4.6 Article

Chemoselective N-arylation of aminobenzamides via copper catalysed Chan-Evans-Lam reactions

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 15, Issue 44, Pages 9288-9292

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob02491f

Keywords

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Funding

  1. National Natural Science Foundation of China [21603150]
  2. Shihezi University [RCZX201543, CXRC201602]
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT_15R46]
  4. Yangtze River Scholar Research Project of Shihezi University [CJXZ201601]

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Chemoselective N-arylation of unprotected aminobenzamides was achieved via Cu-catalysed Chan-Evans-Lam cross-coupling with aryl boronic acids for the first time. Simple copper catalysts enable the selective arylation of amino groups in ortho/meta/para-amino-benzamides under open-flask conditions. The reactions were scalable and compatible with a wide range of functional groups.

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