AR049433A1 - Derivados de naftalina - Google Patents

Derivados de naftalina

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Publication number
AR049433A1
AR049433A1 ARP050102236A ARP050102236A AR049433A1 AR 049433 A1 AR049433 A1 AR 049433A1 AR P050102236 A ARP050102236 A AR P050102236A AR P050102236 A ARP050102236 A AR P050102236A AR 049433 A1 AR049433 A1 AR 049433A1
Authority
AR
Argentina
Prior art keywords
lower alkyl
alkyl
unsubstituted
substituted
group
Prior art date
Application number
ARP050102236A
Other languages
English (en)
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34982058&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR049433(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR049433A1 publication Critical patent/AR049433A1/es

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    • C07D401/02Heterocyclic 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
    • C07D401/10Heterocyclic 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 linked by a carbon chain containing aromatic rings
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
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    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
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    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/20Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
    • C07D211/22Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
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    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente se refiere a compuestos de la formula (1), y las sales farmacéuticamente aceptables de los mismos, la obtencion de tales compuestos y composiciones farmacéuticas que los contienen. Los compuestos son utiles para el tratamiento y/o prevencion de enfermedades asociadas con la modulacion de receptores H3. Reivindicacion 1: Compuestos de la formula general (1) en la que R1 se elige entre el grupo formado por H, alquilo inferior, fenilo sin sustituir o sustituido por uno o dos restos elegidos con independencia entre sí entre el grupo formado por alquilo inferior, halogenoalcoxi inferior e hidroxialquilo inferior, fenil-alquilo inferior, en el que el anillo fenilo está sin sustituir o sustituido por uno o dos restos elegidos con independencia entre sí entre el grupo formado por alquilo inferior, halogeno, alcoxi inferior, e hidroxialquilo inferior, y (alcoxi inferior)alquilo; R2 se elige entre el grupo formado por H, alquilo inferior, cicloalquilo, cicloalquilalquilo inferior, hidroxialquilo inferior, (alcoxi inferior)alquilo, (alquilo inferior)sulfanilalquilo, di(alquilo inferior)aminoalquilo, fenilo sin sustituir o sustituido por uno o dos restos elegidos con independencia entre sí entre el grupo formado por alquilo inferior, halogeno, alcoxi inferior e hidroxialquilo inferior, fenil-alquilo inferior, en el que el anillo fenilo está sin sustituir o sustituido por uno o dos restos elegidos con independencia entre sí entre el grupo formado por alquilo inferior, halogeno, alcoxi inferior, e hidroxialquilo inferior, pirrolidinilo sin sustituir o sustituido por un resto elegido entre alquilo inferior o halogeno, heteroarilalquilo inferior, en el que el anillo heteroarilo está sin sustituir o sustituido por uno o dos restos alquilo inferior, y heterociclilalquilo inferior, en el que el anillo heterocíclico está sin sustituir o sustituido por uno o dos restos alquilo inferior; o bien R1 y R2 junto con el átomo de N al que están unidos forman un anillo heterocíclico de 4, 5, 6 o 7 eslabones, saturado o parcialmente insaturado que contiene opcionalmente otro heteroátomo elegido entre N, O y S, dicho anillo heterocíclico saturado está sin sustituir o sustituido por uno, dos o tres restos elegidos con independencia entre sí entre el grupo formado por alquilo inferior, halogeno, halogeno-alquilo, hidroxi, hidroxialquilo inferior, alcoxi inferior, oxo, fenilo, bencilo, piridilo, dialquilamino, carbamoílo, alquilsulfonilo inferior y (halogenoalquilo inferior)carbonilamino, o está condensado con un anillo fenilo, dicho anillo fenilo está sin sustituir o sustituido por uno, dos o tres restos elegidos con independencia entre sí entre alquilo inferior, alcoxi inferior y halogeno; A se elige entre los compuestos del grupo de formulas (2), en la que m es 0, 1 o 2; n es 0, 1 o 2; R3 es H o alquilo inferior; R9 y R10 con independencia entre sí se eligen entre H o alquilo inferior; t es 1 o 2; R4 es H o alquilo inferior; X es O, S o N-R8; siendo R8 H o alquilo inferior; p es 0, 1 o 2; R5 es alquilo inferior o cicloalquilo; q es 0, 1 o 2; R6 es alquilo inferior; s es 0, 1 o 2; R7 es alquilo inferior; y las sales farmacéuticamente aceptables de los mismos.
ARP050102236A 2004-06-02 2005-05-31 Derivados de naftalina AR049433A1 (es)

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