http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2185517-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fd048f86dea957a0403c59240263abcb
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4704
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-18
filingDate 2008-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3931b391500327acdb4aafe8d93742b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f1d797ad47a4e5d6e56784048c902b7
publicationDate 2010-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2185517-A1
titleOfInvention Process for preparing a leukotriene antagonist and an intermediate thereof
abstract Dicyclohexylamine salt of formula (IIa) or a pharmaceutically acceptable solvate thereof, including a hydrate, and its process for preparation. Process for the preparation of montelukast of formula (I) or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate thereof, including a hydrate, comprising the conversion of a salt of formula (IIa) into its form of free acid, followed by reaction with a compound of formula (III) CH3MgX, wherein X is halogen, in a suitable solvent, optionally in the presence of a Lewis acid.
priorityDate 2007-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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