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Synthesis and Antimicrobial Studies of 5-N-alkyl-1,3,4-oxadiazole-2-thiol Derivatives from Fatty Acids

机译:脂肪酸5-正烷基-1,3,4-二氧化唑-2-硫醇衍生物的合成和抗微生物研究

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摘要

The novel 5-N-alkyl-1,3,4-oxadiazole-2-thiol derivatives have been synthesized by esterification of fatty acid followed by reaction the ester with hydrazine hydrate. The acid hydrazide was converted to 1,3,4-oxadiazole by ring closure mechanism. The synthesized compounds have been characterized by physical (melting point and TLC) and spectral (IR, 'H NMR and mass) data. All the compounds were screened for their antimicrobial activity. The compounds 3F1 & 3F4 showed good inhibition activity against all four types of bacteria; while compound 3F2 & 3F3 shown moderate activity.
机译:通过脂肪酸的酯化,然后用肼水合物反应酯化的新型5-N-烷基-1,3,4-恶二唑-2-硫醇衍生物。 通过环闭合机制将酸酰肼转化为1,3,4-恶充唑。 合成化合物的特征在于物理(熔点和TLC)和光谱(IR,'H NMR和质量)数据。 将所有化合物筛选出抗微生物活性。 化合物3F1和3F4对所有四种细菌表现出良好的抑制活性; 虽然化合物3F2和3F3显示了适度的活性。

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