http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2409571-C2

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-337
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D305-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2006-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b617a29f87b0fdfc12a5d7f3f8493f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1a5cb22ab6995f3d42ff93eb5b3629d
publicationDate 2011-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2409571-C2
titleOfInvention Method of cleaning 10-deacetylbaccatine iii from 10-deacetyl-2-debenzoyl-2-pentenoylbaccatine iii
abstract FIELD: chemistry. n SUBSTANCE: invention relates to a method of obtaining 10-deacetylbaccatine III with purity of over 99%, which does not contain 10-deacetyl-2-debenzoyl-2-pentenoylbaccatine III. The disclosed method includes: a) treating crude 10-deacetylbaccatine III with an activated derivative of trichloroacetic acid; b) carrying out chromatography on silica gel and elution of 7,10-bis-trichloroacetyl-10-deacetylbaccatine III with dichloromethane or a dichloromethane/ethylacetate mixture; and c) treatment of 10-deacetyl-7,10-bis-trichloroacetylbaccatine III with an alkali followed by crystallisation. The invention also relates to production of paclitaxel, which involves production of 10-deacetylbaccatine III using the disclosed method and its subsequent conversion to N-debenzoylpaclitaxel with its subsequent benzoylation. n EFFECT: convenient semi-synthesis of anti-tumour agents with a taxane backbone, which enables to avoid laborious methods of removing corresponding 2-debenzoyl-2-pentenoyl analogues. n 7 cl, 1 tbl, 3 ex
priorityDate 2005-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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