GB893723A - Cyclopentanophenanthrene derivatives and process for their production - Google Patents
Cyclopentanophenanthrene derivatives and process for their productionInfo
- Publication number
- GB893723A GB893723A GB22880/58A GB2288058A GB893723A GB 893723 A GB893723 A GB 893723A GB 22880/58 A GB22880/58 A GB 22880/58A GB 2288058 A GB2288058 A GB 2288058A GB 893723 A GB893723 A GB 893723A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- keto
- hydroxy
- androsten
- acyloxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes for the preparation of steroids in general
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
Abstract
The invention comprises 11a -methyl-11b -hydroxy steroids of the general formula <FORM:0893723/IV (b)/1> wherein X is a D 4 : 5 bond or a saturated 4 : 5 a -linkage R is keto, or a - or b -hydroxy or acyloxy, R1 is keto, b -hydroxy or acyloxy, or b -hydroxy together with an a -methyl group, the acyloxy groups being derived from hydrocarbon carboxylic acids of less than 12 carbon atoms, with the proviso that R1 is not keto when R is keto; also 3-n-pyrrolidyl-11a - methyl - D 3,5 - androstadien-11b -ol-17-one and the corresponding 17-methyl-17b -ol compound, together with a process for the preparation of compounds of the above general formula by reacting the corresponding 11-keto compounds with methyl lithium, preferably under nitrogen and in ethereal solution. Detailed examples illustrate the invention and include the preparation of the acetate, propionate cyclopentylpropionate and benzoate esters. 11a - Methyl - D 4 - androsten - 11b - ol - 3, 17 - dione required as an intermediate is prepared by reacting 3, 17 - bis - ethylenedioxy - D 5 - androsten-11-one with methyl lithium and treating the resulting 11a -methyl-3,17-bis-ethylenedioxy-D 5 -androsten-11b -ol with p-toluene sulphonic acid in acetone or with acetic acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MX893723X | 1957-07-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB893723A true GB893723A (en) | 1962-04-11 |
Family
ID=19743143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22880/58A Expired GB893723A (en) | 1957-07-20 | 1958-07-16 | Cyclopentanophenanthrene derivatives and process for their production |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB893723A (en) |
-
1958
- 1958-07-16 GB GB22880/58A patent/GB893723A/en not_active Expired
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