Amidoacetonitrilo derived Compounds, a process for their preparation, a process for the preparation of compounds intermediaries, a composition for Combating parasites, a procedure to combat these parasites, and the use of these derivatives for the preparation of a com

摘要

1. The compounds prepared by ammonium nitroformate used to deal with endo-y outta parallel, as well as nitroformate and isodihydrazide used in hot blooded animals and plants;1. Independent substitutes selected from halogen, nitrogen, cyanogen, C1-6 tar, C1-6 halide, alcoxyl C1-6, haloxyl C1-6, alcoxyl C1-6, alquenilo c2-6, haloalkoxyl c2-6, haloalquenilo c2-6, tar c2-6, C3-6 cyclopropyl calcium oxide C3-6 groups, but not replaced once or more; 6-1, 1-1-1-1, 1-6-1-1-1, 1-1-1, 1-6-1-2-quenil c2-6-uncle Alquenil c2-6-sulfur,1. Haloalquenil c2-6-sulfur, alquenil c2-6-sulfur, haloalquenil c2-6-sulfur, hydrocarbon c1-6-amino, di-acquil c1-6-amino, tar c1-6-sulfur-amine, haloalquenil c1-6-carbonilo, halogel c1-6-carbonilo, alcox c1-6-carbonilo, c1-6-carbon, c1-6-amin, c1-1-6-bonal Not replaced or replaced once or more phenylethylamine; not replaced or replaced once or more methyl benzoate; not replaced or replaced once or more phenylhydroxymethyl ether; not replaced or replaced once or more 1-phenyl-1 Or replace once or more times;unsubstituted or substituted phenylcyanomethyl one or more times; phenyl unsubstituted or substituted one or more times, the substituents being able to be independent of each other and are selected from the group consisting of halogen, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, haloalkoxy C1-6, C1-6-thio alkyl, halo C1-6-thio alkyl, C1-6 alkyl-sulfinyl, haloC 1-6 alkyl sulfinyl, C1-6 alkyl sulfonyl and haloC 1-6 alkyl sulfonyl; phenoxy unsubstituted or substituted one or more times, the substituents being able to be independent of each other and are selected from the group consisting of halogen, nitro, cyano, C1-6 alkyl, haloalkyl C1-6, alkoxy C1-6,C1-6 haloalkoxy, C1-6-thio alkyl, C1-6-thio haloalkyl, C1-6-sulfinyl alkyl, C1-6-alkyl sulfinyl, C1-6-sulfonyl alkyl and C1-6-sulfonyl alkyl; phenylacetylenyl unsubstituted or substituted one or more times, the substituents being able to be independent of each other and are selected from the group consisting of halogen, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 haloalkoxy , C1-6-thio alkyl, halo C1-6-thio alkyl, C1-6 alkyl sulfinyl, haloC 1-6 alkyl sulfinyl, C1-6 alkyl sulfonyl and haloC 1-6 alkyl sulfonyl; and unsubstituted or substituted pyridyloxy one or more times,the substituents may be independent of each other and are selected from the group consisting of halogen, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 haloalkoxy, C1-6-thio alkyl, C1-haloalkyl -6-thio, C 1-6 alkyl sulfinyl, C 1-6 haloalkyl sulfinyl, C 1-6 alkyl sulfonyl and halo C 1-6 alkyl sulfonyl; heteroaryl unsubstituted or substituted one or more times, the substituents being able to be independent of each other and are selected from the group consisting of halogen, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 haloalkoxy , C2-6 alkenyloxy, C2-6 haloalkenyloxy, C1-6-thio alkyl, C1-6-thio haloalkyl, C1-6-sulfinyl alkyl,halo C1-6-sulfinyl, C2-6-thio alkenyl, halo C2-6-thio-alkenyl, C2-6-sulfinyl alkenyl, C2-6-sulfinyl haloalkenyl, C1-6-sulfonyl alkyl and C1-6-sulfonyl haloalkyl , C2-6 alkenyl sulfonyl, C2-6 haloalkenyl sulfonyl, C1-6-amino alkyl and di- C1-6 alkyl alkyl; or naphthyl or quinolyl unsubstituted or substituted one or more times, the substituents being able to be independent of each other and are selected from the group consisting of halogen, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, haloalkoxyl C1-6, C2-6 alkenyloxy, C2-6 haloalkenyloxy, C1-6-thio alkyl, C1-6-thio haloalkyl, C1-6-sulfinyl alkyl, C1-6-halofinalkyl, C2-6-thio alkenyl,C2-6-thio halo-alkenyl, C2-6-sulfinyl alkenyl, C2-6-sulfinyl haloalkenyl, C1-6-sulfonyl and haloC 1-6-sulfonyl alkyl, C2-6-alkenyl sulfonyl, C2-6-sulfonyl haloalkenyl , C2-6 haloalkenyl-sulfonyl, C1-6-amino alkyl and di- C1-6-amino alkyl; R 1 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, allyl or C 1-6 alkoxy-methyl; R2, R3, R4, R5, R6, R7 and R8 either independently of each other,1. Hydrogen, halogen, C1-6 tar, not replaced or replaced with halogen once or more; 2-6 hydrazide, not replaced or replaced with halogen once or more; 2-6 tar, not replaced or replaced with halogen once or more; 1 C1-6 halogen, which has not been replaced or replaced one or more times, or replaced one or more times, can be selected from C1-6 halogen and tar group as independent substitutes, or benzene which has not been replaced or replaced one or more times,the substituents may be independent of one another and is selected from the group consisting of halogen, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 haloalkoxy, C1-6-thio alkyl, C1 haloalkyl -6-thio, C1-6 alkyl sulfinyl, haloC 1-6 alkyl sulfinyl, C1-6 alkyl sulfonyl, haloC 1-6 alkyl sulfonyl, C 1-6 alkyl or di C 1-6 alkyl; or R2 and R3 are together C2-6 alkylene; and X is C (R3) (R4) -C (R5) (R6) or C (R7) = C (R8),A preparation procedure, an intermediate compound preparation procedure, a parasite control ingredient, a parasite control procedure, and the preparation of pharmaceutical ingredients using these derivatives. Active substances have advantages in pesticide properties, especially in the prevention and control of parasites in hot blooded animals.