GB685331A - Improvements in cyclopentanophenanthrene derivatives and process for producing the same - Google Patents
Improvements in cyclopentanophenanthrene derivatives and process for producing the sameInfo
- Publication number
- GB685331A GB685331A GB21136/50A GB2113650A GB685331A GB 685331 A GB685331 A GB 685331A GB 21136/50 A GB21136/50 A GB 21136/50A GB 2113650 A GB2113650 A GB 2113650A GB 685331 A GB685331 A GB 685331A
- Authority
- GB
- United Kingdom
- Prior art keywords
- allopregnane
- dione
- producing
- same
- collidine
- 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
Allopregnane - 17a - ol - 3,20 - dione is produced by treating allopregnane-3b , 17a -diol-20-one with an amide of the formula <FORM:0685331/IV (b)/1> where R is an aromatic or aliphatic radical and X is a bromine or chlorine atom. D 1,2-allopregnene-17a -ol-3,20-dione is obtained from allopregnane-17a -ol-3,20-dione by treating with bromine to produce 2-bromo-allopregnane-17a -ol-3,20-dione and dehydrobrominating. The first step of the reaction may be effected with bromacetamide, bromotoluene-sulphonamide, bromophthalimide, bromosuccimide or chlorosuccimide in the presence of pyridine, collidine, lutidine or diethyl aniline. Dehydrobromination can be effected with collidine, pyridine, lutidine or diethyl aniline.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US685331XA | 1949-09-19 | 1949-09-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB685331A true GB685331A (en) | 1952-12-31 |
Family
ID=22083169
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB21136/50A Expired GB685331A (en) | 1949-09-19 | 1950-08-25 | Improvements in cyclopentanophenanthrene derivatives and process for producing the same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB685331A (en) |
-
1950
- 1950-08-25 GB GB21136/50A patent/GB685331A/en not_active Expired
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