http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8569508-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7b86c0e65ff0cf2731708808aab8441
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-47
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-38
filingDate 2010-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc2a9663c5536a8564febe3e6fa89b7d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_882b732e1688b053ddb153e5874b12b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c940abddb83aba384f4108b750008745
publicationDate 2013-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8569508-B2
titleOfInvention Synthetic method for montelukast sodium intermediate
abstract A synthesis method for preparing Montelukast sodium intermediate 2-(2-(3-(2-(7-chloro-2-quinolyl)vinyl)phenyl-3-oxopropyl)phenyl) propanol is provided. In this method, the target compound is prepared by condensing the starting materials 7-chloroquinaldine and 3-cyanobenzaldehyde, and then reacting the resultant product with 2-(2-ortho-(2-haloethyl)-phenylpropyl)tetrahydropyrane ether. The present invention can easily obtain start materials and is applicable for mass production.
priorityDate 2009-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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