CN102131389A - 三唑并吡啶jak抑制剂化合物和方法 - Google Patents

三唑并吡啶jak抑制剂化合物和方法 Download PDF

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Publication number
CN102131389A
CN102131389A CN2009801324950A CN200980132495A CN102131389A CN 102131389 A CN102131389 A CN 102131389A CN 2009801324950 A CN2009801324950 A CN 2009801324950A CN 200980132495 A CN200980132495 A CN 200980132495A CN 102131389 A CN102131389 A CN 102131389A
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alkyl
cancer
compound
heterocyclyl
optionally substituted
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Chinese (zh)
Inventor
朱炳炎
迈克尔·苏
史蒂文·R·马格努森
理查德·帕斯特
贺海鹰
肖贻崧
郑吉富
胥星
赵军平
克里斯托弗·A·赫尔利
梁军
温迪·刘
约瑟夫·P·利西卡托斯
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Genentech Inc
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Genentech Inc
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Publication of CN102131389A publication Critical patent/CN102131389A/zh
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    • 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
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    • 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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—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 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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    • A61K31/495—Heterocyclic 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
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/5375—1,4-Oxazines, e.g. morpholine
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CN2009801324950A 2008-06-20 2009-06-19 三唑并吡啶jak抑制剂化合物和方法 Pending CN102131389A (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US7450608P 2008-06-20 2008-06-20
US61/074,506 2008-06-20
PCT/US2009/048017 WO2009155551A1 (en) 2008-06-20 2009-06-19 Triazolopyridine jak inhibitor compounds and methods

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CN102131389A true CN102131389A (zh) 2011-07-20

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US (4) US20100048557A1 (https=)
EP (1) EP2288260A4 (https=)
JP (1) JP5512665B2 (https=)
KR (1) KR20110033223A (https=)
CN (1) CN102131389A (https=)
AU (1) AU2009259853A1 (https=)
BR (1) BRPI0910021A2 (https=)
CA (1) CA2727036C (https=)
IL (1) IL209763A0 (https=)
MX (1) MX2010014005A (https=)
PE (1) PE20110545A1 (https=)
RU (1) RU2560153C2 (https=)
SG (1) SG178812A1 (https=)
WO (1) WO2009155551A1 (https=)
ZA (1) ZA201008957B (https=)

Cited By (12)

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CN102317288A (zh) * 2009-02-13 2012-01-11 佛维雅制药公司 作为激酶抑制剂的[1,2,4]三唑并[1,5-a]吡啶
CN104321325A (zh) * 2012-05-24 2015-01-28 诺华股份有限公司 吡咯并吡咯烷酮化合物
WO2015032286A1 (en) * 2013-09-05 2015-03-12 F.Hoffmann-La Roche Ag Triazolopyridine compounds, compositions and methods of use thereof
CN104918945A (zh) * 2012-11-01 2015-09-16 因赛特公司 作为jak抑制剂的三环稠合噻吩衍生物
US9802957B2 (en) 2014-04-30 2017-10-31 Incyte Corporation Processes of preparing a JAK1 inhibitor and new forms thereto
CN107949279A (zh) * 2015-07-06 2018-04-20 得克萨斯系统大学评议会 可用作用于治疗人类癌症的抗癌剂的苯甲酰胺或苯扎明化合物
CN109890817A (zh) * 2016-09-06 2019-06-14 豪夫迈·罗氏有限公司 8-(氮杂环丁烷-1-基)-[1,2,4]三唑并[1,5-a]吡啶基化合物、其组合物和应用方法
CN111465603A (zh) * 2017-12-19 2020-07-28 勃林格殷格翰国际有限公司 作为γ-分泌酶调节剂的三唑并吡啶
CN114008050A (zh) * 2019-06-18 2022-02-01 豪夫迈·罗氏有限公司 Jak激酶的吡唑并嘧啶芳基醚抑制剂及其用途
US11304949B2 (en) 2018-03-30 2022-04-19 Incyte Corporation Treatment of hidradenitis suppurativa using JAK inhibitors
CN114728963A (zh) * 2019-11-25 2022-07-08 株式会社大熊制药 新型三唑吡啶衍生物和包括其的药物组合物
CN115054698A (zh) * 2014-01-14 2022-09-16 约翰斯·霍普金斯大学 包封选择性atp抑制剂的环糊精组合物及其应用

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JP5328816B2 (ja) 2008-02-22 2013-10-30 エフ．ホフマン−ラ ロシュ アーゲー アミロイドβの調節薬
WO2009155565A1 (en) * 2008-06-20 2009-12-23 Genentech, Inc. Triazolopyridine jak inhibitor compounds and methods
CN102131389A (zh) * 2008-06-20 2011-07-20 健泰科生物技术公司 三唑并吡啶jak抑制剂化合物和方法
TWI453207B (zh) 2008-09-08 2014-09-21 Signal Pharm Llc 胺基三唑并吡啶，其組合物及使用其之治療方法
WO2010040661A1 (en) 2008-10-09 2010-04-15 F. Hoffmann-La Roche Ag Modulators for amyloid beta
AU2009312856A1 (en) 2008-11-10 2010-05-14 F. Hoffmann-La Roche Ag Heterocyclic gamma secretase modulators
AU2011211410B2 (en) * 2009-02-13 2013-01-31 Fovea Pharmaceuticals Sa [1,2,4] triazolo [1,5-A] pyridines as kinase inhibitors
EP2438066A2 (en) 2009-06-05 2012-04-11 Cephalon, Inc. PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a]PYRIDINE DERIVATIVES
TWI462920B (zh) * 2009-06-26 2014-12-01 葛萊伯格有限公司 用於治療退化性及發炎疾病之新穎化合物
EP2343294A1 (en) 2009-11-30 2011-07-13 Bayer Schering Pharma AG Substituted triazolopyridines
EP2523949B1 (en) 2010-01-15 2014-08-20 Janssen Pharmaceuticals Inc. Novel substituted triazole derivatives as gamma secretase modulators
US20110190269A1 (en) * 2010-02-01 2011-08-04 Karlheinz Baumann Gamma secretase modulators
US8486967B2 (en) 2010-02-17 2013-07-16 Hoffmann-La Roche Inc. Heteroaryl substituted piperidines
EP2588105A1 (en) 2010-07-01 2013-05-08 Cellzome Limited Triazolopyridines as tyk2 inhibitors
EA201300282A1 (ru) 2010-08-27 2013-08-30 Мерк Патент Гмбх Производные триазолопиразина
JP2014500254A (ja) 2010-11-09 2014-01-09 セルゾーム リミティッド Ｔｙｋ２阻害剤としてのピリジン化合物およびそのアザ類似体
EP2648728B1 (en) * 2010-12-06 2016-04-27 Cephalon, Inc. Janus kinase 2 (jak2) inhibitor for the treatment of lupus
AR086042A1 (es) 2011-04-28 2013-11-13 Galapagos Nv Compuesto util para el tratamiento de enfermedades degenerativas e inflamatorias y composicion farmaceutica
CN104114557B (zh) * 2012-02-21 2017-10-24 默克专利股份公司 作为syk酪氨酸激酶抑制剂和gcn2丝氨酸激酶抑制剂的8‑取代2‑氨基‑[1,2,4]三唑并[1,5‑a]吡嗪
NZ702611A (en) 2012-05-16 2016-10-28 Cellzome Ltd Substituted 3, 4 - dihydro - 2h - pyrido [1, 2 -a] pyrazine - 1, 6 - dione derivatives useful for the treatment of (inter alia) alzheimer’s disease
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