BR112016011844B1 - Derivados de triazolpiridina como moduladores de atividade de tnf - Google Patents

Info

Publication number

BR112016011844B1

BR112016011844B1 BR112016011844-8A BR112016011844A BR112016011844B1 BR 112016011844 B1 BR112016011844 B1 BR 112016011844B1 BR 112016011844 A BR112016011844 A BR 112016011844A BR 112016011844 B1 BR112016011844 B1 BR 112016011844B1

Authority

BR

Brazil

Prior art keywords

alkyl

methyl

optionally substituted

carboxy

heteroaryl

Prior art date

2013-12-09

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• Global Dossier
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• 230000000694 effects Effects 0.000 title abstract description 9
• 238000011282 treatment Methods 0.000 claims abstract description 51
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 21
• 208000035475 disorder Diseases 0.000 claims abstract description 18
• 208000023275 Autoimmune disease Diseases 0.000 claims abstract description 13
• 208000027866 inflammatory disease Diseases 0.000 claims abstract description 9
• 230000002757 inflammatory effect Effects 0.000 claims abstract description 9
• 208000024172 Cardiovascular disease Diseases 0.000 claims abstract description 8
• 208000012902 Nervous system disease Diseases 0.000 claims abstract description 8
• 208000030159 metabolic disease Diseases 0.000 claims abstract description 8
• 208000015122 neurodegenerative disease Diseases 0.000 claims abstract description 8
• 230000000926 neurological effect Effects 0.000 claims abstract description 8
• 208000002193 Pain Diseases 0.000 claims abstract description 7
• 208000030533 eye disease Diseases 0.000 claims abstract description 7
• 230000003040 nociceptive effect Effects 0.000 claims abstract description 7
• 230000000771 oncological effect Effects 0.000 claims abstract description 7
• -1 ethoxycarbonylethyl Chemical group 0.000 claims description 985
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 230
• 150000001875 compounds Chemical class 0.000 claims description 185
• 125000001424 substituent group Chemical group 0.000 claims description 123
• 229910052739 hydrogen Inorganic materials 0.000 claims description 90
• 239000001257 hydrogen Substances 0.000 claims description 90
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 74
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 68
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 67
• 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 61
• 229910052736 halogen Inorganic materials 0.000 claims description 57
• 150000002367 halogens Chemical class 0.000 claims description 57
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 56
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 55
• 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 37
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 34
• 125000001153 fluoro group Chemical group F* 0.000 claims description 31
• 125000004043 oxo group Chemical group O=* 0.000 claims description 31
• 150000003839 salts Chemical class 0.000 claims description 30
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 28
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 27
• 150000001204 N-oxides Chemical class 0.000 claims description 16
• 239000002253 acid Substances 0.000 claims description 14
• 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 14
• 229910052757 nitrogen Inorganic materials 0.000 claims description 14
• 229910052760 oxygen Inorganic materials 0.000 claims description 12
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 10
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 9
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 8
• 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 5
• 239000003937 drug carrier Substances 0.000 claims description 4
• 239000008194 pharmaceutical composition Substances 0.000 claims description 4
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
• 239000003814 drug Substances 0.000 claims description 3
• JLAKCHGEEBPDQI-UHFFFAOYSA-N 4-(4-fluorobenzyl)piperidine Chemical compound C1=CC(F)=CC=C1CC1CCNCC1 JLAKCHGEEBPDQI-UHFFFAOYSA-N 0.000 claims description 2
• 150000002431 hydrogen Chemical group 0.000 claims 4
• 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 2
• 125000004939 6-pyridyl group Chemical group N1=CC=CC=C1* 0.000 claims 1
• 241000282320 Panthera leo Species 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 101000611183 Homo sapiens Tumor necrosis factor Proteins 0.000 abstract description 6
• 230000002265 prevention Effects 0.000 abstract description 6
• 208000025966 Neurological disease Diseases 0.000 abstract description 5
• 230000009286 beneficial effect Effects 0.000 abstract description 5
• 102000057041 human TNF Human genes 0.000 abstract description 5
• NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 abstract description 4
• 201000010099 disease Diseases 0.000 abstract description 3
• 230000003389 potentiating effect Effects 0.000 abstract description 3
• 150000003222 pyridines Chemical class 0.000 abstract description 2
• 239000000126 substance Substances 0.000 description 65
• 125000004890 (C1-C6) alkylamino group Chemical group 0.000 description 64
• 125000004435 hydrogen atom Chemical class [H]* 0.000 description 62
• 125000001072 heteroaryl group Chemical group 0.000 description 47
• 125000003118 aryl group Chemical group 0.000 description 45
• 125000004093 cyano group Chemical group *C#N 0.000 description 36
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 30
• 108060008682 Tumor Necrosis Factor Proteins 0.000 description 30
• 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 description 30
• 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 26
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 25
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 25
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 24
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 23
• 239000000203 mixture Substances 0.000 description 23
• 125000000217 alkyl group Chemical group 0.000 description 22
• 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 description 21
• 239000000543 intermediate Substances 0.000 description 21
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
• 239000002585 base Substances 0.000 description 20
• 125000000753 cycloalkyl group Chemical group 0.000 description 20
• 238000000034 method Methods 0.000 description 20
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
• 125000005213 alkyl heteroaryl group Chemical group 0.000 description 18
• 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 description 17
• 125000004457 alkyl amino carbonyl group Chemical group 0.000 description 17
• 238000006243 chemical reaction Methods 0.000 description 17
• PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 17
• 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 17
• 125000002757 morpholinyl group Chemical group 0.000 description 17
• 125000004366 heterocycloalkenyl group Chemical group 0.000 description 16
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 16
• 239000012453 solvate Substances 0.000 description 16
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
• 125000003806 alkyl carbonyl amino group Chemical group 0.000 description 15
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 15
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 15
• 125000003831 tetrazolyl group Chemical group 0.000 description 15
• 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 15
• 229910020008 S(O) Inorganic materials 0.000 description 14
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 14
• 239000000460 chlorine Substances 0.000 description 14
• 239000000651 prodrug Substances 0.000 description 14
• 229940002612 prodrug Drugs 0.000 description 14
• 239000007787 solid Substances 0.000 description 14
• 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 description 13
• 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 13
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 13
• 125000004453 alkoxycarbonyl group Chemical group 0.000 description 13
• 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 13
• 238000002360 preparation method Methods 0.000 description 13
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
• 239000003054 catalyst Substances 0.000 description 12
• 229910052801 chlorine Inorganic materials 0.000 description 12
• 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 12
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
• 125000004076 pyridyl group Chemical group 0.000 description 12
• 125000001544 thienyl group Chemical group 0.000 description 12
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 11
• 229930182480 glucuronide Natural products 0.000 description 11
• 150000008134 glucuronides Chemical class 0.000 description 11
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 10
• OKKJLVBELUTLKV-MZCSYVLQSA-N Deuterated methanol Chemical compound [2H]OC([2H])([2H])[2H] OKKJLVBELUTLKV-MZCSYVLQSA-N 0.000 description 10
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 10
• 125000004432 carbon atom Chemical group C* 0.000 description 10
• 210000004027 cell Anatomy 0.000 description 10
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 10
• 125000005843 halogen group Chemical group 0.000 description 10
• 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 10
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 10
• 150000007530 organic bases Chemical class 0.000 description 10
• 239000000243 solution Substances 0.000 description 10
• 239000002904 solvent Substances 0.000 description 10
• 229910052717 sulfur Inorganic materials 0.000 description 10
• 125000000335 thiazolyl group Chemical group 0.000 description 10
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
• 125000004448 alkyl carbonyl group Chemical group 0.000 description 9
• 125000002947 alkylene group Chemical group 0.000 description 9
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 9
• 229910052794 bromium Inorganic materials 0.000 description 9
• 125000006310 cycloalkyl amino group Chemical group 0.000 description 9
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 9
• 238000002953 preparative HPLC Methods 0.000 description 9
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• 125000003107 substituted aryl group Chemical group 0.000 description 9
• 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 9
• 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 9
• 229910052723 transition metal Inorganic materials 0.000 description 9
• 150000003624 transition metals Chemical class 0.000 description 9
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 9
• KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 8
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 8
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• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
• IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 8
• 125000002877 alkyl aryl group Chemical group 0.000 description 8
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• 125000005215 cycloalkylheteroaryl group Chemical group 0.000 description 8
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• NXQGGXCHGDYOHB-UHFFFAOYSA-L cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;dichloropalladium;iron(2+) Chemical compound [Fe+2].Cl[Pd]Cl.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NXQGGXCHGDYOHB-UHFFFAOYSA-L 0.000 description 8
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