JP2018524343A5 - - Google Patents
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- Publication number
- JP2018524343A5 JP2018524343A5 JP2017568146A JP2017568146A JP2018524343A5 JP 2018524343 A5 JP2018524343 A5 JP 2018524343A5 JP 2017568146 A JP2017568146 A JP 2017568146A JP 2017568146 A JP2017568146 A JP 2017568146A JP 2018524343 A5 JP2018524343 A5 JP 2018524343A5
- Authority
- JP
- Japan
- Prior art keywords
- dihydro
- methyl
- difluoro
- furo
- carbonyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 113
- 125000000217 alkyl group Chemical group 0.000 claims 94
- 229910052739 hydrogen Inorganic materials 0.000 claims 72
- 239000001257 hydrogen Substances 0.000 claims 71
- 150000003839 salts Chemical class 0.000 claims 65
- 239000011780 sodium chloride Substances 0.000 claims 65
- -1 2,2-dimethyl-1,3-dioxolan-4-yl Chemical group 0.000 claims 51
- UHJCPTUYASMZRC-UHFFFAOYSA-N 1,3-benzodioxole-4-carboxamide Chemical compound NC(=O)C1=CC=CC2=C1OCO2 UHJCPTUYASMZRC-UHFFFAOYSA-N 0.000 claims 38
- 229910052736 halogen Inorganic materials 0.000 claims 38
- 150000002367 halogens Chemical class 0.000 claims 38
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 37
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 35
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 33
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 33
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 26
- 125000001424 substituent group Chemical group 0.000 claims 25
- 125000001188 haloalkyl group Chemical group 0.000 claims 23
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 22
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 22
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 19
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 19
- 125000003277 amino group Chemical compound 0.000 claims 19
- NZNMSOFKMUBTKW-UHFFFAOYSA-N Cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 claims 15
- 229910052799 carbon Inorganic materials 0.000 claims 15
- 125000005605 benzo group Chemical group 0.000 claims 14
- 125000003917 carbamoyl group Chemical compound [H]N([H])C(*)=O 0.000 claims 14
- 229910052757 nitrogen Inorganic materials 0.000 claims 14
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims 13
- 150000002431 hydrogen Chemical class 0.000 claims 12
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 12
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 11
- 239000005711 Benzoic acid Substances 0.000 claims 11
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 11
- 235000010233 benzoic acid Nutrition 0.000 claims 11
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 9
- 239000002253 acid Substances 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- 239000003814 drug Substances 0.000 claims 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 7
- 125000004076 pyridyl group Chemical group 0.000 claims 7
- UDKVMASCRFDIIP-UHFFFAOYSA-N 1,7,9,11-tetrahydroxy-3-methyl-8,13-dioxo-5,6-dihydrobenzo[a]tetracene-2-carboxylic acid Chemical compound O=C1C2=C(O)C=C(O)C=C2C(=O)C2=C1C(O)=C1CCC(C=C(C(=C3O)C(O)=O)C)=C3C1=C2 UDKVMASCRFDIIP-UHFFFAOYSA-N 0.000 claims 6
- 150000003857 carboxamides Chemical class 0.000 claims 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 6
- 125000005466 alkylenyl group Chemical group 0.000 claims 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-M benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-M 0.000 claims 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 5
- DFPAKSUCGFBDDF-UHFFFAOYSA-N nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 5
- 235000005152 nicotinamide Nutrition 0.000 claims 5
- 239000011570 nicotinamide Substances 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 5
- 125000004432 carbon atoms Chemical group C* 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 230000000051 modifying Effects 0.000 claims 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 4
- 125000001544 thienyl group Chemical group 0.000 claims 4
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 201000003883 cystic fibrosis Diseases 0.000 claims 3
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 3
- 125000004029 hydroxymethyl group Chemical compound [H]OC([H])([H])* 0.000 claims 3
- 125000004043 oxo group Chemical group O=* 0.000 claims 3
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
- XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-Methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 claims 2
- FYTHEJLCDOBYCF-VGYIUAJSSA-N FC(OC1=CC2=C([C@@H](C[C@@H](O2)C2=CC=C(C=N2)C(=O)O)NC(=O)[C@]2(COC=3C2=CC2=C(OC(O2)(F)F)C=3)C)C=C1)F Chemical compound FC(OC1=CC2=C([C@@H](C[C@@H](O2)C2=CC=C(C=N2)C(=O)O)NC(=O)[C@]2(COC=3C2=CC2=C(OC(O2)(F)F)C=3)C)C=C1)F FYTHEJLCDOBYCF-VGYIUAJSSA-N 0.000 claims 2
- MLIHJZWVFLXBEU-OXJIQLNZSA-N FC(OC1=CC2=C([C@@H](C[C@@H](O2)[C@@H]2CC[C@H](CC2)C(=O)O)NC(=O)[C@]2(COC=3C2=CC2=C(OC(O2)(F)F)C=3)C)C=C1)F Chemical compound FC(OC1=CC2=C([C@@H](C[C@@H](O2)[C@@H]2CC[C@H](CC2)C(=O)O)NC(=O)[C@]2(COC=3C2=CC2=C(OC(O2)(F)F)C=3)C)C=C1)F MLIHJZWVFLXBEU-OXJIQLNZSA-N 0.000 claims 2
- LETLLRLVJOBSGP-WTGRHJARSA-N FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC(F)(F)F)C1(CC1)C(=O)O)C)F Chemical compound FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC(F)(F)F)C1(CC1)C(=O)O)C)F LETLLRLVJOBSGP-WTGRHJARSA-N 0.000 claims 2
- WZQNDPZOCKJQDQ-WNMGDLKVSA-N FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC(F)(F)F)[C@@H]1CC[C@H](CC1)C(=O)O)C)F Chemical compound FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC(F)(F)F)[C@@H]1CC[C@H](CC1)C(=O)O)C)F WZQNDPZOCKJQDQ-WNMGDLKVSA-N 0.000 claims 2
- JQXRINCXSQPXHM-NBVYDZSDSA-N FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC)[C@@H]1CC[C@H](CC1)C(=O)O)C)F Chemical compound FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC)[C@@H]1CC[C@H](CC1)C(=O)O)C)F JQXRINCXSQPXHM-NBVYDZSDSA-N 0.000 claims 2
- XCELBSHYOAMWHD-RDGZHIGNSA-N FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](O[C@@H](C1)C1=CC=CC=C1)C1=CC=C(C(=O)O)C=C1)C)F Chemical compound FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@@H]1C[C@@H](O[C@@H](C1)C1=CC=CC=C1)C1=CC=C(C(=O)O)C=C1)C)F XCELBSHYOAMWHD-RDGZHIGNSA-N 0.000 claims 2
- XCELBSHYOAMWHD-CNBBWRMGSA-N FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@H]1C[C@H](O[C@H](C1)C1=CC=CC=C1)C1=CC=C(C(=O)O)C=C1)C)F Chemical compound FC1(OC2=C(O1)C=C1C(=C2)[C@](CO1)(C(=O)N[C@H]1C[C@H](O[C@H](C1)C1=CC=CC=C1)C1=CC=C(C(=O)O)C=C1)C)F XCELBSHYOAMWHD-CNBBWRMGSA-N 0.000 claims 2
- MNSCITNYGXTMKY-YJNDVTPQSA-N FC1(OC2=C(O1)C=C1CC[C@@](C1=C2)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC(F)(F)F)[C@@H]1CC[C@H](CC1)C(=O)O)C)F Chemical compound FC1(OC2=C(O1)C=C1CC[C@@](C1=C2)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC(F)(F)F)[C@@H]1CC[C@H](CC1)C(=O)O)C)F MNSCITNYGXTMKY-YJNDVTPQSA-N 0.000 claims 2
- MRDCHUMTOVHGTH-BLJTZWMSSA-N FC1(OC2=C(O1)C=C1CC[C@@](C1=C2)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC)[C@@H]1CC[C@H](CC1)C(=O)O)C)F Chemical compound FC1(OC2=C(O1)C=C1CC[C@@](C1=C2)(C(=O)N[C@@H]1C[C@@H](OC2=C1C=CC(=C2)OC)[C@@H]1CC[C@H](CC1)C(=O)O)C)F MRDCHUMTOVHGTH-BLJTZWMSSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 239000003623 enhancer Substances 0.000 claims 2
- 230000002708 enhancing Effects 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000003566 oxetanyl group Chemical group 0.000 claims 2
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims 2
- DNUTZBZXLPWRJG-UHFFFAOYSA-M piperidine-1-carboxylate Chemical compound [O-]C(=O)N1CCCCC1 DNUTZBZXLPWRJG-UHFFFAOYSA-M 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000000979 2-amino-2-oxoethyl group Chemical compound [H]C([*])([H])C(=O)N([H])[H] 0.000 claims 1
- GTVRGHWZBVNPIG-GAKIBJFNSA-N BrC1=CC=C(C=N1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC Chemical compound BrC1=CC=C(C=N1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC GTVRGHWZBVNPIG-GAKIBJFNSA-N 0.000 claims 1
- GHBMCHCPTGPRTI-OXJIQLNZSA-N BrC=1C(=CC2=C([C@@H](C[C@@H](O2)[C@@H]2CC[C@H](CC2)C(=O)O)NC(=O)[C@]2(COC=3C2=CC2=C(OC(O2)(F)F)C=3)C)C=1)OC Chemical compound BrC=1C(=CC2=C([C@@H](C[C@@H](O2)[C@@H]2CC[C@H](CC2)C(=O)O)NC(=O)[C@]2(COC=3C2=CC2=C(OC(O2)(F)F)C=3)C)C=1)OC GHBMCHCPTGPRTI-OXJIQLNZSA-N 0.000 claims 1
- QSSPSNXRJPGZND-QFIPXVFZSA-N BrC=1C=C(C(N(C=1)C1=CC=C(C(=O)O)C=C1)=O)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C Chemical compound BrC=1C=C(C(N(C=1)C1=CC=C(C(=O)O)C=C1)=O)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C QSSPSNXRJPGZND-QFIPXVFZSA-N 0.000 claims 1
- WFWUVPORXIMFJZ-MGNBDDOMSA-N BrC=1C=C(C(N(C=1)C[C@H](CO)O)=O)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C Chemical compound BrC=1C=C(C(N(C=1)C[C@H](CO)O)=O)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C WFWUVPORXIMFJZ-MGNBDDOMSA-N 0.000 claims 1
- WGJZDEWHMQJLJV-UHFFFAOYSA-N C(#N)C1=CC=C(C=C1)C=1N=C(SC=1)NC(=O)C1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C Chemical compound C(#N)C1=CC=C(C=C1)C=1N=C(SC=1)NC(=O)C1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C WGJZDEWHMQJLJV-UHFFFAOYSA-N 0.000 claims 1
- FZFNCGNJYLSTJL-QHCPKHFHSA-N C(#N)C=1C=C(C=CC=1)C1=C(C=CC(=N1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)C Chemical compound C(#N)C=1C=C(C=CC=1)C1=C(C=CC(=N1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)C FZFNCGNJYLSTJL-QHCPKHFHSA-N 0.000 claims 1
- ZSBXSCGIZFZMND-HAWMADMCSA-N C(#N)C[C@@H](CN1C(=CC2=CC(=C(C=C12)F)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)C(CO)(C)C)O Chemical compound C(#N)C[C@@H](CN1C(=CC2=CC(=C(C=C12)F)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)C(CO)(C)C)O ZSBXSCGIZFZMND-HAWMADMCSA-N 0.000 claims 1
- IRJJHRSBEWJOMD-WTSFKKHRSA-N C(=C)C=1N=CC(=NC=1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC Chemical compound C(=C)C=1N=CC(=NC=1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC IRJJHRSBEWJOMD-WTSFKKHRSA-N 0.000 claims 1
- YSFMNEHGDWYHJC-LXHIVTORSA-N C(C)(=O)C=1C=CC(=NC=1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC Chemical compound C(C)(=O)C=1C=CC(=NC=1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC YSFMNEHGDWYHJC-LXHIVTORSA-N 0.000 claims 1
- GLXXSZLPIOXCHA-PWECECGKSA-N C(C)(C)(C)C=1N(C2=CC(=C(C=C2C=1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)F)C[C@H](CO)O Chemical compound C(C)(C)(C)C=1N(C2=CC(=C(C=C2C=1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)F)C[C@H](CO)O GLXXSZLPIOXCHA-PWECECGKSA-N 0.000 claims 1
- CSIOQDOEGYDFCA-QFIPXVFZSA-N C(C)(C)(C)C=1NC2=CC=C(C=C2C=1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C Chemical compound C(C)(C)(C)C=1NC2=CC=C(C=C2C=1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C CSIOQDOEGYDFCA-QFIPXVFZSA-N 0.000 claims 1
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- QXJSNGXOKUTSMM-LJAQVGFWSA-N C(C1=CC=CC=C1)OCC(C)(C)C=1NC2=CC(=C(C=C2C=1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)F Chemical compound C(C1=CC=CC=C1)OCC(C)(C)C=1NC2=CC(=C(C=C2C=1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)F QXJSNGXOKUTSMM-LJAQVGFWSA-N 0.000 claims 1
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- OPEJBCYWUNQXDF-GYCJOSAFSA-N O[C@H](CN1C(C(=CC(=C1)C1=CC=CC=C1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)=O)CO Chemical compound O[C@H](CN1C(C(=CC(=C1)C1=CC=CC=C1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)=O)CO OPEJBCYWUNQXDF-GYCJOSAFSA-N 0.000 claims 1
- AODKAKLGENMABW-SUMNFNSASA-N O[C@H](CN1C2=C(C=3C=C(C(=CC1=3)F)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C(OCC2(C)C)(C)C)CO Chemical compound O[C@H](CN1C2=C(C=3C=C(C(=CC1=3)F)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C(OCC2(C)C)(C)C)CO AODKAKLGENMABW-SUMNFNSASA-N 0.000 claims 1
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- OGMRGCMUMBRGBI-MGNBDDOMSA-N O[C@H](CNC1=CC=CC(=N1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)CO Chemical compound O[C@H](CNC1=CC=CC(=N1)NC(=O)[C@]1(COC=2C1=CC1=C(OC(O1)(F)F)C=2)C)CO OGMRGCMUMBRGBI-MGNBDDOMSA-N 0.000 claims 1
- GODUAFVFBRPXRL-KJMMEZDOSA-N O[C@H](CO)C=1N=CC(=NC=1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC Chemical compound O[C@H](CO)C=1N=CC(=NC=1)[C@@H]1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC GODUAFVFBRPXRL-KJMMEZDOSA-N 0.000 claims 1
- LZJCYHSDLPCVBN-FUAMEPFCSA-N O[C@H](COC1=CC=C(N=N1)C1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC)CO Chemical compound O[C@H](COC1=CC=C(N=N1)C1OC2=C([C@@H](C1)NC(=O)[C@]1(COC=3C1=CC1=C(OC(O1)(F)F)C=3)C)C=CC(=C2)OC)CO LZJCYHSDLPCVBN-FUAMEPFCSA-N 0.000 claims 1
- 125000002393 azetidinyl group Chemical group 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000005842 heteroatoms Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
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- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 150000002829 nitrogen Chemical group 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
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- 125000004430 oxygen atoms Chemical group O* 0.000 claims 1
- 125000003884 phenylalkyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000001436 propyl group Chemical compound [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002206 pyridazin-3-yl group Chemical compound [H]C1=C([H])C([H])=C(*)N=N1 0.000 claims 1
- PVNIIMVLHYAWGP-UHFFFAOYSA-M pyridine-3-carboxylate Chemical compound [O-]C(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-M 0.000 claims 1
- JAEIBKXSIXOLOL-UHFFFAOYSA-N pyrrolidin-1-ium-3-carboxylate Chemical compound OC(=O)C1CCNC1 JAEIBKXSIXOLOL-UHFFFAOYSA-N 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- YNVOMSDITJMNET-UHFFFAOYSA-N thiophene-3-carboxylic acid Chemical compound OC(=O)C=1C=CSC=1 YNVOMSDITJMNET-UHFFFAOYSA-N 0.000 claims 1
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| US10138227B2 (en) | 2016-06-03 | 2018-11-27 | Abbvie S.Á.R.L. | Heteroaryl substituted pyridines and methods of use |
| US10399940B2 (en) | 2016-10-07 | 2019-09-03 | Abbvie S.Á.R.L. | Substituted pyrrolidines and methods of use |
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| US20200123137A1 (en) | 2016-12-20 | 2020-04-23 | AbbVie S.à.r.l. | Deuterated cftr modulators and methods of use |
| TW201831471A (zh) | 2017-02-24 | 2018-09-01 | 盧森堡商艾伯維公司 | 囊腫纖化症跨膜傳導調節蛋白的調節劑及其使用方法 |
| JP2020518107A (ja) | 2017-04-26 | 2020-06-18 | オーティーアイ ルミオニクス インコーポレーテッドＯｔｉ Ｌｕｍｉｏｎｉｃｓ Ｉｎｃ． | 表面上のコーティングをパターン化する方法およびパターン化されたコーティングを含むデバイス |
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| CN111187197B (zh) * | 2020-01-13 | 2021-10-01 | 苏州旺山旺水生物医药有限公司 | 一种Tezacaftor中间体的合成方法 |
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| WO2022123431A1 (en) | 2020-12-07 | 2022-06-16 | Oti Lumionics Inc. | Patterning a conductive deposited layer using a nucleation inhibiting coating and an underlying metallic coating |
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