WO2009028543A1 - 置換ピラゾール誘導体 - Google Patents

置換ピラゾール誘導体 Download PDF

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Publication number
WO2009028543A1
WO2009028543A1 PCT/JP2008/065286 JP2008065286W WO2009028543A1 WO 2009028543 A1 WO2009028543 A1 WO 2009028543A1 JP 2008065286 W JP2008065286 W JP 2008065286W WO 2009028543 A1 WO2009028543 A1 WO 2009028543A1
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Prior art keywords
group
bonding hand
atom serving
serving
pyrazole derivative
Prior art date
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Ceased
Application number
PCT/JP2008/065286
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English (en)
French (fr)
Inventor
Mitsuhiro Ito
Tomohiko Suzaki
Satoshi Yamamoto
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Takeda Pharmaceutical Co Ltd
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Takeda Pharmaceutical Co Ltd
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Filing date
Publication date
Priority to EP08828418A priority Critical patent/EP2194045A4/en
Priority to CN200880114151A priority patent/CN101842357A/zh
Priority to AU2008292429A priority patent/AU2008292429A1/en
Priority to JP2009530148A priority patent/JPWO2009028543A1/ja
Priority to BRPI0816095-3A2A priority patent/BRPI0816095A2/pt
Priority to MX2010002266A priority patent/MX2010002266A/es
Priority to CA2697663A priority patent/CA2697663A1/en
Priority to US12/675,748 priority patent/US20100227846A1/en
Application filed by Takeda Pharmaceutical Co Ltd filed Critical Takeda Pharmaceutical Co Ltd
Priority to EA201070323A priority patent/EA201070323A1/ru
Publication of WO2009028543A1 publication Critical patent/WO2009028543A1/ja
Priority to TNP2010000091A priority patent/TN2010000091A1/fr
Anticipated expiration legal-status Critical
Priority to MA32720A priority patent/MA31714B1/fr
Ceased legal-status Critical Current

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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/28—Antiandrogens
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    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • C07D401/02—Heterocyclic 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
    • C07D401/06—Heterocyclic 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
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    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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 chain containing hetero atoms as chain links
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    • C07D401/14—Heterocyclic 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 three or more hetero rings
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    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D495/04—Ortho-condensed systems

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  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Pharmacology & Pharmacy (AREA)
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  • Animal Behavior & Ethology (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

 新規ピラゾール誘導体およびそれを含有するアンドロゲン受容体拮抗剤の提供。式(I’) 〔式中、R1は、水素原子、炭素原子を介する基、窒素原子を介する基、酸素原子を介する基、または硫黄原子を介する基;R2は、シアノを有するフェニル基(本フェニル基はシアノ以外の置換基をさらに有していてもよい);R3は、水素原子、炭素原子を介する基、窒素原子を介する基、酸素原子を介する基、または硫黄原子を介する基;R4は、置換基を有していてもよい環状基;およびXは、置換基を有していてもよいメチレン、またはCOを示す。〕で表される化合物、またはその塩。
PCT/JP2008/065286 2007-08-30 2008-08-27 置換ピラゾール誘導体 Ceased WO2009028543A1 (ja)

Priority Applications (11)

Application Number Priority Date Filing Date Title
CA2697663A CA2697663A1 (en) 2007-08-30 2008-08-27 Substituted pyrazole derivative
AU2008292429A AU2008292429A1 (en) 2007-08-30 2008-08-27 Substituted pyrazole derivative
JP2009530148A JPWO2009028543A1 (ja) 2007-08-30 2008-08-27 置換ピラゾール誘導体
BRPI0816095-3A2A BRPI0816095A2 (pt) 2007-08-30 2008-08-27 Composto ou um sal do mesmo, pró-droga, agente farmacêutico, métodos para antagonizar um receptor de androgênio e para prevenir / tratar cãncer, e, uso do composto ou uma pró-droga do mesmo.
MX2010002266A MX2010002266A (es) 2007-08-30 2008-08-27 Derivados de pirazol sustituidos.
EP08828418A EP2194045A4 (en) 2007-08-30 2008-08-27 Substituted pyrazole derivative
CN200880114151A CN101842357A (zh) 2007-08-30 2008-08-27 取代的吡唑衍生物
US12/675,748 US20100227846A1 (en) 2007-08-30 2008-08-27 Substituted pyrazole derivative
EA201070323A EA201070323A1 (ru) 2007-08-30 2008-08-27 Замещенное производное пиразола
TNP2010000091A TN2010000091A1 (en) 2007-08-30 2010-02-23 Substituted pyrazole derivative
MA32720A MA31714B1 (fr) 2007-08-30 2010-03-26 Derive de pyrazole substitue

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007-224910 2007-08-30
JP2007224910 2007-08-30

Publications (1)

Publication Number Publication Date
WO2009028543A1 true WO2009028543A1 (ja) 2009-03-05

Family

ID=40387261

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/065286 Ceased WO2009028543A1 (ja) 2007-08-30 2008-08-27 置換ピラゾール誘導体

Country Status (20)

Country Link
US (2) US20090270359A1 (ja)
EP (1) EP2194045A4 (ja)
JP (1) JPWO2009028543A1 (ja)
KR (1) KR20100046275A (ja)
CN (1) CN101842357A (ja)
AR (1) AR068813A1 (ja)
AU (1) AU2008292429A1 (ja)
BR (1) BRPI0816095A2 (ja)
CA (1) CA2697663A1 (ja)
CL (1) CL2008002521A1 (ja)
CO (1) CO6190530A2 (ja)
DO (1) DOP2010000068A (ja)
EA (1) EA201070323A1 (ja)
EC (1) ECSP10010060A (ja)
MA (1) MA31714B1 (ja)
MX (1) MX2010002266A (ja)
PE (1) PE20090610A1 (ja)
TN (1) TN2010000091A1 (ja)
TW (1) TW200913993A (ja)
WO (1) WO2009028543A1 (ja)

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WO2011051540A1 (en) 2009-10-27 2011-05-05 Orion Corporation Androgen receptor modulating compounds
WO2012053630A1 (ja) 2010-10-22 2012-04-26 アステラス製薬株式会社 変異アンドロゲン受容体拮抗薬
CN102481294A (zh) * 2009-09-11 2012-05-30 拜耳医药股份有限公司 作为抗癌药物的取代(杂芳基甲基)乙内酰硫脲
WO2012127441A1 (en) 2011-03-23 2012-09-27 Semorex Technologies Ltd. Treatment of proliferative disorders with a chemiluminescent agent
WO2012143599A1 (en) 2011-04-21 2012-10-26 Orion Corporation Androgen receptor modulating carboxamides
US8697911B2 (en) 2010-07-07 2014-04-15 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
JP2014125430A (ja) * 2012-12-25 2014-07-07 Dow Corning Toray Co Ltd イミド基含有有機ケイ素化合物の製造方法
US9000154B2 (en) 2010-10-19 2015-04-07 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
US9079880B2 (en) 2010-07-07 2015-07-14 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
JP2017525700A (ja) * 2014-08-15 2017-09-07 ヤンセン ファーマシューティカルズ,インコーポレーテッド ピラゾール類
JP2020516672A (ja) * 2017-04-18 2020-06-11 セルジーン クオンティセル リサーチ,インク. 治療用化合物
CN111499539A (zh) * 2020-04-20 2020-08-07 南昌大学 一种以芳基羧酸为原料的芳基氰化物合成方法
JP2021024798A (ja) * 2019-08-02 2021-02-22 株式会社デ・ウエスタン・セラピテクス研究所 エチルアニリノトルエンスルホン酸誘導体の製造方法
JP2023539034A (ja) * 2020-08-04 2023-09-13 プレシジョン・バイオ-セラピューティクス・エッセ・エッレ・エッレ 胆汁酸受容体及びロイコトリエンシステイニル受容体の選択的及び/又は二重調節剤としてのキノリン化合物
WO2024013690A1 (en) * 2022-07-15 2024-01-18 Chong Kun Dang Pharmaceutical Corp. 1,3,4-oxadiazole triazole compounds as histone deacetylase 6 inhibitor, and pharmaceutical composition comprising the same
RU2858542C2 (ru) * 2022-07-15 2026-03-18 Чонг Кун Данг Фармасьютикал Корп. Соединения 1,3,4-оксадиазолтриазола в качестве ингибитора гистондеацетилазы 6 и фармацевтическая композиция, содержащая их

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JP6105594B2 (ja) 2011-09-30 2017-03-29 エンドゥ ファーマシューティカルズ,インコーポレイティド 癌処置用cyp17阻害剤としてのイミダゾール誘導体
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US10093613B2 (en) 2015-04-21 2018-10-09 Gtx, Inc. Selective androgen receptor degrader (SARD) ligands and methods of use thereof
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MX2018000352A (es) 2015-07-09 2018-08-15 Janssen Pharmaceutica Nv 4-azaindoles sustituidos y su uso como moduladores del receptor glun2b.
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US11230523B2 (en) 2016-06-10 2022-01-25 University Of Tennessee Research Foundation Selective androgen receptor degrader (SARD) ligands and methods of use thereof
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US10806719B2 (en) 2016-06-10 2020-10-20 University Of Tennessee Research Foundation Selective androgen receptor degrader (SARD) ligands and methods of use thereof
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