WO2008084861A1 - 縮合ピリジン化合物 - Google Patents

縮合ピリジン化合物 Download PDF

Info

Publication number
WO2008084861A1
WO2008084861A1 PCT/JP2008/050300 JP2008050300W WO2008084861A1 WO 2008084861 A1 WO2008084861 A1 WO 2008084861A1 JP 2008050300 W JP2008050300 W JP 2008050300W WO 2008084861 A1 WO2008084861 A1 WO 2008084861A1
Authority
WO
WIPO (PCT)
Prior art keywords
compound
jak3
diseases
therapeutic
confirmed
Prior art date
Application number
PCT/JP2008/050300
Other languages
English (en)
French (fr)
Inventor
Shohei Shirakami
Takayuki Inoue
Koichiro Mukoyoshi
Yutaka Nakajima
Hiroyuki Usuda
Hisao Hamaguchi
Yasuyuki Higashi
Keiko Hatanaka
Original Assignee
Astellas Pharma Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Astellas Pharma Inc. filed Critical Astellas Pharma Inc.
Priority to KR1020097016746A priority Critical patent/KR20090106604A/ko
Priority to US12/522,987 priority patent/US20100105661A1/en
Priority to JP2008553128A priority patent/JP5287253B2/ja
Priority to CNA2008800020671A priority patent/CN101578285A/zh
Priority to CA002675288A priority patent/CA2675288A1/en
Priority to MX2009007426A priority patent/MX2009007426A/es
Priority to EP08703164A priority patent/EP2123651A4/en
Publication of WO2008084861A1 publication Critical patent/WO2008084861A1/ja

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/12Heterocyclic 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 three hetero rings
    • C07D471/14Ortho-condensed systems

Abstract

【課題】優れたJAK3阻害作用を有し、自己免疫疾患、炎症性疾患、アレルギー性疾患を含む、種々の免疫性疾患の治療あるいは予防剤の有効成分として有用な化合物の提供。 【解決手段】  本発明者らは、新規な縮合へテロ環誘導体について検討した結果、本発明縮合ピリジン化合物が、優れたJAK3阻害作用を有することを確認し本発明を完成させた。即ち、本発明化合物は、JAK3に対する阻害活性を有していることから、望ましくないサイトカインシグナル伝達によって引き起こされる疾患、例えば生体移植における拒絶、自己免疫疾患、喘息、アトピー性皮膚炎、リウマチ、乾癬、アテローム性動脈硬化症、あるいはサイトカインシグナル伝達異常によって引き起こされる疾患、例えば、癌、白血病等の治療剤若しくは予防剤の有効成分として有用であることが確認された。
PCT/JP2008/050300 2007-01-12 2008-01-11 縮合ピリジン化合物 WO2008084861A1 (ja)

Priority Applications (7)

Application Number Priority Date Filing Date Title
KR1020097016746A KR20090106604A (ko) 2007-01-12 2008-01-11 축합 피리딘 화합물
US12/522,987 US20100105661A1 (en) 2007-01-12 2008-01-11 Condensed pyridine compound
JP2008553128A JP5287253B2 (ja) 2007-01-12 2008-01-11 縮合ピリジン化合物
CNA2008800020671A CN101578285A (zh) 2007-01-12 2008-01-11 稠合吡啶化合物
CA002675288A CA2675288A1 (en) 2007-01-12 2008-01-11 Condensed pyridine compound
MX2009007426A MX2009007426A (es) 2007-01-12 2008-01-11 Compuesto de piridina condensado.
EP08703164A EP2123651A4 (en) 2007-01-12 2008-01-11 CONDENSED PYRIDINE COMPOUND

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007005236 2007-01-12
JP2007-005236 2007-01-12

Publications (1)

Publication Number Publication Date
WO2008084861A1 true WO2008084861A1 (ja) 2008-07-17

Family

ID=39608748

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/050300 WO2008084861A1 (ja) 2007-01-12 2008-01-11 縮合ピリジン化合物

Country Status (10)

Country Link
US (1) US20100105661A1 (ja)
EP (1) EP2123651A4 (ja)
JP (1) JP5287253B2 (ja)
KR (1) KR20090106604A (ja)
CN (1) CN101578285A (ja)
AR (1) AR064879A1 (ja)
CA (1) CA2675288A1 (ja)
MX (1) MX2009007426A (ja)
TW (1) TW200900061A (ja)
WO (1) WO2008084861A1 (ja)

Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010058846A1 (ja) * 2008-11-21 2010-05-27 アステラス製薬株式会社 4,6-ジアミノニコチンアミド化合物
WO2010119875A1 (ja) 2009-04-14 2010-10-21 アステラス製薬株式会社 縮合ピロロピリジン誘導体
WO2010144486A1 (en) 2009-06-08 2010-12-16 Takeda Pharmaceutical Company Limited Dihydropyrrolonaphtyridinone compounds as inhibitors of jak
US7879844B2 (en) 2005-12-28 2011-02-01 Astellas Pharma Inc. Heterocyclic janus kinase 3 inhibitors
JP2011506437A (ja) * 2007-12-13 2011-03-03 メルク・シャープ・エンド・ドーム・コーポレイション Janusキナーゼの阻害剤
US20110201593A1 (en) * 2010-01-12 2011-08-18 Genentech, Inc. Tricyclic heterocyclic compounds, compositions and methods of use thereof
JP2012505152A (ja) * 2008-06-10 2012-03-01 アボット・ラボラトリーズ 新規な三環式化合物
US8163767B2 (en) 2005-07-14 2012-04-24 Astellas Pharma Inc. Heterocyclic Janus Kinase 3 inhibitors
CN102574863A (zh) * 2009-08-27 2012-07-11 拜奥克里斯特制药公司 作为janus激酶抑制剂的杂环化合物
US8329699B2 (en) 2010-05-20 2012-12-11 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
JP2013504532A (ja) * 2009-09-10 2013-02-07 エフ.ホフマン−ラ ロシュ アーゲー Jakの阻害剤
WO2013024895A1 (en) 2011-08-12 2013-02-21 Nissan Chemical Industries, Ltd. Tricyclic heterocyclic compounds and jak inhibitors
JP2013512282A (ja) * 2009-12-01 2013-04-11 アボット・ラボラトリーズ 新規三環式化合物
US8426411B2 (en) 2008-06-10 2013-04-23 Abbott Laboratories Tricyclic compounds
US8481541B2 (en) 2010-03-22 2013-07-09 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
US8518945B2 (en) 2010-03-22 2013-08-27 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
WO2014123167A1 (ja) 2013-02-08 2014-08-14 日産化学工業株式会社 3環性ピロロピリジン化合物及びjak阻害剤
JP2015529242A (ja) * 2012-09-21 2015-10-05 アドヴィヌス セラピューティクス リミテッドAdvinus Therapeutics Limited 置換された縮合三環式化合物、組成物およびその医薬用途
JP2016518344A (ja) * 2013-03-19 2016-06-23 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. ヤヌスキナーゼ阻害剤としてのシクロアルキルニトリルピラゾロピリドン
KR20170003521A (ko) 2014-05-14 2017-01-09 닛산 가가쿠 고교 가부시키 가이샤 3 고리성 화합물 및 jak 저해제
US9879019B2 (en) 2015-10-16 2018-01-30 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
KR20200005562A (ko) * 2017-05-12 2020-01-15 셀론 파르마 에스.에이. 키나아제 jak 저해제로서 피라졸[1,5-a]피리미딘 유도체
US10550126B2 (en) 2015-10-16 2020-02-04 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
CN113631557A (zh) * 2019-03-14 2021-11-09 上海华汇拓医药科技有限公司 Jak激酶抑制剂及其制备方法和在医药领域的应用
US11365198B2 (en) 2015-10-16 2022-06-21 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11512092B2 (en) 2015-10-16 2022-11-29 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11524964B2 (en) 2015-10-16 2022-12-13 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11661422B2 (en) 2020-08-27 2023-05-30 Incyte Corporation Tricyclic urea compounds as JAK2 V617F inhibitors
US11691971B2 (en) 2020-06-19 2023-07-04 Incyte Corporation Naphthyridinone compounds as JAK2 V617F inhibitors
US11753413B2 (en) 2020-06-19 2023-09-12 Incyte Corporation Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors
US11767323B2 (en) 2020-07-02 2023-09-26 Incyte Corporation Tricyclic pyridone compounds as JAK2 V617F inhibitors
US11773106B2 (en) 2015-10-16 2023-10-03 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11780840B2 (en) 2020-07-02 2023-10-10 Incyte Corporation Tricyclic urea compounds as JAK2 V617F inhibitors
US11919908B2 (en) 2020-12-21 2024-03-05 Incyte Corporation Substituted pyrrolo[2,3-d]pyrimidine compounds as JAK2 V617F inhibitors
US11958861B2 (en) 2021-02-25 2024-04-16 Incyte Corporation Spirocyclic lactams as JAK2 V617F inhibitors

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
US9115133B2 (en) 2011-03-22 2015-08-25 Advinus Therapeutics Limited Substituted fused tricyclic compounds, compositions and medicinal applications thereof
EP3822273B1 (en) 2012-06-13 2024-04-10 Incyte Holdings Corporation Substituted tricyclic compounds as fgfr inhibitors
WO2014026125A1 (en) 2012-08-10 2014-02-13 Incyte Corporation Pyrazine derivatives as fgfr inhibitors
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
WO2014146249A1 (en) 2013-03-19 2014-09-25 Merck Sharp & Dohme Corp. Geminally substituted cyanoethylpyrazolo pyridones as janus kinase inhibitors
WO2014146492A1 (en) * 2013-03-19 2014-09-25 Merck Sharp & Dohme Corp. N-(2-cyano heterocyclyl)pyrazolo pyridones as janus kinase inhibitors
RU2015144385A (ru) 2013-03-19 2017-04-26 Мерк Шарп И Доум Корп. Ациклические цианоэтилпиразолопиридоны в качестве ингибиторов янус-киназы
SG10201708520YA (en) 2013-04-19 2017-12-28 Incyte Corp Bicyclic heterocycles as fgfr inhibitors
KR101548492B1 (ko) * 2013-09-23 2015-09-01 건국대학교 산학협력단 야누스 키나아제 1 (Janus kinase 1)의 활성을 선택적으로 저해하는 4-아미노-7-아자인돌-5-카르복사마이드 유도체
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
MX2017010673A (es) 2015-02-20 2018-03-21 Incyte Corp Heterociclos biciclicos como inhibidores de receptores del factor de crecimiento fibroblastico (fgfr).
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
EP3710431A4 (en) 2017-11-03 2021-07-07 Aclaris Therapeutics, Inc. SUBSTITUTED PYRROLOPYRIMIDINE JAK INHIBITORS AND METHODS FOR THEIR MANUFACTURE AND USE
KR102034538B1 (ko) * 2017-11-28 2019-10-21 주식회사한국파마 Jak 저해제 화합물, 및 이의 제조방법
CN112867716A (zh) 2018-05-04 2021-05-28 因赛特公司 Fgfr抑制剂的固体形式和其制备方法
CN112566912A (zh) 2018-05-04 2021-03-26 因赛特公司 Fgfr抑制剂的盐
JP2021534244A (ja) 2018-08-10 2021-12-09 アクラリス セラピューティクス,インコーポレイテッド ピロロピリミジンitk阻害剤
WO2020185532A1 (en) 2019-03-08 2020-09-17 Incyte Corporation Methods of treating cancer with an fgfr inhibitor
MX2021013224A (es) * 2019-05-02 2022-01-06 Aclaris Therapeutics Inc Pirrolopiridinas sustituidas como inhibidores de jak.
KR102286372B1 (ko) * 2019-05-27 2021-08-05 주식회사한국파마 Jak 저해제 화합물, 및 이를 포함하는 의약 조성물
CN112174951A (zh) * 2019-07-02 2021-01-05 深圳美莹基因科技有限公司 作为詹纳斯激酶1选择抑制剂的吡咯并[2,3-b]吡啶衍生物
WO2021007269A1 (en) 2019-07-09 2021-01-14 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
AU2020366006A1 (en) 2019-10-14 2022-04-21 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
EP4069696A1 (en) 2019-12-04 2022-10-12 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
KR20220131900A (ko) 2019-12-04 2022-09-29 인사이트 코포레이션 Fgfr 억제제의 유도체
CN111233751B (zh) * 2020-03-25 2021-02-02 丽水绿氟科技有限公司 一种3,3-二氟-4-氨基哌啶类化合物及其衍生物的制备方法
KR102551758B1 (ko) * 2020-11-30 2023-07-05 주식회사한국파마 신규한 jak 특이 저해제 화합물, 및 이의 제조방법
CN113200983B (zh) * 2021-05-22 2023-01-03 中国药科大学 一种吡咯并吡啶结构的化合物、制备方法和医药用途
US11939331B2 (en) 2021-06-09 2024-03-26 Incyte Corporation Tricyclic heterocycles as FGFR inhibitors
AR127972A1 (es) * 2021-12-17 2024-03-13 Pi Industries Ltd Novedosos compuestos de piridina carboxamida bicíclica sustituida fusionada para combatir hongos fitopatogénicos

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999065909A1 (en) 1998-06-19 1999-12-23 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
WO1999065908A1 (en) 1998-06-19 1999-12-23 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
WO2001042246A2 (en) 1999-12-10 2001-06-14 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
WO2002000661A1 (en) 2000-06-26 2002-01-03 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS AS IMMUNOSUPPRESSIVE AGENTS
WO2004099204A1 (en) 2003-05-09 2004-11-18 Astrazeneca Ab Imidazo and thiazolopyridines as jak3 kinase inhibitors
WO2004099205A1 (en) 2003-05-09 2004-11-18 Astrazeneca Ab Azaindole compounds as kinase inhibitors
WO2006069080A2 (en) 2004-12-22 2006-06-29 Incyte Corporation Pyrrolo[2,3-b]pyridin-4-yl-amines and pyrrolo[2m3-b]pyrimidin-4-yl-amines as janus kinase inhibitors
WO2006087543A1 (en) 2005-02-18 2006-08-24 Astrazeneca Ab Antibacterial piperidine derivatives
WO2006127587A1 (en) 2005-05-20 2006-11-30 Vertex Pharmaceuticals Incorporated Pyrrolopyridines useful as inhibitors of protein kinase
WO2007007919A2 (en) 2005-07-14 2007-01-18 Astellas Pharma Inc. Heterocyclic janus kinase 3 inhibitors
WO2007077949A1 (en) * 2005-12-28 2007-07-12 Astellas Pharma Inc. Heterocyclic janus kinase 3 inhibitors

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR940702451A (ko) * 1991-09-06 1994-08-20 고야 다다시 4-아미로(알킬)시클로헥산-1-카르복사미드 화합물 및 그 용도
US6946473B2 (en) * 1999-01-27 2005-09-20 Wyeth Holdings Corporation Preparation and use of acetylenic ortho-sulfonamido and phosphinic acid amido bicyclic heteroaryl hydroxamic acids as TACE inhibitors

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999065909A1 (en) 1998-06-19 1999-12-23 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
WO1999065908A1 (en) 1998-06-19 1999-12-23 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
WO2001042246A2 (en) 1999-12-10 2001-06-14 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
WO2002000661A1 (en) 2000-06-26 2002-01-03 Pfizer Products Inc. PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS AS IMMUNOSUPPRESSIVE AGENTS
JP2006525998A (ja) * 2003-05-09 2006-11-16 アストラゼネカ・アクチエボラーグ キナーゼ阻害剤としてのアザインドール化合物
WO2004099205A1 (en) 2003-05-09 2004-11-18 Astrazeneca Ab Azaindole compounds as kinase inhibitors
JP2006525997A (ja) * 2003-05-09 2006-11-16 アストラゼネカ・アクチエボラーグ Jak3キナーゼ阻害剤としてのイミダゾ及びチアゾロピリジン
WO2004099204A1 (en) 2003-05-09 2004-11-18 Astrazeneca Ab Imidazo and thiazolopyridines as jak3 kinase inhibitors
WO2006069080A2 (en) 2004-12-22 2006-06-29 Incyte Corporation Pyrrolo[2,3-b]pyridin-4-yl-amines and pyrrolo[2m3-b]pyrimidin-4-yl-amines as janus kinase inhibitors
WO2006087543A1 (en) 2005-02-18 2006-08-24 Astrazeneca Ab Antibacterial piperidine derivatives
WO2006127587A1 (en) 2005-05-20 2006-11-30 Vertex Pharmaceuticals Incorporated Pyrrolopyridines useful as inhibitors of protein kinase
WO2007007919A2 (en) 2005-07-14 2007-01-18 Astellas Pharma Inc. Heterocyclic janus kinase 3 inhibitors
WO2007077949A1 (en) * 2005-12-28 2007-07-12 Astellas Pharma Inc. Heterocyclic janus kinase 3 inhibitors

Non-Patent Citations (9)

* Cited by examiner, † Cited by third party
Title
"Jikken Kagaku Koza (Courses in Experimental Chemistry)", 2003
"Molecular Design", vol. 7, 1990, HIROKAWA PUB. CO., article "Iyakuhin No Kaihatsu (Development of Medicines)", pages: 163 - 198
J. J. 0' SHEA ET AL., CELL, vol. 109, 2002, pages S121
K. OZAKI ET AL., SCIENCE, vol. 298, 2002, pages 1630
P. MACCHI ET AL., NATURE, vol. 377, 1995, pages 65
PROG. MED., vol. 5, 1985, pages 2157 - 2161
S. M. RUSSELL ET AL., SCIENCE, vol. 270, 1995, pages 797
See also references of EP2123651A4
T. W. GREENE; P. G. M. WUTS: "Protective Groups in Organic Synthesis", 1999

Cited By (90)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8163767B2 (en) 2005-07-14 2012-04-24 Astellas Pharma Inc. Heterocyclic Janus Kinase 3 inhibitors
US7879844B2 (en) 2005-12-28 2011-02-01 Astellas Pharma Inc. Heterocyclic janus kinase 3 inhibitors
JP2011506437A (ja) * 2007-12-13 2011-03-03 メルク・シャープ・エンド・ドーム・コーポレイション Janusキナーゼの阻害剤
US9365579B2 (en) 2008-06-10 2016-06-14 Abbvie Inc. Tricyclic compounds
EP3031324A3 (en) * 2008-06-10 2016-09-07 AbbVie Inc. Tricyclic kinase inhibitors
US8426411B2 (en) 2008-06-10 2013-04-23 Abbott Laboratories Tricyclic compounds
JP2012505152A (ja) * 2008-06-10 2012-03-01 アボット・ラボラトリーズ 新規な三環式化合物
US8962629B2 (en) 2008-06-10 2015-02-24 Abbvie Inc. Tricyclic compounds
WO2010058846A1 (ja) * 2008-11-21 2010-05-27 アステラス製薬株式会社 4,6-ジアミノニコチンアミド化合物
EP2420502A4 (en) * 2009-04-14 2012-12-19 Astellas Pharma Inc CONDENSED PYRROLOPYRIDINE DERIVATIVE
EP2420502A1 (en) * 2009-04-14 2012-02-22 Astellas Pharma Inc. Fused pyrrolopyridine derivative
CN102395589A (zh) * 2009-04-14 2012-03-28 安斯泰来制药株式会社 稠合吡咯并吡啶衍生物
WO2010119875A1 (ja) 2009-04-14 2010-10-21 アステラス製薬株式会社 縮合ピロロピリジン誘導体
US8785429B2 (en) 2009-06-08 2014-07-22 Takeda Pharmaceutical Company Limited Dihydropyrrolonaphthyridinone compounds as inhibitors of JAK
WO2010144486A1 (en) 2009-06-08 2010-12-16 Takeda Pharmaceutical Company Limited Dihydropyrrolonaphtyridinone compounds as inhibitors of jak
US8420816B2 (en) 2009-06-08 2013-04-16 Takeda Pharmaceutical Company Limited Dihydropyrrolonaphthyridinone compounds as inhibitors of JAK
CN102574863A (zh) * 2009-08-27 2012-07-11 拜奥克里斯特制药公司 作为janus激酶抑制剂的杂环化合物
JP2013504532A (ja) * 2009-09-10 2013-02-07 エフ.ホフマン−ラ ロシュ アーゲー Jakの阻害剤
JP2013512282A (ja) * 2009-12-01 2013-04-11 アボット・ラボラトリーズ 新規三環式化合物
CN108774237A (zh) * 2009-12-01 2018-11-09 Abbvie 公司 新的三环化合物
US8785639B2 (en) 2009-12-01 2014-07-22 Abbvie Inc. Substituted dihydropyrazolo[3,4-D]pyrrolo[2,3-B]pyridines and methods of use thereof
USRE47221E1 (en) 2009-12-01 2019-02-05 Abbvie Inc. Tricyclic compounds
JP2013517220A (ja) * 2010-01-12 2013-05-16 エフ.ホフマン−ラ ロシュ アーゲー 三環式複素環式化合物、その組成物、及び使用の方法
US8461328B2 (en) * 2010-01-12 2013-06-11 Genentech, Inc. Tricyclic heterocyclic compounds, compositions and methods of use thereof
US20110201593A1 (en) * 2010-01-12 2011-08-18 Genentech, Inc. Tricyclic heterocyclic compounds, compositions and methods of use thereof
US8518945B2 (en) 2010-03-22 2013-08-27 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
US8481541B2 (en) 2010-03-22 2013-07-09 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
US8329699B2 (en) 2010-05-20 2012-12-11 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
US9556187B2 (en) 2011-08-12 2017-01-31 Nissan Chemical Industries, Ltd. Substituted pyrrolo[3′,2′:5,6]pyrido[4,3-d]pyrimidines and JAK inhibitors comprising the same
KR20140059195A (ko) 2011-08-12 2014-05-15 닛산 가가쿠 고교 가부시키 가이샤 트리시클릭 헤테로시클릭 화합물 및 jak 저해제
US9216999B2 (en) 2011-08-12 2015-12-22 Nissan Chemical Industries, Ltd. Substituted pyrrolo[2,3-h][1,6]naphthyridines and compositions thereof as JAK inhibitors
EP3112370A1 (en) 2011-08-12 2017-01-04 Nissan Chemical Industries, Ltd. Tricyclic heterocyclic compounds and jak inhibitors
WO2013024895A1 (en) 2011-08-12 2013-02-21 Nissan Chemical Industries, Ltd. Tricyclic heterocyclic compounds and jak inhibitors
TWI601727B (zh) * 2011-08-12 2017-10-11 日產化學工業股份有限公司 三環雜環化合物及jak(傑納斯激酶)抑制劑
JP2015529242A (ja) * 2012-09-21 2015-10-05 アドヴィヌス セラピューティクス リミテッドAdvinus Therapeutics Limited 置換された縮合三環式化合物、組成物およびその医薬用途
US9475813B2 (en) 2013-02-08 2016-10-25 Nissan Chemical Industries, Ltd. Tricyclic pyrrolopyridine compound, and JAK inhibitor
WO2014123167A1 (ja) 2013-02-08 2014-08-14 日産化学工業株式会社 3環性ピロロピリジン化合物及びjak阻害剤
JP2016518344A (ja) * 2013-03-19 2016-06-23 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. ヤヌスキナーゼ阻害剤としてのシクロアルキルニトリルピラゾロピリドン
KR20170003521A (ko) 2014-05-14 2017-01-09 닛산 가가쿠 고교 가부시키 가이샤 3 고리성 화합물 및 jak 저해제
US10385052B2 (en) 2014-05-14 2019-08-20 Nissan Chemical Corporation Tricyclic compound and JAK inhibitor
US9890165B2 (en) 2014-05-14 2018-02-13 Nissan Chemical Industries, Ltd. Tricyclic compound and JAK inhibitor
US11186584B2 (en) 2015-10-16 2021-11-30 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11535624B2 (en) 2015-10-16 2022-12-27 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US9963459B1 (en) 2015-10-16 2018-05-08 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-alpla]pyrrolo[2,3-e]-pyrazin-8-YL)-N-(2,2,2-Trifluoroethyl)pyrrol and solid state forms thereof
US9951080B2 (en) 2015-10-16 2018-04-24 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-alpha]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10202394B2 (en) 2015-10-16 2019-02-12 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10202393B2 (en) 2015-10-16 2019-02-12 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10344036B2 (en) 2015-10-16 2019-07-09 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-#a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-#carboxamide and solid state forms thereof
US9879018B2 (en) 2015-10-16 2018-01-30 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl and solid state forms thereof
US10519164B2 (en) 2015-10-16 2019-12-31 Abbvie Inc. Processes for the preparation of (3S,4R)-3,ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11976077B2 (en) 2015-10-16 2024-05-07 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms therof
US10550126B2 (en) 2015-10-16 2020-02-04 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10597400B2 (en) 2015-10-16 2020-03-24 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carb oxamide and solid state forms thereof
US11795175B2 (en) 2015-10-16 2023-10-24 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10730883B2 (en) 2015-10-16 2020-08-04 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10981924B2 (en) 2015-10-16 2021-04-20 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10981923B2 (en) 2015-10-16 2021-04-20 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[l,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10995095B2 (en) 2015-10-16 2021-05-04 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carb oxamide and solid state forms thereof
US11787815B1 (en) 2015-10-16 2023-10-17 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US9879019B2 (en) 2015-10-16 2018-01-30 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11198697B1 (en) 2015-10-16 2021-12-14 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11780847B1 (en) 2015-10-16 2023-10-10 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1- carboxamide and solid state forms thereof
US11365198B2 (en) 2015-10-16 2022-06-21 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11780848B2 (en) 2015-10-16 2023-10-10 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1- carboxamide and solid state forms thereof
US11512092B2 (en) 2015-10-16 2022-11-29 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11524964B2 (en) 2015-10-16 2022-12-13 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10017517B2 (en) 2015-10-16 2018-07-10 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-α]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluorethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11535625B2 (en) 2015-10-16 2022-12-27 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11535626B2 (en) 2015-10-16 2022-12-27 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1 carboxamide and solid state forms thereof
US11773106B2 (en) 2015-10-16 2023-10-03 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11773105B2 (en) 2015-10-16 2023-10-03 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]- pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11661425B2 (en) 2015-10-16 2023-05-30 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11767326B2 (en) 2015-10-16 2023-09-26 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11680069B2 (en) 2015-10-16 2023-06-20 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11718627B2 (en) 2015-10-16 2023-08-08 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
KR102533519B1 (ko) 2017-05-12 2023-05-17 셀론 파르마 에스.에이. 키나아제 jak 저해제로서 피라졸[1,5-a]피리미딘 유도체
KR20200005562A (ko) * 2017-05-12 2020-01-15 셀론 파르마 에스.에이. 키나아제 jak 저해제로서 피라졸[1,5-a]피리미딘 유도체
JP2020519631A (ja) * 2017-05-12 2020-07-02 セロン ファーマ エス.アー.Celon Pharma S.A. キナーゼJAK阻害剤としてのピラゾロ[1,5−a]ピリミジン誘導体
JP7157084B2 (ja) 2017-05-12 2022-10-19 セロン ファーマ エス.アー. キナーゼJAK阻害剤としてのピラゾロ[1,5-a]ピリミジン誘導体
CN113631557A (zh) * 2019-03-14 2021-11-09 上海华汇拓医药科技有限公司 Jak激酶抑制剂及其制备方法和在医药领域的应用
JP7248256B2 (ja) 2019-03-14 2023-03-29 上海華匯拓医薬科技有限公司 Jakキナーゼ阻害剤及びその調製方法、並びにその医薬分野での使用
JP2022525749A (ja) * 2019-03-14 2022-05-19 上海華匯拓医薬科技有限公司 Jakキナーゼ阻害剤及びその調製方法、並びにその医薬分野での使用
CN113631557B (zh) * 2019-03-14 2024-03-15 上海华汇拓医药科技有限公司 Jak激酶抑制剂及其制备方法和在医药领域的应用
US11691971B2 (en) 2020-06-19 2023-07-04 Incyte Corporation Naphthyridinone compounds as JAK2 V617F inhibitors
US11753413B2 (en) 2020-06-19 2023-09-12 Incyte Corporation Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors
US11767323B2 (en) 2020-07-02 2023-09-26 Incyte Corporation Tricyclic pyridone compounds as JAK2 V617F inhibitors
US11780840B2 (en) 2020-07-02 2023-10-10 Incyte Corporation Tricyclic urea compounds as JAK2 V617F inhibitors
US11661422B2 (en) 2020-08-27 2023-05-30 Incyte Corporation Tricyclic urea compounds as JAK2 V617F inhibitors
US11919908B2 (en) 2020-12-21 2024-03-05 Incyte Corporation Substituted pyrrolo[2,3-d]pyrimidine compounds as JAK2 V617F inhibitors
US11958861B2 (en) 2021-02-25 2024-04-16 Incyte Corporation Spirocyclic lactams as JAK2 V617F inhibitors

Also Published As

Publication number Publication date
US20100105661A1 (en) 2010-04-29
KR20090106604A (ko) 2009-10-09
AR064879A1 (es) 2009-04-29
MX2009007426A (es) 2009-07-17
EP2123651A4 (en) 2011-05-04
CN101578285A (zh) 2009-11-11
CA2675288A1 (en) 2008-07-17
TW200900061A (en) 2009-01-01
JP5287253B2 (ja) 2013-09-11
EP2123651A1 (en) 2009-11-25
JPWO2008084861A1 (ja) 2010-05-06

Similar Documents

Publication Publication Date Title
WO2008084861A1 (ja) 縮合ピリジン化合物
TW200745108A (en) Condensed pyridine compound
WO2015042078A3 (en) Substituted aminopyrimidine compounds and methods of use
PH12017502171A1 (en) PYRIDO[3,4-d]PYRIMIDINE DERIVATIVE AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
WO2009080638A3 (en) Sulfamides as zap-70 inhibitors
WO2011014795A3 (en) Compounds and compositions as syk kinase inhibitors
WO2011162515A3 (en) Novel fused pyrimidine derivatives for inhibition of tyrosine kinase activity
IN2015DN00827A (ja)
MX347917B (es) Compuestos a base de imidazo[1,2-b]piridazina, composiciones que los comprenden, y metodos para su uso.
WO2015039612A8 (zh) 抑制btk和/或jak3激酶活性的化合物
MY170326A (en) Imidazo [1,2-b] pyridazine derivativea as kinase inhibitors
EP3577116A4 (en) DERIVATIVES OF N-CYCLOALKYL / HETEROCYCLOALKYL-4- (IMIDAZO [1,2-A] PYRIDINE) PYRIMIDINE-2-AMINE AS THERAPEUTICS
GEP20156285B (en) Compounds and compositions as trk inhibitors
WO2006020276A3 (en) Antiviral compounds
WO2015148373A3 (en) TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF
WO2010141796A3 (en) PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a] PYRIDINE DERIVATIVES
EA201890827A1 (ru) Конденсированные производные пиразола в качестве ингибиторов киназы
WO2007058832A3 (en) Pyrrolo (2, 3-b) pyridine derivatives useful as tec kinase inhibitors
WO2011051342A8 (en) IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS
WO2005074375A3 (en) Heparanase inhibitors and uses thereof
GEP20227344B (en) Pyrimidine compound as jak kinase inhibitor
WO2007100610A3 (en) Pyridine, pyrimidine and pyrazine derivatives as cxcr3 receptor modulators
WO2007135026A3 (de) Substituierte pteridine als therapeutika
SA519401827B1 (ar) [3، 4- d] مشتق بيريدو بيريميدين وملح مقبول صيدلانياً منه
WO2016164286A3 (en) TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200880002067.1

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08703164

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2008553128

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 2008703164

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 4042/CHENP/2009

Country of ref document: IN

Ref document number: MX/A/2009/007426

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 2675288

Country of ref document: CA

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 1020097016746

Country of ref document: KR