CO5680479A2 - Derivados de pirimidilsulfonamida como moduladores del receptor de quimiocina, sus composiciones y proceso de obtencion - Google Patents
Derivados de pirimidilsulfonamida como moduladores del receptor de quimiocina, sus composiciones y proceso de obtencionInfo
- Publication number
- CO5680479A2 CO5680479A2 CO05005309A CO05005309A CO5680479A2 CO 5680479 A2 CO5680479 A2 CO 5680479A2 CO 05005309 A CO05005309 A CO 05005309A CO 05005309 A CO05005309 A CO 05005309A CO 5680479 A2 CO5680479 A2 CO 5680479A2
- Authority
- CO
- Colombia
- Prior art keywords
- 6alkyl
- phenyl
- optionally substituted
- substituents independently
- independently selected
- Prior art date
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Abstract
1.- Un compuesto de fórmula (1), sal farmacéuticamente aceptable, solvato o éster hidrolizable in vivo del mismo. En donde R1 es un grupo seleccionado de C3-7carbociclil, C1-8alquil, C2-6alquenil y C2-6alquinil;en donde el grupo es sustituído opcionalmente por 1, 2 o 3 sustituyentes independientemente seleccionados de flúor, nitrilo, -OR4, -NR5R6, -CONR5R6, -COOR7, -NR8COR9, -SR10, -SO2R10, -SO2NR5R6, -NR8SO2R9, fenil o heteroaril; en donde fenil y heteroaril son sustituídos opcionalmente por 1, 2 o 3 sustituyentes independientemente seleccionados de halo, ciano, nitro -OR4, -NR5R6, -CONR5R6, -COOR7, -NR8COR9, -SR10, -SO2R10, -SO2NR5R6, -NR8SO2R9, C1-6alquil y trifluorometil;En donde R2 es C3-7carbociclil, sustituído opcionalmente por 1, 2 o 3 sustituyentes seleccionados independientemente de:(a) flúor, -OR4, -NR5R6, -CONR5R6, -COOR7, -NR8COR9, -SR10, -SO2R10, -SO2NR5R6, -NR8SO2R9;(b) un anillo de 3-8 miembros conteniendo opcionalmente 1, 2 o 3 átomos seleccionados de O, S, -NR8 y en donde el anillo es sustituído opcionalmente por C1-3alquil o flúor; o (c) fenil o heteroaril, cada uno de los cuales es sustituído opcionalmente por 1, 2 o 3 sustituyentes independientemente seleccionados de halo, ciano, nitro, -OR4, -NR5R6, CONR5R6, -NR8COR9, -SO2NR5R6, -NR8SO2R9, C1-6alquil y trifluorometil;o R2 es un grupo seleccionado de C1-8alquil, C2-6alquenil o C2-6alquinil en donde el grupo es sustituido por 1, 2 o 3 sustituyentes independientemente seleccionados de hidroxi, amino, C1-6alcoxi, C1-6alquilamino, di(C1-6alquil)amino, N-(C1-6alquil)-N-(fenil)amino, N-C1-6alquilcarbamoil, N,N-di(C1-6alquil)carbamoil, N-(C1-6alquil)-N-(fenil)carbamoil, carboxi, fenoxicarbonil, NR8COR9, -SO2R10, -SO2NR5R6 y -NR8SO2R9;en donde R3 es hidrógeno o independientemente R2;R4 es hidrógeno o un grupo seleccionado de C1-6alquil y fenil, en donde el grupo es sustituido opcionalmente por 1 o 2 sustituyentes seleccionados independientemente de halo, fenil, -OR11 y -NR12R13; ...
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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GBGB0217431.6A GB0217431D0 (en) | 2002-07-27 | 2002-07-27 | Novel compounds |
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US (2) | US7582644B2 (es) |
EP (1) | EP1527051B1 (es) |
JP (1) | JP4619782B2 (es) |
KR (2) | KR20110033313A (es) |
CN (1) | CN100345829C (es) |
AR (1) | AR040700A1 (es) |
AU (1) | AU2003281684B2 (es) |
BR (1) | BR0312967A (es) |
CA (1) | CA2493785C (es) |
CO (1) | CO5680479A2 (es) |
EG (1) | EG25893A (es) |
ES (1) | ES2392965T3 (es) |
GB (1) | GB0217431D0 (es) |
HK (1) | HK1076465A1 (es) |
IL (1) | IL166290A0 (es) |
IS (1) | IS7697A (es) |
MX (1) | MXPA05000960A (es) |
MY (1) | MY139561A (es) |
NO (1) | NO330531B1 (es) |
NZ (1) | NZ537914A (es) |
PL (1) | PL375400A1 (es) |
RU (1) | RU2342366C2 (es) |
TW (1) | TWI340038B (es) |
UA (1) | UA80283C2 (es) |
WO (1) | WO2004011443A1 (es) |
ZA (1) | ZA200500791B (es) |
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US7288563B2 (en) | 2004-02-19 | 2007-10-30 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
MX2007002240A (es) | 2004-08-28 | 2007-04-20 | Astrazeneca Ab | Derivados de pirimidinosulfonamida como moduladores del receptor quimiocina. |
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RU2007146769A (ru) * | 2005-05-16 | 2009-06-27 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Бициклические производные и их применение в качестве модуляторов ионых каналов |
GB0526255D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
WO2009064938A1 (en) * | 2007-11-16 | 2009-05-22 | Abbott Laboratories | Method of treating arthritis |
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
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WO2009151910A2 (en) * | 2008-05-25 | 2009-12-17 | Wyeth | Combination product of receptor tyrosine kinase inhibitor and fatty acid synthase inhibitor for treating cancer |
MX2011000402A (es) * | 2008-07-16 | 2011-03-15 | Astrazeneca Ab | Derivado de pirimidil sulfonamida y su uso para el tratamiento de enfermedades mediadas por quimiocinas. |
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US20130259830A1 (en) | 2010-07-12 | 2013-10-03 | Ironwood Pharmaceuticals, Inc. | Crth2 modulators |
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WO2012007748A1 (en) | 2010-07-13 | 2012-01-19 | Astrazeneca Ab | New crystalline forms of n-[2-[[(2,3-difluoropheny)methyl)thio]-6-{[(1r,2s)-2,3-dihydroxy-1- methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide |
EA201391626A1 (ru) | 2011-05-04 | 2014-03-31 | Ариад Фармасьютикалз, Инк. | Соединения для ингибирования клеточной пролиферации в egfr-стимулированных типах рака |
SI3255043T1 (sl) | 2011-07-12 | 2021-04-30 | Astrazeneca Ab | N-(6-((2R,3S)-3,4-dihidroksibutan-2-iloksi)-2-(4-fluorobenziltio) pirimidin-4-il)-3-metilazetidin-1-sulfonamid, kot modulator kemokinskega receptorja |
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 |
US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
TW201512171A (zh) | 2013-04-19 | 2015-04-01 | Pfizer Ltd | 化學化合物 |
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2002
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- 2003-07-23 EP EP03740844A patent/EP1527051B1/en not_active Expired - Lifetime
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- 2003-07-23 US US10/522,871 patent/US7582644B2/en not_active Expired - Fee Related
- 2003-07-23 KR KR1020117006101A patent/KR20110033313A/ko not_active Application Discontinuation
- 2003-07-23 UA UAA200500513A patent/UA80283C2/uk unknown
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- 2003-07-25 MY MYPI20032818A patent/MY139561A/en unknown
- 2003-07-28 EG EG2003070726A patent/EG25893A/xx active
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