Synthesis 2014; 46(23): 3256-3262
DOI: 10.1055/s-0034-1378635
paper
© Georg Thieme Verlag Stuttgart · New York

Thioacetamide as an Ammonium Source for Multicomponent Synthesis of Pyridines from Aldehydes and Electron-Deficient Enamines or Alkynes

Authors

  • Jie-Ping Wan*

    a   Key Laboratory of Functional Small Organic Molecule, Ministry of Education, and College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. of China
  • Youyi Zhou

    a   Key Laboratory of Functional Small Organic Molecule, Ministry of Education, and College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. of China
  • Kezhi Jiang

    b   Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou 310012, P. R. of China   Fax: +86(791)88120380   Email: wanjieping@jxnu.edu.cn
  • Hongyan Ye

    a   Key Laboratory of Functional Small Organic Molecule, Ministry of Education, and College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. of China
Further Information

Publication History

Received: 13 June 2014

Accepted after revision: 17 July 2014

Publication Date:
21 August 2014 (online)


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Abstract

A generally applicable multicomponent method has been established for the synthesis of pyridines. In the reactions, thioacetamide is used as a cheap and efficient ammonium source in a multicomponent reaction with aldehydes and electron-deficient enamines or alkynes to give 3,4,5-trisubstituted pyridines in moderate to good yields and with a high product diversity.

Supporting Information