JP2009532486A5 - - Google Patents
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- Publication number
- JP2009532486A5 JP2009532486A5 JP2009504315A JP2009504315A JP2009532486A5 JP 2009532486 A5 JP2009532486 A5 JP 2009532486A5 JP 2009504315 A JP2009504315 A JP 2009504315A JP 2009504315 A JP2009504315 A JP 2009504315A JP 2009532486 A5 JP2009532486 A5 JP 2009532486A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- alkyl
- heteroaryl
- amino
- tautomer
- 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.)
- Withdrawn
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- -1 carbonylamino, aminocarbonyl Chemical group 0.000 claims description 75
- 125000000217 alkyl group Chemical group 0.000 claims description 54
- 125000001072 heteroaryl group Chemical group 0.000 claims description 53
- 150000001875 compounds Chemical class 0.000 claims description 45
- 150000003839 salts Chemical class 0.000 claims description 45
- 125000000623 heterocyclic group Chemical group 0.000 claims description 34
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 32
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 24
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 22
- 125000005843 halogen group Chemical group 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 18
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 18
- 125000004414 alkyl thio group Chemical group 0.000 claims description 16
- 125000003107 substituted aryl group Chemical group 0.000 claims description 16
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
- 125000002252 acyl group Chemical group 0.000 claims description 10
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 10
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 10
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 10
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 10
- 125000004442 acylamino group Chemical group 0.000 claims description 8
- 125000004423 acyloxy group Chemical group 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 125000004104 aryloxy group Chemical group 0.000 claims description 8
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 8
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 8
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 8
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 8
- 125000003441 thioacyl group Chemical group 0.000 claims description 8
- 150000003573 thiols Chemical class 0.000 claims description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000005338 substituted cycloalkoxy group Chemical group 0.000 claims description 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 0 COC1CCN(*)CC1 Chemical compound COC1CCN(*)CC1 0.000 description 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 1
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 101000600756 Homo sapiens 3-phosphoinositide-dependent protein kinase 1 Proteins 0.000 description 1
- 101001117146 Homo sapiens [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial Proteins 0.000 description 1
- 102100024148 [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial Human genes 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79030406P | 2006-04-06 | 2006-04-06 | |
| PCT/US2007/008592 WO2007117607A2 (en) | 2006-04-06 | 2007-04-05 | Quinazolines for pdk1 inhibition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009532486A JP2009532486A (ja) | 2009-09-10 |
| JP2009532486A5 true JP2009532486A5 (https=) | 2010-03-11 |
Family
ID=38476139
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009504315A Withdrawn JP2009532486A (ja) | 2006-04-06 | 2007-04-05 | Ｐｄｋ１阻害のためのキナゾリン類 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US7932262B2 (https=) |
| EP (1) | EP2004615A2 (https=) |
| JP (1) | JP2009532486A (https=) |
| KR (1) | KR20080111114A (https=) |
| CN (1) | CN101454294A (https=) |
| AR (1) | AR060358A1 (https=) |
| AU (1) | AU2007235339A1 (https=) |
| BR (1) | BRPI0710521A2 (https=) |
| CA (1) | CA2648529A1 (https=) |
| CR (1) | CR10427A (https=) |
| EA (1) | EA200870415A1 (https=) |
| EC (1) | ECSP088823A (https=) |
| GT (1) | GT200800202A (https=) |
| MA (1) | MA30358B1 (https=) |
| MX (1) | MX2008012852A (https=) |
| NO (1) | NO20084665L (https=) |
| PE (1) | PE20080059A1 (https=) |
| SM (1) | SMP200800059B (https=) |
| TN (1) | TNSN08375A1 (https=) |
| TW (1) | TW200808739A (https=) |
| WO (1) | WO2007117607A2 (https=) |
| ZA (1) | ZA200808307B (https=) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2673003A1 (en) * | 2006-12-22 | 2008-07-03 | Novartis Ag | Quinazolines for pdk1 inhibition |
| UY31137A1 (es) * | 2007-06-14 | 2009-01-05 | Smithkline Beecham Corp | Derivados de quinazolina como inhibidores de la pi3 quinasa |
| WO2009007984A2 (en) * | 2007-07-11 | 2009-01-15 | Hetero Drugs Limited | An improved process for erlotinib hydrochloride |
| WO2009084695A1 (ja) | 2007-12-28 | 2009-07-09 | Carna Biosciences Inc. | ２－アミノキナゾリン誘導体 |
| ES2375919T3 (es) * | 2008-01-11 | 2012-03-07 | F. Hoffmann-La Roche Ag | Moduladores de beta-amiloide. |
| EP2269993B1 (en) | 2008-04-23 | 2013-02-27 | Kyowa Hakko Kirin Co., Ltd. | 2-aminoquinazoline derivative |
| GEP20125502B (en) | 2008-05-23 | 2012-04-25 | Novartis Ag | Derivatives of quinolines and quinoxalines as protein tyrosine kinase inhibitors |
| JP5599783B2 (ja) | 2008-05-30 | 2014-10-01 | アムジエン・インコーポレーテツド | Ｐｉ３キナーゼの阻害薬 |
| US20100121052A1 (en) * | 2008-06-20 | 2010-05-13 | Rama Jain | Novel compounds for treating proliferative diseases |
| AU2009334869A1 (en) * | 2008-12-29 | 2011-07-14 | Fovea Pharmaceuticals | Substituted quinazoline compounds |
| KR20130141500A (ko) * | 2010-09-29 | 2013-12-26 | 크리스탈지노믹스(주) | 단백질 키나제 억제 활성을 갖는 신규한 아미노퀴나졸린 화합물 |
| WO2013050527A1 (en) | 2011-10-05 | 2013-04-11 | H. Lundbeck A/S | Quinazoline derivatives as pde10a enzyme inhibitors |
| KR101360948B1 (ko) * | 2012-01-17 | 2014-02-12 | 한국과학기술연구원 | 신규한 2-아미노퀴나졸린 유도체 및 이를 유효성분으로 포함하는 항암제 |
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| AU2014308616B2 (en) * | 2013-08-23 | 2018-12-06 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| EP3078660B1 (en) * | 2013-12-06 | 2022-07-13 | MycHunter Therapeutics, Inc. | Novel quinazoline derivative |
| RU2685234C1 (ru) * | 2013-12-09 | 2019-04-17 | Юсб Байофарма Спрл | Конденсированные бициклические гетероароматические производные в качестве модуляторов активности tnf |
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| JP6752715B2 (ja) | 2014-03-26 | 2020-09-09 | アステックス、セラピューティックス、リミテッドＡｓｔｅｘ Ｔｈｅｒａｐｅｕｔｉｃｓ Ｌｉｍｉｔｅｄ | 組合せ |
| US10047037B2 (en) | 2014-09-01 | 2018-08-14 | Nippon Soda Co., Ltd. | Method for producing 2-amino-substituted benzaldehyde compound |
| ES2735087T3 (es) | 2014-12-24 | 2019-12-16 | Gilead Sciences Inc | Compuestos de pirimidina fusionados para el tratamiento de VIH |
| TWI699355B (zh) | 2014-12-24 | 2020-07-21 | 美商基利科學股份有限公司 | 喹唑啉化合物 |
| BR112017013440A2 (pt) | 2014-12-24 | 2018-01-09 | Gilead Sciences, Inc. | compostos de isoquinolina para o tratamento de hiv |
| TWI719960B (zh) | 2015-02-10 | 2021-03-01 | 英商阿斯迪克治療公司 | 新穎組成物 |
| CN107613769A (zh) * | 2015-02-17 | 2018-01-19 | 润新生物公司 | 某些化学实体、组合物和方法 |
| CN106316965B (zh) * | 2015-07-03 | 2021-08-27 | 上海医药集团股份有限公司 | 喹唑啉类化合物、其中间体、制备方法、药物组合物和应用 |
| KR102591886B1 (ko) * | 2015-07-21 | 2023-10-20 | 광저우 맥시노벨 파마수티컬스 씨오., 엘티디. | 축합고리 피리미딘계 화합물, 중간체, 이의 제조 방법, 조성물 및 응용 |
| JP6821670B2 (ja) * | 2015-10-02 | 2021-01-27 | センティネル・オンコロジー・リミテッドＳｅｎｔｉｎｅｌ Ｏｎｃｏｌｏｇｙ Ｌｉｍｉｔｅｄ | 薬学的化合物 |
| CN105753793B (zh) * | 2016-01-19 | 2018-09-04 | 河北医科大学 | 芳甲酰脲偶联喹唑啉类化合物及其制备方法、药物组合物及药物用途 |
| CN109843858B (zh) | 2016-08-15 | 2023-05-05 | 润新生物公司 | 某些化学实体、组合物及方法 |
| GB201705263D0 (en) * | 2017-03-31 | 2017-05-17 | Probiodrug Ag | Novel inhibitors |
| GB201709840D0 (en) | 2017-06-20 | 2017-08-02 | Inst Of Cancer Research: Royal Cancer Hospital | Methods and medical uses |
| RU2761824C2 (ru) * | 2018-08-03 | 2021-12-13 | Закрытое Акционерное Общество "Биокад" | Ингибиторы CDK8/19 |
| CN110872243B (zh) * | 2018-08-31 | 2023-03-31 | 四川科伦博泰生物医药股份有限公司 | 磺酰胺类化合物、其制备方法及用途 |
| CN109320511A (zh) * | 2018-10-26 | 2019-02-12 | 广安凯特制药有限公司 | 一种高纯度帕博西尼中间体产品及其制备方法 |
| EP4025585A4 (en) * | 2019-06-05 | 2024-01-03 | Advanced technologies for novel therapeutics, LLC | MODIFIED PEPTIDES AND RELATED METHODS OF USE |
| EP4090663A1 (en) * | 2020-01-15 | 2022-11-23 | Blueprint Medicines Corporation | Map4k1 inhibitors |
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| CN114315798B (zh) * | 2020-09-29 | 2025-03-25 | 安思科(苏州)医药科技有限公司 | 喹唑啉类化合物及其药物组合物 |
| US20230406864A1 (en) * | 2020-11-09 | 2023-12-21 | Merck Sharp & Dohme Llc | 7-azole substituted 2-aminoquinazoline inhibitors of hpk1 |
| EP4240363A4 (en) * | 2020-11-09 | 2024-10-23 | Merck Sharp & Dohme LLC | 2-AMINOQUINAZOLINE 7-PHENYL SUBSTITUTED, HPK1 INHIBITORS |
| KR20230160350A (ko) * | 2021-03-24 | 2023-11-23 | 아토스 테라퓨틱스, 인크. | 키나제-관련 질환의 치료를 위한 소분자 |
| WO2022222951A1 (zh) * | 2021-04-22 | 2022-10-27 | 浙江海正药业股份有限公司 | 芳香稠合环类衍生物及其制备方法和用途 |
| CN115583946B (zh) * | 2021-07-06 | 2026-01-16 | 赛诺哈勃药业（成都）有限公司 | 杂环化合物及其作为cdk抑制剂的用途 |
| CN113999206B (zh) * | 2021-12-31 | 2022-04-12 | 北京鑫开元医药科技有限公司 | 异喹啉-1,3-二胺类似物、制备方法、药物组合物及其应用 |
| CN114533733A (zh) * | 2021-12-31 | 2022-05-27 | 北京鑫开元医药科技有限公司 | 一种异喹啉-1,3-二胺类似物药物制剂及其制备方法 |
| WO2023138412A1 (en) * | 2022-01-20 | 2023-07-27 | Insilico Medicine Ip Limited | Fused pyrimidin-2-amine compounds as cdk20 inhibitors |
| CN116514728A (zh) * | 2022-01-28 | 2023-08-01 | 赛诺哈勃药业（成都）有限公司 | 一种喹唑啉衍生物及其用途 |
| CN116672450A (zh) * | 2022-02-23 | 2023-09-01 | 智宠制药（北京）有限公司 | Hpk1抑制剂在治疗干扰素相关疾病中的应用 |
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-
2007
- 2007-04-04 TW TW096112158A patent/TW200808739A/zh unknown
- 2007-04-04 AR ARP070101448A patent/AR060358A1/es unknown
- 2007-04-05 MX MX2008012852A patent/MX2008012852A/es not_active Application Discontinuation
- 2007-04-05 SM SM200800059T patent/SMP200800059B/it unknown
- 2007-04-05 JP JP2009504315A patent/JP2009532486A/ja not_active Withdrawn
- 2007-04-05 AU AU2007235339A patent/AU2007235339A1/en not_active Abandoned
- 2007-04-05 EP EP07755008A patent/EP2004615A2/en not_active Withdrawn
- 2007-04-05 CN CNA2007800195027A patent/CN101454294A/zh active Pending
- 2007-04-05 CA CA002648529A patent/CA2648529A1/en not_active Abandoned
- 2007-04-05 US US12/295,967 patent/US7932262B2/en not_active Expired - Fee Related
- 2007-04-05 BR BRPI0710521-5A patent/BRPI0710521A2/pt not_active IP Right Cessation
- 2007-04-05 KR KR1020087026508A patent/KR20080111114A/ko not_active Withdrawn
- 2007-04-05 EA EA200870415A patent/EA200870415A1/ru unknown
- 2007-04-05 WO PCT/US2007/008592 patent/WO2007117607A2/en not_active Ceased
- 2007-04-09 PE PE2007000418A patent/PE20080059A1/es not_active Application Discontinuation
-
2008
- 2008-09-25 TN TNP2008000375A patent/TNSN08375A1/en unknown
- 2008-09-29 ZA ZA200808307A patent/ZA200808307B/xx unknown
- 2008-10-01 GT GT200800202A patent/GT200800202A/es unknown
- 2008-10-15 EC EC2008008823A patent/ECSP088823A/es unknown
- 2008-10-27 MA MA31336A patent/MA30358B1/fr unknown
- 2008-11-05 CR CR10427A patent/CR10427A/es not_active Application Discontinuation
- 2008-11-05 NO NO20084665A patent/NO20084665L/no not_active Application Discontinuation
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