In this work, ethyl 4-(4-chloro phenyl)-6-methyl-2-oxo-l ,2,3,4-tetrahydro
pyrimidine-5-carboxylatc (1) was prepared from condensation of 4-chloro
benzaldehyde, urea with ethyl acetoacctate in the presence of LaCl.7H2O and then
converted into the carbohydrazide (2). The azomethines (3-11) were prepared from
the corresponding aryl aldehydes or ketones with the carbohydrazide derivative (2).
The reactions of some new Schiff bases (3-11) with anhydrous acetic acid and
mercapto acetic acid afforded 5-(4-acetyl-5-aryl-4,5-dihydro-l,3,4-oxadiazol-2-yl)-
4-(4-chloro phenyl)-6-methyl-3, 4-dihydro pyrimidine-[lH]-2-ones (12-15) and 4-
(4-chloro phenyl)-6-methyl-2-oxo-N- (4-oxo-2-aryl-l,3- thiazolidin-3-yl)-1,2,3,4-
tetrahydro pyrimidine-5-carboxamide (16-18) respectively.The synthesized
compounds were confirmed by IR and UV spectral data |