GB799343A - Preparation of steroid compounds - Google Patents
Preparation of steroid compoundsInfo
- Publication number
- GB799343A GB799343A GB23574/56A GB2357456A GB799343A GB 799343 A GB799343 A GB 799343A GB 23574/56 A GB23574/56 A GB 23574/56A GB 2357456 A GB2357456 A GB 2357456A GB 799343 A GB799343 A GB 799343A
- Authority
- GB
- United Kingdom
- Prior art keywords
- progesterone
- dione
- keto
- hydroxyhydrocortisone
- pregnadiene
- 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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
D 1,4-3-keto-steroids are obtained by contacting a 3-keto-steroid having conjugated with said keto group one A ring double bond, with selenium dioxide at an elevated temperature in an inert organic solvent. As starting compounds there may be used cortisone, hydrocortisone, progesterone, desoxycorticosterone, corticosterone, 14-hydroxycortisone, 14-hydroxyhydrocortisone, 14 - hydroxy - 15 - bromocortisone, 14,15 - dihydroxyhydrocortisone, 9a -fluorocortisone, 9a - bromohydrocorisone, D 6-progesterone, D 14 - dehydrocortisone, D 9(11)-progesterone, 9 - hydroxyhydrocortisone and esters of those compounds having a 21-hydroxy group, e.g. the benzoates, acetates, propionates, butyrates and phthalates. As solvents there may be used ethylene glycol diethers, phenetole, xylene, dioxane and naphthalene. The addition of pyridine, dimethylaniline, diethylaniline, N - propylaniline, N - propyltoluidine, or dimethyltoluidine prevents decomposition of both the starting compounds and the produc.ts Examples disclose the preparation of D 1,4-pregnadiene - 3,20 - dione - 17a ,21 - diol acetate, D 1-dehydrocortisone acetate, D 1,4 - 9 - chloro-11,17,21 - trihydroxy - pregnadiene - 3,20-dione, D 1,4 - androstadiene - 3,17 - dione, D 1,4,7,22 ergostateraene - 3 - one, and D 1,4 - cholestadiene-3-one.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US799343XA | 1955-08-05 | 1955-08-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB799343A true GB799343A (en) | 1958-08-06 |
Family
ID=22153744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23574/56A Expired GB799343A (en) | 1955-08-05 | 1956-07-31 | Preparation of steroid compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB799343A (en) |
-
1956
- 1956-07-31 GB GB23574/56A patent/GB799343A/en not_active Expired
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