Process for the recovery of ampicillin
    35.
    发明授权
    Process for the recovery of ampicillin 失效
    氨苄青霉素回收方法

    公开(公告)号:US5916762A

    公开(公告)日:1999-06-29

    申请号:US940984

    申请日:1997-09-30

    CPC classification number: C07D499/00 C12P37/04

    Abstract: Process for the recovery of ampicillin from a mixture containing ampicillin and 6-aminopenicillic acid (6-APA), in which a mixture of ampicillin and 6-APA, with a pH higher than 7, which apart from any solid ampicillin being present is homogeneous at a pH between 7 and 8.5, is subjected to a pH lowering till a pH lower than 8.2 is reached, and the solid substance present is recovered. The process is in particular suitable to be applied to the reaction mixture which is obtained after the enzymatic acylation reaction of 6-APA with a phenylglycidine derivative as acylation agent. Pure ampicillin can thus be recovered in a simple way.

    Abstract translation: 从含有氨苄青霉素和6-氨基青蒿酸(6-APA)的混合物中回收氨苄青霉素的方法,其中氨苄西林和6-APA的混合物,pH高于7,除了存在任何固体氨苄青霉素之外 在pH7〜8.5之间,进行pH降低,直至达到低于8.2的pH值,并回收存在的固体物质。 该方法特别适用于6-APA与苯基甘氨啶衍生物作酰化剂的酰化反应后获得的反应混合物。 因此,可以简单的方式回收纯氨苄青霉素。

    Process for the recovery of cephalexin
    36.
    发明授权
    Process for the recovery of cephalexin 失效
    回收头孢氨苄的方法

    公开(公告)号:US5874571A

    公开(公告)日:1999-02-23

    申请号:US903879

    申请日:1997-07-31

    CPC classification number: C12P35/00 C07D501/00

    Abstract: The disclosed process is for the recovery of cephalexin from a mixture containing cephalexin and 7-aminodesacetoxy cephalosporanic acid (7-ADCA), wherein a mixture of cephalexin and 7-ADCA, with a pH higher than 7, which apart from any solid cephalexin being present is homogeneous at a pH between 7 and 8.5, is subjected to a pH modification until a pH lower than 7.8 is reached, and the solid substance is recovered. The disclosed process is particularly suited for application to a reaction mixture obtained after the enzymatic acylation reaction of 7-ADCA with a phenylglycine derivative as an acylation agent. Pure cephalexin can thus be recovered in a simple manner.

    Abstract translation: 所公开的方法是从含有头孢氨苄和7-氨基二乙酰氧基头孢菌酸(7-ADCA)的混合物中回收头孢氨苄,其中除了任何固体头孢氨苄之外,pH高于7的头孢氨苄和7-ADCA的混合物 在pH7-7.5之间存在是均相的,经过pH调节,直到达到低于7.8的pH,并回收固体物质。 所公开的方法特别适用于7-ADCA与作为酰化剂的苯基甘氨酸衍生物进行酶酰化反应后得到的反应混合物。 因此可以简单的方式回收纯头孢氨苄。

    Acylation method for penicillins and cephalosporins
    37.
    发明授权
    Acylation method for penicillins and cephalosporins 失效
    青霉素和头孢菌素的酰化方法

    公开(公告)号:US5753458A

    公开(公告)日:1998-05-19

    申请号:US596166

    申请日:1996-02-07

    CPC classification number: C12P37/04 C12P35/04

    Abstract: A method for providing a semisynthetic .beta.-lactam antibiotic by enzyme catalyzed acylation of the parent .beta.-lactam with an activated derivative of the side chain acid wherein a modulator, which consists of one or more compounds different from the reactants and the reaction product and which suppresses the hydrolysis of the activated derivative of the side chain acid and the desired product more than it suppresses the synthesis of the desired product, is added to the reaction mixture, at the beginning of the reaction process, in a concentration from about 0.2 to 100.times.10.sup.3 .mu.m.

    Abstract translation: PCT No.PCT / EP95 / 02277 Sec。 371日期:1996年1月7日 102(e)日期1996年1月7日PCT提交1995年6月12日PCT公布。 公开号WO95 / 34675 PCT 日期1995年12月21日一种提供半合成β-内酰胺抗生素的方法,其通过用活化的侧链酸衍生物酶催化母体β-内酰胺酰化,其中调节剂由一种或多种不同于反应物的化合物组成, 在反应过程开始时,将反应产物并且抑制侧链酸和所需产物的活化衍生物的水解比抑制所需产物合成更多的方法加入到反应混合物中,浓度 约0.2〜100×103亩。

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