NO322746B1 - Indoliner, substituert i 6-stilling, og farmasoytisk preparat, samt anvendelse og fremstilling derav. - Google Patents
Indoliner, substituert i 6-stilling, og farmasoytisk preparat, samt anvendelse og fremstilling derav. Download PDFInfo
- Publication number
- NO322746B1 NO322746B1 NO20021719A NO20021719A NO322746B1 NO 322746 B1 NO322746 B1 NO 322746B1 NO 20021719 A NO20021719 A NO 20021719A NO 20021719 A NO20021719 A NO 20021719A NO 322746 B1 NO322746 B1 NO 322746B1
- Authority
- NO
- Norway
- Prior art keywords
- group
- alkyl
- phenyl
- amino
- methylene
- Prior art date
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- 238000002360 preparation method Methods 0.000 title description 11
- 150000002476 indolines Chemical class 0.000 title description 3
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- -1 C 1-3 -Alkoxy Chemical group 0.000 claims description 197
- 150000001875 compounds Chemical class 0.000 claims description 142
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 124
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 120
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 114
- 125000000217 alkyl group Chemical group 0.000 claims description 97
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 90
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 69
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 64
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 62
- 229910052757 nitrogen Inorganic materials 0.000 claims description 51
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 50
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 46
- 125000003545 alkoxy group Chemical group 0.000 claims description 38
- 229910052801 chlorine Inorganic materials 0.000 claims description 38
- 229910052717 sulfur Inorganic materials 0.000 claims description 36
- 125000004434 sulfur atom Chemical group 0.000 claims description 36
- 125000006563 (C1-3) alkylaminocarbonyl group Chemical group 0.000 claims description 35
- 150000003839 salts Chemical class 0.000 claims description 34
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 33
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 32
- 239000000460 chlorine Substances 0.000 claims description 32
- 229910052760 oxygen Inorganic materials 0.000 claims description 32
- 239000001301 oxygen Substances 0.000 claims description 32
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 30
- 125000001072 heteroaryl group Chemical group 0.000 claims description 30
- 238000006243 chemical reaction Methods 0.000 claims description 29
- 229910052731 fluorine Inorganic materials 0.000 claims description 29
- 239000011737 fluorine Substances 0.000 claims description 29
- 125000006698 (C1-C3) dialkylamino group Chemical group 0.000 claims description 28
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 27
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims description 26
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 25
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 25
- 125000006576 di-(C1-C3-alkyl)-aminocarbonyl group Chemical group 0.000 claims description 24
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 24
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 22
- 125000003282 alkyl amino group Chemical group 0.000 claims description 22
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 21
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 21
- 125000006239 protecting group Chemical group 0.000 claims description 21
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 20
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 20
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 20
- 229910052740 iodine Inorganic materials 0.000 claims description 20
- 125000006602 (C1-C3) alkylsulfonylamino group Chemical group 0.000 claims description 19
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 19
- 229910052794 bromium Inorganic materials 0.000 claims description 18
- 239000007790 solid phase Substances 0.000 claims description 17
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 16
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 16
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 claims description 15
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 15
- 125000004744 butyloxycarbonyl group Chemical group 0.000 claims description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 14
- 125000003277 amino group Chemical group 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 14
- 150000003951 lactams Chemical group 0.000 claims description 14
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 14
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 13
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 13
- 125000006842 cycloalkyleneimino group Chemical group 0.000 claims description 13
- NALBLJLOBICXRH-UHFFFAOYSA-N dinitrogen monohydride Chemical group N=[N] NALBLJLOBICXRH-UHFFFAOYSA-N 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 125000001153 fluoro group Chemical group F* 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
- JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical compound C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 claims description 11
- 125000002950 monocyclic group Chemical group 0.000 claims description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 9
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 9
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 claims description 8
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 8
- 125000002883 imidazolyl group Chemical group 0.000 claims description 8
- 125000001624 naphthyl group Chemical group 0.000 claims description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 8
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 8
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 8
- 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 8
- 125000006603 (C1-C3) alkylaminosulfonyl group Chemical group 0.000 claims description 7
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 7
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 7
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 7
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 7
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 6
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 6
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 6
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims description 6
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims description 6
- 125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims description 6
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 6
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- 239000002243 precursor Substances 0.000 claims description 6
- 125000006850 spacer group Chemical group 0.000 claims description 6
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 6
- 125000001425 triazolyl group Chemical group 0.000 claims description 6
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims description 5
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 5
- 230000009435 amidation Effects 0.000 claims description 5
- 238000007112 amidation reaction Methods 0.000 claims description 5
- 239000000969 carrier Substances 0.000 claims description 5
- 230000004663 cell proliferation Effects 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 230000032050 esterification Effects 0.000 claims description 5
- 238000005886 esterification reaction Methods 0.000 claims description 5
- ORCLOYHXQJNMMX-IZHYLOQSSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C=C1 ORCLOYHXQJNMMX-IZHYLOQSSA-N 0.000 claims description 5
- GUSPUPJKTCNHOJ-VHXPQNKSSA-N methyl (3z)-3-[[4-(ethylaminomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CNCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O GUSPUPJKTCNHOJ-VHXPQNKSSA-N 0.000 claims description 5
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims description 5
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 4
- 230000010933 acylation Effects 0.000 claims description 4
- 238000005917 acylation reaction Methods 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000001246 bromo group Chemical group Br* 0.000 claims description 4
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 150000001721 carbon Chemical group 0.000 claims description 4
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims description 4
- RTLQNDXPILJVLA-UHFFFAOYSA-N ethyl 2-hydroxy-3-[C-phenyl-N-[4-(piperidin-1-ylmethyl)phenyl]carbonimidoyl]-1H-indole-6-carboxylate Chemical compound CCOC(=O)C1=CC2=C(C=C1)C(=C(N2)O)C(=NC3=CC=C(C=C3)CN4CCCCC4)C5=CC=CC=C5 RTLQNDXPILJVLA-UHFFFAOYSA-N 0.000 claims description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000005935 hexyloxycarbonyl group Chemical group 0.000 claims description 4
- 230000007062 hydrolysis Effects 0.000 claims description 4
- 238000006460 hydrolysis reaction Methods 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 claims description 4
- CPMDPSXJELVGJG-UHFFFAOYSA-N methyl 2-hydroxy-3-[N-[4-[methyl-[2-(4-methylpiperazin-1-yl)acetyl]amino]phenyl]-C-phenylcarbonimidoyl]-1H-indole-6-carboxylate Chemical compound OC=1NC2=CC(=CC=C2C=1C(=NC1=CC=C(C=C1)N(C(CN1CCN(CC1)C)=O)C)C1=CC=CC=C1)C(=O)OC CPMDPSXJELVGJG-UHFFFAOYSA-N 0.000 claims description 4
- 125000001148 pentyloxycarbonyl group Chemical group 0.000 claims description 4
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims description 4
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 4
- 125000005544 phthalimido group Chemical group 0.000 claims description 4
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000004742 propyloxycarbonyl group Chemical group 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 238000006722 reduction reaction Methods 0.000 claims description 4
- 238000005932 reductive alkylation reaction Methods 0.000 claims description 4
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 3
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 claims description 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- IXKSURGKVWEOIW-DQSJHHFOSA-N ethyl (3z)-3-[[4-[acetyl-[2-(dimethylamino)ethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)C(C)=O)C=C1 IXKSURGKVWEOIW-DQSJHHFOSA-N 0.000 claims description 3
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims description 3
- 125000002541 furyl group Chemical group 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- PJYLAPUQQYSUKA-RQZHXJHFSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(piperidin-1-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCCCC1 PJYLAPUQQYSUKA-RQZHXJHFSA-N 0.000 claims description 3
- UTEHGZFZMLODQF-VHXPQNKSSA-N methyl (3z)-3-[[4-(1-methylimidazol-2-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=NC=CN1C UTEHGZFZMLODQF-VHXPQNKSSA-N 0.000 claims description 3
- PKXSPUDURLLHHG-RQZHXJHFSA-N methyl (3z)-3-[[4-[acetyl-[2-(dimethylamino)-2-oxoethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(=O)N(C)C)C(C)=O)C=C1 PKXSPUDURLLHHG-RQZHXJHFSA-N 0.000 claims description 3
- PWDPLHOKCYLVIC-RQZHXJHFSA-N methyl (3z)-3-[[4-[acetyl-[2-(dimethylamino)ethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)C(C)=O)C=C1 PWDPLHOKCYLVIC-RQZHXJHFSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 3
- 150000007522 mineralic acids Chemical class 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 238000006277 sulfonation reaction Methods 0.000 claims description 3
- 125000006597 (C1-C3) alkylcarbonylamino group Chemical group 0.000 claims description 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 2
- 125000006164 6-membered heteroaryl group Chemical group 0.000 claims description 2
- 230000002159 abnormal effect Effects 0.000 claims description 2
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 2
- 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 description 2
- IVIFECJEIKPXDF-RQZHXJHFSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)S(C)(=O)=O)C=C1 IVIFECJEIKPXDF-RQZHXJHFSA-N 0.000 claims description 2
- NETCICHFVHZSSG-ZIADKAODSA-N ethyl (3z)-3-[[4-[acetyl-[3-(dimethylamino)propyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCCN(C)C)C(C)=O)C=C1 NETCICHFVHZSSG-ZIADKAODSA-N 0.000 claims description 2
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- ZQQCIGZFIKNSLX-RQZHXJHFSA-N methyl (3z)-3-[[4-[3-(dimethylamino)propyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCCN(C)C)S(C)(=O)=O)C=C1 ZQQCIGZFIKNSLX-RQZHXJHFSA-N 0.000 claims description 2
- VBLVPTZXOOSQHZ-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 VBLVPTZXOOSQHZ-QPLCGJKRSA-N 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 2
- CREXVNNSNOKDHW-UHFFFAOYSA-N azaniumylideneazanide Chemical group N[N] CREXVNNSNOKDHW-UHFFFAOYSA-N 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- KUZBKIYSYFCFOT-QPLCGJKRSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)S(C)(=O)=O)C=C1 KUZBKIYSYFCFOT-QPLCGJKRSA-N 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 837
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 729
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 227
- 239000000741 silica gel Substances 0.000 description 227
- 229910002027 silica gel Inorganic materials 0.000 description 227
- 238000000119 electrospray ionisation mass spectrum Methods 0.000 description 185
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 182
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 90
- 238000001819 mass spectrum Methods 0.000 description 80
- 229920005989 resin Polymers 0.000 description 80
- 239000011347 resin Substances 0.000 description 80
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 65
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 62
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 59
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 55
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 54
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 45
- 239000000203 mixture Substances 0.000 description 40
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- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 4
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- PXQKFKVOLJRXCJ-IZHYLOQSSA-N ethyl (3z)-2-oxo-3-[phenyl-[4-(triazol-2-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1N=CC=N1 PXQKFKVOLJRXCJ-IZHYLOQSSA-N 0.000 description 1
- FEKDGMBDLGAOAF-KTMFPKCZSA-N ethyl (3z)-2-oxo-3-[phenyl-[4-[(2-piperazin-1-ylacetyl)-propan-2-ylamino]anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C(C)C)C(=O)CN1CCNCC1 FEKDGMBDLGAOAF-KTMFPKCZSA-N 0.000 description 1
- MIEFLTZYAPOBFN-MVJHLKBCSA-N ethyl (3z)-2-oxo-3-[phenyl-[4-[(2-piperidin-1-ylacetyl)-propan-2-ylamino]anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C(C)C)C(=O)CN1CCCCC1 MIEFLTZYAPOBFN-MVJHLKBCSA-N 0.000 description 1
- HBJVBPWUOTUJLJ-ZIADKAODSA-N ethyl (3z)-3-[(4-benzylanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CC1=CC=CC=C1 HBJVBPWUOTUJLJ-ZIADKAODSA-N 0.000 description 1
- PHZAEELHHMVCBJ-VHXPQNKSSA-N ethyl (3z)-3-[(4-ethoxyanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(OCC)C=C1 PHZAEELHHMVCBJ-VHXPQNKSSA-N 0.000 description 1
- OAQGXSYPNXOVNI-FCQUAONHSA-N ethyl (3z)-3-[(4-methoxyanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(OC)C=C1 OAQGXSYPNXOVNI-FCQUAONHSA-N 0.000 description 1
- IFFQFGXSWOSXKP-FCQUAONHSA-N ethyl (3z)-3-[(4-methylanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C)C=C1 IFFQFGXSWOSXKP-FCQUAONHSA-N 0.000 description 1
- SZNAKLOSBCUWEK-FCQUAONHSA-N ethyl (3z)-3-[(4-methylsulfanylanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(SC)C=C1 SZNAKLOSBCUWEK-FCQUAONHSA-N 0.000 description 1
- SVTNYGVEBCIXBO-XDOYNYLZSA-N ethyl (3z)-3-[1-[4-[(dimethylamino)methyl]anilino]butylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C/1NC2=CC(C(=O)OCC)=CC=C2C\1=C(/CCC)NC1=CC=C(CN(C)C)C=C1 SVTNYGVEBCIXBO-XDOYNYLZSA-N 0.000 description 1
- JRGQSUPXYLJIGB-JCMHNJIXSA-N ethyl (3z)-3-[1-[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]ethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(/C)NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 JRGQSUPXYLJIGB-JCMHNJIXSA-N 0.000 description 1
- HRDUWDJLEWNFMR-ATJXCDBQSA-N ethyl (3z)-3-[1-[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]propylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(/CC)NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 HRDUWDJLEWNFMR-ATJXCDBQSA-N 0.000 description 1
- FPCAYZUZSJHFLE-LCUIJRPUSA-N ethyl (3z)-3-[1-[4-[acetyl-[3-(dimethylamino)propyl]amino]anilino]butylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C/1NC2=CC(C(=O)OCC)=CC=C2C\1=C(/CCC)NC1=CC=C(N(CCCN(C)C)C(C)=O)C=C1 FPCAYZUZSJHFLE-LCUIJRPUSA-N 0.000 description 1
- QERMALCKFDOHQZ-ULJHMMPZSA-N ethyl (3z)-3-[1-[4-[acetyl-[3-(dimethylamino)propyl]amino]anilino]ethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(/C)NC1=CC=C(N(CCCN(C)C)C(C)=O)C=C1 QERMALCKFDOHQZ-ULJHMMPZSA-N 0.000 description 1
- HPRDNJKLSHVSFW-BZZOAKBMSA-N ethyl (3z)-3-[1-[4-[acetyl-[3-(dimethylamino)propyl]amino]anilino]propylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(/CC)NC1=CC=C(N(CCCN(C)C)C(C)=O)C=C1 HPRDNJKLSHVSFW-BZZOAKBMSA-N 0.000 description 1
- YGASJVGLHJEVQF-IZHYLOQSSA-N ethyl (3z)-3-[[3,5-dibromo-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC(Br)=C(CN(C)C)C(Br)=C1 YGASJVGLHJEVQF-IZHYLOQSSA-N 0.000 description 1
- KGLGZLLAQXVHMY-IZHYLOQSSA-N ethyl (3z)-3-[[3,5-dichloro-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC(Cl)=C(CN(C)C)C(Cl)=C1 KGLGZLLAQXVHMY-IZHYLOQSSA-N 0.000 description 1
- VIVWCLZPYSFYDJ-RQZHXJHFSA-N ethyl (3z)-3-[[3-acetamido-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(NC(C)=O)=C1 VIVWCLZPYSFYDJ-RQZHXJHFSA-N 0.000 description 1
- GHWFWNCLIGQYCE-RQZHXJHFSA-N ethyl (3z)-3-[[3-amino-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(N)=C1 GHWFWNCLIGQYCE-RQZHXJHFSA-N 0.000 description 1
- TZJRNTBXNYWUCH-IZHYLOQSSA-N ethyl (3z)-3-[[3-bromo-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(Br)=C1 TZJRNTBXNYWUCH-IZHYLOQSSA-N 0.000 description 1
- MGHYPWDVRBOKQH-RQZHXJHFSA-N ethyl (3z)-3-[[3-bromo-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(Br)=C1 MGHYPWDVRBOKQH-RQZHXJHFSA-N 0.000 description 1
- WQRLCUGPDYKDFJ-IZHYLOQSSA-N ethyl (3z)-3-[[3-carbamoyl-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(C(N)=O)=C1 WQRLCUGPDYKDFJ-IZHYLOQSSA-N 0.000 description 1
- LMRDUCHWJWIOCU-RQZHXJHFSA-N ethyl (3z)-3-[[3-carbamoyl-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(C(N)=O)=C1 LMRDUCHWJWIOCU-RQZHXJHFSA-N 0.000 description 1
- GCYBFBVHWMONRI-IZHYLOQSSA-N ethyl (3z)-3-[[3-chloro-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(Cl)=C1 GCYBFBVHWMONRI-IZHYLOQSSA-N 0.000 description 1
- POPQNWNIUXXQCA-RQZHXJHFSA-N ethyl (3z)-3-[[3-chloro-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(Cl)=C1 POPQNWNIUXXQCA-RQZHXJHFSA-N 0.000 description 1
- KEUFNMADPSPXCP-QPLCGJKRSA-N ethyl (3z)-3-[[3-cyano-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(C#N)=C1 KEUFNMADPSPXCP-QPLCGJKRSA-N 0.000 description 1
- ZPXLBJWBFHUKTE-IZHYLOQSSA-N ethyl (3z)-3-[[4-(1,3-diamino-3-oxopropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CC(N)=O)C=C1 ZPXLBJWBFHUKTE-IZHYLOQSSA-N 0.000 description 1
- HMGLXPMTOJSFCU-IZHYLOQSSA-N ethyl (3z)-3-[[4-(1,3-diaminopropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCN)C=C1 HMGLXPMTOJSFCU-IZHYLOQSSA-N 0.000 description 1
- GYBLBBSLEFEACO-QPLCGJKRSA-N ethyl (3z)-3-[[4-(1,4-diaminobutyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCN)C=C1 GYBLBBSLEFEACO-QPLCGJKRSA-N 0.000 description 1
- CCUTYSBBHLIUID-IZHYLOQSSA-N ethyl (3z)-3-[[4-(1-amino-3-hydroxypropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCO)C=C1 CCUTYSBBHLIUID-IZHYLOQSSA-N 0.000 description 1
- AMXWKHKQGZBFAX-QPLCGJKRSA-N ethyl (3z)-3-[[4-(1-amino-3-methoxypropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCOC)C=C1 AMXWKHKQGZBFAX-QPLCGJKRSA-N 0.000 description 1
- XIAOKDVXMUAJLG-KTMFPKCZSA-N ethyl (3z)-3-[[4-(1-benzylimidazol-2-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=NC=CN1CC1=CC=CC=C1 XIAOKDVXMUAJLG-KTMFPKCZSA-N 0.000 description 1
- ANZDFYNJBOYQLG-IZHYLOQSSA-N ethyl (3z)-3-[[4-(1-methylimidazol-2-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=NC=CN1C ANZDFYNJBOYQLG-IZHYLOQSSA-N 0.000 description 1
- JPVQTOCCDAXLPQ-IZHYLOQSSA-N ethyl (3z)-3-[[4-(1h-imidazol-5-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=CNC=N1 JPVQTOCCDAXLPQ-IZHYLOQSSA-N 0.000 description 1
- MQSZSNUWQIYNCH-RQZHXJHFSA-N ethyl (3z)-3-[[4-(3-acetamido-1-aminopropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCNC(C)=O)C=C1 MQSZSNUWQIYNCH-RQZHXJHFSA-N 0.000 description 1
- BSENHRCAKJZRCG-DQSJHHFOSA-N ethyl (3z)-3-[[4-(4-acetamido-1-aminobutyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCNC(C)=O)C=C1 BSENHRCAKJZRCG-DQSJHHFOSA-N 0.000 description 1
- LRKHTNZONLERKV-RQZHXJHFSA-N ethyl (3z)-3-[[4-(4-methylpiperazin-1-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N1CCN(C)CC1 LRKHTNZONLERKV-RQZHXJHFSA-N 0.000 description 1
- ZZRFQLQDQIIOEP-FCQUAONHSA-N ethyl (3z)-3-[[4-(aminomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN)C=C1 ZZRFQLQDQIIOEP-FCQUAONHSA-N 0.000 description 1
- XCQJIAXZZGZBHA-QPLCGJKRSA-N ethyl (3z)-3-[[4-(azetidin-1-ylmethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC1 XCQJIAXZZGZBHA-QPLCGJKRSA-N 0.000 description 1
- QHUDIXGJTODSBM-DQSJHHFOSA-N ethyl (3z)-3-[[4-(cyclohexylamino)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1NC1CCCCC1 QHUDIXGJTODSBM-DQSJHHFOSA-N 0.000 description 1
- XZMSFBYAWRFVKO-RQZHXJHFSA-N ethyl (3z)-3-[[4-(diethylaminomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(CC)CC)C=C1 XZMSFBYAWRFVKO-RQZHXJHFSA-N 0.000 description 1
- UAHPGQHLSDDKQC-IZHYLOQSSA-N ethyl (3z)-3-[[4-(ethylaminomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CNCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OCC)C=C2NC\1=O UAHPGQHLSDDKQC-IZHYLOQSSA-N 0.000 description 1
- CGJLGJPXRMRVDR-VHXPQNKSSA-N ethyl (3z)-3-[[4-(methanesulfonamidomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CNS(C)(=O)=O)C=C1 CGJLGJPXRMRVDR-VHXPQNKSSA-N 0.000 description 1
- MQKCTOHUDXGOFG-RQZHXJHFSA-N ethyl (3z)-3-[[4-[(2-acetamidoacetyl)-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CNC(C)=O)C=C1 MQKCTOHUDXGOFG-RQZHXJHFSA-N 0.000 description 1
- JSWBWTGNRWEANH-IZHYLOQSSA-N ethyl (3z)-3-[[4-[(2-aminoacetyl)-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN)C=C1 JSWBWTGNRWEANH-IZHYLOQSSA-N 0.000 description 1
- AGRUGIBTTDRWNM-RQZHXJHFSA-N ethyl (3z)-3-[[4-[(3-hydroxypyrrolidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC(O)C1 AGRUGIBTTDRWNM-RQZHXJHFSA-N 0.000 description 1
- ZFVWQYNIVJRCIG-KARKAFJISA-N ethyl (3z)-3-[[4-[(4-benzoylpiperazin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN(CC1)CCN1C(=O)C1=CC=CC=C1 ZFVWQYNIVJRCIG-KARKAFJISA-N 0.000 description 1
- XMPWEPBXDKUKDD-DQSJHHFOSA-N ethyl (3z)-3-[[4-[(4-hydroxypiperidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC(O)CC1 XMPWEPBXDKUKDD-DQSJHHFOSA-N 0.000 description 1
- JNFMCZHQSYIZKU-ZIADKAODSA-N ethyl (3z)-3-[[4-[(4-methoxypiperidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC(OC)CC1 JNFMCZHQSYIZKU-ZIADKAODSA-N 0.000 description 1
- OTTBHEFDQWWXLM-FCQUAONHSA-N ethyl (3z)-3-[[4-[(carbamoylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CNC(N)=O)C=C1 OTTBHEFDQWWXLM-FCQUAONHSA-N 0.000 description 1
- NWHXMHYMDFNAOQ-FCQUAONHSA-N ethyl (3z)-3-[[4-[(diaminomethylideneamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CNC(N)=N)C=C1 NWHXMHYMDFNAOQ-FCQUAONHSA-N 0.000 description 1
- PLZZBWOORXREMY-QPLCGJKRSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-(methanesulfonamido)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(NS(C)(=O)=O)=C1 PLZZBWOORXREMY-QPLCGJKRSA-N 0.000 description 1
- KIIQDBPXYINGHU-IZHYLOQSSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-(trifluoromethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(C(F)(F)F)=C1 KIIQDBPXYINGHU-IZHYLOQSSA-N 0.000 description 1
- PDUQRDIYTOIXCO-RQZHXJHFSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-ethoxycarbonylanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(C(=O)OCC)=C1 PDUQRDIYTOIXCO-RQZHXJHFSA-N 0.000 description 1
- PXEKBKUCLHQUIM-IZHYLOQSSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-fluoroanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(F)=C1 PXEKBKUCLHQUIM-IZHYLOQSSA-N 0.000 description 1
- TXPJKUCTZAGEKA-IZHYLOQSSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-hydroxyanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(O)=C1 TXPJKUCTZAGEKA-IZHYLOQSSA-N 0.000 description 1
- YTQGMVPOQZVHPK-QPLCGJKRSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-methoxyanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(OC)=C1 YTQGMVPOQZVHPK-QPLCGJKRSA-N 0.000 description 1
- YOWHTRAZMMBOBZ-QPLCGJKRSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-methylanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(C)=C1 YOWHTRAZMMBOBZ-QPLCGJKRSA-N 0.000 description 1
- FZYJUDWSHZQXIT-IZHYLOQSSA-N ethyl (3z)-3-[[4-[(dimethylamino)methyl]-3-nitroanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C([N+]([O-])=O)=C1 FZYJUDWSHZQXIT-IZHYLOQSSA-N 0.000 description 1
- ACMBPOUTCUNNEI-QPLCGJKRSA-N ethyl (3z)-3-[[4-[1-amino-3-(methanesulfonamido)propyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCNS(C)(=O)=O)C=C1 ACMBPOUTCUNNEI-QPLCGJKRSA-N 0.000 description 1
- DIWHRMJVZVOQMR-DQSJHHFOSA-N ethyl (3z)-3-[[4-[1-amino-4-(dimethylamino)butyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCN(C)C)C=C1 DIWHRMJVZVOQMR-DQSJHHFOSA-N 0.000 description 1
- LPVZNMSLQKJADJ-RQZHXJHFSA-N ethyl (3z)-3-[[4-[1-amino-4-(methanesulfonamido)butyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCNS(C)(=O)=O)C=C1 LPVZNMSLQKJADJ-RQZHXJHFSA-N 0.000 description 1
- LMPDBUQWXPQWRU-RQZHXJHFSA-N ethyl (3z)-3-[[4-[2-(1h-imidazol-5-yl)ethyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CCC1=CNC=N1 LMPDBUQWXPQWRU-RQZHXJHFSA-N 0.000 description 1
- UHKVEGYQVGJASB-ZIADKAODSA-N ethyl (3z)-3-[[4-[2-(4-hydroxypiperidin-1-yl)ethyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CCN1CCC(O)CC1 UHKVEGYQVGJASB-ZIADKAODSA-N 0.000 description 1
- PVQSVNCLFZCJRA-KARKAFJISA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-(2-methoxybenzoyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(CCN(C)C)C(=O)C1=CC=CC=C1OC PVQSVNCLFZCJRA-KARKAFJISA-N 0.000 description 1
- KMSWNGUOBCAPQD-ZIADKAODSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-(2-methylpropanoyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)C(=O)C(C)C)C=C1 KMSWNGUOBCAPQD-ZIADKAODSA-N 0.000 description 1
- BKWXEEZBTJQHOJ-FLWNBWAVSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-(furan-2-carbonyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(CCN(C)C)C(=O)C1=CC=CO1 BKWXEEZBTJQHOJ-FLWNBWAVSA-N 0.000 description 1
- RTTCGZGAJZHUIX-DQSJHHFOSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-ethylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)S(=O)(=O)CC)C=C1 RTTCGZGAJZHUIX-DQSJHHFOSA-N 0.000 description 1
- AYECMIXQKVZTGO-RQZHXJHFSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)CCN(C)C)C=C1 AYECMIXQKVZTGO-RQZHXJHFSA-N 0.000 description 1
- UCVDESGYVWSIKY-HKWRFOASSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-methylsulfonylamino]anilino]methylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C\NC1=CC=C(N(CCN(C)C)S(C)(=O)=O)C=C1 UCVDESGYVWSIKY-HKWRFOASSA-N 0.000 description 1
- UXEOJRZPJFJGEN-ZIADKAODSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethyl-propan-2-ylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)S(=O)(=O)C(C)C)C=C1 UXEOJRZPJFJGEN-ZIADKAODSA-N 0.000 description 1
- ZXPFMRZTJDKPPB-FLWNBWAVSA-N ethyl (3z)-3-[[4-[2-(dimethylamino)ethylsulfonyl-[2-(dimethylamino)-2-oxoethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(=O)N(C)C)S(=O)(=O)CCN(C)C)C=C1 ZXPFMRZTJDKPPB-FLWNBWAVSA-N 0.000 description 1
- WJSIKXOMOMYGEP-IZHYLOQSSA-N ethyl (3z)-3-[[4-[2-amino-1-(dimethylamino)-1-oxopropan-2-yl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(C)(N)C(=O)N(C)C)C=C1 WJSIKXOMOMYGEP-IZHYLOQSSA-N 0.000 description 1
- GMMCUXSRHGXTGE-FLWNBWAVSA-N ethyl (3z)-3-[[4-[3-(dimethylamino)propanoyl-propan-2-ylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C(C)C)C(=O)CCN(C)C)C=C1 GMMCUXSRHGXTGE-FLWNBWAVSA-N 0.000 description 1
- OKYBZVUDULWEDR-DQSJHHFOSA-N ethyl (3z)-3-[[4-[3-(dimethylamino)propyl-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)CCCN(C)C)C=C1 OKYBZVUDULWEDR-DQSJHHFOSA-N 0.000 description 1
- YHIXYTDHADFYNE-DQSJHHFOSA-N ethyl (3z)-3-[[4-[3-(dimethylamino)propyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCCN(C)C)S(C)(=O)=O)C=C1 YHIXYTDHADFYNE-DQSJHHFOSA-N 0.000 description 1
- JZGMCNWSYULLGN-YHZPTAEISA-N ethyl (3z)-3-[[4-[3-[benzyl(methyl)amino]propanoyl-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CCN(C)CC1=CC=CC=C1 JZGMCNWSYULLGN-YHZPTAEISA-N 0.000 description 1
- QILYYCRNPGJUOB-MVJHLKBCSA-N ethyl (3z)-3-[[4-[4-(dimethylamino)butanoyl-[2-(dimethylamino)-2-oxoethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(=O)N(C)C)C(=O)CCCN(C)C)C=C1 QILYYCRNPGJUOB-MVJHLKBCSA-N 0.000 description 1
- YVFLJBZTBGIMCY-QPLCGJKRSA-N ethyl (3z)-3-[[4-[[(2-amino-2-oxoethyl)-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CC(N)=O)C=C1 YVFLJBZTBGIMCY-QPLCGJKRSA-N 0.000 description 1
- KPLNAMNDLNVERF-DQSJHHFOSA-N ethyl (3z)-3-[[4-[[(2-ethoxy-2-oxoethyl)-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(C)CC(=O)OCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OCC)C=C2NC\1=O KPLNAMNDLNVERF-DQSJHHFOSA-N 0.000 description 1
- BLZAOVRTMUHFRB-DQSJHHFOSA-N ethyl (3z)-3-[[4-[[1,3-dioxolan-2-ylmethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN(C)CC1OCCO1 BLZAOVRTMUHFRB-DQSJHHFOSA-N 0.000 description 1
- LPDUXWXQCAKPHG-KXYMVQBMSA-N ethyl (3z)-3-[[4-[[2-(4-benzylpiperazin-1-yl)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CN(CC1)CCN1CC1=CC=CC=C1 LPDUXWXQCAKPHG-KXYMVQBMSA-N 0.000 description 1
- PVADCVQLBCMSHD-KTMFPKCZSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)-2-oxoethyl]-[3-(dimethylamino)propylsulfonyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(=O)N(C)C)S(=O)(=O)CCCN(C)C)C=C1 PVADCVQLBCMSHD-KTMFPKCZSA-N 0.000 description 1
- UNBQUTRCPHSDIA-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)-2-oxoethyl]-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(=O)N(C)C)S(C)(=O)=O)C=C1 UNBQUTRCPHSDIA-RQZHXJHFSA-N 0.000 description 1
- HUJGOHAHCWRDTA-ZIADKAODSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-ethoxycarbonylanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(C(=O)OCC)=C1 HUJGOHAHCWRDTA-ZIADKAODSA-N 0.000 description 1
- FWVNYIJGAKFLPG-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-fluoroanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(F)=C1 FWVNYIJGAKFLPG-RQZHXJHFSA-N 0.000 description 1
- BBAKZSSKRFAYHQ-DQSJHHFOSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-methoxyanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(OC)=C1 BBAKZSSKRFAYHQ-DQSJHHFOSA-N 0.000 description 1
- VWEFBNRKWBWVSJ-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-nitroanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C([N+]([O-])=O)=C1 VWEFBNRKWBWVSJ-RQZHXJHFSA-N 0.000 description 1
- SWRUJBCJOYDYCW-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 SWRUJBCJOYDYCW-RQZHXJHFSA-N 0.000 description 1
- RXSMTEABPKZJSU-UYRXBGFRSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]methylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C\NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 RXSMTEABPKZJSU-UYRXBGFRSA-N 0.000 description 1
- KLGREXUHOWSUCI-ZIADKAODSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-propan-2-ylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C(C)C)C(=O)CN(C)C)C=C1 KLGREXUHOWSUCI-ZIADKAODSA-N 0.000 description 1
- XETGZBDAWRWVNO-DQSJHHFOSA-N ethyl (3z)-3-[[4-[[2-(dimethylamino)ethyl-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCN(C)C)C=C1 XETGZBDAWRWVNO-DQSJHHFOSA-N 0.000 description 1
- NGDNHJZYQZUQFE-QPLCGJKRSA-N ethyl (3z)-3-[[4-[[2-(methanesulfonamido)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CNS(C)(=O)=O)C=C1 NGDNHJZYQZUQFE-QPLCGJKRSA-N 0.000 description 1
- VUWZNUSAPAMEIA-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[2-(methanesulfonamido)ethyl-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCNS(C)(=O)=O)C=C1 VUWZNUSAPAMEIA-RQZHXJHFSA-N 0.000 description 1
- BKKLUEPLYLXSEH-FLWNBWAVSA-N ethyl (3z)-3-[[4-[[2-[2-(dimethylamino)ethyl-methylamino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)CCN(C)C)C=C1 BKKLUEPLYLXSEH-FLWNBWAVSA-N 0.000 description 1
- VCSOYTCDZBZUNQ-ZIADKAODSA-N ethyl (3z)-3-[[4-[[2-[2-methoxyethyl(methyl)amino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)CCOC)C=C1 VCSOYTCDZBZUNQ-ZIADKAODSA-N 0.000 description 1
- UOTYYZPXQGKBHV-ZIADKAODSA-N ethyl (3z)-3-[[4-[[2-[bis(2-hydroxyethyl)amino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(CCO)CCO)C=C1 UOTYYZPXQGKBHV-ZIADKAODSA-N 0.000 description 1
- KOVXOBIYGAPUII-QPLCGJKRSA-N ethyl (3z)-3-[[4-[[2-aminoethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCN)C=C1 KOVXOBIYGAPUII-QPLCGJKRSA-N 0.000 description 1
- COIPPHYWTDFRLX-QPLCGJKRSA-N ethyl (3z)-3-[[4-[[2-hydroxyethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCO)C=C1 COIPPHYWTDFRLX-QPLCGJKRSA-N 0.000 description 1
- OEHGVRVGLUGFRP-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[2-methoxyethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCOC)C=C1 OEHGVRVGLUGFRP-RQZHXJHFSA-N 0.000 description 1
- GKLZWJVAGURZJE-ZIADKAODSA-N ethyl (3z)-3-[[4-[[3-(dimethylamino)propyl-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCCN(C)C)C=C1 GKLZWJVAGURZJE-ZIADKAODSA-N 0.000 description 1
- YDWTZPKQPNXBBU-ZIADKAODSA-N ethyl (3z)-3-[[4-[[3-acetamidopropyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCCNC(C)=O)C=C1 YDWTZPKQPNXBBU-ZIADKAODSA-N 0.000 description 1
- JTLUINUGLRLOCP-ZIADKAODSA-N ethyl (3z)-3-[[4-[[4-(hydroxymethyl)piperidin-1-yl]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC(CO)CC1 JTLUINUGLRLOCP-ZIADKAODSA-N 0.000 description 1
- JCORLWNCVJPPSB-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[bis(2-hydroxyethyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(CCO)CCO)C=C1 JCORLWNCVJPPSB-RQZHXJHFSA-N 0.000 description 1
- MJUKTKWSJVXXJB-ZIADKAODSA-N ethyl (3z)-3-[[4-[[bis(2-methoxyethyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(CCOC)CCOC)C=C1 MJUKTKWSJVXXJB-ZIADKAODSA-N 0.000 description 1
- ZQWXMEXHUFYHHO-FLWNBWAVSA-N ethyl (3z)-3-[[4-[[hexyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(C)CCCCCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OCC)C=C2NC\1=O ZQWXMEXHUFYHHO-FLWNBWAVSA-N 0.000 description 1
- QIAFNXKHWWOBRX-MVJHLKBCSA-N ethyl (3z)-3-[[4-[[methyl(2-phenylethyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN(C)CCC1=CC=CC=C1 QIAFNXKHWWOBRX-MVJHLKBCSA-N 0.000 description 1
- HBRJGBCAONZVFS-RQZHXJHFSA-N ethyl (3z)-3-[[4-[[methyl-[2-(methylamino)-2-oxoethyl]amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CC(=O)NC)C=C1 HBRJGBCAONZVFS-RQZHXJHFSA-N 0.000 description 1
- ZKQOGXXXRNWYQT-DQSJHHFOSA-N ethyl (3z)-3-[[4-[acetyl-[2-(dimethylamino)ethyl]amino]-3-aminoanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OCC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)C(C)=O)C(N)=C1 ZKQOGXXXRNWYQT-DQSJHHFOSA-N 0.000 description 1
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- MILPOVQHFLFZLJ-LNVKXUELSA-N methyl (3z)-2-oxo-3-[1-[4-(piperidin-1-ylmethyl)anilino]propylidene]-1h-indole-6-carboxylate Chemical compound O=C/1NC2=CC(C(=O)OC)=CC=C2C\1=C(/CC)NC(C=C1)=CC=C1CN1CCCCC1 MILPOVQHFLFZLJ-LNVKXUELSA-N 0.000 description 1
- JQSVEWLFMVTAGS-ZROIWOOFSA-N methyl (3z)-2-oxo-3-[[4-(2h-tetrazol-5-yl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C\NC(C=C1)=CC=C1C1=NN=NN1 JQSVEWLFMVTAGS-ZROIWOOFSA-N 0.000 description 1
- LNJSJWOCLRJVIA-ZHZULCJRSA-N methyl (3z)-2-oxo-3-[[4-(piperidin-1-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C\NC(C=C1)=CC=C1CN1CCCCC1 LNJSJWOCLRJVIA-ZHZULCJRSA-N 0.000 description 1
- KHEQXLHVUPKNQU-QPLCGJKRSA-N methyl (3z)-2-oxo-3-[[4-[(1-oxo-1,4-thiazinan-4-yl)methyl]anilino]-phenylmethylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCS(=O)CC1 KHEQXLHVUPKNQU-QPLCGJKRSA-N 0.000 description 1
- FQRRZZGWVKENKU-QPLCGJKRSA-N methyl (3z)-2-oxo-3-[[4-[(3-oxopiperazin-1-yl)methyl]anilino]-phenylmethylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCNC(=O)C1 FQRRZZGWVKENKU-QPLCGJKRSA-N 0.000 description 1
- NHKGMLKDGQJHNN-QPLCGJKRSA-N methyl (3z)-2-oxo-3-[phenyl-(4-pyridin-2-ylanilino)methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=CC=CC=N1 NHKGMLKDGQJHNN-QPLCGJKRSA-N 0.000 description 1
- QDSBLMNXFRUSAC-QPLCGJKRSA-N methyl (3z)-2-oxo-3-[phenyl-(4-pyridin-3-ylanilino)methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=CC=CN=C1 QDSBLMNXFRUSAC-QPLCGJKRSA-N 0.000 description 1
- PHIGDVCYFZLICL-VHXPQNKSSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(1,2,4-triazol-1-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1C=NC=N1 PHIGDVCYFZLICL-VHXPQNKSSA-N 0.000 description 1
- IQEQBXQGCPVPOO-DQSJHHFOSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(2-piperidin-1-ylethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CCN1CCCCC1 IQEQBXQGCPVPOO-DQSJHHFOSA-N 0.000 description 1
- UNEIROSAOKXQCW-MRCUWXFGSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(2h-tetrazol-5-yl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=NN=NN1 UNEIROSAOKXQCW-MRCUWXFGSA-N 0.000 description 1
- WFWFAKWTVKMAJE-IZHYLOQSSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(propylaminomethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound C1=CC(CNCCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O WFWFAKWTVKMAJE-IZHYLOQSSA-N 0.000 description 1
- WIBHRANONYESRM-RQZHXJHFSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(pyridin-4-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CC1=CC=NC=C1 WIBHRANONYESRM-RQZHXJHFSA-N 0.000 description 1
- SKQVWHWWKSQUPK-QPLCGJKRSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(pyrrolidin-1-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCCC1 SKQVWHWWKSQUPK-QPLCGJKRSA-N 0.000 description 1
- IYORXXKXXWXNMT-QPLCGJKRSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(thiomorpholin-4-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCSCC1 IYORXXKXXWXNMT-QPLCGJKRSA-N 0.000 description 1
- BTAQJYBUIQPDQB-VHXPQNKSSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(triazol-1-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1C=CN=N1 BTAQJYBUIQPDQB-VHXPQNKSSA-N 0.000 description 1
- HFTBELNGYZLFND-VHXPQNKSSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(triazol-2-ylmethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1N=CC=N1 HFTBELNGYZLFND-VHXPQNKSSA-N 0.000 description 1
- FTWGZBDWDBQXAG-MRCUWXFGSA-N methyl (3z)-2-oxo-3-[phenyl-[4-(trifluoromethyl)anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(F)(F)F)C=C1 FTWGZBDWDBQXAG-MRCUWXFGSA-N 0.000 description 1
- YMDHFSHAFSDHGC-FLWNBWAVSA-N methyl (3z)-2-oxo-3-[phenyl-[4-[(2-piperazin-1-ylacetyl)-propan-2-ylamino]anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C(C)C)C(=O)CN1CCNCC1 YMDHFSHAFSDHGC-FLWNBWAVSA-N 0.000 description 1
- IIIGSXYVAHIXRD-KTMFPKCZSA-N methyl (3z)-2-oxo-3-[phenyl-[4-[(2-piperidin-1-ylacetyl)-propan-2-ylamino]anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C(C)C)C(=O)CN1CCCCC1 IIIGSXYVAHIXRD-KTMFPKCZSA-N 0.000 description 1
- IWCWQRLASYFOIU-IZHYLOQSSA-N methyl (3z)-2-oxo-3-[phenyl-[4-[(propan-2-ylamino)methyl]anilino]methylidene]-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CNC(C)C)C=C1 IWCWQRLASYFOIU-IZHYLOQSSA-N 0.000 description 1
- GCMYYSATKUWOGV-DQSJHHFOSA-N methyl (3z)-3-[(4-benzylanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CC1=CC=CC=C1 GCMYYSATKUWOGV-DQSJHHFOSA-N 0.000 description 1
- PVQLMANNFBZOFB-MRCUWXFGSA-N methyl (3z)-3-[(4-bromoanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(Br)C=C1 PVQLMANNFBZOFB-MRCUWXFGSA-N 0.000 description 1
- ORRNEYOVWFPWAP-MRCUWXFGSA-N methyl (3z)-3-[(4-chloroanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(Cl)C=C1 ORRNEYOVWFPWAP-MRCUWXFGSA-N 0.000 description 1
- NQROFBRJNJSXKA-DQRAZIAOSA-N methyl (3z)-3-[(4-cyanoanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C#N)C=C1 NQROFBRJNJSXKA-DQRAZIAOSA-N 0.000 description 1
- OHCAWFMXYUNPGZ-FCQUAONHSA-N methyl (3z)-3-[(4-ethoxyanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(OCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O OHCAWFMXYUNPGZ-FCQUAONHSA-N 0.000 description 1
- WLLXCGQUQRIENQ-MRCUWXFGSA-N methyl (3z)-3-[(4-fluoroanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(F)C=C1 WLLXCGQUQRIENQ-MRCUWXFGSA-N 0.000 description 1
- JZQXIZWXSRTLAM-MRCUWXFGSA-N methyl (3z)-3-[(4-iodoanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(I)C=C1 JZQXIZWXSRTLAM-MRCUWXFGSA-N 0.000 description 1
- NQOXUALBKFUCJF-DQRAZIAOSA-N methyl (3z)-3-[(4-methoxyanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(OC)C=C1 NQOXUALBKFUCJF-DQRAZIAOSA-N 0.000 description 1
- NIGSGKHDAXWGET-DQRAZIAOSA-N methyl (3z)-3-[(4-methylsulfanylanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(SC)C=C1 NIGSGKHDAXWGET-DQRAZIAOSA-N 0.000 description 1
- UQAMDWYLNNWLHK-MRCUWXFGSA-N methyl (3z)-3-[(4-nitroanilino)-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C([N+]([O-])=O)C=C1 UQAMDWYLNNWLHK-MRCUWXFGSA-N 0.000 description 1
- UKDNXXZAGVDGLC-ATJXCDBQSA-N methyl (3z)-3-[1-[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]butylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C/1NC2=CC(C(=O)OC)=CC=C2C\1=C(/CCC)NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 UKDNXXZAGVDGLC-ATJXCDBQSA-N 0.000 description 1
- VAHWEVGCUFXVQK-STZFKDTASA-N methyl (3z)-3-[1-[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]ethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(/C)NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 VAHWEVGCUFXVQK-STZFKDTASA-N 0.000 description 1
- AHFOHWWSQSLKQH-QOCHGBHMSA-N methyl (3z)-3-[1-[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]propylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C/1NC2=CC(C(=O)OC)=CC=C2C\1=C(/CC)NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 AHFOHWWSQSLKQH-QOCHGBHMSA-N 0.000 description 1
- PSBOWDCVRMIKJN-KQWNVCNZSA-N methyl (3z)-3-[1-[4-[acetyl-[3-(dimethylamino)propyl]amino]anilino]ethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(/C)NC1=CC=C(N(CCCN(C)C)C(C)=O)C=C1 PSBOWDCVRMIKJN-KQWNVCNZSA-N 0.000 description 1
- FCLITXSPSUOHHD-VHXPQNKSSA-N methyl (3z)-3-[[3,5-dibromo-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC(Br)=C(CN(C)C)C(Br)=C1 FCLITXSPSUOHHD-VHXPQNKSSA-N 0.000 description 1
- SNUSQQNGMPGWRB-IZHYLOQSSA-N methyl (3z)-3-[[3,5-dibromo-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC(Br)=C(N(C)C(=O)CN(C)C)C(Br)=C1 SNUSQQNGMPGWRB-IZHYLOQSSA-N 0.000 description 1
- UYRMFXGNPAOJJM-VHXPQNKSSA-N methyl (3z)-3-[[3,5-dichloro-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC(Cl)=C(CN(C)C)C(Cl)=C1 UYRMFXGNPAOJJM-VHXPQNKSSA-N 0.000 description 1
- GJZOCJMBIIKQIK-DQSJHHFOSA-N methyl (3z)-3-[[3-acetamido-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(NC(C)=O)=C1 GJZOCJMBIIKQIK-DQSJHHFOSA-N 0.000 description 1
- FQPQINWPSPWZJS-QPLCGJKRSA-N methyl (3z)-3-[[3-amino-4-[2-(dimethylamino)ethyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)S(C)(=O)=O)C(N)=C1 FQPQINWPSPWZJS-QPLCGJKRSA-N 0.000 description 1
- MDHPVJCMQBSWTC-QPLCGJKRSA-N methyl (3z)-3-[[3-bromo-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(Br)=C1 MDHPVJCMQBSWTC-QPLCGJKRSA-N 0.000 description 1
- HPNQZONFUXLKDA-VHXPQNKSSA-N methyl (3z)-3-[[3-chloro-4-[(dimethylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(Cl)=C1 HPNQZONFUXLKDA-VHXPQNKSSA-N 0.000 description 1
- PYWYMRSZOWDEDS-QPLCGJKRSA-N methyl (3z)-3-[[3-chloro-4-[2-(dimethylamino)ethyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)S(C)(=O)=O)C(Cl)=C1 PYWYMRSZOWDEDS-QPLCGJKRSA-N 0.000 description 1
- LITNYBZNPBBUDL-RQZHXJHFSA-N methyl (3z)-3-[[3-cyano-4-[[2-(dimethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(C#N)=C1 LITNYBZNPBBUDL-RQZHXJHFSA-N 0.000 description 1
- CSMAMMGWSPPCFM-VHXPQNKSSA-N methyl (3z)-3-[[4-(1,3-diaminopropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCN)C=C1 CSMAMMGWSPPCFM-VHXPQNKSSA-N 0.000 description 1
- CMEKJNNNRKFNAH-IZHYLOQSSA-N methyl (3z)-3-[[4-(1,4-diaminobutyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCN)C=C1 CMEKJNNNRKFNAH-IZHYLOQSSA-N 0.000 description 1
- IKNSSCDVQASFBP-VHXPQNKSSA-N methyl (3z)-3-[[4-(1-amino-3-hydroxypropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCO)C=C1 IKNSSCDVQASFBP-VHXPQNKSSA-N 0.000 description 1
- YAPOARLAMRUWED-IZHYLOQSSA-N methyl (3z)-3-[[4-(1-amino-3-methoxypropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(C(N)CCOC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O YAPOARLAMRUWED-IZHYLOQSSA-N 0.000 description 1
- KFQUQGPGBSRWLL-FLWNBWAVSA-N methyl (3z)-3-[[4-(1-benzylimidazol-2-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=NC=CN1CC1=CC=CC=C1 KFQUQGPGBSRWLL-FLWNBWAVSA-N 0.000 description 1
- QRYXUASSWIFHFW-IZHYLOQSSA-N methyl (3z)-3-[[4-(1-ethylimidazol-2-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound CCN1C=CN=C1C(C=C1)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O QRYXUASSWIFHFW-IZHYLOQSSA-N 0.000 description 1
- BGNCLMXCLORXLK-FCQUAONHSA-N methyl (3z)-3-[[4-(1h-imidazol-2-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=NC=CN1 BGNCLMXCLORXLK-FCQUAONHSA-N 0.000 description 1
- QYUVQENLWCRKLV-VHXPQNKSSA-N methyl (3z)-3-[[4-(1h-imidazol-5-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C1=CNC=N1 QYUVQENLWCRKLV-VHXPQNKSSA-N 0.000 description 1
- XXBZVVHKDMBPQL-IZHYLOQSSA-N methyl (3z)-3-[[4-(1h-imidazol-5-ylmethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CC1=CNC=N1 XXBZVVHKDMBPQL-IZHYLOQSSA-N 0.000 description 1
- FSZGHRMXKHMOCA-IZHYLOQSSA-N methyl (3z)-3-[[4-(2-acetamidoethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CCNC(C)=O)C=C1 FSZGHRMXKHMOCA-IZHYLOQSSA-N 0.000 description 1
- DOOGGJTZJJJMTJ-FCQUAONHSA-N methyl (3z)-3-[[4-(2-amino-2-oxoethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CC(N)=O)C=C1 DOOGGJTZJJJMTJ-FCQUAONHSA-N 0.000 description 1
- BRESLQOHIMDFJC-FCQUAONHSA-N methyl (3z)-3-[[4-(2-aminoethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CCN)C=C1 BRESLQOHIMDFJC-FCQUAONHSA-N 0.000 description 1
- WYPKJAANQARQNV-RQZHXJHFSA-N methyl (3z)-3-[[4-(3,6-dihydro-2h-pyridin-1-ylmethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC=CC1 WYPKJAANQARQNV-RQZHXJHFSA-N 0.000 description 1
- UKZBPRXAASHSDP-VHXPQNKSSA-N methyl (3z)-3-[[4-(3-amino-3-oxopropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CCC(N)=O)C=C1 UKZBPRXAASHSDP-VHXPQNKSSA-N 0.000 description 1
- YKZFJSOJAKUINN-VHXPQNKSSA-N methyl (3z)-3-[[4-(3-aminopropyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CCCN)C=C1 YKZFJSOJAKUINN-VHXPQNKSSA-N 0.000 description 1
- ZRVRRMHTQYERBN-RQZHXJHFSA-N methyl (3z)-3-[[4-(4-acetamido-1-aminobutyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCNC(C)=O)C=C1 ZRVRRMHTQYERBN-RQZHXJHFSA-N 0.000 description 1
- OKBAJDUJXQITPZ-BZZOAKBMSA-N methyl (3z)-3-[[4-(5-methyl-1h-imidazol-4-yl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C=1N=CNC=1C OKBAJDUJXQITPZ-BZZOAKBMSA-N 0.000 description 1
- FOZZNPZXSKJEQN-DQSJHHFOSA-N methyl (3z)-3-[[4-(anilinomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CNC1=CC=CC=C1 FOZZNPZXSKJEQN-DQSJHHFOSA-N 0.000 description 1
- LAVIABVORHCAAD-DQSJHHFOSA-N methyl (3z)-3-[[4-(azepan-1-ylmethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCCCCC1 LAVIABVORHCAAD-DQSJHHFOSA-N 0.000 description 1
- GKJAQZQLIADODD-IZHYLOQSSA-N methyl (3z)-3-[[4-(azetidin-1-ylmethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC1 GKJAQZQLIADODD-IZHYLOQSSA-N 0.000 description 1
- XWJDCUCFMSIPPA-RQZHXJHFSA-N methyl (3z)-3-[[4-(cyclohexanecarbonyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C(=O)C1CCCCC1 XWJDCUCFMSIPPA-RQZHXJHFSA-N 0.000 description 1
- YXQMTPXIYODTOH-RQZHXJHFSA-N methyl (3z)-3-[[4-(cyclohexylamino)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1NC1CCCCC1 YXQMTPXIYODTOH-RQZHXJHFSA-N 0.000 description 1
- LCAMDNGTCFSSHD-QPLCGJKRSA-N methyl (3z)-3-[[4-(diethylaminomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(CC)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O LCAMDNGTCFSSHD-QPLCGJKRSA-N 0.000 description 1
- XHYDNVCBHSFLQR-FCQUAONHSA-N methyl (3z)-3-[[4-(methanesulfonamidomethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CNS(C)(=O)=O)C=C1 XHYDNVCBHSFLQR-FCQUAONHSA-N 0.000 description 1
- IDWZQYHNNILFMO-QPLCGJKRSA-N methyl (3z)-3-[[4-(morpholin-4-ylmethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCOCC1 IDWZQYHNNILFMO-QPLCGJKRSA-N 0.000 description 1
- BEULZLALWAJZNR-QPLCGJKRSA-N methyl (3z)-3-[[4-[(1,1-dioxo-1,4-thiazinan-4-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCS(=O)(=O)CC1 BEULZLALWAJZNR-QPLCGJKRSA-N 0.000 description 1
- MFMREZXKGGWAGY-FCQUAONHSA-N methyl (3z)-3-[[4-[(2,5-dioxoimidazolidin-4-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CC1NC(=O)NC1=O MFMREZXKGGWAGY-FCQUAONHSA-N 0.000 description 1
- URNUEBLYEXQFTO-WVVAYPLRSA-N methyl (3z)-3-[[4-[(2,5-dioxoimidazolidin-4-ylidene)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1C=C1NC(=O)NC1=O URNUEBLYEXQFTO-WVVAYPLRSA-N 0.000 description 1
- XBUCECOAKVVLNR-ZIADKAODSA-N methyl (3z)-3-[[4-[(2,6-dimethylpiperidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1C(C)CCCC1C XBUCECOAKVVLNR-ZIADKAODSA-N 0.000 description 1
- SEZYXLIMGCZJMT-VHXPQNKSSA-N methyl (3z)-3-[[4-[(2-amino-2-oxoethyl)-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(N)=O)S(C)(=O)=O)C=C1 SEZYXLIMGCZJMT-VHXPQNKSSA-N 0.000 description 1
- ZUWLEBRSSYJVEQ-VHXPQNKSSA-N methyl (3z)-3-[[4-[(2-aminoacetyl)-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN)C=C1 ZUWLEBRSSYJVEQ-VHXPQNKSSA-N 0.000 description 1
- FTJZNXYBEQOVKI-QPLCGJKRSA-N methyl (3z)-3-[[4-[(2-methylpropylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CNCC(C)C)C=C1 FTJZNXYBEQOVKI-QPLCGJKRSA-N 0.000 description 1
- GMJWQWHGELZQIQ-ZIADKAODSA-N methyl (3z)-3-[[4-[(3,5-dimethylpiperidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CC(C)CC(C)C1 GMJWQWHGELZQIQ-ZIADKAODSA-N 0.000 description 1
- JOJRRLVBVACGHK-QPLCGJKRSA-N methyl (3z)-3-[[4-[(3-hydroxypyrrolidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC(O)C1 JOJRRLVBVACGHK-QPLCGJKRSA-N 0.000 description 1
- RTBGMEMZIPGYHB-MVJHLKBCSA-N methyl (3z)-3-[[4-[(4-benzoylpiperazin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN(CC1)CCN1C(=O)C1=CC=CC=C1 RTBGMEMZIPGYHB-MVJHLKBCSA-N 0.000 description 1
- DWQMEXHZENVEEZ-RQZHXJHFSA-N methyl (3z)-3-[[4-[(4-hydroxypiperidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC(O)CC1 DWQMEXHZENVEEZ-RQZHXJHFSA-N 0.000 description 1
- HMDBPOYXPOSDJX-DQSJHHFOSA-N methyl (3z)-3-[[4-[(4-methoxypiperidin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1CC(OC)CCN1CC(C=C1)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O HMDBPOYXPOSDJX-DQSJHHFOSA-N 0.000 description 1
- IRIFEJWVQKJYPO-RQZHXJHFSA-N methyl (3z)-3-[[4-[(4-methylpiperazin-1-yl)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCN(C)CC1 IRIFEJWVQKJYPO-RQZHXJHFSA-N 0.000 description 1
- VLVSTMQEIKJUIB-ZIADKAODSA-N methyl (3z)-3-[[4-[(benzylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CNCC1=CC=CC=C1 VLVSTMQEIKJUIB-ZIADKAODSA-N 0.000 description 1
- MZQVUAAURXIYRD-DQSJHHFOSA-N methyl (3z)-3-[[4-[(cyclohexylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CNC1CCCCC1 MZQVUAAURXIYRD-DQSJHHFOSA-N 0.000 description 1
- NJSMNIIVGXCSBI-KXYMVQBMSA-N methyl (3z)-3-[[4-[(dibenzylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN(CC=1C=CC=CC=1)CC1=CC=CC=C1 NJSMNIIVGXCSBI-KXYMVQBMSA-N 0.000 description 1
- UDUBGBJOQMFORB-VHXPQNKSSA-N methyl (3z)-3-[[4-[(dimethylamino)methyl]-3-(trifluoromethyl)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(C(F)(F)F)=C1 UDUBGBJOQMFORB-VHXPQNKSSA-N 0.000 description 1
- QXMDRRDVEIGIAL-VHXPQNKSSA-N methyl (3z)-3-[[4-[(dimethylamino)methyl]-3-fluoroanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(F)=C1 QXMDRRDVEIGIAL-VHXPQNKSSA-N 0.000 description 1
- AFUUYWZKISIIDQ-VHXPQNKSSA-N methyl (3z)-3-[[4-[(dimethylamino)methyl]-3-hydroxyanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(O)=C1 AFUUYWZKISIIDQ-VHXPQNKSSA-N 0.000 description 1
- NQFDXCBVWXJEFE-IZHYLOQSSA-N methyl (3z)-3-[[4-[(dimethylamino)methyl]-3-methylanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)C)C(C)=C1 NQFDXCBVWXJEFE-IZHYLOQSSA-N 0.000 description 1
- IZTCGPDAIPBHGU-BOPFTXTBSA-N methyl (3z)-3-[[4-[(dimethylamino)methyl]anilino]methylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C\NC1=CC=C(CN(C)C)C=C1 IZTCGPDAIPBHGU-BOPFTXTBSA-N 0.000 description 1
- RPPPXRUSARQHLC-DQSJHHFOSA-N methyl (3z)-3-[[4-[(dipropylamino)methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(CCC)CCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O RPPPXRUSARQHLC-DQSJHHFOSA-N 0.000 description 1
- POJVTYBLLXHLQL-QPLCGJKRSA-N methyl (3z)-3-[[4-[1-amino-3-(dimethylamino)propyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCN(C)C)C=C1 POJVTYBLLXHLQL-QPLCGJKRSA-N 0.000 description 1
- ZLYZTANYDSIYPC-IZHYLOQSSA-N methyl (3z)-3-[[4-[1-amino-3-(methanesulfonamido)propyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCNS(C)(=O)=O)C=C1 ZLYZTANYDSIYPC-IZHYLOQSSA-N 0.000 description 1
- BTHGXGDWQASQRP-RQZHXJHFSA-N methyl (3z)-3-[[4-[1-amino-4-(dimethylamino)butyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCN(C)C)C=C1 BTHGXGDWQASQRP-RQZHXJHFSA-N 0.000 description 1
- VWANDBSUBUHNFW-QPLCGJKRSA-N methyl (3z)-3-[[4-[1-amino-4-(methanesulfonamido)butyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(C(N)CCCNS(C)(=O)=O)C=C1 VWANDBSUBUHNFW-QPLCGJKRSA-N 0.000 description 1
- ZYKDYALDSSSEKC-QPLCGJKRSA-N methyl (3z)-3-[[4-[2-(1h-imidazol-5-yl)ethyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CCC1=CNC=N1 ZYKDYALDSSSEKC-QPLCGJKRSA-N 0.000 description 1
- QXRQSNFYTPRXMN-DQSJHHFOSA-N methyl (3z)-3-[[4-[2-(4-hydroxypiperidin-1-yl)ethyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CCN1CCC(O)CC1 QXRQSNFYTPRXMN-DQSJHHFOSA-N 0.000 description 1
- ZBGGFGDKVXCEJA-DQSJHHFOSA-N methyl (3z)-3-[[4-[2-(diethylamino)ethyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCN(CC)CC)S(C)(=O)=O)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O ZBGGFGDKVXCEJA-DQSJHHFOSA-N 0.000 description 1
- YPCNHVIKYWKTMT-IZHYLOQSSA-N methyl (3z)-3-[[4-[2-(dimethylamino)-2-oxoethyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CC(=O)N(C)C)C=C1 YPCNHVIKYWKTMT-IZHYLOQSSA-N 0.000 description 1
- UDRYCALAFSXOJU-IZHYLOQSSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethoxy]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(OCCN(C)C)C=C1 UDRYCALAFSXOJU-IZHYLOQSSA-N 0.000 description 1
- UGZDSGPCUPMYNG-MVJHLKBCSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-(2-methoxybenzoyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(CCN(C)C)C(=O)C1=CC=CC=C1OC UGZDSGPCUPMYNG-MVJHLKBCSA-N 0.000 description 1
- NSEGQXXOKNFRQH-KARKAFJISA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-(2-phenylacetyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(CCN(C)C)C(=O)CC1=CC=CC=C1 NSEGQXXOKNFRQH-KARKAFJISA-N 0.000 description 1
- UXPGGJLMVUQWLH-FLWNBWAVSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-(pyridine-3-carbonyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(CCN(C)C)C(=O)C1=CC=CN=C1 UXPGGJLMVUQWLH-FLWNBWAVSA-N 0.000 description 1
- UTISDSYHQVSJSO-RQZHXJHFSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-ethylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCN(C)C)S(=O)(=O)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O UTISDSYHQVSJSO-RQZHXJHFSA-N 0.000 description 1
- NSJWGYJIQYLIMC-QPLCGJKRSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)CCN(C)C)C=C1 NSJWGYJIQYLIMC-QPLCGJKRSA-N 0.000 description 1
- WJZTXYKYCJDGGW-DQSJHHFOSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-propanoylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCN(C)C)C(=O)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O WJZTXYKYCJDGGW-DQSJHHFOSA-N 0.000 description 1
- AGQVXLYIQBWXIE-DQSJHHFOSA-N methyl (3z)-3-[[4-[2-(dimethylamino)ethyl-propylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCN(C)C)S(=O)(=O)CCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O AGQVXLYIQBWXIE-DQSJHHFOSA-N 0.000 description 1
- XNJPIGSAHQKNRZ-QPLCGJKRSA-N methyl (3z)-3-[[4-[2-(ethylamino)ethyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCNCC)S(C)(=O)=O)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O XNJPIGSAHQKNRZ-QPLCGJKRSA-N 0.000 description 1
- HUKMKKIFMCLRLL-IZHYLOQSSA-N methyl (3z)-3-[[4-[2-(methylamino)ethyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCNC)S(C)(=O)=O)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O HUKMKKIFMCLRLL-IZHYLOQSSA-N 0.000 description 1
- IIWXYHWYUFXQBW-VHXPQNKSSA-N methyl (3z)-3-[[4-[2-(methylamino)ethyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CCNC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O IIWXYHWYUFXQBW-VHXPQNKSSA-N 0.000 description 1
- JLDXMMDMAJYUIJ-VHXPQNKSSA-N methyl (3z)-3-[[4-[2-aminoethyl(methylsulfonyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN)S(C)(=O)=O)C=C1 JLDXMMDMAJYUIJ-VHXPQNKSSA-N 0.000 description 1
- MXFOZFBVTXOVHM-ZIADKAODSA-N methyl (3z)-3-[[4-[3-(diethylamino)propanoyl-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CCN(CC)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O MXFOZFBVTXOVHM-ZIADKAODSA-N 0.000 description 1
- CXURIOROSJWAMI-QPLCGJKRSA-N methyl (3z)-3-[[4-[3-(dimethylamino)propoxy]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(OCCCN(C)C)C=C1 CXURIOROSJWAMI-QPLCGJKRSA-N 0.000 description 1
- KNRKOFDOYIKJGR-RQZHXJHFSA-N methyl (3z)-3-[[4-[3-(dimethylamino)propyl-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)CCCN(C)C)C=C1 KNRKOFDOYIKJGR-RQZHXJHFSA-N 0.000 description 1
- HQVUFGHRHRIQHU-QPLCGJKRSA-N methyl (3z)-3-[[4-[3-(dimethylamino)propyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CCCN(C)C)C=C1 HQVUFGHRHRIQHU-QPLCGJKRSA-N 0.000 description 1
- QTEFTUGUGQMXBI-QPLCGJKRSA-N methyl (3z)-3-[[4-[3-(methylamino)propyl-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCCNC)S(C)(=O)=O)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O QTEFTUGUGQMXBI-QPLCGJKRSA-N 0.000 description 1
- QWHWQOKJBPYICM-IZHYLOQSSA-N methyl (3z)-3-[[4-[3-aminopropanoyl(methyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CCN)C=C1 QWHWQOKJBPYICM-IZHYLOQSSA-N 0.000 description 1
- AOZQUABEISRQBJ-KTMFPKCZSA-N methyl (3z)-3-[[4-[4-(dimethylamino)butanoyl-[2-(dimethylamino)-2-oxoethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(=O)N(C)C)C(=O)CCCN(C)C)C=C1 AOZQUABEISRQBJ-KTMFPKCZSA-N 0.000 description 1
- UTKGHSVTHCHCCU-IZHYLOQSSA-N methyl (3z)-3-[[4-[[(2-amino-2-oxoethyl)-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CC(N)=O)C=C1 UTKGHSVTHCHCCU-IZHYLOQSSA-N 0.000 description 1
- BTUACWQNCVFDMG-DQSJHHFOSA-N methyl (3z)-3-[[4-[[2-(diethylamino)-2-oxoethyl]-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CC(=O)N(CC)CC)S(C)(=O)=O)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O BTUACWQNCVFDMG-DQSJHHFOSA-N 0.000 description 1
- BAUFJTXWLJKPAR-DQSJHHFOSA-N methyl (3z)-3-[[4-[[2-(diethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CN(CC)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O BAUFJTXWLJKPAR-DQSJHHFOSA-N 0.000 description 1
- LGPFPZWGWQZVGL-FLWNBWAVSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)-2-oxoethyl]-[3-(dimethylamino)propylsulfonyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CC(=O)N(C)C)S(=O)(=O)CCCN(C)C)C=C1 LGPFPZWGWQZVGL-FLWNBWAVSA-N 0.000 description 1
- RXHZDTGOOZYYRM-DQSJHHFOSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)-2-oxoethyl]-propanoylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CC(=O)N(C)C)C(=O)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O RXHZDTGOOZYYRM-DQSJHHFOSA-N 0.000 description 1
- VJLJKPGFMIFONZ-RQZHXJHFSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-ethylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C(=O)CN(C)C)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O VJLJKPGFMIFONZ-RQZHXJHFSA-N 0.000 description 1
- HOXJEHKBYSZHDT-RQZHXJHFSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-(methanesulfonamido)anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(NS(C)(=O)=O)=C1 HOXJEHKBYSZHDT-RQZHXJHFSA-N 0.000 description 1
- WAUCSJCPUORSTC-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-fluoroanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(F)=C1 WAUCSJCPUORSTC-QPLCGJKRSA-N 0.000 description 1
- HQGFACIJAOUSHR-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-hydroxyanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(O)=C1 HQGFACIJAOUSHR-QPLCGJKRSA-N 0.000 description 1
- KKQAKFFHVQJBRP-RQZHXJHFSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-methylanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C(C)=C1 KKQAKFFHVQJBRP-RQZHXJHFSA-N 0.000 description 1
- WZSPHJSIBQNMLK-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]-3-nitroanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)C)C([N+]([O-])=O)=C1 WZSPHJSIBQNMLK-QPLCGJKRSA-N 0.000 description 1
- WDLKBZLGTNDINZ-PDGQHHTCSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-methylamino]anilino]methylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C\NC1=CC=C(N(C)C(=O)CN(C)C)C=C1 WDLKBZLGTNDINZ-PDGQHHTCSA-N 0.000 description 1
- FVQJAAAWWIGEMK-DQSJHHFOSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)acetyl]-propylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C(=O)CN(C)C)CCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O FVQJAAAWWIGEMK-DQSJHHFOSA-N 0.000 description 1
- CLMURYIACIHACU-RQZHXJHFSA-N methyl (3z)-3-[[4-[[2-(dimethylamino)ethyl-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCN(C)C)C=C1 CLMURYIACIHACU-RQZHXJHFSA-N 0.000 description 1
- CXDYWQZLHPBBQY-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-(ethylamino)-2-oxoethyl]-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CC(=O)NCC)S(C)(=O)=O)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O CXDYWQZLHPBBQY-QPLCGJKRSA-N 0.000 description 1
- OEYMBRUKBJIOJL-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-(ethylamino)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CNCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O OEYMBRUKBJIOJL-QPLCGJKRSA-N 0.000 description 1
- RTXFTXQHTXRSSM-IZHYLOQSSA-N methyl (3z)-3-[[4-[[2-(methanesulfonamido)acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CNS(C)(=O)=O)C=C1 RTXFTXQHTXRSSM-IZHYLOQSSA-N 0.000 description 1
- TXANJRRNRHLIGN-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-(methanesulfonamido)ethyl-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCNS(C)(=O)=O)C=C1 TXANJRRNRHLIGN-QPLCGJKRSA-N 0.000 description 1
- WZOBASBNPSNEQM-IZHYLOQSSA-N methyl (3z)-3-[[4-[[2-(methylamino)-2-oxoethyl]-methylsulfonylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CC(=O)NC)S(C)(=O)=O)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O WZOBASBNPSNEQM-IZHYLOQSSA-N 0.000 description 1
- USVLUTIAGKLFLC-RQZHXJHFSA-N methyl (3z)-3-[[4-[[2-[(2-amino-2-oxoethyl)-methylamino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)CC(N)=O)C=C1 USVLUTIAGKLFLC-RQZHXJHFSA-N 0.000 description 1
- LLRYASAHXGEORL-ZIADKAODSA-N methyl (3z)-3-[[4-[[2-[2-(dimethylamino)ethyl-methylamino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(C)CCN(C)C)C=C1 LLRYASAHXGEORL-ZIADKAODSA-N 0.000 description 1
- SUBBBPXDIJNZNV-DQSJHHFOSA-N methyl (3z)-3-[[4-[[2-[2-methoxyethyl(methyl)amino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CN(C)CCOC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O SUBBBPXDIJNZNV-DQSJHHFOSA-N 0.000 description 1
- RZNYISXKOSUPRU-DQSJHHFOSA-N methyl (3z)-3-[[4-[[2-[bis(2-hydroxyethyl)amino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)C(=O)CN(CCO)CCO)C=C1 RZNYISXKOSUPRU-DQSJHHFOSA-N 0.000 description 1
- XTHMDGVWHHKQOE-RQZHXJHFSA-N methyl (3z)-3-[[4-[[2-[ethyl(methyl)amino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CN(C)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O XTHMDGVWHHKQOE-RQZHXJHFSA-N 0.000 description 1
- GCSYCCHPGMVUKA-ZIADKAODSA-N methyl (3z)-3-[[4-[[2-[ethyl(propyl)amino]acetyl]-methylamino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CN(CC)CCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O GCSYCCHPGMVUKA-ZIADKAODSA-N 0.000 description 1
- FKSICKKKGOVLIS-RQZHXJHFSA-N methyl (3z)-3-[[4-[[2-acetamidoethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCNC(C)=O)C=C1 FKSICKKKGOVLIS-RQZHXJHFSA-N 0.000 description 1
- RIJRLDYGGPGPOI-IZHYLOQSSA-N methyl (3z)-3-[[4-[[2-aminoethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCN)C=C1 RIJRLDYGGPGPOI-IZHYLOQSSA-N 0.000 description 1
- QFVUURLADURDAG-IZHYLOQSSA-N methyl (3z)-3-[[4-[[2-hydroxyethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCO)C=C1 QFVUURLADURDAG-IZHYLOQSSA-N 0.000 description 1
- QFDIOUCLNGGUQP-QPLCGJKRSA-N methyl (3z)-3-[[4-[[2-methoxyethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(C)CCOC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O QFDIOUCLNGGUQP-QPLCGJKRSA-N 0.000 description 1
- RXZWGNDZZXCZGH-DQSJHHFOSA-N methyl (3z)-3-[[4-[[3-acetamidopropyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CCCNC(C)=O)C=C1 RXZWGNDZZXCZGH-DQSJHHFOSA-N 0.000 description 1
- PVDDHMABBCZBCT-DQSJHHFOSA-N methyl (3z)-3-[[4-[[4-(hydroxymethyl)piperidin-1-yl]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN1CCC(CO)CC1 PVDDHMABBCZBCT-DQSJHHFOSA-N 0.000 description 1
- YWPMQYDTEUFJMU-RQZHXJHFSA-N methyl (3z)-3-[[4-[[[2-(dimethylamino)-2-oxoethyl]-methylamino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C)CC(=O)N(C)C)C=C1 YWPMQYDTEUFJMU-RQZHXJHFSA-N 0.000 description 1
- VGFCLVZQGXFUBP-FLWNBWAVSA-N methyl (3z)-3-[[4-[[benzyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN(C)CC1=CC=CC=C1 VGFCLVZQGXFUBP-FLWNBWAVSA-N 0.000 description 1
- GZQQQXWKMMUNAW-DQSJHHFOSA-N methyl (3z)-3-[[4-[[bis(2-methoxyethyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(CCOC)CCOC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O GZQQQXWKMMUNAW-DQSJHHFOSA-N 0.000 description 1
- FQHSDNRZQHBVIC-DQSJHHFOSA-N methyl (3z)-3-[[4-[[di(propan-2-yl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(CN(C(C)C)C(C)C)C=C1 FQHSDNRZQHBVIC-DQSJHHFOSA-N 0.000 description 1
- RVDUOGHPXADGKD-IZHYLOQSSA-N methyl (3z)-3-[[4-[[ethyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(C)CC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O RVDUOGHPXADGKD-IZHYLOQSSA-N 0.000 description 1
- AOUHPEGJMFYYFU-RQZHXJHFSA-N methyl (3z)-3-[[4-[[ethyl(propyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(CC)CCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O AOUHPEGJMFYYFU-RQZHXJHFSA-N 0.000 description 1
- YMPRIZDZHDMBLD-ZIADKAODSA-N methyl (3z)-3-[[4-[[hexyl(methyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(C)CCCCCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O YMPRIZDZHDMBLD-ZIADKAODSA-N 0.000 description 1
- OULCGLUBKXTBRA-KTMFPKCZSA-N methyl (3z)-3-[[4-[[methyl(2-phenylethyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1CN(C)CCC1=CC=CC=C1 OULCGLUBKXTBRA-KTMFPKCZSA-N 0.000 description 1
- VAIRUXVDRLLXEU-QPLCGJKRSA-N methyl (3z)-3-[[4-[[methyl(propyl)amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(C)CCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O VAIRUXVDRLLXEU-QPLCGJKRSA-N 0.000 description 1
- PJHMTIYWQHYUSZ-QPLCGJKRSA-N methyl (3z)-3-[[4-[[methyl-[2-(methylamino)-2-oxoethyl]amino]methyl]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(CN(C)CC(=O)NC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O PJHMTIYWQHYUSZ-QPLCGJKRSA-N 0.000 description 1
- LGYZWMSAASYNAN-IZHYLOQSSA-N methyl (3z)-3-[[4-[acetyl(2-aminoethyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN)C(C)=O)C=C1 LGYZWMSAASYNAN-IZHYLOQSSA-N 0.000 description 1
- ICWCEAPXTJICQR-FLWNBWAVSA-N methyl (3z)-3-[[4-[acetyl-(2-oxo-2-piperidin-1-ylethyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C(C)=O)CC(=O)N1CCCCC1 ICWCEAPXTJICQR-FLWNBWAVSA-N 0.000 description 1
- BAIGDZLJOJIQHO-RQZHXJHFSA-N methyl (3z)-3-[[4-[acetyl-[2-(dimethylamino)ethyl]amino]-3-bromoanilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCN(C)C)C(C)=O)C(Br)=C1 BAIGDZLJOJIQHO-RQZHXJHFSA-N 0.000 description 1
- PTQKFPKUOYEZHW-QPLCGJKRSA-N methyl (3z)-3-[[4-[acetyl-[2-(methylamino)ethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C(C)=O)CCNC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O PTQKFPKUOYEZHW-QPLCGJKRSA-N 0.000 description 1
- IZTXKRFGALXQFK-KTMFPKCZSA-N methyl (3z)-3-[[4-[benzenesulfonyl-[2-(dimethylamino)ethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(CCN(C)C)S(=O)(=O)C1=CC=CC=C1 IZTXKRFGALXQFK-KTMFPKCZSA-N 0.000 description 1
- INOGNMCSLFRZAV-KTMFPKCZSA-N methyl (3z)-3-[[4-[benzoyl-[2-(dimethylamino)ethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(CCN(C)C)C(=O)C1=CC=CC=C1 INOGNMCSLFRZAV-KTMFPKCZSA-N 0.000 description 1
- KNAYESYOVINZLR-KNWKATPGSA-N methyl (3z)-3-[[4-[benzyl-(2-piperidin-1-ylacetyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C(=O)CN1CCCCC1)CC1=CC=CC=C1 KNAYESYOVINZLR-KNWKATPGSA-N 0.000 description 1
- RZRQHIPUCVMBGN-DTTHWBISSA-N methyl (3z)-3-[[4-[benzyl-[2-[benzyl(methyl)amino]acetyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C(=O)CN(C)CC=1C=CC=CC=1)CC1=CC=CC=C1 RZRQHIPUCVMBGN-DTTHWBISSA-N 0.000 description 1
- RWLCROIPWSUHJF-ZIADKAODSA-N methyl (3z)-3-[[4-[butyl-[2-(dimethylamino)acetyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C(=O)CN(C)C)CCCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O RWLCROIPWSUHJF-ZIADKAODSA-N 0.000 description 1
- AAEHNSZVCCLBDC-ZIADKAODSA-N methyl (3z)-3-[[4-[butylsulfonyl-[2-(dimethylamino)ethyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(CCN(C)C)S(=O)(=O)CCCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O AAEHNSZVCCLBDC-ZIADKAODSA-N 0.000 description 1
- UFVYHADLRPSKQD-ZIADKAODSA-N methyl (3z)-3-[[4-[methyl(3-piperazin-1-ylpropanoyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CCN1CCNCC1 UFVYHADLRPSKQD-ZIADKAODSA-N 0.000 description 1
- GYWGUXFFONDEKI-FLWNBWAVSA-N methyl (3z)-3-[[4-[methyl(3-piperidin-1-ylpropanoyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CCN1CCCCC1 GYWGUXFFONDEKI-FLWNBWAVSA-N 0.000 description 1
- UEIQMVYRNFWKTR-FCQUAONHSA-N methyl (3z)-3-[[4-[methyl(methylsulfonyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(C)S(C)(=O)=O)C=C1 UEIQMVYRNFWKTR-FCQUAONHSA-N 0.000 description 1
- QQJODNJZFHWZML-RQZHXJHFSA-N methyl (3z)-3-[[4-[methyl(piperidine-1-carbonyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)N1CCCCC1 QQJODNJZFHWZML-RQZHXJHFSA-N 0.000 description 1
- STMBVXYQKYKAOW-DQSJHHFOSA-N methyl (3z)-3-[[4-[methyl-(2-piperazin-1-ylacetyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CN1CCNCC1 STMBVXYQKYKAOW-DQSJHHFOSA-N 0.000 description 1
- ZDVTYZZJKKLFIY-ZIADKAODSA-N methyl (3z)-3-[[4-[methyl-(2-piperidin-1-ylacetyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CN1CCCCC1 ZDVTYZZJKKLFIY-ZIADKAODSA-N 0.000 description 1
- LGSYSPALXTUAJL-DQSJHHFOSA-N methyl (3z)-3-[[4-[methyl-(2-pyrrolidin-1-ylacetyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CN1CCCC1 LGSYSPALXTUAJL-DQSJHHFOSA-N 0.000 description 1
- CKSHKSLNZDHHFF-IZHYLOQSSA-N methyl (3z)-3-[[4-[methyl-[2-(methylamino)acetyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CNC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O CKSHKSLNZDHHFF-IZHYLOQSSA-N 0.000 description 1
- UXGZKMOVOLAAPN-DQSJHHFOSA-N methyl (3z)-3-[[4-[methyl-[2-[methyl(propyl)amino]acetyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CN(C)CCC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O UXGZKMOVOLAAPN-DQSJHHFOSA-N 0.000 description 1
- XSPAJBFOMCBXQS-QPLCGJKRSA-N methyl (3z)-3-[[4-[methyl-[3-(methylamino)propanoyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound C1=CC(N(C)C(=O)CCNC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(=O)OC)C=C2NC\1=O XSPAJBFOMCBXQS-QPLCGJKRSA-N 0.000 description 1
- VPJPIDGNIJXAFS-ZIADKAODSA-N methyl (3z)-3-[[4-[methylsulfonyl(2-piperidin-1-ylethyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(S(C)(=O)=O)CCN1CCCCC1 VPJPIDGNIJXAFS-ZIADKAODSA-N 0.000 description 1
- LPFSELPFSKESFN-DQSJHHFOSA-N methyl (3z)-3-[[4-[methylsulfonyl(2-pyrrolidin-1-ylethyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(S(C)(=O)=O)CCN1CCCC1 LPFSELPFSKESFN-DQSJHHFOSA-N 0.000 description 1
- GAPKEPIGKOPJOC-DQSJHHFOSA-N methyl (3z)-3-[[4-[methylsulfonyl-(2-morpholin-4-yl-2-oxoethyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(S(C)(=O)=O)CC(=O)N1CCOCC1 GAPKEPIGKOPJOC-DQSJHHFOSA-N 0.000 description 1
- CFSALSHJYOGOLL-DQSJHHFOSA-N methyl (3z)-3-[[4-[methylsulfonyl-(2-oxo-2-pyrrolidin-1-ylethyl)amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(S(C)(=O)=O)CC(=O)N1CCCC1 CFSALSHJYOGOLL-DQSJHHFOSA-N 0.000 description 1
- ZHKJEDPUXSVIFH-IZHYLOQSSA-N methyl (3z)-3-[[4-[methylsulfonyl-[3-[(2,2,2-trifluoroacetyl)amino]propyl]amino]anilino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=C(N(CCCNC(=O)C(F)(F)F)S(C)(=O)=O)C=C1 ZHKJEDPUXSVIFH-IZHYLOQSSA-N 0.000 description 1
- VXYDONSUAPNUAL-MRCUWXFGSA-N methyl (3z)-3-[[methyl(piperidin-4-yl)amino]-phenylmethylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\N(C)C1CCNCC1 VXYDONSUAPNUAL-MRCUWXFGSA-N 0.000 description 1
- ILLAFQLVCWQSQA-MRCUWXFGSA-N methyl (3z)-3-[anilino(phenyl)methylidene]-2-oxo-1h-indole-6-carboxylate Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC1=CC=CC=C1 ILLAFQLVCWQSQA-MRCUWXFGSA-N 0.000 description 1
- YLFLCTBGQLPNCU-UHFFFAOYSA-N methyl 2-(2-methoxy-2-oxoethyl)-5-nitrobenzoate Chemical compound COC(=O)CC1=CC=C([N+]([O-])=O)C=C1C(=O)OC YLFLCTBGQLPNCU-UHFFFAOYSA-N 0.000 description 1
- QUOAYJYCXJEUSP-UHFFFAOYSA-N methyl 2-[(4-nitrophenyl)methylamino]acetate Chemical compound COC(=O)CNCC1=CC=C([N+]([O-])=O)C=C1 QUOAYJYCXJEUSP-UHFFFAOYSA-N 0.000 description 1
- QABLOFMHHSOFRJ-UHFFFAOYSA-N methyl 2-chloroacetate Chemical compound COC(=O)CCl QABLOFMHHSOFRJ-UHFFFAOYSA-N 0.000 description 1
- SHWVZUGUOIRBTR-UHFFFAOYSA-N methyl 2-hydroxy-3-[N-[4-[(2-oxopyrrolidin-1-yl)methyl]phenyl]-C-phenylcarbonimidoyl]-1H-indole-6-carboxylate Chemical compound COC(=O)C1=CC2=C(C=C1)C(=C(N2)O)C(=NC3=CC=C(C=C3)CN4CCCC4=O)C5=CC=CC=C5 SHWVZUGUOIRBTR-UHFFFAOYSA-N 0.000 description 1
- YUGAQWBIOKQVPV-UHFFFAOYSA-N methyl 3-[N-[4-[acetyl-[3-(dimethylamino)propyl]amino]phenyl]-C-phenylcarbonimidoyl]-2-hydroxy-1H-indole-6-carboxylate Chemical compound CC(=O)N(CCCN(C)C)C1=CC=C(C=C1)N=C(C2=CC=CC=C2)C3=C(NC4=C3C=CC(=C4)C(=O)OC)O YUGAQWBIOKQVPV-UHFFFAOYSA-N 0.000 description 1
- FPUPGTDVGVCPMU-DCXSSQDFSA-N methyl 3-amino-3-[4-[[(z)-(6-carbamoyl-2-oxo-1h-indol-3-ylidene)-phenylmethyl]amino]phenyl]propanoate;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.C1=CC(C(N)CC(=O)OC)=CC=C1N\C(C=1C=CC=CC=1)=C/1C2=CC=C(C(N)=O)C=C2NC\1=O FPUPGTDVGVCPMU-DCXSSQDFSA-N 0.000 description 1
- AXLYJLKKPUICKV-UHFFFAOYSA-N methyl 3-nitrobenzoate Chemical compound COC(=O)C1=CC=CC([N+]([O-])=O)=C1 AXLYJLKKPUICKV-UHFFFAOYSA-N 0.000 description 1
- DCDSLKRPXTVJSA-UHFFFAOYSA-N methyl 4-(2-methoxy-2-oxoethyl)-3-nitrobenzoate Chemical compound COC(=O)CC1=CC=C(C(=O)OC)C=C1[N+]([O-])=O DCDSLKRPXTVJSA-UHFFFAOYSA-N 0.000 description 1
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- 239000008108 microcrystalline cellulose Substances 0.000 description 1
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- 230000011278 mitosis Effects 0.000 description 1
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19949208A DE19949208A1 (de) | 1999-10-13 | 1999-10-13 | In 6-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
DE2000142696 DE10042696A1 (de) | 2000-08-31 | 2000-08-31 | In 6-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
PCT/EP2000/009867 WO2001027081A1 (de) | 1999-10-13 | 2000-10-09 | In 6-stellung substituierte indolinone, ihre herstellung und ihre verwendung als arzneimittel |
Publications (3)
Publication Number | Publication Date |
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NO20021719L NO20021719L (no) | 2002-04-11 |
NO20021719D0 NO20021719D0 (no) | 2002-04-11 |
NO322746B1 true NO322746B1 (no) | 2006-12-04 |
Family
ID=26006858
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
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NO20021719A NO322746B1 (no) | 1999-10-13 | 2002-04-11 | Indoliner, substituert i 6-stilling, og farmasoytisk preparat, samt anvendelse og fremstilling derav. |
NO2015009C NO2015009I1 (no) | 1999-10-13 | 2015-03-18 | Nintedanib, tautomere og salter derav, spesielt Nintedanib og fysiologiske akseptable salter derav, spesielt Nintedanib esilat; 3-Z-[l-(4-(N-((4-metylpiperazin-1-yl)-metylkarbonyl)-N-metylamino)- anilino)-1-fenylmetylen]-6-metoksykarbonyl-2-indolinon - Se blant annet kravene 1, 2, 5 (t) og 6 i basispatentet |
NO2023033C NO2023033I1 (no) | 1999-10-13 | 2023-09-05 | Nintedanib |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
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NO2015009C NO2015009I1 (no) | 1999-10-13 | 2015-03-18 | Nintedanib, tautomere og salter derav, spesielt Nintedanib og fysiologiske akseptable salter derav, spesielt Nintedanib esilat; 3-Z-[l-(4-(N-((4-metylpiperazin-1-yl)-metylkarbonyl)-N-metylamino)- anilino)-1-fenylmetylen]-6-metoksykarbonyl-2-indolinon - Se blant annet kravene 1, 2, 5 (t) og 6 i basispatentet |
NO2023033C NO2023033I1 (no) | 1999-10-13 | 2023-09-05 | Nintedanib |
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JP2020512364A (ja) | 2017-03-28 | 2020-04-23 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 筋ジストロフィーの処置方法において使用するためのニンテダニブ |
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KR20220107973A (ko) | 2021-01-25 | 2022-08-02 | 주식회사 나이벡 | 섬유화 예방 및 치료용 펩타이드 |
EP4098246A1 (en) | 2021-05-31 | 2022-12-07 | Lotus Pharmaceutical Co., Ltd. | Formulation of nintedanib |
CN115703758B (zh) * | 2021-08-12 | 2024-03-26 | 中国医学科学院药物研究所 | 一类用作激酶抑制剂的化合物及其制备方法和用途 |
WO2024037982A1 (en) | 2022-08-16 | 2024-02-22 | Boehringer Ingelheim International Gmbh | Pharmaceutical formulations of nintedanib for intraocular use |
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BE558210A (bg) * | 1956-06-08 | |||
CA2166722A1 (en) * | 1994-05-06 | 1995-11-16 | Manoj L. Maniar | Use of vitamin e tocopheryl derivatives in ophthalmic compositions |
US5880141A (en) * | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
HUP9800757A3 (en) * | 1996-01-17 | 1998-08-28 | Taiho Pharmaceutical Co Ltd | Intimal thickening inhibitors containing oxyindole derivatives and pharmaceutical compositions containing them |
GB9718913D0 (en) * | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
DE19815020A1 (de) * | 1998-04-03 | 1999-10-07 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
DE19816624A1 (de) * | 1998-04-15 | 1999-10-21 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
DE19824922A1 (de) * | 1998-06-04 | 1999-12-09 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
GB9904933D0 (en) * | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Compounds |
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