JP2016523963A5 - - Google Patents
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- Publication number
- JP2016523963A5 JP2016523963A5 JP2016525377A JP2016525377A JP2016523963A5 JP 2016523963 A5 JP2016523963 A5 JP 2016523963A5 JP 2016525377 A JP2016525377 A JP 2016525377A JP 2016525377 A JP2016525377 A JP 2016525377A JP 2016523963 A5 JP2016523963 A5 JP 2016523963A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- oxazol
- methoxy
- amino
- alkyl
- 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.)
- Pending
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- 125000000217 alkyl group Chemical group 0.000 claims 62
- 239000001257 hydrogen Substances 0.000 claims 34
- 229910052739 hydrogen Inorganic materials 0.000 claims 34
- 125000005843 halogen group Chemical group 0.000 claims 32
- -1 3-methoxy-4- (oxazol-5-yl) phenyl Chemical group 0.000 claims 18
- 150000002431 hydrogen Chemical class 0.000 claims 18
- 125000003545 alkoxy group Chemical group 0.000 claims 17
- 125000000623 heterocyclic group Chemical group 0.000 claims 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 15
- 150000003839 salts Chemical class 0.000 claims 11
- 239000011780 sodium chloride Substances 0.000 claims 11
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 9
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 9
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 8
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 7
- 125000003277 amino group Chemical group 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 6
- IPWFJLQDVFKJDU-UHFFFAOYSA-N pentanamide Chemical compound CCCCC(N)=O IPWFJLQDVFKJDU-UHFFFAOYSA-N 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 125000004433 nitrogen atoms Chemical group N* 0.000 claims 4
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims 3
- 125000003282 alkyl amino group Chemical group 0.000 claims 3
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 3
- 125000004043 oxo group Chemical group O=* 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- 208000004296 Neuralgia Diseases 0.000 claims 2
- 208000002193 Pain Diseases 0.000 claims 2
- 125000004429 atoms Chemical group 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- GCTFTMWXZFLTRR-GFCCVEGCSA-N (2R)-2-amino-N-[3-(difluoromethoxy)-4-(1,3-oxazol-5-yl)phenyl]-4-methylpentanamide Chemical compound FC(F)OC1=CC(NC(=O)[C@H](N)CC(C)C)=CC=C1C1=CN=CO1 GCTFTMWXZFLTRR-GFCCVEGCSA-N 0.000 claims 1
- 206010001897 Alzheimer's disease Diseases 0.000 claims 1
- 206010004938 Bipolar disease Diseases 0.000 claims 1
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- NNTQFSCEOOALNU-UHFFFAOYSA-N CC(C)CC(N)C(=O)Nc1ccc(-c2cn[nH]c2)c(OC(F)F)c1 Chemical compound CC(C)CC(N)C(=O)Nc1ccc(-c2cn[nH]c2)c(OC(F)F)c1 NNTQFSCEOOALNU-UHFFFAOYSA-N 0.000 claims 1
- RWEDLJNZVWUSIL-UHFFFAOYSA-N CC(C)CC(N)C(=O)Nc1ccc(-c2cnco2)c(c1)N(C)C Chemical compound CC(C)CC(N)C(=O)Nc1ccc(-c2cnco2)c(c1)N(C)C RWEDLJNZVWUSIL-UHFFFAOYSA-N 0.000 claims 1
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- CXLFHMWVLCIDID-UHFFFAOYSA-N COc1cc(NC(=O)C(CC(C)C)NC2CNC2)ccc1-c1cnco1 Chemical compound COc1cc(NC(=O)C(CC(C)C)NC2CNC2)ccc1-c1cnco1 CXLFHMWVLCIDID-UHFFFAOYSA-N 0.000 claims 1
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- DJCYAXSHHCNYJO-UHFFFAOYSA-N COc1cc(NC(=O)C(N)CC(C)(C)C)c(F)cc1-c1cnco1 Chemical compound COc1cc(NC(=O)C(N)CC(C)(C)C)c(F)cc1-c1cnco1 DJCYAXSHHCNYJO-UHFFFAOYSA-N 0.000 claims 1
- PDVKHILCGNDSQD-UHFFFAOYSA-N COc1cc(NC(=O)C(N)CC(C)(C)F)ccc1-c1cnco1 Chemical compound COc1cc(NC(=O)C(N)CC(C)(C)F)ccc1-c1cnco1 PDVKHILCGNDSQD-UHFFFAOYSA-N 0.000 claims 1
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| MX2016012829A (es) | 2014-04-02 | 2017-01-05 | Bristol Myers Squibb Co | Inhibidores de biaril cinasa. |
| EP3356330B1 (en) | 2015-10-01 | 2019-11-20 | Bristol-Myers Squibb Company | Biaryl kinase inhibitors |
| CN112142655A (zh) | 2015-10-01 | 2020-12-29 | 百时美施贵宝公司 | 联芳基激酶抑制剂 |
| KR20210108416A (ko) | 2018-12-19 | 2021-09-02 | 레오 파마 에이/에스 | Il-17의 소분자 조절제로서의 아미노산 아닐라이드 |
| CN116209664A (zh) * | 2020-06-12 | 2023-06-02 | 利奥制药有限公司 | Il-17的小分子调节剂 |
| CN112266328B (zh) * | 2020-12-09 | 2023-11-03 | 郑州萃智医药科技有限公司 | 3-氟-4-硝基苯甲醛的合成路线及制备方法 |
| CN113321577A (zh) * | 2021-06-28 | 2021-08-31 | 上海立科化学科技有限公司 | 5-溴-2-氯苯甲酸的制备方法 |
| WO2023220967A1 (en) * | 2022-05-18 | 2023-11-23 | Anheart Therapeutics (Hangzhou) Co., Ltd. | Method for producing 3,6-disubstituted-imidazo[1,2-b]pyridazine compounds |
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| WO2003086325A2 (en) | 2002-04-05 | 2003-10-23 | Boehringer Ingelheim Pharmaceuticals, Inc. | Cyanamides useful as reversible inhibitors of cysteine proteases |
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| WO2004072018A1 (ja) | 2003-02-12 | 2004-08-26 | Takeda Pharmaceutical Company Limited | アミン誘導体 |
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| CN100494167C (zh) | 2005-08-02 | 2009-06-03 | 天津大学 | 抗乙肝病毒的叔胺氧化物及制备方法和制备药物的应用 |
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| US7723336B2 (en) | 2005-09-22 | 2010-05-25 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
| JP2007217408A (ja) | 2006-01-19 | 2007-08-30 | Tanabe Seiyaku Co Ltd | 医薬組成物 |
| SI2674428T1 (sl) | 2006-04-07 | 2016-07-29 | Vertex Pharmaceuticals Incorporated | Modulatorji transporterjev atp-vezavne kasete |
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| US20110038835A1 (en) * | 2007-12-21 | 2011-02-17 | The Scripps Research Institute | Anilides and analogs as rho kinase inhibitors |
| EP2149565A1 (de) | 2008-07-24 | 2010-02-03 | Bayer Schering Pharma AG | Sulfonsubstituierte Chinazolinderivate als Immunmodulatoren zur Behandlung von enzündlichen und allergischen Erkrankungen |
| CA2765012A1 (en) | 2009-07-06 | 2011-01-13 | Syngenta Participations Ag | Insecticidal compounds |
| US8497271B2 (en) | 2009-10-07 | 2013-07-30 | Bristol-Myers Squibb Company | Modulators of G protein-coupled receptor 88 |
| US8304577B2 (en) | 2009-10-09 | 2012-11-06 | Bristol-Myers Squibb Company | Modulators of G protein-coupled receptor 88 |
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| EP2552922A1 (en) * | 2010-03-31 | 2013-02-06 | Bristol-Myers Squibb Company | Substituted pyrrolotriazines as protein kinase inhibitors |
| US8703953B2 (en) | 2012-03-09 | 2014-04-22 | Bristol-Myers Squibb Company | Aryl ether-base kinase inhibitors |
| US20140080834A1 (en) | 2012-03-09 | 2014-03-20 | Thomas Herbert Lanthorn | Inhibition of adaptor associated kinase 1 for the treatment of pain |
| US8901305B2 (en) | 2012-07-31 | 2014-12-02 | Bristol-Myers Squibb Company | Aryl lactam kinase inhibitors |
| CN105121445A (zh) | 2013-02-22 | 2015-12-02 | 百时美施贵宝公司 | 作为连接蛋白相关激酶1(AAK1)抑制剂的5H-色烯并[3,4-c]吡啶 |
| WO2015026574A1 (en) | 2013-08-20 | 2015-02-26 | Bristol-Myers Squibb Company | Imidazopyridazine kinase inhibitors useful to treating a disease or disorder mediated by aak1, such as alzheimer's disease, bipolar disorder, pain, schizophrenia |
| EA029744B1 (ru) | 2013-09-11 | 2018-05-31 | Бристол-Майерс Сквибб Компани | Ингибиторы киназ на основе простых ариловых эфиров |
| ES2693771T3 (es) | 2014-01-29 | 2018-12-13 | Bristol-Myers Squibb Company | Inhibidores de aril lactama quinasa |
| ES2701903T3 (es) | 2014-01-31 | 2019-02-26 | Bristol Myers Squibb Co | Inhibidores de cinasa a base de quinolina |
| MX2016012829A (es) | 2014-04-02 | 2017-01-05 | Bristol Myers Squibb Co | Inhibidores de biaril cinasa. |
| EP3177604A1 (en) | 2014-08-05 | 2017-06-14 | Bristol-Myers Squibb Company | Heterocyclic kinase inhibitors |
| EP3200797A1 (en) | 2014-09-30 | 2017-08-09 | Bristol-Myers Squibb Company | Quinazoline-based kinase inhibitors |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7383598B2 (ja) | 2017-07-21 | 2023-11-20 | カドモン コーポレイション，リミティド ライアビリティ カンパニー | Ｒｈｏ関連コイルドコイル含有プロテインキナーゼの阻害剤 |
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