CN1934112A - 稠合的杂环化合物及其作为代谢型谷氨酸受体拮抗剂的应用 - Google Patents

稠合的杂环化合物及其作为代谢型谷氨酸受体拮抗剂的应用 Download PDF

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Publication number
CN1934112A
CN1934112A CN200580008454.2A CN200580008454A CN1934112A CN 1934112 A CN1934112 A CN 1934112A CN 200580008454 A CN200580008454 A CN 200580008454A CN 1934112 A CN1934112 A CN 1934112A
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China
Prior art keywords
alkyl
triazolo
oxadiazol
compound
tetrahydro
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Pending
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CN200580008454.2A
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English (en)
Chinese (zh)
Inventor
M·约翰松
D·温斯博
A·米尼迪斯
K·斯塔夫
A·克尔斯
L·爱德华兹
M·伊萨克
T·斯特法纳克
A·斯拉西
D·麦克莱奥
T·辛
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AstraZeneca AB
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AstraZeneca AB
NPS Pharmaceuticals Inc
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Publication of CN1934112A publication Critical patent/CN1934112A/zh
Pending legal-status Critical Current

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    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
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    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

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  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Obesity (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Psychiatry (AREA)
  • Pulmonology (AREA)
  • Hematology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Psychology (AREA)
  • Urology & Nephrology (AREA)
  • Reproductive Health (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Endocrinology (AREA)
  • Vascular Medicine (AREA)
  • Pregnancy & Childbirth (AREA)
  • Dermatology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Hospice & Palliative Care (AREA)
CN200580008454.2A 2004-02-18 2005-02-17 稠合的杂环化合物及其作为代谢型谷氨酸受体拮抗剂的应用 Pending CN1934112A (zh)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US54528804P 2004-02-18 2004-02-18
US60/545,288 2004-02-18
US54558004P 2004-02-19 2004-02-19
US60/545,580 2004-02-19

Publications (1)

Publication Number Publication Date
CN1934112A true CN1934112A (zh) 2007-03-21

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ID=34886171

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CN200580008454.2A Pending CN1934112A (zh) 2004-02-18 2005-02-17 稠合的杂环化合物及其作为代谢型谷氨酸受体拮抗剂的应用

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Country Link
US (1) US20070185095A1 (https=)
EP (1) EP1716152B1 (https=)
JP (1) JP2007523183A (https=)
KR (1) KR20070026380A (https=)
CN (1) CN1934112A (https=)
AT (1) ATE402935T1 (https=)
BR (1) BRPI0507495A (https=)
CA (1) CA2556320A1 (https=)
DE (1) DE602005008558D1 (https=)
DK (1) DK1716152T3 (https=)
ES (1) ES2309718T3 (https=)
HR (1) HRP20080480T3 (https=)
IL (1) IL177291A0 (https=)
MY (1) MY152888A (https=)
PL (1) PL1716152T3 (https=)
PT (1) PT1716152E (https=)
RU (1) RU2006129324A (https=)
SI (1) SI1716152T1 (https=)
UA (1) UA82435C2 (https=)
WO (1) WO2005080397A2 (https=)
ZA (1) ZA200606508B (https=)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103906750A (zh) * 2011-10-03 2014-07-02 欧洲筛选有限公司 作为选择性NK-3受体拮抗剂的新型手性N-酰基-5,6,7,(8-取代的)-四氢-[1,2,4]三唑并[4,3-a]吡嗪、药物组合物、用于NK-3受体介导的疾病中的方法及其手性合成
CN108434147A (zh) * 2013-07-17 2018-08-24 赫普泰雅治疗有限公司 4-(3-氰基苯基)-6-吡啶基嘧啶mglu5调节剂

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IL166510A0 (en) 2002-08-09 2006-01-15 Nps Pharma Inc 1,2,4"oxadiazole as modulators of metabotropic glutamate receptor-5
US7807706B2 (en) 2005-08-12 2010-10-05 Astrazeneca Ab Metabotropic glutamate-receptor-potentiating isoindolones
AR058807A1 (es) 2005-09-29 2008-02-27 Astrazeneca Ab 5-(fenilisoxazoletoxi)-triazol-3-il piridinas sustituidas, para el tratamiento de trastornos mediados por el receptor mglur5
TW200808800A (en) * 2006-05-05 2008-02-16 Astrazeneca Ab MGluR5 modulators V
TW200811179A (en) * 2006-05-05 2008-03-01 Astrazeneca Ab mGluR5 modulators VI
TW200811157A (en) 2006-05-05 2008-03-01 Astrazeneca Ab mGluR5 modulators I
EP2119719A1 (en) * 2006-12-26 2009-11-18 Daiichi Sankyo Company, Limited Thiazepine derivative
TWI417100B (zh) * 2007-06-07 2013-12-01 Astrazeneca Ab 二唑衍生物及其作為代謝型麩胺酸受體增效劑-８４２之用途
TW200911255A (en) 2007-06-07 2009-03-16 Astrazeneca Ab Metabotropic glutamate receptor oxadiazole ligands and their use as potentiators-841
WO2009054791A1 (en) * 2007-10-26 2009-04-30 Astrazeneca Ab Fused pyrrolidine 1,2,4-triazole derivatives as modulators of mglur5
WO2009054792A1 (en) * 2007-10-26 2009-04-30 Astrazeneca Ab Aminopyridine derivatives as modulators of mglur5
TW200922586A (en) * 2007-10-26 2009-06-01 Astrazeneca Ab Thiophene 1,2,4-triazole derivatives as modulators of mGluR5
WO2009054789A1 (en) * 2007-10-26 2009-04-30 Astrazeneca Ab 1,2,3-triazole pyrrolidine derivatives as modulators of mglur5
WO2009054786A1 (en) * 2007-10-26 2009-04-30 Astrazeneca Ab 1,2,4-triazole aryl n-oxides derivatives as modulators of mglur5
SA109300358B1 (ar) 2008-06-06 2012-11-03 استرازينيكا ايه بي مقويات مستقبل جلوتامات ذي انتحاء أيضي من أيزو إندولون
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
ES2472446T3 (es) 2009-11-30 2014-07-01 Novartis Ag Derivados de imidazol como inhibidores de aldosterona sintasa
ES2443578T3 (es) 2009-12-29 2014-02-19 Eli Lilly And Company Compuestos de tetrahidrotriazolopiridina como potenciadores de receptores selectivos de mGlu5 útiles para el tratamiento de la esquizofrenia
WO2011092290A1 (en) 2010-02-01 2011-08-04 Novartis Ag Pyrazolo[5,1b]oxazole derivatives as crf-1 receptor antagonists
AR080056A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de ciclohexil-amida como antagonistas de los receptores de crf
EP2531490B1 (en) 2010-02-02 2014-10-15 Novartis AG Cyclohexyl amide derivatives as crf receptor antagonists
EP2552920B1 (en) 2010-04-02 2017-03-15 Ogeda Sa Novel nk-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in nk-3 receptors mediated disorders
US10065960B2 (en) 2010-04-02 2018-09-04 Ogeda Sa NK-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in NK-3 receptors mediated disorders
KR20130094179A (ko) * 2010-04-30 2013-08-23 아스트라제네카 아베 대사형 글루탐산 수용체 양성 알로스테릭 조정자의 다형체
US10183948B2 (en) 2013-03-29 2019-01-22 Ogeda Sa N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists
ES2711143T3 (es) 2013-03-29 2019-04-30 Ogeda Sa N-acil-(3-sustituido)-5,6,7,8-tetrahidro-[1,2,4]triazolo[4,3-a]pirazinas como antagonistas selectivos del receptor de NK-3, composición farmacéutica, métodos para su uso en los trastornos mediados por el receptor de NK-3
JP6275242B2 (ja) 2013-03-29 2018-02-07 オゲダ エス．エー． 選択的ＮＫ−３受容体拮抗薬としての新規なＮ−アシル−（３位置換）−（８−メチル）−５，６−ジヒドロ−［１，２，４］トリアゾロ［４，３−ａ］ピラジン、その医薬組成物、ＮＫ−３受容体媒介性障害で使用する方法
PT2948455T (pt) 2013-03-29 2017-11-15 Ogeda S A N-acil-(3-substituído)-(8-substituído)-5,6-diidro-[1,2,4]triazolo[4,3-a]pirazinas como antagonistas de recetor nk-3 seletivos, composição farmacêutica, métodos para utilização em distúrbios mediados por recetor nk-3
NZ730295A (en) 2014-09-25 2023-05-26 Ogeda Sa Novel chiral synthesis of n-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines

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NZ517221A (en) * 1999-08-19 2004-01-30 Nps Pharma Inc Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists
AU2003264018A1 (en) * 2002-08-09 2004-02-25 Astrazeneca Ab Compounds having an activity at metabotropic glutamate receptors

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103906750A (zh) * 2011-10-03 2014-07-02 欧洲筛选有限公司 作为选择性NK-3受体拮抗剂的新型手性N-酰基-5,6,7,(8-取代的)-四氢-[1,2,4]三唑并[4,3-a]吡嗪、药物组合物、用于NK-3受体介导的疾病中的方法及其手性合成
CN108434147A (zh) * 2013-07-17 2018-08-24 赫普泰雅治疗有限公司 4-(3-氰基苯基)-6-吡啶基嘧啶mglu5调节剂
CN108434147B (zh) * 2013-07-17 2021-02-02 赫普泰雅治疗有限公司 4-(3-氰基苯基)-6-吡啶基嘧啶mglu5调节剂

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SI1716152T1 (sl) 2008-12-31
BRPI0507495A (pt) 2007-07-10
ES2309718T3 (es) 2008-12-16
ATE402935T1 (de) 2008-08-15
JP2007523183A (ja) 2007-08-16
EP1716152B1 (en) 2008-07-30
RU2006129324A (ru) 2008-04-10
WO2005080397A2 (en) 2005-09-01
ZA200606508B (en) 2007-11-28
EP1716152A2 (en) 2006-11-02
CA2556320A1 (en) 2005-09-01
IL177291A0 (en) 2006-12-10
DK1716152T3 (da) 2008-11-03
UA82435C2 (uk) 2008-04-10
WO2005080397A8 (en) 2006-06-22
US20070185095A1 (en) 2007-08-09
DE602005008558D1 (de) 2008-09-11
WO2005080397A3 (en) 2005-12-22
HK1098460A1 (en) 2007-07-20
MY152888A (en) 2014-11-28
KR20070026380A (ko) 2007-03-08
HRP20080480T3 (hr) 2008-11-30
PT1716152E (pt) 2008-10-02

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