http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101575300-B

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6a201fbfc9902838caa46fbbe2b73ef2
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-18
filingDate 2009-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f058d5e6615349667547a3b1c9cafa51
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49b56e1db237f14e191088d6c42b7ed0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa8a58e4178c68a66d3aacf08fbbcdda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3357cf90035dd507b350148d4f2d9fef
publicationDate 2012-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101575300-B
titleOfInvention The production method of S-2-aminobutanamide
abstract The invention discloses a production method of S-2-aminobutyramide, which belongs to the technical field of chemical synthesis. The invention uses L-(+)-methionine as a raw material, and in the presence of alcohol or ether solvents, through chlorine-containing organic Carboxylate effect, demethylation thiohydroxylation and formation of S-2-amino-4-hydroxybutyric acid hydrochloride, followed by hydroxyl bromination to give S-2-amino-4-bromobutyric acid hydrobromide, S-2-amino-4-bromobutyric acid methyl ester hydrochloride is obtained by carboxymethyl esterification, nickel-catalyzed hydrogenation dehalogenation is converted into S-2-aminobutyric acid methyl ester, and finally aminolysis generates S-2-amino Butanamide. The invention has the advantages of high yield and good safety.
priorityDate 2009-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421410965
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7015191

Total number of triples: 18.