| abstract |
In general terms, the anthranilamide derivatives (1) of the present invention have A and B as O or S; J is substituted phenyl or naphthyl; or J is a 5- or 6-membered heteroaromatic ring or an 8-, 9-, or 10-membered aromatic condensed heterobicyclic ring system optionally substituted; n = 1 to 4; R1 is hydrogen, alkyl, alkenyl, alkynyl or cycloalkyl optionally substituted or R1 is alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl or C (= A) J; R2 is hydrogen or alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, cycloalkylamino, alkoxycarbonyl or alkylcarbonyl; R3 is hydrogen; G is a substitute; alkyl, alkenyl, alkynyl, cycloalkyl optionally substituted, or phenyl, phenoxy, or a 5- or 6-membered heteroaromatic group optionally substituted; alkoxyalkylamino, dialkylamino, cycloalkylamino, alkoxycarbonyl or alkylcarbonyl or R2 and R3 together with the nitrogen atom to which they are attached, in which case they form a further atom, namely a nitrogen, sulfur or oxygen atom ring, substituted; R4 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, haloalkenyl, haloalkynyl, halo-cycloalkyl, halogen, cyano, nitro, hydroxy, alkoxy, haloalkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, haloalkylthio, haloalkylsulfinyl, haloalkylsulfonyl, alkylamino, dialkylamino, cycloalkylamino or trialkylsilyl or R4 is phenyl, benzyl or phenoxy optionally substituted, G is substituted non-aromatic carbocyclic or heterocyclic ring. The present invention also relates to a method of treating anthropodicide composition concentrates containing the compounds of formula (I) as active ingredients. HE |