Synthesis 2015; 47(01): 65-70
DOI: 10.1055/s-0034-1379201
paper
© Georg Thieme Verlag Stuttgart · New York

Highly Efficient, Environment-Friendly, One-Pot Synthesis of 2-Substituted 4-Formylimidazoles from 4-Acylaminoisoxazoles

Authors

  • Feng Gao*

    a   Department of Chinese Traditional Herbal, Agronomy College, Sichuan Agricultural University, No 211, Huimin Road, Wenjing Region, Chengdu 611130, P. R. of China   Fax: +86(28)86290870   eMail: gaofeng@sicau.edu.cn
  • Xin-Chuan Tian

    a   Department of Chinese Traditional Herbal, Agronomy College, Sichuan Agricultural University, No 211, Huimin Road, Wenjing Region, Chengdu 611130, P. R. of China   Fax: +86(28)86290870   eMail: gaofeng@sicau.edu.cn
  • Xiao-Xia Qu

    a   Department of Chinese Traditional Herbal, Agronomy College, Sichuan Agricultural University, No 211, Huimin Road, Wenjing Region, Chengdu 611130, P. R. of China   Fax: +86(28)86290870   eMail: gaofeng@sicau.edu.cn
  • Dan Wang

    a   Department of Chinese Traditional Herbal, Agronomy College, Sichuan Agricultural University, No 211, Huimin Road, Wenjing Region, Chengdu 611130, P. R. of China   Fax: +86(28)86290870   eMail: gaofeng@sicau.edu.cn
  • Dong Pu

    b   State Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, P. R. of China
Weitere Informationen

Publikationsverlauf

Received: 27. Juli 2014

Accepted after revision: 01. September 2014

Publikationsdatum:
30. September 2014 (online)


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Abstract

A highly efficient and environment-friendly one-pot synthesis of 2-substituted 4-formylimidazoles was accomplished. Raney nickel catalyzed hydrogenation of 4-acylaminoisoxazoles in ethanol, followed by sodium hydroxide promoted recyclization of the ring-opened intermediates, afforded the functionalized imidazoles.

Supporting Information