微波辐射下Suzuki偶联反应高效合成5-(4-(取代[1,1 ' -联苯]-4-酰基甲氧基)苄基)噻唑烷-2,4-二酮及其生物筛选

Mitesh B. Vekariya, Tejal D. Bhatt, H. Joshi
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摘要

本文研究了一种高效、绿色的微波辐射合成5-(4-(取代[1,1 ' -联苯]-4-酰基甲氧基)苄基)-噻唑烷-2,4-二酮的方法。本文报道了5-(4-((4-溴苄基)氧苄基)噻唑烷-2,4-二酮,取代芳基硼酸和K2CO3在甲苯:水:乙醇溶剂存在下,在常规加热方法和微波辐照方法下的一锅反应。所有化合物均通过ft - ir、1H NMR、13C NMR和质谱分析进行了表征。抗菌评价研究显示对使用过的微生物有中等活性。
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Efficient Synthesis of 5-(4-(Substituted [1,1′-Biphenyl]-4-yl-methoxy)benzyl)thiazolidine- 2,4-diones under Microwave Irradiation using Suzuki Coupling Reaction and their Biological Screening
In present study, an efficient and greener protocol is developed for the synthesis of 5-(4-(substituted [1,1′-biphenyl]-4-yl-methoxy)benzyl)-thiazolidine-2,4-diones by using microwave irradiations. Here, a one-pot reaction between 5-(4-((4-bromobenzyl)oxy)benzyl)thiazolidine-2,4-dione, substituted aryl boronic acid and K2CO3 in the presence of toluene:water:ethanol solvents under conventional heating methods and microwave irradiation methods is reported. All the final compounds were characterized by FT-IR, 1H NMR, 13C NMR and mass spectroscopic analysis. The antimicrobial evaluation studies show moderate activities against used microbes.
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