GB928552A - New heterocyclic hydrazine compounds and process for their manufacture - Google Patents
New heterocyclic hydrazine compounds and process for their manufactureInfo
- Publication number
- GB928552A GB928552A GB3608861A GB3608861A GB928552A GB 928552 A GB928552 A GB 928552A GB 3608861 A GB3608861 A GB 3608861A GB 3608861 A GB3608861 A GB 3608861A GB 928552 A GB928552 A GB 928552A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- acid addition
- trifluoromethyl
- alkoxy
- halogen
- 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
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B47/00—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase
- C06B47/02—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase the components comprising a binary propellant
- C06B47/08—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase the components comprising a binary propellant a component containing hydrazine or a hydrazine derivative
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
- C07D285/18—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines
- C07D285/20—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems
- C07D285/22—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D285/24—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with oxygen atoms directly attached to the ring sulfur atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Abstract
The invention comprises 4-hydrazino-2-H-1,2,3-benzothiadiazine-1 : 1-dioxides which are substituted in one or more of the 6-, 7- and 8-positions by alkyl, alkoxy, halogen or trifluoromethyl; their acid addition salts (including salts with methionine, tryptophan, lysine and arginine); the preparation thereof by reacting a 2 cyanobenzene-sulphonic acid chloride substituted in at least one of the 4-, 5- and 6-positions by alkyl, alkoxy, halogen or trifluoromethyl, with hydrazine hydrate, then subjecting the 2-sulphone-hydrazido-benzoic acid hydrazidine so produced to ring closure, if necessary in acid medium and, if desired, converting the resulting acid addition salt into the base or the resulting fue base into acid addition salts; and pharmaceutical compositions containing the heterocyclic hydrazines. The intermediate hydrazine may be isolated before ring closure. Pharmaceutical compositions comprise the compounds of the invention in admixture or in conjunction with a suitable pharmaceutical carrier and may be formulated as tablets, dragees, solutions, suspensions or emulsions and may contain other thereapeutically valuable substances. The compounds exhibit a sustained hyposensitive effect in addition to diuretic, adrenolytic and fungistatic effects.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1129360A CH393340A (en) | 1960-10-07 | 1960-10-07 | Process for the preparation of new 4-hydrazino-2H-1,2,3-benzothiadiazine-1,1-dioxydes |
CH884061 | 1961-07-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB928552A true GB928552A (en) | 1963-06-12 |
Family
ID=25703840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3608861A Expired GB928552A (en) | 1960-10-07 | 1961-10-06 | New heterocyclic hydrazine compounds and process for their manufacture |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB928552A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3407197A (en) * | 1966-08-10 | 1968-10-22 | Upjohn Co | 2h-1, 2, 3-benzothiadiazine-1, 1-dioxides and process for their production |
US3407198A (en) * | 1966-08-10 | 1968-10-22 | Upjohn Co | 2h-1, 2, 3-benzothiadiazine-1, 1-dioxides |
-
1961
- 1961-10-06 GB GB3608861A patent/GB928552A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3407197A (en) * | 1966-08-10 | 1968-10-22 | Upjohn Co | 2h-1, 2, 3-benzothiadiazine-1, 1-dioxides and process for their production |
US3407198A (en) * | 1966-08-10 | 1968-10-22 | Upjohn Co | 2h-1, 2, 3-benzothiadiazine-1, 1-dioxides |
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