Synthesis 2016; 48(05): 687-696
DOI: 10.1055/s-0035-1560395
paper
© Georg Thieme Verlag Stuttgart · New York

Metal-Free Oxidative Deamination Cross-Coupling of Imidazo­heterocycles with 2-Aminobenzothiazoles

Authors

  • Xiao-Ming Ji

    a   Department of Applied Chemistry, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, P. R. of China
    b   College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, P. R. of China   eMail: rytang@scau.edu.cn
  • Li Xu

    a   Department of Applied Chemistry, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, P. R. of China
  • Yun Yan

    a   Department of Applied Chemistry, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, P. R. of China
  • Fan Chen

    b   College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, P. R. of China   eMail: rytang@scau.edu.cn
  • Ri-Yuan Tang*

    a   Department of Applied Chemistry, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, P. R. of China
Weitere Informationen

Publikationsverlauf

Received: 22. Oktober 2015

Accepted after revision: 11. Dezember 2015

Publikationsdatum:
05. Januar 2016 (online)


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Abstract

A metal-free oxidative deamination–cross-coupling of imidazoheterocycles with 2-aminobenzothiazoles in the presence of tert-butyl nitrite is reported for the first time. This simple protocol tolerates a wide range of functional groups to afford various benzothiazole–imidazoheterocycles in moderate to excellent yields, with the release of nitrogen and water as benign byproducts.

Supporting Information