http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1723133-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_76a4701c8636c6a7a16ca4612510c33d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-87
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-87
filingDate 2004-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0479db9ed7071fcca13e8f103e35dfa9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7522d53afc2d92661ca0c2f1999a717d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_05c701037b7094bd15ff551b808d1f17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bdf91ddfc255845855e65ad2716ed8fe
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9c87060adeddab20e040514855f67c7c
publicationDate 2006-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1723133-A1
titleOfInvention One pot synthesis of citalopram from 5-cyanophthalide
abstract A process for one pot synthesis of citalopram is disclosed. The process comprises subjecting 5-cyano phthalide to Grignard reduction followed cyclization and followed by C-alkylation reaction to obtain citalopram without isolation and purification of any intermediates. In another embodiment, 5-cyano phthalide is subjected to sequential Grignard reactions followed by cyclization to obtain citalopram without isolation and purification of any intermediate stages.
priorityDate 2004-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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