인듐과 주석 금속을 이용한 세팜 유도체 및 그의 제조 방법
    26.
    发明公开
    인듐과 주석 금속을 이용한 세팜 유도체 및 그의 제조 방법 失效
    CEPHAM衍生物使用印度和锡和其制备方法

    公开(公告)号:KR1020000067451A

    公开(公告)日:2000-11-15

    申请号:KR1019990015261

    申请日:1999-04-28

    CPC classification number: Y02P20/55

    Abstract: PURPOSE: Cepham derivatives prepared by the reaction of 3-hydroxy cephem derivatives and allylhalide or acetylene halide in a solvent in the presence of a metal catalyst and process for the preparation method thereof are provided which can be used as an intermediate for the manufacture of cephem antibiotics. CONSTITUTION: Cepham derivatives of formula (I) useful as an intermediate for producing cephem antibiotics are prepared by the reaction of 3-hydroxy cephem derivatives of formula (V) and allylhalide (III) or acetylene halide in a solvent in the presence of a metal catalyst at 0 to 100°C for 1 to 96 hr. In formula, R1 represents phenylacetyl, 2-£2-amino(1,3-thiazole-4-yl)-2-(hydroxyalkoxyimino)ethinyl, 2-£2-amino(1,3-thiazole-4-yl)-2-(alkoxyimino)ethinyl or 4-hydroxyphenylglycine derivative, R2 is H, carboxylic acid salts (sodium and potassium salt as inorganic salts, alkylamine salt, aromatic amine salt as organic salts), a molecular protecting group in the cephalosporin field of 4-methoxybenzyl, diphenylbenzyl, diphenylmethyl, 4-nitrobenzyl, allyl as a carboxyl protecting group, in a Q compound, R3, R4 and R5 represent each H, halogen, methyl, ethyl, hydroxy, phenyl or alkoxycarbonyl.

    Abstract translation: 目的:提供在金属催化剂存在下,通过3-羟基头孢烯衍生物和烯丙基卤或乙炔卤化物在溶剂中反应制备的Cepham衍生物,其制备方法可用作中间体,用于制备头孢烯 抗生素。 构成:通过式(Ⅴ)的3-羟基头孢烯衍生物与烯丙基卤(III)或炔酰卤在溶剂中在金属存在下的反应制备用作产生头孢类抗生素的中间体的式(I)的头孢类衍生物 催化剂在0〜100℃下反应1〜96小时。 在式中,R 1表示苯乙酰基,2- {2-氨基(1,3-噻唑-4-基)-2-(羟基烷氧基亚氨基)乙炔基,2-(2-氨基(1,3-噻唑-4-基) 2-(烷氧基亚氨基)乙炔基或4-羟基苯基甘氨酸衍生物,R2是H,羧酸盐(作为无机盐的钠盐和钾盐,烷基胺盐,作为有机盐的芳族胺盐),四氢呋喃的头孢菌素领域中的分子保护基, 甲氧基苄基,二苯基苄基,二苯基甲基,4-硝基苄基,烯丙基作为羧基保护基,在Q化合物中,R 3,R 4和R 5各自表示H,卤素,甲基,乙基,羟基,苯基或烷氧基羰基。

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