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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-06
filingDate 1996-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71b283d89c8b7276d6142b5baede3c32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3386b61e3a6b952d25acc3d003da7e7e
publicationDate 2001-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2162085-C2
titleOfInvention Method of preparing enantiomerically pure imidazolyl compounds, enantiomerically pure acid addition salt of imidazolyl and d-or l-pyroglutamic acid, and hydrochloride monohydrate of enantiomerically pure imidazolyl compounds
abstract FIELD: biochemistry. SUBSTANCE: described is method of preparing enantiomerically pure imidazolyl of general formula I: , enantiomerically pure addition salt of imidazolyl and hydrochloride monohydrate of enantiomerically pure imidazolyl compound of general formula I wherein R 1 is as defined above. The resulting compounds have biological activity with respect to 5HT antagonists. EFFECT: more efficient preparation method. 18 cl, 5 ex
priorityDate 1995-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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