http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103073613-A

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_33bc06c3426a944a9ca92d281bcb7784
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J31-00
filingDate 2012-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5569cfb6a8e2cbecdffdf5fc4e86a342
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94130228764cba4c7f7208f70371e3d3
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publicationDate 2013-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103073613-A
titleOfInvention A kind of synthetic method of fluticasone derivative
abstract The invention discloses a method for synthesizing fluticasone derivatives represented by formula (I). The compound represented by formula (II) is subjected to decarboxylation and fluorination under the action of a monovalent metal silver salt catalyst and a selective fluorination reagent. The substitution reaction produces fluticasone derivatives as shown in formula (I). The traditional preparation of propionic acid (furoic acid) fluticasone (I) is generally obtained from (III) by condensation of bromofluoromethane, but bromofluoromethane has high cost, high toxicity and serious environmental hazards. The reagents used in the invention are relatively cheap and easy to obtain, with little environmental pollution, mild reaction conditions, good selectivity and high reaction yield.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111662353-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111751455-A
priorityDate 2012-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8049021-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102219638-A
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Total number of triples: 25.