Syntheses and biological properties of 8-carbamoylimidazo[1,2-c]pyrimidines and their heterocyclic analogs

Pharmazie. 1987 Jun;42(6):381-3.

Abstract

N-substituted 8-carbamoylimidazo[1,2-c]pyrimidines, 9-carbamoylpyrimido[1,2-c]pyrimidines and 8-carbamoyloxazolo[2,3-c]pyrimidines were obtained by the reaction of N-substituted 5-carbamoyl-2-hydroxy-4-mercapto-6-methylpyrimidines with aminoalcohols or ethylene chlorohydrin. Some of the described compounds exhibit weak antiinflammatory and analgetic effects.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemical synthesis*
  • Anti-Inflammatory Agents, Non-Steroidal / toxicity
  • Bacteria / drug effects
  • Chemical Phenomena
  • Chemistry
  • Heterocyclic Compounds / chemical synthesis*
  • Heterocyclic Compounds / pharmacology
  • Heterocyclic Compounds / toxicity
  • Imidazoles / chemical synthesis*
  • Imidazoles / pharmacology
  • Imidazoles / toxicity
  • Lethal Dose 50
  • Magnetic Resonance Spectroscopy
  • Microbial Sensitivity Tests
  • Pyrimidines / chemical synthesis*
  • Pyrimidines / pharmacology
  • Pyrimidines / toxicity
  • Rats

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Heterocyclic Compounds
  • Imidazoles
  • Pyrimidines