GB754845A - Improvements in or relating to pteridines - Google Patents
Improvements in or relating to pteridinesInfo
- Publication number
- GB754845A GB754845A GB651454A GB651454A GB754845A GB 754845 A GB754845 A GB 754845A GB 651454 A GB651454 A GB 651454A GB 651454 A GB651454 A GB 651454A GB 754845 A GB754845 A GB 754845A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amyl
- acid
- prepared
- indoxyl
- refluxing
- 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
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises 2,4-diamino-11-n-amyl-indols-(21,31-6,7) -pteridine and the preparation thereof by condensing 5-nitroso-2,4,6-triaminopyrimidine with an N-n-amyl-O-acyl-indoxyl in solution or suspension in a solvent in the presence of an acid binding condensing agent. In an example 2,4-diamino-11-n - amyl - indolo - (21,31 - 6,7) - pteridine is prepared using N - n - amyl - O - acetyl - indoxyl for reaction with the substituted pyrimidine in the presence of piperidine as the condensing agent. N - n - amyl - anthranilic acid is prepared by refluxing anthranilic acid, n-amyl iodide, potassium carbonate and water. N - n - amyl - N - phenyl - glycine - 2 - carboxylic acid is prepared by refluxing N-n-amylanthranilic acid, monochloroacetic acid, sodium carbonate and water. N - n - amyl - O - acetyl - indoxyl is prepared by refluxing N - n - amyl - N - phenyl - glycine-2-carboxylic acid, sodium acetate and acetic anhydride in the presence of a few drops of concentrated sulphuric acid. Other N-n-amyl-O-acyl-indoxyls may be prepared by a similar method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB651454A GB754845A (en) | 1954-03-05 | 1954-03-05 | Improvements in or relating to pteridines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB651454A GB754845A (en) | 1954-03-05 | 1954-03-05 | Improvements in or relating to pteridines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB754845A true GB754845A (en) | 1956-08-15 |
Family
ID=9815899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB651454A Expired GB754845A (en) | 1954-03-05 | 1954-03-05 | Improvements in or relating to pteridines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB754845A (en) |
-
1954
- 1954-03-05 GB GB651454A patent/GB754845A/en not_active Expired
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