嘧啶[4,5-d][1,3,4]噻二唑[3,2-a]嘧啶二酮的合成及抗菌活性研究

G. Khansole, S. S. Choudhare, Swapnil S.Nawhate, V. Bhosale
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引用次数: 1

摘要

以1-丁基-3-甲基咪唑氯[BMIM]Cl为绿色催化剂,以巴比妥酸、取代芳香醛和2-氨基5-(4-氯苯基)-1,3,4-噻二唑为原料,在乙醇-水中进行一锅三组分缩合反应,合成了一种简单、高效、绿色的嘧啶[4,5-d][1,3,4]噻二唑[3,2- A]嘧啶二酮衍生物。对新合成的化合物进行了光谱分析,并对其抗菌活性进行了筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF PYRIMIDO [4,5-d] [1,3,4] THIADIAZOLO[3,2-a]PYRIMIDINEDIONE
A simple, most efficient and green procedure has been developed for the synthesis of pyrimido [4,5-d] [1,3,4] thiadiazolo [3,2-a] pyrimidinedione derivatives from one-pot three component condensation reactions of barbituric acid, substituted aromatic aldehydes, and 2-amino 5-(4-chlorophenyl)-1,3,4-thiadiazole using 1-Butyl-3-methyl Imidazolium Chloride [BMIM]Cl as a green catalyst in ethanol-water. The newly synthesized compounds evaluated by their spectral techniques and screened for their Antimicrobial activity.
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