One-Pot Reductive Alkylation of 2,4-Dihydroxy Quinolines and Pyridines

J Org Chem. 2021 May 21;86(10):7148-7162. doi: 10.1021/acs.joc.1c00496. Epub 2021 Apr 29.

Abstract

A one-pot, Hantzsch ester-mediated Knoevenagel condensation-reduction reaction has been developed for alkylation of a wide range of substituted 2,4-quinoline diols and 2,4-pyridine diols with aldehydes. The process is operationally simple to perform, scalable, and provides highly useful C-3 alkylated quinoline and pyridine diols in yields of 58-92%. The alkylation products can be converted to 2,4-dihaloquinoline and pyridine substrates for further functionalization.

MeSH terms

  • Alcohols
  • Aldehydes
  • Alkylation
  • Pyridines*
  • Quinolines*

Substances

  • Alcohols
  • Aldehydes
  • Pyridines
  • Quinolines