[go: up one dir, main page]

NO20080059L - Indol-3-karbonyl-spiro-piperidinderivater som V1A-reseptorantagonister - Google Patents

Indol-3-karbonyl-spiro-piperidinderivater som V1A-reseptorantagonister

Info

Publication number
NO20080059L
NO20080059L NO20080059A NO20080059A NO20080059L NO 20080059 L NO20080059 L NO 20080059L NO 20080059 A NO20080059 A NO 20080059A NO 20080059 A NO20080059 A NO 20080059A NO 20080059 L NO20080059 L NO 20080059L
Authority
NO
Norway
Prior art keywords
spiro
carbonyl
receptor antagonists
piperidine derivatives
indole
Prior art date
Application number
NO20080059A
Other languages
English (en)
Inventor
Patrick Schnider
Hasane Ratni
Caterina Bissantz
Christophe Grundschober
Mark Rogers-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 NO20080059L publication Critical patent/NO20080059L/no

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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • 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
    • A61P15/08Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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
    • 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
    • C07D401/06Heterocyclic 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 only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (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)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Reproductive Health (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Endocrinology (AREA)
  • Pain & Pain Management (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pregnancy & Childbirth (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Urology & Nephrology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Foreliggende oppfinnelse angår indol-3-yl-karbonyl-spiro-piperidin-derivater som virker som V1a-reseptorantagonister og som er representert ved formel I: hvor spiro-piperidin-hodegruppen A og residuene R1, R2 og R3 er som definert her. Oppfinnelsen angår videre farmasøytiske preparater inneholdende slike forbindelser, anvendelse av dem i medikamenter mot dysmenorré, hypertensjon, kronisk hjertesvikt, upassende sekresjon av vasopressin, lever-cirrhose, nefrotisk syndrom, obsessiv-kompulsiv lidelse, angst og depresjonslidelser, og metoder for fremstilling derav. 290
NO20080059A 2005-07-14 2008-01-04 Indol-3-karbonyl-spiro-piperidinderivater som V1A-reseptorantagonister NO20080059L (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP05106443 2005-07-14
EP05109364 2005-10-07
PCT/EP2006/063846 WO2007006688A1 (en) 2005-07-14 2006-07-04 Indol-3-carbonyl-spiro-piperidine derivatives as v1a receptor antagonists

Publications (1)

Publication Number Publication Date
NO20080059L true NO20080059L (no) 2008-04-02

Family

ID=37001896

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20080059A NO20080059L (no) 2005-07-14 2008-01-04 Indol-3-karbonyl-spiro-piperidinderivater som V1A-reseptorantagonister

Country Status (25)

Country Link
US (2) US7332501B2 (no)
EP (1) EP1904477B1 (no)
JP (1) JP4927079B2 (no)
KR (1) KR100974967B1 (no)
CN (1) CN101253164B (no)
AR (1) AR054830A1 (no)
AT (1) ATE421511T1 (no)
AU (1) AU2006268724B2 (no)
BR (1) BRPI0612988A2 (no)
CA (1) CA2615726C (no)
CY (1) CY1108996T1 (no)
DE (1) DE602006004997D1 (no)
DK (1) DK1904477T3 (no)
ES (1) ES2317558T3 (no)
IL (1) IL188478A (no)
MX (1) MX2008000585A (no)
MY (1) MY144684A (no)
NO (1) NO20080059L (no)
PL (1) PL1904477T3 (no)
PT (1) PT1904477E (no)
RU (1) RU2414466C2 (no)
SI (1) SI1904477T1 (no)
TW (1) TWI312780B (no)
WO (1) WO2007006688A1 (no)
ZA (1) ZA200800320B (no)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI1904477T1 (sl) * 2005-07-14 2009-06-30 Hoffmann La Roche Derivati indol-3-karbonil-spiro-piperidina kot antagonisti V1A receptorja
AU2006298828B2 (en) * 2005-09-28 2011-12-01 F. Hoffmann-La Roche Ag Indol-3-yl-carbonyl-azaspiro derivatives as vasopressin receptor antagonists
US7351706B2 (en) 2006-01-05 2008-04-01 Hoffmann-La Roche Inc. Indol-3-yl-carbonyl-spiro-piperidine derivatives
ES2344131T3 (es) 2006-12-07 2010-08-18 F. Hoffmann-La Roche Ag Derivados de espiro-piperidina como antagonistas del receptor v1a.
US20080139617A1 (en) 2006-12-08 2008-06-12 Caterina Bissantz Indoles
CN101563324A (zh) * 2006-12-22 2009-10-21 弗·哈夫曼-拉罗切有限公司 螺-哌啶衍生物
CN101583615B (zh) * 2007-01-12 2012-07-04 弗·哈夫曼-拉罗切有限公司 螺哌啶甘氨酰胺衍生物
TW200940547A (en) * 2007-12-13 2009-10-01 Speedel Experimenta Ag Organic compounds
WO2011137024A1 (en) * 2010-04-26 2011-11-03 Merck Sharp & Dohme Corp. Novel spiropiperidine prolylcarboxypeptidase inhibitors
BR112013023068B8 (pt) 2011-03-10 2022-11-22 Zoetis Llc Derivados de isoxazolina espirocíclica, seu uso e seu processo de preparação, e composições veterinárias
RU2475489C1 (ru) * 2011-10-07 2013-02-20 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Чувашский государственный университет имени И.Н. Ульянова" Способ получения 8-амино-1-имино-6-морфолин-4-ил-2-окса-7-азаспиро[4,4]нона-3,6,8-триен-9-карбонитрилов
BR112014022780A8 (pt) 2012-03-16 2021-06-15 Vitae Pharmaceuticals Inc composto modulador de receptor de fígado x, composição farmacêutica que o compreende e seu uso
EP2825541B1 (en) 2012-03-16 2016-06-22 Vitae Pharmaceuticals, Inc. Liver x receptor modulators
JO3109B1 (ar) * 2012-05-10 2017-09-20 Ferring Bv منبهات لمستقبلات v1a
KR101698124B1 (ko) * 2015-05-29 2017-01-19 한국외국어대학교 연구산학협력단 3-(메틸아미노)-3-((r)-피롤리딘-3-일)프로판니트릴 또는 이의 염의 제조방법
JP6990657B2 (ja) * 2016-02-08 2022-01-13 エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト Ddr1阻害剤としてのスピロインドリノン
US20180002344A1 (en) 2016-06-16 2018-01-04 Genentech, Inc. Heteroaryl estrogen receptor modulators and uses thereof
CA3037222C (en) 2016-09-21 2024-02-13 Vectus Biosystems Limited Compositions for the treatment of hypertension and/or fibrosis
HU231206B1 (hu) 2017-12-15 2021-10-28 Richter Gedeon Nyrt. Triazolobenzazepinek
TW201938171A (zh) 2017-12-15 2019-10-01 匈牙利商羅特格登公司 作為血管升壓素V1a受體拮抗劑之三環化合物
CN113563255B (zh) * 2020-04-29 2023-08-18 成都倍特药业股份有限公司 瑞芬沙星中间体的制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5686624A (en) * 1992-01-30 1997-11-11 Sanofi 1-benzenesulfonyl-1,3-dihydro-indol-2-one derivatives, their preparation and pharmaceutical compositions in which they are present
HUT72076A (en) * 1992-12-11 1996-03-28 Merck & Co Inc Process for preparing spiro piperidines and homologs which promote release of growth hormone and pharmaceutical compositions containing them
WO2002058143A2 (en) * 2001-01-22 2002-07-25 Morgan Chemical Products, Inc. Cvd diamond enhanced microprocessor cooling system
SI1904477T1 (sl) * 2005-07-14 2009-06-30 Hoffmann La Roche Derivati indol-3-karbonil-spiro-piperidina kot antagonisti V1A receptorja

Also Published As

Publication number Publication date
CA2615726C (en) 2014-05-27
DK1904477T3 (da) 2009-03-16
ZA200800320B (en) 2009-02-25
EP1904477A1 (en) 2008-04-02
IL188478A (en) 2012-01-31
AU2006268724A1 (en) 2007-01-18
US20070027173A1 (en) 2007-02-01
MY144684A (en) 2011-10-31
KR20080024231A (ko) 2008-03-17
BRPI0612988A2 (pt) 2010-12-14
CY1108996T1 (el) 2014-07-02
RU2008100082A (ru) 2009-08-20
SI1904477T1 (sl) 2009-06-30
PT1904477E (pt) 2009-03-12
MX2008000585A (es) 2008-03-14
US7332501B2 (en) 2008-02-19
US20080146557A1 (en) 2008-06-19
RU2414466C2 (ru) 2011-03-20
TWI312780B (en) 2009-08-01
DE602006004997D1 (de) 2009-03-12
AU2006268724B2 (en) 2011-06-02
PL1904477T3 (pl) 2009-07-31
CN101253164A (zh) 2008-08-27
EP1904477B1 (en) 2009-01-21
WO2007006688A1 (en) 2007-01-18
AR054830A1 (es) 2007-07-18
KR100974967B1 (ko) 2010-08-09
HK1123554A1 (en) 2009-06-19
ES2317558T3 (es) 2009-04-16
US7629353B2 (en) 2009-12-08
CN101253164B (zh) 2012-05-16
TW200726469A (en) 2007-07-16
CA2615726A1 (en) 2007-01-18
IL188478A0 (en) 2008-04-13
JP4927079B2 (ja) 2012-05-09
JP2009501185A (ja) 2009-01-15
ATE421511T1 (de) 2009-02-15

Similar Documents

Publication Publication Date Title
NO20080059L (no) Indol-3-karbonyl-spiro-piperidinderivater som V1A-reseptorantagonister
NO20082733L (no) Indol-3-yl-karbonyl-spiro-piperidinderivater
NO20080291L (no) Indol-3-yl-karbonyl-piperidin-benzomidazolderivater som Via reseptorantagonister
NO20080316L (no) Indol-3-yl-karbonylpiperidin- og piperazinderivater
NO20071660L (no) Nye pyridinonderivater og deres anvendelse som positive allosteriske modulatorer av MGLUR2-reseptorer
WO2010036613A8 (en) Novel cyclic benzimidazole derivatives useful anti-diabetic agents
NO20064579L (no) Bifenylforbindelser anvendelige som muskariniske receptorantagonister
NO20083500L (no) 1,4-disubstituerte 3-cyano-pyridonderivater og deres anvendelse som positiv-allosteriske modulatorer av mGluR2 receptorer
NO20076060L (no) Piperidin-4-yl-amidderivater og deres anvendelse som SST-reseptor subtype 5-antagonister
NO20092762L (no) 2-aza-bicyklo[3.1.0]heksanderivater
NO20072978L (no) Nye betuinderivater, preparat derav og anvendelse derav
WO2006021213A3 (en) Vasopressin v1a antagonists
WO2007115077A3 (en) Bicyclic benzimidazole compounds and their use as metabotropic glutamate receptor potentiators
NO20073019L (no) Pyrasolonforbindelser som metabotrope glutamatreseptor-antagonister for behandlingen av nevrotiske og psykiatriske lidelser
CY1108880T1 (el) Παραγωγα καρβοξαμιδιου ως ανταγωνιστες μουσκαρινικου υποδοχεα
EP2548568A3 (en) Melanocortin receptor ligands
NO20073876L (no) Pyrazolopyrimidinderivater som mGluR2-antagonister
WO2009024989A3 (en) A novel hydrated form of erlotinib free base and a process for preparation of erlotinib hydrochloride polymorph form a substantially free of polymorph form b
WO2008099072A3 (fr) Nouveaux derives de 2, 4-dianilinopyrimidines, leur preparation, a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
WO2004041806A3 (en) Substituted 4-amino-1-(pyridylmethyl) piperidine as muscarinic receptor antagonists
NO20083583L (no) Heterosykliske antivirale forbindelser
WO2007067875A3 (en) Pyridinyl sulfonamide modulators of chemokine receptors
EA200701687A1 (ru) Гидрохлорид аморфного лерканидипина
WO2010131192A3 (en) Novel oxazolidinone derivatives and their use as orexin receptor antagonists
WO2008059513A3 (en) Compounds suitable as modulators of hdl

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application