AR064730A1 - Derivados de 2,4-dianilinopirimidinas, su preparacion, composiciones farmaceuticas y usos como inhibidores de ikk - Google Patents
Derivados de 2,4-dianilinopirimidinas, su preparacion, composiciones farmaceuticas y usos como inhibidores de ikkInfo
- Publication number
- AR064730A1 AR064730A1 ARP080100012A ARP080100012A AR064730A1 AR 064730 A1 AR064730 A1 AR 064730A1 AR P080100012 A ARP080100012 A AR P080100012A AR P080100012 A ARP080100012 A AR P080100012A AR 064730 A1 AR064730 A1 AR 064730A1
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- AR
- Argentina
- Prior art keywords
- radicals
- optionally substituted
- radical
- alkyl
- different
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title 1
- -1 alkyl radical Chemical class 0.000 abstract 22
- 150000003254 radicals Chemical class 0.000 abstract 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 17
- 125000005843 halogen group Chemical group 0.000 abstract 16
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 229910003827 NRaRb Inorganic materials 0.000 abstract 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
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Abstract
Procesos de obtencion y composiciones farmacéuticas que los contienen. Reivindicacion 1: Productos de formula (1), en la que: R representa un átomo de hidrogeno o de halogeno, R2, R3 y R4, idénticos o diferentes, son tales que uno representa un átomo de halogeno o CF3 y los otros dos, idénticos o diferentes, representan un átomo de hidrogeno o un átomo de halogeno o un radical alquilo o un radical alcoxi opcionalmente sustituidos por uno o varios átomos de halogeno; R5 representa un átomo de hidrogeno o un átomo de halogeno; Z representa CO o SO2; estando el ciclo (N) sustituido en el mismo átomo de carbono por R1 y R6, que tiene 4 a 7 eslabones, estando saturado y pudiendo además contener un puente carbonado constituido por 1 a 3 carbonos, entendiéndose que R1 y R6 representan una de las 6 alternativas siguientes i) a vi): i) R1 representa -X1-R7, representando X1 -(CH2)m- y R7 representa un ciclo heterocicloalquilo, arilo o heteroarilo, todos opcionalmente sustituidos y R6 representa el átomo de hidrogeno o los radicales: hidroxilo, metilo, metoxi, -(CH2)mOH, -CO-NRaRb, -CH2-NRaRb, -CO2H y -CO2alq; ii) R1 representa -X2-R7, representando X2: -O-; -O-(CH2)m-; -CH(OH)-(Ch2)n-; -CO-;-CO-NRc-; -CO-NRc-O-; -CH(NRaRb)-; - C=NOH-; -C=N-NH2-; -(CH2)n1-NRc-(CH2)n2- y R7 representa un ciclo heterocicloalquilo, arilo o heteroarilo, todos opcionalmente sustituidos y R6 representa hidrogeno o el radical metilo; iii) R1 representa -NRc-W, representando W el átomo de hidrogeno o un radical alquilo C1-4, lineal o ramificado a partir de 3 átomos de carbono, opcionalmente sustituido por un radical elegido entre: -PO(OEt)2, -OH, -OaIq, -CF3, -CO-NR8R9 y SO2-alq y R6 representa hidrogeno; entendiéndose que cuando W representa un átomo de hidrogeno entonces z representa CO; iv) R1 representa -CH2-NRc-W, representando W el átomo de hidrogeno o un radical alquilo que tiene de 1 a 4 átomos de carbono, lineal o ramificado a partir de 3 átomos de carbono y opcionalmente sustituido por un radical elegido entre: -PO(OEt)2, -OH, -OEt, -CF3, -CO-N(alq)2 y SO2-alq y R6 representa hidrogeno; v) R1 representa -CO-N(Rc)-OR'c y R6 representa hidrogeno; vi) R1 representa X3-R7, representando X3: -CH(OH)-(CH2)n- ; -CO-; -CH(NRaRb)-; -C=NOH-; -C=N-NH2- y R7 representa un ciclo heterocicloalquilo, arilo o heteroarilo, todos opcionalmente sustituidos y R6 representa el átomo de hidrogeno o los radicales: hidroxilo, metilo, metoxi, -(CH2)mOH, -CO-NRaRb, -CH2- NRaRb y -CO2alq; representando n, n1 y n2, idénticos o diferentes, un numero entero de 0 a 3; m representa un numero entero de 1 a 3; Rc y R'c, idénticos o diferentes, representan el átomo de hidrogeno o un radical alquilo C1-4, opcionalmente sustituido por uno o varios átomos de halogeno; NRaRb es tal que Ra y Rb, idénticos o diferentes, representan el átomo de hidrogeno o un radical alquilo C1-4 o un radical cicloalquilo, estando estos radicales alquilo y cicloalquilo opcionalmente sustituidos por uno o varios átomos de halogeno, un radical hidroxilo o un radical NH2, NHalquilo o N(alquilo)2; formando Ra y Rb con el átomo de nitrogeno al que están unidos una amina cíclica que puede contener opcionalmente uno o dos heteroátomos distintos elegidos entre: O, S, N o NR10, formándose así la amina cíclica opcionalmente sustituida por uno o varios radicales idénticos o diferentes elegidos entre los átomos de halogeno y los radicales oxo; hidroxilo; alquilo opcionalmente sustituidos por uno o varios átomos de halogeno o incluso por un radical metilo y un radical hidroxilo sobre el mismo carbono; estando todos los radicales heterocicloalquilo, arilo y heteroarilo opcionalmente sustituidos por uno o varios radicales, idénticos o diferentes, elegidos entre: átomos de halogeno; radicales hidroxilo; ciano; NR8R9 y los radicales: alquilo, cicloalquilo, alcoxi, fenilo, heterocicloalquilo y heteroarilo, opcionalmente sustituidos por uno o varios radicales idénticos o diferentes elegidos entre los átomos de halogeno y los radicales: hidroxilo, alcoxi, alquilo, hidroxialquilo, alcoxialquilo, CN, CF3, OCF3 o NRaRb; NR8R9 es tal que R8 y R9, idénticos o diferentes, son tales que R8 representa el átomo de hidrogeno o un radical alquilo C1-4 o un radical cicloalquilo, estando estos radicales alquilo y cicloalquilo opcionalmente sustituidos por uno o varios átomos de halogeno, un radical hidroxilo o un radical NH2, NHalquilo o N(alquilo)2 y R9 representa el átomo de hidrogeno y los radicales: alquilo, cicloalquilo o heterocicloalquilo opcionalmente sustituidos por uno o varios radicales idénticos o diferentes, elegidos entre los átomos de halogeno y los radicales: hidroxilo, alcoxi, NH2, NHalquilo, N(alquilo)2, estando los radicales alquilo que representa R9 además opcionalmente sustituidos por un radical: fenilo, heterocicloalquilo o heteroarilo opcionalmente sustituidos por uno o varios radicales elegidos entre los átomos de halogeno y los radicales: hidroxilo, alcoxi, alquilo, hidroxialquilo, alcoxialquilo, CN, CF3, OCF3, NH2, NHalq o N(alq)2; formando R8 y R9 con el átomo de nitrogeno al que están unidos una amina cíclica que puede contener opcionalmente uno o dos heteroátomos diferentes elegidos entre: O, S, N o NR10, estando la amina cíclica así formada opcionalmente sustituida por uno o varios radicales idénticos o diferentes, elegidos entre los átomos de halogeno y los radicales alquilo opcionalmente sustituidos por uno o varios átomos de halogeno; todos los radicales heterocicloalquilo y heteroarilo anteriores opcionalmente sustituidos como se indico anteriormente, estando constituidos por 4 a 10 eslabones y con 1 a 3 heteroátomos elegido(s) entre: O, S, N y NR10; R10 representa un átomo de hidrogeno o un radical alquilo, estando dichos productos de formula (1) en todas las formas isomeras posibles: racémicos, enantiomeros y diastereoisomeros, así como las sales de adicion de los ácidos minerales y orgánicos de dichos productos de formula (1).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0700064A FR2911138B1 (fr) | 2007-01-05 | 2007-01-05 | Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk |
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| US (1) | US20100093668A1 (es) |
| EP (1) | EP2118092A1 (es) |
| JP (1) | JP2010514821A (es) |
| CN (1) | CN101605783A (es) |
| AR (1) | AR064730A1 (es) |
| CA (1) | CA2672959A1 (es) |
| CL (1) | CL2008000020A1 (es) |
| FR (1) | FR2911138B1 (es) |
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| DK1976828T3 (en) | 2005-12-29 | 2017-03-06 | Celtaxsys Inc | DIAMINE DERIVATIVES AS INhibitors of Leukotriene A4 HYDROLASE |
| PL2300013T5 (pl) * | 2008-05-21 | 2025-04-28 | Takeda Pharmaceutical Company Limited | Pochodne fosforu jako inhibitor kinazy |
| US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| JP5607241B2 (ja) | 2010-05-21 | 2014-10-15 | ケミリア・エービー | 新規ピリミジン誘導体 |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| EP2688883B1 (en) | 2011-03-24 | 2016-05-18 | Noviga Research AB | Pyrimidine derivatives |
| EP2704572B1 (en) | 2011-05-04 | 2015-12-30 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| CN103204827B (zh) * | 2012-01-17 | 2014-12-03 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的苯并噻二唑化合物及其制备方法和用途 |
| JP6469567B2 (ja) | 2012-05-05 | 2019-02-13 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Egfr発動性がんの細胞増殖阻害用化合物 |
| CN103833771A (zh) * | 2012-11-22 | 2014-06-04 | 天津滨江药物研发有限公司 | 作为蛋白激酶Mek抑制剂的苯并五元杂环化合物及其制备方法和用途 |
| JP6527851B2 (ja) | 2013-03-12 | 2019-06-05 | セルタクシス,インコーポレイテッド | ロイコトリエンa4加水分解酵素を阻害する方法 |
| MX2015011677A (es) | 2013-03-14 | 2016-07-08 | Celtaxsys Inc | Inhibidores de leucotrieno a4 hidrolasa. |
| EP2970309A4 (en) | 2013-03-14 | 2016-11-09 | Celtaxsys Inc | INHIBITORS OF LEUCOTRIENE A4 HYDROLASE |
| MX2015011676A (es) | 2013-03-14 | 2016-04-25 | Celtaxsys Inc | Inhibidores de leucotrieno a4 hidrolasa. |
| US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
| BR112016029662B1 (pt) | 2014-06-19 | 2023-10-24 | Takeda Pharmaceutical Company Limited | COMPOSTO DE FÓRMULA Bf OU UMA FORMA FARMACEUTICAMENTE ACEITÁVEL DO MESMO, COMPOSIÇÃO FARMACÊUTICA COMPREENDENDO O MESMO E SEU USO |
| ES2846833T3 (es) | 2016-07-18 | 2021-07-29 | Janssen Pharmaceutica Nv | Ligandos de obtención de imágenes de tau por PET |
| GB201617758D0 (en) * | 2016-10-20 | 2016-12-07 | Almac Discovery Limited | Pharmaceutical compounds |
| WO2019222093A1 (en) | 2018-05-14 | 2019-11-21 | Ariad Pharmaceuticals, Inc. | Pharmaceutical salts of pyrimidine derivatives and method of treating disorders |
| AU2019278935B2 (en) | 2018-05-31 | 2025-02-13 | Celltaxis, Llc | Method of reducing pulmonary exacerbations in respiratory disease patients |
| EP3890715A4 (en) * | 2018-12-04 | 2023-03-29 | The Board Of Regents Of The University Of Texas System | Therapeutics targeting mutant adenomatous polyposis coli (apc) for the treatment of cancer |
| HUE069128T2 (hu) | 2019-12-06 | 2025-02-28 | Vertex Pharma | Szubsztituált tetrahidrofurán vegyületek mint nátriumcsatornák modulátorai |
| AU2022284886A1 (en) | 2021-06-04 | 2023-11-30 | Vertex Pharmaceuticals Incorporated | N-(hydroxyalkyl (hetero)aryl) tetrahydrofuran carboxamides as modulators of sodium channels |
| KR102789906B1 (ko) * | 2023-06-29 | 2025-04-01 | (주)아이젠사이언스 | 신규 피리미딘 유도체 |
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| GB0004890D0 (en) * | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| GB0004888D0 (en) * | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| EP1598343A1 (de) * | 2004-05-19 | 2005-11-23 | Boehringer Ingelheim International GmbH | 2-Arylaminopyrimidine als PLK Inhibitoren |
| AU2005295788A1 (en) * | 2004-10-13 | 2006-04-27 | Wyeth | N-benzenesulfonyl substituted anilino-pyrimidine analogs |
| BRPI0613452A2 (pt) * | 2005-07-11 | 2011-01-11 | Sanofi Aventis | derivados de 2,4-dianilino pirimidinas, o respectivo preparo, a tìtulo de medicamentos, composições farmacêuticas e notadamente como inibidores de ikk |
| FR2911137B1 (fr) * | 2007-01-05 | 2009-02-20 | Sanofi Aventis Sa | Nouveaux derives de 2,4-dianilinopyrimides, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk |
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- 2007-01-05 FR FR0700064A patent/FR2911138B1/fr not_active Expired - Fee Related
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2008
- 2008-01-02 EP EP08750461A patent/EP2118092A1/fr not_active Withdrawn
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Also Published As
| Publication number | Publication date |
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| CN101605783A (zh) | 2009-12-16 |
| EP2118092A1 (fr) | 2009-11-18 |
| FR2911138A1 (fr) | 2008-07-11 |
| TW200900068A (en) | 2009-01-01 |
| WO2008099073A1 (fr) | 2008-08-21 |
| CL2008000020A1 (es) | 2009-01-23 |
| FR2911138B1 (fr) | 2009-02-20 |
| US20100093668A1 (en) | 2010-04-15 |
| CA2672959A1 (fr) | 2008-08-21 |
| JP2010514821A (ja) | 2010-05-06 |
| UY30857A1 (es) | 2008-09-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |