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AR096640A1 - Derivados de indolin-2-ona o pirrolo-piridin / pirimidin-2-ona - Google Patents

Derivados de indolin-2-ona o pirrolo-piridin / pirimidin-2-ona

Info

Publication number
AR096640A1
AR096640A1 ARP140102299A ARP140102299A AR096640A1 AR 096640 A1 AR096640 A1 AR 096640A1 AR P140102299 A ARP140102299 A AR P140102299A AR P140102299 A ARP140102299 A AR P140102299A AR 096640 A1 AR096640 A1 AR 096640A1
Authority
AR
Argentina
Prior art keywords
lower alkyl
halogen
disorders
cycloalkyl
substituted
Prior art date
Application number
ARP140102299A
Other languages
English (en)
Inventor
Brunner Daniela
Hilpert Hans
Kolczewski Sabine
Limberg Anja
Malberg Jessica
Prinssen Eric
Riemer Claus
G Shankar Bavani
Stoll Theodor
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR096640A1 publication Critical patent/AR096640A1/es

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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
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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
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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Abstract

Los compuestos se pueden utilizar para el tratamiento de ciertos trastornos del sistema nervioso central que son síntomas positivos (psicosis) y negativos de la esquizofrenia, el abuso de sustancias, adicción al alcohol y las drogas, los trastornos obsesivo-compulsivos, deterioro cognitivo, trastornos bipolares, trastornos del estado de ánimo, depresión mayor, depresión resistente al tratamiento, trastornos de ansiedad, enfermedad de Alzheimer, autismo, enfermedad de Parkinson, dolor crónico, trastorno límite de la personalidad, trastornos del sueño, síndrome de fatiga crónica, rigidez, efectos antiinflamatorios en artritis y problemas de equilibrio. Reivindicación 1: Un compuesto de fórmula (1) en el que Ar es un grupo heteroarilo, que contiene uno, dos o tres heteroátomos, seleccionados a partir de N, S ó O; R¹ es hidrógeno, alquilo inferior, halógeno, amino, dimetilamino, ciano, alquilo inferior sustituido por halógeno, alquilo inferior sustituido por hidroxi, CH(OH)CF₃, (CH₂)ₒ-alcoxi inferior, cicloalquilo opcionalmente sustituido por CF₃ o heterocicloalquilo opcionalmente sustituido por alquilo inferior; R² es hidrógeno, alquilo inferior, (CH₂)ₒ-cicloalquilo, (CH₂)ₒ-O-cicloalquilo, (CH₂)ₒ-alcoxi inferior, (CH₂)ₒ-alcoxi inferior sustituido por halógeno, (CH₂)ₒ-heterocicloalquilo opcionalmente sustituido por alquilo inferior, (CH₂)ₒ-S(O)₂-cicloalquilo, alquilo inferior sustituido por uno o dos hidroxi, alquilo inferior sustituido por uno o dos alcoxi inferior, (CH₂)ₒ-S(O)₂-alquilo inferior, alquilo inferior sustituido por halógeno o CH₂CH(OH)CF₃; R³ es halógeno o alquilo inferior; X es CH o N; X¹ es CH o N; n es 1 ó 2; o es 0, 1, 2 ó 3; m es 0, 1 ó 2; y la línea de puntos es un enlace o puede no serlo; así como con sales farmacéuticamente aceptables de los mismos, con una mezcla racémica, o con su correspondiente enantiómero y/o isómero óptico y/o estereoisómero de los mismos.
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