Design and synthesis of 4-alkynyl pyrazoles as inhibitors of PDE4: a practical access via Pd/C-Cu catalysis

Bioorg Med Chem Lett. 2012 Apr 1;22(7):2480-7. doi: 10.1016/j.bmcl.2012.02.008. Epub 2012 Feb 13.

Abstract

The design and synthesis of 4-alkynyl pyrazole derivatives has led to the identification of new class of PDE4 inhibitors. All these compounds were accessed for the first time via a facile Pd/C-CuI-PPh(3) mediated C-C bond forming reaction between an appropriate pyrazole iodide and various terminal alkynes. In vitro PDE4B inhibitory properties and molecular modeling studies of some of the compounds synthesized indicated that 4-alkynyl pyrazole could be a promising template for the discovery of novel PDE4 inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Alkynes / pharmacology
  • Antidepressive Agents / chemical synthesis
  • Antidepressive Agents / pharmacology
  • Catalysis
  • Computer Simulation
  • Copper / chemistry
  • Cyclic Nucleotide Phosphodiesterases, Type 4 / chemistry*
  • Dose-Response Relationship, Drug
  • Drug Design
  • Humans
  • Iodides / chemistry
  • Models, Molecular
  • Palladium / chemistry
  • Phosphodiesterase 4 Inhibitors / chemical synthesis*
  • Phosphodiesterase 4 Inhibitors / pharmacology
  • Pyrazoles / chemical synthesis*
  • Pyrazoles / pharmacology
  • Rolipram / pharmacology

Substances

  • Alkynes
  • Antidepressive Agents
  • Iodides
  • Phosphodiesterase 4 Inhibitors
  • Pyrazoles
  • Palladium
  • Copper
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • Rolipram