ZA200708775B - Substituted amide derivatives as protein kinase inhibitors - Google Patents
Substituted amide derivatives as protein kinase inhibitors Download PDFInfo
- Publication number
- ZA200708775B ZA200708775B ZA200708775A ZA200708775A ZA200708775B ZA 200708775 B ZA200708775 B ZA 200708775B ZA 200708775 A ZA200708775 A ZA 200708775A ZA 200708775 A ZA200708775 A ZA 200708775A ZA 200708775 B ZA200708775 B ZA 200708775B
- Authority
- ZA
- South Africa
- Prior art keywords
- optionally substituted
- phenyl
- alkyl
- methyl
- carboxamide
- Prior art date
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- 150000001408 amides Chemical class 0.000 title description 2
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title description 2
- 239000003909 protein kinase inhibitor Substances 0.000 title description 2
- -1 diastereomers Chemical class 0.000 claims description 268
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 258
- 125000000217 alkyl group Chemical group 0.000 claims description 192
- 125000001424 substituent group Chemical group 0.000 claims description 192
- 125000000623 heterocyclic group Chemical group 0.000 claims description 182
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 150
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 142
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 142
- 150000001875 compounds Chemical class 0.000 claims description 114
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 109
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 108
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 107
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 106
- 125000003118 aryl group Chemical group 0.000 claims description 66
- 125000004076 pyridyl group Chemical group 0.000 claims description 54
- 150000003839 salts Chemical class 0.000 claims description 54
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 53
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 51
- 125000003003 spiro group Chemical group 0.000 claims description 50
- 125000001544 thienyl group Chemical group 0.000 claims description 50
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 48
- 150000002825 nitriles Chemical class 0.000 claims description 36
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 36
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims description 35
- 125000001246 bromo group Chemical group Br* 0.000 claims description 34
- 125000001153 fluoro group Chemical group F* 0.000 claims description 34
- 125000005843 halogen group Chemical group 0.000 claims description 30
- 206010028980 Neoplasm Diseases 0.000 claims description 27
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 26
- 229910052799 carbon Inorganic materials 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- 102100021866 Hepatocyte growth factor Human genes 0.000 claims description 23
- 125000001072 heteroaryl group Chemical group 0.000 claims description 22
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 22
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 19
- 125000006534 ethyl amino methyl group Chemical group [H]N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 claims description 18
- 125000000304 alkynyl group Chemical group 0.000 claims description 17
- 125000001188 haloalkyl group Chemical class 0.000 claims description 16
- 125000003342 alkenyl group Chemical group 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 125000003282 alkyl amino group Chemical group 0.000 claims description 12
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 12
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 10
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 10
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- 239000012453 solvate Substances 0.000 claims description 8
- 201000011510 cancer Diseases 0.000 claims description 7
- 206010027476 Metastases Diseases 0.000 claims description 6
- 150000001204 N-oxides Chemical class 0.000 claims description 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 6
- 230000001404 mediated effect Effects 0.000 claims description 6
- 230000009401 metastasis Effects 0.000 claims description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 4
- 125000003418 alkyl amino alkoxy group Chemical group 0.000 claims description 4
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 4
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims description 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 125000005191 hydroxyalkylamino group Chemical group 0.000 claims description 4
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 claims description 4
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 2
- 125000004946 alkenylalkyl group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 2
- 125000005335 azido alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 2
- 125000001624 naphthyl 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
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 9
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 9
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 7
- 239000003795 chemical substances by application Substances 0.000 claims 6
- 125000006533 methyl amino methyl group Chemical group [H]N(C([H])([H])[H])C([H])([H])* 0.000 claims 6
- 239000011570 nicotinamide Substances 0.000 claims 6
- 229960003966 nicotinamide Drugs 0.000 claims 5
- 239000003814 drug Substances 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 2
- 229940100198 alkylating agent Drugs 0.000 claims 2
- 239000002168 alkylating agent Substances 0.000 claims 2
- 239000002256 antimetabolite Substances 0.000 claims 2
- 229940125697 hormonal agent Drugs 0.000 claims 2
- 239000000677 immunologic agent Substances 0.000 claims 2
- 229940124541 immunological agent Drugs 0.000 claims 2
- AVOHPVUAPGVLAY-UHFFFAOYSA-N n-[3-fluoro-4-(7-methoxyquinolin-4-yl)oxyphenyl]-3-oxo-4-phenylmorpholine-2-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)OCCN1C1=CC=CC=C1 AVOHPVUAPGVLAY-UHFFFAOYSA-N 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- GKTQKQTXHNUFSP-UHFFFAOYSA-N thieno[3,4-c]pyrrole-4,6-dione Chemical compound S1C=C2C(=O)NC(=O)C2=C1 GKTQKQTXHNUFSP-UHFFFAOYSA-N 0.000 claims 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 1
- NJQRAAHKQQPUIT-UHFFFAOYSA-N 1,2-dihydropyridine-3-carboxamide Chemical compound NC(=O)C1=CC=CNC1 NJQRAAHKQQPUIT-UHFFFAOYSA-N 0.000 claims 1
- HLYLVLPUVNOQHH-UHFFFAOYSA-N 1-(2-aminoethyl)-n-[3-fluoro-4-(7-methoxyquinolin-4-yl)oxyphenyl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=C(C)N(CCN)N1C1=CC=CC=C1 HLYLVLPUVNOQHH-UHFFFAOYSA-N 0.000 claims 1
- KLWBNEIPBOZAOQ-UHFFFAOYSA-N 1-(2-chlorophenyl)-n-[3-fluoro-4-(7-methoxyquinolin-4-yl)oxyphenyl]-2,3-dimethyl-5-oxopyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=C(C)N(C)N1C1=CC=CC=C1Cl KLWBNEIPBOZAOQ-UHFFFAOYSA-N 0.000 claims 1
- POEZAPIQLMNFDN-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropyl)-4-[7-(7-methoxyquinolin-4-yl)oxy-2,3-dihydro-1,4-benzoxazine-4-carbonyl]-5-methyl-2-phenylpyrazol-3-one Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C=C1OCC2)=CC=C1N2C(=O)C(C1=O)=C(C)N(CC(C)(C)O)N1C1=CC=CC=C1 POEZAPIQLMNFDN-UHFFFAOYSA-N 0.000 claims 1
- IIZIRGJCJMFRDM-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropyl)-N-[5-(7-hydroxyquinolin-4-yl)oxypyridin-2-yl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound CC(O)(C)CN1C(C)=C(C(=O)NC=2N=CC(OC=3C4=CC=C(O)C=C4N=CC=3)=CC=2)C(=O)N1C1=CC=CC=C1 IIZIRGJCJMFRDM-UHFFFAOYSA-N 0.000 claims 1
- DSTCGXWRQMWOLU-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropyl)-n-[4-(7-methoxyquinolin-4-yl)sulfanylphenyl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1SC(C=C1)=CC=C1NC(=O)C(C1=O)=C(C)N(CC(C)(C)O)N1C1=CC=CC=C1 DSTCGXWRQMWOLU-UHFFFAOYSA-N 0.000 claims 1
- NXVHOYBQFPQTBF-UHFFFAOYSA-N 1-(3-amino-2-hydroxypropyl)-n-[3-fluoro-4-(7-methoxyquinolin-4-yl)oxyphenyl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=C(C)N(CC(O)CN)N1C1=CC=CC=C1 NXVHOYBQFPQTBF-UHFFFAOYSA-N 0.000 claims 1
- BGLJTUOUNXPWKK-GOSISDBHSA-N 1-[(2r)-2-fluoropropyl]-n-[5-(7-methoxyquinolin-4-yl)oxypyridin-2-yl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C=N1)=CC=C1NC(=O)C(C1=O)=C(C)N(C[C@@H](C)F)N1C1=CC=CC=C1 BGLJTUOUNXPWKK-GOSISDBHSA-N 0.000 claims 1
- GODQNRDRRFCJJI-SANMLTNESA-N 1-[(2r)-2-hydroxy-3-methylbutyl]-n-[5-(7-methoxyquinolin-4-yl)oxypyridin-2-yl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C=N1)=CC=C1NC(=O)C(C1=O)=C(C)N(C[C@H](O)C(C)C)N1C1=CC=CC=C1 GODQNRDRRFCJJI-SANMLTNESA-N 0.000 claims 1
- PUVFWTQKDQUFCP-FQEVSTJZSA-N 1-[(2s)-2-(dimethylamino)propyl]-n-[3-fluoro-4-(7-methoxyquinolin-4-yl)oxyphenyl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=C(C)N(C[C@H](C)N(C)C)N1C1=CC=CC=C1 PUVFWTQKDQUFCP-FQEVSTJZSA-N 0.000 claims 1
- NEOAGSZQQLXWTO-UHFFFAOYSA-N 1-benzyl-2-oxo-5-phenylpyridine-3-carboxamide Chemical compound O=C1C(C(=O)N)=CC(C=2C=CC=CC=2)=CN1CC1=CC=CC=C1 NEOAGSZQQLXWTO-UHFFFAOYSA-N 0.000 claims 1
- XUJAABYTWJFTEW-UHFFFAOYSA-N 1-benzyl-5-bromo-n-[2-chloro-4-(6,7-dimethoxyquinolin-4-yl)oxyphenyl]-2-oxopyridine-3-carboxamide Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C=C1Cl)=CC=C1NC(=O)C(C1=O)=CC(Br)=CN1CC1=CC=CC=C1 XUJAABYTWJFTEW-UHFFFAOYSA-N 0.000 claims 1
- DQOIOXHXYBCWOD-UHFFFAOYSA-N 1-benzyl-n-[4-(6,7-dimethoxyquinolin-4-yl)oxy-3-fluorophenyl]-2-oxo-5-pyrimidin-2-ylpyridine-3-carboxamide Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=CC(C=2N=CC=CN=2)=CN1CC1=CC=CC=C1 DQOIOXHXYBCWOD-UHFFFAOYSA-N 0.000 claims 1
- BSFMLWRRSOWTEQ-UHFFFAOYSA-N 1-benzyl-n-[5-(6,7-dimethoxyquinolin-4-yl)oxypyridin-2-yl]-4-(2-methoxyethylamino)-2-oxopyridine-3-carboxamide Chemical compound O=C1C(C(=O)NC=2N=CC(OC=3C4=CC(OC)=C(OC)C=C4N=CC=3)=CC=2)=C(NCCOC)C=CN1CC1=CC=CC=C1 BSFMLWRRSOWTEQ-UHFFFAOYSA-N 0.000 claims 1
- XOUIDBCXNCBWRA-UHFFFAOYSA-N 1-benzyl-n-[5-(7-methoxyquinolin-4-yl)oxypyridin-2-yl]-5-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C=N1)=CC=C1NC(=O)C(C(N1C=2C=CC=CC=2)=O)=C(C)N1CC1=CC=CC=C1 XOUIDBCXNCBWRA-UHFFFAOYSA-N 0.000 claims 1
- ZVXKYWHJBYIYNI-UHFFFAOYSA-N 1h-pyrazole-4-carboxamide Chemical compound NC(=O)C=1C=NNC=1 ZVXKYWHJBYIYNI-UHFFFAOYSA-N 0.000 claims 1
- HPAXBNHGBRPUCO-UHFFFAOYSA-N 2,3-dihydro-1h-pyrazole-4-carboxamide Chemical compound NC(=O)C1=CNNC1 HPAXBNHGBRPUCO-UHFFFAOYSA-N 0.000 claims 1
- SLAASIAWHQRRKL-UHFFFAOYSA-N 2-phenyl-1-propyl-3h-pyrazole-4-carboxamide Chemical compound CCCN1C=C(C(N)=O)CN1C1=CC=CC=C1 SLAASIAWHQRRKL-UHFFFAOYSA-N 0.000 claims 1
- ONWIGSJBMCHKOV-UHFFFAOYSA-N 3-benzyl-n-[4-(6,7-dimethoxyquinolin-4-yl)oxy-3-fluorophenyl]-2-oxoimidazolidine-1-carboxamide Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C(=C1)F)=CC=C1NC(=O)N(C1=O)CCN1CC1=CC=CC=C1 ONWIGSJBMCHKOV-UHFFFAOYSA-N 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- NDKGNYXCMKDBKK-UHFFFAOYSA-N 3-oxo-2-phenyl-1h-pyrazole-4-carboxamide Chemical compound O=C1C(C(=O)N)=CNN1C1=CC=CC=C1 NDKGNYXCMKDBKK-UHFFFAOYSA-N 0.000 claims 1
- AKLARZWWYXICKZ-UHFFFAOYSA-N 4-(2-methoxyethylamino)-n-[5-(7-methoxyquinolin-4-yl)oxypyridin-2-yl]-2-oxo-1-phenylpyridine-3-carboxamide Chemical compound O=C1C(C(=O)NC=2N=CC(OC=3C4=CC=C(OC)C=C4N=CC=3)=CC=2)=C(NCCOC)C=CN1C1=CC=CC=C1 AKLARZWWYXICKZ-UHFFFAOYSA-N 0.000 claims 1
- WEEMSRUOVNMUPV-UHFFFAOYSA-N 4-anilino-n-[5-(6,7-dimethoxyquinolin-4-yl)oxypyridin-2-yl]-2-oxo-1-phenylpyridine-3-carboxamide Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C=N1)=CC=C1NC(=O)C(C(N(C=1C=CC=CC=1)C=C1)=O)=C1NC1=CC=CC=C1 WEEMSRUOVNMUPV-UHFFFAOYSA-N 0.000 claims 1
- RYQBKVFFHMNFTM-UHFFFAOYSA-N 5-(aminomethyl)-n-[3-fluoro-4-(7-methoxyquinolin-4-yl)oxyphenyl]-1-methyl-3-oxo-2-phenylpyrazole-4-carboxamide Chemical compound C=1C=NC2=CC(OC)=CC=C2C=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=C(CN)N(C)N1C1=CC=CC=C1 RYQBKVFFHMNFTM-UHFFFAOYSA-N 0.000 claims 1
- XHAJFXSLJHVISJ-UHFFFAOYSA-N 5-bromo-n-[4-(6,7-dimethoxyquinolin-4-yl)oxy-3-fluorophenyl]-1-(3-methylphenyl)-2-oxopyridine-3-carboxamide Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=CC(Br)=CN1C1=CC=CC(C)=C1 XHAJFXSLJHVISJ-UHFFFAOYSA-N 0.000 claims 1
- HBLJLTPJXZQZCK-UHFFFAOYSA-N 7-[2-fluoro-4-[[1-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenylpyrazole-4-carbonyl]amino]phenoxy]-n-(2-methoxyethyl)thieno[3,2-b]pyridine-2-carboxamide Chemical compound C=12SC(C(=O)NCCOC)=CC2=NC=CC=1OC(C(=C1)F)=CC=C1NC(=O)C(C1=O)=C(C)N(CC(C)(C)O)N1C1=CC=CC=C1 HBLJLTPJXZQZCK-UHFFFAOYSA-N 0.000 claims 1
- AZIBPFHNLVDQOV-DKXQDJALSA-N CCCN1C(C)=C(C(=O)N[C@@H]2CC[C@@H](CC2)OC=2C3=CC=C(OC)C=C3N=CC=2)C(=O)N1C1=CC=CC=C1 Chemical compound CCCN1C(C)=C(C(=O)N[C@@H]2CC[C@@H](CC2)OC=2C3=CC=C(OC)C=C3N=CC=2)C(=O)N1C1=CC=CC=C1 AZIBPFHNLVDQOV-DKXQDJALSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- 101000713575 Homo sapiens Tubulin beta-3 chain Proteins 0.000 claims 1
- 229910019567 Re Re Inorganic materials 0.000 claims 1
- 102100036790 Tubulin beta-3 chain Human genes 0.000 claims 1
- 125000001539 acetonyl group Chemical group [H]C([H])([H])C(=O)C([H])([H])* 0.000 claims 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000005518 carboxamido group Chemical group 0.000 claims 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000005322 morpholin-1-yl group Chemical group 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- QTSXUAWJQYJGBT-UHFFFAOYSA-N n-[2-chloro-4-(6,7-dimethoxyquinolin-4-yl)oxyphenyl]-6-methyl-3-oxo-2-phenylpyridazine-4-carboxamide Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C=C1Cl)=CC=C1NC(=O)C(C1=O)=CC(C)=NN1C1=CC=CC=C1 QTSXUAWJQYJGBT-UHFFFAOYSA-N 0.000 claims 1
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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