GB803062A - Improved method for preparation of 3, 4-dimethyl-5-sulfanilamido-isoxazole - Google Patents
Improved method for preparation of 3, 4-dimethyl-5-sulfanilamido-isoxazoleInfo
- Publication number
- GB803062A GB803062A GB3602/57A GB360257A GB803062A GB 803062 A GB803062 A GB 803062A GB 3602/57 A GB3602/57 A GB 3602/57A GB 360257 A GB360257 A GB 360257A GB 803062 A GB803062 A GB 803062A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dimethyl
- isoxazole
- chlorosulphonylphenyl
- water
- amidophosphoryl
- 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
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/14—Nitrogen atoms
- C07D261/16—Benzene-sulfonamido isoxazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
3 : 4 - Dimethyl - 5 - sulphanilamido - isoxazole (p - chlorosulphonylphenyl) - amidophosphoryldichloride, ClSO2.C6H4.NH.POCl2, with 3 : 4-dimethyl - 5 - amino - isoxazole, in the presence of water and hydrolysing the product by heating in an acid medium. The condensation reaction is preferably carried out in the presence of a tertiary organic base and in the presence of a water-miscible solvent. In examples: (1) 3 : 4 - dimethyl - 5 - aminoisoxazole, dissolved in acetone containing a minor amount of water, is treated with moist (p-chlorosulphonylphenyl) amidophosphoryl dichloride and the reaction product is heated with hydrochloric acid to give 3 : 4 - dimethyl - 5 - sulphanilamido - isoxazole; and (2) the process of (1) is carried out using pyridine as a condensing agent in the first stage. Starting materials. p-(Chlorosulphonylphenyl)-amidophosphoryl dichloride is made by the action of phosphorus pentachloride on sulphanilic acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT803062X | 1956-12-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB803062A true GB803062A (en) | 1958-10-15 |
Family
ID=11316915
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3602/57A Expired GB803062A (en) | 1956-12-22 | 1957-02-01 | Improved method for preparation of 3, 4-dimethyl-5-sulfanilamido-isoxazole |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB803062A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5226952A (en) * | 1991-05-17 | 1993-07-13 | Pechiney Electrometallurgie | Nitride process for refining calcium |
-
1957
- 1957-02-01 GB GB3602/57A patent/GB803062A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5226952A (en) * | 1991-05-17 | 1993-07-13 | Pechiney Electrometallurgie | Nitride process for refining calcium |
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