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    • 专利摘要:
    The present invention relates to 4-haloalkyl-3-heterocyclylpyridine and 4-haloalkyl-5-heterocyclyl-pyrimidine, methods for their preparation, compositions comprising them, and their use as pesticides. The present invention relates to 4-haloalkyl-3-heterocyclylpyridine and 4-haloalkyl-5-heterocyclyl-pyrimidine of the general formula (I), methods for their preparation, compositions comprising them, and animal pests, in particular insects, spiders It relates to the use of these compounds to control ticks, external parasites and worms. In formula (I), Q is a 5-membered heterocyclic group optionally substituted by halogen or organic radicals, Y is halogen- (C 1 -C 6 ) -alkyl, X is CH or N, m is 0 or Is 1: Formula I
    公开号:KR20010013830A
    申请号:KR1019997011850
    申请日:1998-06-03
    公开日:2001-02-26
    发明作者:티에베스외르그；탑켄토마스；록부르크하르트；케른만프레트；산프트울리히
    申请人:슈미트, 루츠；훽스트 쉐링 아그레보 게엠베하；
    IPC主号:
    专利说明:

    4-haloalkyl-3-heterocyclylpyridine and 4-haloalkyl-5-heterocyclylpyrimidine, processes for their preparation, compositions comprising them, and their use as insecticides {4-HALOALKYL-3-HETEROCYCLYLPYRIDINES AND 4- HALOALKYL-5-HETEROCYCLYLPYRIMIDINES, METHOD FOR THE PRODUCTION THEREOF, AGENTS CONTAINING THE SAME AND THEIR USE AS PESTICIDES}
    It is already known that suitably substituted pyridine or pyrimidine are acaricide and insecticidal. Accordingly, WO 95/07891 discloses pyridine in which the cycloalkyl radical is connected at the 4 position via a heteroatom in which the 3 position is located and a group of various substituents. WO 93/19050 discloses 4-cycloalkylamino- and 4-cycloalkoxypyrimidines having, in particular, alkyl, alkoxy or haloalkoxy groups at the 5 position. However, the desired activity against harmful organisms is not always sufficient. In addition, these compounds often have undesirable toxicity to mammals and aquatic animals.
    Pyridyl-1,2,4-thiadiazole having fungicidal properties is disclosed in German Patent Application No. 42 39 727. The compounds disclosed herein carry a thiadiazole ring at the 2, 3 or 4 position of the unsubstituted pyridine.
    EP 0 371 925 discloses 1,3,4-oxadiazole- and 1,3,4-thiadiazolyl-pyrimidine having nematicidal and fungicidal properties. In the biologically effective compounds disclosed in this document, the pyrimidine has an axadiazolyl or thiadiazolyl ring in a) position 5, optionally substituted by a thiomethyl group in position 2, or b) in position 2, optionally And at each of the 4 and 6 positions are substituted by a methyl group.
    Aryltriazole derivatives useful as insecticides are known from EP 0 185 256. In addition to the particularly preferred phenyltriazoles, three haloalkyl-3-pyridyltriazoles are disclosed:
    3- (2-chlorophenyl) -1-methyl-5- (4-trifluoromethyl-3-pyridyl) -1H-1,2,4-triazole;
    3- (2,6-difluorophenyl) -1-methyl-5- (4-trifluoromethyl-3-pyridyl) -1H-1,2,4-triazole; And
    3- (2-chloro-4-fluorophenyl) -1-methyl-5- (4-trifluoromethyl-3-pyridyl) -1H-1,2,4-triazole.
    However, at low sparging rates, this desired activity is not always satisfactory, particularly when controlling insects and spider mites.
    Several commercially available 4-haloalkyl-3-heterocyclylpyridines are described in Maybridge Catalog 1996/1997, Maybridge Chemical Co. LTD., Trevillett Tintagel, GB, and the compounds are as follows:
    3- (3,5-dichlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (4-trifluoromethyl-3-pyridyl) -3-phenyl-1,2,4-oxadiazole;
    3- (4-trifluoromethyl-3-pyridyl) -5-phenyl-1,2,4-oxadiazole;
    5- (2-chlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3-chlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (4-chlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (2-fluorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (4-fluorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (2,4-dichlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3,4-dichlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3,5-dichlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (2,6-dichloro-4-pyridyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3,5-bistrifluoromethylphenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    2- (2-chlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (3-chlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (4-chlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (2-trifluoromethoxyphenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (4-trifluoromethoxyphenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (4-trifluoromethyl-3-pyridyl) -5-phenyl-1,3,4-oxadiazole;
    2- (4-trifluoromethyl-3-pyridyl) -4-methylthiazolecarbohydrazide;
    Ethyl 2- (4-trifluoromethyl-3-pyridyl) -4-methylthiazole carboxylate;
    N- (4-chlorophenyl) carbonyl-N '-[2- (4-trifluoromethyl-3-pyridyl) -4-methyl-5-thiazolyl] carbonylhydrazine;
    2- (4-trifluoromethyl-3-pyridyl) -4-thiazolecarbohydrazide;
    4- (4-chlorophenyl) -2- (4-trifluoromethyl-3-pyridyl) thiazole;
    4- (4-cyanophenyl) -2- (4-trifluoromethyl-3-pyridyl) thiazole;
    N- (4-trifluoromethylphenyl) carbonyl-N '-[2- (4-trifluoromethyl-3-pyridyl) -4-thiazolyl] carbonylhydrazine;
    2- (2- (4-trifluoromethyl-3-pyridyl) thiazolyl) -5-chloro-3-methylbenzo [b] thiophene;
    2- (4-chlorophenylmethylthio) -5- (4-trifluoromethyl-3-pyridyl) -1-methyl-1H-1,3,4-triazole;
    2- (4-chlorophenylcarbonylmethylthio) -5- (4-trifluoromethyl-3-pyridyl) -1-methyl-1H-1,3,4-triazole and
    2-ethoxycarbonylmethylthio-5- (4-trifluoromethyl-3-pyridyl) -1-methyl-1H-1,3,4-triazole.
    However, no biological activity against harmful organisms has ever been disclosed.
    The present invention relates to 4-haloalkyl-3-heterocyclylpyridine and 4-haloalkyl-5-heterocyclyl-pyrimidine, methods for their preparation, compositions comprising them, and certain insects, spider mites, external It relates to the use of new or known 4-haloalkyl-3-heterocyclylpyridine and 4-haloalkyl-5-heterocyclylpyrimidine for controlling animal pests in parasites and intestinal parasites.
    It is an object of the present invention to provide compounds having low toxicity to mammals and aquatic animals with good pesticidal properties and acaricide.
    It has been found by the present invention that the compounds of formula (I), optionally as salts, have a wide range of activity against animal pests, while at the same time being more toxic to mammals and aquatic animals than to compounds of the prior art:
    Where
    Y is halo-C 1 -C 6 -alkyl;
    X is CH or N;
    m is 0 or 1;
    Q is a 5-membered heterocyclic group ego;
    Where a) X 1 = W, X 2 = NR a , X 3 = CR b R 1, or b) X 1 = NR a , X 2 = CR b R 1 , X 3 = W, or c) X 1 = V, X 2 = CR a R 1 , X 3 = NR b or d) X 1 = V, X 2 = CR a R 2 , X 3 = CR b R 3, or e) X 1 = V, X 2 = CR 4 R 5 , X 3 = CR 6 R 7 , or f) X 1 = NR a , X 2 = CR b R 1 , X 3 = NR 8 ; At this time
    R a and R b together form a single bond;
    V is oxygen, sulfur or NR 9 ;
    W is oxygen or sulfur;
    R 1 is hydrogen, (C 1 -C 20 ) -alkyl, (C 2 -C 20 ) -alkenyl, (C 2 -C 20 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the last six radicals mentioned are halogen, cyano, nitro, hydroxyl, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -NR 10 C (= W) OR 10 , -C (= W) NR 10 -NR 10 2 , -C (= W) NR 10 -NR 10 [C (= W) R 10 ], -NR 10 -C (= W) NR 10 2 , -NR 10 -NR 10 C (= W) R 10 , -NR 10 -N [C (= W) R 10 ] 2 , -N [(C = W) R 10 ] -NR 10 2 , -NR 10 -NR 10 [(C = W) R 10 ], -NR 10 -NR 10 [(C = W) WR 10 ], -NR 10 -R 10 [(C = W) NR 10 2 ], -NR 10 (C = NR 10 ) R 10 , -NR 10 (C = NR 10 ) NR 10 2 , -ONR 10 2 , -O-NR 10 (C = W) R 10 , -SO 2 NR 10 2 , -NR 10 SO 2 R 10 , -SO 2 OR 10 , -OSO 2 R 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -SeR 10 , -PR 10 2 , -P (= W) R 10 2 , -SOR 10 , -SO 2 R 10, -PW 2 R 10 2 , -PW 3 R 10 2, aryl and heteroaryl Cycle reels are optionally substituted by one or more radicals selected from the group consisting of, where the two radicals mentioned last is (C 1 -C 6) alkyl, (C 2 -C 6) - alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, (C 1 -C 6 ) -halo Alkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, halogen, -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -SOR 10 , -SO 2 R 10 , at least one radical selected from the group consisting of nitro, cyano and hydroxyl Optionally substituted by
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are halogen, cyano, nitro, halogen, -C (= W) R 10 , -C (= W) Optionally substituted by one or more radicals selected from the group consisting of OR 10 , -C (= W) NR 10 2 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ; , Halogen, cyano, nitro, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C ( = W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 ,- NR 10 C (= W) OR 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -PR 10 2 , -SOR 10 , -SO 2 R 10 , -PW 2 R 10 2 and Aryl optionally substituted by one or more radicals selected from the group consisting of -PW 3 R 10 2 ,
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are cyano, nitro, halogen, -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -OC (= W) R 10 , -OC (= W) Optionally substituted by one or more radicals selected from the group consisting of OR 10 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ], halogen, cyano, nitro, -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OR 10 , -NR 10 2 , -SR 10 , -SOR Heterocyclyl optionally substituted by one or more radicals selected from the group consisting of 10 and —SO 2 R 10 ,
    -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 , -SO 2 R 10 , -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -NR 10 C (= W) OR 10 , -C (= W) NR 10 -NR 10 2 , -C (= W) NR 10 -NR 10 [ C (= W) R 10 ], -NR 10 -C (= W) NR 10 2 , -NR 10 -NR 10 C (= W) R 10 , -NR 10 -NC (= W) R 10 2 ,- N (C = W) R 10 -NR 10 2 , -NR 10 -NR 10 [(C = W) R 10 ], -NR 10 -NR 10 [(C = W) WR 10 ], -NR 10 -NR 10 [(C = W) NR 10 2 ], -NR 10 (C = NR 10 ) R 10 , -NR 10 (C = NR 10 ) NR 10 2 , -O-NR 10 2 , -O-NR 10 ( C = W) R 10 , -SO 2 NR 10 2 , -NR 10 SO 2 R 10 , -SO 2 OR 10 , -OSO 2 R 10 , -SC (= W) R 10 , -SC (= W) OR 10 , -SC (= W) R 10 , -PR 10 2 , -PW 2 R 10 2 , -PW 3 R 10 2 , SiR 10 3 or halogen;
    R 2 and R 3 independently of each other have the definition given to R 1 ; R 2 and R 3 together form a 5 to 7 membered ring which is partially or fully unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are directly adjacent to each other Ring is optionally substituted by 1 to 5 radicals R 1 ;
    R 4 and R 6 independently of each other have the definition given to R 1 ; R 4 and R 6 together form a 4-7 membered ring which is partially or fully unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are directly adjacent to each other Ring is optionally substituted by 1 to 5 radicals R 1 ;
    R 5 and R 7 independently of one another are hydrogen, (C 1 -C 20 ) -alkyl, (C 2 -C 20 ) -alkenyl, (C 2 -C 20 ) -alkynyl, (C 3 -C 8 ) -Cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned last are halogen, cyano, nitro, hydroxyl, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC ( = W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -NR 10 C (= W) OR 10 , -C (= W) NR 10 -NR 10 2 , -C (= W) NR 10 -NR 10 [C (= W) R 10 ], -NR 10 -C (= W) NR 10 2 , -NR 10 -NR 10 C (= W) R 10 , -NR 10 -N [C (= W) R 10 ] 2 , -N [(C = W) R 10 ] -NR 10 2 , -NR 10 -NR 10 [ (C = W) R 10 ], -NR 10 -NR 10 [(C = W) WR 10 ], -NR 10 -NR 10 [(C = W) NR 10 2 ], -NR 10 (C = NR 10 ) R 10 , -NR 10 (C = NR 10 ) NR 10 2 , -ONR 10 2 , -O-NR 10 (C = W) R 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3, -SeR 10, -PR 10 2, -P (= W) R 10 2, -SOR 10, -SO 2 R 10, -PW 2 R 10 2, -PW 3 R 10 2, aryl, and heterocyclyl Group of reels It is optionally substituted by one or more radicals selected from, where the last two radicals mentioned are (C 1 -C 6) alkyl, (C 2 -C 6) - alkenyl, (C 2 -C 6) - alkynyl Nyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, (C 1 -C 6 ) -haloalkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, halogen, -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -C (= W) R 10 Optionally substituted by one or more radicals selected from the group consisting of -C (= W) OR 10 , -C (= W) NR 10 2 , -SOR 10 , -SO 2 R 10 , nitro, cyano and hydroxyl do],
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl and (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are halogen, cyano, nitro, halogen, -C (= W) R 10 , -C (= W) Optionally substituted by one or more radicals selected from the group consisting of OR 10 , -C (= W) NR 10 2 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ; , Halogen, cyano, nitro, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C ( = W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 ,- NR 10 C (= W) OR 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -PR 10 2 , -SOR 10 , -SO 2 R 10 , -PW 2 R 10 2 and Aryl optionally substituted by one or more radicals selected from the group consisting of -PW 3 R 10 2 ,
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl and (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are cyano, nitro, halogen, -C (= W) R 10 , -C (= W) OR 10 Is optionally substituted by one or more radicals selected from the group consisting of -C (= W) NR 10 2 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 . , Cyano, nitro, -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OR 10 , -NR 10 Pyridyl optionally substituted by one or more radicals selected from the group consisting of 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ,
    -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 or halogen ego;
    R 4 and R 5 together form a 4-7 membered ring which is partially unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are not directly adjacent to each other The ring is optionally substituted by 1 to 5 radicals R 1 ; R 4 and R 5 together form one of the groups = O, = S and = NR 9 ;
    R 6 and R 7 together form a five to seven membered ring which is partially unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are not directly adjacent to each other , The ring is optionally substituted by 1 to 5 radicals R 1 ; R 6 and R 7 together form one of the groups = O, = S and = NR 9 ;
    R 8 is hydrogen, (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -Alkyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alky Nyl- (C 3 -C 8 ) -cycloalkyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenyl, (C 2 -C 6 ) -alkenyl- (C 4- C 8 ) -cycloalkenyl [wherein the last mentioned radicals are 14 halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -Haloalkynyloxy, (C 3 -C 8 ) -cycloalkoxy, (C 4 -C 8 ) -company Icycloalkenyloxy, (C 3 -C 8 ) -halocycloalkoxy, (C 4 -C 8 ) -halocycloalkenyloxy, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 )- Alkoxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkoxy, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyloxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyloxy, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkoxy, (C 2 -C 6 )- alkenyl, - (C 3 -C 8) - cycloalkoxy, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkoxy, (C 1 -C 6) - alkyl, - (C 4 - C 8 ) -cycloalkenyloxy, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenyloxy, (C 1 -C 4 ) -alkoxy- (C 1 -C 6 ) -Alkoxy, (C 1 -C 4 ) -alkoxy- (C 2 -C 6 ) -alkenyloxy, carbamoyl, (C 1 -C 6 ) -mono- or di-alkylcarbamoyl, (C 1 -C 6 ) -mono- or di-haloalkylcarbamoyl, (C 3 -C 8 ) -mono- or di-cycloalkylcarbamoyl, (C 1 -C 6 ) -alkoxycarbonyl, (C 3 -C 8 ) Cycloalkoxycarbonyl, (C 1 -C 6 ) -alkanoyloxy, (C 3 -C 8 ) -cycloalkanoyloxy, (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1 -C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanamido, (C 2 -C 6 ) -alkenamido, (C 3 -C 8 ) -cycloalkanamido, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkanamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -alkenylthio, (C 2 -C 6 ) -Alkynylthio, (C 1 -C 6 ) -haloalkylthio, (C 2 -C 6 ) -haloalkenylthio, (C 2 -C 6 ) -haloalkynylthio, (C 3 -C 8 ) -Cycloalkylthio, (C 4 -C 8 ) -cycloalkenylthio, (C 3 -C 8 ) -halocycloalkthio, (C 4 -C 8 ) -halocycloalkenylthio, (C 3- C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylthio, (C 3 -C 8 ) -cyclo Alkyl- (C 2 -C 4 ) -alkenylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylthio, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylthio, (C 2 -C 6) - alkenyl, - (C 3 -C 8) - cycloalkyl, thio, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkyl, thio, (C 1 -C 6) -Alkyl- (C 4 -C 8 ) -cycloalkenylthio, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylthio, (C 1 -C 6 ) -alkylsulphi Neyl, (C 2 -C 6 ) -alkenylsulfinyl, (C 2 -C 6 ) -alkynylsulfinyl, (C 1 -C 6 ) -haloalkylsulfinyl, (C 2 -C 6 ) -halo Alkenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl, (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3- C 8 ) -halocycloalksulfinyl, (C 4 -C 8 ) -halocycloalkenylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfinyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfinyl, (C 4- C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfinyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 2 -C 6 ) -Alkenyl- (C 3 -C 8 ) -cycloalkylsulfinyl, ( C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 1 -C 6 ) -alkylsulfonyl, (C 2 -C 6 ) -alkenylsulfonyl, (C 2- C 6 ) -alkynylsulfonyl, (C 1 -C 6 ) -haloalkylsulfonyl, (C 2 -C 6 ) -haloalkenylsulfonyl, (C 2 -C 6 ) -haloalkynylsulfonyl, (C 3 -C 8 ) -cycloalkylsulfonyl, (C 4 -C 8 ) -cycloalkenylsulfonyl, (C 3 -C 8 ) -halocycloalksulfonyl, (C 4 -C 8 ) -halocycloalkenylsulfonyl , (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfonyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfonyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 )- alkynyl, - (C 3 -C 8) - cycloalkyl Kilseol sulfonyl, (C 1 -C 6) - alkyl, - (C 4 -C 8) - cycloalkyl sulfonyl nilseol alkenyl, (C 2 -C 6) - alkenyl, - (C 4 -C 8) - cycloalkyl alkenyl nilseol sulfonyl, (C 1 -C 6 ) -alkylamino, (C 2 -C 6 ) -alkenylamino, (C 2 -C 6 ) -alkynylamino, (C 1 -C 6 ) -haloalkylamino, (C 2 -C 6 ) -haloalkenylamino, (C 2 -C 6 ) -haloalkynylamino, (C 3 -C 8 ) -cycloalkylamino, (C 4 -C 8 ) -cycloalkenylamino, (C 3 -C 8 ) -halocycloalkamino, (C 4 -C 8 ) -halocycloalkenylamino, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylamino, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylamino, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylamino, (C 4 -C 8 ) -Cycloalkenyl- (C 1 -C 4 ) -alkenylamino, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylamino, (C 1 -C 6 ) -alkyl- (C 4 -C 8) - Alkenyl cycle roal amino, (C 2 -C 6) - alkenyl, - (C 4 -C 8) - cycloalkenyl-amino, (C 1 -C 6) - trialkylsilyl, aryl, aryloxy, arylthio, aryl Amino, arylcarbamoyl, aroyl, aroyloxy, aryloxycarbonyl, aryl- (C 1 -C 4 ) -alkoxy, aryl- (C 2 -C 4 ) -alkenyloxy, aryl- (C 1- C 4 ) -alkylthio, aryl- (C 2 -C 4 ) -alkenylthio, aryl- (C 1 -C 4 ) -alkylamino, aryl- (C 2 -C 4 ) -alkenylamino, aryl- (C 1 -C 6) - di-alkylsilyl, diaryl - (C 1 -C 6) - alkylsilyl, triarylsilyl and 5- or 6-membered heterocycle reels are optionally substituted by one or more radicals selected from the group consisting of Wherein the last 19 radicals mentioned are halogen, cyano, nitro, amino, hydroxyl, thio, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4) -alkoxy, (C 1 -C 4) - haloalkoxy, (C 1 -C 4) - alkylthio, (C 1 -C 4) haloalkylthio, (C 1 -C 4) - alkyl Mino, (C 1 -C 4) - haloalkyl, amino, formyl, and (C 1 -C 4) - is optionally substituted in the cyclic moiety by one or more radicals selected from the group consisting of alkanoyl],
    Halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy , (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -haloalkynyloxy, (C 3 -C 8 ) -cycloalkoxy, (C 4 -C 8 ) -cycloalkenyloxy, (C 3 -C 8 ) -halocycloalkoxy, (C 4 -C 8 ) -halocycloalkenyloxy, carbamoyl, (C 1 -C 6 )- mono- or di-alkyl carbamoyl, (C 1 -C 6) - alkoxycarbonyl, (C 1 -C 6) - alkanoyloxy, (C 1 -C 6) - mono- or di-haloalkyl carbamoyl , (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1 -C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanami (C 2 -C 6 ) -alkenamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -alkenylthio, (C 2 -C 6 ) -alkynylthio, ( C 1 -C 6) - haloalkylthio, (C 2 -C 6) - haloalkenyl thio, (C 2 -C 6) - haloalkynyl thio, (C 3 -C 8) - cycloalkyl, O, (C 4 -C 8) - cycloalkenyl thio, (C 3 -C 8) - cycloalkyl halo alk thio, (C 3 -C 8) - halo-cycloalkenyl thio, (C 1 -C 6) - Alkylsulfinyl, (C 2 -C 6 ) -alkenylsulfinyl, (C 2 -C 6 ) -alkynylsulfinyl, (C 1 -C 6 ) -haloalkylsulfinyl, (C 2 -C 6 ) -Haloalkenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl, (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3 -C 8 ) -halocycloalksulfinyl, (C 4 -C 8 ) -halocycloalkenylsulfinyl, (C 1 -C 6 ) -alkylsulfonyl, (C 2 -C 6 ) -alkenylsulfonyl , (C 2 -C 6 ) -alkynylsulfonyl, (C 1 -C 6 ) -haloalkylsulfonyl, (C 2 -C 6 ) -haloalkenylsulfonyl, (C 2 -C 6 ) -haloalkynylsul Ponyl, (C 3 -C 8 ) -cycloalkylsulfonyl, (C 4 -C 8 ) -cycloalkenylsulfonyl, (C 3 -C 8 ) -halocycloalksulfonyl, (C 4 -C 8 )- halo-alkenyl cycloalkyl nilseol sulfonyl, (C 1 -C 6) - alkylamino, (C 2 -C 6) - alkenyl, amino, (C 2 -C 6) - alkynyl, amino , (C 1 -C 6) - haloalkyl, amino, (C 2 -C 6) - haloalkenyl amino, (C 2 -C 6) - haloalkynyl amino, (C 3 -C 8) - cycloalkyl-amino , (C 4 -C 8) - cycloalkenyl-amino, (C 3 -C 8) - cycloalkyl alk halo, amino and (C 4 -C 8) - by one or more radicals selected from halo cycloalkenyl group consisting of amino Optionally substituted aryl,
    -C (= W) R 11 , OR 11 or NR 11 2 ;
    R 9 is (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4- C 8 ) -cycloalkenyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkyl , (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyl or (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyl [wherein The nine radicals mentioned are halogen, cyano, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy and (C 1 -C 6 ) -haloalkyloxy, optionally substituted by one or more radicals selected from the group consisting of;
    R 10 is hydrogen, (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -Alkyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alky Nyl- (C 3 -C 8 ) -cycloalkyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenyl, (C 2 -C 6 ) -alkenyl- (C 4- C 8 ) -cycloalkenyl [the last 14 radicals mentioned are halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -Alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -halo alkynyloxy, (C 3 -C 8) - cycloalkoxy, (C 4 -C 8) - four Claw alkenyloxy, (C 3 -C 8) - cycloalkoxy halo, (C 4 -C 8) - cycloalkyl halo-alkenyloxy, (C 3 -C 8) - cycloalkyl, - (C 1 -C 4) - Alkoxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkoxy, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyloxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyloxy, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkoxy, (C 2 -C 6 )- alkenyl, - (C 3 -C 8) - cycloalkoxy, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkoxy, (C 1 -C 6) - alkyl, - (C 4 - C 8 ) -cycloalkenyloxy, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenyloxy, (C 1 -C 4 ) -alkoxy- (C 1 -C 6 ) -Alkoxy, (C 1 -C 4 ) -alkoxy- (C 2 -C 6 ) -alkenyloxy, carbamoyl, (C 1 -C 6 ) -mono- or di-alkylcarbamoyl, (C 1 -C 6 ) -mono- or di-haloalkylcarbamoyl, (C 3 -C 8 ) -mono- or di-cycloalkylcarbamoyl, (C 1 -C 6 ) -alkoxycarbonyl, (C 3 -C 8 ) Cycloalkoxycarbonyl, (C 1 -C 6 ) -alkanoyloxy, (C 3 -C 8 ) -cycloalkanoyloxy, (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1 -C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanamido, (C 2 -C 6 ) -alkenamido, (C 3 -C 8 ) -cycloalkanamido, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkanamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -alkenylthio, (C 2 -C 6 ) -Alkynylthio, (C 1 -C 6 ) -haloalkylthio, (C 2 -C 6 ) -haloalkenylthio, (C 2 -C 6 ) -haloalkynylthio, (C 3 -C 8 ) -Cycloalkylthio, (C 4 -C 8 ) -cycloalkenylthio, (C 3 -C 8 ) -halocycloalkthio, (C 4 -C 8 ) -halocycloalkenylthio, (C 3- C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylthio, (C 3 -C 8 ) -cyclo Alkyl- (C 2 -C 4 ) -alkenylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylthio, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylthio, (C 2- C 6) - alkenyl, - (C 3 -C 8) - cycloalkyl, thio, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkyl, thio, (C 1 -C 6) - Alkyl- (C 4 -C 8 ) -cycloalkenylthio, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylthio, (C 1 -C 6 ) -alkylsulfinyl , (C 2 -C 6) - alkenyl, sulfinyl, (C 2 -C 6) - alkynyl, sulfinyl, (C 1 -C 6) - haloalkyl sulfinyl, (C 2 -C 6) - haloalkenyl Kenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl, (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3 -C 8 ) -halocycloalksulfinyl, (C 4 -C 8 ) -halocycloalkenylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfinyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfinyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfinyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 2 -C 6 ) -Alkenyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 2- C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 1 -C 6 ) -alkylsulfonyl, (C 2 -C 6 ) -alkenylsulfonyl, (C 2 -C 6 ) -alkynylsulfonyl, (C 1 -C 6 ) -haloalkylsulfonyl, (C 2 -C 6 ) haloalkenylsulfonyl, (C 2 -C 6 ) -haloalkynylsulfonyl, (C 3 -C 8 ) -cycloalkylsulfonyl, (C 4 -C 8 ) -cycloalkenylsulfonyl, (C 3 -C 8 ) -halocycloalksulfonyl, (C 4 -C 8 ) -halocycloalkenylsulfonyl, ( C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfonyl, (C 3- C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfonyl, (C 1 -C 6 ) -Alkyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 ) -alkynyl - (C 8 -C 3) - cycloalkenyl Sulfonyl, (C 1 -C 6) - alkyl, - (C 4 -C 8) - cycloalkyl sulfonyl nilseol alkenyl, (C 2 -C 6) - alkenyl, - (C 4 -C 8) - cycloalkyl alkenyl nilseol sulfonyl, (C 1 -C 6 ) -alkylamino, (C 2 -C 6 ) -alkenylamino, (C 2 -C 6 ) -alkynylamino, (C 1 -C 6 ) -haloalkylamino, (C 2 -C 6 ) -haloalkenylamino, (C 2 -C 6 ) -haloalkynylamino, (C 3 -C 8 ) -cycloalkylamino, (C 4 -C 8 ) -cycloalkenylamino, (C 3 -C 8 ) -halocycloalkamino, (C 4 -C 8 ) -halocycloalkenylamino, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylamino, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylamino, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylamino, (C 4 -C 8 ) -Cycloalkenyl- (C 1 -C 4 ) -alkenylamino, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylamino, (C 1 -C 6 ) -alkyl- (C 4 -C 8 )-4 Ichloroalkenylamino, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylamino, (C 1 -C 6 ) -trialkylsilyl, aryl, aryloxy, arylthio, aryl Amino, aryl- (C 1 -C 4 ) -alkoxy, aryl- (C 2 -C 4 ) -alkenyloxy, aryl- (C 1 -C 4 ) -alkylthio, aryl- (C 2 -C 4 ) -Alkenylthio, aryl- (C 1 -C 4 ) -alkylamino, aryl- (C 2 -C 4 ) -alkenylamino, aryl- (C 1 -C 6 ) -dialkylsilyl, diaryl- ( Optionally substituted by one or more radicals selected from the group consisting of C 1 -C 6 ) -alkylsilyl, triarylsilyl and 5 or 6 membered heterocyclyl, wherein the cyclic moieties of the last 14 radicals mentioned are halogen, Furnace, nitro, amino, hydroxyl, thio, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 3 -C 8 ) -cycloalkyl, (C 1 -C 4 ) -Alkoxy, (C 1 -C 4 ) -haloalkoxy, (C 1 -C 4 ) -alkylthio, (C 1 -C 4 ) -haloalkylthio, (C 1 -C 4 ) -alkylamino, (C 1 -C 4 ) -do Optionally substituted by one or more radicals selected from the group consisting of roalkylamino, formyl and (C 1 -C 4 ) -alkanoyl],
    Aryl, 5- or 6-membered heteroaromatic [where the two radicals mentioned last are halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2- C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -haloalkynyloxy, (C 3 -C 8 ) -cycloalkoxy, (C 4 -C 8 ) -cycloalkenyloxy, (C 3 -C 8 ) -halocycloalkoxy, (C 4 -C 8 ) -Halocycloalkenyloxy, carbamoyl, (C 1 -C 6 ) -mono- or di-alkylcarbamoyl, (C 1 -C 6 ) -alkoxycarbonyl, (C 1 -C 6 ) -alkanoyl Oxy, (C 1 -C 6 ) -mono- or di-haloalkylcarbamoyl, (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1- C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanamido, (C 2 -C 6 ) -alkenamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -Alkenylthio, (C 2 -C 6 ) -alkynylthio, (C 1 -C 6 ) -haloalkylthio, (C 2 -C 6 ) -Haloalkenylthio, (C 2 -C 6 ) -haloalkynylthio, (C 3 -C 8 ) -cycloalkylthio, (C 4 -C 8 ) -cycloalkenylthio, (C 3 -C 8 ) -halocycloalkthio, (C 4 -C 8 ) -halocycloalkenylthio, (C 1 -C 6 ) -alkylsulfinyl, (C 2 -C 6 ) -alkenylsulfinyl, (C 2 -C 6 ) -alkynylsulfinyl, (C 1 -C 6 ) -haloalkylsulfinyl, (C 2 -C 6 ) -haloalkenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl , (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3 -C 8 ) -halocycloalksulfinyl, (C 4 -C 8 )- halo cycloalkenyl sulfinyl, (C 1 -C 6) - alkylsulfonyl, (C 2 -C 6) - alkenyl nilseol sulfonyl, (C 2 -C 6) - alkynyl nilseol sulfonyl, (C 1 -C 6) -haloalkyl-sulfonyl, (C 2 -C 6) - haloalkenyl nilseol sulfonyl, (C 2 -C 6) - haloalkynyl nilseol sulfonyl, (C 3 -C 8) - cycloalkyl, sulfonyl, (C 4 -C 8) -cycloalkyl alkenyl nilseol sulfonyl, (C 3 -C 8) - halo-cycloalkenyl keuseol sulfonyl, (C 4 -C 8) - halo-cycloalkenyl sulfonate , (C 1 -C 6) - alkylamino, (C 2 -C 6) - alkenyl, amino, (C 2 -C 6) - alkynyl, amino, (C 1 -C 6) - haloalkyl, amino, (C 2 -C 6 ) -haloalkenylamino, (C 2 -C 6 ) -haloalkynylamino, (C 3 -C 8 ) -cycloalkylamino, (C 4 -C 8 ) -cycloalkenylamino, ( Optionally substituted by one or more radicals selected from the group consisting of C 3 -C 8 ) -halocycloalkamino and (C 4 -C 8 ) -halocycloalkenylamino;
    R 11 is (C 1 -C 10 ) -alkyl, haloalkyl, aryl (which is halo, cyano, nitro, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkyl, amino, (C 1 -C 4) - is D is optionally substituted by one or more radicals selected from the group consisting of alkylamino), NR 10 2, oR 10 or SR 10 - monoalkyl-amino and (C 1 -C 4).
    The term "halogen" includes fluorine, chlorine, bromine and iodine.
    The term “(C 1 -C 4 ) -alkyl” refers to straight or branched chain hydrocarbon radicals having 1 to 4 carbon atoms, for example methyl, ethyl, propyl, isopropyl, 1-butyl, 2-butyl, 2-methylpropyl Or as a t-butyl radical. Correspondingly, alkyl radicals having a wide range of carbon atoms are to be understood as straight or branched chain saturated hydrocarbon radicals containing carbon numbers corresponding to the stated ranges. Thus, the term “(C 1 -C 6 ) -alkyl” is the alkyl radical mentioned above and includes, for example, pentyl, 2-methylbutyl, 1,1-dimethylpropyl, hexyl radical. The term "(C 1 -C 10 ) -alkyl" includes the above-mentioned alkyl radicals such as nonyl, 1-decyl or 2-decyl radicals and the term "(C 1 -C 20 ) -alkyl" It is to be understood as the aforementioned alkyl radicals, for example undecyl, dodecyl, pentadecyl or eicosyl radicals.
    "(C 1 -C 4) - haloalkyl" refers to the same number of identical or different halogen atoms at least one of the hydrogen atoms, for example, the term optionally substituted by fluorine or chlorine "(C 1 -C 4) - alkyl" Alkyl groups mentioned in, for example trifluoromethyl, 1-fluoroethyl, 2,2,2-trifluoroethyl, chloromethyl, fluoromethyl, difluoromethyl and 1,1,2,2- It should be understood as a tetrafluoroethyl group.
    "(C 1 -C 4 ) -alkoxy" is to be understood as an alkoxy group wherein the hydrocarbon radical has the meaning given in the term "(C 1 -C 4 ) -alkyl". Alkoxy groups containing a wide range of carbon atoms should be understood correspondingly.
    The terms "alkenyl" and "alkynyl" with prefixes referring to a range of carbon atoms refer to a number of carbon sources corresponding to the stated range, including one or more polyvalent bonds that may be at any position of the unsaturated radical in question. It means a straight or branched chain hydrocarbon radical having a rule. Thus, "(C 2 -C 4 ) -alkenyl" is, for example, a vinyl, allyl, 2-methyl-2-propene or 2-butenyl group; "(C 2 -C 6 ) -alkenyl" means a radical mentioned above, for example a pentenyl, 2-methylpentenyl or hexenyl group. The term "(C 2 -C 20 ) -alkenyl" is to be understood as the radicals mentioned above, for example 2-desenyl or 2-eicosenyl groups. "(C 2 -C 4 ) -alkynyl" is, for example, an ethynyl, propargyl, 2-methyl-2-propane or 2-butynyl group. The term "(C 2 -C 6 ) -alkynyl" refers to such radicals, for example 2-pentynyl- or 2-hexynyl groups and "(C 2 -C 20 ) -alkynyl" refers to the radicals mentioned above For example, as 2-octynyl or 2-decynyl group.
    The term “(C 3 -C 8 ) -cycloalkyl” refers to monocyclic alkyl radicals such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl radicals and acyclic alkyl radicals (eg : Norbornyl radical).
    The term "(C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkyl" should be understood as, for example, cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl, cyclohexylethyl and cyclohexylbutyl radicals And the term “(C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkyl” for example 1-methylcyclopropyl, 1-methylcyclopentyl, 1-methylcyclohexyl, 3- Hexylcyclobutyl and 4-t-butyl-cyclohexyl radicals.
    The term “(C 1 -C 4 ) -alkoxy- (C 1 -C 6 ) -alkoxy” is an alkoxy group as defined above substituted by a further alkoxy group, for example 1-ethoxyethoxy. .
    The term "(C 3 -C 8 ) -cycloalkoxy" or "(C 3 -C 8 ) -cycloalkylthio" refers to the aforementioned (C 3 -C 8 ) -cycloalkyl radicals linked via an oxygen or sulfur atom Should be understood as one of.
    "(C 3 -C 8 ) -cycloalkyl- (C 1 -C 6 ) -alkoxy" is for example cyclopropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, cyclohexylmethoxy, cyclohexylethoxy Or a cyclohexyl butoxy group.
    The term “(C 1 -C 4 ) -alkyl- (C 3 -C 8 ) -cycloalkoxy” is a methylcyclopropyloxy, methylcyclobutyloxy or butylcyclohexyloxy group.
    The term "(C 1 -C 6 ) -alkylthio" is an alkylthio group in which the hydrocarbon radical has the meaning given under "(C 1 -C 6 ) -alkyl".
    Correspondingly, the term “(C 1 -C 6 ) -alkylsulfinyl” is for example methyl-, ethyl-, propyl-, isopropyl-, butyl-, isobutyl-, s-butyl- or t- Butylsulfinyl group, and the term "(C 1 -C 6 ) -alkylsulfonyl" is for example methyl-, ethyl-, propyl-, isopropyl-, butyl-, isobutyl-, s-butyl- or t -Butylsulfonyl group.
    "(C 1 -C 6) - alkylamino" is a nitrogen atom substituted by one or two identical or different alkyl radicals of the above definition.
    The term "(C 1 -C 6 ) -mono- or di-alkylcarbamoyl" has the definition of "(C 1 -C 6 ) -alkyl" and in the case of two hydrocarbon radicals one or two identical or different Carbamoyl group having a hydrocarbon radical.
    Correspondingly is, "(C 1 -C 6) - alkyl carbamoyl dihalo" is two (C 1 -C 6) according to the definition - a haloalkyl radical or one according to the definition (C 1 -C 6 Carbamoyl group with) -haloalkyl radical and one (C 1 -C 6 ) -alkyl radical.
    “(C 1 -C 6 ) -alkanoyl” is, for example, an acetyl, propionyl, butyryl or 2-methylbutyryl group.
    The term "aryl" is an isocyclic aromatic radical having 6 to 14 carbon atoms, in particular 6 to 12 carbon atoms, for example phenyl, naphthyl or biphenylyl, preferably phenyl. Thus, the term "aroyl" is an aryl radical as defined above attached via a carbonyl group, an example of which is a benzoyl group.
    The term “heterocyclyl” is a cyclic radical that is fully saturated, partially unsaturated or fully unsaturated, and which may be interrupted by one or more identical atoms selected from nitrogen, sulfur and oxygen, wherein the oxygen atoms are then directly Are not adjacent and one or more carbon atoms are present in the ring, for example thiophene, furan, pyrrole, thiazole, oxazole, imidazole, isothiazole, isoxazole, pyrazole, 1,3,4-oxa Diazole, 1,3,4-thiadiazole, 1,3,4-triazole, 1,2,4-oxadiazole, 1,2,4-thiadiazole, 1,2,4-triazole , 1,2,3-triazole, 1,2,3,4-tetrazole, benzo [b] thiophene, benzo [b] furan, indole, benzo [c] thiophene, benzo [c] furan, iso Indole, benzoxazole, benzothiazole, benzimidazole, benzisoxazole, benzisothiazole, benzopyrazole, benzothiadiazole, benzotriazole, dibenzofuran, dibenzothiophene, carbazole, Pyridine, pyrazine, pyrimidine, pyridazine, 1,3,5-triazine, 1,2,4-triazine, 1,2,4,5-triazine, quinoline, isoquinoline, quinoxaline, quinazoline, Cinnoline, 1,8-naphthyridine, 1,5-naphthyridine, 1,6-naphthyridine, 1,7-naphthyridine, phthalazine, pyridopyrimidine, purine, pteridine 4H-quinolizine ; Piperidine, pyrrolidine, oxazoline, tetrahydrofuran, tetrahydropyran, isoxazolidine or thiazolidine radical. Thus, the term "heteroaromatic" includes in each case fully unsaturated aromatic heterocyclic compounds in the meaning referred to in "heterocyclyl".
    The term “aryl- (C 1 -C 4 ) -alkoxy” is an aryl radical attached via a (C 1 -C 4 ) -alkoxy group, for example benzyloxy, phenylethoxy, phenylbutoxy or naphthylmethoxy There is a radical.
    "Arylthio" is an aryl radical attached through a sulfur atom, examples of which are phenylthio or 1- or 2-naphthylthio radicals. Correspondingly, "aryloxy" is for example a phenoxy or 1- or 2-naphthyloxy radical.
    “Aryl- (C 1 -C 4 ) -alkylthio” is an aryl radical attached through an alkylthio radical, for example benzylthio, naphthylmethylthio or phenylethylthio radicals.
    The term "(C 1 -C 6 ) -trialkylsilyl" means a silicon atom carrying three identical or different alkyl radicals according to the above definition. Correspondingly, the "aryl - (C 1 -C 6) - dialkyl silyl" and the silicon atom is accompanied by one aryl radical and two identical or different radicals according to the above definition, "diaryl - (C 1 - C 6 ) -alkylsilyl "is a silicon atom carrying one alkyl radical and two identical or different aryl radicals according to the above definition, and" triarylsilyl "carries three identical or different aryl radicals according to the above definition Is a silicon atom.
    If two or more radicals R 10 are present in a substituent, for example -C (= W) NR 10 2 , these radicals may be the same or different.
    Preference is given to compounds of the formula I as follows:
    Y is C 1 -C 6 -alkyl mono- or polysubstituted by chlorine and / or fluorine;
    m is 0;
    Q is a 5-membered heterocyclic group ego;
    Where a) X 2 = NR a and X 3 = CR b R 1, or b) X 2 = CR a R 2 and X 3 = CR b R 3, or c) X 2 = CR 4 R 5 and X 3 = CR 6 R 7 ;
    R a and R b together form a single bond;
    R 1 , R 2 , R 3 , R 4 and R 6 are each independently of each other hydrogen, halogen, C 1 -C 12 -alkyl, (C 3 -C 8 ) -cycloalkyl, (C 2 -C 8 )- Alkenyl, (C 2 -C 8 ) -alkynyl [wherein the last four hydrocarbon radicals mentioned are C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -alkylamino, C 1 -C 6 -alkylcarbonylamino, C 1 -C 6 -alkylsulfonylamino, phenyl, furyl, pyryl, Optionally mono- or polysubstituted by the same or different radicals selected from the group A1 consisting of thienyl, halogen, cyano, phenyloxy, phenylthio and phenylamino, wherein the eleven radicals mentioned first in the group A1 are each To the same or different radicals selected from the group B1 consisting of halogen, cyano, C 1 -C 3 -alkoxy and phenyl, which is optionally mono- or polysubstituted by one or more halogen atoms Optionally mono- or polysubstituted by each of the three radicals mentioned in the group A1 are selected from the group B2 consisting of halogen, cyano, nitro, C 1 -C 3 -alkyl and C 1 -C 3 -alkoxy Mono- or polysubstituted by the same or different radicals]
    (C 1 -C 6 ) -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxycarbonyl, phenyl, pyridyl, furyl, thienyl, pyryl (the last 8 mentioned) Radicals are optionally mono- or polysubstituted by the same or different radicals selected from group B 1), or
    OR 10 , SR 10 or N (R 10 ) 2 ;
    R 5 and R 7 are each independently of the other hydrogen, halogen, (C 1 -C 12 ) -alkyl, (C 3 -C 8 ) -cycloalkyl, C 2 -C 8 -alkenyl, C 2 -C 8- Alkynyl [wherein the last four hydrocarbon radicals mentioned are C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkyl Selected from the group A2 consisting of thio, C 1 -C 6 -alkylamino, C 1 -C 6 -alkylcarbonylamino, phenyl, furyl, pyryl, thienyl, halogen, cyano, phenyloxy, phenylthio and phenylamino Optionally mono- or polysubstituted by the same or different radicals, wherein the ten radicals mentioned first in group A 2 are each optionally mono- or poly-substituted by the same or different radicals selected from group B 1 and in group A 2 The last three radicals mentioned are each optionally monosubstituted by the same or different radicals selected from group B2 Is multi-substituted, or
    (C 1 -C 6 ) -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxycarbonyl, phenyl, pyridyl, furyl, thienyl, pyryl (the last 8 mentioned) Radicals are optionally mono- or polysubstituted by the same or different radicals selected from group B 1), or
    OR 10 , SR 10 or N (R 10 ) 2 ;
    R 10 is hydrogen, benzyl, C 1 -C 6 -alkyl, C 1 -C 6 -cycloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, phenyl, C 1 -C 6- Alkylcarbonyl or C 1 -C 6 -alkylsulfonyl, wherein the eight radicals mentioned last are optionally mono- or polysubstituted by the same or different halogen atoms.
    Especially preferred are compounds of formula I,
    Y is trifluoromethyl;
    R 1 , R 2 , R 3 , R 4 and R 6 are each independently of the other halogen, C 1 -C 12 -alkyl, C 2 -C 12 -alkenyl [the last two radicals mentioned are C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylamino, C 1 -C 4 The same selected from the group A3 consisting of -alkylcarbonylamino, C 1 -C 4 -alkylsulfonylamino, phenyl, furyl, pyryl, thienyl, fluorine, chlorine, bromine, cyano, phenyloxy, phenylthio and phenylamino Or optionally monosubstituted or polysubstituted by different radicals, wherein the eleven radicals mentioned first in group A3 are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B1 and the last in group A3 The three radicals mentioned in are each optionally monosubstituted or substituted by the same or different radicals selected from group B2. Is ring], or is OR 10, SR 10 or N (R 10) 2, and;
    R 5 and R 7 are each independently of the other halogen, (C 1 -C 12 ) -alkyl, C 2 -C 12 -alkenyl, wherein the two radicals mentioned at the end are C 1 -C 4 -alkylcarbonyl , C 1 -C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylamino, C 1 -C 4 -alkylcarbonylamino, phenyl Optionally mono- or polysubstituted by the same or different radicals selected from group A4 consisting of furyl, pyryl, thienyl, fluorine, chlorine, bromine, cyano, phenyloxy, phenylthio and phenylamino, the first of group A4 The ten radicals mentioned in are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B1, and the three radicals mentioned last in group A4 are each selected by the same or different radicals selected from group B2 or a mono-substituted or multi-substituted], or oR 10, SR 10 or N (R 10) 2 And;
    R 10 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, phenyl, C 1 -C 4 -alkylcarbonyl or C 1 -C 4 -alkyl Sulfonyl, wherein the six radicals mentioned last are optionally mono- or polysubstituted by the same or different halogen atoms.
    Very particular preference is given to compounds of formula I, wherein R 1 , R 2 , R 3 , R 4 and R 6 are each independently of each other C 1 -C 10 -alkyl or C 2 -C 10 -alkenyl, wherein The two radicals mentioned are C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 - A5 from the group consisting of alkyl sulfonylamino, phenyl, fluorine, chlorine, bromine, cyano, phenyloxy, phenylthio and phenylamino-alkylamino, C 1 -C 4 -alkyl-carbonyl-amino, C 1 -C 4 Optionally monosubstituted or polysubstituted by the same or different radicals selected, wherein the eight radicals mentioned first in group A5 are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B1, and group A5 The last of the three radicals mentioned are each of the same or different radicals selected from group B2. Optionally substituted with one or multi-substituted;
    R 5 and R 7 are each independently of one another C 1 -C 10 -alkyl or C 2 -C 10 -alkenyl, wherein the two radicals mentioned last are C 1 -C 4 -alkylcarbonyl, C 1- C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylamino, C 1 -C 4 -alkylcarbonylamino, phenyl, fluorine, chlorine , Optionally mono- or polysubstituted by the same or different radicals selected from group A6 consisting of bromine, cyano, phenyloxy, phenylthio and phenylamino, wherein the seven radicals mentioned last in group A6 are each group B1 Optionally monosubstituted or polysubstituted by the same or different radicals selected from, and the three radicals mentioned last in group A6 are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B2.
    Depending on the nature of the substituents described above, the compounds of formula (I) can be acidic or basic and form salts. For example, if the compounds of formula (I) have hydroxyl, carboxyl and other groups that induce acidicity, these compounds can be reacted with a base to form salts. For example, suitable bases are hydroxides, carbonates, bicarbonates of alkali metals and alkaline earth metals, in particular sodium, potassium, magnesium and calcium, ammonia with further (C 1 -C 4 ) -alkyl radicals, primary, secondary And mono-, di- and trialkanolamines of tertiary amines and also of (C 1 -C 4 ) -alkanols. For example, if the compounds of formula (I) have amino, alkylamino and other groups that induce basicity, these compounds can react with acids to form salts. For example, suitable acids are mineral acids (eg hydrochloric acid, sulfuric acid and phosphoric acid), organic acids (eg acetic acid and oxalic acid) and acid salts (eg NaHSO 4 and KHSO 4 ). Salts obtainable in this way have insecticide, acaricide and nematicide properties.
    Compounds of formula (I) may have one or more asymmetric carbon atoms or stereoisomers on the double bond. Thus, enantiomers or diastereomers may be present. The present invention includes pure isomers and mixtures thereof. Mixtures of diastereomers may be separated into isomers by conventional methods such as selective crystallization from a suitable solvent or chromatography. Racemates can be separated into enantiomers by conventional methods.
    The invention also provides a process for the preparation of compounds of formula (I):
    In the presence of a base, an activated derivative of an acid of formula II is reacted with a compound of formula III, wherein a) X 1 = W, X 2 = NR a , X 3 = CR b R 1 and R a , R b , where R 1 is as defined above and W is oxygen.
    Where
    The radical R 1 is as defined in formula (I),
    X and Y are as defined above.
    Suitable activated derivatives are for example acyl halides, esters and anhydrides. Suitable bases are amines such as triethylamine, diisopropylethylamine, pyridine or rutidine, alkali metal hydroxides, alkali metal alkoxides such as sodium ethoxide or potassium tert-butoxide, or alkyl Metal compounds such as butyllithium.
    Depending on the conditions, the reactions described above may be carried out in one step or two steps via intermediates of formula IV:
    Compounds of formula IV can be cyclized to 1,2,4-oxadiazoles by heating with an inert solvent at temperatures below 180 ° C. Compounds of formula IV can be prepared using the acid of formula II using dehydrating reagents such as dicyclohexylcarbodiimide, 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide or N, N'-carbonyldiimidazole; It can be obtained directly from amidoxime of formula III.
    Acids of formula II and amidoxime of formula III are commercially available or can be prepared by methods known in the literature (see Houben-Weyl, Methoden der organischen Chemie, Volume X / 4, pages 209-212; EP -A 0580374; GF Holland, JNPereira, J. Med. Chem., 1967, 10,149).
    In the case of a) described above, when W is sulfur, hydroxylamine-O-sulfonic acid can be obtained by methods known from the literature (Y. Lin, SA Lang, SR Petty, J. Org. Chem. 1980, 45, 3750). The compounds of formula (I) can be obtained by reacting the same electrophilic amination agent with a compound of formula (VII):

    Compounds of formula (VII) required as starting materials for the reaction include thioamides of formula (VIII) and dialkylamide dialkyl acetals of formula (IX) wherein R 1 is as defined above and R 12 and R 13 are each C 1 -C 4 -alkyl).

    The amidoxime of Formula (V) is reacted with an activated derivative of the acid of Formula (VI) or the acid of Formula (VI) itself to yield a compound of Formula (I) wherein X 1 = NR a , X 2 = CR b R 1 , X 3 = W, where R a , R b and R 1 are as defined above).

    In an inert solvent such as toluene, N, N'-diacylhydrazine of formula (XIII) is converted to a Labeson reagent (AA. El-Barbary, S. Scheibyl, SO Lawesson, H. Fritz, Acta Chem. Scand. 1980, 597) Cyclized with a thiolating agent to yield a compound of formula I wherein c) X 1 = V, X 2 = CR a R 1 , X 3 = NR b , wherein R a , R b and R 1 are as defined above; , V is sulfur).

    In the case of b) above, when W is oxygen, the acid of formula (II) is used with an activator such as phosphorus oxychloride or phosphorus pentachloride to give the hydrazide of formula (X) wherein R 1 is as defined above May be reacted with to form a compound of formula (I):

    It is also possible to react an acid hydrazide of formula (XI) with an ortho ester of formula (XII) wherein R 1 is as defined above and R 12 is (C 1 -C 4 ) -alkyl:

    The reaction can be carried out depending on the presence of a solvent or the presence of an activator. Suitable solvents are hydrocarbons such as toluene, or ethers such as 1,2-dimethoxyoxyethane. Suitable activators are for example phosphorus oxychloride. The reaction temperature is generally the reflux temperature of the solvent.
    A compound of formula (IV) is reacted with a dehydration reagent to give a compound of formula (I) wherein X 1 = V, X 2 = CR a R 2 , X 3 = CR b R 3 , and R a , R b and R 3 Is as defined above and V is oxygen).

    Suitable dehydration reagents are inorganic acyl chlorides (e.g. phosphorus oxychloride or thionyl chloride), inorganic acids (e.g. sulfuric acid or polyphosphoric acid) or mixtures of phosphoric acid and acetic anhydride (Houben-Weyl, Methoden der organischen Chemie, Volume E8a, pages 935-941).
    The reaction can be carried out depending on the presence or absence of a solvent. Suitable solvents are inert solvents such as toluene, benzene, dimethoxyethane, dimethylformamide, dimethylacetamide and chlorobenzene. The reaction temperature is advantageously in the range of 50 to 150 ° C. For example, it is possible to obtain compounds of formula XIV by oxidation of the corresponding hydroxyl compounds of formula XV and to use all reagents commonly used for organic chemistry purposes (Milos Hudlicky, “Oxidations in Organic Chemistry ", ACS Monograph 186, American Chemical Society, Washington, DC, 1990):

    In the case of d) above, when V is sulfur, the thioamide of formula XVII and the carbonyl derivative of formula XVIII (Z is halogen, in particular chlorine or bromine, acyloxy or sulfonyloxy, in particular methanesulfonyloxy or Compound of formula (I) can be prepared by condensation reaction of tolylsulfonyloxy):

    In a solvent such as tetrahydrofuran and 1,4-dioxane, the compound of formula (XV) is subjected to Burgess' reagent (GM Atkins, EM Burgess, J. Am. Chem. Soc) in the range of room temperature to reflux temperature of the solvent. 1968, 90, 4744.) and reacted with a cyclizing agent such as e) wherein X 1 = V, X 2 = CR 4 R 5 , X 3 = CR 6 R 7 , R 4 , R 5 , R 6 and R 7 are as defined above and V is oxygen.

    If appropriate, the activated derivative of the acid of formula II can be reacted with β-aminoalcohol of formula XVI in the presence of a base such as triethylamine in an inert solvent such as dichloromethane to give a compound of formula XV:
    Acyl halides or anhydrides can be used as activated derivatives of the acid. Many β-aminoalcohols of formula XVI are commercially available. Many preparation procedures for the reduction of α-amino acids are found in B.M. Trost "Comprehensive Organic Synthesis, Reduction", Volume 8, Pergamon Press, Oxford, 1991.
    In the case of e) described above, when V is sulfur, a compound of formula (I) is prepared by reacting formula (XVII) with a compound of formula (XIX) wherein two substituents Z are as defined above and both are the same or different (AR Katritzky "Comprehensive Heterocyclic Chemistry", Volume 6, pages 306-312, Pergamon Press, Oxford).

    Thioamides of formula (XVII) are commercially available or can be obtained by adding hydrogen sulfide to the corresponding carbonitriles in the presence of a base (A.E.S. Fairfull, J.L.Low, D.A.Peak, J. Chem. Soc. 1952, 742).
    A hydrazide of formula (XX) is reacted with a compound of formula (XXI) or a thioamide of formula (XXII), wherein f is a compound of formula (I) wherein X 1 = NR a , X 2 = CR b R 1 , X 3 = NR 8 and R a , R b , R 1 and R 8 are as defined above (Houben-Weyl, Methoden der organischen Chemie, Volume E8d, pages 510-512):
    The reaction can be carried out with or without solvents and suitable solvents are alcohols such as ethanol and propanol or aromatic hydrocarbons such as toluene and xylene. If the reaction is carried out in a solvent, the reaction temperature selected is advantageously the reflux temperature of the solvent. On the other hand, if the reaction is carried out without solvent, it can suitably be heated to 200 ° C or less.
    When group Q is prepared by condensation, cyclic or ring reaction, the radicals R 1 to R 9 can be further derived, if desired, using extensive collection of organic chemical synthesis methods.
    Compounds of formula I can be prepared by treating compounds of formula I, wherein m is 0, with oxidants such as meta-chloroperbenzoic acid, where m is 1.
    Compounds of formula (I, or hereinafter referred to herein as "active compounds") have excellent plant resistance to aquatic organisms, good serotoxicity and advantageous properties and are suitable for pest animals, especially insects, arthropods (ticks), worms And molluscs, which are highly desirable for controlling insects and arthropods, which live in agriculture, animal husbandry, forestry, preservation and hygiene compartments of stored products. They are usually sensitive and active against the resistant class and all or individual development. The pests mentioned above include the following:
    Acarina (e.g., Acarus siro, Argas spp., Ornithodoros spp., Dermanyssus gallinae, Eriophyes ribis) ), Phyllocoptruta oleivora, Bophillus spp., Ripicephalus spp., Amblyomma spp., Hyaloma spp., Hyalomma spp, Ixodes spp., Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Brio Bryobia praetiosa, Panonicus spp., Tetranychus spp., Eotetranychus spp., Oligonychus spp. And Eutetranichus spp.],
    Isopoda (e.g. Oniscus asselus, Armadium vlgar and Porcellio scaber),
    Diloplopoda (e.g. Blaniulus guttulatus),
    Chilopoda (e.g., Geophilus carpophagus and Scutigera spp.),
    Symphyla (e.g. Scutigerella immaculata),
    Thysanura (e.g. Lepisma saccharina),
    Collembola (e.g. Onychiurus armatus),
    Orthoptera (e.g. Blata orientalis, Periplaneta americana, Leucophaea madeirae, Platella germanica, Arceta) Acheta domesticus, Gryllotalpa spp., Locusta migratoria migratorioides, Melanoplus differentialis and Skistoserca gre Schistocerca gregaria],
    Isoptera (eg, Reticulitermes spp.),
    Anoplura (e.g. Phylloera vastatrix, Pemphigus spp., Pediculus humanus corporis, Haematopinus spp. And Reno Gnatus species (Linognathus spp.)],
    Mallophaga (e.g. Trichodectes spp. And Damalinea spp.),
    Thysanoptera (e.g. Hercinothrips femoralis, Tripps tabaci and Frankliniella spp.),
    Heteroptera (e.g., Eurygaster spp., Dysdercus intermedius, Piesma quadrata, Cimax lectularius, Rodneys phurlic) Rhodnius prolixus and Triatoma spp.],
    Cicada (Homoptera) (e.g. Aleurodes brassicae, Bemisia tabaci, Trialeurodes vaporarirum, Apis spp., Brevico Brevicoryne brassicae, Cryptomyzus ribis, Doralis fabae, Doralis pomi, Eriosoma lanigerum, Hyalloprus aran Hyniopterus arandinis, Macrosiphum avenae, Myzus spp., Phorodon humuli, Rhopalosiphum padi, Empoasca spp. .), Euscelus bilobatus, Nephotettix cincticeps, Lecanium corni, Saissetia oleae, Lao delfax striatel Laodelphax striatellus, Nilaparv ata lugens, Aonidiella aurantii, Aspiciotus hederae, Pseudococcus spp. and Psylla spp.],
    Lepidoptera (e.g., Pectinophora gossypiella, Bupalus piniarius, Cheimatobia brumata, Lithocolletis blancardella, Hipono Hyponomeuta padella, Flutella maculipennis, Malacosoma neustria, Euroctis chrysorrhoea, Lymantria spp. Buculatrix thurberiella, Phyllocnistis citrella, Agrotis spp, Euxoa spp., Feltia spp., Erias Earias insulana, Heliothis spp., Laphygma exigua, Mamestra brassicae, Panolis flammea, Prodenia litura litura) , Spodoptera spp., Trichoplusia ni, Carpocapsa pomonella, Pieris spp., Chilo spp., Pirastar nubilla Pyrausta nubilalis, Ephestia kuehniella, Galleria mellonella, Cacoacia podana, Capua reticulana, Coristoneura fumi Chorastoneura fumiferana, Clysia ambiguella, Homona magnanima, Tortrix viridana, Cuaphalocrocis spp. And Manduca species ( Manduca spp.)],
    Coleoptera (e.g. Anobium punctatum, Rizoperta dominica, Bruchidius obtectus, Acanthoscelides obtectus, Hilotru Hylotrupes bajulus, Agelastica alni, Leptinotarsa decemlineata, Phaedon cochlearae, Diabrotica spp. Psylloides chrysocephala, Epilachna varivestis, Atomaria spp., Oryzaephilus surinmensis, Antonumus spp. , Sitophilus spp., Otiorrhynchus sulcatus, Cosmopolites sordidus, Cethorthorchus assimilis, Hyperapo Hypera postica, Dermestes spp., Trogoderrma, Anthrenus spp., Attagenus spp., Lyctus spp. ), Meligethes aeneus, Ptinus spp., Niptus hololeucus, Gibbium psylloides, Tribolium spp. , Tenebrio molitor, Agriotes spp., Conoderus spp., Melolontha melolontha, Amphimallon solstitialis, Kos Telestera zealandica and Lissorhoptus spp.],
    Hymenoptera (e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis and Vespa spp) .)],
    Diptera (e.g., Aedes spp., Anopheles spp., Culex spp., Drosophila melanogaster, Musca species spp.), Fannia spp., Califora erythrocephala, Lucilia spp., Chrysomyia spp., Cuterebra spp., Gastrophilus spp., Hypobosca spp., Stomoxys spp., Oestrus spp., Hypoderma spp., Tabanus spp., Taniaa spp., Bibio hortulanus, Oscinella frit, Phorbia spp., Pegomia hyaciami Pegomyia hyoscyami, Ceratitis capitata, Dacus oleae and Tipula paludosa],
    Siphoaptera (eg, Xenopsylla cheopsis and Ceratophyllus spp.),
    Arachnida (e.g. Scorpio maurus and Latrodectus mactans),
    Helminthes (e.g. Heemonchus, Trichostrongulus, Ostertagia, Couperia, Cabertia, Strongiloides ), Oesophagostomum, Hyostrongulus, Acylostoma, Ascaris and Heterakis, and also Fasciola,
    Gastropoda (e.g. Deroceras spp., Arion spp., Limnaea spp., Galba spp., Succinea spp. ), Biomphalaria spp., Bulinus spp. And Oncomelania spp.],
    Bivalve (eg Dreissena spp.).
    Examples of plant-parasitic nematodes that may be controlled in accordance with the present invention include root-parasitic soil nematodes, such as Meloidogyne (rooted nematodes, such as Meloidogyne insognita, Melido) Melodogyne hapla and Meloidogyne javanica, Heterodera and Grolobodera (cystic nematodes, such as Globoderra rostochiensis, Globoderra pallida, Heterodera trifolii, and
    Radopholus (e.g. Radopholus similis, Pratylenkus) (e.g. Pratilenchus neglectus, Pratilenkus penetrans) ) And Pratylenkus curvitatus), Tylenchulus (e.g. Tylenchulus semipenetrans), Tylencholinus (e.g. Tylenechorhynchus dubius) And Tylenechorhynchus claytoni, Rotylenchus (e.g. Rotylenchus robustus), Heliocotylenchus (e.g. (Heliocotylenchus multicinctus), Belonoaimus (e.g. Belonoaimus longicaudatus), Rondorus (e.g. Longidorus elongatus), Trichodoru Trichodorus (e.g. Trichodorus primitivus) and Xiphinema (e.g. Xiphinema index).
    The compounds according to the invention are also useful in the nematode Ditylenchus (stem parasites, such as Ditylenchus dipsaci and Ditylenchus destructor), Aphelenchoides ( Oral nematodes such as Aphelenchoides ritzemabosi) and Anguina (oral-hox nematodes such as Anguina tritici).
    The invention also relates to compositions, in particular pesticidal and acaricide compositions, which comprise a compound of formula (I) and suitable formulation auxiliaries.
    The composition according to the invention generally comprises the active substance of formula (I) in a proportion of 1 to 95% by weight. They can be combined in various ways depending on the well-known biological and / or chemical and physical parameters. Thus, the following combinations may be suitable:
    Wettable powder (WP), emulsifiable concentrate (EC), aqueous solution (SL), emulsion, sprayable solution, oil-based or water-based dispersion (SC), suspension emulsion (SE) dust powder (DP), Seed-dressing products, granules in the form of micro granules, spray granules, coated and adsorbent granules, water dispersible granules (WG), ULV formulations, microcapsules, waxes or baits.
    These individual types of formulations are mainly known and described in the following literature:
    Winnacker-Kuchler, "Chemische Technologie" [Chemical Technology], Volume 7, C. Hauser Verlag Munich, 4th ed. 1986;
    Van Falkenberg, "Pesticides Formulations", Marcel Dekker N.Y. 2nd ed. 1972-73;
    K. Martens, "Spray Drying Handbook", 3rd ed. 1979, G. Goodwin Ltd. London.
    Necessary formulation auxiliaries such as inerts, surfactants, solvents and other additives, ie carrier materials and surfactants, are known as above and are known in the following literature:
    Watkins, "Handbook of Insecticide Dust Diluents and Carriers", 2nd ed., Darland Books, Caldwell N.J .;
    Olphen, "Introduction to Clay Colloid Chemistry", 2nd ed., J. Wiley & Sons, N.Y .;
    Marsden, Solvents Guide, 2nd ed., Interscience, N.Y. 1950;
    McCutcheon, "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood N. J .;
    Sisley and Wood, "Encyclopedia of Surface Active Agents", Chem. Publ. Co. Inc., N.Y. 1964;
    Schonfeldt, "Grenzflachenaktive Ahylenoxidaddukte" [Surface-Active Ethylene oxide adducts], Wiss. Verlagsgesell., Stuttgart 1967;
    Binnacker-kuchler, "Chemische Technologie", Volume 7, C. Hauser Verlag Munich, 4th ed. 1986.
    Based on these formulations, they may also be prepared in combination with other pesticidal substances, fertilizers and / or growth regulators (such as in the form of premixes or tank mixtures). Wettable powders are preparations that are singly dispersible in water, which are further actives and also diluents or inerts, moisturizers (e.g. polyethoxylated alkylphenols, polyethoxylated fatty alcohols, alkyl- or alkylphenols). Sulfonates) and dispersants such as sodium ligninsulfonate or sodium 2,2'-dinaphthylmethane-6,6'-disulfonate. Emulsifiable concentrates are prepared by dissolving the active substance with the addition of one or more emulsifiers in an organic solvent (eg butanol, cyclohexanone, dimethylformamide, xylene or a high boiling aromatic compound or hydrocarbon). As emulsifiers, for example calcium alkylarylsulfonates (such as calcium dodecylbenzenesulfonate) or nonionic emulsifiers (such as fatty acid polyglycol esters), alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide / ethylene oxide condensation Products, alkyl polyethers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters or polyoxyethylene sorbitan esters can be used.
    Dusting agents are obtained by grinding the active compound together with finely divided solid materials such as talc, natural clays such as kaolin, benzonitite, polyfillite or diatomaceous earth. Granules may be used to grind the active material onto an adsorbent granulated inert material, or adhesives (eg, polyvinyl alcohol or sodium polyacrylate) on the surface of the carrier material (eg sand or kaolinite) or on the surface of the granulated inert material. Or mineral oils can be used to apply the active substance concentrate. Suitable active compounds can also be granulated in conventional manner for the preparation of fertilizer granules, if necessary, in admixture with fertilizers.
    In the wettable powders, the concentration of the active compound is, for example, about 10 to 90% by weight, with the remainder being formulated such that 100% by weight of conventional formulation components. In the case of emulsifiable concentrates, the concentration of active substance can be from about 5 to 80% by weight. Dust-like formulations typically comprise from 5 to 20% by weight of active material and from about 2 to 20% by weight of a sprayable solution. In the case of granules, the content of the active compound depends in part on whether the active compound is in liquid or solid form and depends on the granule aids, fillers and the like used.
    In addition, the formulations of the above-mentioned active compounds include, where appropriate, tackifiers, humectants, dispersions, emulsifiers, penetrants, solvents, fillers or carriers conventionally used in each case.
    Commercially available concentrates are, if appropriate, diluted with water in a manner customary for their use, such as wettable powders, emulsifiable concentrates, dispersions and any micro granules. Sprayable solutions as well as dust-like and granule formulations are typically not diluted with any other inerts prior to use.
    The required application rate depends on external conditions (eg temperature and humidity). For example, the active substance may be varied within a wide range of 0.0005 to 10.0 kg / ha or more but preferably 0.001 to 5 kg / ha.
    The active compounds according to the invention are commercially available formulations and in the form of applications prepared from these formulations, i.e. with other active substances (e.g. May be present as a mixture.
    Examples of pesticides include phosphate esters, carbamates, carboxylic acid esters, formamidines, tin compounds and materials produced by the microorganisms themselves.
    Preferred mixing components are as follows:
    1.Groups of phosphorus compounds (e.g. acetate, azametiphos, azinfos-ethyl, azinfos-methyl, bromophos, bromophos-ethyl, chlorfenbinfos, chlormefos, chlorpyrifos, chlorpyri Force-methyl, demethone, demethone-S-methyl, demethone-S-methylsulfone, dialilifos, diazinone, dichlorbose, dicrotophos, O, O-1,2,2,2-tetra Chloroethyl phosphorothioate (SD 208 304), Dimethoate, Disulfotone, EPN, Ethion, Etoprophos, Etrifoss, Pampur, Phenamiphos, Phentriiothione, Pensulpotion, Pention, Phonophos, Formomothione, Heptenophos, Isozofos, Isothioate, Isoxation, Malathion, Metacriphos, Metamidophos, Metidathione, Salityon, Mevinforce, Monoclotophos, Naled , Ometoate, oxydemethone-methyl, parathion, parathion-methyl, pentoate, forate, phoslon, phospholane, phosph , Phosphamidone, bombardment, pyrimifos, pyrimifos-ethyl, pyrimifos-methyl, propenofoss, propaphos, proetasphos, prothiophos, pyraclophos, pyridapention, Quinal force, sulfprophos, temefos, perbufos, tetrachlorbinfos, thiomethone, triazofoss, trichlorpon, bamidothione);
    2. Groups of carbamate (eg aldicarb, 2-tert-butylphenyl methylcarbamate (BPMC), carbaryl, carbofuran, carbosulphan, clotocarb, benpracarb, thiophencarb, Furathiocarb, isoprocarb, metomil, 5-methyl-meth-cumenylbutyryl (methyl) carbamate, oxamyl, pyrimikab, propoxur, thiodicarb, thiocarnox, ethyl 4,6,9-tria-4-benzyl-6,10-dimethyl-8-oxa-7-oxo-5,11-dithia-9-dodecenoate (OK 135), 1-methylthio (ethyl Lideneamino) -N-methyl-N- (morpholinothio) carbamate (UC 51717));
    3. Groups containing carboxylic esters, such as alletrin, alphamethrin, 5-benzyl-3-furylmethyl (E)-(1R) -cis-2,2-dimethyl-3- (2-oxothiolane- 3-ylidenemethyl) cyclopropanecarboxylate, bioaletrin, bioaletrin ((S) -cyclopentyl isomer), bioresmethrin, biphenate, (RS) -1-cyano-1- (6-phenoxy Cy-2-pyridyl) methyl (1RS) -trans-3- (4-tert-butyl-phenyl) -2,2-dimethylcyclopropanecarboxylate (NCI 85193), cycloprotrin, cyhalothrin, Cytitrin, cypermethrin, cyphenotrin, deltamethrin, empentrin, espen valerate, fenflutrin, phenpropatrine, fenvallate, flucitalinate, flumethrin, flu Valinate (D-isomer), permethrin, peotrin ((R) -isomer), d-prarethrin, pyrethrins (natural product), resmethrin, tefluthrin, tetramethrin, tralomethrin) ;
    4. a group of amidines (eg amitraz, chlordimeform);
    5. group of tin compounds (eg cyhexatin, fenbutatin oxide);
    6. Other groups (eg Abamectin, Bacillus thuringiensis, Bensultap, Vinapacryl, Bromopropylate, Buprofezin, Caffechlor, Cartop, Chlorobenzylate, Chlorfluazuron, 2- (4) -Chlorophenyl) -4,5-diphenylthiophene (UBI-T 930), chlorpentazine, 2-naphthylmethyl cyclopropanecarboxylate (Ro 12-0470), cyromazine, N- (3,5- Dichloro-4- (1,1,2,3,3,3-hexafluoro-1-propyloxy) phenyl) carbamoyl) -2-chlorobenzocarboximide ethyl ester, DDT, dicopol, N- ( N- (3,5-dichloro-4- (1,1,2,2-tetrafluoroethoxy) phenylamino) carbonyl) -2,6-difluorobenzamide (XRD 473), diflubenzuron , N- (2,3-dihydro-3-methyl-1,3-thiazol-2-ylidene) -2,4-xyldine, dinobutone, dinocap, endosulfan, etofenprox, (4 -Ethoxy-phenyl) (dimethyl) (3- (3-phenoxyphenyl) propyl) silane, (4-ethoxyphenyl) (3- (4-fluoro-3-phenoxyphenyl) propyl) dimethylsilane,Oxycarb, 2-fluoro-5- (4- (4-ethoxyphenyl) -4-methyl-1-pentyl) -diphenyl ether (MTI 800), granulosis and nucleus polyhedrosis virus (nuclear) polygedrosis virus), penthiocarb, flubenzimine, flucycloxonon, flufenoxuron, gamma-HCH, hexthiaxans, hydrammethylnon (AC 217300), ivermectin, 2-nitromethyl- 4,5-dihydro-6H-thiazine (DS 52618), 2-nitromethyl-3,4-dihydrothiazole (SD 35651), 2-nitromethylene-1,2-thiazinan-3-ylcarbam Aldehydes (WL 108477), propargite, teflubenzuron, tetradipon, tetrasul, thiocyclam, tripufuron and imidacloprid).
    The above mentioned mixing partners are active compounds, most of which are described in Ch. R. Worthing and SB Walker, The Pesticide Manual, 7th Edition (1983), British Crop Protection Crop Protection Council. have.
    The content of the active compound in the form used in the commercial formulation can be from 0.00000001 to 95% by weight of the active compound, preferably from 0.00001 to 1% by weight.
    The active compound is used in a conventional manner consistent with the form used.
    The active compounds according to the invention are also suitable for controlling external and internal parasites in the veterinary or livestock sector. The active substances according to the invention can be administered in known manner, such as in the form of tablets, capsules, potions or granules, immersion, spraying, pouring-on and spotting- epidermal administration, such as on) and dusting, and also parenteral administration, such as injection forms.
    Thus, the novel compounds of formula (I) according to the invention can also be advantageously used in particular for livestock (eg poultry such as cattle, sheep, pigs, chickens and geese). In a preferred embodiment of the present invention, the novel compounds are administered to the oral cavity of the animal, if appropriate, with a suitable formulation (ie, such a formulation) and, where appropriate, with a drink or food. Since it is secreted in an active manner upon defecation, the development of insects in the feces of the animal can be prevented in a very easy manner. Suitable dosages and formulations in each case depend in particular on the type of animal and the stage of growth, and the extent of infection, and can be easily determined and fixed by conventional methods. For cattle, the novel compounds can be used at dosages of 0.01 to 1 mg / kg of body weight.
    In addition to the aforementioned methods of application, the active compounds of formula (I) according to the invention also have good lineage activity. Thus, the active compounds may also be below the ground and above the ground of the plant (roots, stems, leaves) when they are treated in liquid or solid form on the ground of the plant (eg when applied with granules of contaminants in flood-infested rice fields). Can be induced through the plant.
    Moreover, the active compounds according to the present invention are capable of reducing the caliber, grounding and tuber of vegetable and developing multiplying stems, such as, for example, seeds of cereals, plants, cotton, rice, beets and other crops, and other vegetable multiplying and ornamental plants. It is particularly useful for processing. For this purpose, prior to sowing or transplanting (eg by seed seeding techniques, seed dressing or seed box treatment in liquid or solid form) by a specific application technique (eg seed heat treatment), during sowing or transplanting or sowing. Or after transplantation. Depending on the application, the amount of active compound treated can be relatively wide. In general, the application rate is 1 g to 10 kg of active compound per ha of contaminated area.
    The following examples illustrate the invention.
    A. Formulation Example
    (a) 10 parts by weight of active compound and 90 parts by weight of talc as inert material were mixed and the mixture was ground in an impact mill to obtain a dusting powder.
    (b) a wettable powder easily dispersible in water, 25 parts by weight of the active compound, 65 parts by weight of kaolin-containing quartz as inert material, 10 parts by weight of potassium ligninsulfonate as wetting agent and dispersant and 1 part by weight of sodium oleylmethyltauride The parts are mixed and obtained by grinding the mixture on a pinned disk mill.
    (c) a dispersion concentrate easily dispersible in water is mixed with 40 parts by weight of the active compound, 7 parts by weight of sulfosuccinic acid monoester, 2 parts by weight of sodium lingininesulfonate, and 51 parts by weight of water, and the grinding bead mill obtained by grinding the mixture to a powder degree of less than 5 μm in a bead mill).
    (d) Emulsifiable concentrates can be prepared from 15% by weight of active compound, 75% by weight of cyclohexane as solvent and 10% by weight of ethoxylated nonylphenol (10 EO) as emulsifier.
    (e) Granules may be prepared from 2 to 15 parts by weight of the active compound and an inert granule carrier material such as attapulgite, fumeis granules and / or quartz sand. A suspension of the wettable powder from example b) with a solids content of 30% is conveniently used, after spraying on the surface of the atepulgite granules, the components are dried and mixed uniformly. The content of the wettable powder is about 5% by weight and the content of inert carrier material is about 95% by weight of the final granules.
    B. Preparation of Chemicals
    Example 1
    3-isopropyl-5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole (No. 81 in Table 1)
    First 2 g of methyl 4-trifluoromethylnicotinate and 1.56 g of isobutyramide oxime were charged in 15 ml of ethanol and cooled to 0 ° C. 10 ml of a 1.2 mole sodium ethoxide solution was added dropwise to the solution. The mixture was allowed to warm to room temperature for 2 hours and then continued to stir at this temperature until the reaction was complete according to TLC.
    The reaction mixture was concentrated and the residue was dissolved in saturated ammonium chloride solution and extracted with diethyl ether. The crude product was chromatographed to afford the title compound as a yellow oil.
    Example 2
    3-isopropyl-5- (4-trifluoromethyl-5-pyrimidyl) -1,2,4-oxadiazole (No. 189 in Table 1)
    First, 2 g of ethyl 4-trifluoromethylpyridine-5-carboxylate and 1.56 g of isobutyramide oxime were charged into 15 ml of ethanol and cooled to 0 ° C. 10 ml of a 1.2 mole sodium ethoxide solution was added dropwise to this solution. The mixture was allowed to warm to room temperature for 1 hour and then refluxed until complete by TLC. The reaction mixture was concentrated and the residue was dissolved in saturated ammonium chloride solution and extracted with diethyl ether. The crude product was chromatographed to afford the title compound as a yellow oil.
    Example 3
    2-methyl-5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole (No. 549 in Table 1)
    500 mg of 4-trifluoromethylniconic acid hydrazide was heated under reflux in 3.5 ml of triethyl orthoacetate for 2 hours. The reaction mixture was then concentrated and the residue was carefully mixed with 2 ml of phosphorus oxychloride. The mixture was stirred for 1 hour at room temperature, then poured onto ice and extracted with ethyl acetate. The crude product obtained after drying and concentration was chromatographed to afford the title compound as a yellow oil:
    Example 4
    4- (ethoxycarbonylmethyl) -2- (4-trifluoromethyl-3-pyridyl) thiazole (No. 688 in Table 4)
    500 mg of 4-trifluoromethylpyridine-3-thiocarboxamide and 440 mg of ethyl 4-chloroacetate were dissolved in 5 ml of dimethylformamide and heated to 100 ° C. for 4 hours. After cooling, the reaction mixture was poured into cold water and extracted with diethyl ether. The diethyl ether phase was dried (with MgSO 4 ), filtered and concentrated and the residue was purified by chromatography. This procedure gave the title compound in the pure form of a colorless oil.
    Example 5
    4-ethyl-5- (4-trifluoromethyl-3-pyridyl) oxazole (No. 762 in Table 4)
    2.6 g of 4-trifluoromethylnicotinic acid were mixed with 20 ml of thionyl chloride and heated to reflux for 1 hour. After cooling, the excess thionyl chloride was distilled off, and the acyl chloride remaining as light yellow oil was dissolved in 30 ml of dichloromethane. This solution was then added dropwise to 2.4 g of 2-amino-1-butanol and 2.75 g of triethylamine in 30 ml of dichloromethane cooled in an ice bath. After completion of the dropping, stirring was continued for about 2 hours at room temperature. The mixture was poured into ammonium chloride solution and extracted with ethyl acetate. The crude N- (1-hydroxy-2-butyl) -4-trifluoromethylnicotinamide (2.3 g) obtained after drying and concentration was dissolved in 100 ml of dichloromethane at room temperature and dried periodinane (des- It was mixed with 4.6 g of Dess-Martin reagent. After completion of the reaction according to TLC, the reaction mixture was concentrated and purified by column chromatography. The resulting 2- (trifluoromethylpyridine-3-amido) butanol (1.5 g) was dissolved in 30 ml of dimethylformamide, mixed with 2.72 g of phosphorus oxychloride and heated to 90 ° C. for 15 minutes. Then the solution was poured on ice and extracted with diethyl ether. The diethyl ether phase was dried and concentrated and the residue was chromatographed to afford the product as a brown oil.
    Example 6
    4-ethyl-2- (4-trifluoromethyl-3-pyridyl) -4,5-dihydrooxazole (Table 5, No. 876)
    1 g of 4-trifluoromethylnicotinic acid was mixed with 8 ml of thionyl chloride and heated to reflux for 1 hour. After cooling, the excess thionyl chloride was distilled off, and the acyl chloride remaining as light yellow oil was dissolved in 10 ml of dichloromethane. This solution was then added dropwise to 930 mg of 2-amino-1-butanol and 1.06 g of triethylamine in 10 ml of dichloromethane cooled in an ice bath. After completion of the dropping, stirring was continued for about 2 hours at room temperature. The mixture was poured into ammonium chloride solution and extracted with ethyl acetate. After drying and concentrating the ethyl acetate phase, the crude N- (1-hydroxy-2-butyl) -4-trifluoromethylnicotinamide (1.03 g) obtained was dissolved in 6 ml of tetrahydrofuran at room temperature, It was mixed with 1.09 g of N-[(triethylamonio) sulfonyl] -methylcarbamate (buges reagent). The mixture was stirred at 60 ° C. for 3 hours. After cooling, the batch was concentrated and the residue was dissolved in water and extracted with ethyl acetate. The crude product was chromatographed to afford the product as a colorless oil.
    Example 7
    2- (3-thienylmethyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole (No. 572 of Table 3)
    880 mg of thiophene-3-acetic acid hydrazide was added to 960 mg of a solution of 4-trifluoromethylpyridine-3-carboxylic acid in 5 ml of phosphorus oxychloride, and the mixture was heated to reflux for 2 hours. The reaction mixture was then added dropwise to cold water, neutralized with concentrated ammonia solution and then extracted with ethyl acetate. After drying (with Na 2 SO 4 ), concentrated and purified by chromatography to give 624 mg of the title product as a light brown oil.
    Example 8
    5-methyl-3- (4-trifluoromethyl-3-pyridyl) -1H-1,2,4-triazole (Table 6, no. 947)
    100 mg of a mixture of 290 mg of ethylacetimidade hydrochloride and sodium hydroxide in 2 ml of ethanol was filtered and added to 500 mg of 4-trifluoromethyl-3-pyridinecarbohydrazide, and then the mixture was added for 3 hours. Heated under reflux. The reaction mixture was concentrated and the residue suspended in xylene and refluxed for 4 hours. For workup, the batch was diluted with ethyl acetate and washed with water. Purification by chromatography gave the pure product as a colorless solid.
    Example 9
    3- (N-isopropylcarbamoylmethyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole
    Step 1: tert-butyl-3-amino-3- (4-trifluoromethyl-3-pyridinecarbonyloxy-imino) propionate
    First, 30 g of 4-trifluoromethyl-3-pyridinecarboxylic acid was charged into 150 mL of anhydrous THF, and mixed with 25.3 g of carbonyl diimidazole almost simultaneously. The mixture was stirred for 30 minutes at room temperature. Then, 27.2 g of tert-butoxycarbonylacetamide oxime dissolved in 150 mL of THF was added dropwise. The mixture was stirred overnight, the solvent was evaporated and the residue was dissolved in ethyl acetate, washed three times with 1M sulfuric acid and once with saturated sodium bicarbonate solution. The ethyl acetate phase was concentrated to give 28 g of product as pale yellow solid.
    Step 2: 3- (tert-butoxycarbonylmethyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole
    28 g of tert-butyl-3-amino-3- (4-trifluoromethyl-3-pyridinecarbonyloxy-imido) propionate was dissolved in 380 ml of toluene and heated at reflux for 17 h. The residue was concentrated and purified by chromatography on silica gel to give 14.4 g of the product as light brown oil.
    Step 3: 3- (hydroxycarbonylmethyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole
    Dissolve 12.4 g of 3- (tert-butoxycarbonylmethyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole in 110 ml of dichloromethane, and Mix with 57 ml of fluoroacetic acid. The reaction mixture was stirred at rt for 1.5 h and then concentrated under reduced pressure. The residue was repeatedly dissolved in dichloromethane and reconcentrated to remove any residual trifluoroacetic acid. The mixture was finally triturated with diethyl ether to give 8.1 g of product as a white solid.
    Step 4: 3- (N-isopropylcarbamoylmethyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole
    1 g of the previous step was dissolved in 10 ml of THF and mixed with 0.59 g of carbonyldiimidazole. The mixture was stirred for 10 minutes at room temperature, 0.22 g of isopropylamine was added dropwise, and the mixture was reacted for another 1.5 hours at room temperature with stirring. The reaction mixture was then concentrated and the residue was dissolved in ethyl acetate, washed three times with 1M sulfuric acid and once with saturated sodium bicarbonate solution. After drying and concentration of the ethyl acetate phase, the obtained solid residue was recrystallized from tert-butyl methyl ether to give 0.46 g of pure product as a light yellow solid.
    Example 10
    3- (N, N-dimethylaminocarbamoyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole
    Step 1: ethyl 2-amino-2- (4-trifluoromethyl-3-pyridinecarbonyloxyimino) acetate
    First, 17.3 g of carbonyldiimidazole was charged into 200 ml of 1,4-dioxane and mixed with 20 g of 4-trifluoromethyl-3-pyridinecarboxylic acid almost simultaneously. The mixture was stirred at rt for 1 h and then heated to 45 ° C. for 2 h. After cooling to 30 ° C., 14.5 g of ethoxycarbonylformamide oxime was added and the mixture was stirred at 45 ° C. for 3 hours. The precipitated solid was aspirated and filtered off, the filtrate was concentrated to 50 ml and added to 250 ml of ice water with solids. The solid was suctioned off and dried at 50 ° C. under reduced pressure. This gave 28.7 g of the product as a white solid having a melting point of 172 to 174 ° C.
    Step 2: 3-ethoxycarbonyl-5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole
    20 g of ethyl 2-amino-2- (4-trifluoromethyl-3-pyridinecarbonyloxyimido) -acetate were dissolved in 200 ml of a mixture of xylene and toluene and mixed with 5 g of Amberlyst 15. Boiling at 125-130 ° C. for 6 hours using a Dean-Stark apparatus. After the reaction was completed, the mixture was cooled down and mixed with a small amount of diethyl ether. The mixture was filtered under suction in glass filter fritz and the solution was then concentrated. This gave 15.8 g of a yellow oil product.
    Step 3: 5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole-3-carboxylic acid
    First, 15.8 g of 3-ethoxycarbonyl-5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole was charged in 13 ml of methanol and ice-cooled at 0 ° C. And 2.8 g of lithium hydroxide solution in 50 ml of water was added dropwise. The mixture was stirred for 2 hours at room temperature, 20 ml of ice water was added and the mixture was extracted with 200 ml of diethyl ether. The aqueous phase was adjusted to pH 2 with diluted HCL and the precipitated product was filtered off by suction. After drying, 13.8 g of 5- (4-trifluoro methyl-3-pyridyl) -1,2,4-oxadiazole-3-carboxylic acid was obtained as a white solid having a melting point of 157 to 159 ° C.
    Step 4: N, N-dimethyl-5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole-3-carboxamide
    Initially, 5.8 g of carbonyldiimidazole was charged into 90 mL of tetrahydrofuran, and almost simultaneously with 9 g of 5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxydiazole-3-carboxylic acid Mixed. The mixture was stirred at room temperature for 15 minutes and then heated to 50 ° C. for 2 hours. After cooling to room temperature, 2.3 g of dimethylamine were introduced in the gas stream for 2 hours. After reacting for 12 hours, the mixture was concentrated and dissolved in 200 ml of diethyl ether. The mixture was washed with ice-cold ½ concentrated hydrochloric acid solution, washed with saturated sodium bicarbonate solution, dried over magnesium sulfate and concentrated under reduced pressure. This procedure yielded a pale yellow oil, which gave a solid with a melting point of 52 to 54 ° C. after several days.
    In a similar manner, the compounds shown in Tables 1 to 6 can be prepared.
    The abbreviations used below are:
    Ph: Phenyl
    THP: 2-tetrahydropyranyl.
    TABLE 1









    TABLE 2

    TABLE 3


    TABLE 4


    TABLE 5
    TABLE 6

    C. Biological Examples
    Example 1
    A petri dish was prepared with the bottom covered with filter paper and containing about 5 ml of medium. A piece of filter paper containing eggs of US tobacco caterpillar (Heliothis virescens) grown about 30, 24 hours was immersed in an aqueous solution of the formulated formulation to be tested for 5 seconds and then placed in a petri dish. Further 200 μl of aqueous solution was sprinkled onto the medium. The Petri dish was sealed and kept at about 25 ° C. in a conditioned chamber. After storage for 6 days, the effect of the formulation on eggs and the larvae resulting therefrom were determined. At concentrations of 300 ppm (based on the content of active compound), the formulations of Examples 79 and 88 resulted in a mortality of 90 to 100%.
    Example 2
    Germinated seed beans (Vicia faba) with roots were transferred to a brown glass bottle containing tap water, and then sprinkled with about 100 black bean aphids (Aphis fabae). The plants and aphids are then immersed for 5 minutes in an aqueous solution of the formulated formulation to be tested. After removing the solution, the plants and animals were placed in a conditioned chamber (25 ° C., 40-60% relative humidity for 16 hours night and day). After storage for 3 and 6 days, the effect of the formulation on aphids was measured. Examples 79, 78, 80, 81, 83, 84, 88, 133, 135, 136, 137, 138, 139, 1117, 1229, 1230, 1231, 1246 at concentrations of 300 ppm And the formulation of 1254 exhibited a mortality of 90 to 100% for aphids.
    Example 3
    Twelve rice leaves with a stem length of 8 cm were soaked for 5 seconds in an aqueous solution of the formulated formulation to be tested. After the solution was drained off, the rice treated in this way was placed in a Petri dish and sprinkled with about 20 rice leaf locust species, Nilaparvata lugens. The Tetri dishes were sealed and stored in a conditioned chamber (25 ° C., atmospheric humidity: 40-60% for 16 hours of night / day). After 6 days of storage, the mortality of leaf locust larvae was measured. At a concentration of 300 ppm (based on the content of active compound), the lethal dose of the formulations of Examples 88, 139 and 927 was 90 to 100%.
    Example 4
    Germinated seed beans (Bycia pava) with roots were transferred to a brown glass jar of tap water. 4 ml of the aqueous solution of the formulated formulation to be tested was pipetted into a brown glass bottle. Then, sprinkled apricots with about 100 black bean aphids. The plants and animals were then placed in a conditioned chamber (16 hours of day / night, 25 ° C., 40-60% relative humidity). After storage for 3 and 6 days, the root-penetrating activity of the formulation against aphids was measured. Examples 78, 79, 80, 81, 83, 84, 88, 133, 135, 136, 137, 138, 139, 187, 1117, 1229, 1230, 1231 at concentrations of 300 ppm (based on the content of active compound) Formulations 1246 and 1254 showed a mortality of 90 to 100% of aphids by root-penetrating action.
    权利要求:
    Claims (12)
    [1" claim-type="Currently amended] 4-haloalkyl-3-heterocyclylpyridine or 4-haloalkyl-5-heterocyclylpyrimidine of formula (I), or optionally their salts:
    Formula I

    Where
    Y is halo-C 1 -C 6 -alkyl;
    X is CH or N;
    m is 0 or 1;
    Q is a 5-membered heterocyclic group ego;
    Where a) X 1 = W, X 2 = NR a , X 3 = CR b R 1, or b) X 1 = NR a , X 2 = CR b R 1 , X 3 = W, or c) X 1 = V, X 2 = CR a R 1 , X 3 = NR b or d) X 1 = V, X 2 = CR a R 2 , X 3 = CR b R 3, or e) X 1 = V, X 2 = CR 4 R 5 , X 3 = CR 6 R 7 , or f) X 1 = NR a , X 2 = CR b R 1 , X 3 = NR 8 ; At this time
    R a and R b together form a single bond;
    V is oxygen, sulfur or NR 9 ;
    W is oxygen or sulfur;
    R 1 is hydrogen, (C 1 -C 20 ) -alkyl, (C 2 -C 20 ) -alkenyl, (C 2 -C 20 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the last six radicals mentioned are halogen, cyano, nitro, hydroxyl, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -NR 10 C (= W) OR 10 , -C (= W) NR 10 -NR 10 2 , -C (= W) NR 10 -NR 10 [C (= W) R 10 ], -NR 10 -C (= W) NR 10 2 , -NR 10 -NR 10 C (= W) R 10 , -NR 10 -N [C (= W) R 10 ] 2 , -N [(C = W) R 10 ] -NR 10 2 , -NR 10 -NR 10 [(C = W) R 10 ], -NR 10 -NR 10 [(C = W) WR 10 ], -NR 10 -R 10 [(C = W) NR 10 2 ], -NR 10 (C = NR 10 ) R 10 , -NR 10 (C = NR 10 ) NR 10 2 , -ONR 10 2 , -O-NR 10 (C = W) R 10 , -SO 2 NR 10 2 , -NR 10 SO 2 R 10 , -SO 2 OR 10 , -OSO 2 R 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -SeR 10 , -PR 10 2 , -P (= W) R 10 2 , -SOR 10 , -SO 2 R 10, -PW 2 R 10 2 , -PW 3 R 10 2, aryl and heteroaryl Cycle reels are optionally substituted by one or more radicals selected from the group consisting of, where the two radicals mentioned last is (C 1 -C 6) alkyl, (C 2 -C 6) - alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, (C 1 -C 6 ) -halo Alkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, halogen, -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -SOR 10 , -SO 2 R 10 , at least one radical selected from the group consisting of nitro, cyano and hydroxyl Optionally substituted by
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are halogen, cyano, nitro, halogen, -C (= W) R 10 , -C (= W) Optionally substituted by one or more radicals selected from the group consisting of OR 10 , -C (= W) NR 10 2 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ; , Halogen, cyano, nitro, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C ( = W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 ,- NR 10 C (= W) OR 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -PR 10 2 , -SOR 10 , -SO 2 R 10 , -PW 2 R 10 2 and Aryl optionally substituted by one or more radicals selected from the group consisting of -PW 3 R 10 2 ,
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are cyano, nitro, halogen, -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -OC (= W) R 10 , -OC (= W) Optionally substituted by one or more radicals selected from the group consisting of OR 10 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ], halogen, cyano, nitro, -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OR 10 , -NR 10 2 , -SR 10 , -SOR Heterocyclyl optionally substituted by one or more radicals selected from the group consisting of 10 and —SO 2 R 10 ,
    -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 , -SO 2 R 10 , -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -NR 10 C (= W) OR 10 , -C (= W) NR 10 -NR 10 2 , -C (= W) NR 10 -NR 10 [ C (= W) R 10 ], -NR 10 -C (= W) NR 10 2 , -NR 10 -NR 10 C (= W) R 10 , -NR 10 -NC (= W) R 10 2 ,- N (C = W) R 10 -NR 10 2 , -NR 10 -NR 10 [(C = W) R 10 ], -NR 10 -NR 10 [(C = W) WR 10 ], -NR 10 -NR 10 [(C = W) NR 10 2 ], -NR 10 (C = NR 10 ) R 10 , -NR 10 (C = NR 10 ) NR 10 2 , -O-NR 10 2 , -O-NR 10 ( C = W) R 10 , -SO 2 NR 10 2 , -NR 10 SO 2 R 10 , -SO 2 OR 10 , -OSO 2 R 10 , -SC (= W) R 10 , -SC (= W) OR 10 , -SC (= W) R 10 , -PR 10 2 , -PW 2 R 10 2 , -PW 3 R 10 2 , SiR 10 3 or halogen;
    R 2 and R 3 independently of each other have the definition given to R 1 ; R 2 and R 3 together form a 5 to 7 membered ring which is partially or fully unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are directly adjacent to each other Ring is optionally substituted by 1 to 5 radicals R 1 ;
    R 4 and R 6 independently of each other have the definition given to R 1 ; R 4 and R 6 together form a 4-7 membered ring which is partially or fully unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are directly adjacent to each other Ring is optionally substituted by 1 to 5 radicals R 1 ;
    R 5 and R 7 independently of one another are hydrogen, (C 1 -C 20 ) -alkyl, (C 2 -C 20 ) -alkenyl, (C 2 -C 20 ) -alkynyl, (C 3 -C 8 ) -Cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned last are halogen, cyano, nitro, hydroxyl, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC ( = W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 , -NR 10 C (= W) OR 10 , -C (= W) NR 10 -NR 10 2 , -C (= W) NR 10 -NR 10 [C (= W) R 10 ], -NR 10 -C (= W) NR 10 2 , -NR 10 -NR 10 C (= W) R 10 , -NR 10 -N [C (= W) R 10 ] 2 , -N [(C = W) R 10 ] -NR 10 2 , -NR 10 -NR 10 [ (C = W) R 10 ], -NR 10 -NR 10 [(C = W) WR 10 ], -NR 10 -NR 10 [(C = W) NR 10 2 ], -NR 10 (C = NR 10 ) R 10 , -NR 10 (C = NR 10 ) NR 10 2 , -ONR 10 2 , -O-NR 10 (C = W) R 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3, -SeR 10, -PR 10 2, -P (= W) R 10 2, -SOR 10, -SO 2 R 10, -PW 2 R 10 2, -PW 3 R 10 2, aryl, and heterocyclyl Group of reels It is optionally substituted by one or more radicals selected from, where the last two radicals mentioned are (C 1 -C 6) alkyl, (C 2 -C 6) - alkenyl, (C 2 -C 6) - alkynyl Nyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 6 -C 8 ) -cycloalkynyl, (C 1 -C 6 ) -haloalkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, halogen, -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -C (= W) R 10 Optionally substituted by one or more radicals selected from the group consisting of -C (= W) OR 10 , -C (= W) NR 10 2 , -SOR 10 , -SO 2 R 10 , nitro, cyano and hydroxyl do],
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl and (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are halogen, cyano, nitro, halogen, -C (= W) R 10 , -C (= W) Optionally substituted by one or more radicals selected from the group consisting of OR 10 , -C (= W) NR 10 2 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ; , Halogen, cyano, nitro, -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C ( = W) NR 10 2 , -OC (= W) R 10 , -OC (= W) OR 10 , -NR 10 C (= W) R 10 , -N [C (= W) R 10 ] 2 ,- NR 10 C (= W) OR 10 , -OR 10 , -NR 10 2 , -SR 10 , -SiR 10 3 , -PR 10 2 , -SOR 10 , -SO 2 R 10 , -PW 2 R 10 2 and Aryl optionally substituted by one or more radicals selected from the group consisting of -PW 3 R 10 2 ,
    (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -Cycloalkenyl and (C 6 -C 8 ) -cycloalkynyl, wherein the six radicals mentioned above are cyano, nitro, halogen, -C (= W) R 10 , -C (= W) OR 10 Is optionally substituted by one or more radicals selected from the group consisting of -C (= W) NR 10 2 , -OR 10 , -NR 10 2 , -SR 10 , -SOR 10 and -SO 2 R 10 . , Cyano, nitro, -C (= W) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 , -OC (= W) R 10 , -OR 10 , -NR 10 Pyridyl optionally substituted by one or more radicals selected from the group consisting of 2 , -SR 10 , -SOR 10 and -SO 2 R 10 ,
    -C (= W) R 10 , -C (= NOR 10 ) R 10 , -C (= NNR 10 2 ) R 10 , -C (= W) OR 10 , -C (= W) NR 10 2 or halogen ego;
    R 4 and R 5 together form a 4-7 membered ring which is partially unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are not directly adjacent to each other The ring is optionally substituted by 1 to 5 radicals R 1 ; R 4 and R 5 together form one of the groups = O, = S and = NR 9 ;
    R 6 and R 7 together form a five to seven membered ring which is partially unsaturated and can be interrupted by one or more atoms selected from the group consisting of nitrogen, oxygen and sulfur, wherein the oxygen atoms are not directly adjacent to each other , The ring is optionally substituted by 1 to 5 radicals R 1 ; R 6 and R 7 together form one of the groups = O, = S and = NR 9 ;
    R 8 is hydrogen, (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -Alkyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alky Nyl- (C 3 -C 8 ) -cycloalkyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenyl, (C 2 -C 6 ) -alkenyl- (C 4- C 8 ) -cycloalkenyl [wherein the last 14 radicals mentioned are halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -Haloalkynyloxy, (C 3 -C 8 ) -cycloalkoxy, (C 4 -C 8 ) -company Icycloalkenyloxy, (C 3 -C 8 ) -halocycloalkoxy, (C 4 -C 8 ) -halocycloalkenyloxy, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 )- Alkoxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkoxy, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyloxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyloxy, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkoxy, (C 2 -C 6 )- alkenyl, - (C 3 -C 8) - cycloalkoxy, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkoxy, (C 1 -C 6) - alkyl, - (C 4 - C 8 ) -cycloalkenyloxy, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenyloxy, (C 1 -C 4 ) -alkoxy- (C 1 -C 6 ) -Alkoxy, (C 1 -C 4 ) -alkoxy- (C 2 -C 6 ) -alkenyloxy, carbamoyl, (C 1 -C 6 ) -mono- or di-alkylcarbamoyl, (C 1 -C 6 ) -mono- or di-haloalkylcarbamoyl, (C 3 -C 8 ) -mono- or di-cycloalkylcarbamoyl, (C 1 -C 6 ) -alkoxycarbonyl, (C 3 -C 8 ) Cycloalkoxycarbonyl, (C 1 -C 6 ) -alkanoyloxy, (C 3 -C 8 ) -cycloalkanoyloxy, (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1 -C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanamido, (C 2 -C 6 ) -alkenamido, (C 3 -C 8 ) -cycloalkanamido, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkanamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -alkenylthio, (C 2 -C 6 ) -Alkynylthio, (C 1 -C 6 ) -haloalkylthio, (C 2 -C 6 ) -haloalkenylthio, (C 2 -C 6 ) -haloalkynylthio, (C 3 -C 8 ) -Cycloalkylthio, (C 4 -C 8 ) -cycloalkenylthio, (C 3 -C 8 ) -halocycloalkthio, (C 4 -C 8 ) -halocycloalkenylthio, (C 3- C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylthio, (C 3 -C 8 ) -cyclo Alkyl- (C 2 -C 4 ) -alkenylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylthio, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylthio, (C 2 -C 6) - alkenyl, - (C 3 -C 8) - cycloalkyl, thio, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkyl, thio, (C 1 -C 6) -Alkyl- (C 4 -C 8 ) -cycloalkenylthio, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylthio, (C 1 -C 6 ) -alkylsulphi Neyl, (C 2 -C 6 ) -alkenylsulfinyl, (C 2 -C 6 ) -alkynylsulfinyl, (C 1 -C 6 ) -haloalkylsulfinyl, (C 2 -C 6 ) -halo Alkenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl, (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3- C 8 ) -halocycloalksulfinyl, (C 4 -C 8 ) -halocycloalkenylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfinyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfinyl, (C 4- C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfinyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 2 -C 6 ) -Alkenyl- (C 3 -C 8 ) -cycloalkylsulfinyl, ( C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 1 -C 6 ) -alkylsulfonyl, (C 2 -C 6 ) -alkenylsulfonyl, (C 2- C 6 ) -alkynylsulfonyl, (C 1 -C 6 ) -haloalkylsulfonyl, (C 2 -C 6 ) -haloalkenylsulfonyl, (C 2 -C 6 ) -haloalkynylsulfonyl, (C 3 -C 8 ) -cycloalkylsulfonyl, (C 4 -C 8 ) -cycloalkenylsulfonyl, (C 3 -C 8 ) -halocycloalksulfonyl, (C 4 -C 8 ) -halocycloalkenylsulfonyl , (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfonyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfonyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 )- alkynyl, - (C 3 -C 8) - cycloalkyl Kilseol sulfonyl, (C 1 -C 6) - alkyl, - (C 4 -C 8) - cycloalkyl sulfonyl nilseol alkenyl, (C 2 -C 6) - alkenyl, - (C 4 -C 8) - cycloalkyl alkenyl nilseol sulfonyl, (C 1 -C 6 ) -alkylamino, (C 2 -C 6 ) -alkenylamino, (C 2 -C 6 ) -alkynylamino, (C 1 -C 6 ) -haloalkylamino, (C 2 -C 6 ) -haloalkenylamino, (C 2 -C 6 ) -haloalkynylamino, (C 3 -C 8 ) -cycloalkylamino, (C 4 -C 8 ) -cycloalkenylamino, (C 3 -C 8 ) -halocycloalkamino, (C 4 -C 8 ) -halocycloalkenylamino, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylamino, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylamino, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylamino, (C 4 -C 8 ) -Cycloalkenyl- (C 1 -C 4 ) -alkenylamino, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylamino, (C 1 -C 6 ) -alkyl- (C 4 -C 8) - Alkenyl cycle roal amino, (C 2 -C 6) - alkenyl, - (C 4 -C 8) - cycloalkenyl-amino, (C 1 -C 6) - trialkylsilyl, aryl, aryloxy, arylthio, aryl Amino, arylcarbamoyl, aroyl, aroyloxy, aryloxycarbonyl, aryl- (C 1 -C 4 ) -alkoxy, aryl- (C 2 -C 4 ) -alkenyloxy, aryl- (C 1- C 4 ) -alkylthio, aryl- (C 2 -C 4 ) -alkenylthio, aryl- (C 1 -C 4 ) -alkylamino, aryl- (C 2 -C 4 ) -alkenylamino, aryl- (C 1 -C 6) - di-alkylsilyl, diaryl - (C 1 -C 6) - alkylsilyl, triarylsilyl and 5- or 6-membered heterocycle reels are optionally substituted by one or more radicals selected from the group consisting of Wherein the last 19 radicals mentioned are halogen, cyano, nitro, amino, hydroxyl, thio, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4) -alkoxy, (C 1 -C 4) - haloalkoxy, (C 1 -C 4) - alkylthio, (C 1 -C 4) haloalkylthio, (C 1 -C 4) - alkyl Mino, (C 1 -C 4) - haloalkyl, amino, formyl, and (C 1 -C 4) - is optionally substituted in the cyclic moiety by one or more radicals selected from the group consisting of alkanoyl],
    Halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy , (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -haloalkynyloxy, (C 3 -C 8 ) -cycloalkoxy, (C 4 -C 8 ) -cycloalkenyloxy, (C 3 -C 8 ) -halocycloalkoxy, (C 4 -C 8 ) -halocycloalkenyloxy, carbamoyl, (C 1 -C 6 )- mono- or di-alkyl carbamoyl, (C 1 -C 6) - alkoxycarbonyl, (C 1 -C 6) - alkanoyloxy, (C 1 -C 6) - mono- or di-haloalkyl carbamoyl , (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1 -C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanami (C 2 -C 6 ) -alkenamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -alkenylthio, (C 2 -C 6 ) -alkynylthio, ( C 1 -C 6) - haloalkylthio, (C 2 -C 6) - haloalkenyl thio, (C 2 -C 6) - haloalkynyl thio, (C 3 -C 8) - cycloalkyl, O, (C 4 -C 8) - cycloalkenyl thio, (C 3 -C 8) - cycloalkyl halo alk thio, (C 3 -C 8) - halo-cycloalkenyl thio, (C 1 -C 6) - Alkylsulfinyl, (C 2 -C 6 ) -alkenylsulfinyl, (C 2 -C 6 ) -alkynylsulfinyl, (C 1 -C 6 ) -haloalkylsulfinyl, (C 2 -C 6 ) -Haloalkenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl, (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3 -C 8 ) -halocycloalksulfinyl, (C 4 -C 8 ) -halocycloalkenylsulfinyl, (C 1 -C 6 ) -alkylsulfonyl, (C 2 -C 6 ) -alkenylsulfonyl , (C 2 -C 6 ) -alkynylsulfonyl, (C 1 -C 6 ) -haloalkylsulfonyl, (C 2 -C 6 ) -haloalkenylsulfonyl, (C 2 -C 6 ) -haloalkynylsul Ponyl, (C 3 -C 8 ) -cycloalkylsulfonyl, (C 4 -C 8 ) -cycloalkenylsulfonyl, (C 3 -C 8 ) -halocycloalksulfonyl, (C 4 -C 8 )- halo-alkenyl cycloalkyl nilseol sulfonyl, (C 1 -C 6) - alkylamino, (C 2 -C 6) - alkenyl, amino, (C 2 -C 6) - alkynyl, amino , (C 1 -C 6) - haloalkyl, amino, (C 2 -C 6) - haloalkenyl amino, (C 2 -C 6) - haloalkynyl amino, (C 3 -C 8) - cycloalkyl-amino , (C 4 -C 8) - cycloalkenyl-amino, (C 3 -C 8) - cycloalkyl alk halo, amino and (C 4 -C 8) - by one or more radicals selected from halo cycloalkenyl group consisting of amino Optionally substituted aryl,
    -C (= W) R 11 , OR 11 or NR 11 2 ;
    R 9 is (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4- C 8 ) -cycloalkenyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkyl , (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyl or (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyl [wherein The nine radicals mentioned are halogen, cyano, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy and (C 1 -C 6 ) -haloalkyloxy, optionally substituted by one or more radicals selected from the group consisting of;
    R 10 is hydrogen, (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -Alkyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkyl, (C 2 -C 6 ) -alky Nyl- (C 3 -C 8 ) -cycloalkyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenyl, (C 2 -C 6 ) -alkenyl- (C 4- C 8 ) -cycloalkenyl [the last 14 radicals mentioned are halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -Alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -halo alkynyloxy, (C 3 -C 8) - cycloalkoxy, (C 4 -C 8) - four Claw alkenyloxy, (C 3 -C 8) - cycloalkoxy halo, (C 4 -C 8) - cycloalkyl halo-alkenyloxy, (C 3 -C 8) - cycloalkyl, - (C 1 -C 4) - Alkoxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkoxy, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenyloxy, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenyloxy, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkoxy, (C 2 -C 6 )- alkenyl, - (C 3 -C 8) - cycloalkoxy, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkoxy, (C 1 -C 6) - alkyl, - (C 4 - C 8 ) -cycloalkenyloxy, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenyloxy, (C 1 -C 4 ) -alkoxy- (C 1 -C 6 ) -Alkoxy, (C 1 -C 4 ) -alkoxy- (C 2 -C 6 ) -alkenyloxy, carbamoyl, (C 1 -C 6 ) -mono- or di-alkylcarbamoyl, (C 1 -C 6 ) -mono- or di-haloalkylcarbamoyl, (C 3 -C 8 ) -mono- or di-cycloalkylcarbamoyl, (C 1 -C 6 ) -alkoxycarbonyl, (C 3 -C 8 ) Cycloalkoxycarbonyl, (C 1 -C 6 ) -alkanoyloxy, (C 3 -C 8 ) -cycloalkanoyloxy, (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1 -C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanamido, (C 2 -C 6 ) -alkenamido, (C 3 -C 8 ) -cycloalkanamido, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkanamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -alkenylthio, (C 2 -C 6 ) -Alkynylthio, (C 1 -C 6 ) -haloalkylthio, (C 2 -C 6 ) -haloalkenylthio, (C 2 -C 6 ) -haloalkynylthio, (C 3 -C 8 ) -Cycloalkylthio, (C 4 -C 8 ) -cycloalkenylthio, (C 3 -C 8 ) -halocycloalkthio, (C 4 -C 8 ) -halocycloalkenylthio, (C 3- C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylthio, (C 3 -C 8 ) -cyclo Alkyl- (C 2 -C 4 ) -alkenylthio, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylthio, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylthio, (C 2- C 6) - alkenyl, - (C 3 -C 8) - cycloalkyl, thio, (C 2 -C 6) - alkynyl, - (C 3 -C 8) - cycloalkyl, thio, (C 1 -C 6) - Alkyl- (C 4 -C 8 ) -cycloalkenylthio, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylthio, (C 1 -C 6 ) -alkylsulfinyl , (C 2 -C 6) - alkenyl, sulfinyl, (C 2 -C 6) - alkynyl, sulfinyl, (C 1 -C 6) - haloalkyl sulfinyl, (C 2 -C 6) - haloalkenyl Kenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl, (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3 -C 8 ) -halocycloalksulfinyl, (C 4 -C 8 ) -halocycloalkenylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfinyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfinyl, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfinyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfinyl, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 2 -C 6 ) -Alkenyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylsulfinyl, (C 1 -C 6 ) -alkyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 2- C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 1 -C 6 ) -alkylsulfonyl, (C 2 -C 6 ) -alkenylsulfonyl, (C 2 -C 6 ) -alkynylsulfonyl, (C 1 -C 6 ) -haloalkylsulfonyl, (C 2 -C 6 ) haloalkenylsulfonyl, (C 2 -C 6 ) -haloalkynylsulfonyl, (C 3 -C 8 ) -cycloalkylsulfonyl, (C 4 -C 8 ) -cycloalkenylsulfonyl, (C 3 -C 8 ) -halocycloalksulfonyl, (C 4 -C 8 ) -halocycloalkenylsulfonyl, ( C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylsulfonyl, (C 3- C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylsulfonyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkenylsulfonyl, (C 1 -C 6 ) -Alkyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylsulfonyl, (C 2 -C 6 ) -alkynyl - (C 8 -C 3) - cycloalkenyl Sulfonyl, (C 1 -C 6) - alkyl, - (C 4 -C 8) - cycloalkyl sulfonyl nilseol alkenyl, (C 2 -C 6) - alkenyl, - (C 4 -C 8) - cycloalkyl alkenyl nilseol sulfonyl, (C 1 -C 6 ) -alkylamino, (C 2 -C 6 ) -alkenylamino, (C 2 -C 6 ) -alkynylamino, (C 1 -C 6 ) -haloalkylamino, (C 2 -C 6 ) -haloalkenylamino, (C 2 -C 6 ) -haloalkynylamino, (C 3 -C 8 ) -cycloalkylamino, (C 4 -C 8 ) -cycloalkenylamino, (C 3 -C 8 ) -halocycloalkamino, (C 4 -C 8 ) -halocycloalkenylamino, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 4 ) -alkylamino, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkylamino, (C 3 -C 8 ) -cycloalkyl- (C 2 -C 4 ) -alkenylamino, (C 4 -C 8 ) -Cycloalkenyl- (C 1 -C 4 ) -alkenylamino, (C 1 -C 6 ) -alkyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkenyl- (C 3 -C 8 ) -cycloalkylamino, (C 2 -C 6 ) -alkynyl- (C 3 -C 8 ) -cycloalkylamino, (C 1 -C 6 ) -alkyl- (C 4 -C 8 )-4 Ichloroalkenylamino, (C 2 -C 6 ) -alkenyl- (C 4 -C 8 ) -cycloalkenylamino, (C 1 -C 6 ) -trialkylsilyl, aryl, aryloxy, arylthio, aryl Amino, aryl- (C 1 -C 4 ) -alkoxy, aryl- (C 2 -C 4 ) -alkenyloxy, aryl- (C 1 -C 4 ) -alkylthio, aryl- (C 2 -C 4 ) -Alkenylthio, aryl- (C 1 -C 4 ) -alkylamino, aryl- (C 2 -C 4 ) -alkenylamino, aryl- (C 1 -C 6 ) -dialkylsilyl, diaryl- ( Optionally substituted by one or more radicals selected from the group consisting of C 1 -C 6 ) -alkylsilyl, triarylsilyl and 5 or 6 membered heterocyclyl, wherein the cyclic moieties of the last 14 radicals mentioned are halogen, Furnace, nitro, amino, hydroxyl, thio, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 3 -C 8 ) -cycloalkyl, (C 1 -C 4 ) -Alkoxy, (C 1 -C 4 ) -haloalkoxy, (C 1 -C 4 ) -alkylthio, (C 1 -C 4 ) -haloalkylthio, (C 1 -C 4 ) -alkylamino, (C 1 -C 4 ) -do Optionally substituted by one or more radicals selected from the group consisting of roalkylamino, formyl and (C 1 -C 4 ) -alkanoyl],
    Aryl, 5- or 6-membered heteroaromatic [where the two radicals mentioned last are halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 ) -alkoxy, (C 2- C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 1 -C 6 ) -haloalkyloxy, (C 2 -C 6 ) -haloalkenyloxy, (C 2 -C 6 ) -haloalkynyloxy, (C 3 -C 8 ) -cycloalkoxy, (C 4 -C 8 ) -cycloalkenyloxy, (C 3 -C 8 ) -halocycloalkoxy, (C 4 -C 8 ) -Halocycloalkenyloxy, carbamoyl, (C 1 -C 6 ) -mono- or di-alkylcarbamoyl, (C 1 -C 6 ) -alkoxycarbonyl, (C 1 -C 6 ) -alkanoyl Oxy, (C 1 -C 6 ) -mono- or di-haloalkylcarbamoyl, (C 1 -C 6 ) -haloalkoxycarbonyl, (C 1 -C 6 ) -haloalkanoyloxy, (C 1- C 6 ) -alkanamido, (C 1 -C 6 ) -haloalkanamido, (C 2 -C 6 ) -alkenamido, (C 1 -C 6 ) -alkylthio, (C 2 -C 6 ) -Alkenylthio, (C 2 -C 6 ) -alkynylthio, (C 1 -C 6 ) -haloalkylthio, (C 2 -C 6 ) -Haloalkenylthio, (C 2 -C 6 ) -haloalkynylthio, (C 3 -C 8 ) -cycloalkylthio, (C 4 -C 8 ) -cycloalkenylthio, (C 3 -C 8 ) -halocycloalkthio, (C 4 -C 8 ) -halocycloalkenylthio, (C 1 -C 6 ) -alkylsulfinyl, (C 2 -C 6 ) -alkenylsulfinyl, (C 2 -C 6 ) -alkynylsulfinyl, (C 1 -C 6 ) -haloalkylsulfinyl, (C 2 -C 6 ) -haloalkenylsulfinyl, (C 2 -C 6 ) -haloalkynylsulfinyl , (C 3 -C 8 ) -cycloalkylsulfinyl, (C 4 -C 8 ) -cycloalkenylsulfinyl, (C 3 -C 8 ) -halocycloalksulfinyl, (C 4 -C 8 )- halo cycloalkenyl sulfinyl, (C 1 -C 6) - alkylsulfonyl, (C 2 -C 6) - alkenyl nilseol sulfonyl, (C 2 -C 6) - alkynyl nilseol sulfonyl, (C 1 -C 6) -haloalkyl-sulfonyl, (C 2 -C 6) - haloalkenyl nilseol sulfonyl, (C 2 -C 6) - haloalkynyl nilseol sulfonyl, (C 3 -C 8) - cycloalkyl, sulfonyl, (C 4 -C 8) -cycloalkyl alkenyl nilseol sulfonyl, (C 3 -C 8) - halo-cycloalkenyl keuseol sulfonyl, (C 4 -C 8) - halo-cycloalkenyl sulfonate , (C 1 -C 6) - alkylamino, (C 2 -C 6) - alkenyl, amino, (C 2 -C 6) - alkynyl, amino, (C 1 -C 6) - haloalkyl, amino, (C 2 -C 6 ) -haloalkenylamino, (C 2 -C 6 ) -haloalkynylamino, (C 3 -C 8 ) -cycloalkylamino, (C 4 -C 8 ) -cycloalkenylamino, ( Optionally substituted by one or more radicals selected from the group consisting of C 3 -C 8 ) -halocycloalkamino and (C 4 -C 8 ) -halocycloalkenylamino;
    R 11 is (C 1 -C 10 ) -alkyl, haloalkyl, aryl (halo, cyano, nitro, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkyl, amino, (C 1 -C 4) - monoalkyl amino and (C 1 -C 4) - D is optionally substituted by one or more radicals selected from the group consisting of alkylamino), NR 10 2, oR 10 or SR 10, or to only the listed Compounds are not included:
    3- (2-chlorophenyl) -1-methyl-5- (4-trifluoromethyl-3-pyridyl) -1H-1,2,4-triazole;
    3- (2,6-difluorophenyl) -1-methyl-5- (4-trifluoromethyl-3-pyridyl) -1H-1,2,4-triazole;
    3- (2-chloro-4-fluorophenyl) -1-methyl-5- (4-trifluoromethyl-3-pyridyl) -1H-1,2,4-triazole;
    3- (3,5-dichlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (4-trifluoromethyl-3-pyridyl) -3-phenyl-1,2,4-oxadiazole;
    3- (4-trifluoromethyl-3-pyridyl) -5-phenyl-1,2,4-oxadiazole;
    5- (2-chlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3-chlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (4-chlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (2-fluorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (4-fluorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (2,4-dichlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3,4-dichlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3,5-dichlorophenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (2,6-dichloro-4-pyridyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    5- (3,5-bistrifluoromethylphenyl) -3- (4-trifluoromethyl-3-pyridyl) -1,2,4-oxadiazole;
    2- (2-chlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (3-chlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (4-chlorophenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (2-trifluoromethoxyphenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (4-trifluoromethoxyphenyl) -5- (4-trifluoromethyl-3-pyridyl) -1,3,4-oxadiazole;
    2- (4-trifluoromethyl-3-pyridyl) -5-phenyl-1,3,4-oxadiazole;
    2- (4-trifluoromethyl-3-pyridyl) -4-methylthiazolecarbohydrazide;
    Ethyl 2- (4-trifluoromethyl-3-pyridyl) -4-methylthiazole carboxylate;
    N- (4-chlorophenyl) carbonyl-N '-[2- (4-trifluoromethyl-3-pyridyl) -4-methyl-5-thiazolyl] carbonylhydrazine;
    2- (4-trifluoromethyl-3-pyridyl) -4-thiazolecarbohydrazide;
    4- (4-chlorophenyl) -2- (4-trifluoromethyl-3-pyridyl) thiazole;
    4- (4-cyanophenyl) -2- (4-trifluoromethyl-3-pyridyl) thiazole;
    N- (4-trifluoromethylphenyl) carbonyl-N '-[2- (4-trifluoromethyl-3-pyridyl) -4-thiazolyl] carbonylhydrazine;
    2- (2- (4-trifluoromethyl-3-pyridyl) thiazolyl) -5-chloro-3-methylbenzo [b] thiophene;
    2- (4-chlorophenylmethylthio) -5- (4-trifluoromethyl-3-pyridyl) -1-methyl-1H-1,3,4-triazole;
    2- (4-chlorophenylcarbonylmethylthio) -5- (4-trifluoromethyl-3-pyridyl) -1-methyl-1H-1,3,4-triazole and
    2-ethoxycarbonylmethylthio-5- (4-trifluoromethyl-3-pyridyl) -1-methyl-1H-1,3,4-triazole.
    [2" claim-type="Currently amended] The method of claim 1,
    Y is C 1 -C 6 -alkyl mono- or polysubstituted by chlorine and / or fluorine;
    m is 0;
    Q is a 5-membered heterocyclic group ego,
    Where a) X 2 = NR a and X 3 = CR b R 1, or b) X 2 = CR a R 2 and X 3 = CR b R 3, or c) X 2 = CR 4 R 5 and X 3 = CR 6 R 7 ;
    R a and R b together form a single bond;
    R 1 , R 2 , R 3 , R 4 and R 6 are each independently of each other hydrogen, halogen, C 1 -C 12 -alkyl, (C 3 -C 8 ) -cycloalkyl, (C 2 -C 8 )- Alkenyl, (C 2 -C 8 ) -alkynyl [wherein the last four hydrocarbon radicals mentioned are C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -alkylamino, C 1 -C 6 -alkylcarbonylamino, C 1 -C 6 -alkylsulfonylamino, phenyl, furyl, pyryl, Optionally mono- or polysubstituted by the same or different radicals selected from the group A1 consisting of thienyl, halogen, cyano, phenyloxy, phenylthio and phenylamino, wherein the eleven radicals mentioned first in the group A1 are each To the same or different radicals selected from the group B1 consisting of halogen, cyano, C 1 -C 3 -alkoxy and phenyl, which is optionally mono- or polysubstituted by one or more halogen atoms Optionally monosubstituted or polysubstituted, the last three radicals mentioned in group A1 are each selected from group B2 consisting of halogen, cyano, nitro, C 1 -C 3 -alkyl and C 1 -C 3 -alkoxy Mono- or polysubstituted by the same or different radicals] (C 1 -C 6 ) -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxycarbonyl, phenyl, pyridyl, furyl, thienyl, pyryl (the last 8 mentioned) Radicals are optionally mono- or polysubstituted by the same or different radicals selected from group B 1), or
    OR 10 , SR 10 or N (R 10 ) 2 ;
    R 5 and R 7 are each independently of each other hydrogen, halogen, (C 1 -C 12 ) -alkyl, (C 3 -C 8 ) -cycloalkyl, C 2 -C 8 -alkenyl, C 2 -C 8- Alkynyl [wherein the last four hydrocarbon radicals mentioned are C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkyl Selected from the group A2 consisting of thio, C 1 -C 6 -alkylamino, C 1 -C 6 -alkylcarbonylamino, phenyl, furyl, pyryl, thienyl, halogen, cyano, phenyloxy, phenylthio and phenylamino Optionally mono- or polysubstituted by the same or different radicals, wherein the ten radicals mentioned first in group A 2 are each optionally mono- or poly-substituted by the same or different radicals selected from group B 1 and in group A 2 The last three radicals mentioned are each optionally monosubstituted by the same or different radicals selected from group B2 Is multi-substituted, or
    (C 1 -C 6 ) -alkylcarbonyl, C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkoxycarbonyl, phenyl, pyridyl, furyl, thienyl, fluorine, chlorine, bromine, pyryl (The last eight radicals mentioned are optionally monosubstituted or polysubstituted by the same or different radicals selected from group B1), or
    OR 10 , SR 10 or N (R 10 ) 2 ;
    R 10 is hydrogen, benzyl, C 1 -C 6 -alkyl, C 1 -C 6 -cycloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, phenyl, C 1 -C 6- Alkylcarbonyl or C 1 -C 6 -alkylsulfonyl, wherein the eight radicals mentioned last are optionally mono- or polysubstituted by the same or different halogen atoms
    4-haloalkyl-3-heterocyclylpyridine or 4-haloalkyl-5-heterocyclylpyrimidine.
    [3" claim-type="Currently amended] The method of claim 2,
    Y is trifluoromethyl;
    R 1 , R 2 , R 3 , R 4 and R 6 are each independently of the other halogen, C 1 -C 12 -alkyl, C 2 -C 12 -alkenyl [the last two radicals mentioned are C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylamino, C 1 -C 4 The same selected from the group A3 consisting of -alkylcarbonylamino, C 1 -C 4 -alkylsulfonylamino, phenyl, furyl, pyryl, thienyl, fluorine, chlorine, bromine, cyano, phenyloxy, phenylthio and phenylamino Or optionally monosubstituted or polysubstituted by different radicals, wherein the eleven radicals mentioned first in group A3 are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B1 and the last in group A3 The three radicals mentioned in are each optionally monosubstituted or substituted by the same or different radicals selected from group B2. Is ring], or is OR 10, SR 10 or N (R 10) 2, and;
    R 5 and R 7 are each independently of the other halogen, (C 1 -C 12 ) -alkyl, C 2 -C 12 -alkenyl [wherein the two radicals mentioned last are C 1 -C 4 -alkylcarbonyl , C 1 -C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylamino, C 1 -C 4 -alkylcarbonylamino, phenyl Optionally mono- or polysubstituted by the same or different radicals selected from group A4 consisting of furyl, pyryl, thienyl, fluorine, chlorine, bromine, cyano, phenyloxy, phenylthio and phenylamino, the first of group A4 The ten radicals mentioned in are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B1, and the three radicals mentioned last in group A4 are each selected by the same or different radicals selected from group B2 or a mono-substituted or multi-substituted], or oR 10, SR 10 or N (R 10) 2 And;
    R 10 is hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, phenyl, C 1 -C 4 -alkylcarbonyl or C 1 -C 4 -alkyl Sulfonyl, wherein the six radicals mentioned last are optionally mono- or polysubstituted by the same or different halogen atoms
    4-haloalkyl-3-heterocyclylpyridine or 4-haloalkyl-5-heterocyclylpyrimidine.
    [4" claim-type="Currently amended] The method of claim 3, wherein
    R 1 , R 2 , R 3 , R 4 and R 6 are each independently of each other C 1 -C 10 -alkyl or C 2 -C 10 -alkenyl, wherein the two radicals mentioned last are C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylamino, C 1 -C 4 -alkyl Optionally monosubstituted by the same or different radicals selected from the group A5 consisting of carbonylamino, C 1 -C 4 -alkylsulfonylamino, phenyl, fluorine, chlorine, bromine, cyano, phenyloxy, phenylthio and phenylamino Or polysubstituted, wherein the eight radicals mentioned first in group A5 are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B1, and the three radicals mentioned last in group A5 are each group Optionally mono- or polysubstituted by the same or different radicals selected from B 2;
    R 5 and R 7 are each independently of each other C 1 -C 10 -alkyl or C 2 -C 10 -alkenyl, wherein the two radicals mentioned last are C 1 -C 4 -alkylcarbonyl, C 1- C 4 -alkylaminocarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylamino, C 1 -C 4 -alkylcarbonylamino, phenyl, fluorine, chlorine , Optionally mono- or polysubstituted by the same or different radicals selected from group A6 consisting of bromine, cyano, phenyloxy, phenylthio and phenylamino, wherein the seven radicals mentioned last in group A6 are each group B1 Optionally monosubstituted or polysubstituted by the same or different radicals selected from, and the last three radicals mentioned in group A6 are each optionally monosubstituted or polysubstituted by the same or different radicals selected from group B2
    4-haloalkyl-3-heterocyclylpyridine or 4-haloalkyl-5-heterocyclylpyrimidine.
    [5" claim-type="Currently amended] A) when X 1 = O, X 2 = NR a , X 3 = CR b R 1 , react the activated derivative of the acid of formula II with a compound of formula III in the presence of a base;
    Formula II

    Formula III

    (Wherein
    X, Y and R 1 are as defined in formula (I).)
    B) when X 1 = S, X 2 = NR a , X 3 = CR b R 1 , the compound of formula VII is reacted with an electrophilic amination agent;

    C) when X 1 = NR a , X 2 = CR b R 1 , X 3 = O, the amidoxime of Formula V is reacted with an activated derivative of the acid of Formula VI or the acid of Formula VI itself;

    D) When X 1 = S, X 2 = CR a R 1 , X 3 = NR b , the N, N'-acylhydrazine of the formula (XIII) is dissolved in an inert solvent with a thiolating agent such as Lawesson reagent. React;

    E) When X 1 = O, X 2 = CR a R 1 , X 3 = NR b , using an activator such as phosphorus oxychloride or phosphorus pentachloride, the acid of formula II is converted to hydrazide of formula Wherein R 1 is as defined above, or the acid hydrazide of formula XI is ortho ester of formula XII wherein R 1 is as defined above and R 12 is (C 1 -C 4 ) -alkyl);


    F) When X 1 = O, X 2 = CR a R 2 , X 3 = CR b R 3 , wherein R a , R b and R 3 are as defined above, dehydration of the compound of formula XIV React with reagents such as inorganic acid chlorides, inorganic acids and anhydrides;

    G) When X 1 = S, X 2 = CR a R 2 , X 3 = CR b R 3 , the thioamide of formula XVII is a carbonyl derivative of formula XVIII wherein Z is halogen, in particular chlorine or bromine , Acyloxy or sulfonyloxy, especially methanesulfonyloxy or tolylsulfonyloxy);

    H) When X 1 = S, X 2 = CR 4 R 5 , X 3 = CR 6 R 7 , the thioamide of formula XVII is substituted with a compound of formula XIX wherein the two substituents Z are as defined above May be the same or different);

    I) when X 1 = NR a , X 2 = CR b R 1 , X 3 = NR 8 , where R a , R b , R 1 and R 8 are as defined above, Reacting a drazide with a compound of formula XXI or a thioamide of formula XXII
    Formula XX

    Formula XXI

    Formula XXII

    Process for the preparation of compounds of formula (I) according to any one of claims 1 to 4.
    [6" claim-type="Currently amended] A composition having insecticidal, acaricide and / or nematicidal action, comprising at least one compound according to any one of claims 1 to 4.
    [7" claim-type="Currently amended] The method of claim 6,
    A composition having insecticidal, acaricide and / or nematicidal action, mixed with a carrier and / or surfactant.
    [8" claim-type="Currently amended] The method according to claim 6 or 7,
    A composition comprising a further active compound selected from the group consisting of acaricides, fungicides, herbicides, insecticides, nematicides or growth regulators.
    [9" claim-type="Currently amended] A compound according to any one of claims 1 to 4 or a composition according to claim 6, for use as a veterinary medicament, preferably for exterminating external and enteric parasites.
    [10" claim-type="Currently amended] Control of pests, ticks and nematodes, comprising applying an effective amount of a compound according to any one of claims 1 to 4 or a composition according to any one of claims 6 to 8 to the area in need of treatment. Way.
    [11" claim-type="Currently amended] A method for protecting a plant useful against the unwanted action of pests, mites and nematodes, comprising using at least one compound according to any one of claims 1 to 4 to treat seeds of a useful plant.
    [12" claim-type="Currently amended] Use of a compound according to any one of claims 1 to 4 or a composition according to any one of claims 6 to 8 for controlling pests, ticks and nematodes.
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    同族专利:
    公开号 | 公开日
    ZA9805180B|1998-12-17|
    EP0991648A1|2000-04-12|
    HU0002729A3|2001-02-28|
    KR100583260B1|2006-05-24|
    AU754182B2|2002-11-07|
    CA2294888A1|1998-12-23|
    AR014102A1|2001-02-07|
    NZ501792A|2002-03-28|
    TR199903102T2|2000-04-21|
    ID26589A|2001-01-18|
    US6239160B1|2001-05-29|
    US20020013326A1|2002-01-31|
    BR9810139A|2000-08-08|
    WO1998057969A1|1998-12-23|
    PL337695A1|2000-08-28|
    JP2002504127A|2002-02-05|
    IL133531D0|2001-04-30|
    CO5040002A1|2001-05-29|
    CN1260793A|2000-07-19|
    CN1102149C|2003-02-26|
    DE19725450A1|1998-12-17|
    AU8624398A|1999-01-04|
    AP9901716A0|1999-12-31|
    US6521610B2|2003-02-18|
    HU0002729A2|2000-11-28|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1997-06-16|Priority to DE19725450A
    1997-06-16|Priority to DE19725450.0
    1998-06-03|Application filed by 슈미트, 루츠, 훽스트 쉐링 아그레보 게엠베하
    1998-06-03|Priority to PCT/EP1998/003321
    2001-02-26|Publication of KR20010013830A
    2006-05-24|Application granted
    2006-05-24|Publication of KR100583260B1
    优先权:
    申请号 | 申请日 | 专利标题
    DE19725450A|DE19725450A1|1997-06-16|1997-06-16|4-Haloalkyl-3-heterocyclylpyridines and 4-haloalkyl-5-heterocyclylpyrimidines, processes for their preparation, compositions containing them and their use as pesticides|
    DE19725450.0|1997-06-16|
    PCT/EP1998/003321|WO1998057969A1|1997-06-16|1998-06-03|4-haloalkyl-3- heterocyclylpyridines and 4-haloalkyl -5-heterocyclylpyridines, method for the production thereof, agents containing the same and their use as pesticides|
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