一些新型苯并咪唑-氧噻唑烷衍生物抗结核药物的合成:常规与微波辅助方法

S. Dubey, Sakshi Bhardwaj
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引用次数: 0

摘要

设计合成了N-(4-烷基-4-氧-1,3-噻唑烷-3-基)-2-(5-硝基- 1h -苯并咪唑-1-基)乙酰胺衍生物。采用常规方法和微波辅助合成方法合成了12种新型衍生物。本文报道了两种方法在时间、溶剂使用和收率方面的比较。结果表明,绿色化学合成方法在时间和收率方面是更有效的合成方法。对合成的化合物进行抗结核阿拉马尔蓝试验。其中一些已经显示出有希望的活动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of some Novel Benzimidazole-Oxothiazolidine Derivatives as Anti-Tubercular agents: Conventional Vs Microwave Assisted Approach
N-(4-alkyl-4-oxo-1,3-thiazolidin-3-yl)-2-(5-nitro-1H-benzimidazole-1-yl)acetamide derivatives were designed and synthesis. Twelve novel derivatives were synthesized using conventional approach and Microwave-assisted synthesis. Herein we report the comparisonbetween the two approaches in terms of time, solvents used and yield. As evident from the results obtained the green chemistry approach for the synthesis is the more efficient way of synthesis in terms of time and yield. The synthesized compounds were subjected to anti tubercular Alamar Blue Assay. Some of them have shown promising activity.
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