微波辅助合成1,3,4-恶二唑衍生物及其抑菌活性评价

Deepak Swarnkar, R. Ameta, Ritu Vyas
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引用次数: 7

摘要

以二苯乙酸肼为原料,在微波照射下,在不同的反应条件下合成了一系列取代的1,3,4-恶二唑衍生物(3a-f)和(6a-f)。通过元素分析、红外光谱和核磁共振氢谱确定了合成化合物的结构。与氨苄西林和灰黄霉素作为标准药物相比,对这些靶向化合物的抗菌和抗真菌活性进行了测试。化合物3a、3e、3f、6c、6d、6e和6d抑菌活性最强,化合物3b、3c、3d、3e、6a、6d和6e抑菌活性最强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microwave-Assisted Synthesis of Some 1,3,4-Oxadiazole Derivatives and Evaluation of Their Antibacterial and Antifungal Activity
A series of substituted 1,3,4-oxadiazole derivatives (3a–f) and (6a–f) have been synthesized from diphenylacetic acid hydrazide under microwave irradiation in various reaction conditions. The structures of the synthesized compounds were assigned on the basis of elemental analysis, IR, and 1H NMR. These targeted compounds have been tested for their antibacterial and antifungal activities compared to ampicillin and griseofulvin as standard drug. Compounds 3a, 3e, 3f, 6c, 6d, 6e, and 6d exhibited the maximum antibacterial activities while 3b, 3c, 3d, 3e, 6a, 6d, and 6e exhibited the maximum antifungal activities.
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