MA32486B1 - Derives de 4,5- dihydrooxazol-2-yle - Google Patents

Derives de 4,5- dihydrooxazol-2-yle

Info

Publication number
MA32486B1
MA32486B1 MA33533A MA33533A MA32486B1 MA 32486 B1 MA32486 B1 MA 32486B1 MA 33533 A MA33533 A MA 33533A MA 33533 A MA33533 A MA 33533A MA 32486 B1 MA32486 B1 MA 32486B1
Authority
MA
Morocco
Prior art keywords
disorders
halogen
lower alkyl
chr
substituted
Prior art date
Application number
MA33533A
Other languages
Arabic (ar)
English (en)
Inventor
Guido Galley
Annick Goergler
Zbinden Katrin Groebke
Roger Norcross
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41066683&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA32486(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA32486B1 publication Critical patent/MA32486B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08—Heterocyclic 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
    • C07D263/16—Heterocyclic 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
    • C07D263/28—Nitrogen atoms not forming part of a nitro radical
    • 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
    • A61K31/41—Heterocyclic 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
    • A61K31/42—Oxazoles
    • A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Psychology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Addiction (AREA)
  • Nutrition Science (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Cette invention concerne des composés de formule (i), r1 étant hydrogène, alkyle inférieur, alcoxy inférieur, alkyle inférieur substitué par halogène, alcoxy inférieur substitué par halogène, halogène, cyano, nitro, hydroxy, c(o)o-alkyle inférieur, s(o)2-alkyle inférieur, c(o)och2-phényle, och2-phényle, tétrazol-1-yl, phényle éventuellement substitué par halogène, ou est phényloxy éventuellement substitué par halogène, ou est benzyle éventuellement substitué par halogène ou est benzyloxy éventuellement substitué par halogène, les substituants de n > 1 pouvant être identiques ou différents; x est -o-(ch2)2-, -o-chr'-ch2-, -o-ch2-chr', -o-cr''2-ch2-, -(ch2)2-chr', -chr'-(ch2)2-, -cr » 2-(ch2)2-, -ch2-chr'-ch2-, -ch2-cr''2-ch2-, -chr »-o-ch2-, -ch2-o-ch2-, -cr''2-o-ch2-, -cf2(ch2)2-, -cr » 2-ch2-, -sir » 2-(ch2)2-, -s-(ch2)2-, -s(o)2-(ch2)2-, -(ch2)4-, -ch2-o-(ch2)2-, lorsque m vaut 0, 1, 2 ou 3; r' est alkyle inférieur, alcoxy inférieur ou alkyle inférieur substitué par halogène; r'' est alkyle inférieur ou alkyle inférieur substitué par halogène; r2 est hydrogène ou alkyle inférieur; y est aryle, cycloalkyle ou hétéroaryle; n vaut 1, 2 ou 3; ou un sel d'addition acide pharmaceutiquement approprié. Les composés décrits dans la formule (i) peuvent être utilisés dans le traitement de maladies associées à la fonction biologique des récepteurs associés à une amine de trace, lesdites maladies étant la dépression, les troubles de l'angoisse, les troubles bipolaires, les troubles déficitaires de l'attention avec hyperactivité, les troubles associés au stress, les troubles psychotiques, la schizophrénie, les maladies neurologiques, la maladie de parkinson, les troubles neurodégénératifs, la maladie d'alzheimer, l'épilepsie, la migraine, la toxicomanie et les troubles métaboliques, les troubles de l'alimentation, le diabète, les complications diabétiques, l'obésité, la dyslipidémie, les troubles de la consommation et de l'assimilation énergétique, les troubles et les dysfonctionnements de l'homéostasie (température corporelle), les troubles du sommeil et du rythme circadien et les affections cardiovasculaires.
MA33533A 2008-07-24 2011-01-18 Derives de 4,5- dihydrooxazol-2-yle MA32486B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08161060 2008-07-24
PCT/EP2009/059026 WO2010010014A1 (fr) 2008-07-24 2009-07-15 Dérivés de 4,5-dihydrooxazol-2-yle

Publications (1)

Publication Number Publication Date
MA32486B1 true MA32486B1 (fr) 2011-07-03

Family

ID=41066683

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33533A MA32486B1 (fr) 2008-07-24 2011-01-18 Derives de 4,5- dihydrooxazol-2-yle

Country Status (22)

Country Link
US (2) US20100041686A1 (fr)
EP (1) EP2321287B1 (fr)
JP (1) JP5547187B2 (fr)
KR (1) KR101307007B1 (fr)
CN (1) CN102083805A (fr)
AR (1) AR072876A1 (fr)
AU (1) AU2009273324A1 (fr)
BR (1) BRPI0916363A2 (fr)
CA (1) CA2728480A1 (fr)
CL (1) CL2011000137A1 (fr)
CO (1) CO6331336A2 (fr)
CR (1) CR11843A (fr)
EC (1) ECSP11010782A (fr)
ES (1) ES2556633T3 (fr)
IL (1) IL209423A0 (fr)
MA (1) MA32486B1 (fr)
MX (1) MX2011000464A (fr)
PE (1) PE20110215A1 (fr)
RU (1) RU2513086C2 (fr)
TW (1) TW201008916A (fr)
WO (1) WO2010010014A1 (fr)
ZA (1) ZA201008657B (fr)

Families Citing this family (13)

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US8426447B2 (en) 2008-09-11 2013-04-23 Amgen Inc. Spiro-tricyclic ring compounds as beta-secretase modulators and methods of use
US8354441B2 (en) * 2009-11-11 2013-01-15 Hoffmann-La Roche Inc. Oxazoline derivatives
US9452980B2 (en) 2009-12-22 2016-09-27 Hoffmann-La Roche Inc. Substituted benzamides
US8883782B2 (en) 2010-03-15 2014-11-11 Amgen Inc. Spiro-tetracyclic ring compounds as beta-secretase modulators and methods of use
JP5584352B2 (ja) 2010-03-15 2014-09-03 アムジエン・インコーポレーテツド β−セクレターゼ調節剤としてのアミノ−ジヒドロオキサジン系およびアミノ−ジヒドロチアジン系スピロ化合物ならびにそれらの医学的用途
US9132136B2 (en) 2010-08-02 2015-09-15 Hoffmann-La Roche Inc. Pharmaceutical combination
US8673950B2 (en) * 2010-11-02 2014-03-18 Hoffmann-Laroche Inc. Dihydrooxazol-2-amine derivatives
US9346827B2 (en) 2011-02-07 2016-05-24 Amgen Inc. 5-amino-oxazepine and 5-amino-thiazepane compounds as beta secretase antagonists and methods of use
JP2014526560A (ja) 2011-09-21 2014-10-06 アムジエン・インコーポレーテツド β‐セクレターゼ調節因子としてのアミノオキサジン化合物およびアミノジヒドロチアジン化合物および使用方法
WO2014078314A1 (fr) 2012-11-15 2014-05-22 Amgen Inc. Composés d'amino-oxazine et d'amino-dihydrothiazine jouant le rôle de modulateurs de bêta-sécrétase et procédés d'utilisation
JP6814814B2 (ja) 2016-03-17 2021-01-20 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ Ｔａａｒのアゴニストとしての活性を有する５−エチル−４−メチル−ピラゾール−３−カルボキサミド誘導体
US10858326B2 (en) 2016-05-04 2020-12-08 Purdue Pharma L.P. Oxazoline pseudodimers, pharmaceutical compositions and the use thereof
EP3463359A4 (fr) * 2016-06-02 2020-08-26 Purdue Pharma LP Agonistes du récepteur 1 associé à une amine à l'état de trace et agonistes partiels pour le traitement de la douleur

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Also Published As

Publication number Publication date
JP5547187B2 (ja) 2014-07-09
MX2011000464A (es) 2011-03-01
RU2011104433A (ru) 2012-08-27
WO2010010014A1 (fr) 2010-01-28
ZA201008657B (en) 2011-10-26
RU2513086C2 (ru) 2014-04-20
EP2321287A1 (fr) 2011-05-18
BRPI0916363A2 (pt) 2018-05-29
ECSP11010782A (es) 2011-02-28
US20100041686A1 (en) 2010-02-18
CA2728480A1 (fr) 2010-01-28
KR20110020936A (ko) 2011-03-03
KR101307007B1 (ko) 2013-09-11
TW201008916A (en) 2010-03-01
JP2011528685A (ja) 2011-11-24
AR072876A1 (es) 2010-09-29
ES2556633T3 (es) 2016-01-19
EP2321287B1 (fr) 2015-11-11
PE20110215A1 (es) 2011-03-31
CN102083805A (zh) 2011-06-01
US20120165294A1 (en) 2012-06-28
CR11843A (es) 2011-02-16
IL209423A0 (en) 2011-01-31
AU2009273324A1 (en) 2010-01-28
CO6331336A2 (es) 2011-10-20
CL2011000137A1 (es) 2011-07-15

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