In this article presents Synthesis of 2-R5-oxo 5-H 6 -Carbomorpholin 7-phenyl 1,3,4-thiadiazolo-[3,2-a] pyrimidine through reaction of 2-R 5 -Oxo 5 -H 6-EthylCarboxilate 7 -phenyl -1, 3,4 -Thiadiazolo-[3,2-a] pyrimidine with morpholin. in particular,for the new antibacterial drugs in these homologousseries of compounds, we have synthesized 2-R5-oxo 5-H 6 -Carbomorpholin 7-phenyl 1,3,4-thiadiazolo-[3,2-a] pyrimidine .The structures of the compounds obtained are set NMR, 13 C, IR-spectroscopy.Keywords: 2-R 5-oxo 5-H 6 -Carbomorpholin 7-phenyl 1,3,4-thiadiazolo-[3,2-a] pyrimidine -2-R 5-Oxo 5-H 6-EthylCarboxilate 7 -phenyl -1, 3, pyrimidine -Morpholin -Synthesis -The reaction.and numerous repor tshave appeared in the literature [8][9][10][11][12]
The synthesis of 2-R 5-oxo 5-H 6 -carbohydrazin 7-phenyl 1, 3,4-thiadiazolo-[3,2-a] pyrimidine is described. This compound exhibits a broad spectrum of antimicrobial action and can be useful in the search for new antimicrobial drugs.Reactions of 2-R 5 -Oxo 5-H 6-EthylCarboxilate 7-phenyl -1, 3,4 -Thiadiazolo-[3,2-a] pyrimidine with hydrazine produce 2-R 5-oxo 5-H 6 -carbohydrazin 7-phenyl 1,3,4-thiadiazolo-[3,2-a] pyrimidine. The structures of the compounds obtained are set NMR, 13C, IR-spectroscopy.
In this article presents Synthesis of 2-R5-oxo 5-H 6-Carboxamid 7-phenyl 1,3,4-thiadiazolo-[3,2-a] pyrimidine through reaction of 2-R 5-Oxo 5-H 6-EthylCarboxilate 7-phenyl-1, 3,4-Thiadiazolo-[3,2-a] pyrimidine with amine. The structures of the compounds obtained are set NMR, 13 C, IR-spectroscopy.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.