Synthesis 2016; 48(03): 351-356
DOI: 10.1055/s-0035-1560375
paper
© Georg Thieme Verlag Stuttgart · New York

Zinc Iodide Catalyzed Synthesis of 3-Aminoimidazo[1,2-a]pyridines from 2-Aminopyridines and α-Amino Carbonyl Compounds

Authors

  • Xu Han

    a   State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, Lanzhou, Gansu, 730000, P. R. of China   Email: hgs@lzu.edu.cn
  • Chaowei Ma

    a   State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, Lanzhou, Gansu, 730000, P. R. of China   Email: hgs@lzu.edu.cn
    b   Department of Chemistry and Environmental Engineering, Xinjiang Institute of Engineering, Urumqi, Xinjiang, 830091, P. R. of China
  • Zhaoyang Wu

    a   State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, Lanzhou, Gansu, 730000, P. R. of China   Email: hgs@lzu.edu.cn
  • Guosheng Huang*

    a   State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, Lanzhou, Gansu, 730000, P. R. of China   Email: hgs@lzu.edu.cn
Further Information

Publication History

Received: 01 September 2015

Accepted after revision: 23 October 2015

Publication Date:
26 November 2015 (online)


Graphical Abstract

Abstract

A concise approach to 3-aminoimidazo[1,2-a]pyridines is developed via the zinc iodide catalyzed reaction of 2-aminopyridines and α-amino carbonyl compounds in the presence of oxygen. This novel and user-friendly protocol employing diverse and easily available substrates affords the desired products in good to excellent yields.

Supporting Information