Visible-Light-Enabled Direct Decarboxylative N-Alkylation

Angew Chem Int Ed Engl. 2020 May 11;59(20):7921-7927. doi: 10.1002/anie.201916710. Epub 2020 Mar 17.

Abstract

The development of efficient and selective C-N bond-forming reactions from abundant feedstock chemicals remains a central theme in organic chemistry owing to the key roles of amines in synthesis, drug discovery, and materials science. Herein, we present a dual catalytic system for the N-alkylation of diverse aromatic carbocyclic and heterocyclic amines directly with carboxylic acids, by-passing their preactivation as redox-active esters. The reaction, which is enabled by visible-light-driven, acridine-catalyzed decarboxylation, provides access to N-alkylated secondary and tertiary anilines and N-heterocycles. Additional examples, including double alkylation, the installation of metabolically robust deuterated methyl groups, and tandem ring formation, further demonstrate the potential of the direct decarboxylative alkylation (DDA) reaction.

Keywords: amination; carboxylic acids; copper catalysis; photocatalysis; visible light.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acridines / chemistry
  • Alkylation
  • Amines / chemistry*
  • Aniline Compounds / chemistry
  • Catalysis
  • Heterocyclic Compounds / chemistry*
  • Oxidation-Reduction

Substances

  • Acridines
  • Amines
  • Aniline Compounds
  • Heterocyclic Compounds
  • aniline