HRP20080087T5 - Trisupstituirani arilni i heteroarilni derivati kao modulatori metabolizma i profilaksa i liječenje poremećaja koji su s tim povezani - Google Patents
Trisupstituirani arilni i heteroarilni derivati kao modulatori metabolizma i profilaksa i liječenje poremećaja koji su s tim povezani Download PDFInfo
- Publication number
- HRP20080087T5 HRP20080087T5 HR20080087T HRP20080087T HRP20080087T5 HR P20080087 T5 HRP20080087 T5 HR P20080087T5 HR 20080087 T HR20080087 T HR 20080087T HR P20080087 T HRP20080087 T HR P20080087T HR P20080087 T5 HRP20080087 T5 HR P20080087T5
- Authority
- HR
- Croatia
- Prior art keywords
- yloxy
- pyrimidin
- methyl
- fluoro
- phenoxy
- Prior art date
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- 125000001072 heteroaryl group Chemical group 0.000 title claims abstract description 212
- 125000003118 aryl group Chemical group 0.000 title claims abstract description 45
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title claims description 67
- 208000035475 disorder Diseases 0.000 title claims description 43
- 238000011282 treatment Methods 0.000 title claims description 23
- 230000004060 metabolic process Effects 0.000 title claims description 12
- 238000011321 prophylaxis Methods 0.000 title claims description 12
- -1 hydroxy-carbamimidoyl Chemical group 0.000 claims abstract description 518
- 150000001875 compounds Chemical class 0.000 claims abstract description 315
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 193
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 176
- 150000002367 halogens Chemical class 0.000 claims abstract description 176
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 170
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 166
- 125000001424 substituent group Chemical group 0.000 claims abstract description 166
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims abstract description 162
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims abstract description 156
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 139
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 138
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 137
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 136
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims abstract description 128
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 103
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 claims abstract description 74
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims abstract description 70
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 68
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims abstract description 57
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 57
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical group FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims abstract description 53
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims abstract description 42
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims abstract description 42
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims abstract description 42
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims abstract description 42
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims abstract description 41
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 41
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 40
- 229940124530 sulfonamide Drugs 0.000 claims abstract description 39
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 claims abstract description 37
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 35
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 31
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 30
- 150000003839 salts Chemical class 0.000 claims abstract description 27
- 125000000714 pyrimidinyl group Chemical group 0.000 claims abstract description 24
- 125000003373 pyrazinyl group Chemical group 0.000 claims abstract description 23
- 125000002098 pyridazinyl group Chemical group 0.000 claims abstract description 23
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 22
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 22
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims abstract description 21
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims abstract description 21
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims abstract description 21
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims abstract description 21
- 125000004306 triazinyl group Chemical group 0.000 claims abstract description 21
- 239000012453 solvate Substances 0.000 claims abstract description 18
- 150000004677 hydrates Chemical class 0.000 claims abstract description 16
- 150000001204 N-oxides Chemical class 0.000 claims abstract description 15
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims abstract description 14
- 125000005431 alkyl carboxamide group Chemical group 0.000 claims abstract description 13
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 11
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract description 10
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims abstract description 10
- 150000002825 nitriles Chemical class 0.000 claims abstract description 8
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims abstract description 7
- 125000003831 tetrazolyl group Chemical group 0.000 claims abstract description 7
- 150000003857 carboxamides Chemical class 0.000 claims description 94
- 229910020008 S(O) Inorganic materials 0.000 claims description 82
- 241000282414 Homo sapiens Species 0.000 claims description 69
- 238000000034 method Methods 0.000 claims description 69
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 63
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 58
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 56
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 56
- 125000000217 alkyl group Chemical group 0.000 claims description 51
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 46
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 39
- 239000008194 pharmaceutical composition Substances 0.000 claims description 34
- 150000003456 sulfonamides Chemical class 0.000 claims description 33
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 26
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims description 24
- 238000004519 manufacturing process Methods 0.000 claims description 24
- 239000003814 drug Substances 0.000 claims description 22
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 20
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 19
- 239000008103 glucose Substances 0.000 claims description 19
- 230000008569 process Effects 0.000 claims description 16
- 208000011580 syndromic disease Diseases 0.000 claims description 16
- 241001465754 Metazoa Species 0.000 claims description 15
- 229910052794 bromium Inorganic materials 0.000 claims description 15
- 229910052801 chlorine Inorganic materials 0.000 claims description 15
- 201000001421 hyperglycemia Diseases 0.000 claims description 15
- 208000031226 Hyperlipidaemia Diseases 0.000 claims description 14
- 206010022489 Insulin Resistance Diseases 0.000 claims description 14
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 14
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 claims description 14
- 239000003937 drug carrier Substances 0.000 claims description 13
- 208000032928 Dyslipidaemia Diseases 0.000 claims description 12
- 208000017170 Lipid metabolism disease Diseases 0.000 claims description 12
- 230000037406 food intake Effects 0.000 claims description 12
- 235000012631 food intake Nutrition 0.000 claims description 12
- 208000006575 hypertriglyceridemia Diseases 0.000 claims description 12
- 230000036186 satiety Effects 0.000 claims description 12
- 235000019627 satiety Nutrition 0.000 claims description 12
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 11
- 238000002560 therapeutic procedure Methods 0.000 claims description 11
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 9
- 125000004429 atom Chemical group 0.000 claims description 9
- 230000004584 weight gain Effects 0.000 claims description 8
- 235000019786 weight gain Nutrition 0.000 claims description 8
- 208000035150 Hypercholesterolemia Diseases 0.000 claims description 7
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 7
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 6
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 6
- 230000001939 inductive effect Effects 0.000 claims description 6
- 208000030159 metabolic disease Diseases 0.000 claims description 6
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 101100240527 Caenorhabditis elegans nhr-22 gene Proteins 0.000 claims description 4
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 3
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 claims description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 3
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- 125000005929 isobutyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])OC(*)=O 0.000 claims description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 13
- XCKPUZAGEYMHKH-UHFFFAOYSA-N 1-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-methoxypropan-2-ol Chemical compound C1CN(CC(O)COC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C XCKPUZAGEYMHKH-UHFFFAOYSA-N 0.000 claims 2
- KBRFTJUEHZNTLD-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-pyridin-2-ylethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=CC=N1 KBRFTJUEHZNTLD-UHFFFAOYSA-N 0.000 claims 2
- DQDOQWDMORTGOE-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-thiophen-2-ylethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=CS1 DQDOQWDMORTGOE-UHFFFAOYSA-N 0.000 claims 2
- IUORNUVLBGKOPB-UHFFFAOYSA-N tert-butyl 3-[[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]oxymethyl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCC1COC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O IUORNUVLBGKOPB-UHFFFAOYSA-N 0.000 claims 2
- GNXFVIIWULQUBL-UHFFFAOYSA-N (2-chloropyridin-3-yl)-[4-[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]oxypiperidin-1-yl]methanone Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)C=2C(=NC=CC=2)Cl)=C1[N+]([O-])=O GNXFVIIWULQUBL-UHFFFAOYSA-N 0.000 claims 1
- SUTRBBYEBJZKSL-HXUWFJFHSA-N (2r)-1-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-methyl-2-(methylamino)butan-1-one Chemical compound C1CN(C(=O)[C@@H](C(C)C)NC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C SUTRBBYEBJZKSL-HXUWFJFHSA-N 0.000 claims 1
- SUTRBBYEBJZKSL-FQEVSTJZSA-N (2s)-1-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-methyl-2-(methylamino)butan-1-one Chemical compound C1CN(C(=O)[C@H](C(C)C)NC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C SUTRBBYEBJZKSL-FQEVSTJZSA-N 0.000 claims 1
- NVAUAEAIPCUOBK-UHFFFAOYSA-N (5-methyl-2-propan-2-ylcyclohexyl) 4-[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound CC(C)C1CCC(C)CC1OC(=O)N1CCC(OC=2C(=C(NC=3C=CC(=CC=3)S(C)(=O)=O)N=CN=2)[N+]([O-])=O)CC1 NVAUAEAIPCUOBK-UHFFFAOYSA-N 0.000 claims 1
- JCZNELDPUPQIOL-UHFFFAOYSA-N (6-aminopyridin-3-yl)-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]methanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1C(=O)C1=CC=C(N)N=C1 JCZNELDPUPQIOL-UHFFFAOYSA-N 0.000 claims 1
- BZCKFTOJAAQFTA-UHFFFAOYSA-N 1-(1,4-dioxan-2-yl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1COCCO1 BZCKFTOJAAQFTA-UHFFFAOYSA-N 0.000 claims 1
- NXZKANMZWSPFMK-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-dioxin-2-yl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1COC=CO1 NXZKANMZWSPFMK-UHFFFAOYSA-N 0.000 claims 1
- RVZFZQWLTJQPLS-UHFFFAOYSA-N 1-(2,4-dimethoxyphenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound COC1=CC(OC)=CC=C1C(=O)CN1CCC(OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)CC1 RVZFZQWLTJQPLS-UHFFFAOYSA-N 0.000 claims 1
- BYOVXZGDVJRLSG-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound CC1=CC(C)=CC=C1C(=O)CN1CCC(OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)CC1 BYOVXZGDVJRLSG-UHFFFAOYSA-N 0.000 claims 1
- FXCOOELGVLFKQL-UHFFFAOYSA-N 1-(2,5-dimethoxyphenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound COC1=CC=C(OC)C(C(=O)CN2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)=C1 FXCOOELGVLFKQL-UHFFFAOYSA-N 0.000 claims 1
- ZGQWNYLFEIIJJA-UHFFFAOYSA-N 1-(2-chlorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=CC=C1Cl ZGQWNYLFEIIJJA-UHFFFAOYSA-N 0.000 claims 1
- AGYJGOBTVGVHCQ-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(Cl)C(Cl)=C1 AGYJGOBTVGVHCQ-UHFFFAOYSA-N 0.000 claims 1
- WTRLCDYYFXPAPD-UHFFFAOYSA-N 1-(3,4-difluorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(F)C(F)=C1 WTRLCDYYFXPAPD-UHFFFAOYSA-N 0.000 claims 1
- PHJXLUZEMQGAHL-UHFFFAOYSA-N 1-(3-chlorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=CC(Cl)=C1 PHJXLUZEMQGAHL-UHFFFAOYSA-N 0.000 claims 1
- AKFARRXTBWPOSU-UHFFFAOYSA-N 1-(4-chloro-3-methylphenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound C1=C(Cl)C(C)=CC(C(=O)CN2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)=C1 AKFARRXTBWPOSU-UHFFFAOYSA-N 0.000 claims 1
- BMIUMSRQZZKLPW-UHFFFAOYSA-N 1-(4-chlorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(Cl)C=C1 BMIUMSRQZZKLPW-UHFFFAOYSA-N 0.000 claims 1
- VOQZIYNVRLBGCV-UHFFFAOYSA-N 1-[4-(1-benzylazetidin-3-yl)oxy-6-[(6-methylsulfonylpyridin-3-yl)amino]pyrimidin-5-yl]ethanone Chemical compound N1=CN=C(OC2CN(CC=3C=CC=CC=3)C2)C(C(=O)C)=C1NC1=CC=C(S(C)(=O)=O)N=C1 VOQZIYNVRLBGCV-UHFFFAOYSA-N 0.000 claims 1
- OILAFPLLAZHETH-UHFFFAOYSA-N 1-[4-(diethylamino)phenyl]-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)CN1CCC(OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)CC1 OILAFPLLAZHETH-UHFFFAOYSA-N 0.000 claims 1
- GDBJBLFDRZEHSX-UHFFFAOYSA-N 1-[4-(difluoromethoxy)phenyl]-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(OC(F)F)C=C1 GDBJBLFDRZEHSX-UHFFFAOYSA-N 0.000 claims 1
- RFTMNFALQNCBJY-UHFFFAOYSA-N 1-[4-[5-ethynyl-6-[2-fluoro-4-(1,2,4-triazol-1-yl)phenoxy]pyrimidin-4-yl]oxypiperidin-1-yl]-3-pyridin-2-ylpropan-1-one Chemical compound FC1=CC(N2N=CN=C2)=CC=C1OC(C=1C#C)=NC=NC=1OC(CC1)CCN1C(=O)CCC1=CC=CC=N1 RFTMNFALQNCBJY-UHFFFAOYSA-N 0.000 claims 1
- OTEOXAURHOATIC-UHFFFAOYSA-N 1-[4-[6-(2-fluoro-4-methylsulfonylanilino)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-methylbutan-1-one Chemical compound C1CN(C(=O)CC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C OTEOXAURHOATIC-UHFFFAOYSA-N 0.000 claims 1
- XYTIQXINBAEKPT-UHFFFAOYSA-N 1-[4-[6-(2-fluoro-4-methylsulfonylanilino)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]butan-1-one Chemical compound C1CN(C(=O)CCC)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C XYTIQXINBAEKPT-UHFFFAOYSA-N 0.000 claims 1
- RIAXTBCAPSTEGQ-UHFFFAOYSA-N 1-[4-[6-(2-fluoro-4-methylsulfonylanilino)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]pentan-1-one Chemical compound C1CN(C(=O)CCCC)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C RIAXTBCAPSTEGQ-UHFFFAOYSA-N 0.000 claims 1
- XRVMQLBTZWLEMK-UHFFFAOYSA-N 1-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-2-[4-(trifluoromethoxy)phenoxy]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1C(=O)COC1=CC=C(OC(F)(F)F)C=C1 XRVMQLBTZWLEMK-UHFFFAOYSA-N 0.000 claims 1
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- IBNIPRMVXVNXAW-UHFFFAOYSA-N 1-[4-[[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]amino]piperidin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCC1NC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O IBNIPRMVXVNXAW-UHFFFAOYSA-N 0.000 claims 1
- GGMJFGFKFRAWTH-UHFFFAOYSA-N 2,2-dimethyl-1-[4-[[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]amino]piperidin-1-yl]propan-1-one Chemical compound C1CN(C(=O)C(C)(C)C)CCC1NC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O GGMJFGFKFRAWTH-UHFFFAOYSA-N 0.000 claims 1
- JVKNQSNKBPRGGO-UHFFFAOYSA-N 2-[3-fluoro-4-[5-methyl-6-(1-propan-2-yloxycarbonylpiperidin-4-yl)oxypyrimidin-4-yl]oxyphenyl]acetic acid Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CC(O)=O)=CC=2)F)=C1C JVKNQSNKBPRGGO-UHFFFAOYSA-N 0.000 claims 1
- KMRWDTYHXJTJMK-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-(3-fluorophenyl)ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=CC(F)=C1 KMRWDTYHXJTJMK-UHFFFAOYSA-N 0.000 claims 1
- XBUBBGIMTPSSQO-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-(4-fluorophenyl)ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(F)C=C1 XBUBBGIMTPSSQO-UHFFFAOYSA-N 0.000 claims 1
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- HYARXWARKOIYRN-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-(4-methylphenyl)ethanone Chemical compound C1=CC(C)=CC=C1C(=O)CN1CCC(OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)CC1 HYARXWARKOIYRN-UHFFFAOYSA-N 0.000 claims 1
- MJQKSBDLAPJBIJ-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-(4-methylsulfonylphenyl)ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(S(C)(=O)=O)C=C1 MJQKSBDLAPJBIJ-UHFFFAOYSA-N 0.000 claims 1
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- VGKJEXKKZYGQGF-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-[4-(trifluoromethoxy)phenyl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(OC(F)(F)F)C=C1 VGKJEXKKZYGQGF-UHFFFAOYSA-N 0.000 claims 1
- GCSBEPIRNMWBPR-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-[4-(trifluoromethyl)phenyl]ethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(C(F)(F)F)C=C1 GCSBEPIRNMWBPR-UHFFFAOYSA-N 0.000 claims 1
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- ILUJEJKVTTZYGJ-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-phenylethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=CC=C1 ILUJEJKVTTZYGJ-UHFFFAOYSA-N 0.000 claims 1
- HUBNTPOXFSZGTG-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-pyridin-3-ylethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=CN=C1 HUBNTPOXFSZGTG-UHFFFAOYSA-N 0.000 claims 1
- VQAKENAYCYDJEL-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-pyridin-4-ylethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=NC=C1 VQAKENAYCYDJEL-UHFFFAOYSA-N 0.000 claims 1
- FHMHSBNXXPGLBG-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1-thiophen-3-ylethanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C=1C=CSC=1 FHMHSBNXXPGLBG-UHFFFAOYSA-N 0.000 claims 1
- XZXFZWYWQSKEFG-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-n-(4-methoxyphenyl)acetamide Chemical compound C1=CC(OC)=CC=C1NC(=O)CN1CCC(OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)CC1 XZXFZWYWQSKEFG-UHFFFAOYSA-N 0.000 claims 1
- VTXXGGZSMRSJOR-UHFFFAOYSA-N 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-n-(4-propan-2-ylphenyl)acetamide Chemical compound C1=CC(C(C)C)=CC=C1NC(=O)CN1CCC(OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)CC1 VTXXGGZSMRSJOR-UHFFFAOYSA-N 0.000 claims 1
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- MCPSLCJANOFXEW-UHFFFAOYSA-N 2-[[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]methyl]prop-2-enoic acid Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC1CCN(CC(=C)C(O)=O)CC1 MCPSLCJANOFXEW-UHFFFAOYSA-N 0.000 claims 1
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- QABYRZYSSGZTSE-UHFFFAOYSA-N 2-methylpropyl 4-[5-cyano-6-(4-methylsulfonylanilino)pyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC(C)C)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1C#N QABYRZYSSGZTSE-UHFFFAOYSA-N 0.000 claims 1
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- MDZBNPSMIWSWGH-UHFFFAOYSA-N 3,3-dimethyl-1-[4-[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]oxypiperidin-1-yl]butan-2-one Chemical compound C1CN(CC(=O)C(C)(C)C)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O MDZBNPSMIWSWGH-UHFFFAOYSA-N 0.000 claims 1
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- LWNRMDVXXLXCFI-UHFFFAOYSA-N 3-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-oxopropane-1-sulfonic acid Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC1CCN(C(=O)CCS(O)(=O)=O)CC1 LWNRMDVXXLXCFI-UHFFFAOYSA-N 0.000 claims 1
- ILSMGGRXRKWAEN-UHFFFAOYSA-N 3-amino-1-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-4-methylpentan-1-one Chemical compound C1CN(C(=O)CC(N)C(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C ILSMGGRXRKWAEN-UHFFFAOYSA-N 0.000 claims 1
- GGUXFXPGTFEOGQ-UHFFFAOYSA-N 3-ethyl-5-[4-[5-ethynyl-6-(2-fluoro-4-methylsulfonylphenoxy)pyrimidin-4-yl]oxypiperidin-1-yl]-1,2,4-oxadiazole Chemical compound CCC1=NOC(N2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C#C)=N1 GGUXFXPGTFEOGQ-UHFFFAOYSA-N 0.000 claims 1
- ZICSYHWVNYHXEV-UHFFFAOYSA-N 3-ethyl-5-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-1,2,4-oxadiazole Chemical compound CCC1=NOC(N2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)=N1 ZICSYHWVNYHXEV-UHFFFAOYSA-N 0.000 claims 1
- KZMAXLPGELOJRP-UHFFFAOYSA-N 3-fluoro-4-[5-methyl-6-(1-propan-2-yloxycarbonylpiperidin-4-yl)oxypyrimidin-4-yl]oxybenzenesulfonic acid Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(O)(=O)=O)F)=C1C KZMAXLPGELOJRP-UHFFFAOYSA-N 0.000 claims 1
- GYVQSDVQPGRVGW-UHFFFAOYSA-N 3-fluoro-4-[5-methyl-6-(1-propan-2-yloxycarbonylpiperidin-4-yl)oxypyrimidin-4-yl]oxybenzoic acid Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C(O)=O)F)=C1C GYVQSDVQPGRVGW-UHFFFAOYSA-N 0.000 claims 1
- MBPWZHDZEVESMX-UHFFFAOYSA-N 4-(1-butylpiperidin-4-yl)oxy-6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidine Chemical compound C1CN(CCCC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C MBPWZHDZEVESMX-UHFFFAOYSA-N 0.000 claims 1
- AZQKDCFSKVWQQO-UHFFFAOYSA-N 4-(1-formylpiperidin-4-yl)oxy-6-(4-methylsulfonylanilino)pyrimidine-5-carbonitrile Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C=O)=C1C#N AZQKDCFSKVWQQO-UHFFFAOYSA-N 0.000 claims 1
- PGHCNXHAKQGQKA-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-5-methyl-6-(1-pentylpiperidin-4-yl)oxypyrimidine Chemical compound C1CN(CCCCC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C PGHCNXHAKQGQKA-UHFFFAOYSA-N 0.000 claims 1
- NUCBMLTYQHSURX-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-5-methyl-6-[1-(2-pyridin-3-ylethyl)piperidin-4-yl]oxypyrimidine Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CCC1=CC=CN=C1 NUCBMLTYQHSURX-UHFFFAOYSA-N 0.000 claims 1
- WKDDGTJMOBLSEP-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-5-methyl-6-[1-(3-methylbutyl)piperidin-4-yl]oxypyrimidine Chemical compound C1CN(CCC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C WKDDGTJMOBLSEP-UHFFFAOYSA-N 0.000 claims 1
- TUTHICCOPAUTTP-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-5-methyl-6-[1-(4-methylpentyl)piperidin-4-yl]oxypyrimidine Chemical compound C1CN(CCCC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C TUTHICCOPAUTTP-UHFFFAOYSA-N 0.000 claims 1
- JZQGRHDMONUUBS-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-5-methyl-6-[1-(5-methylhexyl)piperidin-4-yl]oxypyrimidine Chemical compound C1CN(CCCCC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C JZQGRHDMONUUBS-UHFFFAOYSA-N 0.000 claims 1
- HSWSVHVEPTZPHW-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-6-(1-hexylpiperidin-4-yl)oxy-5-methylpyrimidine Chemical compound C1CN(CCCCCC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C HSWSVHVEPTZPHW-UHFFFAOYSA-N 0.000 claims 1
- DKAKENLLKAAJLB-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-6-[1-(3-methoxypropyl)piperidin-4-yl]oxy-5-methylpyrimidine Chemical compound C1CN(CCCOC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C DKAKENLLKAAJLB-UHFFFAOYSA-N 0.000 claims 1
- FMPWSSDQCGMCEM-UHFFFAOYSA-N 4-(2-fluoro-4-methylsulfonylphenoxy)-6-[1-(4-methoxycyclohexyl)piperidin-4-yl]oxy-5-methylpyrimidine Chemical compound C1CC(OC)CCC1N1CCC(OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)CC1 FMPWSSDQCGMCEM-UHFFFAOYSA-N 0.000 claims 1
- DBOSVHCPPHXLBM-UHFFFAOYSA-N 4-(4-methylsulfonylanilino)-6-[1-(oxolane-2-carbonyl)piperidin-4-yl]oxypyrimidine-5-carbonitrile Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)C2OCCC2)=C1C#N DBOSVHCPPHXLBM-UHFFFAOYSA-N 0.000 claims 1
- FLKMZINWQJKEFD-UHFFFAOYSA-N 4-(4-methylsulfonylanilino)-6-[1-(pyridine-2-carbonyl)piperidin-4-yl]oxypyrimidine-5-carbonitrile Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)C=2N=CC=CC=2)=C1C#N FLKMZINWQJKEFD-UHFFFAOYSA-N 0.000 claims 1
- YINWJAMYSUYNSJ-UHFFFAOYSA-N 4-(4-methylsulfonylanilino)-6-[1-(pyridine-3-carbonyl)piperidin-4-yl]oxypyrimidine-5-carbonitrile Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)C=2C=NC=CC=2)=C1C#N YINWJAMYSUYNSJ-UHFFFAOYSA-N 0.000 claims 1
- LIGNNMGXVMPANI-UHFFFAOYSA-N 4-[1-(3,3-dimethyl-2-oxobutyl)piperidin-4-yl]oxy-6-(4-methylsulfonylanilino)pyrimidine-5-carbonitrile Chemical compound C1CN(CC(=O)C(C)(C)C)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1C#N LIGNNMGXVMPANI-UHFFFAOYSA-N 0.000 claims 1
- OXSWPFICEVAYLI-UHFFFAOYSA-N 4-[2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]acetyl]benzonitrile Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)C1=CC=C(C#N)C=C1 OXSWPFICEVAYLI-UHFFFAOYSA-N 0.000 claims 1
- UZBYFVFRWANJMR-UHFFFAOYSA-N 4-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-4-oxobutanoic acid Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC1CCN(C(=O)CCC(O)=O)CC1 UZBYFVFRWANJMR-UHFFFAOYSA-N 0.000 claims 1
- JRFBERKQAWMFIA-UHFFFAOYSA-N 4-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]butanoic acid Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC1CCN(CCCC(O)=O)CC1 JRFBERKQAWMFIA-UHFFFAOYSA-N 0.000 claims 1
- OPVUBJGKKGMRHF-UHFFFAOYSA-N 4-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]cyclohexane-1-carboxylic acid Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1C1CCC(C(O)=O)CC1 OPVUBJGKKGMRHF-UHFFFAOYSA-N 0.000 claims 1
- WUAPNOGRFMNQBW-UHFFFAOYSA-N 4-[5-ethynyl-6-[1-(3-propan-2-yl-1,2,4-oxadiazol-5-yl)piperidin-4-yl]oxypyrimidin-4-yl]oxy-3-fluorobenzonitrile Chemical compound CC(C)C1=NOC(N2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)C#N)F)N=CN=2)C#C)=N1 WUAPNOGRFMNQBW-UHFFFAOYSA-N 0.000 claims 1
- WEDVKQHNZJJEMJ-UHFFFAOYSA-N 4-[5-methyl-6-(1-propan-2-yloxycarbonylpiperidin-4-yl)oxypyrimidin-4-yl]oxybenzenesulfonic acid Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C=CC(=CC=2)S(O)(=O)=O)=C1C WEDVKQHNZJJEMJ-UHFFFAOYSA-N 0.000 claims 1
- GHLZCPGUOZCNKM-UHFFFAOYSA-N 4-[[5-ethynyl-6-[1-(3-propan-2-yl-1,2,4-oxadiazol-5-yl)piperidin-4-yl]oxypyrimidin-4-yl]amino]-3-fluorobenzonitrile Chemical compound CC(C)C1=NOC(N2CCC(CC2)OC=2C(=C(NC=3C(=CC(=CC=3)C#N)F)N=CN=2)C#C)=N1 GHLZCPGUOZCNKM-UHFFFAOYSA-N 0.000 claims 1
- HIQWBSMZSYOGER-UHFFFAOYSA-N 5-[4-[5-ethynyl-6-(2-fluoro-4-methylsulfonylphenoxy)pyrimidin-4-yl]oxypiperidin-1-yl]-3-propan-2-yl-1,2,4-oxadiazole Chemical compound CC(C)C1=NOC(N2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C#C)=N1 HIQWBSMZSYOGER-UHFFFAOYSA-N 0.000 claims 1
- ZWNVNAGORNWSJM-UHFFFAOYSA-N 5-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-methyl-1,2,4-oxadiazole Chemical compound CC1=NOC(N2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)=N1 ZWNVNAGORNWSJM-UHFFFAOYSA-N 0.000 claims 1
- OZKKNPMLZOJSHG-UHFFFAOYSA-N 5-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-propan-2-yl-1,2,4-oxadiazole Chemical compound CC(C)C1=NOC(N2CCC(CC2)OC=2C(=C(OC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)=N1 OZKKNPMLZOJSHG-UHFFFAOYSA-N 0.000 claims 1
- JOMRUCMOWQYVPH-UHFFFAOYSA-N 5-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-4-oxopentanenitrile Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC1CCN(CC(=O)CCC#N)CC1 JOMRUCMOWQYVPH-UHFFFAOYSA-N 0.000 claims 1
- GOTPPKKRNYLGNE-UHFFFAOYSA-N 5-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-4-oxopentanoic acid Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC1CCN(CC(=O)CCC(O)=O)CC1 GOTPPKKRNYLGNE-UHFFFAOYSA-N 0.000 claims 1
- DSEYJRQXCPNOQS-UHFFFAOYSA-N 5-[4-[6-(4-bromo-2-fluorophenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-3-propan-2-yl-1,2,4-oxadiazole Chemical compound CC(C)C1=NOC(N2CCC(CC2)OC=2C(=C(OC=3C(=CC(Br)=CC=3)F)N=CN=2)C)=N1 DSEYJRQXCPNOQS-UHFFFAOYSA-N 0.000 claims 1
- OTCNORQDEKFSQJ-UHFFFAOYSA-N 5-ethynyl-n-(2-fluoro-4-methylsulfonylphenyl)-6-[1-(3-propan-2-yl-1,2,4-oxadiazol-5-yl)piperidin-4-yl]oxypyrimidin-4-amine Chemical compound CC(C)C1=NOC(N2CCC(CC2)OC=2C(=C(NC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C#C)=N1 OTCNORQDEKFSQJ-UHFFFAOYSA-N 0.000 claims 1
- WUUPHVSVAJFGQY-UHFFFAOYSA-N 6-(1-butylsulfonylpiperidin-4-yl)oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound C1CN(S(=O)(=O)CCCC)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O WUUPHVSVAJFGQY-UHFFFAOYSA-N 0.000 claims 1
- ASBQCOPKXJXJBA-UHFFFAOYSA-N 6-(1-hexylpiperidin-4-yl)oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound C1CN(CCCCCC)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O ASBQCOPKXJXJBA-UHFFFAOYSA-N 0.000 claims 1
- VUQXEBQXNBVHSC-UHFFFAOYSA-N 6-[1-(1-methylimidazol-4-yl)sulfonylpiperidin-4-yl]oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound CN1C=NC(S(=O)(=O)N2CCC(CC2)OC=2C(=C(NC=3C=CC(=CC=3)S(C)(=O)=O)N=CN=2)[N+]([O-])=O)=C1 VUQXEBQXNBVHSC-UHFFFAOYSA-N 0.000 claims 1
- AMORTYLNSDSJNK-UHFFFAOYSA-N 6-[1-(2-ethoxyethyl)piperidin-4-yl]oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound C1CN(CCOCC)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O AMORTYLNSDSJNK-UHFFFAOYSA-N 0.000 claims 1
- UGGSPMQRNUCNBE-UHFFFAOYSA-N 6-[1-(3,3-dimethylbutyl)piperidin-4-yl]oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound C1CN(CCC(C)(C)C)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O UGGSPMQRNUCNBE-UHFFFAOYSA-N 0.000 claims 1
- VGLGTLBVYJRXMY-UHFFFAOYSA-N 6-[1-(3-methylbutyl)piperidin-4-yl]oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound C1CN(CCC(C)C)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O VGLGTLBVYJRXMY-UHFFFAOYSA-N 0.000 claims 1
- FZIQGTZAADXHTO-UHFFFAOYSA-N 6-[1-(cyclopropylmethyl)piperidin-4-yl]oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC3CC3)CC2)=C1[N+]([O-])=O FZIQGTZAADXHTO-UHFFFAOYSA-N 0.000 claims 1
- XHCKZJIDLWYGSV-UHFFFAOYSA-N 6-[1-[(2,4-dimethyl-1,3-thiazol-5-yl)sulfonyl]piperidin-4-yl]oxy-n-(4-methylsulfonylphenyl)-5-nitropyrimidin-4-amine Chemical compound S1C(C)=NC(C)=C1S(=O)(=O)N1CCC(OC=2C(=C(NC=3C=CC(=CC=3)S(C)(=O)=O)N=CN=2)[N+]([O-])=O)CC1 XHCKZJIDLWYGSV-UHFFFAOYSA-N 0.000 claims 1
- RNPWVVWMMDDDDF-UHFFFAOYSA-N 6-n-(4-methylsulfonylphenyl)-5-nitro-4-n-piperidin-4-ylpyrimidine-4,6-diamine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(NC2CCNCC2)=C1[N+]([O-])=O RNPWVVWMMDDDDF-UHFFFAOYSA-N 0.000 claims 1
- AYBBTCLLYOYTHS-MRXNPFEDSA-N [(3r)-oxolan-3-yl] 4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1C(=O)O[C@@H]1CCOC1 AYBBTCLLYOYTHS-MRXNPFEDSA-N 0.000 claims 1
- AYBBTCLLYOYTHS-INIZCTEOSA-N [(3s)-oxolan-3-yl] 4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1C(=O)O[C@H]1CCOC1 AYBBTCLLYOYTHS-INIZCTEOSA-N 0.000 claims 1
- VWVLGJIQPZRFQV-UHFFFAOYSA-N [4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-(oxolan-2-yl)methanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1C(=O)C1CCCO1 VWVLGJIQPZRFQV-UHFFFAOYSA-N 0.000 claims 1
- HDOUIWSXXJZLNT-UHFFFAOYSA-N [4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]-[6-(2-pyrrolidin-1-ylethyl)pyridin-3-yl]methanone Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1C(=O)C(C=N1)=CC=C1CCN1CCCC1 HDOUIWSXXJZLNT-UHFFFAOYSA-N 0.000 claims 1
- DADMJFSLSPECRO-UHFFFAOYSA-N [4-[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]oxypiperidin-1-yl]-pyridin-2-ylmethanone Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)C=2N=CC=CC=2)=C1[N+]([O-])=O DADMJFSLSPECRO-UHFFFAOYSA-N 0.000 claims 1
- ZOGSDONAVGUYKY-UHFFFAOYSA-N [4-[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]oxypiperidin-1-yl]-pyridin-3-ylmethanone Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)C=2C=NC=CC=2)=C1[N+]([O-])=O ZOGSDONAVGUYKY-UHFFFAOYSA-N 0.000 claims 1
- GVBFWCNJDPQJJX-UHFFFAOYSA-N ethyl 2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]acetate Chemical compound C1CN(CC(=O)OCC)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C GVBFWCNJDPQJJX-UHFFFAOYSA-N 0.000 claims 1
- ZPFPHIJNUJHJIJ-UHFFFAOYSA-N ethyl 4-[5-cyano-6-(4-methylsulfonylanilino)pyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1C#N ZPFPHIJNUJHJIJ-UHFFFAOYSA-N 0.000 claims 1
- HNESUBILRWZIJH-UHFFFAOYSA-N ethyl 4-[6-(4-methylsulfonylanilino)-5-nitropyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O HNESUBILRWZIJH-UHFFFAOYSA-N 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- MIKPNFRHUSSWPW-UHFFFAOYSA-N n-(2-fluoro-4-methylsulfonylphenyl)-5-methyl-6-[1-(3-propan-2-yl-1,2,4-oxadiazol-5-yl)piperidin-4-yl]oxypyrimidin-4-amine Chemical compound CC(C)C1=NOC(N2CCC(CC2)OC=2C(=C(NC=3C(=CC(=CC=3)S(C)(=O)=O)F)N=CN=2)C)=N1 MIKPNFRHUSSWPW-UHFFFAOYSA-N 0.000 claims 1
- MPRPMZLALGYKSX-UHFFFAOYSA-N n-(3,5-dichlorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]acetamide Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)NC1=CC(Cl)=CC(Cl)=C1 MPRPMZLALGYKSX-UHFFFAOYSA-N 0.000 claims 1
- XYTXYHSAIKDPLR-UHFFFAOYSA-N n-(3-chlorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]acetamide Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)NC1=CC=CC(Cl)=C1 XYTXYHSAIKDPLR-UHFFFAOYSA-N 0.000 claims 1
- SSJBYJPJNQVDTE-UHFFFAOYSA-N n-(4-chlorophenyl)-2-[4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidin-1-yl]acetamide Chemical compound N1=CN=C(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)C(C)=C1OC(CC1)CCN1CC(=O)NC1=CC=C(Cl)C=C1 SSJBYJPJNQVDTE-UHFFFAOYSA-N 0.000 claims 1
- RGSZNJSURQGKFN-UHFFFAOYSA-N n-(4-methylsulfonylphenyl)-5-nitro-6-(1-propylsulfonylpiperidin-4-yl)oxypyrimidin-4-amine Chemical compound C1CN(S(=O)(=O)CCC)CCC1OC1=NC=NC(NC=2C=CC(=CC=2)S(C)(=O)=O)=C1[N+]([O-])=O RGSZNJSURQGKFN-UHFFFAOYSA-N 0.000 claims 1
- VRBVIBUXYLJGPL-UHFFFAOYSA-N n-(4-methylsulfonylphenyl)-5-nitro-6-(1-pyridin-2-ylpiperidin-4-yl)oxypyrimidin-4-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C=2N=CC=CC=2)=C1[N+]([O-])=O VRBVIBUXYLJGPL-UHFFFAOYSA-N 0.000 claims 1
- OGIWNXGYRVBJBD-UHFFFAOYSA-N n-(4-methylsulfonylphenyl)-5-nitro-6-(1-thiophen-2-ylsulfonylpiperidin-4-yl)oxypyrimidin-4-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)S(=O)(=O)C=2SC=CC=2)=C1[N+]([O-])=O OGIWNXGYRVBJBD-UHFFFAOYSA-N 0.000 claims 1
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- RLTJJAPYYDVBHI-UHFFFAOYSA-N propan-2-yl 4-[5-methyl-6-[2-methyl-6-(2-propan-2-yloxyethyl)pyridin-3-yl]oxypyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound CC1=NC(CCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C RLTJJAPYYDVBHI-UHFFFAOYSA-N 0.000 claims 1
- ZPWICAYIOJFSAF-UHFFFAOYSA-N propan-2-yl 4-[5-methyl-6-[2-methyl-6-(2-propan-2-yloxyethylamino)pyridin-3-yl]oxypyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound CC1=NC(NCCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C ZPWICAYIOJFSAF-UHFFFAOYSA-N 0.000 claims 1
- WSSOKQLEYYKNIE-UHFFFAOYSA-N propan-2-yl 4-[5-methyl-6-[2-methyl-6-(2-propan-2-yloxyethylsulfonyl)pyridin-3-yl]oxypyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound CC1=NC(S(=O)(=O)CCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C WSSOKQLEYYKNIE-UHFFFAOYSA-N 0.000 claims 1
- BHJOPJYQRQJFEX-UHFFFAOYSA-N propan-2-yl 4-[5-methyl-6-[2-methyl-6-(2-pyridin-2-ylethoxy)pyridin-3-yl]oxypyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=NC(OCCC=3N=CC=CC=3)=CC=2)C)=C1C BHJOPJYQRQJFEX-UHFFFAOYSA-N 0.000 claims 1
- YEFYWAQUIUARHT-UHFFFAOYSA-N propan-2-yl 4-[5-methyl-6-[2-methyl-6-(3-methylsulfonylpyrrolidin-1-yl)pyridin-3-yl]oxypyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=NC(=CC=2)N2CC(CC2)S(C)(=O)=O)C)=C1C YEFYWAQUIUARHT-UHFFFAOYSA-N 0.000 claims 1
- QEMUYKYQTXITIU-UHFFFAOYSA-N propan-2-yl 4-[5-methyl-6-[2-methyl-6-[methyl(2-methylsulfonylethyl)amino]pyridin-3-yl]oxypyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=NC(=CC=2)N(C)CCS(C)(=O)=O)C)=C1C QEMUYKYQTXITIU-UHFFFAOYSA-N 0.000 claims 1
- PXAAOZABLFMNNP-UHFFFAOYSA-N propan-2-yl 4-[5-methyl-6-[2-methyl-6-[methyl(2-propan-2-yloxyethyl)amino]pyridin-3-yl]oxypyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound CC1=NC(N(C)CCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C PXAAOZABLFMNNP-UHFFFAOYSA-N 0.000 claims 1
- NSLQLEXVLQPFCZ-UHFFFAOYSA-N propan-2-yl 4-[6-(2,4-difluorophenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(F)=CC=2)F)=C1C NSLQLEXVLQPFCZ-UHFFFAOYSA-N 0.000 claims 1
- FUVPFNOSJYGLPK-UHFFFAOYSA-N propan-2-yl 4-[6-(2,5-difluoro-4-morpholin-4-ylanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=C(F)C=2)N2CCOCC2)F)=C1C FUVPFNOSJYGLPK-UHFFFAOYSA-N 0.000 claims 1
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- ZJWHLPLVFLFBFU-UHFFFAOYSA-N propan-2-yl 4-[6-(2-amino-4-ethylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound NC1=CC(S(=O)(=O)CC)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C ZJWHLPLVFLFBFU-UHFFFAOYSA-N 0.000 claims 1
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- YHHAHJJSDRQSRI-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-methylsulfonylanilino)-5-(n'-hydroxycarbamimidoyl)pyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C(=N)NO YHHAHJJSDRQSRI-UHFFFAOYSA-N 0.000 claims 1
- CETAULDFJQHIIO-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-methylsulfonylanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C CETAULDFJQHIIO-UHFFFAOYSA-N 0.000 claims 1
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- FEGPUMZPRQGWFH-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(C)(=O)=O)F)=C1C FEGPUMZPRQGWFH-UHFFFAOYSA-N 0.000 claims 1
- DNEKWRVZWQYSII-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-morpholin-4-ylanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)N2CCOCC2)F)=C1C DNEKWRVZWQYSII-UHFFFAOYSA-N 0.000 claims 1
- UAGMIFWTVRQHCS-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-morpholin-4-ylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)N2CCOCC2)F)=C1C UAGMIFWTVRQHCS-UHFFFAOYSA-N 0.000 claims 1
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- KJILYXWVLTZHIG-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-pyridin-4-ylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C=2C=CN=CC=2)F)=C1C KJILYXWVLTZHIG-UHFFFAOYSA-N 0.000 claims 1
- UHAQXZNFHIKJSK-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-pyrimidin-5-ylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C=2C=NC=NC=2)F)=C1C UHAQXZNFHIKJSK-UHFFFAOYSA-N 0.000 claims 1
- AUPWVYJZIQROJT-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluoro-4-sulfamoylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)S(N)(=O)=O)F)=C1C AUPWVYJZIQROJT-UHFFFAOYSA-N 0.000 claims 1
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- WRUCYROGZMLUFE-UHFFFAOYSA-N propan-2-yl 4-[6-(2-fluorophenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC=CC=2)F)=C1C WRUCYROGZMLUFE-UHFFFAOYSA-N 0.000 claims 1
- RYCBZUIEKBLZGV-UHFFFAOYSA-N propan-2-yl 4-[6-(4-bromo-2,5-difluoroanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(Br)=C(F)C=2)F)=C1C RYCBZUIEKBLZGV-UHFFFAOYSA-N 0.000 claims 1
- CMXAMJYUNZOYQN-UHFFFAOYSA-N propan-2-yl 4-[6-(4-bromo-2-fluorophenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(Br)=CC=2)F)=C1C CMXAMJYUNZOYQN-UHFFFAOYSA-N 0.000 claims 1
- WBDSWKYSCKAMGZ-UHFFFAOYSA-N propan-2-yl 4-[6-(4-carbamimidoyl-2,5-difluoroanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=C(F)C=2)C(N)=N)F)=C1C WBDSWKYSCKAMGZ-UHFFFAOYSA-N 0.000 claims 1
- VWBNSZCNUFREEU-UHFFFAOYSA-N propan-2-yl 4-[6-(4-carbamoyl-2,5-difluoroanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=C(F)C=2)C(N)=O)F)=C1C VWBNSZCNUFREEU-UHFFFAOYSA-N 0.000 claims 1
- MBRPHWHMCQYIGF-UHFFFAOYSA-N propan-2-yl 4-[6-(4-carbamoyl-2-fluorophenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C(N)=O)F)=C1C MBRPHWHMCQYIGF-UHFFFAOYSA-N 0.000 claims 1
- IIKFADUSHOWPEI-UHFFFAOYSA-N propan-2-yl 4-[6-(4-cyano-2,5-difluoroanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=C(F)C=2)C#N)F)=C1C IIKFADUSHOWPEI-UHFFFAOYSA-N 0.000 claims 1
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- YYTDPKRUHUGFKM-UHFFFAOYSA-N propan-2-yl 4-[6-(4-cyano-2-fluoroanilino)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)C#N)F)=C1C YYTDPKRUHUGFKM-UHFFFAOYSA-N 0.000 claims 1
- RROARNPQYHNTRB-UHFFFAOYSA-N propan-2-yl 4-[6-(4-cyano-2-fluorophenoxy)-5-ethynylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C#N)F)=C1C#C RROARNPQYHNTRB-UHFFFAOYSA-N 0.000 claims 1
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- AQVCVWMEYVQWBA-UHFFFAOYSA-N propan-2-yl 4-[6-(6-amino-2-methylpyridin-3-yl)oxy-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=NC(N)=CC=2)C)=C1C AQVCVWMEYVQWBA-UHFFFAOYSA-N 0.000 claims 1
- CLODCVKGSVBCJT-UHFFFAOYSA-N propan-2-yl 4-[6-(6-chloro-2-methylpyridin-3-yl)oxy-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=NC(Cl)=CC=2)C)=C1C CLODCVKGSVBCJT-UHFFFAOYSA-N 0.000 claims 1
- AZOJZEMNGYADTQ-UHFFFAOYSA-N propan-2-yl 4-[6-[(6-chloro-2-methylpyridin-3-yl)amino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=NC(Cl)=CC=2)C)=C1C AZOJZEMNGYADTQ-UHFFFAOYSA-N 0.000 claims 1
- JDJIIACNAVDGRO-UHFFFAOYSA-N propan-2-yl 4-[6-[(6-chloro-4-fluoropyridin-3-yl)amino]-5-cyanopyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(Cl)=NC=2)F)=C1C#N JDJIIACNAVDGRO-UHFFFAOYSA-N 0.000 claims 1
- ZLAWJAASCHLJCK-UHFFFAOYSA-N propan-2-yl 4-[6-[(6-chloro-4-methylpyridin-3-yl)amino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(Cl)=NC=2)C)=C1C ZLAWJAASCHLJCK-UHFFFAOYSA-N 0.000 claims 1
- RLRZXOMUGOGMKA-UHFFFAOYSA-N propan-2-yl 4-[6-[2,3-difluoro-4-(2-methylsulfonylethyl)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=C(F)C(CCS(C)(=O)=O)=CC=2)F)=C1C RLRZXOMUGOGMKA-UHFFFAOYSA-N 0.000 claims 1
- BMQSCHGXCKJSKE-UHFFFAOYSA-N propan-2-yl 4-[6-[2,3-difluoro-4-(2-methylsulfonylethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=C(F)C(CCS(C)(=O)=O)=CC=2)F)=C1C BMQSCHGXCKJSKE-UHFFFAOYSA-N 0.000 claims 1
- CTOMSGBVBCDWOU-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-(2-methoxyethoxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1=C(F)C(OCCOC)=CC(F)=C1NC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C CTOMSGBVBCDWOU-UHFFFAOYSA-N 0.000 claims 1
- BBVNUJZNCLCSPS-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-(2-methylsulfonylethyl)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(CCS(C)(=O)=O)=C(F)C=2)F)=C1C BBVNUJZNCLCSPS-UHFFFAOYSA-N 0.000 claims 1
- TWOGYGUGMDXEQY-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-(2-methylsulfonylethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCS(C)(=O)=O)=C(F)C=2)F)=C1C TWOGYGUGMDXEQY-UHFFFAOYSA-N 0.000 claims 1
- JNLNGMYUDUZZRW-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-(2-morpholin-4-ylethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCN3CCOCC3)=C(F)C=2)F)=C1C JNLNGMYUDUZZRW-UHFFFAOYSA-N 0.000 claims 1
- AXIAZYZEGMRUNR-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-(n'-hydroxycarbamimidoyl)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=C(F)C=2)C(=N)NO)F)=C1C AXIAZYZEGMRUNR-UHFFFAOYSA-N 0.000 claims 1
- QGCFLMKKPXDPKJ-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-(trifluoromethoxy)phenoxy]-5-ethynylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(OC(F)(F)F)=C(F)C=2)F)=C1C#C QGCFLMKKPXDPKJ-UHFFFAOYSA-N 0.000 claims 1
- VEBXRJLVZHNWFN-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-(trifluoromethoxy)phenoxy]-5-prop-1-ynylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound N1=CN=C(OC=2C(=CC(OC(F)(F)F)=C(F)C=2)F)C(C#CC)=C1OC1CCN(C(=O)OC(C)C)CC1 VEBXRJLVZHNWFN-UHFFFAOYSA-N 0.000 claims 1
- PISKBNYLTUJSMW-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-[2-(1,2,4-triazol-1-yl)ethyl]anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(CCN3N=CN=C3)=C(F)C=2)F)=C1C PISKBNYLTUJSMW-UHFFFAOYSA-N 0.000 claims 1
- OZJQWYFHVNLWGV-UHFFFAOYSA-N propan-2-yl 4-[6-[2,5-difluoro-4-[2-(1,2,4-triazol-1-yl)ethyl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCN3N=CN=C3)=C(F)C=2)F)=C1C OZJQWYFHVNLWGV-UHFFFAOYSA-N 0.000 claims 1
- HAXGOWDKEMRTJS-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-hydroxyethoxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(OCCO)=CC=2)F)=C1C HAXGOWDKEMRTJS-UHFFFAOYSA-N 0.000 claims 1
- YMLFKNYAQKEKMT-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-hydroxyethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCO)=CC=2)F)=C1C YMLFKNYAQKEKMT-UHFFFAOYSA-N 0.000 claims 1
- HETOYGUJFDGINB-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-imidazol-1-ylethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCN3C=NC=C3)=CC=2)F)=C1C HETOYGUJFDGINB-UHFFFAOYSA-N 0.000 claims 1
- VSWMTWPKJUWSID-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-methoxyethoxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(OCCOC)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C VSWMTWPKJUWSID-UHFFFAOYSA-N 0.000 claims 1
- KTUPQVPEEPMWCU-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-methoxyethylamino)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(NCCOC)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C KTUPQVPEEPMWCU-UHFFFAOYSA-N 0.000 claims 1
- IOIOUGPZHCNRGS-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-methoxyethylcarbamoyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(C(=O)NCCOC)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C IOIOUGPZHCNRGS-UHFFFAOYSA-N 0.000 claims 1
- RNCHRLLIKRUBPX-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-methylsulfonylethoxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(OCCS(C)(=O)=O)=CC=2)F)=C1C RNCHRLLIKRUBPX-UHFFFAOYSA-N 0.000 claims 1
- OAZAGUDHDAWCOR-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-methylsulfonylethyl)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(CCS(C)(=O)=O)=CC=2)F)=C1C OAZAGUDHDAWCOR-UHFFFAOYSA-N 0.000 claims 1
- VGCRHIKAKZKWOF-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-methylsulfonylethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCS(C)(=O)=O)=CC=2)F)=C1C VGCRHIKAKZKWOF-UHFFFAOYSA-N 0.000 claims 1
- AJHLWZLACIOZMR-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-methylsulfonylethylamino)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(NCCS(C)(=O)=O)=CC=2)F)=C1C AJHLWZLACIOZMR-UHFFFAOYSA-N 0.000 claims 1
- XVLAZRKHCAGQJJ-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-morpholin-4-ylethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCN3CCOCC3)=CC=2)F)=C1C XVLAZRKHCAGQJJ-UHFFFAOYSA-N 0.000 claims 1
- UNPIQRIPQOOGHZ-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-phosphonooxyethyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCOP(O)(O)=O)=CC=2)F)=C1C UNPIQRIPQOOGHZ-UHFFFAOYSA-N 0.000 claims 1
- CHSMDZOJSOXXBI-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-propan-2-yloxyethoxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(OCCOC(C)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C CHSMDZOJSOXXBI-UHFFFAOYSA-N 0.000 claims 1
- XPJGMUJGHYDECJ-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-propan-2-yloxyethoxy)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(OCCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C XPJGMUJGHYDECJ-UHFFFAOYSA-N 0.000 claims 1
- HOQBUTBSIIHOCH-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-propan-2-yloxyethylamino)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(NCCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C HOQBUTBSIIHOCH-UHFFFAOYSA-N 0.000 claims 1
- ZXPCYPDCHABJBF-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-propan-2-yloxyethylsulfamoyl)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(S(=O)(=O)NCCOC(C)C)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C ZXPCYPDCHABJBF-UHFFFAOYSA-N 0.000 claims 1
- UEZRYSSOLPIHEX-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(2-pyridin-2-ylethoxy)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(OCCC=3N=CC=CC=3)=CC=2)F)=C1C UEZRYSSOLPIHEX-UHFFFAOYSA-N 0.000 claims 1
- PGKJGOFQPMALGJ-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(3-methoxypropoxy)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(OCCCOC)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C PGKJGOFQPMALGJ-UHFFFAOYSA-N 0.000 claims 1
- OMLJEUKKPUKHNB-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(3-methoxypropylsulfonyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(S(=O)(=O)CCCOC)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C OMLJEUKKPUKHNB-UHFFFAOYSA-N 0.000 claims 1
- WMZJVGAPOFVIPY-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(3-methoxypyridin-2-yl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound COC1=CC=CN=C1C(C=C1F)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C WMZJVGAPOFVIPY-UHFFFAOYSA-N 0.000 claims 1
- GZZYBQOCRCVABA-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(4-propan-2-ylpiperazine-1-carbonyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C(=O)N2CCN(CC2)C(C)C)F)=C1C GZZYBQOCRCVABA-UHFFFAOYSA-N 0.000 claims 1
- CZZOGDHQLJVGGT-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(5-methoxypyridin-2-yl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound N1=CC(OC)=CC=C1C(C=C1F)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C CZZOGDHQLJVGGT-UHFFFAOYSA-N 0.000 claims 1
- FNXAERGVGRIRPJ-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(5-methoxypyridin-3-yl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound COC1=CN=CC(C=2C=C(F)C(OC=3C(=C(OC4CCN(CC4)C(=O)OC(C)C)N=CN=3)C)=CC=2)=C1 FNXAERGVGRIRPJ-UHFFFAOYSA-N 0.000 claims 1
- JHJZKZFLAKFXNO-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(6-methoxypyridin-3-yl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1=NC(OC)=CC=C1C(C=C1F)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C JHJZKZFLAKFXNO-UHFFFAOYSA-N 0.000 claims 1
- RLKURVUAVXZLFI-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(methanesulfonamido)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(NS(C)(=O)=O)=CC=2)F)=C1C RLKURVUAVXZLFI-UHFFFAOYSA-N 0.000 claims 1
- QKQJBMVIEJGIOY-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(oxan-4-yloxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(OC3CCOCC3)=CC=2)F)=C1C QKQJBMVIEJGIOY-UHFFFAOYSA-N 0.000 claims 1
- UMCWFDFYNNIRQR-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(oxan-4-yloxy)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(OC3CCOCC3)=CC=2)F)=C1C UMCWFDFYNNIRQR-UHFFFAOYSA-N 0.000 claims 1
- MTKZPBCCWLLISS-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(oxolan-2-ylmethoxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(OCC3OCCC3)=CC=2)F)=C1C MTKZPBCCWLLISS-UHFFFAOYSA-N 0.000 claims 1
- IIIXUUQXURBVAR-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(oxolan-2-ylmethylamino)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(NCC3OCCC3)=CC=2)F)=C1C IIIXUUQXURBVAR-UHFFFAOYSA-N 0.000 claims 1
- MSTPEBZHISIWGK-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(oxolan-2-ylmethylamino)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(NCC3OCCC3)=CC=2)F)=C1C MSTPEBZHISIWGK-UHFFFAOYSA-N 0.000 claims 1
- ITQKJDJHZHDFBJ-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(propanoylsulfamoyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(S(=O)(=O)NC(=O)CC)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C ITQKJDJHZHDFBJ-UHFFFAOYSA-N 0.000 claims 1
- BOJBCSGXZJNGMP-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(propylamino)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(NCCC)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C BOJBCSGXZJNGMP-UHFFFAOYSA-N 0.000 claims 1
- DKKNGXJPBDPDPJ-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(pyridin-2-ylmethoxy)anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(OCC=3N=CC=CC=3)=CC=2)F)=C1C DKKNGXJPBDPDPJ-UHFFFAOYSA-N 0.000 claims 1
- MZRJRANLKQTSCY-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(pyridine-2-carbonyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C(=O)C=2N=CC=CC=2)F)=C1C MZRJRANLKQTSCY-UHFFFAOYSA-N 0.000 claims 1
- ADTXKBXANHVSEM-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-(thiophene-2-carbonyl)phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)C(=O)C=2SC=CC=2)F)=C1C ADTXKBXANHVSEM-UHFFFAOYSA-N 0.000 claims 1
- KGLUMNMAISAVHF-SFHVURJKSA-N propan-2-yl 4-[6-[2-fluoro-4-[(4r)-2-oxo-1,3-oxazolidin-4-yl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)[C@H]2NC(=O)OC2)F)=C1C KGLUMNMAISAVHF-SFHVURJKSA-N 0.000 claims 1
- KGLUMNMAISAVHF-GOSISDBHSA-N propan-2-yl 4-[6-[2-fluoro-4-[(4s)-2-oxo-1,3-oxazolidin-4-yl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(=CC=2)[C@@H]2NC(=O)OC2)F)=C1C KGLUMNMAISAVHF-GOSISDBHSA-N 0.000 claims 1
- OCSZWDWXPKBLIU-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[2-(2-hydroxyethylamino)-2-oxoethyl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CC(=O)NCCO)=CC=2)F)=C1C OCSZWDWXPKBLIU-UHFFFAOYSA-N 0.000 claims 1
- TZLYKVMHYOOBQU-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[2-(2-methylpropoxy)ethoxy]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(OCCOCC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C TZLYKVMHYOOBQU-UHFFFAOYSA-N 0.000 claims 1
- CMPLAQWCNXONKG-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[2-(triazol-1-yl)ethyl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCN3N=NC=C3)=CC=2)F)=C1C CMPLAQWCNXONKG-UHFFFAOYSA-N 0.000 claims 1
- DCTPZDGHGAHJOX-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[2-[(2-methylpropan-2-yl)oxy]ethoxy]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(OCCOC(C)(C)C)=CC=2)F)=C1C DCTPZDGHGAHJOX-UHFFFAOYSA-N 0.000 claims 1
- MWORHDZZZNKAQP-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[2-oxo-2-(2-propan-2-yloxyethylamino)ethyl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(CC(=O)NCCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C MWORHDZZZNKAQP-UHFFFAOYSA-N 0.000 claims 1
- FZVLKVYJGJARPW-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[5-(propan-2-yloxymethyl)-1,2,4-oxadiazol-3-yl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound O1C(COC(C)C)=NC(C=2C=C(F)C(OC=3C(=C(OC4CCN(CC4)C(=O)OC(C)C)N=CN=3)C)=CC=2)=N1 FZVLKVYJGJARPW-UHFFFAOYSA-N 0.000 claims 1
- NMNURQZBLKKXDM-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[methyl(2-methylsulfonylethyl)amino]anilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(NC=2C(=CC(=CC=2)N(C)CCS(C)(=O)=O)F)=C1C NMNURQZBLKKXDM-UHFFFAOYSA-N 0.000 claims 1
- AJZUWEHTCVVXJG-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-4-[n'-(2-propan-2-yloxyethyl)carbamimidoyl]phenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(C(=N)NCCOC(C)C)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C AJZUWEHTCVVXJG-UHFFFAOYSA-N 0.000 claims 1
- PFJDFXKWNAFGNO-UHFFFAOYSA-N propan-2-yl 4-[6-[2-fluoro-n-(2-methoxyethyl)-4-methylsulfonylanilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound N=1C=NC(OC2CCN(CC2)C(=O)OC(C)C)=C(C)C=1N(CCOC)C1=CC=C(S(C)(=O)=O)C=C1F PFJDFXKWNAFGNO-UHFFFAOYSA-N 0.000 claims 1
- BUOFPIKGFFDFBG-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(2-amino-2-oxoethyl)-2-fluorophenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CC(N)=O)=CC=2)F)=C1C BUOFPIKGFFDFBG-UHFFFAOYSA-N 0.000 claims 1
- HMGKNQLILIKVCU-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(2-cyclopropyloxyethoxy)-2-fluorophenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(OCCOC3CC3)=CC=2)F)=C1C HMGKNQLILIKVCU-UHFFFAOYSA-N 0.000 claims 1
- OQDMPMMIRNANGW-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(2-ethoxyethoxy)-2-fluoroanilino]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(OCCOCC)=CC=C1NC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C OQDMPMMIRNANGW-UHFFFAOYSA-N 0.000 claims 1
- VODFVJZYYILJHH-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(2-ethoxyethoxy)-2-fluorophenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound FC1=CC(OCCOCC)=CC=C1OC1=NC=NC(OC2CCN(CC2)C(=O)OC(C)C)=C1C VODFVJZYYILJHH-UHFFFAOYSA-N 0.000 claims 1
- VLEWEXAJLISORE-UHFFFAOYSA-N propan-2-yl 4-[6-[4-[2-(dimethylamino)-2-oxoethyl]-2-fluorophenoxy]-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CC(=O)N(C)C)=CC=2)F)=C1C VLEWEXAJLISORE-UHFFFAOYSA-N 0.000 claims 1
- WGEATORUYINAEO-UHFFFAOYSA-N propan-2-yl 4-[6-[4-fluoro-6-(2-methylsulfonylethyl)pyridin-3-yl]oxy-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCS(C)(=O)=O)=NC=2)F)=C1C WGEATORUYINAEO-UHFFFAOYSA-N 0.000 claims 1
- CXXCDNSAIZTFEO-UHFFFAOYSA-N propan-2-yl 4-[6-[4-fluoro-6-(2-morpholin-4-ylethyl)pyridin-3-yl]oxy-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=CC(CCN3CCOCC3)=NC=2)F)=C1C CXXCDNSAIZTFEO-UHFFFAOYSA-N 0.000 claims 1
- JWMZGUNZIJMGJJ-UHFFFAOYSA-N propan-2-yl 4-[6-[6-(2-cyclopropyloxyethylamino)-2-methylpyridin-3-yl]oxy-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=NC(NCCOC3CC3)=CC=2)C)=C1C JWMZGUNZIJMGJJ-UHFFFAOYSA-N 0.000 claims 1
- CGTLTGSMTRRXDP-UHFFFAOYSA-N propan-2-yl 4-[6-[6-(2-fluoroethyl)-2-methylpyridin-3-yl]oxy-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1OC1=NC=NC(OC=2C(=NC(CCF)=CC=2)C)=C1C CGTLTGSMTRRXDP-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
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- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
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- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
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- Communicable Diseases (AREA)
- Oncology (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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PCT/US2004/022327 WO2005007647A1 (en) | 2003-07-11 | 2004-07-09 | Trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto |
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Families Citing this family (138)
Publication number | Priority date | Publication date | Assignee | Title |
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US7407955B2 (en) | 2002-08-21 | 2008-08-05 | Boehringer Ingelheim Pharma Gmbh & Co., Kg | 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions |
NZ540612A (en) | 2003-01-14 | 2008-02-29 | Arena Pharm Inc | 1,2,3-Trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto such as diabetes and hyperglycemia |
AR045047A1 (es) * | 2003-07-11 | 2005-10-12 | Arena Pharm Inc | Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos |
US7501426B2 (en) | 2004-02-18 | 2009-03-10 | Boehringer Ingelheim International Gmbh | 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions |
WO2005121121A2 (en) * | 2004-06-04 | 2005-12-22 | Arena Pharmaceuticals, Inc. | Substituted aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto |
DE102004042607A1 (de) | 2004-09-03 | 2006-03-09 | Bayer Healthcare Ag | Substituierte Phenylaminothiazole und ihre Verwendung |
DE102004054054A1 (de) | 2004-11-05 | 2006-05-11 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine |
BRPI0516407A (pt) * | 2004-12-24 | 2008-09-02 | Prosidion Ltd | agonistas de receptor acoplado à proteìna g (gpr116) e uso destes para o tratamento de obesidade e diabetes |
DOP2006000010A (es) * | 2005-01-10 | 2006-07-31 | Arena Pharm Inc | Procedimiento para preparar eteres aromáticos |
DOP2006000008A (es) * | 2005-01-10 | 2006-08-31 | Arena Pharm Inc | Terapia combinada para el tratamiento de la diabetes y afecciones relacionadas y para el tratamiento de afecciones que mejoran mediante un incremento de la concentración sanguínea de glp-1 |
MY148521A (en) | 2005-01-10 | 2013-04-30 | Arena Pharm Inc | Substituted pyridinyl and pyrimidinyl derivatives as modulators of metabolism and the treatment of disorders related thereto |
AU2006244203B2 (en) | 2005-05-09 | 2012-05-03 | Achillion Pharmaceuticals, Inc. | Thiazole compounds and methods of use |
CA2613235A1 (en) * | 2005-06-30 | 2007-01-11 | Prosidion Limited | Gpcr agonists |
CA2613236A1 (en) * | 2005-06-30 | 2007-01-11 | Prosidion Limited | G-protein coupled receptor agonists |
DE102005035891A1 (de) | 2005-07-30 | 2007-02-08 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel |
WO2007035355A2 (en) * | 2005-09-16 | 2007-03-29 | Arena Pharmaceuticals, Inc. | Modulators of metabolism and the treatment of disorders related thereto |
JP4854253B2 (ja) * | 2005-09-30 | 2012-01-18 | 国立大学法人佐賀大学 | 脂質代謝改善用組成物 |
CN101384568B (zh) | 2006-02-15 | 2012-12-12 | 雅培制药有限公司 | 乙酰辅酶a羧化酶(acc)抑制剂及其在糖尿病、肥胖症和代谢综合征中的应用 |
US8748627B2 (en) | 2006-02-15 | 2014-06-10 | Abbvie Inc. | Acetyl-CoA carboxylase (ACC) inhibitors and their use in diabetes, obesity and metabolic syndrome |
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