http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S60222496-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P5-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-585
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J51-00
filingDate 1984-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0e8aeca64aef36694cd29e4760de040
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa0f786a6c2b6c2f23907f73fb8bae55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa636d60c41d1e14feb94ef4bc3c5175
publicationDate 1985-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S60222496-A
titleOfInvention Steroid derivative having aldosterone antagonism
abstract NEW MATERIAL:A compound shown by the formula I (X is hydroxy, Y is alkali metallic salt of carboxyethyl, or X and Y together with neighboring carbon atom form lactone ring shown by the formula II). n EXAMPLE: 17-Hydroxy-6β-,7β-methylene-3-oxo-17α-pregna-1, 4, 11-triene-21-carboxylic acid.γ-lactone. n USE: A hypotensive diuretic. Useful for remedying hypertension, renal edema, etc. n PREPARATION: 3-17-Bis(ethylene dioxide)-androsta-5,11-diene as a starting raw material is deketalized, reacted with a secondary amine to give enamine shown by the formula III, which is processed into a compound shown by the formula IV, to give a halohydrin shown by the formula V. The compound shown by the formula V is processed into an allyl alcohol derivative, and converted into a silyl ether. Then, β-methylene group is introduced to the compound shown by the formula VI, the prepared silyl ether is processed into a hydroxyl compound, and oxidized, to give the desired substance. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1984-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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