4.6 Article

Potassium carbonate-mediated tandem C-S and C-N coupling reaction for the synthesis of phenothiazines under transition-metal-free and ligand-free conditions

Journal

RSC ADVANCES
Volume 6, Issue 29, Pages 24257-24260

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra01295g

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Funding

  1. Priority Academic Program for the Development of Jiangsu Higher Education Institutions
  2. Project of Scientific and Technologic Infrastructure of Suzhou [SZS201207]
  3. National Natural Science Foundation of China [21072143]

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An efficient potassium carbonate-mediated tandem C-S and C-N coupling reaction between N-(2-iodophenyl) acetamides and 2-halo-benzenethiols has been developed. This protocol affords a simple and efficient approach for the construction of phenothiazine derivatives without the need for addition of transition-metal catalyst or ligand for the first time. Furthermore, the reaction can be easily performed on a large scale.

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