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    • 6. 发明申请
    • Method of Making 6-Aminocaproic Acid As Active Pharmaceutical Ingredient
    • 制备6-氨基己酸作为活性药物成分的方法
    • US20140039219A1
    • 2014-02-06
    • US13660126
    • 2012-10-25
    • Jien-Heh TienChu-yi Pang
    • Jien-Heh TienChu-yi Pang
    • C07C227/22
    • C07C227/22C07C227/38
    • The present invention provides a method for making 6-aminocaproic acid as an active pharmaceutical ingredient. The method comprises: performing a hydrolysis procedure to have ε-caprolactam react with acid or base to generate a first reaction mixture, performing a modification procedure to have a solubility regulating agent reacts with 6-aminocaproic acid in the first reaction mixture to form a second reaction mixture including an aminocaproic acid intermediate, performing a separation procedure to have the intermediate separated from the second reaction mixture and performing a hydrogenation procedure to have the aminocaproic acid intermediate hydrogenated to form a 6-aminocaproic acid product.
    • 本发明提供了制备6-氨基己酸作为活性药物成分的方法。 该方法包括:进行水解步骤以使ε-己内酰胺与酸或碱反应以产生第一反应混合物,进行修饰方法以使第一反应混合物中的溶解度调节剂与6-氨基己酸反应形成第二反应混合物 反应混合物包括氨基己酸中间体,进行分离步骤以使中间体与第二反应混合物分离,并进行氢化方法使氨基己酸中间体氢化形成6-氨基己酸产物。
    • 10. 发明申请
    • Method Of Separately Collecting Optically Active Amino Acid Amide And Optically Active Amino Acid
    • 分开收集光活性氨基酸酰胺和光活性氨基酸的方法
    • US20070213559A1
    • 2007-09-13
    • US11587006
    • 2005-04-22
    • Atsushi InoueAkinori TanakaSatoshi Nanba
    • Atsushi InoueAkinori TanakaSatoshi Nanba
    • C07C227/40
    • C07C227/38C07C231/24C12P13/04C07C229/08C07C237/06
    • The present invention is a method for separately collecting an optically active amino acid amide and an optically active amino acid from an aqueous solution containing the optically active amino acid amide and the optically active amino acid together with at least one member selected from the group consisting of an acid, a base and a salt: comprising a neutralization step of neutralizing an acid or a base when the aqueous solution contains the acid or the base; a desalting step of removing a salt contained in the aqueous solution and/or formed in the neutralization step; and a step of collecting the optically active amino acid amide and the optically active amino acid separately from the aqueous solution which has been desalted in the desalting step, by a process which takes advantage of a difference in solubility between the two components in an organic solvent. The desalting step is preferably performed by an electrodialysis process optionally in the state where ammonia is added to the aqueous solution. According to the present invention, an optically active amino acid amide and an optically active amino acid, which are important as intermediates in the production of pharmaceuticals, agricultural chemicals, and various industrial chemicals, can be separately collected with high efficiency by use of an organic solvent.
    • 本发明是从含有光学活性氨基酸酰胺和光学活性氨基酸的水溶液中分别收集光学活性氨基酸酰胺和光学活性氨基酸的方法,以及选自以下的至少一种: 酸,碱和盐:包含当水溶液含有酸或碱时中和酸或碱的中和步骤; 去除水溶液中含有的盐和/或在中和步骤中形成的脱盐步骤; 以及通过利用有机溶剂中的两种成分之间的溶解度差异的方法,在脱盐步骤中从脱盐的水溶液中分离收集光学活性氨基酸酰胺和光学活性氨基酸的步骤 。 脱盐步骤优选通过电渗析方法进行,任选地在向水溶液中加入氨的状态下进行。 根据本发明,可以通过使用有机物以高效率单独收集作为药物,农药和各种工业化学品生产中的中间体的光学活性氨基酸酰胺和光学活性氨基酸 溶剂。