首页> 外国专利> Composition for controlling animal pests comprises a synergistic combination of a nicotinergic acetylcholine receptor agonist or antagonist and an anthranilamide derivative

Composition for controlling animal pests comprises a synergistic combination of a nicotinergic acetylcholine receptor agonist or antagonist and an anthranilamide derivative

机译:用于防治动物害虫的组合物包含烟碱能乙酰胆碱受体激动剂或拮抗剂与蒽酰胺衍生物的协同组合。

摘要

Composition comprising a synergistic combination of a nicotinergic acetylcholine receptor agonist or antagonist (I) and an anthranilamide derivative (II) is new. Composition comprising a synergistic combination of a nicotinergic acetylcholine receptor agonist or antagonist of formula (I) and an anthranilamide derivative of formula (II) is new. [Image] R : H or optionally substituted acyl, alkyl, aryl, aralkyl, heterocyclyl, heteroaryl or heteroarylalkyl; A : H, acyl, alkyl or aryl or a bifunctional group bonded to Z; E : an electron-withdrawing group; X : CH or N, or C bonded to Z; Z : alkyl, OR, SR or N(R) 2, or a bifunctional group bonded to A or X; A 1, A 2O or S; X 1N or CR 1 0; R 1H or optionally substituted C1-C6-Alkyl, C2-C6-Alkenyl, C2-C6-Alkynyl or C3-C6-Cycloalkyl; R 2H, C1-C6-Alkyl, C2-C6-Alkenyl, C2-C6-Alkynyl, C3-C6-Cycloalkyl, C1C4-Alkoxy, C1-C4-Alkylamino, C2-C8-Dialkylamino, C3-C6-Cycloalkylamino, C2-C6 Alkoxycarbonyl or C1-C6-Alkylcarbonyl; R 3H, R 1 1 or optionally substituted C1-C6-Alkyl, C2-C6-Alkenyl, C2-C6-Alkynyl, C3-C6-Cycloalkyl; R 2+R3 : a ring M; R 4H, C1-C6-Alkyl, C2-C6-Alkenyl, C2-C6-Alkynyl, C3-C6-Cycloalkyl, C1-C6 Haloalkyl, C2-C6-Haloalkenyl, C2-C6-Haloalkynyl, C3-C6-Halocycloalkyl, Halogen, Cyano, Nitro, Hydroxy, C1-C4-Alkoxy, C1-C4-Haloalkoxy, C1-C4-Alkylthio, C1-C4-Alkylsulfinyl, C1-C4-Alkylsulfonyl, C1-C4-Haloalkylthio, C1-C4-Haloalkylsulfinyl, C1-C4-Haloalkylsulfonyl, C1-C4-Alkylamino, C2-C8-Dialkylamino, C3-C6-Cycloalkylamino, C3-C6-Trialkylsilyl or optionally substituted Phenyl, Benzyl or Phenoxy; R 5, R 8H, Halogen or optionally substituted C1-C4-Alkyl, C1-C4-Haloalkyl, R 1 2, G, J, -OJ, -OG, -S(O) p-J, -S(O) p-G, -S(O)p-phenyl; G : a 5- or 6-membered non-aromatic carbocyclic or heterocyclic ring optionally containing 1 or 2 C(=O), SO or S(=O)Z ring members and optionally substituted; J : an optionally substituted 5- or 6-membered heteroaromatic ring; R 6-C(=E 1)R 1 9, -LC(=E 1) 1 9, C(=E 1)LR 1 9, -LC(=E 1)LR 1 9, -OP(=Q)(OR 1 9)2, -SO 2LR 1 8 or -LSO 2LR 1 9; E 1O, S, N-R 1 5, N-OR 1 5, N-N(R 1 5) 2, N-S=O, N-CN or N-NO 2; R 7H, C1-C4-Alkyl, C1-C4-Haloalkyl, Halogen, C1-C4-Alkoxy, C1-C4 Haloalkoxy, C1-C4-Alkylthio, C1-C4-Alkylsulfinyl, C1-C4-Alkylsulfonyl, C1-C4 Haloalkylthio, C1-C4-Haloalkylsulfinyl, C1-C4-Haloalkylsulfonyl; R 9C1-C4-Haloalkyl, C1-C4-Haloalkoxy, C1-C4-Haloalkylsulfinyl or Halogen; R 1 0H, C1-C4-Alkyl, C1-C4-Haloalkyl, Halogen, Cyano or C1-C4 Haloalkoxy; R 1 1optionally mono- to trisubstituted C1-C6-Alkylthio, C1-C6-Alkylsulfenyl, C1-C6-Haloalkythio, C1-C6 Haloalkylsulfenyl, Phenylthio or Phenylsulfenyl; L : O, NR 1 8 or S; R 1 2-B(OR 1 7) 2, Amino, SH, Thiocyanato, C3-C8 Trialkylsilyloxy, C1-C4-Alkyldisulfide, -SF 5, -C(=E)R 1 9, -LC(=E)R 1 9, -C(=E)LR 1 9, -LC(=E)LR 1 9, -OP(=Q)(OR 1 9) 2, -SO 2LR 1 9 or -LSO 2LR 1 9; Q : O or S; R 1 3H or optionally substituted C1-C6-Alkyl, C2-C6-Alkenyl, C2-C6-Alkynyl or C3-C6 Cycloalkyl; R 1 4optionally substituted C1-C20-Alkyl, C2-C20-Alkenyl, C2-C20-Alkynyl or C3-C6-Cycloalkyl; R 1 5H or optionally substituted C1-C6-Haloalkyl or C1-C6-Alkyl, or N(R 1 5) 2 forms a ring M; R 1 6C1-C12-Alkyl or C1-C12-Haloalkyl, or N(R 1 6) 2 forms a ring M; R 1 7H or C1-C4-Alkyl, or B(OR 1 7) 2 is a ring in which both O atoms are connected with a chain of 2-3 C atoms, optionally substituted with 1 or 2 of methyl oder C2-C6 Alkoxycarbonyl; R 1 8H, C1-C6 Alkyl or C1-C6-Haloalkyl, or N(R 1 3)(R 1 8) forms a ring M; R 1 9H or optionally substituted C1-C6-Alkyl; M : an optionally substituted ring comprising an N atom, 2-6 C atoms and optionally another N, O or S atom; n : 0 or 1; p : 0, 1 or 2; when (a) R 5H, C1-C6-Alkyl, C1-C6-Haloalkyl, C2-C6 Haloalkenyl, C2-C6-Haloalkynyl, C1-C4-Haloalkoxy, C1-C4-Haloalkylthio or Halogen steht and (b) R 8 = H, C1-C6-Alkyl, C1-C6-Haloalkyl, C2-C6-Haloalkenyl, C2-C6 Haloalkynyl, C1-C4-Haloalkoxy, C1-C4-Haloalkylthio, Halogen, C2-C4-Alkylcarbonyl, C2-C6 Alkoxycarbonyl, C2-C6-Alkylaminocarbonyl or C3-C8 Dialkylaminocarbonyl, (c) at least one of R 6, R 1 1 and R 1 2 is present and (d) R 1 2 is not present, then R 6 or R 1 1 is not C2-C6-Alkylcarbonyl, C2-C6 Alkoxycarbonyl, C2-C6-Alkylaminocarbonyl or C3-C8-Dialkylaminocarbonyl. Full definitions are given in the Definitions Field (Full Definitions). ACTIVITY : Insecticide; Acaricide; Nematocide. MECHANISM OF ACTION : Nicotinergic acetylcholine receptor agonist; Nicotinergic acetylcholine receptor antagonist.
机译:包含烟碱能乙酰胆碱受体激动剂或拮抗剂(I)和邻氨基苯甲酰胺衍生物(II)的协同组合的组合物是新的。包含式(I)的烟碱能乙酰胆碱受体激动剂或拮抗剂与式(II)的邻氨基苯甲酰胺衍生物的协同组合的组合物是新的。 [图像] R:H或任选取代的酰基,烷基,芳基,芳烷基,杂环基,杂芳基或杂芳基烷基; A:H,酰基,烷基或芳基或与Z键合的双官能团; E:吸电子基团; X:CH或N,或C键合至Z; Z:烷基,OR,SR或N(R)2,或与A或X键合的双官能团; A 1>,A 2> O或S; X 1> N或CR 1> 0>; R 1> H或任选取代的C 1 -C 6烷基,C 2 -C 6烯基,C 2 -C 6炔基或C 3 -C 6环烷基; R 2> H,C1-C6-烷基,C2-C6-链烯基,C2-C6-烷基,C3-C6-环烷基,C1C4-烷氧基,C1-C4-烷基氨基,C2-C8-二烷基氨基,C3-C6-环烷基氨基,C2-C6烷氧羰基或C1-C6-烷氧羰基; R 3> H,R 1> 1>或任选取代的C 1 -C 6烷基,C 2 -C 6烯基,C 2 -C 6炔基,C 3 -C 6环烷基; R 2> + R 3:环M; R 4> H,C1-C6-烷基,C2-C6-烯基,C2-C6-炔基,C3-C6-环烷基,C1-C6卤代烷基,C2-C6-卤代烯基,C2-C6-卤代炔基,C3-C6-卤代环烷基,卤素,氰基,硝基,羟基,C 1 -C 4烷氧基,C 1 -C 4卤代烷氧基,C 1 -C 4烷硫基,C 1 -C 4烷基亚磺酰基,C 1 -C 4烷基磺酰基,C 1 -C 4卤代烷硫基,C 1 -C 4卤代烷基亚磺酰基,C 1 -C 4卤代烷基磺酰基,C 1 -C 4烷基氨基,C 2 -C 8-二烷基氨基,C 3 -C 6环烷基氨基,C 3 -C 6三烷基甲硅烷基或任选取代的苯基,苄基或苯氧基; R 5>,R 8> H,卤素或任选取代的C1-C4-烷基,C1-C4-卤代烷基,R 1> 2>,G,J,-OJ,-OG,-S(O)pJ,-S (O)pG,-S(O)对苯基; G:5或6元非芳族碳环或杂环,其任选地含有1或2个C(= O),SO或S(= O)Z环成员并且任选地被取代; J:任选取代的5或6元杂芳族环; R 6> -C(= E 1>)R 1> 9>,-LC(= E 1>)1> 9>,C(= E 1>)LR 1> 9>,-LC(= E 1> )LR 1> 9>,-OP(= Q)(OR 1> 9>)2,-SO 2LR 1> 8>或-LSO 2LR 1> 9>; E 1> O,S,N-R 1> 5>,N-OR 1> 5>,N-N(R 1> 5>)2,N-S = O,N-CN或N-NO 2; R 7> H,C 1 -C 4烷基,C 1 -C 4卤代烷基,卤素,C 1 -C 4烷氧基,C 1 -C 4卤代烷氧基,C 1 -C 4烷硫基,C 1 -C 4烷基亚磺酰基,C 1 -C 4烷基磺酰基,C 1 C4卤代烷硫基,C1-C4-卤代烷基亚磺酰基,C1-C4-卤代烷基磺酰基; R 9> C1-C4-卤代烷基,C1-C4-卤代烷氧基,C1-C4-卤代烷基亚磺酰基或卤素; R 1> 0> H,C 1 -C 4烷基,C 1 -C 4卤代烷基,卤素,氰基或C 1 -C 4卤代烷氧基; R 1> 1>任选地为单取代至三取代的C 1 -C 6烷硫基,C 1 -C 6烷基亚硫基,C 1 -C 6卤代烷硫基,C 1 -C 6卤代烷基亚硫基,苯硫基或苯硫基; L:O,NR 1> 8>或S; R 1> 2> -B(OR 1> 7>)2,氨基,SH,硫氰酸根,C3-C8三烷基甲硅烷氧基,C1-C4-烷基二硫化物,-SF 5,-C(= E)R 1> 9>,- LC(= E)R 1> 9>,-C(= E)LR 1> 9>,-LC(= E)LR 1> 9>,-OP(= Q)(OR 1> 9>)2, -SO 2LR 1> 9>或-LSO 2LR 1> 9>;问:O或S; R 1> 3> H或任选取代的C 1 -C 6烷基,C 2 -C 6烯基,C 2 -C 6炔基或C 3 -C 6环烷基; R 1> 4>任选取代的C 1 -C 20烷基,C 2 -C 20烷基,C 2 -C 20烷基或C 3 -C 6环烷基; R 1> 5> H或任选取代的C 1 -C 6卤代烷基或C 1 -C 6烷基,或N(R 1> 5>)2形成环M; R 1> 6> C 1〜C 12烷基或C 1〜C 12卤代烷基,或N(R 1> 6>)2形成环M; R 1> 7> H或C1-C4-烷基,或B(OR 1> 7>)2是这样一个环,其中两个O原子均与2-3个C原子的链相连,并任选地被1个或2个C取代甲基C2-C6烷氧羰基; R 1> 8> H,C1-C6烷基或C1-C6-卤代烷基或N(R 1> 3>)(R 1> 8>)形成环M; R 1> 9> H或任选取代的C 1 -C 6烷基; M:包含N原子,2-6个C原子和任选地另一个N,O或S原子的任选取代的环; n:0或1; p:0、1或2; (a)R 5> H,C1-C6-烷基,C1-C6-卤代烷基,C2-C6卤代烯基,C2-C6-卤代炔基,C1-C4-卤代烷氧基,C1-C4-卤代烷硫基或卤代卤R 8> = H,C 1 -C 6烷基,C 1 -C 6卤代烷基,C 2 -C 6卤代烯基,C 2 -C 6卤代炔基,C 1 -C 4卤代烷氧基,C 1 -C 4卤代烷硫基,卤素,C 2 -C 4烷基羰基,C 2 -C6烷氧羰基,C2-C6-烷基氨基羰基或C3-C8二烷基氨基羰基,(c)存在R 6>,R 1> 1>和R 1> 2>中的至少一个,并且(d)R 1> 2>不存在如果存在,则R 6>或R 1> 1>不是C2-C6-烷基羰基,C2-C6烷氧基羰基,C2-C6-烷基氨基羰基或C3-C8-二烷基氨基羰基。完整定义在“定义”字段(完整定义)中给出。活性:杀虫剂;杀螨剂杀线虫剂。作用机理:烟碱能乙酰胆碱受体激动剂。烟碱能乙酰胆碱受体拮抗剂。

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