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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-252
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-252
filingDate 1988-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1989-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a46bab678cf689957ff7b626277cec4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5085fe92aef052f5edae2c77052f11fd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20584eac8b71ba6521ce63bbc34b8fe0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_464dee99029447d6499bb6e8afb6eac2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f942afe3b08088d48ab08ca8e749dcc
publicationDate 1989-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4889926-A
titleOfInvention Method for the synthesis of (2"R)-4'-O-tetra-hydropyranyladriamycim using 14-chloro-daunomycin as an intermediate
abstract A new compound, i.e., 14-chlorodaunomycin, and its method of preparation are provided. The new compound, useful as an antitumor agent and as an intermediate in the preparation of (2"R)-4'-O-tetrahydropyranyladriamycin, is obtained by reaction of daunomycin with an alkyl ortho-formate and a brominating agent to produce a 14-bromo-13-dialkylketaldaunomycin, hydrolysis of the latter compound, then adding an excess of a solid metal/chloride to produce an acid addition salt of 14-chlorodaunomycin and concurrently salting out the latter compound from the reaction solution, followed by recovering the 14-chlorodaunomycin acid addition salt.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111675738-A
priorityDate 1987-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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