PE20071009A1 - Compuestos derivados de fenoxipiperidinas como antagonistas de histamina h3 - Google Patents

Compuestos derivados de fenoxipiperidinas como antagonistas de histamina h3

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Publication number
PE20071009A1
PE20071009A1 PE2006001648A PE2006001648A PE20071009A1 PE 20071009 A1 PE20071009 A1 PE 20071009A1 PE 2006001648 A PE2006001648 A PE 2006001648A PE 2006001648 A PE2006001648 A PE 2006001648A PE 20071009 A1 PE20071009 A1 PE 20071009A1
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PE
Peru
Prior art keywords
alkyl
halo
histamine
antagonists
phenoxipiperidines
Prior art date
Application number
PE2006001648A
Other languages
English (en)
Inventor
Mwangi W Mutahi
Robert G Aslanian
Michael Y Berlin
Christopher W Boyce
Lera Ruiz Manuel De
Kevin D Mccormick
Daniel M Solomon
Henry A Vaccaro
Junying Zheng
Purakkattle Biju
Younong Yu
Wei Zhou
Xiaohong Zhu
Original Assignee
Schering Corp
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 Schering Corp filed Critical Schering Corp
Publication of PE20071009A1 publication Critical patent/PE20071009A1/es

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    • C07D471/02Heterocyclic 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
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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Abstract

REFERIDA A UN COMPUESTO DE FORMULA I, DONDE a ES 0-4; b ES 0-3; M ES CH; n ES 1-2; p ES 0-2; U y W SON CADA UNO CH; X ES UN ENLACE, ALQUILENO, C(O), ENTRE OTROS; Y ES O, CH2, (CH2)2, C(O), ENTRE OTROS; Z ES UN ENLACE, CH(R9)-(R10-ALQUILENO C1-C5), CH(R9)-CH(R9)-O-, ENTRE OTROS; R1 ES R11-ALQUILO, R11-CICLOALQUILO, R11-ARILO, ENTRE OTROS; R2 ES R13-ALQUILO, R13-ALQUENILO, R13-ARILO, R13-ARILALQUILO, ENTRE OTROS; R3 ES H, ALQUILO, HALO, OH, ALCOXI, ENTRE OTROS; R4 ES H, HALO, ALQUILO, HALOALQUILO, ENTRE OTROS; R9 ES H, ALQUILO, HALOALQUILO; R10 ES 1-3 SUSTITUYENTES SELECCIONADOS DE HALO, -CN, -OH, ALCOXI, ENTRE OTROS; R11 ES 1-4 SUSTITUYENTES SELECCIONADOS DE H, HALO, ALQUILO, ALCOXI, ENTRE OTROS. UN COMPUESTO PREFERIDO ES: 4-[2-(2-PIRIDINA)-3H-IMIDAZO[4,5-b]PIRIDINA-3-IL]-FENOXI-4-IL[N-METIL-(2-AMINOPIRIDIN-4-IL)]PIPERIDINA. REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS SON ANTAGONISTAS DE HISTAMINA H3 Y SON UTILES EN TRATAMIENTO DE ENFERMEDADES INFLAMATORIAS, AFECCIONES ALERGICAS, DIABETES, OBESIDAD, TRASTORNO DEL SISTEMA CARDIOVASCULAR Y SISTEMA NERVIOSO CENTRAL
PE2006001648A 2005-12-21 2006-12-19 Compuestos derivados de fenoxipiperidinas como antagonistas de histamina h3 PE20071009A1 (es)

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US (1) US7638531B2 (es)
EP (1) EP1976848A2 (es)
JP (1) JP2009521448A (es)
KR (1) KR20080087833A (es)
CN (1) CN101426777A (es)
AU (1) AU2006331882A1 (es)
CA (1) CA2634250A1 (es)
IL (1) IL192309A0 (es)
MX (1) MX2008008337A (es)
PE (1) PE20071009A1 (es)
TW (1) TW200734337A (es)
WO (1) WO2007075629A2 (es)

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