AR067673A1 - Derivados de 1,3 oxazinan - 2 - ona como inhibidores ciclicos de la 11 beta -hidroxiesteroide deshidrogenasa 1. composiciones farmaceuticas. - Google Patents
Derivados de 1,3 oxazinan - 2 - ona como inhibidores ciclicos de la 11 beta -hidroxiesteroide deshidrogenasa 1. composiciones farmaceuticas.Info
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- AR067673A1 AR067673A1 ARP080103215A ARP080103215A AR067673A1 AR 067673 A1 AR067673 A1 AR 067673A1 AR P080103215 A ARP080103215 A AR P080103215A AR P080103215 A ARP080103215 A AR P080103215A AR 067673 A1 AR067673 A1 AR 067673A1
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- alkyl
- cycloalkyl
- alkoxy
- 2nhc
- nhs
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Abstract
Composiciones farmacéuticas de los mismos para el tratamiento terapéutico de enfermedades asociadas con la modulacion o inhibicion de 11beta-HSD1 en mamíferos. Reivindicacion 1: Un compuesto de formula (1) en la que: R está (a) ausente o (b) se selecciona entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-3-alcoxi C1-3 o alcoxi C1-3-alquilo C1-3 y está opcionalmente sustituido hasta con cuatro grupos seleccionados independientemente entre fluor, ciano, oxo, R4, R4O-, (R4)2N-, R4O2C-, R4S, R4S(=O)-, R4S(=O)2-, R4C(=O)NR4-, (R4)2NC(=O)-, (R4)2NC(=O)O-, (R4)2NC(=O)NR4-, R4OC(=O)NR4-, (R4)2NC(=NCN)NR4-, (R4O)2P(=O)O-, (R4O)2P(=O)NR4-, R4OS(=O)2NR4-, (R4)2NS(=O)2O-, (R4)2NS(=O)2NR4-, R4S(=O)2NR4-, R4S(=O)2NHC(=O)-, R4S(=O)2NHC(=O)O-, R4S(=O)2NHC(=O)NR4-, R4OS(=O)2NHC(=O)-, R4OS(=O)2NHC(=O)O-, R4OS(=O)2NHC(=O)NR4-, (R4)2NS(=O)2NHC(=O)-, (R4)2NS(=O)2NHC(=O)O-, (R4)2NS(=O)2NHC(=O)NR4-, R4C(=O)NHS(=O)2-, R4C(=O)NHS(=O)2O-, R4C(=O)NHS(=O)2NR4, R4OC(=O)NHS(=O)2-, R4OC(=O)NHS(=O)2O-, R4OC(=O)NHS(=O)2NR4-, (R4)2NC(=O)NHS(=O)2, (R4)2NC(=O)NHS(=O)2O- (R4)2NC(=O)NHS(=O)2NR4-, heterociclilo, heteroarilo, arilamino y heteroarilamino; A1 es (a) un enlace, o. (b) alquileno C1-3, CH2CH2O, donde el oxigeno está unido a Cy1 o CH2C(=O),donde el carbono del carbonilo está unido a Cy1; Cy1 es arilo, heteroarilo, cicloalquilo monocíclico o heterociclilo monociclico y está opcionalmente sustituido con 1 a 4 grupos seleccionados independientemente entre fluor, cloro, bromo, .yodo ciano, nitro, amino, hidroxi, carboxi, alquilo C1-6, hidroxialquilo C1-6, cicloalquilo C3-6, hidroxicicloalquilo C3-6, cicloalquilalquilo C4-7, alquenilo C2-6, haloalquenilo C2-6, hidroxialquenilo C2-6, alquinilo C2-6, cicloalquil C3-6-alquinilo C2-4, haloalquilo C1-6, halocicloalquilo C3-6, halocicloalquilalquilo C4-7, alcoxi C1-6, cicloalcoxi C3-6, cicloalquilalcoxi C4-7, haloalcoxi C1-6, halocicloalcoxi C3-6, halocicloalquilalcoxi C4-7, alquiltio C1-6, cicloalquiltio C3-6, cicloalquilalquiltio C4-7, haloalquiltio C1-6, halocicloalquiltio C3-6, halocicloalquilalquiltio C4-7, alcanosulfinilo C1-6, cicloalcanosulfinilo C3-6, cicloalquilalcanosulfinilo C4-7, haloalcanosulfinilo C1-6, halocicloalcanosulfinilo C3-6, halocicloalquilalcanosulfinilo C4-7, alcanosulfonilo C1-6, cicloalcanosulfonilo C3-6, cicloalquilalcanosulfonilo C4-7, haloalcanosulfonilo C1-6, halocicloalcanosulfonilo C3-6, halocicloalquilalcanosulfonilo C4-7, alquilamino C1-6, dialquilamino C1-6, aIcoxi C1-6-alcoxi C1-6, haloalcoxi C1-6-alcoxi C1-6, alcoxicarbonilo C1-6, H2NCO, H2NSO2, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, alcoxi C1-3-alquilaminocarbonilo C1-3, heterociclilcarbonilo, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C1-6, heterociclosulfonilo, alquilcarbonilamino C1-6, alquilcarbonilamino C1-6-alquilo C1-6, alquilsulfonilamino C1-6, alquilsulfonilamino C1-6-alquilo C1-6, alcoxicarbonil C1-6-alcoxi C1-6, alcoxi C1-6-alquilo C1-6, haloalcoxi C1-6-alquilo C1-6, hidroxialcoxi C1-6, heteroarilo, oxo, aminoalquilo C1-6, alquilamino C1-6-alquilo C1-6, dialquilamino C1-6-alquilamino C1-6-alcoxi C2-6, alquilamino C1-6-alcoxi C2-6, dialquilamino C1-6-alcoxi C2-6, alquilcarbonilo C1-6, cicloalquilcarbonilo C3-6, dicloalquilaminocarbonilo C3-6, cicloalquil C3-6-alquil C1-6-aminocarbonilo, dicicloalquilaminocarbonilo C3-6, cicloalquilaminosulfonilo C3-6, cicloalquil C3-6-alquil C1-6-aminosulfonilo, dicicloalquilaminosulfonilo C3-6, cianoalquilo C1-6, aminocarbonilalquilo C1-6, alquilaminocarbonil C1-6-alquilo C1-6, dialquilaminocarbonil C1-6-alquilo C1-6, cicloalquilaminocarbonil C3-6-alquilo C1-6, cicloalquil C3-6-alquil C1-6-aminocarbonilalquilo C1-6 y dicicloalquilaminocarbonil C3-6-alquilo C1-6; A2 es (a) un enlace, O, S o NR4 o (b) alquileno C1-3 o alquilenooxi C1-2, estando cada uno opcionalmente sustituido con 1 a 4 grupos seleccionados independientemente entre metilo, etilo, trifluorometilo u oxo; Cy2 es (a) hidrogeno o (b) arilo, heteroarilo, cicloalquilo o heterociclilo y está opcionalmente sustituido con 1 a 4 grupos seleccionados independientemente entre fluor, cloro, bromo, yodo, ciano, nitro, amino, hidroxi, carboxi, alquilo C1-6, hidroxialquilo C1-6, cicloalquilo C3-6, hidroxicicloalquilo C3-6, cicloalquilalquilo C4-7, alquenilo C2-6, haloalquenilo C2-6, hidroxialquenilo C2-6, alquinilo C2-6, cicloalquil C3-6-alquinilo C2-4, haloalquilo C1-6, halocicloalquilo C3-6, halocicloalquilalquilo C4-7, alcoxi C1-6, cicloalcoxi C3-6, cicloalquilalcoxi C4-7, haloalcoxi C1-6, halocicloalcoxi C3-6, halocicloalquilalcoxi C4-7, alquiltio C1-6, cicloalquiltio C3-6, cicloalquilalquiltio C4-7, haloalquiltio C1-6, halocicloalquiltio C3-6, halocicloalquilalquiltio C4-7, alcanosulfinilo C1-6, cicloalcanosulfinilo C3-6, cicloalquilalcanosulfinilo C4-7, haloalcanosulfinilo C1-6, halocicloalcanosulfinilo C3-6, halocicloalquilalcanosulfinilo C4-7, alcanosulfonilo C1-6, cicloalcanosulfonilo C3-6, cicloalquilalcanosulfonilo C4-7, haloalcanosulfonilo C1-6, halocicloalcanosulfonilo C3-6, halocicloalquilalcanosulfonilo C4-7, alquilamino C1-6, dialquilamino C1-6, aIcoxi C1-6-alcoxi C1-6, haloalcoxi C1-6-alcoxi C1-6, alcoxicarbonilo C1-6, H2NCO, H2NSO2, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, alcoxi C1-3-alquilaminocarbonilo C1-3, heterociclilcarbonilo, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C1-6, heterociclosulfonilo, alquilcarbonilamino C1-6, alquilcarbonilamino C1-6-alquilo C1-6, alquilsulfonilamino C1-6, alquilsulfonilamino C1-6-alquilo C1-6, alcoxicarbonil C1-6-alcoxi C1-6, alcoxi C1-6-alquilo C1-6, haloalcoxi C1-6-alquilo C1-6, hidroxialcoxi C1-6, heteroarilo, oxo, aminoalquilo C1-6, alquilamino C1-6-alquilo C1-6, dialquilamino C1-6-alquilamino C1-6-alcoxi C2-6, alquilamino C1-6-alcoxi C2-6, dialquilamino C1-6-alcoxi C2-6, alquilcarbonilo C1-6, cicloalquilcarbonilo C3-6, cicloalquilaminocarbonilo C3-6, cicloalquil C3-6-alquil C1-6-aminocarbonilo, dicicloalquilaminocarbonilo C3-6, cicloalquilaminosulfonilo C3-6, cicloalquil C3-6-alquil C1-6-aminosulfonilo, dicicloalquilaminosulfonilo C3-6, cianoalquilo C1-6, aminocarbonilalquilo C1-6, alquilaminocarbonil C1-6-alquilo C1-6, dialquilaminocarbonil C1-6-alquilo C1-6, cicloalquilaminocarbonil C3-6-alquilo C1-6, cicloalquil C3-6-alquil C1-6-aminocarbonilalquilo C1-6 y dicicloalquilaminocarbonil C3-6-alquilo C1-6; en un aspecto, el heterociclilo representado por Cy2 es distinto de tiazolidina-2,4-dionilo opcionalmente sustituido; Y es alquilo C1-6, haloalquilo C1-6 u oxo; n es 0, 1 o 2; E es (a) un enlace o (b) alquileno C1-3 o alquileniloxi C1-2, donde el O está unido a R2, estando cada uno opcionalmente sustituido con 1 a 4 grupos seleccionados independientemente entre metilo, etilo, trifluorometilo u oxo; R2 es alquilo C1-6, arilo, heteroarilo, cicloalquilo o heterociclilo y está opcionalmente sustituido hasta con 4 grupos seleccionados independientemente entre fluor, cloro, bromo, yodo, ciano, nitro, amino, hidroxi, carboxi, alquilo C1-6, hidroxialquilo C1-6, cicloalquilo C3-6, hidroxicicloalquilo C3-6, cicloalquilalquilo C4-7, alquenilo C2-6, haloalquenilo C2-6, hidroxialquenilo C2-6, alquinilo C2-6, cicloalquil C3-6-alquinilo C2-4, haloalquilo C1-6, halocicloalquilo C3-6, halocicloalquilalquilo C4-7, alcoxi C1-6, cicloalcoxi C3-6, cicloalquilalcoxi C4-7, haloalcoxi C1-6, halocicloalcoxi C3-6, halocicloalquilalcoxi C4-7, alquiltio C1-6, cicloalquiltio C3-6, cicloalquilalquiltio C4-7, haloalquiltio C1-6, halocicloalquiltio C3-6, halocicloalquilalquiltio C4-7, alcanosulfinilo C1-6, cicloalcanosulfinilo C3-6, cicloalquilalcanosulfinilo C4-7, haloalcanosulfinilo C1-6, halocicloalcanosulfinilo C3-6, halocicloalquilalcanosulfinilo C4-7, alcanosulfonilo C1-6, cicloalcanosulfonilo C3-6, cicloalquilalcanosulfonilo C4-7, haloalcanosulfonilo C1-6, halocicloalcanosulfonilo C3-6, halocicloalquilalcanosulfonilo C4-7, alquilamino C1-6, dialquilamino C1-6, aIcoxi C1-6-alcoxi C1-6, haloalcoxi C1-6-alcoxi C1-6, alcoxicarbonilo C1-6, H2NCO, H2NSO2, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, alcoxi C1-3-alquilaminocarbonilo C1-3, heterociclilcarbonilo, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C1-6, heterociclosulfonilo, alquilcarbonilamino C1-6, alquilcarbonilamino C1-6-alquilo C1-6, alquilsulfonilamino C1-6, alquilsulfonilamino C1-6-alquilo C1-6, alcoxicarbonil C1-6-alcoxi C1-6, alcoxi C1-6-alquilo C1-6, haloalcoxi C1-6-alquilo C1-6, hidroxialcoxi C1-6, heteroarilo, oxo, aminoalquilo C1-6, alquilamino C1-6-alquilo C1-6, dialquilamino C1-6-alquilo C1-6-aminoalcoxi C2-6, alquilamino C1-6-alcoxi C2-6, dialquilamino C1-6-alcoxi C2-6, alquilcarbonilo C1-6, cicloalquilcarbonilo C3-6, cicloalquilaminocarbonilo C3-6, cicloalquil C3-6-alquil C1-6-aminocarbonilo, dicicloalquilaminocarbonilo C3-6, cicloalquilaminosulfonilo C3-6, cicloalquil C3-6-alquil C1-6-aminosulfonilo, dicicloalquilaminosulfonilo C3-6, cianoalquilo C1-6, aminocarbonilalquilo C1-6, alquilaminocarbonil C1-6-alquilo C1-6, dialquilaminocarbonil C1-6-alquilo C1-6, cicloalquilaminocarbonil C3-6-alquilo C1-6, cicloalquil C3-6-alquil C1-6-aminocarbonilalquilo C1-6 y dicicloalquilaminocarbonil C3-6-alquilo C1-6; R3 se selecciona entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquil C3-5-alquilo C1-4, alcoxi C1-3-alcoxi C1-3 o alcoxi C1-3-alquilo C1-3 y está opcionalmente sustituido hasta con cuatro grupos seleccionados independientemente entré fluor, ciano, oxo, R4, R4O-, (R4)2N-, R4O2C-, R4O(=O)O-, R4S(=O)2-, R4C(=O)NR4-, (R4)2NC(=O)-, (R4)2NC(=O)O-, (R4)2NC(=O)NR4-, R4OC(=O)NR4-, (R4)2NC(=NCN)NR4-, (R4O)2P(=O)O-, (R4O)2P(=O)NR4-, R4OS(=O)2NR4-, (R4)2NS(=O)2O-, (R4)2NS(=O)2NR4-, R4S(=O)2NR4-, R4S(=O)2NHC(=O)-, R4S(=O)2NHC(=O)O-, R4S(=O)2NHC(=O)NR4-, R4OS(=O)2NHC(=O)-, R4OS(=O)2NHC(=O)O-, R4OS(=O)2NHC(=O)NR4-, (R4)2NS(=O)2NHC(=O)-, (R4)2NS(=O)2NHC(=O)O-, (R4)2NS(=O)2NHC(=O)NR4-, R4C(=O)NHS(=O)2-, R4C(=O)NHS(=O)2O-, R4C(=O)NHS(=O)2NR4, R4OC(=O)NHS(=O)2-, R4OC(=O)NHS(=O)2O-, R4OC(=O)NHS(=O)2NR4-, (R4)2NC(=O)NHS(=O)2, (R4)2NC(=O)NHS(=O)2O- (R4
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-
2008
- 2008-07-25 EP EP08794755A patent/EP2183229B1/en not_active Not-in-force
- 2008-07-25 JP JP2010518233A patent/JP5470557B2/ja not_active Expired - Fee Related
- 2008-07-25 US US12/670,205 patent/US8575156B2/en not_active Expired - Fee Related
- 2008-07-25 CA CA2697168A patent/CA2697168A1/en not_active Abandoned
- 2008-07-25 ES ES08794755T patent/ES2395081T3/es active Active
- 2008-07-25 AR ARP080103215A patent/AR067673A1/es unknown
- 2008-07-25 CA CA2697147A patent/CA2697147A1/en not_active Abandoned
- 2008-07-25 TW TW097128296A patent/TW200911796A/zh unknown
- 2008-07-25 WO PCT/US2008/009048 patent/WO2009017671A1/en not_active Ceased
- 2008-07-25 JP JP2010518226A patent/JP5451611B2/ja not_active Expired - Fee Related
- 2008-07-25 CL CL2008002199A patent/CL2008002199A1/es unknown
- 2008-07-25 EP EP08794727.1A patent/EP2183228B1/en not_active Not-in-force
- 2008-07-25 AT AT08794755T patent/ATE554078T1/de active
- 2008-07-25 WO PCT/US2008/009017 patent/WO2009017664A1/en not_active Ceased
- 2008-07-25 US US12/670,209 patent/US8329897B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| TW200911796A (en) | 2009-03-16 |
| US20110015157A1 (en) | 2011-01-20 |
| CA2697147A1 (en) | 2009-02-05 |
| ATE554078T1 (de) | 2012-05-15 |
| US20100256363A1 (en) | 2010-10-07 |
| JP2010534654A (ja) | 2010-11-11 |
| JP5451611B2 (ja) | 2014-03-26 |
| JP2010534656A (ja) | 2010-11-11 |
| US8575156B2 (en) | 2013-11-05 |
| ES2395081T3 (es) | 2013-02-08 |
| EP2183229B1 (en) | 2012-04-18 |
| WO2009017664A1 (en) | 2009-02-05 |
| CA2697168A1 (en) | 2009-02-05 |
| EP2183228A1 (en) | 2010-05-12 |
| WO2009017671A1 (en) | 2009-02-05 |
| CL2008002199A1 (es) | 2009-10-23 |
| EP2183228B1 (en) | 2014-08-20 |
| JP5470557B2 (ja) | 2014-04-16 |
| US8329897B2 (en) | 2012-12-11 |
| EP2183229A1 (en) | 2010-05-12 |
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