Methyl 5-(4-acetoxyphenyl)-2-(2-bromobenzylidine)-7-methyl-3-oxo-2,3- dihydro-5H-1,3-thiazolo[3,2-a]pyrimidine-6-carboxylate

Abstract

In the title molecule, C24H19BrN2O5S, the pyrimidine ring is in a flattened half-chair conformation and the 4-acetoxyphenyl group is substituted axially to this ring. The thiazole ring is essentially planar [with a maximum deviation of 0.012 (2) Å for the N atom] and forms dihedral angles of 17.65 (13) and 88.95 (11)° with the bromo- and acetoxy-substituted benzene rings, respectively. The dihedral angle between the benzene rings is 81.84 (13) Å. In the crystal, pairs of weak C - H⋯O hydrogen bonds lead to the formation of inversion dimers. A weak C - H⋯π interaction and π-π stacking interactions with centroid-centroid distances of 3.5903 (14) Å are observed.