Nitroepoxides as versatile precursors to 1,4-diamino heterocycles

Org Lett. 2014 Mar 21;16(6):1752-5. doi: 10.1021/ol500444z. Epub 2014 Mar 3.

Abstract

Nitroepoxides are easily transformed into 1,4-diamino heterocycles such as quinoxalines and pyrazines by treatment with 1,2-benzenediamines and ammonia, respectively. Additionally, related saturated heterocycles, such as piperazines and tetrahydroquinoxalines, can be accessed by treatment with 1,2-diamines and a reducing agent. These transformations are efficient, provide access privileged, bioactive structures, and produce minimal waste.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Diamines / chemistry*
  • Epoxy Compounds / chemistry*
  • Molecular Structure
  • Nitro Compounds / chemistry*
  • Piperazines / chemical synthesis*
  • Piperazines / chemistry
  • Pyrazines / chemical synthesis
  • Pyrazines / chemistry
  • Quinoxalines / chemical synthesis*
  • Quinoxalines / chemistry
  • Stereoisomerism

Substances

  • Diamines
  • Epoxy Compounds
  • Nitro Compounds
  • Piperazines
  • Pyrazines
  • Quinoxalines