Multicomponent Strategy to Pyrazolo[3,4-e]indolizine Derivatives under Microwave Irradiation

J Org Chem. 2015 Aug 21;80(16):8435-42. doi: 10.1021/acs.joc.5b01314. Epub 2015 Aug 12.

Abstract

A simple and efficient one-pot construction of pyrazolo[3,4-e]indolizine derivatives via a diethylamine-catalyzed three-component domino reaction of arylglyoxals, cyclic 1,3-diones, and 5-aminopyrazoles under microwave irradiation is described. In this one-pot transformation, seven bonds and two new rings are efficiently formed. This synthesis was confirmed to follow the group-assisted-purification (GAP) chemistry process, which can avoid traditional recrystallization or chromatography purification methods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cyclization
  • Diethylamines / chemistry*
  • Indolizines / chemical synthesis*
  • Indolizines / chemistry
  • Microwaves
  • Molecular Structure
  • Pyrazoles / chemical synthesis*
  • Pyrazoles / chemistry

Substances

  • Diethylamines
  • Indolizines
  • Pyrazoles
  • Pyrazolo(3,4-e)indolizine