PL91826B1 - - Google Patents
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- Publication number
- PL91826B1 PL91826B1 PL1972175670A PL17567072A PL91826B1 PL 91826 B1 PL91826 B1 PL 91826B1 PL 1972175670 A PL1972175670 A PL 1972175670A PL 17567072 A PL17567072 A PL 17567072A PL 91826 B1 PL91826 B1 PL 91826B1
- Authority
- PL
- Poland
- Prior art keywords
- dione
- benzodiazepine
- dimethylphosphinylmethyl
- tetrahydro
- phenyl
- Prior art date
Links
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 3
- 239000012442 inert solvent Substances 0.000 claims description 3
- 150000007530 organic bases Chemical group 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- SXYFKXOFMCIXQW-UHFFFAOYSA-N propanedioyl dichloride Chemical compound ClC(=O)CC(Cl)=O SXYFKXOFMCIXQW-UHFFFAOYSA-N 0.000 claims description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 3
- NFCPRRWCTNLGSN-UHFFFAOYSA-N 2-n-phenylbenzene-1,2-diamine Chemical class NC1=CC=CC=C1NC1=CC=CC=C1 NFCPRRWCTNLGSN-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229940053197 benzodiazepine derivative antiepileptics Drugs 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 claims 1
- -1 1- (dimethylphosphinylmethyl) -5- (4'-methoxyphenyl) -1,2,4,5-tetrahydro -3H-1,5-benzodiazepine--2,4-dione Chemical compound 0.000 description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WJUSNAMQSJDCJF-UHFFFAOYSA-N CP(C)(CN(C(C=CC(Cl)=C1)=C1N(C1=CC=CC=C1)C(C1)=O)C1=O)=O Chemical compound CP(C)(CN(C(C=CC(Cl)=C1)=C1N(C1=CC=CC=C1)C(C1)=O)C1=O)=O WJUSNAMQSJDCJF-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 150000001557 benzodiazepines Chemical class 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- FNJLLAIBRXOHTM-UHFFFAOYSA-N 1-(dimethylphosphorylmethyl)-5-phenyl-7-(trifluoromethyl)-1,5-benzodiazepine-2,4-dione Chemical compound CP(=O)(C)CN1C(CC(N(C2=C1C=CC(=C2)C(F)(F)F)C2=CC=CC=C2)=O)=O FNJLLAIBRXOHTM-UHFFFAOYSA-N 0.000 description 1
- XNCMQRWVMWLODV-UHFFFAOYSA-N 1-phenylbenzimidazole Chemical class C1=NC2=CC=CC=C2N1C1=CC=CC=C1 XNCMQRWVMWLODV-UHFFFAOYSA-N 0.000 description 1
- SWMBNKSGZGEGRY-UHFFFAOYSA-N 6-chloro-1-phenylbenzimidazole Chemical compound C12=CC(Cl)=CC=C2N=CN1C1=CC=CC=C1 SWMBNKSGZGEGRY-UHFFFAOYSA-N 0.000 description 1
- MIZWBTZOVFDFBL-UHFFFAOYSA-N CP(=O)(C)CN1C(CC(N(C2=C1C=CC=C2)C1=CC=CC=C1)=O)=O Chemical compound CP(=O)(C)CN1C(CC(N(C2=C1C=CC=C2)C1=CC=CC=C1)=O)=O MIZWBTZOVFDFBL-UHFFFAOYSA-N 0.000 description 1
- QAOKTWYBHFEPSO-UHFFFAOYSA-N CP(C)(CCCN(C(C=CC(Cl)=C1)=C1N(C1=CC=CC=C1)C(C1)=O)C1=O)=O Chemical compound CP(C)(CCCN(C(C=CC(Cl)=C1)=C1N(C1=CC=CC=C1)C(C1)=O)C1=O)=O QAOKTWYBHFEPSO-UHFFFAOYSA-N 0.000 description 1
- YKBBNLWVMQGWHA-UHFFFAOYSA-M CP(C)(CN1C(C=CC(Cl)=C2)=C2[N+](C2=CC=CC=C2)=C1)=O.[Cl-] Chemical compound CP(C)(CN1C(C=CC(Cl)=C2)=C2[N+](C2=CC=CC=C2)=C1)=O.[Cl-] YKBBNLWVMQGWHA-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 229940049706 benzodiazepine Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- VACOMSNNWGXHSF-UHFFFAOYSA-N chloro(dimethylphosphoryl)methane Chemical compound CP(C)(=O)CCl VACOMSNNWGXHSF-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 208000020016 psychiatric disease Diseases 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000003385 ring cleavage reaction Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/53—Organo-phosphine oxides; Organo-phosphine thioxides
- C07F9/5304—Acyclic saturated phosphine oxides or thioxides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712118262 DE2118262C3 (de) | 1971-04-15 | 1,5-Benzodtazepinphosphorverbindungen, Verfahren zu ihrer Herstellung und diese enthaltende Mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL91826B1 true PL91826B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1977-03-31 |
Family
ID=5804787
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1972175670A PL91826B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-04-15 | 1972-04-14 | |
| PL1972154735A PL85047B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-04-15 | 1972-04-14 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1972154735A PL85047B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-04-15 | 1972-04-14 |
Country Status (29)
-
1971
- 1971-05-06 US US00140978A patent/US3718645A/en not_active Expired - Lifetime
- 1971-05-06 SE SE7105875A patent/SE373857B/xx unknown
- 1971-05-06 DK DK220871A patent/DK138542C/da active
- 1971-05-06 FI FI711265A patent/FI51351C/fi active
-
1972
- 1972-04-06 CS CS7200002299A patent/CS181707B2/cs unknown
- 1972-04-06 CS CS7600004994A patent/CS181744B2/cs unknown
- 1972-04-10 ES ES401632A patent/ES401632A1/es not_active Expired
- 1972-04-11 CA CA139,384A patent/CA966483A/en not_active Expired
- 1972-04-11 BG BG023632A patent/BG20373A3/xx unknown
- 1972-04-11 EG EG143/72A patent/EG10547A/xx active
- 1972-04-11 BG BG020195A patent/BG20110A3/xx unknown
- 1972-04-12 RO RO70521A patent/RO62303A/ro unknown
- 1972-04-12 CH CH1345375A patent/CH572066A5/xx not_active IP Right Cessation
- 1972-04-12 CH CH535772A patent/CH570414A5/xx not_active IP Right Cessation
- 1972-04-12 RO RO7200078192A patent/RO63622A/ro unknown
- 1972-04-12 JP JP47036826A patent/JPS5750799B1/ja active Pending
- 1972-04-13 IL IL39208A patent/IL39208A/xx unknown
- 1972-04-13 YU YU00996/72A patent/YU99672A/xx unknown
- 1972-04-13 IT IT23096/72A patent/IT1051356B/it active
- 1972-04-13 AR AR241445A patent/AR192762A1/es active
- 1972-04-13 NL NL7204983A patent/NL7204983A/xx not_active Application Discontinuation
- 1972-04-13 AU AU41084/72A patent/AU459339B2/en not_active Expired
- 1972-04-13 GB GB1710172A patent/GB1391288A/en not_active Expired
- 1972-04-14 PL PL1972175670A patent/PL91826B1/pl unknown
- 1972-04-14 SU SU1773202A patent/SU459889A3/ru active
- 1972-04-14 PL PL1972154735A patent/PL85047B1/pl unknown
- 1972-04-14 AT AT327272A patent/AT315853B/de not_active IP Right Cessation
- 1972-04-14 FR FR7213212A patent/FR2133751B1/fr not_active Expired
- 1972-04-14 HU HUHO1472A patent/HU165360B/hu unknown
- 1972-04-14 ZA ZA722518A patent/ZA722518B/xx unknown
- 1972-04-14 DD DD162308A patent/DD98677A5/xx unknown
- 1972-04-14 IE IE492/72A patent/IE36291B1/xx unknown
- 1972-04-14 BR BR722216A patent/BR7202216D0/pt unknown
- 1972-04-17 BE BE782213A patent/BE782213A/xx not_active IP Right Cessation
-
1973
- 1973-02-10 AR AR246383A patent/AR210976A1/es active
-
1978
- 1978-10-26 YU YU02501/78A patent/YU250178A/xx unknown
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