Preparation and novel reduction reactions of vinamidinium salts

J Org Chem. 2001 Jan 12;66(1):251-5. doi: 10.1021/jo005656p.

Abstract

Substituted acetic acids and formamides react in the presence of phosphorus oxychloride to yield the vinamidinium hexafluorophosphate salts 5a-d, 6a-d, and 7 in moderate to good unoptimized recrystallized yields (40-67%) as easily handled nonhygroscopic solids. The 1,3-differentially substituted vinamidinium salts 8 was prepared by amine exchange in 81% yield as are the cyclic diazapinium salts 9 and 10 in > 76% yield. The symmetrical 2-chlorovinamidinium 11 was prepared by displacement of 3 in 71% yield. The 2-chlorovinamidinium salts are cleanly reduced to the parent vinamidinium salts 12-16 using HI or PPh3/pTSA in up to 99% assay yield.

MeSH terms

  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / chemical synthesis*
  • Cyclooxygenase Inhibitors / chemistry
  • Etoricoxib
  • Indicators and Reagents
  • Isoenzymes
  • Oxidation-Reduction
  • Piperidines / chemical synthesis*
  • Piperidines / chemistry
  • Prostaglandin-Endoperoxide Synthases
  • Pyridines / chemical synthesis*
  • Pyridines / chemistry
  • Sulfones / chemical synthesis*
  • Sulfones / chemistry

Substances

  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Indicators and Reagents
  • Isoenzymes
  • Piperidines
  • Pyridines
  • Sulfones
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Etoricoxib