NO343376B1 - 8-metoksy-9H-isotiazolo[5,4-b]kinolin-3,4-dioner, farmasøytisk preparater omfattende slike samt slike forbindelser og preparater for anvendelse ved behandling eller forhindring av infeksjoner - Google Patents

Info

Publication number

NO343376B1

NO343376B1 NO20081005A NO20081005A NO343376B1 NO 343376 B1 NO343376 B1 NO 343376B1 NO 20081005 A NO20081005 A NO 20081005A NO 20081005 A NO20081005 A NO 20081005A NO 343376 B1 NO343376 B1 NO 343376B1

Authority

NO

Norway

Prior art keywords

cyclopropyl

dione

quinoline

fluoro

pyrrolidin

Prior art date

2005-07-27

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• 150000001875 compounds Chemical class 0.000 title claims description 233
• 238000002360 preparation method Methods 0.000 title claims description 39
• 208000015181 infectious disease Diseases 0.000 title claims description 28
• 230000002265 prevention Effects 0.000 title claims description 6
• TYDQUACGVFCRFY-UHFFFAOYSA-N 8-methoxy-9h-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=CC=CC(C2=O)=C1NC1=C2C(=O)NS1 TYDQUACGVFCRFY-UHFFFAOYSA-N 0.000 title description 4
• 239000008194 pharmaceutical composition Substances 0.000 title description 4
• -1 hydroxy, amino Chemical group 0.000 claims description 93
• 150000003839 salts Chemical class 0.000 claims description 87
• 125000001424 substituent group Chemical group 0.000 claims description 58
• 125000000217 alkyl group Chemical group 0.000 claims description 51
• 125000003118 aryl group Chemical group 0.000 claims description 47
• 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 37
• 229910052717 sulfur Inorganic materials 0.000 claims description 31
• 125000001188 haloalkyl group Chemical group 0.000 claims description 30
• 229910052760 oxygen Inorganic materials 0.000 claims description 29
• 150000002367 halogens Chemical class 0.000 claims description 27
• 125000005842 heteroatom Chemical group 0.000 claims description 27
• 239000000825 pharmaceutical preparation Substances 0.000 claims description 27
• 229910052736 halogen Inorganic materials 0.000 claims description 26
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 25
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 24
• 125000003545 alkoxy group Chemical group 0.000 claims description 22
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 21
• 125000004043 oxo group Chemical group O=* 0.000 claims description 21
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 17
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 15
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 14
• 239000003814 drug Substances 0.000 claims description 14
• 239000001257 hydrogen Substances 0.000 claims description 14
• 229910052739 hydrogen Inorganic materials 0.000 claims description 14
• 125000003386 piperidinyl group Chemical group 0.000 claims description 14
• 125000003282 alkyl amino group Chemical group 0.000 claims description 13
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 13
• 229910052757 nitrogen Inorganic materials 0.000 claims description 13
• 239000000654 additive Substances 0.000 claims description 12
• 125000002619 bicyclic group Chemical group 0.000 claims description 11
• 239000003085 diluting agent Substances 0.000 claims description 11
• 230000001580 bacterial effect Effects 0.000 claims description 10
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
• 239000003937 drug carrier Substances 0.000 claims description 10
• 125000004193 piperazinyl group Chemical group 0.000 claims description 10
• 150000002431 hydrogen Chemical class 0.000 claims description 9
• 239000006188 syrup Substances 0.000 claims description 9
• 235000020357 syrup Nutrition 0.000 claims description 9
• 239000007788 liquid Substances 0.000 claims description 8
• 125000002757 morpholinyl group Chemical group 0.000 claims description 8
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
• 125000004076 pyridyl group Chemical group 0.000 claims description 8
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
• 208000035143 Bacterial infection Diseases 0.000 claims description 6
• 230000000996 additive effect Effects 0.000 claims description 6
• 208000022362 bacterial infectious disease Diseases 0.000 claims description 6
• 125000001153 fluoro group Chemical group F* 0.000 claims description 6
• 229940054534 ophthalmic solution Drugs 0.000 claims description 6
• 239000002997 ophthalmic solution Substances 0.000 claims description 6
• 125000003003 spiro group Chemical group 0.000 claims description 6
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 5
• 239000002775 capsule Substances 0.000 claims description 5
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
• 239000006071 cream Substances 0.000 claims description 5
• 239000011737 fluorine Substances 0.000 claims description 5
• 229910052731 fluorine Inorganic materials 0.000 claims description 5
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
• 125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
• 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 4
• 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 4
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
• 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 4
• 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 4
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
• PHXQIAWFIIMOKG-UHFFFAOYSA-N NClO Chemical compound NClO PHXQIAWFIIMOKG-UHFFFAOYSA-N 0.000 claims description 4
• 239000000443 aerosol Substances 0.000 claims description 4
• 125000005843 halogen group Chemical group 0.000 claims description 4
• 125000004366 heterocycloalkenyl group Chemical group 0.000 claims description 4
• 208000028172 protozoa infectious disease Diseases 0.000 claims description 4
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
• 125000006448 cycloalkyl cycloalkyl group Chemical group 0.000 claims description 3
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
• 239000006187 pill Substances 0.000 claims description 3
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
• 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims description 2
• 125000006536 (C1-C2)alkoxy group Chemical group 0.000 claims description 2
• 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims description 2
• VJVQHNNWFIAYBE-UHFFFAOYSA-N 1-(9-cyclopropyl-6-fluoro-8-methoxy-3,4-dioxo-[1,2]thiazolo[5,4-b]quinolin-7-yl)-4-methylpyrrolidine-3-carbonitrile Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC(C)C(C#N)C1 VJVQHNNWFIAYBE-UHFFFAOYSA-N 0.000 claims description 2
• GDFMGXHNHLDERN-UHFFFAOYSA-N 7-(1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl)-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2CC3NCCCC3C2)C(F)=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 GDFMGXHNHLDERN-UHFFFAOYSA-N 0.000 claims description 2
• IPNXHUCBRZCASH-UHFFFAOYSA-N 7-(3-aminoazetidin-1-yl)-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC(N)C1 IPNXHUCBRZCASH-UHFFFAOYSA-N 0.000 claims description 2
• FUIWHAOIPKPCER-SNVBAGLBSA-N 7-[(3r)-3-(1-aminocyclopropyl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound NC1([C@@H]2CCN(C2)C2=C(C3=C(C(C=4C(=O)NSC=4N3C3CC3)=O)C=C2F)OC)CC1 FUIWHAOIPKPCER-SNVBAGLBSA-N 0.000 claims description 2
• XREWPHQHZZBTEH-LLVKDONJSA-N 7-[(3r)-3-(1-aminocyclopropyl)pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@@H](CC2)C2(N)CC2)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 XREWPHQHZZBTEH-LLVKDONJSA-N 0.000 claims description 2
• OEFVEGDPRVNFMP-QVDQXJPCSA-N 7-[(3r)-3-(1-aminoethyl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC[C@@H](C(C)N)C1 OEFVEGDPRVNFMP-QVDQXJPCSA-N 0.000 claims description 2
• TXJCKZMAAWYMSB-RRKGBCIJSA-N 7-[(3r)-3-(1-aminoethyl)pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@@H](CC2)C(C)N)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 TXJCKZMAAWYMSB-RRKGBCIJSA-N 0.000 claims description 2
• CECJUHKZSOSOJJ-SNVBAGLBSA-N 7-[(3r)-3-(2-aminopropan-2-yl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC[C@@H](C(C)(C)N)C1 CECJUHKZSOSOJJ-SNVBAGLBSA-N 0.000 claims description 2
• LESPJGYGFNKEAR-LLVKDONJSA-N 7-[(3r)-3-(2-aminopropan-2-yl)pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@@H](CC2)C(C)(C)N)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 LESPJGYGFNKEAR-LLVKDONJSA-N 0.000 claims description 2
• LNKKKLISQOGUFB-SNVBAGLBSA-N 7-[(3r)-3-(2-aminopropan-2-yl)pyrrolidin-1-yl]-9-ethyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C2N(CC)C=3SNC(=O)C=3C(=O)C2=CC(F)=C1N1CC[C@@H](C(C)(C)N)C1 LNKKKLISQOGUFB-SNVBAGLBSA-N 0.000 claims description 2
• KNDXGEBFIJOZPT-SECBINFHSA-N 7-[(3r)-3-(aminomethyl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC[C@H](CN)C1 KNDXGEBFIJOZPT-SECBINFHSA-N 0.000 claims description 2
• LBAVESGGMJDWHK-SNVBAGLBSA-N 7-[(3r)-3-(aminomethyl)pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@@H](CN)CC2)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 LBAVESGGMJDWHK-SNVBAGLBSA-N 0.000 claims description 2
• TXJCKZMAAWYMSB-GHMZBOCLSA-N 7-[(3r)-3-[(1r)-1-aminoethyl]pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@@H](CC2)[C@@H](C)N)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 TXJCKZMAAWYMSB-GHMZBOCLSA-N 0.000 claims description 2
• TXJCKZMAAWYMSB-WDEREUQCSA-N 7-[(3r)-3-[(1s)-1-aminoethyl]pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@@H](CC2)[C@H](C)N)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 TXJCKZMAAWYMSB-WDEREUQCSA-N 0.000 claims description 2
• LLSPDVCBZDPWSM-ARLHGKGLSA-N 7-[(3r)-3-[1-(cyclopentylamino)ethyl]pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound CC([C@@H]1CCN(C1)C1=C(C2=C(C(C=3C(=O)NSC=3N2C2CC2)=O)C=C1F)OC)NC1CCCC1 LLSPDVCBZDPWSM-ARLHGKGLSA-N 0.000 claims description 2
• PAGNERNSMOUOJL-MRVPVSSYSA-N 7-[(3r)-3-aminopyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC[C@@H](N)C1 PAGNERNSMOUOJL-MRVPVSSYSA-N 0.000 claims description 2
• DAQDKAXGYLAAJD-SECBINFHSA-N 7-[(3r)-3-aminopyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@H](N)CC2)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 DAQDKAXGYLAAJD-SECBINFHSA-N 0.000 claims description 2
• CECJUHKZSOSOJJ-JTQLQIEISA-N 7-[(3s)-3-(2-aminopropan-2-yl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC[C@H](C(C)(C)N)C1 CECJUHKZSOSOJJ-JTQLQIEISA-N 0.000 claims description 2
• LESPJGYGFNKEAR-NSHDSACASA-N 7-[(3s)-3-(2-aminopropan-2-yl)pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@H](CC2)C(C)(C)N)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 LESPJGYGFNKEAR-NSHDSACASA-N 0.000 claims description 2
• KNDXGEBFIJOZPT-VIFPVBQESA-N 7-[(3s)-3-(aminomethyl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC[C@@H](CN)C1 KNDXGEBFIJOZPT-VIFPVBQESA-N 0.000 claims description 2
• LBAVESGGMJDWHK-JTQLQIEISA-N 7-[(3s)-3-(aminomethyl)pyrrolidin-1-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@H](CN)CC2)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 LBAVESGGMJDWHK-JTQLQIEISA-N 0.000 claims description 2
• WPSPHFQYFAYZRY-RISCZKNCSA-N 7-[(4ar,7ar)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-9-cyclopropyl-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@@H]3NCCC[C@@H]3C2)C=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 WPSPHFQYFAYZRY-RISCZKNCSA-N 0.000 claims description 2
• GDFMGXHNHLDERN-IINYFYTJSA-N 7-[(4as,7as)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound COC1=C(N2C[C@H]3NCCC[C@H]3C2)C(F)=CC(C(C=2C(=O)NSC=22)=O)=C1N2C1CC1 GDFMGXHNHLDERN-IINYFYTJSA-N 0.000 claims description 2
• CECJUHKZSOSOJJ-UHFFFAOYSA-N 7-[3-(2-aminopropan-2-yl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CCC(C(C)(C)N)C1 CECJUHKZSOSOJJ-UHFFFAOYSA-N 0.000 claims description 2
• SUMJLCCIRRARQW-UHFFFAOYSA-N 7-[3-(aminomethyl)-4-methylpyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC(C)C(CN)C1 SUMJLCCIRRARQW-UHFFFAOYSA-N 0.000 claims description 2
• OXJQXSMVBYVHFL-UHFFFAOYSA-N 7-[3-(aminomethyl)azetidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC(CN)C1 OXJQXSMVBYVHFL-UHFFFAOYSA-N 0.000 claims description 2
• KNDXGEBFIJOZPT-UHFFFAOYSA-N 7-[3-(aminomethyl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CCC(CN)C1 KNDXGEBFIJOZPT-UHFFFAOYSA-N 0.000 claims description 2
• SHQYLHQRWSZIMO-UHFFFAOYSA-N 7-[3-amino-3-(hydroxymethyl)pyrrolidin-1-yl]-9-cyclopropyl-6-fluoro-8-methoxy-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CCC(N)(CO)C1 SHQYLHQRWSZIMO-UHFFFAOYSA-N 0.000 claims description 2
• BLXRXCUUZCJCNX-SECBINFHSA-N 9-cyclopropyl-6-fluoro-8-methoxy-7-[(3r)-3-(methylamino)pyrrolidin-1-yl]-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound C1[C@H](NC)CCN1C1=C(F)C=C2C(=O)C(C(=O)NS3)=C3N(C3CC3)C2=C1OC BLXRXCUUZCJCNX-SECBINFHSA-N 0.000 claims description 2
• SOJRULJEVFPUAA-GHMZBOCLSA-N 9-cyclopropyl-6-fluoro-8-methoxy-7-[(3r)-3-[(1r)-1-(methylamino)ethyl]pyrrolidin-1-yl]-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound C1[C@H]([C@@H](C)NC)CCN1C1=C(F)C=C2C(=O)C(C(=O)NS3)=C3N(C3CC3)C2=C1OC SOJRULJEVFPUAA-GHMZBOCLSA-N 0.000 claims description 2
• BIFUBTLJPKQHCM-IAQYHMDHSA-N 9-cyclopropyl-6-fluoro-8-methoxy-7-[(3r)-3-[(1r)-1-(methylamino)propyl]pyrrolidin-1-yl]-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound C1[C@H]([C@H](NC)CC)CCN1C1=C(F)C=C2C(=O)C(C(=O)NS3)=C3N(C3CC3)C2=C1OC BIFUBTLJPKQHCM-IAQYHMDHSA-N 0.000 claims description 2
• SOJRULJEVFPUAA-WDEREUQCSA-N 9-cyclopropyl-6-fluoro-8-methoxy-7-[(3r)-3-[(1s)-1-(methylamino)ethyl]pyrrolidin-1-yl]-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound C1[C@H]([C@H](C)NC)CCN1C1=C(F)C=C2C(=O)C(C(=O)NS3)=C3N(C3CC3)C2=C1OC SOJRULJEVFPUAA-WDEREUQCSA-N 0.000 claims description 2
• BIFUBTLJPKQHCM-ABAIWWIYSA-N 9-cyclopropyl-6-fluoro-8-methoxy-7-[(3r)-3-[(1s)-1-(methylamino)propyl]pyrrolidin-1-yl]-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound C1[C@H]([C@@H](NC)CC)CCN1C1=C(F)C=C2C(=O)C(C(=O)NS3)=C3N(C3CC3)C2=C1OC BIFUBTLJPKQHCM-ABAIWWIYSA-N 0.000 claims description 2
• SOJRULJEVFPUAA-RRKGBCIJSA-N 9-cyclopropyl-6-fluoro-8-methoxy-7-[(3r)-3-[1-(methylamino)ethyl]pyrrolidin-1-yl]-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound C1[C@H](C(C)NC)CCN1C1=C(F)C=C2C(=O)C(C(=O)NS3)=C3N(C3CC3)C2=C1OC SOJRULJEVFPUAA-RRKGBCIJSA-N 0.000 claims description 2
• MQFPHOIGJGZROC-ZGTCLIOFSA-N 9-cyclopropyl-6-fluoro-8-methoxy-7-[(3r)-3-[1-(propan-2-ylamino)ethyl]pyrrolidin-1-yl]-[1,2]thiazolo[5,4-b]quinoline-3,4-dione Chemical compound FC1=CC(C(C=2C(=O)NSC=2N2C3CC3)=O)=C2C(OC)=C1N1CC[C@@H](C(C)NC(C)C)C1 MQFPHOIGJGZROC-ZGTCLIOFSA-N 0.000 claims description 2
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