synthesis Synthesis and Characterization ( Oxazepine , Thiazine and Quinazoline ) Derivatives and Study the Biological Activity as Antibacteria

S. Adnan, A. jasim
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Abstract

This research. Included the preparation. and characterization some novel. Six and seven membered Heterocyclic. Compounds ( oxazepine , thiazine , quinazoline ) The first step in clode react 2-amino-6- methoxybenzothiazole with 4- amino acetophenone to get Schiff base derivative (1). The second step react (1) with 4 -hydroxy acetophenone to get schiff base derivative (2) the last step involve react (2) with ( Phthalic , Maleic , Succinic) anhydride to .get oxazepine derivatives (3,4and 5) also react (2) with(2-amino benzoic acid) and (2-mercaptobenzoic acid ) to get quinazoline (6)and thiazine (7) derivatives respectively .the physical; properties of the prepared; These Compounds. Were Identification (FT-IR) ,(1H-NMR) and (13C-NMR) by spectroscopy thene study their biological effect on two types of bacteria Staphylococcus aureuses (Gram positive) and Escherichia coli (Gram Negative)
恶氮平、噻嗪和喹唑啉衍生物的合成、表征及抗菌活性研究
这项研究。包括准备工作。还有一些新颖的人物塑造。六元和七元杂环。化合物(恶氮平、噻嗪、喹唑啉)第一步与4-氨基苯乙酮反应2-氨基-6-甲氧基苯并噻唑得到希夫碱衍生物(1),第二步与4-羟基苯乙酮反应(1)得到希夫碱衍生物(2),最后一步与(邻苯二甲酸、丙烯二甲酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸、丙烯二酸反应(2)。丁二酸酐得到恶氮平衍生物(3,4和5),并与(2-氨基苯甲酸)和(2-巯基苯甲酸)分别反应(2)得到喹唑啉(6)和噻嗪(7)衍生物。制备物的性质;这些化合物。通过光谱鉴定(FT-IR)、(1H-NMR)和(13C-NMR),研究了它们对金黄色葡萄球菌(革兰氏阳性)和大肠杆菌(革兰氏阴性)两种细菌的生物学作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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