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AR048315A1 - Compuestos heterociclicos inhibidores de la produccion de citocinas; composiciones farmaceuticas que los contienen y su uso en el tratamiento de enfermedades inflamatorias y oncologicas. - Google Patents

Compuestos heterociclicos inhibidores de la produccion de citocinas; composiciones farmaceuticas que los contienen y su uso en el tratamiento de enfermedades inflamatorias y oncologicas.

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Publication number
AR048315A1
AR048315A1 ARP050100899A ARP050100899A AR048315A1 AR 048315 A1 AR048315 A1 AR 048315A1 AR P050100899 A ARP050100899 A AR P050100899A AR P050100899 A ARP050100899 A AR P050100899A AR 048315 A1 AR048315 A1 AR 048315A1
Authority
AR
Argentina
Prior art keywords
alkyl
optionally
alkoxy
substituted
cr7r8
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
ARP050100899A
Other languages
English (en)
Inventor
Ming Hong Hao
Victor Kamhi
Matthew Netherton
Alan D Swinamer
Creig Andrew Miller
Derek A Cogan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boehringer Ingelheim Pharma GmbH Co KG
Boehringer Ingelheim Pharmaceuticals Inc
Original Assignee
Boehringer Ingelheim Pharma GmbH Co KG
Boehringer Ingelheim Pharmaceuticals Inc
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 Boehringer Ingelheim Pharma GmbH Co KG, Boehringer Ingelheim Pharmaceuticals Inc filed Critical Boehringer Ingelheim Pharma GmbH Co KG
Publication of AR048315A1 publication Critical patent/AR048315A1/es
Pending legal-status Critical Current

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    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07—ORGANIC CHEMISTRY
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    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
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    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D471/02—Heterocyclic 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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    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

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Abstract

Compuestos descriptos de la formula (1), que inhiben la produccion de citocinas implicadas en procesos inflamatorios y que, por lo tanto, son utiles para tratar enfermedades y afecciones patologicas que implican inflamacion, como la enfermedad inflamatoria cronica. También se describen composiciones farmacéuticas que comprenden estos compuestos utilizables para el tratamiento de enfermedades oncologicas además de las ya mencionadas. Reivindicacion 1: Un compuesto de la formula (1), en el que: Ar1 se selecciona entre i), ii) y iii) a continuacion: i) un carbociclo sustituido con R1, R2 y Rx; ii) una formula (2), en el que uno de E o F es nitrogeno y el otro es carbono, R1 está covalentemente unido o bien a E o F y, cuando nitrogeno es N-R1, no está presente el enlace doble entre E y F; iii) una formula (3) en el que c es un anillo benzo condensado al anillo d que es un anillo heterocíclico de 5-7 miembros opcionalmente sustituido con un grupo oxo (=O), y uno a dos grupos R, siendo cada uno independientemente H o alquilo C1-3; R1 se selecciona entre hidrogeno, NO2, -N(Rc)2, J-C(O)-N(Rc)-, J-S(O)m-N(Rc)-, alquiloC1-6S(O)m-; o R1 se selecciona entre alquilo C1-6, cicloalquilo C3-7, alcoxilo C1-5 o cicloalcoxilo C3-7, alquiltiol C1-5 o cicicloalquiltiol C3-7, acilo C1-5, alcoxicarbonilo C1-5, aciloxi C1-5, acilamino C1-5, alquenilo C2-5, alquinilo C2-5, heterociclo, heterocicloalquilo C1-6, heteroarilo, heteroarilalquilo C1-6 y nitrilo; cada uno de los anteriormente mencionados, cuando es posible, está opcionalmente parcial o totalmente halogenado o está opcionalmente sustituido además con alquilsulfonilamino, aminocarboxilo, alcoxilo, amino, alquilamino, dialquilamino, hidroxilo, oxo, nitro o nitrilo; R2 se selecciona entre: hidrogeno, halogeno, nitrilo, alquiloC1-5S(O)m-, ariloS(O)m, J-O-C(O)-O-, N(Rc)2-C(O)-(CH2)n-, acetilo C1-6, aroilo, alcoxicarbonilo C1-6, alquilo C1-6, cicloalquilo C3-7, alcoxi C1-6, cicloalcoxi C3-5, alquilo C1- 5alcoxiC1-5, hidroxi, hidroxialquilo C1-5 y amino opcionalmente mono o di-sustituido C1-5, arilo o arilalquilo C1-5; cada uno de los ya mencionados, cuando es posible, está opcionalmente parcial o totalmente halogenado u opcionalmente también sustituido con alquilo C1-3, alquilsulfonilamino, alcoxilo, amino, alquilamino, dialquilamino, hidroxilo, oxo, nitro o nitrilo; cada Rx se selecciona entre alquilo C1-6 o cicloalquilo C3-7, estando cada uno opcionalmente sustituido con alquilo C1-3 y opcionalmente parcial o totalmente halogenado, acilo C1-4, aroilo, alcoxi C1-4, alquiloC1-5S(O)m-, en los que cada uno puede estar opcionalmente parcial o totalmente halogenado, halogeno, alcoxicarbonilo C1-6, carbociclosulfonilo; cada Rc es indepedientemente hidrogeno o alquilo C1-5; D, A y B del resto de formula (4) de la formula (1) se seleccionan cada uno independientemente entre N o CH, en los que el átomo de hidrogeno está opcionalmente reemplazado con R6; Het es un anillo de heteroarilo o heterocíclico, en el que Het está opcionalmente sustituido con uno a tres R5; m es 0, 1 o 2; J se selecciona entre alquilo C1-10 y cicloalquilo C3-7, cada uno opcionalmente sustituido con Rb; R3, R4, R6, R7 y R8 se seleccionan cada uno independientemente entre hidrogeno, halogeno, alquilo C1-5, alcoxi C1-5, alquiloC1-5alcoxiC1-5, hidroxi, hidroxialquilo C1-5 o amino opcionalmente mono o di-sustituido con alquilo C1-5, arilo o arilalquilo C1-5; R5 es: Ra, -O-Ra, -S(O)m-Ra, -N(Ra)2, -C(O)-Ra, -NH(CR7R8)n-Ra, N(Ra)2-(CH2)1-2-, -(CR7R8)n-Ra, -O(CR7R8)n-Ra, -C(O)-O(CR7R8)n-Ra, -C(O)(CR7R8)n-Ra, -C(O)C(O)Ra, -C(O)C(O)ORa, -C(O)NHRa o -C(O)NH(CR7R8)n-, cada uno opcionalmente sustituido con alquilo C1-3, halogeno o hidroxi; en los que n es 1-5; o R5 es arilo, heteroarilo o heterociclilo, cada uno opcionalmente sustituido con Ra; Ra y Rb se seleccionan cada uno independientemente entre hidrogeno, alquilo C1-6, hidroxialquilo C1-5, alquenilo C2-5, alquinilo C2-5, carbociclo, carbocicloalquilo C0-2, arilo, heterociclo, heteroarilo, alcoxi C1-5, alquiltio C1-5, amino, alquilamino C1-5, dialquilamino C1-5, arilamino, arilalquilamino C1-5, diarilamino, acilo C1-5, alcoxicarbonilo C1-5, aciloxi C1-5, acilamino C1-5, en los que cada uno de los ya mencionados está opcionalmente parcial o totalmente halogenado, o Ra y Rb se seleccionan entre alquilsulfonilamino C1-5, hidroxi, oxo, halogeno, CF3, -CH2-CF3, nitro y nitrilo, en los que cada carbociclo, heterociclo o heteroarilo C1-3, halogeno o hidroxi; y X es O o S; o sus sales farmacéuticamente aceptables.
ARP050100899A 2004-03-09 2005-03-09 Compuestos heterociclicos inhibidores de la produccion de citocinas; composiciones farmaceuticas que los contienen y su uso en el tratamiento de enfermedades inflamatorias y oncologicas. Pending AR048315A1 (es)

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US55144504P 2004-03-09 2004-03-09

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AR048315A1 true AR048315A1 (es) 2006-04-19

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AR (1) AR048315A1 (es)
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ATE532770T1 (de) 2006-09-05 2011-11-15 Kyowa Hakko Kirin Co Ltd Imidazolderivat
PE20090837A1 (es) * 2007-07-02 2009-07-24 Boehringer Ingelheim Int Nuevos compuestos quimicos
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