An expeditious synthesis of series of novel 1,3,5-thiadiazine (5a-f) and (6a-f) derivatives have been
described. These compounds were synthesized by reaction of 1-(N-((6-methyl-2-(p-tolyloxy)quinoline-
3-yl)methylene)carbamimidoyl)-3-arylthiourea (3a-b) derivatives with N-aryl isocyanodichloride (4a-c)
in chloroform followed by basification with dilute NH4OH to give the target compounds 5a-f; which
were acetylated further to afford six novel 1,3,5-thiadiazin-3-(6H)-yl)ethanone (6a-f) derivatives. Synthesis
of intermediate compounds 3a-b was obtained by reacting 6-methyl-2-(p-tolyloxy)quinoline-3-
carbaldehyde (2a) and 1-carbamimidoyl-3-aryllthiourea (1a-b) in chloroform. Structures of compounds
5a-f and 6a-f were established by FTIR, 1H & 13C NMR, mass spectra and further supported by elemental
analysis. All synthesized compounds were investigated for their in vitro antimicrobial screening against
a panel of pathogenic microorganism comprising S. aureus as Gram positive while E. coli, P. vulgaris, S.
typhi as Gram-negative bacterial strains.