SG192944A1 - Triazolopyridine compounds as pim kinase inhibitors - Google Patents

Info

Publication number

SG192944A1

SG192944A1 SG2013064324A SG2013064324A SG192944A1 SG 192944 A1 SG192944 A1 SG 192944A1 SG 2013064324 A SG2013064324 A SG 2013064324A SG 2013064324 A SG2013064324 A SG 2013064324A SG 192944 A1 SG192944 A1 SG 192944A1

Authority

SG

Singapore

Prior art keywords

alkyl

alkoxy

formula

compound

methyl

Prior art date

2011-02-25

Links

• Espacenet
• Global Dossier
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• 150000008523 triazolopyridines Chemical class 0.000 title description 3
• 229940043355 kinase inhibitor Drugs 0.000 title description 2
• 239000003757 phosphotransferase inhibitor Substances 0.000 title description 2
• 150000001875 compounds Chemical class 0.000 claims abstract description 246
• 101001001642 Xenopus laevis Serine/threonine-protein kinase pim-3 Proteins 0.000 claims abstract description 40
• 238000011282 treatment Methods 0.000 claims abstract description 34
• 101100297651 Mus musculus Pim2 gene Proteins 0.000 claims abstract description 26
• 101100297652 Coturnix japonica PIM3 gene Proteins 0.000 claims abstract description 24
• 230000001404 mediated effect Effects 0.000 claims abstract description 17
• 108091000080 Phosphotransferase Proteins 0.000 claims abstract description 6
• 102000020233 phosphotransferase Human genes 0.000 claims abstract description 6
• 125000000217 alkyl group Chemical group 0.000 claims description 364
• -1 tetrahydropyranyloxy Chemical group 0.000 claims description 279
• 125000003545 alkoxy group Chemical group 0.000 claims description 247
• 238000002360 preparation method Methods 0.000 claims description 213
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 155
• 239000000203 mixture Substances 0.000 claims description 101
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 88
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 82
• 238000006243 chemical reaction Methods 0.000 claims description 78
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 60
• 229910052739 hydrogen Inorganic materials 0.000 claims description 60
• 238000000034 method Methods 0.000 claims description 58
• 125000001153 fluoro group Chemical group F* 0.000 claims description 57
• 229910052736 halogen Inorganic materials 0.000 claims description 40
• 150000002367 halogens Chemical class 0.000 claims description 40
• 206010028980 Neoplasm Diseases 0.000 claims description 36
• 239000002585 base Substances 0.000 claims description 35
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 35
• PQIOSYKVBBWRRI-UHFFFAOYSA-N methylphosphonyl difluoride Chemical group CP(F)(F)=O PQIOSYKVBBWRRI-UHFFFAOYSA-N 0.000 claims description 34
• 150000003839 salts Chemical class 0.000 claims description 34
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 32
• 125000003396 thiol group Chemical group [H]S* 0.000 claims description 31
• 239000003153 chemical reaction reagent Substances 0.000 claims description 30
• 208000023275 Autoimmune disease Diseases 0.000 claims description 29
• 125000004429 atom Chemical group 0.000 claims description 28
• 229910052731 fluorine Inorganic materials 0.000 claims description 28
• 201000006417 multiple sclerosis Diseases 0.000 claims description 26
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 23
• 201000011510 cancer Diseases 0.000 claims description 20
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 20
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 20
• 229910052757 nitrogen Inorganic materials 0.000 claims description 20
• 241000124008 Mammalia Species 0.000 claims description 18
• 230000008878 coupling Effects 0.000 claims description 17
• 238000010168 coupling process Methods 0.000 claims description 17
• 238000005859 coupling reaction Methods 0.000 claims description 17
• 208000022559 Inflammatory bowel disease Diseases 0.000 claims description 16
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 16
• 208000027866 inflammatory disease Diseases 0.000 claims description 16
• 125000004432 carbon atom Chemical group C* 0.000 claims description 15
• 206010025135 lupus erythematosus Diseases 0.000 claims description 13
• 229910052740 iodine Inorganic materials 0.000 claims description 12
• 230000002757 inflammatory effect Effects 0.000 claims description 11
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 11
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 11
• 125000006239 protecting group Chemical group 0.000 claims description 11
• 125000004414 alkyl thio group Chemical group 0.000 claims description 10
• 239000003054 catalyst Substances 0.000 claims description 10
• 239000003638 chemical reducing agent Substances 0.000 claims description 9
• 206010039073 rheumatoid arthritis Diseases 0.000 claims description 9
• 239000012453 solvate Substances 0.000 claims description 9
• 125000006242 amine protecting group Chemical group 0.000 claims description 8
• 125000000623 heterocyclic group Chemical group 0.000 claims description 8
• YUCFVHQCAFKDQG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH] YUCFVHQCAFKDQG-UHFFFAOYSA-N 0.000 claims description 7
• 229910052760 oxygen Inorganic materials 0.000 claims description 7
• 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 claims description 6
• HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 6
• 125000005842 heteroatom Chemical group 0.000 claims description 6
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
• PBVFROWIWWGIFK-UHFFFAOYSA-N fluoromethyl-(2-hydroxyethyl)-dimethylazanium Chemical compound FC[N+](C)(C)CCO PBVFROWIWWGIFK-UHFFFAOYSA-N 0.000 claims description 5
• 125000005647 linker group Chemical group 0.000 claims description 5
• 125000003566 oxetanyl group Chemical group 0.000 claims description 5
• 125000001424 substituent group Chemical group 0.000 claims description 5
• 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 4
• ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
• 239000003085 diluting agent Substances 0.000 claims description 4
• 239000011630 iodine Substances 0.000 claims description 4
• 229910052763 palladium Inorganic materials 0.000 claims description 4
• 230000008569 process Effects 0.000 claims description 4
• 239000002841 Lewis acid Substances 0.000 claims description 3
• 125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
• 150000007517 lewis acids Chemical class 0.000 claims description 3
• 239000003446 ligand Substances 0.000 claims description 3
• 229910052751 metal Inorganic materials 0.000 claims description 3
• 239000002184 metal Substances 0.000 claims description 3
• 125000000962 organic group Chemical group 0.000 claims description 3
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 3
• NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 2
• 150000008065 acid anhydrides Chemical class 0.000 claims description 2
• 229910052698 phosphorus Inorganic materials 0.000 claims description 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 23
• 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 49
• 201000010099 disease Diseases 0.000 abstract description 39
• 239000003112 inhibitor Substances 0.000 abstract description 14
• OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 abstract 1
• OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 abstract 1
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 316
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 260
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 174
• 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 141
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 136
• 239000000243 solution Substances 0.000 description 128
• 239000007787 solid Substances 0.000 description 122
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 116
• 235000019439 ethyl acetate Nutrition 0.000 description 105
• 125000004939 6-pyridyl group Chemical group N1=CC=CC=C1* 0.000 description 88
• NJPNCMOUEXEGBL-UHFFFAOYSA-N pyrrolidin-1-ium-3-ylazanium;dichloride Chemical compound Cl.Cl.NC1CCNC1 NJPNCMOUEXEGBL-UHFFFAOYSA-N 0.000 description 80
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 67
• 239000012267 brine Substances 0.000 description 61
• HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 61
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 58
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 55
• 125000004356 hydroxy functional group Chemical group O* 0.000 description 53
• 239000012044 organic layer Substances 0.000 description 51
• 239000011541 reaction mixture Substances 0.000 description 49
• 238000010992 reflux Methods 0.000 description 48
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 47
• WXFAZCYUMXZXBA-UHFFFAOYSA-N 8-methoxyquinoline-2-carbaldehyde Chemical compound C1=C(C=O)N=C2C(OC)=CC=CC2=C1 WXFAZCYUMXZXBA-UHFFFAOYSA-N 0.000 description 46
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 45
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 45
• 229910052938 sodium sulfate Inorganic materials 0.000 description 45
• 235000011152 sodium sulphate Nutrition 0.000 description 45
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 42
• 238000001816 cooling Methods 0.000 description 42
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 40
• 239000000741 silica gel Substances 0.000 description 40
• 229910002027 silica gel Inorganic materials 0.000 description 40
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 39
• 238000003818 flash chromatography Methods 0.000 description 38
• 239000002904 solvent Substances 0.000 description 38
• 210000004027 cell Anatomy 0.000 description 36
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 34
• JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 32
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 30
• YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 29
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 28
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 27
• 210000001744 T-lymphocyte Anatomy 0.000 description 27
• 239000000706 filtrate Substances 0.000 description 27
• 239000010410 layer Substances 0.000 description 27
• 238000003556 assay Methods 0.000 description 26
• NPPLFOLRHWBLKV-UHFFFAOYSA-N pyrrolidin-3-amine;hydrochloride Chemical compound Cl.NC1CCNC1 NPPLFOLRHWBLKV-UHFFFAOYSA-N 0.000 description 26
• JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 26
• 239000003921 oil Substances 0.000 description 24
• 238000001914 filtration Methods 0.000 description 23
• 238000004366 reverse phase liquid chromatography Methods 0.000 description 23
• 239000011734 sodium Substances 0.000 description 23
• JHHZLHWJQPUNKB-UHFFFAOYSA-N pyrrolidin-3-ol Chemical compound OC1CCNC1 JHHZLHWJQPUNKB-UHFFFAOYSA-N 0.000 description 21
• SOGQXABASMLRNX-WCQYABFASA-N tert-butyl n-[(3s)-1-[(1r)-2,2,2-trifluoro-1-(6-hydrazinylpyridin-3-yl)ethyl]pyrrolidin-3-yl]carbamate Chemical compound C1[C@@H](NC(=O)OC(C)(C)C)CCN1[C@@H](C(F)(F)F)C1=CC=C(NN)N=C1 SOGQXABASMLRNX-WCQYABFASA-N 0.000 description 21
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 20
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 20
• 239000001257 hydrogen Substances 0.000 description 19
• 241000699670 Mus sp. Species 0.000 description 18
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 17
• 238000004440 column chromatography Methods 0.000 description 17
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 16
• NGXSWUFDCSEIOO-UHFFFAOYSA-N pyrrolidin-3-amine Chemical compound NC1CCNC1 NGXSWUFDCSEIOO-UHFFFAOYSA-N 0.000 description 16
• WIEJVMZWPIUWHO-QMMMGPOBSA-N tert-butyl n-[[(3s)-pyrrolidin-3-yl]methyl]carbamate Chemical compound CC(C)(C)OC(=O)NC[C@H]1CCNC1 WIEJVMZWPIUWHO-QMMMGPOBSA-N 0.000 description 16
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
• UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 14
• KUPHUIFUXRACHJ-UHFFFAOYSA-N 8-propan-2-yloxyquinoline-2-carbaldehyde Chemical compound C1=C(C=O)N=C2C(OC(C)C)=CC=CC2=C1 KUPHUIFUXRACHJ-UHFFFAOYSA-N 0.000 description 14
• VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 14
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
• 235000011114 ammonium hydroxide Nutrition 0.000 description 14
• 210000004877 mucosa Anatomy 0.000 description 14
• PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 14
• 239000012074 organic phase Substances 0.000 description 14
• 102000004127 Cytokines Human genes 0.000 description 13
• 108090000695 Cytokines Proteins 0.000 description 13
• 229910052801 chlorine Inorganic materials 0.000 description 13
• 238000000746 purification Methods 0.000 description 13
• 239000000725 suspension Substances 0.000 description 13
• DQQJBEAXSOOCPG-ZETCQYMHSA-N tert-butyl n-[(3s)-pyrrolidin-3-yl]carbamate Chemical compound CC(C)(C)OC(=O)N[C@H]1CCNC1 DQQJBEAXSOOCPG-ZETCQYMHSA-N 0.000 description 13
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 13
• 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 12
• JSTPXQLNMGIGGW-UHFFFAOYSA-N 8-(cyclopropylmethoxy)quinoline-2-carbaldehyde Chemical compound C12=NC(C=O)=CC=C2C=CC=C1OCC1CC1 JSTPXQLNMGIGGW-UHFFFAOYSA-N 0.000 description 12
• ZPVSAUSAHRIAQM-UHFFFAOYSA-N 8-ethyl-2-methylquinoline Chemical compound C1=C(C)N=C2C(CC)=CC=CC2=C1 ZPVSAUSAHRIAQM-UHFFFAOYSA-N 0.000 description 12
• 229910002091 carbon monoxide Inorganic materials 0.000 description 12
• 208000037765 diseases and disorders Diseases 0.000 description 12
• 239000000047 product Substances 0.000 description 12
• UDVPQRRWUGKGQY-XQHVRGAUSA-N (e)-but-2-enal Chemical compound C\C=C\C=O.C\C=C\C=O UDVPQRRWUGKGQY-XQHVRGAUSA-N 0.000 description 11
• 238000002965 ELISA Methods 0.000 description 11
• 210000003719 b-lymphocyte Anatomy 0.000 description 11
• FMKOJHQHASLBPH-UHFFFAOYSA-N isopropyl iodide Chemical compound CC(C)I FMKOJHQHASLBPH-UHFFFAOYSA-N 0.000 description 11
• 239000012071 phase Substances 0.000 description 11
• 238000003756 stirring Methods 0.000 description 11
• 238000010790 dilution Methods 0.000 description 10
• 239000012895 dilution Substances 0.000 description 10
• 208000035475 disorder Diseases 0.000 description 10
• 239000003814 drug Substances 0.000 description 10
• 230000000694 effects Effects 0.000 description 10
• 239000000284 extract Substances 0.000 description 10
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 10
• WFKAJVHLWXSISD-UHFFFAOYSA-N isobutyramide Chemical compound CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 description 10
• JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 10
• 229910000027 potassium carbonate Inorganic materials 0.000 description 10
• RWJAYFXVJJUQMA-UHFFFAOYSA-N pyrrolidin-3-amine trihydrochloride Chemical compound Cl.Cl.[Cl-].N1CC(CC1)[NH3+] RWJAYFXVJJUQMA-UHFFFAOYSA-N 0.000 description 10
• 238000000926 separation method Methods 0.000 description 10
• YZUPZGFPHUVJKC-UHFFFAOYSA-N 1-bromo-2-methoxyethane Chemical compound COCCBr YZUPZGFPHUVJKC-UHFFFAOYSA-N 0.000 description 9
• ZBIKORITPGTTGI-UHFFFAOYSA-N [acetyloxy(phenyl)-$l^{3}-iodanyl] acetate Chemical compound CC(=O)OI(OC(C)=O)C1=CC=CC=C1 ZBIKORITPGTTGI-UHFFFAOYSA-N 0.000 description 9
• 238000004296 chiral HPLC Methods 0.000 description 9
• 238000004587 chromatography analysis Methods 0.000 description 9
• 238000004519 manufacturing process Methods 0.000 description 9
• MLJLUBLVRXPCKT-UHFFFAOYSA-N 7-bromo-8-fluoro-2-methylquinoline Chemical compound C1=CC(Br)=C(F)C2=NC(C)=CC=C21 MLJLUBLVRXPCKT-UHFFFAOYSA-N 0.000 description 8
• BDLLDGUBELPPAD-UHFFFAOYSA-N 8-cyclopropylquinoline-2-carbaldehyde Chemical compound C12=NC(C=O)=CC=C2C=CC=C1C1CC1 BDLLDGUBELPPAD-UHFFFAOYSA-N 0.000 description 8
• QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 8
• 239000000908 ammonium hydroxide Substances 0.000 description 8
• 229910052794 bromium Inorganic materials 0.000 description 8
• 201000002491 encephalomyelitis Diseases 0.000 description 8
• 230000002489 hematologic effect Effects 0.000 description 8
• 230000035755 proliferation Effects 0.000 description 8
• 108010083755 proto-oncogene proteins pim Proteins 0.000 description 8
• SOGQXABASMLRNX-AMGKYWFPSA-N tert-butyl n-[(3s)-1-[2,2,2-trifluoro-1-(6-hydrazinylpyridin-3-yl)ethyl]pyrrolidin-3-yl]carbamate Chemical compound C1[C@@H](NC(=O)OC(C)(C)C)CCN1C(C(F)(F)F)C1=CC=C(NN)N=C1 SOGQXABASMLRNX-AMGKYWFPSA-N 0.000 description 8
• DHRYTVOGXFGKFJ-XNUZUHMRSA-N tert-butyl n-[(3s)-1-[2,2,2-trifluoro-1-[3-(8-methoxyquinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl]ethyl]pyrrolidin-3-yl]carbamate Chemical compound N1=C2C(OC)=CC=CC2=CC=C1C(N1C=2)=NN=C1C=CC=2C(C(F)(F)F)N1CC[C@H](NC(=O)OC(C)(C)C)C1 DHRYTVOGXFGKFJ-XNUZUHMRSA-N 0.000 description 8
• DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 8
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 7
• 125000004575 3-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 7
• CYSXPNMJJBGOAL-UHFFFAOYSA-N 6-fluoro-8-propan-2-yloxyquinoline-2-carbaldehyde Chemical compound C1=C(C=O)N=C2C(OC(C)C)=CC(F)=CC2=C1 CYSXPNMJJBGOAL-UHFFFAOYSA-N 0.000 description 7
• 241000282414 Homo sapiens Species 0.000 description 7
• 230000001594 aberrant effect Effects 0.000 description 7
• 239000008346 aqueous phase Substances 0.000 description 7
• 230000016396 cytokine production Effects 0.000 description 7
• 238000005516 engineering process Methods 0.000 description 7
• 210000002865 immune cell Anatomy 0.000 description 7
• MVYIDFCWKYEFLL-UHFFFAOYSA-N methyl 2-(2-methylquinolin-8-yl)acetate Chemical compound C1=C(C)N=C2C(CC(=O)OC)=CC=CC2=C1 MVYIDFCWKYEFLL-UHFFFAOYSA-N 0.000 description 7
• 108090000623 proteins and genes Proteins 0.000 description 7
• 102000004169 proteins and genes Human genes 0.000 description 7
• 230000004044 response Effects 0.000 description 7
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