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2-Amino-N-(7-substituted Benzo [d] thiazol-2yl) benzamide: Synthesis and characterization of novel antibacterial compounds

机译:2-氨基-N-(7-取代的苯并[d]噻唑-2基)苯甲酰胺:新型抗菌化合物的合成与表征

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Various 2-Amino-N-(7-subtituted Benzo [d] thiazol-2yl) benzamide containing different secondary amines have been synthesized by treating aniline with KSCN in presence of bromine in glacial acetic acid and ammonia to get to get 2-aminobenzothiazole which was treated with anthranillic acid in presence of dry pyridine to get N- (Benzo [d] thiazol-2-yl) benzamide. To the above appropriate amine in equimolar Quantities were refluxed for 2-6 hrs in an oil bath in the Presence of DMF to get colorless crystalline Derivatives 3 A-E. The derivatives were characterized by melting point, IR, 1HNMR, and mass spectral studies. The compounds were tested for antimicrobial activity against Staphylococcus aureus (MTCC 83), Streptococcus pyogen (MTCC 442), Escherichia coli (MTCC443), Pseudomonas aeruginosa (MTCC 741), Aspergillus niger (MTCC 134), Candida albicans (MTCC 183) taking Ceftizoxime, Ampilicilline, Gentamicin and Fluconazole as standard drugs and showed significant activity.
机译:在冰醋酸和氨水中,在溴的存在下,用KSCN处理苯胺,合成了各种含不同仲胺的2-氨基-N-(7-取代的苯并[d]噻唑-2基)苯甲酰胺,得到2-氨基苯并噻唑,其中在干燥的吡啶存在下,用邻氨基苯甲酸对苯甲酰胺处理,得到N-(苯并[d]噻唑-2-基)苯甲酰胺。在DMF存在下,在油浴中将等摩尔量的上述胺在上述适当的胺中回流2-6小时,得到无色结晶衍生物3A-E。通过熔点,IR,1 HNMR和质谱研究表征衍生物。测试了这些化合物对金黄色葡萄球菌(MTCC 83),化脓性链球菌(MTCC 442),大肠杆菌(MTCC443),铜绿假单胞菌(MTCC 741),黑曲霉(MTCC 134),白色念珠菌(MTCCox 183)的抗菌活性,氨苄西林,庆大霉素和氟康唑为标准药物,并显示出明显的活性。

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