JP2007505875A5 - - Google Patents
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- Publication number
- JP2007505875A5 JP2007505875A5 JP2006526686A JP2006526686A JP2007505875A5 JP 2007505875 A5 JP2007505875 A5 JP 2007505875A5 JP 2006526686 A JP2006526686 A JP 2006526686A JP 2006526686 A JP2006526686 A JP 2006526686A JP 2007505875 A5 JP2007505875 A5 JP 2007505875A5
- Authority
- JP
- Japan
- Prior art keywords
- quinazoline
- chloro
- piperidin
- oxy
- methoxy
- 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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- 150000003246 quinazolines Chemical class 0.000 claims 46
- -1 cyano, nitro, hydroxy, amino, carboxy, sulfamoyl Chemical group 0.000 claims 31
- 125000000217 alkyl group Chemical group 0.000 claims 23
- 229910052739 hydrogen Inorganic materials 0.000 claims 20
- 239000001257 hydrogen Substances 0.000 claims 20
- 150000003839 salts Chemical class 0.000 claims 18
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000000524 functional group Chemical group 0.000 claims 13
- 125000005843 halogen group Chemical group 0.000 claims 10
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims 10
- 125000003545 alkoxy group Chemical group 0.000 claims 9
- 125000003282 alkyl amino group Chemical group 0.000 claims 9
- 125000001153 fluoro group Chemical group F* 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 7
- 239000003814 drug Substances 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 206010028980 Neoplasm Diseases 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
- 125000000304 alkynyl group Chemical group 0.000 claims 4
- 238000006243 chemical reaction Methods 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- SHSMZPYXZURMEE-UHFFFAOYSA-N 2-[4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-(4-methylpiperazin-1-yl)ethanone Chemical compound C=12C=C(OC3CCN(CC(=O)N4CCN(C)CC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=CC(Cl)=C1F SHSMZPYXZURMEE-UHFFFAOYSA-N 0.000 claims 2
- QRVGWOQDGHNNOJ-UHFFFAOYSA-N 2-[4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-piperazin-1-ylethanone Chemical compound C=12C=C(OC3CCN(CC(=O)N4CCNCC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=CC(Cl)=C1F QRVGWOQDGHNNOJ-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- 125000005236 alkanoylamino group Chemical group 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000006239 protecting group Chemical group 0.000 claims 2
- DFJSJLGUIXFDJP-UHFFFAOYSA-N sapitinib Chemical compound C1CN(CC(=O)NC)CCC1OC(C(=CC1=NC=N2)OC)=CC1=C2NC1=CC=CC(Cl)=C1F DFJSJLGUIXFDJP-UHFFFAOYSA-N 0.000 claims 2
- 150000003335 secondary amines Chemical class 0.000 claims 2
- TUJMSLXGODIOSJ-UHFFFAOYSA-N 2-[4-[4-(3-chloro-2,4-difluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-(4-methylpiperazin-1-yl)ethanone Chemical compound C=12C=C(OC3CCN(CC(=O)N4CCN(C)CC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1F TUJMSLXGODIOSJ-UHFFFAOYSA-N 0.000 claims 1
- OYVGKMHHOZESFV-UHFFFAOYSA-N 2-[4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-morpholin-4-ylethanone Chemical compound C=12C=C(OC3CCN(CC(=O)N4CCOCC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=CC(Cl)=C1F OYVGKMHHOZESFV-UHFFFAOYSA-N 0.000 claims 1
- QJKLDSLAYNMJPH-UHFFFAOYSA-N 2-[4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-morpholin-4-ylethanone Chemical compound C=12C=C(OC3CCN(CC(=O)N4CCOCC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 QJKLDSLAYNMJPH-UHFFFAOYSA-N 0.000 claims 1
- YAMOXVHULRXADY-UHFFFAOYSA-N 2-[4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-pyrrolidin-1-ylethanone Chemical compound C=12C=C(OC3CCN(CC(=O)N4CCCC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 YAMOXVHULRXADY-UHFFFAOYSA-N 0.000 claims 1
- DWKBIQXIOVLREL-UHFFFAOYSA-N 2-[4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-n,n-dimethylacetamide Chemical compound C=12C=C(OC3CCN(CC(=O)N(C)C)CC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 DWKBIQXIOVLREL-UHFFFAOYSA-N 0.000 claims 1
- UUHJZHSXOPNXJK-UHFFFAOYSA-N 2-[4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-n-methylacetamide Chemical compound C1CN(CC(=O)NC)CCC1OC(C(=CC1=NC=N2)OC)=CC1=C2NC1=CC=C(F)C(Cl)=C1 UUHJZHSXOPNXJK-UHFFFAOYSA-N 0.000 claims 1
- BPJGLRNTMKLTFV-UHFFFAOYSA-N 2-[4-[4-(3-chloro-4-fluoroanilino)quinazolin-6-yl]oxypiperidin-1-yl]-1-morpholin-4-ylethanone Chemical compound C1=C(Cl)C(F)=CC=C1NC(C1=C2)=NC=NC1=CC=C2OC1CCN(CC(=O)N2CCOCC2)CC1 BPJGLRNTMKLTFV-UHFFFAOYSA-N 0.000 claims 1
- KFLQUVCHGBIZNL-UHFFFAOYSA-N 2-[4-[4-(3-chloro-4-fluoroanilino)quinazolin-6-yl]oxypiperidin-1-yl]-n,n-dimethylacetamide Chemical compound C1CN(CC(=O)N(C)C)CCC1OC1=CC=C(N=CN=C2NC=3C=C(Cl)C(F)=CC=3)C2=C1 KFLQUVCHGBIZNL-UHFFFAOYSA-N 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- AJGCCHYJVIYICA-UHFFFAOYSA-N 3-[4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-morpholin-4-ylpropan-1-one Chemical compound C=12C=C(OC3CCN(CCC(=O)N4CCOCC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 AJGCCHYJVIYICA-UHFFFAOYSA-N 0.000 claims 1
- VDDLIDPTQSBAAT-UHFFFAOYSA-N 4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxy-n-(2-pyrrolidin-1-ylethyl)piperidine-1-carboxamide Chemical compound C=12C=C(OC3CCN(CC3)C(=O)NCCN3CCCC3)C(OC)=CC2=NC=NC=1NC1=CC=CC(Cl)=C1F VDDLIDPTQSBAAT-UHFFFAOYSA-N 0.000 claims 1
- LYTUHALVDRDFOK-UHFFFAOYSA-N 4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxy-n-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1OC(C(=CC1=NC=N2)OC)=CC1=C2NC1=CC=CC(Cl)=C1F LYTUHALVDRDFOK-UHFFFAOYSA-N 0.000 claims 1
- WMBRKFRXBSLUHE-UHFFFAOYSA-N 4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxy-n,n-diethylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)N(CC)CC)CCC1OC(C(=CC1=NC=N2)OC)=CC1=C2NC1=CC=C(F)C(Cl)=C1 WMBRKFRXBSLUHE-UHFFFAOYSA-N 0.000 claims 1
- IQGVKORQJHVGOB-UHFFFAOYSA-N 4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxy-n,n-dimethylpiperidine-1-carboxamide Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N(C)C)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 IQGVKORQJHVGOB-UHFFFAOYSA-N 0.000 claims 1
- MLCJKARGBIMLJM-UHFFFAOYSA-N 4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxy-n-ethylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NCC)CCC1OC(C(=CC1=NC=N2)OC)=CC1=C2NC1=CC=C(F)C(Cl)=C1 MLCJKARGBIMLJM-UHFFFAOYSA-N 0.000 claims 1
- BDCBLXLWPRFFPU-UHFFFAOYSA-N 4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxy-n-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1OC(C(=CC1=NC=N2)OC)=CC1=C2NC1=CC=C(F)C(Cl)=C1 BDCBLXLWPRFFPU-UHFFFAOYSA-N 0.000 claims 1
- TYDXNUIFLUEDFR-UHFFFAOYSA-N 4-[4-(3-chloro-4-fluoroanilino)quinazolin-6-yl]oxy-n,n-dimethylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)N(C)C)CCC1OC1=CC=C(N=CN=C2NC=3C=C(Cl)C(F)=CC=3)C2=C1 TYDXNUIFLUEDFR-UHFFFAOYSA-N 0.000 claims 1
- OPXXBONXLXHZNU-UHFFFAOYSA-N 4-[4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-1-morpholin-4-ylbutan-1-one Chemical compound C=12C=C(OC3CCN(CCCC(=O)N4CCOCC4)CC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 OPXXBONXLXHZNU-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- SNUHGTFGVZBUPD-UHFFFAOYSA-N [4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-morpholin-4-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=CC(Cl)=C1F SNUHGTFGVZBUPD-UHFFFAOYSA-N 0.000 claims 1
- BHKSATWJMGPDRI-UHFFFAOYSA-N [4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-pyrrolidin-1-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCCC3)C(OC)=CC2=NC=NC=1NC1=CC=CC(Cl)=C1F BHKSATWJMGPDRI-UHFFFAOYSA-N 0.000 claims 1
- HGQSWGUVSJUFJD-UHFFFAOYSA-N [4-[4-(3-chloro-4-fluoroanilino)-7-(2-methoxyethoxy)quinazolin-6-yl]oxypiperidin-1-yl]-morpholin-4-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCOCC3)C(OCCOC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 HGQSWGUVSJUFJD-UHFFFAOYSA-N 0.000 claims 1
- IWYSVFZTNXLAOF-UHFFFAOYSA-N [4-[4-(3-chloro-4-fluoroanilino)-7-ethoxyquinazolin-6-yl]oxypiperidin-1-yl]-morpholin-4-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCOCC3)C(OCC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 IWYSVFZTNXLAOF-UHFFFAOYSA-N 0.000 claims 1
- XFVIYGALQWSYAD-UHFFFAOYSA-N [4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-(4-methylpiperazin-1-yl)methanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCN(C)CC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XFVIYGALQWSYAD-UHFFFAOYSA-N 0.000 claims 1
- SGPQZLAIXLGTBH-UHFFFAOYSA-N [4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-morpholin-4-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 SGPQZLAIXLGTBH-UHFFFAOYSA-N 0.000 claims 1
- GCFQYHBVQUQWIX-UHFFFAOYSA-N [4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-piperidin-1-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCCCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 GCFQYHBVQUQWIX-UHFFFAOYSA-N 0.000 claims 1
- AKGOXFWKPNRRRD-UHFFFAOYSA-N [4-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-pyrrolidin-1-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 AKGOXFWKPNRRRD-UHFFFAOYSA-N 0.000 claims 1
- OTYKNBPRZBCEBA-UHFFFAOYSA-N [4-[4-(3-chloro-4-fluoroanilino)quinazolin-6-yl]oxypiperidin-1-yl]-morpholin-4-ylmethanone Chemical compound C1=C(Cl)C(F)=CC=C1NC(C1=C2)=NC=NC1=CC=C2OC1CCN(C(=O)N2CCOCC2)CC1 OTYKNBPRZBCEBA-UHFFFAOYSA-N 0.000 claims 1
- COUMVWRRFZOSEJ-UHFFFAOYSA-N [4-[4-(3-ethynylanilino)-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]-morpholin-4-ylmethanone Chemical compound C=12C=C(OC3CCN(CC3)C(=O)N3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 COUMVWRRFZOSEJ-UHFFFAOYSA-N 0.000 claims 1
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 125000003302 alkenyloxy group Chemical group 0.000 claims 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 230000029936 alkylation Effects 0.000 claims 1
- 238000005804 alkylation reaction Methods 0.000 claims 1
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 230000001028 anti-proliverative effect Effects 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 238000003776 cleavage reaction Methods 0.000 claims 1
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 230000002062 proliferating effect Effects 0.000 claims 1
- 238000006268 reductive amination reaction Methods 0.000 claims 1
- 230000007017 scission Effects 0.000 claims 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Chemical group 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 C*C(N(*)*)=O Chemical compound C*C(N(*)*)=O 0.000 description 3
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03292309 | 2003-09-19 | ||
| EP04291248 | 2004-05-14 | ||
| PCT/GB2004/003937 WO2005028469A1 (en) | 2003-09-19 | 2004-09-15 | Quinazoline derivatives |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007240846A Division JP2008037874A (ja) | 2003-09-19 | 2007-09-18 | キナゾリン誘導体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007505875A JP2007505875A (ja) | 2007-03-15 |
| JP2007505875A5 true JP2007505875A5 (cg-RX-API-DMAC7.html) | 2007-07-05 |
| JP4036885B2 JP4036885B2 (ja) | 2008-01-23 |
Family
ID=34379392
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006526686A Expired - Fee Related JP4036885B2 (ja) | 2003-09-19 | 2004-09-15 | キナゾリン誘導体 |
| JP2007240846A Pending JP2008037874A (ja) | 2003-09-19 | 2007-09-18 | キナゾリン誘導体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007240846A Pending JP2008037874A (ja) | 2003-09-19 | 2007-09-18 | キナゾリン誘導体 |
Country Status (32)
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200813014A (en) * | 2002-03-28 | 2008-03-16 | Astrazeneca Ab | Quinazoline derivatives |
| US6924285B2 (en) | 2002-03-30 | 2005-08-02 | Boehringer Ingelheim Pharma Gmbh & Co. | Bicyclic heterocyclic compounds, pharmaceutical compositions containing these compounds, their use and process for preparing them |
| GB0317665D0 (en) | 2003-07-29 | 2003-09-03 | Astrazeneca Ab | Qinazoline derivatives |
| BRPI0414489A8 (pt) | 2003-09-16 | 2019-01-15 | Astrazeneca Ab | derivado de quinazolina, composição farmacêutica, uso de um derivado de quinazolina, e, processo para a preparação de um derivado de quinazolina |
| ATE353888T1 (de) * | 2003-09-19 | 2007-03-15 | Astrazeneca Ab | Chinazolinderivate |
| DK1667992T3 (da) | 2003-09-19 | 2007-04-30 | Astrazeneca Ab | Quinazolinderivater |
| CA2540008A1 (en) * | 2003-09-25 | 2005-04-07 | Astrazeneca Ab | Quinazoline derivatives |
| GB0322409D0 (en) * | 2003-09-25 | 2003-10-29 | Astrazeneca Ab | Quinazoline derivatives |
| GB0326459D0 (en) | 2003-11-13 | 2003-12-17 | Astrazeneca Ab | Quinazoline derivatives |
| WO2005075439A1 (en) | 2004-02-03 | 2005-08-18 | Astrazeneca Ab | Quinazoline derivatives |
| DE602005026865D1 (de) * | 2004-12-14 | 2011-04-21 | Astrazeneca Ab | Pyrazolopyrimidinverbindungen als antitumormittel |
| WO2006090163A1 (en) * | 2005-02-26 | 2006-08-31 | Astrazeneca Ab | Quinazoline derivatives as tyrosine kinase inhibitors |
| CN101175733A (zh) * | 2005-05-12 | 2008-05-07 | 黄文林 | 一种酪氨酸激酶抑制剂、其制备方法及作为抗肿瘤药物的应用 |
| EP1957468A2 (en) * | 2005-09-06 | 2008-08-20 | T.K. Signal Ltd. | Polyalkylene glycol derivatives of 4 - (phenylamino)quinazolines useful as irreversible inhibitors of epidermal growth factor receptor tyrosine kinase |
| WO2007068552A1 (de) * | 2005-12-12 | 2007-06-21 | Boehringer Ingelheim International Gmbh | Bicyclische heterocyclen, diese verbindungen enthaltende arzneimittel, deren verwendung und verfahren zu ihrer herstellung |
| EP1921070A1 (de) * | 2006-11-10 | 2008-05-14 | Boehringer Ingelheim Pharma GmbH & Co. KG | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstelllung |
| BRPI0807234A2 (pt) | 2007-02-06 | 2014-06-03 | Boehringer Ingelheim Int | Heterociclos bicíclicos, composições farmacêuticas que contêm estes compostos, o uso dos mesmos e processos para a preparação dos mesmos |
| KR20100111291A (ko) | 2008-02-07 | 2010-10-14 | 베링거 인겔하임 인터내셔날 게엠베하 | 스피로사이클릭 헤테로사이클, 상기 화합물을 함유하는 약제, 이의 용도 및 이의 제조 방법 |
| WO2009138779A1 (en) * | 2008-05-13 | 2009-11-19 | Astrazeneca Ab | Combination comprising 4- (3-chloro-2-fluoroanilino) -7-meth0xy-6- { [1- (n-methylcarbamoylmethyl) piperidin- 4-yl] oxyjquinazoline |
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2012
- 2012-09-10 US US13/607,999 patent/US20120329795A1/en not_active Abandoned