JP2011529918A5 - - Google Patents

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Publication number
JP2011529918A5
JP2011529918A5 JP2011521361A JP2011521361A JP2011529918A5 JP 2011529918 A5 JP2011529918 A5 JP 2011529918A5 JP 2011521361 A JP2011521361 A JP 2011521361A JP 2011521361 A JP2011521361 A JP 2011521361A JP 2011529918 A5 JP2011529918 A5 JP 2011529918A5
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JP
Japan
Prior art keywords
compound
aryl
heteroaryl
lower alkyl
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2011521361A
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English (en)
Japanese (ja)
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JP2011529918A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2009/052449 external-priority patent/WO2010014930A2/en
Publication of JP2011529918A publication Critical patent/JP2011529918A/ja
Publication of JP2011529918A5 publication Critical patent/JP2011529918A5/ja
Pending legal-status Critical Current

Links

JP2011521361A 2008-08-01 2009-07-31 Jak3阻害剤としてのピペリジン誘導体 Pending JP2011529918A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US8570508P 2008-08-01 2008-08-01
US61/085,705 2008-08-01
US9856208P 2008-09-19 2008-09-19
US61/098,562 2008-09-19
PCT/US2009/052449 WO2010014930A2 (en) 2008-08-01 2009-07-31 Therapeutic agents

Publications (2)

Publication Number Publication Date
JP2011529918A JP2011529918A (ja) 2011-12-15
JP2011529918A5 true JP2011529918A5 (cg-RX-API-DMAC7.html) 2012-09-06

Family

ID=41170025

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011521361A Pending JP2011529918A (ja) 2008-08-01 2009-07-31 Jak3阻害剤としてのピペリジン誘導体

Country Status (13)

Country Link
US (1) US20110165183A1 (cg-RX-API-DMAC7.html)
EP (1) EP2324020A2 (cg-RX-API-DMAC7.html)
JP (1) JP2011529918A (cg-RX-API-DMAC7.html)
KR (1) KR20110050654A (cg-RX-API-DMAC7.html)
CN (1) CN102171211A (cg-RX-API-DMAC7.html)
AU (1) AU2009276420A1 (cg-RX-API-DMAC7.html)
BR (1) BRPI0916931A2 (cg-RX-API-DMAC7.html)
CA (1) CA2732628A1 (cg-RX-API-DMAC7.html)
IL (1) IL210990A0 (cg-RX-API-DMAC7.html)
MX (1) MX2011001259A (cg-RX-API-DMAC7.html)
NZ (1) NZ590922A (cg-RX-API-DMAC7.html)
RU (1) RU2011105768A (cg-RX-API-DMAC7.html)
WO (1) WO2010014930A2 (cg-RX-API-DMAC7.html)

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EP2825533B1 (en) 2012-03-13 2016-10-19 Basf Se Fungicidal pyrimidine compounds
LT3181567T (lt) 2012-09-10 2019-07-25 Principia Biopharma Inc. Pirazolpirimidino junginiai kaip kinazės slopikliai
AU2013348217B2 (en) * 2012-11-20 2016-10-06 Glaxosmithkline Llc Novel compounds
EP2935216B1 (en) * 2012-12-17 2018-06-27 Sun Pharmaceutical Industries Limited Process for the preparation of tofacitinib and intermediates thereof
WO2014102826A1 (en) * 2012-12-28 2014-07-03 Glenmark Pharmaceuticals Limited; The present invention relates to process for the preparation of tofacitinib and intermediates thereof.
CN105722833A (zh) 2013-09-16 2016-06-29 巴斯夫欧洲公司 杀真菌的嘧啶化合物
WO2015036059A1 (en) 2013-09-16 2015-03-19 Basf Se Fungicidal pyrimidine compounds
EP3049086A4 (en) * 2013-09-27 2017-02-22 Nimbus Iris, Inc. Irak inhibitors and uses thereof
PT3539965T (pt) * 2013-12-09 2021-04-07 Unichem Lab Ltd Processo melhorado para a preparação de (3r,4r)-(1-benzil-4-metilpiperidin-3-il)-metilamina
KR20220027271A (ko) 2014-02-21 2022-03-07 프린시피아 바이오파마, 인코퍼레이티드 Btk 억제제의 염 및 고체 형태
CN104860950A (zh) * 2014-02-24 2015-08-26 重庆医药工业研究院有限责任公司 一种制备4-氯吡咯[2,3-d]并嘧啶的方法
CN104059016A (zh) * 2014-06-20 2014-09-24 湖南天地恒一制药有限公司 制备托法替布的中间体及所述中间体的制备方法
KR101710127B1 (ko) * 2014-08-29 2017-02-27 한화제약주식회사 야누스인산화효소 억제제로서의 치환된 N-(피롤리딘-3-일)-7H-피롤로[2,3-d]피리미딘-4-아민
ES2843323T3 (es) 2014-12-18 2021-07-16 Principia Biopharma Inc Tratamiento de pénfigo
CN105732637B (zh) * 2014-12-30 2020-04-21 广东东阳光药业有限公司 杂芳化合物及其在药物中的应用
EP3078665A1 (en) 2015-04-10 2016-10-12 OLON S.p.A. Efficient method for the preparation of tofacitinib citrate
CN107709327A (zh) 2015-06-22 2018-02-16 小野药品工业株式会社 Brk抑制性化合物
US20180305350A1 (en) 2015-06-24 2018-10-25 Principia Biopharma Inc. Tyrosine kinase inhibitors
WO2017004134A1 (en) * 2015-06-29 2017-01-05 Nimbus Iris, Inc. Irak inhibitors and uses thereof
CN105622616A (zh) * 2016-02-25 2016-06-01 上海雅本化学有限公司 一种4-氯吡咯并嘧啶的制备方法
CN109600989B (zh) 2016-06-29 2022-11-04 普林斯匹亚生物制药公司 2-[3-[4-氨基-3-(2-氟-4-苯氧基-苯基)吡唑并[3,4-d]嘧啶-1-基]哌啶-1-羰基]-4-甲基-4-[4-(氧杂环丁烷-3-基)哌嗪-1-基]戊-2-烯腈的改性的释放制剂
GB201617758D0 (en) 2016-10-20 2016-12-07 Almac Discovery Limited Pharmaceutical compounds
JP7710223B2 (ja) 2018-04-16 2025-07-18 深▲チェン▼市塔吉瑞生物医薬有限公司 置換ピロロトリアジン系化合物およびその医薬組成物並びにそれらの使用
KR20220080179A (ko) 2019-10-14 2022-06-14 프린시피아 바이오파마, 인코퍼레이티드 (R)-2-[3-[4-아미노-3-(2-플루오로-4-페녹시-페닐)피라졸로[3,4-d]피리미딘-1-일]피페리딘-1-카르보닐]-4-메틸-4-[4-(옥세탄-3-일)피페라진-1-일]펜트-2-엔니트릴을 투여하여 면역 혈소판 감소증을 치료하는 방법
KR20220130184A (ko) 2020-01-22 2022-09-26 프린시피아 바이오파마, 인코퍼레이티드 2-[3-[4-아미노-3-(2-플루오로-4-페녹시-페닐)-1H-피라졸로[3,4-d]피리미딘-1-일]피페리딘-1-카르보닐]-4-메틸-4-[4-(옥세탄-3-일)피페라진-1-일]펜트-2-엔니트릴의 결정질 형태
CN116768908B (zh) * 2022-03-10 2025-11-18 石家庄迪斯凯威医药科技有限公司 一种含n多环化合物及其制备方法与用途
CN117164519A (zh) * 2023-08-18 2023-12-05 杭州小蓓医药科技有限公司 一种l-肌肽的合成方法
CN117534603A (zh) * 2023-11-10 2024-02-09 江苏海悦康医药科技有限公司 一种托法替布中间体的制备方法

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CN100351253C (zh) * 2000-06-26 2007-11-28 辉瑞产品公司 作为免疫抑制剂的吡咯并[2,3-d]嘧啶化合物
US7301023B2 (en) * 2001-05-31 2007-11-27 Pfizer Inc. Chiral salt resolution
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KR100824193B1 (ko) * 2003-04-29 2008-04-21 화이자 인코포레이티드 고혈압 치료에 유용한5,7-디아미노피라졸로[4,3-d]피리미딘
MXPA06005882A (es) * 2003-11-25 2006-06-27 Pfizer Prod Inc Metodo de tratamiento de la aterosclerosis.
AR054416A1 (es) * 2004-12-22 2007-06-27 Incyte Corp Pirrolo [2,3-b]piridin-4-il-aminas y pirrolo [2,3-b]pirimidin-4-il-aminas como inhibidores de las quinasas janus. composiciones farmaceuticas.
EP1910358A2 (en) * 2005-07-14 2008-04-16 Astellas Pharma Inc. Heterocyclic janus kinase 3 inhibitors
NL2000291C2 (nl) * 2005-11-10 2009-02-17 Pfizer Prod Inc 1-(1-(2-ethoxyethyl)-3-ethyl-7-(4-methylpyridin-2-ylamino)-1H- pyrazool(4,3-d)pyrimidine-5-yl)piperidine-4-carbonzuur en zouten daarvan.
TW201111385A (en) * 2009-08-27 2011-04-01 Biocryst Pharm Inc Heterocyclic compounds as janus kinase inhibitors
PH12013500661A1 (en) * 2010-10-08 2017-08-23 Abbvie Inc FURO[3,2-d]PYRIMIDINE COMPOUNDS

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