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      Synthesis and anti-inflammatory activities of some thiazolo[3,2-a]pyrimidine derivatives.

      Farmaco (Società chimica italiana : 1989)
      Animals, Anti-Inflammatory Agents, Non-Steroidal, chemical synthesis, chemistry, pharmacology, Female, Magnetic Resonance Spectroscopy, Male, Mass Spectrometry, Mice, Pyrimidines, Spectrophotometry, Infrared

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          Abstract

          Sixteen new 2-benzylidene-7-methyl-3-oxo-5-(substituted phenyl)-2, 3-dihydro-5H-thiazolo[3,2-a]pyrimidine-6-carboxylic acid methyl esters (1a-4d) have been synthesized by reacting 1,2,3,4-tetrahydropyrimidine-2-thiones (1-4) with chloroacetic acid and appropriate benzaldehydes in a single step. Their structures have been proved by IR, 1H NMR, mass spectra and elemental analysis. The compounds were tested for their anti-inflammatory activities. Test results revealed that compounds 1b, 1c, 4a and 4c exerted moderate anti-inflammatory activity at the 100 mg/kg dose level compared with indomethacin.

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