http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105130875-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a544c49cadf466ab6f2337003140df2e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_385f84ec011382ecd8628ec07c5fea83
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-52
filingDate 2014-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82e7fa147c683907ffcea93800b59654
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf155690bcbd223f0f4406d319f823f2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a700eaeac29b0d3712e8f774430a41d5
publicationDate 2015-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105130875-A
titleOfInvention Saxagliptin and saxagliptin salt preparation method
abstract The present invention discloses a saxagliptin and saxagliptin salt preparation method, which includes the following reaction shown in the specification, and is characterized in that: according reaction a, a compound of formula III is reacted with cyanuric chloride in an organic solvent to produce a compound of formula II. The method has the advantages of safe and easy operation, available and cheap raw materials, easy-control and mild reaction conditions, simple reaction post-processing, high yield, and the like, can achieve the requirements of low-cost, large-scale production of high purity saxagliptin, and has significant industrial value.
priorityDate 2014-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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