N-(苯并噻唑-2-基)-4-((5-氯苯并恶唑-2-基)氨基)丁酰胺

Molbank Pub Date : 2024-07-23 DOI:10.3390/m1854
Hugo Pilotzi-Xahuentitla, Gabriela Canche-Naal, Rolffy Ortiz-Andrade, Gabriel Navarrete-Vázquez, Emanuel Hernández-Núñez
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引用次数: 0

摘要

苯并唑(如苯并恶唑和苯并噻唑)是具有重要生物和药理活性的化合物,也是重要的合成中间体。本报告介绍了 5-氯-2-氨基苯并恶唑和 2-氨基苯并噻唑通过 4-氯丁酰氯连接而得到的丁酰胺的合成过程。利用可获得的起始材料和两步反应的方法,我们获得了相应的化合物 N-(苯并噻唑-2-基)-4-((5-氯苯并恶唑-2-基)氨基丁酰胺,总收率为 76%。此外,我们还对该化合物与 3-TOP 蛋白进行了对接研究,以探索其作为抗糖尿病药物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
N-(Benzothiazol-2-yl)-4-((5-chlorobenzoxazol-2-yl)amino)butanamide
Benzazoles, such as benzoxazoles and benzothiazoles, are compounds with important biological and pharmacological activities and important intermediaries in synthesis. This report presents the synthesis of a butanamide derived from linking 5-chloro-2-aminobenzoxazole and 2-aminobenzothiazole via 4-chlorobutanoyl chloride. The corresponding compound N-(benzothiazol-2-yl)-4-((5-chlorobenzoxazol-2-yl)aminobutanamide was obtained at a 76% global yield using accessible starting materials and a methodology in two reaction steps. Furthermore, we conducted docking studies of this compound on 3-TOP protein to explore its potential as an antidiabetic agent.
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