首页> 外文期刊>Bulletin of the Korean Chemical Society >New Thiazolo[3,2-b][1,2,4]triazole Derivatives : Useful Compounds for the Preparation of 7-Substituted Cephalosporins
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New Thiazolo[3,2-b][1,2,4]triazole Derivatives : Useful Compounds for the Preparation of 7-Substituted Cephalosporins

机译:新的噻唑并[3,2-b] [1,2,4]三唑衍生物:用于制备7位取代的头孢菌素的有用化合物

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We have synthesized several bicyclic heteroaromatic compounds with bridgehead nitrogen from N-amine salts of heteroaromatic amines. 2-Amino and 2-unsubstituted thiazolo[3,2-b][l,2,4]triazole derivatives 2a-b were prepared by the cyclization reaction from N-amine salts of aminothiazole-5-yl(N-methoxyimino)acetate with cyanogen bromide and formamidine acetic acid salt, respectively. 2-Methylthiazolo[3,2-b][1,2,4]triazole 2c was obtained from N-acetylated N-amine salt of aminothiazole-5-yl(N-methoxyimino)acetate by the cyclization reaction in the presence of polyphosphoric acid (PPA). 2-Substituted and 2-unsubstituted thiazole[3,2-b][1,2,4]triazole derivatives 2a-c were coupled with 7-aminocephalosporanic acid (7-ACA). Coupled cephalosporin derivatives 1a-c did not have good antibacterial activities in vitro.
机译:我们已经从杂芳族胺的N-胺盐中合成了几种具有桥头氮的双环杂芳族化合物。由氨基噻唑-5-基(N-甲氧基亚氨基)乙酸盐的N-胺盐通过环化反应制备2-氨基和2-未取代的噻唑并[3,2-b] [1,2,4]三唑衍生物2a-b与溴化氰和甲am乙酸盐分别。在多磷酸的存在下,通过环化反应,从氨基噻唑-5-基(N-甲氧基亚氨基)乙酸酯的N-乙酰化N-胺盐获得2-甲基噻唑并[3,2-b] [1,2,4]三唑2c。酸(PPA)。将2-取代和2-未取代的噻唑[3,2-b] [1,2,4]三唑衍生物2a-c与7-氨基头孢烷酸(7-ACA)偶联。偶合的头孢菌素衍生物1a-c在体外不具有良好的抗菌活性。

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