JP2017526711A5 - - Google Patents

Download PDF

Info

Publication number
JP2017526711A5
JP2017526711A5 JP2017513448A JP2017513448A JP2017526711A5 JP 2017526711 A5 JP2017526711 A5 JP 2017526711A5 JP 2017513448 A JP2017513448 A JP 2017513448A JP 2017513448 A JP2017513448 A JP 2017513448A JP 2017526711 A5 JP2017526711 A5 JP 2017526711A5
Authority
JP
Japan
Prior art keywords
compound
pharmaceutically acceptable
hydrogen
acceptable salt
dihydropyridin
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.)
Granted
Application number
JP2017513448A
Other languages
English (en)
Japanese (ja)
Other versions
JP2017526711A (ja
JP6538153B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/CN2015/089332 external-priority patent/WO2016037578A1/en
Publication of JP2017526711A publication Critical patent/JP2017526711A/ja
Publication of JP2017526711A5 publication Critical patent/JP2017526711A5/ja
Application granted granted Critical
Publication of JP6538153B2 publication Critical patent/JP6538153B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017513448A 2014-09-10 2015-09-10 Rearranged during transfection(ret)阻害剤としての新規な化合物 Expired - Fee Related JP6538153B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CNPCT/CN2014/000834 2014-09-10
CN2014000834 2014-09-10
PCT/CN2015/089332 WO2016037578A1 (en) 2014-09-10 2015-09-10 Novel compounds as rearranged during transfection (ret) inhibitors

Publications (3)

Publication Number Publication Date
JP2017526711A JP2017526711A (ja) 2017-09-14
JP2017526711A5 true JP2017526711A5 (cg-RX-API-DMAC7.html) 2018-10-18
JP6538153B2 JP6538153B2 (ja) 2019-07-03

Family

ID=55458357

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017513448A Expired - Fee Related JP6538153B2 (ja) 2014-09-10 2015-09-10 Rearranged during transfection(ret)阻害剤としての新規な化合物

Country Status (23)

Country Link
US (2) US9879021B2 (cg-RX-API-DMAC7.html)
EP (1) EP3191449B1 (cg-RX-API-DMAC7.html)
JP (1) JP6538153B2 (cg-RX-API-DMAC7.html)
KR (1) KR20170046180A (cg-RX-API-DMAC7.html)
CN (1) CN107250110B (cg-RX-API-DMAC7.html)
AU (1) AU2015316438B2 (cg-RX-API-DMAC7.html)
BR (1) BR112017004897A2 (cg-RX-API-DMAC7.html)
CA (1) CA2960730A1 (cg-RX-API-DMAC7.html)
CL (1) CL2017000589A1 (cg-RX-API-DMAC7.html)
CO (1) CO2017002378A2 (cg-RX-API-DMAC7.html)
CR (1) CR20170094A (cg-RX-API-DMAC7.html)
DK (1) DK3191449T3 (cg-RX-API-DMAC7.html)
DO (1) DOP2017000067A (cg-RX-API-DMAC7.html)
EA (1) EA032030B1 (cg-RX-API-DMAC7.html)
ES (1) ES2819871T3 (cg-RX-API-DMAC7.html)
IL (1) IL250923B (cg-RX-API-DMAC7.html)
MX (1) MX381233B (cg-RX-API-DMAC7.html)
MY (1) MY187169A (cg-RX-API-DMAC7.html)
PE (1) PE20170677A1 (cg-RX-API-DMAC7.html)
PH (1) PH12017500454A1 (cg-RX-API-DMAC7.html)
SG (1) SG11201701695UA (cg-RX-API-DMAC7.html)
UA (1) UA123084C2 (cg-RX-API-DMAC7.html)
WO (1) WO2016037578A1 (cg-RX-API-DMAC7.html)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT3205654T (pt) 2010-05-20 2019-04-22 Array Biopharma Inc Compostos macrocíclicos como inibidores de cinases trk
WO2016037578A1 (en) 2014-09-10 2016-03-17 Glaxosmithkline Intellectual Property Development Limited Novel compounds as rearranged during transfection (ret) inhibitors
EP3517526B1 (en) 2014-09-10 2020-08-19 GlaxoSmithKline Intellectual Property Development Limited Pyridinones as rearranged during transfection (ret) inhibitors
US10202365B2 (en) 2015-02-06 2019-02-12 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as RET inhibitors
EA035049B1 (ru) 2015-07-16 2020-04-22 Аррэй Байофарма Инк. СОЕДИНЕНИЯ ЗАМЕЩЕННОГО ПИРАЗОЛО[1,5-a]ПИРИДИНА В КАЧЕСТВЕ ИНГИБИТОРОВ RET КИНАЗЫ
EP3371171B1 (en) 2015-11-02 2023-10-25 Blueprint Medicines Corporation Inhibitors of ret
WO2017145050A1 (en) * 2016-02-23 2017-08-31 Glaxosmithkline Intellectual Property Development Limited Pyridylpyridone derivative useful as a ret kinase inhibitor in the treatment of ibs and cancer
WO2017152117A1 (en) * 2016-03-03 2017-09-08 Cornell University Small molecule ire1-alpha inhibitors
UY37155A (es) 2016-03-17 2017-10-31 Blueprint Medicines Corp Inhibidores de ret
WO2018017983A1 (en) 2016-07-22 2018-01-25 Blueprint Medicines Corporation Compounds useful for treating disorders related to ret
JP2018052878A (ja) * 2016-09-29 2018-04-05 第一三共株式会社 ピリジン化合物
JOP20190077A1 (ar) 2016-10-10 2019-04-09 Array Biopharma Inc مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret
TWI704148B (zh) 2016-10-10 2020-09-11 美商亞雷生物製藥股份有限公司 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物
TWI795381B (zh) 2016-12-21 2023-03-11 比利時商健生藥品公司 作為malt1抑制劑之吡唑衍生物
CA3049136C (en) 2017-01-18 2022-06-14 Array Biopharma Inc. Substituted pyrazolo[1,5-a]pyrazine compounds as ret kinase inhibitors
WO2018136663A1 (en) 2017-01-18 2018-07-26 Array Biopharma, Inc. Ret inhibitors
JOP20190213A1 (ar) 2017-03-16 2019-09-16 Array Biopharma Inc مركبات حلقية ضخمة كمثبطات لكيناز ros1
EP3624802A1 (en) 2017-05-15 2020-03-25 Blueprint Medicines Corporation Combinations of ret inhibitors and mtorc1 inhibitors and uses thereof for the treatment of cancer mediated by aberrant ret activity
TWI791053B (zh) 2017-10-10 2023-02-01 美商亞雷生物製藥股份有限公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物
TWI812649B (zh) 2017-10-10 2023-08-21 美商絡速藥業公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物
CN111630054B (zh) 2018-01-18 2023-05-09 奥瑞生物药品公司 作为RET激酶抑制剂的取代的吡唑并[3,4-d]嘧啶化合物
EP3740486A1 (en) 2018-01-18 2020-11-25 Array Biopharma, Inc. Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors
EP3740491A1 (en) 2018-01-18 2020-11-25 Array Biopharma, Inc. Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors
WO2019195471A1 (en) 2018-04-03 2019-10-10 Blueprint Medicines Corporation Ret inhibitor for use in treating cancer having a ret alteration
CN109096264B (zh) * 2018-08-28 2019-08-23 山东理工职业学院 Ret抑制剂及其制备方法、组合物和用途
ES2922314T3 (es) 2018-09-10 2022-09-13 Array Biopharma Inc Compuestos heterocíclicos condensados como inhibidores de cinasa RET
WO2020083311A1 (zh) * 2018-10-24 2020-04-30 南京明德新药研发有限公司 作为ret抑制剂的吡嗪衍生物
CN109678724A (zh) * 2018-12-18 2019-04-26 常州大学 一种2-甲基-1-取代苯基-2-丙胺类化合物的新合成方法
KR20210151880A (ko) * 2019-04-11 2021-12-14 얀센 파마슈티카 엔.브이. Malt1 억제제로서의 피리딘 고리 함유 유도체
US12433876B2 (en) 2019-08-30 2025-10-07 University Of Rochester Septin inhibitors for treatment of cancers
CN110950898B (zh) * 2019-12-12 2022-11-11 江苏华益科技有限公司 一种含氮的氘代甲基化合物的合成方法
CN111187257B (zh) * 2020-02-17 2021-03-16 山东理工职业学院 Ret受体酪氨酸激酶抑制剂
CA3183728A1 (en) 2020-05-29 2021-12-02 Blueprint Medicines Corporation Solid forms of pralsetinib
CN115803316B (zh) * 2020-07-23 2024-12-06 深圳晶泰科技有限公司 吡啶酮类化合物及其制备方法和应用
KR20230124555A (ko) 2020-11-06 2023-08-25 알리고스 테라퓨틱스 인코포레이티드 갑상선 호르몬 수용체 조절제로서의 2-피리돈
CN114539065B (zh) * 2020-11-25 2023-07-25 帕潘纳(北京)科技有限公司 制备4-硝基-2-三氟甲基苯乙酮的方法
WO2022256284A1 (en) 2021-06-02 2022-12-08 Fmc Corporation Fused pyridines for controlling invertebrate pests
CN113896650A (zh) * 2021-10-27 2022-01-07 成都科圣原医药科技有限公司 一种辛波莫德中间体的合成方法
AU2022457759A1 (en) 2022-05-09 2024-11-14 Maxunitech Inc. Method for preparing 2-substituted aryl acetonitrile compound and use thereof
CN116283748A (zh) * 2023-02-21 2023-06-23 康化(上海)新药研发有限公司 2,5-二氯-3-甲氧基吡啶的合成方法

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120046290A1 (en) * 1997-12-22 2012-02-23 Jacques Dumas Inhibition of p38 kinase activity using substituted heterocyclic ureas
US20070244120A1 (en) * 2000-08-18 2007-10-18 Jacques Dumas Inhibition of raf kinase using substituted heterocyclic ureas
JP4403482B2 (ja) 1997-12-22 2010-01-27 バイエル コーポレイション 置換複素環尿素合成のための中間体およびその製造方法
CZ299156B6 (cs) * 1997-12-22 2008-05-07 Bayer Corporation Substituované heterocyklické mocoviny, farmaceutické prípravky je obsahující a jejich použití
JP2003507329A (ja) 1999-08-12 2003-02-25 フアルマシア・イタリア・エツセ・ピー・アー 3(5)−アミノ−ピラゾール誘導体、それらの製造方法および抗腫瘍薬としてのそれらの使用
JP2004517840A (ja) 2000-11-27 2004-06-17 フアルマシア・イタリア・エツセ・ピー・アー フェニルアセトアミド−ピラゾール誘導体およびそれの抗腫瘍薬としての使用
DE10201764A1 (de) 2002-01-18 2003-07-31 Bayer Cropscience Ag Substituierte 4-Aminopyridin-Derivate
TW200406374A (en) * 2002-05-29 2004-05-01 Novartis Ag Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases
JPWO2004024694A1 (ja) * 2002-09-10 2006-01-05 杏林製薬株式会社 4−置換アリール−5−ヒドロキシイソキノリノン誘導体
BRPI0413757A (pt) 2003-08-22 2006-10-31 Boehringer Ingelheim Pharma métodos para o tratamento de copd e da hipertensão pulmonar
US7968574B2 (en) 2004-12-28 2011-06-28 Kinex Pharmaceuticals, Llc Biaryl compositions and methods for modulating a kinase cascade
EP2001892B1 (en) * 2006-03-17 2013-04-24 Ambit Biosciences Corporation Imidazolothiazole compounds for the treatment of proliferative diseases
DK2041071T3 (da) 2006-06-29 2014-09-01 Kinex Pharmaceuticals Llc Biarylsammensætninger og fremgangsmåder til modulering af en kinasekaskade
WO2008046802A1 (en) 2006-10-16 2008-04-24 Novartis Ag Phenylacetamides useful as protein kinase inhibitors
CA2701959C (en) 2006-11-15 2016-01-05 Ym Biosciences Australia Pty Ltd Inhibitors of kinase activity
KR20120059558A (ko) 2009-08-19 2012-06-08 암비트 바이오사이언시즈 코포레이션 바이아릴 화합물 및 이의 사용 방법
EP2651930B1 (en) 2010-12-16 2015-10-28 Boehringer Ingelheim International GmbH Biarylamide inhibitors of leukotriene production
ES2616655T3 (es) * 2013-03-15 2017-06-13 Glaxosmithkline Intellectual Property Development Limited Derivados de piridina como inhibidores de quinasa reorganizada durante la transfección (RET)
AR095308A1 (es) 2013-03-15 2015-10-07 Glaxosmithkline Ip Dev Ltd Compuesto de 2-piridona, composición farmacéutica que lo comprende y su uso para preparar un medicamento
WO2016037578A1 (en) 2014-09-10 2016-03-17 Glaxosmithkline Intellectual Property Development Limited Novel compounds as rearranged during transfection (ret) inhibitors
EP3517526B1 (en) 2014-09-10 2020-08-19 GlaxoSmithKline Intellectual Property Development Limited Pyridinones as rearranged during transfection (ret) inhibitors

Similar Documents

Publication Publication Date Title
JP2017526711A5 (cg-RX-API-DMAC7.html)
JP2017527578A5 (cg-RX-API-DMAC7.html)
US20190345138A1 (en) Heterocyclic amides as kinase inhibitors
HRP20190815T1 (hr) Piridonski derivati korišteni kao inhibitori kinaze reorganizirane tijekom transfekcije (ret)
JP2014504646A5 (cg-RX-API-DMAC7.html)
JP2016512515A5 (cg-RX-API-DMAC7.html)
JP2017502940A5 (cg-RX-API-DMAC7.html)
JP2013543896A5 (cg-RX-API-DMAC7.html)
JP2011529049A5 (cg-RX-API-DMAC7.html)
JP2009529541A5 (cg-RX-API-DMAC7.html)
NZ627750A (en) Carbamate compounds and of making and using same
JP2015503529A5 (cg-RX-API-DMAC7.html)
JP2007504160A5 (cg-RX-API-DMAC7.html)
JP2016525136A5 (cg-RX-API-DMAC7.html)
JP2011519854A5 (cg-RX-API-DMAC7.html)
JP2015531774A5 (cg-RX-API-DMAC7.html)
JP2014525470A5 (cg-RX-API-DMAC7.html)
JP2013531055A5 (cg-RX-API-DMAC7.html)
JP2013510859A5 (cg-RX-API-DMAC7.html)
CN109790158A (zh) 作为jak抑制剂杂环化合物,该化合物的盐类及其治疗用途
JP2010540602A5 (cg-RX-API-DMAC7.html)
JP2012507535A5 (cg-RX-API-DMAC7.html)
JP2012530765A5 (cg-RX-API-DMAC7.html)
JP2014510133A (ja) 1−(3−シアノ−1−イソプロピル−インドール−5−イル)ピラゾール−4−カルボン酸の結晶形とその製造方法
JP2016529264A5 (cg-RX-API-DMAC7.html)