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Synthesis and biological evaluation of some 1,3,4-oxadiazole derivatives.

机译:某些1,3,4-恶二唑衍生物的合成及生物学评价。

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摘要

The acid hydrazides (2) derived from ibuprofen and 4-methylthiophenyl acetic acids have been subjected to cyclization with carbon disulphide under basic conditions to yield 1,3,4-oxadiazol-2-thiones (3) which on aminomethylation with formaldehyde and secondary amines afforded a series of Mannich bases (4 and 5). Purity of the compounds has been confirmed by TLC. Structures of these compounds were established on the basis of elemental analyses and spectral studies. The newly synthesized compounds were evaluated for their anti-inflammatory, analgesic, ulcerogenic and antimicrobial activities.
机译:衍生自布洛芬和4-甲基硫代苯基乙酸的酰肼(2)在碱性条件下与二硫化碳进行环化反应,生成1,3,4-恶二唑-2-硫酮(3),该甲醛在与甲醛和仲胺进行氨基甲基化后提供了一系列的曼尼希基地(4和5)。化合物的纯度已通过TLC证实。这些化合物的结构是在元素分析和光谱研究的基础上确定的。评价了新合成的化合物的抗炎,镇痛,促溃疡和抗菌活性。

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