AR087328A1 - Derivados de imidazo[1,2-b]piridazina e imidazo[4,5-b]piridina como inhibidores de jak - Google Patents

Derivados de imidazo[1,2-b]piridazina e imidazo[4,5-b]piridina como inhibidores de jak

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Publication number
AR087328A1
AR087328A1 ARP110104376A AR087328A1 AR 087328 A1 AR087328 A1 AR 087328A1 AR P110104376 A ARP110104376 A AR P110104376A AR 087328 A1 AR087328 A1 AR 087328A1
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group
hydroxyalkyl
haloalkyl
cycloalkyl
linear
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Inventor
Juan Bernat Vidal
Gispert Laura Vidal
TAÑA Jordi BACH
Rodriguez Jacob Gonzalez
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Almirall Sa
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Application filed by Almirall Sa filed Critical Almirall Sa
Publication of AR087328A1 publication Critical patent/AR087328A1/es

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    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
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    • C07D487/04Ortho-condensed systems
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
    • A61K9/2018Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2059Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
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    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems

Abstract

Los compuestos son útiles para terapia de enfermedades de tipo inmune e inflamatoria.Reivindicación 1: Un compuesto de fórmula (1), o una sal farmacéuticamente aceptable, o solvato, o N-óxido, o estereoisómero o derivado deuterado o tautómero del mismo, donde, m es 0 o un número entero de 1 a 3; cada uno de X e Y independientemente representa un átomo de nitrógeno o un grupo -CR7, en donde al menos uno de X e Y representa un grupo -CR7; uno de G1 y G2 representa un átomo de nitrógeno y el otro representa un átomo de carbono; cada uno de R1 y R2 independientemente representa un átomo de hidrógeno, un átomo de halógeno, un grupo hidroxi, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-10, un grupo cicloalquenilo C3-10, un grupo arilo monocíclico o policíclico C5-14, un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, un grupo heterocíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos alquilo, haloalquilo, hidroxialquilo, cicloalquilo, cicloalquenilo, arilo, heteroarilo, y heterocíclico están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo alquilsulfonilo C1-4, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; o cada uno de R1 y R2 independientemente representa un grupo -(CH2)0-2OR9, un grupo -O-(CH2)1-2OR9, o un grupo -NR8R9; R3 representa un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-10, un grupo cicloalquenilo C3-10, un grupo arilo monocíclico o policíclico C5-14, un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, un grupo heterocíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos alquilo, haloalquilo, hidroxialquilo, cicloalquilo, cicloalquenilo, arilo, heteroarilo, y heterocíclico están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo, un grupo piperidilo, un grupo -(CH2)nOR9, un grupo -NR8R9, un grupo -C(O)-(CH2)n-R8, un grupo -C(O)-(CH2)n-NR8R9, un grupo -S(O)2(CH2)nR9 o un grupo -S(O)2(CH2)nNR8R9; en donde cada n es 0, 1 ó 2; R4 representa un átomo de hidrógeno, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo C1-6 lineal o ramificado, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; cada uno de R5 y R6 independientemente representa un átomo de hidrógeno, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo lineal o ramificado C1-6, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; R7 representa un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-10, un grupo cicloalquenilo C3-10, un grupo arilo monocíclico o policíclico C5-14, un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, un grupo heterocíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos alquilo, haloalquilo, hidroxialquilo, cicloalquilo, cicloalquenilo, arilo, heteroarilo, y heterocíclico están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; R8 representa un átomo de hidrógeno, un grupo ciano, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo lineal o ramificado C1-6, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; R9 representa un átomo de hidrógeno, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo lineal o ramificado C1-6, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo.
ARP110104376 2010-11-26 2011-11-24 Derivados de imidazo[1,2-b]piridazina e imidazo[4,5-b]piridina como inhibidores de jak AR087328A1 (es)

Applications Claiming Priority (1)

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EP20100382318 EP2463289A1 (en) 2010-11-26 2010-11-26 Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors

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AR087328A1 true AR087328A1 (es) 2014-03-19

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US (1) US9133200B2 (es)
EP (2) EP2463289A1 (es)
JP (1) JP5809704B2 (es)
KR (1) KR20140004637A (es)
CN (1) CN103228654A (es)
AR (1) AR087328A1 (es)
AU (1) AU2011334146A1 (es)
BR (1) BR112013012965A2 (es)
CA (1) CA2815029A1 (es)
CL (1) CL2013001464A1 (es)
CO (1) CO6781467A2 (es)
CR (1) CR20130210A (es)
EA (1) EA201300620A1 (es)
GT (1) GT201300137A (es)
IL (1) IL225232A0 (es)
MX (1) MX2013005257A (es)
NZ (1) NZ608718A (es)
PE (1) PE20140390A1 (es)
SG (1) SG190042A1 (es)
TW (1) TW201236683A (es)
UY (1) UY33752A (es)
WO (1) WO2012069202A1 (es)

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IL225232A0 (en) 2013-06-27
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US20130309200A1 (en) 2013-11-21
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EP2643321A1 (en) 2013-10-02
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UY33752A (es) 2012-05-31
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