TWI485146B - Novel piperidine compounds or salts thereof - Google Patents
Novel piperidine compounds or salts thereof Download PDFInfo
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- TWI485146B TWI485146B TW102106767A TW102106767A TWI485146B TW I485146 B TWI485146 B TW I485146B TW 102106767 A TW102106767 A TW 102106767A TW 102106767 A TW102106767 A TW 102106767A TW I485146 B TWI485146 B TW I485146B
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- methyl
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- 150000003839 salts Chemical class 0.000 title claims description 55
- 150000003053 piperidines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 210
- -1 piperidine compound Chemical class 0.000 claims description 74
- 239000000556 agonist Substances 0.000 claims description 42
- 102000029749 Microtubule Human genes 0.000 claims description 41
- 108091022875 Microtubule Proteins 0.000 claims description 41
- 210000004688 microtubule Anatomy 0.000 claims description 41
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 39
- 125000001424 substituent group Chemical group 0.000 claims description 36
- 230000000259 anti-tumor effect Effects 0.000 claims description 33
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 26
- 239000002246 antineoplastic agent Substances 0.000 claims description 24
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 23
- 229910052731 fluorine Inorganic materials 0.000 claims description 21
- 125000001153 fluoro group Chemical group F* 0.000 claims description 21
- 229910052801 chlorine Inorganic materials 0.000 claims description 19
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 19
- CKJNUZNMWOVDFN-UHFFFAOYSA-N methanone Chemical compound O=[CH-] CKJNUZNMWOVDFN-UHFFFAOYSA-N 0.000 claims description 18
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 15
- 125000005843 halogen group Chemical group 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 13
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 13
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 12
- 239000003623 enhancer Substances 0.000 claims description 11
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical group C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims description 10
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 9
- SRJOCJYGOFTFLH-UHFFFAOYSA-N isonipecotic acid Chemical compound OC(=O)C1CCNCC1 SRJOCJYGOFTFLH-UHFFFAOYSA-N 0.000 claims description 9
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 8
- 125000002393 azetidinyl group Chemical group 0.000 claims description 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 7
- 229940124639 Selective inhibitor Drugs 0.000 claims description 7
- 125000002720 diazolyl group Chemical group 0.000 claims description 7
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 239000012830 cancer therapeutic Substances 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 229940124597 therapeutic agent Drugs 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 3
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical group C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims description 3
- BMILXMRPPSTLQP-UHFFFAOYSA-N ClC=1C(=C(C(C2=CC=CC=C2)N2CCC(CC2)(C(=O)O)CC2=NC(=C(C=C2)F)NC2=NNC=C2)C=CC1)F Chemical compound ClC=1C(=C(C(C2=CC=CC=C2)N2CCC(CC2)(C(=O)O)CC2=NC(=C(C=C2)F)NC2=NNC=C2)C=CC1)F BMILXMRPPSTLQP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 3
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 claims 2
- 125000001781 1,3,4-oxadiazolyl group Chemical group 0.000 claims 1
- VEASMXJHQLRFHB-UHFFFAOYSA-N ClC=1C(=C(C(C2=CC=CC=C2)N2CCC(CC2)(C(=O)O)CC2=NC(=C(C=C2)F)NC2=NNC(=C2)C)C=CC1)F Chemical compound ClC=1C(=C(C(C2=CC=CC=C2)N2CCC(CC2)(C(=O)O)CC2=NC(=C(C=C2)F)NC2=NNC(=C2)C)C=CC1)F VEASMXJHQLRFHB-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 111
- 238000000034 method Methods 0.000 description 60
- 238000006243 chemical reaction Methods 0.000 description 42
- 238000000746 purification Methods 0.000 description 40
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- 238000003786 synthesis reaction Methods 0.000 description 27
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- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 26
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- 230000000704 physical effect Effects 0.000 description 23
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- 239000005441 aurora Substances 0.000 description 22
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- 210000004027 cell Anatomy 0.000 description 21
- 238000004519 manufacturing process Methods 0.000 description 21
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- 230000000694 effects Effects 0.000 description 19
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- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
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- 230000005764 inhibitory process Effects 0.000 description 18
- 239000003795 chemical substances by application Substances 0.000 description 17
- 238000002425 crystallisation Methods 0.000 description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 16
- 230000008025 crystallization Effects 0.000 description 16
- 238000000926 separation method Methods 0.000 description 16
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 15
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- 238000004587 chromatography analysis Methods 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 15
- 238000000638 solvent extraction Methods 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 14
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- DKPFODGZWDEEBT-QFIAKTPHSA-N taxane Chemical class C([C@]1(C)CCC[C@@H](C)[C@H]1C1)C[C@H]2[C@H](C)CC[C@@H]1C2(C)C DKPFODGZWDEEBT-QFIAKTPHSA-N 0.000 description 14
- 239000002585 base Substances 0.000 description 13
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 12
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- RQCNHUCCQJMSRG-UHFFFAOYSA-N tert-butyl piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1 RQCNHUCCQJMSRG-UHFFFAOYSA-N 0.000 description 1
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| TWI485146B (zh) * | 2012-02-29 | 2015-05-21 | Taiho Pharmaceutical Co Ltd | Novel piperidine compounds or salts thereof |
| US9012475B2 (en) | 2013-08-27 | 2015-04-21 | Taiho Pharmaceutical Co., Ltd. | Method for enhancing anti-tumor effect of a microtubule-targeting drug, and a method for treatment of tumor |
| KR101430209B1 (ko) * | 2014-03-06 | 2014-08-14 | 강원대학교산학협력단 | 단백질 키나아제 활성 측정 방법 및 이를 위한 키트 |
| TWI693218B (zh) * | 2014-11-14 | 2020-05-11 | 美商美國禮來大藥廠 | 極光ａ激酶抑制劑 |
| CN104758286B (zh) * | 2015-03-05 | 2016-09-14 | 南京工业大学 | 1-苄基-4-(2,4-二氯苯乙胺基)哌啶在制备抗肿瘤药物中的应用 |
| JP6937322B2 (ja) * | 2016-12-22 | 2021-09-22 | 大鵬薬品工業株式会社 | 置換ピペリジン化合物の塩 |
| WO2019230679A1 (ja) | 2018-05-29 | 2019-12-05 | 大鵬薬品工業株式会社 | 抗腫瘍剤及び腫瘍治療方法 |
| CN112239465A (zh) | 2019-07-16 | 2021-01-19 | 微境生物医药科技(上海)有限公司 | 极光激酶抑制剂及其用途 |
| CN112898292A (zh) * | 2019-12-03 | 2021-06-04 | 微境生物医药科技(上海)有限公司 | 新型极光激酶抑制剂及其用途 |
| TWI785474B (zh) * | 2020-01-22 | 2022-12-01 | 大陸商北京加科思新藥研發有限公司 | 用作選擇性Aurora A抑制劑的新型雜環化合物 |
| TW202321215A (zh) * | 2021-07-28 | 2023-06-01 | 大陸商北京加科思新藥研發有限公司 | Aurora a 選擇性抑制劑的多晶型及其用途 |
| EP4504209A1 (en) | 2022-04-08 | 2025-02-12 | Eli Lilly and Company | Method of treatment including kras g12c inhibitors and aurora a inhibitors |
| WO2024088193A1 (en) * | 2022-10-26 | 2024-05-02 | Js Innopharm (Suzhou) Ltd. | Combination of aurora a and parp inhibitors for treatment of cancers |
| WO2024088192A1 (en) * | 2022-10-26 | 2024-05-02 | Js Innopharm (Suzhou) Ltd. | An aurora a inhibitor for use in treatments of cancers |
| CN121039117A (zh) * | 2023-05-05 | 2025-11-28 | 苏州信诺维医药科技股份有限公司 | 杂环类化合物、其药物组合物和其应用 |
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| WO2009104802A1 (en) * | 2008-02-22 | 2009-08-27 | Banyu Pharmaceutical Co., Ltd. | Novel aminopyridine derivatives having aurora a selective inhibitory action |
| CN101528731A (zh) * | 2006-08-31 | 2009-09-09 | 万有制药株式会社 | 具有AuroraA选择性抑制作用的新型氨基吡啶衍生物 |
| WO2010111050A1 (en) * | 2009-03-23 | 2010-09-30 | Banyu Pharmaceutical Co., Ltd. | Novel aminopyridine derivatives having aurora a selective inhibitory action |
| WO2010111056A1 (en) * | 2009-03-24 | 2010-09-30 | Banyu Pharmaceutical Co., Ltd. | Novel aminopyridine derivatives having aurora a selective inhibitory action |
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| EP1345925B1 (en) * | 2000-12-21 | 2006-05-17 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| SE0302486D0 (sv) | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
| AU2005297848B2 (en) * | 2004-10-29 | 2011-03-17 | Msd K.K. | Novel aminopyridine derivatives having selective Aurora-A inhibitory effect |
| GB0509227D0 (en) * | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Intracellular enzyme inhibitors |
| CA2619517A1 (en) | 2005-08-18 | 2007-02-22 | Michael Mortimore | Pyrazine kinase inhibitors |
| EP1917258A2 (en) * | 2005-08-26 | 2008-05-07 | SmithKline Beecham Corporation | Pyrimidinyl-pyrazole inhibitors of aurora kinases |
| WO2007041358A2 (en) | 2005-09-30 | 2007-04-12 | Miikana Therapeutics, Inc. | Substituted pyrazole compounds |
| CA2645728A1 (en) * | 2006-03-20 | 2007-09-27 | Edward Boyd (Deceased) | Phthalazinone pyrazole derivatives, their manufacture and use as pharmaceutical agents |
| CA2645583A1 (en) | 2006-03-20 | 2007-09-27 | F. Hoffman-La Roche Ag | Methods of inhibiting btk and syk protein kinases |
| GB0705656D0 (en) | 2007-03-23 | 2007-05-02 | Addex Pharmaceuticals Sa | Novel compounds E1 |
| AU2008266960A1 (en) | 2007-06-20 | 2008-12-24 | Merck Sharp & Dohme Corp. | Diphenyl substituted alkanes |
| TWI485146B (zh) * | 2012-02-29 | 2015-05-21 | Taiho Pharmaceutical Co Ltd | Novel piperidine compounds or salts thereof |
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2013
- 2013-02-26 TW TW102106767A patent/TWI485146B/zh active
- 2013-02-27 KR KR1020147023717A patent/KR101677823B1/ko active Active
- 2013-02-27 PT PT137552295T patent/PT2821406T/pt unknown
- 2013-02-27 HU HUE13755229A patent/HUE028495T2/hu unknown
- 2013-02-27 US US14/381,814 patent/US9346787B2/en active Active
- 2013-02-27 MY MYPI2014702424A patent/MY169179A/en unknown
- 2013-02-27 SG SG11201405318PA patent/SG11201405318PA/en unknown
- 2013-02-27 IN IN7283DEN2014 patent/IN2014DN07283A/en unknown
- 2013-02-27 AU AU2013227024A patent/AU2013227024B2/en active Active
- 2013-02-27 EP EP13755229.5A patent/EP2821406B1/en active Active
- 2013-02-27 DK DK13755229.5T patent/DK2821406T3/en active
- 2013-02-27 PL PL13755229.5T patent/PL2821406T3/pl unknown
- 2013-02-27 CN CN201380011842.0A patent/CN104159893B/zh active Active
- 2013-02-27 MX MX2014010395A patent/MX344276B/es active IP Right Grant
- 2013-02-27 ES ES13755229.5T patent/ES2576497T3/es active Active
- 2013-02-27 JP JP2013523421A patent/JP5323289B1/ja active Active
- 2013-02-27 WO PCT/JP2013/055064 patent/WO2013129443A1/ja not_active Ceased
- 2013-02-27 BR BR112014021519-7A patent/BR112014021519B1/pt active IP Right Grant
- 2013-02-27 CA CA2865875A patent/CA2865875C/en active Active
- 2013-02-27 RU RU2014138987/04A patent/RU2581834C1/ru active
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2016
- 2016-04-18 US US15/131,372 patent/US10092556B2/en active Active
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2018
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101528731A (zh) * | 2006-08-31 | 2009-09-09 | 万有制药株式会社 | 具有AuroraA选择性抑制作用的新型氨基吡啶衍生物 |
| WO2009104802A1 (en) * | 2008-02-22 | 2009-08-27 | Banyu Pharmaceutical Co., Ltd. | Novel aminopyridine derivatives having aurora a selective inhibitory action |
| WO2010111050A1 (en) * | 2009-03-23 | 2010-09-30 | Banyu Pharmaceutical Co., Ltd. | Novel aminopyridine derivatives having aurora a selective inhibitory action |
| WO2010111056A1 (en) * | 2009-03-24 | 2010-09-30 | Banyu Pharmaceutical Co., Ltd. | Novel aminopyridine derivatives having aurora a selective inhibitory action |
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