AR039698A1 - Agonistas de los receptores cannabinoides - Google Patents

Agonistas de los receptores cannabinoides

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Publication number
AR039698A1
AR039698A1 ARP030102152A ARP030102152A AR039698A1 AR 039698 A1 AR039698 A1 AR 039698A1 AR P030102152 A ARP030102152 A AR P030102152A AR P030102152 A ARP030102152 A AR P030102152A AR 039698 A1 AR039698 A1 AR 039698A1
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Argentina
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substituted
unsubstituted
group
heteroaryl
cycloalkyl
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ARP030102152A
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English (en)
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Schering Corp
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Publication of AR039698A1 publication Critical patent/AR039698A1/es

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
    • C07D213/6432-Phenoxypyridines; Derivatives thereof
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07D209/04Indoles; Hydrogenated indoles
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    • C07D209/04Indoles; Hydrogenated indoles
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    • C07D209/04Indoles; Hydrogenated indoles
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/70Sulfur atoms
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    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three 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
    • C07D307/64Sulfur atoms
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    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
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    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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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Abstract

Compuestos antagonistas de receptores cannabinoides, sus composiciones farmacéuticas, métodos para preparar dichas composiciones farmacéuticas y métodos de uso de las mismas. Reivindicación 1: Un compuesto representado por la fórmula estructural (1) o su sal o solvato farmacéuticamente aceptable; en la cual: R1 se selecciona entre el grupo que consiste en hidrógeno, alquilo sustituido o insustituido, alquenilo sustituido o insustituido, haloalquilo, -N(R7)2, cicloalquilo sustituido o insustituido, cicloheteroalquilo sustituido o insustituido, arilo sustituido o insustituido, y heteroarilo sustituido o insustituido, en donde el término "sustituido" significa estando sustituido con (X)p; R2 se selecciona entre el grupo que consiste en hidrógeno, alquilo sustituido o insustituido, alquenilo sustituido o insustituido, haloalquilo, -N(R7)2, cicloalquilo sustituido o insustituido, cicloheteroalquilo sustituido o insustituido, arilo sustituido o insustituido, y heteroarilo sustituido o insustituido, en donde el término "sustituido" significa estando sustituido con (X)p; R3 se selecciona entre el grupo que consiste en alquilo, heteroalquilo, arilo, heteroarilo, Br, Cl, F, CF3, OCF2H, OCF3 y alcoxi, en donde R3 puede ser igual o diferente y se selecciona independientemente cuando n > 1; R4 se selecciona entre el grupo que consiste en H, alquilo sustituido o insustituido, alquenilo sustituido o insustituido, cicloalquilo sustituido o insustituido, cicloheteroalquilo sustituido o insustituido, arilo sustituido o insustituido, y heteroarilo sustituido o insustituido, en donde el término "sustituido" significa estando sustituido con (X)p; R5 y R6, los cuales pueden ser iguales o diferentes, se seleccionan independientemente entre el grupo que consiste en H, alquilo sustituido o insustituido, alquenilo sustituido o insustituido, cicloalquilo sustituido o insustituido, cicloheteroalquilo sustituido o insustituido, arilo sustituido o insustituido, y heteroarilo sustituido o insustituido, en donde el término "sustituido" significa estando sustituido con (X)p; R7 se selecciona entre el grupo que consiste en hidrógeno, alquilo sustituido o insustituido, alquenilo sustituido o insustituido, haloalquilo, cicloalquilo sustituido o insustituido, cicloheteroalquilo, arilo sustituido o insustituido, y heteroarilo sustituido o insustituido, o dos grupos R7 pueden formar un anillo de 4-7 átomos de carbono, en donde el término "sustituido" significa estando sustituido con (X)p; L1 se selecciona entre el grupo que consiste en -C(R2)2, -C(O)-, -(CH(OR2))-, -S(O2), -S(O)-, -S-, -O-, -N(R2)-, -C(O)N(H)-, -N(H)C(O)-, CF2-, -CH=N-O-R2 y -CH(NHOR2)-; L2 se selecciona entre el grupo que consiste en un enlace covalente, -CH2-, -CH(CH3)-, -C(CH3)2-, -CH=N-O-R2, -S(O2)-, -S(O), -S-, -C(O)-, -O-, -N(R2)-, -C(O)N(H)- y -N(H)C(O)-; M es una porción heteroarilo; n es 0-4; p es 0-5; X puede ser igual o diferente y se selecciona entre el grupo que consiste en Br, Cl, F, CF3, OH, OCF2H, OCF3, alcoxi, alquilo, cicloalquilo, -O-cicloalquilo, heteroalquilo, -C(O)N(R7)2, -S(O2)R2 y -OS(O2)R2, en donde X se selecciona independientemente cuando p > 1; Y se selecciona entre el grupo que consiste en un enlace covalente, -CH2-, -S(O2)- y -C(O)-; y Z se selecciona entre el grupo que consiste en un enlace covalente, -CH2-, -S(O2)- y -C(O)-, con las siguientes condiciones: cuando L2 es un enlace covalente, M está directamente ligado a R4; cuando Y es un enlace covalente, R1 está directamente ligado al átomo de nitrógeno mostrando en la fórmula (1); y cuando Z es un enlace covalente, R2 está directamente ligado al átomo de nitrógeno mostrando en la fórmula (1).
ARP030102152A 2002-06-19 2003-06-18 Agonistas de los receptores cannabinoides AR039698A1 (es)

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AR039698A1 true AR039698A1 (es) 2005-03-09

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US (1) US7217732B2 (es)
EP (1) EP1539693B9 (es)
JP (1) JP2005533809A (es)
CN (1) CN1662496A (es)
AR (1) AR039698A1 (es)
AT (1) ATE388937T1 (es)
AU (1) AU2003243637A1 (es)
CA (1) CA2487346A1 (es)
DE (1) DE60319714T2 (es)
ES (1) ES2303599T3 (es)
MX (1) MXPA04012704A (es)
PE (1) PE20040574A1 (es)
TW (1) TW200405892A (es)
WO (1) WO2004000807A1 (es)

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US7217732B2 (en) 2007-05-15
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JP2005533809A (ja) 2005-11-10
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CA2487346A1 (en) 2003-12-31
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US20040044051A1 (en) 2004-03-04
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