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Design, Synthesis, and Antimicrobial Activity of Novel Fluorine-Containing Imidazolones
Russian Journal of Organic Chemistry ( IF 0.8 ) Pub Date : 2021-07-18 , DOI: 10.1134/s1070428021060142
N. C. Desai 1 , H. K. Mehta 1 , K. R. Wadekar 2 , U. P. Pandit 3
Affiliation  

Abstract

A simple synthetic protocol have been developed for the preparation of novel N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydro-1H-imidazol-1-yl)-N′-phenylthiourea derivatives by the reaction of 4-benzylidene-2-phenyl-4,5-dihydro-1,3-oxazol-5-ones with N-(3-chloro-4-fluorophenyl)- and N-[3-(trifluoromethyl)phenyl)hydrazinecarbothioamides. The synthesized imidazolones have been characterized by using different spectroscopic techniques and evaluated for their antimicrobial activity against some bacterial and fungal strains. Imidazolone derivatives containing 2-nitrobenzylidene and 4-methoxybenzylidene substituents were found to be potent against fungal strains Candida albicans and Aspergillus clavatus..



中文翻译:

新型含氟咪唑酮的设计、合成和抗菌活性

摘要

一个简单的合成方案已被开发用于新颖的制备ñ - (4-苯亚甲基-5-氧代-2-苯基-4,5-二氢-1- ħ -咪唑-1-基)ñ由'-phenylthiourea衍生物4-benzylidene-2-phenyl-4,5-dihydro-1,3-oxazol-5-ones 与N- (3-chloro-4-fluorophenyl)- 和N- [3-(trifluoromethyl)phenyl)hydrazinecarbothioamides 的反应. 合成的咪唑酮已通过使用不同的光谱技术进行表征,并评估了它们对某些细菌和真菌菌株的抗菌活性。发现含有 2-硝基亚苄基和 4-甲氧基亚苄基取代基的咪唑酮衍生物对真菌菌株白色念珠菌棒状曲霉..

更新日期:2021-07-19
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