@Article{, title={Synthesis of new N-Substituted -3- chloro -2- azetidinones for 2, 4-Diamino-6-phenyl-1,3,5-triazine}, author={Tamador A. Mahmood}, journal={journal of the college of basic education مجلة كلية التربية الاساسية}, volume={21}, number={88 / علمي}, pages={1-12}, year={2015}, abstract={

The current study involved synthesis of several new N-Substituted -3- chloro -2- azetidinones for 2,4-Diamino-6-phenyl-1,3,5-triazine by two steps. The first step includes preparation of Schiff bases (A1-A6) by condensation of 2,4-Diamino-6-phenyl-1,3,5-triazine with many substituted aldehydes, then the second step includes preparation new six azetidinone compounds (B1-B6) by reaction of chloro acetyl chloride with the prepared Schiff bases in first step. The prepared compounds were characterized by physical properties, FT-IR, UV and some of them by 1H-NMR, 13C-NMR spectroscopy were recorded.Keywords: 2, 4-Diamino-6-phenyl-1, 3, 5-triazine, Schiffbase, azetidinones.Introduction:Schiff bases are characterized by the (N=CH) imines group which important compounds in medicinal and pharmaceutical field [1]. They show biological activities including antibacterial, antifungal [2,3] , anticancer [4] and herbicidal activities [5] figure (1) shows the stricture for this component. Fur their more Schiff bases have been widely used as protective group of amino group in organic synthesis [6, 7]. Schiff bases react with chloroacetyl chloride to give (β – Lactam) 3-chloro-2-azetidinones.} }