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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c3fab15895eb59644225598b1c9b9aea
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-56
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-56
filingDate 2010-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6532ea3116c469f0954f8695ae4c1d48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_606e0f4405d0b91b661cb73f32c42214
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b8ad76026455cc322bf61696b3f50d5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a46f061fe6ad25e128a11011b3362edc
publicationDate 2013-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102120733-B
titleOfInvention Preparation method of Febuxostat
abstract The invention relates to a preparation method of Febuxostat. In the preparation method, 2,4-dihalogenated phenol (a compound 1) which is cheap and is easy to obtain is used as a starting material, and the Febuxostat is synthesized by means of a new route comprising the steps of alkylation, cyaniding, sulfo-formylation, cyclization, and deprotection. The preparation method provided by the invention has a short route, and low-toxicity cuprous cyanide is used for cyaniding and virulent compounds such as potassium cyanide, sodium cyanide and the like are avoided, so that the process safety is greatly improved.
priorityDate 2010-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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