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PE20081662A1 - DERIVADOS DE 6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-ILO - Google Patents

DERIVADOS DE 6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-ILO

Info

Publication number
PE20081662A1
PE20081662A1 PE2008000215A PE2008000215A PE20081662A1 PE 20081662 A1 PE20081662 A1 PE 20081662A1 PE 2008000215 A PE2008000215 A PE 2008000215A PE 2008000215 A PE2008000215 A PE 2008000215A PE 20081662 A1 PE20081662 A1 PE 20081662A1
Authority
PE
Peru
Prior art keywords
azepin
dibenzo
oxo
dihydro
propyl
Prior art date
Application number
PE2008000215A
Other languages
English (en)
Inventor
Alexander Flohr
Roland Jacob-Roetne
Wolfgang Wostl
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=39332521&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20081662(A1) "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 PE20081662A1 publication Critical patent/PE20081662A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/18—Dibenzazepines; Hydrogenated dibenzazepines
    • 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
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • 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
    • A61P35/00—Antineoplastic agents

Landscapes

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

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE 6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-ILO DE FORMULA (I) DONDE R1 ES H O ALQUILO INFERIOR(C1-C7) SUSTITUIDO POR HALOGENO; R2 ES ALQUILO INFERIOR(C1-C7); R3 ES ALQUILO INFERIOR(C1-C7) SUSTITUIDO CON HALOGENO, -(CH2)n-CICLOALQUILO(C3-C6) O -(CH2)n-FENILO OPCIONALMENTE SUSTITUIDO CON HALOGENO, EN DONDE n ES DE 0 A 2. SON COMPUESTOS PREFERIDOS: (R)-2-HIDROXI-2-METIL-N-((S)-6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-IL)-N'-(2,2,3,3,3-PENTAFLUOR-PROPIL)-MALONAMIDA, (S)-2-HIDROXI-2-METIL-N-((S)-6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-IL)-N'-(3,3,3-TRIFLUOR-PROPIL)-MALONAMIDA, (R/S)-2-HIDROXI-N-((S)-6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-IL)-N-(2,2,3,3,3-PENTAFLUOR-PROPIL)-2-PROPIL-MALONAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA SECRETASA ? SIENDO UTILES EN EL TRATAMIENTO DE LA ENFERMEDAD DE ALZHEIMER, CANCER
PE2008000215A 2007-02-02 2008-01-30 DERIVADOS DE 6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-ILO PE20081662A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP07101658 2007-02-02

Publications (1)

Publication Number Publication Date
PE20081662A1 true PE20081662A1 (es) 2008-11-22

Family

ID=39332521

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008000215A PE20081662A1 (es) 2007-02-02 2008-01-30 DERIVADOS DE 6-OXO-6,7-DIHIDRO-5H-DIBENZO[b,d]AZEPIN-7-ILO

Country Status (15)

Country Link
US (1) US7544679B2 (es)
EP (1) EP2109604A1 (es)
JP (1) JP2010517954A (es)
KR (1) KR101150574B1 (es)
CN (1) CN101622232A (es)
AR (1) AR065129A1 (es)
AU (1) AU2008209861B2 (es)
BR (1) BRPI0807341A2 (es)
CA (1) CA2676160A1 (es)
CL (1) CL2008000254A1 (es)
IL (1) IL199973A0 (es)
MX (1) MX2009007864A (es)
PE (1) PE20081662A1 (es)
TW (1) TW200846005A (es)
WO (1) WO2008092786A1 (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8309299B2 (en) * 2010-05-19 2012-11-13 Hoffmann-La Roche Inc. Combination therapy and method for assessing resistance to treatment
AR087107A1 (es) * 2011-07-27 2014-02-12 Lilly Co Eli Compuesto inhibidor de la señalizacion de la trayectoria notch
EP2897960B1 (en) 2012-09-21 2016-08-03 Bristol-Myers Squibb Company Tricyclic heterocyclic compounds as notch inhibitors
US9273075B2 (en) 2012-09-21 2016-03-01 Bristol-Myers Squibb Company Prodrugs of 1,4-benzodiazepinone compounds
US9133139B2 (en) 2012-09-21 2015-09-15 Bristol-Myers Squibb Company Fluoroalkyl-1,4-benzodiazepinone compounds
WO2014047370A1 (en) * 2012-09-21 2014-03-27 Bristol-Myers Squibb Company Fluoroalkyl dibenzodiazepinone compounds
WO2014047393A1 (en) 2012-09-21 2014-03-27 Bristol-Myers Squibb Company N-substituted bis(fluoroalkyl)-1,4-benzodiazepinone compounds as notch inhibitors
US9242941B2 (en) 2012-09-21 2016-01-26 Bristol-Myers Squibb Company Alkyl, fluoroalkyl-1,4-benzodiazepinone compounds
US9187434B2 (en) 2012-09-21 2015-11-17 Bristol-Myers Squibb Company Substituted 1,5-benzodiazepinones compounds
JP2015529253A (ja) 2012-09-21 2015-10-05 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Ｎｏｔｃｈ阻害剤としてのフルオロアルキルおよびフルオロシクロアルキル１，４−ベンゾジアゼピノン化合物
CN102911118B (zh) * 2012-11-09 2014-04-09 天津商业大学 一类苯并氮杂卓类衍生物及其制备方法和用途
EP2981267A1 (en) 2013-04-04 2016-02-10 Bristol-Myers Squibb Company Combination therapy for the treatment of proliferative diseases
WO2015073524A1 (en) * 2013-11-12 2015-05-21 Drexel University Novel methods of treating or preventing alzheimer's disease
WO2017075264A1 (en) * 2015-10-30 2017-05-04 Inception 3, Inc. Dibenzo azepine compounds and their use in the treatment of otic diseases and disorders
CN109320456A (zh) * 2018-11-16 2019-02-12 天津商业大学 新晶型的抗肿瘤化合物及其制备方法和含其的组合物

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993003011A1 (fr) 1991-08-08 1993-02-18 Yamanouchi Pharmaceutical Co., Ltd. Derive d'uree
EP1218377A1 (en) 1999-10-08 2002-07-03 Bristol-Myers Squibb Pharma Company AMINO LACTAM SULFONAMIDES AS INHIBITORS OF A$g(b) PROTEIN PRODUCTION
AU2001253090A1 (en) * 2000-04-03 2001-10-15 Bristol-Myers Squibb Pharma Company Cyclic lactams as inhibitors of abeta protein production
JP2004500419A (ja) 2000-04-11 2004-01-08 デュポン　ファーマシューティカルズ　カンパニー Ａβタンパク質産生阻害剤としての置換ラクタム
GB0012671D0 (en) 2000-05-24 2000-07-19 Merck Sharp & Dohme Therapeutic agents
DE602004015415D1 (de) * 2003-02-04 2008-09-11 Hoffmann La Roche Malonamidderivate als gamma-secretaseinhibitoren
DE602004020680D1 (de) * 2003-09-09 2009-05-28 Hoffmann La Roche Die aktivität von gamma-secretase blockierende malonamidderivate
DK1673347T3 (en) 2003-10-06 2015-10-12 Hoffmann La Roche SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USED AS GAMMA SECRETASE INHIBITORS
US7211573B2 (en) * 2004-12-08 2007-05-01 Hoffmann-La Roche Inc. Malonamide derivatives
EP2018368B1 (en) * 2006-03-27 2012-12-05 F. Hoffmann-La Roche AG Malonamide derivatives as gamma secretase inhibitors
BRPI0717587A2 (pt) * 2006-09-20 2013-10-29 Hoffmann La Roche Derivados de 4-oxo-2,3,4,5-tetra-hidro-benzo[b][1,4]diazepina

Also Published As

Publication number Publication date
EP2109604A1 (en) 2009-10-21
MX2009007864A (es) 2009-07-31
KR20090104916A (ko) 2009-10-06
KR101150574B1 (ko) 2012-05-30
IL199973A0 (en) 2010-04-15
US7544679B2 (en) 2009-06-09
CA2676160A1 (en) 2008-08-07
TW200846005A (en) 2008-12-01
CL2008000254A1 (es) 2008-08-08
AR065129A1 (es) 2009-05-20
WO2008092786A1 (en) 2008-08-07
JP2010517954A (ja) 2010-05-27
BRPI0807341A2 (pt) 2014-05-20
AU2008209861B2 (en) 2012-08-09
CN101622232A (zh) 2010-01-06
AU2008209861A1 (en) 2008-08-07
US20080188463A1 (en) 2008-08-07

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