CA2897200C - Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors - Google Patents
Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors Download PDFInfo
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- CA2897200C CA2897200C CA2897200A CA2897200A CA2897200C CA 2897200 C CA2897200 C CA 2897200C CA 2897200 A CA2897200 A CA 2897200A CA 2897200 A CA2897200 A CA 2897200A CA 2897200 C CA2897200 C CA 2897200C
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- Prior art keywords
- alkyl
- amino
- compound
- pharmaceutically acceptable
- acceptable salt
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- -1 Bicyclic aromatic carboxamide compounds Chemical class 0.000 title claims description 206
- 229940043355 kinase inhibitor Drugs 0.000 title description 6
- 239000003757 phosphotransferase inhibitor Substances 0.000 title description 6
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- 239000000203 mixture Substances 0.000 claims abstract description 317
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 63
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- 201000011510 cancer Diseases 0.000 claims abstract description 22
- 230000000694 effects Effects 0.000 claims abstract description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 213
- 150000003839 salts Chemical class 0.000 claims description 139
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 105
- 125000001424 substituent group Chemical group 0.000 claims description 102
- 229910052736 halogen Inorganic materials 0.000 claims description 99
- 150000002367 halogens Chemical group 0.000 claims description 94
- ZEXKKIXCRDTKBF-UHFFFAOYSA-N quinoline-2-carboxamide Chemical compound C1=CC=CC2=NC(C(=O)N)=CC=C21 ZEXKKIXCRDTKBF-UHFFFAOYSA-N 0.000 claims description 79
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 69
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 64
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 63
- 229910052739 hydrogen Inorganic materials 0.000 claims description 54
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 52
- 229910052757 nitrogen Inorganic materials 0.000 claims description 49
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 48
- 125000003118 aryl group Chemical group 0.000 claims description 39
- 125000004432 carbon atom Chemical group C* 0.000 claims description 38
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 35
- 125000005843 halogen group Chemical group 0.000 claims description 35
- 229910052799 carbon Inorganic materials 0.000 claims description 34
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 32
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 31
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 29
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 28
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 27
- CZWUESRDTYLNDE-UHFFFAOYSA-N (2z)-2-[(2e,4e,6e)-7-[1-(5-carboxypentyl)-3,3-dimethyl-5-sulfoindol-1-ium-2-yl]hepta-2,4,6-trienylidene]-1-ethyl-3,3-dimethylindole-5-sulfonate Chemical compound CC1(C)C2=CC(S([O-])(=O)=O)=CC=C2N(CC)\C1=C/C=C/C=C/C=C/C1=[N+](CCCCCC(O)=O)C2=CC=C(S(O)(=O)=O)C=C2C1(C)C CZWUESRDTYLNDE-UHFFFAOYSA-N 0.000 claims description 24
- 150000001408 amides Chemical class 0.000 claims description 22
- 125000003277 amino group Chemical group 0.000 claims description 21
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- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
- 125000006413 ring segment Chemical group 0.000 claims description 14
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 14
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
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- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 claims description 7
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical class C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 7
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- DXASQZJWWGZNSF-UHFFFAOYSA-N n,n-dimethylmethanamine;sulfur trioxide Chemical group CN(C)C.O=S(=O)=O DXASQZJWWGZNSF-UHFFFAOYSA-N 0.000 claims description 4
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- VMWJCFLUSKZZDX-UHFFFAOYSA-N n,n-dimethylmethanamine Chemical compound [CH2]N(C)C VMWJCFLUSKZZDX-UHFFFAOYSA-N 0.000 claims description 2
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| US201361791275P | 2013-03-15 | 2013-03-15 | |
| US61/791,275 | 2013-03-15 | ||
| PCT/US2014/011487 WO2014110574A1 (en) | 2013-01-14 | 2014-01-14 | Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors |
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| WO2014110574A1 (en) | 2014-07-17 |
| CA2897200A1 (en) | 2014-07-17 |
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| HK1216316A1 (en) | 2016-11-11 |
| JP2016505021A (ja) | 2016-02-18 |
| US20160137626A1 (en) | 2016-05-19 |
| US9676750B2 (en) | 2017-06-13 |
| EP2943485B1 (en) | 2017-09-20 |
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| JP6437452B2 (ja) | 2018-12-12 |
| EP2943485A1 (en) | 2015-11-18 |
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