GB956592A - Improvements in or relating to trifluoromethyl-1,4-benzodiazepine derivatives - Google Patents
Improvements in or relating to trifluoromethyl-1,4-benzodiazepine derivativesInfo
- Publication number
- GB956592A GB956592A GB1301161A GB1301161A GB956592A GB 956592 A GB956592 A GB 956592A GB 1301161 A GB1301161 A GB 1301161A GB 1301161 A GB1301161 A GB 1301161A GB 956592 A GB956592 A GB 956592A
- Authority
- GB
- United Kingdom
- Prior art keywords
- trifluoromethyl
- alkyl
- general formula
- acid addition
- halogen atom
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/74—Quinazolines; Hydrogenated quinazolines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
- C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
- C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
- C07D243/20—Nitrogen atoms
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 compounds of the general formula: <FORM:0956592/C2/1> (wherein R1 is a hydrogen atom or a C1-4 alkyl, C2-4 alkenyl, hydroxy-C1-4 alkyl, C1-4 alkoxy-C1-4 alkyl, benzyl or phenethyl group, R2 is a hydrogen atom or a C1-4 alkyl group, and R3 is a hydrogen or halogen atom or a trifluoromethyl, methyl or methoxy group) and pharmaceutically-acceptable acid addition salts thereof, and their preparation by reacting a trifluoromethylquinazoline of the general formula <FORM:0956592/C2/2> (wherein X is a halogen atom) with R1NH2, optionally followed by acid addition salt formation. The processes of the examples are summarized in the following reaction scheme: The compounds of the invention have central nervous system activity and are useful as ataractic, antidepressant and tranquilizing agents; they also have anticonvulsant and muscle relaxant activity. <FORM:0956592/C2/3> The trifluoromethyl-substituted o-aminobenzophenone starting materials are prepared (a) from the corresponding trifluoromethyl-o-nitroaniline via the trifluoromethyl-o-nitrobenzonitrile and trifluoromethyl-o-aminobenzonitrile, or (b) by the following process: <FORM:0956592/C2/4>
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US2338660A | 1960-04-20 | 1960-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB956592A true GB956592A (en) | 1964-04-29 |
Family
ID=21814782
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1301161A Expired GB956592A (en) | 1960-04-20 | 1961-04-11 | Improvements in or relating to trifluoromethyl-1,4-benzodiazepine derivatives |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1445134A1 (en) |
GB (1) | GB956592A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2034577A1 (en) * | 1969-02-28 | 1970-12-11 | Upjohn Co | |
US3649617A (en) * | 1970-07-20 | 1972-03-14 | Upjohn Co | 2-substituted amino-5-phenyl-3h-1 4-benzodiazepines |
-
1961
- 1961-04-11 GB GB1301161A patent/GB956592A/en not_active Expired
- 1961-04-20 DE DE19611445134 patent/DE1445134A1/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2034577A1 (en) * | 1969-02-28 | 1970-12-11 | Upjohn Co | |
US3649617A (en) * | 1970-07-20 | 1972-03-14 | Upjohn Co | 2-substituted amino-5-phenyl-3h-1 4-benzodiazepines |
Also Published As
Publication number | Publication date |
---|---|
DE1445134A1 (en) | 1968-10-24 |
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