Premium
Preparation and Reactions of 2‐Methyl‐7‐(3‐methyl‐5‐oxo‐1‐phenyl‐2‐pyrazolin‐4‐yl)‐5‐arylthiazolo[3,2‐ a ]‐pyrimido[4,5‐ d ]oxazin‐4(5 H )‐one
Author(s) -
Youssef Mohamed Salah K.,
Abbady Mohamed S.,
Ahmed Ragaa A.,
Omar Ahmed A.
Publication year - 2011
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.201180268
Subject(s) - chemistry , acetic anhydride , sodium hydroxide , reagent , pyrimidine , hydrolysis , aryl , salt (chemistry) , medicinal chemistry , organic chemistry , catalysis , stereochemistry , alkyl
Ethyl 7‐amino‐3‐(3‐methyl‐5‐oxo‐1‐phenyl‐2‐pyrazolin‐4‐yl)‐5‐aryl‐5 H ‐thiazolo[3,2‐ a ]pyrimidine‐6‐carboxylate was hydrolyzed with an ethanolic sodium hydroxide and the sodium salt thus formed underwent cyclization with acetic anhydride to afford 2‐methyl‐7‐(3‐methyl‐5‐oxo‐1‐phenyl‐2‐pyrazolin‐4‐yl)‐5‐arylthiazolo[3,2‐ a ]pyrimido[4,5‐ d ]oxazin‐4(5 H )‐one. This compound was transformed to related heterocyclic systems via its reaction with various reagents. The biological activity of the prepared compounds was tested against Gram positive and Gram negative bacteria as well as yeast‐like and filamentous fungi. They revealed in some cases excellent biocidal properties.