Indoles synthesized from amines via copper catalysis

Org Lett. 2013 Apr 5;15(7):1666-9. doi: 10.1021/ol400444g. Epub 2013 Mar 13.

Abstract

N-substituted indoles are synthesized from primary amines through a tandem reaction sequence. Initial condensation of the amine with an α-(o-haloaryl)ketone or aldehyde is followed by intramolecular aryl amination catalyzed by CuI. A variety of anilines and alkyl amines, including those with significant steric demands, are converted to indoles in high yields and with varying indole substitution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Amines / chemistry*
  • Aniline Compounds / chemistry
  • Catalysis
  • Combinatorial Chemistry Techniques
  • Copper / chemistry*
  • Indoles / chemical synthesis*
  • Indoles / chemistry
  • Molecular Structure

Substances

  • Amines
  • Aniline Compounds
  • Indoles
  • Copper
  • aniline