An efficient and large-scale enantioselective synthesis of PNP405: a purine nucleoside phosphorylase inhibitor

J Org Chem. 2002 Sep 20;67(19):6612-7. doi: 10.1021/jo020256i.

Abstract

An efficient and large-scale enantioselective synthesis of PNP405 (1), a purine nucleoside phosphorylase inhibitor, is described. This synthesis of 1 involved eight steps starting from o-fluorophenylacetic acid with a 21.6% overall yield and >99.5% enantiopurity. The key stereogenic center with (R)-configuration was created using Evans' asymmetric alkylation methodology. This synthesis also features the racemization-free reductive removal of the chiral auxiliary in 5 using sodium borohydride, protection of the gamma-cyano alcohol 6 as the trityl ether by a new water-assisted tritylation with trityl chloride and triethylamine or with trityl alcohol and catalytic trifluoroacetic acid, and an efficient one-pot cyclo-guanidinylation of 10 using cyanamide as the guanidinylating agent.

MeSH terms

  • Catalysis
  • Combinatorial Chemistry Techniques / methods*
  • Enzyme Inhibitors / chemical synthesis*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Fluorobenzenes / chemical synthesis*
  • Fluorobenzenes / chemistry
  • Fluorobenzenes / pharmacology*
  • Molecular Structure
  • Purine-Nucleoside Phosphorylase / antagonists & inhibitors*
  • Pyrimidinones / chemical synthesis*
  • Pyrimidinones / chemistry
  • Pyrimidinones / pharmacology*
  • Stereoisomerism

Substances

  • Enzyme Inhibitors
  • Fluorobenzenes
  • PNP405
  • Pyrimidinones
  • Purine-Nucleoside Phosphorylase