http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2476676-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B57-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-20
filingDate 2010-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ffe33f60cbb0c9a146571fabd5c491f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_606e0f4405d0b91b661cb73f32c42214
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98f540506b68b6240809ad3cc5a62d71
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b8ad76026455cc322bf61696b3f50d5
publicationDate 2012-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2476676-A1
titleOfInvention S-5-substituent-n-2'-(thiophene-2-yl)ethyl-tetralin-2-amine or chiral acid salts thereof and use for preparing rotigotine
abstract The chiral compound S-5-substituted-N-2-(thienyl-2-yl-)ethyl-tetralin-2-amine or its chiral acid salts and preparation method thereof are disclosed, and the method for preparing Rotigotine by using the chiral compound is also disclosed. Racemic 5-substituted-N-2'-(thien-2-yl-)ethyl-tetralin-2-amine (compound 1 ) is resolved by using a conventional chiral acid to obtain an optically pure chiral acid salt of S-5-substituted-N,2'-(thien-2-yl-)ethyl-tetralin-2-amine, which is then dissociated to obtain S-5-substituted-N-2'-(thien-2-yl-)ethyl-tetralin-2-amine (compound 2 ). The compound 2 or chiral acid salt thereof is alkylated and deprotected to produce rotigotine (compound 5 ).
priorityDate 2009-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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