N-acetonyl-substituted-naphthyl-amides
AssigneeRohm and Haas Company
InventorAshok K. Sharma
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Abstract
Certain N-acetonyl-substituted-amides of the formula: ##STR1## wherein A naphthyl; X, Y and Z are selected from the group consisting of hydrogen, halo, cyano, thiocyano, isothiocyano, thio(C.sub.1 -C.sub.2)alkyl, (C.sub.1 -C.sub.2)alkoxy, carbamoyl, dithiocarbomoyl, hydroxy, azide, thiophenyl, imidazolyl or triazolyl group as described herein; R.sup.1 and R.sup.2 are each independently a hydrogen atom or a (C.sub.1 -C.sub.6)alkyl group; and compositions containing these amides are fungicidally active, particularly against phytopathogenic fungi.
Claims1
A compound of the structure ##STR18## wherein A is naphthyl which may be substituted with up to three substituents independently selected from halo, trifluoromethyl, fluorosulfonyl, methyl, ethyl, methoxy or phenyl group;
- x is chloro, bromo, iodo, fluoro, cyano, thiocyano, isothiocyano, methylsulfonyloxy, thio(C.sub.1 -C.sub.2)alkyl, (C.sub.1 -C.sub.2)alkoxy, carbamoyl, dithiocarbomoyl, hydroxy, azido, (C.sub.1 -C.sub.4)alkylcarbonyloxy, phenylcarbonyloxy, trifluoromethylcarbonyloxy, phenoxy, phenylthio, imidazolyl or triazolyl group, when X is a phenylcarbonyloxy, phenoxy or phenylthio substituent, the phenyl moiety may be substituted with up to one substituent selected from chloro, fluoro, bromo, iodo or methyl group;
- Y and Z are each independently hydrogen, bromo, chloro, iodo, fluoro, cyano, thiocyano, isothiocyano, methylsulfonyloxy, thio(C.sub.1 -C.sub.2)alkyl, (C.sub.1 -C.sub.2)alkoxy, carbamoyl, hydroxy, azido or thio(C.sub.1 -C.sub.4)alkylcarbonyloxy group and either Y or Z may be imidazolyl or triazolyl group;
- and
- R.sup.1 and R.sup.2 are each independently selected from a hydrogen atom and (C.sub.1 -C.sub.6)alkyl group.
Dependencies are inferred from the claim text.