JP2015531401A - イミダゾピラジノン骨格を有するｐｄｅ９ｉ - Google Patents
イミダゾピラジノン骨格を有するｐｄｅ９ｉ Download PDFInfo
- Publication number
- JP2015531401A JP2015531401A JP2015535994A JP2015535994A JP2015531401A JP 2015531401 A JP2015531401 A JP 2015531401A JP 2015535994 A JP2015535994 A JP 2015535994A JP 2015535994 A JP2015535994 A JP 2015535994A JP 2015531401 A JP2015531401 A JP 2015531401A
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- JP
- Japan
- Prior art keywords
- imidazo
- pyrazin
- methyl
- azetidin
- fluorophenyl
- 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.)
- Pending
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- MPWOBEOETVOESI-UHFFFAOYSA-N imidazo[4,5-b]pyrazin-2-one Chemical group N1=CC=NC2=NC(=O)N=C21 MPWOBEOETVOESI-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 96
- 238000000034 method Methods 0.000 claims abstract description 19
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 17
- 239000003937 drug carrier Substances 0.000 claims abstract description 9
- 238000002360 preparation method Methods 0.000 claims abstract description 8
- 230000004770 neurodegeneration Effects 0.000 claims abstract description 6
- 208000015122 neurodegenerative disease Diseases 0.000 claims abstract description 6
- -1 8-oxo-3-phenyl-7H-imidazo [1,5-A] pyrazin-6-yl Chemical group 0.000 claims description 65
- 229910052801 chlorine Inorganic materials 0.000 claims description 25
- 229910052731 fluorine Inorganic materials 0.000 claims description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000001072 heteroaryl group Chemical group 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
- 208000024827 Alzheimer disease Diseases 0.000 claims description 15
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 claims description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 13
- 239000003085 diluting agent Substances 0.000 claims description 12
- 201000010099 disease Diseases 0.000 claims description 12
- 238000007363 ring formation reaction Methods 0.000 claims description 10
- 125000004104 aryloxy group Chemical group 0.000 claims description 9
- 239000003814 drug Substances 0.000 claims description 9
- 208000028017 Psychotic disease Diseases 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims description 7
- 241000218236 Cannabis Species 0.000 claims description 7
- 208000036626 Mental retardation Diseases 0.000 claims description 7
- 230000007000 age related cognitive decline Effects 0.000 claims description 7
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 7
- 229960003920 cocaine Drugs 0.000 claims description 7
- 239000000380 hallucinogen Substances 0.000 claims description 7
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 6
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 claims description 6
- 229940025084 amphetamine Drugs 0.000 claims description 6
- 229940005483 opioid analgesics Drugs 0.000 claims description 6
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 claims description 6
- 229950010883 phencyclidine Drugs 0.000 claims description 6
- 208000011963 Substance-induced psychotic disease Diseases 0.000 claims description 5
- 231100000393 Substance-induced psychotic disorder Toxicity 0.000 claims description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- UIIQLHYXQBZHDU-UHFFFAOYSA-N 3-phenyl-6-[(3-phenylazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1CN(C1)CC1C1=CC=CC=C1 UIIQLHYXQBZHDU-UHFFFAOYSA-N 0.000 claims description 2
- ZLOQDIDEFDRYEQ-UHFFFAOYSA-N 3-phenyl-6-[(3-pyrazin-2-yloxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1CN(C1)CC1OC1=CN=CC=N1 ZLOQDIDEFDRYEQ-UHFFFAOYSA-N 0.000 claims description 2
- UJWXNBFXBBWNBN-UHFFFAOYSA-N 3-phenyl-6-[(3-pyrimidin-2-yloxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1CN(C1)CC1OC1=NC=CC=N1 UJWXNBFXBBWNBN-UHFFFAOYSA-N 0.000 claims description 2
- OZWPMNOQMHSJRL-UHFFFAOYSA-N 3-phenyl-6-[(3-quinoxalin-2-yloxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound N=1C=C2C(=O)NC(CN3CC(C3)OC=3N=C4C=CC=CC4=NC=3)=CN2C=1C1=CC=CC=C1 OZWPMNOQMHSJRL-UHFFFAOYSA-N 0.000 claims description 2
- OLZQZZXWANRKEL-UHFFFAOYSA-N 3-phenyl-6-[1-(3-phenylazetidin-1-yl)ethyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1C1=CC=CC=C1 OLZQZZXWANRKEL-UHFFFAOYSA-N 0.000 claims description 2
- DWJFOZLYWSESSK-UHFFFAOYSA-N 3-phenyl-6-[1-(3-pyrimidin-2-yloxyazetidin-1-yl)ethyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1OC1=NC=CC=N1 DWJFOZLYWSESSK-UHFFFAOYSA-N 0.000 claims description 2
- YDZCIMPTHKZBJC-UHFFFAOYSA-N 6-(1-benzyl-4-methylpyrrolidin-3-yl)-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(C=2NC(=O)C3=CN=C(N3C=2)C=2C=CC=CC=2)C(C)CN1CC1=CC=CC=C1 YDZCIMPTHKZBJC-UHFFFAOYSA-N 0.000 claims description 2
- QVLJPVCBNMVOLX-UHFFFAOYSA-N 6-[(3-anilinopyrrolidin-1-yl)methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1CN(C1)CCC1NC1=CC=CC=C1 QVLJPVCBNMVOLX-UHFFFAOYSA-N 0.000 claims description 2
- UWMJSOJFERDASH-UHFFFAOYSA-N 6-[(3-methoxyazetidin-1-yl)methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(OC)CN1CC(NC1=O)=CN2C1=CN=C2C1=CC=CC=C1 UWMJSOJFERDASH-UHFFFAOYSA-N 0.000 claims description 2
- MNFIXJUASSBZOW-UHFFFAOYSA-N 6-[1-(3-methoxyazetidin-1-yl)ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(OC)CN1C(C)C(NC1=O)=CN2C1=CN=C2C1=CC=CC=C1 MNFIXJUASSBZOW-UHFFFAOYSA-N 0.000 claims description 2
- WMIPWRFZOVGSAJ-UHFFFAOYSA-N 6-[1-(3-phenoxyazetidin-1-yl)ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1OC1=CC=CC=C1 WMIPWRFZOVGSAJ-UHFFFAOYSA-N 0.000 claims description 2
- KYRKGOCWXBDKBD-UHFFFAOYSA-N 6-[1-[3-(2-fluorophenoxy)azetidin-1-yl]ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1OC1=CC=CC=C1F KYRKGOCWXBDKBD-UHFFFAOYSA-N 0.000 claims description 2
- YMFXDBVYLGTEJF-UHFFFAOYSA-N 6-[1-[3-(3-fluorophenoxy)azetidin-1-yl]ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1OC1=CC=CC(F)=C1 YMFXDBVYLGTEJF-UHFFFAOYSA-N 0.000 claims description 2
- BYUYQURHJNXKRJ-UHFFFAOYSA-N 6-[1-[3-(4-ethylphenyl)azetidin-1-yl]ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(CC)=CC=C1C1CN(C(C)C=2NC(=O)C3=CN=C(N3C=2)C=2C=CC=CC=2)C1 BYUYQURHJNXKRJ-UHFFFAOYSA-N 0.000 claims description 2
- BGGBTQOCEKKJHN-UHFFFAOYSA-N 6-[1-[3-(4-fluorophenoxy)azetidin-1-yl]ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1OC1=CC=C(F)C=C1 BGGBTQOCEKKJHN-UHFFFAOYSA-N 0.000 claims description 2
- FKKWWRNYEOOBSX-UHFFFAOYSA-N 6-[1-[3-(4-fluorophenyl)azetidin-1-yl]ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1C1=CC=C(F)C=C1 FKKWWRNYEOOBSX-UHFFFAOYSA-N 0.000 claims description 2
- BOPIZTALPMZROL-UHFFFAOYSA-N 6-[1-[3-(6-fluoropyridin-2-yl)oxyazetidin-1-yl]ethyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1OC1=CC=CC(F)=N1 BOPIZTALPMZROL-UHFFFAOYSA-N 0.000 claims description 2
- DXOVFJHHONEJOL-UHFFFAOYSA-N 6-[[3-(2-fluorophenoxy)azetidin-1-yl]methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound FC1=CC=CC=C1OC1CN(CC=2NC(=O)C3=CN=C(N3C=2)C=2C=CC=CC=2)C1 DXOVFJHHONEJOL-UHFFFAOYSA-N 0.000 claims description 2
- OMKMXPNRMOBLJW-UHFFFAOYSA-N 6-[[3-(3-fluorophenoxy)azetidin-1-yl]methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound FC1=CC=CC(OC2CN(CC=3NC(=O)C4=CN=C(N4C=3)C=3C=CC=CC=3)C2)=C1 OMKMXPNRMOBLJW-UHFFFAOYSA-N 0.000 claims description 2
- BCFBUHSRTSXNFB-UHFFFAOYSA-N 6-[[3-(4,6-dimethylpyrimidin-2-yl)oxyazetidin-1-yl]methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound CC1=CC(C)=NC(OC2CN(CC=3NC(=O)C4=CN=C(N4C=3)C=3C=CC=CC=3)C2)=N1 BCFBUHSRTSXNFB-UHFFFAOYSA-N 0.000 claims description 2
- OAMBWTBJNZOALP-UHFFFAOYSA-N 6-[[3-(4-ethylphenyl)azetidin-1-yl]methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(CC)=CC=C1C1CN(CC=2NC(=O)C3=CN=C(N3C=2)C=2C=CC=CC=2)C1 OAMBWTBJNZOALP-UHFFFAOYSA-N 0.000 claims description 2
- CPWSTVGPJSYNMA-UHFFFAOYSA-N 6-[[3-(4-fluorophenoxy)azetidin-1-yl]methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1OC1CN(CC=2NC(=O)C3=CN=C(N3C=2)C=2C=CC=CC=2)C1 CPWSTVGPJSYNMA-UHFFFAOYSA-N 0.000 claims description 2
- MAKIYAKALMRMOD-UHFFFAOYSA-N 6-[[3-(6-fluoropyridin-2-yl)oxyazetidin-1-yl]methyl]-3-phenyl-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound FC1=CC=CC(OC2CN(CC=3NC(=O)C4=CN=C(N4C=3)C=3C=CC=CC=3)C2)=N1 MAKIYAKALMRMOD-UHFFFAOYSA-N 0.000 claims description 2
- DMIUQICEZBGJHR-UHFFFAOYSA-N methyl 1-benzyl-4-(8-oxo-3-phenyl-7h-imidazo[1,5-a]pyrazin-6-yl)pyrrolidine-3-carboxylate Chemical compound C1C(C=2NC(=O)C3=CN=C(N3C=2)C=2C=CC=CC=2)C(C(=O)OC)CN1CC1=CC=CC=C1 DMIUQICEZBGJHR-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims description 2
- 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 claims 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 3
- FKZBSXUJAGAAGL-UHFFFAOYSA-N 1-bromo-3-(4-chlorophenyl)-6-[1-[(4-fluorophenyl)methyl]-4-methylpyrrolidin-3-yl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(C=2NC(=O)C3=C(Br)N=C(N3C=2)C=2C=CC(Cl)=CC=2)C(C)CN1CC1=CC=C(F)C=C1 FKZBSXUJAGAAGL-UHFFFAOYSA-N 0.000 claims 1
- LYDLONHBBHMLKV-UHFFFAOYSA-N 1-bromo-3-(4-fluorophenyl)-6-[1-[(4-fluorophenyl)methyl]-4-methylpyrrolidin-3-yl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(C=2NC(=O)C3=C(Br)N=C(N3C=2)C=2C=CC(F)=CC=2)C(C)CN1CC1=CC=C(F)C=C1 LYDLONHBBHMLKV-UHFFFAOYSA-N 0.000 claims 1
- WZEBNPXEWQABBM-UHFFFAOYSA-N 3-(3,5-difluorophenyl)-6-[[3-(4-methoxyphenyl)azetidin-1-yl]methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(OC)=CC=C1C1CN(CC=2NC(=O)C3=CN=C(N3C=2)C=2C=C(F)C=C(F)C=2)C1 WZEBNPXEWQABBM-UHFFFAOYSA-N 0.000 claims 1
- QWXPAEULRAXJME-UHFFFAOYSA-N 3-(4,4-difluorocyclohexyl)-6-[(3-methoxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(OC)CN1CC(NC1=O)=CN2C1=CN=C2C1CCC(F)(F)CC1 QWXPAEULRAXJME-UHFFFAOYSA-N 0.000 claims 1
- XEVNPWFTIMDURN-UHFFFAOYSA-N 3-(4,4-difluorocyclohexyl)-6-[[3-(4-methoxyphenyl)azetidin-1-yl]methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(OC)=CC=C1C1CN(CC=2NC(=O)C3=CN=C(N3C=2)C2CCC(F)(F)CC2)C1 XEVNPWFTIMDURN-UHFFFAOYSA-N 0.000 claims 1
- QUVZKCAAXZEUKT-UHFFFAOYSA-N 3-(4-chlorophenyl)-6-[1-[(4-fluorophenyl)methyl]-4-methylpyrrolidin-3-yl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(C=2NC(=O)C3=CN=C(N3C=2)C=2C=CC(Cl)=CC=2)C(C)CN1CC1=CC=C(F)C=C1 QUVZKCAAXZEUKT-UHFFFAOYSA-N 0.000 claims 1
- FXDZYGQOMMBTKL-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[(3-phenoxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(C3)OC=3C=CC=CC=3)=CN12 FXDZYGQOMMBTKL-UHFFFAOYSA-N 0.000 claims 1
- FGZIMOPQPLAICG-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[(3-phenoxypyrrolidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(CC3)OC=3C=CC=CC=3)=CN12 FGZIMOPQPLAICG-UHFFFAOYSA-N 0.000 claims 1
- YRNHKKWWMGNSJH-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[(3-phenylmethoxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(C3)OCC=3C=CC=CC=3)=CN12 YRNHKKWWMGNSJH-UHFFFAOYSA-N 0.000 claims 1
- BJRLUBFRQQIWDK-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[(3-pyrazin-2-yloxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(C3)OC=3N=CC=NC=3)=CN12 BJRLUBFRQQIWDK-UHFFFAOYSA-N 0.000 claims 1
- OPPJESMUQLKXLM-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[(3-pyridin-4-yloxyazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(C3)OC=3C=CN=CC=3)=CN12 OPPJESMUQLKXLM-UHFFFAOYSA-N 0.000 claims 1
- FQTKUALMFWAFOT-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[(3-pyrimidin-2-ylazetidin-1-yl)methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(C3)C=3N=CC=CN=3)=CN12 FQTKUALMFWAFOT-UHFFFAOYSA-N 0.000 claims 1
- KZXQDNGEOOWVOT-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[1-(3-methoxyazetidin-1-yl)ethyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(OC)CN1C(C)C(NC1=O)=CN2C1=CN=C2C1=CC=C(F)C=C1 KZXQDNGEOOWVOT-UHFFFAOYSA-N 0.000 claims 1
- VURKBBXXUCMNNY-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[1-(3-propan-2-yloxyazetidin-1-yl)ethyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(OC(C)C)CN1C(C)C(NC1=O)=CN2C1=CN=C2C1=CC=C(F)C=C1 VURKBBXXUCMNNY-UHFFFAOYSA-N 0.000 claims 1
- IXXFEEXROAIYKE-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[1-[(4-fluorophenyl)methyl]-4-methylpyrrolidin-3-yl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(C=2NC(=O)C3=CN=C(N3C=2)C=2C=CC(F)=CC=2)C(C)CN1CC1=CC=C(F)C=C1 IXXFEEXROAIYKE-UHFFFAOYSA-N 0.000 claims 1
- DECWKGNPLGHKNM-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[1-[3-(4-methoxyphenyl)azetidin-1-yl]ethyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(OC)=CC=C1C1CN(C(C)C=2NC(=O)C3=CN=C(N3C=2)C=2C=CC(F)=CC=2)C1 DECWKGNPLGHKNM-UHFFFAOYSA-N 0.000 claims 1
- QAWRXXWLFINXRI-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[1-[3-[4-(trifluoromethoxy)phenoxy]azetidin-1-yl]ethyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C=1N2C(C=3C=CC(F)=CC=3)=NC=C2C(=O)NC=1C(C)N(C1)CC1OC1=CC=C(OC(F)(F)F)C=C1 QAWRXXWLFINXRI-UHFFFAOYSA-N 0.000 claims 1
- KQUHRFKFEIWQQX-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[4-methyl-1-(pyridin-2-ylmethyl)pyrrolidin-3-yl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1C(C=2NC(=O)C3=CN=C(N3C=2)C=2C=CC(F)=CC=2)C(C)CN1CC1=CC=CC=N1 KQUHRFKFEIWQQX-UHFFFAOYSA-N 0.000 claims 1
- RQTYTKFUFIQXRT-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[[3-(4-methoxyphenyl)azetidin-1-yl]methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(OC)=CC=C1C1CN(CC=2NC(=O)C3=CN=C(N3C=2)C=2C=CC(F)=CC=2)C1 RQTYTKFUFIQXRT-UHFFFAOYSA-N 0.000 claims 1
- SNADRBGYEUKACC-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[[3-(6-fluoropyridin-2-yl)oxyazetidin-1-yl]methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(C3)OC=3N=C(F)C=CC=3)=CN12 SNADRBGYEUKACC-UHFFFAOYSA-N 0.000 claims 1
- OQOLKOFSTBTOOE-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-[[3-[3-(trifluoromethyl)phenoxy]azetidin-1-yl]methyl]-7h-imidazo[1,5-a]pyrazin-8-one Chemical compound C1=CC(F)=CC=C1C1=NC=C2C(=O)NC(CN3CC(C3)OC=3C=C(C=CC=3)C(F)(F)F)=CN12 OQOLKOFSTBTOOE-UHFFFAOYSA-N 0.000 claims 1
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- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- C—CHEMISTRY; METALLURGY
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2011001692 | 2011-10-10 | ||
| PCT/EP2012/069936 WO2013053690A1 (en) | 2011-10-10 | 2012-10-09 | Pde9i with imidazo pyrazinone backbone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2015531401A true JP2015531401A (ja) | 2015-11-02 |
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| JP2015535994A Pending JP2015531401A (ja) | 2011-10-10 | 2012-10-09 | イミダゾピラジノン骨格を有するｐｄｅ９ｉ |
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|---|---|
| US (2) | US9643970B2 (https=) |
| EP (2) | EP3121178B1 (https=) |
| JP (1) | JP2015531401A (https=) |
| CN (2) | CN106905324B (https=) |
| AU (2) | AU2012323085B2 (https=) |
| BR (1) | BR112015007731B1 (https=) |
| CA (1) | CA2886885C (https=) |
| HK (1) | HK1211023A1 (https=) |
| IL (2) | IL237836A (https=) |
| IN (1) | IN2015DN02829A (https=) |
| MA (1) | MA37958B1 (https=) |
| MX (2) | MX381326B (https=) |
| SG (1) | SG11201502728WA (https=) |
| TN (1) | TN2015000100A1 (https=) |
| WO (1) | WO2013053690A1 (https=) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019534324A (ja) * | 2016-10-18 | 2019-11-28 | ハー・ルンドベック・アクチエゼルスカベット | Ｐｄｅ１阻害剤としてのイミダゾピラジノン、ピラゾロピリミジノンおよびピラゾロピリジノン |
| JP2019536762A (ja) * | 2016-10-28 | 2019-12-19 | ハー・ルンドベック・アクチエゼルスカベット | 精神疾患及び／又は認知障害の治療のためのイミダゾピラジノンを含む併用療法 |
| JP2020500841A (ja) * | 2016-10-28 | 2020-01-16 | ハー・ルンドベック・アクチエゼルスカベット | イミダゾピラジノンの投与を含む併用療法 |
| KR20200016891A (ko) * | 2017-05-26 | 2020-02-17 | 이마라 인크. | Pde9 억제제의 제조 방법 및 사용 방법 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG11201502728WA (en) * | 2011-10-10 | 2015-05-28 | Lundbeck & Co As H | Pde9i with imidazo pyrazinone backbone |
| MX373103B (es) | 2014-02-13 | 2020-04-17 | Incyte Holdings Corp | Ciclopropilaminas como inhibidores de desmetilasa específica de lisina 1 (lsd1). |
| US9527835B2 (en) | 2014-02-13 | 2016-12-27 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
| SI3105218T1 (sl) | 2014-02-13 | 2019-11-29 | Incyte Corp | Ciklopropilamini kot inhibitorji LSD1 |
| EP3105219B9 (en) | 2014-02-13 | 2018-10-03 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| TW201613925A (en) | 2014-07-10 | 2016-04-16 | Incyte Corp | Imidazopyrazines as LSD1 inhibitors |
| WO2016007722A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
| WO2016007727A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
| TWI687419B (zh) | 2014-07-10 | 2020-03-11 | 美商英塞特公司 | 作為ｌｓｄ１抑制劑之咪唑并吡啶及咪唑并吡嗪 |
| TW201629064A (zh) | 2014-10-10 | 2016-08-16 | Ｈ 朗德貝克公司 | 作爲ｐｄｅ１抑制劑之三唑並吡酮 |
| EP3277689B1 (en) | 2015-04-03 | 2019-09-04 | Incyte Corporation | Heterocyclic compounds as lsd1 inhibitors |
| JO3627B1 (ar) | 2015-04-30 | 2020-08-27 | H Lundbeck As | إيميدازو بيرازينونات على هيئة مثبطات pde1 |
| HRP20240082T1 (hr) * | 2015-07-07 | 2024-03-29 | H. Lundbeck A/S | Inhibitor pde9 s okosnicom imidazopirazinona za liječenje perifernih bolesti |
| TW201717948A (zh) * | 2015-08-10 | 2017-06-01 | Ｈ 朗德貝克公司 | 包括給予２－胺基－３，５，５－三氟－３，４，５，６－四氫吡啶的聯合治療 |
| LT3334709T (lt) | 2015-08-12 | 2025-03-10 | Incyte Holdings Corporation | Lsd1 inhibitoriaus druskos |
| RS60155B1 (sr) * | 2015-11-09 | 2020-05-29 | Astrazeneca Ab | Derivati dihidroimidazopirazinona korisni za upotrebu u tretmanu raka |
| TWI729109B (zh) | 2016-04-12 | 2021-06-01 | 丹麥商Ｈ 朗德貝克公司 | 作爲PDE1抑制劑的1,5-二氫-4H-吡唑并[3,4-d]嘧啶-4-酮和1,5-二氫-4H-吡唑并[4,3-c]吡啶-4-酮 |
| JP6999574B2 (ja) | 2016-04-22 | 2022-01-18 | インサイト・コーポレイション | Ｌｓｄ１阻害剤の製剤 |
| TN2018000383A1 (en) | 2016-07-06 | 2020-06-15 | H Lundbeck As | Pde9 inhibitors for treatment of peripheral diseases. |
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