http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103243130-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ac31afbea1cbbb03498644721ffb4a62
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-14
filingDate 2013-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fd5985d8fd9b66320610a9160c4dde9
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publicationDate 2013-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103243130-A
titleOfInvention A kind of one pot method prepares the method for γ-glutamine compound
abstract The invention discloses a method for preparing γ-glutamine compounds in one pot. The method comprises the following steps: using 5-carboxyethyl hydantoin and amine compounds for amidation reaction in water phase to form 5-carboxyethyl hydantoin amide compounds; The bacterium with carbamylase is used as a catalyst to carry out enzymatic hydrolysis and acyclic reaction to obtain γ-glutamine compounds. In the present invention, hydantoin rings are used to co-protect the α-amino and α-carboxyl groups of glutamic acid, and only the γ-carboxyl groups are exposed, which ensures the site specificity of the amidation reaction; the intermediate product does not need to be extracted and separated directly Carry out the next step of enzymatic reaction, the "one pot" reaction process can effectively improve the total yield of the reaction, and at the same time, the aqueous phase reaction also avoids the environmental pollution caused by organic solvents; the use of enzymatic hydrolysis and ring opening avoids most of the chemical synthesis. Repeated protection and deprotection steps reduce the occurrence of side reactions.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106916858-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113278660-B
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priorityDate 2013-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 24.