AR039445A1 - Derivados de pirazina sustituida y su uso - Google Patents

Derivados de pirazina sustituida y su uso

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Publication number
AR039445A1
AR039445A1 ARP030101432A ARP030101432A AR039445A1 AR 039445 A1 AR039445 A1 AR 039445A1 AR P030101432 A ARP030101432 A AR P030101432A AR P030101432 A ARP030101432 A AR P030101432A AR 039445 A1 AR039445 A1 AR 039445A1
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AR
Argentina
Prior art keywords
substituted
heteroaryl
heterocycloalkyl
aryl
cycloalkyl
Prior art date
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ARP030101432A
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English (en)
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Upjohn Co
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Publication of AR039445A1 publication Critical patent/AR039445A1/es

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    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
    • C07D241/20Nitrogen atoms
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S206/00Special receptacle or package
    • Y10S206/828Medicinal content

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Abstract

Son antagonistas de los receptores CRF1, incluyendo los receptores CRF1 humanos. También está relacionada con el uso de los compuestos para tratar un trastorno o afección cuyo tratamiento se puede lograr o facilitar antagonizando un receptor del CRF, tales como los trastornos o enfermedades del sistema nervioso central, especialmente los trastornos de ansiedad, y la depresión y trastornos relacionados al estrés. Reivindicación 1: Un compuesto de fórmula (1), o un estereoisómero, de dicho compuesto, una sal farmacéuticamente aceptable de dicho compuesto, o un profármaco de dicho compuesto, en donde en la fórmula (1): R1 y R2 se seleccionan independientemente entre halógeno, -NO2,-CN, -Ra, -ORa, -S(O)mRa, -NRaRa, -C(O)NRaRa, -C(S)NRaRa, -S(O)mNRaRa, -NRaS(O)mRa, -NRaC(O)ORa, -NRaC(S)ORa, -OC(O)NRaRa, -OC(S)NRaRa, -NRaC(O)NRaRa, -NRaC(S)NRaRa, -C(O)ORa, -C(S)ORa, OC(O)ORa, o CRaRaAr; X se selecciona entre -NR3R4, -OR3, -CR3R4R5, -C(O)R3, -C(S)R3, -S(O)mR3, -NR3C(O)R4, -NR3C(S)R4, -NR3S(O)mR4, o R3; R3, R4 y R5 se seleccionan independientemente entre Ra, alquilo sustituido, arilo sustituido, heteroarilo sustituido, cicloalquilo sustituido, heterocicloalquilo sustituido, aril-cicloalquilo, aril-cicloalquilo sustituido, heteroaril-cicloalquilo, heteroaril-cicloalquilo sustituido, aril-heterocicloalquilo, aril-heterocicloalquilo sustituido, heteroaril-heterocicloalquilo, o heteroaril-heterocicloalquilo sustituido, cada Ra se selecciona entre H, alquilo, cicloalquilo, haloalquilo, arilo, heteroarilo, o heterocicloalquilo, en donde cada Ra puede estar opcionalmente sustituido con 1 a 5 grupos entre Rt, -ORt, -S(O)mRt, -NRtRt, oxo (=O), tiona (=S); cada Rt se selecciona entre H, halógeno, -NO2, -NH2, -OH, -SH, -CN, -C(O)NH2, -C(S)NH2, -C(O)NHalquilo, -C(S)NHalquilo, -C(O)Nalquilalquilo, -C(S)Nalquilalquilo, -Oalquilo, -NHalquilo, -Nalquilalquilo, -S(O)malquilo, -SO2NH2, -SO2NHalquilo y -SO2Nalquilalquilo, alquilo, cicloalquilo, haloalquilo, fenilo, bencilo, heteroarilo, o heterocicloalquilo en donde el fenilo, bencilo, heteroarilo, y heterocicloalquilo pueden estar opcionalmente sustituidos con alquilo o halógeno; G se selecciona entre un resto del grupo de fórmulas (2) en donde cada grupo G puede tener 1 a 6 sustituyentes independientemente seleccionados entre halógeno, -CN, -NO2, oxo(=O), tiona(=S), -OR5, -SR5, -NR5R5, -C(O)R5, -C(S)R5, -C(O)OR5, -C(S)OR5, -C(O)NR5R5, -C(S)NR5R5, -S(O)mR5, -S(O)2NR5R5, -NR5C(O)R5, -NR5C(S)R5, -NR5C(O)OR5, -NR5C(S)OR5, -NR5C(O)NR5R5, -NR5C(S)NR5R5, -NR5S(O)2R5, -OC(O)R5, -OC(S)R5, -OC(O)OR5, -OC(S)OR5, -OC(O)NR5R5, -OC(S)NR5R5, -CR5R5Ar, alquilo, alquilo sustituido, cicloalquilo, cicloalquilo sustituido, arilo, arilo sustituido, heteroarilo, heteroarilo sustituido, heterocicloalquilo, o heterocicloalquilo sustituido, y en donde cada grupo G puede tener hasta un enlace doble en su anillo no aromático; Ar se selecciona entre arilo, arilo sustituido, heteroarilo y heteroarilo sustituido; m es 0, 1 ó 2; y n es 0, 1, ó 2.
ARP030101432A 2002-04-26 2003-04-24 Derivados de pirazina sustituida y su uso AR039445A1 (es)

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US37603102P 2002-04-26 2002-04-26

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US (1) US6964965B2 (es)
EP (1) EP1499599A1 (es)
JP (1) JP2005533014A (es)
AR (1) AR039445A1 (es)
AU (1) AU2003223475A1 (es)
BR (1) BR0309551A (es)
CA (1) CA2480497A1 (es)
MX (1) MXPA04008384A (es)
TW (1) TW200307672A (es)
WO (1) WO2003091225A1 (es)

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CA2524519A1 (en) * 2003-05-09 2004-11-18 Pharmacia & Upjohn Company Llc Compounds as crf1 receptor antagonists
US20060211710A1 (en) * 2005-03-17 2006-09-21 Pfizer Inc Substituted aryl 1,4-pyrazine derivatives
US7319152B2 (en) 2005-09-19 2008-01-15 Wyeth 5-Aryl-indan-1-one and analogs useful as progesterone receptor modulators
US7414142B2 (en) 2005-09-19 2008-08-19 Wyeth 5-aryl-indan-1-one oximes and analogs useful as progesterone receptor modulators
ES2385404T3 (es) * 2006-04-14 2012-07-24 Abbott Laboratories Procedimiento para la preparación de ureas de indazolilo que inhiben los receptores vaniloides de subtipo 1 (VR1)
WO2009006245A2 (en) * 2007-07-02 2009-01-08 Smithkline Beecham Corporation Calcilytic compounds

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EP1499599A1 (en) 2005-01-26
CA2480497A1 (en) 2003-11-06
US6964965B2 (en) 2005-11-15
JP2005533014A (ja) 2005-11-04
TW200307672A (en) 2003-12-16
BR0309551A (pt) 2005-02-09

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