Process for the manufacture of 7-amino-3-cephem-4-carboxylic acid derivatives
    1.
    发明授权
    Process for the manufacture of 7-amino-3-cephem-4-carboxylic acid derivatives 失效
    制备7-氨基-3-头孢烯-4-羧酸衍生物的方法

    公开(公告)号:US3928331A

    公开(公告)日:1975-12-23

    申请号:US39287773

    申请日:1973-08-30

    Applicant: HOECHST AG

    CPC classification number: C07D499/00

    Abstract: Process for the manufacture of 7-amino-3-cephem-4-carboxylic acids and the esters thereof of the formula I

    in which A stands for hydrogen, alkyl, acyloxy, alkyloxy or hydroxy and R stands for hydrogen, optionally substituted linear or branched alkyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, alkoxyalkyl, acryloxyalkyl, aroylalkyl, or a heterocyclic radical and the salts thereof which comprises reacting 7-acylamino-3cephem-4-carboxylic acid esters of the general formula II

    in which R'' stands for optionally substituted alkyl, aryl, aralkyl, aryloxyalkyl, alkoxyalkyl or a heterocyclic radical and R'''' has the meaning given for R but cannot stand for hydrogen and A is defined as above, in an inert solvent with a silylating agent in the presence of a base, converting the amido group activated by the silylation into the iminohalide by adding a halogenating agent, allowing it to react with an alcohol to yield the iminoether hydrohalide, hydrolyzing the iminoether hydrohalide and optionally splitting the 7-amino-3-cephem-4carboxylic acid ester of the general formula I to yield the free acid, the esters obtained being valuable intermediates.

    Abstract translation: 制备7-氨基-3-头孢烯-4-羧酸的方法及其分子式Ⅰ的酯,其中A代表氢,烷基,酰氧基,烷氧基或羟基,R代表氢,任选取代的直链或支链 烷基,环烷基,芳基,芳烷基,芳氧基烷基,烷氧基烷基,丙烯酰氧基烷基,芳酰基烷基或杂环基及其盐,其包括使通式II的7-酰基氨基-3-头孢烯-4-羧酸酯与R' 对于任选取代的烷基,芳基,芳烷基,芳氧基烷基,烷氧基烷基或杂环基,R“具有R给出的含义,但不能代表氢,A如上所定义,在惰性溶剂中,在甲硅烷基化剂存在下, 碱,通过加入卤化剂将通过甲硅烷基活化的酰氨基转化成亚胺基卤化物,使其与醇反应得到亚氨基醚氢卤酸盐,水解亚氨基醚氢卤酸盐和任选的 制备通式I的7-氨基-3-头孢烯-4-羧酸酯,得到游离酸,得到的酯是有价值的中间体。

    Acylamino-cephem-carboxylic acids and process for preparing them
    2.
    发明授权
    Acylamino-cephem-carboxylic acids and process for preparing them 失效
    酰氨基 - 头孢烯羧酸及其制备方法

    公开(公告)号:US3920640A

    公开(公告)日:1975-11-18

    申请号:US35646673

    申请日:1973-05-02

    Applicant: HOECHST AG

    CPC classification number: C07D239/06 C07D233/22 C07D233/26 C07D333/38

    Abstract: IN WHICH R1, R2 and R3 represent hydrogen or lower alkyl groups and R1 and R2 may form together an alkylene group which may be substituted, R4 represents a linear or branched alkyl radical of 1 to 5 carbon atoms, a cyclo-alkyl radical of 3 to 7 carbon atoms which may be interrupted by heteroatoms, X represents a single bond or NH, A represents a phenylene or thienylene group which may be substituted and Y represents a single bond or oxygen, and their physiologically tolerated salts; the novel compounds have very good anti-bacterial properties.

    Acylamino-cephem-carboxylic acids of the general formula

    Abstract translation: 酰基氨基 - 头孢烯羧酸,其通式为R 1,R 2和R 3表示氢或低级烷基,R 1和R 2可以一起形成可被取代的亚烷基,R 4表示1至5的直链或支链烷基 碳原子,可被杂原子中断的3-7个碳原子的环烷基,X表示单键或NH,A表示可被取代的亚苯基或亚噻吩基,Y表示单键或氧,以及 他们的生理耐受盐; 新型化合物具有非常好的抗菌性能。

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