2H, m), 6.90-6.82 (1H, m), 4.41 (2H, s), 3.55 (3H, s) , 2.12 (3H, s), 1.82-1.67 (1H, m), 0.80-0.67 (2H, m), 0.64-0.55 (2H, m).
[2596] Physical property: Paste form.
[2597] Example 499 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl phenoxyacetate (Compound No. 2758)
[2598] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.42 (1H, s), 7.29-7.25 (2H, m), 7.23-6.96 (5H, m), 6.89-6.83 (1H, m), 5.00 (2H, s), 2.08 (3H, s), 1.73-1.64 (1H, m), 0.71-0.54 (4H, m).
[2599] Properties: Caramel statue.
[2600] Example 500 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-phenoxypropanoate (Compound No. 2764)
[2601] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.33 (1H, s), 7.25-7.19 (2H, m), 7.17-7.04 (2H, m), 7.00-6.91 (3H, m), 6.86-6.82 ( 1H, m), 5.09 (1H, q, J = 6.6 Hz), 2.05 (3H, s), 1.84 (3H, d, J = 6.6 Hz), 1.64-1.58 (1H, m), 0.68-0.52 (4H , m).
[2602] Properties: Caramel statue.
[2603] Example 501 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methoxy (phenyl) acetate (Compound No. 2770)
[2604] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56-7.51 (2H, m), 7.40-7.30 (4H, m), 7.12-7.02 (2H, m), 6.83-6.78 (1H, m), 5.10 ( 1H, s), 3.52 (3H, s), 2.01 (3H, s), 1.67-1.50 (1H, m), 0.70-0.43 (4H, m).
[2605] Physical property: Paste form.
[2606] Example 502 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3- (methylsulfanyl) propanoate (Compound No. 2776)
[2607] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.42 (1H, s), 7.10-7.00 (2H, m), 6.90-6.77 (1H, m), 3.07-2.83 (4H, m), 2.17 (3H, s), 2.12 (3H, s), 1.85-1.65 (1H, m), 0.80-0.50 (4H, m).
[2608] Properties: Caramel statue.
[2609] Example 503 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl oxo (2-thienyl) acetate (Compound No. 2782)
[2610] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.07 (1H, dd, J = 1.5 Hz, 4.1 Hz), 7.77 (1H, dd, J = 1.5 Hz, 4.1 Hz), 7.58 (1H, s), 7.22 (1H, t, J = 4.0 Hz), 7.10-7.02 (2H, m), 6.90-6.77 (1H, m), 2.15 (3H, s), 1.90-1.70 (1H, m), 0.85-0.50 (4H , m).
[2611] Properties: Caramel statue.
[2612] Example 504 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-fluorobenzoate (Compound No. 2788)
[2613] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.17-8.09 (1H, m), 7.73-7.62 (1H, m), 7.57 (1H, s), 7.36-7.20 (2H, m), 7.09-7.07 ( 2H, m), 6.87-6.82 (1H, m), 2.16 (3H, s), 1.85-1.72 (1H, m), 0.76-0.56 (4H, m).
[2614] Physical property: Amorphous.
[2615] Example 505 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-bromobenzoate (Compound No. 2805)
[2616] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.20-8.05 (1H, m), 7.85-7.70 (1H, m), 7.59 (1H, s), 7.55-7.38 (2H, m), 7.15-7.00 ( 2H, m), 6.90-6.80 (1H, m), 2.17 (3H, s), 1.88-1.70 (1H, m), 0.80-0.50 (4H, m).
[2617] Properties: Caramel statue.
[2618] Example 506 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-iodobenzoate (Compound No. 2814)
[2619] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.20-8.05 (2H, m), 7.60-7.44 (2H, m), 7.35-7.20 (1H, m), 7.13-7.00 (2H, m), 6.90- 6.78 (1 H, m), 2.17 (3 H, s), 1.90-1.72 (1 H, m), 0.85-0.50 (4 H, m).
[2620] Properties: Caramel statue.
[2621] Example 507 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2- (trifluoromethyl) benzoate (Compound No. 2820)
[2622] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.13-8.09 (1H, m), 7.91-7.86 (1H, m), 7.76-7.72 (2H, m), 7.55 (1H, s), 7.11-7.06 ( 2H, m), 6.88-6.83 (1H, m), 2.16 (3H, s), 1.86-1.71 (1H, m), 0.75-0.56 (4H, m).
[2623] Properties: Caramel statue.
[2624] Example 508 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-benzylbenzoate (Compound No. 2826)
[2625] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.22-8.18 (1H, d, J = 7.2 Hz), 7.62-7.54 (1H, t, J = 7.6 Hz), 7.44-7.06 (10H, m), 6.85 -6.81 (1H, m), 4.46 (1H, s), 2.11 (3H, s), 1.80-1.67 (1H, m), 0.75-0.64 (2H, m), 0.60-0.52 (2H, m).
[2626] Physical property: Paste form.
[2627] Example 509 Bis [6-chloro-3- (2-methylphenoxy) -4-pyridazinyl] phthalate (Compound No. 2827)
[2628] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.06 (2H, dd, J = 6.0, 3.4 Hz), 7.57 (2H, s), 7.25-7.15 (8H, m), 7.05-7.01 (2H, m) , 2.14 (6H, s).
[2629] Melting point (° C): 157-158.
[2630] Example 510 1- [6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] 2-methyl 1,2-piperidinedicarboxylate (Compound No. 3642)
[2631] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.60 (0.5H, s), 7.59 (0.5H, s), 7.14-7.03 (2H, m), 6.92-6.80 (1H, m), 5.10-4.90 ( 1H, m), 4.32-4.06 (1H, m), 3.73 (1.5H, s), 3.71 (1.5H, s), 3.40-3.05 (1H, m), 2.43-2.20 (1H, m), 2.15 ( 1.5H, s), 2.13 (1.5H, s), 2.00-1.20 (6H, m), 0.80-0.50 (4H, m).
[2632] Properties: Caramel statue.
[2633] Example 511 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-nitrobenzoate (Compound No. 2850)
[2634] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.15-8.05 (1H, m), 7.95-7.72 (3H, m), 7.65 (1H, s), 7.14-7.05 (2H, m), 6.90-6.80 ( 1H, m), 2.15 (3H, s), 1.85-1.70 (1H, m), 0.78-0.65 (2H, m), 0.65-0.50 (2H, m).
[2635] Properties: Oily substance.
[2636] Example 512 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-phenoxybenzoate (Compound No. 2856)
[2637] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.35 (1H, dd, J = 8.2, 1.8 Hz), 8.15 (1H, dd, J = 8.0, 1.8 Hz), 7.74 (1H, dt, J = 7.0, 1.4 Hz), 7.61-7.21 (5H, m), 7.15-6.98 (4H, m), 6.84-6.79 (1H, m), 2.09 (3H, s), 1.80-1.68 (1H, m), 0.70-0.71 (2H, m), 0.59-0.51 (2H, m).
[2638] Physical property: Paste form.
[2639] Example 513 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-chlorobenzoate (Compound No. 2868)
[2640] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.18 (1H, d, J = 1.8 Hz), 8.10 (1H, d, J = 8.1 Hz), 7.68 (1H, br.d, J = 9.2 Hz), 7.57 (1H, s), 7.50 (1H, t, J = 8.1 Hz), 7.08 (1H, d, J = 5.8 Hz), 7.07 (1H, d, J = 3.7 Hz), 6.85 (1H, dd, J = 5.8, 3.7 Hz), 2.15 (3H, s), 1.85-1.66 (1H, m), 0.80-0.50 (4H, m).
[2641] Physical property: Amorphous.
[2642] Example 514 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-fluorobenzoate (Compound No. 2862)
[2643] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.02 (1H, dd, J = 6.2, 1.5 Hz), 7.89 (1H, br.d, J = 8.8 Hz), 7.60-7.34 (2H, m), 7.59 (1H, s), 7.13-7.04 (2H, m), 6.90-6.78 (1H, m), 2.15 (3H, s), 1.83-1.68 (1H, m), 0.80-0.50 (4H, m).
[2644] Properties: Oily substance.
[2645] Example 515 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-bromobenzoate (Compound No. 2874)
[2646] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.33 (1H, s), 8.14 (1H, d, J = 8.0 Hz), 7.82 (1H, d, J = 8.0 Hz), 7.56 (1H, s), 7.43 (1H, t, J = 8.0 Hz), 7.13-7.03 (2H, m), 6.90-6.80 (1H, m), 2.15 (3H, s), 1.85-1.68 (1H, m), 0.80-0.50 ( 4H, m).
[2647] Properties: Caramel statue.
[2648] Example 516 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-iodobenzoate (Compound No. 2880)
[2649] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.54 (1H, d, J = 1.8 Hz), 8.20-8.15 (1H, m), 8.03 (1H, d, J = 8.1 Hz), 7.56 (1H, s ), 7.34-7.26 (1H, m), 7.13-7.05 (2H, m), 6.89-6.82 (1H, m), 2.15 (3H, s), 1.83-1.71 (1H, m), 0.80-0.68 (2H) m), 0.65-0.52 (2H, m).
[2650] Physical property: Amorphous.
[2651] Example 517 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3- (trifluoromethyl) benzoate (Compound No. 2900)
[2652] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.47 (1H, s), 8.41 (1H, d, J = 7.7 Hz), 7.96 (1H, d, J = 7.3 Hz), 7.75-7.67 (1H, m ), 7.58 (1H, s), 7.12-7.06 (2H, m), 6.89-6.82 (1H, m), 2.16 (3H, s), 1.84-1.71 (1H, m), 0.80-0.53 (4H, m) ).
[2653] Properties: Caramel statue.
[2654] Example 518 Bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] isophthalate (Compound No. 2906)
[2655] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.02 (1H, s), 8.53 (2H, d, J = 8.2 Hz), 7.78 (1H, t, J = 7.8 Hz), 7.58 (2H, s), 7.08-7.06 (4H, m), 6.86-6.82 (2H, m), 2.14 (6H, s), 1.83-1.68 (2H, m), 0.78-0.69 (4H, m), 0.60-0.53 (4H, m ).
[2656] Physical property: Paste form.
[2657] Example 519 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-nitrobenzoate (Compound No. 2918)
[2658] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.05-9.04 (1H, m), 8.59-8.52 (2H, m), 7.79 (1H, t, J = 7.7 Hz), 7.59 (1H, s), 7.13 -7.07 (2H, m), 6.89-6.82 (1H, m), 2.15 (3H, s), 1.83-1.72 (1H, m), 0.80-0.54 (4H, m).
[2659] Properties: Caramel statue.
[2660] Example 520 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-phenoxybenzoate (Compound No. 2924)
[2661] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.95-7.90 (1H, m), 7.80-7.78 (1H, m), 7.57 (1H, s), 7.50 (1H, t, J = 8.0 Hz), 7.40 -7.30 (3H, m), 7.17-7.10 (1H, m), 7.09-7.03 (3H, m), 7.07 (1H, s), 6.87-6.82 (1H, m), 2.13 (3H, s), 1.81 -1.67 (1 H, m), 0.78-0.66 (2 H, m). 0.59-0.54 (2H, m).
[2662] Physical property: Paste form.
[2663] Example 521 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-fluorobenzoate (Compound No. 2930)
[2664] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.30-8.18 (2H.m), 7.59 (1H, s), 7.30-7.15 (2H, m), 7.15-7.02 (2H, m), 6.90-6.78 ( 1H, m), 2.15 (3H, s), 1.85-1.70 (1H, m), 0.80-0.50 (4H, m).
[2665] Properties: Caramel statue.
[2666] Example 522 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-ethylbenzoate (Compound No. 2961)
[2667] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.13 (2H, d, J = 8.5 Hz), 7.60 (1H, s), 7.36 (2H, d, J = 8.5 Hz), 7.12-7.04 (2H, m ), 6.88-6.81 (1H, m), 2.75 (2H, q, J = 7.6 Hz), 2.04 (3H, s), 1.85-1.71 (1H, m), 1.28 (3H, t, J = 7.6 Hz) , 0.79-0.65 (2H, m), 0.61-0.52 (2H, m).
[2668] Physical property: Paste form.
[2669] Example 523 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-propylbenzoate (Compound No. 2970)
[2670] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.12 (2H, d, J = 8.4 Hz), 7.59 (1H, s), 7.34 (2H, d, J = 8.4 Hz), 7.12-7.05 (2H, m ), 6.88-6.81 (1H, m), 2.69 (2H, t, J = 7.3 Hz), 2.16 (3H, s), 1.85-1.60 (3H, m), 0.96 (3H, t, J = 7.3 Hz) , 0.80-0.68 (2H, m), 0.63-0.52 (2H, m).
[2671] Physical property: Paste form.
[2672] Example 524 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-isopropylbenzoate (Compound No. 2976)
[2673] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.14 (2H, d, J = 8.4 Hz), 7.59 (1H, s), 7.40 (2H, d, J = 8.4 Hz), 7.12-7.05 (2H, m ), 6.90-6.82 (1H, m), 3.01 (1H, septet, J = 7.0 Hz), 2.15 (3H, s), 1.85-1.70 (1H, m), 1.29 (6H, d, J = 7.0 Hz) , 0.80-0.65 (2H, m), 0.63-0.52 (2H, m).
[2674] Physical property: Paste form.
[2675] Example 525 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-butylbenzoate (Compound No. 2982)
[2676] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.12 (2H, d, J = 8.1 Hz), 7.59 (1H, s), 7.35 (2H, d, J = 8.1 Hz), 7.12-7.03 (2H, m ), 6.89-6.81 (1H, m), 2.72 (2H, t, J = 7.3 Hz), 2.16 (3H, s), 1.85-1.57 (3H, m), 1.47-1.22 (2H, m), 0.94 ( 3H, t, J = 7.3 Hz, 0.80-0.68 (2H, m), 0.65-0.55 (2H, m).
[2677] Physical property: Paste form.
[2678] Example 526 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (trifluoromethyl) benzoate (Compound No. 2988)
[2679] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.34 (2H, d, J = 8.8 Hz), 7.83 (2H, d, J = 8.8 Hz), 7.60 (1H, s), 7.14-7.07 (2H, m ), 6.89-6.83 (1H, m), 2.15 (3H, s), 1.83-1.72 (1H, m), 0.79-0.71 (2H, m), 0.63-0.54 (2H, m).
[2680] Melting point (° C.): 127-128.
[2681] Example 527 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-cyanobenzoate (Compound No. 2994)
[2682] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.33 (2H, d, J = 8.8 Hz), 7.86 (2H, d, J = 8.8 Hz), 7.60 (1H, s), 7.14-7.07 (2H, m ), 6.89-6.83 (1H, m), 2.14 (3H, s), 1.82-1.68 (1H, m), 0.79-0.53 (4H, m).
[2683] Properties: Caramel statue.
[2684] Example 528 Bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] terephthalate (Compound No. 3001)
[2685] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.39 (4H, s), 7.62 (2H, s), 7.10-7.07 (4H, m), 6.87-6.83 (2H, m), 2.15 (6H, s) , 1.81-1.68 (2H, m), 0.78-0.70 (4H, m), 0.61-0.53 (4H, m).
[2686] Melting point (° C): 247-249.
[2687] Example 529 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl [1,1'-biphenyl] -4-carboxylate (Compound No. 3016)
[2688] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.31-8.23 (2H, m), 7.79-7.74 (2H, m), 7.67-7.62 (3H, m), 7.54-7.42 (3H, m), 7.09- 7.06 (2H, m), 6.87-6.82 (1H, m), 2.17 (3H, s), 1.84-1.75 (1H, m), 0.77-0.56 (4H, m).
[2689] Melting Point (° C): 135-137.
[2690] Example 530 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (trifluoromethoxy) benzoate (Compound No. 3022)
[2691] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.28 (2H, d, J = 9.2 Hz), 7.59 (1H, s), 7.38 (2H, d, J = 9.2 Hz), 7.14-7.04 (2H, m ), 6.89-6.82 (1H, m), 2.15 (3H, s), 1.83-1.69 (1H, m), 0.78-0.65 (2H, m), 0.62-0.53 (2H, m).
[2692] Physical property: Paste form.
[2693] Example 531 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (benzyloxy) benzoate (Compound No. 3028)
[2694] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.16 (2H, d, J = 9.2 Hz), 7.60 (1H, s), 7.50-7.30 (5H, m), 7.10-7.03 (4H, m), 6.89 -6.82 (1H, m), 5.17 (2H, s), 2.15 (3H, s), 1.85-1.72 (1H, m), 0.80-0.68 (2H, m), 0.65-0.53 (2H, m).
[2695] Physical property: Paste form.
[2696] Example 532 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,3-difluorobenzoate (Compound No. 3034)
[2697] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.93-7.85 (1H, m), 7.57 (1H, s), 7.57-7.44 (1H, m), 7.32-7.21 (1H, m), 7.10-7.05 ( 2H, m), 6.87-6.82 (1H, m), 2.15 (3H, s), 1.81-1.73 (1H, m), 0.76-0.72 (2H, m), 0.60-0.56 (2H, m).
[2698] Physical property: Paste form.
[2699] Example 533 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-fluoro-3- (trifluoromethyl) benzoate (Compound No. 3040)
[2700] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.36-8.28 (1H, m), 7.99-7.92 (1H, m), 7.56 (1H, s), 7.49-7.41 (1H, m), 7.13-7.05 ( 2H, m), 6.89-6.83 (1H, m), 2.15 (3H, s), 1.84-1.72 (1H, m), 0.80-0.54 (4H, m).
[2701] Physical property: Amorphous.
[2702] Example 534 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,3-dimethylbenzoate (Compound No. 3046)
[2703] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.00-7.96 (1H, m), 7.54 (1H, s), 7.45-7.41 (1H, m), 7.27-7.20 (1H, m), 7.14-7.05 ( 2H, m), 6.89-6.82 (1H, m), 2.57 (3H, s), 2.37 (3H, s), 2.16 (3H, s), 1.86-1.72 (1H, m), 0.79-0.69 (2H, m), 0.61-0.53 (2H, m).
[2704] Physical property: Paste form.
[2705] Example 535 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-chloro-2-methylbenzoate (Compound No. 3052)
[2706] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.04 (1H, d, J = 8.1 Hz), 7.65 (1H, d, J = 8.1 Hz), 7.54 (1H, s), 7.33-7.25 (1H, m ), 7.13-7.06 (2H, m), 6.89-6.83 (1H, m), 2.73 (3H, s), 2.15 (3H, s), 1.83-1.71 (1H, m), 0.79-0.68 (2H, m) ), 0.65-0.53 (2H, m).
[2707] Physical property: Amorphous.
[2708] Example 536 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,4-difluorobenzoate (Compound No. 3058)
[2709] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.23-8.12 (1H, m), 7.56 (1H, s), 7.10-6.94 (4H, m), 6.87-6.82 (1H, m), 2.15 (3H, s), 1.81-1.73 (1H, m), 0.75-0.56 (4H, m).
[2710] Physical property: Amorphous.
[2711] Example 537 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-chloro-2-fluorobenzoate (Compound No. 3064)
[2712] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.07 (1H, dd, J = 7.4 Hz, 8.5 Hz), 7.55 (1H, s), 7.38-7.22 (2H, m), 7.14-7.03 (2H, m ), 6.90-6.78 (1H, m), 2.15 (3H, s), 1.85-1.68 (1H, m), 0.80-0.50 (4H, m).
[2713] Properties: Caramel statue.
[2714] Example 538 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-fluoro-4- (trifluoromethyl) benzoate (Compound No. 3070)
[2715] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.30-8.22 (1H, m), 7.61-7.52 (2H, m), 7.57 (1H, s), 7.14-7.05 (2H, m), 6.87-6.82 ( 1H, m), 2.15 (3H, m), 1.83-1.69 (1H, m), 0.78-0.70 (2H, m), 0.65-0.55 (2H, m).
[2716] Physical property: Paste form.
[2717] Example 539 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-chloro-4-fluorobenzoate (Compound No. 3076)
[2718] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.25-8.18 (1H, m), 7.57 (1H, s), 7.34-7.29 (1H, m), 7.19-7.05 (3H, m), 6.89-6.82 ( 1H, m), 2.15 (3H, m), 1.84-1.70 (1H, m), 0.79-0.68 (2H, m), 0.64-0.53 (2H, m).
[2719] Physical property: Paste form.
[2720] Example 540 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-bromo-2-chlorobenzoate (Compound No. 3082)
[2721] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.01 (1H, d, J = 8.4), 7.76 (1H, d, J = 1.8), 7.60-7.55 (2H, m), 7.10-7.07 (2H, m ), 6.87-6.83 (1H, m), 2.15 (3H, s), 1.83-1.71 (1H, m), 0.77-0.71 (2H, m), 0.62-0.56 (2H, m).
[2722] Physical property: Paste form.
[2723] Example 541 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-bromo-2-methylbenzoate (Compound No. 3088)
[2724] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.05 (1H, d, J = 8.4), 7.56-7.48 (3H, m), 7.09-7.07 (2H, m), 6.86-6.82 (1H, m), 2.14 (3H, s), 2.04 (3H, s), 1.85-1.72 (1H, m), 0.79-0.71 (2H, m), 0.64-0.55 (2H, m).
[2725] Physical property: Paste form.
[2726] Example 542 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,4-dimethylbenzoate (Compound No. 3094)
[2727] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.11 (1H, d, J = 8.9 Hz), 7.57 (1H, s), 7.16-7.13 (2H, m), 7.09-7.05 (2H, m), 6.88 -6.81 (1H, m), 2.65 (3H, s), 2.41 (3H, s), 2.15 (3H, s), 1.85-1.71 (1H, m), 0.80-0.68 (2H, m), 0.67-0.55 (2H, m).
[2728] Physical property: Paste form.
[2729] Example 543 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,5-dichlorobenzoate (Compound No. 3100)
[2730] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.10 (1H, d, J = 2.2 Hz), 7.60-7.45 (3H, m), 7.15-7.04 (2H, m), 6.90-6.78 (1H, m) , 2.15 (3H, s), 1.85-1.70 (1H, m), 0.80-0.50 (4H, m).
[2731] Melting Point (° C): 128-130.
[2732] Example 544 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-bromo-2-chlorobenzoate (Compound No. 3106)
[2733] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.20 (1H, d, J = 2.2 Hz), 7.68 (1H, dd, J = 2.2 Hz, 8.4 Hz), 7.54 (1H, s), 7.43 (1H, d, J = 8.4 Hz), 7.14-7.03 (2H, m), 6.92-6.80 (1H, m), 2.15 (3H, s), 1.87-1.70 (1H, m), 0.85-0.50 (4H, m) .
[2734] Properties: Caramel statue.
[2735] Example 545 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-bromo-5-methoxybenzoate (Compound No. 3112)
[2736] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.67-7.57 (3H, m), 7.12-7.00 (3H, m), 6.87-6.82 (1H, m), 3.85 (3H, s), 2.16 (3H, s), 1.87-1.75 (1H, m), 0.80-0.68 (2H, m), 0.65-0.55 (2H, m).
[2737] Physical property: Paste form.
[2738] Example 546 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,5-dimethylbenzoate (Compound No. 3129)
[2739] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.99 (1H, s), 7.54 (1H, s), 7.37-7.30 (1H, m), 7.25-7.21 (1H, m), 7.13-7.05 (2H, m), 6.89-6.82 (1H, m), 2.63 (3H, s), 2.40 (3H, s), 2.16 (3H, s), 1.86-1.72 (1H, m), 0.80-0.70 (2H, m) , 0.62-0.54 (2H, m).
[2740] Properties: Oily substance.
[2741] Example 547 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,6-difluorobenzoate (Compound No. 3138)
[2742] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.68-7.50 (2H, m), 7.15-7.00 (4H, m), 6.90-6.77 (1H, m), 2.15 (3H, s), 1.90-1.70 ( 1 H, m), 0.85-0.50 (4 H, m).
[2743] Properties: Caramel statue.
[2744] Example 548 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-chloro-6-fluorobenzoate (Compound No. 3144)
[2745] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.57-7.00 (5H, m), 6.90-6.78 (1H, m), 2.16 (3H, s), 1.90-1.75 (1H, m), 0.80-0.50 (4H, m).
[2746] Properties: Caramel statue.
[2747] Example 549 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,6-dichlorobenzoate (Compound No. 3150)
[2748] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.43-7.41 (3H, m), 7.11-7.08 (2H, m), 6.88-6.83 (1H, m), 2.17 (3H, s), 1.85-1.77 (1H, m), 0.74-0.56 (4H, m).
[2749] Physical property: Amorphous.
[2750] Example 550 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,6-dimethylbenzoate (Compound No. 3156)
[2751] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.48 (1H, s), 7.32 (1H, dd, J = 8.4, 7.0 Hz), 7.15-7.07 (3H, m), 6.87-6.83 (1H, m) 2.53 (6H, s), 2.16 (3H, s), 1.84-1.76 (1H, m), 0.75-0.69 (2H, m), 0.62-0.57 (2H, m).
[2752] Physical property: Paste form.
[2753] Example 551 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,6-dimethoxybenzoate (Compound No. 3162)
[2754] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.39 (1H, t, J = 8.8 Hz), 7.09-7.07 (2H, m), 6.85-6.81 (1H, m), 6.62 (2H, d, J = 6.6 Hz), 3.84 (6H, s), 2.17 (3H, s), 1.96-1.81 (1H, m), 0.74-0.55 (4H, m).
[2755] Melting point (° C.): 127-128.
[2756] Example 552 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,4-difluorobenzoate (Compound No. 3168)
[2757] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.10-7.99 (2H, m), 7.58 (1H, s), 7.43-7.25 (1H, m), 7.15-7.02 (2H, m), 6.90-6.80 ( 1H, m), 2.15 (3H, s), 1.83-1.67 (1H, m), 0.80-0.50 (4H, m).
[2758] Properties: Caramel statue.
[2759] Example 553 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-fluoro-4-methylbenzoate (Compound No. 3185)
[2760] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.90 (1H, d, J = 8.1 Hz), 7.83 (1H, d, J = 9.9 Hz), 7.59 (1H, s), 7.37 (1H, dd, J = 7.3 Hz, 7.7 Hz), 7.15-7.00 (2H, m), 6.90-6.78 (1H, m), 2.39 (3H, d, 1.5 Hz), 2.15 (3H, s), 1.85-1.67 (1H, m) ), 0.80-0.50 (4H, m).
[2761] Properties: Caramel statue.
[2762] Example 554 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,4-dichlorobenzoate (Compound No. 3194)
[2763] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.29 (1H, d, J = 1.8 Hz), 8.03 (1H, dd, J = 8.4, 2.2 Hz), 7.65 (1H, d, J = 8.4 Hz), 7.57 (1H, s), 7.15-7.02 (2H, m), 6.90-6.80 (1H, m), 2.15 (3H, s), 1.82-1.68 (1H, m), 0.78-0.47 (4H, m).
[2764] Physical property: Amorphous.
[2765] Example 555 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-chloro-3-nitrobenzoate (Compound No. 3200)
[2766] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.69 (1H, d, J = 1.8 Hz), 8.33 (1H, dd, J = 8.4, 1.8 Hz), 7.78 (1H, d, J = 8.4 Hz), 7.57 (1H, s), 7.10-7.05 (2H, m), 6.87-6.82 (1H, m), 2.14 (3H, s), 1.77-1.69 (1H, m), 0.75-0.56 (4H, m).
[2767] Physical property: Amorphous.
[2768] Example 556 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,5-difluorobenzoate (Compound No. 3217)
[2769] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.80-7.65 (2H, m), 7.58 (1H, s), 7.32-7.00 (3H, m), 6.90-6.80 (1H, m), 2.15 (3H, s), 1.85-1.65 (1H, m), 0.80-0.50 (4H, m).
[2770] Physical property: Amorphous.
[2771] Example 557 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,5-dichlorobenzoate (Compound No. 3226)
[2772] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.07 (2H, d, J = 2.0 Hz), 7.69 (1H, t, J = 2.0 Hz), 7.55 (1H, s), 7.13-7.00 (2H, m ), 6.89-6.82 (1H, m), 2.15 (3H, s), 1.83-1.60 (1H, m), 0.80-0.70 (2H, m), 0.63-0.55 (2H, m).
[2773] Melting point (° C.): 168-174.
[2774] Example 558 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,5-dimethylbenzoate (Compound No. 3243)
[2775] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.82 (2H, s), 7.56 (1H, s), 7.32 (1H, s,), 7.13-7.04 (2H, m), 6.89-6.82 (1H, m ), 2.41 (6H, s), 2.16 (3H, s), 1.85-1.72 (1H, m), 0.80-0.70 (2H, m), 0.63-0.53 (2H, m).
[2776] Melting Point (° C): 117-119.
[2777] Example 559 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,5-dimethoxybenzoate (Compound No. 3252)
[2778] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.34 (1H, s), 7.33 (1H, s), 7.08-7.06 (2H, m), 6.87-6.82 (1H, m) , 6.78-6.75 (1H, m), 3.86 (6H, s), 2.16 (3H, s), 1.86-1.72 (1H, m), 0.80-0.72 (2H, m), 0.63-0.54 (2H, m) .
[2779] Physical property: Paste form.
[2780] Example 560 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,4,6-trichlorobenzoate (Compound No. 3258)
[2781] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.55 (1H, s), 7.46 (2H, s), 7.15-7.05 (2H, m), 6.90-6.82 (1H, m), 2.16 (3H, s) , 1.86-1.72 (1H, m), 0.78-0.67 (2H, m), 0.65-0.55 (2H, m).
[2782] Physical property: Paste form.
[2783] Example 561 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3,4,5-trimethoxybenzoate (Compound No. 3264)
[2784] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.45 (2H, s), 7.14-7.04 (2H, m), 6.89-6.83 (1H, m), 3.96 (3H, s) , 3.94 (6H, s), 2.16 (3H, s), 1.85-1.72 (1H, m), 0.80-0.67 (2H, m), 0.63-0.54 (2H, m).
[2785] Physical property: Amorphous.
[2786] Example 562 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-naphthoate (Compound No. 3270)
[2787] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.02 (1H, d, J = 8.4 Hz), 8.55 (1H, d, J = 7.3 Hz), 8.17 (1H, d, J = 8.0 Hz), 7.95 ( 1H, d, J = 8.0 Hz), 7.75-7.54 (4H, m), 7.13-7.00 (2H, m), 6.90-6.80 (1H, m), 2.18 (3H, s), 1.93-1.75 (1H, m), 0.83-0.52 (4H, m).
[2788] Physical property: Amorphous.
[2789] Example 563 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-naphthoate (Compound No. 3276)
[2790] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.81 (1H, s), 8.18 (1H, dd, J = 1.5 Hz, 8.5 Hz), 8.05-7.87 (3H, m), 7.70-7.52 (3H, m ), 7.10-7.00 (2H, m), 6.90-6.77 (1H, m), 2.18 (3H, s), 1.90-1.73 (1H, m), 0.83-0.53 (4H, m).
[2791] Physical property: Amorphous.
[2792] Example 564 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-methyl-1H-pyrrole-2-carboxylate (Compound No. 3282)
[2793] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.25 (1H, s), 7.08-7.06 (2H, m), 6.96 (1H, s), 6.86-6.81 (1H, m) , 6.24-6.21 (1H, m), 3.97 (3H, s), 2.15 (3H, s), 1.87-1.72 (1H, m), 0.80-0.70 (2H, m), 0.63-0.52 (2H, m) .
[2794] Melting point (° C): 143-144.
[2795] Example 565 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-bromo-2-furoate (Compound No. 3288)
[2796] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.53 (1H, s), 7.43 (1H, d, J = 3.7 Hz), 7.15-7.03 (2H, m), 6.90-6.78 (1H, m), 6.59 (1H, d, J = 3.7 Hz), 2.15 (3H, s), 1.83-1.70 (1H, m), 0.80-0.50 (4H, m).
[2797] Properties: Caramel statue.
[2798] Example 566 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-furoate (Compound No. 3294)
[2799] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.30 (1H, t, J = 0.7 Hz), 7.57-7.53 (1H, m), 7.55 (1H, s), 7.13-7.04 (2H, m), 6.92 -6.81 (2H, m), 2.15 (3H, s), 1.83-1.69 (1H, s), 0.80-0.53 (4H, m).
[2800] Physical property: Paste form.
[2801] Example 567 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-tert-butyl-2-methyl-3-furoate (Compound No. 3300)
[2802] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.09-7.07 (2H, m), 6.87-6.83 (1H, m), 6.33 (1H, s), 2.64 (3H, s) , 2.15 (3H, s), 1.78-1.73 (1H, m), 1.29 (9H, s), 0.75-0.57 (4H, m).
[2803] Properties: Caramel statue.
[2804] Example 568 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-methyl-2- (trifluoromethyl) -3-furoate (Compound No. 3306 )
[2805] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.53 (1H, s), 7.13-7.04 (2H, m), 6.89-6.82 (1H, m), 6.64 (1H, s), 2.42 (3H, s) 2.13 (3H, s), 1.81-1.67 (1H, m), 0.78-0.68 (2H, m), 0.65-0.53 (2H, m).
[2806] Physical property: Paste form.
[2807] Example 569 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5- (4-chlorophenyl) -2- (trifluoromethyl) -3-furo Eight (Compound No. 3312)
[2808] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.70-7.66 (2H, m), 7.56 (1H, s), 7.47-7.42 (2H, m), 7.19 (1H, s), 7.14-7.05 (2H, m), 6.90-6.82 (1H, m), 2.14 (3H, s), 1.83-1.69 (1H, m), 0.80-0.68 (2H, m), 0.65-0.53 (2H, m).
[2809] Physical property: Paste form.
[2810] Example 570 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-chloro-2-thiophencarboxylate (Compound No. 3318)
[2811] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.68 (1H, d, J = 5.5 Hz), 7.58 (1H, s), 7.14 (1H, d, J = 5.5 Hz), 7.11-7.03 (2H, m ), 6.90-6.80 (1H, m), 2.16 (3H, s), 1.85-1.70 (1H, m), 0.85-0.50 (4H, m).
[2812] Properties: Caramel statue.
[2813] Example 571 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-methyl-2-thiophencarboxylate (Compound No. 3324)
[2814] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.65-7.55 (2H, m), 7.13-6.95 (3H, m), 6.90-6.80 (1H, m), 2.63 (3H, s), 2.16 (3H, s), 1.90-1.70 (1H, m), 0.85-0.50 (4H, m).
[2815] Physical property: Amorphous.
[2816] Example 572 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-ethoxy-2-thiophencarboxylate (Compound No. 3330)
[2817] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.62 (1H, s), 7.59 (1H, d, J = 5.5 Hz), 7.08-7.06 (2H, m), 6.90 (1H, d, J = 5.5 Hz ), 6.86-6.81 (1H, m), 4.26 (2H, q, J = 7.0 Hz), 2.17 (3H, s), 1.86-1.75 (1H, m), 1.46 (3H, t, J = 7.0 Hz) , 0.75-0.55 (4H, m).
[2818] Properties: Caramel statue.
[2819] Example 573 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-chloro-2-thiophencarboxylate (Compound No. 3336)
[2820] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.86 (1H, d, J = 4.0 Hz), 7.57 (1H, s), 7.14-7.03 (3H, m), 6.90-6.83 (1H, m), 2.15 (3H, m), 1.83-1.68 (1H, m), 0.80-0.68 (2H, m), 0.65-0.53 (2H, m).
[2821] Physical property: Paste form.
[2822] Example 574 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-bromo-2-thiophenecarboxylate (Compound No. 3342)
[2823] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.80 (1H, d, J = 4.0 Hz), 7.57 (1H, s), 7.19 (1H, d, J = 4.0 Hz), 7.10-7.00 (2H, m ), 6.90-6.80 (1H, m), 2.15 (3H, s), 1.85-1.65 (1H, m), 0.80-0.50 (4H, m).
[2824] Properties: Caramel statue.
[2825] Example 575 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-methyl-2-thiophencarboxylate (Compound No. 3348)
[2826] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.87 (1H, d, J = 3.7 Hz), 7.57 (1H, s), 7.12-7.00 (2H, m), 6.93-6.87 (2H, m), 2.58 (3H, s), 2.15 (3H, s), 1.85-1.70 (1H, m), 0.80-0.50 (4H, m).
[2827] Properties: Caramel statue.
[2828] Example 576 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-acetyl-2-thiophencarboxylate (Compound No. 3354)
[2829] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.02 (1H, d, J = 4.0 Hz), 7.72 (1H, d, J = 4.0 Hz), 7.58 (1H, s), 7.10-7.07 (2H, m ), 6.87-6.83 (1H, m), 2.63 (3H, s), 2.15 (3H, s), 1.79-1.71 (1H, m), 0.75-0.56 (4H, m).
[2830] Physical property: Amorphous.
[2831] Example 577 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-nitro-3-thiophenecarbocylate (Compound No. 3360)
[2832] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.52 (1H, d, J = 1.8 Hz), 8.43 (1H, d, J = 1.8 Hz), 7.56 (1H, s), 7.13-7.05 (2H, m ), 6.90-6.80 (1H, m), 2.14 (3H, s), 1.85-1.65 (1H, m), 0.85-0.50 (4H, m).
[2833] Physical property: Amorphous.
[2834] Example 578 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4,5-dibromo-2-thiophenecarboxylate (Compound No. 3366)
[2835] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.84 (1H, s), 7.56 (1H, s), 7.14-7.05 (2H, m), 6.90-6.83 (1H, m), 2.14 (3H, s) , 1.83-1.69 (1H, m), 0.79-0.68 (2H, m), 0.65-0.55 (2H, m).
[2836] Physical property: Amorphous.
[2837] Example 579 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-thiophenecarboxylate (Compound No. 3372)
[2838] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.42-8.40 (1H, m), 7.70-7.66 (1H, m), 7.58 (1H, s), 7.47-7.41 (1H, m), 7.13-7.05 ( 2H, m), 6.88-6.82 (1H, m), 2.15 (3H, s), 1.84-1.70 (1H, m), 0.80-0.68 (2H, m), 0.64-0.55 (2H, m).
[2839] Physical property: Paste form.
[2840] Example 580 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methoxy-3-thiophencarboxylate (Compound No. 3378)
[2841] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.33 (1H, d, J = 3.5 Hz), 7.59 (1H, s), 7.09-7.06 (2H, m), 6.87-6.82 (1H, m), 6.38 (1H, d, J = 3.5 Hz), 3.93 (3H, s), 2.16 (3H, s), 1.82-1.74 (1H, m), 0.75-0.56 (4H, m).
[2842] Melting Point (° C): 146-149.
[2843] Example 581 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-benzyl-3-tert-butyl-1H-pyrazole-5-carboxylate ( Compound number 3384)
[2844] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.44 (1H, s), 7.21 (5H, s), 7.09-7.06 (2H, m), 6.98 (1H, s), 6.85-6.80 (1H, m) , 5.72 (2H, s), 2.08 (3H, s), 1.76-1.64 (1H, m), 1.36 (9H, s), 0.75-0.64 (2H, m), 0.59-0.50 (2H, m).
[2845] Physical property: Paste form.
[2846] Example 582 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-chloro-1,3-dimethyl-1H-pyrazole-4-carboxylate ( Compound number 3390)
[2847] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.62 (1H, s), 7.09-7.07 (2H, m), 6.87-6.82 (1H, m), 3.86 (3H, s), 2.52 (3H, s) , 2.14 (3H, s), 1.84-1.77 (1H, m), 0.75-0.67 (2H, m), 0.60-0.53 (2H, m).
[2848] Physical property: Paste form.
[2849] Example 583 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3- (2-chlorophenyl) -5-methyl-4-isoxazole carboxylate ( Compound number 3396)
[2850] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.53 (1H, s), 7.48-7.42 (2H, m), 7.41-7.30 (2H, m), 7.08-7.06 (2H, m), 6.83-6.78 ( 1H, m), 2.89 (3H, s), 2.02 (3H, s), 1.67-1.53 (1H, m), 0.68-0.50 (4H, m).
[2851] Physical property: Amorphous.
[2852] Example 584 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4-methyl-1,2,3-thiadiazole-5-carboxylate (compound Number 3402)
[2853] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.15-7.05 (2H, m), 6.91-6.84 (1H, m), 3.08 (3H, s), 2.14 (3H, s) , 1.80-1.65 (1H, m), 0.80-0.72 (2H, m), 0.64-0.53 (2H, m).
[2854] Physical property: Paste form.
[2855] Example 585 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 6-methyl-2-pyridinecarboxylate (Compound No. 3408)
[2856] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.12 (1H, d, J = 7.7 Hz), 7.82 (1H, t, J = 7.7 Hz), 7.55 (1H, s), 7.46 (1H, d, J = 7.7 Hz), 7.12-7.02 (2H, m), 6.85-6.76 (1H, m), 2.71 (3H, s), 2.15 (3H, s), 1.87-1.74 (1H, m), 0.82-0.52 ( 4H, m).
[2857] Properties: Caramel statue.
[2858] Example 586 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5-butyl-2-pyridinecarboxylate (Compound No. 3414)
[2859] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.67 (1H, br.s), 8.22 (1H, d, J = 7.7 Hz), 7.74 (1H, br.d, J = 7.7 Hz), 7.53 (1H , s), 7.08-7.05 (2H, m), 6.83-6.78 (1H, m), 2.75 (2H, t, J = 7.7 Hz), 2.15 (3H, s), 1.84-1.59 (3H, m), 1.48-1.32 (2H, m), 0.95 (3H, t, J = 7.0 Hz), 0.75-0.54 (4H, m).
[2860] Properties: Caramel statue.
[2861] Example 587 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl nicotinate (Compound No. 3420)
[2862] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.42-9.41 (1H, m), 8.91 (1H, dd, J = 4.8, 0.8 Hz), 8.50-8.44 (1H, m), 7.60 (1H, s) , 7.56-7.49 (1H, m), 7.13-7.04 (2H, m), 6.88-6.78 (1H, m), 2.15 (3H, s), 1.90-1.70 (1H, m), 0.81-0.70 (2H, m), 0.63-0.55 (2H, m).
[2863] Physical property: Paste form.
[2864] Example 588 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-chloronicotinate (Compound No. 3426)
[2865] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.66 (1H, dd, J = 4.8, 2.0 Hz), 8.45 (1H, dd, J = 7.7, 2.0 Hz), 7.59 (1H, s), 7.45 (1H , dd, J = 7.7, 4.8 Hz), 7.14-7.06 (2H, m), 6.89-6.83 (1H, m), 2.15 (3H, s), 1.84-1.70 (1H, m), 0.80-0.52 (4H , m).
[2866] Properties: Caramel statue.
[2867] Example 589 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-methylnicotinate (Compound No. 3432)
[2868] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.74 (1H, dd, J = 4.8, 1.5 Hz), 8,46 (1H, dd, J = 7.7, 1.5 Hz), 7.58 (1H, s), 7.34 (1H, dd, J = 7.7, 4.8 Hz), 7.13-7.05 (2H, m), 6.89-6.83 (1H, m), 2.93 (3H, s), 2.15 (3H, s), 1.83-1.67 (1H m), 0.80-0.68 (2H, m), 0.65-0.55 (2H, m).
[2869] Physical property: Paste form.
[2870] Example 590 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-phenoxynicotinate (Compound No. 3438)
[2871] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.50 (1H, dd, J = 7.8, 2.2 Hz), 8.39 (1H, dd, J = 4.8, 2.2 Hz), 7.61 (1H, s), 7.46-7.38 (2H, m), 7.29-7.20 (1H, m), 7.19-7.04 (5H, m), 6.86-6.81 (1H, m), 2.14 (3H, s), 1.85-1.72 (1H, m), 1.36 (9H, s), 0.75-0.65 (2H, m), 0.58-0.52 (2H, m).
[2872] Physical property: Paste form.
[2873] Example 591 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2- (methylsulfanyl) nicotinate (Compound No. 3444)
[2874] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.70 (1H, dd, J = 4.9, 1.8 Hz), 8.47 (1H, dd, J = 7.7, 1.8 Hz), 7.63 (1H, s), 7.16 (1H , dd, J = 7.7, 4.8 Hz), 7.12-7.05 (2H, m), 6.89-6.82 (1H, m), 2.59 (3H, s), 2.16 (3H, s), 1.84-1.71 (1H, m ), 0.80-0.70 (2H, m), 0.65-0.53 (2H, m).
[2875] Physical property: Paste form.
[2876] Example 592 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2- (allylsulfanyl) nicotinate (Compound No. 3450)
[2877] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.67 (1H, dd, J = 4.8, 1.8 Hz), 8.46 (1H, dd, J = 8.2, 1.8 Hz), 7.62 (1H, s), 7.16 (1H , dd, J = 8.2, 4.8 Hz), 7.09-7.04 (2H, m), 6.89-6.82 (1H, m), 6.10-5.90 (1H, m), 5.33 (1H, dd, J = 16.8, 1.6 Hz ), 5.12 (1H, dd, J = 11.0, 1.2 Hz), 3.91 (1H, dd, J = 6.8, 1.2 Hz), 2.15 (3H, s), 1.85-1.70 (1H, m), 0.78-0.71 ( 2H, m), 0.60-0.51 (2H, m).
[2878] Physical property: Paste form.
[2879] Example 593 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2- (phenylsulfanyl) nicotinate (Compound No. 3456)
[2880] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.50 (1H, s), 8.47 (1H, d, J = 2.6 Hz), 7.65 (1H, s), 7.59-7.51 (2H, m), 7.48-7.41 (3H, m), 7.17-7.05 (3H, m), 6.90-6.82 (1H, m), 2.18 (3H, s), 1.89-1.74 (1H, m), 0.82-0.70 (2H, m), 0.65 -0.54 (2H, m).
[2881] Physical property: Paste form.
[2882] Example 594 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (trifluoromethyl) nicotinate (Compound No. 3462)
[2883] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.42 (1H, s), 9.08 (1H, d, J = 5.1 Hz), 7.79 (1H, d, J = 5.1 Hz), 7.57 (1H, s), 7.14-7.06 (2H, m), 6.90-6.84 (1H, m), 2.16 (3H, s), 1.84-1.72 (1H, m), 0.79-0.71 (2H, m), 0.63-0.55 (2H, m ).
[2884] Melting Point (° C): 92-93.
[2885] Example 595 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 6-chloronicotinate (Compound No. 3468)
[2886] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.19 (1H, d, J = 2.0), 8.40 (1H, dd, J = 8.4, 2.6), 7.59 (1H, s), 7.54 (1H, d, J = 8.4 Hz), 7.10-7.08 (1H, m), 7.07 (1H, s), 6.87-6.82 (1H, m), 2.14 (3H, s), 1.79-1.65 (1H, m), 0.79-0.70 ( 2H, m), 0.62-0.53 (2H, m).
[2887] Physical property: Paste form.
[2888] Example 596 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,6-dichloronicotinate (Compound No. 3474)
[2889] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.46 (1H, d, J = 8.1 Hz), 7.67 (1H, s), 7.52 (1H, d, J = 8.1 Hz), 7.13-7.02 (2H, m ), 6.90-6.75 (1H, m), 2.14 (3H, s), 1.85-1.68 (1H, m), 0.85-0.48 (4H, m).
[2890] Physical property: Amorphous.
[2891] Example 597 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-chloro-6-methylnicotinate (Compound No. 3480)
[2892] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.37 (1H, d, J = 7.7 Hz), 7.58 (1H, s), 7.27 (1H, d, J = 7.7 Hz), 7.14-7.08 (2H, m ), 6.89-6.80 (1H, m), 2.65 (3H, s), 2.15 (3H, s), 1.83-1.69 (1H, m), 0.80-0.70 (2H, m), 0.68-0.55 (2H, m) ).
[2893] Physical property: Paste form.
[2894] Example 598 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 5,6-dichloronicotinate (Compound No. 3486)
[2895] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.07 (1H, d, J = 2.2 Hz), 8.50 (1H, d, J = 2.2 Hz), 7.57 (1H, s), 7.10-7.07 (2H, m ), 6.87-6.82 (1H, m), 2.13 (3H, s), 1.80-1.65 (1H, m), 0.75-0.70 (2H, m), 0.58-0.55 (2H, m).
[2896] Physical property: Paste form.
[2897] Example 599 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2-chloroisonicotinate (Compound No. 3492)
[2898] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.68 (1H, d, J = 5.0 Hz), 8.05 (1H, s), 7.95-7.92 (1H, m), 7.57 (1H, s), 7.10-7.07 (2H, m), 6.87-6.83 (1H, m), 2.14 (3H, s), 1.77-1.68 (1H, m), 0.75-0.71 (2H, m), 0.58-0.56 (2H, m).
[2899] Physical property: Paste form.
[2900] Example 600 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-benzofuran-2-carboxylate (Compound No. 3498)
[2901] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.86-7.75 (2H, m), 7.68-7.51 (3H, m), 7.38 (1H, dd, J = 7.7, 7.0 Hz), 7.12-7.05 (2H, m), 6.89-6.80 (1H, m), 2.17 (3H, s), 1.86-1.73 (1H, m), 0.80-0.68 (2H, m), 0.64-0.55 (2H, m).
[2902] Physical property: Amorphous.
[2903] Example 601 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-benzothiophene-2-carboxylate (Compound No. 3504)
[2904] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.34 (1H, s), 7.94 (2H, m), 7.64 (1H, s), 7.59-7.42 (2H, m), 7.09-7.07 (2H, m) , 6.87-6.83 (1H, m), 2.18 (3H, s), 1.88-1.72 (1H, m), 0.77-0.71 (2H, m), 0.61-0.53 (2H, m).
[2905] Melting point (° C): 105-107.
[2906] Example 602 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1,3-benzothiazole-6-carboxylate (Compound No. 3510)
[2907] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 9.24 (1H, s), 8.89 (1H, d, J = 1.4 Hz), 8.36 (1H, dd, J = 8.4, 1.4 Hz), 8.28 (1H, d , J = 8.4 Hz), 7.65 (1H, s), 7.09-7.06 (2H, m), 6.87-6.82 (1H, m), 2.17 (3H, s), 1.86-1.73 (1H, m), 0.78- 0.72 (2H, m), 0.63-0.55 (2H, m).
[2908] Physical property: Amorphous.
[2909] Example 603 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1,3-benzodioxol-5-carboxylate (Compound No. 3516)
[2910] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.85 (1H, dd, J = 8.4, 1.8 Hz), 7.60-7.59 (2H, m), 7.09-7.06 (2H, m), 6.93 (1H, d, J = 8.0 Hz), 6.86-6.82 (1H, m), 6.10 (2H, s), 2.15 (3H, s), 1.86-1.74 (1H, m), 0.79-0.70 (2H, m), 0.62-0.53 (2H, m).
[2911] Physical property: Paste form.
[2912] Example 604 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-isoquinolinecarboxylate (Compound No. 3522)
[2913] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.45 (1H, d, J = 8.1 Hz), 7.78-7.70 (2H, m), 7.61-7.53 (2H, m), 7.16 (1H, d, J = 7.7 Hz), 7.12-7.05 (2H, m), 6.90-6.83 (1H, m), 6.66 (1H, d, J = 7.3 Hz), 2.15 (3H, s), 1.81-1.66 (1H, m), 0.79-0.67 (2H, m), 0.63-0.53 (2H, m).
[2914] Physical property: Amorphous.
[2915] Example 605 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyltert-butyl (methyl) carbamate (Compound No. 3528)
[2916] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.51 (1H, s), 7.15-7.03 (2H, m), 6.90-6.80 (1H, m), 3.11 (3H, s), 2.14 (3H, s) , 1.85-1.70 (1H, m), 1.47 (9H, s), 0.80-0.50 (4H, m).
[2917] Melting point (° C.): 113-115.
[2918] Example 606 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl dibutylcarbamate (Compound No. 3534)
[2919] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.15-7.03 (2H, m), 6.90-6.78 (1H, m), 3.50-3.26 (4H, m), 2.13 (3H, s), 1.87-1.50 (5H, m), 1.50-1.15 (4H, m), 1.10-0.85 (6H, m), 0.80-0.54 (4H, m).
[2920] Properties: Caramel statue.
[2921] Example 607 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl benzyl (methyl) carbamate (Compound No. 3540)
[2922] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (0.5H, s), 7.57 (0.5H, s), 7.40-7.20 (5H, m), 7.15-7.03 (2H, m), 6.92-6.80 ( 1H, m), 4.68 (1H, s), 4.57 (1H, s), 3.08 (1.5H, s), 3.02 (1.5H, s), 2.15 (1.5H, s), 2.13 (1.5H, s) , 1.85-1.65 (1H, m), 0.80-0.45 (4H, m).
[2923] Properties: Caramel statue.
[2924] Example 608 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl cyanomethyl (methyl) carbamate (Compound No. 3546)
[2925] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (0.4 H, s), 7.56 (0.6 H, s), 7.15-7.04 (2H, m), 6.90-6.80 (1 H, m), 4.42 (0.8 H , s), 4.36 (1.2H, s), 3.30 (1.8H, s), 3.19 (1.2H, s), 2.14 (3H, s), 1.85-1.62 (1H, m), 0.80-0.53 (4H, m).
[2926] Properties: Caramel statue.
[2927] Example 609 Ethyl N-({[6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] oxy} carbonyl) -N-methylglycinate (compound Number 3552)
[2928] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.61 (0.5H, s), 7.60 (0.5H, s), 7.15-7.02 (2H, m), 6.90-6.80 (1H, m), 4.28-4.11 ( 4H, m), 3.23 (1.5H, s), 3.13 (1.5H, s), 2.15 (1.5H, s), 2.13 (1.5H, s), 1.85-1.65 (1H, m), 1.31-1.18 ( 3H, m), 0.80-0.50 (4H, m).
[2929] Properties: Caramel statue.
[2930] Example 610 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methyl (2-pyridinyl) carbamate (Compound No. 3558)
[2931] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.35-8.25 (1H, m), 7.70-7.55 (1H, m), 7.05-6.90 (5H, m), 6.85-6.74 (1H, m), 3.56 ( 3H, s), 2.03 (3H, s), 1.72-1.55 (1H, m), 0.75-0.45 (4H, m).
[2932] Melting point (° C.): 140-147.
[2933] Example 611 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-piperidinecarboxylate (Compound No. 3636)
[2934] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56 (1H, s), 7.15-7.03 (2H, m), 6.90-6.80 (1H, m), 3.70-3.60 (2H, m), 3.60-3.45 ( 2H, m), 2.15 (3H, s), 1.86-1.70 (1H, m), 1.70-1.50 (6H, m), 0.80-0.53 (4H, m).
[2935] Properties: Caramel statue.
[2936] Example 612 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl bis (2-chloroethyl) carbamate (Compound No. 3570)
[2937] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.58 (1H, s), 7.15-7.05 (2H, m), 6.92-6.82 (1H, m), 3.98-3.70 (8H, m), 2.13 (3H, s), 1.82-1.65 (1H, m), 0.80-0.50 (4H, m).
[2938] Melting point (° C): 166-167.
[2939] Example 613 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl diallylcarbamate (Compound No. 3576)
[2940] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.56 (1H, s), 7.12-7.04 (2H, m), 6.88-6.80 (1H, m), 6.00-5.70 (2H, m), 5.30-5.15 ( 4H, m), 4.10-3.93 (4H, m), 2.13 (3H, s), 1.85-1.68 (1H, m), 0.80-0.52 (4H, m).
[2941] Properties: Caramel statue.
[2942] Example 614 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl bis (cyanomethyl) carbamate (Compound No. 3582)
[2943] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.18-7.05 (2H, m), 6.90-6.80 (1H, m), 4.54 (2H, s), 4.48 (2H, s) , 2.13 (3H, s), 1.80-1.65 (1H, m), 0.80-0.50 (4H, m).
[2944] Properties: Caramel statue.
[2945] Example 615 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl bis (2-cyanoethyl) carbamate (Compound No. 3588)
[2946] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.61 (1H, s), 7.18-7.05 (2H, m), 6.92-6.82 (1H, m), 3.91 (2H, t, J = 6.6 Hz), 3.77 (2H, t, J = 6.2 Hz), 2.85 (2H, t, J = 6.6 Hz), 2.78 (2H, t, J = 6.2 Hz), 2.13 (3H, s), 1.80-1.63 (1H, m) , 0.82-0.53 (4H, m).
[2947] Melting Point (° C): 159-161.
[2948] Example 616 Ethyl N-({[6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] oxy} carbonyl) -N- (2-ethoxy- 2-oxoethyl) glycinate (Compound No. 3594)
[2949] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.65 (1H, s), 7.13-7.03 (2H, m), 6.90-6.80 (1H, m), 4.33-4.05 (8H, m), 2.12 (3H, s), 1.83-1.65 (1H, m), 1.28 (3H, t, J = 7.3 Hz), 1.19 (3H, t, J = 7.3 Hz), 0.80-0.50 (4H, m).
[2950] Properties: Caramel statue.
[2951] Example 617 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl bis (2-methoxyethyl) carbamate (Compound No. 3600)
[2952] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.15-7.05 (2H, m), 6.90-6.80 (1H, m), 3.80-3.50 (8H, m), 3.32 (6H, s), 2.15 (3H, s), 1.86-1.69 (1H, m), 0.80-0.52 (4H, m).
[2953] Properties: Caramel statue.
[2954] Example 618 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl bis (2-ethoxyethyl) carbamate (Compound No. 3606)
[2955] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.57 (1H, s), 7.15-7.03 (2H, m), 6.90-6.80 (1H, m), 3.78-3.55 (8H, m), 3.46 (4H, q, J = 6.9 Hz, 2.14 (3H, s), 1.87-1.65 (1H, m), 1.15 (3H, t, J = 6.9 Hz), 1.14 (3H, t, J = 6.9 Hz), 0.80- 0.53 (4H, m).
[2956] Properties: Caramel statue.
[2957] Example 619 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-azetidinecarboxylate (Compound No. 3612)
[2958] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.53 (1H, s), 7.13-7.02 (2H, m), 6.90-6.78 (1H, m), 4.38-4.05 (4H, m), 2.45-2.29 ( 2H, m), 2.15 (3H, s), 1.85-1.67 (1H, m), 0.80-0.50 (4H, m).
[2959] Melting point (° C.): 134-136.
[2960] Example 620 1- [6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] 2-methyl 1,2-pyrrolidinedicarboxylate (Compound No. 3618)
[2961] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.65 (0.5H, s), 7.62 (0.5H, s), 7.15-7.02 (2H, m), 6.90-6.78 (1H, m), 4.63-4.57 ( 0.5H, m), 4.51-4.44 (0.5H, m), 3.91-3.55 (2H, m), 3.75 (1.5H, s), 3.65 (1.5H, s), 2.50-1.90 (4H, m), 2.15 (1.5H, s), 2.13 (1.5H, s), 1.90-1.69 (1H, m), 0.80-0.50 (4H, m).
[2962] Properties: Caramel statue.
[2963] Example 621 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 3-hydroxy-1-pyrrolidinecarboxylate (Compound No. 3624)
[2964] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.60 (1H, s), 7.13-7.03 (2H, m), 6.90-6.80 (1H, m), 4.65-4.52 (1H, m), 3.85-3.55 ( 4H, m), 2.14 (3H, s), 2.13-2.00 (2H, m), 1.87-1.70 (2H, m), 0.80-0.50 (4H, m).
[2965] Properties: Caramel statue.
[2966] Example 622 6-Chloro-3- (2-cyclopropyl-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1126)
[2967] (1) 2,3,5-trimethylphenyl acetate
[2968] 15.09 g (0.1108 mol) of 2,3,5-trimethylphenol was dissolved in dichloromethane (150 mL), 17.82 mL (0.2204 mol) of pyridine was added, followed by 20.78 mL (0.2202 mol) of acetic anhydride, and the mixture was stirred overnight to room temperature. . The reaction mixture was poured into water and extracted with dichloromethane. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Wako Gel C-100, hexanes: ethyl acetate gradient) to give 20.08 g (0.1127 mol, quantitative yield) of 2,3,5-trimethylphenyl acetate. Got it.
[2969] (2) 1- (2-hydroxy-3,4,6-trimethylphenyl) ethanone
[2970] To 13.83 g (77.60 mmol) of 2,3,5-trimethylphenyl acetate obtained in (1), 20.69 g (155.2 mmol) of aluminum chloride were added little by little while stirring under ice cooling. The mixture was stirred overnight while heating to 100 ° C. After cooling, the reaction mixture was slowly added to ice-cold water. The mixture was extracted with dichloromethane, the organic layers were combined, washed with water, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (WACO gel C-100, hexane: ethyl acetate gradient) to give 1- (2-hydroxy-3,4,6-trimethylphenyl) eta. 12.75 g (71.55 mmol, the yield 92.20%) were obtained for rice fields.
[2971] (3) 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone
[2972] 8.00 g (44.9 mmol) of 1- (2-hydroxy-3,4,6-trimethylphenyl) ethanone obtained in (2) were dissolved in acetone (100 mL), followed by 18.6 g (135 mmol) of potassium carbonate, followed by iodide 8.40 mL (135 mmol) methyl was added and heated to reflux for 27 hours 30 minutes. Furthermore, 18.6 g (135 mmol) of potassium carbonate and 8.40 mL (135 mmol) of methyl iodide were added, and the mixture was heated to reflux for 6 hours. The reaction mixture was concentrated under reduced pressure, water (100 mL) was added to the residue, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (Daisogel 1001W, hexane: ethyl acetate gradient) to obtain 8.04 g of 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone. (41.9 mmol, yield 93.3%) were obtained.
[2973] (4) 1- (2-methoxy-3,4,6-trimethylphenyl) ethanol
[2974] 5.01 g (26.1 mmol) of 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone obtained in (3) was dissolved in methanol (100 mL) and, under ice cooling, 1.00 g (26.5 mmol) of sodium borohydride. ) Was added, and the mixture was stirred for 2 hours and 30 minutes under ice cooling. The reaction mixture was poured into 400 mL of ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and 4.35 g (22.4 mmol, yield 85.8%) of 1- (2-methoxy-3,4,6-trimethylphenyl) ethanol were obtained.
[2975] (5) 2- (1-chloroethyl) -3-methoxy-1,4,5-trimethylbenzene
[2976] 0.150 mL (1.72 mmol) of oxalyl chloride was added dropwise to 0.652 g (3.36 mmol) of 1- (2-methoxy-3,4,6-trimethylphenyl) ethanol obtained in (4), followed by stirring at 100 ° C for 2 hours. It was. Dichloromethane (1 mL) and triethylamine (3 mL) were then added to the reaction mixture, which was stirred for 3 hours at 100 ° C. The reaction mixture was poured into 60 ml of ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 0.620 g (2.91 mmol, yield 86.6%) of 2- (1-chloroethyl) -3-methoxy-1,4,5-trimethylbenzene.
[2977] (6) 3-methoxy-1,2,5-trimethyl-4-vinylbenzene
[2978] 0.620 g (2.91 mmol) of 2- (1-chloroethyl) -3-methoxy-1,4,5-trimethylbenzene obtained in (5) was dissolved in N, N-dimethylformamide (DMF, 6 mL), 1.20 g (8.70 mmol) of potassium carbonate were added and heated to reflux for 9 hours. The reaction mixture was poured into 50 ml of ice cold water and extracted with hexane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Daisogel 1001W, hexane: ethyl acetate gradient) to give 0.360 g (2.05) of 3-methoxy-1,2,5-trimethyl-4-vinylbenzene. Mmol, yield 70.4%).
[2979] (7) 2-cyclopropyl-3-methoxy-1,4,5-trimethylbenzene
[2980] 3.07 mL (3.04 mmol) of diethylzinc (0.99 mol / L hexane solution) was added to dry dichloromethane (5 mL), and a solution of 0.23 mL (3.0 mmol) of dichloromethane (2.5 mL) in trifluoroacetic acid was stirred under ice-cooling. Was slowly added dropwise. After completion of the dropwise addition, the mixture was stirred for 30 minutes under ice-cooling, and 0.24 mL (3.0 mmol) of diiodomethane was added dropwise. Subsequently, a solution of 0.268 g (1.52 mmol) of dichloromethane (3 mL) of 3-methoxy-1,2,5-trimethyl-4-vinylbenzene obtained in (6) was added dropwise, followed by stirring for 1 hour under ice-cooling. The reaction mixture was poured into water, made acidic with diluted hydrochloric acid, and then extracted with dichloromethane. The organic layers were combined, washed with water, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by MERCK, 1.05717, use of 2 sheets, and developed with hexane: ethyl acetate = 25: 1), 2-cyclopropyl-3-methoxy-1 0.212 g (1.12 mmol, yield 73.7%) of, 4,5-trimethylbenzene was obtained.
[2981] (8) 2-cyclopropyl-3,5,6-trimethylphenol
[2982] Under nitrogen atmosphere, 134 mg (3.35 mmol) of 60% sodium hydride was suspended in dry N, N-dimethylformamide (5 mL), and 0.26 mL (3.5 mmol) of ethanethiol was slowly added dropwise to the suspension. After stirring for 30 minutes, a solution of 0.212 g (1.12 mmol) of dry N, N-dimethylformamide (5 mL) of 2-cyclopropyl-3-methoxy-1,4,5-trimethylbenzene obtained by (7) was prepared. It was dripped and stirred at 160 degreeC for 5 hours. After allowing to cool, the reaction mixture was poured into water, diluted with hydrochloric acid, acidified, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (The product made by MERCK, 1.05744, 3 pieces, expansion with ethyl acetate: hexane = 25: 1), 2-cyclopropyl-3,5,6. 179 mg (1.02 mmol, yield 91.1%) of -trimethylphenol were obtained.
[2983] (9) 6-chloro-3- (2-cyclopropyl-3,5,6-trimethylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-cyclopropyl-3,5,6- Trimethylphenoxy) pyridazine 1-oxide mixture (step B-2)
[2984] 179 mg (1.02 mmol) of 2-cyclopropyl-3,5,6-trimethylphenol, 1,4-dioxane (5 mL) and dimethylsulfoxide (5 mL) were mixed and to this mixture potassium tert-butoxide 125 mg (1.12 mmol) was added and stirred for 10 minutes. 167 mg (1.01 mmol) of 3,6-dichloropyridazine 1-oxides were added to this mixture, and it was left to stand at room temperature for 3 days. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by MERCK, 1.05717, use of 2 sheets, and developed as hexane: ethyl acetate = 2: 1), and 6-chloro-3- (2-cyclopropyl A mixture of -3,5,6-trimethylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-cyclopropyl-3,5,6-trimethylphenoxy) pyridazine 1-oxide was prepared. mg obtained.
[2985] (10) 4,6-dichloro-3- (2-cyclopropyl-3,5,6-trimethylphenoxy) pyridazine (Step B-3)
[2986] 6-chloro-3- (2-cyclopropyl-3,5,6-trimethylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-cyclopropyl-3,5 obtained by (9) 263 mg of a mixture of, 6-trimethylphenoxy) pyridazine 1-oxide, and 3.0 mL (32 mmol) of phosphorus oxychloride were mixed and stirred at room temperature overnight. Dichloromethane and water were added to the reaction mixture, which was then stirred and extracted with dichloromethane. The organic layers were combined, washed with water, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (made by MERCK, 1.05717, use of 2 sheets, and developed as hexane: ethyl acetate = 2: 1), and 4,6-dichloro-3- (2- 198 mg (0.613 mmol, yield 60.7% from 3,6-dichloropyridazine 1-oxide) of cyclopropyl-3,5,6-trimethylphenoxy) pyridazine were obtained. Further 3-chloro-6- (2 43.8 mg (0.144 mmol, yield 14.2% from 3,6-dichloropyridazine 1-oxide) of -cyclopropyl-3,5,6-trimethylphenoxy) pyridazine 1-oxide were obtained.
[2987] (11) 6-chloro-3- (2-cyclopropyl-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1126, steps A-3 and A-4)
[2988] 198 mg (0.613 mmol) of 4,6-dichloro-3- (2-cyclopropyl-3,5,6-trimethylphenoxy) pyridazine obtained in (10) were dissolved in dimethyl sulfoxide (10 mL), and sodium acetate 251 mg (3.06 mmol) was added and stirred at 120 ° C. for 4 hours. The reaction mixture was cooled, poured into water, and made acidic with diluted hydrochloric acid. The mixture was extracted with ethyl acetate, the organic layers were combined, washed with water, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by MERCK Corporation, 1.05717, use of 2 sheets, developed as hexane: ethyl acetate = 1: 2), and 6-chloro-3- (2-cyclopropyl). 116 mg (0.380 mmol, yield 62.0%) of -3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1126) were obtained.
[2989] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.67 (1H, s), 6.62 (1H, s), 2.22 (3H, s), 2.16 (3H, s), 2.05 (3H, s), 1.85- 1.65 (1 H, m), 0.75-0.62 (2 H, m), 0.60-0.45 (2 H, m).
[2990] Melting point (° C): 212-219.
[2991] Example 623 6-Chloro-3- (2-methoxy-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1128)
[2992] (1) 1- [2- (benzyloxy) -3,4,6-trimethylphenyl] ethanone
[2993] 2.00 g (11.2 mmol) of 1- (2-hydroxy-3,4,6-trimethylphenyl) ethanone obtained in Example 622 (2) were dissolved in N, N-dimethylformamide (8 mL). 0.488 g (11.2 mmol) of 60% sodium hydride was added to this solution under ice-cooling, and after stirring for 10 minutes under ice-cooling, 1.92 g (11.2 mmol) of benzyl bromide was slowly added dropwise and stirred overnight at room temperature. The reaction mixture was poured into ice-cold water, and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate gradient) to obtain 1- [2- (benzyloxy) -3,4,6-trimethylphenyl ] 2.36 g (8.81 mmol, yield 78.7%) of ethanone were obtained.
[2994] (2) 2- (benzyloxy) -3,4,6-trimethylphenyl acetate
[2995] 500 mg (1.87 mmol) of 1- [2- (benzyloxy) -3,4,6-trimethylphenyl] ethanone obtained in (1) were dissolved in dichloromethane (3 mL), and 921 mg (purity) of m-chloroperbenzoic acid was obtained. A solution of 70-75%, 3.73-3.99 mmol) of dichloromethane (6 mL) was added and stirred at room temperature for 2 days. The reaction mixture was poured into saturated aqueous sodium sulfite solution, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 560 mg of 2- (benzyloxy) -3,4,6-trimethylphenyl acetate.
[2996] (3) 2- (benzyloxy) -3,4,6-trimethylphenol
[2997] 560 mg of 2- (benzyloxy) -3,4,6-trimethylphenyl acetate obtained in (2) was dissolved in ethanol (15 mL), an aqueous solution of 2 N sodium hydroxide was added thereto, and the mixture was stirred at room temperature overnight at 60 ° C. for 4 hours. It was. The reaction mixture was cooled to room temperature and poured into water. 1 N hydrochloric acid was added to make this acid, and it extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 290 mg of 2- (benzyloxy) -3,4,6-trimethylphenol. (1.20 mmol, the yield 64.2% from 1- [2- (benzyloxy) -3,4,6-trimethylphenyl] ethanone) were obtained.
[2998] (4) 3- (benzyloxy) -2-methoxy-1,4,5-trimethylbenzene
[2999] 290 mg (1.20 mmol) of 2- (benzyloxy) -3,4,6-trimethylphenol obtained in (3) was dissolved in acetone (3 mL), and 350 mg (2.54 mmol) of potassium carbonate was added thereto for 15 minutes at room temperature. Stirred. 0.180 mL (2.89 mmol) of methyl iodide was then added and stirred overnight at room temperature. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (The product made by MERCK, 1.05744, 3 pieces, development with ethyl acetate: hexane = 10: 1), 3- (benzyloxy) -2-meth 196 mg (0.766 mmol, yield 63.8%) of oxy-1,4,5-trimethylbenzene was obtained.
[3000] (5) 2-methoxy-3,5,6-trimethylphenol
[3001] 180 mg (0.703 mmol) of 3- (benzyloxy) -2-methoxy-1,4,5-trimethylbenzene obtained in (4) were dissolved in methanol (3 mL), and 0.10 g of 5% palladium-carbon in this solution. Was added and stirred under hydrogen atmosphere (1 atm) for 4 hours. The reaction mixture was filtered through celite and the filtrate was concentrated. 90.7 mg (0.546 mmol, yield 77.7%) of 2-methoxy-3,5,6-trimethylphenol were obtained.
[3002] (6) 6-chloro-3- (2-methoxy-3,5,6-trimethylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-methoxy-3,5,6- Trimethylphenoxy) pyridazine 1-oxide mixture (step B-2)
[3003] 90.0 mg (0.542 mmol) of 2-methoxy-3,5,6-trimethylphenol obtained in (5), 1,4-dioxane (1.5 mL) and dimethyl sulfoxide (1.5 mL) were mixed and added to this mixture. 73.5 mg (0.656 mmol) of potassium tert-butoxide were added and stirred for 15 minutes under ice-cooling. 93.2 mg (0.565 mmol) of 3,6-dichloropyridazine 1-oxide was added to the mixture, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (The product made by MERCK, 1.05744, 3 pieces, and developed as hexane: ethyl acetate = 2: 1). 6-chloro- 3- (2-methoxy- 140 mg of a mixture of 3,5,6-trimethylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-methoxy-3,5,6-trimethylphenoxy) pyridazine 1-oxide Got it.
[3004] (7) 4,6-dichloro-3- (2-methoxy-3,5,6-trimethylphenoxy) pyridazine (Step B-3)
[3005] 6-chloro-3- (2-methoxy-3,5,6-trimethylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-methoxy-3,5 obtained by (6) 140 mg of a mixture of, 6-trimethylphenoxy) pyridazine 1-oxide and 0.25 mL (2.7 mmol) of phosphorus oxychloride were mixed and stirred at room temperature overnight. The reaction mixture was poured into water and extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (The product made by MERCK, 1.05744, 3 pieces, and developed as hexane: ethyl acetate = 2: 1), and 4,6- dichloro-3- (2- 111 mg (0.355 mmol, yield 62.8% from 3,6-dichloropyridazine 1-oxide) of methoxy-3,5,6-trimethylphenoxy) pyridazine were obtained. Also, 38.3 mg (0.130 mmol, 3,6-dichloropyridazine 1-oxide of 3-chloro-6- (2-methoxy-3,5,6-trimethylphenoxy) pyridazine 1-oxide Yield 23.0%).
[3006] (8) 6-chloro-3- (2-methoxy-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1128, step B-4)
[3007] 2 mol in 111 mg (0.355 mmol) of dimethylsulfoxide (10 mL) solution of 4,6-dichloro-3- (2-methoxy-3,5,6-trimethylphenoxy) pyridazine obtained by (7) 0.3 mL (0.6 mmol) of / L sodium hydroxide aqueous solution were added, and it stirred at room temperature for 2 hours and 30 minutes. The reaction mixture was poured into ice-cold 1 mol / L aqueous sodium hydroxide solution, and extracted with ethyl acetate. The aqueous layer was separated, concentrated with hydrochloric acid under ice cooling, acidified, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over magnesium sulfate. The residue obtained by distilling off the solvent was washed with ether to give 38.9 mg of 6-chloro-3- (2-methoxy-3,5,6-trimethylphenoxy) -4-pyridazinol (Compound No. 1128). (0.132 mmol, yield 37.2%) were obtained.
[3008] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 6.73 (1H, s), 6.67 (1H, s), 3.69 (3H, s), 2.29 (3H, s), 2.15 (3H, s), 2.09 ( 3H, s).
[3009] Melting point (° C): 209-210.
[3010] Example 624 6-chloro-3- [2- (1-isopropylvinyl) phenoxy] -4-pyridazinol (Compound No. 2529) and 6-chloro-3- [2- (1,2- Dimethyl-1-propenyl) phenoxy] -4-pyridazinol (Compound No. 2542)
[3011] (1) 1- [2- (methoxymethoxy) phenyl] ethanone
[3012] 3.39 g (24.9 mmol) of commercially available 1- (2-hydroxyphenyl) ethanone were dissolved in N, N-dimethylformamide (25 mL), and 1.52 g (38.0 mmol) of 60% sodium hydride was added under ice cooling, followed by ice cooling. Stir under 20 minutes. To this, 3.00 mL (39.5 mmol) of chloro (methoxy) methane was slowly added dropwise and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 4.33 g of 1- [2- (methoxymethoxy) phenyl] ethanone. (24.1 mmol, yield 96.8%) was obtained.
[3013] (2) 2- [2- (methoxymethoxy) phenyl] -3-methyl-2-butanol
[3014] 1.00 g (5.56 mmol) of 1- [2- (methoxymethoxy) phenyl] ethanone obtained in (1) was dissolved in dry tetrahydrofuran (3 mL), and cooled in ice under nitrogen atmosphere to 2 mol / L isopropyl. 2.8 mL (5.6 mmol) of tetrahydrofuran solution of magnesium bromide was added dropwise. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 1 hour 30 minutes. The reaction mixture was poured into water, made acidic with diluted hydrochloric acid, and then extracted with ether. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to give 2- [2- (methoxymethoxy) phenyl] -3-methyl- 0.522 g (2.33 mmol, yield 41.9%) of 2-butanol were obtained.
[3015] (3) 6-chloro-3- [2- (1-isopropylvinyl) phenoxy] pyridazine 1-oxide and 6-chloro-3- [2- (1,2-dimethyl-1-propenyl) Phenoxy] pyridazine 1-oxide and the like
[3016] 0.522 g (2.33 mmol) of 2- [2- (methoxymethoxy) phenyl] -3-methyl-2-butanol obtained in (2) was dissolved in dichloromethane (3 mL), and 0.50 mL of triethylamine under ice-cooling ( 3.6 mmol), then 0.25 mL (3.2 mmol) of methanesulfonylchloride was added and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with dichloromethane. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (Wako gel C-100, hexane: ethyl acetate gradient) to include 2- (1,2-dimethyl-1-propenyl) phenol and the like. 186 mg of crude product were obtained. 132 mg of this crude product were mixed with 1,4-dioxane (2 mL) and dimethylsulfoxide (2 mL), and 100 mg (0.893 mmol) of potassium tert-butoxide were added to this mixture. Subsequently, 119 mg (0.721 mmol) of 3,6-dichloropyridazine 1-oxides were added to the mixture, followed by stirring at room temperature for 5 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane: ethyl acetate gradient) to give 6-chloro-3- [2- (1-isopropylvinyl) phenoxy. 220 mg of a mixture containing] pyridazine 1-oxide and 6-chloro-3- [2- (1,2-dimethyl-1-propenyl) phenoxy] pyridazine 1-oxide and the like was obtained.
[3017] (4) 4,6-dichloro-3- [2- (1-isopropylvinyl) phenoxy] pyridazine and 4,6-dichloro-3- [2- (1,2-dimethyl-1-propenyl) Phenoxy] pyridazine (Process B-3)
[3018] 6-chloro-3- [2- (1-isopropylvinyl) phenoxy] pyridazine 1-oxide and 6-chloro-3- [2- (1,2-dimethyl-1-prop) obtained in (3). 200 mg of a mixture containing phenyl) phenoxy] pyridazine 1-oxide and the like was dissolved in chloroform (0.4 mL), and 0.40 mL (4.3 mmol) of phosphorus oxychloride was mixed and stirred at 70 ° C. for 2 hours. The reaction mixture was poured into water and extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (manufactured by MERCK Corporation, 1.05744, use of 3 pieces, developed three times with hexane: acetone = 20: 1) to obtain 4,6-dichloro-3- [2. -(1-isopropylvinyl) phenoxy] pyridazine (purity 86%, containing 4% 4,6-dichloro-3- [2- (1,2-dimethyl-1-propenyl) phenoxy] pyridazine 23 mg, and 4,6-dichloro-3- [2- (1,2-dimethyl-1-propenyl) phenoxy] pyridazine (81% purity, 4,6-dichloro-3- [2]) 50 mg of-(1-isopropylvinyl) phenoxy] pyridazine containing 19%) was obtained.
[3019] (5) 6-chloro-3- [2- (1-isopropylvinyl) phenoxy] -4-pyridazinol (Compound No. 2529, steps A-3 and A-4)
[3020] 4,6-dichloro-3- [2- (1-isopropylvinyl) phenoxy] pyridazine obtained in (4) (purity 86%, 4,6-dichloro-3- [2- (1,2-dimethyl 23 mg of 1-propenyl) phenoxy] pyridazine was dissolved in dimethylsulfoxide (1 mL), and 80 mg (0.98 mmol) of sodium acetate was added thereto, followed by stirring at 60 ° C for 9 hours. The reaction mixture was cooled, poured into water, and made acidic with diluted hydrochloric acid. The mixture was extracted with ethyl acetate, the organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (manufactured by MERCK Corporation, 1.05744, use of 2 sheets, developed with hexane: ethyl acetate = 1: 1) to give 6-chloro-3- [2- (1 -Isopropylvinyl) phenoxy] -4-pyridazinol (Compound No. 2529, 91% purity, 9% 6-chloro-3- [2- (1,2-dimethyl-1-propenyl) phenoxy] 4.5 mg of 4-pyridazinol) was obtained. Further, 6-chloro-3- [2- (1-isopropylvinyl) phenoxy] -4-pyridazinol (23% 6-chloro-3- [2- (1,2-dimethyl) with a purity of 77% 1-1-mg of 1-propenyl) phenoxy] -4-pyridazinol) was obtained.
[3021] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.40-7.05 (4H, m), 6.59 (1H, s), 5.90 (1H, s), 5.04 (1H, s), 2.71 (1H, septet, J = 6.9 Hz), 0.98 (6H, d, J = 6.9 Hz).
[3022] Physical property: Amorphous.
[3023] (6) 6-chloro-3- [2- (1,2-dimethyl-1-propenyl) phenoxy] -4-pyridazinol (Compound No. 2542, steps A-3 and A-4)
[3024] 4,6-dichloro-3- [2- (1,2-dimethyl-1-propenyl) phenoxy] pyridazine obtained in (4) (81% purity, 4,6-dichloro-3- [2- ( 50 mg of 1-isopropylvinyl) phenoxy] pyridazine) was dissolved in dimethylsulfoxide (2 mL), 68 mg (0.83 mmol) of sodium acetate was added thereto, and the mixture was stirred at 50 ° C for 11 hours. The reaction mixture was cooled, poured into water, and made acidic with diluted hydrochloric acid. The mixture was extracted with ethyl acetate, the organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by MERCK Corporation, 1.05744, use of 2 sheets, developed with hexane: ethyl acetate = 2: 1), and 6-chloro-3- [2- (1 , 2-dimethyl-1-propenyl) phenoxy] -4-pyridazinol (compound 2542, purity 86%, 14% 6-chloro-3- [2- (1-isopropylvinyl) phenoxy]- 40.2 mg) of 4-pyridazinol) was obtained. In addition, 6-chloro-3- [2- (1,2-dimethyl-1-propenyl) phenoxy] -4-pyridazinol (73% of 6-chloro-3- [2- ( 3.7 mg of 1-isopropylvinyl) phenoxy] -4-pyridazinol) was obtained.
[3025] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.38-7.05 (4H, m), 6.59 (1H, s), 1.78 (3H, s), 1.62 (3H, s), 1.46 (3H, s).
[3026] Physical property: Amorphous.
[3027] Example 625 6-chloro-3- [2- (2-methyl-1-propenyl) phenoxy] -4-pyridazinol (Compound No. 2540)
[3028] (1) 1- (2-methoxyphenyl) -2-methyl-1-propanol
[3029] To a commercially available 2-methoxybenzaldehyde 1.01 g (7.43 mmol), dry tetrahydrofuran (3 mL) was added and ice-cooled under nitrogen atmosphere. 3.8 mL (7.6 mmol) of a tetrahydrofuran solution of 2 mol / L isopropylmagnesium bromide was added dropwise thereto. After completion of the dropwise addition, the reaction mixture was stirred for 1 hour under ice-cooling. The reaction mixture was poured into water, made acidic with diluted hydrochloric acid, and then extracted with ether. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate gradient) to obtain 1- (2-methoxyphenyl) -2-methyl-1-propanol. 1.00 g (5.56 mmol, yield 74.8%) were obtained.
[3030] (2) 1- (1-chloro-2-methylpropyl) -2-methoxybenzene
[3031] 630 mg (3.50 mmol) of 1- (2-methoxyphenyl) -2-methyl-1-propanol obtained in (1) were dissolved in dichloromethane (3 mL), followed by 0.70 mL (5.0 mmol) of triethylamine, followed by methane. 0.35 mL (4.5 mmol) of sulfonylchloride was added and stirred for 1 hour. The reaction mixture was poured into water and extracted with dichloromethane. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 720 mg of 1- (1-chloro-2-methylpropyl) -2-methoxybenzene.
[3032] (3) 1-methoxy-2- (2-methyl-1-propenyl) benzene
[3033] 410 mg of 1- (1-chloro-2-methylpropyl) -2-methoxybenzene obtained in (2) was dissolved in dry N, N-dimethylformamide (8 mL), and then potassium tert-butoxide under ice-cooling. 395 mg (3.52 mmol) was added. The reaction mixture was heated to reflux for 2 hours, then cooled to room temperature and poured into water. The organic layers obtained by extraction with hexane were combined, washed successively with water and brine. The mixture was dried over anhydrous magnesium sulfate, and the solvent was distilled off to obtain 460 mg of 1-methoxy-2- (2-methyl-1-propenyl) benzene.
[3034] (4) 2- (2-methyl-1-propenyl) phenol
[3035] Under a nitrogen atmosphere, 60.0 mg (1.50 mmol) of 60% sodium hydride was suspended in dry N, N-dimethylformamide (3 mL), and 0.11 mL (1.5 mmol) of ethanethiol was slowly added dropwise to the suspension under ice cooling. After stirring for 10 minutes, a dry N, N-dimethylformamide (0.5 mL) solution of 200 mg of 1-methoxy-2- (2-methyl-1-propenyl) benzene obtained in (3) was added dropwise, and 2 It was heated to reflux for 30 minutes. After cooling, the reaction mixture was poured into water, diluted with hydrochloric acid, and acidified, and extracted with hexane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 220 mg of 2- (2-methyl-1-propenyl) phenol.
[3036] (5) 6-chloro-3- [2- (2-methyl-1-propenyl) phenoxy] pyridazine 1-oxide and 3-chloro-6- [2- (2methyl-1-propenyl) Phenoxy] pyridazine 1-oxide mixture (Step B-2)
[3037] 200 mg of 2- (2-methyl-1-propenyl) phenol obtained in (4), 1,4-dioxane (2 mL) and dimethylsulfoxide (2 mL) were mixed, and to this mixture potassium tert-butoxide 151 mg (1.35 mmol) of seeds were added and stirred under ice cooling for 15 minutes. 207 mg (1.25 mmol) of 3,6-dichloropyridazine 1-oxide were added to the mixture, and the mixture was stirred for 15 minutes under ice cooling, followed by 4 hours at room temperature. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to give 6-chloro-3- [2- (2-methyl-1-propenyl). 90.0 mg (0.325 mmol, 1-) of a mixture of phenoxy] pyridazine 1-oxide and 3-chloro-6- [2- (2-methyl-1-propenyl) phenoxy] pyridazine 1-oxide Yield 41.2% from (2-methoxyphenyl) -2-methyl-1-propanol).
[3038] (6) 4,6-dichloro-3- [2- (2-methyl-1-propenyl) phenoxy] pyridazine (Step B-3)
[3039] 6-chloro-3- [2- (2-methyl-1-propenyl) phenoxy] pyridazine 1-oxide and 3-chloro-6- [2- (2-methyl-1- obtained in (5) 90.0 mg (0.325 mmol) of a mixture of propenyl) phenoxy] pyridazine 1-oxide was dissolved in chloroform (0.2 mL), 0.20 mL (2.2 mmol) of phosphorus oxychloride was mixed and stirred at 70 ° C for 2 hours. The reaction mixture was poured into water and extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (The product made by MERCK, 1.05744, 3 pieces, and developed with hexane: ethyl acetate = 9: 1), and 4,6- dichloro-3- [2- 85.0 mg (0.288 mmol, yield 88.6%) of (2-methyl-1-propenyl) phenoxy] pyridazine were obtained.
[3040] (7) 6-chloro-3- [2- (2-methyl-1-propenyl) phenoxy] -4-pyridazinol (Compound No. 2540, steps A-3 and A-4)
[3041] 85.0 mg (0.288 mmol) of 4,6-dichloro-3- [2- (2-methyl-1-propenyl) phenoxy] pyridazine obtained in (6) was dissolved in dimethyl sulfoxide (3 mL), and sodium acetate 122 mg (1.49 mmol) was added and stirred at 120 ° C. for 2 hours. The reaction mixture was cooled to room temperature, poured into water, and made acidic with diluted hydrochloric acid. The mixture was extracted with ethyl acetate, the organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by MERCK, 1.05744, use of 2 pieces, developed with ethyl acetate) to give 6-chloro-3- [2- (2-methyl-1-prop Phenyl) phenoxy] -4-pyridazinol (Compound No. 2540) was obtained 39.6 mg (0.143 mmol, yield 49.7%).
[3042] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.35-7.15 (3H, m), 7.15-7.05 (1H, m), 6.65 (1H, s), 6.05 (1H, s), 1.76 (3H, s ), 1.70 (3H, s).
[3043] Melting point (° C.): 149-152.
[3044] Example 626 6-Chloro-3- (3-hydroxyphenoxy) -4-pyridazinol (Compound No. 2544)
[3045] (1) 1- {3-[(6-chloro-1-oxide-3-pyridazinyl) oxy] phenyl} ethanone and 1- {3-[(6-chloro-2-oxide-3- Mixture of pyridazinyl) oxy] phenyl} ethanone
[3046] 306 mg (2.25 mmol) of 1- (3-hydroxyphenyl) ethanone, 1,4-dioxane (6 mL) and dimethylsulfoxide (6 mL) were mixed and 297 mg of potassium tert-butoxide was added to the mixture. (2.65 mmol) was added and the mixture was stirred for 15 minutes under ice cooling. 342 mg (2.07 mmol) of 3,6-dichloropyridazine 1-oxide was added to the mixture under ice cooling, and the mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain 1- {3-[(6-chloro-1-oxide-3- 400 mg (1.51 mmol, yield 72.9%) of a mixture of pyridazinyl) oxy] phenyl} ethanone and 1- {3-[(6-chloro-2-oxide-3-pyridazinyl) oxy] phenyl} ethanone )
[3047] (2) 3-[(6-chloro-1-oxide-3-pyridazinyl) oxy] phenyl acetate and 3-[(6-chloro-2-oxide-3-pyridazinyl) oxy] phenyl acetate Mixture of
[3048] 1- {3-[(6-chloro-1-oxide-3-pyridazinyl) oxy] phenyl} ethanone obtained in (1) and 1- {3-[(6-chloro-2-oxide- 400 mg (1.51 mmol) of a mixture of 3-pyridazinyl) oxy] phenyl} ethanone are dissolved in 3 mL of dichloromethane, where 1.1 g (purity 70-75%, 4.5-4.8 mmol) of m-chloroperbenzoic acid is added thereto. (3 mL) was added and stirred at room temperature for 4 days. Saturated aqueous sodium sulfite solution was added to the reaction mixture, followed by stirring, followed by extraction with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain the raw material and 3-[(6-chloro-1-oxide-3-pyridine). 330 mg of a mixture of dazinyl) oxy] phenyl acetate and 3-[(6-chloro-2-oxide-3-pyridazinyl) oxy] phenyl acetate were obtained. 280 mg of this mixture was dissolved in dichloromethane (3 mL), and 1.1 g (purity 70-75%, 4.5-4.8 mmol) of m-chloroperbenzoic acid was added thereto, followed by stirring at room temperature overnight. The reaction mixture was poured into 10% aqueous sodium sulfite solution and extracted with dichloromethane. The organic layer was washed with water and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was washed with hexane to give 3-[(6-chloro-1-oxide-3-pyridazinyl) oxy] phenyl acetate and 3-[(6-chloro-2-oxide- 310 mg of a mixture of 3-pyridazinyl) oxy] phenyl acetate was obtained.
[3049] (3) 3-[(4,6-dichloro-3-pyridazinyl) oxy] phenyl acetate (step B-3)
[3050] 3-[(6-chloro-1-oxide-3-pyridazinyl) oxy] phenyl acetate and 3-[(6-chloro-2-oxide-3-pyridazinyl) oxy] obtained in (2). 310 mg of a mixture of phenyl acetate was mixed with chloroform (0.4 mL), 0.40 mL (4.3 mmol) of phosphorus oxychloride was mixed and stirred at 70 ° C. for 3 hours. The reaction mixture was poured into water, stirred, and extracted with dichloromethane. The organic layers were combined, washed with water and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain 3-[(4,6-dichloro-3-pyridazinyl) oxy]. 46.0 mg (0.154 mmol, 1- {3-[(6-chloro-1-oxide-3-pyridazinyl) oxy] phenyl} ethanone and 1- {3-[(6-chloro-2) -9.6% of the yield from the mixture of -oxide-3-pyridazinyl) oxy] phenyl} ethanone) was obtained.
[3051] (4) 6-chloro-3- (3-hydroxyphenoxy) -4-pyridazinol (Compound No. 2544, steps A-3 and A-4)
[3052] 40.0 mg (0.134 mmol) of 3-[(4,6-dichloro-3-pyridazinyl) oxy] phenyl acetate obtained in (3) were dissolved in dimethyl sulfoxide (1 mL), and 56.0 mg (0.683 mmol) of sodium acetate. Was added and stirred at 120 ° C. for 1 hour. After cooling to room temperature, the reaction mixture was poured into 0.5 mol / L aqueous sodium hydroxide solution, and washed with ethyl acetate. The aqueous layer was made acidic with 4 mol / L hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the solvent was distilled off to obtain 30 mg (0.126 mmol, yield 94.0%) of 6-chloro-3- (3-hydroxyphenoxy) -4-pyridazinol (Compound No. 2544).
[3053] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.25-7.10 (1 H, m), 6.70-6.57 (4 H, m).
[3054] Melting point (° C): 248-251.
[3055] Example 627 6-Chloro-3- (2-iodo-3-methoxyphenoxy) -4-pyridazinol (Compound No. 2551)
[3056] (1) 1-methoxy-3- (methoxymethoxy) benzene
[3057] 3.68 g (29.7 mmol) of commercial 3-methoxyphenol was dissolved in N, N-dimethylformamide (50 mL), and 1.81 g (45.4 mmol) of 60% sodium hydride was added under ice cooling, followed by stirring for 20 minutes under ice cooling. To this, 4.05 mL (53.3 mmol) of chloro (methoxy) methane was slowly added dropwise under ice-cooling, and the mixture was stirred overnight at room temperature. Saturated aqueous ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako Gel C-100, hexane-ethyl acetate gradient) to obtain 4.81 g of 1-methoxy-3- (methoxymethoxy) benzene. 28.6 mmol, yield 96.3%).
[3058] (2) 2-iodo-1-methoxy-3- (methoxymethoxy) benzene
[3059] 3.70 g (22.0 mmol) of 1-methoxy-3- (methoxymethoxy) benzene obtained in (1) was dissolved in dry ether (50 mL), cooled to -78 ° C under nitrogen atmosphere, and tetramethylethylenediamine 5.60 mL (37.2 mmol) was added followed by 22.0 mL (35.2 mmol) of n-butyllithiumhexane solution (1.60 M). After stirring at −78 ° C. for 30 minutes, followed by 0 ° C. for 30 minutes, it was cooled to −78 ° C. and 9.80 g (38.6 mmol) of iodine were added. It stirred at -78 degreeC for 30 minutes, The saturated aqueous ammonium chloride solution was added to the reaction mixture, and it extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium thiosulfate solution and dried over anhydrous magnesium sulfate. The solvent was distilled off and 6.59 g of 2-iodo-1-methoxy-3- (methoxymethoxy) benzene was obtained.
[3060] (3) 2-iodo-3-methoxyphenol
[3061] 6.59 g of 2-iodo-1-methoxy-3- (methoxymethoxy) benzene obtained in (2) was dissolved in methanol (70 mL), and concentrated hydrochloric acid (0.18 mL) was added dropwise thereto at 65 ° C for 1 hour. The mixture was heated and stirred for 15 minutes. Further concentrated hydrochloric acid (0.20 mL) was added and the mixture was heated and stirred at 65 ° C. for 2 hours and 40 minutes. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate gradient) to obtain 4.61 g (18.4 mmol, 1) of 2-iodo-3-methoxyphenol. 83.6% of yield from -methoxy-3- (methoxymethoxy) benzene).
[3062] (4) 6-chloro-3- (2-iodo-3-methoxyphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-iodo-3-methoxyphenoxy) pyridazine Mixture of 1-oxides (Step B-2)
[3063] 298 mg (1.19 mmol) of 2-iodo-3-methoxyphenol obtained in (3), 1,4-dioxane (2.5 mL) and dimethyl sulfoxide (2.5 mL) were mixed, and to this mixture potassium tert- 215 mg (1.92 mmol) of butoxide were added and stirred for 10 minutes under ice-cooling. 196 mg (1.19 mmol) of 3,6-dichloropyridazine 1-oxides were added to this mixture under ice cooling, and it stirred at room temperature for 3 days. Saturated aqueous ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 3: 1, followed by hexane: ethyl acetate = 1: 1), and 6-chloro-3- (2-iodo 324 mg (0.855 mmol, yield) of a mixture of 3-methoxyphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-iodo-3-methoxyphenoxy) pyridazine 1-oxide 71.8%).
[3064] (5) 4,6-dichloro-3- (2-iodo-3-methoxyphenoxy) pyridazine (Step B-3)
[3065] 6-chloro-3- (2-iodo-3-methoxyphenoxy) pyridazine 1-oxide and 3-chloro-6- (2-iodo-3-methoxyphenoxy) obtained in (4). 1.0 mL (1.1 mmol) of phosphorus oxychloride was added to 324 mg (0.855 mmol) of the mixture of pyridazine 1-oxide, and stirred overnight at room temperature. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate = 5: 1) to give 4,6-dichloro-3- (2-iodo-3- 225 mg (0.567 mmol, yield 66.3%) of methoxyphenoxy) pyridazine were obtained.
[3066] (6) 6-chloro-3- (2-iodo-3-methoxyphenoxy) -4-pyridazinol (Compound No. 2551, steps A-3 and A-4)
[3067] 105 mg (0.264 mmol) of 4,6-dichloro-3- (2-iodo-3-methoxyphenoxy) pyridazine obtained in (5) were dissolved in dimethyl sulfoxide (2 mL), and 118 mg of sodium acetate ( 1.44 mmol) was added and stirred at 120 ° C. for 1 hour 30 minutes. After cooling to room temperature, 4 mol / L aqueous hydrochloric acid solution was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layers were combined and washed with saturated brine. After drying over anhydrous magnesium sulfate, the residue obtained by distilling off the solvent was washed with isopropyl ether to give 6-chloro-3- (2-iodo-3-methoxyphenoxy) -4-pyridazinol (compound No. 2551) was obtained 51.2 mg (0.135 mmol, yield 51.1%).
[3068] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.39 (1H, t, J = 8.4 Hz), 6.84 (2H, br.t, J = 8.4 Hz), 6.73 (1H, s), 3.90 (3H, s).
[3069] Melting point (° C): 231-234.
[3070] Example 628 6-chloro-3-{[7- (3-hydroxypropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} -4-pyri Dazinol (Compound No. 2555)
[3071] (1) 2-iodo-3-methoxyphenyl trifluoromethanesulfonate
[3072] 3.75 g (15.0 mmol) of 2-iodo-3-methoxyphenol obtained in Example 627 (3) were dissolved in dry dichloromethane, and 7.28 mL (90.0 mmol) of pyridine was added. The mixture was cooled to -20 deg. C, 5.40 mL (32.2 mmol) of trifluoromethanesulfonic anhydride was added, followed by stirring for 3 hours and 50 minutes. The reaction mixture was poured into water, and extracted with dichloromethane, followed by ethyl acetate. The organic layers were combined, washed successively with 4 mol / L hydrochloric acid, water, and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate = 10: 1) to give 2-iodo-3-methoxyphenyl trifluoromethanesulfonate 5.52 g (14.5 mmol, yield 96.7%) was obtained.
[3073] (2) tert-butyl [(8-methoxy-2,3,4,4a-tetrahydro-8 bH-benzo [3,4] cyclobuta [1,2-b] pyran-8b-yl) oxy] Dimethylsilane
[3074] 1.10 g (2.88 mmol) of 2-iodo-3-methoxyphenyl trifluoromethanesulfonate obtained in (1) were dissolved in dry tetrahydrofuran (15 mL), and commercially available tert-butyl (3, 1.00 mL (4.37 mmol) of 4-dihydro-2H-pyran-6-yloxy) dimethylsilane were added. The mixture was cooled to −78 ° C., and 4.50 mL (7.20 mmol) of n-butyllithium hexane solution (1.60 M) was added and stirred for 20 minutes. The reaction mixture was poured into a pH 7 buffer (prepared by dissolving 9.1 g KH ₂ PO ₄ and 4.3 g Na ₂ HPO ₄ in 1 L of water) and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Wako gel C-100, hexane-ethyl acetate = 50: 1) to give tert-butyl [(8-methoxy-2,3,4 0.897 g (2.79 mmol, yield 96.9%) of 4a-tetrahydro-8bH-benzo [3,4] cyclobuta [1,2-b] pyran-8b-yl) oxy] dimethylsilane were obtained.
[3075] (3) 8- (3-hydroxypropyl) -5-methoxybicyclo [4.2.0] octa-1,3,5-trien-7-one
[3076] Tert-butyl [(8-methoxy-2,3,4,4a-tetrahydro-8bH-benzo [3,4] cyclobuta [1,2-b] pyran-8b-yl) oxy obtained in (2). ] 897 mg (2.79 mmol) of dimethylsilane was dissolved in acetonitrile (12 mL), and 0.30 mL (7.96-8.30 mmol) of 46-47% hydrofluoric acid aqueous solution was added thereto under ice cooling, followed by stirring for 30 minutes. The reaction mixture was poured into a saturated aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate = 7: 3) to give 8- (3-hydroxypropyl) -5-methoxybicyclo 446 mg (2.17 mmol, yield 77.8%) of [4.2.0] octa-1,3,5-trien-7-one were obtained.
[3077] (4) 8- (3-chloropropyl) -5-methoxybicyclo [4.2.0] octa-1,3,5-trien-7-one
[3078] 474 mg (2.30 mmol) of 8- (3-hydroxypropyl) -5-methoxybicyclo [4.2.0] octa-1,3,5-trien-7-one obtained in (3) was converted to dichloromethane (22 mL), 467 mg (3.49 mmol) of N-chlorosuccinimide and 917 mg (3.5 mmol) of triphenylphosphine were added, followed by stirring at room temperature for 1 hour. The reaction mixture was poured into water, saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate = 20: 1) to give 8- (3-chloropropyl) -5-methoxybicyclo [ 4.2.0] 409 mg (1.82 mmol, yield 79.1%) of octa-1,3,5-trien-7-one was obtained.
[3079] (5) 7- (3-chloropropyl) -2-methoxybicyclo [4.2.0] octa-1,3,5-triene
[3080] 111 mg (0.408 mmol) of mercury chloride (HgCl ₂ ) was added to dissolve water (6 mL), and 4.00 g (6.12 mmol) of zinc powder was added thereto, followed by stirring at room temperature for 50 minutes. The remaining solid was washed once with water, except the supernatant. To this, water (6.0 mL), followed by concentrated hydrochloric acid (5.0 mL) was slowly added, and also acetic acid (2.4 mL), finally obtained from 8- (3-chloropropyl) -5-methoxybicyclo [4.2]. .0] 409 mg (1.82 mmol) of octa-1,3,5-trien-7-one was added in toluene (2 mL) and ethanol (2 mL). The mixture was stirred at 115 ° C. overnight and cooled to room temperature. Toluene (20 mL) was added and stirred for 30 minutes, and the organic layer was separated. The obtained organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate = 20: 1) to give 7- (3-chloropropyl) -2-methoxybicyclo [4.2]. .0] octa-1,3,5-triene was obtained as 304 mg (1.44 mmol, yield 79.1%).
[3081] (6) 7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-ol
[3082] Dissolve 304 mg (1.44 mmol) of 7- (3-chloropropyl) -2-methoxybicyclo [4.2.0] octa-1,3,5-triene obtained in (5) in dichloromethane (2.0 mL), 0.50 mL (5.32 mmol) of boron tribromide was added while stirring under ice cooling, and the mixture was stirred for 1 hour under ice cooling. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed with brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate = 4: 1) to obtain 7- (3-chloropropyl) bicyclo [4.2.0] octa 303 mg (1.54 mmol, yield quantitative) of -1,3,5-trien-2-ol were obtained.
[3083] (7) 6-chloro-3-{[7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} pyridazine 1-oxide and Mixture of 3-chloro-6-{[7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} pyridazine 1-oxide (process B-2)
[3084] 303 mg (1.54 mmol) of 7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-ol obtained in (6), 1,4-dioxane (2.0 mL ) And dimethyl sulfoxide (2.0 mL) were added, and 275 mg (2.46 mmol) of potassium tert-butoxide were added to the mixture, which was stirred for 10 minutes under ice cooling. To this mixture was added 254 mg (1.54 mmol) of 3,6-dichloropyridazine 1-oxide under ice-cooling and stirred at room temperature overnight. Saturated aqueous ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 3: 1) to give 6-chloro-3-{[7- (3-chloropropyl) bicyclo [4.2. 0] octa-1,3,5-trien-2-yl] oxy} pyridazine 1-oxide and 3-chloro-6-{[7- (3-chloropropyl) bicyclo [4.2.0] octa 364 mg (1.12 mmol, yield 72.7%) of a mixture of -1,3,5-trien-2-yl] oxy} pyridazine 1-oxide were obtained.
[3085] (8) 4,6-dichloro-3-{[7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} pyridazine (process B -3)
[3086] 6-chloro-3-{[7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} pyridazine 1-jade obtained in (7). Seed and mixture of 3-chloro-6-{[7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} pyridazine 1-oxide 1.0 mL (11 mmol) of phosphorus oxychloride was added to 364 mg (1.12 mmol), and the mixture was stirred at room temperature for 7 hours and 15 minutes. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 2: 1) to give 4,6-dichloro-3-{[7- (3-chloropropyl) bicyclo [ 4.2.0] 253 mg (0.735 mmol, yield 65.6%) of octa-1,3,5-trien-2-yl] oxy} pyridazine were obtained.
[3087] (9) 6-chloro-3-{[7- (3-hydroxypropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} -4-pyridazinol (Compound No. 2555, Steps A-3 and A-4)
[3088] 4,6-dichloro-3-{[7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} pyridazine 253 obtained in (8). mg (0.735 mmol) was dissolved in dimethyl sulfoxide (5.0 mL), and 250 mg (3.05 mmol) of sodium acetate were added thereto, followed by heating and stirring at 120 ° C. for 2 hours. After cooling to room temperature, 4 mol / L aqueous hydrochloric acid solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined and washed with saturated brine. After drying over anhydrous magnesium sulfate, the residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 2: 1) to give 6-chloro-3-{[7- (3-hydrate). 48.5 mg (0.158 mmol, Yield 21.5%) of oxypropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} -4-pyridazinol (Compound No. 2555) were obtained. . Furthermore, 28.2 mg of 6-chloro-3-{[7- (3-chloropropyl) bicyclo [4.2.0] octa-1,3,5-trien-2-yl] oxy} -4-pyridage Nol and 3- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] bicyclo [4.2.0] octa-1,3,5-trien-7-yl} propyl acetate A mixture of was obtained.
[3089] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.22-7.18 (1H, m), 6.98-6.94 (2H, m), 6.70 (1H, s), 3.62-3.56 (2H, m), 3.46 (1H , br.s), 3.34 (1H, br.s), 3.18 (1H, dd, J = 13.9, 5.5 Hz), 2.62 (1H, dd, J = 13.9, 2.2 Hz), 1.81-1.62 (4H, m ).
[3090] Properties: Oily substance.
[3091] Example 629 6-chloro-3-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] -4-pyridazinol (compound Number 2556)
[3092] (1) 5-methoxy-8,8-dimethylbicyclo [4.2.0] octa-1,3,5-trien-7-one
[3093] 723 mg (1.89 mmol) of 2-iodo-3-methoxyphenyl trifluoromethanesulfonate obtained in the method of Example 628 (1) were dissolved in dry tetrahydrofuran (10 mL), and sold under a nitrogen atmosphere, commercially available [ 0.50 mL (2.47 mmol) of (1-methoxy-2-methyl-1-propynyl) oxy] (trimethyl) silane was added. The mixture was cooled to -78 ° C, 2.70 mL (4.32 mmol) of n-butyllithium hexane solution (1.60 M) was added and stirred for 20 minutes. The reaction mixture was poured into a pH 7 buffer (prepared by dissolving 9.1 g KH ₂ PO ₄ and 4.3 g Na ₂ HPO ₄ in 1 L of water) and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and tetrahydrofuran (2.0 mL), water (0.2 mL), acetic acid (2.0 mL) were added to the residue, and the mixture was stirred at room temperature for 1 hour. Ether was added to the reaction mixture, which was washed sequentially with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 2: 1) to give 5-methoxy-8,8-dimethylbicyclo [4.2.0] octa-1, 182 mg (1.03 mmol, yield 54.5%) of 3,5-trien-7-one were obtained.
[3094] (2) 2-methoxy-7,7-dimethylbicyclo [4.2.0] octa-1,3,5-triene
[3095] 109 mg (0.401 mmol) of mercury chloride (HgCl ₂ ) was added thereto to dissolve water (6 mL), and 3.98 g (6.09 mmol) of zinc powder was added thereto, followed by stirring at room temperature for 1 hour. The remaining solid, excluding the supernatant, was washed once with water. To this, water (6.0 mL), followed by concentrated hydrochloric acid (5.0 mL) was slowly added, and acetic acid (2.4 mL), and finally 5-methoxy-8,8-dimethylbicyclo [4.2.0] obtained in (1). ] 182 mg (1.03 mmol) of octa-1,3,5-trien-7-one were added in toluene (2 mL) and ethanol (2 mL). The mixture was stirred at 115 ° C. overnight and cooled to room temperature. Toluene (20 mL) was added and stirred for 20 minutes, and the organic layer was separated. The obtained organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 25: 1) to give 2-methoxy-7,7-dimethylbicyclo [4.2.0] octa-1, 85.1 mg (0.525 mmol, yield 51.0%) of 3,5-triene were obtained.
[3096] (3) 7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-ol
[3097] 85.1 mg (0.525 mmol) of 2-methoxy-7,7-dimethylbicyclo [4.2.0] octa-1,3,5-triene obtained in (2) are dissolved in dichloromethane (5.0 mL), and ice-cooled. 0.20 mL (2.12 mmol) of boron tribromide was added while stirring, and it stirred under ice cooling for 2 hours and 10 minutes. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 97.6 mg of 7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-ol.
[3098] (4) 6-chloro-3-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] pyridazine 1-oxide and 3-chloro -6-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] pyridazine 1-oxide (step B-2)
[3099] 97.6 mg of 7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-ol obtained in (3), 1,4-dioxane (1.5 mL) and dimethyl sulfoxide (1.5 mL) was mixed, and 97.8 mg (0.873 mmol) of potassium tert-butoxide was added to the mixture, which was stirred for 10 minutes under ice cooling. To this mixture was added 90.2 mg (0.547 mmol) of 3,6-dichloropyridazine 1-oxide under ice-cooling and stirred at room temperature overnight. Saturated aqueous ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (developed twice with hexane: ethyl acetate = 3: 1) to give 6-chloro-3-[(7,7-dimethylbicyclo [4.2.0]. ] Octa-1,3,5-trien-2-yl) oxy] pyridazine 1-oxide and 3-chloro-6-[(7,7-dimethylbicyclo [4.2.0] octa-1,3 61.7 mg (0.223 mmol, 2-methoxy-7,7-dimethylbicyclo [4.2.0] octa-1,3, containing 6,5 trien-2-yl) oxy] pyridazine 1-oxide mixture Yield 42.5% from 5-triene) was obtained.
[3100] (5) 4,6-dichloro-3-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] pyridazine (Step B-3)
[3101] 6-chloro-3-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] pyridazine 1-oxide and 3 obtained in (4). 61.7 mg (0.223 mmol) of a mixture of -chloro-6-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] pyridazine 1-oxide To the reaction was added 0.50 mL (5.4 mmol) of phosphorus oxychloride, followed by stirring at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 5: 1) to give 4,6-dichloro-3-[(7,7-dimethylbicyclo [4.2.0]. 43.7 mg (0.148 mmol, yield 66.4%) of octa-1,3,5-trien-2-yl) oxy] pyridazine were obtained.
[3102] (6) 6-chloro-3-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] -4-pyridazinol (Compound No. 2556 , Process A-3 and process A-4)
[3103] 43.7 mg (0.148) of 4,6-dichloro-3-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5-trien-2-yl) oxy] pyridazine obtained in (5) Mmol) was dissolved in dimethyl sulfoxide (2.0 mL), and 63.1 mg (0.770 mmol) of sodium acetate were added thereto, and the resulting mixture was heated and stirred at 120 ° C for 2 hours. After cooling to room temperature, 4 mol / L aqueous hydrochloric acid solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the residue obtained by distilling off the solvent was washed with isopropyl ether to give 6-chloro-3-[(7,7-dimethylbicyclo [4.2.0] octa-1,3,5 31.6 mg (0.114 mmol, yield 77.0%) of -trien-2-yl) oxy] -4-pyridazinol (Compound No. 2556).
[3104] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.26-7.19 (1H, m), 6.97-6.89 (2H, m), 6.71 (1H, s), 2.81 (2H, s), 1.41 (6H, s ).
[3105] Melting Point (° C): 197-199.
[3106] Example 630 4-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -3-methylphenyl acetate (Compound No. 2572)
[3107] (1) 1- {4-[(6-chloro-1-oxide-3-pyridazinyl) oxy] -3-methylphenyl} ethanone and 1- {4-[(6-chloro-2-oxide A mixture of -3-pyridazinyl) oxy] -3-methylphenyl} ethanone (step B-2)
[3108] Commercially available 1- (4-hydroxy-3-methylphenyl) ethanone 784 mg (5.23 mmol), 1,4-dioxane (5 mL) and dimethylsulfoxide (5 mL) were mixed and potassium tert was added to the mixture. -938 mg (8.38 mmol) of butoxide were added and stirred for 10 minutes under ice-cooling. 861 mg (5.22 mmol) of 3,6-dichloropyridazine 1-oxide was added to the mixture under ice-cooling, and the mixture was stirred overnight at room temperature. Saturated aqueous ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate = 5: 1) to give 1- {4-[(6-chloro-1-oxide A mixture of -3-pyridazinyl) oxy] -3-methylphenyl} ethanone and 1- {4-[(6-chloro-2-oxide-3-pyridazinyl) oxy] -3-methylphenyl} ethanone 758 mg (2.74 mmol, yield 52.5%) were obtained.
[3109] (2) 4-[(6-chloro-1-oxide-3-pyridazinyl) oxy] -3-methylphenyl acetate and 4-[(6-chloro-2-oxide-3-pyridazinyl) oxy ] -3-methylphenyl acetate
[3110] 1- {4-[(6-chloro-1-oxide-3-pyridazinyl) oxy] -3-methylphenyl} ethanone obtained in (1) and 1- {4-[(6-chloro-2- 758 mg (2.74 mmol) of the oxide-3-pyridazinyl) oxy] -3-methylphenyl} ethanone mixture are dissolved in 1,2-dichloroethane (13 mL) and 1.1 g (purity 70-75) of m-chloroperbenzoic acid. %, 4.5-4.8 mmol) dichloromethane (3 mL) solution was added, and stirred at room temperature for 4 days. Saturated aqueous sodium sulfite solution was added to the reaction mixture, followed by stirring, followed by extraction with ethyl acetate. The organic layer was washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to obtain the raw material and 3-[(6-chloro-1-oxide-3-pyridine). 330 mg of a mixture of dazinyl) oxy] phenyl acetate and 3-[(6-chloro-2-oxide-3-pyridazinyl) oxy] phenyl acetate were obtained. 280 mg of this mixture was dissolved in dichloromethane (3 mL), and 2.62 g (purity 70-75%, 10.6-11.4 mmol) of m-chloroperbenzoic acid was added thereto, followed by stirring at room temperature for 4 hours 45 minutes. Furthermore, 1.20 g (purity 70-75%, 4.86-5.20 mmol) m-chloro perbenzoic acid was added, and it stirred at room temperature overnight. The reaction mixture was poured into 10% aqueous sodium sulfite solution, and extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium carbonate solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Waco gel C-100, hexane-ethyl acetate = 5: 1) to obtain the starting material and 4-[(6-chloro-1-oxide-3). 622 mg of a mixture of -pyridazinyl) oxy] -3-methylphenyl acetate and 4-[(6-chloro-2-oxide-3-pyridazinyl) oxy] -3-methylphenyl acetate were obtained. 0.5 mL (4.85 mmol) of 30% hydrogen peroxide water was mixed with 1,2-dichloroethane (2.2 mL), and 3.2 mL (22.7 mmol) of trifluoroacetic anhydride were added dropwise under ice cooling, followed by stirring at room temperature. This mixture was prepared from firstly obtained raw materials and 4-[(6-chloro-1-oxide-3-pyridazinyl) oxy] -3-methylphenyl acetate and 4-[(6-chloro-2-oxide-3- 622 mg of a mixture of pyridazinyl) oxy] -3-methylphenyl acetate was dissolved in 1,2-dichloroethane (2.2 mL) and added under ice cooling, and the mixture was stirred for 1 hour at room temperature overnight under ice cooling. The reaction mixture was poured into 10% aqueous sodium sulfite solution, and extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium carbonate solution, water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to give 4-[(6-chloro-1-oxide-3-pyridazinyl 413 mg (1.40 mmol, yield 51.1%) of a mixture of) oxy] -3-methylphenyl acetate and 4-[(6-chloro-2-oxide-3-pyridazinyl) oxy] -3-methylphenyl acetate were obtained.
[3111] (3) 4-[(4,6-dichloro-3-pyridazinyl) oxy] -3-methylphenyl acetate (step B-3)
[3112] 4-[(6-chloro-1-oxide-3-pyridazinyl) oxy] -3-methylphenyl acetate and 4-[(6-chloro-2-oxide-3-pyridazinyl) obtained in (2). 413 mg (1.40 mmol) of a mixture of) oxy] -3-methylphenyl acetate were dissolved in chloroform (2 mL), 2.0 mL (22 mmol) of phosphorus oxychloride was mixed and stirred at 80 ° C for 3 hours. The reaction mixture was diluted with dichloromethane and then poured into water. This mixture was extracted with dichloromethane and then ethyl acetate. The organic layers were combined, washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Wako gel C-100, hexane-ethyl acetate, hexane-ethyl acetate = 6: 1) to obtain 4-[(4,6-dichloro- 336 mg (1.07 mmol, yield 76.4%) of 3-pyridazinyl) oxy] -3-methylphenyl acetate were obtained.
[3113] (4) 4-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -3-methylphenyl acetate (Compound No. 2572, steps A-3 and A-4)
[3114] 160 mg (0.511 mmol) of 4-[(4,6-dichloro-3-pyridazinyl) oxy] -3-methylphenyl acetate obtained in (3) were dissolved in dimethyl sulfoxide (1.5 mL), and 136 mg of sodium acetate ( 1.66 mmol) was added and stirred at 120 ° C. for 2 hours. After cooling to room temperature, 4 mol / L aqueous hydrochloric acid solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the residue obtained by distilling off the solvent was washed with isopropyl ether to give 4-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] -3-methylphenyl acetate ( 37.3 mg (0.126 mmol) of the compound No. 2572 were obtained. The yield was 24.7%.
[3115] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.13-6.94 (3H, m), 6.70 (1H, s), 2.27 (3H, s), 2.17 (3H, s).
[3116] Melting point (° C.): 255 (decomposition).
[3117] Example 631 6-Chloro-3- [2- (difluoromethyl) -6-methylphenoxy] -4-pyridazinol (Compound No. 2576)
[3118] (1) 2- (methoxymethoxy) -3-methylbenzaldehyde
[3119] 4.96 g (36.5 mmol) of 2-hydroxy-3-methylbenzaldehyde was dissolved in N, N-dimethylformamide (50 mL), and 2.19 g (54.6 mmol) of 60% sodium hydride was added thereto under ice cooling, followed by stirring for 10 minutes. Under ice-cooling, 3.59 mL (47.3 mmol) of chloro (methoxy) methane was added thereto, and the mixture was stirred at room temperature for 1 hour 30 minutes. The reaction mixture was poured into a saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (Daisogel 1001W, hexane: ethyl acetate = 50: 1) to give 6.60 g (36.6 mmol) of 2- (methoxymethoxy) -3-methylbenzaldehyde. , Yield 100%) was obtained.
[3120] (2) 1- (difluoromethyl) -2- (methoxymethoxy) -3-methylbenzene
[3121] 589 mg (3.27 mmol) of 2- (methoxymethoxy) -3-methylbenzaldehyde obtained in (1) were dissolved in dichloromethane (10 mL), and (diethylamino) sulfurtrifluoride (DAST) under nitrogen atmosphere. 0.863 mL (6.52 mmol) was added and the mixture was stirred at room temperature for 3 hours. After standing at room temperature overnight, the reaction mixture was poured into water and extracted with dichloromethane. The organic layers were combined, washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (Daisogel 1001W, hexane: ethyl acetate = 10: 1) to give 1- (difluoromethyl) -2- (methoxymethoxy) -3 229 mg (1.13 mmol, yield 34.6%) of -methylbenzene were obtained.
[3122] (3) 2- (difluoromethyl) -6-methylphenol
[3123] 229 mg (1.13 mmol) of 1- (difluoromethyl) -2- (methoxymethoxy) -3-methylbenzene obtained in (2) was dissolved in methanol (5 mL), and 2 drops of concentrated hydrochloric acid was added at room temperature. It stirred for 30 minutes at 60 degreeC. The reaction mixture was cooled to room temperature and the solvent was distilled off under reduced pressure. Ethyl acetate was added to the residue, washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off and 135 mg (0.854 mmol, yield 75.6%) of 2- (difluoromethyl) -6-methylphenols were obtained.
[3124] (4) 6-chloro-3- [2- (difluoromethyl) -6-methylphenoxy] pyridazine 1-oxide and 3-chloro-6- [2- (difluoromethyl) -6- Methylphenoxy] pyridazine 1-oxide (Step B-1)
[3125] 135 mg (0.854 mmol) of 2- (difluoromethyl) -6-methylphenol obtained in (3) are dissolved in 1,4-dioxane (1.5 mL) and dimethylsulfoxide (1.5 mL), and ice-cold in this mixture. Under, 115 mg (1.03 mmol) of potassium tert-butoxide were added and stirred for 5 minutes. To this mixture was added 141 mg (0.855 mmol) of 3,6-dichloropyridazine 1-oxide under ice-cooling and stirred at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off a solvent was developed by silica gel column chromatography (eluted with hexane: ethyl acetate = 2: 1) and preparative thin layer chromatography (1.05744 3 pieces of MERCK Co., Ltd. use hexane: ethyl acetate = 2: 1). 6-chloro-3- [2- (difluoromethyl) -6-methylphenoxy] pyridazine 1-oxide and 3-chloro-6- [2- (difluoromethyl)- 28.6 mg (0.0997 mmol, yield 11.7%) of a mixture of 6-methylphenoxy] pyridazine 1-oxide was obtained.
[3126] (5) 4,6-dichloro-3- [2- (difluoromethyl) -6-methylphenoxy] pyridazine (Step B-3)
[3127] 6-chloro-3- [2- (difluoromethyl) -6-methylphenoxy] pyridazine 1-oxide and 3-chloro-6- [2- (difluoromethyl)-obtained in (4). 28.6 mg (0.0997 mmol) of a mixture of 6-methylphenoxy] pyridazine 1-oxide was dissolved in chloroform (0.5 mL), and 76.5 mg (0.50 mmol) of phosphorus oxychloride was added to the mixture under heating for 8 hours. After standing at room temperature overnight, water and dichloromethane were added to the reaction mixture, which was stirred for 30 minutes. This was extracted with dichloromethane, the organic layers were combined, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developed as MERCK Co., Ltd. 1.05744 hexane: ethyl acetate = 4: 1) to obtain 4,6-dichloro-3- [2- (difluoromethyl) 19.1 mg (0.0626 mmol, yield 62.8%) of -6-methylphenoxy] pyridazine were obtained.
[3128] (6) 6-chloro-3- [2- (difluoromethyl) -6-methylphenoxy] -4-pyridazinol (Compound No. 2576)
[3129] 19.1 mg (0.0626 mmol) of 4,6-dichloro-3- [2- (difluoromethyl) -6-methylphenoxy] pyridazine obtained in (5) was dissolved in dimethyl sulfoxide (0.5 mL), and sodium acetate 25.7 mg (0.313 mmol) was added and the mixture was heated and stirred at 120 ° C for 2 hours. After cooling to room temperature, water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous sodium sulfate, the residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (developed with 1.05744 ethyl acetate manufactured by MERCK), and then 6-chloro-3- [2- (difluoromethyl) -6 17.8 mg (0.0620 mmol, yield 99.0%) of -methylphenoxy-4-pyridazinol (Compound No. 2576) were obtained.
[3130] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.55-7.25 (3H, m), 6.83 (1H, t, J = 55.1 Hz). 2.15 (3H, s).
[3131] Melting point (° C): 204-205.
[3132] Example 632 6-Chloro-3- [2,4-dibromo-5- (ethylsulfanyl) phenoxy] -4-pyridazinol (Compound No. 2596)
[3133] (1) 4,6-dichloro-3- [2,4-dibromo-5- (ethylsulfanyl) phenoxy] pyridazine
[3134] 2.05 g (8.84 mmol) of commercially available 1-bromo-2-methoxy-4-nitrobenzene and water (200 mL) were mixed, followed by 11.4 g (213 mmol) of ammonium chloride followed by 4.78 g (73.2 of zinc powder). Mmol). After stirring at room temperature for 5 hours, the mixture was filtered through celite and the filtrate was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 1.78 g of residue.
[3135] This residue was mixed with water (9 mL), 47% aqueous hydrobromic acid solution (3 mL), and an aqueous solution of 655 mg (9.49 mmol) of sodium nitrite (3.6 mL of water) was added dropwise while stirring under ice-cooling. It stirred for 10 minutes after completion | finish of dripping, and what melt | dissolved 973 mg (6.80 mmol) of cuprous cuprous bromide in 47% aqueous hydrobromic acid solution (3.6 mL) was dripped. The reaction mixture was stirred at 110 ° C. for 2 hours 30 minutes, then cooled to room temperature, water was added, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was subjected to silica gel column chromatography (Wako gel C-100, hexane: ethyl acetate = 10: 1) and preparative thin layer chromatography (1.05717 hexane: ethyl acetate = 4: 1 manufactured by MERCK). Purification to give 751 mg of crude product.
[3136] Under a nitrogen atmosphere, 339 mg (8.46 mmol) of 60% sodium hydride was suspended in dry N, N-dimethylformamide (5 mL), and 0.65 mL (8.78 mmol) of ethanethiol was slowly added dropwise to this suspension. After stirring for 30 minutes, 751 mg of the previous crude product was dissolved in N, N-dimethylformamide (8 mL), and stirred for 5 hours at 160 ° C. The reaction mixture was allowed to stand at room temperature overnight. The mixture was poured into water, diluted hydrochloric acid was made acidic, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was purified by preparative thin layer chromatography (manufactured by MERCK Corporation, 1.05744, use of three, multiple development as hexane: ethyl acetate = 4: 1) to give 109 mg of phenolic crude product.
[3137] 109 mg of the obtained phenolic crude product was mixed with 1,4-dioxane (3 mL) and dimethyl sulfoxide (3 mL), and 53.5 mg (0.478 mmol) of potassium tert-butoxide were added to the mixture, and the mixture was cooled under ice cooling. Stirred for a minute. To this mixture was added 71.2 mg (0.432 mmol) of 3,6-dichloropyridazine 1-oxide under ice-cooling and stirred at room temperature overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (manufactured by MERCK Corporation, 1.05744, use of three, multiple development as hexane: ethyl acetate = 2: 1) to give 71.5 mg of an ethereal crude product.
[3138] 44.8 mg of an ethereal crude product was dissolved in phosphorus oxychloride (3 mL) and stirred at 60 ° C. for 21 hours. Water and dichloromethane were added to the reaction mixture, followed by stirring, followed by extraction with dichloromethane. The organic layers were combined, washed with water, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (manufactured by MERCK, 1.05744, used in 2 pieces, developed with hexane: ethyl acetate = 2: 1) to obtain 4,6-dichloro-3- [2. 14.4 mg (0.0314 mmol, yield 0.567%) of, 4-dibromo-5- (ethylsulfanyl) phenoxy] pyridazine were obtained.
[3139] (2) 6-chloro-3- [2,4-dibromo-5- (ethylsulfanyl) phenoxy] -4-pyridazinol (Compound No. 2596, steps A-3 and A-4)
[3140] 33.4 mg (0.0728 mmol) of 4,6-dichloro-3- [2,4-dibromo-5- (ethylsulfanyl) phenoxy] pyridazine obtained in (1) were dissolved in dimethyl sulfoxide (3 mL). 29.8 mg (0.363 mmol) of sodium acetate were added, and the mixture was heated and stirred at 120 ° C. for 4 hours 30 minutes. After standing at room temperature overnight, water was added to the reaction mixture, diluted hydrochloric acid was made acidic, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (multiple development with 1.05744 ethyl acetate manufactured by MERCK Co., Ltd.) to obtain 6-chloro-3- [2,4-dibromo- 13.1 mg (0.0297 mmol, yield 40.8%) of 5- (ethylsulfanyl) phenoxy] -4-pyridazinol (Compound No. 2596) was obtained.
[3141] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.84 (1H, s), 7.21 (1H, s), 6.72 (1H, s), 2.97 (2H, q, J = 7.3 Hz), 1.33 (3H, t, J = 7.3 Hz).
[3142] Melting point (° C): 225-228.
[3143] Example 633 6-Chloro-3- (2,3,5-trimethyl-6-vinylphenoxy) -4-pyridazinol (Compound No. 2603)
[3144] (1) 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone
[3145] 2.00 g of 1- (2-hydroxy-3,4,6-trimethylphenyl) ethanone, which may be prepared by the method described in Chemical Research in Toxicology, 1997, Vol. 10, No. 3, pages 335-343. (11.2 mmol) was dissolved in acetone (30 mL), and 3.10 g (22.4 mmol) potassium carbonate was added followed by 1.40 mL (22.5 mmol) methyl iodide and heated to reflux for 5 hours. After cooling to room temperature, the reaction mixture was concentrated, the residue was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (WACO gel C-100, hexane: ethyl acetate gradient) to give 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone. 1.90 g (9.90 mmol, yield 88.4%) were obtained.
[3146] (2) 1- (2-methoxy-3,4,6-trimethylphenyl) ethanol
[3147] 1.00 g (5.21 mmol) of 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone obtained in (1) was dissolved in methanol (8 mL) and 170 mg (4.50 mmol) of sodium borohydride while stirring. Was added little by little. After confirming the disappearance of the raw material by analytical thin layer chromatography (TLC), the reaction mixture was poured into water, and hydrochloric acid was added to make acid. The mixture was extracted with hexane, the organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 1.0 g of 1- (2-methoxy-3,4,6-trimethylphenyl) ethanol.
[3148] (3) 2- (1-chloroethyl) -3-methoxy-1,4,5-trimethylbenzene
[3149] 1.0 g of 1- (2-methoxy-3,4,6-trimethylphenyl) ethanol obtained in (2) was dissolved in dichloromethane (10 mL), followed by stirring under ice-cooling, 1.10 mL (7.91 mmol) of triethylamine, followed by 0.56 mL (7.21 mmol) methanesulfonylchloride was added. The reaction mixture was stirred at room temperature for 20 minutes, poured into water and extracted with dichloromethane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and 1.2 g of 2- (1-chloroethyl) -3-methoxy-1,4,5-trimethylbenzene was obtained.
[3150] (4) 3-methoxy-1,2,5-trimethyl-4-vinylbenzene
[3151] 1.2 g of 2- (1-chloroethyl) -3-methoxy-1,4,5-trimethylbenzene obtained in (3) was dissolved in dry N, N-dimethylformamide (12 mL) and stirred under ice-cooling, 1.14 g (10.2 mmol) of potassium tert-butoxide were added. The reaction mixture was stirred for 30 minutes at room temperature and then for 30 minutes under heating to reflux. After cooling to room temperature, the mixture was poured into water and extracted with hexane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 870 mg of 3-methoxy-1,2,5-trimethyl-4-vinylbenzene.
[3152] (5) 2,3,5-trimethyl-6-vinylphenol and 2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenol
[3153] Under a nitrogen atmosphere, 270 mg (6.75 mmol) of 60% sodium hydride was suspended in dry N, N-dimethylformamide (8 mL), and 0.60 mL (8.10 mmol) of ethanethiol was slowly added dropwise to the suspension. After stirring for 15 minutes, 400 mg (2.27 mmol) of 3-methoxy-1,2,5-trimethyl-4-vinylbenzene obtained in (4) were added to this mixture in dry N, N-dimethylformamide (1.5 mL). The melted product was added and heated to reflux for 1 hour. After cooling to room temperature, the reaction mixture was poured into water, made acidic by adding hydrochloric acid, and extracted with hexane. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was developed by silica gel column chromatography (Wako gel C-100, hexane: ethyl acetate = 20: 1) and preparative thin layer chromatography (1.05744 hexane: ethyl acetate = 8: 1 manufactured by MERCK). Purified by), 63.0 mg (0.389 mmol, yield 16.2% from 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone) of 2,3,5-trimethyl-6-vinylphenol and 2 Yield 61.4% from 330 mg (1.47 mmol, 1- (2-methoxy-3,4,6-trimethylphenyl) ethanone-[1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenol )
[3154] (6) 6-chloro-3- (2,3,5-trimethyl-6-vinylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2,3,5-trimethyl-6-vinylphenoxy A mixture of pyridazine 1-oxides (step B-2)
[3155] 43.0 mg (0.265 mmol) of 2,3,5-trimethyl-6-vinylphenol obtained in (5) are dissolved in 1,4-dioxane (0.4 mL) and dimethylsulfoxide (0.4 mL), and the mixture is cooled with ice. , 36.0 mg (0.321 mmol) of potassium tert-butoxide were added, followed by stirring for 10 minutes. To this mixture was added 47.6 mg (0.288 mmol) of 3,6-dichloropyridazine 1-oxide under ice-cooling and stirred at room temperature for 4 hours. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (developing with MERCK Corporation 1.05744 two use hexane: ethyl acetate = 2: 1), and 6-chloro-3- (2,3,5-trimethyl 27.6 mg (0.0949 mmol, of a mixture of 6-vinylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2,3,5-trimethyl-6-vinylphenoxy) pyridazine 1-oxide Yield 35.8%).
[3156] (7) 4,6-dichloro-3- (2,3,5-trimethyl-6-vinylphenoxy) pyridazine (Step B-3)
[3157] 6-chloro-3- (2,3,5-trimethyl-6-vinylphenoxy) pyridazine 1-oxide and 3-chloro-6- (2,3,5-trimethyl-6- obtained in (6) To 27.6 mg (0.0949 mmol) of a mixture of vinylphenoxy) pyridazine 1-oxide, 0.02 mL (0.22 mmol) of phosphorus oxychloride was added and stirred at room temperature for 2 hours. 0.4 mL of chloroform was added thereto, and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated and 0.2 mL (2.2 mmol) of phosphorus oxychloride was added to the residue and stirred at room temperature for 5 hours. The reaction mixture was concentrated, and the residue was purified by preparative thin layer chromatography (developed with MERCK Co., Ltd. 1.05744 1 use hexane: ethyl acetate = 5: 1) to obtain 4,6-dichloro-3- (2,3,5 5.0 mg (0.016 mmol, yield 17%) of -trimethyl-6-vinylphenoxy) pyridazine was obtained.
[3158] (8) 6-chloro-3- (2,3,5-trimethyl-6-vinylphenoxy) -4-pyridazinol (Compound No. 2603, steps A-3 and A-4)
[3159] 5.0 mg (0.016 mmol) of 4,6-dichloro-3- (2,3,5-trimethyl-6-vinylphenoxy) pyridazine obtained in (7) were dissolved in dimethyl sulfoxide (1 mL), and sodium acetate 10.3 mg (0.126 mmol) was added and the mixture was heated and stirred at 120 ° C for 2 hours. After cooling to room temperature, the reaction mixture was poured into water, made acidic by adding hydrochloric acid, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the residue obtained by distilling off the solvent was purified by preparative thin layer chromatography (developed with 1.05744 one from Merck Co., Ltd. using ethyl acetate), and then 6-chloro-3- (2,3,5- 1.5 mg (0.0052 mmol) of 33% of trimethyl-6-vinylphenoxy) -4-pyridazinol (Compound No. 2603) were obtained.
[3160] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.25 (1H, s), 6.67 (1H, dd, J = 11.0 Hz, 17.6 Hz), 6.56 (1H, s), 5.66 (1H, dd, J = 1.5 Hz, 17.6 Hz), 5.10 (1H, dd, J = 1.5 Hz, 11.0 Hz), 2.29 (3H, s), 2.20 (3H, s), 2.04 (3H, s).
[3161] Physical property: Amorphous.
[3162] Example 634 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenoxy} -4-pyridazinol (Compound No. 2606)
[3163] (1) 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenoxy} -4-methoxypyridazine (step D-1)
[3164] 150 mg (0.670 mmol) of 2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenol obtained in Example 633 (5) were treated with 1,4-dioxane (2 mL) and dimethyl sulfoxide. (2 mL) was dissolved in a mixed solvent, and under ice-cooling, 93 mg (0.83 mmol) of potassium tert-butoxide was added to the solution, followed by stirring at room temperature for 20 minutes. The mixture was ice-cooled again, and 120 mg (0.670 mmol) of 3,6-dichloro-4-methoxypyridazine were added and stirred overnight at room temperature. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was developed by silica gel chromatography (Wako gel C-100, hexane-ethyl acetate gradient), and preparative thin layer chromatography (1.05744 two pieces use of MERCK company hexane: ethyl acetate = 2: 1). Purified)) to 26.7 mg (0.0728 mmol, 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenoxy} -4-methoxypyridazine Yield 10.9%). Also, 60.0 mg (0.163 mmol, yield 24.3%) of 3-chloro-6- {2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenoxy} -4-methoxypyridazine Got it.
[3165] (2) 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenoxy} -4-pyridazinol (Compound No. 2606, step D-2)
[3166] 34.0 mg (0.358 mmol) of 2-hydroxypyridine was dissolved in dimethyl sulfoxide (1 mL), and 41.0 mg (0.366 mmol) of potassium tert-butoxide was added to the solution at room temperature, followed by stirring at room temperature for 20 minutes. 26.7 mg (0.0728) of 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -3,5,6-trimethylphenoxy} -4-methoxypyridazine obtained by (1) Mmol) solution of dimethyl sulfoxide (1 mL) was added and stirred at 60 ° C. After the reaction was completed, the reaction mixture was allowed to cool and poured into water. After adding hydrochloric acid to make it acidic, it extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the solvent was distilled off. The obtained residue was purified by preparative thin layer chromatography (manufactured by MERCK, 1.05744, developed with ethyl acetate) to give 6-chloro-3- {2- [1- (ethylsulfanyl) ethyl] -3,5,6 6.6 mg (0.019 mmol, yield 26%) of -trimethylphenoxy} -4-pyridazinol (Compound No. 2606) was obtained.
[3167] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.20 (2H, s), 6.64 (1H, s), 2.40-2.15 (8H, m), 2.03 (3H, s), 1.40 (3H, d, J = 7.0 Hz), 1.24 (1H, m), 1.03 (3H, t, J = 7.3 Hz).
[3168] Physical property: Amorphous.
[3169] (Example 635) 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazole -5-yl phthalate (Compound No. 1625) and bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] phthalate (Compound No. 2838, step I)
[3170] 207 mg (0.726 mmol) of (2,4-dichlorophenyl) (5-hydroxy-1,3-dimethyl-1H-pyrazol-4-yl) methanone are suspended in acetonitrile (3 mL), 1, 81.6 mg (0.729 mmol) of 4-diazabicyclo [2.2.2] octane were added and stirred. 105 µL (0.729 mmol) of phthaloyl dichloride was added thereto, stirred at room temperature for 1 hour, and then 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol 200 mg (0.722 mmol) was added and the mixture was stirred at room temperature for 1 hour 30 minutes. The reaction mixture was poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (Daisogel 1001W, hexane: ethyl acetate gradient) to give 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridine. 28.0 mg (0.0405 mmol, yield 5.61%) and bis [6-chloro in 2 mg of dizinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl phthalate (Compound No. 1625) 163 mg (0.238 mmol, yield 33.0%) of 3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] phthalate (Compound No. 2838) were obtained.
[3171] 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl phthalate (Compound No. 1625):
[3172] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.01-7.96 (1H, m), 7.89-7.68 (3H, m), 7.57 (1H, s), 7.29-7.06 (5H, m), 6.90-6.83 ( 1H, m), 3.71 (3H, s), 2.27 (3H, s), 2.13 (3H, s), 1.82-1.68 (1H, m), 0.77-0.53 (4H, m).
[3173] Physical property: Amorphous.
[3174] Bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] phthalate (Compound No. 2838):
[3175] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.13-8.06 (2H, m), 7.84-7.78 (2H, m), 7.58 (2H, s), 7.15-7.06 (4H, m), 6.90-6.83 ( 2H, m), 2.13 (6H, s), 1.82-1.68 (2H, m), 0.73-0.52 (8H, m).
[3176] Physical property: Amorphous.
[3177] Example 636 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazole -5-yl 1,3-benzenedisulfonate (Compound No. 2333) and bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] 1,3-benzene Disulfonate (Compound No. 3755, Process I)
[3178] 122 mg (0.428 mmol) of (2,4-dichlorophenyl) (5-hydroxy-1,3-dimethyl-1H-pyrazol-4-yl) methanone are suspended in acetonitrile (4 mL) and under ice-cooling 72.0 mg (0.643 mmol) of 1,4-diazabicyclo [2.2.2] octane were added followed by 117 mg (0.425 mmol) of 1,3-benzenedisulfonyl dichloride, followed by stirring at room temperature for 30 minutes. The reaction mixture was ice-cooled, and 100 mg (0.361 mmol) of 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol was added thereto, followed by stirring at room temperature for 1 hour. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane: ethyl acetate gradient) to give 6-chloro-3- (2-cyclopropyl-6-methylphenoxy)-. 135 mg (0.177 mmol, 4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl 1,3-benzenedisulfonate (Compound No. 2333), Yield 49.0%) and 38.0 mg (0.0503) of bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] 1,3-benzenedisulfonate (Compound No. 3755) Mmol, yield 13.9%).
[3179] 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl 1 , 3-benzenedisulfonate (Compound No. 2333):
[3180] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.67 (1H, t, J = 1.9 Hz), 8.40-8.34 (1H, m), 8.31-8.24 (1H, m), 7.86 (1H, t, J = 8.0 Hz), 7.56 (1H, s), 7.37 (1H, d, J = 1.9 Hz), 7.29-7.23 (1H, m), 7.15-7.00 (3H, m), 6.85-6.78 (1H, m), 3.81 (3H, s), 2.00 (3H, s), 1.94 (3H, s), 1.70-1.52 (1H, m), 0.73-0.45 (4H, m).
[3181] Physical property: Amorphous.
[3182] Bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] 1,3-benzenedisulfonate (Compound No. 3755):
[3183] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.77 (1H, dd, J = 1.8 Hz, 1.8 Hz), 8.41 (2H, dd, J = 7.7 Hz, 1.8 Hz), 7.88 (1H, t, J = 8.0 Hz), 7.48 (2H, s), 7.15-6.95 (4H, m), 6.90-6.75 (2H, m), 1.97 (6H, s), 1.67-1.46 (2H, m), 0.75-0.44 (8H , m).
[3184] Physical property: Amorphous.
[3185] Example 637 bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] pentanediate (Compound No. 2746) and 6-chloro-3- (2- Cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl pentanedioate (Compound No. 2739)
[3186] 241 mg (0.870 mmol) of 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol are suspended in acetonitrile (8 mL) and 1,4-diazabicyclo under ice-cooling [2.2.2] octane 139 mg (1.23 mmol) followed by 146 mg (0.864 mmol) pentanedoyl dichloride, followed by (2,4-dichlorophenyl) (5-hydroxy-1,3-dimethyl-1H-pyra 244 mg (0.856 mmol) of zol-4-yl) methanone were added and stirred at room temperature. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was subjected to silica gel column chromatography (Wako gel C-100, hexane: ethyl acetate gradient) and preparative thin layer chromatography (1.05744 two pieces by MERCK Co., Ltd. use hexane: ethyl acetate = 2: 1 or 1). Purified by: 1), 42.0 mg (0.0646 mmol) of bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] pentanediate (Compound No. 2746) , Yield 7.48%) and 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyra 35.0 mg (0.0532 mmol, yield 6.21%) of sol-5-yl pentanedioate (Compound No. 2739) were obtained.
[3187] Bis [6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl] pentanediate (Compound No. 2746):
[3188] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.23 (2H, s), 7.14-7.02 (4H, m), 6.83 (2H, dd, J = 6.6, 2.9 Hz), 2.89 (4H, t, J = 7.0 Hz), 2.25 (2H, quintet, J = 7.0 Hz), 2.10 (6H, s), 1.80-1.65 (2H, m), 0.78-0.52 (8H, m).
[3189] Properties: Caramel statue.
[3190] 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-1H-pyrazol-5-yl pentane Dioate (Compound No. 2739):
[3191] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.45-7.17 (4H, m), 7.14-7.00 (2H, m), 6.90-6.75 (1H, m), 3.53 (3H, s), 2.83 (2H, t, J = 7.0 Hz, 2.57 (2H, t, J = 7.0 Hz), 2.20-2.00 (2H, m), 2.11 (3H, s), 2.10 (3H, s), 1.80-1.65 (1H, m ), 0.80-0.50 (4H, m).
[3192] Physical property: Amorphous.
[3193] Example 638 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 1-pyrrolidinecarboxylate (Compound No. 1937)
[3194] 200 mg (0.722 mmol) of 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol were mixed with toluene (3 mL) and ice-cooled. 60 µL (0.742 mmol) of pyridine was added thereto followed by 0.67 mL (0.724 mmol) of 1.08 mol / L phosgenetoluene solution under stirring in a nitrogen atmosphere, followed by stirring at room temperature for 15 minutes. The reaction mixture was ice-cooled, and 60 µL (0.722 mmol) of pyridine was added followed by 60 µL (0.719 mmol) of pyrrolidine and stirred at room temperature for 1 hour. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (developing as 1.05744 four pieces use hexane: ethyl acetate = 2: 1 by Merck Corporation), and 6-chloro-3- (2-cyclopropyl-6- 190 mg (0.508 mmol, yield 70.7%) of methylphenoxy) -4-pyridazinyl 1-pyrrolidinecarboxylate (Compound No. 1937) were obtained.
[3195] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.59 (1H, s), 7.15-7.03 (2H, m), 6.90-6.80 (1H, m), 3.62 (2H, dd, J = 6.6 Hz, 6.9 Hz ), 3.51 (2H, dd, J = 6.9 Hz, 6.6 Hz), 2.15 (3H, s), 2.05-1.90 (4H, m), 1.88-1.68 (1H, m), 0.80-0.50 (4H, m) .
[3196] Melting point (° C): 115-118.
[3197] Example 639 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl methoxy (methyl) carbamate (Compound No. 3564)
[3198] 200 mg (0.722 mmol) of 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol were mixed with toluene (3 mL) and ice-cooled. 60 µL (0.742 mmol) of pyridine was added thereto followed by 0.67 mL (0.724 mmol) of 1.08 mol / L phosgenetoluene solution under stirring in a nitrogen atmosphere, followed by stirring at room temperature for 15 minutes. The reaction mixture was ice-cooled, and 120 μL (1.48 mmol) of pyridine was added followed by 70.4 mg (0.722 mmol) of N, O-dimethylhydroxylamine hydrochloride and stirred at room temperature for 1 hour. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography (WACO gel C-100, hexane: ethyl acetate gradient) to give 6-chloro-3- (2-cyclopropyl-6-methylphenoxy)-. 100 mg (0.275 mmol, Yield 38.1%) of 4-pyridazinyl methoxy (methyl) carbamate (Compound No. 3564) was obtained.
[3199] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 7.53 (1H, s), 7.15-7.03 (2H, m), 6.90-6.82 (1H, m), 3.84 (3H, s), 3.35 (3H, s) , 2.15 (3H, s), 1.87-1.67 (1H, m), 0.80-0.52 (4H, m).
[3200] Melting Point (° C): 63-64.5.
[3201] Example 640 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinyl 2,5-dimethyl-1H-pyrrole-1-carboxylate (Compound No. 3630)
[3202] 37.4 mg (0.393 mmol) of 2,5-dimethyl-1H-pyrrole were mixed with toluene (1 mL) and 40.0 μL (0.407 mmol) of pyridine with stirring under ice cooling followed by 0.34 mL (0.367 mmol) of 1.08 mol / L phosgenetoluene solution. ) Was added and stirred for 1 hour. To this was added 40.0 μL (0.407 mmol) of pyridine, followed by 100 mg (0.361 mmol) of 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol and stirred for 3 hours. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed with water, and dried over anhydrous magnesium sulfate. The residue obtained by distilling a solvent off was refine | purified by preparative thin layer chromatography (developing with MERCK Co., Ltd. 1.05744 two pieces use hexane: ethyl acetate = 2: 1), and 6-chloro-3- (2-cyclopropyl-6- 24.0 mg (0.0603 mmol, yield 16.7%) of methylphenoxy) -4-pyridazinyl 2,5-dimethyl-1H-pyrrole-1-carboxylate (Compound No. 3630) were obtained.
[3203] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.20-8.03 (1H, m), 7.63 (1H, s), 7.13-7.00 (2H, m), 6.90-6.80 (1H, m), 6.36 (1H, d, J = 2.9 Hz), 2.55 (3H, s), 2.22 (3H, s), 2.15 (3H, s), 1.90-1.70 (1H, m), 0.80-0.50 (4H, m).
[3204] Melting Point (° C): 208-210.
[3205] Example 641 4-{[4- (benzoyloxy) -6-chloro-3-pyridazinyl] oxy} -3-methylphenyl benzoate (Compound No. 3850)
[3206] (1) 6-chloro-3- (4-hydroxy-2-methylphenoxy) -4-pyridazinol
[3207] 173 mg (0.553 mmol) of 4-[(4,6-dichloro-3-pyridazinyl) oxy] -3-methylphenyl acetate obtained in Example 630 (3) was dissolved in 1,4-dioxane (1.4 mL). , 0.7 mL (2.1 mmol) and 3 mol / L sodium hydroxide solution and dimethylsulfoxide (2.8 mL) were added and stirred overnight at room temperature. 4 mol / L aqueous hydrochloric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the solvent was distilled off. The resulting residue was purified by preparative thin layer chromatography (developed as dichloromethane: methanol = 36: 1) to give 6-chloro-3- (4-hydroxy-2-methylphenoxy) -4-pyridazinol 66.8. mg obtained.
[3208] (2) 4-{[4- (benzoyloxy) -6-chloro-3-pyridazinyl] oxy} -3-methylphenyl benzoate (Compound No. 3850)
[3209] 66.8 mg of 6-chloro-3- (4-hydroxy-2-methylphenoxy) -4-pyridazinol obtained in (1) was dissolved in acetonitrile (1.0 mL), and 1,4-diazabicyclo [2.2 .2] 60.0 mg (0.536 mmol) of octane were added, followed by 61 µL (0.523 mmol) of benzoyl chloride, followed by stirring at room temperature for 1 hour 30 minutes. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine. After drying over anhydrous magnesium sulfate, the solvent was distilled off. The resulting residue was purified by preparative thin layer chromatography (developed as hexane: ethyl acetate = 5: 1) to give 4-{[4- (benzoyloxy) -6-chloro-3-pyridazinyl] oxy} -3- 36.9 mg (0.0800 mmol, yield 14.5% from 4-[(4,6-dichloro-3-pyridazinyl) oxy] -3-methylphenyl acetate) of methylphenyl benzoate (Compound No. 3850) were obtained.
[3210] ¹ H-NMR (200 MHz, CDCl ₃ ) δ ppm: 8.21-8.17 (4H, m), 7.72-7.48 (7H, m), 7.22-7.07 (3H, m), 2.21 (3H, s).
[3211] Melting Point (° C): 118-120.
[3212] Example 642 3- (2-aminophenoxy) -3-chloro-4-pyridazinol (Compound No. 377)
[3213] (1) 2-[(6-chloro-4-methoxy-3-pyridazinyl) oxy] aniline (step D-1)
[3214] 670 mg (6.15 mmol) of 2-aminophenol are dissolved in a mixed solvent of 1,4-dioxane (7 mL) and dimethyl sulfoxide (7 mL) and 690 mg (6.16 mmol) of potassium tert-butoxide in this solution under ice-cooling. ) Was added and stirred for 10 minutes. 1000 mg (5.59 mmol) of 3, 6- dichloro-4- methoxypyridazines were added to this mixture, and it stirred at room temperature for 5 hours. The reaction mixture was poured into ice-cold water, brine was added, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel chromatography (WACO gel C-100, hexane-ethyl acetate gradient) to give 2-[(6-chloro-4-methoxy-3-pyridazinyl) 328 mg (1.30 mmol, yield 23.3%) of oxy] aniline and 2-[(6-chloro-4-methoxy-3-pyridazinyl) oxy] aniline and 2-[(6-chloro-5-methoxy 100 mg of a mixture of -3-pyridazinyl) oxy] aniline were obtained.
[3215] (2) 3- (2-aminophenoxy) -3-chloro-4-pyridazinol (Compound No. 377, step D-2)
[3216] 50.0 mg (0.198 mmol) of 2-[(6-chloro-4-methoxy-3-pyridazinyl) oxy] aniline obtained in (1) were dissolved in dimethyl sulfoxide (0.4 mL), and dissolved in 2 mol / L hydroxide. An aqueous sodium solution (0.4 mL, 0.4 mmol) was added and stirred at room temperature for 5 hours. The reaction mixture was poured into saturated brine and extracted with tetrahydrofuran. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developing with 1.05744 two pieces of dichloromethane: methanol = 10: 1 manufactured by MERCK), and then 3- (2-aminophenoxy) -3-chloro- 17.0 mg (0.0714 mmol, yield 36.1%) of 4-pyridazinol (Compound No. 377) were obtained.
[3217] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.50-6.94 (2H, m), 6.90-6.82 (1H, m), 6.85-6.63 (2H, m).
[3218] Melting point (° C.): 249-250.
[3219] Example 643 N- {2-[(6-chloro-4-hydroxy-3-pyridazinyl) oxy] phenyl} acetamide (Compound No. 380)
[3220] 18.0 mg (0.0756 mmol) of 3- (2-aminophenoxy) -3-chloro-4-pyridazinol obtained in Example 641 are mixed with dichloromethane (0.8 mL) and 0.050 mL of triethylamine while stirring under ice-cooling. (0.36 mmol), and then 0.010 mL (0.14 mmol) of acetyl chloride were added and stirred at room temperature for 3 hours. The reaction mixture was poured into saturated brine and extracted with tetrahydrofuran. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developing as 1.05715 dichloromethane: methanol = 10: 1 manufactured by MERCK), and N- {2-[(6-chloro-4-hydroxy-3 3.6 mg (0.0129 mmol, yield 17.1%) of -pyridazinyl) oxy] phenyl} acetamide (Compound No. 380) was obtained.
[3221] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 8.10-8.00 (1H, m), 7.25-7.08 (3H, m), 6.60 (1H.s), 2.12 (3H, s).
[3222] Melting point (° C.): 135.
[3223] Example 644 N, N, N-tributyl-1-butananium 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinoate (Compound No. 3798)
[3224] 0.19 mL (0.38 mmol) aqueous 2 mol / L aqueous sodium hydroxide solution in 105 mg (0.379 mmol) ethanol (2 mL) solution of 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol ), Then 106 mg (0.381 mmol) of tetrabutylammonium chloride were added, followed by stirring at 60 ° C for 5 hours. The reaction mixture was left at room temperature overnight, and the solids were removed by filtration. Concentrate the filtrate and replace N, N, N-tributyl-1-butananium 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinoate (Compound No. 3798). 197 mg (0.380 mmol, yield 100%) were obtained.
[3225] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.05-6.95 (2H, m), 6.80-6.73 (1H, m), 6.43 (1H, s), 3.30-3.15 (8H, m), 2.14 (3H , s), 2.00-1.85 (1H, m), 1.76-1.53 (8H, m), 1.50-1.30 (8H, m), 1.02 (9H, t, J = 7.1 Hz), 0.78-0.63 (2H, m ), 0.63-0.48 (2H, m).
[3226] Melting Point (° C): 113-114.
[3227] Example 645 Sodium 6-Chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinoate (Compound No. 3805)
[3228] 0.18 mL (0.36 mmol) of 2 mol / L aqueous sodium hydroxide solution in 100 mg (0.361 mmol) ethanol (2 mL) solution of 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol ) Was added and stirred at 50 ° C for 4 hours. The reaction mixture was concentrated to give 108 mg (0.361 mmol, yield 100%) of sodium 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinoate (Compound No. 3805).
[3229] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.05-6.95 (2H, m), 6.77 (1H, dd, J = 6.4, 3.1 Hz), 6.43 (1H, s), 2.14 (3H, s), 2.00-1.82 (1H, m), 0.78-0.63 (2H, m), 0.63-0.48 (2H, m).
[3230] Melting Point (℃):> 260.
[3231] Example 646 5-Bromo-6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol (Compound No. 3843)
[3232] N-bromosuccin was added to a solution of 157 mg (0.567 mmol) of N, N-dimethylformamide (2 mL) in 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol. 108 mg (0.607 mmol) of mead were added, and the mixture was stirred at room temperature for 3 hours 30 minutes. To the reaction mixture was added water, followed by 4 mol / L aqueous hydrochloric acid solution, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by preparative thin layer chromatography (developed as MERCK Corporation 1.05744 hexane: ethyl acetate = 2: 1) to give 5-bromo-6-chloro-3- (2-cyclopropyl- 123 mg (0.346 mmol, yield 61.0%) of 6-methylphenoxy) -4-pyridazinol (Compound No. 3843) were obtained.
[3233] ¹ H-NMR (200 MHz, CD ₃ OD) δ ppm: 7.08-7.05 (2H, m), 6.85-6.80 (1H, m), 2.14 (3H, s), 1.88-1.76 (1H, m), 0.82-0.72 (2H, m), 0.60-0.56 (2H, m).
[3234] Physical property: Amorphous.
[3235] Compounds of Nos. 1 and 6 can be prepared according to the method of Example 2.
[3236] Compound No. 123-127, 130-138, 144, 145, 151, 163, 173, 184, 202, 217, 226, 249, 264, 265, 266, 267, 269-275, 279, 280, 284, 287, 288, 292, 293, 300, 304, 305, 306, 307, 308, 309, 311, 315, 324, 325, 329, 330, 334, 336, 339, 344, 348, 349, 355, 356, 359, 361, 362, 364-370, 375, 376, 379, 383, 385-387, 390, 391, 396, 399-401, 403, 410, 412, 413, 415-425, 426, 427, 430, 432- 438, 441, 443, 446, 450, 453, 454, 456, 458-460, 472, 491, 498, 503, 505, 506, 507, 510, 513, 514, 520, 521, 527-529, 531, 532, 534-536, 538-541, 544, 547, 549, 552, 556, 557, 558, 559, 562, 566, 567, 571, 614, 618, 621, 623, 626-629, 635, 640, 642, 650, 653, 658, 659, 662-664, 667, 679, 680, 692, 700, 701, 702, 707-712, 716, 717, 719, 731-733, 734, 735-737, 740, 746, 754, 756, 758, 759, 762, 775, 778, 780-782, 802-804, 834, 844-846, 850, 890, 894, 896, 911, 914, 931, 964, 965, 979, 982, 987, 998, 1000, 1007, 1009, 1013, 1016, 1020, 1023, 1027, 1040, 1050, 1052, 1053, 1055, 1058, 1060, 1061, 1063, 1064, 1066, 1069 , 1073, 1080, 1083, 1086, 1088, 1089, 1091, 1096, 1099, 1100, 1102,1115, 1118-1120, 1122-1125, 1129, 1133, 2519, 2547, 2548, 2565, 2568, 2570, 2571 The compounds of Nos. 2574, 2577, 2585, 2587, 2589, 2592, 2597, 2599, 2600, 2601, 2605, 2607, 2608, 2609, and 2614 can be used in Examples 1, 6, 13, 16, It can manufacture according to the method of Example 21, Example 22, or Example 23.
[3237] Compound No. 1140, 1151, 1160, 1172, 1178, 1184, 1207, 1251, 1260, 1266, 1286, 1298, 1334, 1340, 1358, 1364, 1382, 1387, 1391, 1396, 1417, 1441, 1446, 1448, 1450, 1455-1459, 1461, 1481, 1509, 1522, 1531, 1537, 1543, 1549, 1553, 1554, 1566, 1575, 1593, 1599, 1603, 1616, 1643, 1649, 1658, 1706, 1710, 1757, 1770, 1789, 1811, 1840, 1877, 1879, 1881, 1898, 1924, 1981, 1985, 2010, 2034, 2038, 2040, 2042, 2051, 2060, 2066, 2072, 2106, 2136, 2147, 2151, 2176, 2198-2200, 2212, 2220-2224, 2230-2232, 2234-2238, 2240, 2245-2249, 2263, 2265, 2287, 2289, 2300, 2309, 2315, 2321, 2351, 2662, 2671, 2677, 2697, 2703, 2709, 2715, 2721, 2727, 2752, 2758, 2764, 2770, 2776, 2782, 2788, 2805, 2814, 2820, 2826, 2850, 2856, 2862, 2868, 2874, 2880, 2900, 2906, 2918, 2924, 2930, 2961, 2970, 2976, 2982, 2988, 2994, 3016, 3022, 3028, 3034, 3040, 3046, 3052, 3058, 3064, 3070, 3076, 3082, 3088, 3094, 3100, 3106, 3112, 3129, 3138, 3144, 3150, 3156, 3162, 3168, 3185, 3194, 3200, 3217, 3226, 3243, 3252, 3258, 3264, 3270, 3276, 3282, 3288, 3294, 3300, 3306, 3312, 3318, 3324, 3330, 3336, 3342, 3348, 3354, 3360, 3366, 3372, 3378, 3384, 3390, 3396, 3402, 3408, 3414, The compounds of Nos. 3420, 3426, 3432, 3438, 3444, 3450, 3456, 3462, 3468, 3474, 3480, 3486, 3492, 3498, 3504,3510, 3516, 3780, 3786, 3792 and 3856 are in Example 26, Example It can manufacture according to the method as described in 27 or Example 28.
[3238] The compound of compound number 2402 can be manufactured according to the method described in Example 33.
[3239] Compounds of Compound Nos. 2418 and 2431 can be prepared according to the methods described in Example 1, Example 6, or Example 22.
[3240] The compound of compound number 2478 can be manufactured according to the method described in Example 35, Example 36, Example 37, Example 39, or Example 40.
[3241] The compound of compound number 2492 can be manufactured according to the method described in Example 41.
[3242] Compounds of Nos. 1620, 1631, 2827 and 3001 can be prepared according to the method described in Example 635.
[3243] Compound No. 1891, 1911, 1920, 1946, 1952, 1958, 3522, 3528, 3534, 3540, 3546, 3552, 3558, 3570, 3576, 3582, 3588, 3594, 3600, 3606, 3612, 3618, 3624, 3636, The compounds of Nos. 3642, 3648, 3654, 3660, 3666, 3672, 3678, 3684, 3690, 3696, 3702, 3708, 3714 and 3720 may be prepared in Examples 26, 27, 28, 638, 663 or It can manufacture according to the method described in Example 640.
[3244] The compound of compound number 2327 can be prepared according to the method described in Example 636.
[3245] The compound of compound number 2733 can be prepared according to the method described in Example 637.
[3246] The compound of compound number 3811 can be manufactured according to the method described in Example 645.
[3247] Compounds of Nos. 3837 and 3849 can be prepared according to the methods described in Example 646.
[3248] In the following formulation examples, "%" represents weight%.
[3249] (Example 1)
[3250] Hydrating agent
[3251] Example 1 Compound (10 parts by weight) of Compound (128), Kaplex # 80D (manufactured by Shionogi Seiyaku Co., Ltd., 10 parts by weight), Gosenol GL05 (manufactured by Nippon Kosei Kagaku Co., Ltd., 2 parts by weight) ), New call 291PG (dioctylsulfosuccinate sodium salt, Nippon Yukazai Kabuki Seiki Co., Ltd., 0.5 parts by weight), neogen powder (Daiichi Kogyo Seiyaku Kabuki Seiki Co., Ltd., 5 parts by weight), Radiolite # 200 (Showagawa Kogyo Co., Ltd., 10 parts by weight) and H fine powder (Keiwa Rozai Kabuki Seiki Co., Ltd., 62.5 parts by weight) are sufficiently mixed, Example KII-1 type (Fuji Powder Co., Ltd.) Preparative) to obtain a hydrating agent.
[3252] (Example 2)
[3253] Granulation
[3254] Example 61 Compound (5 parts by weight) of Compound (136), Sodium tripolyphosphate (manufactured by Mitsui Chemicals, 2 parts by weight), Amichol No. 1 (dextrin, manufactured by Nippon Denbun Chemical Co., Ltd.), 1.5 parts by weight), bentonite (manufactured by Horus Kogyo Co., Ltd., 25 parts by weight) and calcium carbonate calpin 600 (Adachi Sekai Co., Ltd., 66.5 parts by weight) were kneaded with a kneader (manufactured by Mt. Fuji Kagoshi Co., Ltd., FM- NW-5 type) was mixed, combined water (13 parts by weight) was added, further mixed, and extruded using a dome gran (manufactured by Fuji Powder Co., Ltd., screen 1.0 mmφ). The granulated material thus obtained was dried with a shelf dryer (Tabai Kabushiki Kaisha, PERFECT OVEN PS-222 type, 60 ° C.), and then sieved to 600 to 1190 mm to obtain granules.
[3255] (Example 3)
[3256] Granule hydration
[3257] Example 7 Compound (80 parts by weight) of Compound (140), Geropon SC / 213 (polycarboxylic acid surfactant, manufactured by Rhodia Co., Ltd., 7 parts by weight), Neopelex No. 6F powder (dodecylbenzenesulfonate, Kao Kabuki Kaisha, 3 parts by weight), Amichol No. 1 (5 parts by weight) and titanium oxide (Saga Kagaku Kogyo Co., Ltd., 5 parts by weight) were mixed and pulverized with an air mill (manufactured by Seishin Co., Ltd., SK-JET O MIZER model 0101), followed by It was added in a rotary mixer and water was granulated by spraying. When most became 1.00 mm-0.15 mm, the granules were taken out, dried by the shelf type dryer, and sieved, and the granules hydrate of 1.00 mm-0.15 mm was obtained.
[3258] (Example 4)
[3259] Aqueous suspensions
[3260] Example 171 (Compound No. 506), Compound (10 parts by weight), Nucol 291PG (1 part by weight), Perlex CP (calcium lignin sulfonate salt, manufactured by Nippon Seishi, 10 parts by weight), propylene glycol (Nippon Yuka 10 parts by weight) and water (69 parts by weight) were manufactured and mixed together in an attritor (Mitsui Koyama Co., Ltd.) until the diameter of the solid particles was 5 μm or less. 0.05% (W / W) xanthan gum aqueous solution (10 parts by weight) was added to this ground slurry (90 parts by weight) and mixed to obtain an aqueous suspending agent.
[3261] (Example 5)
[3262] Hydrating agent
[3263] Example 6 (Compound No. 139), Compound A (10 parts by weight), Compound A (10 parts by weight), Kaplex # 80D (manufactured by Shionogi Seiyaku Co., Ltd., 10 parts by weight), Gosenol GL05-S (Nibbon Kosei Kagaku Co., Ltd., 2 parts by weight), New Cole 291PG (Dioctylsulfosuccinate sodium salt, Nippon Yukazai Kabuki Seiki Co., Ltd., 0.5 parts by weight), Neogen powder , 5 parts by weight), Radiolite # 200 (manufactured by Showa Kagaku Kogyo Co., Ltd., 10 parts by weight) and H fine powder (manufactured by Keiwa Rozai Co., Ltd., 52.5 parts by weight) were sufficiently mixed. The mixture was pulverized with an air mill (manufactured by Seishin Co., Ltd., SK-JET O MIZER model 0101) to obtain a mixed hydrate of Compound (10%) and Compound A (10%) of Example 6.
[3264] (Example 6)
[3265] Hydrating agent
[3266] Example 23 (10 parts by weight) of Compound (Compound No. 806), Compound B (10 parts by weight), Capplex # 80D (manufactured by Shionogi Seiyaku Co., Ltd., 10 parts by weight), Kosenol GL05-S (Nibbon Kosei Kagaku Co., Ltd., 2 parts by weight), New Cole 291PG (Dioctylsulfosuccinate sodium salt, Nippon Yukazai Kabuki Seiki Co., Ltd., 0.5 parts by weight), Neogen powder , 5 parts by weight), Radiolite # 200 (manufactured by Showa Kagaku Kogyo Co., Ltd., 10 parts by weight) and H fine powder (manufactured by Keiwa Rozai Co., Ltd., 52.5 parts by weight) were sufficiently mixed. The mixture was pulverized with an air mill (manufactured by Seishin Kogyo Co., Ltd., SK-JET O MIZER model 0101) to obtain a mixed wetting agent of Compound (10%) and Compound B (10%) in Example 23.
[3267] (Example 7)
[3268] Granulation
[3269] Compound A (61.22 parts by weight), Nucol 291PG (0.85 parts by weight) and water (37.93 parts by weight) were mixed and pulverized with an attritor (manufactured by Mitsui Kosan Co., Ltd.) until the particle size was about 2 μm. Got it. Toxanone (Sanyo Kasei Co., Ltd. make, 2 weight part) was added to this slurry (98 weight part), and it mixed, and obtained the slurry 2. Example 171 (Compound No. 506), Compound (5 parts by weight), Sodium tripolyphosphate (manufactured by Mitsui Chemicals, 2 parts by weight), Amichol No. 1 (dextrin, Nippon Denbun Chemicals, Ltd.) 1.5 parts by weight), bentonite (manufactured by Horus Kogyo Co., Ltd., 25 parts by weight) and calcium carbonate calpin 600 (Adachi Sekai Co., Ltd., 61.27 parts by weight) were kneaded by Fuji Sangyo Co., Ltd., FM- NW-5 type), and further slurry 2 (8.33 parts by weight) was added and mixed. The granules obtained by extruding the mixture using a dome gran (manufactured by Fuji Powder Co., Ltd., screen 1.0 mmφ) were dried with a shelf dryer (made by Taba Kabuki Co., Ltd., PERFECT OVEN PS-222, 60 ° C). Thereafter, the mixture was sieved to 600 to 1190 mm to obtain a mixed granule of the compound (5%) and the compound A (5%) of Example 171.
[3270] (Example 8)
[3271] Aqueous suspensions
[3272] Example 1 Compound (11.11 parts by weight), Compound C (11.11 parts by weight), Nucol 291PG (1 part by weight), calcium lignin sulfonic acid salt (Perlex CP, manufactured by Nippon Seishi KK, Ltd., 10 parts by weight) ), Propylene glycol (10 parts by weight of Nippon Yukazai Co., Ltd.) and water (56.78 parts by weight) are mixed and the attritor until the diameter of the solid particles is 5 μm or less (Mitsui Kosan Kabuki Seiki Co., Ltd.) It grind | pulverized in the middle and obtained the slurry. 0.05% xanthan gum aqueous solution (10 parts by weight) was added to this slurry (90 parts) and mixed to obtain a mixed aqueous suspending agent of the compound (10%) and compound C (10%) of Example 1.
[3273] (Example 9)
[3274] Hydrating agent
[3275] Example 23 Compound (10 parts by weight) of Compound No. 806, Compound D (2 parts by weight), Capplex # 80D (manufactured by Shionogi Seiyaku Co., Ltd., 10 parts by weight), Gosenol GL05-S (Nibbon Kosei Kagaku Co., Ltd., 2 parts by weight), New Cole 291PG (Dioctylsulfosuccinate sodium salt, Nippon Yukazai Kabuki Seiki Co., Ltd., 0.5 parts by weight), Neogen powder , 5 parts by weight), Radiolite # 200 (manufactured by Showa Kagaku Kogyo Co., Ltd., 10 parts by weight) and H fine powder (manufactured by Keiwa Rozai Co., Ltd., 60.5 parts by weight) were sufficiently mixed. The mixture was pulverized with an air mill (manufactured by Seishin Co., Ltd., SK-JET O MIZER model 0101) to obtain a mixed hydration agent of the compound of Example 23 (10%) and compound D (2%).
[3276] (Example 10)
[3277] Hydrating agent
[3278] Example 23 Compound (10 parts by weight) of Compound No. 806, Compound E (8 parts by weight), Carplex # 80D (manufactured by Shionogi Seiyaku Co., Ltd., 10 parts by weight), Gosenol GL05-S (Nibbon Kosei Kagaku Co., Ltd., 2 parts by weight), New Cole 291PG (Dioctylsulfosuccinate sodium salt, Nippon Yukazai Kabuki Seiki Co., Ltd., 0.5 parts by weight), Neogen powder , 5 parts by weight), Radiolite # 200 (10,5 parts by weight, manufactured by Showa Kagaku Kogyo Co., Ltd.), and H fine powder (54.5 parts by weight of Keiwa Rozai Co., Ltd.) were sufficiently mixed. The mixture was pulverized with an air mill (manufactured by Seishin Co., Ltd., SK-JET O MIZER model 0101) to obtain a mixed hydrating agent of the compound of Example 23 (10%) and compound E (8%).
[3279] (Example 11)
[3280] Hydrating agent
[3281] A mixed hydration agent of the compound (10%) and the compound F (8%) of Example 23 was obtained in the same manner as in Formulation Example 10, except that Compound F was used instead of Compound E.
[3282] (Test Example 1)
[3283] Herbicidal Effect and Weakness Test on Transplanted Rice
[3284] Filled with 1 / 10,000 a pots of paddy soil, seeded dormant bark, tadpoles, and annual broadleaf weeds (grass and bark) blended to 1 cm of surface layer. In addition, tubers of germinated beetles were planted, and seedlings of 2.2 leafy rice were transplanted and grown in a greenhouse as fresh water. Three days after transplantation, a predetermined amount of the hydrating agent prepared according to Formulation Example 1 was diluted in water, and the spray solution was treated with fresh water soil, and 25 days after the treatment, the herbicidal effect and the damage to the transplanted rice were measured. In addition, 3- (2-allylphenoxy) -6-chloro-4-methoxypyridazine described in Chemical Pharmaceutical Bulletin, 1972, 20, 10, pages 2191-2203 was used as comparative compound. . The results are shown in Table 2 below. In addition, the herbicidal effect and the damage to transplanted rice are determined by the following criteria, and "-" in a table | surface shows no test.
[3285] Criteria
[3286] 0: growth inhibition rate 0 to 10%
[3287] 1: growth inhibition rate of 11 to 30%
[3288] 2: growth inhibition rate of 31-50%
[3289] 3: growth inhibition rate of 51 to 70%
[3290] 4: growth inhibition rate 71-90%
[3291] 5: 91 to 100% growth inhibition rate.
[3292]
[3293]
[3294]
[3295]
[3296]
[3297]
[3298] (Test Example 2)
[3299] Test of herbicidal effect (soil treatment)
[3300] Field soil was charged to a 150 cm 2 pot, and the bark and lampshade were sown and grown in a greenhouse. The next day of sowing, a predetermined amount of the hydrating agent prepared according to Formulation Example 1 was diluted with water and treated with soil. After 21 days of treatment, the herbicidal effect was determined according to the criterion of Example 1 and shown in Table 3 below.
[3301]
[3302] (Test Example 3)
[3303] Test of herbicidal effect (foliage treatment)
[3304] Field soil was charged to a 150 cm ² pot, and seedlings, tall morning glory, pods, crows, and furs were sown and grown in greenhouses. After the weeds were grown to about 10 to 15 cm, a predetermined amount of the hydrating agent prepared according to Formulation Example 1 was diluted with water containing 0.05% of Gramine S and treated with foliage. After 14 days of treatment, the herbicidal effect was determined according to the criterion of Test Example 1, and is shown in Table 4 below. In addition, "-" in a table | surface shows no test.
[3305]
[3306] (Test Example 4)
[3307] Herbicidal Effect and Weakness Test on Transplanted Rice
[3308] Filling paddy soil with a 1/5000 a Wagner pot, seeded dormant bark, tadpoles and annual broadleaf weeds (grass and knotweed) blended to 1 cm of surface layer. Also, tubers of dormant agitated beetles, snares, and taverns were planted, seedlings of 2.2 leafy rice were transplanted, and grown in fresh water in a greenhouse. After 3 days of transplantation, a predetermined amount of the hydrating agent prepared according to Formulation Example 5 was diluted with water, treated with fresh water soil, and 25 days later, the herbicidal effect and the damage to the transplanted rice were judged according to the following criteria. Table 5 below. In addition, "-" in a table | surface shows the composition which does not contain the said active ingredient.
[3309] Criteria
[3310] 0: growth inhibition rate from 0 to 15%
[3311] 1: growth inhibition rate 16-35%
[3312] 2: growth inhibition rate 36-55%
[3313] 3: growth inhibition rate 56-75%
[3314] 4: growth inhibition rate 76-95%
[3315] 5: 96 to 100% growth inhibition rate.
[3316]
[3317]
[3318]
[3319] (Test Example 5)
[3320] Weeding effect and pesticide test on field crops (soil treatment)
[3321] Field soil was charged to a 150 cm ² pot, and barks, varieties of varieties, mother-of-pearl, crows, tall morning glory and corn were sown and grown in greenhouses. The day after sowing, the predetermined amount of the hydrating agent adjusted according to Formulation Example 5 was diluted with water, and the soil was treated. After 21 days of treatment, the herbicidal effect and the damage to corn were determined according to the following criteria, and the results are shown in Tables 6 to 8 below. In addition, "-" in a table | surface shows that it does not contain the said active ingredient.
[3322] Criteria
[3323] 0: growth inhibition rate from 0 to 9%
[3324] 1: growth inhibition rate 10-19%
[3325] 2: growth inhibition rate from 20 to 29%
[3326] 3: growth inhibition rate 30-39%
[3327] 4: growth inhibition rate 40-49%
[3328] 5: 50% to 59% growth inhibition rate
[3329] 6: growth inhibition rate 60-69%
[3330] 7: Growth inhibition rate 70-79%
[3331] 8: Growth inhibition rate 80-89%
[3332] 9: growth inhibition rate 90-98%
[3333] 10: 99 to 100% growth inhibition rate.
[3334]
[3335]
[3336]
[3337]
[3338] (Test Example 6)
[3339] Herbicide effect and pesticide test on field crops (foliar treatment)
[3340] Field soil was charged to a 150 cm ² pot, and barks, varieties of varieties, mother-of-pearl, crows, tall morning glory and corn were sown and grown in greenhouses. After the weeds were grown to about 10-15 cm, the predetermined amount of the hydrating agent adjusted according to Formulation Example 5 was diluted with water containing 0.05% of Gramine S and treated with foliage. After 14 days of treatment, the herbicidal effect and the weakness were determined in accordance with the criterion of Test Example 5, and are shown in Tables 9 and 10 below. In addition, "-" in a table | surface shows that it does not contain the said active ingredient.
[3341]
[3342]
[3343] The compounds of the present invention have a herbicidal action and can be used as herbicides in rice fields, fields, orchards, grasslands, grasses, forests or non-cropland.
[3344] The compound of the present invention is a variety of weeds that are problematic in rice fields, for example, annual herb leaf weeds, such as turfgrass, paddygrass, bark flower, water starch, coot, mantis grass, dorsal grass, and moth bud; Perennial peels and weeds such as snares, peels, and taxa; Annual herbaceous weeds such as Geumbang-dong and Malbang-dong; Perennial gilts and weeds such as ox bones, tadpoles, beetles, and beetles; Or it shows herbicidal activity against annual and perennial rice and weeds such as bark and buckthorn, and does not show a harmful problem to rice.
[3345] In addition, the compounds of the present invention exhibit herbicidal activity against various weeds that are problematic in soil treatment and foliage treatment of field farming.
[3346] In addition, it can be used not only in rice fields and fields, but also in orchards, mulberry fields and non-crop lands.
[3347] In addition, the herbicidal composition of the present invention is mixed with the active ingredient 3-phenoxy-4-pyridazinol derivative and the second herbicidal active compound, so that the width of the herbicide is extended beyond the application range obtained by each single agent. . The herbicidal width of the composition of the present invention extends to perennial weeds such as rice plants, annual broad-leaved weeds and bark, and fast-growing poultry family. In addition, the composition of the present invention has a high safety against rice and field crops, and a wide spread time. Moreover, the composition of this invention shows synergistic effect in the herbicidal effect, and fully exhibits the effect by mixing of much lower doses than the dose when using each active ingredient as a single agent. As a result, the composition of the present invention increases the herbicidal effect to a sufficient degree as a one-time treatment agent, and its effect lasts for a long time. In addition, the composition of the present invention is harmless to rice, and treatment before and after transplantation is also possible.

权利要求:
Claims (21)
[1" claim-type="Currently amended] The compounds represented by the following formula (I), salts thereof and ester derivatives thereof.
<Formula I>

Wherein R ¹ represents a hydrogen atom, a halogen atom, a C1 to C6 alkyl group, a C1 to C6 haloalkyl group, a C3 to C6 cycloalkyl group, a C2 to C6 alkenyl group, a cyano group, a C2 to C7 alkylcarbonyl group, a di (C1 to C6 alkyl) ) Carbamoyl group, a phenyl group which may be substituted (this substituent is a substituent selected from Substituent Group A), a 5 or 6 membered heterocyclic group (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring) And may also contain 1 to 2 nitrogen atoms), a C1 to C6 alkoxy group, a phenoxy group which may be substituted (this substituent is a substituent selected from Substituent Group A below) or 5 or 6 which may be substituted Circle heterocyclic oxy groups (This heterocycle contains one nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain one to two nitrogen atoms, and this substituent may be substituted with a benzoyl group The substituent is And it may be substituted) by a moiety selected from the group consisting of the substituent) and a C1 to C6 alkyl group is selected from the ventilation group A,
R ² is a hydrogen atom, a halogen atom, a C1 to C6 alkyl group, a (C1 to C6 alkoxy) C1 to C6 alkyl group, a benzoyl group which may be substituted (this substituent is a substituent selected from substituent group A below), C2 to C7 alkoxy A carbonyl group, a phenoxy group which may be substituted (this substituent is a substituent selected from substituent group A below), a phenylthio group which may be substituted (this substituent is a substituent selected from substituent group A below) or a tree (C1 to C6) Alkyl) silicon group,
R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each independently a hydrogen atom, a halogen atom, a C 1 to C 6 alkyl group which may be substituted (this substituent is a substituent selected from Substituent Group B below), C2 to C6 alkenyl group (this substituent is a cyano group or nitro group), C2 to C6 alkynyl group, C3 to C6 cycloalkyl group which may be substituted (this substituent is a substituent selected from substituent group C below), C4 to C10 bicycloalkyl group, cyano group, formyl group, C2 to C7 alkylcarbonyl group, benzoyl group which may be substituted (this substituent is a substituent selected from Substituent Group A), carboxyl group, C2 to C7 alkoxycarbonyl group, carbamoyl group, A di (C1-C6 alkyl) carbamoyl group, a phenyl group which may be substituted (this substituent is a substituent selected from Substituent Group A below), a 3- to 6-membered heterocyclic group which may be substituted (this heterocyclic ring is one Nitrogen atom , Containing an oxygen atom or a sulfur atom, and may also contain 1 to 2 nitrogen atoms, may be condensed with a benzene ring, which substituent is a substituent selected from the following substituent group E), an amino group which may be substituted ( This substituent is a substituent selected from the following substituent group D), nitro group, hydroxyl group, C1 to C6 alkoxy group, C1 to C6 haloalkoxy group, (C1 to C6 alkoxy) C1 to C6 alkoxy group, phenoxy group which may be substituted (This substituent is a pyridazinyloxy group substituted by a hydroxyl group or a halogen atom and a C1 to C6 alkoxy group), a 5- to 6-membered heterocyclic oxy group which may be substituted (this heterocycle has one nitrogen atom, oxygen in the ring An atom or a sulfur atom, and may also contain 1 to 2 nitrogen atoms, the substituent being a substituent selected from the following substituent group E, a phenylsulfonyloxy group which may be substituted Or a C1 to C6 alkylthio group, a C1 to C6 alkylsulfinyl group, a C1 to C6 alkylsulfonyl group or a tri (C1 to C6 alkyl) silicon group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ each represent a 3 to 6 membered cyclic hydrocarbon group which may be substituted together with the carbon atoms to which it is bonded, each of which is selected from the group consisting of nitrogen atom, oxygen atom and sulfur atom Interrupted by the same or different 1 to 2 heteroatoms, which substituents are halogen atoms, C1 to C6 alkyl groups, hydroxy C1 to C6 alkyl groups, C1 to C6 alkoxy groups, oxo groups, hydroxyimino groups or C1 to A C6 alkoxyimino group and substituted with a C1 to C6 alkyl group, it may be combined with a different C1 to C6 alkyl group or a cyclic carbon atom to form a new three-membered ring),
m and n represent 0 or 1 independently of each other,
Substituent group A is a group consisting of a halogen atom, a C1 to C6 alkyl group, a C1 to C6 haloalkyl group, a C3 to C6 cycloalkyl group, a cyano group, and a tri (C1 to C6 alkyl) silicon group,
Substituent group B is a halogen atom, C3 to C6 cycloalkyl group, cyano group, C2 to C7 alkylcarbonyl group, C2 to C7 alkoxycarbonyl group, phenyl group, C1 to C6 alkoxy group, C1 to C6 alkylthio group, C1 to C6 alkylsulfinyl group, C1 to C6 alkylsulfonyl group, C1 to C4 alkylenedioxy group, hydroxyimino group and C1 to C6 alkoxyimino group,
Substituent group C is a halogen atom, a C1 to C6 alkyl group which may be substituted (the substituent is a substituent selected from the substituent group B), a C3 to C6 cycloalkyl group, a C2 to C6 alkenyl group, a cyano group, a C2 to C7 alkylcarbonyl group , Benzoyl group, carboxyl group, C2 to C7 alkoxycarbonyl group, carbamoyl group, di (C1 to C6 alkyl) carbamoyl group, phenyl group which may be substituted (this substituent is a substituent selected from Substituent Group A), 5 or 6 Circle heterocyclic group (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and may also contain 1 to 2 nitrogen atoms), an amino group which may be substituted (this substituent is the following substituent group) Substituents selected from D), nitro groups, hydroxyl groups, C1 to C6 alkoxy groups, C1 to C6 haloalkoxy groups, phenoxy groups, C1 to C6 alkylthio groups, phenylthio groups, C1 to C6 alkylsulfinyl groups and C1 to C6 It is a group which consists of an alkylsulfonyl group,
Substituent group D is a group consisting of a C1 to C6 alkyl group, a C2 to C7 alkylcarbonyl group, a C2 to C7 alkoxycarbonyl group, a di (C1 to C6 alkyl) carbamoyl group, and a C1 to C6 alkylsulfonyl group,
Substituent group E is a halogen atom, a C1 to C6 alkyl group, a C1 to C6 haloalkyl group, a hydroxyl group, a phenylsulfonyl group which may be substituted (this substituent is a substituent selected from Substituent Group A) and di (C1 to C6 alkyl) It is a group consisting of pamoyl group.
[2" claim-type="Currently amended] The compound of claim 1, wherein R ¹ is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (the halogen atom is 1 to 3 fluorine atoms), a cyclopropyl group, C2 To C3 alkenyl group, cyano group, C2 to C4 alkylcarbonyl group, di (C1 to C3 alkyl) carbamoyl group, a phenyl group which may be substituted (this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, C3 haloalkyl group (this halogen atom is the same or different from 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group, cyano group and tri (C1 to C3 alkyl) silicon group The same or different 1 to 2 substituents selected from), furyl group, thienyl group, C1 to C3 alkoxy group, phenoxy group which may be substituted (the substituents are fluorine atom, chlorine atom, bromine atom, C1 To C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is 1 to 3 fluorine atoms), cyclopropyl group, cyano group, and the same or different 1 to 2 selected from the group consisting of tri (C1 to C3 alkyl) silicon groups Substituents) or substituted pyrazolyloxy groups, which substituents are one benzoyl group and two C1 to C3 alkyl groups substituted by two chlorine atoms, salts thereof and ester derivatives thereof.
[3" claim-type="Currently amended] The compound, a salt thereof, and an ester derivative thereof according to claim 1, wherein R ¹ is a chlorine atom, bromine atom, trifluoromethyl group or cyano group.
[4" claim-type="Currently amended] The compound, a salt thereof, and an ester derivative thereof according to claim 1, wherein R ¹ is a chlorine atom or a bromine atom.
[5" claim-type="Currently amended] 2. Compounds, salts thereof and ester derivatives thereof according to claim 1, wherein R ¹ is a chlorine atom.
[6" claim-type="Currently amended] The R ² is hydrogen atom, fluorine atom, chlorine atom, bromine atom, iodine atom, C1 to C3 alkyl group, (C1 to C3 alkoxy) C1 to C3 alkyl group, to be substituted. Benzoyl group (this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (the halogen atom is the same or different from 1 to 3 selected from the group consisting of Halogen atoms), a cyclopropyl group, a cyano group, and the same or different 1 to 2 substituents selected from the group consisting of tri (C1 to C3 alkyl) silicon groups), a C2 to C4 alkoxycarbonyl group, a phenoxy group which may be substituted (This substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group. (This halogen atom is composed of a fluorine atom, a chlorine atom and a bromine atom. And the same or different 1 to 2 halogen atoms selected from the same or different 1 to 2 halogen atoms selected from the group consisting of a cyclopropyl group, a cyano group and a tri (C1 to C3 alkyl) silicon group), Phenylthio group (this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (this halogen atom is the same or different from one to three selected from the group consisting of fluorine atom, chlorine atom and bromine atom A halogen atom), a cyclopropyl group, a cyano group, and the same or different 1 to 2 substituents selected from the group consisting of tri (C1 to C3 alkyl) silicon groups) or a tri (C1 to C3 alkyl) silicon group, salts thereof And ester derivatives thereof.
[7" claim-type="Currently amended] The compound according to any one of claims 1 to 5, wherein R ² is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethoxycarbonyl group or a trimethylsilyl group, a salt thereof and an ester derivative thereof.
[8" claim-type="Currently amended] The compound according to any one of claims 1 to 5, wherein R ² is a hydrogen atom, a salt thereof, and an ester derivative thereof.
[9" claim-type="Currently amended] The compound according to any one of claims 1 to 8, wherein R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ may be independently of each other a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, or a substituted group. C1 to C4 alkyl group (the substituent being the same or different from 1 to 3 substituents selected from the group consisting of fluorine atom, chlorine atom and bromine atom, or C3 to C4 cycloalkyl group, C1 to C3 alkylthio group or C1 to C3 alkoxyimide No group), C2 to C3 alkenyl group, C2 to C3 alkynyl group, C3 to C5 cycloalkyl group which may be substituted (this substituent is a fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group, C3 to C4 cycloalkyl group, cya The same or different 1 to 3 substituents selected from the group consisting of a no group, a C1 to C3 alkoxy group and a C1 to C3 alkylthio group), a C6 to C7 bicycloalkyl group, a cyano group, a C2 to C4 alkylcarbonyl group, C2 A C4 alkoxycarbonyl group, a phenyl group which may be substituted (this substituent is selected from the group consisting of fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group or C1 to C3 haloalkyl group (this halogen atom is selected from the group consisting of fluorine atom, chlorine atom and bromine atom) The same or different from 1 to 3 halogen atoms), a 5-6 membered heterocyclic group which may be substituted (this heterocycle contains 1 nitrogen atom, oxygen atom or sulfur atom in the ring, and also 1 to 2 It may contain a nitrogen atom, this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group and a C1 to C3 haloalkyl group (the halogen atom is the same or different selected from the group consisting of fluorine atom, chlorine atom and bromine atom) The same or different 1 to 2 substituents selected from the group consisting of 1 to 3 halogen atoms), a nitro group, C1 to C 3 alkoxy group, C1 to C3 haloalkoxy group (this halogen atom is the same or different from 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), phenoxy group which may be substituted (this substituent is fluorine A pyridazinyloxy group substituted by an atom, a chlorine atom, a bromine atom and a C1 to C3 alkoxy group) or a C1 to C3 alkylthio group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are adjacent to each other. Two together with the carbon atom to which each is bonded -CH ₂ CH _2- , -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -CH ₂ CH ₂ CH ₂ CH ₂ -,- CH = CH-CH = CH-, -OCH ₂ CH _2- , -OCH = CH-, -OCH = C (CH ₃ )-, -SCH = CH-, -N = CH-CH = CH-, -OCH ₂ O-, -OCH ₂ CH ₂ O-,

Group compounds, salts thereof and ester derivatives thereof.
[10" claim-type="Currently amended] The compound according to any one of claims 1 to 8, wherein R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ may be independently of each other a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, or a substituted group. C1 to C4 alkyl group (this substituent is 1 to 3 fluorine atoms or 1 cyclopropyl group), C3 to C4 cycloalkyl group which may be substituted (the substituents are fluorine atom, chlorine atom, bromine atom, C1 to C2 alkyl group, The same 1 to 2 substituents selected from the group consisting of a cyclopropyl group and a C1 to C2 alkoxy group), a cyano group, a C2 to C3 alkoxycarbonyl group, a nitro group, a C1 to C3 alkoxy group or a trifluoromethoxy group, or R Two adjacent to each other, ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ , together with the carbon atom to which they are bonded -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -OCH ₂ CH _2- , -OCH = CH- or

Wherein R ³ is not a hydrogen atom, salts thereof and ester derivatives thereof.
[11" claim-type="Currently amended] The compound according to any one of claims 1 to 8, wherein R ³ , R ⁴ , R ⁵ , R ^6, and R ⁷ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, C1 to C3. An alkyl group, a C3 to C4 cycloalkyl group which may be substituted (this substituent is the same 1 to 2 substituents selected from the group consisting of a chlorine atom and a C1 to C2 alkoxy group), a cyano group or a C1 to C2 alkoxy group, or R ³ , Two adjacent groups of R ⁴ , R ⁵ , R ⁶ and R ⁷ are each represented by —CH ₂ CH ₂ CH ₂ — or —OCH═CH— with the carbon atom to which each is bonded, provided that R ³ is hydrogen Non-atom compounds, salts thereof and ester derivatives thereof.
[12" claim-type="Currently amended] The compound according to any one of claims 1 to 8, wherein R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group or an ethyl group. , Isopropyl group, a cyclopropyl group which may be substituted (this substituent is two chlorine atoms) or a cyano group, or two adjacent groups of R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each bonded Together with a carbon atom to represent —CH ₂ CH ₂ CH ₂ —, wherein R ³ is not a hydrogen atom, a salt thereof, and an ester derivative thereof.
[13" claim-type="Currently amended] The compound according to any one of claims 1 to 12, wherein m and n are both 0, salts thereof and ester derivatives thereof.
[14" claim-type="Currently amended] The compound of claim 1, wherein R ¹ is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, a C1 to C3 haloalkyl group (the halogen atom is 1 to 3 fluorine atoms), a cyclopropyl group, C2 To C3 alkenyl group, cyano group, C2 to C4 alkylcarbonyl group, di (C1 to C3 alkyl) carbamoyl group, a phenyl group which may be substituted (this substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group, C3 haloalkyl group (this halogen atom is the same or different from 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group, cyano group and tri (C1 to C3 alkyl) silicon group The same or different 1 to 2 substituents selected from), furyl group, thienyl group, C1 to C3 alkoxy group, phenoxy group which may be substituted (the substituents are fluorine atom, chlorine atom, bromine atom, C1 To C3 alkyl group, C1 to C3 haloalkyl group (this halogen atom is 1 to 3 fluorine atoms), cyclopropyl group, cyano group, and the same or different 1 to 2 selected from the group consisting of tri (C1 to C3 alkyl) silicon group Substituents) or a substituted pyrazolyloxy group (which is one benzoyl group and two C1 to C3 alkyl groups substituted by two chlorine atoms),
R ² is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C3 alkyl group, a (C1 to C3 alkoxy) C1 to C3 alkyl group, a benzoyl group which may be substituted (this substituent is a fluorine atom, a chlorine atom, Bromine atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is the same or different 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group, cyano group and tree (C1 to C3 alkyl) same or different 1 to 2 substituents selected from the group consisting of silicon groups, C2 to C4 alkoxycarbonyl groups, phenoxy groups which may be substituted (the substituents are fluorine atoms, chlorine atoms, bromine atoms, C1 To C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is one or three same or different selected from the group consisting of fluorine atom, chlorine atom and bromine atom) A halogen atom), a cyclopropyl group, a cyano group, and one or two substituents selected from the group consisting of tri (C1 to C3 alkyl) silicon groups), and a phenylthio group which may be substituted (this substituent is a fluorine atom) , Chlorine atom, bromine atom, C1 to C3 alkyl group, C1 to C3 haloalkyl group (the halogen atom is the same or different 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom), cyclopropyl group, The same or different 1 to 2 substituents selected from the group consisting of a cyano group and a tri (C1 to C3 alkyl) silicon group) or a tri (C1 to C3 alkyl) silicon group,
R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ independently of one another are a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C4 alkyl group which may be substituted (this substituent is a fluorine atom, a chlorine atom And the same or different 1 to 3 substituents selected from the group consisting of bromine atoms, or C3 to C4 cycloalkyl group, C1 to C3 alkylthio group or C1 to C3 alkoxyimino group), C2 to C3 alkenyl group, C2 to C3 alkoxy Nyl group, C3 to C5 cycloalkyl group which may be substituted (This substituent is a fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group, C3 to C4 cycloalkyl group, cyano group, C1 to C3 alkoxy group and C1 to C3 alkylthio group The same or different 1 to 3 substituents selected from the group consisting of), C6 to C7 bicycloalkyl group, cyano group, C2 to C4 alkylcarbonyl group, C2 to C4 alkoxycarbonyl group, which may be substituted Phenyl group (this substituent is a fluorine atom, chlorine atom, bromine atom, C1 to C3 alkyl group or C1 to C3 haloalkyl group (this halogen atom is the same or different from 1 to 3 halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom) Substituting a 5-6 membered heterocyclic group which may contain 1 nitrogen atom, oxygen atom or sulfur atom in the ring and may also contain 1 to 2 nitrogen atoms The substituent is a fluorine atom, a chlorine atom, a bromine atom, a C1 to C3 alkyl group and a C1 to C3 haloalkyl group (the halogen atom is the same or different from one to three halogen atoms selected from the group consisting of fluorine atom, chlorine atom and bromine atom) The same or different 1 to 2 substituents selected from the group consisting of), nitro group, C1 to C3 alkoxy group, C1 to C3 haloalkoxy group The gen atom is the same or different from 1 to 3 halogen atoms selected from the group consisting of fluorine atoms, chlorine atoms and bromine atoms, phenoxy groups which may be substituted (the substituents being fluorine atoms, chlorine atoms, bromine atoms and C1 to C3 alkoxy); Is a pyridazinyloxy group substituted by a group) or a C1 to C3 alkylthio group, or two adjacent R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are each -CH together with the carbon atom to which they are bonded. ₂ CH _2- , -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -CH ₂ CH ₂ CH ₂ CH _2- , -CH = CH-CH = CH-, -OCH ₂ CH _2- , -OCH = CH-, -OCH = C (CH ₃ )-, -SCH = CH-, -N = CH-CH = CH-, -OCH ₂ O-, -OCH ₂ CH ₂ O-,

Is a group represented by
m and n are both 0, salts thereof and ester derivatives thereof.
[15" claim-type="Currently amended] The compound of claim 1, wherein R ¹ is a hydrogen atom, a bromine atom, a trifluoromethyl group, or a cyano group,
R ² is a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethoxycarbonyl group or a trimethylsilyl group,
R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ independently of one another are a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C4 alkyl group which may be substituted (this substituent is 1 to 3 fluorine An atom or one cyclopropyl group), a C3 to C4 cycloalkyl group which may be substituted (this substituent is selected from the group consisting of fluorine atoms, chlorine atoms, bromine atoms, C1 to C2 alkyl groups, cyclopropyl groups and C1 to C2 alkoxy groups) The same 1 to 2 substituents), cyano group, C2 to C3 alkoxycarbonyl group, nitro group, C1 to C3 alkoxy group or trifluoromethoxy group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are Two adjacent groups, together with the carbon atom to which each is bonded, are -CH ₂ CH ₂ CH _2- , -CH (CH ₃ ) CH ₂ CH _2- , -OCH ₂ CH _2- , -OCH = CH- or

In which R ³ is not a hydrogen atom,
m and n are both 0, salts thereof and ester derivatives thereof.
[16" claim-type="Currently amended] The compound according to claim 1, wherein R ¹ is a hydrogen atom or a bromine atom,
R ² is a hydrogen atom,
R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are independently of each other a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a C1 to C3 alkyl group, a C3 to C4 cycloalkyl group which may be substituted (this substituent Is the same 1 to 2 substituents selected from the group consisting of a chlorine atom and a C1 to C2 alkyl group), a cyano group or a C1 to C2 alkoxy group, or R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are adjacent Two of which together with the carbon atom to which each are bonded are a group represented by -CH ₂ CH ₂ CH ₂ -or -OCH = CH-, provided that R ³ is not a hydrogen atom,
m and n are both 0, salts thereof and ester derivatives thereof.
[17" claim-type="Currently amended] The compound according to claim 1, wherein R ¹ is a hydrogen atom,
R ² is a hydrogen atom,
R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are independently of each other a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethyl group, an isopropyl group, a cyclopropyl group which may be substituted (this The substituent is two chlorine atoms) or a methoxy group, or two adjacent groups of R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ each represent -CH ₂ CH ₂ CH ₂ -together with the carbon atom to which it is bonded Represented by the proviso that R ³ is not a hydrogen atom,
m and n are both 0, salts thereof and ester derivatives thereof.
[18" claim-type="Currently amended] 18. The compound of any of claims 1-17, wherein 6-chloro-3- (2-iodophenoxy) -4-pyridazinol, 6-chloro-3- (2-methylphenoxy) -4 -Pyridazinol, 6-chloro-3- (2-cyclopropylphenoxy) -4-pyridazinol, 6-chloro-3- (2,3-dihydro-1H-inden-4-yloxy)- 4-pyridazinol, 3- (1-benzofuran-7-yloxy) -6-chloro-4-pyridazinol, 6-chloro-3- (2-methoxy-5-methylphenoxy) -4 -Pyridazinol, 6-chloro-3- (2-chloro-6-cyclopropylphenoxy) -4-pyridazinol, 3- (2-bromo-6-methylphenphenoxy) -6-chloro- 4-pyridazinol, 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol and 6-chloro-3- (2-cyclopropyl-3,5-dimethylphenoxy ) -4-pyridazinol compounds, salts thereof and ester derivatives thereof.
[19" claim-type="Currently amended] A pesticide containing the compound as described in any one of Claims 1-18, its salt, and its ester derivative as an active ingredient.
[20" claim-type="Currently amended] One or two or more 3-phenoxy-4-pyridazinol derivatives selected from the group consisting of the compound according to any one of claims 1 to 18, salts thereof and ester derivatives thereof, and
4- (2,4-Dichlorobenzoyl) -1,3-dimethyl-5-pyrazolyl-p-toluenesulfonate, 2- [4- (2,4-dichlorobenzoyl) -1,3-dimethylpyrazole- 5-yloxy] acetophenone, 2- [4- (2,4-dichloro-m-toluoyl) -1,3-dimethylpyrazol-5-yloxy] -4'-methylacetophenone, 5-cyclo Propyl-1,2-oxazol-4-yl α, α, α-trifluoro-2-methyl-p-tolyl ketone, 2- (2-chloro-4-mesylbenzoyl) cyclohexane-1,3- In the group consisting of dione, 2- (4-mesyl-2-nitrobenzoyl) cyclohexane-1,3-dione and 4-chloro-2- (methylsulfonyl) phenyl 5-cyclopropyl-4-isooxazolyl ketone A herbicidal composition containing one or two or more selected second herbicidal active compounds as active ingredients.
[21" claim-type="Currently amended] The herbicidal composition of claim 20 wherein the second herbicidal active compound is 4- (2,4-dichlorobenzoyl) -1,3-dimethyl-5-pyrazolyl-p-toluenesulfonate.

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KR100879693B1|2009-01-21|

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TWI254708B|2006-05-11|

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EP1426365A4|2004-12-08|

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US20100041555A1|2010-02-18|

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EP1426365B9|2009-10-21|

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CA2457575A1|2003-02-27|

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US20050037925A1|2005-02-17|

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KR100910691B1|2009-08-04|

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WO2003016286A1|2003-02-27|

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CN1543455B|2012-07-11|

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AU2002327096B2|2007-11-22|

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ES2330089T3|2009-12-04|

引用文献:

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公开号 | 申请日 | 公开日 | 申请人 | 专利标题

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法律状态:
2001-08-17|Priority to JP2001248014

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2001-08-17|Priority to JPJP-P-2001-00248014

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2002-03-25|Priority to JPJP-P-2002-00082219

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2002-03-25|Priority to JP2002082219

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2002-08-14|Application filed by 상꾜 아그로 가부시키가이샤

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2002-08-14|Priority to PCT/JP2002/008278

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2004-06-14|Publication of KR20040050061A

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2009-08-04|Application granted

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2009-08-04|Publication of KR100910691B1

优先权:

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申请号 | 申请日 | 专利标题

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JP2001248014|2001-08-17|

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JPJP-P-2001-00248014|2001-08-17|

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JPJP-P-2002-00082219|2002-03-25|

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JP2002082219|2002-03-25|

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PCT/JP2002/008278|WO2003016286A1|2001-08-17|2002-08-14|3-phenoxy-4-pyridazinol derivative and herbicide composition containing the same|