JP2003535859A5 - - Google Patents
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- JP2003535859A5 JP2003535859A5 JP2002501890A JP2002501890A JP2003535859A5 JP 2003535859 A5 JP2003535859 A5 JP 2003535859A5 JP 2002501890 A JP2002501890 A JP 2002501890A JP 2002501890 A JP2002501890 A JP 2002501890A JP 2003535859 A5 JP2003535859 A5 JP 2003535859A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- group
- formula
- pyrrolidin
- amino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- -1 cyano, isocyano, nitro, hydroxy, mercapto, amino, formyl Chemical group 0.000 claims description 653
- 125000000217 alkyl group Chemical group 0.000 claims description 350
- 125000001424 substituent group Chemical group 0.000 claims description 146
- 125000000623 heterocyclic group Chemical group 0.000 claims description 89
- 229910052739 hydrogen Inorganic materials 0.000 claims description 76
- 239000001257 hydrogen Substances 0.000 claims description 76
- 229910052760 oxygen Inorganic materials 0.000 claims description 75
- 229910052757 nitrogen Inorganic materials 0.000 claims description 67
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 60
- 125000003545 alkoxy group Chemical group 0.000 claims description 49
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 47
- 125000003118 aryl group Chemical group 0.000 claims description 42
- 125000001072 heteroaryl group Chemical group 0.000 claims description 39
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 39
- 125000001153 fluoro group Chemical group F* 0.000 claims description 37
- 125000005843 halogen group Chemical group 0.000 claims description 35
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 34
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 30
- 229910052717 sulfur Inorganic materials 0.000 claims description 25
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 24
- 125000005236 alkanoylamino group Chemical group 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 20
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 20
- 125000002947 alkylene group Chemical group 0.000 claims description 19
- 238000003780 insertion Methods 0.000 claims description 19
- 230000037431 insertion Effects 0.000 claims description 19
- 125000003282 alkyl amino group Chemical group 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 16
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 16
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 16
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 14
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 125000003342 alkenyl group Chemical group 0.000 claims description 13
- 125000000304 alkynyl group Chemical group 0.000 claims description 13
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 9
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 9
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 7
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims 28
- 150000003246 quinazolines Chemical class 0.000 claims 25
- 150000002431 hydrogen Chemical class 0.000 claims 15
- 239000002253 acid Substances 0.000 claims 12
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 12
- 125000001589 carboacyl group Chemical group 0.000 claims 11
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 claims 10
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 10
- 125000004414 alkyl thio group Chemical group 0.000 claims 10
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 10
- 125000001246 bromo group Chemical group Br* 0.000 claims 10
- 125000004423 acyloxy group Chemical group 0.000 claims 9
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 8
- 125000000524 functional group Chemical group 0.000 claims 8
- 125000004043 oxo group Chemical group O=* 0.000 claims 8
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 5
- LCIYFINKFGDAHD-UHFFFAOYSA-N azepane;3-nitrobenzoic acid Chemical compound C1CCCNCC1.OC(=O)C1=CC=CC([N+]([O-])=O)=C1 LCIYFINKFGDAHD-UHFFFAOYSA-N 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 238000006243 chemical reaction Methods 0.000 claims 4
- 125000006239 protecting group Chemical group 0.000 claims 4
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims 4
- 125000002619 bicyclic group Chemical group 0.000 claims 3
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 3
- 125000000464 thioxo group Chemical group S=* 0.000 claims 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 238000003776 cleavage reaction Methods 0.000 claims 2
- 230000008878 coupling Effects 0.000 claims 2
- 238000010168 coupling process Methods 0.000 claims 2
- 238000005859 coupling reaction Methods 0.000 claims 2
- 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- QPKZNXSXCNZSDC-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine Chemical compound ClC1=CC=C2OCOC2=C1NC(C1=C(OC2CCOCC2)C=2)=NC=NC1=CC=2OCCN1CCCC1 QPKZNXSXCNZSDC-UHFFFAOYSA-N 0.000 claims 2
- HLILQABBLFGERM-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine Chemical compound ClC1=CC=C2OCOC2=C1NC(C1=C(OC2CCOCC2)C=2)=NC=NC1=CC=2OCCCN1CCCC1 HLILQABBLFGERM-UHFFFAOYSA-N 0.000 claims 2
- NNTCPBYVAUSUOH-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-7-[3-(4-methylpiperazin-1-yl)propoxy]-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound C1CN(C)CCN1CCCOC1=CC(OC2CCOCC2)=C(C(NC=2C(=CC=C3OCOC3=2)Cl)=NC=N2)C2=C1 NNTCPBYVAUSUOH-UHFFFAOYSA-N 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- OUKYUETWWIPKQR-UHFFFAOYSA-N saracatinib Chemical compound C1CN(C)CCN1CCOC1=CC(OC2CCOCC2)=C(C(NC=2C(=CC=C3OCOC3=2)Cl)=NC=N2)C2=C1 OUKYUETWWIPKQR-UHFFFAOYSA-N 0.000 claims 2
- 230000007017 scission Effects 0.000 claims 2
- VCVITBJRYVJDMQ-DEOSSOPVSA-N (2s)-1-[2-[4-(2-bromo-5-methoxyanilino)-5-(oxan-4-yloxy)quinazolin-7-yl]oxyethyl]-n-methylpyrrolidine-2-carboxamide Chemical compound CNC(=O)[C@@H]1CCCN1CCOC1=CC(OC2CCOCC2)=C(C(NC=2C(=CC=C(OC)C=2)Br)=NC=N2)C2=C1 VCVITBJRYVJDMQ-DEOSSOPVSA-N 0.000 claims 1
- CZVCRAPDCDORMP-UHFFFAOYSA-N 1-[4-(2-chloro-5-methoxyanilino)-5-(oxan-4-yloxy)quinazolin-7-yl]oxy-3-(4-methylpiperazin-1-yl)propan-2-ol Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OC4CCOCC4)C=C(OCC(O)CN4CCN(C)CC4)C=C3N=CN=2)=C1 CZVCRAPDCDORMP-UHFFFAOYSA-N 0.000 claims 1
- BDKVXBWNXMYXMM-UHFFFAOYSA-N 1-[4-(2-chloro-5-methoxyanilino)-5-(oxan-4-yloxy)quinazolin-7-yl]oxy-3-morpholin-4-ylpropan-2-ol Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OC4CCOCC4)C=C(OCC(O)CN4CCOCC4)C=C3N=CN=2)=C1 BDKVXBWNXMYXMM-UHFFFAOYSA-N 0.000 claims 1
- MJPPGVVIDGQOQT-UHFFFAOYSA-N 2-bromo-5-(2-bromo-2-nitroethenyl)furan Chemical compound [O-][N+](=O)C(Br)=CC1=CC=C(Br)O1 MJPPGVVIDGQOQT-UHFFFAOYSA-N 0.000 claims 1
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 230000029936 alkylation Effects 0.000 claims 1
- 238000005804 alkylation reaction Methods 0.000 claims 1
- 125000005530 alkylenedioxy group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 230000001740 anti-invasion Effects 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 238000007796 conventional method Methods 0.000 claims 1
- 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 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- VSCFUBQXHXHWBU-UHFFFAOYSA-N n-(2,4-dichloro-5-methoxyphenyl)-5-(oxan-4-yloxy)-7-(2-piperidin-1-ylethoxy)quinazolin-4-amine Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=C(OC4CCOCC4)C=C(OCCN4CCCCC4)C=C3N=CN=2)=C1Cl VSCFUBQXHXHWBU-UHFFFAOYSA-N 0.000 claims 1
- RIDMECZKUSOYKF-UHFFFAOYSA-N n-(2,4-dichloro-5-methoxyphenyl)-5-(oxan-4-yloxy)-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=C(OC4CCOCC4)C=C(OCCN4CCCC4)C=C3N=CN=2)=C1Cl RIDMECZKUSOYKF-UHFFFAOYSA-N 0.000 claims 1
- BLIYFWIFLLWOIW-UHFFFAOYSA-N n-(2,4-dichloro-5-methoxyphenyl)-7-(2-morpholin-4-ylethoxy)-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=C(OC4CCOCC4)C=C(OCCN4CCOCC4)C=C3N=CN=2)=C1Cl BLIYFWIFLLWOIW-UHFFFAOYSA-N 0.000 claims 1
- PEZRZHSAIHVJIJ-UHFFFAOYSA-N n-(2,4-dichloro-5-methoxyphenyl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=C(OC4CCOCC4)C=C(OCCN4CCN(C)CC4)C=C3N=CN=2)=C1Cl PEZRZHSAIHVJIJ-UHFFFAOYSA-N 0.000 claims 1
- LWYABZMGKZJVCX-UHFFFAOYSA-N n-(2,4-dichloro-5-methoxyphenyl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine Chemical compound C=12C(NC=3C(=CC(Cl)=C(OC)C=3)Cl)=NC=NC2=CC(OC)=CC=1OC1CCN(C)CC1 LWYABZMGKZJVCX-UHFFFAOYSA-N 0.000 claims 1
- WCGMYDZBHJUBAI-UHFFFAOYSA-N n-(2,5-dimethoxyphenyl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine Chemical compound COC1=CC=C(OC)C(NC=2C3=C(OC4CCN(C)CC4)C=C(OC)C=C3N=CN=2)=C1 WCGMYDZBHJUBAI-UHFFFAOYSA-N 0.000 claims 1
- AUPJMWGAXBDLAF-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-5-(oxan-4-yloxy)-7-(2-piperidin-1-ylethoxy)quinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCOCC4)C=C(OCCN4CCCCC4)C=C3N=CN=2)=C1 AUPJMWGAXBDLAF-UHFFFAOYSA-N 0.000 claims 1
- AIRJDVWSRXGZLJ-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-5-(oxan-4-yloxy)-7-(2-pyridin-4-yloxyethoxy)quinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCOCC4)C=C(OCCOC=4C=CN=CC=4)C=C3N=CN=2)=C1 AIRJDVWSRXGZLJ-UHFFFAOYSA-N 0.000 claims 1
- RWCQVHHBOZOVOB-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-5-(oxan-4-yloxy)-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCOCC4)C=C(OCCN4CCCC4)C=C3N=CN=2)=C1 RWCQVHHBOZOVOB-UHFFFAOYSA-N 0.000 claims 1
- QHSJVBSZHSXNSA-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-5-(oxan-4-yloxy)-7-(pyridin-4-ylmethoxy)quinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCOCC4)C=C(OCC=4C=CN=CC=4)C=C3N=CN=2)=C1 QHSJVBSZHSXNSA-UHFFFAOYSA-N 0.000 claims 1
- RWICHPXUBOMASG-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-7-(3-methylsulfonylpropoxy)-5-piperidin-4-yloxyquinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCNCC4)C=C(OCCCS(C)(=O)=O)C=C3N=CN=2)=C1 RWICHPXUBOMASG-UHFFFAOYSA-N 0.000 claims 1
- LXCFBQWFFIUKPN-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCOCC4)C=C(OCCN4CCN(C)CC4)C=C3N=CN=2)=C1 LXCFBQWFFIUKPN-UHFFFAOYSA-N 0.000 claims 1
- IXDJANRWLQKZKC-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCN(C)CC4)C=C(OC)C=C3N=CN=2)=C1 IXDJANRWLQKZKC-UHFFFAOYSA-N 0.000 claims 1
- KBCHXRRWXCXHDE-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-7-methoxy-5-(piperidin-4-ylmethoxy)quinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OCC4CCNCC4)C=C(OC)C=C3N=CN=2)=C1 KBCHXRRWXCXHDE-UHFFFAOYSA-N 0.000 claims 1
- KFRSXMUSYAQULP-UHFFFAOYSA-N n-(2-bromo-5-methoxyphenyl)-7-phenylmethoxy-5-piperidin-4-yloxyquinazolin-4-amine Chemical compound COC1=CC=C(Br)C(NC=2C3=C(OC4CCNCC4)C=C(OCC=4C=CC=CC=4)C=C3N=CN=2)=C1 KFRSXMUSYAQULP-UHFFFAOYSA-N 0.000 claims 1
- JNYZPLVVZJKPNU-UHFFFAOYSA-N n-(2-chloro-5-methoxyphenyl)-5,7-bis(3-morpholin-4-ylpropoxy)quinazolin-4-amine Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OCCCN4CCOCC4)C=C(OCCCN4CCOCC4)C=C3N=CN=2)=C1 JNYZPLVVZJKPNU-UHFFFAOYSA-N 0.000 claims 1
- UKFYOXMBPXQXJR-UHFFFAOYSA-N n-(2-chloro-5-methoxyphenyl)-7-(3-morpholin-4-ylpropoxy)-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OC4CCOCC4)C=C(OCCCN4CCOCC4)C=C3N=CN=2)=C1 UKFYOXMBPXQXJR-UHFFFAOYSA-N 0.000 claims 1
- DWMMULHPJUKYRJ-UHFFFAOYSA-N n-(2-chloro-5-methoxyphenyl)-7-(3-morpholin-4-ylpropoxy)-5-(oxolan-3-yloxy)quinazolin-4-amine Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OC4COCC4)C=C(OCCCN4CCOCC4)C=C3N=CN=2)=C1 DWMMULHPJUKYRJ-UHFFFAOYSA-N 0.000 claims 1
- KSOSADFISSODEE-UHFFFAOYSA-N n-(2-chloro-5-methoxyphenyl)-7-[3-(4-methylpiperazin-1-yl)propoxy]-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OC4CCOCC4)C=C(OCCCN4CCN(C)CC4)C=C3N=CN=2)=C1 KSOSADFISSODEE-UHFFFAOYSA-N 0.000 claims 1
- YNFZBOQQNNBILJ-UHFFFAOYSA-N n-(2-chloro-5-methoxyphenyl)-7-[3-(4-methylpiperazin-1-yl)propoxy]-5-(oxolan-3-yloxy)quinazolin-4-amine Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OC4COCC4)C=C(OCCCN4CCN(C)CC4)C=C3N=CN=2)=C1 YNFZBOQQNNBILJ-UHFFFAOYSA-N 0.000 claims 1
- UDMCXVWGJLMNDD-UHFFFAOYSA-N n-(2-chloro-5-methoxyphenyl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine Chemical compound COC1=CC=C(Cl)C(NC=2C3=C(OC4CCN(C)CC4)C=C(OC)C=C3N=CN=2)=C1 UDMCXVWGJLMNDD-UHFFFAOYSA-N 0.000 claims 1
- SRUFFEXENVBMCO-UHFFFAOYSA-N n-(3-chloro-1-benzofuran-7-yl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine Chemical compound C=12C(NC=3C=4OC=C(Cl)C=4C=CC=3)=NC=NC2=CC(OC)=CC=1OC1CCN(C)CC1 SRUFFEXENVBMCO-UHFFFAOYSA-N 0.000 claims 1
- VCVHFPAOHFDEOW-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(2-piperidin-1-ylethoxy)quinazolin-4-amine Chemical compound ClC1=CC=C2OCOC2=C1NC(C1=C(OC2CCOCC2)C=2)=NC=NC1=CC=2OCCN1CCCCC1 VCVHFPAOHFDEOW-UHFFFAOYSA-N 0.000 claims 1
- UUUXOMVMDSIRMB-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(2-pyridin-4-yloxyethoxy)quinazolin-4-amine Chemical compound ClC1=CC=C2OCOC2=C1NC(C1=C(OC2CCOCC2)C=2)=NC=NC1=CC=2OCCOC1=CC=NC=C1 UUUXOMVMDSIRMB-UHFFFAOYSA-N 0.000 claims 1
- UTOOQZAPEDMMFY-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(piperidin-4-ylmethoxy)quinazolin-4-amine Chemical compound ClC1=CC=C2OCOC2=C1NC(C1=C(OC2CCOCC2)C=2)=NC=NC1=CC=2OCC1CCNCC1 UTOOQZAPEDMMFY-UHFFFAOYSA-N 0.000 claims 1
- WETSNLOXQAQKPO-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-5-cyclopentyloxy-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine Chemical compound ClC1=CC=C2OCOC2=C1NC(C1=C(OC2CCCC2)C=2)=NC=NC1=CC=2OCCN1CCCC1 WETSNLOXQAQKPO-UHFFFAOYSA-N 0.000 claims 1
- QLPARMMDOPNDPN-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-5-piperidin-4-yloxyquinazolin-4-amine Chemical compound ClC1=CC=C2OCOC2=C1NC(C=12)=NC=NC2=CC=CC=1OC1CCNCC1 QLPARMMDOPNDPN-UHFFFAOYSA-N 0.000 claims 1
- YQPAFFIGFWEPLF-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-7-[(1-methylpiperidin-4-yl)methoxy]-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound C1CN(C)CCC1COC1=CC(OC2CCOCC2)=C(C(NC=2C(=CC=C3OCOC3=2)Cl)=NC=N2)C2=C1 YQPAFFIGFWEPLF-UHFFFAOYSA-N 0.000 claims 1
- PVOAJSAAENFMPF-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-7-fluoro-5-(oxan-4-yloxy)quinazolin-4-amine Chemical compound C=12C(NC=3C(=CC=C4OCOC4=3)Cl)=NC=NC2=CC(F)=CC=1OC1CCOCC1 PVOAJSAAENFMPF-UHFFFAOYSA-N 0.000 claims 1
- VVKSFHCTJLSWTD-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine Chemical compound C=12C(NC=3C(=CC=C4OCOC4=3)Cl)=NC=NC2=CC(OC)=CC=1OC1CCN(C)CC1 VVKSFHCTJLSWTD-UHFFFAOYSA-N 0.000 claims 1
- QQZMLTXRSKBBOH-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-7-methoxy-5-(piperidin-4-ylmethoxy)quinazolin-4-amine Chemical compound C=12C(NC=3C(=CC=C4OCOC4=3)Cl)=NC=NC2=CC(OC)=CC=1OCC1CCNCC1 QQZMLTXRSKBBOH-UHFFFAOYSA-N 0.000 claims 1
- RHICODWVWUTRSH-UHFFFAOYSA-N n-(5-chloro-1,3-benzodioxol-4-yl)-7-methoxy-5-piperidin-4-yloxyquinazolin-4-amine Chemical compound C=12C(NC=3C(=CC=C4OCOC4=3)Cl)=NC=NC2=CC(OC)=CC=1OC1CCNCC1 RHICODWVWUTRSH-UHFFFAOYSA-N 0.000 claims 1
- AWTKDKXDACFEHT-UHFFFAOYSA-N n-(5-chloronaphthalen-1-yl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine Chemical compound C=12C(NC=3C4=CC=CC(Cl)=C4C=CC=3)=NC=NC2=CC(OC)=CC=1OC1CCN(C)CC1 AWTKDKXDACFEHT-UHFFFAOYSA-N 0.000 claims 1
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-
2001
- 2001-01-06 UA UA2003010151A patent/UA73993C2/uk unknown
- 2001-06-01 PL PL360745A patent/PL210852B1/pl unknown
- 2001-06-01 CZ CZ20023961A patent/CZ301987B6/cs not_active IP Right Cessation
- 2001-06-01 AU AU2001260482A patent/AU2001260482B2/en not_active Ceased
- 2001-06-01 BR BR0111335-6A patent/BR0111335A/pt not_active IP Right Cessation
- 2001-06-01 AU AU6048201A patent/AU6048201A/xx active Pending
- 2001-06-01 CN CNB01810830XA patent/CN100345844C/zh not_active Expired - Lifetime
- 2001-06-01 EP EP01934176A patent/EP1292594B1/en not_active Expired - Lifetime
- 2001-06-01 SK SK1702-2002A patent/SK286748B6/sk not_active IP Right Cessation
- 2001-06-01 HU HU0301046A patent/HU229290B1/hu not_active IP Right Cessation
- 2001-06-01 WO PCT/GB2001/002424 patent/WO2001094341A1/en not_active Ceased
- 2001-06-01 ES ES01934176T patent/ES2225545T3/es not_active Expired - Lifetime
- 2001-06-01 CA CA002407371A patent/CA2407371C/en not_active Expired - Fee Related
- 2001-06-01 DE DE60105295T patent/DE60105295T2/de not_active Expired - Lifetime
- 2001-06-01 JP JP2002501890A patent/JP3774438B2/ja not_active Expired - Lifetime
- 2001-06-01 MX MXPA02011765A patent/MXPA02011765A/es active IP Right Grant
- 2001-06-01 PT PT01934176T patent/PT1292594E/pt unknown
- 2001-06-01 SI SI200130193T patent/SI1292594T1/xx unknown
- 2001-06-01 DK DK01934176T patent/DK1292594T3/da active
- 2001-06-01 NZ NZ522204A patent/NZ522204A/en not_active IP Right Cessation
- 2001-06-01 US US10/275,382 patent/US7049438B2/en not_active Expired - Lifetime
- 2001-06-01 KR KR1020087002129A patent/KR20080015055A/ko not_active Withdrawn
- 2001-06-01 KR KR1020027016508A patent/KR100807162B1/ko not_active Expired - Fee Related
- 2001-06-01 AT AT01934176T patent/ATE275145T1/de active
- 2001-06-01 IL IL15275401A patent/IL152754A0/xx unknown
- 2001-06-01 EE EEP200200673A patent/EE05481B1/xx not_active IP Right Cessation
- 2001-06-05 MY MYPI20012632 patent/MY127369A/en unknown
- 2001-06-06 AR ARP010102704A patent/AR030937A1/es active IP Right Grant
- 2001-06-06 TW TW090113714A patent/TWI288748B/zh not_active IP Right Cessation
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2002
- 2002-11-11 IL IL152754A patent/IL152754A/en not_active IP Right Cessation
- 2002-11-28 BG BG107332A patent/BG65836B1/bg unknown
- 2002-12-02 IS IS6647A patent/IS2114B/is unknown
- 2002-12-02 NO NO20025792A patent/NO324838B1/no not_active IP Right Cessation
- 2002-12-30 CO CO02117241A patent/CO5700751A2/es active IP Right Grant
-
2005
- 2005-11-21 US US11/283,415 patent/US7696214B2/en not_active Expired - Lifetime
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2010
- 2010-01-29 US US12/696,489 patent/US20100280042A1/en not_active Abandoned
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