[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

PE20071023A1 - Azaciclilaminas-n-sustituidas como antagonistas de histamina-3 - Google Patents

Azaciclilaminas-n-sustituidas como antagonistas de histamina-3

Info

Publication number
PE20071023A1
PE20071023A1 PE2007000268A PE2007000268A PE20071023A1 PE 20071023 A1 PE20071023 A1 PE 20071023A1 PE 2007000268 A PE2007000268 A PE 2007000268A PE 2007000268 A PE2007000268 A PE 2007000268A PE 20071023 A1 PE20071023 A1 PE 20071023A1
Authority
PE
Peru
Prior art keywords
halogen
oxo
nitro
alkyl
optionally substituted
Prior art date
Application number
PE2007000268A
Other languages
English (en)
Inventor
Derek Cecil Cole
Magda Asselin
Joseph Raymond Stock
Albert Jean Robichaud
Ji-In Kim
William Ronald Solvibile
Jonathan Laird Gross
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Publication of PE20071023A1 publication Critical patent/PE20071023A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14Ortho-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Child & Adolescent Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE AZACICLILAMINA N-SUSTITUIDOS DE FORMULA (I) DONDE X ES CO, CH2 O SOm, DONDE m ES DE 0 A 2; n Y p SON CADA UNO DE 1 A 3; R1 Y R2 SON CADA UNO H, ALQUILO(C1-C10) O R1 Y R2 SON TOMADOS JUNTO AL ATOMO AL CUAL ESTAN UNIDOS PARA FORMAR UN ANILLO DE 4 A 7 MIEMBROS QUE TIENE DE 1 A 2 HETEROATOMOS SELECCIONADOS DE N, O U S, OPCIONALMENTE SUSTITUIDOS CON HALOGENO, NITRO, CN, OXO, OH, ENTRE OTROS; R3 ES NR4R5, ARILO(C6-C20) O HETEROARILO DE 5 A 11 MIEMBROS OPCIONALMENTE SUSTITUIDOS CON HALOGENO, NITRO, CN, OXO, OH, ENTRE OTROS, DONDE R4 Y R5 SON TOMADOS JUNTO CON EL ATOMO AL CUAL ESTAN UNIDOS PARA FORMAR UN ANILLO BICICLICO, TRICICLICO O TETRACICLICO DE 9 A 15 MIEMBROS QUE CONTIENE DE 1 A 3 HETEROATOMOS SELECCIONADOS DE N, O U S; R6 Y R7 SON CADA UNO H, HALOGENO, ALQUILO(C1-C10), CICLOALQUILO(C3-C10), ENTRE OTROS, OPCIONALMENTE SUSTITUIDOS CON HALOGENO, NITRO, CN, OXO, OH, ENTRE OTROS; R8 Y R9 SON CADA UNO H, ALQUILO(C1-C10), CICLOALQUILO(C3-C10) O ARILO(C6-C20) OPCIONALMENTE SUSTITUIDOS CON HALOGENO, NITRO, CN, OXO, OH, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N,N-DIMETIL-1-{4-[(2-FENIL-1H-BENCIMIDAZOL-1-IL)METIL]-BENZOIL}PIRROLIDIN-3-ILAMINA, N,N-DIMETIL-1-{4-[(6-FLUORO-1H-BENCIMIDAZOL-1-IL)METIL]-BENZOIL}PIRROLIDIN-3-ILAMINA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS SON INHIBIDORES DEL RECEPTOR DE HISTAMINA H3 SIENDO UTILES EN EL TRATAMIENTO DE LA ENFERMEDAD DE ALZHEIMER
PE2007000268A 2006-03-15 2007-03-13 Azaciclilaminas-n-sustituidas como antagonistas de histamina-3 PE20071023A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US78251306P 2006-03-15 2006-03-15
US85907906P 2006-11-15 2006-11-15

Publications (1)

Publication Number Publication Date
PE20071023A1 true PE20071023A1 (es) 2007-10-03

Family

ID=38353957

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2007000268A PE20071023A1 (es) 2006-03-15 2007-03-13 Azaciclilaminas-n-sustituidas como antagonistas de histamina-3

Country Status (11)

Country Link
US (1) US7820825B2 (es)
EP (1) EP1994022A2 (es)
JP (1) JP2009530274A (es)
AR (1) AR059905A1 (es)
AU (1) AU2007227681A1 (es)
BR (1) BRPI0709612A2 (es)
CA (1) CA2645731A1 (es)
MX (1) MX2008011791A (es)
PE (1) PE20071023A1 (es)
TW (1) TW200800958A (es)
WO (1) WO2007108936A2 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7423147B2 (en) * 2004-03-31 2008-09-09 Janssen Pharmaceutical, N.V. Pyridine compounds as histamine H3 modulators
CA2645731A1 (en) 2006-03-15 2007-09-27 Wyeth N-substituted-azacyclylamines as histamine-3 antagonists
CA2649913A1 (en) 2006-05-19 2007-11-29 Wyeth N-benzoyl- and n-benzylpyrrolidin-3-ylamines as histamine-3 antagonists
JP5285603B2 (ja) 2006-05-30 2013-09-11 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ヒスタミンh3受容体のモジュレーターとしての置換ピリジルアミド化合物
EP2038269A1 (en) * 2006-06-29 2009-03-25 Janssen Pharmaceutica N.V. Substituted benzamide modulators of the histamine h3 receptor
PE20081152A1 (es) 2006-10-06 2008-08-10 Wyeth Corp Azaciclilaminas n-sustituidas como antagonistas de histamina-3
TW200823204A (en) * 2006-10-17 2008-06-01 Arena Pharm Inc Biphenyl sulfonyl and phenyl-heteroaryl sulfonyl modulators of the histamine H3-receptor useful for the treatment of disorders related thereto
EP2155719A1 (en) * 2007-05-24 2010-02-24 Wyeth LLC Azacyclylbenzamide derivatives as histamine-3 antagonists
PE20090812A1 (es) 2007-07-16 2009-06-14 Wyeth Corp Derivados de aminoalquilazol como antagonistas de histamina-3
EP2220045A1 (en) * 2007-11-20 2010-08-25 Janssen Pharmaceutica, N.V. Substituted pyridyl amide compounds as modulators of the histamine h3 receptor
KR101546712B1 (ko) 2007-11-20 2015-08-24 얀센 파마슈티카 엔.브이. 히스타민 h3 수용체의 조절제로서 사이클로알킬옥시- 및 헤테로사이클로알킬옥시피리딘 화합물
BRPI1011258A2 (pt) * 2009-06-26 2016-03-22 Sanofi Sa sais de fumarato, uso destes, composição farmacêutica que os compreende e processos para preparação da dita composição e de difumarato mono-hidratado de 2-(ciclo-hexilmetil)-n-{2-[(2s)-1-metilporrolidin-2-il]etil}-1,2,3,4-tetra-hirdoisoquinolina-7-sulfonamida
CA2825134A1 (en) 2011-01-25 2012-08-02 Kissei Pharmaceutical Co., Ltd. Indole derivative, and pharmacologically acceptable salt thereof
PT2875013T (pt) * 2012-07-17 2018-02-28 Glaxosmithkline Ip No 2 Ltd Indolecarbonitrilos como moduladores seletivos do recetor androgénio
ES2774517T3 (es) 2015-06-09 2020-07-21 Abbvie Inc Moduladores del receptor nuclear (ROR) para el tratamiento de enfermedades inflamatorias y autoinmunes
EP3886854A4 (en) 2018-11-30 2022-07-06 Nuvation Bio Inc. PYRROLE AND PYRAZOLE COMPOUNDS AND METHODS OF USE THERE

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1416872A (en) 1972-03-10 1975-12-10 Wyeth John & Brother Ltd 4-aminoquinoline derivatives
US3933829A (en) * 1974-08-22 1976-01-20 John Wyeth & Brother Limited 4-Aminoquinoline derivatives
US4166853A (en) * 1978-05-05 1979-09-04 The Upjohn Company Antihypertensive 7-trifluoromethyl-4-aminoquinolones
US4159331A (en) * 1978-05-05 1979-06-26 The Upjohn Company Antihypertensive 4-aminoquinolines
AU7759591A (en) * 1990-04-13 1991-11-11 Smithkline Beecham Corporation Substituted benzimidazoles
AU674207B2 (en) 1993-04-07 1996-12-12 Otsuka Pharmaceutical Co., Ltd. N-acylated 4-amino piperidine derivatives
IL117149A0 (en) * 1995-02-23 1996-06-18 Schering Corp Muscarinic antagonists
US6034093A (en) * 1995-06-07 2000-03-07 Rhone-Poulenc Rorer Pharmaceuticals Inc. Substituted sulfonic acid N-[(aminoiminomethyl)phenylalkyl]-azaheterocyclylamide compounds
EP1019047B1 (en) * 1997-05-01 2003-11-05 Eli Lilly And Company Antithrombotic agents
US6699873B1 (en) * 1999-08-04 2004-03-02 Millennium Pharmaceuticals, Inc. Melanocortin-4 receptor binding compounds and methods of use thereof
US7375125B2 (en) * 1999-08-04 2008-05-20 Ore Pharmaceuticals, Inc. Melanocortin-4 receptor binding compounds and methods of use thereof
WO2001042224A1 (en) 1999-12-09 2001-06-14 Mitsubishi Pharma Corporation Carboxyamido derivatives
AU2001247906A1 (en) 2000-03-31 2001-10-15 Ortho-Mcneil Pharmaceutical, Inc. Phenyl-substituted indoles and indazoles
EP1341768A1 (en) * 2000-12-07 2003-09-10 AstraZeneca AB Therapeutic benzimidazole compounds
HN2002000156A (es) 2001-07-06 2003-11-27 Inc Agouron Pharmaceuticals Derivados de benzamida tiazol y composiciones farmaceuticas para inhibir la proliferacion de celulas y metodos para su utilización.
NZ535985A (en) 2002-03-29 2007-04-27 Chiron Corp Substituted benzazoles and use thereof as RAF kinase inhibitors
EA009680B1 (ru) 2003-03-14 2008-02-28 Эвидекс Лимитед Иммуномодулирующие гетероциклические соединения
ATE454372T1 (de) * 2004-04-01 2010-01-15 Lilly Co Eli Am histamin-h3-rezeptor wirksame mittel, herstellung und therapeutische anwendungen
MY139355A (en) * 2004-05-14 2009-09-30 Millennium Pharm Inc Compounds and methods for inhibiting mitotic progression by inhibition of aurora kinase
TW200602314A (en) 2004-05-28 2006-01-16 Tanabe Seiyaku Co A novel pyrrolidine compound and a process for preparing the same
US20060014733A1 (en) * 2004-07-19 2006-01-19 Pfizer Inc Histamine-3 agonists and antagonists
SI1786790T1 (sl) 2004-07-26 2009-10-31 Lilly Co Eli Derivati oksazola kot agenti histamin h3 receptorja, priprava in terapevtska uporaba
CA2577061C (en) 2004-08-23 2014-02-18 Eli Lilly And Company Histamine h3 receptor agents, preparation and therapeutic uses
WO2006028269A2 (en) * 2004-09-09 2006-03-16 Astellas Pharma Inc. Thiazole derivatives having vap-1 ihibitory activity
UY29149A1 (es) 2004-10-07 2006-05-31 Boehringer Ingelheim Int Tiazolil-dihidro-indazoles
US7381732B2 (en) * 2004-10-26 2008-06-03 Bristol-Myers Squibb Company Pyrazolobenzamides and derivatives as factor Xa inhibitors
CA2595157A1 (en) * 2005-01-21 2006-07-27 Schering Corporation Imidazole and benzimidazole derivatives useful as histamine h3 antagonists
WO2006113140A2 (en) * 2005-04-15 2006-10-26 Elan Pharmaceuticals, Inc. Novel compounds useful for bradykinin b1 receptor antagonism
CA2645731A1 (en) 2006-03-15 2007-09-27 Wyeth N-substituted-azacyclylamines as histamine-3 antagonists
WO2007107539A1 (en) 2006-03-20 2007-09-27 Glaxo Group Limited Compounds which potentiate ampa receptor and uses thereof in medicine
US20070238718A1 (en) 2006-04-06 2007-10-11 Matthias Grauert Thiazolyl-dihydro-indazole
CA2649913A1 (en) * 2006-05-19 2007-11-29 Wyeth N-benzoyl- and n-benzylpyrrolidin-3-ylamines as histamine-3 antagonists
PE20081152A1 (es) * 2006-10-06 2008-08-10 Wyeth Corp Azaciclilaminas n-sustituidas como antagonistas de histamina-3

Also Published As

Publication number Publication date
US20070219240A1 (en) 2007-09-20
JP2009530274A (ja) 2009-08-27
BRPI0709612A2 (pt) 2011-07-19
EP1994022A2 (en) 2008-11-26
WO2007108936A2 (en) 2007-09-27
WO2007108936A3 (en) 2007-11-01
AU2007227681A1 (en) 2007-09-27
AR059905A1 (es) 2008-05-07
TW200800958A (en) 2008-01-01
US7820825B2 (en) 2010-10-26
MX2008011791A (es) 2008-09-25
CA2645731A1 (en) 2007-09-27

Similar Documents

Publication Publication Date Title
PE20071023A1 (es) Azaciclilaminas-n-sustituidas como antagonistas de histamina-3
CR9459A (es) Derivados benzodioxano y benzodioxolano y usos de los mismos
PE20081152A1 (es) Azaciclilaminas n-sustituidas como antagonistas de histamina-3
PE20091734A1 (es) Compuestos de 2-imino-3-metilpirrolopirimidinona fenilo-sustituida como inhibidores de bace-1, composiciones y su uso
AR061015A1 (es) Compuesto y composicion farmaceutica para el tratamiento de un trastorno del sistema nervioso central relacionado con o afectado por el receptor histamina-3 y para la inhibicion del receptor h3 y proceso para la preparacion del compuesto
PE20120833A1 (es) Compuestos sustituidos de espiro-amida
PE20120693A1 (es) Compuestos heterociclos como moduladores de la piruvato cinasa m2 (pkm2)
PE20130306A1 (es) Morfolinopirimidinas y su uso en terapia
UY28578A1 (es) Derivados de amida
DE602006006712D1 (de) Thiazolylpiperidin-derivate nützlich als h3 rezeptor modulatoren
EA201000946A1 (ru) Бициклические производные для применения при лечении состояний, связанных с андрогенным рецептором
GT200600165A (es) Derivados dihidrobenzofuranos y usos de los mismos
AR054485A1 (es) ARIL-ALQUILAMINAS Y HETEROARIL-ALQUILAMINAS COMO INHIBIDORES DE PROTEINA QUINASA A Y B, UN PROCESO PARA SU PREPARACION, COMPOSICIONES FARMACEUTICAS QUE LAS CONTIENEN Y SU USO EN LA FABRICACIoN DE MEDICAMENTOS PARA EL TRATAMIENTO O PROFILAXIS DE ENFERMEDADES ORIGINADAS EN EL CRECIMIENTO ANORMAL DE LA
CO5031253A1 (es) Antagonistas receptores y5 de neuropeptidos composiciones farmaceuticas que las contienen
CL2008002864A1 (es) Compuestos derivados de 2-amino-quinolina, antagonistas del receptor de serotonina 5-ht 5a; procedimiento de preparacion;composicion farmaceutica; y uso de los compuestos en la prevencion o el tratamiento de depresion,trastornos de ansiedad,esquizofrenia,trastornos de panico,trastornos de memoria,demencia,entre otros.
PE20071177A1 (es) Derivados de 3,5-piridina como inhibidores de renina
PE20081876A1 (es) Aminoamidas como antagonistas de orexina
AR049398A1 (es) Derivados de sulfamato y sulfamida; una composicion farmaceutica que los contiene y su uso en la preparacion de un medicamento util para el tratamiento de la epilepsia y trastornos relacionados.
AR083831A1 (es) Antagonistas del receptor del cgrp de piperidinona carboxamida azaindano
PE20080277A1 (es) Derivados de azaindol espirociclicos y sustituidos
UY31712A1 (es) Nuevos derivados de diosmetina, su procedimiento de preparacion y las composiciones farmacéuticas que los contienen
UY29301A1 (es) Derivados amida
PE20081665A1 (es) Antagonistas del receptor de dopamina 2 de rapida disociacion
PE20090651A1 (es) Derivados de isoquinolinilo e isoindolinilo como antagonistas de histamina-3
UY30577A1 (es) Derivados de éter diarilico y usos de los mismos

Legal Events

Date Code Title Description
FD Application declared void or lapsed