http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S57139098-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J7-00
filingDate 1981-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38670ef1339793e0feb67c054fca5682
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2e71b2ccb8fac6dbf0139ac76f1dc9e
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publicationDate 1982-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S57139098-A
titleOfInvention Preparation of intermediate for preparing corticoid
abstract PURPOSE: To obtain the titled intermediate for preparing adrenocortical hormones in short steps, by bringing a novel dihalogenated steroid obtained from androsta-4,9(11)-diene-3,17-dione, etc. into contact with a metallic powder, e.g. zinc or iron. n CONSTITUTION: A novel dihalogenated steroid, e.g. 17α-dihydroxy-21,21-dibromopregna-1,4-diene-3,20-dione 17-acetate, of formulaI(the dotted line is single or double bond; X is halogen; Y is acyloxy) obtained from androsta-4,9(11)-diene- 3,17-dione easily derived from 9α-hydroxyandrost-4-ene-3,17-dione as a raw material is brought into contact with a metallic powder, e.g. zinc or iron, in a molar amount of preferably 5W20 times that of the dihalogenated steroid to give the aimed pregnane steroid of formula II. n USE: Useful as a leuteohormone itself. n COPYRIGHT: (C)1982,JPO&Japio
priorityDate 1981-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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