METHOD FOR PRODUCING OXIDIZED GAMMA-GLUTAMYLCYSTEINE AND OXIDIZED GLUTATHIONE

    公开(公告)号:US20170145466A1

    公开(公告)日:2017-05-25

    申请号:US15323144

    申请日:2015-07-02

    CPC classification number: C12P21/02 C12N9/00

    Abstract: The technical problem to be solved by the present invention is to provide a method for producing oxidized glutathione, GSSG and a precursor thereof, i.e., oxidized γ-glutamylcysteine, by a simple process. As a means for solving the problem, the method for producing GSSG according to the present invention comprises step A′ of reacting L-cystine and L-glutamic acid to produce oxidized γ-glutamylcysteine and step B′ of reacting oxidized γ-glutamylcysteine and glycine to produce GSSG.

    METHOD FOR PRODUCING OPTICALLY ACTIVE 3-AMINOPIPERIDINE OR SALT THEREOF

    公开(公告)号:US20130079525A1

    公开(公告)日:2013-03-28

    申请号:US13682840

    申请日:2012-11-21

    CPC classification number: C07D211/60 C07B57/00 C07D211/56 C12P17/12 C12P41/006

    Abstract: The present invention relates to a method for producing an optically active 3-aminopiperidine or salt thereof. In the method, a racemic nipecotamide is stereoselectively hydrolyzed to obtain an optically active nipecotamide and an optically active nipecotic acid in the presence of an enzyme source derived from an organism, and then the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by aroylation, Hofmann rearrangement, deprotection of the amino group and further deprotection; or the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by selective protection with BOC, Hofmann rearrangement and further deprotection. It is possible by the present invention to produce an optically active 3-aminopiperidine or salt thereof useful as a pharmaceutical intermediate from an inexpensive and easily available starting material by easy method applicable to industrial manufacturing.

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