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Conventional and microwave assisted synthesis of new benzotriazole derivatives and their antimicrobial potential

机译:常规和微波辅助合成新的苯并三唑衍生物及其抗菌潜力

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摘要

The cyclization reaction of 5-[2-(l,2,3-benzotriazole)-l-yl-methyl]-substituted arylidene-hydrazino-1,3',4'-thiodiazoles (starting material) using thioglycolic acid has afforded the corresponding 5-[2-(l,2,3-benzotriazole)-l-yl-methyl]-2' [2"-(substituted phenyl)-4"-oxo-l",3"-thiazolidine]-1,3',4'-thiadia-zoles, la-k which is further condensed with various aromatic aldehydes in presence of suitable base to yield 5-[2-(l,2,3-benzotriazole)-l-yl-methyl]-2'-[5"-(benzylidene)-2"-substituted phenyl-4"-oxo-l ",3"-thiazolidine]-l ',3',4'-thiadiazoles, 2a-k. These compounds have been synthesized by conventional as well as microwave assisted methods and the structures are established on the basis of spectral and analytical data. All the synthesized compounds have been screened for their antimicrobial activities and are found to possess significant antibacterial activity against Bacillus subtillus, Escherichia coli, Klebsiella pneumoniae and Staphylococcus aureus and antifungal activity against Aspergillus niger, Aspergillus flavus, Fusarium oxyporum and Trichoderma viride.
机译:使用巯基乙酸对5- [2-(1,2,3-苯并三唑)-1-基-甲基]-取代的亚芳基-肼基-1,3',4'-硫代二唑(起始原料)进行环化反应相应的5- [2-(1,2,3-苯并三唑)-1-基-甲基] -2'[2“-(取代的苯基)-4”-氧代-1“,3”-噻唑烷] -1, 3',4'-噻二唑-la-k,其在合适的碱存在下进一步与各种芳族醛缩合,生成5- [2-(1,2,3-苯并三唑)-1-基-甲基]- 2'-[5“-(亚苄基)-2”-取代的苯基-4“-氧代-1”,3“-噻唑烷] -1',3',4'-噻二唑,2a-k。通过常规和微波辅助合成方法合成,并通过光谱和分析数据确定结构,筛选出所有合成化合物的抗菌活性,发现它们对枯草芽孢杆菌,大肠杆菌,克雷伯菌具有显着的抗菌活性。肺炎和金黄色葡萄球菌及其抗真菌活性黑曲霉,黄曲霉,尖孢镰刀菌和绿色木霉。

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