DD139581A5 - Verfahren zur herstellung neuer 4-phenyl-thieno-eckige klammer auf 2,3-c eckige klammer zu-piperidine - Google Patents
Verfahren zur herstellung neuer 4-phenyl-thieno-eckige klammer auf 2,3-c eckige klammer zu-piperidine Download PDFInfo
- Publication number
- DD139581A5 DD139581A5 DD78208420A DD20842078A DD139581A5 DD 139581 A5 DD139581 A5 DD 139581A5 DD 78208420 A DD78208420 A DD 78208420A DD 20842078 A DD20842078 A DD 20842078A DD 139581 A5 DD139581 A5 DD 139581A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- thieno
- hydrogen
- general formula
- item
- carbon atoms
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 13
- 238000002360 preparation method Methods 0.000 title description 5
- 150000003053 piperidines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000000460 chlorine Substances 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
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- 239000002253 acid Substances 0.000 claims description 8
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- 150000003839 salts Chemical class 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
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- 150000002431 hydrogen Chemical class 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
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- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
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- 239000002244 precipitate Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 210000003568 synaptosome Anatomy 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- PUGUQINMNYINPK-UHFFFAOYSA-N tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCN(C(=O)CCl)CC1 PUGUQINMNYINPK-UHFFFAOYSA-N 0.000 description 1
- 230000001519 thymoleptic effect Effects 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772746443 DE2746443C2 (de) | 1977-10-15 | 1977-10-15 | 4-Phenyl-thieno-[2,3-c]-piperidine, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zusammensetzungen |
| DE19782833378 DE2833378A1 (de) | 1978-07-29 | 1978-07-29 | Neue 4-phenyl-thieno-eckige klammer auf 2,3-c eckige klammer zu -piperidine, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zusammensetzungen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD139581A5 true DD139581A5 (de) | 1980-01-09 |
Family
ID=25772905
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD78208420A DD139581A5 (de) | 1977-10-15 | 1978-10-12 | Verfahren zur herstellung neuer 4-phenyl-thieno-eckige klammer auf 2,3-c eckige klammer zu-piperidine |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US4322423A (cs) |
| JP (1) | JPS5470296A (cs) |
| AT (1) | AT368504B (cs) |
| AU (1) | AU522759B2 (cs) |
| BG (1) | BG28715A3 (cs) |
| CA (1) | CA1113095A (cs) |
| CH (1) | CH644126A5 (cs) |
| CS (1) | CS204036B2 (cs) |
| DD (1) | DD139581A5 (cs) |
| DK (1) | DK150158C (cs) |
| ES (1) | ES474218A1 (cs) |
| FI (1) | FI63942C (cs) |
| FR (1) | FR2405948A1 (cs) |
| GB (1) | GB2007219B (cs) |
| GR (1) | GR65251B (cs) |
| HU (1) | HU176486B (cs) |
| IE (1) | IE47455B1 (cs) |
| IL (1) | IL55727A (cs) |
| IT (1) | IT1109215B (cs) |
| LU (1) | LU80366A1 (cs) |
| NL (1) | NL7810307A (cs) |
| NO (1) | NO151324C (cs) |
| NZ (1) | NZ188645A (cs) |
| PL (1) | PL126597B1 (cs) |
| PT (1) | PT68656A (cs) |
| RO (1) | RO75532A (cs) |
| SE (1) | SE442510B (cs) |
| SU (1) | SU718011A3 (cs) |
| YU (1) | YU240178A (cs) |
| ZA (1) | ZA785769B (cs) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2927294A1 (de) * | 1979-07-06 | 1981-01-08 | Boehringer Sohn Ingelheim | Neue 4-phenyl-4,5,6,7-tetrahydropyrrolo eckige klammer auf 2,3-c eckige klammer zu pyridine, verfahren zu ihrer herstellung und pharmazeutische zusammensetzungen |
| US4282227A (en) * | 1980-05-22 | 1981-08-04 | Smithkline Corporation | Renal vasodilating 3,4-dihydroxyphenyltetrahydrothienopyridines |
| DD210278A5 (de) * | 1982-03-05 | 1984-06-06 | Boehringer Ingelheim Kg | Verfahren zur herstellung neuer basisch substituierter 4-phenyl-4,5,6,7-tetrahydro-thieno-(2,3-c)pyridine |
| IL71661A0 (en) * | 1983-04-27 | 1984-07-31 | Boehringer Ingelheim Kg | 4-phenyl-tetrahydro-furano-pyridines,their preparation and pharmaceutical compositions containing them |
| US4572911A (en) * | 1984-08-02 | 1986-02-25 | Mcneilab, Inc. | Hexahydroindolinzine compounds, pharmaceutical compositions and methods and intermediates |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3651068A (en) * | 1969-11-13 | 1972-03-21 | Colgate Palmolive Co | Derivatives of 1 2 3 4-tetrahydrobenzothieno(2 3-c)pyridines |
| FR2315274A1 (fr) * | 1975-06-27 | 1977-01-21 | Parcor | Nouveaux derives de la thieno (2,3-c) pyridine, leur preparation et leurs applications |
| FR2358150A1 (fr) * | 1976-07-13 | 1978-02-10 | Parcor | Nouvelles thieno (2,3-c) et (3,2-c) pyridines, leur procede de preparation et leur application |
| GB1576511A (en) * | 1977-03-29 | 1980-10-08 | Parcor | Thieno(2,3 - c) and (3,2 - c) pyridines process for their preparation and therapeutic applications thereof |
-
1978
- 1978-10-03 AT AT0710978A patent/AT368504B/de not_active IP Right Cessation
- 1978-10-05 GR GR57383A patent/GR65251B/el unknown
- 1978-10-10 RO RO7895375A patent/RO75532A/ro unknown
- 1978-10-10 SU SU782673554A patent/SU718011A3/ru active
- 1978-10-11 CH CH1056578A patent/CH644126A5/de not_active IP Right Cessation
- 1978-10-12 DD DD78208420A patent/DD139581A5/de unknown
- 1978-10-12 YU YU02401/78A patent/YU240178A/xx unknown
- 1978-10-13 LU LU80366A patent/LU80366A1/de unknown
- 1978-10-13 PL PL1978210271A patent/PL126597B1/pl unknown
- 1978-10-13 CS CS786668A patent/CS204036B2/cs unknown
- 1978-10-13 SE SE7810728A patent/SE442510B/sv not_active IP Right Cessation
- 1978-10-13 HU HU78BO1740A patent/HU176486B/hu unknown
- 1978-10-13 IE IE2050/78A patent/IE47455B1/en unknown
- 1978-10-13 GB GB7840431A patent/GB2007219B/en not_active Expired
- 1978-10-13 BG BG041084A patent/BG28715A3/xx unknown
- 1978-10-13 FR FR7829335A patent/FR2405948A1/fr active Granted
- 1978-10-13 PT PT68656A patent/PT68656A/pt unknown
- 1978-10-13 CA CA313,339A patent/CA1113095A/en not_active Expired
- 1978-10-13 DK DK458078A patent/DK150158C/da not_active IP Right Cessation
- 1978-10-13 NO NO783481A patent/NO151324C/no unknown
- 1978-10-13 JP JP12605578A patent/JPS5470296A/ja active Pending
- 1978-10-13 IL IL55727A patent/IL55727A/xx unknown
- 1978-10-13 ZA ZA785769A patent/ZA785769B/xx unknown
- 1978-10-13 IT IT51501/78A patent/IT1109215B/it active
- 1978-10-13 AU AU40698/78A patent/AU522759B2/en not_active Expired
- 1978-10-13 NL NL7810307A patent/NL7810307A/xx not_active Application Discontinuation
- 1978-10-13 NZ NZ188645A patent/NZ188645A/xx unknown
- 1978-10-13 FI FI783125A patent/FI63942C/fi not_active IP Right Cessation
- 1978-10-14 ES ES474218A patent/ES474218A1/es not_active Expired
-
1980
- 1980-03-27 US US06/134,441 patent/US4322423A/en not_active Expired - Lifetime
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