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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J75-00
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filingDate 1968-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_865ad8e79f568720a5568fa5d29ab147
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d073994752a4b870013b2295ebec36ca
publicationDate 1971-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-514564-A
titleOfInvention Process for making 9B, 10x steroids
abstract Steroids of formula (I) R = a 3-keto-DELTA4-, 3-keto-DELTA4,6-, 3-keto-DELTA1,4-, 3-keto-DELTA1,4,6-, 3-alkoxy-DELTA3,5-, 3-alkoxy-DELTA4,6-, 3-acyloxy-DELTA3,5-, 3-acyloxy-DELTA4,6-, 3-acyloxy-DELTA2,4,6- or 3-hydroxy-DELTA4,6-system. R' = H or acyl (I) have hormonal, esp. progestative, activity and in animal experiments have an effect on gonadotropin levels and display antiestrogenic activity; they can be used e.g. for regulating the menstrual cycle. (a) By treating (II) with a reducing agent: (b) By treating (III) with a chlorinating agent: (where R3 = a 3-acyloxy-DELTA3,5-, 3-alkoxy-DELTA3,5- or 3-keto-DELTA4,6-system). (c) (I; R' = H, R = 3-hydroxy-DELTA4,6) can be partially oxidised to (I; R' = H, R = 3-keto-DELTA4,6); (I; R = 3-keto-DELTA4 or 3-keto-DELTA4,6) can be dehydrogenated in at least one of the positions 1 (2) and 6(7); the 20-hydroxy group of (I; R' = H, R = 3-keto-DELTA4, 3-keto-DELTA1,4, 3-keto-DELTA4,6 or 3-keto-DELTA1,4,6) can be acylated; the acyloxy group of (I ; R' = acyl, R = 3-keto-DELTA4, 3-keto-DELTA1,4, 3-keto-DELTA4,6 or 3-keto-DELTA1,4,6) can be saponified; a free hydroxy group in (I; R = 3-hydroxy-DELTA4,6) can be acylated; the 3-hydroxy group in (I; R = 3-hydroxy-DELTA4,6) can be alkylated; (I; R = 3-keto-DELTA4) can be enol-etherified; and (I; R = 3-keto-DELTA4 or 3-keto-DELTA4,6) can be enolesterified.
priorityDate 1968-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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