GB850424A - 6-methyl steroid compounds - Google Patents
6-methyl steroid compoundsInfo
- Publication number
- GB850424A GB850424A GB2135059A GB2135059A GB850424A GB 850424 A GB850424 A GB 850424A GB 2135059 A GB2135059 A GB 2135059A GB 2135059 A GB2135059 A GB 2135059A GB 850424 A GB850424 A GB 850424A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dione
- methyl
- hours
- organic solvent
- inert organic
- 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
- C07J43/00—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton
-
- 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
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
-
- 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 6a : dimethylpregna-4 : 16-dien-3 : 20-dione and 6a -methyl-16a : 17a -(21 : 31-diazacyclopent-21-eno)-pregn-4 ene-3 : 20-dione, and the preparation of the former by reacting 6a -methyl-pregna-4 : 16-diene-3 : 20-dione with diazomethane to yield the diaza compound and then thermally decomposing this. The first process is preferably performed in an inert organic solvent such as diethyl ether and the reaction mixture allowed to stand at room temperature for periods of 16 to 40 hours. The thermal decomposition is advantageously performed at reflux temperature in an inert organic solvent of b.p. approximately the same as the m.p. of the diaza compound for a duration of 3 to 5 hours, suitable solvents being dibutyl ether, p-cymene and ethylene glycol. An example is given.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH7512359A CH377810A (en) | 1958-07-09 | 1959-06-30 | Process for the preparation of 6a, 16-dimethylpregna-4,16-diene-3,20-dione |
GB2135059A GB850424A (en) | 1959-07-09 | 1959-07-09 | 6-methyl steroid compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2135059A GB850424A (en) | 1959-07-09 | 1959-07-09 | 6-methyl steroid compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB850424A true GB850424A (en) | 1960-10-05 |
Family
ID=10161410
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2135059A Expired GB850424A (en) | 1958-07-09 | 1959-07-09 | 6-methyl steroid compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB850424A (en) |
-
1959
- 1959-07-09 GB GB2135059A patent/GB850424A/en not_active Expired
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