http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009247760-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_07addebfc9446dc5a9a77692ebf4dac1
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C235-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-77
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-00
filingDate 2009-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebca871b3cff044e29b6b91e8ffc3683
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6451ec36eb25761d5e51c69dd108d651
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f364d2cbe01728f96c441ca7aeffcddd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c7018364ffa5dea05402927bcf94421
publicationDate 2009-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2009247760-A1
titleOfInvention Preparation of Amides from an Acid and Amine for Intermediates in the Synthesis of Morphinans
abstract The present invention is directed to processes for the synthesis of morphinans. In particular, a process for coupling a carboxylic acid compound with an amine compound to form an amide product that can then be isolated or the crude amide product can be cyclized to form a 3,4-dihydroisoquinoline. In one embodiment, the carboxylic acid contains a phenol moiety protected with a labile protecting group. The protected phenol reduces reaction times, simplifies work-up of the product, and reduces the amount of cyclizing agent, POCl 3 that is necessary to form the 3,4-dihydroisoquinoline.
priorityDate 2006-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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