http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1010031-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J75-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J75-00
filingDate 1964-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1965-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1010031-A
titleOfInvention Improvements in or relating to the preparation of steroids
abstract A steroid 21-dialkali phosphate is obtained by treating a 21-hydroxy steroid with an organic phosphate ester in the presence of a dehydrating agent to obtain the corresponding steroid 21-organophosphate, cleaving the latter in an aqueous base to obtain the corresponding steroid 21-dialkali phosphate in aqueous solution and purifying the latter compound by selective extraction alternately with n-butanol, ether, water containing alternately hydrogen and sodium ions and freeze-drying the aqueous solution containing the 21-dialkali phosphate salt of the steroid. As organic phosphate ester there may be used an ethyl phosphate of the formula <FORM:1010031/C2/1> wherein R is hydrogen or lower alkyl and 2 is a strongly electronegative substituent, e.g. b -cyanoethyl phosphate, and as dehydrating agent a carbodiimide, e.g. dicyclohexyl carbodiimide, may be used. The preferred 21-hydroxy steroid is 6a -methylprednisolone. Pyridinium b -cyanoethyl phosphate is obtained by adding a mixture of pyridine and b -hydroxy-propionitrile to a solution of POCl3 in ether, treating the reaction mixture with barium acetate to obtain barium cyanoethyl phosphate, treating the latter with an acid ion exchange resin to obtain b -cyanoethyl phosphoric acid which with pyridine yields the desired pyridinium b -cyanoethyl phosphate.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0106115-A2
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priorityDate 1963-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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