http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SE-324563-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e737b999245afb461a9a9e552e8f3a1e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J75-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J1-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J75-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J1-00 |
| filingDate | 1966-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9179821ac84ac8f3e1be6efe7feab81c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a95d94cf61697aa3cecd42195964aaf |
| publicationDate | 1970-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SE-324563-B |
| abstract | Novel steroids having in the 17-position the structure <FORM:1074369/C2/1> (wherein R is C1- 5 alkyl; and R1 is H, methyl, ethyl or tetrahydropyranyl) are prepared by alkylation under anhydrous conditions of a metal derivative of the corresponding 17a -butadiynyl-17b -OR1 steroids. This process may be effected with an alkali metal derivative and an alkyl halide. The alkali metal derivative may conveniently be formed by adding a solution of the steroid in tetrahydrofuran to the amide of the alkali metal in liquid ammonia, and when in this method a molar ratio of sodamide to a 17-hydroxy-steroid not less than about 2:1 is used the hydroxy group is alkylated as well as the butadiynyl group; while with equimolar quantities a mixture of products is obtained which can be separated by thin layer chromatography and/or fractional crystallization. 17b -tetrahydropyranyloxy products may be acid hydrolysed to the free 17b -ols, which may be alkylated. The steroids may belong to the androstane or 19-nor-androstane (estrane) series and may optionally contain substituents and/or double bonds in the steroid nucleus, such as D 1, D 2, D 3, D 4, D 5, D 5(10), D 6, D 7, D 8, D 9, D 9(11), D 11 and D 14 double bonds, hydroxyl at positions 1, 3, 4, 5, 6 and 11, or acyloxy group, alkyl or alkenyl at positions 1, 2, 4, 6, 7 or 16, and carbonyl at positions 2, 3, 6, 11 and 12. Hydroxy groups may be alkylated during the process unless protected as tetrahydropyranyloxy groups; acyloxy groups may be hydrolysed; and carbonyl groups may interfere with the process and are preferably protected by conversion to ketals. Products containing a D 2,5(10)-3-alkoxy grouping may be hydrolysed directly or via the D 5(10)-3-ones to the D 4-3-ones, and D 3,5-3-enol ethers may be hydrolysed to the D 4-3-ones as may D 5-3-ketals. 3b ,17b - bis - (Tetrahydro - 21 - pyranyloxy) - 17a - butadiynyl - androst - 5 - ene is prepared from the diol and dihydropyran. 17b -(Tetrahydro - 21 - pyranyloxy) - 17a - butadiynyl - 4 - methyl - estra - 1,3,5(10) - triene, 17a - butadiynyl - 3 - methoxy - 17b - (tetrahydro - 21 - pyranyloxy) - estra - 1,3,5(10) - triene, a mixture of D 5- and D 5(10) - 17a - butadiynyl - 17b - (tetrahydro - 21 - pyranyloxy) - 3 - ethylenedioxy - 19 - nor-androstene (the parent 17b -ols of which are prepared from the D 4-3-one and ethyleneglycol), 17a - butadiynyl - 17b - (tetrahydro - 21 - pyranyloxy) - 3 - ethylenedioxy - androst - 5 - ene (the parent 17b -ol of which is prepared from the D 4-3-one and ethyleneglycol), and 17a -butadiynyl-3,17b - bis(tetrahydro - 21 - pyranyloxy) - estra-1,3,5(10)-triene are prepared similarly. The steroids of the invention, which may possess estrogenic, progestational, claudogenic, ovulation-inhibiting and gonadotrophin-inhibiting properties, may be administered as tablets, pills, injections or vaginal tampons. |
| priorityDate | 1965-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.