http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-184576-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-22
filingDate 1981-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f27161fc949293bd9ec7ee2536305ec8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71852dbd12d8e0d35992e7aa0aa1adac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41e04ade255a6d664a98b2011345b48f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61294fc398ad81d5a43edab989896d7f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52c201fd4a2314a529451b07a5ee3826
publicationDate 1984-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-184576-B
titleOfInvention Process for preparing 14,15-dihydro-d-nor-eburnamenine derivatives
abstract FIELD OF THE INVENTION The present invention relates to a novel 14,15 dihydro-D-norburbamenine derivative of the formula Ia and / or Ic, wherein R2 is (C1-C4 alkoxy) carbonyl or a cyano group such that i) a - optionally an acid addition salt of formula IIb, wherein X "is an anion-free anion-liberated l-ethylindolo (3,2-g) indolizine derivative, an acrylic acid derivative of formula III wherein Y is halogen, R2 is the reaction product is hydrogenated by chemical reduction and, if desired, the resulting mixture is separated; for the preparation of a (C 1 -C 4) alkoxy) carbomyl group, optionally 11b from an acid addition salt of the general formula wherein X 'is the in situ release of the 1-ethylindolo [3,2-g] indolizine derivative with an acrylic acid derivative of formula IIP wherein R 1 is (C 1 -C 4 alkoxy) carbonyl; And Y is as defined below, by reacting the resulting 14,15-dihydro-H '-1-
priorityDate 1981-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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