AR059136A1 - Derivados de indol-3-il-carbonil-espiro-piperidina - Google Patents

Derivados de indol-3-il-carbonil-espiro-piperidina

Info

Publication number
AR059136A1
AR059136A1 ARP070100032A ARP070100032A AR059136A1 AR 059136 A1 AR059136 A1 AR 059136A1 AR P070100032 A ARP070100032 A AR P070100032A AR P070100032 A ARP070100032 A AR P070100032A AR 059136 A1 AR059136 A1 AR 059136A1
Authority
AR
Argentina
Prior art keywords
alkyl
optionally substituted
halogen
nririi
alkoxy
Prior art date
Application number
ARP070100032A
Other languages
English (en)
Inventor
Caterina Bissantz
Christophe Grundschober
Hasane Ratni
Patrick Schnider
Mark Reogers-Evans
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 AR059136A1 publication Critical patent/AR059136A1/es

Links

Classifications

    • 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
    • C07D471/10Spiro-condensed systems
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/02Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
    • A61P5/04Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin for decreasing, blocking or antagonising the activity of the hypothalamic hormones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/02Non-specific cardiovascular stimulants, e.g. drugs for syncope, antihypotensives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/10Spiro-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Hospice & Palliative Care (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Reproductive Health (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Urology & Nephrology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Reivindicacion 1: Compuestos de la formula general (1) en la A se elige los siguientes grupos (a), (b), (c), (d), (e) y (f): X puede ser igual o diferente y es CRiiiRiv, NRiii u O, en las que en (a), solamente una X puede ser O, la otra es CRiiiEiv o NRiii; R1 es H, alquilo C1-6 opcionalmente sustituido por CN, o es arilo, heteroarilo de 5 o 6 eslabones o sulfonilarilo, que están opcionalmente sustituidos por uno o más B, o es -(CH2)m-Ra, en el que Ra es: R3 es H, o es halogeno, o es -(CO)-Rc, en el que Rc es: alquilo C1-6, -(CH2)n-NRiRii, -(CH2)n-NRiiiRiv, heterocicloalquilo de 5 o 6 eslabones opcionalmente sustituido por alquilo C1-6, o es alquilo C1-6 o arilo, que están opcionalmente sustituidos por halogeno, -O(CO)-alquilo C1-6, o por -NH(CO)Rd, en el que Rd es alquilo C1-6 opcionalmente sustituido por halogeno o nitro o Rd es arilo o un heteroarilo de 5 o 6 eslabones, que están opcionalmente sustituidos por halogeno, nitro, alquilo C1-6 o haloalquilo C1-6; R4 es uno o más de H, halogeno, alquilo C1-6 o alcoxi C1-6, CN o dos R4 pueden formar un puente oxo o dioxo junto con el anillo fenilo al que están unidos, B es halogeno, CN, NRiRii, alquilo C1-6 opcionalmente sustituido por CN, halogeno o alcoxi C1-6, alcoxi C1-6, haloalcoxi C1-6, cicloalquilo C3-6, -C(O)O-alquilo C1-6, -C(O)-NRiRii, -C(O)-alquilo C1-6, -S(O)2-alquilo C1-6, -S(O)2-NRiRii, (CRiiiRiv)n-fenilo o (CRiiiRIV)n-heteroarilo de 5 o 6 eslabones, dichos restos fenilo o heteroarilo de 5 o 6 eslabones están opcionalmente sustituidos por uno o más sustituyentes elegidos entre el grupo formado por: halogeno, CN, NRiRii, alquilo C1-6 opcionalmente sustituido por CN o alcoxi C1-6, alcoxi C1-6, haloalcoxi C1-6, cicloalquilo C3-6, -C(O)O-alquilo C1-6, - C(O)-NRiRii, -C(O)-alquilo C1-6, -S(O)2-alquilo C1-6, -S(O)2-NRiRii; Ri y Rii son H, alquilo C1-6, alquileno C1-6-NRiiiRiv, -(CO)O-alquilo C1-6, -C(O)-NRiiiRiv, -C(O)-alquilo C1-6, -S(O)2-alquilo C1-6 o -S(O)2-NRiiiRiv; Riii es H, alquilo C1-6 o alquileno C1-6-N(Riv)2; Riv es H o alquilo C1-6; m es un numero de 1 a 6; n es un numero de 0 a 4, así como las sales farmacéuticamente aceptables de los mismos. La invencion se refiere además a composiciones farmacéuticas que contienen dichos compuestos, a su utilizacion en medicamentos contra dismenorrea, hipertension, fallo cardíaco cronico, secrecion inapropiada de vasopresina, cirrosis hepática, síndrome nefrotico, trastorno obsesivo-compulsivo, ansiedad y trastornos depresivos y a métodos para la obtencion de dichos compuestos
ARP070100032A 2006-01-05 2007-01-04 Derivados de indol-3-il-carbonil-espiro-piperidina AR059136A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06100118 2006-01-05

Publications (1)

Publication Number Publication Date
AR059136A1 true AR059136A1 (es) 2008-03-12

Family

ID=37989141

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP070100032A AR059136A1 (es) 2006-01-05 2007-01-04 Derivados de indol-3-il-carbonil-espiro-piperidina

Country Status (15)

Country Link
US (1) US7351706B2 (es)
EP (1) EP1973913A1 (es)
JP (1) JP2009522318A (es)
KR (1) KR101121349B1 (es)
CN (1) CN101356174B (es)
AR (1) AR059136A1 (es)
AU (1) AU2006334423B2 (es)
BR (1) BRPI0620951A2 (es)
CA (1) CA2634120A1 (es)
IL (1) IL192401A0 (es)
NO (1) NO20082733L (es)
RU (1) RU2420529C2 (es)
TW (1) TW200734343A (es)
WO (1) WO2007077122A1 (es)
ZA (1) ZA200805574B (es)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6374762B1 (en) * 1997-10-27 2002-04-23 Correct Craft, Inc. Water sport towing apparatus
MX2007002033A (es) * 2004-08-19 2007-04-26 Vertex Pharma Moduladores de receptores muscarinicos.
US7786141B2 (en) * 2004-08-19 2010-08-31 Vertex Pharmaceuticals Incorporated Dihydrospiroindene modulators of muscarinic receptors
AU2005309365B2 (en) * 2004-11-29 2011-10-06 Vertex Pharmaceuticals Incorporated Modulators of muscarinic receptors
DE602006018334D1 (de) * 2005-09-28 2010-12-30 Hoffmann La Roche Indol-3-ylcarbonylazaspiroderivate als vasopressinrezeptorantagonisten
WO2007076070A2 (en) * 2005-12-22 2007-07-05 Vertex Pharmaceuticals Incorporated Modulators of muscarinic receptors
RU2008137593A (ru) 2006-02-22 2010-03-27 Вертекс Фармасьютикалз Инкорпорейтед (Us) Модуляторы мускариновых рецепторов
WO2008021375A2 (en) * 2006-08-15 2008-02-21 Vertex Pharmaceuticals Incorporated Modulators of muscarinic receptors
CA2660974A1 (en) * 2006-08-18 2008-02-21 Vertex Pharmaceuticals Incorporated Modulators of muscarinic receptors
JP2010511654A (ja) 2006-12-07 2010-04-15 エフ.ホフマン−ラ ロシュ アーゲー スピロ−ピペリジン誘導体
JP2010540640A (ja) * 2007-10-03 2010-12-24 バーテックス ファーマシューティカルズ インコーポレイテッド ムスカリン作用性レセプターのモジュレーター
US8846684B2 (en) 2011-03-31 2014-09-30 The Regents Of The University Of Michigan Arbovirus inhibitors and uses thereof
WO2013138565A1 (en) 2012-03-16 2013-09-19 Vitae Pharmaceuticals, Inc. Liver x receptor modulators
KR102069913B1 (ko) 2012-03-16 2020-01-23 비타이 파마슈티컬즈, 엘엘씨 간 x 수용체 조절제
KR102353431B1 (ko) 2013-12-19 2022-01-20 에프. 호프만-라 로슈 아게 스피로-옥사졸론
MX2020002436A (es) * 2017-09-05 2020-07-13 Blackthorn Therapeutics Inc Antagonistas del receptor de vasopresina y productos y metodos relacionados a los mismos.
WO2020048826A1 (en) 2018-09-03 2020-03-12 Bayer Aktiengesellschaft 5-substituted 1-oxa-3,9-diazaspiro[5.5]undecan-2-one compounds
TW202024083A (zh) 2018-09-03 2020-07-01 德商拜耳廠股份有限公司 3,9-二氮雜螺[5.5]十一烷化合物
WO2020048830A1 (en) 2018-09-03 2020-03-12 Bayer Aktiengesellschaft 5-aryl-3,9-diazaspiro[5.5]undecan-2-one compounds
WO2020048831A1 (en) 2018-09-03 2020-03-12 Bayer Aktiengesellschaft 5-aryl-3,9-diazaspiro[5.5]undecan-2-one compounds
WO2020048828A1 (en) 2018-09-03 2020-03-12 Bayer Pharma Aktiengesellschaft 5-heteroaryl-3,9-diazaspiro[5.5]undecane compounds

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4349549A (en) * 1981-05-18 1982-09-14 Syntex (U.S.A.) Inc. Anti-hypertensive 1-substituted spiro(piperidine-oxobenzoxazine)s
EP1009405A4 (en) 1997-08-28 2001-05-09 Merck & Co Inc MODULATORS OF PYRROLIDINE AND PIPERIDINE OF CHEMOKINE RECEPTOR ACTIVITY
US6013652A (en) 1997-12-04 2000-01-11 Merck & Co., Inc. Spiro-substituted azacycles as neurokinin antagonists
WO2001022919A2 (en) 1999-09-30 2001-04-05 Merck & Co., Inc. Spiro[bicyclic -azacycloalkyl and -cycloalkyl] derivatives and uses thereof
GB0003397D0 (en) 2000-02-14 2000-04-05 Merck Sharp & Dohme Therapeutic agents
BR0315047A (pt) 2002-10-03 2005-08-23 Hoffmann La Roche Composto, composição fermacêutica que compreende o mesmo, processo para a preparação da composição farmacêutica, utilização dos compostos, método de tratamento e processo para a preparação do composto
BRPI0612988A2 (pt) 2005-07-14 2010-12-14 Hoffmann La Roche derivados de indol-3-il-carbonil-espiro-piperidina como antagonistas de receptor v1a

Also Published As

Publication number Publication date
AU2006334423A1 (en) 2007-07-12
ZA200805574B (en) 2009-12-30
CA2634120A1 (en) 2007-07-12
RU2420529C2 (ru) 2011-06-10
CN101356174B (zh) 2011-11-23
BRPI0620951A2 (pt) 2011-11-29
NO20082733L (no) 2008-10-02
US20070155761A1 (en) 2007-07-05
AU2006334423B2 (en) 2011-09-22
KR101121349B1 (ko) 2012-03-09
EP1973913A1 (en) 2008-10-01
KR20080073364A (ko) 2008-08-08
TW200734343A (en) 2007-09-16
CN101356174A (zh) 2009-01-28
US7351706B2 (en) 2008-04-01
RU2008125813A (ru) 2010-02-10
IL192401A0 (en) 2008-12-29
WO2007077122A1 (en) 2007-07-12
JP2009522318A (ja) 2009-06-11

Similar Documents

Publication Publication Date Title
AR059136A1 (es) Derivados de indol-3-il-carbonil-espiro-piperidina
AR057086A1 (es) Derivados de indol-3- il-carbonil-piperidina y piperazina, composicion farmaceutica y proceso de preparacion del compuesto
ES2552320T3 (es) Nuevas piridín-2-onas y piridazín-3-onas sustituidas
AR047056A1 (es) Derivados de pirimidinas condensadas. composiciones farmacéuticas
AR047456A1 (es) Derivados de amidas, procesos para su preparacion y uso como insecticidas
AR041672A1 (es) Compuesto biciclico de benzamida, composicion farmaceutica que lo comprende, su uso para la fabricacion de un medicamento y procedimiento para prepararlo
AR048055A1 (es) Derivados de pirimidina como inhibidores de dipeptidil peptidasa
AR047902A1 (es) Compuestos como inhibidores de ns3 serina proteasa del virus de hepatitis c
AR078163A1 (es) Utilizacion de aminodihidrotiazinas para el tratamiento o prevencion de la diabetes
AR051092A1 (es) Derivados heterociclicos y su uso como inhibidores de la estearoil-coa
CO6160296A2 (es) Derivados de acido benzoazepin-oxi-acetico como agonistas de receptores activados por proliferador de peroxisona delta usados para incrementar la lipoproteina de alta densidad-colesterol-colesterol reducir la lipoproteina de baja densidad-colesterol
CO5640135A2 (es) Derivados de 4-(4-(heterociclilalcoxi)-1-(heterociclil-carbonil)piperidina y compuestos relacionados como antagonistas de histamina h3 para el tratamiento de enfermedades neurologicas tales como alzheimer
AR060173A1 (es) Derivados de piridina y de pirimidina como antagonistas del mglur2, metodos para su preparacion, composiciones farmaceuticas que los contienen y su uso en la fabricacion de medicamentos para el tratamiento de trastornos del snc.
AR052568A1 (es) Derivados de pirazolo -pirimidina como antagonstas de mglur2
CO5700754A2 (es) Derivados de piperazina y su uso en el tratamiento de enfermedades neurologicas y psiquiatricas
AR056188A1 (es) Derivados indol-3-il-carbonil-piperidin-benzoimidazol como antagonistas del receptor v1a
AR058776A1 (es) Compuesto de piridina condensado
RS51471B (en) BIPHYNYLOXYXIC ACID DERIVATIVES FOR TREATMENT OF RESPIRATORY DISEASES
AR051202A1 (es) Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa
AR041297A1 (es) Derivados de 4-pirrolidino- fenil- bencil eter
AR066669A1 (es) Derivados de imidazolona como inhibidores de bencimidazolona quimasa. composiciones farmaceuticas.
AR057197A1 (es) Derivados de 1, 1-dioxo-tiomorfolinil-indolil-metanona
AR068376A1 (es) Amidas heterociclicas utiles para inhibir la via hedgehog.
AR057136A1 (es) Derivados de indol-3-il-carbonil-azaespiro
AR055420A1 (es) Derivados de pirimidina sustituidos

Legal Events

Date Code Title Description
FA Abandonment or withdrawal