Development of a regioselective N-methylation of (benz)imidazoles providing the more sterically hindered isomer

J Org Chem. 2013 Dec 6;78(23):12220-3. doi: 10.1021/jo401978b. Epub 2013 Nov 12.

Abstract

An efficient and highly regioselective N-methylation of (NH)-(benz)imidazoles furnishing the sterically more hindered, less stable, and usually minor regioisomer has been developed. The methodology involves very mild reaction conditions and tolerates a wide range of functional groups.

MeSH terms

  • Benzimidazoles / chemical synthesis*
  • Benzimidazoles / chemistry
  • Methylation
  • Molecular Structure
  • Stereoisomerism

Substances

  • Benzimidazoles
  • benzimidazole