SU461502A3 - Способ получени 1-арил-3н-1, 4-бензодиазепин-2,5-(1н,4н)дионов - Google Patents
Способ получени 1-арил-3н-1, 4-бензодиазепин-2,5-(1н,4н)дионовInfo
- Publication number
- SU461502A3 SU461502A3 SU1955543A SU1955543A SU461502A3 SU 461502 A3 SU461502 A3 SU 461502A3 SU 1955543 A SU1955543 A SU 1955543A SU 1955543 A SU1955543 A SU 1955543A SU 461502 A3 SU461502 A3 SU 461502A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- aryl
- benzodiazepin
- obtaining
- dyons
- diones
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- GOPYZMJAIPBUGX-UHFFFAOYSA-N [O-2].[O-2].[Mn+4] Chemical class [O-2].[O-2].[Mn+4] GOPYZMJAIPBUGX-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 229940053197 benzodiazepine derivative antiepileptics Drugs 0.000 description 1
- 125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- -1 nitro, amino Chemical group 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2165311A DE2165311A1 (de) | 1971-12-29 | 1971-12-29 | Neue 1-aryl-3h-1,4-benzodiazepin2,5-(1h,4h)-dione |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU461502A3 true SU461502A3 (ru) | 1975-02-25 |
Family
ID=5829591
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1955543A SU461502A3 (ru) | 1971-12-29 | 1972-12-20 | Способ получени 1-арил-3н-1, 4-бензодиазепин-2,5-(1н,4н)дионов |
| SU1860137*7A SU452098A3 (ru) | 1971-12-29 | 1972-12-20 | Способ получени 1-арил-3н-1,4 -бензодиазепин-2,5-(1н,4н)-дионов |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1860137*7A SU452098A3 (ru) | 1971-12-29 | 1972-12-20 | Способ получени 1-арил-3н-1,4 -бензодиазепин-2,5-(1н,4н)-дионов |
Country Status (23)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1319144C (en) * | 1986-11-14 | 1993-06-15 | Quirico Branca | Tetrahydronaphthalene derivatives |
| RU2687556C1 (ru) * | 2018-12-24 | 2019-05-15 | Акционерное общество "Федеральный научно-производственный центр "Алтай" | Способ получения 7-хлор-1,3-дигидро-1-метил-5-фенил-2Н-1,4-бензодиазепин-2-она |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT280290B (de) * | 1967-11-24 | 1970-04-10 | Boehringer Sohn Ingelheim | Verfahren zur Herstellung von neuen 1-Phenyl-4-alkyl-3H-1,4-benzodiazepin-2,5-[1H,4H]-dionen |
-
0
- BE BE793460D patent/BE793460A/xx unknown
-
1971
- 1971-12-29 DE DE2165311A patent/DE2165311A1/de active Pending
-
1972
- 1972-12-19 AT AT228574*1A patent/AT324345B/de not_active IP Right Cessation
- 1972-12-19 AT AT1080772A patent/AT327912B/de not_active IP Right Cessation
- 1972-12-19 RO RO7200073207A patent/RO62852A/ro unknown
- 1972-12-20 SU SU1955543A patent/SU461502A3/ru active
- 1972-12-20 SU SU1860137*7A patent/SU452098A3/ru active
- 1972-12-21 DK DK641872AA patent/DK129655B/da unknown
- 1972-12-26 BG BG022240A patent/BG19805A3/xx unknown
- 1972-12-26 JP JP47129704A patent/JPS4885587A/ja active Pending
- 1972-12-26 BG BG025578A patent/BG20375A3/xx unknown
- 1972-12-27 CH CH1887672A patent/CH587830A5/xx not_active IP Right Cessation
- 1972-12-27 CH CH250676A patent/CH583208A5/xx not_active IP Right Cessation
- 1972-12-27 ZA ZA729073A patent/ZA729073B/xx unknown
- 1972-12-27 DD DD168055*A patent/DD106384A5/xx unknown
- 1972-12-27 ES ES410057A patent/ES410057A1/es not_active Expired
- 1972-12-28 PL PL1972175731A patent/PL84244B1/pl unknown
- 1972-12-28 GB GB5988172A patent/GB1395772A/en not_active Expired
- 1972-12-28 FI FI3686/72A patent/FI54920C/fi active
- 1972-12-28 CA CA160,145A patent/CA1028702A/en not_active Expired
- 1972-12-28 PL PL1972159831A patent/PL85284B1/pl unknown
- 1972-12-28 SE SE7217089A patent/SE405120B/xx unknown
- 1972-12-28 NO NO4808/72A patent/NO138089C/no unknown
- 1972-12-28 HU HUBO5306A patent/HU165306B/hu unknown
- 1972-12-28 IL IL41198A patent/IL41198A/en unknown
- 1972-12-29 NL NL7217795A patent/NL7217795A/xx not_active Application Discontinuation
- 1972-12-29 FR FR7247013A patent/FR2166204B1/fr not_active Expired
- 1972-12-29 IE IE1805/72A patent/IE37815B1/xx unknown
-
1974
- 1974-04-16 ES ES425329A patent/ES425329A1/es not_active Expired
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