GB997150A - A process for the purification of 4,6-dimethyl-2-sulfanilamidopyrimidine - Google Patents
A process for the purification of 4,6-dimethyl-2-sulfanilamidopyrimidineInfo
- Publication number
- GB997150A GB997150A GB2969463A GB2969463A GB997150A GB 997150 A GB997150 A GB 997150A GB 2969463 A GB2969463 A GB 2969463A GB 2969463 A GB2969463 A GB 2969463A GB 997150 A GB997150 A GB 997150A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sodium hydroxide
- dimethyl
- sulphadimidine
- decolourized
- sodium
- 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
4,6 - Dimethyl - 2 - sulphanilamidopyrimidine (sulphadimidine) is purified by adding to a filtered, decolourized aqueous solution of the crude product (synthesized by known methods and subsequently separated as the sodium salt by addition to the reaction mixture of dilute sodium hydroxide) sodium hydroxide until a sodium hydroxide concentration of 21-22% is attained, followed by cooling to precipitate substantially completely sodium sulphadimidine, which is then separated, dissolved in water, decolourized and treated with mineral acid to precipitate the desired product.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL295796D NL295796A (en) | 1963-07-26 | ||
GB2969463A GB997150A (en) | 1963-07-26 | 1963-07-26 | A process for the purification of 4,6-dimethyl-2-sulfanilamidopyrimidine |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2969463A GB997150A (en) | 1963-07-26 | 1963-07-26 | A process for the purification of 4,6-dimethyl-2-sulfanilamidopyrimidine |
Publications (1)
Publication Number | Publication Date |
---|---|
GB997150A true GB997150A (en) | 1965-07-07 |
Family
ID=10295624
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2969463A Expired GB997150A (en) | 1963-07-26 | 1963-07-26 | A process for the purification of 4,6-dimethyl-2-sulfanilamidopyrimidine |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB997150A (en) |
NL (1) | NL295796A (en) |
-
0
- NL NL295796D patent/NL295796A/xx unknown
-
1963
- 1963-07-26 GB GB2969463A patent/GB997150A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NL295796A (en) |
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