Reaction of methyl 3-phenyl-3-chloro-2-oxopropionate with thiosemicarbazones
摘要:
The reaction of methyl 3-phenyl-3-chloro-2-oxopropionate with thiosemicarbazones proceeds via the intermediate formation of methyl [S-(1'-alkylideneiso-thiosemicarbazidyl)]-3-phenyl-2-oxopropionate hydrochlorides, which then cyclize to novel 4-methoxycarbonyl-5-phenyl-2-substituted thiazoles. Hydrolysis of the intermediate products and the thiazoles obtained therefrom with simultaneous distillation of the carbonyl compound affords 2-hydrazino-4-methoxycarbonyl-5-phenylthiazole.
Synthesis and reactions of 2-amino-5-carbomethoxy-6-phenyl-6H-1,3,4-thiadiazine
作者:V. A. Mamedov、L. V. Krokhina、E. A. Berdnikov、Ya. A. Levin
DOI:10.1007/bf01164718
日期:1996.9
Reaction of methyl 3-phenyl-3-chloro-2-oxopropionate with thiosemicarbazones
作者:V. A. Mamedov、V. N. Valeeva、L. A. Antokhina、I. A. Nuretdinov
DOI:10.1007/bf00961310
日期:1991.6
The reaction of methyl 3-phenyl-3-chloro-2-oxopropionate with thiosemicarbazones proceeds via the intermediate formation of methyl [S-(1'-alkylideneiso-thiosemicarbazidyl)]-3-phenyl-2-oxopropionate hydrochlorides, which then cyclize to novel 4-methoxycarbonyl-5-phenyl-2-substituted thiazoles. Hydrolysis of the intermediate products and the thiazoles obtained therefrom with simultaneous distillation of the carbonyl compound affords 2-hydrazino-4-methoxycarbonyl-5-phenylthiazole.