http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102887934-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f593503a63e122fc0c61002f0c1bc9b7
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J53-00
filingDate 2012-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5a9993602aa5ad559ad3a0c901fe2b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0c3d3bebd5d83890640428240149bed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9040163d30d86b012b5c14ab4c23817f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_402397f078bc4b23cc97c64fb7719a05
publicationDate 2015-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102887934-B
titleOfInvention Preparation method of drospirenone
abstract The invention discloses a preparation method of drospirenone, which aims at solving the problems of high production cost, low yield, and poor product quality in the existing preparation method of the drospirenone. The preparation method comprises the steps of: taking 3beta, 5-dyhydroxy-15beta, 16beta-methylene-5beta-androstane-6 alkene-17-ketone as materials, firstly, reacting with diiodomethane and zinc-copper couple, introducing 6beta and 7beta cyclopropane structures, then orderly carrying out condensation reaction and esterification reaction in THF (tetrahydrofuran) solution of lithium metal and 3-methyl bromopropionate and DMF (dimethyl formamide) solution of sodium ethoxide, finally oxidizing by sodium hypochlorite, and dewatering the toluenesulfonic acid to obtain the drospirenone. According to the preparation method, the efficiency is high, the production cost is low, by-products are few, special demands on production equipment do not exist, the reaction condition is mild, the process is stable, the operation is convenient, the environment is prevented from being damaged, and the large-scale industrial production is facilitated. The product obtained by the method is stable in quality, high in yield and purity and free of purification.
priorityDate 2012-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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