Reactions of 4-acyl-1-alkoxyaryl-5-aryl-3-hydroxy-2,5-dihydro-1H-pyrrol-2-ones with nucleophilic reagents
作者:V. L. Gein、N. L. Fedorova、E. B. Levandovskaya、M. I. Vakhrin
DOI:10.1134/s1070428011010118
日期:2011.1
4-Acetyl-1-alkoxyaryl-5-aryl-3-hydroxy-2,5-dihydro-1H-pyrrol-2-ones reacted with amines to give 1-alkoxyaryl-5-aryl-4-(1-R-aminoethylidene)pyrrolidine-2,3-diones. Reactions of amines with 4-benzoyl-substituted analogs involve nucleophilic attack on the C(3) atom in the heteroring to produce the corresponding 3-R-amino-1-alkoxyaryl-5-aryl-4-benzoyl-2,5-dihydro-1H-pyrrol-2-ones. Reactions of the title compounds with hydrazine hydrate, regardless on the substituent on C(4), afforded 4-aryl-3-methyl(phenyl)-5-[2(4)-methoxy-phenyl]- 4,6-dihydropyrrolo[3,4-c]pyrazol-6-ones.