WO2008084861A1 - 縮合ピリジン化合物 - Google Patents
縮合ピリジン化合物 Download PDFInfo
- 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
Links
Classifications
-
- 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
- A61K31/4353—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
Abstract
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)
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 |
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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 |
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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 |
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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 |
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MX2021013224A (es) * | 2019-05-02 | 2022-01-06 | Aclaris Therapeutics Inc | Pirrolopiridinas sustituidas como inhibidores de jak. |
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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 |
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WO1999065909A1 (en) | 1998-06-19 | 1999-12-23 | Pfizer Products Inc. | PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS |
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-
2008
- 2008-01-11 CA CA002675288A patent/CA2675288A1/en not_active Abandoned
- 2008-01-11 AR ARP080100145A patent/AR064879A1/es unknown
- 2008-01-11 JP JP2008553128A patent/JP5287253B2/ja not_active Expired - Fee Related
- 2008-01-11 WO PCT/JP2008/050300 patent/WO2008084861A1/ja active Application Filing
- 2008-01-11 KR KR1020097016746A patent/KR20090106604A/ko not_active Application Discontinuation
- 2008-01-11 MX MX2009007426A patent/MX2009007426A/es not_active Application Discontinuation
- 2008-01-11 TW TW097101243A patent/TW200900061A/zh unknown
- 2008-01-11 CN CNA2008800020671A patent/CN101578285A/zh active Pending
- 2008-01-11 US US12/522,987 patent/US20100105661A1/en not_active Abandoned
- 2008-01-11 EP EP08703164A patent/EP2123651A4/en not_active Withdrawn
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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 |
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