Two-step iron(0)-mediated N-demethylation of N-methyl alkaloids

J Org Chem. 2010 Jul 16;75(14):4806-11. doi: 10.1021/jo1008492.

Abstract

A mild and simple two-step Fe(0)-mediated N-demethylation of a number of tertiary N-methyl alkaloids is described. The tertiary N-methylamine is first oxidized to the corresponding N-oxide, which is isolated as the hydrochloride salt. Subsequent treatment of the N-oxide hydrochloride with iron powder readily provides the N-demethylated amine. Representative substrates include a number of opiate and tropane alkaloids. Key intermediates in the synthesis of semisynthetic 14-hydroxy pharmaceutical opiates such as oxycodone and oxymorphone are also readily N-demethylated using this method.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemistry*
  • Iron / chemistry*
  • Methylamines / chemistry*
  • Methylation
  • Molecular Structure
  • Nitrogen Oxides / chemistry*
  • Oxidation-Reduction

Substances

  • Alkaloids
  • Methylamines
  • Nitrogen Oxides
  • Iron