AR088352A1 - Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina - Google Patents

Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina

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Publication number
AR088352A1
AR088352A1 ARP120103852A AR088352A1 AR 088352 A1 AR088352 A1 AR 088352A1 AR P120103852 A ARP120103852 A AR P120103852A AR 088352 A1 AR088352 A1 AR 088352A1
Authority
AR
Argentina
Prior art keywords
unsubstituted
substituted
alkyl
substituents selected
cycloalkyl
Prior art date
Application number
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English (en)
Original Assignee
Merck Sharp & Dohme
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 Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of AR088352A1 publication Critical patent/AR088352A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Abstract

Usos de los compuestos de 2-piridil-oxi-4-nitrilo descriptos en la presente en el tratamiento o prevención de trastornos y enfermedades neurológicas y psiquiátricas en las que están implicados receptores de orexina, y composiciones farmacéuticas que comprenden estos compuestos. Reivindicación 1: Un compuesto de la fórmula (1), en la que: A se selecciona entre el grupo que consiste en fenilo, naftilo y heteroarilo; R¹ᵃ, R¹ᵇ y R¹ᶜ se seleccionan independientemente entre el grupo que consiste en: (i) hidrógeno, (ii) halógeno, (iii) hidroxilo, (iv) -(C=O)ₘ-Oₙ-alquilo C₁₋₆, donde m es 0 ó 1, n es 0 ó 1 (donde si m es 0 o n es 0, está presente un enlace) y donde el alquilo está sin sustituir o sustituido con uno o más sustituyentes seleccionados entre R⁴, (v) -(C=O)ₘ-Oₙ-cicloalquilo C₃₋₆, donde el cicloalquilo está sin sustituir o sustituido con uno o más sustituyentes seleccionados entre R⁴, (vi) -(C=O)ₘ-alquenilo C₂₋₄, donde el alquenilo está sin sustituir o sustituido con uno o más sustituyentes seleccionados entre R⁴, (vii) -(C=O)ₘ-alquinilo C₂₋₄, donde el alquinilo está sin sustituir o sustituido con uno o más sustituyentes seleccionados entre R⁴, (viii) -(C=O)ₘ-Oₙ-fenilo o -(C=O)ₘ-Oₙ-naftilo, donde el fenilo o el naftilo están sin sustituir o sustituidos con uno o más sustituyentes seleccionados entre R⁴, (ix) -(C=O)ₘ-Oₙ-heterociclo, donde el heterociclo está sin sustituir o sustituido con uno o más sustituyentes seleccionados entre R⁴, (x) -(C=O)ₘ-NR¹⁰R¹¹, donde R¹⁰ y R¹¹ se seleccionan independientemente entre el grupo que consiste en: (a) hidrógeno, (b) alquilo C₁₋₆, que está sin sustituir o sustituido con R⁴, (c) alquenilo C₃₋₆, que está sin sustituir o sustituido con R⁴, (d) alquinilo C₃₋₆, que está sin sustituir o sustituido con R⁴, (e) cicloalquilo C₃₋₆ que está sin sustituir o sustituido con R⁴, (f) fenilo, que está sin sustituir o sustituido con R¹⁴, y (g) heterociclo, que está sin sustituir o sustituido con R⁴, (xi) -S(O)₂NR¹⁰R¹¹, (xii) -S(O)q-R¹², donde q es 0, 1 ó 2 y donde R¹² se selecciona entre las definiciones de R¹⁰ y R¹¹, (xiii) -CO₂H, (xiv) -CN, y (xv) -NO₂; R³ se selecciona entre alquilo C₁₋₆ y cicloalquilo C₃₋₆, que está sin sustituir o sustituido con uno o más sustituyentes seleccionados entre R⁴; R⁴ se selecciona entre el grupo que consiste en: (i) hidroxilo, (ii) halógeno, (iii) alquilo C₁₋₆, (iv) -cicloalquilo C₃₋₆, (v) -O-alquilo C₁₋₆, (vi) -O(C=O)-alquilo C₁₋₆, (vii) -NH₂, (viii) -NH-alquilo C₁₋₆, (ix) -NO₂, (x) fenilo, (xi) heterociclo, (xii) -CO₂H, y (xiii) -CN; o una sal farmacéuticamente aceptable de los mismos.
ARP120103852 2011-10-19 2012-10-16 Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina AR088352A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161548883P 2011-10-19 2011-10-19

Publications (1)

Publication Number Publication Date
AR088352A1 true AR088352A1 (es) 2014-05-28

Family

ID=47116466

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP120103852 AR088352A1 (es) 2011-10-19 2012-10-16 Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina

Country Status (11)

Country Link
US (1) US9156819B2 (es)
EP (1) EP2768823B1 (es)
JP (1) JP5947906B2 (es)
CN (1) CN103874695B (es)
AR (1) AR088352A1 (es)
AU (1) AU2012326275B2 (es)
BR (1) BR112014009486A2 (es)
CA (1) CA2852425C (es)
IN (1) IN2014CN02515A (es)
TW (1) TW201317228A (es)
WO (1) WO2013059222A1 (es)

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US20130102619A1 (en) 2013-04-25
EP2768823B1 (en) 2017-09-06
AU2012326275A1 (en) 2014-04-17
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IN2014CN02515A (es) 2015-07-31
AU2012326275B2 (en) 2016-12-01
CN103874695B (zh) 2017-12-15
JP2014532624A (ja) 2014-12-08
TW201317228A (zh) 2013-05-01
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