HRP20110655T1 - 2-amino-7,8-dihidro-6h-pirido(4,3-d)pirimidin-5-oni, postupak njihove proizvodnje i farmaceutski sastavi koji ih sadrže - Google Patents
2-amino-7,8-dihidro-6h-pirido(4,3-d)pirimidin-5-oni, postupak njihove proizvodnje i farmaceutski sastavi koji ih sadrže Download PDFInfo
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- HRP20110655T1 HRP20110655T1 HR20110655T HRP20110655T HRP20110655T1 HR P20110655 T1 HRP20110655 T1 HR P20110655T1 HR 20110655 T HR20110655 T HR 20110655T HR P20110655 T HRP20110655 T HR P20110655T HR P20110655 T1 HRP20110655 T1 HR P20110655T1
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- Prior art keywords
- amino
- phenyl
- pyrimidin
- methyl
- fluoro
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- 238000000034 method Methods 0.000 title claims 2
- 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
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 50
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 30
- 239000001257 hydrogen Substances 0.000 claims abstract 30
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 23
- 125000003118 aryl group Chemical group 0.000 claims abstract 21
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 14
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract 14
- 150000003839 salts Chemical class 0.000 claims abstract 13
- 125000000392 cycloalkenyl group Chemical group 0.000 claims abstract 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 10
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract 6
- 150000002367 halogens Chemical class 0.000 claims abstract 6
- 150000001356 alkyl thiols Chemical class 0.000 claims abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 4
- 150000003573 thiols Chemical class 0.000 claims abstract 4
- -1 2-methyl-2-morpholinopropyl Chemical group 0.000 claims 320
- 150000002431 hydrogen Chemical group 0.000 claims 11
- 206010028980 Neoplasm Diseases 0.000 claims 10
- 125000001475 halogen functional group Chemical group 0.000 claims 10
- 201000011510 cancer Diseases 0.000 claims 9
- 125000001041 indolyl group Chemical group 0.000 claims 7
- 125000003373 pyrazinyl 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
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000003545 alkoxy group Chemical group 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
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 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
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 125000002098 pyridazinyl group Chemical group 0.000 claims 3
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 3
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 3
- 125000001425 triazolyl group Chemical group 0.000 claims 3
- 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
- MVWLENRNKYYEID-MRXNPFEDSA-N (7r)-2-amino-7-[2-(2,3-dimethoxyphenyl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=CC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1OC MVWLENRNKYYEID-MRXNPFEDSA-N 0.000 claims 2
- OWKFMMGDGVSSCH-CQSZACIVSA-N (7r)-2-amino-7-[2-(2,4-dimethoxypyrimidin-5-yl)-4-fluorophenyl]-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=NC(OC)=NC=C1C1=CC(F)=CC=C1[C@@H]1NC(=O)C2=CN=C(N)N=C2C1 OWKFMMGDGVSSCH-CQSZACIVSA-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
- BGTRYMGNQMHSTP-CQSZACIVSA-N (7r)-2-amino-7-[2-(4-ethoxy-5-fluoropyrimidin-2-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C1=C(F)C(OCC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 BGTRYMGNQMHSTP-CQSZACIVSA-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
- 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 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
- 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 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
- 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
- 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 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
- GZHQNPWPYAHOLX-SECBINFHSA-N (7r)-2-amino-7-[5-(6-methoxypyrazin-2-yl)-1,3-thiazol-4-yl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CN=CC(C2=C(N=CS2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=N1 GZHQNPWPYAHOLX-SECBINFHSA-N 0.000 claims 2
- PSRJRRKMWYGYOW-LLVKDONJSA-N 2-[(7r)-2-amino-4-methyl-5-oxo-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-7-yl]-5-fluorobenzonitrile Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)C)=CC=C(F)C=C1C#N PSRJRRKMWYGYOW-LLVKDONJSA-N 0.000 claims 2
- BDTRIDKONHOQQN-UHFFFAOYSA-N 4h-pyrimidin-5-one Chemical compound O=C1CN=CN=C1 BDTRIDKONHOQQN-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-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
- 101100074998 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) nmp-2 gene Proteins 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 201000011243 gastrointestinal stromal tumor Diseases 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
- 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
- BMKDZUISNHGIBY-ZETCQYMHSA-N (+)-dexrazoxane Chemical compound C([C@H](C)N1CC(=O)NC(=O)C1)N1CC(=O)NC(=O)C1 BMKDZUISNHGIBY-ZETCQYMHSA-N 0.000 claims 1
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- CNWJBTHUHMAMCT-CQSZACIVSA-N (7r)-2-amino-7-(2-cyclopentyloxy-4-fluorophenyl)-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=C1OC1CCCC1 CNWJBTHUHMAMCT-CQSZACIVSA-N 0.000 claims 1
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- IHBWMFSUJZBNHS-CQSZACIVSA-N (7r)-2-amino-7-(2-cyclopentyloxyphenyl)-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=C1OC1CCCC1 IHBWMFSUJZBNHS-CQSZACIVSA-N 0.000 claims 1
- WDXWMNUYDISCET-GFCCVEGCSA-N (7r)-2-amino-7-(4-fluoro-2-propan-2-yloxyphenyl)-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound CC(C)OC1=CC(F)=CC=C1[C@@H]1NC(=O)C2=C(C)N=C(N)N=C2C1 WDXWMNUYDISCET-GFCCVEGCSA-N 0.000 claims 1
- GTSUIIPROYHHQL-SNVBAGLBSA-N (7r)-2-amino-7-(4-fluorophenyl)-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=C1 GTSUIIPROYHHQL-SNVBAGLBSA-N 0.000 claims 1
- UDGCXCCSDQNGSM-SNVBAGLBSA-N (7r)-2-amino-7-(4-fluorophenyl)-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=C1 UDGCXCCSDQNGSM-SNVBAGLBSA-N 0.000 claims 1
- XCIDJUGADVTBOY-ZCFIWIBFSA-N (7r)-2-amino-7-(5-bromo-1,3-thiazol-4-yl)-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C=1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2)C)N=CSC=1Br XCIDJUGADVTBOY-ZCFIWIBFSA-N 0.000 claims 1
- WYLBBGPVCWUWRF-QGZVFWFLSA-N (7r)-2-amino-7-[2-(2,4-dimethoxypyrimidin-5-yl)-4-fluorophenyl]-6-ethyl-4-methyl-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@@H]2N(C(C3=C(C)N=C(N)N=C3C2)=O)CC)=CC=C(F)C=C1C1=CN=C(OC)N=C1OC WYLBBGPVCWUWRF-QGZVFWFLSA-N 0.000 claims 1
- QIVRZIJNOSPKAE-CYBMUJFWSA-N (7r)-2-amino-7-[2-(2-ethoxy-1,3-thiazol-4-yl)-4-fluorophenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound S1C(OCC)=NC(C=2C(=CC=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 QIVRZIJNOSPKAE-CYBMUJFWSA-N 0.000 claims 1
- 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
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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
- SDSLCGXITKIRSW-LJQANCHMSA-N (7r)-2-amino-7-[2-(5,6-dimethoxypyrazin-2-yl)-4-fluorophenyl]-4-methyl-6-(2-methylpropyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(OC)C(OC)=NC=C1C1=CC(F)=CC=C1[C@@H]1N(CC(C)C)C(=O)C2=C(C)N=C(N)N=C2C1 SDSLCGXITKIRSW-LJQANCHMSA-N 0.000 claims 1
- DSICYNWBHUOVGE-HXUWFJFHSA-N (7r)-2-amino-7-[2-(5,6-dimethoxypyrazin-2-yl)-4-fluorophenyl]-4-methyl-6-(3-methylbutyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(OC)C(OC)=NC=C1C1=CC(F)=CC=C1[C@@H]1N(CCC(C)C)C(=O)C2=C(C)N=C(N)N=C2C1 DSICYNWBHUOVGE-HXUWFJFHSA-N 0.000 claims 1
- 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
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- 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
- 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
- KWVBOJGVFKJJON-CQSZACIVSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-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(OC)=N1 KWVBOJGVFKJJON-CQSZACIVSA-N 0.000 claims 1
- CMXWDYUOYPGVEA-GOSISDBHSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)-4-fluorophenyl]-4-methyl-6-(2-methylpropyl)-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(C)C)=C1 CMXWDYUOYPGVEA-GOSISDBHSA-N 0.000 claims 1
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- 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
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- GDBNZMPFCWOYAX-OAQYLSRUSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)-4-fluorophenyl]-6-[(2-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=CC=2)F)=C1 GDBNZMPFCWOYAX-OAQYLSRUSA-N 0.000 claims 1
- 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
- YLEHSXNUGPZEFG-GFCCVEGCSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)-4-fluorophenyl]-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=CN=C(N)N=C3C2)=C1 YLEHSXNUGPZEFG-GFCCVEGCSA-N 0.000 claims 1
- OJZOYJQVXDIAEP-CYBMUJFWSA-N (7r)-2-amino-7-[2-(5-amino-6-methoxypyrazin-2-yl)-4-methoxyphenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound C=1C(OC)=CC=C([C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)C=1C1=CN=C(N)C(OC)=N1 OJZOYJQVXDIAEP-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
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- 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
- YBVKFZNMXWXMGY-CQSZACIVSA-N (7r)-2-amino-7-[2-[5-(dimethylamino)-6-methoxypyrazin-2-yl]phenyl]-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=CC=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 YBVKFZNMXWXMGY-CQSZACIVSA-N 0.000 claims 1
- VAGCKOKNGOHQSF-CYBMUJFWSA-N (7r)-2-amino-7-[2-[6-methoxy-5-(methylamino)pyrazin-2-yl]phenyl]-4-methyl-7,8-dihydro-6h-pyrido[4,3-d]pyrimidin-5-one Chemical compound N1=C(OC)C(NC)=NC=C1C1=CC=CC=C1[C@@H]1NC(=O)C2=C(C)N=C(N)N=C2C1 VAGCKOKNGOHQSF-CYBMUJFWSA-N 0.000 claims 1
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- BNRHCGPVINGNTO-OAHLLOKOSA-N (7r)-2-amino-7-[4-ethoxy-2-(6-methoxypyrazin-2-yl)phenyl]-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=CC(OC)=N1 BNRHCGPVINGNTO-OAHLLOKOSA-N 0.000 claims 1
- SDVZGIHLCGTWNP-QGZVFWFLSA-N (7r)-2-amino-7-[4-ethoxy-2-(6-methoxypyridin-2-yl)phenyl]-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=CC=CC(OC)=N1 SDVZGIHLCGTWNP-QGZVFWFLSA-N 0.000 claims 1
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- ARFDWRCGNZTJPI-HXUWFJFHSA-N (7r)-2-amino-7-[4-fluoro-2-(2-fluoropyridin-3-yl)phenyl]-4-methyl-6-(3-methylbutyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound C1([C@@H]2N(C(C3=C(C)N=C(N)N=C3C2)=O)CCC(C)C)=CC=C(F)C=C1C1=CC=CN=C1F ARFDWRCGNZTJPI-HXUWFJFHSA-N 0.000 claims 1
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- BNOYRDUPHFYYTI-GFCCVEGCSA-N (7r)-2-amino-7-[4-fluoro-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=C(F)C=2)[C@@H]2NC(=O)C3=C(C)N=C(N)N=C3C2)=C1 BNOYRDUPHFYYTI-GFCCVEGCSA-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
- 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
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- 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
- 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 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
- XCZWEHQTNQUMSG-HXUWFJFHSA-N (7r)-2-amino-7-[4-fluoro-2-(4-methoxypyridin-3-yl)phenyl]-4-methyl-6-(2-methylpropyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=NC=C1C1=CC(F)=CC=C1[C@@H]1N(CC(C)C)C(=O)C2=C(C)N=C(N)N=C2C1 XCZWEHQTNQUMSG-HXUWFJFHSA-N 0.000 claims 1
- RBWYWCZCZNEVKM-OAQYLSRUSA-N (7r)-2-amino-7-[4-fluoro-2-(4-methoxypyridin-3-yl)phenyl]-4-methyl-6-(3-methylbutyl)-7,8-dihydropyrido[4,3-d]pyrimidin-5-one Chemical compound COC1=CC=NC=C1C1=CC(F)=CC=C1[C@@H]1N(CCC(C)C)C(=O)C2=C(C)N=C(N)N=C2C1 RBWYWCZCZNEVKM-OAQYLSRUSA-N 0.000 claims 1
- 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
- OYZQWJNSTBRXOZ-LJQANCHMSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyrazin-2-yl)phenyl]-4-methyl-6-(2-methylpropyl)-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)CC(C)C)=N1 OYZQWJNSTBRXOZ-LJQANCHMSA-N 0.000 claims 1
- 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
- CPEKJNQQDIZMGS-OAQYLSRUSA-N (7r)-2-amino-7-[4-fluoro-2-(6-methoxypyrazin-2-yl)phenyl]-4-methyl-6-(pyridin-3-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)CC=2C=NC=CC=2)=N1 CPEKJNQQDIZMGS-OAQYLSRUSA-N 0.000 claims 1
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- 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
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- 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
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- 208000005017 glioblastoma Diseases 0.000 claims 1
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- 208000032839 leukemia Diseases 0.000 claims 1
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- XORCKRYJJZITCJ-QGZVFWFLSA-N tert-butyl n-[3-[(7r)-2-amino-7-(2-bromo-4-fluorophenyl)-4-methyl-5-oxo-7,8-dihydropyrido[4,3-d]pyrimidin-6-yl]propyl]carbamate Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2CCCNC(=O)OC(C)(C)C)C)=CC=C(F)C=C1Br XORCKRYJJZITCJ-QGZVFWFLSA-N 0.000 claims 1
- PEBJOMJDRGXVDW-JOCHJYFZSA-N tert-butyl n-[3-[(7r)-2-amino-7-(4-fluoro-2-pyridin-3-ylphenyl)-4-methyl-5-oxo-7,8-dihydropyrido[4,3-d]pyrimidin-6-yl]propyl]carbamate Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2CCCNC(=O)OC(C)(C)C)C)=CC=C(F)C=C1C1=CC=CN=C1 PEBJOMJDRGXVDW-JOCHJYFZSA-N 0.000 claims 1
- RYSYTOBNIUXVME-OAQYLSRUSA-N tert-butyl n-[3-[(7r)-2-amino-7-[4-fluoro-2-(2-fluoropyridin-3-yl)phenyl]-4-methyl-5-oxo-7,8-dihydropyrido[4,3-d]pyrimidin-6-yl]propyl]carbamate Chemical compound C1([C@H]2CC=3N=C(N)N=C(C=3C(=O)N2CCCNC(=O)OC(C)(C)C)C)=CC=C(F)C=C1C1=CC=CN=C1F RYSYTOBNIUXVME-OAQYLSRUSA-N 0.000 claims 1
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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)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (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)
- Hydrogenated Pyridines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| 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 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20110655T1 true HRP20110655T1 (hr) | 2011-10-31 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20110655T HRP20110655T1 (hr) | 2005-09-30 | 2011-09-13 | 2-amino-7,8-dihidro-6h-pirido(4,3-d)pirimidin-5-oni, postupak njihove proizvodnje i farmaceutski sastavi koji ih sadrže |
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|---|---|
| US (2) | US7671059B2 (ja) |
| EP (1) | EP1928875B1 (ja) |
| JP (2) | JP5036002B2 (ja) |
| KR (1) | KR101311757B1 (ja) |
| AR (1) | AR058072A1 (ja) |
| AT (1) | ATE514694T1 (ja) |
| AU (1) | AU2006297124B2 (ja) |
| BR (1) | BRPI0616701A2 (ja) |
| CA (1) | CA2624253C (ja) |
| CR (1) | CR9846A (ja) |
| CY (1) | CY1112028T1 (ja) |
| DK (1) | DK1928875T3 (ja) |
| EA (1) | EA016152B1 (ja) |
| EC (1) | ECSP088324A (ja) |
| GE (1) | GEP20115231B (ja) |
| HK (1) | HK1118823A1 (ja) |
| HR (1) | HRP20110655T1 (ja) |
| IL (1) | IL190446A0 (ja) |
| JO (1) | JO2783B1 (ja) |
| MA (1) | MA29885B1 (ja) |
| ME (1) | ME01952B (ja) |
| MY (1) | MY143604A (ja) |
| NO (1) | NO342258B1 (ja) |
| NZ (1) | NZ566914A (ja) |
| PE (1) | PE20070621A1 (ja) |
| PL (1) | PL1928875T3 (ja) |
| PT (1) | PT1928875E (ja) |
| RS (1) | RS51795B (ja) |
| SM (1) | SMP200800029B (ja) |
| TN (1) | TNSN08143A1 (ja) |
| TW (1) | TWI373471B (ja) |
| WO (1) | WO2007041362A1 (ja) |
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| 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 |
| GEP20125718B (en) * | 2008-02-01 | 2012-12-25 | Takeda Pharmaceuticals Co | Oxim derivatives as hsp90 inhibitors |
| US8759010B2 (en) | 2008-09-26 | 2014-06-24 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Host cell kinases as targets for antiviral therapies against HCV infection |
| CA2742743C (en) * | 2008-11-28 | 2017-05-23 | Novartis Ag | Pharmaceutical combinations comprising a pyrido [4,3-d] pyrimidine derived hsp90-inhibitor and a her2 inhibitor |
| JP2012510444A (ja) * | 2008-11-28 | 2012-05-10 | ノバルティス アーゲー | 治療的処置のためのＨｓｐ９０阻害剤 |
| CA2744937C (en) * | 2008-11-28 | 2017-02-28 | Novartis Ag | Pharmaceutical combination comprising a hsp 90 inhibitor and a mtor inhibitor |
| 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 |
| SG10201407012XA (en) * | 2009-10-29 | 2014-11-27 | Genosco | Kinase inhibitors |
| WO2012104823A2 (en) | 2011-02-04 | 2012-08-09 | Novartis Ag | Pyridopyrimidinone compounds in the treatment of neurodegenerative diseases |
| RU2017119219A (ru) | 2011-10-14 | 2018-11-02 | Новартис Аг | 2-карбоксамид циклоамино производные мочевины в комбинации с ингибиторами hsp90 для лечения пролиферативных заболеваний |
| 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 |
| IN2015DN04175A (ja) | 2012-11-07 | 2015-10-16 | Novartis Ag | |
| 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 |
| EP3053578B1 (en) | 2013-09-30 | 2020-12-23 | Taiho Pharmaceutical Co., Ltd. | Combination cancer therapy using azabicyclo compound |
| 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 |
| CN115916752A (zh) * | 2020-06-26 | 2023-04-04 | 日本农药株式会社 | 芳基四氢吡啶衍生物或其盐类、和含有该化合物的杀虫剂及其使用方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| 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 |
| US4734418A (en) * | 1984-12-14 | 1988-03-29 | Mitsui Petrochemical Industries, Ltd. | Quinazoline compounds and antihypertensives |
| IL85347A0 (en) | 1987-02-11 | 1988-07-31 | May & Baker Ltd | Cyclic diones |
| ATE305303T1 (de) * | 2001-02-12 | 2005-10-15 | Hoffmann La Roche | 6-substituierte pyridopyrimidine |
| DE102004018198A1 (de) * | 2004-04-15 | 2005-11-03 | Merck Patent Gmbh | Sulfonamide |
| CA2584507C (en) | 2004-10-20 | 2016-04-26 | Resverlogix Corp. | Flavanoids and isoflavanoids for the prevention and treatment of cardiovascular diseases |
| US20100152206A1 (en) * | 2005-01-07 | 2010-06-17 | Ralph Mazitschek | Bicyclic Dihydropyrimidines and Uses Thereof |
| AU2006236557A1 (en) * | 2005-04-14 | 2006-10-26 | Novartis Vaccines And Diagnostics Inc. | 2-amino-quinazolin-5-ones as HSP90 inhibitors useful in treating proliferation diseases |
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