AR082112A1 - Derivados de imidazopiridina, su procedimiento de preparacion y su aplicacion en terapeutica - Google Patents

Derivados de imidazopiridina, su procedimiento de preparacion y su aplicacion en terapeutica

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Publication number
AR082112A1
AR082112A1 ARP110102398A ARP110102398A AR082112A1 AR 082112 A1 AR082112 A1 AR 082112A1 AR P110102398 A ARP110102398 A AR P110102398A AR P110102398 A ARP110102398 A AR P110102398A AR 082112 A1 AR082112 A1 AR 082112A1
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Argentina
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alk
group
coor5
alkyl
nr5r6
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ARP110102398A
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Chantal Alcouffe
Reinhard Kirsch
Corentin Herbert
Gilbert Lassale
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Sanofi Sa
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Application filed by Sanofi Sa filed Critical Sanofi Sa
Publication of AR082112A1 publication Critical patent/AR082112A1/es

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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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    • A61K31/437—Heterocyclic 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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    • A61K31/5375—1,4-Oxazines, e.g. morpholine
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    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2013—Organic compounds, e.g. phospholipids, fats
    • A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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    • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/82—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
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    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Procedimiento de preparación y aplicación en terapéutica.Reivindicación 1: Compuesto de fórmula (1), en la que: R1 representa un átomo de hidrógeno o de halógeno; un grupo alquilo sustituido opcionalmente con -COOR5; un grupo alquenilo sustituido opcionalmente con -COOR5; un grupo -COOR5, -CONR5R6; un grupo -NR5COR6, -NR5-SO2R6; o un grupo arilo, en particular fenilo, o heteroarilo, estando dicho grupo arilo o heteroarilo sustituido opcionalmente con uno o varios grupos elegidos entre: los átomos de halógeno, los grupos alquilos, los grupos cicloalquilos, -COOR5, -CF3, -OCF3, -CN, -C(NH2)NOH, -OR5, -O-Alk-COOR5, -O-Alk-NR5R6, -O-Alk-NR7R8, -Alk-OR5, -Alk-COOR5, -CONR5R6, -CO-NR5-OR6, -CO-NR5-SO2R7, -CONR5-Alk-NR5R6, -CONR5-Alk-NR7R8, -Alk-NR5R6, -NR5R6, -NC(O)N(CH3)2, -CO-Alk, -CO(OAlk)nOH, COO-AlkNR5R6, COO-AIkNR7R8 y los grupos heteroarilos de 5 eslabones, estando dichos grupos heteroarilos sustituidos opcionalmente con uno o varios grupos elegidos entre los átomos de halógeno y los grupos alquilos, -CF3, -CN, -COOR5, -Alk-OR5, -Alk-COOR5, -CONR5R6, -CONR7R8, -CO-NR5-OR6, -CO-NR5-SO2R6 y -NR5R6, -Alk-NR5R6, o con un grupo hidroxilo o con un átomo de oxígeno; n es un número entero que va de 1 a 3; R2 y R3 forman conjuntamente, con los átomos de carbono del núcleo fenilo al que están unidos, un heterociclo nitrogenado de 6 eslabones que responde a una de las fórmulas (2), (3) ó (4), en las que los trazos ondulados representan el núcleo fenilo al que están unidos R2 y R3 y: Ra representa un átomo de hidrógeno o un grupo alquilo, halógenoalquilo, -Alk-CF3, -Alk-COOR5, -Alk’-COOR5, -Alk-CONR5R6, -Alk’-CONR5R6, -Alk-CONR7R8, -Alk-NR5R6, -AIkCONR5-OR6, -Alk-NR7R8, -Alk-cicloalquilo, -Alk-O-R5, -Alk-S-R5, -Alk-CN, -OR5, -OAIkCOOR5, -NR5R6, -NR5-COOR6, -Alk-arilo, -Alk-O-arilo, -Alk-O-heteroarilo, -Alk-heteroarilo o heteroarilo en el que el grupo arilo o heteroarilo está sustituido opcionalmente con uno o varios átomos de halógeno y/o grupos alquilos, cicloalquilos, -CF3, -OCF3, -O-R5 o -S-R5; Ra’ representa un átomo de hidrógeno o un grupo alquilo, lineal, ramificado, cíclico o parcialmente cíclico, o un grupo -Alk-OR5 o -Alk-NR5R6, -Alk-NR7R8, estando Ra’ sustituido opcionalmente con uno o varios átomos de halógeno; Rb representa un átomo de hidrógeno o un grupo alquilo o -Alk-COOR5; Rb’ representa un átomo de hidrógeno o un grupo alquilo, halógenoalquilo, cicloalquilo, fenilo o -Alk-COOR5; Rc representa un átomo de hidrógeno o un grupo alquilo, -CN, -COOR5, -CO-NR5R6, -CONR7R8 -CO-NR5-Alk-NR5R6, -CONR5-Alk-OR5, -CONR5SO2R5, o -Alk-arilo, -Alk-heteroarilo, en el que el grupo arilo o heteroarilo está sustituido opcionalmente con uno o varios átomos de halógeno y/o grupos alquilos, cicloalquilos, -CF3, -OCF3, -O-alquilo o -S-alquilo; Rc’ representa un átomo de hidrógeno o un grupo alquilo; Rc’’ representa un átomo de hidrógeno o un grupo alquilo, alquenilo, halógenoalquilo, cicloalquilo, -Alk-NR5R6, -Alk-NR7R8, -Alk-OR5, -Alk-SR5; R4, situado en la posición 6, 7 u 8 del núcleo imidazopiridina, representa: un átomo de hidrógeno; un grupo -COOR5; un grupo -CO-NR5-Alk-NR5R6; un grupo -CO-NR5-Alk-NR7R8; o un grupo -CO-NR5-Alk-OR6; R5 y R6, idénticos o diferentes, representan átomos de hidrógeno, grupos halógenoalquilos o grupos alquilos, grupos cicloalquilos, un grupo Ms; R7 y R8, idénticos o diferentes, representan átomos de hidrógeno o grupos alquilos o fenilos, o bien R7 y R8 forman conjuntamente un ciclo saturado de 3 a 8 eslabones que puede contener opcionalmente un heteroátomo; Alk representa una cadena alquileno lineal o ramificada; y Alk’ representa una cadena alquileno lineal, ramificada, cíclica o parcialmente cíclica; opcionalmente en la forma de una de sus sales farmacéuticamente aceptables.
ARP110102398A 2010-07-06 2011-07-05 Derivados de imidazopiridina, su procedimiento de preparacion y su aplicacion en terapeutica AR082112A1 (es)

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FR1055475A FR2962437B1 (fr) 2010-07-06 2010-07-06 Derives d'imidazopyridine, leur procede de preparation et leur application en therapeutique

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US (2) US8759344B2 (es)
EP (1) EP2590976B1 (es)
JP (1) JP5889295B2 (es)
KR (1) KR101820548B1 (es)
CN (1) CN103080111B (es)
AR (1) AR082112A1 (es)
AU (1) AU2011275427B2 (es)
BR (1) BR112013000273B1 (es)
CA (1) CA2804915C (es)
CL (1) CL2013000016A1 (es)
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