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Synthesis and biological activities of 3,6-disubstituted-1,2,4-triazolo-1,3,4- thiadiazole derivatives

机译:3,6-二取代的-1,2,4-三唑-1,3,4-噻二唑衍生物的合成和生物活性

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摘要

Twelve novel triazolothiadiazole derivatives were synthesized from 4-amino-5-substituted-4H-1,2,4-triazole-3-thiols with various aromatic carboxylic acids by cyclization in the presence of phosphorous oxychloride. All the newly synthesized compounds were characterized by FTIR, 1H NMR, mass spectroscopy and elemental analysis. The antimicrobial activities of the title compounds were examined by disc diffusion method against Escherichia coli, Staphylococcus aureus, Pyricularia oryzae and Rhizoctnia solani. The bioassay indicated all synthesized triazolothiadiazole derivatives possessed moderate to good antibacterial and antifungal activities against the tested organisms. Especially, compounds 2e and 2k exhibited excellent antibacterial and antifungal activities among these triazolothiadiazole derivatives.
机译:通过环化在氯氧化磷酸氯化物存在下通过环化由4-氨基-5-取代-4H-1,2,4-三唑-3- 1,2,4-三唑-3-硫醇合成12个新的三唑噻唑衍生物。所有新合成的化合物的特征在于FTIR,1H NMR,质谱和元素分析。通过对大肠杆菌,金黄色葡萄球菌,浮尾草柚子和rhizoctnia solani检查标题化合物的抗微生物活性。生物测定表明所有合成的三唑噻唑衍生物具有中度至良好的抗菌和抗真菌活性的对抗测试的生物。特别是,化合物2E和2K在这些三唑噻唑衍生物中表现出优异的抗菌和抗真菌活性。

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