CN112020496A - 作为rho激酶抑制剂的苯并吡唑类化合物 - Google Patents

作为rho激酶抑制剂的苯并吡唑类化合物 Download PDF

Info

Publication number
CN112020496A
CN112020496A CN201980026510.7A CN201980026510A CN112020496A CN 112020496 A CN112020496 A CN 112020496A CN 201980026510 A CN201980026510 A CN 201980026510A CN 112020496 A CN112020496 A CN 112020496A
Authority
CN
China
Prior art keywords
compound
reaction
isomer
pharmaceutically acceptable
acceptable salt
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
CN201980026510.7A
Other languages
English (en)
Other versions
CN112020496B (zh
Inventor
吴凌云
尹军
王才林
肖哲明
黎健
陈曙辉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Medshine Discovery Inc
Original Assignee
Medshine Discovery 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 Medshine Discovery Inc filed Critical Medshine Discovery Inc
Publication of CN112020496A publication Critical patent/CN112020496A/zh
Application granted granted Critical
Publication of CN112020496B publication Critical patent/CN112020496B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

公开了一类作为RHO激酶抑制剂的苯并吡唑类化合物,其药物组合物以及它们在制备RHO抑制药物中的应用,具体公开了式I‑1所示化合物、其药学上可接受的盐或异构体。

Description

PCT国内申请,说明书已公开。

Claims (30)

  1. PCT国内申请,权利要求书已公开。
CN201980026510.7A 2018-04-18 2019-04-18 作为rho激酶抑制剂的苯并吡唑类化合物 Active CN112020496B (zh)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
CN201810349362 2018-04-18
CN201810349362X 2018-04-18
CN201811221303 2018-10-19
CN2018112213030 2018-10-19
PCT/CN2019/083210 WO2019201297A1 (zh) 2018-04-18 2019-04-18 作为rho激酶抑制剂的苯并吡唑类化合物

Publications (2)

Publication Number Publication Date
CN112020496A true CN112020496A (zh) 2020-12-01
CN112020496B CN112020496B (zh) 2023-04-28

Family

ID=68239949

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201980026510.7A Active CN112020496B (zh) 2018-04-18 2019-04-18 作为rho激酶抑制剂的苯并吡唑类化合物

Country Status (5)

Country Link
US (1) US11345678B2 (zh)
EP (1) EP3782987A4 (zh)
JP (1) JP7187575B2 (zh)
CN (1) CN112020496B (zh)
WO (1) WO2019201297A1 (zh)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021038419A1 (en) * 2019-08-23 2021-03-04 Insilico Medicine Ip Limited Kinase inhibitors and methods of synthesis and treatment
WO2021073592A1 (zh) * 2019-10-18 2021-04-22 南京明德新药研发有限公司 作为rho激酶抑制剂的苯并吡唑类化合物的盐型、晶型及其制备方法
CN116438175A (zh) * 2020-11-11 2023-07-14 南京明德新药研发有限公司 苯并脲环衍生物及其制备方法和应用
CN113214172A (zh) * 2021-04-25 2021-08-06 西南大学 氟康唑中间体还原胺化产物的制备方法
CN114181139B (zh) * 2021-12-27 2023-12-08 四川仁安药业有限责任公司 一种5-卤代烟酸的合成方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005074643A2 (en) * 2004-01-30 2005-08-18 Smithkline Beecham Corporation Benzamide compounds useful as rock inhibitors

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CR9465A (es) 2005-03-25 2008-06-19 Surface Logix Inc Compuestos mejorados farmacocineticamente
EP1979353A2 (en) 2006-01-19 2008-10-15 OSI Pharmaceuticals, Inc. Fused heterobicyclic kinase inhibitors
WO2008054599A2 (en) 2006-09-27 2008-05-08 Surface Logix, Inc. Rho kinase inhibitors
KR20100032886A (ko) * 2007-06-08 2010-03-26 아보트 러보러터리즈 키나제 억제제로서의 5-헤테로아릴 치환된 인다졸
CN101903349B (zh) * 2007-08-27 2014-01-08 Abbvie德国有限责任两合公司 4-(4-吡啶基)-苯甲酰胺及其作为rock活性调节剂的应用
AU2010222848A1 (en) 2009-03-09 2011-10-20 Surface Logix, Inc. Rho kinase inhibitors
DK2987487T3 (da) * 2009-08-10 2020-12-07 Samumed Llc Indazolinhibitorer af wnt-signalvejen og terapeutiske anvendelser deraf
WO2011050245A1 (en) 2009-10-23 2011-04-28 Yangbo Feng Bicyclic heteroaryls as kinase inhibitors
WO2012135697A2 (en) 2011-03-30 2012-10-04 H. Lee Moffitt Cancer Center & Research Institute Inc. Novel rho kinase inhibitors and methods of use
US9815820B2 (en) 2012-10-05 2017-11-14 Kadmon Corporation, Llc Rho kinase inhibitors
AR094929A1 (es) 2013-02-28 2015-09-09 Bristol Myers Squibb Co Derivados de fenilpirazol como inhibidores potentes de rock1 y rock2
ES2838573T3 (es) 2014-08-21 2021-07-02 Bristol Myers Squibb Co Derivados de benzamida ligados como inhibidores potentes de ROCK
AU2017351216C1 (en) * 2016-10-24 2021-10-14 Translational Drug Development, Llc Amide compounds as kinase inhibitors

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005074643A2 (en) * 2004-01-30 2005-08-18 Smithkline Beecham Corporation Benzamide compounds useful as rock inhibitors

Also Published As

Publication number Publication date
JP2021522201A (ja) 2021-08-30
EP3782987A1 (en) 2021-02-24
JP7187575B2 (ja) 2022-12-12
CN112020496B (zh) 2023-04-28
EP3782987A4 (en) 2021-05-19
US11345678B2 (en) 2022-05-31
WO2019201297A1 (zh) 2019-10-24
US20210371393A1 (en) 2021-12-02

Similar Documents

Publication Publication Date Title
CN113365988B (zh) Shp2抑制剂及其应用
CN112020496A (zh) 作为rho激酶抑制剂的苯并吡唑类化合物
CN103097340B (zh) 治疗活性组合物及其使用方法
JP6419990B2 (ja) ブロモドメイン阻害剤としてのベンゾイミダゾール誘導体
CN113474338A (zh) 吡嗪类衍生物及其在抑制shp2中的应用
JP7012078B2 (ja) 化合物
WO2020011246A1 (zh) 含苯环的化合物、其制备方法及应用
JP2022547952A (ja) Brd9二機能性分解誘導薬及びその使用方法
WO2015124063A1 (zh) 丙肝病毒抑制剂及其制药用途
CN104136411A (zh) 治疗活性化合物及其使用方法
CN115515947B (zh) Shp2抑制剂及其组合物和应用
EP3538528A1 (en) Pyrrole amides as alpha v integrin inhibitors
CN102770425A (zh) 用作β-类胰蛋白酶抑制剂的吲哚基-哌啶基苄胺类化合物
WO2022166890A1 (zh) 取代的哒嗪苯酚类衍生物
CN109311891A (zh) 作为jak抑制剂的吡咯并嘧啶化合物的结晶
TW202227422A (zh) 組織蛋白酶c小分子抑制劑及其醫藥用途
CN113348168A (zh) 杂环衍生物
CN102046618A (zh) 羟基喹喔啉甲酰胺衍生物
CN116768861A (zh) Sos1蛋白降解靶向嵌合体及其组合物、制剂和用途
WO2023072301A1 (zh) 吡唑[3,4-d]嘧啶-3-酮类化合物及其医药用途
CN113698390B (zh) 用作ret激酶抑制剂的化合物及其应用
JP7358372B2 (ja) イミダゾピロロン化合物及びその使用
WO2021110076A1 (zh) 草酰胺类衍生物、其制备方法及其在医药上的应用
WO2020259613A1 (zh) 作为dna-pk抑制剂的喹啉和噌啉衍生物
WO2024067744A1 (zh) 杂环取代喹唑啉及其制备方法和应用

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
REG Reference to a national code

Ref country code: HK

Ref legal event code: DE

Ref document number: 40038573

Country of ref document: HK

GR01 Patent grant
GR01 Patent grant