JP6474166B2 - 化合物及び使用方法 - Google Patents
化合物及び使用方法 Download PDFInfo
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- JP6474166B2 JP6474166B2 JP2016544111A JP2016544111A JP6474166B2 JP 6474166 B2 JP6474166 B2 JP 6474166B2 JP 2016544111 A JP2016544111 A JP 2016544111A JP 2016544111 A JP2016544111 A JP 2016544111A JP 6474166 B2 JP6474166 B2 JP 6474166B2
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- Prior art keywords
- chloro
- mmol
- phenyl
- pyridyl
- cancer
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- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical group N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims 1
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- 239000011541 reaction mixture Substances 0.000 description 265
- 239000000243 solution Substances 0.000 description 208
- 230000015572 biosynthetic process Effects 0.000 description 196
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 174
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 169
- 230000002829 reductive effect Effects 0.000 description 160
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- 235000019439 ethyl acetate Nutrition 0.000 description 132
- 239000012044 organic layer Substances 0.000 description 132
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 131
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 129
- 238000004809 thin layer chromatography Methods 0.000 description 111
- 239000012043 crude product Substances 0.000 description 109
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 107
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 93
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- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 90
- 239000007787 solid Substances 0.000 description 82
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 71
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 66
- 239000012267 brine Substances 0.000 description 65
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 65
- PVNIIMVLHYAWGP-UHFFFAOYSA-M nicotinate Chemical compound [O-]C(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-M 0.000 description 61
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 58
- 229910052757 nitrogen Inorganic materials 0.000 description 57
- 125000000217 alkyl group Chemical group 0.000 description 55
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 53
- 238000002360 preparation method Methods 0.000 description 49
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 46
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 45
- 125000001424 substituent group Chemical group 0.000 description 42
- 239000003480 eluent Substances 0.000 description 40
- 238000011282 treatment Methods 0.000 description 40
- OCARFFAPQGYGBP-UHFFFAOYSA-N methyl 4-aminopyridine-3-carboxylate Chemical compound COC(=O)C1=CN=CC=C1N OCARFFAPQGYGBP-UHFFFAOYSA-N 0.000 description 36
- 235000005152 nicotinamide Nutrition 0.000 description 36
- 239000011570 nicotinamide Substances 0.000 description 36
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 35
- 125000001072 heteroaryl group Chemical group 0.000 description 34
- 125000003545 alkoxy group Chemical group 0.000 description 33
- 125000003118 aryl group Chemical group 0.000 description 33
- 125000000623 heterocyclic group Chemical group 0.000 description 33
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 32
- 239000012299 nitrogen atmosphere Substances 0.000 description 32
- 125000000753 cycloalkyl group Chemical group 0.000 description 30
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 30
- 238000004007 reversed phase HPLC Methods 0.000 description 29
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 27
- 238000004440 column chromatography Methods 0.000 description 27
- 125000000547 substituted alkyl group Chemical group 0.000 description 27
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 26
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 26
- 238000004587 chromatography analysis Methods 0.000 description 24
- 239000000741 silica gel Substances 0.000 description 24
- 229910002027 silica gel Inorganic materials 0.000 description 24
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 23
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 20
- 229910052736 halogen Inorganic materials 0.000 description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 20
- 229920006395 saturated elastomer Polymers 0.000 description 20
- HXKKHQJGJAFBHI-GSVOUGTGSA-N (2R)-1-aminopropan-2-ol Chemical compound C[C@@H](O)CN HXKKHQJGJAFBHI-GSVOUGTGSA-N 0.000 description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 19
- 239000000460 chlorine Substances 0.000 description 19
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- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 16
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 16
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 16
- CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 16
- HXKKHQJGJAFBHI-VKHMYHEASA-N (2s)-1-aminopropan-2-ol Chemical compound C[C@H](O)CN HXKKHQJGJAFBHI-VKHMYHEASA-N 0.000 description 15
- 125000003342 alkenyl group Chemical group 0.000 description 15
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 15
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 15
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- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 15
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
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- 125000000304 alkynyl group Chemical group 0.000 description 14
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- GGTUVWGMCFXUAS-UHFFFAOYSA-N (5-chloro-2-fluorophenyl)boronic acid Chemical compound OB(O)C1=CC(Cl)=CC=C1F GGTUVWGMCFXUAS-UHFFFAOYSA-N 0.000 description 12
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 230000000875 corresponding effect Effects 0.000 description 12
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 12
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 12
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 11
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 11
- 125000004104 aryloxy group Chemical group 0.000 description 11
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 11
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 239000002552 dosage form Substances 0.000 description 11
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- 238000002953 preparative HPLC Methods 0.000 description 11
- 125000003107 substituted aryl group Chemical group 0.000 description 11
- 238000006467 substitution reaction Methods 0.000 description 11
- GTKLTAYQGIKYTN-UHFFFAOYSA-N 2-(4,6-dichloropyridin-3-yl)propan-2-ol Chemical compound ClC1=C(C=NC(=C1)Cl)C(C)(C)O GTKLTAYQGIKYTN-UHFFFAOYSA-N 0.000 description 10
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- LICNVQCUUJKYJN-UHFFFAOYSA-N 4-chloro-2-(5-chloro-2-fluorophenyl)-5-prop-1-en-2-ylpyridine Chemical compound ClC1=CC(=NC=C1C(=C)C)C1=C(C=CC(=C1)Cl)F LICNVQCUUJKYJN-UHFFFAOYSA-N 0.000 description 9
- 206010016654 Fibrosis Diseases 0.000 description 9
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- 125000004429 atom Chemical group 0.000 description 9
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- 125000000392 cycloalkenyl group Chemical group 0.000 description 9
- 229910052740 iodine Inorganic materials 0.000 description 9
- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 9
- 238000000746 purification Methods 0.000 description 9
- 230000002441 reversible effect Effects 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
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- 239000000126 substance Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 8
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- 230000000893 fibroproliferative effect Effects 0.000 description 8
- 125000001153 fluoro group Chemical group F* 0.000 description 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 8
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 8
- 229910000160 potassium phosphate Inorganic materials 0.000 description 8
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- JZIQNDFHVVKMQW-UHFFFAOYSA-N 2,4-dichloro-5-prop-1-en-2-ylpyridine Chemical compound ClC1=NC=C(C(=C1)Cl)C(=C)C JZIQNDFHVVKMQW-UHFFFAOYSA-N 0.000 description 7
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- YJPVAMGGHWRIBR-LURJTMIESA-N 4-amino-N-[(2S)-2-hydroxypropyl]pyridine-3-carboxamide Chemical compound NC1=C(C=NC=C1)C(=O)NC[C@H](C)O YJPVAMGGHWRIBR-LURJTMIESA-N 0.000 description 7
- IASBMUIXBJNMDW-UHFFFAOYSA-N 4-aminonicotinic acid Chemical compound NC1=CC=NC=C1C(O)=O IASBMUIXBJNMDW-UHFFFAOYSA-N 0.000 description 7
- 108091005735 TGF-beta receptors Proteins 0.000 description 7
- 102000016715 Transforming Growth Factor beta Receptors Human genes 0.000 description 7
- 208000003721 Triple Negative Breast Neoplasms Diseases 0.000 description 7
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- 229910052794 bromium Inorganic materials 0.000 description 7
- 230000008878 coupling Effects 0.000 description 7
- 238000010168 coupling process Methods 0.000 description 7
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
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- 239000000543 intermediate Substances 0.000 description 7
- JEJMDUMJSZTJTI-UHFFFAOYSA-N methyl 4,6-dichloropyridine-3-carboxylate Chemical compound COC(=O)C1=CN=C(Cl)C=C1Cl JEJMDUMJSZTJTI-UHFFFAOYSA-N 0.000 description 7
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 7
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- VDXWCRIARMBDOX-UHFFFAOYSA-N (4,6-dichloropyridin-3-yl)methanol Chemical compound OCC1=CN=C(Cl)C=C1Cl VDXWCRIARMBDOX-UHFFFAOYSA-N 0.000 description 6
- CPHMTWAGYKYGDE-UHFFFAOYSA-N 1-(4,6-dichloropyridin-3-yl)ethanol Chemical compound CC(O)C1=C(Cl)C=C(Cl)N=C1 CPHMTWAGYKYGDE-UHFFFAOYSA-N 0.000 description 6
- TUIXUFOQXGRSKJ-UHFFFAOYSA-N 1-[4-chloro-6-(5-chloro-2-fluorophenyl)pyridin-3-yl]ethanol Chemical compound CC(O)C1=C(Cl)C=C(N=C1)C1=C(F)C=CC(Cl)=C1 TUIXUFOQXGRSKJ-UHFFFAOYSA-N 0.000 description 6
- NUIPNTORHOXPGS-UHFFFAOYSA-N 2-[6-(5-chloro-2-fluorophenyl)pyridin-3-yl]propan-2-ol Chemical compound ClC=1C=CC(=C(C1)C1=CC=C(C=N1)C(C)(C)O)F NUIPNTORHOXPGS-UHFFFAOYSA-N 0.000 description 6
- FBGVTWONYOCYGA-UHFFFAOYSA-N 4,6-dichloropyridin-3-amine Chemical compound NC1=CN=C(Cl)C=C1Cl FBGVTWONYOCYGA-UHFFFAOYSA-N 0.000 description 6
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