GB881627A - N-(ú=-chlorobenzenesulphonyl)-n-(ú=-dimethylaminophenyl) urea, and its preparation - Google Patents
N-(ú=-chlorobenzenesulphonyl)-n-(ú=-dimethylaminophenyl) urea, and its preparationInfo
- Publication number
- GB881627A GB881627A GB40077/59A GB4007759A GB881627A GB 881627 A GB881627 A GB 881627A GB 40077/59 A GB40077/59 A GB 40077/59A GB 4007759 A GB4007759 A GB 4007759A GB 881627 A GB881627 A GB 881627A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dimethylaminophenyl
- urea
- chlorobenzenesulphonyl
- preparation
- alkali
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/64—Sulfonylureas, e.g. glibenclamide, tolbutamide, chlorpropamide
-
- 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
- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
- C07C311/52—Y being a hetero atom
- C07C311/54—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea
-
- 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
- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
- C07C311/52—Y being a hetero atom
- C07C311/54—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea
- C07C311/57—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings
- C07C311/60—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings having nitrogen atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises: N-(p-chlorobenzenesulphonyl)-N1-(p-dimethylaminophenyl) -urea and its alkali metal salts; pharmaceutical compositions containing them (see Group VI); and the preparation of N-(p-chlorobenzenesulphonyl)-N1-(p-dimethylaminophenyl)-urea by reacting p-chlorobenzenesulphonamide, or an alkali metal salt thereof, with p-dimethylaminophenyl isocyanate, or with an N,N-diaryl-N1-(p-dimethylaminophenyl)-urea, or with an aryl-N-(p-dimethylaminophenyl)-carbamate or -thiocarbamate. Other standard methods of preparation are also outlined. p-Chlorobenzenesulphonamide may be prepared by ammonolysis of the corresponding sulphochloride, and may be converted into alkali or alkaline-earth metal salts by the action of basic alkali and alkaline-earth metal compounds.ALSO:Pharmaceutical compositions for the oral treatment of diabetes comprise N-(p-chlorobenzenesulphonyl) - N1 - (p - dimethylaminophenyl)-urea or an alkali metal salt thereof, in admixture with a pharmaceutically acceptable carrier or diluent. They may take the form of capsules, tablets, lozenges, troches, aqueous suspensions or elixirs.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB40077/59D GB922696A (en) | 1959-11-25 | 1959-11-25 | Improvements in or relating to calculating devices |
FR844600A FR1280670A (en) | 1959-11-25 | 1960-11-22 | Multiplication factor calculator with predetermined values |
CH1306760A CH383040A (en) | 1959-11-25 | 1960-11-22 | Accounting facility |
DEN19238A DE1183283B (en) | 1959-11-25 | 1960-11-24 | Booking or similar calculating machine with electrical constant factor multiplication |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US77618558A | 1958-11-25 | 1958-11-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB881627A true GB881627A (en) | 1961-11-08 |
Family
ID=25106700
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB40077/59A Expired GB881627A (en) | 1958-11-25 | 1959-11-25 | N-(ú=-chlorobenzenesulphonyl)-n-(ú=-dimethylaminophenyl) urea, and its preparation |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1283825B (en) |
FR (1) | FR285M (en) |
GB (1) | GB881627A (en) |
-
1959
- 1959-11-25 DE DEP23945A patent/DE1283825B/en active Pending
- 1959-11-25 GB GB40077/59A patent/GB881627A/en not_active Expired
-
1960
- 1960-08-25 FR FR836748A patent/FR285M/en active Active
Also Published As
Publication number | Publication date |
---|---|
DE1283825B (en) | 1968-11-28 |
FR285M (en) | 1961-03-13 |
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