http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1223156-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-71
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-255
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filingDate 1996-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee7c0f8c766b41dec96ed73606e81d03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c476dd11a28ee8b866004c5e12dfdf04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ab46cb8be551ad351a9ee70d35049ac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6745f6950f9bbbb7f336b35242308d6a
publicationDate 2002-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1223156-A1
titleOfInvention Use of 4-substituted 2-butanones to prepare nabumetone
abstract The palladium-catalyzed coupling of aryl and vinyl halides with vinylicncompounds is disclosed. A preferred embodiment relating to the palladium catalyzed couplingnof 4-substituted and 6-substituted-2-methoxynaphthalene to form nabumetone is also disclosed.nThe beauty of this novel reaction is that methylvinylketone, normally employed by the artndirectly as-is for the preparation of nabumetone, is formed in situ . We have discovered anmechanism to take advantage of the in situ formation of methylvinylketone, thus avoiding thenuse of expensive, toxic, and unstable methyl vinyl ketone feed. This reaction may be employednfor a variety of pharmaceutically active and non-pharmaceutical compounds.
priorityDate 1995-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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