4.4 Article

A convenient synthesis of 2-acyl benzothiazoles/thiazoles from benzothiazole/thiazole and N,N′-carbonyldiimidazole activated carboxylic acids

期刊

TETRAHEDRON LETTERS
卷 60, 期 25, 页码 1667-1670

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2019.05.043

关键词

2-Acyl thiazoles; 2-Acyl benzothiazoles; Grignard reagents; Acylation

资金

  1. Natural Science Foundation of Jiangsu Province [BK20171184]
  2. Jiangsu Planned Projects for Postdoctoral Research Funds [1701132C]
  3. Technology Plan Projects of Xuzhou [KC17091]
  4. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX18-2203]

向作者/读者索取更多资源

A convenient and efficient strategy for the synthesis of 2-acyl benzothiazoles/thiazoles has been developed. The treatment of benzothiazole/thiazole with allylic Grignard reagents readily generates the corresponding 2-Grignard reagents, which is followed by a reaction with N,N'-carbonyldiimidazole activated carboxylic acids to afford various 2-acyl benzothiazoles/thiazoles products. The synthetic method is applicable to a wide array of carboxylic acids and allows easy access to 2-acyl benzothiazoles/thiazoles with considerable yields under mild reaction conditions. (C) 2019 Elsevier Ltd. All rights reserved.

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