http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2161253-A3

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filingDate 2007-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6451ec36eb25761d5e51c69dd108d651
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publicationDate 2010-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2161253-A3
titleOfInvention Process for the preparation of 3,4-dihydroisoquinolines in the synthesis of morphinans
abstract The present invention is directed to processes for the synthesis of morphinans. In particular, a process tor 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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