Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles

Molecules. 2020 Apr 14;25(8):1788. doi: 10.3390/molecules25081788.

Abstract

A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C-N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations revealed that the synthetic pathway involves a copper-based desulphurization/nucleophilic substitution and a subsequent domino intra and intermolecular C-N cross-coupling reactions. Some of the issues typically encountered during the synthesis of 2-arylaminobezimidazoles, including the use of expensive catalytic systems and the low reactivity of bromo precursors, were addressed using this newly developed copper-catalyzed method. The reaction procedure is simple, generally with excellent substrate tolerance, and provides good to high yields of the desired products.

Keywords: 2-aminoaryl benzimidazole; copper catalyst; desulfurization; domino C–Ncross-coupling; homogeneous catalysis.

MeSH terms

  • Benzimidazoles / chemical synthesis*
  • Benzimidazoles / chemistry
  • Benzimidazoles / pharmacology
  • Catalysis
  • Chemistry Techniques, Synthetic*
  • Copper / chemistry*
  • Molecular Structure

Substances

  • Benzimidazoles
  • Copper