GB810264A - Manufacture of a 17-hydroxysteroid - Google Patents
Manufacture of a 17-hydroxysteroidInfo
- Publication number
- GB810264A GB810264A GB3857/56A GB385756A GB810264A GB 810264 A GB810264 A GB 810264A GB 3857/56 A GB3857/56 A GB 3857/56A GB 385756 A GB385756 A GB 385756A GB 810264 A GB810264 A GB 810264A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- per
- pregnene
- acid
- acetylamine
- 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
D 5 - 17 a - Hydroxy - pregnene - ol - (3b ) - one-(20) is prepared by oxidizing D 5 : 17(20)-pregnadiene - ol - (3b ) - acylamine - (20) - acylate with an organic per-acid to form 17,20-oxido- D 5 - pregnene - ol - (3b ) - acetylamine - (20) - acylate which is then hydrolysed. Suitable organic per-acids are aromatic per-acids such as perbenzoic and monoperphthalic acids and saturated aliphatic per-acids such as performic, peracetic and persuccinic acids. The per-acid may be formed in situ by the addition of a peroxide, for example, sodium or barium peroxide, to the corresponding organic acid, or a mixture of hydrogen peroxide and glacial acetic acid may be used. The hydrolysis may be carried out with dilute alkalies such as dilute sodium or potassium hydroxide solution. In the example D 5 - 17a - hydroxy - pregnene - ol - (3b ) - one - (20) is prepared from D 5 : 17(20)-pregnadiene-ol -(3b ) - acetylamine - (20) - acetate, the intermediate compound being 17 : 20-oxido- D 5 - pregnene - ol - (3b ) - acetylamine - (20) - acetate. Specification 780,970 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE810264X | 1955-02-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB810264A true GB810264A (en) | 1959-03-11 |
Family
ID=6724237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3857/56A Expired GB810264A (en) | 1955-02-07 | 1956-02-07 | Manufacture of a 17-hydroxysteroid |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB810264A (en) |
-
1956
- 1956-02-07 GB GB3857/56A patent/GB810264A/en not_active Expired
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