A Viedma ripening route to an enantiopure building block for Levetiracetam and Brivaracetam

Org Biomol Chem. 2018 Dec 19;17(1):35-38. doi: 10.1039/c8ob02660b.

Abstract

A simple route to enantiomerically pure (S)-2-aminobutyramide - the chiral component of the anti-epileptic drugs Levetiracetam and Brivaracetam has been developed. This approach is based on the rational design and application of a Viedma ripening process. The practical potential of the process is demonstrated on a large scale.

MeSH terms

  • Amides / chemistry
  • Aminobutyrates / chemistry
  • Animals
  • Anticonvulsants / chemical synthesis*
  • Humans
  • Levetiracetam / chemical synthesis*
  • Pyrrolidinones / chemical synthesis*
  • Stereoisomerism

Substances

  • Amides
  • Aminobutyrates
  • Anticonvulsants
  • Pyrrolidinones
  • Levetiracetam
  • alpha-aminobutyric acid
  • brivaracetam