PL2367812T3 - [4-(5-aminometylo-2-fluorofenylo)piperydyn-1-ylo]-[7-fluoro-1-(2-metoksyetylo)-4-trifluorometoksy-1H-indol-3-ilo]metanon jako inhibitor tryptazy komórek tucznych - Google Patents
[4-(5-aminometylo-2-fluorofenylo)piperydyn-1-ylo]-[7-fluoro-1-(2-metoksyetylo)-4-trifluorometoksy-1H-indol-3-ilo]metanon jako inhibitor tryptazy komórek tucznychInfo
- Publication number
- PL2367812T3 PL2367812T3 PL09791693T PL09791693T PL2367812T3 PL 2367812 T3 PL2367812 T3 PL 2367812T3 PL 09791693 T PL09791693 T PL 09791693T PL 09791693 T PL09791693 T PL 09791693T PL 2367812 T3 PL2367812 T3 PL 2367812T3
- Authority
- PL
- Poland
- Prior art keywords
- fluoro
- methanone
- indol
- piperidin
- aminomethyl
- Prior art date
Links
- 102000001400 Tryptase Human genes 0.000 title 1
- 108060005989 Tryptase Proteins 0.000 title 1
- WCJRDLYNOVMUTE-UHFFFAOYSA-N [4-[5-(aminomethyl)-2-fluorophenyl]piperidin-1-yl]-[7-fluoro-1-(2-methoxyethyl)-4-(trifluoromethoxy)indol-3-yl]methanone Chemical compound C12=C(OC(F)(F)F)C=CC(F)=C2N(CCOC)C=C1C(=O)N(CC1)CCC1C1=CC(CN)=CC=C1F WCJRDLYNOVMUTE-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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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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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Neurology (AREA)
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- Immunology (AREA)
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- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
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- Heart & Thoracic Surgery (AREA)
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9101108P | 2008-08-22 | 2008-08-22 | |
| US9101808P | 2008-08-22 | 2008-08-22 | |
| EP09791693.6A EP2367812B1 (en) | 2008-08-22 | 2009-08-20 | [4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-[7-fluoro-1-(2-methoxy-ethyl)-4trifluoromethoxy-1h-indol-3-yl]methanone as an inhibitor of mast cell tryptase |
| PCT/US2009/054381 WO2010022196A2 (en) | 2008-08-22 | 2009-08-20 | [4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-[7-fluoro-1-(2-methoxy-ethyl)-4-trifluoromethoxy-1h-indol-3-yl]-methanone as an inhibitor of mast cell tryptase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2367812T3 true PL2367812T3 (pl) | 2016-03-31 |
Family
ID=41198646
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL09791693T PL2367812T3 (pl) | 2008-08-22 | 2009-08-20 | [4-(5-aminometylo-2-fluorofenylo)piperydyn-1-ylo]-[7-fluoro-1-(2-metoksyetylo)-4-trifluorometoksy-1H-indol-3-ilo]metanon jako inhibitor tryptazy komórek tucznych |
Country Status (36)
| Country | Link |
|---|---|
| US (2) | US8217178B2 (pl) |
| EP (1) | EP2367812B1 (pl) |
| JP (1) | JP5656834B2 (pl) |
| KR (1) | KR101630217B1 (pl) |
| CN (2) | CN102149705B (pl) |
| AR (1) | AR073117A1 (pl) |
| AU (1) | AU2009282884B8 (pl) |
| BR (1) | BRPI0916920A2 (pl) |
| CA (1) | CA2734877C (pl) |
| CL (1) | CL2009001759A1 (pl) |
| CO (1) | CO6341624A2 (pl) |
| CR (1) | CR20110093A (pl) |
| CY (1) | CY1117261T1 (pl) |
| DK (1) | DK2367812T3 (pl) |
| DO (1) | DOP2011000055A (pl) |
| EC (1) | ECSP11010841A (pl) |
| ES (1) | ES2556764T3 (pl) |
| HR (1) | HRP20151338T1 (pl) |
| HU (1) | HUE026331T2 (pl) |
| IL (2) | IL211265A (pl) |
| MA (1) | MA32639B1 (pl) |
| MX (1) | MX2011001135A (pl) |
| MY (1) | MY150599A (pl) |
| NI (1) | NI201100024A (pl) |
| NZ (1) | NZ591234A (pl) |
| PE (1) | PE20100235A1 (pl) |
| PL (1) | PL2367812T3 (pl) |
| PT (1) | PT2367812E (pl) |
| RS (1) | RS54413B1 (pl) |
| RU (1) | RU2509766C2 (pl) |
| SI (1) | SI2367812T1 (pl) |
| TW (1) | TWI473613B (pl) |
| UA (1) | UA104148C2 (pl) |
| UY (1) | UY32069A (pl) |
| WO (1) | WO2010022196A2 (pl) |
| ZA (1) | ZA201100597B (pl) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102149705B (zh) | 2008-08-22 | 2013-08-07 | 赛诺菲-安万特 | 作为肥大细胞类胰蛋白酶抑制剂的[4-(5-氨基甲基-2-氟苯基)-哌啶-1-基]-[7-氟-1-(2-甲氧基乙基)-4-三氟甲氧基-1h-吲哚-3-基]-甲酮 |
| FR2955324A1 (fr) * | 2010-01-15 | 2011-07-22 | Sanofi Aventis | [4-(5-aminomethyl-phenyl)-piperidin-1-yl]-1h-indol-3-yl]-methanones disubstituees |
| JP2013515724A (ja) * | 2009-12-23 | 2013-05-09 | サノフイ | ベータ−トリプターゼ阻害剤としてのトロピノンベンジルアミン類 |
| WO2011078983A1 (en) * | 2009-12-23 | 2011-06-30 | Sanofi | Treatment for inflammatory bowel disease |
| MY155980A (en) * | 2009-12-23 | 2015-12-31 | Sanofi Sa | Prodrugs of [4[4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-(1h-pyrrolo-pyridin-yl)-methanones and synthesis thereof |
| CA2784894A1 (en) * | 2009-12-23 | 2011-06-30 | Sanofi | Indolyl-piperidinyl benzylamines as beta-tryptase inhibitors |
| BR112012020965A2 (pt) * | 2010-02-24 | 2016-05-03 | Sanofi Sa | tratamento de condições alérgicas dermatológicas |
| EP2397074B1 (en) | 2010-06-19 | 2012-10-24 | M Stenqvist AB | A system and computer readable medium for determination of transpulmonary pressure in a patient connected to a breathing apparatus |
| CN103842356B (zh) | 2011-10-07 | 2017-03-15 | 武田药品工业株式会社 | 用于治疗神经变性疾病的1‑芳基羰基‑4‑氧‑哌啶化合物 |
| DE102020120900A1 (de) * | 2020-08-07 | 2022-02-10 | Drägerwerk AG & Co. KGaA | Vorrichtung und Verfahren zur Messung der Lungen-Compliance |
| IL304924A (en) | 2021-02-10 | 2023-10-01 | Iolyx Therapeutics Inc | Methods for ophthalmic delivery of roflumilast |
| MX2024003580A (es) | 2021-09-22 | 2024-04-05 | Iolyx Therapeutics Inc | Metodos de tratamiento de enfermedades inflamatorias oculares. |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| GB8804164D0 (en) * | 1988-02-23 | 1988-03-23 | Tucker J M | Bandage for administering physiologically active compound |
| US5008110A (en) * | 1988-11-10 | 1991-04-16 | The Procter & Gamble Company | Storage-stable transdermal patch |
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| US5352456A (en) * | 1991-10-10 | 1994-10-04 | Cygnus Therapeutic Systems | Device for administering drug transdermally which provides an initial pulse of drug |
| CA2123809A1 (en) * | 1991-12-18 | 1993-06-24 | Debra L. Wilfong | Multilayered barrier structures |
| US5451569A (en) * | 1994-04-19 | 1995-09-19 | Hong Kong University Of Science And Technology R & D Corporation Limited | Pulmonary drug delivery system |
| RU2278115C2 (ru) * | 1999-05-21 | 2006-06-20 | Сайос Инк. | ПРОИЗВОДНЫЕ ИНДОЛЬНОГО РЯДА В КАЧЕСТВЕ ИНГИБИТОРОВ p38 КИНАЗЫ |
| HU227630B1 (hu) * | 2000-05-22 | 2011-10-28 | Aventis Pharma Inc | Arilmetilamin-származékok triptáz gátlóként való alkalmazásra és ezeket tartalmazó gyógyszerkészítmények |
| GB0012362D0 (en) * | 2000-05-22 | 2000-07-12 | Aventis Pharma Ltd | Chemical compounds |
| EP1571150A1 (en) * | 2004-03-02 | 2005-09-07 | Aventis Pharma Deutschland GmbH | Process for the preparation of tryptase inhibitors |
| DOP2005000039A (es) * | 2004-03-26 | 2005-10-31 | Aventis Pharma Inc | Hidrocloruro de [4-(5-aminometil-2-fluoro-fenil)- piperidin-1-il]-(4-bomo-3-metil-5-propoxi-tiofen-2-il)-metanona como un inhibidor de la triptasa de mastocitos |
| AR065859A1 (es) * | 2007-03-29 | 2009-07-08 | Sanofi Aventis | Ester de 2,5-dioxo-pirrolidin-1-ilo de acido 4-bromo-3-metil-5-propoxitiofen-2- carboxilico ,su sintesis regioespecifica y un intermedio del mismo |
| AR065858A1 (es) * | 2007-03-29 | 2009-07-08 | Sanofi Aventis | Metodo para preparar el inhibidor de triptasa [ 4-(5-aminoetil-2-fluoro-fenil)-piperidin-1-il]-(4-bromo-3-metil-5-propoxi-tiofen-2-il)-metanona. |
| CN102149705B (zh) | 2008-08-22 | 2013-08-07 | 赛诺菲-安万特 | 作为肥大细胞类胰蛋白酶抑制剂的[4-(5-氨基甲基-2-氟苯基)-哌啶-1-基]-[7-氟-1-(2-甲氧基乙基)-4-三氟甲氧基-1h-吲哚-3-基]-甲酮 |
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