ME01952B - 2-amino-7,8-dihydro-6h-pyrido[4,3-d] pyrimidin-5-ones - Google Patents
2-amino-7,8-dihydro-6h-pyrido[4,3-d] pyrimidin-5-onesInfo
- Publication number
- ME01952B ME01952B MEP-2011-334A MEP33411A ME01952B ME 01952 B ME01952 B ME 01952B ME P33411 A MEP33411 A ME P33411A ME 01952 B ME01952 B ME 01952B
- Authority
- ME
- Montenegro
- Prior art keywords
- amino
- pyrimidin
- phenyl
- methyl
- fluoro
- Prior art date
Links
- CZOQBGHFZWUWPV-UHFFFAOYSA-N 2-amino-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical class O=C1NCCC2=NC(N)=NC=C21 CZOQBGHFZWUWPV-UHFFFAOYSA-N 0.000 title 1
- -1 2-methyl-2-morpholinopropyl Chemical group 0.000 claims 309
- 150000001875 compounds Chemical class 0.000 claims 43
- 229910052739 hydrogen Inorganic materials 0.000 claims 28
- 239000001257 hydrogen Substances 0.000 claims 28
- 125000001072 heteroaryl group Chemical group 0.000 claims 19
- 125000003118 aryl group Chemical group 0.000 claims 18
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 11
- 125000005843 halogen group Chemical group 0.000 claims 11
- 150000002431 hydrogen Chemical class 0.000 claims 11
- 150000003839 salts Chemical group 0.000 claims 11
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- 125000003277 amino group Chemical group 0.000 claims 8
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- BDTRIDKONHOQQN-UHFFFAOYSA-N 4h-pyrimidin-5-one Chemical compound O=C1CN=CN=C1 BDTRIDKONHOQQN-UHFFFAOYSA-N 0.000 claims 7
- 125000001041 indolyl group Chemical group 0.000 claims 7
- 125000004076 pyridyl group Chemical group 0.000 claims 7
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 7
- 125000000335 thiazolyl group Chemical group 0.000 claims 7
- 125000001544 thienyl group Chemical group 0.000 claims 7
- 206010028980 Neoplasm Diseases 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 201000011510 cancer Diseases 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000003373 pyrazinyl group Chemical group 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 150000002357 guanidines Chemical class 0.000 claims 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 3
- 125000001617 2,3-dimethoxy phenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C(OC([H])([H])[H])=C1[H] 0.000 claims 3
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims 3
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 3
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 3
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims 3
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims 3
- 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims 3
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 3
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims 3
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 3
- RRXSYZFVDIRTFB-UHFFFAOYSA-N C[CH]C1=CC=C(OC)C=C1 Chemical group C[CH]C1=CC=C(OC)C=C1 RRXSYZFVDIRTFB-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 150000001356 alkyl thiols Chemical class 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 125000000842 isoxazolyl group Chemical group 0.000 claims 3
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims 3
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims 3
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims 3
- 125000002971 oxazolyl group Chemical group 0.000 claims 3
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 229940002612 prodrug Drugs 0.000 claims 3
- 239000000651 prodrug Chemical class 0.000 claims 3
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 3
- 150000003573 thiols Chemical class 0.000 claims 3
- 125000001425 triazolyl group Chemical group 0.000 claims 3
- VBWJSOZNRRIJKW-CYBMUJFWSA-N (7r)-2-amino-4-ethyl-7-[2-(2-methoxy-1,3-thiazol-4-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=CC=C1C1=CSC(OC)=N1 VBWJSOZNRRIJKW-CYBMUJFWSA-N 0.000 claims 2
- ZSOOONHJQCGYGH-CQSZACIVSA-N (7r)-2-amino-4-ethyl-7-[2-(6-methoxypyrazin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=CC=C1C1=CN=CC(OC)=N1 ZSOOONHJQCGYGH-CQSZACIVSA-N 0.000 claims 2
- PUZHLUJYTGUFDZ-MRXNPFEDSA-N (7r)-2-amino-4-ethyl-7-[2-(6-methoxypyridin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=CC=C1C1=CC=CC(OC)=N1 PUZHLUJYTGUFDZ-MRXNPFEDSA-N 0.000 claims 2
- XQNIXHZQURVQNY-CYBMUJFWSA-N (7r)-2-amino-4-ethyl-7-[4-fluoro-2-(2-methoxy-1,3-thiazol-4-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=C(F)C=C1C1=CSC(OC)=N1 XQNIXHZQURVQNY-CYBMUJFWSA-N 0.000 claims 2
- PYGDPDNOWJKHBZ-CQSZACIVSA-N (7r)-2-amino-4-ethyl-7-[4-fluoro-2-(6-methoxypyrazin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=C(F)C=C1C1=CN=CC(OC)=N1 PYGDPDNOWJKHBZ-CQSZACIVSA-N 0.000 claims 2
- QHJOJAPTTNUTLH-MRXNPFEDSA-N (7r)-2-amino-4-ethyl-7-[4-fluoro-2-(6-methoxypyridin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=C(F)C=C1C1=CC=CC(OC)=N1 QHJOJAPTTNUTLH-MRXNPFEDSA-N 0.000 claims 2
- ZRFMJIRKTWKFFF-LLVKDONJSA-N (7r)-2-amino-7-(2-bromo-4-fluorophenyl)-4-ethyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=C(F)C=C1Br ZRFMJIRKTWKFFF-LLVKDONJSA-N 0.000 claims 2
- JHRBZBFFNJGBDX-SNVBAGLBSA-N (7r)-2-amino-7-(2-bromophenyl)-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)C)=CC=CC=C1Br JHRBZBFFNJGBDX-SNVBAGLBSA-N 0.000 claims 2
- JETRSAYBEYEUMV-OAHLLOKOSA-N (7r)-2-amino-7-(4-fluoro-2-pyridin-3-ylphenyl)-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@@H]2NC(=O)C3=CN=C(N=C3C2)N)=CC=C(F)C=C1C1=CC=CN=C1 JETRSAYBEYEUMV-OAHLLOKOSA-N 0.000 claims 2
- JHPAFJTVQHGETR-GFCCVEGCSA-N (7r)-2-amino-7-[2-(2-methoxy-1,3-thiazol-4-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound S1C(OC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 JHPAFJTVQHGETR-GFCCVEGCSA-N 0.000 claims 2
- XDHFEFLWTMOYPX-MRXNPFEDSA-N (7r)-2-amino-7-[2-(3,4-dimethoxyphenyl)-4-fluorophenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=CN=C(N)N=C2C1 XDHFEFLWTMOYPX-MRXNPFEDSA-N 0.000 claims 2
- WWZWNASCKPLORW-CYBMUJFWSA-N (7r)-2-amino-7-[2-(4,5-dimethoxypyrimidin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(OC)C(OC)=CN=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=C(C)N=C(N)N=C2C1 WWZWNASCKPLORW-CYBMUJFWSA-N 0.000 claims 2
- ZHLGDCNNFNWSIN-CQSZACIVSA-N (7r)-2-amino-7-[2-(4-ethoxypyrimidin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CCOC1=CC=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 ZHLGDCNNFNWSIN-CQSZACIVSA-N 0.000 claims 2
- OCTZNELAVPCHKI-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5,6-dimethoxypyrazin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(OC)C(OC)=NC=C1C1=CC=CC=C1[C@@H]1NC(=O)C2=C(C)N=C(N)N=C2C1 OCTZNELAVPCHKI-CYBMUJFWSA-N 0.000 claims 2
- CBHLHQSZYFOTRD-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5-amino-6-ethoxypyrazin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OCC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 CBHLHQSZYFOTRD-CYBMUJFWSA-N 0.000 claims 2
- VBTGUWFNLIKXPW-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5-amino-6-ethoxypyrazin-2-yl)-4-fluorophenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OCC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=C1 VBTGUWFNLIKXPW-CYBMUJFWSA-N 0.000 claims 2
- JRUMJUOFDGKDDW-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5-amino-6-ethoxypyrazin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OCC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 JRUMJUOFDGKDDW-CYBMUJFWSA-N 0.000 claims 2
- ZREUAANSOWEBLC-OAHLLOKOSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyridin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(N)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 ZREUAANSOWEBLC-OAHLLOKOSA-N 0.000 claims 2
- JDERYWBTAWGGPK-OAHLLOKOSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyridin-2-yl)-4-fluorophenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(N)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=C1 JDERYWBTAWGGPK-OAHLLOKOSA-N 0.000 claims 2
- MEGJRXVVTLBCOM-OAHLLOKOSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyridin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(N)C(OC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 MEGJRXVVTLBCOM-OAHLLOKOSA-N 0.000 claims 2
- GSOFQMUSKWIILK-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5-chloro-4-methoxypyrimidin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(Cl)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 GSOFQMUSKWIILK-CYBMUJFWSA-N 0.000 claims 2
- CTCIDUPLFJLLEX-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5-fluoro-4-methoxypyrimidin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(F)C(OC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 CTCIDUPLFJLLEX-CYBMUJFWSA-N 0.000 claims 2
- GEVQNWGODDAVJD-OAHLLOKOSA-N (7r)-2-amino-7-[2-(6-ethoxypyrazin-2-yl)-4-fluorophenyl]-4-ethyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CCOC1=CN=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(CC)N=C(N)N=C3C2)=N1 GEVQNWGODDAVJD-OAHLLOKOSA-N 0.000 claims 2
- JRWDAMDIXNLHPV-CQSZACIVSA-N (7r)-2-amino-7-[2-(6-ethoxypyrazin-2-yl)-4-fluorophenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CCOC1=CN=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=N1 JRWDAMDIXNLHPV-CQSZACIVSA-N 0.000 claims 2
- BGOLLOXAKPBNOR-CQSZACIVSA-N (7r)-2-amino-7-[2-(6-ethoxypyrazin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CCOC1=CN=CC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 BGOLLOXAKPBNOR-CQSZACIVSA-N 0.000 claims 2
- YZMLUOHUAMGPGS-MRXNPFEDSA-N (7r)-2-amino-7-[2-(6-ethoxypyridin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CCOC1=CC=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 YZMLUOHUAMGPGS-MRXNPFEDSA-N 0.000 claims 2
- KVFSDPAXFWZEOO-CYBMUJFWSA-N (7r)-2-amino-7-[2-(6-methoxypyrazin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CN=CC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 KVFSDPAXFWZEOO-CYBMUJFWSA-N 0.000 claims 2
- LQRMWIFHAFUBHY-CYBMUJFWSA-N (7r)-2-amino-7-[2-(6-methoxypyrazin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CN=CC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=N1 LQRMWIFHAFUBHY-CYBMUJFWSA-N 0.000 claims 2
- XTFUULJHEFTUJD-OAHLLOKOSA-N (7r)-2-amino-7-[2-(6-methoxypyridin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=CC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=N1 XTFUULJHEFTUJD-OAHLLOKOSA-N 0.000 claims 2
- WJIVZYGWMWGPEU-QGZVFWFLSA-N (7r)-2-amino-7-[4-fluoro-2-(3-methylphenyl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CC1=CC=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=C1 WJIVZYGWMWGPEU-QGZVFWFLSA-N 0.000 claims 2
- URIQODZTLUYWGV-MRXNPFEDSA-N (7r)-2-amino-7-[4-fluoro-2-(4-fluoro-2-methoxyphenyl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC(F)=CC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=CN=C(N)N=C2C1 URIQODZTLUYWGV-MRXNPFEDSA-N 0.000 claims 2
- BKSRJXJPZGILQE-CYBMUJFWSA-N (7r)-2-amino-7-[4-fluoro-2-(4-methoxypyrimidin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 BKSRJXJPZGILQE-CYBMUJFWSA-N 0.000 claims 2
- DAUZFWLDXPXYFO-QGZVFWFLSA-N (7r)-2-amino-7-[4-fluoro-2-(4-methylphenyl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=CC(C)=CC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=CN=C(N)N=C2C1 DAUZFWLDXPXYFO-QGZVFWFLSA-N 0.000 claims 2
- NYVDVTHQVSBUIY-MRXNPFEDSA-N (7r)-2-amino-7-[4-fluoro-2-(4-pyrrolidin-1-ylpyrimidin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)C)=CC=C(F)C=C1C(N=1)=NC=CC=1N1CCCC1 NYVDVTHQVSBUIY-MRXNPFEDSA-N 0.000 claims 2
- DKQUDOVNDMRXNZ-CYBMUJFWSA-N (7r)-2-amino-7-[4-fluoro-2-(5-methoxythiophen-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound S1C(OC)=CC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=C(C)N=C(N)N=C2C1 DKQUDOVNDMRXNZ-CYBMUJFWSA-N 0.000 claims 2
- 206010051066 Gastrointestinal stromal tumour Diseases 0.000 claims 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 201000011243 gastrointestinal stromal tumor Diseases 0.000 claims 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 229910052727 yttrium Inorganic materials 0.000 claims 2
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- KLQLELHYCUTHSY-CQSZACIVSA-N (7r)-2-amino-7-[2-(2-ethoxy-1,3-thiazol-4-yl)-4-methoxyphenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound S1C(OCC)=NC(C=2C(=CC=C(OC)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 KLQLELHYCUTHSY-CQSZACIVSA-N 0.000 claims 1
- XREFELMPQYYTQL-CYBMUJFWSA-N (7r)-2-amino-7-[2-(2-ethoxy-1,3-thiazol-4-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound S1C(OCC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 XREFELMPQYYTQL-CYBMUJFWSA-N 0.000 claims 1
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- UWFWRCHZCOUSLE-CQSZACIVSA-N (7r)-2-amino-7-[2-(4-methoxy-5-methylpyrimidin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(C)C(OC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 UWFWRCHZCOUSLE-CQSZACIVSA-N 0.000 claims 1
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- ABDXUMYYQCZDEM-OAHLLOKOSA-N (7r)-2-amino-7-[2-(5-amino-6-ethoxypyrazin-2-yl)-4-ethoxyphenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C=1C(OCC)=CC=C([C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)C=1C1=CN=C(N)C(OCC)=N1 ABDXUMYYQCZDEM-OAHLLOKOSA-N 0.000 claims 1
- KTNKZWOMALPZFU-CQSZACIVSA-N (7r)-2-amino-7-[2-(5-amino-6-ethoxypyrazin-2-yl)-4-fluorophenyl]-4-ethyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OCC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(CC)N=C(N)N=C3C2)=C1 KTNKZWOMALPZFU-CQSZACIVSA-N 0.000 claims 1
- ZKSUZLKXPDCNJT-CQSZACIVSA-N (7r)-2-amino-7-[2-(5-amino-6-ethoxypyrazin-2-yl)-4-methoxyphenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OCC)=NC(C=2C(=CC=C(OC)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 ZKSUZLKXPDCNJT-CQSZACIVSA-N 0.000 claims 1
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- DZVNPRWMBZCFPD-CQSZACIVSA-N (7r)-2-amino-7-[2-(5-amino-6-ethylpyrazin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(CC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 DZVNPRWMBZCFPD-CQSZACIVSA-N 0.000 claims 1
- UBZCNOJGKIKFTO-GFCCVEGCSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 UBZCNOJGKIKFTO-GFCCVEGCSA-N 0.000 claims 1
- ZTXPMQQFANTVSM-OAQYLSRUSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)-4-fluorophenyl]-6-[(2-chlorophenyl)methyl]-4-methyl-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2N(C(=O)C3=C(C)N=C(N)N=C3C2)CC=2C(=CC=CC=2)Cl)=C1 ZTXPMQQFANTVSM-OAQYLSRUSA-N 0.000 claims 1
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- LHIAMNXIPIYSRC-OAQYLSRUSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)-4-fluorophenyl]-6-[(4-fluorophenyl)methyl]-4-methyl-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2N(C(=O)C3=C(C)N=C(N)N=C3C2)CC=2C=CC(F)=CC=2)=C1 LHIAMNXIPIYSRC-OAQYLSRUSA-N 0.000 claims 1
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- ZOJAOSAXIHOMRQ-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)phenyl]-4-ethyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)CC)=CC=CC=C1C1=CN=C(N)C(OC)=N1 ZOJAOSAXIHOMRQ-CYBMUJFWSA-N 0.000 claims 1
- URKCHWNTUXQPQT-GFCCVEGCSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 URKCHWNTUXQPQT-GFCCVEGCSA-N 0.000 claims 1
- XIXQWXAXKHFMOV-GFCCVEGCSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N)C(OC)=NC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=C1 XIXQWXAXKHFMOV-GFCCVEGCSA-N 0.000 claims 1
- AMCUQIOCNNSZOX-CQSZACIVSA-N (7r)-2-amino-7-[2-(6-ethoxypyrazin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CCOC1=CN=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 AMCUQIOCNNSZOX-CQSZACIVSA-N 0.000 claims 1
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- YYVZNVJHYCNNAS-OAHLLOKOSA-N (7r)-2-amino-7-[2-(6-methoxypyridin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=CC(C=2C(=CC=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 YYVZNVJHYCNNAS-OAHLLOKOSA-N 0.000 claims 1
- DQKUYPMPRLSRJL-CQSZACIVSA-N (7r)-2-amino-7-[2-[5-(dimethylamino)-6-methoxypyrazin-2-yl]-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(N(C)C)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 DQKUYPMPRLSRJL-CQSZACIVSA-N 0.000 claims 1
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- NEBIQJIIOIAQDK-CQSZACIVSA-N (7r)-2-amino-7-[4-fluoro-2-(2-fluoropyridin-3-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)C)=CC=C(F)C=C1C1=CC=CN=C1F NEBIQJIIOIAQDK-CQSZACIVSA-N 0.000 claims 1
- ZDVWPCBCFQRVOL-GFCCVEGCSA-N (7r)-2-amino-7-[4-fluoro-2-(2-methoxy-1,3-thiazol-5-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound S1C(OC)=NC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=C(C)N=C(N)N=C2C1 ZDVWPCBCFQRVOL-GFCCVEGCSA-N 0.000 claims 1
- KALCIQWJZRPDNY-MRXNPFEDSA-N (7r)-2-amino-7-[4-fluoro-2-(2-methoxyphenyl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=CC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=CN=C(N)N=C2C1 KALCIQWJZRPDNY-MRXNPFEDSA-N 0.000 claims 1
- RGMRIVCMJKMUGX-HXUWFJFHSA-N (7r)-2-amino-7-[4-fluoro-2-(2-methoxypyridin-3-yl)phenyl]-4-methyl-6-(2-methylpropyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=NC=CC=C1C1=CC(F)=CC=C1[C@@H]1N(CC(C)C)C(=O)C2=C(C)N=C(N)N=C2C1 RGMRIVCMJKMUGX-HXUWFJFHSA-N 0.000 claims 1
- XPUWYJKHTWTOBQ-OAQYLSRUSA-N (7r)-2-amino-7-[4-fluoro-2-(2-methoxypyridin-3-yl)phenyl]-4-methyl-6-(3-methylbutyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=NC=CC=C1C1=CC(F)=CC=C1[C@@H]1N(CCC(C)C)C(=O)C2=C(C)N=C(N)N=C2C1 XPUWYJKHTWTOBQ-OAQYLSRUSA-N 0.000 claims 1
- KDONHFIXUCEHJH-QGZVFWFLSA-N (7r)-2-amino-7-[4-fluoro-2-(2-methylphenyl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CC1=CC=CC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=CN=C(N)N=C2C1 KDONHFIXUCEHJH-QGZVFWFLSA-N 0.000 claims 1
- MJWHLLCUDBSQTP-QGZVFWFLSA-N (7r)-2-amino-7-[4-fluoro-2-(4-fluoro-2-methylphenyl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CC1=CC(F)=CC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=CN=C(N)N=C2C1 MJWHLLCUDBSQTP-QGZVFWFLSA-N 0.000 claims 1
- IAKZMEKRMJBGOI-CQSZACIVSA-N (7r)-2-amino-7-[4-fluoro-2-(4-methoxy-5-methylpyrimidin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(C)C(OC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 IAKZMEKRMJBGOI-CQSZACIVSA-N 0.000 claims 1
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- FJMVDJBVWSKJEB-LLVKDONJSA-N (7r)-2-amino-7-[4-fluoro-2-(5-methoxy-1,3,4-oxadiazol-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound O1C(OC)=NN=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=C(C)N=C(N)N=C2C1 FJMVDJBVWSKJEB-LLVKDONJSA-N 0.000 claims 1
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- MIOGXGVTLHKICS-HXUWFJFHSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyrazin-2-yl)phenyl]-4-methyl-6-(3-methylbutyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CN=CC(C=2C(=CC=C(F)C=2)[C@@H]2N(C(=O)C3=C(C)N=C(N)N=C3C2)CCC(C)C)=N1 MIOGXGVTLHKICS-HXUWFJFHSA-N 0.000 claims 1
- AQUWQQXPWXUZFH-OAQYLSRUSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyrazin-2-yl)phenyl]-4-methyl-6-(oxan-4-ylmethyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CN=CC(C=2C(=CC=C(F)C=2)[C@@H]2N(C(=O)C3=C(C)N=C(N)N=C3C2)CC2CCOCC2)=N1 AQUWQQXPWXUZFH-OAQYLSRUSA-N 0.000 claims 1
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- XRFHWSYKRFEPRA-CYBMUJFWSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyrazin-2-yl)phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CN=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 XRFHWSYKRFEPRA-CYBMUJFWSA-N 0.000 claims 1
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- HGAWINPTRRJJMQ-CYBMUJFWSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyrazin-2-yl)phenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CN=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=CN=C(N)N=C3C2)=N1 HGAWINPTRRJJMQ-CYBMUJFWSA-N 0.000 claims 1
- QDKJJHPEDAWSFV-HXUWFJFHSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyridin-2-yl)phenyl]-4-methyl-6-(2-methylpropyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=CC(C=2C(=CC=C(F)C=2)[C@@H]2N(C(=O)C3=C(C)N=C(N)N=C3C2)CC(C)C)=N1 QDKJJHPEDAWSFV-HXUWFJFHSA-N 0.000 claims 1
- SHRULSHFCCBDNO-OAQYLSRUSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyridin-2-yl)phenyl]-4-methyl-6-(3-methylbutyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=CC(C=2C(=CC=C(F)C=2)[C@@H]2N(C(=O)C3=C(C)N=C(N)N=C3C2)CCC(C)C)=N1 SHRULSHFCCBDNO-OAQYLSRUSA-N 0.000 claims 1
- QANWJNBGIFWSKZ-JOCHJYFZSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyridin-2-yl)phenyl]-4-methyl-6-(oxan-4-ylmethyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=CC(C=2C(=CC=C(F)C=2)[C@@H]2N(C(=O)C3=C(C)N=C(N)N=C3C2)CC2CCOCC2)=N1 QANWJNBGIFWSKZ-JOCHJYFZSA-N 0.000 claims 1
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- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims 1
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 1
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- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims 1
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 claims 1
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- 208000008839 Kidney Neoplasms Diseases 0.000 claims 1
- 239000005517 L01XE01 - Imatinib Substances 0.000 claims 1
- 239000005551 L01XE03 - Erlotinib Substances 0.000 claims 1
- 239000002147 L01XE04 - Sunitinib Substances 0.000 claims 1
- 239000005511 L01XE05 - Sorafenib Substances 0.000 claims 1
- 208000028018 Lymphocytic leukaemia Diseases 0.000 claims 1
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- 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 claims 1
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims 1
- 208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims 1
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 1
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- 229940123237 Taxane Drugs 0.000 claims 1
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- 229940122803 Vinca alkaloid Drugs 0.000 claims 1
- 229940045799 anthracyclines and related substance Drugs 0.000 claims 1
- VSRXQHXAPYXROS-UHFFFAOYSA-N azanide;cyclobutane-1,1-dicarboxylic acid;platinum(2+) Chemical compound [NH2-].[NH2-].[Pt+2].OC(=O)C1(C(O)=O)CCC1 VSRXQHXAPYXROS-UHFFFAOYSA-N 0.000 claims 1
- 210000000481 breast Anatomy 0.000 claims 1
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- 210000003679 cervix uteri Anatomy 0.000 claims 1
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims 1
- 229960004316 cisplatin Drugs 0.000 claims 1
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- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 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
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 229960004397 cyclophosphamide Drugs 0.000 claims 1
- 229960000605 dexrazoxane Drugs 0.000 claims 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229960001433 erlotinib Drugs 0.000 claims 1
- AAKJLRGGTJKAMG-UHFFFAOYSA-N erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 claims 1
- 210000003238 esophagus Anatomy 0.000 claims 1
- 229960002949 fluorouracil Drugs 0.000 claims 1
- VVIAGPKUTFNRDU-ABLWVSNPSA-N folinic acid Chemical compound C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-ABLWVSNPSA-N 0.000 claims 1
- 235000008191 folinic acid Nutrition 0.000 claims 1
- 239000011672 folinic acid Substances 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 210000000232 gallbladder Anatomy 0.000 claims 1
- 229960005277 gemcitabine Drugs 0.000 claims 1
- SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 claims 1
- 208000005017 glioblastoma Diseases 0.000 claims 1
- 210000003128 head Anatomy 0.000 claims 1
- KTUFNOKKBVMGRW-UHFFFAOYSA-N imatinib Chemical compound C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 claims 1
- 229960002411 imatinib Drugs 0.000 claims 1
- 229960004768 irinotecan Drugs 0.000 claims 1
- UWKQSNNFCGGAFS-XIFFEERXSA-N irinotecan Chemical compound C1=C2C(CC)=C3CN(C(C4=C([C@@](C(=O)OC4)(O)CC)C=4)=O)C=4C3=NC2=CC=C1OC(=O)N(CC1)CCC1N1CCCCC1 UWKQSNNFCGGAFS-XIFFEERXSA-N 0.000 claims 1
- 201000010982 kidney cancer Diseases 0.000 claims 1
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- 208000003747 lymphoid leukemia Diseases 0.000 claims 1
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- 238000000034 method Methods 0.000 claims 1
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- 208000025113 myeloid leukemia Diseases 0.000 claims 1
- 208000025189 neoplasm of testis Diseases 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 210000001672 ovary Anatomy 0.000 claims 1
- 210000000496 pancreas Anatomy 0.000 claims 1
- 210000004197 pelvis Anatomy 0.000 claims 1
- 210000003800 pharynx Anatomy 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 210000002307 prostate Anatomy 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 206010038038 rectal cancer Diseases 0.000 claims 1
- 201000001275 rectum cancer Diseases 0.000 claims 1
- 229960004641 rituximab Drugs 0.000 claims 1
- 210000000813 small intestine Anatomy 0.000 claims 1
- 229960003787 sorafenib Drugs 0.000 claims 1
- 210000002784 stomach Anatomy 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 229960001796 sunitinib Drugs 0.000 claims 1
- WINHZLLDWRZWRT-ATVHPVEESA-N sunitinib Chemical compound CCN(CC)CCNC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C WINHZLLDWRZWRT-ATVHPVEESA-N 0.000 claims 1
- 201000003120 testicular cancer Diseases 0.000 claims 1
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- 229960000303 topotecan Drugs 0.000 claims 1
- UCFGDBYHRUNTLO-QHCPKHFHSA-N topotecan Chemical compound C1=C(O)C(CN(C)C)=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 UCFGDBYHRUNTLO-QHCPKHFHSA-N 0.000 claims 1
- 229960000575 trastuzumab Drugs 0.000 claims 1
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- YCOYDOIWSSHVCK-UHFFFAOYSA-N vatalanib Chemical compound C1=CC(Cl)=CC=C1NC(C1=CC=CC=C11)=NN=C1CC1=CC=NC=C1 YCOYDOIWSSHVCK-UHFFFAOYSA-N 0.000 claims 1
- 229950000578 vatalanib Drugs 0.000 claims 1
- 208000024051 villous adenoma of colon Diseases 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/86—Oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72279605P | 2005-09-30 | 2005-09-30 | |
| US83688606P | 2006-08-09 | 2006-08-09 | |
| PCT/US2006/038181 WO2007041362A1 (en) | 2005-09-30 | 2006-09-28 | 2-amino-7,8-dihydro-6h-pyrido[4,3-d] pyrimidin-5-ones |
| EP06825272A EP1928875B1 (en) | 2005-09-30 | 2006-09-28 | 2-amino-7,8-dihydro-6H-pyrido(4,3-d)pyrimidin-5-ones, process for their preparation and pharmaceutical compositions containing the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME01952B true ME01952B (en) | 2011-12-31 |
Family
ID=37661234
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2011-334A ME01952B (en) | 2005-09-30 | 2006-09-28 | 2-amino-7,8-dihydro-6h-pyrido[4,3-d] pyrimidin-5-ones |
Country Status (31)
| Country | Link |
|---|---|
| US (2) | US7671059B2 (OSRAM) |
| EP (1) | EP1928875B1 (OSRAM) |
| JP (2) | JP5036002B2 (OSRAM) |
| KR (1) | KR101311757B1 (OSRAM) |
| AR (1) | AR058072A1 (OSRAM) |
| AT (1) | ATE514694T1 (OSRAM) |
| AU (1) | AU2006297124B2 (OSRAM) |
| BR (1) | BRPI0616701A2 (OSRAM) |
| CA (1) | CA2624253C (OSRAM) |
| CR (1) | CR9846A (OSRAM) |
| CY (1) | CY1112028T1 (OSRAM) |
| DK (1) | DK1928875T3 (OSRAM) |
| EA (1) | EA016152B1 (OSRAM) |
| EC (1) | ECSP088324A (OSRAM) |
| GE (1) | GEP20115231B (OSRAM) |
| HR (1) | HRP20110655T1 (OSRAM) |
| IL (1) | IL190446A0 (OSRAM) |
| JO (1) | JO2783B1 (OSRAM) |
| MA (1) | MA29885B1 (OSRAM) |
| ME (1) | ME01952B (OSRAM) |
| MY (1) | MY143604A (OSRAM) |
| NO (1) | NO342258B1 (OSRAM) |
| NZ (1) | NZ566914A (OSRAM) |
| PE (1) | PE20070621A1 (OSRAM) |
| PL (1) | PL1928875T3 (OSRAM) |
| PT (1) | PT1928875E (OSRAM) |
| RS (1) | RS51795B (OSRAM) |
| SM (1) | SMP200800029B (OSRAM) |
| TN (1) | TNSN08143A1 (OSRAM) |
| TW (1) | TWI373471B (OSRAM) |
| WO (1) | WO2007041362A1 (OSRAM) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CL2007002994A1 (es) * | 2006-10-19 | 2008-02-08 | Wyeth Corp | Compuestos derivados heterociclicos que contienen sulfamoilo, inhibidores de hsp90; composicion farmaceutica; y uso para el tratamiento del cancer, tal como cancer de mama, de colon y prostata, entre otros. |
| CN101225083A (zh) * | 2007-01-16 | 2008-07-23 | 北京摩力克科技有限公司 | 四氢喹唑啉酮类化合物及其用于制备治疗和预防病毒性疾病的药物的用途 |
| GB2449293A (en) | 2007-05-17 | 2008-11-19 | Evotec | Compounds having Hsp90 inhibitory activity |
| US8071766B2 (en) * | 2008-02-01 | 2011-12-06 | Takeda Pharmaceutical Company Limited | HSP90 inhibitors |
| EP2334379A2 (en) | 2008-09-26 | 2011-06-22 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Host cell kinases as targets for antiviral therapies against hcv infection |
| EP2370103B1 (en) * | 2008-11-28 | 2016-03-23 | Novartis AG | Pharmaceutical combinations comprising an isoxazole derived hsp90-inhibitor and the her2 inhibitor trastuzumab |
| DK2370076T3 (en) * | 2008-11-28 | 2017-04-03 | Novartis Ag | Pharmaceutical combination comprising an Hsp 90 inhibitor and an mTOR inhibitor |
| CN102227220A (zh) * | 2008-11-28 | 2011-10-26 | 诺瓦提斯公司 | 用于治疗性治疗的Hsp90抑制剂 |
| AR075180A1 (es) | 2009-01-29 | 2011-03-16 | Novartis Ag | Formulaciones orales solidas de una pirido-pirimidinona |
| AR077405A1 (es) | 2009-07-10 | 2011-08-24 | Sanofi Aventis | Derivados del indol inhibidores de hsp90, composiciones que los contienen y utilizacion de los mismos para el tratamiento del cancer |
| FR2949467B1 (fr) | 2009-09-03 | 2011-11-25 | Sanofi Aventis | Nouveaux derives de 5,6,7,8-tetrahydroindolizine inhibiteurs d'hsp90, compositions les contenant et utilisation |
| KR101690358B1 (ko) | 2009-10-29 | 2017-01-09 | 제노스코 | 키나아제 억제제 |
| WO2012104823A2 (en) | 2011-02-04 | 2012-08-09 | Novartis Ag | Pyridopyrimidinone compounds in the treatment of neurodegenerative diseases |
| EP2766015A1 (en) | 2011-10-14 | 2014-08-20 | Novartis AG | 2-carboxamide cycloamino urea derivatives in combination with hsp90 inhibitors for the treatment of proliferative diseases |
| ITTO20111013A1 (it) | 2011-11-03 | 2013-05-04 | Dac Srl | Composti farmaceutici |
| CN103664938A (zh) * | 2012-09-12 | 2014-03-26 | 山东亨利医药科技有限责任公司 | 含有嘧啶并环的syk抑制剂 |
| RU2015121424A (ru) | 2012-11-07 | 2016-12-27 | Новартис Аг | Комбинированная терапия |
| US9677907B2 (en) * | 2013-03-14 | 2017-06-13 | Itron Inc | Intelligent receptacle |
| GB201306610D0 (en) * | 2013-04-11 | 2013-05-29 | Almac Discovery Ltd | Pharmaceutical compounds |
| KR101767859B1 (ko) * | 2013-09-30 | 2017-08-11 | 다이호야쿠힌고교 가부시키가이샤 | 아자 2 고리형 화합물을 사용한 암 병용 요법 |
| JP2017525734A (ja) * | 2014-09-02 | 2017-09-07 | ピエール、ファーブル、メディカマン | 癌の治療において有用なイソキノリノン誘導体 |
| KR20160035411A (ko) * | 2014-09-23 | 2016-03-31 | 주식회사 오스코텍 | LRRK2 (Leucine Rich Repeat Kinase 2) 키나제 억제제로서의 피리도피리미딘 유도체 화합물 |
| KR101653560B1 (ko) * | 2016-02-02 | 2016-09-12 | 한국화학연구원 | 신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물 |
| RU2629599C1 (ru) * | 2016-09-28 | 2017-08-30 | Государственное бюджетное учреждение здравоохранения Московской области "Московский областной научно-исследовательский клинический институт им. М.Ф. Владимирского" (ГБУЗ МО МОНИКИ им. М.Ф. Владимирского) | Способ химиолучевого лечения опухолей прямой кишки и анального канала |
| JP7229158B2 (ja) | 2017-06-09 | 2023-02-27 | 中外製薬株式会社 | Ｎ－置換アミノ酸を含むペプチドの合成方法 |
| US20230295108A1 (en) * | 2020-06-26 | 2023-09-21 | Nihon Nohyaku Co., Ltd. | Aryltetrahydropyridine derivative or salt thereof, insecticidal agent containing the compound, and method of use thereof |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6165873A (ja) * | 1984-09-07 | 1986-04-04 | Mitsui Petrochem Ind Ltd | ２−ピペラジノピリミジン誘導体 |
| CA1307786C (en) | 1984-12-14 | 1992-09-22 | Keiichi Yokoyama | Quinazoline derivatives and antihypertensive preparations containing same as effective components |
| MA21177A1 (fr) * | 1987-02-11 | 1988-10-01 | May & Baker Ltd | Diones cycliques. |
| KR100639772B1 (ko) * | 2001-02-12 | 2006-10-30 | 에프. 호프만-라 로슈 아게 | 6-치환된 피리도-피리미딘 |
| DE102004018198A1 (de) | 2004-04-15 | 2005-11-03 | Merck Patent Gmbh | Sulfonamide |
| EP2332527A3 (en) | 2004-10-20 | 2011-11-16 | Resverlogix Corp. | Flavanoids and Isoflavanoids for the prevention and treatment of cardiovascular diseases |
| WO2006074293A2 (en) | 2005-01-07 | 2006-07-13 | President And Fellows Of Harvard College | Bicyclic dihydropyrimidines as eg5 inhibitors |
| US20070027150A1 (en) | 2005-04-14 | 2007-02-01 | Bellamacina Cornelia R | 2-Amino-quinazolin-5-ones |
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- 2006-09-28 SM SM200800029T patent/SMP200800029B/it unknown
- 2006-09-28 KR KR1020087010134A patent/KR101311757B1/ko not_active Expired - Fee Related
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- 2006-09-28 AR ARP060104292A patent/AR058072A1/es unknown
- 2006-09-28 US US11/541,462 patent/US7671059B2/en active Active
- 2006-09-28 PL PL06825272T patent/PL1928875T3/pl unknown
- 2006-09-28 RS RS20110334A patent/RS51795B/sr unknown
- 2006-09-28 AU AU2006297124A patent/AU2006297124B2/en not_active Ceased
- 2006-09-28 PE PE2006001177A patent/PE20070621A1/es not_active Application Discontinuation
- 2006-09-28 AT AT06825272T patent/ATE514694T1/de active
- 2006-09-28 MY MYPI20080862A patent/MY143604A/en unknown
- 2006-09-29 TW TW095136162A patent/TWI373471B/zh not_active IP Right Cessation
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2008
- 2008-03-26 IL IL190446A patent/IL190446A0/en not_active IP Right Cessation
- 2008-03-28 CR CR9846A patent/CR9846A/es unknown
- 2008-03-28 EC EC2008008324A patent/ECSP088324A/es unknown
- 2008-03-28 TN TNP2008000143A patent/TNSN08143A1/en unknown
- 2008-04-24 MA MA30873A patent/MA29885B1/fr unknown
- 2008-04-30 NO NO20082069A patent/NO342258B1/no not_active IP Right Cessation
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2009
- 2009-07-31 US US12/462,302 patent/US20100004237A1/en not_active Abandoned
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2011
- 2011-08-09 CY CY20111100758T patent/CY1112028T1/el unknown
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2012
- 2012-05-25 JP JP2012119613A patent/JP2012158611A/ja not_active Withdrawn
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