GB569140A - Sulphanilamide derivative - Google Patents
Sulphanilamide derivativeInfo
- Publication number
- GB569140A GB569140A GB963243A GB963243A GB569140A GB 569140 A GB569140 A GB 569140A GB 963243 A GB963243 A GB 963243A GB 963243 A GB963243 A GB 963243A GB 569140 A GB569140 A GB 569140A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetal
- aminobenzenesulphonamidopyrimidine
- ethoxyacrolein
- aminobenzenesulphonyl
- guanidine
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/69—Benzenesulfonamido-pyrimidines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
2-Para-aminobenzenesulphonamidopyrimidine is prepared by reacting p-aminobenzenesulphonyl guanidine with an acetal of b -alkoxyacrolein. Suitable acetals are the diethyl acetal, the dimethyl acetal of b -ethoxyacrolein, and also the acetals of b -methoxyacrolein and b -propyloxy-acrolein. In an example, b -ethoxyacrolein diethyl acetal is heated with p-aminobenzenesulphonyl-guanidine in amyl alcohol-glacial acetic acid solution. The ethyl alcohol liberated is evaporated off and the residue extracted with aqueous caustic soda. On acidification, crude 2-p-aminobenzenesulphonamidopyrimidine separated and is purified by recrystallisation. Specification 552,887 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB963243A GB569140A (en) | 1943-06-16 | 1943-06-16 | Sulphanilamide derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB963243A GB569140A (en) | 1943-06-16 | 1943-06-16 | Sulphanilamide derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
GB569140A true GB569140A (en) | 1945-05-07 |
Family
ID=9875728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB963243A Expired GB569140A (en) | 1943-06-16 | 1943-06-16 | Sulphanilamide derivative |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB569140A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3037977A (en) * | 1958-10-25 | 1962-06-05 | Basf Ag | Production of compounds of the pyrimidine series |
-
1943
- 1943-06-16 GB GB963243A patent/GB569140A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3037977A (en) * | 1958-10-25 | 1962-06-05 | Basf Ag | Production of compounds of the pyrimidine series |
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