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    • 专利摘要:
    1. New carbostyril derivatives of general formula see diagramm : EP0003771,P26,F1 wherein W represents a vinylene group (optionally substituted by a methyl group) or the ethylene group, m represents the number 0, 1 or 2, D represents a straight-chained or branched alkylene group with 2 to 6 carbon atoms, whilst there must be at least 2 carbon atoms between the oxygen atom and the SOm group, or a xylylene group, R1 represents a cycloalkyl group with 3 to 6 carbon atoms ; an aryl group with 6 to 10 carbon atoms or an aralkyl group with 7 to 11 carbon atoms, whilst the above-mentioned aromatic nuclei may be monosubstituted by an alkyl group with 1 to 4 carbon atoms, by a hydroxy, methoxy, amino, acetylamino, nitro, carboxyl, cyclohexyl or phenyl group or by a halogen atom and, additionally, the above-mentioned monosubstituted phenyl groups may be mono- or disubstituted by alkyl groups with 1 to 4 carbon atoms and/or by halogen atoms (whilst the substituents of the phenyl nucleus may be identical or different) ; an N-methyl-cyclohexylamino-carbonylmethyl, amino-iminomethylene, pyridyl, pyridylmethyl, furfuryl, benzimidazolyl, benzothiazolyl, pyrimidyl, quinolyl, quinazolin-4-on-yl, 4,5-bis-(p-chlorophenyl)-oxazol-2-yl, pyridyloxide, triazolyl, methyl-pyridyl, methoxy-pyridyl, fluoropyridyl, chloropyridyl, aminopyridyl, acetylaminopyridyl or triphenyl-methyl group, or also a tert. butyl group, if m represents the number 1, and R2 and R3 , which may be identical or different, represent hydrogen or halogen atoms, alkyl groups with 1 to 4 carbon atoms, amino, acetylamino or nitro groups.
    公开号:SU843739A3
    申请号:SU792716799
    申请日:1979-01-31
    公开日:1981-06-30
    发明作者:Мюллер Эрих；Никль Иозеф；Рох Иозеф；Нарр Бертхольд；Харманн Вальтер；Максимилиан Вейзенбергер Иоганнес
    申请人:Карл Томэ Гмбх (Фирма)；
    IPC主号:
    专利说明:

    (54-) METHOD FOR OBTAINING CARBOSTYLENE OR OXINDOL DERIVATIVES
    up to 4 and / or halogen atoms, and the originators of the phenyl core may be the same or different. 1,2,4-triazolyl-, pyridyl-oxide, triphenylmethyl-, 4,5-bis- (para-chlorophenyl) -oxazol-2-yl-, N-methyl-cyclohexylamino-carbonylmethyl or amino-iminomethyl group or also an alkyl group with the number of carbon atoms from 1 to 6, if
    m is the number 1 or
    O means a linear or branched oxyalkylene group with 3 to 6 carbon atoms, or a xylylene group;
    R and R, which may be the same or different and mean hydrogen atoms or gadogen, alkyl groups with carbon numbers from 1 to 4, amino, aylamino or nitro groups.
    Under the expression mentioned in the description of the radicals RJ, RO, and R
    halogen atom should be understood in particular fluorine, chlorine, bromine or iodine atom.
    The method consists in the interaction of the oxo compound of the general formula (I I)
    (AND)
    R4
    where r
    RI
    Ri and W
    have above u
    These values or its salts with inorganic or tertiary organic bases with a compound of the general formula (III)
    Z - o - 50 - R,
    where D, R and m are as defined above;
    Z means a nucleophilic substitutable group such as a halogen atom or a sulfonic acid ester radical, for example a chlorine, bromine, iodine atom, para-toluenesul1, a fonyloxy or methanesulfonyloxy group.
    The reaction is expediently carried out in a solvent such as dioxane, tetrahydrofuran, chloroform or: an oluol, preferably anhydrous, an aprotic solvent such as acetone, dimethylformamide or dimethyl sulfoxide, or in the presence of an alkaline base such as sodium carbonate, potassium carbonate or sodium hydroxide. The reaction temperature is from room temperature to.
    Example 1. Preparation of b- (4-feiylsulfinylbutoxy) -3,4-dihydrocarbostyril.
    32.6 g (0.2 mol) of b-hydroxy-3,4-dihydrocarbostyril and 27.6 g (0.2 mol of potassium carbonate is mixed with 600 ml of dimethyl sulfoxide dried over a molecular sieve for 5 minutes and then added 52.2 g 4-phenylsulfinylbutyl bromide (0.2 mol), obtained from thiophenol and 1,4-dibromobutane, followed by oxidation with hydrogen peroxide in glacial acetic acid as in Example 2, gives an oily substance that solidifies on standing in a refrigerator. Stir for 15 hours at 25 ° C and pour the reaction mixture into 6 l of water. Stir for another 30 minutes, suck in the Separate the product and rinse well with water. After drying it is recrystallized upon treatment with charcoal from approximately 600 ml of xylene. White crystals are obtained with mp 144.5-145. Yield 49 g (71/3% of theory).
    Example 2. 6- (4-Phenylmercapto-butoxy) -3,4-dihydro-carbostyril is prepared analogously to example 1 of 6-hydroxy-3, 4-dihydrocarbostyril and 4- (phenylmercapto) butyl bromide, QQ. 02 96 -103 ° C, derived from thiophenol and 1,4-dibromobutane. M.p. 121.5-123 ° C. Output 75.6% of theory.
    Example 3. 6- (4-Phenylsulfonyl-butoxy) -3,4-dihydrocarbostyril is prepared as in Example 1 from 6-hydroxy-3, 4-dihydro-carbostyril and 4-phenyl-sulfonyl-butyl bromide, obtained from 4- (phenylmercapto) -butyl bromide by oxidation as in Example 3. M.p. 157.5-158c. Output 65.1% of theory.
    Example 4. 7- (4-Phenylmercaptobutoxy) -3,4-dihydrocarbostyryl is prepared analogously to example 1 of 7-hydroxy-3, 4-dihydrocarbostyril and 4-phenylmercapto-butyl bromide, bp. 0.02 96-1030С. M.p. 121-123 With the yield of 72% of theory.
    Example 5. 7- (4-phenylsulfinyl-butoxy) -3,4-dihydrocarbostyril was prepared as in Example 1 from 7-hydroxy-3, 4-dihydrocarbostyril and 4-phenylsulfinylbutyl bromide. M.p. 134-136 C. Exit 80% of theory.
    Example 6. 7- (4-Phenylsulfonyl-butoxy) -3,4-dihydrocarbostyryl was prepared as in Example 1 from 7-hydroxy-3, 4-digrocarbostyril and 4-phenylsulfonylbutylbromide. M.p. 178.5-179 ,. Exit 74 from the theory.
    Example 7. 8- (4-Phenylmercaptobutoxy) -3,4-dihydrocarbostyryl is prepared analogously to example 1 of 8-hydroxy-3, 4-dihydrocarbostyril and 4-phenylmercapto-butyl bromide, bp., 96-103 ° C. M.p. 101-1020С. 75% yield of theory ..
    Example 8. 8- (4-Phenylsulfinyl-butoxy) -3,4-dihydrocarbostyril is prepared as in Example 1 from 8-hydroxy-3, 4-dihydrocarbostyril and phenylsulfinylbutyl bromide. A colorless resin is obtained. Output 60% of theory.
    Rf value: 0.60 (thin layer chromatography on silica gel, solvent: benzene / ethanol / concentrated ammonia 75/25/1).
    Example 9. 5- (4-Phenylmercapto-butoxy) -3,4-dihydrocarbostyril is prepared as in Example 1 from 5-hydroxy-3,4-dihydrocarbstyryl and / 4-phenylmercaptobutyl bromide. M.p. 155-157C. Output 64% of theory
    Example 10. 5- (4-Phenylsulfinyl-butoxy) -3,4-dihydrocarbostyri prepared analogously to example 1 of 5-hydroxy-3, 4-dihydrocarbostyryl and 4-phenylsulfinylbutyl bromide. M.p. 136-138 ° C. Output 64% of theory
    EXAMPLE 11. 5- (4-Phenylsulfonyl-butoxy) -3,4-dihydrocarbostyryl is prepared, as in Example 1, from 5-hydroxy-3, 4-di hydrocarbostyril and 4-phenylsulfonylbutyl bromide. M.p. 187-189 ° C. Output 73% of theory
    Example 12. Obtaining 5- (4-Phenylmercapto-butoxy) -carbostyril
    49g of 4-phenylmercaptobutylbromide was added to a mixture of 32.3 g of 5-hydroxycarbostyril, 30 g of potassium carbonate and 650 ml of dimethyl sulfoxide dried over a molecular sieve. The mixture is stirred for 20 hours, diluted with 3 liters of water and the crystals are filtered off with suction. called reaction product. mp. 185187С (from toluene). Output 45.0 g (70% of theory).
    Example 13. 6- (4-Phenylmercapto-butoxy) -carbostil was prepared analogously to example 12 of 6-hydroxycarbostyril and 4-phenylmercaptobutyl bromide. M.p. 161-163 C. Output 78% of theory.
    Example 14. 6- (4-Phenylsulfinyl-butoxy) -carbostil was prepared analogously to example 12 of 6-hydroxycarbostyril and 4-phenylsulfinylbutyl bromide. M.p. 181-182 ° C. Yield 71% of theory.
    . Example 15. Obtaining 4-methyl-6- (4-phenylmercapto-butoxy) -carbostyril. 5.25 g (0.03 mol) of 4-methyl-6-hydrocarbostyril: mp. 326-330 ° C), 8.09 g (.0.033 mol of 4-phenylmercaptobutyl bromide and 6.22 g (0.045 mol) potassium carbonate is stirred in 70 ml of dimethyl sulfoxide at a room temperature of 16 h, then it is diluted with water and the separated crystals are recrystallized from toluene after drying, mp 148-150 ° C, yield 6.2 g (61.2% of theory).
    Example 16. 4-Methyl-6- (4-phenylsulfinyl-butoxy) -carbostyril is prepared as in Example 15 from
    4-methyl-6-hydroxycarbostyril (mp. 323.33-WZ C) and 4-phenylsulfinylbutyl bromide. M.p. 167-168 ° C. Output 47.3% of theory.
    EXAMPLE 17 4-Methyl-6- (4-phenylsulfonyl-butoxy) -carbostyril is prepared, as in Example 15, from 4-methyl-6-hydroxycarbostyril (mp. 326.33.34-C) and 4-phenylsulfonylbutyl bromide. M.p. 217-219 C. Output 66.6% of theory.
    o
    Example 18. 5- (4-Phenylmercapto-butoxy-oxindol is prepared analogously to Example 15 of 5-hydroxyoxindol and 4-phenylmercaptobutyl bromide. Mp. 131-132 ° C. Yield 13% of theory.
    Example 19. Obtaining 6-C25 - (phenylmercapto-methyl) -benzyloxy-3 .4-dihydro-carbostyryl.
    A mixture of 67.1 g of phthalide, 51.3 ml of thiophenol, 35.1 g of potassium methylate and
    0 250 ml of methanol is heated under reflux. Fc of the resulting 2-phenylmercaptomethylbenzoic acid (78% of theoretical, mp. 108-110 ° C) of methanol / thionyl chloride is added in succession, leaving
    5 at. After standing overnight, methyl 2-phenylmercaptomethylbenzoic acid (89% yield of theory, bp) is obtained, which is converted into 2-phenylmercapto-methyl-phenyl- by reduction of lithium aluminum hydride carbinol (yield 97% of theory, mp. 64-65s).
    This compound is converted to para5 toluenesulfonyl chloride to the ester of 2-phenylmercaptomethyl-phenylcarbitol with nol-p-toluenesulfonic acid (thin layer chromatography: silica gel; solvent: chloroform / acetic
    0 broadcast 1: 1; Rf O, 8,, yield 55% of theory). This ester is inverted analogously to Example 1 of 6-hydroxy-3,4-dihydrocarbostyril in (phenylmercaptomethyl) benzyloxy-3,4-dihydro-, carbostyryl (thin-layer chromatography 5 rafi: silica gel: solvent:: chloroform / ethyl acetate 1: 1 ; Rf 0,35; yield 64% of theory).
    Example 20. Obtaining 6-G4- (phenylmercaptomethyl) -benzyloxyJ0 -3,4-dihydrocarbostyril.
    In dimethyl sulfoxide, in the presence of excess potassium carbonate, para-xylylene dichloride and thiophenol are converted in a molar ratio
    5 1: 1 at room temperature in 4-phenylmercaptomethyl-benzyl chloride (checked by thin-layer chromatogram), which successively, without separation from the reaction solution, are reacted with 6-hydroxy-3,4-dihydrocarbatiryl in the same way as in Example 12. So pl. 139-141 C. Output 52% of theory.
    Similarly, receive the following
    5 compounds: 6-t4- (2-pyridyl mercapto) butoxy | -3, 4-dihydrocarbostyryl, m.p. 123 124.5 ° C; (4-fluorophenylmercapto) butoxy-3, 4-dihydrocarbostyryl, m.p. 139,140 ° C; 6-14- (4: 7methylphenyl-mercapto) -butoxy-3, 4-dihydrocarbostyryl, m.p. 120-121 ° C .; (3-Methylphenylmercapto) -blue C-3,4 -dihydrocarbatiri l, so pl. 95960С; 6- 4- (4-chlorophenyl mercapto) -butoxy-3, 4-dihydrocarbostyryl, m.p. 144 (3,4-dichlorophenyl mercapto) butoxy-3, 4-dihydrocarbostyryl, mp. 116.5-118 ° C; (2-metoxyphenylmethyl) -butyric - 3,4-dihydrocarboxyryl, so pl. 130.5-133 ° C .; (3-methoxyphenylmercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 93.5-97 ° C; (4-methoxyphenylmercapto) -but oxy-3,4-dihydrocarbostyryl, m.p. 130.5-133 ° C; , 4-dimethoxyphenylmercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 117-119®C; b- 4- {4-biphenylylmercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 179.5-181C; b- (6-phenylmercapto-hexoxy) -3,4-dihydrocarbostyryl, m.p. 112, 6- (2-hydroxy-3-phenylmercapto-propoxy) -3,4-dihydrocarbostyryl, m.p. 14 1490С; (2-quinolyl mercapto) butoxy-3,4-dihydrocarbostyryl, m.p. (2-quinazolin-4-one-yl-mercapto) butoxy-3,4-dihydrocarbostyril, m.p. 184.5-188 seconds; 6- (4-triphenylmethyl mercapto-butoxy) -3,4-dihydrocarbostyryl, mp. 169 software ° C; b-f2- (2-naphthylmercapto) -ethoxy-3, 4-dihydrocarboxyryl so pl. 147.5147, 8 ° C; b- 2- (4-biphenylylmercapto) -ethoxy-3/4-dihydrocarboxyryl, m.p. 192 194 "C: b-Hz- (2-pyridyl mercapto) -proximate-3, 4-dihydrocarbrostyl, m.p. 108 1b8, (2-naphthylmercapto) butoxy7-3, 4f dihydrocarbostyryl, m.p. 108% 109, | O.C; 6- (4-cyclohexylmercaptobutoxy) -3, 4-ligidrocarbostyril, mp 1141150 ° C; 6- (4-beisyl mercapto-butoxy) -3,4-dihydrocarbostyryl mp; 77.578, 50С; (2-furylmethylmercapto) -blue C-3.4-dihydrocarbostyryl so pl. 7980WC; 6-f4- (M-oxide-2-pyridyl mercapto) butoxy-3,4-dihydrocarbostyryl mp; 179.5-181CC; 6-C4- (2-pyridyl-mercapto) -butoxy 3, 4-dihydrocarbostyryl so pl. 154ISe C: 6- 4- (4-pyridylmercapto) -butoxy} -3, 4.-dihydr6carbostyryl mp; 128129 ° C; b- {4- (2-benzimidazolylmercapto) -butoxy-3,4-dihydrocarbostyryl, mp 100-103 ° C; 6-14- (benethiazolyl-mercapto) -butoxy-3., 4-dihydrocarbostyryl, m.p. 1571580С; 6- (2-phenylmercapto-ethoxy) -3,4-dihydrocarbosteryl, so pl. 132133, 5 ° C; 6- (3-phenylmercapto-propoxy) -3,4-dihydrocarbostyryl, m.p. 111-112 ° C; 1-methyl-6- (4-phenylmercapto-butoxy) -3,4-dihydrocarbostyryl, m.p. 79.580, 5 “C; b- (4-phenylmercapto-butoxy) -carbostil, so pl. 1b2-164 ° C; 5- (4-phenylmercapto-butoxy) -carbostyril, so pl. 185-187 ° C (from toluene); 8- (4-phenylmercapto-butoxy) carbostyryl, mp. 119-120-C; b- (4-amino-iminomethylmercapto-butoxy) -3,4-dihydrocarbostyryl, m.p. 140-141,800; b- (4-ben zilmercapto-butoxy) -3,4-dihydrocarbostyril, so pl. 7b-78C; b- (5-phenylmercaptopentoxy) -3,4-dihydrocarbostyryl, m.p. 117119®C; b- 5- (2-pyridyl-mercapto) -pentoxy-3, 4-dihydrocarboxyryl, m.p. 113-114.8 ° C; 5- (2-hydroxy-3-phenylmercapto-propoxy) -3,4-dihydrocarbostyryl, m.p. 135-1370С; (4-hydroxyphenylmercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 191.5-193, OOS; (4-acetaminophenylmercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 162.5-163, 6-C4- (4,5-di-p-chlorophenyl-oxazol-2-yl-mercapt) -butoxy-3,4-dihydrocarbostyryl, m.p. 110-115С; 7- (4-phenylmercapto-butoxy) -carbstyryl, m.p. 157.5-158.5 ° C; 6-14- (2,5-dichlorophenylmercapto) -butoxy-3, 4-dihydrocaroylryl, m.p. 133-134C; (4-hydroxy-3,5-di-tert.butyl-feiylmercapto) -butoxy 3,4-dihydrocarbostyryl, m.p. 146-147 0; (2-carboxyphenylmercapto) -butoxy-3, 4-dihydrocarbostyril, mp 176-179 ° C; b- (3-benzylmercapto-propoxy) -3,4-dihydrocarbostyryl, m.p. 87,599, OOS; 5- (3-tert.butylmercapto-2-hydroxy-propoxy) -3,4-dihydrocarbostyryl, m.p. , 105-109 0;
    4-methyl-6-14- (2-pyridyl mercapto) -butoxy-carboxyryl, m.p. 149ISl C;
    4-methyl-b- 4- (2-quinolylmercapto) -butoxy-carbostyryl, m.p. 162163 C;
    (4-chlorophenylmercapto) -butoxy-carboxyryl, m.p. 1b8-170 C;
     (3,4-dichlorophenyl mercapto) -butoxy-carbostyryl, m.p. 149152 С:
     (2,5-dichlorophenylmercapto) -butoxyT-carbostyryl, m.p. 175176 С:
    (4-fluorophenylmercapto) -butoxy-carboxyryl, m.p. 149-150 ° C;
    (4-hydroxy-3,5-di-tert.butyl-phenylmercapto) butoxy-carbostyryl, m.p. 172-173 ° C;
    6- 4- (4-biphenylyl-mercapto) -butoxy-carboxyryl, m.p. 191-192 C;
    (4-nitrophenylmercapto) -butoxyT-carbostyryl, m.p. 184ISS C:
    6-t4- (2-quinolyl mercapto) -butoxy-carboxyryl, m.p.
    b- (4-cyclohexylmercapto-butoxy-carbostyril, mp 153-159 ° C;
    (4-bromophenylmercapto) butoxy-carbostyryl, m.p. 156-158 ° C;
    6- {4- (3-methyl-4-bromo-phenylmercapto) -butoxy-carbostyryl, m.p. 1671690s:
    6-L4- (1,2,4-triazole-3-yl-adercapto) butoxy 1-carbostyryl, m.p. 203Yub C:
     (2,4, 5-trichlorophenylmercapto. -Butoxy-carbostyril, mp 1771780s;
    (3,5-dibrom-4-amino-phenylmercapto) -butoxy 3 -3,4-dihydrocarbostyryl, m.p. 90-92 ° C;
    (3,5-dibrom-4-amino-phenylmercapto) -butoxy-carbostyryl, m.p. 153-155 ° C;
    b- 4- (4-bromo-3-methyl-phenylmercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 1С4-109С;
    6 - 4 -. (2,5-dibromophenylmercapto) -butoxy-3, 4-dihydrocarboxyryl, m.p. 127-129 ° C;
    (2,5-dibromo-phenylmercapto) -butoxy-carbostyryl, m.p. 178-. 1850С;
    (3,4-ichloro-phenylmercapto) -propoxy-3, 4-dihydrocarbosyryl, m.p. 106-107 ° C;
    (4-cyclohexyl-phenylmercapto) -butoxy-3,4-dihydrocarbostyryl, m.p. 118-120 oc;
    (4-cyclohexyl-phenylmercapto) -butoxy-carbostyryl. m.p. 1651670s;
    (4-tert.butyl-phenylmercapto) -butoxy-3,4-dihydrocarbostyryl, m.p. 126-12700;
    (4-tert.butyl-phenylmercapto) -butoxy-carboxyryl, m.p. 156158 “С; .
    6-G2- (N-methyl-N-cyclohexyl-carbamidomethyl mercapto) -ethoxy-carbostyryl, Rf value: 0.41 (silica gel luminescent plate; solvent: ethylene chloride / methanol 95: 5). .
    6-5 - (3,5-dichlorf nilmerk ap-to) -pentoxy-3, 4-dihydrocarboxyryl, m.p. 101-1040С;
    (2-methyl-4-tert.butyl-phenylmercapto) butoxy-3,4-dihydrocarbostyril, pl. 81-85;
    (3,5-dichloro-4-hydroxy-phenylmercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 110-114C;
    5-bromo-b- (4-phenylmercaptobutoxy) -carbostyryl, m.p. 209-213 C;
    5-nitro-b- (4-phenylmercaptobutoxy) -carbostyryl, m.p. 228-230 ° Cj
    5-acetamino-6- (4-phenylmercaptobutoxy) -carbostyril, mp 238-240 ° C; 6-C4- (1,2,4-triazole-3-yl-mercapto) -butoxy3-3,4-dihydrocarbostyryl, m.p. 152-154 ° C;
    (2,4,5-trichlorophenyl mercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 144-145С;
     (3,4-dichlorophenyl mercapto) -2-hydroxy-propoxy-3, 4-dihydrocarbostyryl, m.p. 175-1760C;
     (Z-hydroxy-pyrid-2-yl-mercapto) butoxy-3,4-dihydrocarbostyryl, m.p. 211-2160C;
    6- 2- (N-methyl-M-cyc. Hexyl-carbamidomethyl mercapto) -ethoxy-3,4-dihydrocarbostyryl, Rf — value: 0.46 (silica gel luminescent plate; solvent: ethylene chloride / methanol 95/5);
    (2-pyridylsulfinyl) -butoxy-3, 4-dihydrocarbostyryl, so pl. 144.5-14 ° C;
    (4-Fluorophenylsulfinyl) -butoxy J- 3,4-dihydrocarbostyryl, m.p. 184.5-18BS;
    (4-methylphenylsulfinyl) -butoxy-3, 4-dihydrocarbostyryl, tr. 149.5-1500С;
    (3-methylphenylsulfinyl) -butoxy-3,4-dihydrocarbostyryl, Rf value: 0.48 (thin-layer chromatography on silica gel - solvent: benzene (ethanol) concentrated ammonia 75/25/1).
    6 -1 | 4 - (4-chlorofen n ilusul fi n and il) butoxy-3, 4-dihydrocarbostyryl, m.p. 148-149,50С;
    (3,4-dichlorophenylsulfinyl) -butoxy} -3, 4-dihydrocarbostyryl, m.p. 106.5-1081 C;
    (2-methoxyphenylsulfinyl) butoxy-3,4-dihydrocarbostyryl, m.p. 162-1630С;
    (3-methoxyphenylsulfonyl) -butoxy-3, 4-dihydrocarbostyryl, m.p. 147-1480C;
    6-t4- (4-methoxyphenylsulfinyl) -butoxy-3, 4-dihydroxy arbostil, so pl. 132-1330СГ
    (3,4-dimethoxyphenylsulfinyl) -butoxy3-3,4-dihydrocarbostyryl, m.p. 145-147 C;
    b-T4- (4-bifvnilylsulfinyl) -butoxyJ-3, 4-dihydrOcar6ostiril, so pl. 192-192,500;
    6-G4- {2-naphthylsulfinyl) -butoxy-3, 4-dihydrocarboxyryl, m.p. 147.5-148.5 ° C:
    (2-pyridylsulfinyl) -pentoxy-3, 4-dihydrocarbostyril, so pl. 116
    6- (2-methylsulphinloxy) -3,4-dihydrocarbostyryl, m.p. 129131, 50С;
    b- (4-methylsulfinylbutoxy) -3,4-dihydrocarbostyryl, m.p. 128130, 50С;
    6- (4-cyclohexylsulfinyl-butoxy) -3,4-dihydrocarbostyryl, m.p. 153-155,500;
    6- (4-benzylsulfinyl-butoxy) -3, 4-dihydrocarbostyryl, m.p. 141.51420С;
    (2-furylmethylsulfinyl) -butoxy-3, 4-dihydrocarbostyryl, so pl. 135-13b ° C;
    6-t4- (2-pyridylsulfinyl) -butoxy-3, 4-dihydrocarboxyryl, m.p. 154 15BS;
    (2-benimidazolylsulfinyl) -butoxy 3, 4-dihydrocarboxyryl, m.p. 180-1820С;
    (2-benzthiazolylsulfinyl) -butoxy-3, 4-dihydrocarbostyl, so pl. 183-184 ° C;
    6- (2-phenylsulfinyl-ethoxy) -3,4-dihydrocarbostyryl, m.p. 171-172С
    b- (3-phenylsulfinyl-propoxy) -3, 4-dihydrocarbostyryl, m.p. 131.5133, 50С;
    1-methyl-6- (4-phenylsulfinyl-butoxy) -3,4-dihydrocarbostyryl, m.p. 8282, 50s;
    6- {6-phenylsulfinyl-hexoxy) -3,4-dihydrocarbostyryl, m.p. 119.5121, 50С;
    6- (2-hydroxy-3-phenylsulfinylpropoxy) -3,4-dihydrocarbostyryl, m.p. 1851870С;
    6 (2-naphthylsulfinyl) -ethoxy-3, 4-dihydrocarboxyryl, so pl. 186.5187, AIA;
    (4-biphenylyl-sulfinyl) -ethoxyT-3; 4-dihydrocarbostyryl, m.p. 195-19bOs;
     (4-Phenylsulfinyl-butoxy) -carostyryl, m.p. 155-157C;
    TT- (4-phenylsulfinyl) -carbostyryl, m.p. 193-1940C;
    8- (4-feiylsulfinyl-butoxy) -carbostil, so pl. 125.5-126,
    6- (5-phenylsulfinyl-pentoxy) -3, 4-dihydrocarbostyryl, m.p. 104109, AIA;
    5- (2-hydroxy-3-phenylsulfinyl-propoxy) -3,4-dihydrocarbostyryl, tlp. l 186188 ° С;
    (4-hydroxyphenylsulfinyl) -butoxy-3, 4-dihydrocarbostyryl, m.p. 206207, 8 ° C;
    6-f4- (4-acetaminophenylsulfinyl) -buty-3, 4-dihydrocarbostyryl, m.p. 202.0-203,
    b-f4- (2-pyridylsulfinyl) -butoxy-carboxyryl, m.p. 152-154 0;
    6-t4- (2,5-dichlorophenylsulfinyl) -butoxy} -3, 4-dihydrocarboxyryl, m.p. 185-186;
    (2,5-dichlorophenylsulfinyl) butoxy} -3, 4-dihydrocarbostyryl, m.p. 185-18;
    (4-hydroxy-3, 5-di-tert.butyl-phenylsulfinyl) butoxy-3,4-dihydrocarbostyryl, m.p. 170-171-O;
     (2-carboxy-phenylsulfinyl) -butoxy-3, 4-dihydrocarbostyryl, m.p. 194-19600;
     (4-pyridylsulfinyl) -butoxy} -3,4-dihydrocarbostyryl, m.p. 15400;
    6-1z- (3,4-dichlorophenylsulfinyl) -2-hydroxy-propoxy-3, 4-dihydrocarbostyryl, T .. 108-110 0;
    6- (3-benzylsulfinyl-propoxy) -3, 4-dihydrocarbostyryl, m.p. 144.5147, 0 ° 0;
    5- (3-tert.butylsulfinyl-2-hydroxy-propoxy) -3,4-dihydrocarbostyryl, m.p. 175-17700;
    4-methyl-6-1; 4- (2-pyridylsulfinyl) butoxy-carbostyryl, m.p. 167169 0;
    4-methyl-6-t4- (2-pyridylsulfinyl) -butoxy-carbostyryl, m.p. 18919000; . .
    4-methyl-b- 4- (4-biphenylylsulfinyl) -butoxy-carbostyryl, m.p. 16116200;
    6-L4- (4-chlorophenylsulfinyl) tbutok, si-carbostiril, mp-. 157-158®0;
    b- (4- (3,4-dichlorophenylsulfinyl) -butoxy-carbostyryl, mp 191196OO6- 4- (2,5-dichlorophenylsulfinyl) butoxyD-carbostyryl, mp 20020200;
    6- (4- (4-fluorophenylsulfinyl) -butoxyD-carbostyryl, mp 164-165 0;
    (4-hydroxy-3, 5-di-tert.butylphenylsulfinyl) -butoxy-carbostyryl m.p. 192-194 ° 0;
    6-.4- (4-biphenylylsulfinyl) -butoxy-carboxyryl, m.p. 196-197 0;
    (4-nitrophenylsulfinyl) -butoxy-carboxyryl, m.p. 183184 0;
    (2-quinolylsulfinyl) -butoxy-carboxyryl, m.p. 161-162 ° 0;
    5- (4-phenylsulfinyl-butoxy) -oxindol, so pl. 114-116 0;
    6-C2- (phenylsulfinylmethyl) -benzyloxy-3, 4-dihydrocarbostyryl, m.p. 133-13500;
    6-f4- (phenylsulfinyl) -benzyl-3-4, 4-dihydrocarboxyryl, m.p. 179181 0;
    6- (4-cyclohexylsulfinyl-butoxy) -carbostyryl, m.p. 169-170C;
    6- 4- (4-bromophenylsulfinyl) -buto1 Si -carbostyryl, m.p. 168-170 ° C;
    (3-methyl-4-bromo-phenylsulfinyl) -butoxy-carboxyryl, m.p. 1691720s;
    6-f4- (2,4,5-trichlorophenylsulfinyl-butoxy-carbostyryl, mp 206-208
    (3, 5-dibromo-4-aminophenylsulfinyl Ugbutoxy-3.4 dihydrocarbostyryl, mp 115-146 ° C;
    (3,5-dibrom-4-amino-phenylsulfine l) -butoxy 3-carbostyril, mp. 205-2070С;
     (4-bromo-3-methyl-phenylsulfinyl) -butoxy-3,4-dihydrocarbostyryl, m.p. 129-130 ° C;
    (2,5-dibromophenylsulphinyl) butoxy-3, 4-dihydrocarbostyryl, m.p. 182-1840C;
     (2,5-dibromo-phenylsulfinyl) -butoxy-carbostyryl, m.p. 187189 Oc;
    (3, 4-dichlorophenylsulfinyl) -propoxy D-3, 4-dihydrocarbostyryl, m.p. 170-1720С;
    (4-cyclohexylphenylsulfinyl) -butoxy 3 -3,4-dihydrocarbostyryl, m.p. 155-1570С;
    (4-cyclohexyl-phenylsulfonyl) -butoxy I -carbostyryl, m.p. 1881900С;
    (4-tert.butyl-phenylsulfinyl-butoxy-3,4-dihydrocarbostyryl, Black pl. 121-1230С;
    (4-tert.butyl-phenylsulfonyl) -butoxy-carboxyryl, m.p. 164, 1660C;
    (2-quinolylsulfinyl) -butoxy-3,4-dihydrocarbostyryl, m.p. 154157 C67L2- (M-methyl-M-cyclohexyl-carbamidomethylsulfinyl) -ethoxy-3,4-dihydrocarbostyryl, m.p. 143-146 ° С
    6- 2- (N-methyl-N-cycle ohexylcarbamidomethylsulfinyl) -ethoxy-carbostyryl, m.p. 128-1300С; .
    6-t5- (3 ,, 4-dichlorophenylsulfinyl) pentoxy-3, 4-dihydrocarboxyryl, m.p. 165-1660С;
    6-f 4- (2-methyl-4-tert.butyl-phenylsulfinyl) -butoxy-3, 4-dihydrocarbostyryl, Rf-value: 0.54 (silica gel luminescent plate; solvent: ethylene chloride / / methanol 95: 5); 5-nitro-6- (4-phenylsulfinylbutoxy) -carbostyryl, m.p. 192-1940C;
    5-acetamino-6- (4-phenylsulfinylbutoxy) -carbostyryl, m.p. 213-217
    5-bromo-6- (4-phenylsulfonyl by-6) -caIboctipyl, m.p. 190-191 ° C;
    4-methyl-6- 4- (2-pyridylsulfinyl) -6-toxy-carbostil, so pl. 166168 ° C;
    6- (4-tert.butylsulfinyl-butoxy) -3, 4-dihydrocarbostyryl, m.p. 126128t C;
    (1,2,4-triazole-3-yl-sulfinyl) -butoxy-carboxyryl, Rf-value: O, 12 (silica gel luminescent plate; solvent: ethylene chloride / methanol 95: 5);
     (1,2, 4-triazole-3-yl-sulfinyl) -butoxy} -3,4-dihydrocarbostyryl, Rf-value: 0.18 (silica gel luminescent plate; solution5) itel: ethylene chloride / methanol 95: 5);
    6- 4- (2-pyridylsulfonyl) -butoxy 3- 3,4-dihydrocarbostyryl, m.p. 123.8-125 ° C;
     (3,4-dimethoxyphenylsulfonyl) -butoxy-3,4-dihydrocarbostyryl, m.p. 158-160 ° C;
    (2-pyridylsulfonyl) -pentoxy} - 3,4-dihydrocarbostyryl, so pl. 113.5-115, 7- (4-phenylsulfonyl-butoxy) -carbostyryl, m.p. 199-201С;
    6- (2-phenylsulfonyl-ethoxy) -3,4-dihydrocarbostyryl, m.p. 18518bSS;
    1-methyl-6- (4-phenylsulfonyl-butoxy) -3,4-dihydrocarbostyryl, m.p. 108-1090С;
    6- (2-hydroxy-3-phenylsulfonyl-propoxy) -3,4-dihydrocarbostyryl, m.p. 1701720s;
    8- (4-phenylsulfonyl-butoxy) -3,4-dihydrocarbostyril, mp. 114.5115 ° C; .
    (2-Benzthiazolyl-sulfonyl) -butoxy-D3, 4-dihydrocarboxyryl, m.p. 146-1490С;
    6-L4- (2-naphthylsulfonyl) -butoxy-3,4-dihydrocarboxyryl, m.p .; 173175 ° C;
    (4-biphenylylsulfonyl) -butoxy-3; 4-dihydrocarbostyryl, m.p. 23234, 50С;
    5- (4-phenylsulfonyl-butoxy) -carbostil, so pl. 182-183C;
    6- (4-phenylsulfonyl-butoxy) -carbostil, so pl. 212-213 ° C;
    5- (4-phenylsulfonyl-butoxy) -carbostil, so pl. 182-1830С;
    5- (2-hydroxy-3-phenylsulfonyl-propoxy) -3,4-dihydrocarbostyryl, m.p. 168-1700С;
    (4-hydroxyphenylsulfonyl) -butoxy-3,4-dihydrocarbostyryl, m.p. 219-219.5 ° C;
    (4-acetaminophenylsulfonyl) -butoxy3-3, 4-dihydrocarbostyryl, m.p. 143.5-147,
    8- (4-phenylsulfonyl-butoxy) -carbostil, so pl. 146-i47 ° C;
    (2,5-dichlorophenylsulfonyl) -butoxy1-3, 4-dihydrocarbostyryl, m.p. 174.5-175.50С;
    (3,4-Dichlorophenylsulfonyl) t-butoxy-3,4-dihydrocarbostyryl, m.p. 172-1730С ;;
    (4-hydroxy-3,5-di-tert.butyl-phenylsulfonyl) -butoxy-3,4-dihydrocarbostyryl, m.p. 165-167C;
     {4-pyridylsulfonyl) butoxy-3,4-dihydrocarbostyryl, m.p. 179-183 BC;
    5- (3-t.butylsulfonyl-2-oxy-propoxy) -3,4-dihydrocarbostyryl, so pl. 210-2120C;
    (2-pyri or sulphonyl) -butoxy-carbostyryl, m.p. IVS-ISO C;
    4-methyl-6-14- (2-pyridylsulfonyl) -butoxy 3-carbostyryl, m.p. 1951970С; .
    4-methyl-6-i4- (2-quinolylsulfonyl) -butoxy-carbostyryl, m.p. 199203 ° C;
    6-f4- (4-chlorophenylsulfonyl) -butoxy-carboxyryl, m.p. 197-199 C;
    (3,4-Dichlorphenylsulfonyl) -butoxyT-carbostyryl, m.p. 1881900С;
    (2,5-dichlorophenylsulfonyl) -butoxy-carbostyryl, m.p. 203205 ° C6- 4- (4-fluorophenylsulfonyl) -butoxy-carbostyryl, m.p. 209-211 C;
    6- 4- {4-hydroxy-3,5-di-tert.butylphenylsulfonyl) -butoxy-carbostyryl m.p. 242-244 5С;
    6-t4- (4-biphenyl-sulfonyl) -butoxy-carboxyryl, m.p. 213-215 G;
    6- 4- (4-nitrophenylsulfonyl) -butoxy-carbostyryl, m.p. 230-232 ° C;
    (2-quinolylsulfonyl) -butoxy-carbostil, so pl. 197-198 ° C;
    (3-methyl-4-bromo-phenylsulfonyl) -butoxy-carboxyryl, m.p. 163167 S.
    b- 4- (3,5-dibromo-4-amino-phenylsul fonyl) -6ytoKCH -3,4-dihydrocarboster, pl. 157-159 С;
    (3,5-dibromo-4-amino-phenylsulfonyl) -butoxy} -carbostyryl, m.p. 238-241 ° C;
    6-C4- (4-cyclohexyl-phenylsulfonyl) -butoxy-3,4-dihydrocarbostyryl, m.p. 172-1740C;
    6- 4- {4-cyclohexyl-phenylsulfonyl) -butoxy-carbostyryl, m.p. 18518БС7С; ,
    6-G4- (4-tert.butyl-phenylsulfonyl-butoxy-3, 4-dihydrocarbostcryl, mp 198-200C;
    (4-tert.butyl-phenylsulfo-NILE) -butoxy-carboxyryl, m.p. 20320500;
    (4-tert.butyl-phenylsulfonyl K-butoxyT-carboxyryl, m.p.
    205
     (2-quinolylsulfonyl) -butoxy-3,4-aihydrocarbostyril, Rfc3Ha4e: 1p, 50 (silica gel luminescent thyginum; solvent: benzene / / ethanol / concentrated ammonia 75: 25: 2);
    6- 2- (N-methyl-M-cyclohexyl-carbamidomethylsulfonyl) -toxy-3,4-dihydrocarbostyryl, m.p. 110-111 ° C;
    (N-methyl-M-cyclohexyl-carbamidomethylsulfonyl) -ethoxy-carbostil, Rf value: 0.39 (silica gel luminescent plate; solvent: ethylene chloride / methanol 95: 5);
    (3,4-dichlorophenylsulfonyl) -propoxy-3,4-dichlorocarbostyril, m.p. 187-188 ° C;
     (3,4-dichlorophenylsulfonyl) -pentoxy-3, 4-dihydrocarbostyryl, mp. 17b-178 C;
    6- 4- (1,2,4-triazole-3-yl-sulfonyl) -butoxy-3,4-dihydrocarbostyryl, m.p. 217-2240C;
    6- (5-feNilsulfonyl-pentoxy) -3, 4-dihydrocarbostyryl, m.p. 136.5137, 8CC.
    权利要求:
    Claims (1)
    [1]
    1. A method for producing carbostyril or oxindole derivatives of general formula (I)
    v
    where W denotes a vinylene group, unsubstituted or substituted by a methyl group, a methylene or ethylene group;
    m is O, 1 or 2;
    D is a straight or branched alkylene group with 2 to 6 carbon atoms, a straight or branched hydroxy, an alkylene group with 3 to 6 carbon atoms, or a xylylene group;
    R is a hydrogen atom or an alkyl group with 1 to 3 carbon atoms;
    2-cycloalkyl group with the number of carbon atoms from 3 to 6, aryl group with the number of atoms of 5 glerod from 6 to 10, aralkyl group with the number of carbon atoms from 7 to 11, nitrogen atom and / or oxygen atom or sulfur atom, or containing two a nitrogen atom is a heteroaryl group with 4 to 9 carbon atoms or a heteroaralkyl group with 5 to 10 carbon atoms, and the above aromatic nuclei can be monosubstituted with an alkyl group with 1 to 4 carbon atoms, hydroxy, methoxyamino, acetylamino -, nitro, carbosyl-, cyclohex a flax, phenyl group or halogen atom and the aforementioned monosubstituted phenyl group can be mono- or disubstituted with alkyl groups with 1 to 4 carbon atoms and / or halogen atoms (and the substituents of the phenyl core can be the same or different), 1,2 , 4-triazolyl-, pyridi-oxide, triphenylmethyl-, 4,5-bis- (p-chlorophenyl) -oxazol-2-yl, N-methyl-cyclohexylamino-carbonylmethyl or amino-iminomethyl group, or also an alkyl group with the number carbon atoms from 1 to 6, if m is the number 1 or D is a linear or branched oxyalkylene group with 3 to 6 carbon atoms, and a xylylene group; may be identical or different and denote hydrogen atoms or halogen, hypoxy groups with 1 to 4 carbon atoms, amino, acetylamino or nitro groups, characterized in that the hydroxy compound of the general formula (II) f, ri .. and W have the above where R,, R, values, or its salts with inorganic or tertiary organic bases are reacted with a compound of the general formula (III) where O, Rft and m have the aforementioned; Z is a halogen or a radical of a sulfonic acid ester. 2; Method POP.1, characterized in that the reaction is a wire in a solvent at a temperature of 2025 ° C. 3. The method according to Claims 1 and 2.0 tons is based on the fact that the reaction is carried out in the presence of an alkaline base. Priority by featured. 17.02,78. With W, a vinylene group, unsubstituted or substituted by methyl, an ethyl group; m is O, 1 or 2; O is an unbranched or branched alkylene group with 2 to 6 carbon atoms, an unbranched or branched oxyalkylene group with 3 to 6 carbon atoms; R is a hydrogen atom, an alkyl group with 1 to 3 carbon atoms; Rfj is a cycloalkyl group with the number of carbon atoms from 3 to 6, an aryl group with the number of atoms, carbon from 6 to 10, an aralkyl group with 7-11C, a nitrogen atom and / or an oxygen or sulfur atom, or two nitrogen atoms, a heteroaryl group with 4-9 C or a heteroaralkyl group with 5-10 C, and the aromatic cores can be mono-substituted by methyl, hydroxyl, acetylamino, or phenyl group or halogen atom, the monosubstituted phenyl group can be additionally mono- or disubstituted with methyl, and / or atom halogen, and the substituents phenyl cores can be the same or different, pyridyl oxide, triphenylmethyl, 4,5-bis- (para-chlorophenyl) -oxazol-2-yl, amino-aminomethyl group or also an alkyl group from 1-6 C, if m is the number 1 or D - an unbranched or branched oxyalkylene group with 3-6 C; Re, and RA is a hydrogen atom. 09 .. 12.78. When W - methylene group; O - xylidene group; R, - 1,2, 4-triazolyl, N-methyl-cyclohexylaminocarbonylmethyl; Rn and R, are the same or different halogen atoms, alkyl with 1-4C, amino, acetylamino, nitro. Sources of information taken into account in the examination 1. Weigand-Hilgetag. Experimental methods in organic chemistry. M., Himi, 1968, p. 333 and 341.
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    同族专利:
    公开号 | 公开日
    YU36679A|1983-02-28|
    RO82013B|1983-05-30|
    IL56677A|1982-09-30|
    FI69064B|1985-08-30|
    AU523147B2|1982-07-15|
    JPS54132581A|1979-10-15|
    NO152839B|1985-08-19|
    YU41146B|1986-12-31|
    GR66565B|1981-03-27|
    HU177522B|1981-10-28|
    SU852170A3|1981-07-30|
    ES484634A1|1980-05-16|
    MY113785A|1985-12-31|
    RO76683A|1981-05-30|
    PL213471A1|1980-02-25|
    AT374183B|1984-03-26|
    AU4432979A|1979-08-23|
    CA1116600A|1982-01-19|
    ATA93379A|1983-08-15|
    RO82013A|1983-06-01|
    EP0003771A1|1979-09-05|
    FI790507A|1979-08-18|
    PH16698A|1984-01-16|
    DK157017C|1990-03-26|
    JPS6331464B2|1988-06-23|
    DK157017B|1989-10-30|
    PT69244A|1979-03-01|
    NO152839C|1985-11-27|
    EP0003771B1|1982-10-20|
    IE790313L|1979-08-17|
    PL117771B1|1981-08-31|
    DK69679A|1979-08-18|
    DD141829A5|1980-05-21|
    CS227005B2|1984-04-16|
    NO790521L|1979-08-20|
    IE48179B1|1984-10-17|
    PL119423B1|1981-12-31|
    ES477517A1|1980-01-16|
    PL119177B1|1981-12-31|
    DE2963868D1|1982-11-25|
    IL56677D0|1979-05-31|
    FI69064C|1985-12-10|
    NZ189685A|1984-07-06|
    ES484633A1|1980-05-16|
    HK50485A|1985-07-12|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE19782806721|DE2806721A1|1978-02-17|1978-02-17|Substd. alkoxy-carbostyril derivs. - useful as antithrombotic and cardioactive agents, used for treating thromboembolic disorders and arteriosclerosis |
    DE19782853314|DE2853314A1|1978-12-09|1978-12-09|Substd. alkoxy carbostyril, di:hydro-carbostyril and oxindole derivs. - with positive inotropic and antithrombotic activity|
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