AR045551A1 - Compuestos fenil o piridil amida como prostaglandina e2 antagonistas - Google Patents

Compuestos fenil o piridil amida como prostaglandina e2 antagonistas

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Publication number
AR045551A1
AR045551A1 ARP040103132A ARP040103132A AR045551A1 AR 045551 A1 AR045551 A1 AR 045551A1 AR P040103132 A ARP040103132 A AR P040103132A AR P040103132 A ARP040103132 A AR P040103132A AR 045551 A1 AR045551 A1 AR 045551A1
Authority
AR
Argentina
Prior art keywords
groups
group
atoms
alkyl
substituted
Prior art date
Application number
ARP040103132A
Other languages
English (en)
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of AR045551A1 publication Critical patent/AR045551A1/es

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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C233/81—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/82—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/87—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
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Abstract

Compuestos útiles para el tratamiento de patologías mediadas por prostaglandina tales como dolor o similar en mamíferos. Esta proporciona también una co0mposición farmacéutica que comprende el compuesto anterior. Reivindicación 1: Un compuesto de fórmula (1) en la que A representa un grupo fenilo o un grupo piridilo; B representa un grupo arilo o un grupo heteroarilo; E representa un grupo 1,2-fenileno; R1 y R2 representan independientemente un átomo de H, un átomo de halógeno, un grupo alquilo C1-4, un grupo alcoxi C1-4, un grupo haloalquilo C1-4, un grupo haloalcoxi C1-4, un grupo ciano o un grupo aminocarbonilo; R3 y R4 representan independientemente un átomo de H o un grupo alquilo C1-4, o R3 y R4 pueden unirse formando una cadena alquileno C2-6; R5 representa -CO2H, CO2W, o como se muestra en el grupo de fórmulas (2); R6 representa un grupo alquilo C1-6, un grupo cicloalquilo C3-7 átomos de anillo, un grupo arilo o un grupo heteroarilo; X representa un grupo metileno, un átomo de O o un átomo de S; dichos grupos arilo tienen C6-10; dichos grupos heteroarilo son grupos heterocíclicos aromáticos de 5 a 10 miembros que contienen de 1 a 3 heteroátomos seleccionados entre el grupo compuesto por átomos de S, átomos de O y átomos de N; dichos grupos arilo y dichos grupos heteroarilo a los que se hace referencia en las definiciones de B no están sustituidos o están sustituidos con al menos un sustituyente seleccionado entre el grupo compuesto por sustituyentes alfa; dicho grupo 1,4-fenileno al que se hace referencia en la definición de E no está sustituido o está sustituido con al menos un sustituyente seleccionado entre el grupo constituido por sustituyentes beta; dichos grupos arilo y heteroarilo a los que se hace referencia en las definiciones de R6 y alfa no están sustituidos o están sustituidos con al menos un sustituyente seleccionado entre el grupo constituido por sustituyentes beta; dichos sustituyentes alfa se seleccionan entre el grupo compuesto por átomos de halógeno, grupos alquilo C1-4, grupos alcoxi C1-4, grupos haloalquilo C1-4, grupos haloalcoxi C1-4, grupos ciano, grupos alquinilo C2-6, grupos alcanoilo C1-5, grupos cicloalquilo C3-7 átomos de anillo, grupo heteroarilo, grupos arilo, grupos aralcoxi C7-10, grupos arilcarbonilo, dos grupos alfa adyacentes se juntan opcionalmente formando una cadena alquileno o alquenileno C3-4, grupos aminocarbonilo, grupos alquenilo C2-5, grupos alquiltio C1-4, grupos aminosulfinilo, grupos aminosulfonilo, grupos hidroxi, grupos hidroxialquilo C1-4, grupos nitro, grupos amino, grupos carboxi, grupos alcoxicarbonilo C2-5, grupos alcoxialquilo C1-4, grupos alquilsulfonilo C1-4, grupos alcanoilamino C1-4, grupos alcanoil(alquil)amino C1-6, grupos alcanoilaminoalquilo que tiene de 1 a 6 átomos de C en la parte alcanoilo y alquilo, grupos alcanoil(alquil)aminoalquilo que tienen de 1 a 6 átomos de C en la parte alcanoilo y en cada una de las partes alquilo, grupos alquilsulfonilamino C1-4, grupos mono- o di-alquilaminocarbonilo C1-6, grupos mono o di-alquilaminosulfinilo C1-6, grupos mono o dialquilaminosulfonilo C1-6, grupos aminoalquilo C1-4, grupos mono o di-alquilamino C1-6, grupos mono o di- alquilaminoalquilo C1-6 en cada parte alquilo, grupos aralquilo que tienen de 7 a 10 átomos de C, grupos heteroarilalquilo que tienen de 1 a 4 átomos de C en la parte alquilo, grupos heteroarilalcoxi que tienen de 1 a 4 átomos de C en la parte alcoxi y grupos alquilsulfonilamino que tienen de 1 a 4 átomos de C; dichos constituyentes beta se seleccionan entre el grupo compuesto por átomos de halógeno, grupos alquilo C1-4, grupos alcoxi C1-4, grupos haloalquilo C1-4, grupos haloalcoxi C1-4 y grupos ciano; W es un grupo éster profármaco farmacéuticamente aceptable; con la condición de que R1 y R2 no representen un átomo de H simultáneamente; o una sal farmacéuticamente aceptable del mismo.
ARP040103132A 2003-09-03 2004-09-01 Compuestos fenil o piridil amida como prostaglandina e2 antagonistas AR045551A1 (es)

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