ES2546502T3 - 2,6-Diamino-pirimidin-5-il-carboxamidas como inhibidores de syk o JAK quinasas - Google Patents
2,6-Diamino-pirimidin-5-il-carboxamidas como inhibidores de syk o JAK quinasas Download PDFInfo
- Publication number
- ES2546502T3 ES2546502T3 ES09742982T ES09742982T ES2546502T3 ES 2546502 T3 ES2546502 T3 ES 2546502T3 ES 09742982 T ES09742982 T ES 09742982T ES 09742982 T ES09742982 T ES 09742982T ES 2546502 T3 ES2546502 T3 ES 2546502T3
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- Prior art keywords
- formula
- 8alkyl
- 8alkoxy
- halo
- independently
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- VULZVYGZVOMUKU-UHFFFAOYSA-N 2,4-diaminopyrimidine-5-carboxamide Chemical class NC(=O)C1=CN=C(N)N=C1N VULZVYGZVOMUKU-UHFFFAOYSA-N 0.000 title 1
- 102000015617 Janus Kinases Human genes 0.000 title 1
- 108010024121 Janus Kinases Proteins 0.000 title 1
- 102000000551 Syk Kinase Human genes 0.000 title 1
- 108010016672 Syk Kinase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- -1 halo C1-8alkyl Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000005124 aminocycloalkyl group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000005150 heteroarylsulfinyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000003367 polycyclic group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003003 spiro group Chemical group 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—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
- C07D409/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un compuesto que tiene la fórmula (I):**Fórmula** o uno de sus tautómeros o sales farmacéuticamente aceptables, en donde: D1 es fenilo sustituido con heteroarilo; cada E1 está seleccionado de modo independiente del grupo que consiste en alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-8, alquil C1-8-tio, aminocarbonilo, alcoxi C1-8-carbonil-alquileno C1-8, alcoxi C1-8-carbonil C1-8alcoxi C1-8, alcoxi C1-8-carbonilamino, oxo, halo, ciano, haloalquilo C1-8, haloalcoxi C1-8, aminosulfonilo, heteroarilsulfinilo; amino, hidroxilo, arilalquileno C1-8, fenilo, aminoalquilo C1-8, aminocicloalquilo C3-8, heterociclilo, heteroarilo, acilo C1-8, alquil C1-8 sulfonilo, acilamino y heterociclilalquileno C1-8; el subíndice n es 0, 1, 2, 3 ó 4; el resto:**Fórmula** es bien: (a)**Fórmula** y donde X e Y están seleccionados independientemente del grupo que consiste en: CH2, NH, NCOOH3 y S; (b) seleccionado del grupo que consiste en:**Fórmula** y donde cada R8a y R8b es independientemente H, hidroxilo, halo o si están en carbonos adyacentes, pueden combinarse con los átomos a los que están unidos para formar un anillo de benceno fusionado; y cada R9a y R9b es independientemente H, hidroxilo, halo o si están en carbonos adyacentes, pueden combinarse con los átomos a los que están unidos para formar un anillo de benceno fusionado; y la línea ondulada indica el punto de unión al resto de la molécula; o**Fórmula** (c) donde cada R8a y R8b es independientemente H o pueden combinarse con los átomos a los que están unidos para formar un anillo de benceno fusionado; y la línea ondulada indica el punto de unión al resto de la molécula; y "cicloalquilo" se refiere a un grupo hidrocarbonado mono o policíclico alifático, que puede formar un anillo con puente o un anillo espiro, y que puede tener uno o más enlaces dobles o triples.
Applications Claiming Priority (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US120346P | 1999-02-17 | ||
| US4549908P | 2008-04-16 | 2008-04-16 | |
| US4540608P | 2008-04-16 | 2008-04-16 | |
| US4539908P | 2008-04-16 | 2008-04-16 | |
| US45406P | 2008-04-16 | ||
| US45499P | 2008-04-16 | ||
| US45399P | 2008-04-16 | ||
| US12034808P | 2008-12-05 | 2008-12-05 | |
| US12034108P | 2008-12-05 | 2008-12-05 | |
| US12034608P | 2008-12-05 | 2008-12-05 | |
| US120341P | 2008-12-05 | ||
| US120348P | 2008-12-05 | ||
| PCT/US2009/002401 WO2009136995A2 (en) | 2008-04-16 | 2009-04-16 | Inhibitors of syk protein kinase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2546502T3 true ES2546502T3 (es) | 2015-09-24 |
Family
ID=41696952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES09742982T Active ES2546502T3 (es) | 2008-04-16 | 2009-04-16 | 2,6-Diamino-pirimidin-5-il-carboxamidas como inhibidores de syk o JAK quinasas |
Country Status (15)
| Country | Link |
|---|---|
| US (5) | US8063058B2 (es) |
| AU (1) | AU2009244897B2 (es) |
| BR (1) | BRPI0910921B1 (es) |
| CO (1) | CO6331450A2 (es) |
| EA (1) | EA019973B1 (es) |
| EC (1) | ECSP10010608A (es) |
| ES (1) | ES2546502T3 (es) |
| GT (1) | GT201000299A (es) |
| HN (1) | HN2010002121A (es) |
| IL (1) | IL208638A (es) |
| MX (1) | MX2010011463A (es) |
| NI (1) | NI201000175A (es) |
| NZ (1) | NZ589315A (es) |
| PT (1) | PT2323993E (es) |
| ZA (1) | ZA201007046B (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
| US8063058B2 (en) | 2008-04-16 | 2011-11-22 | Portola Pharmaceuticals, Inc. | Inhibitors of syk and JAK protein kinases |
| US8367689B2 (en) * | 2009-05-06 | 2013-02-05 | Portola Pharmaceuticals, Inc. | Inhibitors of JAK |
| WO2012040499A2 (en) * | 2010-09-22 | 2012-03-29 | Surface Logix, Inc. | Metabolic inhibitors |
| EP2621489A1 (en) | 2010-09-30 | 2013-08-07 | Portola Pharmaceuticals, Inc. | Combinations of 4-(cyclopropylamino)-2-(4-(4-(ethylsulfonyl)piperazin-1-yl)phenylamino)pyrimidine-5-carboxamide and fludarabine |
| WO2012044936A1 (en) | 2010-09-30 | 2012-04-05 | Portola Pharmaceuticals, Inc. | Combination therapy with 4-(3-(2h-1,2,3-triazol-2-yl)phenylamino)-2-((1r,2s)-2-aminocyclohexylamino)pyrimidine-5-carboxamide |
| US9139534B2 (en) * | 2011-04-22 | 2015-09-22 | Signal Pharmaceuticals, Llc | Substituted diaminocarboxamide and diaminocarbonitrile pyrimidines, compositions thereof, and methods of treatment therewith |
| MX363551B (es) | 2011-11-23 | 2019-03-27 | Portola Pharmaceuticals Inc Star | Compuestos derivados de pirazina como inhibidores de cinasa. |
| CA2856306A1 (en) * | 2011-11-23 | 2013-05-30 | Portola Pharmaceuticals, Inc. | Selective kinase inhibitors |
| CN104159891B (zh) * | 2012-01-10 | 2016-09-07 | 霍夫曼-拉罗奇有限公司 | 哒嗪酰胺化合物和它们作为syk 抑制剂的用途 |
| AR090650A1 (es) | 2012-04-12 | 2014-11-26 | Alcon Res Ltd | Tratamiento para respuestas inflamatorias inducidas por microbios en el ojo |
| WO2014045029A1 (en) * | 2012-09-18 | 2014-03-27 | Ziarco Pharma Ltd | 2-(2-aminocyclohexyl)amino-pyrimidine-5-carboxamides as spleen tyrosine kinasei(syk) inhibitors |
| AU2013337717B2 (en) | 2012-11-01 | 2018-10-25 | Infinity Pharmaceuticals, Inc. | Treatment of cancers using PI3 kinase isoform modulators |
| EP2970138B1 (en) | 2013-03-13 | 2019-01-16 | Canadian Blood Services | Pyrazole derivatives and their uses thereof |
| WO2014151386A1 (en) | 2013-03-15 | 2014-09-25 | Infinity Pharmaceuticals, Inc. | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
| CA2914284A1 (en) | 2013-05-30 | 2014-12-04 | Infinity Pharmaceuticals, Inc. | Treatment of cancers using pi3 kinase isoform modulators |
| US20160130659A1 (en) * | 2013-06-05 | 2016-05-12 | Merck Sharp & Dohme Corp. | Compositions and methods for treating cancer |
| EP3030241A4 (en) | 2013-08-06 | 2019-06-19 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | INHIBITORS OF ACK1 / TNK2.TYROSINE KINASE |
| PT3052485T (pt) | 2013-10-04 | 2021-10-22 | Infinity Pharmaceuticals Inc | Compostos heterocíclicos e suas utilizações |
| US9751888B2 (en) | 2013-10-04 | 2017-09-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
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| US9834548B2 (en) * | 2014-02-14 | 2017-12-05 | Portola Pharmaceuticals, Inc. | Pyridazine compounds as JAK inhibitors |
| MX382033B (es) | 2014-03-19 | 2025-03-13 | Infinity Pharmaceuticals Inc | Compuestos heterocíclicos para utilizarlos en el tratamiento de trastornos mediados por pi3k-gamma. |
| WO2015148867A1 (en) | 2014-03-28 | 2015-10-01 | Calitor Sciences, Llc | Substituted heteroaryl compounds and methods of use |
| US20150320754A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
| WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| JP2018527362A (ja) | 2015-09-11 | 2018-09-20 | サンシャイン・レイク・ファーマ・カンパニー・リミテッドSunshine Lake Pharma Co.,Ltd. | 置換されたヘテロアリール化合物および使用方法 |
| WO2017048702A1 (en) | 2015-09-14 | 2017-03-23 | Infinity Pharmaceuticals, Inc. | Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same |
| WO2017214269A1 (en) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
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| EP3554499B1 (en) * | 2016-12-14 | 2022-01-26 | Merck Sharp & Dohme Corp. | Aminopyrazoles as janus kinase inhibitors |
| BR112020018377A2 (pt) * | 2018-03-09 | 2021-03-09 | Portola Pharmaceuticals, Inc | Métodos de uso e composições farmacêuticas de um inibidor de syk seletivo |
| WO2022019920A1 (en) | 2020-07-24 | 2022-01-27 | Verastem, Inc. | Treatment of cancers using pi3 kinase isoform modulators |
| TW202227418A (zh) * | 2020-10-12 | 2022-07-16 | 大陸商四川海思科製藥有限公司 | 一種雜環衍生物及其在醫藥上的應用 |
| CA3245866A1 (en) * | 2022-03-14 | 2023-09-21 | Huyabio International, Llc | BLOOD-BRAIN BARRIER CROSSING PROTEIN-PROTEIN INTERACTION INHIBITORS (MLL1-WDR5) AND THEIR USES |
| WO2024026430A1 (en) * | 2022-07-28 | 2024-02-01 | 1910 Genetics Inc. | Substituted pyrimidine compounds as tyk2 inhibitors |
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| HK1155452A1 (en) | 2012-05-18 |
| IL208638A0 (en) | 2010-12-30 |
| AU2009244897B2 (en) | 2014-11-13 |
| ZA201007046B (en) | 2013-09-25 |
| US20120130073A1 (en) | 2012-05-24 |
| US20130165431A1 (en) | 2013-06-27 |
| GT201000299A (es) | 2015-02-09 |
| CO6331450A2 (es) | 2011-10-20 |
| US20100048567A1 (en) | 2010-02-25 |
| MX2010011463A (es) | 2011-06-03 |
| US9579320B2 (en) | 2017-02-28 |
| BRPI0910921A2 (pt) | 2021-04-20 |
| US8318755B2 (en) | 2012-11-27 |
| ECSP10010608A (es) | 2011-02-28 |
| US8349860B2 (en) | 2013-01-08 |
| NZ589315A (en) | 2012-11-30 |
| US8952027B2 (en) | 2015-02-10 |
| AU2009244897A1 (en) | 2009-11-12 |
| US8063058B2 (en) | 2011-11-22 |
| PT2323993E (pt) | 2015-10-12 |
| EA201001618A1 (ru) | 2011-06-30 |
| IL208638A (en) | 2017-03-30 |
| US20120101275A1 (en) | 2012-04-26 |
| NI201000175A (es) | 2011-08-08 |
| EA019973B1 (ru) | 2014-07-30 |
| HN2010002121A (es) | 2013-06-17 |
| US20150297595A1 (en) | 2015-10-22 |
| AU2009244897A2 (en) | 2011-01-20 |
| BRPI0910921B1 (pt) | 2022-06-21 |
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