GB559775A - Preparation of new sulphonamide derivatives - Google Patents
Preparation of new sulphonamide derivativesInfo
- Publication number
- GB559775A GB559775A GB180642A GB180642A GB559775A GB 559775 A GB559775 A GB 559775A GB 180642 A GB180642 A GB 180642A GB 180642 A GB180642 A GB 180642A GB 559775 A GB559775 A GB 559775A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- para
- naphthol
- benzene sulphonyl
- aminobenzene
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
559,775. Para-aminobenzene-sulphonamidonaphthalene compounds. BUTLER, G. C., LOZINSKI, E., and ODELL, A. D. Feb. 11, 1942, No. 1806. [Class 2 (iii)] Para - aminobenzene - sulphonamido naphthalene compounds are prepared by the action of a para acylamino substituted benzene sulphonyl halide on a 4-amino-1-naphthol containing an organic substituent in position - 2 followed by hydrolysis of the acylamino group. In examples (1) 2-Allyl-4-amino-1- naphthol is reacted in dioxane solution with p-acetamino-benzene sulphonyl chloride and the condensation product hydrolysed to give N-(p-aminobenzenesulphonyl)-2-allyl - 4 -amino- 1-naphthol. (2) 1-Hydroxy-4-amino-2-naphthoic acid is reacted in dioxane solution with pacetamino benzene sulphonyl chloride and the reaction product hydrolysed to give N-(paminobenzenesulphonyl)-1-hydroxy-4-amino-2- naphthoic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB180642A GB559775A (en) | 1942-02-11 | 1942-02-11 | Preparation of new sulphonamide derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB180642A GB559775A (en) | 1942-02-11 | 1942-02-11 | Preparation of new sulphonamide derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB559775A true GB559775A (en) | 1944-03-06 |
Family
ID=9728337
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB180642A Expired GB559775A (en) | 1942-02-11 | 1942-02-11 | Preparation of new sulphonamide derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB559775A (en) |
-
1942
- 1942-02-11 GB GB180642A patent/GB559775A/en not_active Expired
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