Skip to Content
MilliporeSigma
  • One-pot synthesis of 2,3-dihydro-pyrrolopyridinones using in situ generated formimines.

One-pot synthesis of 2,3-dihydro-pyrrolopyridinones using in situ generated formimines.

Organic letters (2006-12-01)
Geoffrey Deguest, Alice Devineau, Laurent Bischoff, Corinne Fruit, Francis Marsais
ABSTRACT

A novel one-pot methodology is described for the synthesis of functionalized pyrrolopyridinones using in situ generated formimines and an ortho-lithiated pyridinecarboxamide species. Depending on the reaction conditions, this procedure allows versatile access to aminomethylated pyridinecarboxamides, 2,3-dihydro-pyrrolopyridinones, or 1,1-dialkylated 2,3-dihydro-pyrrolopyridinone derivatives. [reaction: see text]

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
2,2,6,6-Tetramethylpiperidine, ≥99%