Synthesis of a novel fluorinated benzo[a]pyrene: 4,5-difluorobenzo[a]pyrene

Carcinogenesis. 1991 Sep;12(9):1647-50. doi: 10.1093/carcin/12.9.1647.

Abstract

The synthesis of 4,5-difluorobenzo[a]pyrene, as a fluorinated probe to investigate the involvement of the K-region in the further metabolic activation of benzo[a]pyrene metabolites, is described. Benzo[a]pyrene-4,5-dione obtained from 2,3-dichloro-5,6-dicyano-1,4-benzoquinone oxidation of cis-4,5-dihydro-4,5-dihydroxybenzo[a]pyrene was fluorinated with dimethylaminosulfur trifluoride to give 4H,5H,4,4,5,5,-tetra-fluorobenzo[a]pyrene. Defluorination using lithium aluminum hydride in tetrahydrofuran gave 4,5,-difluorobenzo[a]pyrene.

MeSH terms

  • Benzo(a)pyrene / chemistry*
  • Benzo(a)pyrene / pharmacokinetics
  • Benzopyrenes / chemical synthesis*
  • Benzopyrenes / pharmacokinetics

Substances

  • Benzopyrenes
  • 4,5-difluorobenzo(a)pyrene
  • Benzo(a)pyrene