Invention Grant
- Patent Title: Process for the synthesis of L-(+)-ergothioneine
- Patent Title (中): 合成L-(+) - 麦角硫杆菌素的方法
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Application No.: US12240173Application Date: 2008-09-29
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Publication No.: US07767826B2Publication Date: 2010-08-03
- Inventor: Miroslav Trampota
- Applicant: Miroslav Trampota
- Applicant Address: US NJ Fairfield
- Assignee: Pharmatech International, Inc.
- Current Assignee: Pharmatech International, Inc.
- Current Assignee Address: US NJ Fairfield
- Agency: St. Onge Steward Johnston & Reens LLC
- Main IPC: A61K31/4172
- IPC: A61K31/4172 ; C07D233/42

Abstract:
This invention relates to a novel process for the preparation of optically pure L-(+)-ergothioneine. The process for the chemical synthesis of L-ergothioneine comprises steps which consist of reacting L-histidine alkyl ester with an acid halide, chloroformate or pyrocarbonate in the presence of a base, hydrolysis of the alkyl-(S,Z)-2,4,5-triamidopent-4-enoate to obtain a (S)-alkyl 2,5-diamido-4-oxopentanoate, acid catalyzed hydrolysis of the (S)-alkyl 2,5-diamido-4-oxopentanoate followed by reaction with a metal thiocyanate to obtain the thiohistidine, protection of the sulfur of thiohistidine as the tert-butyl thioether, dialkylation of the primary amine to obtain a tertiary amine, quaternization of the tertiary amine, and removal of the protecting group to obtain the desired (S)-3-(2-mercapto-1H-imidazol-5-yl)-2-(trialkylammonio)propanoate (I). This process affords a better yield and is capable of practical application at large scale.
Public/Granted literature
- US20090093642A1 PROCESS FOR THE SYNTHESIS OF L-(+)-ERGOTHIONEINE Public/Granted day:2009-04-09
Information query
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