http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2424752-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_da54f7ebbd2d9d8a82f92aca4d1b4e48
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J21-003
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J41-0088
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J41-00
filingDate 1974-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49824154d0537c8be975fba69ff8d70c
publicationDate 1975-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2424752-A1
titleOfInvention PROCESS FOR THE PRODUCTION OF STEROID SPIRO-LACTONES
abstract Steroid spirolactones of partial formula (I) e.g. 3'-(3-methoxy-1 7 beta-hydroxy-1, 3, 5-(10)-oestratriene-17-yl)-propionic acid (1' 17)-lactone, are prepd. by treating corresp. gamma-hydroxy-propionic acid dimethylamides of partial formula (II), with acidic cation exchangers. The prods. are either biologically active or are intermediates for known biologically active cpds. Thus, 3'-(17 beta-hydroxy-4-androsten-3-on17a-yl)-propio-(1' 17)-lactone may be converted by 6-dehydrogenation and reaction with thioacetic acid into the known aldosterone antagonist 3'-7 alpha-acetylthio-17 beta-hydroxy-3-oxo-4-androsten-17 alpha-yl)-propio-(1' 17)-lactone. The reaction is simple to carry out at room temp., and pure products can be isolated by simply concentrating the reaction mixt. Ketal groups used to protect keto groups during previous reactions are split off during the lactonisation, thus avoiding the need for a separate deprotection step.
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priorityDate 1974-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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