http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103073478-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_53b4d53983adbf56dd0e7d0bf96f8ce5
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-333
filingDate 2013-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_234231736cf75d06eacee10bb8c3f22f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2b974d42a7809274384547eaf00880b
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publicationDate 2015-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103073478-B
titleOfInvention Chemical synthetic method for pyrrole derivatives
abstract The invention relates to a method for synthesizing 4-(formyl-5-hydroxymethyl-1 hydrogen-pyrrole-1-yl) butyric acid, and belongs to the field of organic synthesis. The conventional 4-(formyl-5-hydroxymethyl-1 hydrogen-pyrrole-1-yl) butyric acid can be synthesized by Maillard reaction of monosaccharide and gamma-aminobutyric acid under high pressure at high temperature, but the deficiencies of low yield, low purity, complex process, higher cost and the like exist. The method comprises the steps as follows: reacting 3-deoxyglucosone with gamma-aminobutyric acid, dehydrating to generate 4-(formyl-5-hydroxymethyl-1 hydrogen-pyrrole-1-yl) butyric acid, and purifying with a solid phase extraction method. The method is simple, the yield is increased, few byproducts are generated, and the purity is high.
priorityDate 2013-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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