YU28902A - Fenil- i piridil-tetrahidro-piridini koji imaju tnf-inhibitorsku aktivnost - Google Patents
Fenil- i piridil-tetrahidro-piridini koji imaju tnf-inhibitorsku aktivnostInfo
- Publication number
- YU28902A YU28902A YU28902A YUP28902A YU28902A YU 28902 A YU28902 A YU 28902A YU 28902 A YU28902 A YU 28902A YU P28902 A YUP28902 A YU P28902A YU 28902 A YU28902 A YU 28902A
- Authority
- YU
- Yugoslavia
- Prior art keywords
- group
- hydrogen
- pyridines
- tetrahydro
- pyridyl
- Prior art date
Links
- 230000002401 inhibitory effect Effects 0.000 title 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- A—HUMAN NECESSITIES
- A43—FOOTWEAR
- A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
- A43B7/00—Footwear with health or hygienic arrangements
- A43B7/12—Special watertight footwear
- A43B7/125—Special watertight footwear provided with a vapour permeable member, e.g. a membrane
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- A43B9/02—Footwear stitched or nailed through
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
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- B29D35/0018—Moulds
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B29D35/128—Moulds or apparatus therefor
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
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- B29D35/14—Multilayered parts
- B29D35/142—Soles
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- C—CHEMISTRY; METALLURGY
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
- B29C45/14836—Preventing damage of inserts during injection, e.g. collapse of hollow inserts, breakage
- B29C2045/14844—Layers protecting the insert from injected material
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
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- General Health & Medical Sciences (AREA)
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- Pharmacology & Pharmacy (AREA)
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- Communicable Diseases (AREA)
- Oncology (AREA)
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- Neurology (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Heart & Thoracic Surgery (AREA)
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- Hematology (AREA)
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- Biotechnology (AREA)
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- Psychology (AREA)
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Abstract
Pronalazak se odnosi na jedinjenja formule (I) gde X predstavlja N ili CH; R1 pretstavlja atom vodonika ili halogena ili CF3 grupu; R2 i R3 nezavisno pretstavljaju atom vodonika ili metil grupu; n je O ili 1; A pretstavlja grupu formule (a) ili (b); R4 pretstavlja atom vodonika ili halogena, (C1-C4) alkil grupu, CF3 grupu, amino grupu, mono (C1-C4) alkilamino grupu ili di (C1-C4) alkilamino grupu; R5 pretstavlja atom vodonika ili halogena, (C1-C4) alkoksi grupu, (C1-C4) alkil grupu ili CF3 grupu; R6 pretstavlja atom vodonika, (C1-C4) alkil grupu ili (C1-C4) alkoksi grupu; isto kao i na njihiove soli ili solvate, na farmaceutske preparate koji ih sadrže, na postupak za njihovo dobijanje i na sintezu intermedijera u pomenutom postupku.[The invention concerns compounds of formula (I) wherein: X represents N or CH; R1 represents a hydrogen or halogen atom, or a CF3 group; R2 and R3 independently represent a hydrogen atom or a methyl group; n is 0 or 1; A represents a group of formula (a) or (b) wherein: R4 represents a hydrogen or halogen atom, a C1-C4 alkyl group, a CF3 group, an amino, mono(C1-C4)alkylamino, di(C1- C4)alkylamino; R5 represents a hydrogen or halogen atom, a (C1-C4)alkoxy group, a (C1-C4)alkyl group or a CF3 group; R6 represents a hydrogen atom, a (C1-C4)alkyl group or a (C1-C4)alkoxy group; and their salts or solvates, pharmaceutical compositions containing them, a method for preparing them and the synthesis intermediates in said method.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9913206A FR2800071B1 (fr) | 1999-10-22 | 1999-10-22 | Tetrahydropyridines, procede pour leur preparation et compositions pharmaceutiques les contenant |
| FR0008328A FR2810984B1 (fr) | 2000-06-28 | 2000-06-28 | Pyridyl-tetrahydropyridines, procede pour leur preparation et compositions pharmaceutiques les contenant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| YU28902A true YU28902A (sh) | 2004-11-25 |
| RS50399B RS50399B (sr) | 2009-12-31 |
Family
ID=26212500
Country Status (35)
| Country | Link |
|---|---|
| US (1) | US6509351B1 (sh) |
| EP (1) | EP1226137B8 (sh) |
| JP (1) | JP4831908B2 (sh) |
| KR (1) | KR100755115B1 (sh) |
| CN (1) | CN1158276C (sh) |
| AR (1) | AR026188A1 (sh) |
| AT (1) | ATE271554T1 (sh) |
| AU (1) | AU778306B2 (sh) |
| BG (1) | BG65564B1 (sh) |
| BR (1) | BR0014871A (sh) |
| CA (1) | CA2386417C (sh) |
| CZ (1) | CZ301566B6 (sh) |
| DE (1) | DE60012355T2 (sh) |
| DK (1) | DK1226137T3 (sh) |
| EA (1) | EA004508B1 (sh) |
| EE (1) | EE05055B1 (sh) |
| ES (1) | ES2223594T3 (sh) |
| HK (1) | HK1046532B (sh) |
| HR (1) | HRP20020347B1 (sh) |
| HU (1) | HUP0204444A3 (sh) |
| IL (2) | IL149250A0 (sh) |
| IS (1) | IS2308B (sh) |
| ME (1) | MEP25108A (sh) |
| MX (1) | MXPA02003979A (sh) |
| NO (1) | NO322596B1 (sh) |
| NZ (1) | NZ518112A (sh) |
| PL (1) | PL198421B1 (sh) |
| PT (1) | PT1226137E (sh) |
| RS (1) | RS50399B (sh) |
| SI (1) | SI1226137T1 (sh) |
| SK (1) | SK287098B6 (sh) |
| TR (1) | TR200201075T2 (sh) |
| TW (1) | TWI224097B (sh) |
| UA (1) | UA72934C2 (sh) |
| WO (1) | WO2001029026A1 (sh) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2823748B1 (fr) * | 2001-04-20 | 2004-02-20 | Sanofi Synthelabo | Tetrahydropyridyl-alkyl-benzodiazines, procede pour leur preparation et compositions pharmaceutiques les contenant |
| FR2831166B1 (fr) * | 2001-10-18 | 2004-02-27 | Sanofi Synthelabo | Aralkyl-tetrahydro-pyridines, leur preparation et compositions pharmaceutiques les contenant |
| FR2832405B1 (fr) * | 2001-11-19 | 2004-12-10 | Sanofi Synthelabo | Tetrahydropyridyl-alkyl-heterocycles azotes, procede pour leur preparation et compositions pharmaceutiques les contenant |
| FR2840896B1 (fr) * | 2002-06-18 | 2005-04-08 | Sanofi Synthelabo | Phenyl-et pyridyl-piperazines, procede pour leur preparation et compositions pharmaceutiques les contenant |
| WO2005016910A1 (ja) | 2003-08-18 | 2005-02-24 | Sankio Chemical Co., Ltd. | ピリジルテトラヒドロピリジン類およびピリジルピペリジン類とそれらの製造方法 |
| FR2883285B1 (fr) * | 2005-03-17 | 2007-05-18 | Sanofi Aventis Sa | Sel besylate de la 7-(2-(4-(3-trifluoromethyl-phenyl) -1,2,3,6-tetrahudro-pyrid-1-yl)ethyl) isoquinoleine, sa preparation et son utilisation en therapeutique |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3991061A (en) * | 1975-07-16 | 1976-11-09 | G. D. Searle & Co. | Azanaphthaleneacetic acid derivatives |
| US4704390A (en) * | 1986-02-13 | 1987-11-03 | Warner-Lambert Company | Phenyl and heterocyclic tetrahydropyridyl alkoxy-benzheterocyclic compounds as antipsychotic agents |
| US5118691A (en) * | 1990-09-20 | 1992-06-02 | Warner-Lambert Co. | Substituted tetrahydropyridines as central nervous system agents |
| US5045550A (en) * | 1990-09-20 | 1991-09-03 | Warner-Lambert Co. | Substituted tetrahydropyridines as central nervous system agents |
| US5273977A (en) * | 1990-11-05 | 1993-12-28 | Warner-Lambert Company | Substituted tetrahydropyridines and hydroxypiperidines as central nervous system agents |
| JP2001511764A (ja) * | 1996-04-12 | 2001-08-14 | 住友製薬株式会社 | ピペリジニルピリミジン誘導体 |
| US5776939A (en) * | 1997-06-12 | 1998-07-07 | Eli Lilly And Company | Drug resistance and multidrug resistance modulators |
| US6281216B1 (en) * | 1998-02-09 | 2001-08-28 | Duphar International Research B.V. | 2-aminoquinoline derivatives having d4-agonistic activity |
| FR2803593B1 (fr) * | 2000-01-06 | 2002-02-15 | Sanofi Synthelabo | Nouvelles tetrahydropyridines, procede pour leur preparation et compositions pharmaceutiques les contenant |
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2000
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