UY25965A1 - AMINOMETIL-2 3 8 9-TETRAHIDRO-7H-1 4-DIOXINO [2 3 E] -INDOL-8- ONAS AND DERIVATIVES - Google Patents

AMINOMETIL-2 3 8 9-TETRAHIDRO-7H-1 4-DIOXINO [2 3 E] -INDOL-8- ONAS AND DERIVATIVES

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Publication number
UY25965A1
UY25965A1 UY25965A UY25965A UY25965A1 UY 25965 A1 UY25965 A1 UY 25965A1 UY 25965 A UY25965 A UY 25965A UY 25965 A UY25965 A UY 25965A UY 25965 A1 UY25965 A1 UY 25965A1
Authority
UY
Uruguay
Prior art keywords
alkyl
optionally substituted
hydrogen
detailed
indole
Prior art date
Application number
UY25965A
Other languages
Spanish (es)
Inventor
Gary P Stack
Richard E Mewsaw
Byron A Bravo
Young H Kang
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Priority to UY25965A priority Critical patent/UY25965A1/en
Publication of UY25965A1 publication Critical patent/UY25965A1/en

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Abstract

Los compuestos de la fórmula l (como por ejemplo: 2-(bencilamino)metil-2,3,8,9-tetrahidro-7H-1,4-dioxino[2,3-e]-indol-8-ona) en la cual R1 y R2 son, independientemente, hidrógeno, alquilo, fenilo o benzilo; o R1 y R2, juntos, son bencilideno sustituido opcionalmente por R3 según se lo detalla más abajo, o alquilideno, o R1 y R2 tomados junto al carbono al cual se hallan unidos, forman una porción de carbonilo o un grupo cicloalquilo; R3 es hidrogeno, hidróxido, halo, trifluorometilo, trifluorometoxi, alquilo, alcoxi, aralcoxi,alcanoiloxi,amino, mono o di alquilamino, alcanamido, o alcanosulfonamido, R4 es hidrógeno o alquilo, n es un entero de 0 a 6 inclusive, Z es hidrogeno, hidroxi, alquilo, alquenilo, alquinilo, alcoxi, cicloalquilo, policiclo-alquilo, fenilo sustituido opcionalmente por R3,según se lo detalló anteriormente, fenoxi sustituido opcionalmente por R3, según se lo detalló del grupo heterarilo o heteroariloxi es seleccionado de tiofeno, furano, piridina, pirazina, pirimidina, indol, indazol, imidazo, cromano, cumarina, carboestirilo, quinolina, bencisoxazol, benzoxazol, pirazol, pirrol, tiazo, oxazol, o isoxazol y el anillo heterocíclico es sustituido opcionalmente por R3 según se lo detalló anteriormente, o una sal del mismo, farmacéuticamente aceptable, son útiles para el tratamiento de trastornos del sistema dopaminérgico. Un método para el tratamiento de enfermedades de desregulación de la dopamina cerebral, que implica la administración, oral o parental, de una cantidad de un compuesto de la fórmula l, a un sujeto que padezca ese tipo de trastorno del sistema dopaminérgico.Compounds of formula l (such as: 2- (benzylamino) methyl-2,3,8,9-tetrahydro-7H-1,4-dioxino [2,3-e] -indole-8-one) in which R1 and R2 are independently hydrogen, alkyl, phenyl or benzyl; or R1 and R2, together, are benzylidene optionally substituted by R3 as detailed below, or alkylidene, or R1 and R2 taken together with the carbon to which they are attached, form a carbonyl moiety or a cycloalkyl group; R3 is hydrogen, hydroxide, halo, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, aralkoxy, alkanoyloxy, amino, mono or di alkylamino, alkanido, or alkanesulfonamido, R4 is hydrogen or alkyl, n is an integer from 0 to 6 inclusive, Z is hydrogen, hydroxy, alkyl, alkenyl, alkynyl, alkoxy, cycloalkyl, polycycloalkyl, phenyl optionally substituted by R3, as detailed above, phenoxy optionally substituted by R3, as detailed from the heteroaryl or heteroaryloxy group is selected from thiophene, furan, pyridine, pyrazine, pyrimidine, indole, indazole, imidazo, chroman, coumarin, carbostyril, quinoline, benzisxaxazole, benzoxazole, pyrazole, pyrrole, thiazo, oxazole, or isoxazole and is optionally substituted by R3 as detailed above , or a pharmaceutically acceptable salt thereof, are useful for the treatment of disorders of the dopaminergic system. A method for the treatment of brain dopamine dysregulation diseases, involving the administration, orally or parentally, of an amount of a compound of formula I, to a subject suffering from such a disorder of the dopaminergic system.

UY25965A 2000-01-17 2000-01-17 AMINOMETIL-2 3 8 9-TETRAHIDRO-7H-1 4-DIOXINO [2 3 E] -INDOL-8- ONAS AND DERIVATIVES UY25965A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
UY25965A UY25965A1 (en) 2000-01-17 2000-01-17 AMINOMETIL-2 3 8 9-TETRAHIDRO-7H-1 4-DIOXINO [2 3 E] -INDOL-8- ONAS AND DERIVATIVES

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
UY25965A UY25965A1 (en) 2000-01-17 2000-01-17 AMINOMETIL-2 3 8 9-TETRAHIDRO-7H-1 4-DIOXINO [2 3 E] -INDOL-8- ONAS AND DERIVATIVES

Publications (1)

Publication Number Publication Date
UY25965A1 true UY25965A1 (en) 2001-08-27

Family

ID=38812155

Family Applications (1)

Application Number Title Priority Date Filing Date
UY25965A UY25965A1 (en) 2000-01-17 2000-01-17 AMINOMETIL-2 3 8 9-TETRAHIDRO-7H-1 4-DIOXINO [2 3 E] -INDOL-8- ONAS AND DERIVATIVES

Country Status (1)

Country Link
UY (1) UY25965A1 (en)

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Effective date: 20110802