Volume 19, Issue 2 pp. 149-153
Research Article
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Efficient synthesis of 5H-thiazolo[3,2-a]pyrimidines from reactions of 3,4-dihydropyrimidine-thiones with α-bromoacetone in aqueous media

Zheng-Jun Quan

Zheng-Jun Quan

Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China

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Zhang Zhang

Zhang Zhang

Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China

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Jun-Ke Wang

Jun-Ke Wang

Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China

Key Laboratory of Resources and Environment, Chemistry of West China, Department of Chemistry, Hexi University, Zhangye 734000, People's Republic of China

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Xi-Cun Wang

Corresponding Author

Xi-Cun Wang

Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China

Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of ChinaSearch for more papers by this author
Ya-Juan Liu

Ya-Juan Liu

Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China

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Peng-Yan Ji

Peng-Yan Ji

Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China

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First published: 04 March 2008
Citations: 19

Abstract

An efficient and convenient method for thiazolo[3,2-a]pyrimidines from cyclization reaction of dihydropyrimidine-thiones with α-bromoacetone in aqueous media is described. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:149–153, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20386

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