GB851287A - 5-chlorotoluene-2:4-disulphonamide and alkali metal salts thereof - Google Patents
5-chlorotoluene-2:4-disulphonamide and alkali metal salts thereofInfo
- Publication number
- GB851287A GB851287A GB22148/58A GB2214858A GB851287A GB 851287 A GB851287 A GB 851287A GB 22148/58 A GB22148/58 A GB 22148/58A GB 2214858 A GB2214858 A GB 2214858A GB 851287 A GB851287 A GB 851287A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali metal
- disulphonamide
- chloro
- toluene
- metal salts
- 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
- 229910052783 alkali metal Inorganic materials 0.000 title abstract 3
- -1 alkali metal salts Chemical class 0.000 title abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- RCFKEIREOSXLET-UHFFFAOYSA-N disulfamide Chemical compound CC1=CC(Cl)=C(S(N)(=O)=O)C=C1S(N)(=O)=O RCFKEIREOSXLET-UHFFFAOYSA-N 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- OSOUNOBYRMOXQQ-UHFFFAOYSA-N 1-chloro-3-methylbenzene Chemical compound CC1=CC=CC(Cl)=C1 OSOUNOBYRMOXQQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 239000002934 diuretic Substances 0.000 abstract 1
- 230000001882 diuretic effect Effects 0.000 abstract 1
- 230000001452 natriuretic effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000008024 pharmaceutical diluent Substances 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/32—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of salts of sulfonic acids
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises 5-chloro-toluene-2,4-disulphonamide and alkali metal salts thereof, the preparation thereof by reacting 5-chloro-toluene-2,4-disulphonchloride with ammonia or its chemical equivalents and if desired reacting the resulting sulphonamide with an alkali metal hydroxide, and pharmaceutical preparations containing the products (see Group VI). The products have diuretic and/or natriuretic properties. 5-Chloro-toluene-2,4-disulphonchloride is prepared by reacting m-chlorotoluene with chlorosulphonic acid.ALSO:Pharmaceutical compositions comprise 5-chloro-toluene-2,4-disulphonamide or alkali metal salts thereof with pharmaceutical diluents. Preparations may be in the form of tablets and solutions.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB22148/58A GB851287A (en) | 1958-07-10 | 1958-07-10 | 5-chlorotoluene-2:4-disulphonamide and alkali metal salts thereof |
| FR837316A FR531M (en) | 1958-07-10 | 1960-08-31 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB22148/58A GB851287A (en) | 1958-07-10 | 1958-07-10 | 5-chlorotoluene-2:4-disulphonamide and alkali metal salts thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB851287A true GB851287A (en) | 1960-10-12 |
Family
ID=10174686
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22148/58A Expired GB851287A (en) | 1958-07-10 | 1958-07-10 | 5-chlorotoluene-2:4-disulphonamide and alkali metal salts thereof |
Country Status (2)
| Country | Link |
|---|---|
| FR (1) | FR531M (en) |
| GB (1) | GB851287A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1174286B (en) * | 1960-11-18 | 1964-07-23 | Kyowa Hakko Kogyo Kk | Process for the biotechnological production of 1-isoleucine |
| EP0033042A1 (en) * | 1980-01-28 | 1981-08-05 | Merck & Co. Inc. | Ophthalmic inserts for lowering intraocular pressure comprising carbonic anhydrase inhibitors |
| EP0036351A3 (en) * | 1980-03-04 | 1981-11-04 | Merck & Co. Inc. | Ophthalmic compositions of carbonic anhydrase inhibitors for topical application in the treatment of elevated intraocular pressure |
| WO2004017964A1 (en) | 2002-08-19 | 2004-03-04 | Pfizer Products Inc. | Combination therapy for hyperproliferative diseases |
| US6878703B2 (en) | 2000-11-21 | 2005-04-12 | Sankyo Company, Limited | Pharmaceutical composition |
| WO2007062314A2 (en) | 2005-11-23 | 2007-05-31 | Bristol-Myers Squibb Company | Heterocyclic cetp inhibitors |
| WO2008070496A2 (en) | 2006-12-01 | 2008-06-12 | Bristol-Myers Squibb Company | N- ( (3-benzyl) -2, 2- (bis-phenyl) -propan-1-amine derivatives as cetp inhibitors for the treatment of atherosclerosis and cardiovascular diseases |
| EP2392567A1 (en) | 2005-10-21 | 2011-12-07 | Bristol-Myers Squibb Company | Benzothiazine derivatives and their use as lxr modulators |
| WO2014170786A1 (en) | 2013-04-17 | 2014-10-23 | Pfizer Inc. | N-piperidin-3-ylbenzamide derivatives for treating cardiovascular diseases |
| WO2015012205A1 (en) | 2013-07-23 | 2015-01-29 | 第一三共株式会社 | Medicine for preventing or treating hypertension |
| WO2016055901A1 (en) | 2014-10-08 | 2016-04-14 | Pfizer Inc. | Substituted amide compounds |
| WO2020150473A2 (en) | 2019-01-18 | 2020-07-23 | Dogma Therapeutics, Inc. | Pcsk9 inhibitors and methods of use thereof |
-
1958
- 1958-07-10 GB GB22148/58A patent/GB851287A/en not_active Expired
-
1960
- 1960-08-31 FR FR837316A patent/FR531M/fr active Active
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1174286B (en) * | 1960-11-18 | 1964-07-23 | Kyowa Hakko Kogyo Kk | Process for the biotechnological production of 1-isoleucine |
| EP0033042A1 (en) * | 1980-01-28 | 1981-08-05 | Merck & Co. Inc. | Ophthalmic inserts for lowering intraocular pressure comprising carbonic anhydrase inhibitors |
| EP0036351A3 (en) * | 1980-03-04 | 1981-11-04 | Merck & Co. Inc. | Ophthalmic compositions of carbonic anhydrase inhibitors for topical application in the treatment of elevated intraocular pressure |
| US6878703B2 (en) | 2000-11-21 | 2005-04-12 | Sankyo Company, Limited | Pharmaceutical composition |
| WO2004017964A1 (en) | 2002-08-19 | 2004-03-04 | Pfizer Products Inc. | Combination therapy for hyperproliferative diseases |
| EP2392567A1 (en) | 2005-10-21 | 2011-12-07 | Bristol-Myers Squibb Company | Benzothiazine derivatives and their use as lxr modulators |
| WO2007062314A2 (en) | 2005-11-23 | 2007-05-31 | Bristol-Myers Squibb Company | Heterocyclic cetp inhibitors |
| WO2008070496A2 (en) | 2006-12-01 | 2008-06-12 | Bristol-Myers Squibb Company | N- ( (3-benzyl) -2, 2- (bis-phenyl) -propan-1-amine derivatives as cetp inhibitors for the treatment of atherosclerosis and cardiovascular diseases |
| WO2014170786A1 (en) | 2013-04-17 | 2014-10-23 | Pfizer Inc. | N-piperidin-3-ylbenzamide derivatives for treating cardiovascular diseases |
| WO2015012205A1 (en) | 2013-07-23 | 2015-01-29 | 第一三共株式会社 | Medicine for preventing or treating hypertension |
| WO2016055901A1 (en) | 2014-10-08 | 2016-04-14 | Pfizer Inc. | Substituted amide compounds |
| WO2020150473A2 (en) | 2019-01-18 | 2020-07-23 | Dogma Therapeutics, Inc. | Pcsk9 inhibitors and methods of use thereof |
| EP4470609A2 (en) | 2019-01-18 | 2024-12-04 | Astrazeneca AB | Pcsk9 inhibitors and methods of use thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| FR531M (en) | 1961-05-23 |
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