Synthesis of new 2',3'-dideoxy-6',6'-difluoro-3'-thionucleoside from gem-difluorohomoallyl alcohol

Org Lett. 2004 Oct 28;6(22):3941-4. doi: 10.1021/ol048423j.

Abstract

[reaction: see text] 2',3'-Dideoxy-6',6'-difluoro-3'-thionucleoside 1b, an analogue of 3Tc that has high biological activities against HIV and HBV, has been synthesized from gem-difluorohomoallyl alcohol 3 in an efficient way. The key intermediate 4-amino-3,3-difluorotetrahydrothiophen-2-ylmethyl benzoate 15 was prepared from 2,2-difluoro-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]but-3-en-1-ol 3 in 11 steps. The construction of pyrimidine ring with the amino group of compound 15 gave the target compound 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Alcohols / chemistry
  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / pharmacology
  • Crystallography, X-Ray
  • Fluorocarbons / chemistry*
  • Propanols / chemistry*
  • Pyrimidines / chemistry
  • Thionucleosides / chemical synthesis*
  • Thionucleosides / pharmacology

Substances

  • 2',3'-dideoxy-6',6'-difluoro-3'-thionucleoside
  • Amino Alcohols
  • Antiviral Agents
  • Fluorocarbons
  • Propanols
  • Pyrimidines
  • Thionucleosides
  • allyl alcohol
  • pyrimidine