http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1401815-A1

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filingDate 2002-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c212d99fcecd9c476b10677b57d55c75
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0523e8b564e8ecc56e34dca6de6a32ff
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publicationDate 2004-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1401815-A1
titleOfInvention Process for the preparation of a highly pure pharmaceutical intermediate, 4-(cyclopropylcarbonyl)-alpha,alpha-dimethylphenyl acetic acid
abstract This invention relates to a novel process to obtain hoghly pure 4-(cyclopropylcarbonyl)-α,α-dimethylphenylacetic acid of Formula I through crystallization from a mixture of para and meta regioisomers of Formula I and II in cyclohexane, whereby the amount of undesired meta isomer, 3-(cyclopropylcarbonyl)-α,$g)a)-dimethylphenylacetic acid of Formula II is decreased to below 0.5%. The compound of Formula I is a key intermediate for the preparation of high purity terfenadine carboxylate, which is a known antihistaminic.
priorityDate 2001-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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