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AR076979A1 - 2- aminooxazolinas como ligandos de taar1 - Google Patents

2- aminooxazolinas como ligandos de taar1

Info

Publication number
AR076979A1
AR076979A1 ARP100101977A ARP100101977A AR076979A1 AR 076979 A1 AR076979 A1 AR 076979A1 AR P100101977 A ARP100101977 A AR P100101977A AR P100101977 A ARP100101977 A AR P100101977A AR 076979 A1 AR076979 A1 AR 076979A1
Authority
AR
Argentina
Prior art keywords
disorders
lower alkyl
halogen
disease
formula
Prior art date
Application number
ARP100101977A
Other languages
English (en)
Inventor
Katrin Groebke Zbinden
Roger Norcross
Guillaume Decoret
Guido Galley
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR076979A1 publication Critical patent/AR076979A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D263/28Nitrogen atoms not forming part of a nitro radical
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Los compuestos de la formula 1, son activos en el receptor de TAARI, y así, por lo tanto, son apropiados para el tratamiento de la depresion, los trastornos de la ansiedad, el trastorno bipolar, el trastorno de hiperactividad del déficit de atencion, los trastornos relacionados con el estrés, los trastornos psicoticos, la esquizofrenia, las enfermedades neurologicas, la enfermedad de Parkinson, los trastornos neurodegenerativos, la enfermedad de Alzheimer, la epilepsia, la migrana, el abuso de substancias y los trastornos metabolicos, los trastornos del comer, la diabetes, las complicaciones diabéticas, la obesidad, la dislipemia, los trastornos del consumo y de la asimilacion de energía, los trastornos y el mal funcionamiento de la homeostasis de la temperatura corporal, trastornos del sueno y del ritmo circardiano, y trastornos cardiovasculares. Composiciones farmacéuticas. Reivindicacion 1: Un compuesto de la formula (1) en donde, R1, es halogeno; R2, es alquilo inferior o alquilo inferior sustituido por halogeno; R2', es hidrogeno, alquilo inferior o alquilo inferior sustituido por halogeno; X, es un eslabon, -CH2-, -CH2CH2- o -CH2CH2CH2-; Y, es fenilo o ciclohexilo; y n, es 0, 1 o 2, o una sal de adicion de ácidos de éste, farmacéuticamente aceptable.
ARP100101977A 2009-06-05 2010-06-04 2- aminooxazolinas como ligandos de taar1 AR076979A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP09162061 2009-06-05

Publications (1)

Publication Number Publication Date
AR076979A1 true AR076979A1 (es) 2011-07-20

Family

ID=42342699

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP100101977A AR076979A1 (es) 2009-06-05 2010-06-04 2- aminooxazolinas como ligandos de taar1

Country Status (4)

Country Link
US (1) US20100311798A1 (es)
AR (1) AR076979A1 (es)
TW (1) TW201103538A (es)
WO (1) WO2010139707A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX377836B (es) 2016-03-17 2025-03-11 F Hoffmann La Roche Ag Derivado de 5-etil-4-metil-pirazol-3-carboxamida teniendo actividad como agonista de receptor asociado con aminas trazas (taar).
EP3452473A1 (en) 2016-05-04 2019-03-13 Purdue Pharma L.P. Oxazoline pseudodimers, pharmaceutical compositions and the use thereof
PL240819B1 (pl) * 2020-06-25 2022-06-06 Inst Biologii Doswiadczalnej Im M Nenckiego Polskiej Akademii Nauk Pochodne 4,5-dihydro oksazol-2-ilo aminy do zastosowania w zapobieganiu lub leczeniu choroby alkoholowej

Family Cites Families (30)

* Cited by examiner, † Cited by third party
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US2744909A (en) * 1955-06-27 1956-05-08 Bristol Lab Inc 2-(ortho-phenylbenzyl) imidazoline and acid addition salts
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DE1121054B (de) * 1960-11-23 1962-01-04 Merck Ag E Verfahren zur Herstellung eines neuen Imidazolinderivates und dessen Saeureadditionssalzen
DE1150180B (de) * 1962-04-12 1963-06-12 Merck Ag E Mittel zur Vorbehandlung der Haut fuer die Rasur
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US3586695A (en) * 1968-01-26 1971-06-22 Dow Chemical Co Substituted imidazolinyl indoles
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BE754820R (fr) * 1969-08-13 1971-02-15 Schering Ag Nouveaux derives de pyrimidine, leurs procedes de preparation et leurs
US3818094A (en) * 1969-08-28 1974-06-18 Boehringer Sohn Ingelheim Hypotensive pharmaceutical compositions containing certain 2-anilino-1,3-diazacyclopentenes-(2)
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US4125620A (en) * 1974-10-01 1978-11-14 Boehringer Ingelheim Gmbh 2-[(2',6'-Disubstituted-phenyl)-imino]-imidazolidines and salts thereof
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GB9425211D0 (en) * 1994-12-14 1995-02-15 Ucb Sa Substituted 1H-imidazoles
DE19514579A1 (de) * 1995-04-20 1996-10-24 Boehringer Ingelheim Kg Verwendung von alpha¶1¶¶L¶-Agonisten zur Behandlung der Harninkontinenz
US5610174A (en) * 1995-06-02 1997-03-11 Synaptic Pharmaceutical Corporation Use of α1A -selective adrenoceptor agonists for the treatment of urinary incontinence
US5866579A (en) * 1997-04-11 1999-02-02 Synaptic Pharmaceutical Corporation Imidazole and imidazoline derivatives and uses thereof
CA2328973A1 (en) * 1998-04-23 1999-10-28 Akio Ojida Naphthalene derivatives, their production and use
IL147921A0 (en) * 2002-01-31 2002-08-14 Abdulrazik Mohammad A method for treating central nervous system disorders by ocular dosing
WO2008092785A1 (en) * 2007-02-02 2008-08-07 F. Hoffmann-La Roche Ag Novel 2-aminooxazolines as taar1 ligands for cns disorders

Also Published As

Publication number Publication date
TW201103538A (en) 2011-02-01
WO2010139707A1 (en) 2010-12-09
US20100311798A1 (en) 2010-12-09

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