GB692630A - Improvements in or relating to substituted pteridines - Google Patents
Improvements in or relating to substituted pteridinesInfo
- Publication number
- GB692630A GB692630A GB2411350A GB2411350A GB692630A GB 692630 A GB692630 A GB 692630A GB 2411350 A GB2411350 A GB 2411350A GB 2411350 A GB2411350 A GB 2411350A GB 692630 A GB692630 A GB 692630A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- hydroxy
- sec
- dione
- butyl
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D475/00—Heterocyclic compounds containing pteridine ring systems
- C07D475/06—Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4
- C07D475/08—Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4 with a nitrogen atom directly attached in position 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
The invention comprises pteridines of the general formula <FORM:0692630/IV (b)/1> wherein Y and Y1 each represent the n-propyl radical or an alkyl or cycloalkyl radical containing from 4 to 8 carbon atoms or a benzyl radical, and a process for the preparation of the above compounds by condensing 2,4,5,6-tetraamino-pyrimidine, its acetate or bisulphite with an a -diketone of the general formula <FORM:0692630/IV (b)/2> where Y and Y1 have the above significance. The reaction may be carried out in an acid or an alkaline medium such as an alkali metal carbonate, for example, sodium hydrogen carbonate, or in the presence of an organic base such as piperidine. In the examples compounds of the above general formula are prepared wherein Y and Y1 each represent the n-butyl, n-amyl, iso-butyl, n-propyl, benzyl, sec-butyl, sec-amyl and cyclohexyl radical. Di-n-hexyl-2,4-diaminopteridine is also referred to. 4 - Hydroxy - 3,6 - dimethyloctan - 5 - one is prepared by reacting ethyl sec.-valerate and sodium, and treating the reaction product with sulphuric acid. By a similar method 5-hydroxy - 4,7 - dimethyldecan - 6 - one is prepared from ethyl sec.-caproate and 2-hydroxy-1,4 - dicyclohexylbutan - 3 - one is prepared from ethyl cyclohexylacetate. 3,6 - Dimethyloctan - 4,5 - dione, 4,7 - dimethyldecan - 5,6 - dione and 1,4 - dicyclhexylbutan-2,3-dione are prepared by oxidizing the corresponding hydroxy-ketone referred to above.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2411350A GB692630A (en) | 1950-10-03 | 1950-10-03 | Improvements in or relating to substituted pteridines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2411350A GB692630A (en) | 1950-10-03 | 1950-10-03 | Improvements in or relating to substituted pteridines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB692630A true GB692630A (en) | 1953-06-10 |
Family
ID=10206573
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2411350A Expired GB692630A (en) | 1950-10-03 | 1950-10-03 | Improvements in or relating to substituted pteridines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB692630A (en) |
-
1950
- 1950-10-03 GB GB2411350A patent/GB692630A/en not_active Expired
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