JP2008545660A - プロテインキナーゼ阻害剤として有用なピロロピリジン化合物 - Google Patents

プロテインキナーゼ阻害剤として有用なピロロピリジン化合物 Download PDF

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JP2008545660A
JP2008545660A JP2008512591A JP2008512591A JP2008545660A JP 2008545660 A JP2008545660 A JP 2008545660A JP 2008512591 A JP2008512591 A JP 2008512591A JP 2008512591 A JP2008512591 A JP 2008512591A JP 2008545660 A JP2008545660 A JP 2008545660A
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compound
hydrogen
group
compound according
membered
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JP2008545660A5 (enExample
Inventor
マーク ダブリュー． レデボーア，
マリオン ダブリュー． ワナメーカー，
ルーク ジェイ． ファーマー，
ティエンシェン ワン，
アルバート シー． ピアース，
ガブリエル マルティネス−ボテラ，
ランディー エス． ベシール，
ガイ ダブリュー． ビーミス，
チアン ワン，
フランセスコ ジー． サリトゥロ，
マイケル ジェイ． アーノスト，
ジョン エイチ． カム，
ジェレミー グリーン，
ミシェル スチュワート，
クレイグ マーヘフカ，
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Vertex Pharmaceuticals Inc
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Vertex Pharmaceuticals Inc
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Publication of JP2008545660A publication Critical patent/JP2008545660A/ja
Publication of JP2008545660A5 publication Critical patent/JP2008545660A5/ja
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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    • A61P31/14—Antivirals for RNA viruses
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    • 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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  • Heart & Thoracic Surgery (AREA)
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  • Rheumatology (AREA)
  • Diabetes (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Endocrinology (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Psychiatry (AREA)
  • Communicable Diseases (AREA)
  • Dermatology (AREA)
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  • Reproductive Health (AREA)
  • Gynecology & Obstetrics (AREA)
  • Transplantation (AREA)
  • Molecular Biology (AREA)
  • AIDS & HIV (AREA)
  • Ophthalmology & Optometry (AREA)
JP2008512591A 2005-05-20 2006-05-22 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物 Pending JP2008545660A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US68355405P 2005-05-20 2005-05-20
PCT/US2006/019711 WO2006127587A1 (en) 2005-05-20 2006-05-22 Pyrrolopyridines useful as inhibitors of protein kinase

Related Child Applications (2)

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JP2009123635A Division JP2009179644A (ja) 2005-05-20 2009-05-21 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物
JP2013196681A Division JP2013253114A (ja) 2005-05-20 2013-09-24 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物

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JP2008545660A true JP2008545660A (ja) 2008-12-18
JP2008545660A5 JP2008545660A5 (enExample) 2009-07-30

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JP2008512591A Pending JP2008545660A (ja) 2005-05-20 2006-05-22 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物
JP2009123635A Pending JP2009179644A (ja) 2005-05-20 2009-05-21 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物
JP2013196681A Pending JP2013253114A (ja) 2005-05-20 2013-09-24 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物

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JP2009123635A Pending JP2009179644A (ja) 2005-05-20 2009-05-21 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物
JP2013196681A Pending JP2013253114A (ja) 2005-05-20 2013-09-24 プロテインキナーゼ阻害剤として有用なピロロピリジン化合物

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US (1) US8921376B2 (enExample)
EP (3) EP2354139A1 (enExample)
JP (3) JP2008545660A (enExample)
KR (1) KR20080016659A (enExample)
CN (1) CN101228161B (enExample)
AT (1) ATE540948T1 (enExample)
AU (1) AU2006251623A1 (enExample)
CA (1) CA2609126A1 (enExample)
ES (1) ES2380795T3 (enExample)
IL (1) IL187438A0 (enExample)
MX (1) MX2007014619A (enExample)
NO (1) NO20076502L (enExample)
NZ (1) NZ564065A (enExample)
RU (2) RU2435769C2 (enExample)
WO (1) WO2006127587A1 (enExample)
ZA (1) ZA200710379B (enExample)

Cited By (27)

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JP2009519340A (ja) * 2005-12-13 2009-05-14 インサイト・コーポレイション ＪＡＮＵＳキナーゼ阻害剤としてのヘテロアリール置換ピロロ［２，３−ｂ］ピリジンおよびピロロ［２，３−ｂ］ピリミジン
WO2011013785A1 (ja) * 2009-07-31 2011-02-03 日本たばこ産業株式会社 含窒素スピロ環化合物及びその医薬用途
JP2013501713A (ja) * 2009-08-07 2013-01-17 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規なアザ複素環化合物
JP2013522214A (ja) * 2010-03-10 2013-06-13 インサイト・コーポレイション Ｊａｋ１阻害剤としてのピペリジン−４−イルアゼチジン誘導体
JP2013253114A (ja) * 2005-05-20 2013-12-19 Vertex Pharmaceuticals Inc プロテインキナーゼ阻害剤として有用なピロロピリジン化合物
JP2014500260A (ja) * 2010-11-19 2014-01-09 インサイト・コーポレイション Ｊａｋ阻害剤としてのシクロブチル置換ピロロピリジンおよびピロロピリミジン誘導体
WO2015119126A1 (ja) * 2014-02-04 2015-08-13 大鵬薬品工業株式会社 アザインドール誘導体
JP2016512198A (ja) * 2013-03-06 2016-04-25 アロステロス セラピューティクス， インコーポレイテッド ＣａＭＫＩＩ阻害剤及びその使用
JP2017506656A (ja) * 2014-03-28 2017-03-09 ノバルティス ティーアゲズントハイト アーゲー 新規化合物
US9611269B2 (en) 2011-06-20 2017-04-04 Incyte Corporation Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as JAK inhibitors
US9623029B2 (en) 2009-05-22 2017-04-18 Incyte Holdings Corporation 3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]octane- or heptane-nitrile as JAK inhibitors
US9714233B2 (en) 2013-03-06 2017-07-25 Incyte Corporation Processes and intermediates for making a JAK inhibitor
US9718834B2 (en) 2011-09-07 2017-08-01 Incyte Corporation Processes and intermediates for making a JAK inhibitor
US10561616B2 (en) 2013-08-07 2020-02-18 Incyte Corporation Sustained release dosage forms for a JAK1 inhibitor
US10596161B2 (en) 2017-12-08 2020-03-24 Incyte Corporation Low dose combination therapy for treatment of myeloproliferative neoplasms
KR20200043412A (ko) * 2017-08-23 2020-04-27 스프린트 바이오사이언스 아베 아자인돌릴피리돈 및 디아자인돌릴피리돈 화합물
US10758543B2 (en) 2010-05-21 2020-09-01 Incyte Corporation Topical formulation for a JAK inhibitor
US10759792B2 (en) 2014-09-05 2020-09-01 The Johns Hopkins University CaMKII inhibitors and uses thereof
US10899736B2 (en) 2018-01-30 2021-01-26 Incyte Corporation Processes and intermediates for making a JAK inhibitor
US11213528B2 (en) 2007-06-13 2022-01-04 Incyte Holdings Corporation Salts of the janus kinase inhibitor (R)-3-(4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile
JP2022504988A (ja) * 2018-10-16 2022-01-13 ダナ－ファーバー キャンサー インスティテュート，インコーポレイテッド Ｌｒｒｋ２の野生型および変異型のアザインドール阻害剤
US11304949B2 (en) 2018-03-30 2022-04-19 Incyte Corporation Treatment of hidradenitis suppurativa using JAK inhibitors
US11337927B2 (en) 2012-11-15 2022-05-24 Incyte Holdings Corporation Sustained-release dosage forms of ruxolitinib
JP2022531088A (ja) * 2019-05-02 2022-07-06 アクラリス セラピューティクス，インコーポレイテッド Ｊａｋ阻害剤としての置換ピロロピリジン
JP2023527055A (ja) * 2020-05-26 2023-06-26 サントル ナショナル ドゥ ラ ルシェルシュ シアンティフィック がんの治療に使用するためのｌｉｍｋ及び／又はｒｏｃｋキナーゼ阻害剤としての４－（７ｈ－ピロロ［２，３－ｄ］ピリミジン－４－イル）－３，６－ジヒドロピリジン－１－（２ｈ）－カルボキサミド誘導体
WO2023145372A1 (ja) * 2022-01-28 2023-08-03 日本曹達株式会社 アミド化合物の製造方法
US11833155B2 (en) 2020-06-03 2023-12-05 Incyte Corporation Combination therapy for treatment of myeloproliferative neoplasms

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