ZA200800320B - Indol-3-carbonyl-spiro-piperidine derivatives as Via receptor antagonists - Google Patents

Indol-3-carbonyl-spiro-piperidine derivatives as Via receptor antagonists

Info

Publication number
ZA200800320B
ZA200800320B ZA200800320A ZA200800320A ZA200800320B ZA 200800320 B ZA200800320 B ZA 200800320B ZA 200800320 A ZA200800320 A ZA 200800320A ZA 200800320 A ZA200800320 A ZA 200800320A ZA 200800320 B ZA200800320 B ZA 200800320B
Authority
ZA
South Africa
Prior art keywords
indol
spiro
carbonyl
receptor antagonists
piperidine derivatives
Prior art date
Application number
ZA200800320A
Other languages
English (en)
Inventor
Bissantz Caterina
Ratni Hasane
Schnider Patrick
Grundschober Christophe
Rogers-Evans Mark
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 ZA200800320B publication Critical patent/ZA200800320B/xx

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)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Neurology (AREA)
  • Reproductive Health (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Pregnancy & Childbirth (AREA)
  • Hospice & Palliative Care (AREA)
  • Endocrinology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Urology & Nephrology (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)
ZA200800320A 2005-07-14 2008-01-10 Indol-3-carbonyl-spiro-piperidine derivatives as Via receptor antagonists ZA200800320B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP05106443 2005-07-14
EP05109364 2005-10-07

Publications (1)

Publication Number Publication Date
ZA200800320B true ZA200800320B (en) 2009-02-25

Family

ID=37001896

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA200800320A ZA200800320B (en) 2005-07-14 2008-01-10 Indol-3-carbonyl-spiro-piperidine derivatives as Via receptor antagonists

Country Status (26)

Country Link
US (2) US7332501B2 (pl)
EP (1) EP1904477B1 (pl)
JP (1) JP4927079B2 (pl)
KR (1) KR100974967B1 (pl)
CN (1) CN101253164B (pl)
AR (1) AR054830A1 (pl)
AT (1) ATE421511T1 (pl)
AU (1) AU2006268724B2 (pl)
BR (1) BRPI0612988A2 (pl)
CA (1) CA2615726C (pl)
CY (1) CY1108996T1 (pl)
DE (1) DE602006004997D1 (pl)
DK (1) DK1904477T3 (pl)
ES (1) ES2317558T3 (pl)
HK (1) HK1123554A1 (pl)
IL (1) IL188478A (pl)
MX (1) MX2008000585A (pl)
MY (1) MY144684A (pl)
NO (1) NO20080059L (pl)
PL (1) PL1904477T3 (pl)
PT (1) PT1904477E (pl)
RU (1) RU2414466C2 (pl)
SI (1) SI1904477T1 (pl)
TW (1) TWI312780B (pl)
WO (1) WO2007006688A1 (pl)
ZA (1) ZA200800320B (pl)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK1904477T3 (da) * 2005-07-14 2009-03-16 Hoffmann La Roche Indol-3-carbonyl-spiro-piperodom-derivater som V1A-receptorantagonister
CA2623715A1 (en) * 2005-09-28 2007-04-12 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
EP2102207B1 (en) * 2006-12-07 2010-06-02 F.Hoffmann-La Roche Ag Spiro-piperidine derivatives as via receptor antagonists
US8071622B2 (en) * 2006-12-08 2011-12-06 Hoffman-La Roche Inc. Indoles
AU2007338115A1 (en) * 2006-12-22 2008-07-03 F. Hoffmann-La Roche Ag Spiro-piperidine derivatives
AU2008204491B2 (en) * 2007-01-12 2012-05-03 F. Hoffmann-La Roche Ag Spiropiperidine glycinamide derivatives
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
HUE030785T2 (en) 2012-03-16 2017-06-28 Vitae Pharmaceuticals Inc Liver X receptor modulators
HUE029402T2 (en) 2012-03-16 2017-02-28 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
DK3515895T3 (da) * 2016-09-21 2021-10-18 Vectus Biosystems Ltd Imidazolderivater til behandling af hypertension og/eller fibrose
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 (3)

* 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
US7339791B2 (en) * 2001-01-22 2008-03-04 Morgan Advanced Ceramics, Inc. CVD diamond enhanced microprocessor cooling system
DK1904477T3 (da) * 2005-07-14 2009-03-16 Hoffmann La Roche Indol-3-carbonyl-spiro-piperodom-derivater som V1A-receptorantagonister

Also Published As

Publication number Publication date
CN101253164A (zh) 2008-08-27
TW200726469A (en) 2007-07-16
TWI312780B (en) 2009-08-01
IL188478A0 (en) 2008-04-13
PL1904477T3 (pl) 2009-07-31
CA2615726C (en) 2014-05-27
CA2615726A1 (en) 2007-01-18
SI1904477T1 (sl) 2009-06-30
MY144684A (en) 2011-10-31
US7629353B2 (en) 2009-12-08
CN101253164B (zh) 2012-05-16
AU2006268724A1 (en) 2007-01-18
PT1904477E (pt) 2009-03-12
JP4927079B2 (ja) 2012-05-09
AR054830A1 (es) 2007-07-18
RU2008100082A (ru) 2009-08-20
US20070027173A1 (en) 2007-02-01
JP2009501185A (ja) 2009-01-15
DK1904477T3 (da) 2009-03-16
CY1108996T1 (el) 2014-07-02
KR100974967B1 (ko) 2010-08-09
US7332501B2 (en) 2008-02-19
US20080146557A1 (en) 2008-06-19
RU2414466C2 (ru) 2011-03-20
DE602006004997D1 (de) 2009-03-12
BRPI0612988A2 (pt) 2010-12-14
AU2006268724B2 (en) 2011-06-02
IL188478A (en) 2012-01-31
WO2007006688A1 (en) 2007-01-18
EP1904477B1 (en) 2009-01-21
NO20080059L (no) 2008-04-02
EP1904477A1 (en) 2008-04-02
KR20080024231A (ko) 2008-03-17
ATE421511T1 (de) 2009-02-15
HK1123554A1 (en) 2009-06-19
MX2008000585A (es) 2008-03-14
ES2317558T3 (es) 2009-04-16

Similar Documents

Publication Publication Date Title
ZA200800320B (en) Indol-3-carbonyl-spiro-piperidine derivatives as Via receptor antagonists
ZA200800353B (en) Pyrazine derivatives useful as adenosine receptor antagonists
AP2008004441A0 (en) Piperdin-4-ylpyrazin-2-ylamine derivatives as fastdissociating dopamine 2 receptor antagonists
ZA200708028B (en) Acetylenyl-pyrazolo-pyrimidine derivatives as mGluR2 antagonists
EP1915372A4 (en) INDOLE DERIVATIVES AS CRTH2 RECEPTOR ANTAGONISTS
AP2006003840A0 (en) Indole-2-carboxamidine derivatives as NMDA receptor antagonists
AP1983A (en) Carboxamide derivatives as muscarinic receptor antagonists
IL184816A0 (en) 2-phenyl-indoles as prostaglandin d2 receptor antagonists
ZA200709147B (en) Pyrimidindione derivatives as prokineticin 2 receptor antagonists
IL190686A0 (en) Il-21 receptor antagonists
ZA200806065B (en) Oxazoloisoquinoline derivatives as thrombin receptor antagonists
IL178622A0 (en) Piperazinylpiperidine derivatives as chemokine receptor antagonists
IL198542A0 (en) 2-aminoquinolines as 5-ht(5a)receptor antagonists
PT1912976E (pt) Derivados de indol-3-il-carboni-piperidin-benzimidazole como antagonistas dos receptores v1a
HUP0501169A2 (en) New phenantridine derivatives as selective bradykinin b1 receptor antagonists
ZA200802339B (en) Indol-3-yl-carbonyl-azaspiro derivatives as vasopressin receptor antagonists
ZA200903499B (en) Indoles which act as via receptor antagonists
ZA200903496B (en) Spiro-piperidine derivatives as via receptor antagonists
IL185640A0 (en) Use of 2-anilino-3 ,4-dihydro-quinazolines as 5ht5a receptor antagonists
AP2008004537A0 (en) Muscarinic receptor antagonists
GB0525029D0 (en) Receptor Antagonist
ZA200806223B (en) Muscarinic receptor antagonists
ZA200800516B (en) Indol-3-yl-carbonyl-piperidin-benzoimidazol derivatives as V1a receptor antagonists
GB0516617D0 (en) EP2 Receptor antagonists
ZA200608369B (en) Piperazinylpiperidine derivatives as chemokine receptor antagonists