Synthesis of racemic and enantiomeric 3-pyrrolidinyl derivatives of purine and pyrimidine nucleobases

Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):805-8. doi: 10.1081/ncn-200060287.

Abstract

The present work relates to the synthesis of pyrrolidine nucleoside analogs. Starting from malic acid, we have elaborated a high-yield synthesis of racemic and enantiomeric N-protected 3-pyrrolidinols and their O-mesyl derivatives as key compounds for alkylations of purine and pyrimidine nucleobases. On varying base and solvent, we have found conditions providing both satisfactory N-/O-regioisomeric ratio and acceptable yield for pyrimidine compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antiviral Agents / pharmacology
  • Chemistry, Pharmaceutical / methods
  • Magnetic Resonance Spectroscopy
  • Malates / chemistry
  • Mass Spectrometry
  • Models, Chemical
  • Nucleic Acid Conformation
  • Nucleosides / chemistry*
  • Nucleotides / chemistry
  • Purine Nucleosides / chemistry
  • Purines / chemistry*
  • Pyrimidine Nucleosides / chemistry
  • Pyrimidines / chemistry*
  • Solvents / chemistry
  • Stereoisomerism

Substances

  • Antineoplastic Agents
  • Antiviral Agents
  • Malates
  • Nucleosides
  • Nucleotides
  • Purine Nucleosides
  • Purines
  • Pyrimidine Nucleosides
  • Pyrimidines
  • Solvents
  • malic acid