Novel Synthesis and Antimicrobial Activity of 7-Substituted Derivatives of 7-(methylthio)-5-oxo-2-phenyl-5H-[1,3,4]thiadiazolo[3,2-b]- pyrimidine-6-carbonitrile

Jaman A. Angulwar, G. Khansole, V. Bhosale
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引用次数: 1

Abstract

2-Amino-5-phenyl-1,3,4-thiadiazole on reaction with ethyl-2-cyano-3,3-bis(methylthio)acrylate in the presence of N,N′-dimethyl formamide and catalytic amount of anhydrous potassium carbonate afforded 7-(methylthio)-5-oxo-2-phenyl-5H-[1,3,4]thiadiazolo[3,2-b]pyrimidine- 6-carbonitrile under similar experimental condition, compounds 7-(methylthio)-5-oxo-2-phenyl-5H-[1,3,4]thiadiazolo[3,2-b]pyrimidine-6-carbonitrile on treatment independently with aryl amines/ heteryl amines/phenols containing active methylene group yielded correspon-ding 7-substituted derivatives. All these newly synthesized compounds were screened for antimicrobial activity.
7-(甲基硫)-5-氧-2-苯基- 5h -[1,3,4]噻二唑[3,2-b]-嘧啶-6-碳腈7-取代衍生物的新合成及其抑菌活性
在N,N ' -二甲基甲酰胺存在下,2-氨基-5-苯基-1,3,4-噻二唑与乙基-2-氰基-3,3-双(甲基硫代)丙烯酸酯反应,无水碳酸钾的催化量在类似的实验条件下得到7-(甲基硫代)-5-氧-2-苯基- 5h -[1,3,4]噻二唑[3,2-b]嘧啶- 6-碳腈。化合物7-(甲基硫)-5-氧-2-苯基- 5h -[1,3,4]噻二唑[3,2-b]嘧啶-6-碳腈分别与含有活性亚甲基的芳基胺/杂基胺/酚独立处理,得到相应的7-取代衍生物。对这些新合成的化合物进行了抗菌活性筛选。
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