Efficient pd-catalyzed amination of heteroaryl halides

Org Lett. 2005 Sep 1;7(18):3965-8. doi: 10.1021/ol0514754.

Abstract

The Pd-catalyzed amination of a variety of heteroaryl halides has been accomplished by utilizing bulky electron-rich biaryl phosphine ligands. In particular, we report the first couplings of amines with chloro- and bromoindoles bearing a free NH, as well as the first Pd-catalyzed aminations of a 5-halopyrimidine. [reaction: see text]

Publication types

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

MeSH terms

  • Amination
  • Catalysis
  • Combinatorial Chemistry Techniques*
  • Hydrocarbons, Halogenated / chemistry*
  • Molecular Structure
  • Palladium / chemistry*
  • Phosphines / chemistry
  • Pyrimidines / chemistry

Substances

  • Hydrocarbons, Halogenated
  • Phosphines
  • Pyrimidines
  • Palladium