JP2014503599A5 - - Google Patents
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- JP2014503599A5 JP2014503599A5 JP2013551904A JP2013551904A JP2014503599A5 JP 2014503599 A5 JP2014503599 A5 JP 2014503599A5 JP 2013551904 A JP2013551904 A JP 2013551904A JP 2013551904 A JP2013551904 A JP 2013551904A JP 2014503599 A5 JP2014503599 A5 JP 2014503599A5
- Authority
- JP
- Japan
- Prior art keywords
- octane
- azabicyclo
- oxo
- pyridinecarboxamide
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- -1 pyridone derivative compound Chemical class 0.000 claims 13
- 208000010877 cognitive disease Diseases 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 6
- 239000012453 solvate Substances 0.000 claims 6
- 208000028698 Cognitive impairment Diseases 0.000 claims 5
- 208000024827 Alzheimer disease Diseases 0.000 claims 4
- 206010012289 Dementia Diseases 0.000 claims 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 206010027175 memory impairment Diseases 0.000 claims 2
- TXBNSNBQMZRPLJ-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-chloro-4-methylphenyl)-6-oxopyridine-3-carboxamide Chemical compound ClC1=CC(C)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 TXBNSNBQMZRPLJ-UHFFFAOYSA-N 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 1
- HAIGHIYUARLXHE-UHFFFAOYSA-N 1-azabicyclo[2.2.2]octan-3-yl 1-(2,4-dichlorophenyl)-6-oxopyridine-3-carboxylate Chemical compound ClC1=CC(Cl)=CC=C1N1C(=O)C=CC(C(=O)OC2C3CCN(CC3)C2)=C1 HAIGHIYUARLXHE-UHFFFAOYSA-N 0.000 claims 1
- YWBFTAQQUQNNEN-UHFFFAOYSA-N 1-azabicyclo[2.2.2]octan-3-yl 6-oxo-1-phenylpyridine-3-carboxylate Chemical compound C1N(CC2)CCC2C1OC(=O)C(=C1)C=CC(=O)N1C1=CC=CC=C1 YWBFTAQQUQNNEN-UHFFFAOYSA-N 0.000 claims 1
- 206010065040 AIDS dementia complex Diseases 0.000 claims 1
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- 201000010374 Down Syndrome Diseases 0.000 claims 1
- 201000011240 Frontotemporal dementia Diseases 0.000 claims 1
- 206010061598 Immunodeficiency Diseases 0.000 claims 1
- 208000029462 Immunodeficiency disease Diseases 0.000 claims 1
- 208000020358 Learning disease Diseases 0.000 claims 1
- 208000009829 Lewy Body Disease Diseases 0.000 claims 1
- 201000002832 Lewy body dementia Diseases 0.000 claims 1
- 208000000609 Pick Disease of the Brain Diseases 0.000 claims 1
- 206010036631 Presenile dementia Diseases 0.000 claims 1
- 206010039966 Senile dementia Diseases 0.000 claims 1
- 239000000556 agonist Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 102000047725 alpha7 Nicotinic Acetylcholine Receptor Human genes 0.000 claims 1
- 108700006085 alpha7 Nicotinic Acetylcholine Receptor Proteins 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 1
- 235000010290 biphenyl Nutrition 0.000 claims 1
- 239000004305 biphenyl Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 208000025688 early-onset autosomal dominant Alzheimer disease Diseases 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 150000004677 hydrates Chemical class 0.000 claims 1
- 230000007813 immunodeficiency Effects 0.000 claims 1
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 claims 1
- 201000003723 learning disability Diseases 0.000 claims 1
- 230000007576 microinfarct Effects 0.000 claims 1
- 208000027061 mild cognitive impairment Diseases 0.000 claims 1
- VITIUGRHOWHMGM-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2,3-dichlorophenyl)-6-oxopyridine-3-carboxamide Chemical compound ClC1=CC=CC(N2C(C=CC(=C2)C(=O)NC2C3CCN(CC3)C2)=O)=C1Cl VITIUGRHOWHMGM-UHFFFAOYSA-N 0.000 claims 1
- RASYIHIJXQJJMO-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2,4-dichlorophenyl)-6-oxopyridine-3-carboxamide Chemical compound ClC1=CC(Cl)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 RASYIHIJXQJJMO-UHFFFAOYSA-N 0.000 claims 1
- QMPODIWJSYHWSL-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2,4-difluorophenyl)-6-oxopyridine-3-carboxamide Chemical compound FC1=CC(F)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 QMPODIWJSYHWSL-UHFFFAOYSA-N 0.000 claims 1
- DDUVDNHSVDLAJU-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2,4-dimethoxyphenyl)-6-oxopyridine-3-carboxamide Chemical compound COC1=CC(OC)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 DDUVDNHSVDLAJU-UHFFFAOYSA-N 0.000 claims 1
- WVZAFMPAABWPNK-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2,4-dimethylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CC1=CC(C)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 WVZAFMPAABWPNK-UHFFFAOYSA-N 0.000 claims 1
- CAUBAVMJUSKNEN-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2,5-difluorophenyl)-6-oxopyridine-3-carboxamide Chemical compound FC1=CC=C(F)C(N2C(C=CC(=C2)C(=O)NC2C3CCN(CC3)C2)=O)=C1 CAUBAVMJUSKNEN-UHFFFAOYSA-N 0.000 claims 1
- COJYYJMKGKDCKG-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2,5-dimethoxyphenyl)-6-oxopyridine-3-carboxamide Chemical compound COC1=CC=C(OC)C(N2C(C=CC(=C2)C(=O)NC2C3CCN(CC3)C2)=O)=C1 COJYYJMKGKDCKG-UHFFFAOYSA-N 0.000 claims 1
- UNQSEWXNMUMZMK-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-benzylsulfanylphenyl)-6-oxopyridine-3-carboxamide Chemical compound C1N(CC2)CCC2C1NC(=O)C(=C1)C=CC(=O)N1C1=CC=CC=C1SCC1=CC=CC=C1 UNQSEWXNMUMZMK-UHFFFAOYSA-N 0.000 claims 1
- WFORDZBEUQAAQX-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-chloro-4-fluorophenyl)-6-oxopyridine-3-carboxamide Chemical compound ClC1=CC(F)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 WFORDZBEUQAAQX-UHFFFAOYSA-N 0.000 claims 1
- JLIXVVBMBCSKFY-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-chlorophenyl)-6-oxopyridine-3-carboxamide Chemical compound ClC1=CC=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 JLIXVVBMBCSKFY-UHFFFAOYSA-N 0.000 claims 1
- BHWGHXZYVQLCGE-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-ethylsulfanyl-4-methoxyphenyl)-6-oxopyridine-3-carboxamide Chemical compound CCSC1=CC(OC)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 BHWGHXZYVQLCGE-UHFFFAOYSA-N 0.000 claims 1
- VHKHEEVGGRBHRY-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-ethylsulfanylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CCSC1=CC=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 VHKHEEVGGRBHRY-UHFFFAOYSA-N 0.000 claims 1
- LFAWCYBXKDAZMF-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-fluorophenyl)-6-oxopyridine-3-carboxamide Chemical compound FC1=CC=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 LFAWCYBXKDAZMF-UHFFFAOYSA-N 0.000 claims 1
- AWTCIPZNLYDJNG-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methoxy-5-methylphenyl)-6-oxopyridine-3-carboxamide Chemical compound COC1=CC=C(C)C=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 AWTCIPZNLYDJNG-UHFFFAOYSA-N 0.000 claims 1
- SFAPGJATHZNEHN-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methoxy-5-phenylphenyl)-6-oxopyridine-3-carboxamide Chemical compound C1=C(N2C(C=CC(=C2)C(=O)NC2C3CCN(CC3)C2)=O)C(OC)=CC=C1C1=CC=CC=C1 SFAPGJATHZNEHN-UHFFFAOYSA-N 0.000 claims 1
- MIRAXADPGYARDT-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methoxyphenyl)-6-oxopyridine-3-carboxamide Chemical compound COC1=CC=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 MIRAXADPGYARDT-UHFFFAOYSA-N 0.000 claims 1
- GCMZGSSXTKZLID-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CC1=CC=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 GCMZGSSXTKZLID-UHFFFAOYSA-N 0.000 claims 1
- YYAUEPBIPQDNRT-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methylsulfanyl-4-propan-2-ylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CSC1=CC(C(C)C)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 YYAUEPBIPQDNRT-UHFFFAOYSA-N 0.000 claims 1
- RGVKGPVCJRNFFQ-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methylsulfanyl-4-propylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CSC1=CC(CCC)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 RGVKGPVCJRNFFQ-UHFFFAOYSA-N 0.000 claims 1
- QHSLDQPVNRQAFA-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methylsulfanylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CSC1=CC=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 QHSLDQPVNRQAFA-UHFFFAOYSA-N 0.000 claims 1
- RAAANYVBQXYSII-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(2-methylsulfonylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CS(=O)(=O)C1=CC=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 RAAANYVBQXYSII-UHFFFAOYSA-N 0.000 claims 1
- SKQRFVCNULGLPA-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(3,4-dichlorophenyl)-6-oxopyridine-3-carboxamide Chemical compound C1=C(Cl)C(Cl)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 SKQRFVCNULGLPA-UHFFFAOYSA-N 0.000 claims 1
- CSMDTLICMBAYNO-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(3,4-difluorophenyl)-6-oxopyridine-3-carboxamide Chemical compound C1=C(F)C(F)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 CSMDTLICMBAYNO-UHFFFAOYSA-N 0.000 claims 1
- YDWUPDRVVZDBGP-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(3,4-dimethoxyphenyl)-6-oxopyridine-3-carboxamide Chemical compound C1=C(OC)C(OC)=CC=C1N1C(=O)C=CC(C(=O)NC2C3CCN(CC3)C2)=C1 YDWUPDRVVZDBGP-UHFFFAOYSA-N 0.000 claims 1
- CGLXSVFGSGVZMV-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(3,5-dichlorophenyl)-6-oxopyridine-3-carboxamide Chemical compound ClC1=CC(Cl)=CC(N2C(C=CC(=C2)C(=O)NC2C3CCN(CC3)C2)=O)=C1 CGLXSVFGSGVZMV-UHFFFAOYSA-N 0.000 claims 1
- IMPAVINXBUWCOF-UHFFFAOYSA-N n-(1-azabicyclo[2.2.2]octan-3-yl)-1-(3,5-difluorophenyl)-6-oxopyridine-3-carboxamide Chemical compound FC1=CC(F)=CC(N2C(C=CC(=C2)C(=O)NC2C3CCN(CC3)C2)=O)=C1 IMPAVINXBUWCOF-UHFFFAOYSA-N 0.000 claims 1
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- IWOMEVDOPUPGRQ-KRWDZBQOSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-1-(4-methyl-2-methylsulfanylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CSC1=CC(C)=CC=C1N1C(=O)C=CC(C(=O)N[C@@H]2C3CCN(CC3)C2)=C1 IWOMEVDOPUPGRQ-KRWDZBQOSA-N 0.000 claims 1
- QHSLDQPVNRQAFA-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-(2-methylsulfanylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CSC1=CC=CC=C1N1C(=O)C=CC(C(=O)N[C@H]2C3CCN(CC3)C2)=C1 QHSLDQPVNRQAFA-MRXNPFEDSA-N 0.000 claims 1
- AHKDEACSKUSGKH-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-(4-chloro-2-methylsulfanylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CSC1=CC(Cl)=CC=C1N1C(=O)C=CC(C(=O)N[C@H]2C3CCN(CC3)C2)=C1 AHKDEACSKUSGKH-MRXNPFEDSA-N 0.000 claims 1
- WSAWESCAPBKHKD-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-(4-chlorophenyl)-6-oxopyridine-3-carboxamide Chemical compound C1=CC(Cl)=CC=C1N1C(=O)C=CC(C(=O)N[C@H]2C3CCN(CC3)C2)=C1 WSAWESCAPBKHKD-QGZVFWFLSA-N 0.000 claims 1
- IWOMEVDOPUPGRQ-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-(4-methyl-2-methylsulfanylphenyl)-6-oxopyridine-3-carboxamide Chemical compound CSC1=CC(C)=CC=C1N1C(=O)C=CC(C(=O)N[C@H]2C3CCN(CC3)C2)=C1 IWOMEVDOPUPGRQ-QGZVFWFLSA-N 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 239000004031 partial agonist Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 201000000980 schizophrenia Diseases 0.000 claims 1
- 208000019553 vascular disease Diseases 0.000 claims 1
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| KR10-2011-0008960 | 2011-01-28 | ||
| KR20110008960 | 2011-01-28 | ||
| PCT/KR2012/000648 WO2012102580A1 (en) | 2011-01-28 | 2012-01-30 | Pharmaceutical composition comprising pyridone derivatives |
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| JP2014503599A JP2014503599A (ja) | 2014-02-13 |
| JP2014503599A5 true JP2014503599A5 (cg-RX-API-DMAC7.html) | 2014-12-25 |
| JP5921576B2 JP5921576B2 (ja) | 2016-05-24 |
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| CN (1) | CN103328477B (cg-RX-API-DMAC7.html) |
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| ES (1) | ES2634204T3 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2012102580A1 (cg-RX-API-DMAC7.html) |
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| KR101928505B1 (ko) | 2011-01-28 | 2018-12-12 | 에스케이바이오팜 주식회사 | 피리돈 유도체 및 이를 포함하는 약학적 조성물 |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| CN110452216B (zh) | 2014-04-02 | 2022-08-26 | 英特穆恩公司 | 抗纤维化吡啶酮类 |
| EP3259262A4 (en) * | 2015-02-17 | 2018-08-01 | Mapi Pharma Limited | Process and intermediates for the preparation of perampanel |
| MY195948A (en) | 2016-03-22 | 2023-02-27 | Merck Sharp & Dohme | Allosteric Modulators of Nicotinic Acetylcholine Receptors |
| WO2019028062A1 (en) * | 2017-07-31 | 2019-02-07 | Washington University | PIRFENIDONE DERIVATIVES FOR MODULATION OF B-LYMPHOCYTE ACTIVITY AND PROTECTION OF ORGANS |
| HRP20241704T1 (hr) | 2018-05-01 | 2025-02-14 | Merck Sharp & Dohme Llc | Spiropiperidin alosterični modulatori nikotinskih acetiholinskih receptora |
| CN109293507B (zh) * | 2018-10-12 | 2020-12-18 | 河北科技大学 | 4-甲氧基甲烯基-2-烯戊二酸二甲酯的合成方法及其应用 |
Family Cites Families (9)
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| US4404138A (en) | 1982-06-22 | 1983-09-13 | Warner-Lambert Company | 3-[2-(Azabicyclo) ethyl]-1,2,3,4-tetrahydro-5H-[1]benzopyrano[3,4-c]pyridin-5-ones |
| ES2209825T3 (es) * | 1999-01-29 | 2004-07-01 | Abbott Laboratories | Derivados diazabiciclicos utiles como ligandos del receptor nicotinico de la acetilcolina. |
| SE0000540D0 (sv) * | 2000-02-18 | 2000-02-18 | Astrazeneca Ab | New compounds |
| US6569865B2 (en) | 2001-06-01 | 2003-05-27 | Astrazeneca Ab | Spiro 1-azabicyclo[2.2.2]octane-3,2′(3′h)-furo[2,3-b]pyridine |
| US20040259909A1 (en) * | 2001-10-16 | 2004-12-23 | Mccarthy Dennis | Treatment of fibromyalgia syndrome |
| FR2834511B1 (fr) * | 2002-01-07 | 2004-02-13 | Sanofi Synthelabo | Derives de 5-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, leur preparation et leur application en therapeutique |
| JP5775819B2 (ja) * | 2008-10-09 | 2015-09-09 | ハワード ヒューズ メディカル インスティチュート | 新規なキメラリガンド開口型イオンチャネルおよびその使用方法 |
| EP2364150A1 (en) * | 2008-11-11 | 2011-09-14 | Targacept Inc. | Treatment with alpha 7-selective ligands |
| KR101928505B1 (ko) * | 2011-01-28 | 2018-12-12 | 에스케이바이오팜 주식회사 | 피리돈 유도체 및 이를 포함하는 약학적 조성물 |
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- 2012-01-30 CA CA2824467A patent/CA2824467C/en active Active
- 2012-01-30 WO PCT/KR2012/000648 patent/WO2012102580A1/en not_active Ceased
- 2012-01-30 JP JP2013551904A patent/JP5921576B2/ja active Active
- 2012-01-30 CN CN201280006741.XA patent/CN103328477B/zh active Active
- 2012-01-30 US US13/980,819 patent/US8716309B2/en active Active
- 2012-01-30 ES ES12740018.2T patent/ES2634204T3/es active Active
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