Breaking Bond

  • Author: Asian Journal of Organic Chemistry
  • Published Date: 08 November 2013
  • Source / Publisher: Asian Journal of Organic Chemistry/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
thumbnail image: Breaking Bond

The 2-aminothiazole structural motif, which is prevalent in biologically active compounds, contains two C–H bonds and one nonaromatic C–N bond. Previously, the direct arylation of C–H bonds at the C5-position of thiazoles has been reported. However, the direct arylation of the C4–H bond or the C–N bond of 2-aminothiazoles has not yet been reported.


Junichiro Yamaguchi, Kenichiro Itami, and co-workers, Nagoya University, Japan, have successfully developed a palladium catalyst that can react with the C–H bond at the C4-position of 2-aminothiazoles. This enables a Pd-catalyzed coupling with various aryl groups by using aryl boronic acids. The team also discovered a C–N cleavage/arylation of 2-amino(benzo)thiazoles in the presence of a palladium catalyst. This transformation was achieved when the ligand was simply changed from 1,10-phenanthroline to 2,2’-bipyridine.

Further applications to medicinal chemistry and chemical biology by preparing various arylated thiazoles are the current focus of the group.


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