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芳基叠氮化物合成子:一种用于合成 2-氨基噻唑、1,3-噻唑和 1,3-硒唑支架的多样化方法。

Aryliodoazide Synthons: A Different Approach for Diversified Synthesis of 2-Aminothiazole, 1,3-Thiazole, and 1,3-Selenazole Scaffolds.

机构信息

Department of Chemistry , University of Isfahan , Isfahan 81746-73441 , Iran.

Department of Chemistry and Biochemistry , University of Arkansas , Fayetteville , Arkansas 72701 , United States.

出版信息

ACS Comb Sci. 2019 Jul 8;21(7):516-521. doi: 10.1021/acscombsci.9b00045. Epub 2019 Jun 18.

Abstract

Several straightforward and practical processes have been established for the construction of 2-aminothiazoles, 1,3-thiazoles and 1,3-selenazoles from aryliodoazides. These strategies successfully proceed with a wide spectrum of substituted thioamides and its derivatives producing the resulting five-membered heterocycles obtained in satisfactory yields. The unique features of these protocols are operational simplicity and highly functional group tolerance, which make them convenient and practical routes for the preparation of various libraries of 2-aminothiazoles, 1,3-thiazoles, and 1,3-selenazoles.

摘要

已经建立了几种从芳基碘叠氮化物构建 2-氨基噻唑、1,3-噻唑和 1,3-硒唑的简单实用的方法。这些策略成功地应用于广泛取代的硫代酰胺及其衍生物,以令人满意的产率得到所需的五元杂环。这些方案的独特之处在于操作简单和高度的官能团容忍性,这使得它们成为制备各种 2-氨基噻唑、1,3-噻唑和 1,3-硒唑文库的方便实用的途径。

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