Multisite solid catalyst for cascade reactions: the direct synthesis of benzodiazepines from nitro compounds

Chemistry. 2009 Sep 7;15(35):8834-41. doi: 10.1002/chem.200900492.

Abstract

Substituted 1,5-benzodiazepines are selectively synthesized in one pot from substituted nitroaromatics and ketones. The reaction is performed in the presence of hydrogen and in the absence of solvent by using a bifunctional solid catalyst with a chemoselective hydrogenation functional group capable of reducing the nitro group to a diamino group and an acid functional group, which catalyzes the cyclocondensation of the amino group with the ketone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzodiazepines / chemical synthesis*
  • Benzodiazepines / chemistry
  • Catalysis
  • Molecular Structure
  • Nitro Compounds / chemistry*
  • Oxidation-Reduction
  • Stereoisomerism

Substances

  • Nitro Compounds
  • Benzodiazepines