Enamine-mediated Mannich reaction of cyclic N, O-acetals and amido acetals: the multigram synthesis of pyrrolidine alkaloid precursors

Org Biomol Chem. 2022 Sep 14;20(35):7105-7111. doi: 10.1039/d2ob01276f.

Abstract

The cooperative L-proline/Brønsted acid/base promoted reaction of 2-ethoxypyrrolidines or N-substituted 4,4-diethoxybutan-1-amines with methyl(alkyl/aryl)ketones for the synthesis of 2-(acylmethylene)pyrrolidine derivatives is reported. The key features of the developed protocol are gram-scale synthesis of the target compounds, easily available starting materials, operational simplicity and usage of non-expensive reagents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetals*
  • Alkaloids*
  • Ketones
  • Molecular Structure
  • Pyrrolidines
  • Stereoisomerism

Substances

  • Acetals
  • Alkaloids
  • Ketones
  • Pyrrolidines