AR120173A1 - Inhibidores del factor d del complemento para administración oral - Google Patents

Inhibidores del factor d del complemento para administración oral

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Publication number
AR120173A1
AR120173A1 ARP200102782A ARP200102782A AR120173A1 AR 120173 A1 AR120173 A1 AR 120173A1 AR P200102782 A ARP200102782 A AR P200102782A AR P200102782 A ARP200102782 A AR P200102782A AR 120173 A1 AR120173 A1 AR 120173A1
Authority
AR
Argentina
Prior art keywords
alkyl
cycloalkyl
optionally substituted
aryl
heterocycloalkyl
Prior art date
Application number
ARP200102782A
Other languages
English (en)
Inventor
Pravin L Kotian
Yarlagadda S Babu
Weihe Zhang
Peng Lu
- Spaulding Andrew E Cheng
Wei Lv
zhao Dang
Krishnan Raman
Original Assignee
Biocryst Pharm Inc
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 Biocryst Pharm Inc filed Critical Biocryst Pharm Inc
Publication of AR120173A1 publication Critical patent/AR120173A1/es

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    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • C07D307/80Radicals substituted by oxygen atoms
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    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/4161,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • C07C217/00Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
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    • C07C217/48Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing rings
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    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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    • C07D273/02Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
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    • C07D333/52Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
    • C07D333/54Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Compuestos heterocíclicos arilcondensados con actividad inhibitoria del sistema del complemento, composición farmacéutica que comprende a uno de éstos compuestos y su uso para el tratamiento de enfermedades o afecciones que presentan una actividad aberrante del complemento tales como un trastorno inmunológico o una enfermedad del SNC. Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1), o una sal aceptable farmacéuticamente del mismo, donde: el anillo A es arileno o heteroarileno; el anillo B es arileno o heteroarileno; el anillo A está fusionado al anillo B en dos y solamente dos posiciones adyacentes; el anillo C es arilo o heteroarilo; el anillo D es arilo o heteroarilo; J representa -CH₂-, -NH-, -CH₂CH₂-, -C(O)-, -O-, -S-, -S(O)-, -SO₂-, -N(alquil)-, -CH(alquil)-, -CH(aril)-, -C(alquil)₂-, -CH(cicloalquil)-, o un resto de fórmula (2); K representa una unión, -O-, -NH-, -C(O)-, -CH₂-, -S-, -S(O)-, -SO₂-, -N(alquil)-, -CH(alquil)-, o -CH(cicloalquil)-; donde al menos uno de J y K es una unión, -C(O)-, -CH₂-, -CH₂CH₂-, -CH(alquil)-, o -CH(aril)-; LC representa una unión, -CH₂-, -CH(alquil)-, -CH(cicloalquil)-, -CH(hidroxialquil)-, -CH(haloalquil)-, -CH₂CH₂-, -CF₂-, -CH(F)-, -CF(alquil)-, -C(O)-, -CD₂-, o -CH(D)-; LD representa -CH₂-, -CH₂CH₂-, -CF₂-, -CH(F)-, -CD₂-, -CH(D)-, -CH(alquil)-, -CH(cicloalquil)-, -CHNH₂-, -CH(NH(alquil))-, -CH(NH(cicloalquil))-, o un enlace; RA representa H, halo, hidroxilo, ciano, amino, alquilo, alcoxilo, hidroxialquilo, ariloxi, (ariloxi)alquilo, (cicloalquil)alcoxi, (heterocicloalquil)alcoxi, (heteroaril)alcoxi opcionalmente sustituido, haloalquilo, haloalcoxi, (hidroxi)haloalquilo, alcoxialquilo, aminoalquilo opcionalmente sustituido, alquinilo opcionalmente sustituido, arilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, heteroarilalquilo opcionalmente sustituido, cicloalquilo opcionalmente sustituido, (cicloalquil)alquilo opcionalmente sustituido, (cicloalquil)alquenilo opcionalmente sustituido, heterocicloalquilo opcionalmente sustituido, (heterocicloalquil)alquilo opcionalmente sustituido, -C(O)OH, -C(O)NH₂-, -C(O)N(alquil)₂-, -CH₂C(O)OH, -NO₂, -CH₂NH(alquilo opcionalmente sustituido), -CH₂N(Boc)(alquilo opcionalmente sustituido), -CH₂NH((cicloalquil)alquilo), -CH₂N(alquil)(cicloalquilo), -CH₂N(alquil)((cicloalquil)alquilo), -NH(alquilo opcionalmente sustituido), -NH(cicloalquilo), -NH((cicloalquil)alquilo), -NH((heterocicloalquil)alquilo), -N(alquil)₂, -N(alquil)((cicloalquil)alquilo, -N(alquil)((heterocicloalquil)alquilo, -NH(heteroarilalquilo), -CH₂O(arilo opcionalmente sustituido), -C(O)O(alquilo), -C(O)NH(alquilo opcionalmente sustituido), -C(O)NH((cicloalquil)alquilo), -NHC(O)O(alquilo), o -CH₂N(alquilo)₂; RB representa H, -C(O)O(alquilo), halógeno, ciano, amino, -C(O)OH, -CH₂C(O)OH, -C(O)NH₂, -C(O)NH(cicloalquilo), -C(O)NH(alquilo), -C(O)NH(arilo), -C(O)NH(heteroarilo), -C(O)(alquilo), alquilaminoalquilo, alquilaminocicloalquilo, alcoxialquilo, hidroxialquilo, haloalquilo, (hidroxi)haloalquilo, o tosilo, o alquilo, arilo, heteroarilo, cicloalquilo, (cicloalquil)alquilo, o heterocicloalquilo opcionalmente sustituido; RC representa H, halo, -OH, o amino, o alcoxi, alquilo, cicloalquilo, heterocicloalquilo, o (heteroaril)alcoxi opcionalmente sustituido; RD representa H, halo, hidroxilo, ciano, -NH₂, -NH(Ac), -NH(alquilo), -N(alquil)₂, -NH(CO)(alquilo), -CH₂NH₂, -CH₂NHC(O)(alquilo), -C(O)NH₂, -C(O)OH, o -NHC(O)O(alquilo), o alquilo, alcoxilo, cicloalquilo, (cicloalquil)alquilo, hidroxialquilo, aminoalquilo, haloalcoxilo, o haloalquilo opcionalmente sustituido; R¹ representa H o alquilo opcionalmente sustituido; y m, n, p, y q son independientemente entre sí 0, 1, ó 2.
ARP200102782A 2019-10-09 2020-10-08 Inhibidores del factor d del complemento para administración oral AR120173A1 (es)

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