Issue 54, 2016

A metal-free synthesis of 2-aminobenzothiazoles through aminyl radical addition to aryl isothiocyanates

Abstract

A convenient synthesis of 2-aminobenzothiazoles, starting from aryl isothiocyanates and formamides under metal-free conditions, is described. Various secondary and tertiary amine- and even α-amino acid-derived formamides can be used as amino sources in this process. Mechanistic studies suggest that the reaction is initiated by decarbonylative aminyl radical formation in the presence of n-Bu4NI and TBHP, followed by aminyl radical addition to isothiocyanates and cyclization via sulfur centred radical intermediates.

Graphical abstract: A metal-free synthesis of 2-aminobenzothiazoles through aminyl radical addition to aryl isothiocyanates

Supplementary files

Article information

Article type
Communication
Submitted
25 May 2016
Accepted
07 Jun 2016
First published
08 Jun 2016

Chem. Commun., 2016,52, 8444-8447

A metal-free synthesis of 2-aminobenzothiazoles through aminyl radical addition to aryl isothiocyanates

Y. He, J. Li, S. Luo, J. Huang and Q. Zhu, Chem. Commun., 2016, 52, 8444 DOI: 10.1039/C6CC04394A

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