GB880548A - Dihydro-benzo-thia-diazepine-dioxide and derivatives thereof - Google Patents
Dihydro-benzo-thia-diazepine-dioxide and derivatives thereofInfo
- Publication number
- GB880548A GB880548A GB3901758A GB3901758A GB880548A GB 880548 A GB880548 A GB 880548A GB 3901758 A GB3901758 A GB 3901758A GB 3901758 A GB3901758 A GB 3901758A GB 880548 A GB880548 A GB 880548A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dihydro
- dioxide
- aminobenzylsulphonamide
- benzothiadiazepine
- reaction
- 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
- C07D285/36—Seven-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Abstract
The invention comprises 1,3-dihydro-2,3,5-benzothiadiazepine-2,2-dioxides of the formula <FORM:0880548/IV (b)/1> wherein X is hydrogen or a halogen (e.g. 1,3-dihydro - 2, 3, 5 - benzothiadiazepine - 2; 2 - dioxide and its 8-bromo-derivative) and their preparation by heating a 2-aminobenzylsulphonamide with ethyl orthoformate at 100 DEG C to 130 DEG C, in an inert organic solvent boiling at a higher temperature than that of the reaction, while continuously distilling off the ethanol evolved. 2-Aminobenzylsulphonamide and its halo derivatives used as starting materials are made by treating a 2-nitrobenzyl sulphonyl chloride (obtained by reaction of 2-nitrobenzyl chloride with thiourea and chlorination of the resulting addition product) with ammonia in an inert anhydrous organic solvent and reducing the resulting 2-nitrobenzylsulphonamide by hydrogenation at room temperature and atmospheric pressure, in the presence of a palladium on charcoal catalyst.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3901758A GB880548A (en) | 1958-12-03 | 1958-12-03 | Dihydro-benzo-thia-diazepine-dioxide and derivatives thereof |
CH8061059A CH374079A (en) | 1958-12-03 | 1959-11-13 | Process for the preparation of new heterocyclic compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3901758A GB880548A (en) | 1958-12-03 | 1958-12-03 | Dihydro-benzo-thia-diazepine-dioxide and derivatives thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
GB880548A true GB880548A (en) | 1961-10-25 |
Family
ID=10407091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3901758A Expired GB880548A (en) | 1958-12-03 | 1958-12-03 | Dihydro-benzo-thia-diazepine-dioxide and derivatives thereof |
Country Status (2)
Country | Link |
---|---|
CH (1) | CH374079A (en) |
GB (1) | GB880548A (en) |
-
1958
- 1958-12-03 GB GB3901758A patent/GB880548A/en not_active Expired
-
1959
- 1959-11-13 CH CH8061059A patent/CH374079A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CH374079A (en) | 1963-12-31 |
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