GB686135A - Improvements in cyclopentanophenanthrene derivatives and process for producing the same - Google Patents
Improvements in cyclopentanophenanthrene derivatives and process for producing the sameInfo
- Publication number
- GB686135A GB686135A GB21137/50A GB2113750A GB686135A GB 686135 A GB686135 A GB 686135A GB 21137/50 A GB21137/50 A GB 21137/50A GB 2113750 A GB2113750 A GB 2113750A GB 686135 A GB686135 A GB 686135A
- Authority
- GB
- United Kingdom
- Prior art keywords
- allopregnane
- producing
- same
- diol
- amide
- 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
2 - Halo - allopregnane - 17a - ol - 3,20 - dione having the formula <FORM:0686135/IV (b)/1> wherein X is a chlorine or bromine atom, is produced by reacting allopregnane-3b ,17a -diol-20-one with an amide having the formula <FORM:0686135/IV (b)/2> wherein R is an aromatic or aliphatic radical and X is a chlorine or bromine atom, in the proportion of 1 mol. of allopregnane-3b , 17 a -diol-20-one to 2 mols. of the amide. As amides there may be used bromacetamide, bromotoluenesulphonamide, bromophthalimide, bromosuccinimide or chlorosuccinimide and the reaction is effected in a suitable solvent, e.g. tertiary-butyl alcohol. Specification 685,331 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US686135XA | 1949-09-19 | 1949-09-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB686135A true GB686135A (en) | 1953-01-21 |
Family
ID=22083646
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB21137/50A Expired GB686135A (en) | 1949-09-19 | 1950-08-25 | Improvements in cyclopentanophenanthrene derivatives and process for producing the same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB686135A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3057859A (en) * | 1959-06-09 | 1962-10-09 | British Drug Houses Ltd | 4alpha-methyl-3-oxo-5alpha-steroids and a method for preparation of same |
-
1950
- 1950-08-25 GB GB21137/50A patent/GB686135A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3057859A (en) * | 1959-06-09 | 1962-10-09 | British Drug Houses Ltd | 4alpha-methyl-3-oxo-5alpha-steroids and a method for preparation of same |
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