AR051921A1 - Acidos sustituidos utiles como compuestos farmaceuticos para tratar trastornos respiratorios, composiciones farmaceuticas que los contienen, y procesos para su preparacion - Google Patents

Acidos sustituidos utiles como compuestos farmaceuticos para tratar trastornos respiratorios, composiciones farmaceuticas que los contienen, y procesos para su preparacion

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Publication number
AR051921A1
AR051921A1 ARP050102853A ARP050102853A AR051921A1 AR 051921 A1 AR051921 A1 AR 051921A1 AR P050102853 A ARP050102853 A AR P050102853A AR P050102853 A ARP050102853 A AR P050102853A AR 051921 A1 AR051921 A1 AR 051921A1
Authority
AR
Argentina
Prior art keywords
halogen
alkyl
cycloalkyl
optionally substituted
hydrogen
Prior art date
Application number
ARP050102853A
Other languages
English (en)
Inventor
Roger Victor Bonnert
Stephen Thom
Anil Patel
Timothy Jon Luker
Original Assignee
Astrazeneca Ab
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR051921A1 publication Critical patent/AR051921A1/es

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    • C07D213/24Heterocyclic 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
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Abstract

Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1) o una sal aceptable para uso farmacéutico del mismo, en el cual: T es un enlace, S(O)n (donde n es 0, 1 o 2), CR1R2, NR13; W es O, S(O)n (donde n es 0, 1 o 2), NR13, CR1OR2 o CR1R2; X es hidrogeno, halogeno, ciano, nitro, S(O)nR6, OR12 o C1-6 alquilo que puede ser sustituido por uno o más átomos de halogeno; Y se selecciona entre hidrogeno, halogeno, CN, nitro, SO2R3, OR4, SR4, SOR3, SO2NR4R5, CONR4R5, NR4R5, NR6SO2R3, NR6CO2R6, NR6COR3, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7 o alquilo C1-6, estando los ultimos cuatro grupos optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, OR6 y NR6R7, S(O)nR6 donde n es 0, 1 o 2; Z es arilo o heteroarilo, sustituido optativamente por uno o más sustituyentes seleccionados en forma independiente entre hidrogeno, halogeno, CN, OH, SH, nitro, CO2R6, SO2R9, OR9, SR9, SOR9, SO2NR10R11, CONR10R11, NR10R11, NHSO2R9, NR9SO2R9, NR6CO2R6, NHCOR9, NR9COR9, NR6CONR4R5, NR6SO2NR4R5, arilo, heteroarilo, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, estando los ultimos cuatro grupos optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, OR6, NR6R7, S(O)nR6 (donde n es 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R1 y R2 representan en forma independiente un átomo de hidrogeno, halogeno, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7 o un grupo alquilo C1-6, estando los ultimos cuatro grupos optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, NR6R7, OR6, S(O)nR6 (donde n es 0, 1 o 2); o R1 y R2 jun tos pueden formar un anillo de 3-8 miembros que contiene optativamente uno o más átomos seleccionados entre O, S, NR6 y en sí mismo sustituido optativamente por uno o más alquilo C1-3 o halogeno; R3 representa cicloalquilo C3-7, alquilo C1-6, alquenilo C2-6 o alquinilo C2-6 todos los cuales pueden estar optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R4 y R5 representan en forma independiente hidrogeno, cicloalquilo C3-7 o alquilo C1-6, estando los dos ultimos grupos sustituidos optativamente por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R4 y R5 junto con el átomo de nitrogeno al cual están unidos pueden formar un anillo heterocíclico saturado de 3-8 miembros que contiene optativamente uno o más átomos seleccionados entre O, S(O)n (donde n = 0, 1 o 2), NR8, y en sí mismo sustituido optativamente por halogeno o alquilo C1-3; R6 y R7 representan en forma independiente un átomo de hidrogeno o alquilo C1-6; R8 es hidrogeno, alquilo C1-4, -COalquiloC1-4, CO2alquiloC1-4 o CONR6alquiloC1-4; R9 representa arilo, heteroarilo, cicloalquilo C3-7 o alquilo C1-6, pudiendo los ultimos dos grupos estar sustituidos optativamente por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, arilo heteroarilo, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R10 y R11 representan en forma independiente arilo o heteroarilo, hidrogeno, cicloalquilo C3-7; o alquilo C1-6, estando los dos ultimos grupos sustituidos optativamente por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, arilo, heteroarilo, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; o R10 y R11 junto con el átomo de nitrogeno al cual están unidos pueden formar un anillo heterocíclico saturado de 3-8 miembros que contiene optativamente uno o más átomos seleccionados entre O, S(O)n (donde n = 0, 1 o 2), NR8, y en sí mismo sustituido optativamente por halogeno; o C1-3 alquilo; R12 representa un átomo de hidrogeno o alquilo C1-6 que puede ser sustituido por uno o más átomos de halogeno; y R13 representa un átomo de hidrogeno, alquilo C1-6 que puede ser sustituido por uno o más átomos de halogeno o cicloalquilo C3-7, SO2R6 o COalquiloC1-4, con las siguientes salvedades: cuanto T es carbono o un enlace, el sustituyente en el grupo Z no puede ser NR10R11, donde R10R11 son en forma independiente hidrogeno, arilo, o alquilo; y se excluyen los compuestos ácido 2-[(4-carboxifenil)amino]-4,5-dihidroxi-bencenpropanoico y ácido 4-cloro-2-[(4-clorofenil)tio]-bencenacético.
ARP050102853A 2004-07-08 2005-07-08 Acidos sustituidos utiles como compuestos farmaceuticos para tratar trastornos respiratorios, composiciones farmaceuticas que los contienen, y procesos para su preparacion AR051921A1 (es)

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GB0422057D0 (en) 2004-10-05 2004-11-03 Astrazeneca Ab Novel compounds
ATE517085T1 (de) 2004-11-23 2011-08-15 Astrazeneca Ab Zur behandlung von atemwegserkrankungen geeignete phenoxyessigsäurederivate
GB0510584D0 (en) 2005-05-24 2005-06-29 Novartis Ag Organic compounds
TW200745003A (en) * 2005-10-06 2007-12-16 Astrazeneca Ab Novel compounds
JP5155171B2 (ja) 2005-10-06 2013-02-27 アストラゼネカ・アクチエボラーグ 新規化合物
WO2007052023A2 (en) 2005-11-05 2007-05-10 Astrazeneca Ab Novel compounds
ATE545637T1 (de) 2005-12-15 2012-03-15 Astrazeneca Ab Substituierte diphenylether, -amine, -sulfide und methane zur behandlung von atemwegserkrankungen
UA100983C2 (ru) * 2007-07-05 2013-02-25 Астразенека Аб Бифенилоксипропановая кислота как модулятор crth2 и интермедиаты

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US8022248B2 (en) 2011-09-20
US20080114002A1 (en) 2008-05-15
EP1765768B1 (en) 2013-11-06
WO2006005909A1 (en) 2006-01-19
ES2442677T3 (es) 2014-02-12
HK1171736A1 (en) 2013-04-05
JP4869225B2 (ja) 2012-02-08
CN101014564B (zh) 2012-05-09
CN102557971B (zh) 2015-06-17
CN101014564A (zh) 2007-08-08
GB0415320D0 (en) 2004-08-11
UY29004A1 (es) 2006-02-24
CN102557971A (zh) 2012-07-11
TW200612892A (en) 2006-05-01
JP2008505874A (ja) 2008-02-28

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