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Synthesis, Characterization and Antifungal Activity of Some New 5-Substituted 1,3,4-oxadiazole-2-thiols

机译:一些新的5-取代的1,3,4-恶二唑-2-硫醇的合成,表征和抗真菌活性

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摘要

A series of 5-substituted 1,3,4-oxadiazol-2-thiols (3a-i) was synthesized by refluxing variably substituted organic acids (Ra-i) with methanol to the corresponding esters (1a-i). These esters were then converted to hydrazides (2a-i) by reaction with hydrazine hydrate in the presence of absolute ethanol which was followed by reaction with carbon disulfide and potassium hydroxide. Structure of the synthesized compounds was established by physicochemical and spectral data analysis. Synthesized compounds were subjected to antifungal activity. Antifungal activity was performed against Aspergillus flavus, Mucor species, Aspergillus niger and Aspergillus fumigates, with test compounds at a concentration of 200 μg/mL. Terbinafine was used as the standard drug,
机译:通过将可变取代的有机酸(Ra-i)与甲醇回流至相应的酯(1a-i),合成了一系列5取代的1,3,4-恶二唑-2-硫醇(3a-i)。然后通过在无水乙醇存在下与水合肼反应,然后与二硫化碳和氢氧化钾反应,将这些酯转化为酰肼(2a-i)。通过理化和光谱数据分析确定了合成化合物的结构。合成的化合物具有抗真菌活性。用浓度为200μg/ mL的测试化合物对黄曲霉,Mucor菌种,黑曲霉和熏蒸曲霉进行了抗真菌活性。特比萘芬用作标准药物,

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