Malononitrile compounds

专利摘要:

公开号:AU2006328521A1
申请号:U2006328521
申请日:2006-12-13
公开日:2007-06-28
发明作者:Henricus Maria Martinus Bastiaans；Deborah L. Culbertson；Michael Hofmann；Takeo Hokama；Jurgen Langewald；Hassan Oloumi-Sadeghi；Christopher Palmer；Matthias Pohlman；Michael Rack
申请人:BASF SE；
IPC主号:A01N37-34

专利说明:
WO 2007/071609 PCT/EP2006/069686 1 Malononitrile compounds The present invention relates to compounds of formula I A 0 X R (I) NC CN 5 wherein X is oxygen or S(=O)n; n is 0,1 or 2; 10
R
1 is C1-C6-alkyl, Ci- C 6 -haloalkyl, C2- 06-alkenyl, C2- 0 6 -haloalkenyl, C2- 06-alkynyl, C3- 0 6 -haloalkynyl, C3-06-cycloalkyl, C3-06-halocycloalkyl, C3-06-cycloalkenyl,
C
3 -0 6 -halocycloalkenyl, 15 phenyl or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which heteroaromatic ring is bonded to the X atom via a carbon atom of the ring, and which phenyl or which heteraromatic ring may be bonded via a C1-Co10-alkyl group thus forming an aryl-C1-C0io-alkyl or hetaryl-C 1 -C0o-alkyl moiety, 20 wherein phenyl or the heteroaromatic ring may be fused to a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, 25 wherein the hydrogen atoms in the above groups R 1 may be partially or in total be replaced by any combination of groups R 5 . A is -NRb 2 , -C(=G)GRb, -C(=G)NRb 2 , -C(=NORb)Rb, C(=G)[N=SRb 2 ], -C(=G)NRb 30 NRb 2 , wherein two groups Rb together may form a C 2 -0 6 -alkandiyl, C2-06 alkenediyl or C1-C3-alkyl-G-Cl-C3-alkyl bridge which may be substituted by 1 to 5 groups R 2 , phenyl or a 3- to 7-membered saturated or partially unsaturated heterocyclic ring 35 which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteroaromatic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl, the heterocyclic ring, or the heteroaromatic ring may be fused to 40 a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms WO 2007/071609 PCT/EP2006/069686 2 selected from oxygen, nitrogen and sulfur, wherein phenyl or the 5- to 6-membered heteroaromatic ring or the respective fused ring systems may be unsubstituted or substituted by any combination of 1 5 to 6 groups R 2 . B is a saturated or partially unsaturated hydrocarbon chain with one to 3 carbon chain atoms, wherein the hydrogen atoms of this chain may all or in part be replaced with any combination of groups selected from R 3 ; 10 D is a saturated or partially unsaturated hydrocarbon chain with one to 5 carbon chain atoms or C3-06-cycloalkyl, wherein the hydrogen atoms of this chain or of this cycloalkyl may all or in part be replaced with any combination of groups selected from R 4 15
R
2 is halogen, cyano, nitro, hydroxy, mercapto, amino, C1-C6-alkyl, C2-06 alkenyl, C2-06-alkynyl, C3-06-cycloalkyl, C3-06-cycloalkenyl, C1-C 6 -haloalkyl,
C
2 -0 6 -haloalkenyl, C 2 -0 6 -haloalkynyl, C3-06-halocycloalkyl, C3-06 halocycloalkenyl, C0 1
-C
6 -alkoxy, C2-06-alkenyloxy, C3-06-alkynyloxy, C1-C6 20 haloalkoxy, C 2 -0 6 -haloalkenyloxy, C 3 -0 6 -haloalkynyloxy, C3-06 cycloalkyloxy, C3-06-cycloalkenyloxy, C3-06-halocycloalkyloxy, C3-06 halocycloalkenyloxy, C0 1
-C
6 -alkylthio, C0 1
-C
6 -haloalkylthio, C3-06 cycloalkylthio, C 3 -0 6 -halocycloalkylthio, C1-C6-alkylsulfinyl, C2-06 alkenylsulfinyl, C 3 -0 6 -alkynylsulfinyl, C0 1
-C
6 -haloalkylsulfinyl, C2-06 25 haloalkenylsulfinyl, C 3 -0 6 -haloalkynylsulfinyl, C01-C6-alkylsulfonyl, C2-06 alkenylsulfonyl, C3-06-alkynylsulfonyl, C0 1
-C
6 -haloalkylsulfonyl, C2-06 haloalkenylsulfonyl, C 3 -0 6 -haloalkynylsulfonyl, C01-C6-alkylamino, C2-06 alkenylamino, C2-06-alkynylamino, di(C 1
-C
6 -alkyl)amino, di(C 2 -0 6 alkenyl)amino, di(C 2 -0 6 -alkynyl)amino, tri(Ci-C0io)alkylsilyl, or 30 phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which 35 phenyl and which heteroaromatic ring may be bonded via an oxygen or a sulfur atom or a C01-C4-alkyl-group, wherein the above groups R 2 are unsubstituted, or the hydrogen atoms in these groups may all or in part be replaced with any combination of groups 40 selected from Ra, or WO 2007/071609 PCT/EP2006/069686 3
R
2 is -C(=G)Rb, -C(=G)ORb, -C(=G)NRb 2 , -C(=G)[N=SRb 2 ], -C(=NORb)Rb, -C(=NORb)NRb 2 , -C(=NNRb 2 )Rb, -OC(=G)-OC(=G)ORb, N=SRb 2 , -NRbC(=G)Rb, -N[C(=G)Rb 2 , -NRbC(=G)ORb, -C(=G)NRb-NRb 2 , -C(=G)NRb NRb [C(=G)Rb], -NRb-C(=G)NRb 2 , -NRb-NRbC(=G)Rb, -NRb-N[C(=G)Rb] 2 , 5 N[(C=G)Rb]-NRb 2 , -NRb-NRb[(C=G)GRb], -NRb[(C=G)NRb 2 , -NRb[C
=
NRb]Rb, -NRb(C
=
NRb)NRb 2 , -O-NRb 2 , -O-NRb(C=G)Rb, -SO 2 NRb 2 , -NRbSO 2 Rb, S(=O)Rb, -S(=0) 2 Rb, -SO 2 ORb, or -OSO 2 Rb;
R
3 is halogen, cyano, amino, C1-Cio-alkyl, C 1 -C0 1 o-haloalkyl, C2-Clo-alkenyl, C2 10 Co-haloalkenyl, C2-Clo-alkynyl, C 3 -C0 1 o-haloalkynyl, C3-06-cycloalkyl, C3-06 halocycloalkyl, C3-06-cycloalkenyl, C 3 -0 6 -halocycloalkenyl, C0 1
-C
6 -alkoxy, C2-06-alkenyloxy, C3-06-alkynyloxy, Ci-C 6 -haloalkoxy, C2-06 haloalkenyloxy, C 3 -0 6 -haloalkynyloxy, or 15 phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which phenyl or which heterocyclic or heteroaromatic ring may be bonded via an 20 oxygen or a sulfur atom, or 2 groups R 3 together with the carbon atom of the hydrocarbon chain may form a 3- to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and 25 nitrogen, wherein the above groups R 3 are unsubstituted, or the hydrogen atoms in these groups may all or in part be replaced with any combination of groups selected from Ra, or 30
R
4 is halogen, cyano, amino, Ci-Cio-alkyl, C 1 -C0 1 o-haloalkyl, C2-Clo-alkenyl,
C
2 -C0 1 o-haloalkenyl, C2-Clo-alkynyl, C 3 -C0 1 o-haloalkynyl, C3-06-cycloalkyl, C3 C6-halocycloalkyl, C3-06-cycloalkenyl, C3-06-halocycloalkenyl, C0 1
-C
6 -alkoxy, C2-06-alkenyloxy, C3-06-alkynyloxy, Cl-C 6 -haloalkoxy, C2-06 35 haloalkenyloxy, C 3 -0 6 -haloalkynyloxy, C0 1
-C
6 -alkoxycarbonyl, C1-C6 alkenyloxycarbonyl, C1-C6-alkylamino, di(C-C 6 -alkyl)amino, tri(Ci-Cio)alkylsilyl, or phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic 40 ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which WO 2007/071609 PCT/EP2006/069686 4 phenyl and which heterocyclic or heteroaromatic ring may be bonded via an oxygen or a sulfur atom, wherein the above groups R 4 are unsubstituted, or the hydrogen atoms in 5 these groups may all or in part be replaced with any combination of groups selected from Ra, or the moiety R 4
-D-X-R
1 together may form a saturated or unsaturated ring of formula a 10 D-S which may have 5 to 7 ring members and besides sulfur 1 to 2 further heteroatoms selected from oxygen, sulfur and nitrogen and which ring may be substituted with 1 to 5 groups selected from Ra, or 15 the moiety R 4
-D-X-R
1 together may form a group of formula p wherein x is 1 to 5
(CH
2 )xCH-S containing a saturated or unsaturated ring which may have 5 to 7 ring members and besides sulfur 1 to 2 further heteroatoms selected from 20 oxygen, sulfur and nitrogen and which ring may be substituted with 1 to 5 groups selected from Ra;
R
5 is a group R 3 ; 25 G is oxygen or sulfur; Ra is each independently halogen, cyano, nitro, C01-C6-alkyl, C1-C6 haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C2-06 haloalkynyl, C3-06-cycloalkyl, C3-08-halocycloalkyl, C3-06 30 cycloalkenyl, C3-08-halocycloalkenyl, phenoxy, OR i , SR i , S(=O)R i,
S(=O)
2
R
i , NRiR, -S(=O) 2 NRiR, C(=O)R i , C(=O)OR i , C(=O)NRiRJ, C(=NORi)R, -NRiC(=G)R, -N[C(=G)Ri]2, -NRiC(=G)OR, -C(=G)NR i NRJ 2 , -NRiSO 2 RJ, SiRiyRJ 3 -y (y is 0 to 3), or 35 phenyl or a 5- to 6-membered heteraromatic ring which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, wherein the carbon atoms in phenyl or in the heteroaromatic ring may be substituted with 1 to 5 halogens; WO 2007/071609 PCT/EP2006/069686 5
R
i , Ri are each independently hydrogen, C1-C6-alkyl, C1-C6 haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl,
C
2 -0 6 -haloalkynyl, C3-06-cycloalkyl, C3-08-halocycloalkyl, C3-06-cycloalkenyl, or C3-06-halocycloalkenyl; 5 Rb is each independently C1-C6-alkyl, C0 1
-C
6 -haloalkyl, C2-06-alkenyl, C2
C
6 -haloalkenyl, C2-06-alkynyl, C 2 -0 6 -haloalkynyl, C3-06-cycloalkyl, C3 C8-halocycloalkyl, C3-06-cycloalkenyl, C 3 -0 8 -halocycloalkenyl, C3-06 cycloalkyl-C1-C4-alkyl, or C3-08-halocycloalkyl-C1-C4-alkyl, or 10 phenyl or a 5- to 6-membered heteraromatic ring which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which heteroaromatic ring may be bound via a C01-C4-alkyl-moiety, and wherein the carbon atoms in phenyl or in the heteroaromatic ring may be substituted with 1 to 3 groups Ra; 15 or the enantiomers or diastereomers or salts or N-oxides or polymorphs thereof. In addition, the present invention relates to processes and intermediates for preparing the compounds I, pesticidal compositions comprising compounds I, methods for the 20 control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat or breeding grounds with a pesticidally effective amount of compounds or compositions of formula I. Moreover, the present invention also relates to a method of protecting growing plants 25 from attack or infestation by insects or acarids by applying to the plants, or to the soil or water in which they are growing, with a pesticidally effective amount of compositions or compounds of formula I. This invention also provides a method for treating, controlling, preventing or protecting 30 animals against infestation or infection by parasites which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective amount of compositions or compounds of formula I. In spite of the commercial insecticides, acaricides and nematicides available today, 35 damage to crops, both growing and harvested, caused by insects and nematodes still occurs. Therefore, there is continuing need to develop new and more effective insecticidal, acaricidal and nematicidal agents. It was therefore an object of the present invention to provide new pesticidal 40 compositions, new compounds and new methods for the control of insects, acarids or nematodes and of protecting growing plants from attack or infestation by insects, WO 2007/071609 PCT/EP2006/069686 6 arachnids or nematodes. We have found that these objects are achieved by the compositions and the compounds of formula I. Furthermore, we have found processes and intermediates for 5 preparing the compounds of formula I. Compounds exhibiting a dicyanoalkane moiety have been described in a number of patent applications: JP 2002 284608, WO 02/089579, WO 02/090320, WO 02/090321, WO 04/006677, WO 04/020399, JP 2004 99593, JP 2004 99597, WO 05/068432, 10 WO 05/064823, EP 1555259, and WO 05/063694. Compounds of formula I bearing a chalkogenalkane side chain have not been described in the prior art. 15 Compounds of formula I are obtainable, for example, by a process wherein compound (11) is reacted with compound (111) to give compounds (I): AB H B Ds -R A H 1A B gX NC CN base NC CN (i) (1) wherein A, B, D, X and R 1 are as defined above for compounds of formula I and Z 1 represents a suitable leaving group such as a halogen atom, methanesulfonate, 20 trifluoromethanesulfonate or toluenesulfonate. The reaction is generally carried out in the presence of a base in a solvent. The solvent to be used in the reaction includes, for example, acid amides such as 25 N,N-dimethylformamide, NMP and the like, ethers such as diethyl ether, tetrahydrofuran and the like, sulfoxides and sulfones such as dimethylsulfoxide, sulfolane and the like, halogenated hydrocarbons such as 1,2 -dichloroethane, chlorobenzene and the like, aromatic hydrocarbons such as toluene, xylene and the like, and mixtures thereof. 30 The base to be used in the reaction includes, for example, inorganic bases such as sodium hydride, sodium carbonate, potassium carbonate and the like, alkali metal alkoxides such as potassium t-butoxide and the like, alkali metal amides such as lithium diisopropylamide and the like, and organic bases such as 35 dimethylaminopyridine, 1,4-diazabicyclo[2.2.2]octane, 1,8-diazabicyclo [5.4.0]-7 undecene and the like. The amount of the base that can be used in the reaction is usually 1 to 10 moles WO 2007/071609 PCT/EP2006/069686 7 relative to 1 mole of compound (11). In addition, additives such as crown ethers may be added to accelerate the reaction. The amount of compound (111) to be used in the reaction is usually 1 to 10 moles, 5 preferably 1 to 2 moles relative to 1 mole of compound (11). The reaction temperature is usually in the range of - 78' C to 150' C, preferably in the range of -20'C to 80'C and the reaction time is usually in the range of 1 to 24 hours. 10 The compound (11) can be produced, for example, according to the route represented by the following scheme: CN SCN A.B CN - A'B X H A O step 1 CN step 2 NC CN (IV) (V) (ll) wherein the variables are as defined above for formula I. 15 Step 1: The compound (V) can be produced by reacting compound (IV) with malononitrile (CN(CH 2 )CN; see e.g. Organic Process Research & Development 2005, 9, 133-136). The reaction is generally carried out in the presence of base in a solvent. The solvent to be used in the reaction includes, for example, acid amides such as N,N dimethylformamide and the like, ethers such as diethyl ether, tetrahydrofuran and the 20 like, halogenated hydrocarbons such as chloroform, 1,2-dichloroethane, chlorobenzene and the like, aromatic hydrocarbons such as toluene, xylene and the like, alcohols such as methanol, ethanol, isopropyl alcohol and the like, and mixtures thereof. The base to be used in the reaction includes, for example, tetrabutylammonium 25 hydroxide. The amount of the base that can be used in the reaction is usually 0.01 to 0.5 moles relative to 1 mole of compound (IV). The amount of malononitrile to be used in the reaction is usually 1 to 10 moles relative to 1 mole of compound (IV). The reaction temperature is usually in the range of - 20'C 30 to 200'C, and the reaction time is usually in the range of 1 to 24 hours. The reaction may be carried out with removing the water formed by the reaction from the reaction system, if necessary. 35 After completion of the reaction, the compound of formula (V) can be isolated by employing conventional methods such as adding the reaction mixture to water, extracting with an organic solvent, concentrating the extract and the like. The isolated compound (V) can be purified by a technique such as chromatography, recrystallization WO 2007/071609 PCT/EP2006/069686 8 and the like, if necessary. Step 2: (a) When B is substituted by one or more groups R 3 , then compound (11) can be produced by reacting compound (V) with an organometallic compound R 3 -Q. 5 The reaction is generally carried out in a solvent, and if necessary, in the presence of a copper salt. The solvent to be used in the reaction includes, for example, ethers such as diethyl 10 ether, tetrahydrofuran and the like, aromatic hydrocarbons such as toluene, xylene and the like, and mixtures thereof. The organometallic compound R 3 -Q to be used in the reaction includes, for example, organomagnesium compounds such as methylmagnesium iodide, ethylmagnesium 15 bromide, isopropylmagnesium bromide, vinylmagnesium bromide, ethynylmagnesium bromide, dimethylmagnesium and the like, organolithium compounds such as methyllithium and the like, organozinc compounds such as diethylzinc and the like, and organocopper compounds such as trifluoromethylcopper and the like. The amount of the organometallic compound that can be used in the reaction is usually 1 to 10 moles 20 relative to 1 mole of compound (V). The copper salt to be used in the reaction includes, for example, cuprous (I) iodide, cuprous (I) bromide and the like. The amount of the copper salt to be used in the reaction is usually not more than 1 mole relative to 1 mole of compound (V). 25 The reaction temperature is usually in the range of - 20'C to 100'C, and the reaction time is usually in the range of 1 to 24 hours. After completion of the reaction, the compound of formula (11) can be isolated by employing conventional methods such as adding the reaction mixture to water, 30 extracting with an organic solvent, concentrating the extract and the like. The isolated compound (11) can be purified by a technique such as chromatography, recrystallization and the like, if necessary. Step 2: (b) When B is unsubstituted, the compound (11) can be produced by reacting 35 compound (V) with a reducing agent such as formic acid in the presence of a base as described e.g. in J. Org. Chem. 2005, 70, p. 3591, or with Mg in the presence of ZnCI2 as described in Synlett. 2005, p. 523-525 or any other suitable reducing agent. After completion of the reaction, the compound of formula (11) can be isolated by 40 employing conventional methods such as adding the reaction mixture to water, extracting with an organic solvent, concentrating the extract and the like. The isolated compound (11) can be purified by a technique such as chromatography, recrystallization WO 2007/071609 PCT/EP2006/069686 9 and the like, if necessary. In general, compounds (111), if not commercially available, can be synthesized from alcohols (IV) via conversion to the respective tosylates, mesylates or halides in analogy 5 to methods mentioned in J. March, Advanced Organic Chemistry, 4th edition, Wiley. I RI HOD xR (IV) 1 Dx (111)R Compounds (IV) can be obtained via alkylation of compounds (V) where Z 2 is a suitable leaving group such as a halogen atom, methanesulfonate, trifluoromethanesulfonate or toluenesulfonate, with compounds (VI) which are suitably 10 substituted thiols or alcohols or salts thereof in analogy to procedures described in Can. J. Chem. 1979, 57, p. 1958-1966 and J. Am. Chem. Soc. 1924, 46, p. 1503. HOD Z 2 (V) + R 1X'H (VI) HOD" X'R (IV) Specifically, compounds (111) wherein R 1 is CF 3 , X is sulfur and Z 1 is halogen can also 15 be obtained by reaction of CF 3 -SH with acryl halides CH 2
CH-Z
1 as described in J. Am. Chem. Soc. 1962, 84, p. 3148-3153. Compounds (IV) wherein R 1 is CF 3 and X is sulfur can be prepared for example by alkylation of mercapto alcohols HO-D-SH under irradiation conditions as described in 20 WO 01/36410. Compounds (111) wherein R 1 is CF 3 and X is oxygen can be obtained as described in J. Fluorine Chemistry 1982, 21, p. 133-143 or J. Org. Chem. 2001, 66, p. 1061-1063. 25 Compounds of formula I wherein D is a substituted or unsubstituted C 1 -unit, the synthesis can be carried out by an addition reaction of a dinitrile (II) to a suitable carbonyl compound of formula D=O in analogy to procedures described in US 4581178, J. Fluorine Chemistry 1982, 20, p. 397-418 and European Journal of Organic Chemistry 2004, (19), p. 3992-4002 and subsequent conversion of the obtained 30 alcohols to compounds (I) via conversion of the OH-group of (VII) into a leaving group such as a mesylate-group and subsequent reaction with an alcohol or thiol Ri-XH, X = O or S, in analogy to a procedure in Eur. J. of Org. Chem. 2004, (19), 3992-4002. ,B H D=0 AB D AB D xR A A OH A -> -X NN OHN (ll) (VII) () Compounds (I) of the invention wherein X is S and n is 1 can be obtained from the 35 corresponding compounds (I) wherein X is S and n is 0 via oxidation with oxidizing agents such as 30 % H 2 0 2 , NalO 4 or tBuOCl according to procedures described in J. March, Advanced Organic Chemistry, 4th edition, Wiley, chapter 19, pp. 1201 and literature cited therein. Further oxidation with, for example, KMnO 4 , KHSO 5 or another WO 2007/071609 PCT/EP2006/069686 10 equivalent of 30 % H 2 0 2 as described in the literature cited above, yields compounds (I) wherein X is S and n is 2. If individual compounds I are not obtainable by the routes described above, they can 5 be prepared by derivatization of other compounds I or by customary modifications of the synthesis routes described. After completion of the reaction, the compounds can be isolated by employing conventional methods such as adding the reaction mixture to water, extracting with an 10 organic solvent, concentrating the extract and the like. The isolated compounds can be purified by a technique such as chromatography, recrystallization and the like, if necessary. The preparation of the compounds of formula I may lead to them being obtained as 15 isomer mixtures. If desired, these can be resolved by the methods customary for this purpose, such as crystallization or chromatography, also on optically active adsorbate, to give the pure isomers. The compounds of formula I may be present in different crystalline modifications (polymorphs) which may have different biological activity. These are also subject of this invention. 20 Agronomically acceptable salts of the compounds I can be formed in a customary manner, e.g. by reaction with an acid of the anion in question. In this specification and in the claims, reference will be made to a number of terms that 25 shall be defined to have the following meanings: "Salt" as used herein includes adducts of compounds I with maleic acid, dimaleic acid, fumaric acid, difumaric acid, methane sulfenic acid, methane sulfonic acid, and succinic acid. Moreover, included as "salts" are those that can form with, for example, amines, 30 metals, alkaline earth metal bases or quaternary ammonium bases, including zwitterions. Suitable metal and alkaline earth metal hydroxides as salt formers include the salts of barium, aluminum, nickel, copper, manganese, cobalt zinc, iron, silver, lithium, sodium, potassium, magnesium or calcium. Additional salt formers include chloride, sulfate, acetate, carbonate, hydride, and hydroxide. Desirable salts include 35 adducts of compounds I with maleic acid, dimaleic acid, fumaric acid, difumaric acid, and methane sulfonic acid. "Halogen" will be taken to mean fluoro, chloro, bromo and iodo. 40 The term "alkyl" as used herein refers to a branched or unbranched saturated hydrocarbon group having 1 to 6 carbon atoms, such as C1-C6-alkyl, for example methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1- WO 2007/071609 PCT/EP2006/069686 11 dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2 methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3 dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2 5 ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1 -methylpropyl and 1 ethyl-2-methylpropyl. The term "haloalkyl" as used herein refers to a straight-chain or branched alkyl group having 1 to 6 carbon atoms (as mentioned above), where some or all of the hydrogen 10 atoms in these groups may be replaced by halogen atoms as mentioned above, for example C 1
-C
2 -haloalkyl, such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2 fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2 15 difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl; Similarly, "alkoxy" and "alkylthio" refer to straight-chain or branched alkyl groups having 1 to 6 carbon atoms (as mentioned above) bonded through oxygen or sulfur linkages, respectively, at any bond in the alkyl group. Examples include methoxy, ethoxy, 20 propoxy, isopropoxy, methylthio, ethylthio, propylthio, isopropylthio, and n-butylthio. Similarly, "alkylsulfinyl" and "alkylsulfonyl" refer to straight-chain or branched alkyl groups having 1 to 6 carbon atoms (as mentioned above) bonded through -S(=O)- or S(=O)2-linkages, respectively, at any bond in the alkyl group. Examples include 25 methylsulfinyl and methylsulfonyl. Similarly, "alkylamino" refers to a nitrogen atom which carries 1 or 2 straight-chain or branched alkyl groups having 1 to 6 carbon atoms (as mentioned above) which may be the same or different. Examples include methylamino, dimethylamino, ethylamino, 30 diethylamino, methylethylamino, isopropylamino, or methylisopropylamino. The term "alkylcarbonyl" refers to straight-chain or branched alkyl groups having 1 to 6 carbon atoms (as mentioned above) bonded through a -C(=O)- linkage, respectively, at any bond in the alkyl group. Examples include acetyl and propionyl. 35 The term "alkenyl" as used herein intends a branched or unbranched unsaturated hydrocarbon group having 2 to 6 carbon atoms and a double bond in any position, such as ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1 methyl-1 -propenyl, 2-methyl-1 -propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl; 1 40 pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1 -butenyl, 2-methyl-1 -butenyl, 3 methyl-1 -butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl 3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2- WO 2007/071609 PCT/EP2006/069686 12 dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1 -propenyl, 1-ethyl-2-propenyl, 1 hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-l-pentenyl, 2-methyl-1 pentenyl, 3-methyl-1 -pentenyl, 4-methyl-1 -pentenyl, 1-methyl-2-pentenyl, 2-methyl-2 pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3 5 pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4 pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1 dimethyl-3-butenyl, 1,2-dimethyl-1 -butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3 butenyl, 1,3-dimethyl-l-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2 dimethyl-3-butenyl, 2,3-dimethyl-1 -butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3 10 butenyl, 3,3-dimethyl-1 -butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1 -butenyl, 1-ethyl-2 butenyl, 1-ethyl-3-butenyl, 2-ethyl-l-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2 trimethyl-2-propenyl, 1-ethyl-1 -methyl-2-propenyl, 1-ethyl-2-methyl-l-propenyl and 1 ethyl-2-methyl-2-propenyl; 15 The term "alkynyl" as used herein refers to a branched or unbranched unsaturated hydrocarbon group containing at least one triple bond, such as ethynyl, propynyl, 1 butynyl, 2-butynyl, and the like. Cycloalkyl as used herein refers to monocyclic 3- to 6-membered saturated carbon 20 atom rings, e.g. C3-06-cycloalkyl such as cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl. A 5-or 6-membered heteroaromatic ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur may be a 5-membered heteroaromatic ring containing 25 1 nitrogen atom and 0 to 2 further heteroatoms independently selected from oxygen, nitrogen and sulfur, preferably from oxygen and nitrogen, such as pyrrol, pyrazol, imidazol, triazol, oxazol, isoxazol, oxadiazol, thiazol, isothiazol, thiodiazol; or a 5 membered heteroaromatic ring containing 1 heteroatom selected from oxygen and sulfur, such as furane or thiophen; or a 6-membered heteroaromatic ring containing 1 30 nitrogen atom and 0 to 2 further heteroatoms independently selected from oxygen, nitrogen and sulfur, preferably from oxygen and nitrogen, such as pyridine, pyrazine, pyrimidine, pyridazine or triazine. A 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which 35 may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur is e.g. pyridine, pyrimidine, (1,2,4)-oxadiazole, (1,3,4)-oxadiazole, pyrrole, furan, thiophene, oxazole, thiazole, imidazole, pyrazole, isoxazole, 1,2,4-triazole, tetrazole, pyrazine, pyridazine, oxazoline, thiazoline, tetrahydrofuran, tetrahydropyran, morpholine, piperidine, piperazine, pyrroline, pyrrolidine, oxazolidine, thiazolidine. Most preferably, 40 this ring system is dioxolan, furan, oxazol, thiazol, or tetrahydrofuran.
WO 2007/071609 PCT/EP2006/069686 13 A 5-or 6-membered heteroaromatic ring which contains 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur may be a 5-membered heteroaromatic ring containing 1 nitrogen atom and 0 to 2 further heteroatoms independently selected from oxygen, nitrogen and sulfur, such as pyrrol, pyrazol, imidazol, triazol, oxazol, isoxazol, 5 oxadiazol, thiazol, isothiazol, thiodiazol; or a 5-membered heteroaromatic ring containing 1 heteroatom selected from oxygen and sulfur, such as furane or thiophen; or a 6-membered heteroaromatic ring containing 1 nitrogen atom and 0 to 2 further heteroatoms independently selected from oxygen, nitrogen and sulfur, preferably from nitrogen, such as pyridine, pyrazine, pyrimidine, pyridazine or triazine. 10 When fused to a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, this fused ring system is e.g. pyrimidotriazolyl. A 3- to 7-membered saturated or partially unsaturated heterocyclic ring which may 15 contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen is e.g. a 5- to 7 membered heteroaromatic ring containing 1 nitrogen atom and 0 or 1 further heteroatoms independently selected from oxygen and nitrogen, such as morpholine, piperazin, piperidine, or pyrrolidine. When fused to a 5- to 6-membered saturated, partially unsaturated or aromatic 20 heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, this fused ring system is e.g indoline. Phenyl which is fused to phenyl or a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from 25 oxygen, nitrogen and sulfur is e.g. naphthalin, benzoxazolyl, benzthiazolyl, benzimidazolyl, benzoxadiazolyl, or benzthiadiazolyl. The saturated or unsaturated ring of formula a D-X 30 which may have 5 to 7 ring members and besides X 1 to 2 further heteroatoms selected from oxygen, sulfur and nitrogen, e.g. is furanyl, thiophenyl, tetrahydrofuranyl, tetrahydrothiophenyl, tetrahydrothiophenyl oxide or tetrahydrothiophenyl dioxide. The group of formula p 35 (CH2)x-CH-X (0) which contains a saturated or unsaturated ring which may have 5 to 7 ring members and besides X 1 to 2 further heteroatoms selected from oxygen, sulfur and nitrogen e.g. is -CH 2 -furanyl, -CH 2 -thiophenyl, -CH 2 -tetrahydrofuranyl, -CH 2 tetrahydrothiophenyl, -CH 2 -tetrahydrothiophenyl oxide, -CH 2 -tetrahydrothiophenyl 40 dioxide, -(CH 2
)
2 -furanyl, , -(CH 2
)
2 -thiophenyl, , -(CH 2
)
2 -tetrahydrofuranyl, -(CH 2
)
2
-
WO 2007/071609 PCT/EP2006/069686 14 tetrahydrothiophenyl, , -(CH 2
)
2 -tetrahydrothiophenyl oxide or , -(CH 2
)
2 tetrahydrothiophenyl dioxide. The variable x in group p preferably is 1 or 2. With respect to the intended use of the compounds of formula I, particular preference is 5 given to the following meanings of the substituents, in each case on their own or in combination. For the precursors of the inventive compounds, these preferred substituents or the preferred combination of substituents apply accordingly. A compound of formula I wherein X is oxygen or sulfur. 10 A compound of formula I wherein X is S(=O)n. A compound of formula I wherein X is sulfur. A compound of formula I wherein X is S(=O). 15 A compound of formula I wherein R 1 is C1-C6-alkyl, C 1
-C
6 -haloalkyl or phenyl, preferably C 1
-C
6 -haloalkyl. A compound of formula I wherein R 1 is C01-C6-alkyl, C 1
-C
6 -haloalkyl or phenyl, wherein 20 these groups may be partially or fully halogenated and/or substituted with 1 to 3 groups selected from cyano, C01-C6-alkyl, C 1
-C
6 -haloalkyl, C2-06-alkenyl, C 2
-C
6 -haloalkenyl, C2 C6-alkynyl, C 3
-C
6 -haloalkynyl, C3-06-cycloalkyl, C3-06-halocycloalkyl, C3-06 cycloalkenyl, C3-06-halocycloalkenyl, C0 1
-C
6 -alkoxy, C2-06-alkenyloxy, C3-06-alkynyloxy, C0 1
-C
6 -haloalkoxy, C 2 -0 6 -haloalkenyloxy, or C 3 -0 6 -haloalkynyloxy. 25 A compound of formula I wherein R 1 is C01-C6-alkyl, C0 1
-C
6 -haloalkyl or phenyl, wherein these groups may be partially or fully halogenated and/or substituted with 1 to 3 groups selected from cyano, C01-C6-alkyl, C0 1
-C
6 -haloalkyl, C 1
-C
6 -alkoxy or C0 1
-C
6 -haloalkoxy. 30 A compound of formula I wherein A is -C(=G)GRb, or phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteroaromatic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl, the heterocyclic ring, or the heteroaromatic ring 35 may be fused to a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl or the 5- to 6 membered heteroaromatic ring or the respective fused ring systems may be unsubstituted or substituted by any combination of 1 to 6 groups R 2 . 40 A compound of formula I wherein A is phenyl or a 5- to 6-membered heteroaromatic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, WO 2007/071609 PCT/EP2006/069686 15 wherein phenyl, the heterocyclic ring, or the heteroaromatic ring may be fused to a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl or the 5- to 6-membered heteroaromatic ring or the 5 respective fused ring systems may be unsubstituted or substituted by any combination of 1 to 6 groups R 2 . A compound of formula I wherein B is a hydrocarbon chain with one carbon chain atom, preferably -CH 2 - or -CH(CH 3 )-. 10 A compound of formula I wherein D is a saturated or partially unsaturated hydrocarbon chain with 2 to 4 carbon chain atoms or cyclopropyl, preferably a saturated hydrocarbon chain with 2 to 4 carbon chain atoms. 15 A compound of formula I wherein R 2 is halogen, cyano, C1-C6-alkyl, C2-06-alkenyl, C2 C6-alkynyl, C3-06-cycloalkyl, C3-06-cycloalkenyl, C1-C 6 -haloalkyl, C 2
-C
6 -haloalkenyl, C2
C
6 -haloalkynyl, C3-06-halocycloalkyl, C3-06-halocycloalkenyl, C 1
-C
6 -alkoxy, C2-06 alkenyloxy, C3-06-alkynyloxy, C 1
-C
6 -haloalkoxy, C 2
-C
6 -haloalkenyloxy, C3-06 haloalkynyloxy, C3-06-cycloalkyloxy, C3-06-cycloalkenyloxy, C3-06-halocycloalkyloxy, 20 C3-06-halocycloalkenyloxy, C0 1
-C
6 -alkylthio, C0 1
-C
6 -haloalkylthio, C 3 -0 6 -cycloalkylthio, C1-C6-alkylsulfonyl or C0 1
-C
6 -haloalkylsulfonyl, preferably halogen, cyano, C01-C6-alkyl, C0 1
-C
6 -haloalkyl, C0 1
-C
6 -alkoxy, C 1
-C
6 -haloalkoxy, C0 1
-C
6 -alkylthio or C0 1
-C
6 -haloalkylthio. A compound of formula I wherein R 3 is halogen, cyano, Ci-Cio-alkyl, C1-Co-haloalkyl, 25 C2-Clo-alkenyl, C 2 -C0 1 o-haloalkenyl, C2-C1o-alkynyl, C 3 -C0 1 o-haloalkynyl, C3-06-cycloalkyl, C3-06-halocycloalkyl, C3-06-cycloalkenyl, C3-06-halocycloalkenyl, C0 1
-C
6 -alkoxy, C2-06 alkenyloxy, C3-06-alkynyloxy, C0 1
-C
6 -haloalkoxy, C 2 -0 6 -haloalkenyloxy or C3-06 haloalkynyloxy, preferably halogen, cyano, Ci-Cio-alkyl, C1-Cio-haloalkyl, C0 1
-C
6 -alkoxy or C0 1
-C
6 -haloalkoxy. 30 A compound of formula I wherein R 4 is halogen, cyano, C01-C6-alkyl, C 1
-C
6 -haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C 3 -0 6 -haloalkynyl, C3-06-cycloalkyl, C3-06-halocycloalkyl, C3-06-cycloalkenyl, C3-06-halocycloalkenyl, C0 1
-C
6 -alkoxy, C2-06 alkenyloxy, C3-06-alkynyloxy, C0 1
-C
6 -haloalkoxy, C 2 -0 6 -haloalkenyloxy or C3-06 35 haloalkynyloxy. A compound of formula I wherein R 4 is halogen, cyano, C01-C6-alkyl, C0 1
-C
6 -haloalkyl, C3-06-cycloalkyl, C3-06-halocycloalkyl, C 1
-C
6 -alkoxy or C0 1
-C
6 -haloalkoxy. 40 A compound of formula I wherein Ra is each independently halogen, cyano, C1-C6 alkyl, C0 1
-C
6 -haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C2-06 haloalkynyl, C3-06-cycloalkyl, OR i , SR i , S(=O)R i , S(=0) 2
R
i , NRiR, -S(=0) 2 NRiR, WO 2007/071609 PCT/EP2006/069686 16
C(=O)OR
i , C(=O)NRiRi, or phenyl or a 5- to 6-membered heteraromatic ring which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur. A compound of formula I wherein Ra is each independently halogen, cyano, C1-06 5 alkyl, C1-C 6 -haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C2-06 haloalkynyl or C0 1
-C
6 -alkoxy. A compound of formula I wherein Rb is each independently C01-C6-alkyl, C0 1
-C
6 -haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C 2 -0 6 -haloalkynyl, C3-06-cycloalkyl or 10 C3-06-halocycloalkyl. A compound of formula I wherein D is selected from -CH 2 -, -CH(CH 3 )-, -CH(CF 3 )-, -(CH 2
)
2 -, cyclopropyl, -CH 2
C(CH
3
)
2 -,
-CH(CH
3
)CH
2 -, -CH 2
CH(CH
3 )-, or -(CH 2
)
4 -; 15 X is oxygen, sulfur, S(=O) or S(=O)2; and
R
1 is CH 3 , CH 2 0H 3 , (CH 2
)
2 0H 3 , OH(CH 3
)
2 , (CH 2
)
2 0H 3 , OH 2
CH(CH
3
)
2 , 0(0H 3
)
3 , phenyl, pentachlorophenyl, pentafluorophenyl, CH 2
CCH
2 , cyclopropyl, CH 2 CCH, benzyl, OF 3 , CC13, CH 2 0F 3 , CH 2
CHCC
2 , CF 2 0F 3 , cyclopentyl, cyclohexyl, OH 2
CH(CF
3
)
2 , or the moiety -D-X-R 1 together forms furanyl, tetrahydrofuranyl, thiophenyl, 20 tetrahydrothiophenyl, tetrahydrothiophenyl oxide, tetrahydrothiophenyl dioxide, 3-CF 3 thiophen-1 -yl, 3-CF 3 -tetrahydrothiophen-1 -yl, 3-CF 3 -furan-1 -yl, or 3-CF 3 tetrahydrofuran-1 -yl. A compound of formula I wherein A is selected from table A.
WO 2007/071609 PCT/EP2006/069686 17 Table A a2 a2 R a2 Ra 2 Ra 2 RN N N a N Ral O Ral
R
l N # # Ral 0 # S Ra 3 R A.1 A.2 A.3 A.4 Ra2 R2 Ra Rla Ra2 Ral Ra2 N_ # Ral N Ral S/ S IRa 3 N N R A.5 A.6 A.7 A.8 # Ra2 # RR a 2 # Ra2 O Ral Sz Ral O / Ral S R a l N N N N A.9 A.10 A.11 A.12 ### R l a #
R
a 2 / R a l Ra2
R
a l
R
a 2 Ra' R a 3 yN / Ra2 I a3 R A.13 A.14 A.15 A.16 a #R a2 a2 R a l al N a2 # R a R R R R Ra3NN R NC. NN R a 3 #/ R R a2 A.17 A.18 A.19 A.19a #
R
a2 Ra2 S Ra2 A. 1 9b # denotes the binding site.
WO 2007/071609 PCT/EP2006/069686 18 In the heterocycles A.1 to A.19 of table A, Ral and Ra 2 preferably are each independently hydrogen, CH 3 , CH 2
CH
3 , CH 2
CH
2
CH
3 , CH(CH 3
)
2 , cyclopropyl, 1-methyl cyclopropyl, C(0H 3
)
3 , CH 2
C(CH
3
)
3 , C(CH 3
)
2
CH
2
CH
3 , 1-methylcyclohexyl, cyclohexyl, 1 methylcyclopentyl, cyclopentyl, phenyl, F, CI, Br, CN, NO 2 , OCHF 2 , OCH 3 , OCH 2
CH
3 , 5 OF 3 , OCF 3 , SCH 3 , or SCF 3 , most preferably hydrogen, OH 3 , OH(CH 3
)
2 , C(0H 3
)
3 , phenyl, F, CI, CN, OF 3 or SCF 3 . In the groups A.1 to A.19 of table A, Ra 3 preferably is OH 3 , CH 2
CH
3 , CH 2
CH
2
CH
3 ,
CH(CH
3
)
2 , cyclopropyl, or phenyl. 10 A compound of formula I wherein A is selected from table B. Table B al al N-N N-N Ral Ra Ra O # Ra S O. NS N o ' ONz' " N A.20 A.21 A.22 A.23 # # N-N -N N Ral- N3 ON Ral SN Ral Ra 3 A.24 A.25 A.26 Ral N N Ra3N a N /' Ra3.pN - N - Ral 15 A.27 A.28 # denotes the binding site. In the groups A.20 to A.28 of table B, Ral preferably is hydrogen, OH 3 , CH 2
CH
3 , 20 CH 2
CH
2
CH
3 , OH(CH 3
)
2 , cyclopropyl, C(0H 3
)
3 , CH 2
C(CH
3
)
3 , C(CH 3
)
2
CH
2
CH
3 , 1 methylcyclohexyl, cyclohexyl, 1-methylcyclopentyl, cyclopentyl, OF 3 , phenyl, benzyl,
NH
2 , N(CH 3
)
2 or NHC(=O)CH 3 , most preferably CH 3 , CH 2
CH
3 , CH 2
CH
2
CH
3 , CH(CH 3
)
2 , cyclopropyl, C(0H 3
)
3 , CH 2
C(CH
3
)
3 , C(CH 3
)
2
CH
2
CH
3 , OF 3 , phenyl, benzyl, or
NHC(=O)CH
3 . 25 In the groups A.20 to A.28 of table B, Ra 3 preferably is OH 3 , CH 2
CH
3 , CH 2
CH
2
CH
3 ,
CH(CH
3
)
2 , cyclopropyl, or phenyl.
WO 2007/071609 PCT/EP2006/069686 19 A compound of formula I wherein A is selected from table C. Table C F F CI CI # * F # CI F F CI CI A.29 A.30 Ral Ral Ral Ral # # # 7 N # N N 5 A.31 A.32 A.33 A.34 Ra 2
R
a 2
R
a 2
R
al R ~ al # N Ral Ral Ra 2 A.35 A.36 A.37 A.37a Ra 2 Ra 2 # a # Ral Ral a2 a2 a Ra 2 R R Ra2 A.38 A.39 A.40 # denotes the binding site. 10 In the groups A.31 to A.40 of table C the group Ral is selected from hydrogen, CH 3 ,
CH
2
CH
3 , CHCH 2 , CCH, CH 2
CHCH
2 , CH 2
CH
2
CH
3 , CH(CH 3
)
2 , CH 2
CH
2
CH
2
CH
3 ,
CH(CH
3
)CH
2
CH
3 , C(0H 3
)
3 , OCH(CH 3
)CH
2
CH
3 , benzyl, phenoxy, thiophenyl, S-(4-CH 3
)C
6
H
5 , O-(4-CI)0 6
H
5 , O-(3-Cl)-0 6
H
5 , F, CI, Br, I, CN, NO 2 , OCH 3 , OCF 3 , 15 OCF 2 H, OCH 2
CH
3 , OCH 2
CF
3 , OCF 2
CF
2 H, OCF 2 CI, OCBrF 2 , OCH 2
CH
2
CH
3 ,
OCH
2
CH=CH
2 , OCH(CH 3
)
2 , C(=O)CH 3 , C(=O)OCH 3 , OF 3 , OF(CF 3
)
2
,SCH
3 , SCF 3 , or S0 2 0H 3 , preferably from OH 3 , C(0H 3
)
3 , F, CI, Br, I, CN, OCH 3 , SCF 3 , OF 3 , or OF(CF 3
)
2 Ra 2 is selected from F, CI, OF 3 , OH 3 , OCH 3 , OCF 3 , NO 2 , or phenoxy, preferably from F, 20 CI, or OF 3 . A compound of formula I wherein A is selected from table D.
WO 2007/071609 PCT/EP2006/069686 20 Table D N", # Ra # N # N> R N)N R al 5 R N A.41 A.42 A.43 A.44 N # # l N # R N a Ra N R N~ NI Ra A.45 A.46 A.47 A.48 a l Ral R a l B . # R N R a # R a N # A.49 A.50 A.51 5 # denotes the binding site. In the groups A.41 to A.51 of table D the group Ral is selected from hydrogen, F, Cl, Br, CN, NO 2 , OH 3 , CH 2 F, CHF 2 , OF 3 , CF 2 H, CH 2 F, Et, CCH, OH(CH 3
)
2 , C(0H 3
)
3 , SCH 3 , 10 SCF 3 , SO2CH 3 , SO2CF 3 , OCH 2 CCH, or OCH 2
CCCH
3
.
WO 2007/071609 PCT/EP2006/069686 21 A compound of formula I wherein A is selected from table E. Table E Ra 2
R
al Ra 2
R
al Ra 2
R
al Ra 4 # Ra 4 S Ra 4 N R R Ra 5 Ra 5 R Ra 3 A.52 A.53 A.54 Ra4 Ra2 Ra4 Ral Ra 2 Ral R 5 R alR RaRN, #NN Ra 2 #--N N a4 #-N NN R #N--NNN R A.55 A.56 A.57 Ra Ra 2 Ra Ra 2 R a3N # N LO Ra3 NO A.58 A.59 5 # denotes the binding site. In the groups A.52 to A.57 of table E the groups Ral, Ra 2 , Ra 4 , and Ra 5 preferably are each independently selected from hydrogen, OH 3 , CH 2
CH
3 , (CH 2
)
2
CH
3 , OH(CH 3
)
2 , cyclopropyl, 1-methylcyclopropyl, C(0H 3
)
3 , CH(CH 3
)CH
2
CH
3 , -CH 2
-C(CH
3
)
3 , 10 C(CH 3
)
2
CH
2
CH
3 , 1-methylcyclohexyl, cyclohexyl, 1-methylcyclopentyl, cyclopentyl, phenyl, F, CI, Br, CN, NO 2 , OCHF 2 , OCH 3 , OCH 2
CH
3 , OF 3 , SCH 3 , or SCF 3 , most preferably hydrogen, CN, OH 3 , F, CI, or OF 3 . A compound of formula I wherein A is selected from table F. 15 Table F Ral N0 # A.60 I a 2 R # denotes the binding site. In the group A.60 of table F, Ral is selected from hydrogen, CH 3 , CH 2
CH
3 , (CH 2
)
2
CH
3 , 20 CH(CH 3
)
2 , (CH 2
)
3
CH
3 , C(CH 3
)
3 , CH(CH 3
)CH
2
CH
3 , CH 2
CH(CH
3
)
2 , (CH 2
)
4
CH
3 ,
CH
2
C(CH
3
)
3 , CH(CH 3
)CH(CH
3
)
2 , (CH 2
)
2
CH(CH
3
)
2 , CH 2
CF
3 , (CH 2
)
2
CF
3 , (CH 2
)
3
CF
3
,
WO 2007/071609 PCT/EP2006/069686 22
CH
2
CHCH
2 , CH 2
CHC(CH
3
)
2 , CH 2 CHCHCI, CH 2 CHCBr 2 , CH 2 CCH, CH2cyclopropyl,
CH
2 cyclobutyl, CH2cyclopentyl, CH 2 -cyclohexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, (CH 2
)
2 F, (CH 2
)
3 F, (CH 2
)C
6
H
5 , (CH 2 )(2-Cl-Phenyl), (CH 2 )(3-Cl-Phenyl) or
(CH
2 )(4-Cl-Phenyl). 5 R a 2 is selected from OH 3 , OF 3 , CH 2
CH
3 , (CH 2
)
2
CH
3 , (CH 2
)
3
CH
3 , C(0H 3
)
3 , or phenyl. A compound of formula I wherein A is selected from table G. Table G O O al al R N- # A.61 R O # A.62 10 Ra 2 / # denotes the binding site. In the groups A.61 and A.62 of table G, Ral and Ra 2 each independently are selected from hydrogen, CH 3 , CH 2
CH
3 , (CH 2
)
2
CH
3 , CH(CH 3
)
2 , cyclopropyl, (CH 2
)
3
CH
3 , C(CH 3
)
3 , 15 CH(CH 3
)CH
2
CH
3 , CH 2
CH(CH
3
)
2 , CH 2 CCH, CH 2
CHCH
2 , C(CH 3
)
3 CCH, C 6
H
5 , CH 2 0 6
H
5 ,
CF
3 , CH 2 F, CH 2 CN, CF(CF 3
)
2 , CH 2 0CH 3 , CH 2 0CH 2 F, C(=0)CH 3 , C(=0)C 6
H
5 , S(=0) 2 0 6
H
5 , or S(=0) 2 [(p-CH 3 )C6H 4 ]. Ral preferably is selected from (CH 2
)
2
CH
3 , OH(CH 3
)
2 , cyclopropyl C(CH 3
)
3 , CH 2 CN, or
CH
2 0CH 3 , Ra 2 preferably is selected from hydrogen or CH 3 . 20 A compound of formula I wherein D is selected from -CH 2 -, -CH(CH 3 )-, -CH(CF 3 )-, -(CH 2
)
2 -, cyclopropyl, -CH 2
C(CH
3
)
2 -,
-CH(CH
3
)CH
2 -, -CH 2
CH(CH
3 )-, or -(CH 2
)
4 -; X is oxygen, sulfur, S(=0) or S(=0)2; and 25 R 1 is CH 3 , CH 2 0H 3 , (CH 2
)
2 0H 3 , OH(CH 3
)
2 , (CH 2
)
2 0H 3 , OH 2
CH(CH
3
)
2 , C(0H 3
)
3 , phenyl, pentachlorophenyl, pentafluorophenyl, CH 2
CCH
2 , cyclopropyl, CH 2 CCH, benzyl, OF 3 , CC13, CH 2 0F 3 , CH 2
CHCC
2 , CF 2 0F 3 , cyclopentyl, cyclohexyl, OH 2
CH(CF
3
)
2 , or the moiety -D-X-R 1 together forms furanyl, tetrahydrofuranyl, thiophenyl, tetrahydrothiophenyl, tetrahydrothiophenyl oxide, tetrahydrothiophenyl dioxide, 3-CF 3 30 thiophen-1 -yl, 3-CF 3 -tetrahydrothiophen-1 -yl, 3-CF 3 -furan-1 -yl, or 3-CF 3 tetrahydrofuran-1 -yl.
WO 2007/071609 PCT/EP2006/069686 23 A compound of formula I wherein the moiety D-X-R 1 is selected from table H. Table H No. D X R 1 W-1 -CH 2 - O (CH 2
)
2
CH
3 W-2 -CH(CH 3 )- O (CH 2
)
2
CH
3 W-3 -CH(CH 3
)CH
2 - O (CH 2
)
2
CH
3 W-4 -CH 2
CH(CH
3 )- O (CH 2
)
2
CH
3 W-5 -CH 2 - S (CH 2
)
2
CH
3 W-6 -CH(CH 3 )- S (CH 2
)
2
CH
3 W-7 -CH(CH 3
)CH
2 - S (CH 2
)
2
CH
3 W-8 -CH 2
CH(CH
3 )- S (CH 2
)
2
CH
3 W-9 -CH 2 - S(=O) (CH 2
)
2
CH
3 W-10 -CH(CH 3 )- S(=0) (CH 2
)
2
CH
3 W-11 -CH(CH 3
)CH
2 - S(=O) (CH 2
)
2
CH
3 W-12 -CH 2
CH(CH
3 )- S(=O) (CH 2
)
2
CH
3 W-13 -CH 2 - S(=0O)2 (CH 2
)
2
CH
3 W-14 -CH(CH 3 )- S(=O)2 (CH 2
)
2
CH
3 W-15 -CH(CH 3
)CH
2 - S(=0)2 (CH 2
)
2
CH
3 W-16 -CH 2
CH(CH
3 )- S(=0O)2 (CH 2
)
2
CH
3 W-17 -CH 2 - O CH(CH 3
)
2 W-18 -CH(CH 3 )- O CH(CH 3
)
2 W-19 -CH(CH 3
)CH
2 - O CH(CH 3
)
2 W-20 -CH 2
CH(CH
3 )- O CH(CH 3
)
2 W-21 -CH 2 - S CH(CH 3
)
2 W-22 -CH(CH 3 )- S CH(CH 3
)
2 W-23 -CH(CH 3
)CH
2 - S CH(CH 3
)
2 W-24 -CH 2
CH(CH
3 )- S CH(CH 3
)
2 W-25 -CH 2 - S(=0) CH(CH 3
)
2 W-26 -CH(CH 3 )- S(=0) OH(OH 3
)
2 W-27 -CH(CH 3
)CH
2 - S(=0) CH(CH 3
)
2 W-28 -CH 2
CH(CH
3 )- S(=0) CH(CH 3
)
2 W-29 -CH 2 - S(=0O)2 CH(CH 3
)
2 W-30 -CH(CH 3 )- S(=0O)2 CH(CH 3
)
2 W-31 -CH(CH 3
)CH
2 - S(=0)2 CH(CH 3
)
2 W-32 -CH 2
CH(CH
3 )- S(=0)2 CH(CH 3
)
2 W-33 -CH 2 - O C(CH 3
)
3 W-34 -CH(CH 3 )- O C(CH 3
)
3 W-35 -CH(CH 3
)CH
2 - O C(CH 3
)
3 W-36 -CH 2
CH(CH
3 )- O C(CH 3
)
3 W-37 -CH 2 - S C(CH 3
)
3 WO 2007/071609 PCT/EP2006/069686 24 No. D X R W-38 -OH(0H 3 )- s O(OH 3
)
3 W-39 -OH(0H 3 )0H 2 - s O(0H 3
)
3 W-40 -OH 2 OH(0H 3 )- S O(0H 3
)
3 W-41 -OH 2 - S(=O) O(0H 3
)
3 W-42 -OH(0H 3 )- S(=O) O(0H 3
)
3 W-43 -OH(0H 3 )0H 2 - S(=O) O(0H 3
)
3 W-44 -OH 2 OH(0H 3 )- S(=O) O(0H 3
)
3 W-45 -OH 2 - S(=0)2 O(0H 3
)
3 W-46 -OH(0H 3 )- S(=0)2 O(0H 3
)
3 W-47 -OH(0H 3 )0H 2 - S(=0)2 O(0H 3
)
3 W-48 -OH 2 OH(0H 3 )- S(=0)2 O(0H 3
)
3 W-49 -C H 2 - 0 OF 3 W-50 -OH(0H 3 )- 0 OF 3 W-51 -OH(0H 3 )0H 2 - 0 OF 3 W-52 -OH 2
OH(OH
3 )- 0 OF 3 W-53 -O H 2 - S OF 3 W-54 -OH(0H 3 )- S OF 3 W-55 -OH(0H 3 )0H 2 - S OF 3 W-56 -OH 2 OH(0H 3 )- S OF 3 W-57 -OH 2 - S(=0) OF 3 W-58 -OH(0H 3 )- S(=0) OF 3 W-59 -OH(0H 3 )0H 2 - S(=0) OF 3 W-60 -OH 2 OH(0H 3 )- S(=0) OF 3 W-61 -OH 2 - S(=0)2 OF 3 W-62 -OH(0H 3 )- S(=0)2 OF 3 W-63 -OH(0H 3 )0H 2 - S(=0)2 OF 3 W-64 -OH 2 OH(0H 3 )- S(=0)2 OF 3 W-65 -OH 2 - 0 0H 2 0F 3 W-66 -OH(0H 3 )- 0 0H 2 0F 3 W-67 -OH(0H 3 )0H 2 - 0 0H 2 0F 3 W-68 -OH 2
OH(OH
3 )- 0 OH 2
OF
3 W-69 -OH 2 - S OH 2
OF
3 W-70 -OH(OH 3 )- S OH 2
OF
3 W-71 -OH(OH 3
)OH
2 - S OH 2
OF
3 W-72 -OH 2
OH(OH
3 )- S OH 2
OF
3 W-73 -OH 2 - S(=0) OH 2
OF
3 W-74 -OH(OH 3 )- S(=0) OH 2
OF
3 W-75 -OH(OH 3
)OH
2 - S(=0) OH 2
OF
3 W-76 -OH 2
OH(OH
3 )- S(=0) OH 2
OF
3 W-77 -OH 2 - S(=0)2 OH 2
OF
3 WO 2007/071609 PCT/EP2006/069686 25 No. D X R W-78 -OH(0H 3 )- S(=0)2 CH 2
CF
3 W-79 -OH(0H 3 )0H 2 - S(=0)2 CH 2
CF
3 W-80 -OH 2 OH(0H 3 )- S(=0)2 CH 2
CF
3 W-81 -OH 2 - 0 CYClO-0 5
H
9 W-82 -CH(0H 3 )- 0 CYClO-0 5
H
9 W-83 -CH(0H 3 )0H 2 - 0 CYClO-0 5
H
9 W-84 -CH 2 CH(0H 3 )- 0 CYClO-0 5
H
9 W-85 -OH 2 - s CYClO-0 5
H
9 W-86 -CH(0H 3 )- s CYClO-0 5
H
9 W-87 -CH(0H 3 )0H 2 - S CYClO-0 5
H
9 W-88 -CH 2 CH(0H 3 )- S CYClO-0 5
H
9 W-89 -OH 2 - S(=O) CYClO-0 5
H
9 W-90 -CH(0H 3 )- S(=O) CYClO-0 5
H
9 W-91 -CH(0H 3 )0H 2 - S(=O) CYClO-0 5
H
9 W-92 -CH 2 CH(0H 3 )- S(=O) CYClO-0 5
H
9 W-93 -OH 2 - S(=0)2 CYClO-0 5
H
9 W-94 -CH(0H 3 )- S(=0)2 CYClO-0 5
H
9 W-95 -CH(0H 3 )0H 2 - S(=0)2 CYClO-0 5
H
9 W-96 -CH 2 CH(0H 3 )- S(=0)2 CYClO-0 5
H
9 W-97 -OH 2 - 0 0 6
H
5 W-98 -CH(0H 3 )- 0 0 6
H
5 W-99 -CH(0H 3 )0H 2 - 0 0 6
H
5 W-1 00 -CH 2
CH(CH
3 )- 0 C 6
H
5 W-101 -OH 2 - S C 6
H
5 W-1 02 -CH(CH 3 )- S C 6
H
5 W-1 03 -CH(CH 3
)CH
2 - S C 6
H
5 W-1 04 -OH 2
OH(OH
3 )- S O 6
H
5 W-1 05 -OH 2 - S(=0) O 6
H
5 W-1 06 -OH(OH 3 )- S(=0) O 6
H
5 W-1 07 -OH(OH 3
)OH
2 - S(=0) O 6
H
5 W-1 08 -CH 2
CH(CH
3 )- S(=0) C 6
H
5 W-1 09 -OH 2 - S(=0)2 C 6
H
5 W-1 10 -CH(CH 3 )- S(=0)2 C 6
H
5 W-1 11 -CH(CH 3
)CH
2 - S(=0)2 C 6
H
5 W-1 12 -CH 2
CH(CH
3 )- S(=0)2 C 6
H
5 W-1 13 -OH 2 - 0 CH 2
C
6
H
5 W-1 14 -CH(CH 3 )- 0 CH 2
C
6
H
5 W-1 15 -CH(CH 3
)CH
2 - 0 CH 2
C
6
H
5 W-1 16 -CH 2
CH(CH
3 )- 0 CH 2
C
6
H
5 W-1 17 -OH 2 - S CH 2
C
6
H
5 WO 2007/071609 PCT/EP2006/069686 26 No. D X R W-1 18 -OH(OH 3 )- s OH 2
O
6
H
5 W-1 19 -OH(OH 3
)OH
2 - s OH 2
O
6
H
5 W-120 -OH 2
OH(OH
3 )- S OH 2
O
6
H
5 W-1 21 -OH 2 - S(=O) CH 2
C
6
H
5 W-122 -CH(0H 3 )- S(=O) CH 2
C
6
H
5 W-123 -CH(0H 3 )0H 2 - S(=O) CH 2
C
6
H
5 W-124 -CH 2 CH(0H 3 )- S(=O) CH 2
C
6
H
5 W-125 -OH 2 - S(=0)2 CH 2
C
6
H
5 W-126 -CH(0H 3 )- S(=0)2 CH 2
C
6
H
5 W-127 -CH(0H 3 )0H 2 - S(=0)2 CH 2
C
6
H
5 W-128 -CH 2 CH(0H 3 )- S(=0)2 0H 2 0 6
H
5 W-129 -OH 2 - 0 CF=CF 2 W-1 30 -CH(0H 3 )- 0 CF=CF 2 W-1 31 -CH(0H 3 )0H 2 - 0 CF=0F 2 W-1 32 -CH 2 CH(0H 3 )- 0 CF=0F 2 W-1 33 -OH 2 - s CF=0F 2 W-1 34 -CH(0H 3 )- S CF=0F 2 W-1 35 -CH(0H 3 )0H 2 - S CF=0F 2 W-1 36 -CH 2 CH(0H 3 )- S CF=0F 2 W-1 37 -OH 2 - S(=O) CF=0F 2 W-1 38 -CH(0H 3 )- S(=O) CF=0F 2 W-1 39 -CH(0H 3 )0H 2 - S(=O) CF=0F 2 W-140 -CH 2 CH(0H 3 )- S(=O) CF=0F 2 W-1 41 -OH 2 - S(=0)2 CF=0F 2 W-142 -CH(0H 3 )- S(=0)2 CF=0F 2 W-143 -CH(0H 3 )0H 2 - S(=0)2 CF=0F 2 W-144 -CH 2 CH(0H 3 )- S(=0)2 CF=0F 2 W-145 -OH 2 - 0 0F 2 0F 3 W-146 -CH(0H 3 )- 0 0F 2 0F 3 W-147 -CH(0H 3 )0H 2 - 0 0F 2 0F 3 W-148 -CH 2 CH(0H 3 )- 0 0F 2 0F 3 W-149 -OH 2 - S 0F 2 0F 3 W-1 50 -CH(0H 3 )- S 0F 2 0F 3 W-1 51 -CH(0H 3 )0H 2 - S 0F 2 0F 3 W-1 52 -OH 2
OH(OH
3 )- S OF 2
OF
3 W-1 53 -OH 2 - S(=0) OF 2
OF
3 W-1 54 -OH(OH 3 )- S(=0) OF 2
OF
3 W-1 55 -OH(OH 3
)OH
2 - S(=0) OF 2
OF
3 W-1 56 -OH 2
OH(OH
3 )- S(=0) OF 2
OF
3 W-1 57 -OH 2 - S(=0)2 OF 2
OF
3 WO 2007/071609 PCT/EP2006/069686 27 No. D X R 1 W-158 -CH(CH 3 )- S(=O)2 CF 2
CF
3 W-159 -CH(CH 3
)CH
2 - S(=O)2 CF 2
CF
3 W-160 -CH 2
CH(CH
3 )- S(=O)2 CF 2
CF
3 W-161 -CH 2 - O CF 2 CFCI W-162 -CH(CH 3 )- O CF 2 CFCI W-163 -CH(CH 3
)CH
2 - O CF 2 CFCI W-164 -CH 2
CH(CH
3 )- O CF 2 CFCI W-165 -CH 2 - S CF 2 CFCI W-166 -CH(CH 3 )- S CF 2 CFCI W-167 -CH(CH 3
)CH
2 - S CF 2 CFCI W-168 -CH 2
CH(CH
3 )- S CF 2 CFCI W-169 -CH 2 - S(=0) CF 2 CFCI W-170 -CH(CH 3 )- S(=0) CF 2 CFCI W-171 -CH(CH 3
)CH
2 - S(=0) CF 2 CFCI W-172 -CH 2
CH(CH
3 )- S(=0) CF 2 CFCI W-173 -CH 2 - S(=0)2 CF 2 CFCI W-174 -CH(CH 3 )- S(=O)2 CF 2 CFCI W-175 -CH(CH 3
)CH
2 - S(=O)2 CF 2 CFCI W-176 -CH 2
CH(CH
3 )- S(=O)2 CF 2 CFCI W-177 2-tetrahydrothiophenyl W-178 2-thiophenyl W-179 5-CF 3 -2-tetrahydrothiophenyl W-180 5-CF 3 -2-thiophenyl With respect to their use, particular preference is given to the compounds IA compiled in the tables below. Moreover, the groups mentioned for a substituent in the tables are on their own, independently of the combination in which they are mentioned, a 5 particularly preferred embodiment of the substituent in question. Table 1 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-1, and A corresponds in each case to a row of Table K. ,B W A (IA) 10 NC CN Table 2 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-5, and A corresponds in each case to a row of Table K.
WO 2007/071609 PCT/EP2006/069686 28 Table 3 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-17, and A corresponds in each case to a row of Table K. 5 Table 4 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-21, and A corresponds in each case to a row of Table K. Table 5 10 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-33, and A corresponds in each case to a row of Table K. Table 6 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-37, and A 15 corresponds in each case to a row of Table K. Table 7 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-49, and A corresponds in each case to a row of Table K. 20 Table 8 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-53, and A corresponds in each case to a row of Table K. 25 Table 9 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-65, and A corresponds in each case to a row of Table K. Table 10 30 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-69, and A corresponds in each case to a row of Table K. Table 11 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-81, and A 35 corresponds in each case to a row of Table K. Table 12 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-85, and A corresponds in each case to a row of Table K. 40 WO 2007/071609 PCT/EP2006/069686 29 Table 13 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-97, and A corresponds in each case to a row of Table K. 5 Table 14 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-101, and A corresponds in each case to a row of Table K. Table 15 10 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-113, and A corresponds in each case to a row of Table K. Table 16 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-117, and A 15 corresponds in each case to a row of Table K. Table 17 Compounds of the formula IA wherein B denotes -CH 2 -, W denotes W-129, and A corresponds in each case to a row of Table K. 20 Table 18 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-131, and A corresponds in each case to a row of Table K. 25 Table 19 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-1, and A corresponds in each case to a row of Table K. ,B W A O X(IA) NC CN Table 20 30 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-5, and A corresponds in each case to a row of Table K. Table 21 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-17, and A 35 corresponds in each case to a row of Table K. Table 22 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-21, and A corresponds in each case to a row of Table K. 40 WO 2007/071609 PCT/EP2006/069686 30 Table 23 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-33, and A corresponds in each case to a row of Table K. 5 Table 24 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-37, and A corresponds in each case to a row of Table K. Table 25 10 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-49, and A corresponds in each case to a row of Table K. Table 26 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-53, and A 15 corresponds in each case to a row of Table K. Table 27 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-65, and A corresponds in each case to a row of Table K. 20 Table 28 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-69, and A corresponds in each case to a row of Table K. 25 Table 29 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-81, and A corresponds in each case to a row of Table K. Table 30 30 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-85, and A corresponds in each case to a row of Table K. Table 31 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-97, and A 35 corresponds in each case to a row of Table K. Table 32 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-101, and A corresponds in each case to a row of Table K. 40 WO 2007/071609 PCT/EP2006/069686 31 Table 33 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-113, and A corresponds in each case to a row of Table K. 5 Table 34 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-117, and A corresponds in each case to a row of Table K. Table 35 10 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-129, and A corresponds in each case to a row of Table K. Table 36 Compounds of the formula IA wherein B denotes -CH(CH 3 )-, W denotes W-131, and A 15 corresponds in each case to a row of Table K. Table K No. A Ral Ra 2 IA-1 A.1 H H IA-2 A.1 H CH 3 IA-3 A.1 H C(CH 3
)
3 IA-4 A.1 H C 6
H
5 IA-5 A.1 H cyclo-C3H 5 IA-6 A.1 H Cl IA-7 A.1 CH 3 H IA-8 A.1 C(CH 3
)
3 H IA-9 A.1 C 6
H
5 H IA-10 A.1 cyclo-C3H 5 H IA-11 A.1 Cl H IA-12 A.5 H H IA-13 A.5 H CH 3 IA-14 A.5 H C(CH 3
)
3 IA-15 A.5 H C 6
H
5 IA-16 A.5 H cyclo-C3H 5 IA-17 A.5 H Cl IA-18 A.5 CH 3
H
WO 2007/071609 PCT/EP2006/069686 32 No. A Rai Ra 2 IA-19 A.5 C(CH 3
)
3 H IA-20 A.5 C 6
H
5 H IA-21 A.5 cyclo-C 3
H
5 H IA-22 A.5 CI H IA-23 A.9 H H IA-24 A.9 H CH 3 IA-25 A.9 H C(CH 3
)
3 IA-26 A.9 H C 6
H
5 IA-27 A.9 H cyclo-C 3
H
5 IA-28 A.9 H CI IA-29 A.9 CH 3 H IA-30 A.9 C(CH 3
)
3 H IA-31 A.9 C 6
H
5 H IA-32 A.9 cyclo-C 3
H
5 H IA-33 A.9 CI H IA-34 A.14 H H IA-35 A.14 H CH 3 IA-36 A.14 H C(CH 3
)
3 IA-37 A.14 H C 6
H
5 IA-38 A.14 H cyclo-C 3
H
5 IA-39 A.14 H CI IA-40 A.14 OH 3 H IA-41 A.14 C(CH 3
)
3 H IA-42 A.14 C 6
H
5 H IA-43 A.14 cyclo-C 3
H
5 H IA-44 A.14 CI H IA-45 A.20 4-CI-C 6 H5 IA-46 A.20 OH 3 IA-47 A.20 C(CH 3
)
3 IA-48 A.20 OF 3 IA-49 A.20 cyclo-C 3 H5 IA-50 A.21 OH 3 WO 2007/071609 PCT/EP2006/069686 33 No. A Rai Ra 2 IA-51 A.21 C(CH 3
)
3 IA-52 A.21 CF 3 IA-53 A.21 cyclo-C 3 H5 IA-54 A.22 CH 3 IA-55 A.22 C(CH 3
)
3 IA-56 A.22 CF 3 IA-57 A.22 cyclo-C 3 H5 IA-58 A.29 IA-59 A.30 IA-60 A.31 3-CH 3 IA-61 A.31 3-C(CH 3
)
3 IA-62 A.31 3-OCF 3 IA-63 A.31 3-CF 3 IA-64 A.31 3-CI IA-65 A.31 3-F IA-66 A.31 4-CH 3 IA-67 A.31 4-C(CH 3
)
3 IA-68 A.31 4-OCF 3 IA-69 A.31 4-CF 3 IA-70 A.31 4-CI IA-71 A.31 4-F IA-72 A.33 4-CI IA-73 A.35 CH 3 2-CH 3 IA-74 A.35 C(CH 3
)
3 2-CH 3 IA-75 A.35 OCF 3 2-CH 3 IA-76 A.35 CF 3 2-CH 3 IA-77 A.35 CI 2-CH 3 IA-78 A.35 F 2-CH 3 IA-79 A.35 CH 3 2-CI IA-80 A.35 C(CH 3
)
3 2-CI IA-81 A.35 OCF 3 2-CI IA-82 A.35 CF 3 2-CI WO 2007/071609 PCT/EP2006/069686 34 No. A Ral Ra 2 IA-83 A.35 CI 2-CI IA-84 A.35 F 2-CI IA-85 A.35 CH 3 2-F IA-86 A.35 C(CH 3
)
3 2-F IA-87 A.35 OCF 3 2-F IA-88 A.35 CF 3 2-F IA-89 A.35 Cl 2-F IA-90 A.35 F 2-F IA-91 A.35 CH 3 3-CH 3 IA-92 A.35 C(CH 3
)
3 3-CH 3 IA-93 A.35 OCF 3 3-CH 3 IA-94 A.35 CF 3 3-CH 3 IA-95 A.35 Cl 3-CH 3 IA-96 A.35 F 3-CH 3 IA-97 A.35 CH 3 3-Cl IA-98 A.35 C(CH 3
)
3 3-Cl IA-99 A.35 OCF 3 3-Cl IA-100 A.35 CF 3 3-Cl IA-101 A.35 Cl 3-Cl IA-102 A.35 F 3-Cl IA-103 A.35 CH 3 3-F IA-104 A.35 C(CH 3
)
3 3-F IA-105 A.35 OCF 3 3-F IA-106 A.35 CF 3 3-F IA-107 A.35 Cl 3-F IA-108 A.35 F 3-F IA-109 A.36 CH 3 2-CH 3 IA-110 A.36 C(CH 3
)
3 2-CH 3 IA-111 A.36 OCF 3 2-CH 3 IA-112 A.36 CF 3 2-CH 3 IA-113 A.36 Cl 2-CH 3 IA-114 A.36 F 2-CH 3 WO 2007/071609 PCT/EP2006/069686 35 No. A Rai Ra 2 IA-115 A.36 CH 3 2-CI IA-116 A.36 C(CH 3
)
3 2-CI IA-117 A.36 OCF 3 2-CI IA-118 A.36 CF 3 2-CI IA-119 A.36 Cl 2-CI IA-120 A.36 F 2-CI IA-121 A.36 CH 3 2-F IA-122 A.36 C(CH 3
)
3 2-F IA-123 A.36 OCF 3 2-F IA-124 A.36 CF 3 2-F IA-125 A.36 Cl 2-F IA-126 A.36 F 2-F IA-127 A.36 CH 3 4-CH 3 IA-128 A.36 C(0H 3
)
3 4-CH 3 IA-129 A.36 OCF 3 4-CH 3 IA-130 A.36 CF 3 4-CH 3 IA-131 A.36 Cl 4-CH 3 IA-132 A.36 F 4-CH 3 IA-133 A.36 CH 3 4-CI IA-134 A.36 C(CH 3
)
3 4-CI IA-135 A.36 OCF 3 4-CI IA-136 A.36 CF 3 4-CI IA-137 A.36 Cl 4-CI IA-138 A.36 F 4-CI IA-139 A.36 CH 3 4-F IA-140 A.36 C(CH 3
)
3 4-F IA-141 A.36 OCF 3 4-F IA-142 A.36 CF 3 4-F IA-143 A.36 Cl 4-F IA-144 A.36 F 4-F IA-145 A.37 Cl 6-CI IA-146 A.40 CH 3 2,6-(CH 3
)
2 WO 2007/071609 PCT/EP2006/069686 36 No. A Rai Ra 2 IA-147 A.40 C(CH 3
)
3 2,6-(CH 3
)
2 IA-148 A.40 OCF 3 2,6-(CH 3
)
2 IA-149 A.40 CF 3 2,6-(CH 3
)
2 IA-150 A.40 CI 2,6-(CH 3
)
2 IA-151 A.40 F 2,6-(CH 3
)
2 IA-152 A.40 CH 3 2,6-CI2 IA-153 A.40 C(CH 3
)
3 2,6-CI2 IA-154 A.40 OCF 3 2,6-CI2 IA-155 A.40 CF 3 2,6-CI2 IA-156 A.40 CI 2,6-CI2 IA-157 A.40 F 2,6-CI2 IA-158 A.40 CH 3 2,6-F 2 IA-159 A.40 C(CH 3
)
3 2,6-F 2 IA-160 A.40 OCF 3 2,6-F 2 IA-161 A.40 CF 3 2,6-F 2 IA-162 A.40 CI 2,6-F 2 IA-163 A.40 F 2,6-F 2 IA-164 A.40 CH 3 2-CH 3 -6-F IA-165 A.40 C(CH 3
)
3 2-CH 3 -6-F IA-166 A.40 OCF 3 2-CH 3 -6-F IA-167 A.40 CF 3 2-CH 3 -6-F IA-168 A.40 CI 2-CH 3 -6-F IA-169 A.40 F 2-CH 3 -6-F IA-170 A.40 CH 3 2-CH 3 -6-CI IA-171 A.40 C(CH 3
)
3 2-CH 3 -6-CI IA-172 A.40 OCF 3 2-CH 3 -6-CI IA-173 A.40 CF 3 2-CH 3 -6-CI IA-174 A.40 CI 2-CH 3 -6-CI IA-175 A.40 F 2-CH 3 -6-CI IA-176 A.40 CH 3 2-F-6-CI IA-177 A.40 C(CH 3
)
3 2-F-6-CI IA-178 A.40 OCF 3 2-F-6-CI WO 2007/071609 PCT/EP2006/069686 37 No. A Rai Ra 2 IA-179 A.40 CF 3 2-F-6-CI IA-180 A.40 CI 2-F-6-CI IA-181 A.40 F 2-F-6-CI IA-182 A.48 H IA-183 A.48 F IA-184 A.48 CI IA-185 A.48 Br IA-186 A.48 CF 3 IA-187 A.48 C(CH 3
)
3 IA-188 A.48 F IA-189 A.48 CI IA-190 A.48 Br IA-191 A.48 CF 3 IA-192 A.48 C(CH 3
)
3 IA-193 A.60 CH 3
CH
3 IA-194 A.60 CH(CH 3
)
2
CH
3 IA-195 A.60 C(CH 3
)
3
CH
3 IA-196 A.60 CH 2
CF
3
CH
3 IA-197 A.60 cyclo-C 3
H
5
CH
3 IA-198 A.60 CH 2 -cyclo-C 3
H
5
CH
3 IA-199 A.60 CH 3
CF
3 IA-200 A.60 CH(CH 3
)
2
CF
3 IA-201 A.60 C(CH 3
)
3
CF
3 IA-202 A.60 CH 2
CF
3
CF
3 IA-203 A.60 cyclo-C 3
H
5
CF
3 IA-204 A.60 CH 2 -cyclo-C 3
H
5
CF
3 IA-205 A.61 (CH 2
)
2
CH
3 H IA-206 A.61 CH(CH 3
)
2 H IA-207 A.61 C(CH 3
)
3 H IA-208 A.61 CH 2 CN H IA-209 A.61 cyclo-C 3
H
5 H IA-210 A.61 CH 2 0CH 3
H
WO 2007/071609 PCT/EP2006/069686 38 No. A Ral Ra 2 IA-211 A.61 (CH 2
)
2
CH
3
CH
3 IA-212 A.61 CH(CH 3
)
2
CH
3 IA-213 A.61 C(CH 3
)
3
CH
3 IA-214 A.61 CH 2 CN OH 3 IA-215 A.61 cyclo-C 3
H
5
OH
3 IA-216 A.61 CH 2 0CH 3
OH
3 IA-217 A.62 (CH 2
)
2
CH
3 IA-218 A.62 OH(OH 3
)
2 IA-219 A.62 C(CH 3
)
3 IA-220 A.62 CH 2 CN IA-221 A.62 cyclo-C3H5 IA-222 A.62 CH 2 0CH 3 IA-223 A.62 C(CH 3
)
3 IA-224 A.62 C(CH 3
)
2 CCH The compounds of the formula I are especially suitable for efficiently combating the following pests: 5 insects from the order of the lepidopterans (Lepidoptera), for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea 10 grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma exigua, Leucoptera coffeella, Leucoptera scitella, 15 Lithocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia clerkella, Malacosoma neustria, Mamestra brassicae, Orgyia pseudotsugata, Ostrinia nubilalis, Panolis flammea, Pectinophora gossypiella, Peridroma saucia, Phalera bucephala, Phthorimaea operculella, Phyllocnistis citrella, Pieris brassicae, Plathypena scabra, Plutella xylostella, Pseudoplusia includens, 20 Rhyacionia frustrana, Scrobipalpula absoluta, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Thaumatopoea pityocampa, Tortrix viridana, Trichoplusia ni and Zeiraphera canadensis, WO 2007/071609 PCT/EP2006/069686 39 beetles (Coleoptera), for example Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Aphthona euphoridae, Athous haemorrhoidalis, Atomaria 5 linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Ctenicera ssp., Diabrotica longicornis, Diabrotica semipunctata, Diabrotica 12-punctata Diabrotica speciosa, 10 Diabrotica virgifera, Epilachna varivestis, Epitrix hirtipennis, Eutinobothrus brasiliensis, Hylobius abietis, Hypera brunneipennis, Hypera postica, Ips typographus, Lema bilineata, Lema melanopus, Leptinotarsa decemlineata, Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha melolontha, Oulema oryzae, Ortiorrhynchus sulcatus, 15 Otiorrhynchus ovatus, Phaedon cochleariae, Phyllobius pyri, Phyllotreta chrysocephala, Phyllophaga sp., Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata, Popillia japonica, Sitona lineatus and Sitophilus granaria, flies, mosquitoes (Diptera), e.g. Aedes aegypti, Aedes albopictus, Aedes vexans, 20 Anastrepha ludens, Anopheles maculipennis, Anopheles crucians, Anopheles albimanus, Anopheles gambiae, Anopheles freeborni, Anopheles leucosphyrus, Anopheles minimus, Anopheles quadrimaculatus, Calliphora vicina, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Chrysops discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia hominivorax, Contarinia 25 sorghicola Cordylobia anthropophaga, Culicoides furens, Culex pipiens, Culex nigripalpus, Culex quinquefasciatus, Culex tarsalis, Culiseta inornata, Culiseta melanura, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Delia antique, Delia coarctata, Delia platura, Delia radicum, Dermatobia hominis, Fannia canicularis, Geomyza Tripunctata, Gasterophilus intestinalis, Glossina morsitans, Glossina 30 palpalis, Glossina fuscipes, Glossina tachinoides, Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hylemyia platura, Hypoderma lineata, Leptoconops torrens, Liriomyza sativae, Liriomyza trifolii, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mansonia titillanus, Mayetiola destructor, Musca domestica, Muscina stabulans, Oestrus ovis, Opomyza florum, Oscinella frit, Pegomya hysocyami, 35 Phorbia antiqua, Phorbia brassicae, Phorbia coarctata, Phlebotomus argentipes, Psorophora columbiae, Psila rosae, Psorophora discolor, Prosimulium mixtum, Rhagoletis cerasi, Rhagoletis pomonella, Sarcophaga haemorrhoidalis, Sarcophaga sp., Simulium vittatum, Stomoxys calcitrans, Tabanus bovinus, Tabanus atratus, Tabanus lineola, and Tabanus similis, Tipula oleracea, and Tipula paludosa 40 WO 2007/071609 PCT/EP2006/069686 40 thrips (Thysanoptera), e.g. Dichromothrips corbetti, Dichromothrips ssp , Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci, 5 termites (Isoptera), e.g. Calotermes flavicollis, Leucotermes flavipes, Heterotermes aureus, Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes lucifugus, Termes natalensis, and Coptotermes formosanus, cockroaches (Blattaria - Blattodea), e.g. Blattella germanica, Blattella asahinae, 10 Periplaneta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta australasiae, and Blatta orientalis, true bugs (Hemiptera), e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, 15 Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis , Thyanta perditor, Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis forbesi, Aphis pomi, Aphis gossypii, Aphis grossulariae, Aphis schneideri, Aphis spiraecola, Aphis sambuci, Acyrthosiphon pisum, Aulacorthum solani, Bemisia argentifolii, Brachycaudus cardui, 20 Brachycaudus helichrysi, Brachycaudus persicae, Brachycaudus prunicola, Brevicoryne brassicae, Capitophorus horni, Cerosipha gossypii, Chaetosiphon fragaefolii, Cryptomyzus ribis, Dreyfusia nordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum pseudosolani, Dysaphis plantaginea, Dysaphis pyri, Empoasca fabae, Hyalopterus pruni, Hyperomyzus lactucae, Macrosiphum avenae, 25 Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae, Melanaphis pyrarius, Metopolophium dirhodum, Myzus persicae, Myzus ascalonicus, Myzus cerasi, Myzus varians, Nasonovia ribis-nigri, Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Rhopalosiphum padi, Rhopalosiphum insertum, Sappaphis 30 mala, Sappaphis mali, Schizaphis graminum, Schizoneura lanuginosa, Sitobion avenae, Trialeurodes vaporariorum, Toxoptera aurantiiand, Viteus vitifolii, Cimex lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp., and Arilus critatus. ants, bees, wasps, sawflies (Hymenoptera), e.g. Athalia rosae, Atta cephalotes, Atta 35 capiguara, Atta cephalotes, Atta laevigata, Atta robusta, Atta sexdens, Atta texana, Crematogaster spp., Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharaonis, Solenopsis geminata, Solenopsis invicta, Solenopsis richteri, Solenopsis xyloni, Pogonomyrmex barbatus, Pogonomyrmex californicus, Pheidole megacephala, Dasymutilla occidentalis, Bombus spp. Vespula squamosa, Paravespula vulgaris, 40 Paravespula pennsylvanica, Paravespula germanica, Dolichovespula maculata, Vespa crabro, Polistes rubiginosa, Camponotus floridanus, and Linepithema humile, WO 2007/071609 PCT/EP2006/069686 41 crickets, grasshoppers, locusts (Orthoptera), e.g. Acheta domestica, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Schistocerca americana, Schistocerca gregaria, Dociostaurus 5 maroccanus, Tachycines asynamorus, Oedaleus senegalensis, Zonozerus variegatus, Hieroglyphus daganensis, Kraussaria angulifera, Calliptamus italicus, Chortoicetes terminifera, and Locustana pardalina, Arachnoidea, such as arachnids (Acarina), e.g. of the families Argasidae, Ixodidae and 10 Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Ambryomma maculatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Dermacentor andersoni, Dermacentor variabilis, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Ornithodorus moubata, Ornithodorus hermsi, 15 Ornithodorus turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus sanguineus, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, and Eriophyidae spp. such as Aculus schlechtendali, Phyllocoptrata oleivora and Eriophyes sheldoni; Tarsonemidae spp. such as Phytonemus pallidus and Polyphagotarsonemus latus; Tenuipalpidae spp. 20 such as Brevipalpus phoenicis; Tetranychidae spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and Oligonychus pratensis; Araneida, e.g. Latrodectus mactans, and Loxosceles reclusa, 25 fleas (Siphonaptera), e.g. Ctenocephalides felis, Ctenocephalides canis, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and Nosopsyllus fasciatus, silverfish, firebrat (Thysanura), e.g. Lepisma saccharina and Thermobia domestica, 30 centipedes (Chilopoda), e.g. Scutigera coleoptrata, millipedes (Diplopoda), e.g. Narceus spp., Earwigs (Dermaptera), e.g. forficula auricularia, 35 lice (Phthiraptera), e.g. Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus, 40 Plant parasitic nematodes such as root-knot nematodes, Meloidogyne arenaria, Meloidogyne chitwoodi, Meloidogyne exigua, Meloidogyne hapla, Meloidogyne WO 2007/071609 PCT/EP2006/069686 42 incognita, Meloidogyne javanica and other Meloidogyne species; cyst nematodes, Globodera rostochiensis, Globodera pallida, Globodera tabacum and other Globodera species, Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii, and other Heterodera species; seed gall nematodes, Anguina funesta, Anguina 5 tritici and other Anguina species; stem and foliar nematodes, Aphelenchoides besseyi, Aphelenchoides fragariae, Aphelenchoides ritzemabosi and other Aphelenchoides species; sting nematodes, Belonolaimus longicaudatus and other Belonolaimus species; pine nematodes, Bursaphelenchus xylophilus and other Bursaphelenchus species; ring nematodes, Criconema species, Criconemella species, Criconemoides 10 species, and Mesocriconema species; stem and bulb nematodes, Ditylenchus destructor, Ditylenchus dipsaci, Ditylenchus myceliophagus and other Ditylenchus species; awl nematodes, Dolichodorus species; spiral nematodes, Helicotylenchus dihystera, Helicotylenchus multicinctus and other Helicotylenchus species, Rotylenchus robustus and other Rotylenchus species; sheath nematodes, Hemicycliophora species 15 and Hemicriconemoides species; Hirshmanniella species; lance nematodes, Hoplolaimus columbus, Hoplolaimus galeatus and other Hoplolaimus species; false root-knot nematodes, Nacobbus aberrans and other Nacobbus species; needle nematodes, Longidorus elongates and other Longidorus species; pin nematodes, Paratylenchus species; lesion nematodes, Pratylenchus brachyurus, Pratylenchus 20 coffeae, Pratylenchus curvitatus, Pratylenchus goodeyi, Pratylencus neglectus, Pratylenchus penetrans, Pratylenchus scribneri, Pratylenchus vulnus, Pratylenchus zeae and other Pratylenchus species; Radinaphelenchus cocophilus and other Radinaphelenchus species; burrowing nematodes, Radopholus similis and other Radopholus species; reniform nematodes, Rotylenchulus reniformis and other 25 Rotylenchulus species; Scutellonema species; stubby root nematodes, Trichodorus primitivus and other Trichodorus species; Paratrichodorus minor and other Paratrichodorus species; stunt nematodes, Tylenchorhynchus claytoni, Tylenchorhynchus dubius and other Tylenchorhynchus species and Merlinius species; citrus nematodes, Tylenchulus semipenetrans and other Tylenchulus species; dagger 30 nematodes, Xiphinema americanum, Xiphinema index, Xiphinema diversicaudatum and other Xiphinema species; and other plant parasitic nematode species. The formulations are prepared in a known manner (see e.g. for review US 3,060,084, EP-A 707 445 (for liquid concentrates), Browning, "Agglomeration", Chemical 35 Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and et seq. WO 91/13546, US 4,172,714, US 4,144,050, US 3,920,442, US 5,180,587, US 5,232,701, US 5,208,030, GB 2,095,558, US 3,299,566, Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, Hance et al., Weed Control Handbook, 8th Ed., Blackwell 40 Scientific Publications, Oxford, 1989 and Mollet, H., Grubemann, A., Formulation technology, Wiley VCH Verlag GmbH, Weinheim (Germany), 2001, 2. D. A. Knowles, Chemistry and Technology of Agrochemical Formulations, Kluwer Academic WO 2007/071609 PCT/EP2006/069686 43 Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8), for example by extending the active compound with auxiliaries suitable for the formulation of agrochemicals, such as solvents and/or carriers, if desired emulsifiers, surfactants and dispersants, preservatives, antifoaming agents, anti-freezing agents, for seed treatment formulation 5 also optionally colorants and binders. Examples of suitable solvents are water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, 10 gamma-butyrolactone), pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may also be used. Examples of suitable carriers are ground natural minerals (for example kaolins, clays, 15 talc, chalk) and ground synthetic minerals (for example highly disperse silica, silicates). Suitable emulsifiers are nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates). 20 Examples of dispersants are lignin-sulfite waste liquors and methylcellulose. Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty 25 alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ether, 30 tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose. 35 Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, 40 ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone or water.
WO 2007/071609 PCT/EP2006/069686 44 Also anti-freezing agents such as glycerin, ethylene glycol, propylene glycol and bactericides such as can be added to the formulation. Suitable antifoaming agents are for example antifoaming agents based on silicon or 5 magnesium stearate. Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier. 10 Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, 15 for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers. In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 20 to 90% by weight, of the active compound(s). In this case, the active compound(s) are employed in a purity of from 90% to 100% by weight, preferably 95% to 100% by weight (according to NMR spectrum). The compounds of formula I can be used as such, in the form of their formulations or 25 the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible 30 distribution of the active compound(s) according to the invention. Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can 35 be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. However, it is also possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water. 40 The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1% per weight.
WO 2007/071609 PCT/EP2006/069686 45 The active compound(s) may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives. 5 The following are examples of formulations: 1. Products for dilution with water for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted. 10 A) Water-soluble concentrates (SL, LS) 10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, wetters or other auxiliaries are added. The active compound(s) dissolves upon dilution with water, whereby a formulation with 10 % (wlw) of active compound(s) is obtained. 15 B) Dispersible concentrates (DC) 20 parts by weight of the active compound(s) are dissolved in 75 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion, whereby a formulation with 20 20% (wlw) of active compound(s) is obtained. C) Emulsifiable concentrates (EC) 15 parts by weight of the active compound(s) are dissolved in 75 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in 25 each case 5 parts by weight). Dilution with water gives an emulsion, whereby a formulation with 15% (wlw) of active compound(s) is obtained. D) Emulsions (EW, EO, ES) 40 parts by weight of the active compound(s) are dissolved in 35 parts by weight of 30 xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifier machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion, whereby a formulation with 25% (wlw) of active compound(s) is obtained. 35 E) Suspensions (SC, OD, FS) In an agitated ball mill, 20 parts by weight of the active compound(s) are comminuted with addition of 10 parts by weight of dispersants, wetters and 70 parts by weight of water or of an organic solvent to give a fine active compound(s) suspension. Dilution 40 with water gives a stable suspension of the active compound(s), whereby a formulation with 20% (wlw) of active compound(s) is obtained.
WO 2007/071609 PCT/EP2006/069686 46 F) Water-dispersible granules and water-soluble granules (WG, SG) 50 parts by weight of the active compound(s) are ground finely with addition of 50 parts by weight of dispersants and wetters and made as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, 5 fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound(s), whereby a formulation with 50% (wlw) of active compound(s) is obtained. G) Water-dispersible powders and water-soluble powders (WP, SP, SS, WS) 10 75 parts by weight of the active compound(s) are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound(s) , whereby a formulation with 75% (wlw) of active compound(s) is obtained. 15 2. Products to be applied undiluted for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted. H) Dustable powders (DP, DS) 5 parts by weight of the active compound(s) are ground finely and mixed intimately with 20 95 parts by weight of finely divided kaolin. This gives a dustable product having 5% (wlw) of active compound(s) I) Granules (GR, FG, GG, MG) 0.5 part by weight of the active compound(s) is ground finely and associated with 95.5 25 parts by weightof carriers, whereby a formulation with 0.5% (wlw) of active compound(s) is obtained. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted for foliar use. J) ULV solutions (UL, LS) 30 10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product having 10% (wlw) of active compound(s), which is applied undiluted for foliar use. Various types of oils, wetters, adjuvants, herbicides, fungicides, other pesticides, or 35 bactericides may be added to the active ingredients, if appropriate just immediately prior to use (tank mix). These agents usually are admixed with the agents according to the invention in a weight ratio of 1:10 to 10:1. The compounds of formula I are effective through both contact (via soil, glass, wall, bed 40 net, carpet, plant parts or animal parts), and ingestion (bait, or plant part) and through trophallaxis and transfer.
WO 2007/071609 PCT/EP2006/069686 47 According to a preferred embodiment of the invention, the compounds of formula I are employed via soil application. Soil application is especially favorable for use against ants, termites, crickets, or cockroaches. 5 According to another preferred embodiment of the invention, for use against non crop pests such as ants, termites, wasps, flies, mosquitoes, crickets, locusts, or cockroaches the compounds of formula I are prepared into a bait preparation. The bait can be a liquid, a solid or a semisolid preparation (e.g. a gel). Solid baits can 10 be formed into various shapes and forms suitable to the respective application e.g. granules, blocks, sticks, disks. Liquid baits can be filled into various devices to ensure proper application, e.g. open containers, spray devices, droplet sources, or evaporation sources. Gels can be based on aqueous or oily matrices and can be formulated to particular necessities in terms of stickiness, moisture retention or aging characteristics. 15 The bait employed in the composition is a product which is sufficiently attractive to incite insects such as ants, termites, wasps, flies, mosquitoes, crickets etc. or cockroaches to eat it. This attractant may be chosen from feeding stimulants or para and I or sex pheromones. Suitable feeding stimulants are chosen, for example, from 20 animal and/or plant proteins (meat-, fish- or blood meal, insect parts, crickets powder, egg yolk), from fats and oils of animal and/or plant origin, or mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose, glucose, starch, pectin or even molasses or honey, or from salts such as ammonium sulfate, ammonium carbonate or ammonium acetate. Fresh or decaying parts of fruits, crops, 25 plants, animals, insects or specific parts thereof can also serve as a feeding stimulant. Pheromones are known to be more insect specific. Specific pheromones are described in the literature and are known to those skilled in the art. The compounds of formula I are also suitable for the protection of the seed, plant 30 propagules and the seedlings' roots and shoots, preferably the seeds, against soil pests and also for the treatment plant seeds which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods. Conventional seed treatment formulations include for example flowable concentrates 35 FS, solutions LS, powders for dry treatment DS, water dispersible powders WS or granules for slurry treatment, water soluble powders SS and emulsion ES. Application to the seeds is carried out before sowing, either directly on the seeds. The seed treatment application of the compounds of formula I or formulations 40 containing them is carried out by spraying or dusting the seeds before sowing of the plants and before emergence of the plants.
WO 2007/071609 PCT/EP2006/069686 48 The invention also relates to the propagation product of plants, and especially the treated seed comprising, that is, coated with and/or containing, a compound of formula I or a composition comprising it. The term "coated with and/or containing" generally signifies that the active ingredient is for the most part on the surface of the propagation 5 product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product, depending on the method of application. When the said propagation product is (re)planted, it may absorb the active ingredient. The seed comprises the inventive compounds or compositions comprising them in an 10 amount of from 0,1 g to 10 kg per 100 kg of seed. Compositions of this invention may also contain other active ingredients, for example other pesticides, insecticides, herbicides, fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators, safeners and 15 nematicides. These additional ingredients may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix). For example, the plant(s) may be sprayed with a composition of this invention either before or after being treated with other active ingredients. 20 The following list of pesticides together with which the compounds according to the invention can be used, is intended to illustrate the possible combinations, but not to impose any limitation: A.1. Organo(thio)phosphates: acephate, azamethiphos, azinphos-methyl, chlorpyrifos, 25 chlorpyrifos-methyl, chlorfenvinphos, diazinon, dichlorvos, dicrotophos, dimethoate, disulfoton, ethion, fenitrothion, fenthion, isoxathion, malathion, methamidophos, methidathion, methyl-parathion, mevinphos, monocrotophos, oxydemeton-methyl, paraoxon, parathion, phenthoate, phosalone, phosmet, phosphamidon, phorate, phoxim, pirimiphos-methyl, profenofos, prothiofos, sulprophos, tetrachlorvinphos, 30 terbufos, triazophos, trichlorfon; A.2. Carbamates: alanycarb, aldicarb, bendiocarb, benfuracarb, carbaryl, carbofuran, carbosulfan, fenoxycarb, furathiocarb, methiocarb, methomyl, oxamyl, pirimicarb, propoxur, thiodicarb, triazamate; 35 A.3. Pyrethroids: allethrin, bifenthrin, cyfluthrin, cyhalothrin, cyphenothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, zeta-cypermethrin, deltamethrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, imiprothrin, lambda-cyhalothrin, permethrin, prallethrin, pyrethrin I and II, resmethrin, silafluofen, tau-fluvalinate, 40 tefluthrin, tetramethrin, tralomethrin, transfluthrin; WO 2007/071609 PCT/EP2006/069686 49 A.4. Growth regulators: a) chitin synthesis inhibitors: benzoylureas: chlorfluazuron, cyramazin, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron, triflumuron; buprofezin, diofenolan, hexythiazox, etoxazole, clofentazine; b) ecdysone antagonists: halofenozide, methoxyfenozide, tebufenozide, 5 azadirachtin; c) juvenoids: pyriproxyfen, methoprene, fenoxycarb; d) lipid biosynthesis inhibitors: spirodiclofen, spiromesifen, a tetronic acid derivative of formula F 1 ,
CH
2 CH3 0 O (F 1 ) H3'
OH
3 HO A.5. Nicotinic receptor agonists/antagonists compounds: clothianidin, dinotefuran, imidacloprid, thiamethoxam, nitenpyram, acetamiprid, thiacloprid; 10 A.6. GABA antagonist compounds: acetoprole, endosulfan, ethiprole, fipronil, vaniliprole; A.7. Macrocyclic lactone insecticides: abamectin, emamectin, milbemectin, lepimectin, 15 spinosad; A.8. METI I acaricides: fenazaquin, pyridaben, tebufenpyrad, tolfenpyrad; A.9. METI II and III compounds: acequinocyl, fluacyprim, hydramethylnon; 20 A.10. Uncoupler compounds: chlorfenapyr; A.11. Oxidative phosphorylation inhibitor compounds: cyhexatin, diafenthiuron, fenbutatin oxide, propargite; 25 A.12. Moulting disruptor compounds: cryomazine; A.13. Mixed Function Oxidase inhibitor compounds: piperonyl butoxide; A.14. Sodium channel blocker compounds: indoxacarb, metaflumizone; 30 A.15. Various: benclothiaz, bifenazate, cartap, flonicamid, pyridalyl, pymetrozine, sulfur, thiocyclam, N-R'-2,2-dihalo-1l-R"cyclo-propanecarboxamide-2-(2,6-dichloro amm,c -tri-fluoro-p-tolyl)hydrazone or N-R'-2,2-di(R"')propionamide-2-(2,6-dichloro a ,, -trifluoro-p-tolyl)-hydrazone, wherein R' is methyl or ethyl, halo is chloro or 35 bromo, R" is hydrogen or methyl and R"' is methyl or ethyl, and the aminoisothiazole compounds of formula F 2
,
WO 2007/071609 PCT/EP2006/069686 50 CI R N R
(F
2 ) N-S 0 0 wherein R i is -CH 2 0CH 2
CH
3 or H and R i i is CF 2
CF
2
CF
3 or CH 2
CH(CH
3
)
3 , anthranilamide compounds of formula F 3 B
CH
3 N 2 R H (F3)' ON Cl RB H 5 wherein B 1 is hydrogen, chlorine or cyano, B 2 is a bromine atom or CF 3 , and RB is H,
CH
3 or CH(CH 3
)
2 . Some of the mixtures of compounds I with the above pesticides exhibit a synergistic pesticidal effect. 10 The insects may be controlled by contacting the target parasite/pest, its food supply, habitat, breeding ground or its locus with a pesticidally effective amount of compounds of or compositions of formula I. 15 "Locus" means a habitat, breeding ground, plant, seed, soil, area, material or environment in which a pest or parasite is growing or may grow. In general, "pesticidally effective amount" means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, 20 death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The pesticidally effective amount can vary for the various compounds/compositions used in the invention. A pesticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired pesticidal effect and duration, weather, target species, 25 locus, mode of application, and the like. The compounds or compositions of the invention can also be applied preventively to places at which occurrence of the pests is expected. 30 The compounds of formula I may also be used to protect growing plants from attack or infestation by pests by contacting the plant with a pesticidally effective amount of compounds of formula I. As such, "contacting" includes both direct contact (applying the compounds/compositions directly on the pest and/or plant - typically to the foliage, WO 2007/071609 PCT/EP2006/069686 51 stem or roots of the plant) and indirect contact (applying the compounds/compositions to the locus of the pest and/or plant). In the case of soil treatment or of application to the pests dwelling place or nest, the 5 quantity of active ingredient ranges from 0.0001 to 500 g per 100 m 2 , preferably from 0.001 to 20 g per 100 m 2 . For use in bait compositions, the typical content of active ingredient is from 0.0001 weight % to 15 weight %, desirably from 0.001 weight % to 5% weight % of active 10 compound. The composition used may also comprise other additives such as a solvent of the active material, a flavoring agent, a preserving agent, a dye or a bitter agent. Its attractiveness may also be enhanced by a special color, shape or texture. For use in treating crop plants, the rate of application of the active ingredients of this 15 invention may be in the range of 0.1 g to 4000 g per hectare, desirably from 25 g to 600 g per hectare, more desirably from 50 g to 500 g per hectare. Compounds of formula I and compositions comprising them can also be used for controlling and preventing infestations and infections in animals including warm 20 blooded animals (including humans) and fish. They are for example suitable for controlling and preventing infestations and infections in mammals such as cattle, sheep, swine, camels, deer, horses, pigs, poultry, rabbits, goats, dogs and cats, water buffalo, donkeys, fallow deer and reindeer, and also in fur-bearing animals such as mink, chinchilla and raccoon, birds such as hens, geese, turkeys and ducks and fish 25 such as fresh- and salt-water fish such as trout, carp and eels. Infestations in warm-blooded animals and fish include, but are not limited to, lice, biting lice, ticks, nasal bots, keds, biting flies, muscoid flies, flies, myiasitic fly larvae, chiggers, gnats, mosquitoes and fleas. 30 The compounds of formula I and compositions comprising them are suitable for systemic and/or non-systemic control of ecto- and/or endoparasites. They are active against all or some stages of development. 35 Administration can be carried out both prophylactically and therapeutically. Administration of the active compounds is carried out directly or in the form of suitable preparations, orally, topically/dermally or parenterally. For oral administration to warm-blooded animals, the formula I compounds may be 40 formulated as animal feeds, animal feed premixes, animal feed concentrates, pills, solutions, pastes, suspensions, drenches, gels, tablets, boluses and capsules. In addition, the formula I compounds may be administered to the animals in their drinking WO 2007/071609 PCT/EP2006/069686 52 water. For oral administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the formula I compound, preferably with 0.5 mg/kg to 100 mg/kg of animal body weight per day. 5 Alternatively, the formula I compounds may be administered to animals parenterally, for example, by intraruminal, intramuscular, intravenous or subcutaneous injection. The formula I compounds may be dispersed or dissolved in a physiologically acceptable carrier for subcutaneous injection. Alternatively, the formula I compounds may be formulated into an implant for subcutaneous administration. In addition the formula I 10 compound may be transdermally administered to animals. For parenteral administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the formula I compound. The formula I compounds may also be applied topically to the animals in the form of 15 dips, dusts, powders, collars, medallions, sprays, shampoos, spot-on and pour-on formulations and in ointments or oil-in-water or water-in-oil emulsions. For topical application, dips and sprays usually contain 0.5 ppm to 5,000 ppm and preferably 1 ppm to 3,000 ppm of the formula I compound. In addition, the formula I compounds may be formulated as ear tags for animals, particularly quadrupeds such as cattle and 20 sheep. Suitable preparations are: - Solutions such as oral solutions, concentrates for oral administration after dilution, 25 solutions for use on the skin or in body cavities, pouring-on formulations, gels; - Emulsions and suspensions for oral or dermal administration; semi-solid preparations; - Formulations in which the active compound is processed in an ointment base or in an oil-in-water or water-in-oil emulsion base; 30 - Solid preparations such as powders, premixes or concentrates, granules, pellets, tablets, boluses, capsules; aerosols and inhalants, and active compound-containing shaped articles. Generally it is favorable to apply solid formulations which release compounds of 35 formula I in total amounts of 10 mg/kg to 300 mg/kg, preferably 20 mg/kg to 200 mg/kg. The active compounds can also be used as a mixture with synergists or with other active compounds which act against pathogenic endo- and ectoparasites. In general, the compounds of formula I are applied in parasiticidally effective 40 amountmeaning the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target WO 2007/071609 PCT/EP2006/069686 53 organism. The parasiticidally effective amount can vary for the various compounds/compositions used in the invention. A parasiticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired parasiticidal effect and duration, target species, mode of application, and the like. 5 Synthesis Examples With due modification of the starting compounds, the protocols shown in the synthesis examples below were used for obtaining further compounds I. The resulting 10 compounds, together with physical data, are listed in the Table I which follows. The products were characterized by coupled High Performance Liquid Chromatography / mass spectrometry (HPLC/MS), by NMR or by their melting points. 15 HPLC method 1: Analytical HPLC column: RP-18 column Chromolith Speed ROD from Merck KgaA, Germany). Elution: acetonitrile + 0.1% trifluoroacetic acid (TFA) / water + 0.1% trifluoroacetic acid (TFA) in a ratio of from 5:95 to 95:5 in 5 minutes at 40 'C. MS: Quadrupol electrospray ionisation, 80 V (positiv modus) 20 HPLC method 2: Analytical HPLC column: Zorbax Rapid Resolution Cartridge S-C18 (2.1 x 30mm, 3.5 micron). Elution: acetonitrile I water + 0.02% trifluoroacetic acid in a ratio of from 15:85 to 97:3 in 7 min at 40' C. MS: Quadrupol electrospray ionisation, 80 V (positiv modus) 25 The conditions for preparative HPLC were as follows: Purospher Star RP18e Hibar RT 75-25 column (3 pm), elution: acetonitrile + 0.1% trifluoroacetic acid (TFA) / water + 0.1% trifluoroacetic acid (TFA) in a ratio of from 20:80 to 100:0 in 13 minutes, detection by UV at 205 nm, 214 nm, 254 nm, 280 nm and 400 nm or by MS. 30 Example 1, compound I-1: Preparation of 2-(3,4-dichloro-benzyl)-2 trifluoromethylsulfanylmethyl-malononitrile To 113 mg (0.5 mmol) of 3,4-dichlorobenzylmalonodinitrile and 138 mg (1.0 mmol) of potassium carbonate in 1 mL of dimethylformamide in an 8 mL vial was added 53 pl 35 (75 mg, 0.5 mmol) of trifluoromethylthiomethyl chloride. The mixture was shaken at about 20 to 25'C for 12 hours and then poured into a mixture of diethylether and water. The aqueous layer was separated and extracted twice more with diethylether (2 x 20 ml). The combined ether fractions were dried using phase separating paper and then concentrated by rotoevaporation. The residue was purified by preparative HPLC to give 40 79 mg (0.23 mmol, 46% yield) of I-1.
WO 2007/071609 PCT/EP2006/069686 54 Example 2, compound 1-7: Preparation of 2-(3,4-Dichloro-benzyl)-2-(2 trifluoromethylsulfanyl-ethyl)-malononitrile To 107 pl (146 mg, 1 mmol) of trifluoromethylthioethanol in an 8 mL vial fitted with a 5 septum and needle outlet was added 76 pl (208 mg, 1 mmol) of thionyl bromide. The mixture was heated at about 60'C for 20 min, and was then transferred to a second vial containing 113 mg (0.5 mmol) of 3,4-dichlorobenzylmalonodinitrile and 276 mg (2 mmol) of potassium carbonate in 0.5 mL of dimethylformamide at about 20 to 25'C. After 10 hours shaking, the contents of the vial were poured into diethylether and 10 water. The aqueous layer was separated and extracted twice more with diethylether.The combined ether fractions were dried using phase separating paper and then concentrated by rotoevaporation. The residue was purified by preparative HPLC to give 70 mg (0.2 mmol, 40% yield) of compound 1-7. 15 Example 3, compounds 1-15 and compounds 1-19. Preparation of 2-(3,4-Dichloro benzyl)-2-(2-trifluoromethanesulfinyl-ethyl)-malononitrile (1-15) and 2-(3,4-Dichloro benzyl)-2-(2-trifluoromethanesulfonyl-ethyl)-malononitrile (1-19) 20 Synthesis of trifluoromethylsulfinylethyl p-toluenesulfonate To 1.46 gm (10 mmol) of trifluoromethylthioethanol and 1.4 mL (1.0 mg, 10 mmol) of triethylamine in 30 mL of dichloromethane at O'C was added 1.9 mg (10 mmol) of p-toluenesulfonyl chloride. The reaction was then stirred at 20 to 25'C for 22 hours. 25 The reaction mixture was washed twice with brine solution, and the organic layer was dried using phase separating paper. Removal of solvent by rotoevaporation and purification of the crude product by flash column chromatography on silica gel gave 1.91 mg (6.36 mmol, 64% yield) of trifluoromethylthioethyl p-toluenesulfonate. 30 To 600 mg (2.0 mmol) of trifluoromethylthioethyl p-toluenesulfonate in 10 mL of dichloromethane at 20 to 25'C was added 493 mg (2.2 mmol of peracid) of 77% m chloroperbenzoic acid. After stirring for about 12 hours, the mixture was washed with aqueous sodium sulfite, aqueous sodium bicarbonate, and the organic layer was dried using phase separating paper. Removal of solvent by rotoevaporation gave 630 mg 35 (2.0 mmol, 100% yield) of trifluoromethylsulfinylethyl p-toluenesulfonate. Example 3.1, compound 1-15 To 117mg (0.52 mmol) of 3,4-dichlorobenzylmalonodinitrile and 79 mg (0.57 mmol) of 40 potassium carbonate in 1 mL of DMF was added 165 mg (0.52 mmol) of trifluoromethylsulfinylethyl p-toluenesulfonate. The mixture was shaken for 12 hours at 35'C. After 21 hours, the reaction mixture was added to diethylether and water WO 2007/071609 PCT/EP2006/069686 55 containing 50 pL of formic acid. The aqueous phase was separated and washed twice with diethylether. The combined ether fractions were washed with brine and dried using phase separating paper. The solvent was removed by rotoevaporation, and the residue was dissolved in 1 mL of dichloromethane and filtered using dichloromethane (3 x 3 5 mL) through a short column of silica gel. After concentration of the eluate, 87 mg (0.24 mmol, 46% yield) of 1-15 was recovered as a tan solid, mp 122.5-129.5'C. The compound could be recrystallized from acetonitrile/hexane. Example 3.2, compound 1-19 10 To approximately 92 mg (0.25 mmol) of compound 1-15 in 2 mL of dichloromethane was added 200 mg (0.9 mmol of peracid) of 77% m-chloroperbenzoic acid. After stirring for 12 hours, the reaction mixture was diluted with dichloromethane and washed with aqueous sodium sulfite, aqueous sodium bicarbonate. The organic layer 15 was dried using phase separating paper. Removal of solvent by rotoevaporation and purification of the residue by preparative HPLC gave 75 mg (0.19 mmol, 76% yield) of 1-19 , mp. 164-169'C.
WO 2007/071609 PCT/EP2006/069686 56 ++ + + + 0') LO LO LO a) NCY) CY LO C m C) 1 0I II I E 11 011 -o r- r- N -N N Lo N N N 0 N 0 N 0 cm EE E E E Qc E E opE E C Fn; 0~-~- - - - CY) C) 0 ~0- 0)0~( 0) ~LC)L6 CN LC) LC) L6L6 >< CO CO) C/ CO C ) CO C/ CO/C)C CO) Cl ClCl Cl 00 00 0 0 L I I I L L L co I I I I I m mz0U 0 0 U-0 <~ I / t cyi cyi 4 4 cC C)dN (Y CN _Y_____r O a WO 2007/071609 PCT/EP2006/069686 57 + + + + + ++ + No O LoC r Y CY) LO) 0 mQ 0 N N N N N N N N N N N N N U~ . E E E E E E E E E E E E E E SE E~ E E E E E E E E E E CO f'o - oo N- ,I- r- rl- Q( L ,0 C -D-i I -I- -,I- - r - - I-y) c) co co co co co co co co co co co co co co c U) - - U U) U- - U) U- U) - U U - L 0 00 00 00 00 00 0 00 0 0000000000000 0 0 00 00 00 00 00 0 00 0 0 I < CO Li ) 0 0 N COI 0 L ~ I o UL 00000 0 0-s Co U 0 IN 4 0 0 0 4 4 ) I - 4 N 0) 0 1- LL 0~ ) 0 N 't LO CD r-l_~ -~ CC) 0' C CN mN ;T LO CD CN- OD Z - C C C C WO 2007/071609 PCT/EP2006/069686 58 + + + + + + + + + ++ QY ) ) CV) CN a) CV) N CY) CY) LO NN NY ) 0 CII CI CII) iiII) 0II CII4C4 - c N N N N N N N N N tE E E E E E E (.o E E E r - - - c N 5 c > EH S; S; C: 11 C: EZ E E E H E E E E E UO CV) CY) Mt 0 0N N N CO CV) r N Y 0 N MU) ~L .4 U) S i ~ui 0 iiii i ii i ii ii o SC C CO) C) C) CO) ) CO) 0 0 0) I II III NI IN IN I NNN N IN IN IN 0 0 0 00 0 f 0 If0 0 0 000 N N0 N N NO 0 0 0 0 0 0 0000 I I I I I I I I I I I WO 2007/071609 PCT/EP2006/069686 59 N C,4 LO LO - N U) N y N Y UY C) CU) CN r-4 N N N N N N - tE E E E E E E E CO aO - - (1 'I C >LH C C C' C ,I C U) c U) U) U) s N N _0 0 ii r r r 0 0 00000 000 0 0 0 0 0 0 0 L) , I, 1 0 0 N- No No N N r) rL r- r) r N a 0 0 0 0 US I C)cl) 00000 0 0 0 Eu C') 0 0 00 al) OEu * 0 - N Si- U) 5 cl 0 WO 2007/071609 PCT/EP2006/069686 60 Examples for the action against harmful pests: 1. Activity against Boll weevil (Anthonomus grandis) 5 The active compounds were formulated in 1:3 DMSO : water. 10 to 15 eggs were placed into microtiterplates filled with 2% agar-agar in water and 300 ppm formaline. The eggs were sprayed with 20 pl of the test solution, the plates were sealed with pierced foils and kept at 24-26'C and 75-85% humidity with a day/night cycle for 3 to 5 days. Mortality was assessed on the basis of the remaining unhatched eggs or larvae 10 on the agar surface and/or quantity and depth of the digging channels caused by the hatched larvae. Tests were replicated 2 times. In this test, compounds I-1, 1-2, 1-3, 1-4, 1-5, 1-6, 1-7, 1-8, 1-9, 1-10, 1-11, 1-13, 1-14, 1-15, 1 16, 1-17, 1-18. 1-19, 1-20, 1-21, 1-22, 1-23, 1-24, 1-25, 1-26, 1-27, 1-29, 1-31, 1-32, 1-33, 1-34, 15 and 1-43 at 2500 ppm showed over 75 % mortality compared to 0% mortality of untreated controls. 2. Activity against Mediterranean fruitfly (Ceratitis capitata) 20 The active compounds were formulated in 1:3 DMSO : water. 50 to 80 eggs were placed into microtiterplates filled with 0.5% agar-agar and 14 % diet in water. The eggs were sprayed with 5 pl of the test solution, the plates were sealed with pierced foils and kept at 27-29'C and 75-85% humidity under fluorescent light for 6 days. Mortality was assessed on the baswas of the agility of the hatched larvae. Tests were replicated 2 25 times. In this test, compounds I-1, 1-2, 1-3, 1-4, 1-5, 1-6, 1-7, 1-8, 1-9, 1-10, 1-11, 1-13, 1-14, 1-15, 1 16, 1-17, 1-18. 1-19, 1-20, 1-21, 1-22, 1-23, 1-24, 1-26, 1-27, 1-29, 1-30, 1-31, 1-33, and 1-34 at 2500 ppm showed over 75 % mortality compared to 0% mortality of untreated controls. 30 3. Activity against Tobacco budworm (Heliothis virescens) The active compounds are formulated in 1:3 DMSO : water. 15 to 25 eggs are placed into microtiterplates filled with diet. The eggs are sprayed with 10 pl of the test solution, 35 the plates are sealed with pierced foils and kept at 27-29'C and 75-85% humidity under fluorescent light for 6 days. Mortality is assessed on the basis of the agility and of comparative feeding of the hatched larvae. Tests are replicated 2 times. 4. Activity against Vetch aphid (Megoura viciae) 40 The active compounds were formulated in 1:3 DMSO : water. Bean leaf disks were placed into microtiterplates filled with 0.8% agar-agar and 2.5 ppm OPUSTM. The leaf WO 2007/071609 PCT/EP2006/069686 61 disks were sprayed with 2.5 pl of the test solution and 5 to 8 adult aphids were placed into the microtiterplates which were then closed and kept at 22-24'C and 35-45% under fluorescent light for 6 days. Mortality was assessed on the basis of vital, reproduced aphids. Tests were replicated 2 times. 5 In this test, compounds 1-6, 1-7, 1-8, 1-9, 1-10, 1-11, 1-16, 1-21, 1-24, 1-27, 1-29, 1-31, 1-37, and 1-42 at 2500 ppm showed over 75 % mortality compared to 0% mortality of untreated controls. 10 5. Activity against Wheat aphid (Rhopalosiphum padi) The active compounds are formulated in 1:3 DMSO : water. Barlay leaf disk are placed into microtiterplates filled with 0.8% agar-agar and 2.5 ppm OPUSTM .The leaf disks are sprayed with 2.5 pl of the test solution and 3 to 8 adult aphids are placed into the 15 microtiterplates which are then closed and kept at 22-24'C and 35-45% humidity under fluorescent light for 5 days. Mortality is assessed on the basis of vital aphids. Tests are replicated 2 times. 6. Activity against Cotton aphid (Aphis gossypii) 20 The active compounds are formulated in 50:50 acetone:water and 100 ppm KineticTM surfactant. Cotton plants at the cotyledon stage (one plant per pot) are infested by placing a 25 heavily infested leaf from the main colony on top of each cotyledon. The aphids are allowed to transfer to the host plant overnight, and the leaf used to transfer the aphids is removed. The cotyledons are dipped in the test solution and allowed to dry. After 5 days, mortality counts are made. 30 7. Activity against Southern armyworm (Spodoptera eridania), 2nd instar larvae The active compounds are formulated for testing the activity against insects and arachnids as a 10.000 ppm solution in a mixture of 35% acetone and water, which is diluted with water, if needed. 35 A Sieva lima bean leaf is dipped in the test solution and allowed to dry. The leaf is then placed in a petri dish containing a filter paper on the bottom and ten 2nd instar caterpillars. At 5 days, observations are made of mortality and reduced feeding. 40 8. Activity against Argentine ant (Linepithema humile), harvester ant (Pogonomyrmex californicus), acrobat ant (Crematogaster spp.), carpenter ant (Camponotus floridanus), fire ant (Solenopsis invicta), house fly (Musca domestica), stable fly (Stomoxys WO 2007/071609 PCT/EP2006/069686 62 calcitrans), flesh fly (Sarcophaga sp.), yellowfever mosquito (Aedes aegyptii), house mosquito (Culex quinquefasciatus), malaria mosquito (Anopheles albimanus), German cockroach (Blattella Germanica), cat flea (Ctenocephalides felis), and brown dog tick (Rhipicephalus sanguineus) via glass contact 5 Glass vials are treated with 0.5 ml of a solution of active ingredient in acetone and allowed to dry. Insects or ticks are placed into each vial together with some food and moisture supply. The vials are kept at 22 oC and are observed for treatment effects at various time intervals. 10 9. Activity against yellowfever mosquito (Aedes aegyptii), house mosquito (Culex quinquefasciatus) and malaria mosquito (Anopheles albimanus) larvae via water treatment 15 Well plates are used as test arenas. The active ingredient is dissolved in acetone and diluted with water to obtain the concentrations needed. The final solutions containing appr. 1% acetone are placed into each well. Approximately 10 mosquito larvae (4 t h instars) in 1 ml water are added to each well. Larvae are fed one drop of liver powder each day. The dishes are covered and maintained at 22°C. Mortality is recorded daily 20 and dead larvae and live or dead pupae are removed daily. At the end of the test remaining live larvae are recorded and percent mortality is calculated. 10. Activity against brown planthopper (nilaparvata lugens) 25 The active compounds were formulated in 50:50 acetone:water. Potted rice seedlings were sprayed with 10 ml test solution, air dried, placed in cages and inoculated with 10 adults. Percent mortality was recorded after 24, 72 and 120 hours. In this test, compound 1-35 at 300 ppm showed over 90% mortality. 30

权利要求:
Claims (11)
[1] 1. Compounds of formula I A 0 X R (I) NC CN 5 wherein X is oxygen or S(=O)n; n is 0,1 or 2; 10 R 1 is C 1 -C 6 -alkyl, C 1 - C 6 -haloalkyl, C
[2] 2 - C 6 -alkenyl, C 2 - C 6 -haloalkenyl, C 2 - C 6 alkynyl, C 3 - C 6 -haloalkynyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -halocycloalkyl, C 3 -C 6 cycloalkenyl, C 3 -C 6 -halocycloalkenyl, 15 phenyl or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which heteroaromatic ring is bonded to the X atom via a carbon atom of the ring, and which phenyl or which heteraromatic ring may be bonded via a C 1 -C 1 0 alkyl group thus forming an aryl-C1-C0io-alkyl or hetaryl-C 1 -C 1 o-alkyl moiety, 20 wherein phenyl or the heteroaromatic ring may be fused to a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, 25 wherein the hydrogen atoms in the above groups R 1 may be partially or in total be replaced by any combination of groups R 5 . A is -NRb 2 , -C(=G)GRb, -C(=G)NRb 2 , -C(=NORb)Rb, C(=G)[N=SRb 2 ], 30 -C(=G)NRb-NRb 2 , wherein two groups Rb together may form a C 2 -C 6 alkandiyl, C 2 -C 6 -alkenediyl or C 1 -C 3 -alkyl-G-C i -C 3 -alkyl bridge which may be substituted by 1 to 5 groups R 2 , phenyl or a 3- to 7-membered saturated or partially unsaturated heterocyclic 35 ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteroaromatic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl, the heterocyclic ring, or the heteroaromatic ring may be 40 fused to a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 WO 2007/071609 PCT/EP2006/069686 64 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl or the 5- to 6-membered heteroaromatic ring or the respective fused ring systems may be unsubstituted or substituted by any 5 combination of 1 to 6 groups R 2 . B is a saturated or partially unsaturated hydrocarbon chain with one to 3 carbon chain atoms, wherein the hydrogen atoms of this chain may all or in part be replaced with any combination of groups selected from R 3 ; 10 D is a saturated or partially unsaturated hydrocarbon chain with one to 5 carbon chain atoms or C3-06-cycloalkyl, wherein the hydrogen atoms of this chain or of this cycloalkyl may all or in part be replaced with any combination of groups selected from R 4 15 R 2 is halogen, cyano, nitro, hydroxy, mercapto, amino, C1-C6-alkyl, C2-06-alkenyl, C2-06-alkynyl, C3-06-cycloalkyl, C3-06-cycloalkenyl, C 1 -C 6 -haloalkyl, C 2 -0 6 -haloalkenyl, C 2 -0 6 -haloalkynyl, C3-06 halocycloalkyl, C3-06-halocycloalkenyl, C-C 6 -alkoxy, C2-06 20 alkenyloxy, C3-06-alkynyloxy, C-C 6 -haloalkoxy, C2-06 haloalkenyloxy, C 3 -0 6 -haloalkynyloxy, C3-06-cycloalkyloxy, C3-06 cycloalkenyloxy, C3-06-halocycloalkyloxy, C3-06-halocycloalkenyloxy, C-C 6 -alkylthio, C-C 6 -haloalkylthio, C 3 -0 6 -cycloalkylthio, C3-06 halocycloalkylthio, C1-C 6 -alkylsulfinyl, C 2 -0 6 -alkenylsulfinyl, C3-06 25 alkynylsulfinyl, C-C 6 -haloalkylsulfinyl, C 2 -0 6 -haloalkenylsulfinyl, C 3 -0 6 -haloalkynylsulfinyl, C01-C6-alkylsulfonyl, C 2 -0 6 -alkenylsulfonyl, C3-06-alkynylsulfonyl, C-C 6 -haloalkylsulfonyl, C2-06 haloalkenylsulfonyl, C 3 -0 6 -haloalkynylsulfonyl, C01-C6-alkylamino, C2-06-alkenylamino, C2-06-alkynylamino, di(C-C 6 -alkyl)amino, 30 di(C 2 -0 6 -alkenyl)amino, di(C 2 -0 6 -alkynyl)amino, tri(Ci-Cio)alkylsilyl, or phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from 35 oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which phenyl and which heteroaromatic ring may be bonded via an oxygen or a sulfur atom or a C01-C4-alkyl-group, 40 wherein the above groups R 2 are unsubstituted, or the hydrogen atoms in these groups may all or in part be replaced with any combination of groups selected from Ra, or WO 2007/071609 PCT/EP2006/069686 65 R 2 is -C(=G)Rb, -C(=G)ORb, -C(=G)NRb 2 , -C(=G)[N=SRb 2 ], -C(=NORb)Rb, -C(=NORb)NRb 2 , -C(=NNRb 2 )Rb, -OC(=G)-OC(=G)ORb, N=SRb 2 , -NRbC(=G)Rb, -N[C(=G)Rb] 2 , -NRbC(=G)ORb, -C(=G)NRb-NRb 2 , 5 -C(=G)NRb-NRb [C(=G)Rb], -NRb-C(=G)NRb 2 , -NRb-NRbC(=G)Rb, -NRb-N[C(=G)Rb] 2 , -N[(C=G)Rb]-NRb 2 , -NRb-NRb[(C=G)GRb], -NRb[(C=G)NRb 2 , -NRb[C= NRb]Rb, -NRb(C= NRb)NRb 2 , -O-NRb 2 , -O-NRb(C=G)Rb, -SO 2 NRb 2 , -NRbSO 2 Rb, -S(=0)Rb, -S(=0) 2 Rb, SO20Rb, or -OSO 2 Rb; 10 R 3 is halogen, cyano, amino, C1-Co10-alkyl, C1-C0io-haloalkyl, C2-C010 alkenyl, C 2 -C0 1 o-haloalkenyl, C2-Clo0-alkynyl, C 3 -C10-haloalkynyl, C3-06 cycloalkyl, C3-06-halocycloalkyl, C3-06-cycloalkenyl, C3-06 halocycloalkenyl, C0 1 -C 6 -alkoxy, C2-06-alkenyloxy, C3-06-alkynyloxy, 15 C0 1 -C 6 -haloalkoxy, C 2 -0 6 -haloalkenyloxy, C 3 -0 6 -haloalkynyloxy, or phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring 20 system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which phenyl or which heterocyclic or heteroaromatic ring may be bonded via an oxygen or a sulfur atom, or 2 groups R 3 together with the carbon atom of the hydrocarbon chain 25 may form a 3- to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen, wherein the above groups R 3 are unsubstituted, or the hydrogen 30 atoms in these groups may all or in part be replaced with any combination of groups selected from Ra, or R 4 is halogen, cyano, amino, C01-C6-alkyl, C0 1 -C 6 -haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C 3 -0 6 -haloalkynyl, C3-06-cycloalkyl, 35 C3-06-halocycloalkyl, C3-06-cycloalkenyl, C3-06-halocycloalkenyl, Ci C 6 -alkoxy, C2-06-alkenyloxy, C3-06-alkynyloxy, C0 1 -C 6 -haloalkoxy, C2 C 6 -haloalkenyloxy, C 3 -0 6 -haloalkynyloxy, C0 1 -C 6 -alkoxycarbonyl, Ci C6-alkenyloxycarbonyl, C01-C6-alkylamino, di(C 1 -C 6 -alkyl)amino, tri(Ci-C0io)alkylsilyl, or 40 phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from WO 2007/071609 PCT/EP2006/069686 66 oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which phenyl and which heterocyclic or heteroaromatic ring may be bonded via an oxygen or a sulfur atom, 5 wherein the above groups R 4 are unsubstituted, or the hydrogen atoms in these groups may all or in part be replaced with any combination of groups selected from Ra, or 10 the moiety R 4 -D-X-R 1 together may form a saturated or unsaturated ring of formula a D-S which may have 5 to 7 ring members and besides sulfur 1 to 2 further heteroatoms selected from oxygen, sulfur and nitrogen and which ring 15 may be substituted with 1 to 5 groups selected from Ra, or the moiety R 4 -D-X-R 1 together may form a group of formula P wherein x is 1 to 5, (CH 2 )x-CH-S (B) 20 containing a saturated or unsaturated ring which may have 5 to 7 ring members and besides sulfur 1 to 2 further heteroatoms selected from oxygen, sulfur and nitrogen and which ring may be substituted with 1 to 5 groups selected from Ra; 25 R 5 is a group R 3 ; G is oxygen or sulfur; Ra is each independently halogen, cyano, nitro, C01-C6-alkyl, C1-C6 30 haloalkyl, C2-06-alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C2-06 haloalkynyl, C3-06-cycloalkyl, C3-08-halocycloalkyl, C3-06 cycloalkenyl, C3-08-halocycloalkenyl, phenoxy, OR i , SR i, S(=O)R i , S(=O) 2 R i , NRiRj, -S(=O) 2 NRiR, C(=O)R i , C(=O)OR i, C(=O)NRiR, C(=NORi)R, -NRiC(=G)R, -N[C(=G)Ri]2, 35 -NRiC(=G)OR, -C(=G)NRi-NR 2 , -NRiSO 2 R, SiRiyRJ 3 -y (y is 0 to 3), or phenyl or a 5- to 6-membered heteraromatic ring which may contain 1 to 4 heteroatoms selected from oxygen, 40 nitrogen and sulfur, WO 2007/071609 PCT/EP2006/069686 67 wherein the carbon atoms in phenyl or in the heteroaromatic ring may be substituted with 1 to 5 halogens; 5 R i , Ri are each independently hydrogen, C1-C6-alkyl, C1-C 6 -haloalkyl, C2-06-alkenyl, C 2 -C 6 -haloalkenyl, C2 C6-alkynyl, C 2 -C 6 -haloalkynyl, C3-06-cycloalkyl, C3-08 halocycloalkyl, C3-06-cycloalkenyl, or C3-06 halocycloalkenyl; 10 Rb is each independently C01-C6-alkyl, Cl-C 6 -haloalkyl, C2-06 alkenyl, C 2 -0 6 -haloalkenyl, C2-06-alkynyl, C 2 -0 6 -haloalkynyl, C3-06-cycloalkyl, C3-08-halocycloalkyl, C3-06-cycloalkenyl, C3 C8-halocycloalkenyl, C3-06-cycloalkyl-C1-C4-alkyl, or C3-08 15 halocycloalkyl-C1-C4-alkyl, or phenyl or a 5- to 6-membered heteraromatic ring which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which heteroaromatic ring may be bound via a C1-C4 20 alkyl-moiety, and wherein the carbon atoms in phenyl or in the heteroaromatic ring may be substituted with 1 to 3 groups Ra; or the enantiomers or diastereomers or salts or N-oxides or polymorphs thereof. 25 2. Compounds of formula I according to claim 1 wherein X is oxygen or sulfur.
[3] 3. Compounds of formula I according to claims 1 or 2 wherein D is a saturated or partially unsaturated hydrocarbon chain with 2 to 4 carbon chain atoms. 30
[4] 4. A process for the preparation of compounds of formula I as defined in claims 1 to 3 which comprises reacting compounds (11) with compound (111) in the presence of a base to give compounds (I), AB H B Ds -R A H 1A B gX NC CN base NC CN (11) (I) wherein A, B, D, X and R 1 are as defined in claims 1 to 3 for compounds of 35 formula I and Z' represents a suitable leaving group.
[5] 5. Use of compounds of formula I as defined in claims 1 to 3 for combating insects, acarids, or nematodes. WO 2007/071609 PCT/EP2006/069686 68
[6] 6. A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of compositions or compounds of 5 formula I as defined in claims 1 to 3.
[7] 7. A method of protecting growing plants from attack or infestation by insects, acarids or nematodes by applying to the plants, or to the soil or water in which they are growing, a pesticidally effective amount of compositions or compounds 10 of formula I as defined in claims 1 to 3.
[8] 8. A method for treating, controlling, preventing or protecting animals against infestation or infection by parasites which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective 15 amount of compositions or compounds of formula I as defined in claims 1 to 3 or their enantiomers or veterinarily acceptable salts.
[9] 9. A process for the preparation of a composition for treating, controlling, preventing or protecting animals against infestation or infection by parasites which 20 comprises a parasiticidally effective amount of compositions or compounds of formula I as defined in claims 1 to 3 or their enantiomers or veterinarily acceptable salts.
[10] 10. Compositions comprising a pesticidally or parasiticidally active amount of 25 compounds of formula I as defined in claims 1 to 3 and an agronomically or veterinarily acceptable carrier.
[11] 11. Synergistic mixtures comprising a compound of formula I and a pesticide selected from the organo(thio)phosphates, carbamates, pyrethroids, growth 30 regulators, neonicotinoids, nicotinic receptor agonists/antagonists compounds, GABA antagonist compounds, macrocyclic lactone insecticides, METI I acaricides, METI II and III compounds, oxidative phosphorylation inhibitor compounds, moulting disruptor compounds, mixed function oxidase inhibitor compound, sodium channel blocker compounds, benclothiaz, bifenazate, cartap, 35 flonicamid, pyridalyl, pymetrozine, sulfur, thiocyclam, N-R'-2,2-dihalo-1l-R"cyclo propanecarboxamide-2-(2,6-dichloro- a,a,a -tri-fluoro-p-tolyl)hydrazone or N-R' 2,2-di(R"')propionamide-2-(2,6-dichloro- a,a,a -trifluoro-p-tolyl)-hydrazone, wherein R' is methyl or ethyl, halo is chloro or bromo, R" is hydrogen or methyl and R"' is methyl or ethyl, and anthranilamide compounds of formula F 3 WO 2007/071609 PCT/EP2006/069686 69 CH 3 0 2 B N N-N N Cl (F3) RB H wherein B 1 is hydrogen, chlorine or cyano, B 2 is a bromine atom or CF 3 , and RB is H, CH 3 or CH(CH 3 ) 2 .

类似技术:

---

公开号 | 公开日 | 专利标题

---

US9365543B2|2016-06-14|N-Thio-anthranilamid compounds and their use as pesticides

---

US20090029855A1|2009-01-29|Quinoline Derivatives and Their Use as Pesticides

---

EP1973404B1|2015-10-28|Malononitrile compounds

---

EP2044008A1|2009-04-08|Malononitrile compounds

---

US20090221423A1|2009-09-03|Methods to Use 3-Pyridyl Derivatives as Pesticides

---

US20080227635A1|2008-09-18|Dicyano Alkanoic Acid Amides for Combating Animal Pests

---

WO2007039555A1|2007-04-12|Oxime ether compounds and their use as pesticides

---

WO2006122949A1|2006-11-23|Malononitriles and their use as pesticides

---

WO2007054558A2|2007-05-18|Resorcine derivatives and their use as pesticides

---

MX2008008075A|2008-09-26|Malononitrile compounds

同族专利:

---

公开号 | 公开日

---

JP2009520755A|2009-05-28|

---

BRPI0620246B1|2021-03-23|

---

ZA200806256B|2010-01-27|

---

WO2007071609A1|2007-06-28|

---

EP1973404B1|2015-10-28|

---

JP4960380B2|2012-06-27|

---

CN101384170A|2009-03-11|

---

CA2634601C|2015-05-12|

---

BRPI0620246A2|2013-01-15|

---

ES2557443T3|2016-01-26|

---

US8916592B2|2014-12-23|

---

KR20080085179A|2008-09-23|

---

IL192323D0|2008-12-29|

---

CN101384170B|2012-07-18|

---

CA2634601A1|2007-06-28|

---

KR101372756B1|2014-03-10|

---

EA200801567A1|2009-02-27|

---

EP1973404A1|2008-10-01|

---

US20090326012A1|2009-12-31|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

GB9210632D0|1992-05-19|1992-07-01|Fisons Plc|Compounds|

---

JPH1029966A|1996-07-17|1998-02-03|Mitsubishi Chem Corp|Malononitrile derivative and herbicide containing the derivative as active component|

---

JP2002284608A|2001-01-18|2002-10-03|Sumitomo Chem Co Ltd|Insecticide and method for killing insect|

---

TWI223979B|2001-05-09|2004-11-21|Sumitomo Chemical Co|Malononitrile compounds and pesticide composition containing the same as well as pest controlling method|

---

ES2276090T3|2002-07-17|2007-06-16|Sumitomo Chemical Company, Limited|MALONITRILE COMPOUNDS AND THEIR EMPLOYMENT AS PESTICIDES.|

---

JP2004099593A|2002-07-17|2004-04-02|Sumitomo Chem Co Ltd|Malononitrile compound and use of the same|

---

JP4457588B2|2002-07-17|2010-04-28|住友化学株式会社|Uses of malononitrile compounds|

---

WO2004020399A1|2002-08-29|2004-03-11|Sumitomo Chemical Company, Limited|Malononitrile compound and use thereof as pesticides|

---

AR047410A1|2003-12-26|2006-01-18|Sumitomo Chemical Co|NITRILE DERIVATIVES AND ITS USE IN PEST CONTROL. PESTICIDED COMPOSITIONS.|

---

JP4830301B2|2004-01-16|2011-12-07|住友化学株式会社|Malononitrile compound having nitrogen-containing 5-membered ring and use thereof|

---

JP4670355B2|2004-01-16|2011-04-13|住友化学株式会社|Malononitrile compound having nitrogen-containing 6-membered ring and use thereof|

---

DE602005004040T2|2004-01-16|2008-12-11|Sumitomo Chemical Co., Ltd.|Malononitrile compounds as pesticides|

---

CN1910147B|2004-01-16|2011-04-20|住友化学株式会社|Malononitrile compound and use thereof|

---

RU2347779C2|2004-01-16|2009-02-27|Сумитомо Кемикал Компани, Лимитед|Malononitrile compound as pesticide|KR101440162B1|2006-06-22|2014-09-12|바스프 에스이|Malononitrile compounds|

---

MX2012005612A|2009-11-17|2012-11-30|Merial Ltd|Fluorinated oxa or thia heteroarylalkylsulfide derivatives for combating invertebrate pests.|

---

CN102246797B|2011-05-17|2013-04-10|德强生物股份有限公司|Insecticidal synergistic composition containing imidacloprid|

---

US10292388B2|2012-10-24|2019-05-21|Basf Se|Malononitrile compounds for controlling animal pests|

---

EP2984074A1|2012-12-14|2016-02-17|Basf Se|Malononitrile compounds for controlling animal pests|

---

EP3131398B1|2014-04-17|2019-10-23|Boehringer Ingelheim Animal Health USA Inc.|Use of malononitrile compounds for protecting animals from parasites|

---

WO2017089389A1|2015-11-26|2017-06-01|F. Hoffmann-La Roche Ag|Trypanosomes inhibitors|

法律状态:
2012-07-12| MK4| Application lapsed section 142(2)(d) - no continuation fee paid for the application|

优先权:

---

申请号 | 申请日 | 专利标题

---

US75334605P| true| 2005-12-22|2005-12-22||

---

US60/753,346||2005-12-22||

---

PCT/EP2006/069686|WO2007071609A1|2005-12-22|2006-12-13|Malononitrile compounds|

---