Electro-Oxidative Three-Component Synthesis of 3,5-Disubstituted-1,2,4-Thiadiazoles from Amines, Amidines, and CS2

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC
Peng-Fei Huang, Ying Peng, Jia-Le Fu, Bo Li, Quan Zhou, Yu Liu
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引用次数: 0

Abstract

1,2,4-Thiadiazoles, a significant class of heterocyclic compounds, are widely found in biologically active molecules. Herein, we report a green electrochemical three-component reaction of amines, amidines, and CS2 for the effective synthesis of 3,5-disubstituted-1,2,4-thiadiazoles under metal- and oxidant-free conditions. Both aliphatic and aryl amines are well-tolerated at room temperature in a simple undivided cell. A series of 1,2,4-thiadiazoles are prepared with excellent functional groups.

Abstract Image

1,2,4-噻二唑是一类重要的杂环化合物,广泛存在于生物活性分子中。在此,我们报告了一种胺、脒和 CS2 的绿色电化学三组分反应,可在无金属和氧化剂条件下有效合成 3,5 二甲基二取代的 1,2,4 噻二唑。在室温下,脂肪族胺和芳基胺都能在简单的不分裂电池中得到很好的耐受性。制备出一系列具有优良官能团的 1,2,4-噻二唑。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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