ES2640911T3 - Cicloalquilnitrilpirazolcarboxamidas como inhibidores de la quinasa Janus - Google Patents
Cicloalquilnitrilpirazolcarboxamidas como inhibidores de la quinasa Janus Download PDFInfo
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- ES2640911T3 ES2640911T3 ES12833410.9T ES12833410T ES2640911T3 ES 2640911 T3 ES2640911 T3 ES 2640911T3 ES 12833410 T ES12833410 T ES 12833410T ES 2640911 T3 ES2640911 T3 ES 2640911T3
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
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- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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Abstract
Un compuesto de fórmula I o una sal o un estereoisómero farmacéuticamente aceptables del mismo: cada uno de Ra y R4 se selecciona independientemente entre hidrógeno y alquilo C1-4; A se selecciona entre arilo, y heteroarilo; n es 0, 1,2, 3, o 4; p es 2, 3, o 4; cada uno de R2 y R7 se selecciona independientemente entre hidrógeno, halógeno, alquilo C1-10, alquenilo C2-10, heteroalquilo C1-10, arilalquil C0-10 alquilo C0-10, cicloalquil C3-8 alquilo C0-10, heteroarilalquilo C0-10, heterocicloalquil (C3-8) alquilo C0-10, y en donde cada uno de R2 y R7 está independientemente sustituido con 0, 1,2, 3 o 4 sustituyentes R5a; R5a se selecciona de: halógeno, alquil C1-10 (oxi)0-1(carbonil)0-1alquilo C0-10, heteroalquil C1-10 (oxi)0-1(carbonil)0-1alquilo C0-10, alquenil C2-10 (oxi)0-1(carbonil)0-1alquilo C0-10, aril C0-10 alquil(oxi)0-1(carbonil)0-1alquilo C0-10, aril C2-10 alquenil(oxi)0-1(carbonil)0-1alquilo C0-10, aril C2-10 alquinil(oxi)0-1(carbonil)0-1alquilo C0-10, cicloalquil C3-8 alquil C0-10 (oxi)0-1(carbonil)0-1alquilo C0-10, heteroarilalquil C0-10 (oxi)0-1(carbonil)0-1alquilo C0-10, heterocicloalquil (C3-8)alquil C0-10 (oxi)0-1(carbonil)0-1alquilo C0-10, alquil C1-10 (carbonil)0-1oxi alquilo C0-10, heteroalquil C1-10 (carbonil)0-1oxi alquilo C0-10, alquenil C2-10 (carbonil)0-1oxi alquilo C0-10, heteroalquil C1-10 (carbonil)0-1oxi alquilo C0-10, aril C0-10 alquil (carbonil)0-1oxi alquilo C0-10, cicloalquil (C3-8) alquil C0-10 (carbonil)0-1oxi alquilo C0-10, heteroarilalquil C0-10 (carbonil)0-1oxialquilo C0-10, heterocicloalquil (C3-8) alquil C0-10 (carbonil)0-1oxi alquilo C0-10, (alquil (C0-10))1-2aminocarboniloxi, heteroalquil (C0-10)aminocarboniloxi, arilalquil (C0-10) aminocarboniloxi, cicloalquil (C3-8) alquil (C0-10) aminocarboniloxi, heteroarilalquil (C0-10)aminocarboniloxi, heterocicloalquil (C3-8) alquil (C0-10)aminocarboniloxi, alquil C0-10 amino(oxi)0-1(carbonil)0-1 alquenilo C2-10, alquil C1-10 amino(oxi)0-1(carbonil)0-1 alquilo C0-10, heteroalquil (C0-10)amin(oxi)0-1(carbonil)0-1 alquilo C0-10, cicloalquil C3-8 alquil C0-10 amino(oxi)0-1(carbonil)0-1 alquilo C0-10, arilalquil C0-10 amino(oxi)0-1(carbonil)0-1 alquilo C0-10, heteroarilalquil C0-10 amino((oxi)0-1(carbonil)0-1 alquilo C0-10, heterocicloalquil (C3-8) alquil C0-10 amino(oxi)0-1(carbonil)0-1alquilo C0-10, alquil C1-10 (oxi)0-1(carbonil)0-1aminoalquilo C0-10, heteroalquil C1-10 (oxi)0-1(carbonil)0-1aminoalquilo C0-10, cicloalquil C3-8 alquil C0-10 (oxi)0-1(carbonil)0-1aminoalquilo C0-10, arilalquil C0-10 (oxi)0-1(carbonil)0-1aminoalquilo C0-10, heteroarilalquil C0-10 (oxi)0-1(carbonil)0-1aminoalquilo C0-10, heterocicloalquil (C3-8) alquil C0-10 (oxi)0-1(carbonil)0-1aminoalquilo C0-10, -CO2(alquilo C0-10), -(alquil C0-10)CO2H, Oxo (>=O), formilo, sulfonilo , alquilsulfonilo C1-10, heteroalquilsulfonilo C1-10, cicloalquilsulfonilo (C3-8), cicloheteroalquilsulfonilo (C3-8), heteroarilsulfonilo, arilsulfonilo, aminosulfonilo, -SO2N(alquilo C0-6)1-2, -SO2alquilo C1-6, -SO2CF3, -SO2CF2H, -Si(CH3)3 alquilsulfinilo C1-10, amino, (alquil C0-10)1-2 amino, acil C1-4aminoalquilo C0-10, hidroxilo, (alquilo C1-10)OH, alquil C0-10 alcoxilo, iminoalquilo C0-10, (alquilo C0-10)imino, ciano, alquil C1-6ciano, y haloalquilo C1-6; en donde dos R5a y el átomo al que están unidos pueden formar opcionalmente un sistema de anillo saturado de 3, 4, 5, o 6 miembros; en dondecada R5a está opcionalmente sustituido con 1,2, 3 o 4 sustituyentes R6 y R6 se selecciona independientemente entre:
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161537978P | 2011-09-22 | 2011-09-22 | |
| US201161537978P | 2011-09-22 | ||
| PCT/CN2012/001291 WO2013040863A1 (en) | 2011-09-22 | 2012-09-21 | Cycloalkylnitrile pyrazole carboxamides as janus kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2640911T3 true ES2640911T3 (es) | 2017-11-07 |
Family
ID=47913815
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12833410.9T Active ES2640911T3 (es) | 2011-09-22 | 2012-09-21 | Cicloalquilnitrilpirazolcarboxamidas como inhibidores de la quinasa Janus |
| ES12834379T Active ES2670878T3 (es) | 2011-09-22 | 2012-09-21 | Cianometilpirazol carboxamidas como inhibidores de la Janus quinasa |
| ES12834277.1T Active ES2633793T3 (es) | 2011-09-22 | 2012-09-21 | Pirazol carboxamidas como inhibidores de quinasa Janus |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12834379T Active ES2670878T3 (es) | 2011-09-22 | 2012-09-21 | Cianometilpirazol carboxamidas como inhibidores de la Janus quinasa |
| ES12834277.1T Active ES2633793T3 (es) | 2011-09-22 | 2012-09-21 | Pirazol carboxamidas como inhibidores de quinasa Janus |
Country Status (8)
| Country | Link |
|---|---|
| US (4) | US9328099B2 (es) |
| EP (4) | EP2758050B1 (es) |
| JP (4) | JP6034869B2 (es) |
| AU (4) | AU2012313254B8 (es) |
| CA (4) | CA2849169C (es) |
| ES (3) | ES2640911T3 (es) |
| TR (1) | TR201807973T4 (es) |
| WO (4) | WO2013041042A1 (es) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2640911T3 (es) * | 2011-09-22 | 2017-11-07 | Merck Sharp & Dohme Corp. | Cicloalquilnitrilpirazolcarboxamidas como inhibidores de la quinasa Janus |
| WO2014146249A1 (en) * | 2013-03-19 | 2014-09-25 | Merck Sharp & Dohme Corp. | Geminally substituted cyanoethylpyrazolo pyridones as janus kinase inhibitors |
| AU2014234908B2 (en) * | 2013-03-19 | 2017-08-17 | Merck Sharp & Dohme Corp. | N-(2-cyano heterocyclyl)pyrazolo pyridones as Janus kinase inhibitors |
| TWI719401B (zh) | 2013-05-17 | 2021-02-21 | 美商英塞特公司 | 作為jak抑制劑之聯吡唑衍生物 |
| PE20160434A1 (es) | 2013-09-09 | 2016-05-25 | Peloton Therapeutics Inc | Eteres de arilo y sus usos |
| ES2737148T3 (es) * | 2013-12-16 | 2020-01-10 | Peloton Therapeutics Inc | Análogos de sulfona y sulfoximina cíclicos y usos de los mismos |
| WO2015103355A1 (en) | 2014-01-01 | 2015-07-09 | Medivation Technologies, Inc. | Compounds and methods of use |
| CA2946538A1 (en) | 2014-04-04 | 2015-10-08 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
| NO2721710T3 (es) | 2014-08-21 | 2018-03-31 | ||
| EP3227298A4 (en) | 2014-12-05 | 2018-05-23 | Sun Pharmaceutical Industries Ltd | Process for the preparation of baricitinib and an intermediate thereof |
| US9980945B2 (en) * | 2015-01-13 | 2018-05-29 | Vanderbilt University | Benzoisoxazole-substituted compounds as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
| US10512626B2 (en) | 2015-03-11 | 2019-12-24 | Peloton Therapeautics, Inc. | Compositions for use in treating glioblastoma |
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