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AR068511A1 - Tetrahidro[1,4'] bipiridinil-2'-onas sustituidas, composiciones farmaceuticas que las contienen y usos de las mismas para tratar o prevenir trastornos del sistema nervioso central - Google Patents

Tetrahidro[1,4'] bipiridinil-2'-onas sustituidas, composiciones farmaceuticas que las contienen y usos de las mismas para tratar o prevenir trastornos del sistema nervioso central

Info

Publication number
AR068511A1
AR068511A1 ARP080104003A ARP080104003A AR068511A1 AR 068511 A1 AR068511 A1 AR 068511A1 AR P080104003 A ARP080104003 A AR P080104003A AR P080104003 A ARP080104003 A AR P080104003A AR 068511 A1 AR068511 A1 AR 068511A1
Authority
AR
Argentina
Prior art keywords
alkyl
alkyloxy
substituted
diseases
fluoro
Prior art date
Application number
ARP080104003A
Other languages
English (en)
Original Assignee
Addex Pharmaceuticals S A
Ortho Mcneil 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39930548&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR068511(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Addex Pharmaceuticals S A, Ortho Mcneil Pharm Inc filed Critical Addex Pharmaceuticals S A
Publication of AR068511A1 publication Critical patent/AR068511A1/es

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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    • A61K31/535—Heterocyclic 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
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
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    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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    • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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 directly attached to ring carbon atoms
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Abstract

Los compuestos son moduladores alostéricos positivos de receptores metabotropicos - subtipo 2 (ômGluR2ö) los cuales son utiles para el tratamiento o prevencion de desordenes neurologicos y psiquiátricos asociados a la disfuncion del glutamato y a las enfermedades en las cuales el subtipo mGluR2 de receptores metabotropicos está implicado. Particularmente, tales enfermedades son desordenes del sistema nervioso central seleccionados del cupo de ansiedad, esquizofrenia, jaqueca, depresion, y epilepsia. Composiciones farmacéuticas que los contienen y uso de tales compuestos para la prevencion y el tratamiento de tales enfermedades en las cuales el mGluR2 esté implicado. Reivindicacion 1: Un compuesto que tiene la Formula (1) y las formas estereoquímicamente isomeras del mismo, caracterizado porque R1 es C1-6 alquilo; o C1-3 alquilo sustituido con haluro trifluorometilo o trifluorometoxi; R2 es haluro, trifluorometilo, C1-3 alquilo o ciclopropilo; R3 es hidrogeno, fluoro, hidroxilo, hidroxi C1-3 alquilo, hidroxi C1-3 alquilooxi, fluoro C1-3 alquilo, fluoro C1-3 alquilooxi o ciano; y Ar es fenilo no sustituido; o fenilo sustituido con n radicales R4, donde n es 1,2 o 3; R4 es seleccionado del grupo que consiste de hidrogeno, haluros, C1-3 alquilo, hidroxi C1-3 alquilo, polihaluro C1-3 alquilo, ciano, hidroxilo, amino, carboxilo, C1-3 alquilooxiC1-3 alquilo, C1-3 alquilooxi, polihaluro C1-3 alquilooxi, C1-3 alquilocarbonilo, mono - y di (C1-3 alquilo) amino, y morfolinilo; o dos radicales vecinales R4 tomados juntos forman un radical bivalente de formula -N=CH-NH-(a), -CH=CH-NH-(b), o -O-CH2-CH2-NH-(c); o R3 y un radical R4 en posicion orto tomados juntos forman un radical bivalente de formula -CH2-O-(d), o -O-CH2-(e); o una sal farmacéuticamente aceptable o un solvato del mismo.
ARP080104003A 2007-09-14 2008-09-15 Tetrahidro[1,4'] bipiridinil-2'-onas sustituidas, composiciones farmaceuticas que las contienen y usos de las mismas para tratar o prevenir trastornos del sistema nervioso central AR068511A1 (es)

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Application Number Priority Date Filing Date Title
EP07116390 2007-09-14

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AR068511A1 true AR068511A1 (es) 2009-11-18

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ARP080104003A AR068511A1 (es) 2007-09-14 2008-09-15 Tetrahidro[1,4'] bipiridinil-2'-onas sustituidas, composiciones farmaceuticas que las contienen y usos de las mismas para tratar o prevenir trastornos del sistema nervioso central

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Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0420722D0 (en) 2004-09-17 2004-10-20 Addex Pharmaceuticals Sa Novel allosteric modulators
AR059898A1 (es) 2006-03-15 2008-05-07 Janssen Pharmaceutica Nv Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2
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