NO810721L - Fremgangsmaate for fremstilling av n,n-dimetyl(aza-1-bicyklo(2,2,2)oktyl-3)-10-10h-fenotiazinsulfonamid-2 - Google Patents
Fremgangsmaate for fremstilling av n,n-dimetyl(aza-1-bicyklo(2,2,2)oktyl-3)-10-10h-fenotiazinsulfonamid-2Info
- Publication number
- NO810721L NO810721L NO810721A NO810721A NO810721L NO 810721 L NO810721 L NO 810721L NO 810721 A NO810721 A NO 810721A NO 810721 A NO810721 A NO 810721A NO 810721 L NO810721 L NO 810721L
- Authority
- NO
- Norway
- Prior art keywords
- aza
- bicyclo
- formula
- benzenesulfonamide
- bromo
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 title abstract description 4
- 238000002360 preparation method Methods 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims abstract description 17
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 5
- -1 alkali metal amide Chemical class 0.000 claims abstract description 4
- RHLVCLIPMVJYKS-UHFFFAOYSA-N ethyl n-pentyl ketone Natural products CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 10
- 238000009835 boiling Methods 0.000 claims description 8
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- 239000000010 aprotic solvent Substances 0.000 claims description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
- 150000002466 imines Chemical class 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000012429 reaction media Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 239000012024 dehydrating agents Substances 0.000 claims description 2
- 238000006798 ring closing metathesis reaction Methods 0.000 claims 3
- 238000007363 ring formation reaction Methods 0.000 abstract description 5
- 210000004051 gastric juice Anatomy 0.000 abstract description 2
- 239000003112 inhibitor Substances 0.000 abstract description 2
- 230000028327 secretion Effects 0.000 abstract description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 54
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000008346 aqueous phase Substances 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000002198 insoluble material Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 238000010533 azeotropic distillation Methods 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- 229910000102 alkali metal hydride Inorganic materials 0.000 description 1
- 150000008046 alkali metal hydrides Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8100442A FR2497806A1 (fr) | 1981-01-13 | 1981-01-13 | Nouveau procede de preparation du n,n-dimethyl (aza-1 bicyclo (2,2,2) octyl-3)-10 10h-phenothiazinesulfonamide-2 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO810721L true NO810721L (no) | 1982-07-14 |
Family
ID=9254052
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO810721A NO810721L (no) | 1981-01-13 | 1981-03-03 | Fremgangsmaate for fremstilling av n,n-dimetyl(aza-1-bicyklo(2,2,2)oktyl-3)-10-10h-fenotiazinsulfonamid-2 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4482711A (el) |
| EP (1) | EP0056201B1 (el) |
| JP (1) | JPS57123179A (el) |
| AR (1) | AR226096A1 (el) |
| AT (1) | ATE14733T1 (el) |
| AU (1) | AU537401B2 (el) |
| CA (1) | CA1152067A (el) |
| DE (1) | DE3171646D1 (el) |
| DK (1) | DK109381A (el) |
| ES (1) | ES8205221A1 (el) |
| FI (1) | FI810591L (el) |
| FR (1) | FR2497806A1 (el) |
| GR (1) | GR77287B (el) |
| HU (1) | HU182307B (el) |
| IL (1) | IL62304A (el) |
| MA (1) | MA19089A1 (el) |
| NO (1) | NO810721L (el) |
| PT (1) | PT72667B (el) |
| ZA (1) | ZA811440B (el) |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2909521A (en) * | 1959-10-20 | Phenthiazine derivatives | ||
| CA611405A (en) * | 1960-12-27 | M. Jacob Robert | Phenthiazine derivatives and their preparation | |
| DE1047202B (de) * | 1955-11-23 | 1958-12-24 | Rhone Poulenc Sa | Verfahren zur Herstellung des 10-[2',4'-Bis(dimethylamino)-butyl-(1')]-phenthiazins |
| NL295220A (el) * | 1962-07-19 | |||
| US3534053A (en) * | 1967-05-24 | 1970-10-13 | American Home Prod | Quinuclidine derivatives |
| US3987042A (en) * | 1969-03-03 | 1976-10-19 | Claude Gueremy | Phenothiazine derivative |
| GB1250534A (el) * | 1969-03-03 | 1971-10-20 | ||
| US3563995A (en) * | 1969-04-17 | 1971-02-16 | Ian Wellings | Alkyl esters of 1-azabicyclo(2.2.2)oct-2-ene-3-(4 - chloro-3-sulfamoylanilino)-2-carboxylic acid |
| FR2318638A2 (fr) * | 1975-07-25 | 1977-02-18 | Sogeras | Nouveaux derives de la phenothiazine et procede pour leur preparation |
-
1981
- 1981-01-13 FR FR8100442A patent/FR2497806A1/fr active Granted
- 1981-02-20 DE DE8181400261T patent/DE3171646D1/de not_active Expired
- 1981-02-20 EP EP81400261A patent/EP0056201B1/fr not_active Expired
- 1981-02-20 AT AT81400261T patent/ATE14733T1/de not_active IP Right Cessation
- 1981-02-25 FI FI810591A patent/FI810591L/fi not_active Application Discontinuation
- 1981-03-02 ES ES499984A patent/ES8205221A1/es not_active Expired
- 1981-03-03 NO NO810721A patent/NO810721L/no unknown
- 1981-03-04 ZA ZA00811440A patent/ZA811440B/xx unknown
- 1981-03-05 MA MA19293A patent/MA19089A1/fr unknown
- 1981-03-05 IL IL62304A patent/IL62304A/xx unknown
- 1981-03-06 CA CA000372504A patent/CA1152067A/fr not_active Expired
- 1981-03-10 DK DK109381A patent/DK109381A/da unknown
- 1981-03-11 AR AR284583A patent/AR226096A1/es active
- 1981-03-13 AU AU68361/81A patent/AU537401B2/en not_active Ceased
- 1981-03-16 PT PT72667A patent/PT72667B/pt unknown
- 1981-03-17 HU HU81675A patent/HU182307B/hu unknown
- 1981-03-23 JP JP56042245A patent/JPS57123179A/ja active Pending
- 1981-03-27 GR GR64514A patent/GR77287B/el unknown
-
1982
- 1982-08-02 US US06/404,116 patent/US4482711A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| MA19089A1 (fr) | 1981-10-01 |
| DE3171646D1 (en) | 1985-09-12 |
| HU182307B (en) | 1983-12-28 |
| ATE14733T1 (de) | 1985-08-15 |
| AU537401B2 (en) | 1984-06-21 |
| AU6836181A (en) | 1982-07-22 |
| EP0056201B1 (en) | 1985-08-07 |
| IL62304A (en) | 1984-06-29 |
| FI810591L (fi) | 1982-07-14 |
| PT72667B (fr) | 1982-06-15 |
| US4482711A (en) | 1984-11-13 |
| CA1152067A (fr) | 1983-08-16 |
| IL62304A0 (en) | 1981-05-20 |
| JPS57123179A (en) | 1982-07-31 |
| FR2497806B1 (el) | 1983-06-10 |
| AR226096A1 (es) | 1982-05-31 |
| ZA811440B (en) | 1982-03-31 |
| PT72667A (fr) | 1981-04-01 |
| EP0056201A1 (fr) | 1982-07-21 |
| DK109381A (da) | 1982-07-14 |
| ES499984A0 (es) | 1982-06-01 |
| FR2497806A1 (fr) | 1982-07-16 |
| ES8205221A1 (es) | 1982-06-01 |
| GR77287B (el) | 1984-09-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DK173703B1 (da) | Fremgangsmåder til fremstilling af henholdsvis D,L-(threo)- og D-(treo)-1-aryl-2-acylamido-3-fluor-1-propanoler | |
| NO151876B (no) | Fremgangsmaate og anordning for foring av dyr | |
| NO178396B (no) | Forbedret fremgangsmåte for fremstilling av substituerte indolonderivater og mellomprodukter i fremstillingen derav | |
| NO166712B (no) | Fremgangsmaate ved fremstilling av pyrrolidonderivater. | |
| CA2960473A1 (en) | Processes for the preparation of tadalafil and intermediates thereof | |
| NO810721L (no) | Fremgangsmaate for fremstilling av n,n-dimetyl(aza-1-bicyklo(2,2,2)oktyl-3)-10-10h-fenotiazinsulfonamid-2 | |
| NO761796L (el) | ||
| Ishikawa et al. | Reactions of perfluoro-2-methyl-2-pentene and octafluoroisobutylene with arylamines. | |
| SU639441A3 (ru) | Способ получени мета-бензоилгидратроповой кислоты или ее соли со вторичным амином | |
| US3983162A (en) | Optical resolution of alkyl esters of DL-phenylalanine | |
| CA1088539A (en) | Process for the preparation of 5-(2-chlorobenzyl)-4,5, 6,7-tetrahydrothieno ¬3,2-c| pyridine | |
| NO149353B (no) | Fremgangsmaate ved fremstilling av 6-klor-alfa-metylkarbazol-2-eddiksyre | |
| US2806034A (en) | 3-(heterocyclic-substituted alkyl) thianaphthenes and salts thereof | |
| KR20020035857A (ko) | 인돌 유도체 또는 그의 염의 제조방법 | |
| NO115704B (el) | ||
| US3454626A (en) | Racemic monocarboxylic acid resolution using dehydroabietylamine | |
| CA2028953A1 (en) | Process for the preparation of quinazoline derivatives | |
| US4656289A (en) | 1,3-dibenzyl-4-halohexahydro-1H-thieno[3,4-d]imidazol-2(3H)-one intermediates | |
| NO148372B (no) | Fremgangsmaate til fremstilling av bromheksin. | |
| KR860001878B1 (ko) | 피라졸 유도체의 제법 | |
| SU656511A3 (ru) | Способ получени производных гексагидро-4-индолинола или их солей | |
| NO154635B (no) | Fremgangsmaate for fremstilling av terapeutisk aktive ergotalkaloider. | |
| US4299968A (en) | Novel thiophene compounds | |
| CN117551038A (zh) | 一种硼酸促进4-溴-7-甲基-1h-吲唑关环制备的合成方法 | |
| NO852794L (no) | 9- og 11-substituerte apovincaminsyrederivater og fremgangsmaate for deres fremstilling |