Synthesis and Antioxidant Activity of 2-Amino-5-methylthiazol Derivatives Containing 1,3,4-Oxadiazole-2-thiol Moiety.

ISRN Organic Chemistry Pub Date : 2013-08-19 eCollection Date: 2013-01-01 DOI:10.1155/2013/620718
Kikkeri N Mohana, Chikkur B Pradeep Kumar
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引用次数: 0

Abstract

A series of new 5-(2-amino-5-methylthiazol-4-yl)-1,3,4-oxadiazole-2-thiol derivatives 6(a-j) were designed and synthesized with various substituted aldehydes. The chemical structures were confirmed by elemental analyses, FT-IR, (1)H NMR, and mass spectral studies. The antioxidant activity of the synthesized compounds was evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH), hydroxyl, nitric oxide, and superoxide radical scavenging assay methods. Compounds 6a, 6e, and 6c showed significant radical scavenging potential due to the presence of electron donating substituent on substituted aldehydes.

Abstract Image

Abstract Image

含 1,3,4-恶二唑-2-硫醇分子的 2-氨基-5-甲基噻唑衍生物的合成与抗氧化活性。
本研究设计并合成了一系列新的 5-(2-氨基-5-甲基噻唑-4-基)-1,3,4-恶二唑-2-硫醇衍生物 6(a-j),并用各种取代的醛进行了合成。通过元素分析、傅立叶变换红外光谱、(1)H NMR 和质谱研究确认了这些衍生物的化学结构。合成化合物的抗氧化活性通过 2,2-二苯基-1-苦基肼(DPPH)、羟基、一氧化氮和超氧自由基清除测定法进行了评估。化合物 6a、6e 和 6c 显示出显著的自由基清除潜力,这是因为取代醛上存在电子捐赠取代基。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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