JP2012512246A - Ｃ環修飾型三環式ベンゾナフチリジノン・タンパク質キナーゼ阻害薬及びこれらの使用 - Google Patents
Ｃ環修飾型三環式ベンゾナフチリジノン・タンパク質キナーゼ阻害薬及びこれらの使用 Download PDFInfo
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- JP2012512246A JP2012512246A JP2011542212A JP2011542212A JP2012512246A JP 2012512246 A JP2012512246 A JP 2012512246A JP 2011542212 A JP2011542212 A JP 2011542212A JP 2011542212 A JP2011542212 A JP 2011542212A JP 2012512246 A JP2012512246 A JP 2012512246A
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- Prior art keywords
- naphthyridin
- phenyl
- oxo
- ylamino
- benzamide
- Prior art date
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- MMQLBTDCVNCJBE-UHFFFAOYSA-N 1h-benzo[b][1,8]naphthyridin-2-one Chemical compound C1=CC=C2N=C(NC(=O)C=C3)C3=CC2=C1 MMQLBTDCVNCJBE-UHFFFAOYSA-N 0.000 title abstract 2
- 239000003909 protein kinase inhibitor Substances 0.000 title description 5
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 194
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 36
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- 102000001253 Protein Kinase Human genes 0.000 claims abstract description 18
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- ZXWWZGRGUXBCPW-UHFFFAOYSA-N 1-chloro-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-6-one Chemical compound C1CCCC2=C1C(=O)NC1=C2C(Cl)=CC=N1 ZXWWZGRGUXBCPW-UHFFFAOYSA-N 0.000 claims description 7
- CLFYTABSRQFXOA-UHFFFAOYSA-N 9-chloro-2-trityl-5h-pyrazolo[3,4-c][1,8]naphthyridin-4-one Chemical compound C1=C2C=3C(Cl)=CC=NC=3NC(=O)C2=NN1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CLFYTABSRQFXOA-UHFFFAOYSA-N 0.000 claims description 7
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- UBOIEMIWOMLCGZ-UHFFFAOYSA-N 9-chloro-5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound C1=2C(Cl)=CC=NC=2NC(=O)C2=C1OC=C2 UBOIEMIWOMLCGZ-UHFFFAOYSA-N 0.000 claims description 6
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- LRAWEULWMCQGQZ-UHFFFAOYSA-N ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexene-1-carboxylate Chemical compound C1CCCC(C(=O)OCC)=C1B1OC(C)(C)C(C)(C)O1 LRAWEULWMCQGQZ-UHFFFAOYSA-N 0.000 claims description 6
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- AGIJDZPJJJSYEC-UHFFFAOYSA-N 1-(3-phenylmethoxyanilino)-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-6-one Chemical compound C=12C=3CCCCC=3C(=O)NC2=NC=CC=1NC(C=1)=CC=CC=1OCC1=CC=CC=C1 AGIJDZPJJJSYEC-UHFFFAOYSA-N 0.000 claims description 5
- DJHCEZMMYXJWCS-UHFFFAOYSA-N 1-[(5-chloro-1,3-benzodioxol-4-yl)amino]-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-6-one Chemical compound C1CCCC2=C1C(=O)NC1=C2C(NC2=C3OCOC3=CC=C2Cl)=CC=N1 DJHCEZMMYXJWCS-UHFFFAOYSA-N 0.000 claims description 5
- DMLGTGVDUXJRNS-UHFFFAOYSA-N 5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound O=C1NC2=NC=CC=C2C2=C1C=CO2 DMLGTGVDUXJRNS-UHFFFAOYSA-N 0.000 claims description 5
- RXERALKQELAEBI-UHFFFAOYSA-N 9-anilino-5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound C=12C=3OC=CC=3C(=O)NC2=NC=CC=1NC1=CC=CC=C1 RXERALKQELAEBI-UHFFFAOYSA-N 0.000 claims description 5
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- DUQUMTYYZAUNHP-UHFFFAOYSA-N ethyl 1-benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2h-pyridine-4-carboxylate Chemical compound C1CC(C(=O)OCC)=C(B2OC(C)(C)C(C)(C)O2)CN1CC1=CC=CC=C1 DUQUMTYYZAUNHP-UHFFFAOYSA-N 0.000 claims description 5
- VWIUHGUFSGOXDX-UHFFFAOYSA-N ethyl 2-(trifluoromethylsulfonyloxy)cyclohexene-1-carboxylate Chemical compound CCOC(=O)C1=C(OS(=O)(=O)C(F)(F)F)CCCC1 VWIUHGUFSGOXDX-UHFFFAOYSA-N 0.000 claims description 5
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- DLHUWEHGSBIDBV-UHFFFAOYSA-N 1-(4-fluorophenyl)-2-oxo-n-[4-[(6-oxo-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-1-yl)oxy]phenyl]pyridine-3-carboxamide Chemical compound C1=CC(F)=CC=C1N1C(=O)C(C(=O)NC=2C=CC(OC=3C=4C=5CCCCC=5C(=O)NC=4N=CC=3)=CC=2)=CC=C1 DLHUWEHGSBIDBV-UHFFFAOYSA-N 0.000 claims description 4
- WOXAGWCPBCMTSR-UHFFFAOYSA-N 1-[5-tert-butyl-2-(3-methylphenyl)pyrazol-3-yl]-3-[4-[(6-oxo-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-1-yl)oxy]phenyl]urea Chemical compound CC1=CC=CC(N2C(=CC(=N2)C(C)(C)C)NC(=O)NC=2C=CC(OC=3C=4C=5CCCCC=5C(=O)NC=4N=CC=3)=CC=2)=C1 WOXAGWCPBCMTSR-UHFFFAOYSA-N 0.000 claims description 4
- RSIUBFJHQIJBIQ-UHFFFAOYSA-N 1-[[4-[1-(4-fluorophenyl)-2-oxopyridine-3-carbonyl]-2,3-dihydro-1,4-benzoxazin-7-yl]oxy]-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-6-one Chemical compound C1=CC(F)=CC=C1N1C(=O)C(C(=O)N2C3=CC=C(OC=4C=5C=6CCCCC=6C(=O)NC=5N=CC=4)C=C3OCC2)=CC=C1 RSIUBFJHQIJBIQ-UHFFFAOYSA-N 0.000 claims description 4
- KQHDEZLGUZPPLF-UHFFFAOYSA-N 1-o-tert-butyl 4-o-ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2h-pyridine-1,4-dicarboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCC(C(=O)OCC)=C1B1OC(C)(C)C(C)(C)O1 KQHDEZLGUZPPLF-UHFFFAOYSA-N 0.000 claims description 4
- VOAVTORWJQDFET-UHFFFAOYSA-N 1-o-tert-butyl 5-o-ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2h-pyridine-1,5-dicarboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CC(C(=O)OCC)=C1B1OC(C)(C)C(C)(C)O1 VOAVTORWJQDFET-UHFFFAOYSA-N 0.000 claims description 4
- QBSFHOMPPMKXAV-UHFFFAOYSA-N 1-o-tert-butyl 5-o-ethyl 4-(trifluoromethylsulfonyloxy)-3,6-dihydro-2h-pyridine-1,5-dicarboxylate Chemical compound CCOC(=O)C1=C(OS(=O)(=O)C(F)(F)F)CCN(C(=O)OC(C)(C)C)C1 QBSFHOMPPMKXAV-UHFFFAOYSA-N 0.000 claims description 4
- VYDLSGISEVNDKY-UHFFFAOYSA-N 1-quinolin-7-yloxy-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-6-one Chemical compound C1CCCC2=C1C1=C(OC=3C=C4N=CC=CC4=CC=3)C=CN=C1NC2=O VYDLSGISEVNDKY-UHFFFAOYSA-N 0.000 claims description 4
- CBQGQPAZGVWOOH-UHFFFAOYSA-N 2-bromo-5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound C12=CC=CN=C2NC(=O)C2=C1OC(Br)=C2 CBQGQPAZGVWOOH-UHFFFAOYSA-N 0.000 claims description 4
- KVSQFHQIORLIBZ-UHFFFAOYSA-N 2-fluoro-n-[4-[(6-oxo-7,8,9,10-tetrahydro-5h-benzo[c][1,8]naphthyridin-1-yl)amino]phenyl]-3-(trifluoromethyl)benzamide Chemical compound C1=CC=C(C(F)(F)F)C(F)=C1C(=O)NC(C=C1)=CC=C1NC1=CC=NC2=C1C(CCCC1)=C1C(=O)N2 KVSQFHQIORLIBZ-UHFFFAOYSA-N 0.000 claims description 4
- IJYXPNAXRVDKHS-UHFFFAOYSA-N 5h-thieno[3,2-c][1,8]naphthyridin-4-one Chemical compound O=C1NC2=NC=CC=C2C2=C1C=CS2 IJYXPNAXRVDKHS-UHFFFAOYSA-N 0.000 claims description 4
- XGAUPBFYMFAJIS-UHFFFAOYSA-N 9-(3-chloroanilino)-5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound ClC1=CC=CC(NC=2C=3C=4OC=CC=4C(=O)NC=3N=CC=2)=C1 XGAUPBFYMFAJIS-UHFFFAOYSA-N 0.000 claims description 4
- MCSXIEVZQSGRJD-UHFFFAOYSA-N 9-(3-methoxyanilino)-5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound COC1=CC=CC(NC=2C=3C=4OC=CC=4C(=O)NC=3N=CC=2)=C1 MCSXIEVZQSGRJD-UHFFFAOYSA-N 0.000 claims description 4
- WJTJBXCCDALTRN-UHFFFAOYSA-N 9-(4-chloroanilino)-5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound C1=CC(Cl)=CC=C1NC1=CC=NC2=C1C(OC=C1)=C1C(=O)N2 WJTJBXCCDALTRN-UHFFFAOYSA-N 0.000 claims description 4
- IGXYKNFZOKAVJY-UHFFFAOYSA-N 9-(4-methoxyanilino)-5h-furo[3,2-c][1,8]naphthyridin-4-one Chemical compound C1=CC(OC)=CC=C1NC1=CC=NC2=C1C(OC=C1)=C1C(=O)N2 IGXYKNFZOKAVJY-UHFFFAOYSA-N 0.000 claims description 4
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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Landscapes
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| HRP20181310T1 (hr) | 2011-09-30 | 2018-10-19 | C&C Research Laboratories | Novi heterociklički derivati i njihova uporaba |
| DK3067358T3 (da) | 2012-12-21 | 2019-11-04 | Gilead Sciences Inc | Polycykliske carbamoylpyridon-forbindelser og deres farmaceutiske anvendelse |
| TWI695003B (zh) | 2014-12-23 | 2020-06-01 | 美商基利科學股份有限公司 | 多環胺甲醯基吡啶酮化合物及其醫藥用途 |
| CN115611896A (zh) * | 2021-07-16 | 2023-01-17 | 中国药科大学 | 含四氢萘啶酮或四氢吡啶并嘧啶酮骨架的化合物及其制备方法与制药用途 |
Citations (5)
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|---|---|---|---|---|
| JPS6034967A (ja) * | 1983-05-31 | 1985-02-22 | シエリング・コーポレーシヨン | ナフチリジノン，ピリドンおよびキノロンの融合三環式誘導体ならびに対応するチオン類 |
| US20060035920A1 (en) * | 2004-05-28 | 2006-02-16 | Millennium Pharmaceuticals, Inc. | Chk-1 inhibitors |
| WO2007015837A2 (en) * | 2005-07-22 | 2007-02-08 | Merck & Co., Inc. | Inhibitors of checkpoint kinases |
| WO2008028168A2 (en) * | 2006-09-01 | 2008-03-06 | Cylene Pharmaceuticals, Inc. | Serine-threonine protein kinase and parp modulators |
| JP2011513322A (ja) * | 2008-02-28 | 2011-04-28 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | プロテイン・キナーゼ阻害剤とその利用法 |
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| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
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- 2009-12-02 WO PCT/US2009/066319 patent/WO2010077530A1/en not_active Ceased
- 2009-12-02 CA CA2745071A patent/CA2745071C/en not_active Expired - Fee Related
- 2009-12-02 US US13/140,090 patent/US9938268B2/en not_active Expired - Fee Related
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2011
- 2011-06-16 IL IL213588A patent/IL213588A0/en unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| EP2367821A1 (en) | 2011-09-28 |
| EP2367821B1 (en) | 2015-09-16 |
| IL213588A0 (en) | 2011-07-31 |
| ES2550101T3 (es) | 2015-11-04 |
| JP2015163653A (ja) | 2015-09-10 |
| WO2010077530A1 (en) | 2010-07-08 |
| CA2745071C (en) | 2018-08-28 |
| US9938268B2 (en) | 2018-04-10 |
| CA2745071A1 (en) | 2010-07-08 |
| US20110312951A1 (en) | 2011-12-22 |
| AU2009333653A1 (en) | 2011-06-30 |
| AU2009333653B2 (en) | 2015-09-10 |
| JP6378138B2 (ja) | 2018-08-22 |
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