The condensation of 2,4-dihydro-2,5-disubstituted-3H-pyrazol- 3-ones (1) with substituted benzaldehyde (2) in presence of glacil acetic acid gives 4-arylmethylene-2,4-dihydro-2,5-disubstituted-3H- pyrazol-3-ones (3). Similarly, the 4-arylmethylene-2,4-dihydro-2,5- disubstituted-3H-pyrazol-3-ones (3) reacts with thioureal/ phenyl thiourea / urea/ phenyl urea in presence of alkaline solution of ethanol at reflux temperature to give l,3-disubstituted-4-substituted phenyl-6-imino / phenylimino-4,7 -dihydro-1,3-thiazino / oxazino [5,4-d] pyrazoles. The antibacterial activities of the compounds (4) were tested against S. aureus and B. cereus bacteria.
Copy the following to cite this article:
P. Kedia; V. Singh; P. Singh; M. Singh; V. Upadhyay; D. Singh, "Synthesis and Antibacterial Activity of Some Novel Thiazino / Oxazino Pyrazole Derivatives", Journal of Ultra Chemistry, Volume 5, Issue 2, Page Number 271-278, 2018Copy the following to cite this URL:
P. Kedia; V. Singh; P. Singh; M. Singh; V. Upadhyay; D. Singh, "Synthesis and Antibacterial Activity of Some Novel Thiazino / Oxazino Pyrazole Derivatives", Journal of Ultra Chemistry, Volume 5, Issue 2, Page Number 271-278, 2018Available from: http://journalofchemistry.org/paper/718/