GB908737A - 6-oxygenated pregnane compounds - Google Patents
6-oxygenated pregnane compoundsInfo
- Publication number
- GB908737A GB908737A GB2088460A GB2088460A GB908737A GB 908737 A GB908737 A GB 908737A GB 2088460 A GB2088460 A GB 2088460A GB 2088460 A GB2088460 A GB 2088460A GB 908737 A GB908737 A GB 908737A
- Authority
- GB
- United Kingdom
- Prior art keywords
- steroids
- hydrogen
- formula
- group
- ch3b
- 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)
- Steroid Compounds (AREA)
Abstract
The invention comprises (1) a process for the preparation of steroids of the formula <FORM:0908737/IV (b)/1> (wherein R11 is an acyl group containing up to 10 carbon atoms, R is oxygen, a hydroxyl group and a hydrogen atom or a hydroxyl group and a methyl or ethyl group, and R1 is two hydrogen atoms or a methylidene or ethylidene group) by reacting steroids of the formula <FORM:0908737/IV (b)/2> (where R is hydrogen, methyl or ethyl) with an organic peracid in an inert organic solvent, to give the 6-hydroxy-steroids and, if desired, when R is hydrogen, oxidizing these to the 6-keto-steroids; and (2) steroids of the first formula above having the following values for R, R1 and R11:- (a) R=a CH3b OH, R1=H2, R11=Ac; (b) R=a OHb CH3, R1=H2, R11=Ac; (c) R=a Hb OH, R1=CH2, R11=Ac; (d) R=a CH3b OH, R1=CH2, R11=Ac; and (e) R=O, R1=CH2, R11=Ac. Examples are given. Steroids of the second formula above are prepared by treating the corresponding pregn-4-en-3-ones with acetic anhydride in presence of toluene-p-sulphonic acid. U.S.A. Specification 2,889,342 is referred to. p
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2088460A GB908737A (en) | 1960-06-14 | 1960-06-14 | 6-oxygenated pregnane compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2088460A GB908737A (en) | 1960-06-14 | 1960-06-14 | 6-oxygenated pregnane compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB908737A true GB908737A (en) | 1962-10-24 |
Family
ID=10153382
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2088460A Expired GB908737A (en) | 1960-06-14 | 1960-06-14 | 6-oxygenated pregnane compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB908737A (en) |
-
1960
- 1960-06-14 GB GB2088460A patent/GB908737A/en not_active Expired
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