WO2008129994A1 - 含窒素縮合環誘導体、それを含有する医薬組成物及びその医薬用途 - Google Patents

含窒素縮合環誘導体、それを含有する医薬組成物及びその医薬用途 Download PDF

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WO2008129994A1
WO2008129994A1 PCT/JP2008/057390 JP2008057390W WO2008129994A1 WO 2008129994 A1 WO2008129994 A1 WO 2008129994A1 JP 2008057390 W JP2008057390 W JP 2008057390W WO 2008129994 A1 WO2008129994 A1 WO 2008129994A1
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same
alkylene
pharmaceutical composition
fused ring
prodrug
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PCT/JP2008/057390
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English (en)
French (fr)
Inventor
Shigeru Yonekubo
Takashi Miyagi
Kohsuke Ohno
Mikie Kambara
Nobuhiko Fushimi
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Kissei Pharmaceutical Co., Ltd.
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Priority to CA2680769A priority Critical patent/CA2680769C/en
Priority to KR1020097021440A priority patent/KR101524817B1/ko
Priority to CN2008800125480A priority patent/CN101663302B/zh
Priority to EP08740471.1A priority patent/EP2143724B1/en
Priority to AU2008241853A priority patent/AU2008241853B2/en
Priority to US12/596,313 priority patent/US8217069B2/en
Priority to MX2009010296A priority patent/MX2009010296A/es
Priority to JP2009510849A priority patent/JP5313883B2/ja
Priority to ES08740471.1T priority patent/ES2441196T3/es
Publication of WO2008129994A1 publication Critical patent/WO2008129994A1/ja

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    • 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
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    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
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    • C07D473/30Oxygen atom attached in position 6, e.g. hypoxanthine
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    • C07D487/04Ortho-condensed systems

Abstract

【課題】 本発明は、性ホルモン依存性疾患等の予防又は治療剤として有用な化合物を提供する。 【解決手段】 本発明は、GnRH 拮抗作用を有する下記一般式(I)で表される含窒素縮合環誘導体、プロドラッグ、塩等、それを含有する医薬組成物及びその医薬用途等を提供する。式(I)中、環A及び環Bは、独立して、アリール又はヘテロアリール;RA及びRBは、独立して、ハロゲン、シアノ、アルキル、アルキルスルホニル、−OW1、−SW1、−COW2、−NW3W4、−SO2NW3W4、アリール等;RCは、H又はアルキル;Eは、酸素原子等;Uは、単結合又はアルキレン;Xは、Y、−CO−Y、−SO2−Y、−S−(アルキレン)−Y、−O−(アルキレン)−Y、−SO2−(アルキレン)−Y等(YはZ又はアミノ等;Zは、シクロアルキル、ヘテロシクロアルキル、アリール、ヘテロアリール等);等である。
PCT/JP2008/057390 2007-04-18 2008-04-16 含窒素縮合環誘導体、それを含有する医薬組成物及びその医薬用途 WO2008129994A1 (ja)

Priority Applications (9)

Application Number Priority Date Filing Date Title
CA2680769A CA2680769C (en) 2007-04-18 2008-04-16 Nitrogenated fused ring derivative, pharmaceutical composition comprising the same, and use of the same for medical purposes
KR1020097021440A KR101524817B1 (ko) 2007-04-18 2008-04-16 질소 함유 축합환 유도체, 그것을 함유하는 의약 조성물 및 그 의약 용도
CN2008800125480A CN101663302B (zh) 2007-04-18 2008-04-16 含氮稠环衍生物、包含所述含氮稠环衍生物的药物组合物及其医药用途
EP08740471.1A EP2143724B1 (en) 2007-04-18 2008-04-16 Nitrogenated fused ring derivative, pharmaceutical composition comprising the same, and use of the same for medical purposes
AU2008241853A AU2008241853B2 (en) 2007-04-18 2008-04-16 Nitrogenated fused ring derivative, pharmaceutical composition comprising the same, and use of the same for medical purposes
US12/596,313 US8217069B2 (en) 2007-04-18 2008-04-16 Nitrogenated fused ring derivative, pharmaceutical composition comprising the same, and use of the same for medical purposes
MX2009010296A MX2009010296A (es) 2007-04-18 2008-04-16 Derivado de anillo fusionado nitrogenado, composicion farmaceutica que lo contiene, y uso del mismo para propositos medicos.
JP2009510849A JP5313883B2 (ja) 2007-04-18 2008-04-16 含窒素縮合環誘導体、それを含有する医薬組成物及びその医薬用途
ES08740471.1T ES2441196T3 (es) 2007-04-18 2008-04-16 Derivado de anillo condensado nitrogenado, composiciones farmacéuticas que lo contienen, y su uso con fines médicos

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007-108926 2007-04-18
JP2007108926 2007-04-18

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WO2008129994A1 true WO2008129994A1 (ja) 2008-10-30

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US (1) US8217069B2 (ja)
EP (1) EP2143724B1 (ja)
JP (1) JP5313883B2 (ja)
KR (1) KR101524817B1 (ja)
CN (1) CN101663302B (ja)
AU (1) AU2008241853B2 (ja)
CA (1) CA2680769C (ja)
ES (1) ES2441196T3 (ja)
MX (1) MX2009010296A (ja)
TW (1) TWI402073B (ja)
WO (1) WO2008129994A1 (ja)

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CN103483268A (zh) * 2013-09-17 2014-01-01 常州大学 一种4,6-二氯-2-甲基-5-硝基嘧啶的制备方法
US8846909B2 (en) 2010-05-24 2014-09-30 University Of Rochester Bicyclic heteroaryl kinase inhibitors and methods of use
US8877772B2 (en) 2008-11-25 2014-11-04 University Of Rochester Substituted pyrrolo[2,3-B]pyridines as MLK inhibitors
JP2015199737A (ja) * 2006-08-02 2015-11-12 サイトキネティクス・インコーポレーテッドCytokinetics Incorporated 特定の化学物質、組成物及び方法
JP2015537053A (ja) * 2012-12-12 2015-12-24 バイエル・クロップサイエンス・アクチェンゲゼルシャフト ビス(3−アミノフェニル)ジスルフィド類及び3−アミノチオール類を製造する方法
US9512118B2 (en) 2011-06-22 2016-12-06 Takeda Pharmaceutical Company Limited Crystal of fused heterocyclic compound
WO2017108282A1 (en) 2015-12-22 2017-06-29 Kancera Ab Bicyclic hydroxamic acids useful as inhibitors of mammalian histone deacetylase activity
CN107074860A (zh) * 2014-09-16 2017-08-18 吉利德科学公司 制备toll样受体调节剂的方法
US10485800B2 (en) 2012-11-30 2019-11-26 The University Of Rochester Mixed lineage kinase inhibitors for HIV/AIDS therapies
US10508117B2 (en) 2014-09-16 2019-12-17 Gilead Sciences, Inc. Solid forms of a toll-like receptor modulator
US10766899B2 (en) 2006-08-02 2020-09-08 Cytokinetics, Incorporated Methods for preparing substituted imidazo[4,5-b]pyrazines
US11110091B2 (en) 2008-12-09 2021-09-07 Gilead Sciences, Inc. Modulators of toll-like receptors
US11116774B2 (en) 2014-07-11 2021-09-14 Gilead Sciences, Inc. Modulators of toll-like receptors for the treatment of HIV

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RU2007140903A (ru) * 2005-04-05 2009-05-20 Фармакопия, Инк. (Us) Производные пурина и имидазопиридина для иммуносупрессии
WO2019002473A1 (en) * 2017-06-30 2019-01-03 Antev Limited COMPOSITION FOR THE TREATMENT OF ACUTE URINARY RETENTION
CN115232144B (zh) * 2021-04-22 2024-04-02 长春金赛药业有限责任公司 含氮稠环类衍生物、药物组合物及其制备方法和应用
CN115960073A (zh) * 2022-12-02 2023-04-14 中国药科大学 一种n-卤代乙酰基二苯胺衍生物及其制备方法和医药用途
CN117069662A (zh) * 2023-10-17 2023-11-17 峰成医药科技(天津)有限公司 一种4,6-二氯-2-(二氟甲基)嘧啶的合成方法

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