Reaction of N-aryl-3-oxobutanethioamides with 2-amino-1,3-thiazole and 2-amino-1,3-benzothiazole

被引:0
作者
V. N. Britsun
A. N. Borisevich
A. N. Esipenko
M. O. Lozinskii
机构
[1] National Academy of Sciences of Ukraine,Institute of Organic Chemistry
来源
Russian Journal of Organic Chemistry | 2007年 / 43卷
关键词
Aniline; Thiazole; Nitromethane; Benzothiazole; Ethyl Acetoacetate;
D O I
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摘要
N-Aryl-3-oxobutanethioamides react with 2-amino-1,3-thiazole (2-amino-1,3-benzothiazole) in acetic acid to give mixtures of 7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidine-5-thione (2-methyl-4H-pyrimido-[2,1-b][1,3]benzothiazole-4-thione) and 5-arylimino-7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidines (4-arylimino-2-methyl-4H-pyrimido[2,1-b][1,3]benzothiazoles), whose ratio depends on the nature of the aryl substituent in the initial butanethioamide.
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页码:103 / 107
页数:4
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