MX2007006504A - Derivados de malonamida como inhibidores de gamma-secretasa para el tratamiento de la enfermedad de alzheimer. - Google Patents

Derivados de malonamida como inhibidores de gamma-secretasa para el tratamiento de la enfermedad de alzheimer.

Info

Publication number
MX2007006504A
MX2007006504A MX2007006504A MX2007006504A MX2007006504A MX 2007006504 A MX2007006504 A MX 2007006504A MX 2007006504 A MX2007006504 A MX 2007006504A MX 2007006504 A MX2007006504 A MX 2007006504A MX 2007006504 A MX2007006504 A MX 2007006504A
Authority
MX
Mexico
Prior art keywords
lower alkyl
halogen
hydroxy
alzheimer
disease
Prior art date
Application number
MX2007006504A
Other languages
English (en)
Inventor
Roland Jakob-Roetne
Alexander Flohr
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
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MX2007006504A publication Critical patent/MX2007006504A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D267/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02Seven-membered rings
    • C07D267/08Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D267/14Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/12Heterocyclic 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

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La invencion se refiere a compuestos de la formula general en donde R es halogeno, alquilo inferior o alquilo inferior sustituido por halogeno; R1 es hidrogeno, alquilo inferior o alquilo inferior sustituido por halogeno o hidroxi o es alquenilo inferior, -(CH2)n-cicloalquilo, -(CH2)n-COR?? o es bencilo opcionalmente sustituido por halogeno o es -(CH2)n-morfolinilo; R?? es alcoxi inferior, hidroxi o amino, R2 es hidrogeno, alquilo inferior o di-(alquilo inferior), alquilo inferior sustituido por halogeno o hidroxi o es bencilo o cicloalquilo; R3 es alquilo inferior o alquilo inferior sustituido por halogeno o es bencilo opcionalmente sustituido por dos atomos de halogeno o es -(CH2)n-cicloalquilo o -(CH2)n-piridinilo; X es -CR4R4??- o -CR4R4??-O-; R4/R4?? con independencia entre si son hidrogeno, halogeno, alquilo inferior, alcoxi inferior, hidroxi o -CH2-2-[1,3]dioxalan-; n es 0,1 o 2; a sales de adicion de acido farmaceuticamente aceptables de los mismos y a todas las formas de enantiomeros opticamente puros, racematos o diaestereomeros y mezclas de diaestereomeros de los mismos, para el tratamiento de la enfermedad de Alzheimer.
MX2007006504A 2004-12-08 2005-12-01 Derivados de malonamida como inhibidores de gamma-secretasa para el tratamiento de la enfermedad de alzheimer. MX2007006504A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04106395 2004-12-08
EP05100816 2005-02-07
PCT/EP2005/012834 WO2006061136A2 (en) 2004-12-08 2005-12-01 Malonamide derivatives as inhibitors of gamma-secretase for the treatment of alzheimer’s disease

Publications (1)

Publication Number Publication Date
MX2007006504A true MX2007006504A (es) 2007-06-22

Family

ID=36293585

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2007006504A MX2007006504A (es) 2004-12-08 2005-12-01 Derivados de malonamida como inhibidores de gamma-secretasa para el tratamiento de la enfermedad de alzheimer.

Country Status (23)

Country Link
US (1) US7211573B2 (es)
EP (1) EP1828151B1 (es)
JP (1) JP4979590B2 (es)
KR (1) KR100890678B1 (es)
CN (1) CN101072760B (es)
AR (1) AR053987A1 (es)
AT (1) ATE504580T1 (es)
AU (1) AU2005313582B8 (es)
BR (1) BRPI0518615A2 (es)
CA (1) CA2589196A1 (es)
DE (1) DE602005027388D1 (es)
DK (1) DK1828151T3 (es)
HK (1) HK1114840A1 (es)
IL (1) IL183293A0 (es)
MX (1) MX2007006504A (es)
NO (1) NO20072609L (es)
NZ (1) NZ555184A (es)
PL (1) PL1828151T3 (es)
PT (1) PT1828151E (es)
RU (1) RU2402538C2 (es)
TW (1) TWI349005B (es)
WO (1) WO2006061136A2 (es)
ZA (1) ZA200705018B (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2007299129A1 (en) * 2006-09-20 2008-03-27 F. Hoffmann-La Roche Ag 4-oxo-2,3,4,5-tetrahydro-benzo[b][1,4]diazepine derivatives
AU2008209861B2 (en) 2007-02-02 2012-08-09 F. Hoffmann-La Roche Ag 6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl derivatives
US8741889B2 (en) * 2008-01-11 2014-06-03 Hoffmann-La Roche Inc Method of treating non-small cell lung cancer and colon cancer with gamma-secretase inhibitor
EP2244713A1 (en) * 2008-01-11 2010-11-03 F. Hoffmann-La Roche AG Use of a gamma-secretase inhibitor for treating cancer
WO2016198366A1 (en) 2015-06-11 2016-12-15 F. Hoffmann-La Roche Ag Targeted notch pathway inhibitors
CA3079786A1 (en) 2017-10-24 2019-05-02 The Broad Institute, Inc. 4h-pyrrolo[3,2-c]pyridin-4-one derivatives
EP3878836A4 (en) * 2018-11-07 2022-08-10 Chugai Seiyaku Kabushiki Kaisha PROCESS FOR THE PREPARATION OF O-SUBSTITUTED SERIN DERIVATIVES
US20220378762A1 (en) 2019-04-24 2022-12-01 Bayer Aktiengesellschaft 4h-pyrrolo[3,2-c]pyridin-4-one derivatives
CN117946100A (zh) 2019-04-24 2024-04-30 拜耳股份有限公司 4H-吡咯并[3,2-c]吡啶-4-酮化合物
WO2020216773A1 (en) 2019-04-24 2020-10-29 Bayer Aktiengesellschaft 4h-pyrrolo[3,2-c]pyridin-4-one compounds
CN112300019A (zh) * 2019-07-31 2021-02-02 华东师范大学 一种邻乙酰氨基苯丁酸类化合物的制备方法
WO2021198020A1 (en) 2020-03-31 2021-10-07 Bayer Aktiengesellschaft 3-(anilino)-2-[3-(3-alkoxy-pyridin-4-yl]-1,5,6,7-tetrahydro-4h-pyrrolo[3,2-c]pyridin-4-one derivatives as egfr inhibitors for the treatment of cancer
AU2022234513A1 (en) 2021-03-09 2023-09-21 Basf Se Malonamides and their use as herbicides
KR20240051210A (ko) * 2021-08-25 2024-04-19 바스프 에스이 제초제 말론아미드
KR20240054320A (ko) * 2021-08-31 2024-04-25 바스프 에스이 축합된 고리계를 함유하는 제초성 말론아미드

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002241368A (ja) * 1997-02-18 2002-08-28 Shionogi & Co Ltd 新規ベンゾラクタム誘導体およびそれを含有する医薬組成物
WO1999067219A1 (en) * 1998-06-22 1999-12-29 Elan Pharmaceuticals, Inc. Compounds for inhibiting beta-amyloid peptide release and/or its synthesis
GB0012671D0 (en) 2000-05-24 2000-07-19 Merck Sharp & Dohme Therapeutic agents
SI1511718T1 (sl) * 2002-05-29 2009-08-31 Hoffmann La Roche Derivati n-acilaminobenzena kot selektivni inhibitorji monoaminske oksidaze b
TW200502221A (en) * 2002-10-03 2005-01-16 Astrazeneca Ab Novel lactams and uses thereof
ES2311795T3 (es) 2003-02-04 2009-02-16 F. Hoffmann-La Roche Ag Derivados de malonamida como inhibidores de gamma-secretasa.
US7060698B2 (en) 2003-05-19 2006-06-13 Hoffmann-La Roche Inc. Benzoxazepinone derivatives
KR20070087233A (ko) 2003-09-09 2007-08-27 에프. 호프만-라 로슈 아게 감마-세크리테이즈의 활성을 차단하는 말론아미드 유도체
US7166587B2 (en) 2003-10-06 2007-01-23 Hoffmann-La Roche Inc. Carbamic acid alkyl ester derivatives

Also Published As

Publication number Publication date
DE602005027388D1 (de) 2011-05-19
US20060122168A1 (en) 2006-06-08
EP1828151A2 (en) 2007-09-05
WO2006061136A2 (en) 2006-06-15
ZA200705018B (en) 2010-04-28
KR100890678B1 (ko) 2009-03-26
RU2402538C2 (ru) 2010-10-27
RU2007120211A (ru) 2009-01-20
JP2008522994A (ja) 2008-07-03
ATE504580T1 (de) 2011-04-15
IL183293A0 (en) 2007-09-20
PL1828151T3 (pl) 2011-09-30
CN101072760B (zh) 2011-12-28
CA2589196A1 (en) 2006-06-15
CN101072760A (zh) 2007-11-14
AU2005313582A1 (en) 2006-06-15
US7211573B2 (en) 2007-05-01
JP4979590B2 (ja) 2012-07-18
NZ555184A (en) 2010-01-29
AU2005313582A8 (en) 2011-06-16
WO2006061136A3 (en) 2006-08-03
AU2005313582B8 (en) 2011-06-16
PT1828151E (pt) 2011-06-16
NO20072609L (no) 2007-06-19
TWI349005B (en) 2011-09-21
KR20070086979A (ko) 2007-08-27
BRPI0518615A2 (pt) 2008-11-25
TW200626568A (en) 2006-08-01
EP1828151B1 (en) 2011-04-06
AU2005313582B2 (en) 2011-06-02
AR053987A1 (es) 2007-05-30
DK1828151T3 (da) 2011-05-16
HK1114840A1 (en) 2008-11-14

Similar Documents

Publication Publication Date Title
MX2007006504A (es) Derivados de malonamida como inhibidores de gamma-secretasa para el tratamiento de la enfermedad de alzheimer.
SE0104334D0 (sv) Therapeutic agents
PH12015501925A1 (en) Hydrochloride salt of ((1s,2s,4r)-4-{4-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-7h-pyrrolo [2,3-d]pyrimidin-7-yl}-2-hydroxycyclopentyl)methyl sulfamate
MXPA04009784A (es) Tiazolidin-4-carbonitrilos y analogos y su uso como inhibidores de dipeptidil-peptidas.
TW200614983A (en) 5-substituted-2-phenylamino benzamides as MEK inhibitors
TW200642685A (en) Novel spiroindoline or spiroisoquinoline compounds, methods of use and compositions thereof
TW200716531A (en) Cyclohexanesulfonyl derivatives as GLYT1 inhibitors to treat schizophrenia
MXPA05008172A (es) Derivados de malonamida como inhibidores gamma-secretasa.
PT1678166E (pt) Inibidores de proteína-quinase
JO2282B1 (en) Oxazole derivatives
WO2005012269A8 (ja) 新規アゾール化合物
EA200300333A1 (ru) Новые тиадиазолы и оксадиазолы и их применение в качестве ингибиторов фосфодиэстеразы-7
DE60236719D1 (de) Purinderivate als antagonisten an purinergen rezeptoren
CA2592345A1 (en) Piperidine and azetidine derivatives as glyt1 inhibitors
TW200740760A (en) Malonamide derivatives
MX2008008694A (es) Compuestos conjugados de amina terapeutica-arilsulfonamida.
NO20070837L (no) Pyrido-pyrido pyrimidinderivater, fremstilling derav samt terapeutisk anvendelse for behandling av cancer.
BR0313407A (pt) Novo uso de derivados de benzotiazol
ATE507226T1 (de) 1,3,4-oxadiazol-2-one als ppar-delta-modulatoren und deren verwendung
ATE357453T1 (de) Comt-inhibitoren
WO2001012169A3 (en) Method of cancer treatment
NZ331801A (en) Therapeutic agent for diabetes
ATE399164T1 (de) Antagonisten des opioidrezeptors
TW200612912A (en) Benzyloxy derivatives as maob inhibitors
RS20050954A (en) Use of bycyclo/2.2.1/heptane derivatives for the preparation of neuroprotective pharmaceutical compositions

Legal Events

Date Code Title Description
FG Grant or registration