Synthesis of 3H-pyrazolo[3,4-c]isoquinolines and thieno[3,2-c]isoquinolines via cascade imination/intramolecular decarboxylative coupling

Org Lett. 2013 Oct 4;15(19):5044-7. doi: 10.1021/ol4023722. Epub 2013 Sep 18.

Abstract

A general approach for the synthesis of 3H-pyrazolo[3,4-c]isoquinolines and thieno[3,2-c]isoquinolines is described involving the implementation of a cascade imination/intramolecular decarboxylative coupling between potassium 2-amino(hetero)benzoates and 2-haloarylaldehydes. The reactions of pyrazole-based substrates require a Pd-Cu bimetallic system for superior yields whereas the thienyl-based substrates afford the products in excellent yields with a Pd-catalyst only.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry
  • Carboxylic Acids / chemistry*
  • Catalysis
  • Copper
  • Imines / chemistry*
  • Isoquinolines / chemical synthesis*
  • Isoquinolines / chemistry
  • Molecular Structure
  • Palladium
  • Pyrazoles / chemical synthesis*
  • Pyrazoles / chemistry

Substances

  • Aldehydes
  • Carboxylic Acids
  • Imines
  • Isoquinolines
  • Pyrazoles
  • pyrazole
  • Palladium
  • Copper