Sixteen new 2-benzylidene-7-methyl-3-oxo-5-(substituted phenyl)-2,3-dihydro
-5H-thiazolo[3,2-a]pyrimidine-6-carboxylic acid methyl eaters (1a-4d) have
been synthesized by reacting 1,2,3,4-tetrahydropyrimidine-2-thiones (1-4) w
ith chloroacetic acid and appropriate benzaldehydes in a single step. Their
structures have been proved by IR, H-1 NMR, mass spectra and elemental ana
lysis. The compounds were tested for their anti-inflammatory activities. Te
st results revealed that compounds 1b, 1c, 4a and 4c exerted moderate anti-
inflammatory activity at the 100 mg/kg dose level compared with indomethaci
n. (C) 1999 Elsevier Science S.A. All rights reserved.