FIELD: agriculture. SUBSTANCE: the product includes substituted acylaminobenzamides of the formula: wherein A and B are H, F, Cl, Br, C1-C4-alkyl, C1-C4-alkoxy, halo-(C1-C4)-alkyl provided that both are not H; D and E are H and F; R1 is H, C1-C4-alkyl; R2-C1-C4-alkyl, C1-C4-alkoxy, C6H5, or R1 and R2 are together with the nitrogen atom to which they are attached form a morpholino, piperidino, pyrrolidino or acetidino group optionally substituted with C1-C4-alkyl; R3 is Cl3C, C2-C8-alkyl optionally substituted with halogen, C1-C8-alkoxy and R7; R7 is C1-C4-alkyl, n is O, 1 or 2; cyclopropyl optionally substituted with halogen or C1-C4 alkyl; C2-C8-alkenyl, C2-C8-alkynyl; C1-C8-alkoxy, mono- or di-(C1-C4) alkyl amino group; R8ON= C(CN); R8-C1-C4-alkyl, or R3 together with C(O)N form an azetidine -2-one ring optionally substituted with halogen or alkyl. Reagent 1: a compound of the formula: . Reagent 2: R4COCl. Reaction conditions: in an organic solvent in the presence of a base followed by recovery of the desired product or treatment of I in which R3-C2-C8 is alkyl substituted with halogen or, a base in a two-phase system in the presence of a phase transfer catalyst to recover I in which R3 together with C(O)N form azetidin-2-one. EFFECT: improved properties of the title compounds and improved preparation process thereof. 7 tbl
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Authors
Dates
1995-05-10—Published
1990-02-01—Filed