JP2006520805A5 - - Google Patents
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- JP2006520805A5 JP2006520805A5 JP2006507472A JP2006507472A JP2006520805A5 JP 2006520805 A5 JP2006520805 A5 JP 2006520805A5 JP 2006507472 A JP2006507472 A JP 2006507472A JP 2006507472 A JP2006507472 A JP 2006507472A JP 2006520805 A5 JP2006520805 A5 JP 2006520805A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- optionally substituted
- ylmethoxy
- phenyl
- unsubstituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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- -1 substituted Chemical group 0.000 claims 321
- 150000001875 compounds Chemical class 0.000 claims 54
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 52
- 125000000623 heterocyclic group Chemical group 0.000 claims 44
- 125000001424 substituent group Chemical group 0.000 claims 27
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 24
- 125000000217 alkyl group Chemical group 0.000 claims 22
- 125000004093 cyano group Chemical group *C#N 0.000 claims 20
- 125000001475 halogen functional group Chemical group 0.000 claims 20
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 13
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 13
- 125000003418 alkyl amino alkoxy group Chemical group 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 12
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 12
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 11
- 239000003814 drug Substances 0.000 claims 11
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 125000001041 indolyl group Chemical group 0.000 claims 9
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims 9
- 125000004043 oxo group Chemical group O=* 0.000 claims 9
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 8
- 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 8
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 8
- 125000005956 isoquinolyl group Chemical group 0.000 claims 8
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims 8
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 7
- 238000004519 manufacturing process Methods 0.000 claims 7
- 125000004076 pyridyl group Chemical group 0.000 claims 7
- 229910052717 sulfur Inorganic materials 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000001188 haloalkyl group Chemical group 0.000 claims 6
- 125000003226 pyrazolyl group Chemical group 0.000 claims 6
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 6
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 5
- 229940079593 drug Drugs 0.000 claims 5
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 5
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims 5
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000001624 naphthyl group Chemical group 0.000 claims 5
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 125000003386 piperidinyl group Chemical group 0.000 claims 5
- 125000002098 pyridazinyl group Chemical group 0.000 claims 5
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 5
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims 5
- 125000001544 thienyl group Chemical group 0.000 claims 5
- 125000001425 triazolyl group Chemical group 0.000 claims 5
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims 4
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 4
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims 4
- 125000004103 aminoalkyl group Chemical group 0.000 claims 4
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 4
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 4
- 125000002047 benzodioxolyl group Chemical group O1OC(C2=C1C=CC=C2)* 0.000 claims 4
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 4
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 4
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 4
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 125000000842 isoxazolyl group Chemical group 0.000 claims 4
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 4
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims 4
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 4
- 125000002757 morpholinyl group Chemical group 0.000 claims 4
- 125000005246 nonafluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 claims 4
- 125000003884 phenylalkyl group Chemical group 0.000 claims 4
- 125000004193 piperazinyl group Chemical group 0.000 claims 4
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims 4
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 4
- 125000000335 thiazolyl group Chemical group 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 3
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 claims 3
- 125000005493 quinolyl group Chemical group 0.000 claims 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- XTBAPWCYTNCZTO-UHFFFAOYSA-N 1H-isoindolone Natural products C1=CC=C2C(=O)N=CC2=C1 XTBAPWCYTNCZTO-UHFFFAOYSA-N 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 2
- 125000002619 bicyclic group Chemical group 0.000 claims 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 1
- WGONGMOZFNXPIC-UHFFFAOYSA-N 4-[2-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]anilino]-1-methylbenzimidazol-5-yl]oxy-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(CN5CCN(C)CC5)C(Cl)=CC=4)N(C)C3=CC=2)=C1 WGONGMOZFNXPIC-UHFFFAOYSA-N 0.000 claims 1
- ZKSUUBLMUIKQJD-UHFFFAOYSA-N 4-[[2-[3-[2-(dimethylamino)ethoxy]-4-(trifluoromethyl)anilino]-3h-benzimidazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OCCN(C)C)C(=CC=4)C(F)(F)F)NC3=CC=2)=C1 ZKSUUBLMUIKQJD-UHFFFAOYSA-N 0.000 claims 1
- BTZADJMCMGCPTD-UHFFFAOYSA-N 4-[[2-[4-chloro-3-(piperidin-4-ylmethoxy)anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OCC5CCNCC5)C(Cl)=CC=4)OC3=CC=2)=C1 BTZADJMCMGCPTD-UHFFFAOYSA-N 0.000 claims 1
- ONCNFHJNNVYNMM-UHFFFAOYSA-N 4-[[2-[4-chloro-3-[(1-methylpiperidin-4-yl)methoxy]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OCC5CCN(C)CC5)C(Cl)=CC=4)OC3=CC=2)=C1 ONCNFHJNNVYNMM-UHFFFAOYSA-N 0.000 claims 1
- KMNCFOUKJYOZIF-UHFFFAOYSA-N 4-[[2-[4-chloro-3-[(1-methylpyrrolidin-2-yl)methoxy]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OCC5N(CCC5)C)C(Cl)=CC=4)OC3=CC=2)=C1 KMNCFOUKJYOZIF-UHFFFAOYSA-N 0.000 claims 1
- VAZZXEJSCUQVTN-UHFFFAOYSA-N 4-[[2-[4-chloro-3-[(1-propan-2-ylpiperidin-4-yl)methoxy]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OCC5CCN(CC5)C(C)C)C(Cl)=CC=4)OC3=CC=2)=C1 VAZZXEJSCUQVTN-UHFFFAOYSA-N 0.000 claims 1
- QLGYPFBXPCFQHJ-UHFFFAOYSA-N 4-[[2-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(CN5CCN(C)CC5)C(Cl)=CC=4)OC3=CC=2)=C1 QLGYPFBXPCFQHJ-UHFFFAOYSA-N 0.000 claims 1
- HYVFNIQDPPNFIH-UHFFFAOYSA-N 4-[[2-[4-chloro-3-[2-(dimethylamino)ethoxy]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OCCN(C)C)C(Cl)=CC=4)OC3=CC=2)=C1 HYVFNIQDPPNFIH-UHFFFAOYSA-N 0.000 claims 1
- PPPJFYDGNJWIOT-INIZCTEOSA-N 4-[[2-[4-chloro-3-[[(2s)-1-methylpyrrolidin-2-yl]methoxy]anilino]-1,3-benzoxazol-5-yl]oxy]pyridine-2-carboxamide Chemical compound CN1CCC[C@H]1COC1=CC(NC=2OC3=CC=C(OC=4C=C(N=CC=4)C(N)=O)C=C3N=2)=CC=C1Cl PPPJFYDGNJWIOT-INIZCTEOSA-N 0.000 claims 1
- IEAKVOACBVHQHG-IBGZPJMESA-N 4-[[2-[4-chloro-3-[[(2s)-1-propan-2-ylpyrrolidin-2-yl]methoxy]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OC[C@H]5N(CCC5)C(C)C)C(Cl)=CC=4)OC3=CC=2)=C1 IEAKVOACBVHQHG-IBGZPJMESA-N 0.000 claims 1
- NBAJZYVYCOJEQZ-UHFFFAOYSA-N 4-[[2-[4-chloro-3-[[4-[2-(dimethylamino)ethyl]piperazin-1-yl]methyl]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(CN5CCN(CCN(C)C)CC5)C(Cl)=CC=4)OC3=CC=2)=C1 NBAJZYVYCOJEQZ-UHFFFAOYSA-N 0.000 claims 1
- ABWJVVCPMHFSTN-UHFFFAOYSA-N 4-[[7-chloro-2-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]anilino]-1,3-benzoxazol-5-yl]oxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(CN5CCN(C)CC5)C(Cl)=CC=4)OC3=C(Cl)C=2)=C1 ABWJVVCPMHFSTN-UHFFFAOYSA-N 0.000 claims 1
- JPWMAVZTWDLRIZ-UHFFFAOYSA-N 7-chloro-n-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]phenyl]-5-quinolin-4-yloxy-1,3-benzoxazol-2-amine Chemical compound C1CN(C)CCN1CC1=CC(NC=2OC3=C(Cl)C=C(OC=4C5=CC=CC=C5N=CC=4)C=C3N=2)=CC=C1Cl JPWMAVZTWDLRIZ-UHFFFAOYSA-N 0.000 claims 1
- 206010012689 Diabetic retinopathy Diseases 0.000 claims 1
- 102000014150 Interferons Human genes 0.000 claims 1
- 108010050904 Interferons Proteins 0.000 claims 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims 1
- 241001024304 Mino Species 0.000 claims 1
- 239000002168 alkylating agent Substances 0.000 claims 1
- 229940100198 alkylating agent Drugs 0.000 claims 1
- 125000005466 alkylenyl group Chemical group 0.000 claims 1
- 230000033115 angiogenesis Effects 0.000 claims 1
- 230000000340 anti-metabolite Effects 0.000 claims 1
- 239000002256 antimetabolite Substances 0.000 claims 1
- 229940100197 antimetabolite Drugs 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 230000003115 biocidal effect Effects 0.000 claims 1
- 230000017531 blood circulation Effects 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims 1
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 230000007423 decrease Effects 0.000 claims 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 229940088597 hormone Drugs 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 230000001900 immune effect Effects 0.000 claims 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims 1
- 229940079322 interferon Drugs 0.000 claims 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- DEYZENHJMHXQGD-UHFFFAOYSA-N n-(4-chlorophenyl)-6-(6,7-dimethoxyquinazolin-4-yl)oxy-1h-benzimidazol-2-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=NC=1OC(C=C1N=2)=CC=C1NC=2NC1=CC=C(Cl)C=C1 DEYZENHJMHXQGD-UHFFFAOYSA-N 0.000 claims 1
- CWZBMSLLFXVAJC-UHFFFAOYSA-N n-[3-[(1-methylpyrrolidin-2-yl)methoxy]-4-(trifluoromethyl)phenyl]-5-quinolin-4-yloxy-1,3-benzoxazol-2-amine Chemical compound CN1CCCC1COC1=CC(NC=2OC3=CC=C(OC=4C5=CC=CC=C5N=CC=4)C=C3N=2)=CC=C1C(F)(F)F CWZBMSLLFXVAJC-UHFFFAOYSA-N 0.000 claims 1
- WATHVYRKWVIPDZ-UHFFFAOYSA-N n-[3-[(1-methylpyrrolidin-2-yl)methoxy]-4-(trifluoromethyl)phenyl]-6-quinolin-4-yloxy-1h-benzimidazol-2-amine Chemical compound CN1CCCC1COC1=CC(NC=2NC3=CC=C(OC=4C5=CC=CC=C5N=CC=4)C=C3N=2)=CC=C1C(F)(F)F WATHVYRKWVIPDZ-UHFFFAOYSA-N 0.000 claims 1
- LKRNZKIENIKMKS-UHFFFAOYSA-N n-[4-chloro-3-[(1-methylpyrrolidin-2-yl)methoxy]phenyl]-5-(6,7-dimethoxyquinazolin-4-yl)oxy-1,3-benzoxazol-2-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=NC=1OC(C=C1N=2)=CC=C1OC=2NC(C=1)=CC=C(Cl)C=1OCC1CCCN1C LKRNZKIENIKMKS-UHFFFAOYSA-N 0.000 claims 1
- NRUKDYLILMOFJD-UHFFFAOYSA-N n-[4-chloro-3-[(1-methylpyrrolidin-2-yl)methoxy]phenyl]-5-(6,7-dimethoxyquinolin-4-yl)oxy-1,3-benzoxazol-2-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C=C1N=2)=CC=C1OC=2NC(C=1)=CC=C(Cl)C=1OCC1CCCN1C NRUKDYLILMOFJD-UHFFFAOYSA-N 0.000 claims 1
- CCNMBKXRBDXKJO-UHFFFAOYSA-N n-[4-chloro-3-[(1-methylpyrrolidin-2-yl)methoxy]phenyl]-5-quinolin-4-yloxy-1,3-benzoxazol-2-amine Chemical compound CN1CCCC1COC1=CC(NC=2OC3=CC=C(OC=4C5=CC=CC=C5N=CC=4)C=C3N=2)=CC=C1Cl CCNMBKXRBDXKJO-UHFFFAOYSA-N 0.000 claims 1
- AURLMJBXLIAZKM-UHFFFAOYSA-N n-[4-chloro-3-[(1-propan-2-ylpyrrolidin-2-yl)methoxy]phenyl]-5-(1h-pyrrolo[2,3-b]pyridin-4-yloxy)-1,3-benzoxazol-2-amine Chemical compound CC(C)N1CCCC1COC1=CC(NC=2OC3=CC=C(OC=4C=5C=CNC=5N=CC=4)C=C3N=2)=CC=C1Cl AURLMJBXLIAZKM-UHFFFAOYSA-N 0.000 claims 1
- YCFIPAIIPRUSQE-UHFFFAOYSA-N n-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]phenyl]-5-(1h-pyrrolo[2,3-b]pyridin-4-yloxy)-1,3-benzoxazol-2-amine Chemical compound C1CN(C)CCN1CC1=CC(NC=2OC3=CC=C(OC=4C=5C=CNC=5N=CC=4)C=C3N=2)=CC=C1Cl YCFIPAIIPRUSQE-UHFFFAOYSA-N 0.000 claims 1
- OGLAJZUWRJDROE-UHFFFAOYSA-N n-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]phenyl]-5-(6,7-dimethoxyquinolin-4-yl)oxy-1,3-benzoxazol-2-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C=C1N=2)=CC=C1OC=2NC(C=1)=CC=C(Cl)C=1CN1CCN(C)CC1 OGLAJZUWRJDROE-UHFFFAOYSA-N 0.000 claims 1
- GZXULZRBYRVYLK-UHFFFAOYSA-N n-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]phenyl]-6-(6,7-dimethoxyquinolin-4-yl)oxy-1h-benzimidazol-2-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C=C1N=2)=CC=C1NC=2NC(C=1)=CC=C(Cl)C=1CN1CCN(C)CC1 GZXULZRBYRVYLK-UHFFFAOYSA-N 0.000 claims 1
- NVFBMDKKXKOASI-UHFFFAOYSA-N n-[4-chloro-3-[(4-methylpiperazin-1-yl)methyl]phenyl]-6-quinolin-4-yloxy-1h-benzimidazol-2-amine Chemical compound C1CN(C)CCN1CC1=CC(NC=2NC3=CC=C(OC=4C5=CC=CC=C5N=CC=4)C=C3N=2)=CC=C1Cl NVFBMDKKXKOASI-UHFFFAOYSA-N 0.000 claims 1
- BIJITFOSDDPLRR-KRWDZBQOSA-N n-[4-chloro-3-[[(2s)-1-methylpyrrolidin-2-yl]methoxy]phenyl]-5-(1h-pyrrolo[2,3-b]pyridin-4-yloxy)-1,3-benzoxazol-2-amine Chemical compound CN1CCC[C@H]1COC1=CC(NC=2OC3=CC=C(OC=4C=5C=CNC=5N=CC=4)C=C3N=2)=CC=C1Cl BIJITFOSDDPLRR-KRWDZBQOSA-N 0.000 claims 1
- CZGSISQHBYWGGG-KRWDZBQOSA-N n-[4-chloro-3-[[(2s)-1-methylpyrrolidin-2-yl]methoxy]phenyl]-5-[2-(methylamino)pyridin-4-yl]oxy-1,3-benzoxazol-2-amine Chemical compound C1=NC(NC)=CC(OC=2C=C3N=C(NC=4C=C(OC[C@H]5N(CCC5)C)C(Cl)=CC=4)OC3=CC=2)=C1 CZGSISQHBYWGGG-KRWDZBQOSA-N 0.000 claims 1
- DZPFHDSAWGBFFX-UHFFFAOYSA-N n-methyl-4-[[2-[3-[(1-methylpyrrolidin-2-yl)methoxy]-4-(1,1,2,2,2-pentafluoroethyl)anilino]-3h-benzimidazol-5-yl]oxy]pyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C3N=C(NC=4C=C(OCC5N(CCC5)C)C(=CC=4)C(F)(F)C(F)(F)F)NC3=CC=2)=C1 DZPFHDSAWGBFFX-UHFFFAOYSA-N 0.000 claims 1
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- 125000005415 substituted alkoxy group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 125000004306 triazinyl group Chemical group 0.000 claims 1
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- 2004-03-22 EP EP04758050A patent/EP1638954A1/en not_active Withdrawn
- 2004-03-22 AU AU2004223827A patent/AU2004223827B2/en not_active Ceased
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