JP2017528487A5 - - Google Patents
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- JP2017528487A5 JP2017528487A5 JP2017515059A JP2017515059A JP2017528487A5 JP 2017528487 A5 JP2017528487 A5 JP 2017528487A5 JP 2017515059 A JP2017515059 A JP 2017515059A JP 2017515059 A JP2017515059 A JP 2017515059A JP 2017528487 A5 JP2017528487 A5 JP 2017528487A5
- Authority
- JP
- Japan
- Prior art keywords
- oxo
- methyl
- amino
- chloro
- dihydroquinolin
- 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
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- 150000001875 compounds Chemical class 0.000 claims description 52
- 229910052736 halogen Inorganic materials 0.000 claims description 30
- 150000002367 halogens Chemical class 0.000 claims description 25
- 125000000623 heterocyclic group Chemical group 0.000 claims description 22
- 125000001072 heteroaryl group Chemical group 0.000 claims description 21
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- -1 each C 1 -C 6 alkyl Chemical group 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 229910052805 deuterium Inorganic materials 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- DKGZUENOTCHHGB-UHFFFAOYSA-N 5-[(6-chloro-2-oxo-1H-quinolin-3-yl)methylamino]-6-oxo-1H-pyridine-3-carboxylic acid Chemical compound C1=CC2=C(C=C1Cl)C=C(C(=O)N2)CNC3=CC(=CNC3=O)C(=O)O DKGZUENOTCHHGB-UHFFFAOYSA-N 0.000 claims description 2
- HPOPOVVUDKGCAN-LBPRGKRZSA-N CC(C)OC1=CC2=C(C=C1Cl)C=C([C@H](C)NC1=CC=C(C#N)N(C)C1=O)C(=O)N2 Chemical compound CC(C)OC1=CC2=C(C=C1Cl)C=C([C@H](C)NC1=CC=C(C#N)N(C)C1=O)C(=O)N2 HPOPOVVUDKGCAN-LBPRGKRZSA-N 0.000 claims description 2
- VIKJAIUMEYADPO-UHFFFAOYSA-N CC(NC1=CC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)C=C(OCC1CC(F)(F)C1)C(Cl)=C2 Chemical compound CC(NC1=CC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)C=C(OCC1CC(F)(F)C1)C(Cl)=C2 VIKJAIUMEYADPO-UHFFFAOYSA-N 0.000 claims description 2
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- PJBUFTGEHWYEER-AWEZNQCLSA-N C[C@H](NC1=CC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)C=C(OCC1=NC=CC=C1)C(Cl)=C2 Chemical compound C[C@H](NC1=CC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)C=C(OCC1=NC=CC=C1)C(Cl)=C2 PJBUFTGEHWYEER-AWEZNQCLSA-N 0.000 claims description 2
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- ARMGVRSPXQMERQ-VIFPVBQESA-N C[C@H](NC1=CC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)N=CC(Cl)=C2 Chemical compound C[C@H](NC1=CC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)N=CC(Cl)=C2 ARMGVRSPXQMERQ-VIFPVBQESA-N 0.000 claims description 2
- JEDNKDBKPFUMBB-VIFPVBQESA-N C[C@H](NC1=CC=C(C#N)N(C1=O)C(F)(F)F)C1=CC2=C(NC1=O)C=CC(Cl)=C2 Chemical compound C[C@H](NC1=CC=C(C#N)N(C1=O)C(F)(F)F)C1=CC2=C(NC1=O)C=CC(Cl)=C2 JEDNKDBKPFUMBB-VIFPVBQESA-N 0.000 claims description 2
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- GSMIYCKMLOSJBR-JTQLQIEISA-N C[C@H](NC1=CC=C(N2C=NN=N2)N(C)C1=O)C1=CC2=C(NC1=O)C=CC(Cl)=C2 Chemical compound C[C@H](NC1=CC=C(N2C=NN=N2)N(C)C1=O)C1=CC2=C(NC1=O)C=CC(Cl)=C2 GSMIYCKMLOSJBR-JTQLQIEISA-N 0.000 claims description 2
- UXVGPOVENBADCI-VIFPVBQESA-N C[C@H](NC1=CC=C(NC1=O)C#N)C1=CC2=C(NC1=O)C=CC(Cl)=C2 Chemical compound C[C@H](NC1=CC=C(NC1=O)C#N)C1=CC2=C(NC1=O)C=CC(Cl)=C2 UXVGPOVENBADCI-VIFPVBQESA-N 0.000 claims description 2
- UHPKLGPKLHHNCW-VIFPVBQESA-N C[C@H](NC1=NC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)C=CC(Cl)=C2 Chemical compound C[C@H](NC1=NC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)C=CC(Cl)=C2 UHPKLGPKLHHNCW-VIFPVBQESA-N 0.000 claims description 2
- 101100516568 Caenorhabditis elegans nhr-7 gene Proteins 0.000 claims description 2
- MMEAODLKSRHAIR-UHFFFAOYSA-N ClC1=CC2=C(NC(=O)C(CNC3=CC=C(Br)NC3=O)=C2)C=C1 Chemical compound ClC1=CC2=C(NC(=O)C(CNC3=CC=C(Br)NC3=O)=C2)C=C1 MMEAODLKSRHAIR-UHFFFAOYSA-N 0.000 claims description 2
- BJRNSMBACDBVMT-UHFFFAOYSA-N ClC1=CC2=C(NC(=O)C(CNC3=CC=C(NC3=O)C#N)=C2)C=C1 Chemical compound ClC1=CC2=C(NC(=O)C(CNC3=CC=C(NC3=O)C#N)=C2)C=C1 BJRNSMBACDBVMT-UHFFFAOYSA-N 0.000 claims description 2
- SLCDOTDJNCIYCJ-SECBINFHSA-N ClC1=CC=C2NC(C(=NC2=C1)[C@@H](C)NC1=CC=C(N(C1=O)C)C#N)=O Chemical compound ClC1=CC=C2NC(C(=NC2=C1)[C@@H](C)NC1=CC=C(N(C1=O)C)C#N)=O SLCDOTDJNCIYCJ-SECBINFHSA-N 0.000 claims description 2
- GAGJFBRIVDHXBX-UHFFFAOYSA-N ClC=1C=C2C=C(C(NC2=CC=1)=O)CNC=1C(N(C(=CC=1)C(F)(F)F)C)=O Chemical compound ClC=1C=C2C=C(C(NC2=CC=1)=O)CNC=1C(N(C(=CC=1)C(F)(F)F)C)=O GAGJFBRIVDHXBX-UHFFFAOYSA-N 0.000 claims description 2
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- NSSCFMGYDFCYNL-JTQLQIEISA-N ClC=1C=C2C=C(C(NC2=CC=1OC)=O)[C@H](C)NC1=CC=C(N(C1=O)C)C#N Chemical compound ClC=1C=C2C=C(C(NC2=CC=1OC)=O)[C@H](C)NC1=CC=C(N(C1=O)C)C#N NSSCFMGYDFCYNL-JTQLQIEISA-N 0.000 claims description 2
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- UFQKUWOMVVXDCG-VIFPVBQESA-N ClC=1C=C2C=C(C(NC2=NC=1C)=O)[C@H](C)NC1=CC=C(N(C1=O)C)C#N Chemical compound ClC=1C=C2C=C(C(NC2=NC=1C)=O)[C@H](C)NC1=CC=C(N(C1=O)C)C#N UFQKUWOMVVXDCG-VIFPVBQESA-N 0.000 claims description 2
- JOSPMXZAMORKSR-LBPRGKRZSA-N N1(CCC1)C1=C(C=C2C=C(C(NC2=C1)=O)[C@H](C)NC1=CC=C(N(C1=O)C)C#N)Cl Chemical compound N1(CCC1)C1=C(C=C2C=C(C(NC2=C1)=O)[C@H](C)NC1=CC=C(N(C1=O)C)C#N)Cl JOSPMXZAMORKSR-LBPRGKRZSA-N 0.000 claims description 2
- 101710134866 Quinone reductase Proteins 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- RUZLIIJDZBWWSA-INIZCTEOSA-N methyl 2-[[(1s)-1-(7-methyl-2-morpholin-4-yl-4-oxopyrido[1,2-a]pyrimidin-9-yl)ethyl]amino]benzoate Chemical group COC(=O)C1=CC=CC=C1N[C@@H](C)C1=CC(C)=CN2C(=O)C=C(N3CCOCC3)N=C12 RUZLIIJDZBWWSA-INIZCTEOSA-N 0.000 claims description 2
- NEQYWYXGTJDAKR-JTQLQIEISA-N olutasidenib Chemical compound C[C@H](NC1=CC=C(C#N)N(C)C1=O)C1=CC2=C(NC1=O)C=CC(Cl)=C2 NEQYWYXGTJDAKR-JTQLQIEISA-N 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 8
- 201000010099 disease Diseases 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 102000012011 Isocitrate Dehydrogenase Human genes 0.000 description 4
- 108010075869 Isocitrate Dehydrogenase Proteins 0.000 description 4
- 206010028980 Neoplasm Diseases 0.000 description 3
- 201000010915 Glioblastoma multiforme Diseases 0.000 description 2
- 201000003793 Myelodysplastic syndrome Diseases 0.000 description 2
- 208000006990 cholangiocarcinoma Diseases 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 208000005017 glioblastoma Diseases 0.000 description 2
- 201000007450 intrahepatic cholangiocarcinoma Diseases 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- 239000000651 prodrug Substances 0.000 description 2
- 229940002612 prodrug Drugs 0.000 description 2
- 239000012453 solvate Substances 0.000 description 2
- HWXBTNAVRSUOJR-UHFFFAOYSA-N 2-hydroxyglutaric acid Chemical compound OC(=O)C(O)CCC(O)=O HWXBTNAVRSUOJR-UHFFFAOYSA-N 0.000 description 1
- 208000031261 Acute myeloid leukaemia Diseases 0.000 description 1
- SLCDOTDJNCIYCJ-VIFPVBQESA-N C[C@H](NC1=CC=C(C#N)N(C)C1=O)C1=NC2=CC(Cl)=CC=C2NC1=O Chemical compound C[C@H](NC1=CC=C(C#N)N(C)C1=O)C1=NC2=CC(Cl)=CC=C2NC1=O SLCDOTDJNCIYCJ-VIFPVBQESA-N 0.000 description 1
- 208000005243 Chondrosarcoma Diseases 0.000 description 1
- 208000032612 Glial tumor Diseases 0.000 description 1
- 206010018338 Glioma Diseases 0.000 description 1
- 208000014767 Myeloproliferative disease Diseases 0.000 description 1
- 201000007224 Myeloproliferative neoplasm Diseases 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000002489 hematologic effect Effects 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000002626 targeted therapy Methods 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462053006P | 2014-09-19 | 2014-09-19 | |
| US62/053,006 | 2014-09-19 | ||
| US201562128089P | 2015-03-04 | 2015-03-04 | |
| US62/128,089 | 2015-03-04 | ||
| US201562150812P | 2015-04-21 | 2015-04-21 | |
| US62/150,812 | 2015-04-21 | ||
| PCT/US2015/051055 WO2016044789A1 (en) | 2014-09-19 | 2015-09-18 | Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017528487A JP2017528487A (ja) | 2017-09-28 |
| JP2017528487A5 true JP2017528487A5 (cg-RX-API-DMAC10.html) | 2019-10-10 |
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