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AR067886A1 - Derivados de acido azabifenilaminobenzoico - Google Patents

Derivados de acido azabifenilaminobenzoico

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Publication number
AR067886A1
AR067886A1 ARP080103470A ARP080103470A AR067886A1 AR 067886 A1 AR067886 A1 AR 067886A1 AR P080103470 A ARP080103470 A AR P080103470A AR P080103470 A ARP080103470 A AR P080103470A AR 067886 A1 AR067886 A1 AR 067886A1
Authority
AR
Argentina
Prior art keywords
group
alkyl
cycloalkyl
halogen
atoms
Prior art date
Application number
ARP080103470A
Other languages
English (en)
Inventor
Palomino Laria Julio Cesar Castro
Belart Emma Terricabras
Figueras Aranzazu Cardus
Toribio Maria Estrella Lozoya
Romero Eloisa Navarro
Sola Montserrat Erra
Original Assignee
Almirall Lab
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39764880&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR067886(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from ES200702261A external-priority patent/ES2315185B1/es
Priority claimed from EP08382011A external-priority patent/EP2100881A1/en
Application filed by Almirall Lab filed Critical Almirall Lab
Publication of AR067886A1 publication Critical patent/AR067886A1/es

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    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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    • C07D401/04Heterocyclic 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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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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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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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • C07D213/60Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • Pyridine Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Así como procedimientos para su preparacion, composiciones farmacéuticas que los comprenden y su uso en terapia como inhibidores de la dihidroorotato deshidrogenasa (DHODH). Reivindicacion 1: Un compuesto de formula (1) para uso en el tratamiento o prevencion de un estado patologico o enfermedad susceptible de aliviarse mediante inhibicion de deshidroorotato deshidrogenasa en la que: R1 se selecciona del grupo consistente en átomos de hidrogeno, halogeno, alquilo C1-4, cicloalquilo C3-4, -CF3 y -OCF3, R2 se selecciona del grupo consistente en átomos de hidrogeno, halogeno y grupo alquilo C1-4, R3 se selecciona del grupo consistente en grupos -COOR5, -CONHR5, tetrazolilo, -SO2NHR5 y -CONHSO2R5, donde R5 se selecciona del grupo consistente en un átomo de hidrogeno y grupos alquilo C1-4 lineales o ramificados, R4 se selecciona del grupo consistente en un átomo de hidrogeno y un grupo alquilo C1-4; R9 se selecciona del grupo consistente en un átomo de hidrogeno y un grupo fenilo, G1 representa un grupo seleccionado de N y CR6, donde R6 se selecciona del grupo consistente en átomos de hidrogeno, átomos de halogeno, grupos alquilo C1-4, cicloalquilo C3-4, alcoxi C1-4, -CF3, -OCF3, heteroarilo C5-7 que contiene N monociclico, heterociclilo C3-7 que contiene N monocíclico y un grupo arilo C6-10 que está opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halogeno y un grupo alquilo C1-4, G2 representa un grupo seleccionado de: un átomo de hidrogeno, un grupo hidroxi, un átomo de halogeno, un grupo cicloalquilo C3-4, un grupo alcoxi C1-4 y -NRaRb, donde Ra representa un grupo alquilo C1-4 y Rb se selecciona de un grupo consistente en grupo alquilo C1-4 y grupo alcoxi C1-4-alquilo C1-4, o Ra y Rb junto con el átomo de nitrogeno al que están unidos forman un anillo heterocíclico de 6 a 8 miembros saturado que opcionalmente contiene un átomo de oxígeno como heteroátomo adicional, un anillo heteroaromático de 5 a 10 miembros monocíclico o bicíclico que contiene uno o más átomos de nitrogeno que está opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halogeno, alquilo C1-4, alcoxi C1-4, cicloalquilo C3-4, cicloalcoxi C3-4, -CF3, -OCF3 y -CONR7R8, donde R7 y R8 se seleccionan independientemente de átomo de hidrogeno, grupo alquilo C1-4 lineal o ramificado, grupo cicloalquilo C3-7, o R7 y R8 junto con el átomo de nitrogeno al que están unidos forman un grupo de formula (2) en la que n es un numero entero de 0 a 3, y un grupo fenilo que está opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halogeno, grupos alquilo C1-4, hidroxi, alcoxi C1-4, cicloalquilo C3-4, cicloalcoxi C3-4, ciano, -CF3, -OCF3, -CONR7R8, oxadiazolilo, triazolilo, pirazolilo e imidazolilo, estando los grupos oxadiazolilo, triazolilo, pirazolilo e imidazolilo opcionalmente sustituidos con un grupo alquilo C1-4 o cicloalquilo C3-7 y donde R7 y R8 se seleccionan independientemente de átomo de hidrogeno, grupo alquilo C1-4 lineal o ramificado, grupo cicloalquilo C3-7, o R7 y R8 junto con el átomo de nitrogeno al que están unidos forman un grupo de formula (2) en la que n es un numero entero de 0 a 3 o, G2 junto con R6 forma un grupo carbocíclico C5-10 no aromático o un grupo arilo C6-10, y sus sales y N-oxidos farmacéuticamente aceptables.
ARP080103470A 2007-08-10 2008-08-08 Derivados de acido azabifenilaminobenzoico AR067886A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES200702261A ES2315185B1 (es) 2007-08-10 2007-08-10 Nuevos derivados del acido azabifenilaminobenzoico.
EP08382011A EP2100881A1 (en) 2008-03-13 2008-03-13 Pyrimidyl- or pyridinylaminobenzoic acid derivatives

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AR067886A1 true AR067886A1 (es) 2009-10-28

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EP (1) EP2178840B1 (es)
JP (1) JP5367707B2 (es)
KR (1) KR20100046001A (es)
CN (1) CN101801931B (es)
AR (1) AR067886A1 (es)
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Families Citing this family (63)

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Publication number Priority date Publication date Assignee Title
ES2319596B1 (es) 2006-12-22 2010-02-08 Laboratorios Almirall S.A. Nuevos derivados de los acidos amino-nicotinico y amino-isonicotinico.
EP2135610A1 (en) * 2008-06-20 2009-12-23 Laboratorios Almirall, S.A. Combination comprising DHODH inhibitors and methotrexate
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