GB718640A - Cyclopentanophenanthrene compounds and a process for the manufacture thereof - Google Patents
Cyclopentanophenanthrene compounds and a process for the manufacture thereofInfo
- Publication number
- GB718640A GB718640A GB11010/52A GB1101052A GB718640A GB 718640 A GB718640 A GB 718640A GB 11010/52 A GB11010/52 A GB 11010/52A GB 1101052 A GB1101052 A GB 1101052A GB 718640 A GB718640 A GB 718640A
- Authority
- GB
- United Kingdom
- Prior art keywords
- allopregnan
- triol
- dione
- carboxylic acid
- aliphatic carboxylic
- 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
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises 21-aliphatic carboxylic acid esters and 3,21-dialiphatic carboxylic acid esters of allopregnan-3b ,17a ,21-triol-11,20-dione, a process for the preparation of the 21-monoesters by hydrogenating the corresponding 21-esters of allopregnan-17a ,21-diol-3,11,20-trione in the presence of Raney nickel catalyst, and a process for the preparation of the 3,21-diesters by acylating the 21-monoesters with an aliphatic carboxylic acid anhydride. The ester radicals may be derived from aliphatic carboxylic acids containing not more than 6 carbon atoms. The reduction is preferably carried out in an inert solvent, e.g. a mixture of dioxane and alcohol, by shaking with Raney nickel in an atmosphere of hydrogen. The esterification step is preferably carried out with an esterification catalyst, e.g. pyridine. In the example, allopregnan - 3b ,17a ,21 - triol - 11,20 - dione 21 - acetate and allopregnan - 3b ,17a ,21 - triol - 11,20 - dione 3,21 - diacetate are prepared. Specification 712,058 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US718640XA | 1951-05-09 | 1951-05-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB718640A true GB718640A (en) | 1954-11-17 |
Family
ID=22104091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB11010/52A Expired GB718640A (en) | 1951-05-09 | 1952-05-01 | Cyclopentanophenanthrene compounds and a process for the manufacture thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB718640A (en) |
-
1952
- 1952-05-01 GB GB11010/52A patent/GB718640A/en not_active Expired
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