CN102574864B - 稠合的氨基二氢嘧啶酮衍生物 - Google Patents
稠合的氨基二氢嘧啶酮衍生物 Download PDFInfo
- Publication number
- CN102574864B CN102574864B CN201080034140.0A CN201080034140A CN102574864B CN 102574864 B CN102574864 B CN 102574864B CN 201080034140 A CN201080034140 A CN 201080034140A CN 102574864 B CN102574864 B CN 102574864B
- Authority
- CN
- China
- Prior art keywords
- amino
- fluorophenyl
- compound
- pyrimidin
- oxo
- 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.)
- Expired - Fee Related
Links
- 0 C*C(*(C)C([C@]1(C)[C@@](C)OC2)=O)=*[C@]12c1cc(*C(C2=C*C(OC)=C*2)=O)ccc1N Chemical compound C*C(*(C)C([C@]1(C)[C@@](C)OC2)=O)=*[C@]12c1cc(*C(C2=C*C(OC)=C*2)=O)ccc1N 0.000 description 3
- WJZGQRSIPFDCJX-UHFFFAOYSA-N COC(c(nc1)ccc1C#N)=O Chemical compound COC(c(nc1)ccc1C#N)=O WJZGQRSIPFDCJX-UHFFFAOYSA-N 0.000 description 2
- NSAMNCHBMLWXCJ-CKFHNAJUSA-N CCN(C([C@@H]1[C@@H](C(F)(F)F)OC2)=O)C(NC(OC(C)(C)C)=O)=N[C@]12c(cc(cc1)N)c1F Chemical compound CCN(C([C@@H]1[C@@H](C(F)(F)F)OC2)=O)C(NC(OC(C)(C)C)=O)=N[C@]12c(cc(cc1)N)c1F NSAMNCHBMLWXCJ-CKFHNAJUSA-N 0.000 description 1
- OQNWMNJBAFGVQC-CKFHNAJUSA-N CCN(C([C@@H]1[C@@H](C(F)(F)F)OC2)=O)C(NC(OC(C)(C)C)=O)=N[C@]12c(cccc1)c1F Chemical compound CCN(C([C@@H]1[C@@H](C(F)(F)F)OC2)=O)C(NC(OC(C)(C)C)=O)=N[C@]12c(cccc1)c1F OQNWMNJBAFGVQC-CKFHNAJUSA-N 0.000 description 1
- OPESXDGRIQENKI-UHFFFAOYSA-N CN(C(C1COC2)=O)C(N)=NC12c(cc(cc1)NC(c(nc2)ccc2OC)=O)c1F Chemical compound CN(C(C1COC2)=O)C(N)=NC12c(cc(cc1)NC(c(nc2)ccc2OC)=O)c1F OPESXDGRIQENKI-UHFFFAOYSA-N 0.000 description 1
- RUAOHUXOMQONIA-TWOQFEAHSA-N CN(C([C@@H]1[C@@H](C(F)(F)F)OC2)=O)C(N)=N[C@]12c(cc(cc1)NC(c(nc2)ccc2C#N)=O)c1F Chemical compound CN(C([C@@H]1[C@@H](C(F)(F)F)OC2)=O)C(N)=N[C@]12c(cc(cc1)NC(c(nc2)ccc2C#N)=O)c1F RUAOHUXOMQONIA-TWOQFEAHSA-N 0.000 description 1
- JEURNBCYNWNADN-UHFFFAOYSA-N COC(c(nc1)ccc1Br)=O Chemical compound COC(c(nc1)ccc1Br)=O JEURNBCYNWNADN-UHFFFAOYSA-N 0.000 description 1
- DUHLYQRYFBXMNZ-YZSZRTLCSA-N C[C@H]([C@H]12)OC[C@]1(c(cc(cc1)NC(c(nc3)cnc3OC)=O)c1F)N=C(N)N(C)C2=O Chemical compound C[C@H]([C@H]12)OC[C@]1(c(cc(cc1)NC(c(nc3)cnc3OC)=O)c1F)N=C(N)N(C)C2=O DUHLYQRYFBXMNZ-YZSZRTLCSA-N 0.000 description 1
- PLEYYFYZOHUESQ-YZSZRTLCSA-N C[C@H]([C@H]12)OC[C@]1(c(cc(cc1)NC(c3ccc(C(F)(F)F)cn3)=O)c1F)N=C(N)N(C)C2=O Chemical compound C[C@H]([C@H]12)OC[C@]1(c(cc(cc1)NC(c3ccc(C(F)(F)F)cn3)=O)c1F)N=C(N)N(C)C2=O PLEYYFYZOHUESQ-YZSZRTLCSA-N 0.000 description 1
- OLVPERMJEQUNSI-MPSXMAJESA-N C[C@H]([C@H]12)OC[C@]1(c(cc(cc1)[N+]([O-])=O)c1F)N=C(NC(OC(C)(C)C)=O)N(C)C2=O Chemical compound C[C@H]([C@H]12)OC[C@]1(c(cc(cc1)[N+]([O-])=O)c1F)N=C(NC(OC(C)(C)C)=O)N(C)C2=O OLVPERMJEQUNSI-MPSXMAJESA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0912777.0 | 2009-07-22 | ||
| GB0912777A GB0912777D0 (en) | 2009-07-22 | 2009-07-22 | Fused aminodihydropyrimidone derivatives |
| PCT/EP2010/060586 WO2011009897A1 (en) | 2009-07-22 | 2010-07-21 | Fused aminodihydropyrimidone derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102574864A CN102574864A (zh) | 2012-07-11 |
| CN102574864B true CN102574864B (zh) | 2015-04-29 |
Family
ID=41058390
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201080034140.0A Expired - Fee Related CN102574864B (zh) | 2009-07-22 | 2010-07-21 | 稠合的氨基二氢嘧啶酮衍生物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9139594B2 (https=) |
| EP (1) | EP2456771A1 (https=) |
| JP (1) | JP5699146B2 (https=) |
| KR (1) | KR20120052343A (https=) |
| CN (1) | CN102574864B (https=) |
| AU (1) | AU2010275196B2 (https=) |
| CA (1) | CA2768881A1 (https=) |
| GB (1) | GB0912777D0 (https=) |
| IN (1) | IN2012DN00688A (https=) |
| WO (1) | WO2011009897A1 (https=) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| RU2416603C9 (ru) | 2005-10-25 | 2012-06-20 | Сионоги Энд Ко., Лтд. | Производные аминодигидротиазина |
| EP2151435A4 (en) | 2007-04-24 | 2011-09-14 | Shionogi & Co | PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF ALZHEIMER'S DISEASE |
| EP2147914B1 (en) | 2007-04-24 | 2014-06-04 | Shionogi&Co., Ltd. | Aminodihydrothiazine derivatives substituted with cyclic groups |
| RU2476431C2 (ru) | 2008-01-18 | 2013-02-27 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Конденсированное производное аминодигидротиазина |
| WO2009151098A1 (ja) | 2008-06-13 | 2009-12-17 | 塩野義製薬株式会社 | βセクレターゼ阻害作用を有する含硫黄複素環誘導体 |
| EP2318416B1 (en) | 2008-07-28 | 2013-09-04 | Eisai R&D Management Co., Ltd. | Spiroaminodihydrothiazine derivatives |
| KR20110076965A (ko) | 2008-09-30 | 2011-07-06 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 신규한 축합 아미노 디하이드로티아진 유도체 |
| CN102186841A (zh) | 2008-10-22 | 2011-09-14 | 盐野义制药株式会社 | 具有bace1抑制活性的2-氨基嘧啶-4-酮及2-氨基吡啶衍生物 |
| GB0912778D0 (en) | 2009-07-22 | 2009-08-26 | Eisai London Res Lab Ltd | Fused aminodihydro-oxazine derivatives |
| GB0912777D0 (en) | 2009-07-22 | 2009-08-26 | Eisai London Res Lab Ltd | Fused aminodihydropyrimidone derivatives |
| UA108363C2 (uk) | 2009-10-08 | 2015-04-27 | Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування | |
| US8563543B2 (en) | 2009-10-08 | 2013-10-22 | Merck Sharp & Dohme Corp. | Iminothiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| EP2485920B1 (en) | 2009-10-08 | 2016-04-27 | Merck Sharp & Dohme Corp. | Pentafluorosulfur imino heterocyclic compounds as bace-1 inhibitors, compositions, and their use |
| EP2485590B1 (en) | 2009-10-08 | 2015-01-07 | Merck Sharp & Dohme Corp. | Pentafluorosulfur imino heterocyclic compounds as bace-1 inhibitors, compositions, and their use |
| TWI488852B (zh) | 2009-12-11 | 2015-06-21 | Shionogi & Co | 衍生物 |
| JP5816630B2 (ja) | 2010-10-29 | 2015-11-18 | 塩野義製薬株式会社 | ナフチリジン誘導体 |
| JP5766198B2 (ja) | 2010-10-29 | 2015-08-19 | 塩野義製薬株式会社 | 縮合アミノジヒドロピリミジン誘導体 |
| GB201100181D0 (en) | 2011-01-06 | 2011-02-23 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
| US8426584B2 (en) | 2011-01-21 | 2013-04-23 | Eisai R&D Management Co., Ltd. | Methods and compounds useful in the synthesis of fused aminodihydrothiazine derivatives |
| GB201101140D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
| GB201101139D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
| EP2694489B1 (en) | 2011-04-07 | 2017-09-06 | Merck Sharp & Dohme Corp. | C5-c6 oxacyclic-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| EP2694521B1 (en) | 2011-04-07 | 2015-11-25 | Merck Sharp & Dohme Corp. | Pyrrolidine-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| TW201247635A (en) | 2011-04-26 | 2012-12-01 | Shionogi & Co | Oxazine derivatives and a pharmaceutical composition for inhibiting BAC1 containing them |
| RU2014111055A (ru) | 2011-08-22 | 2015-09-27 | Мерк Шарп И Доум Корп. | 2-спирозамещенные иминотиазины и их моно- и диоксиды в качестве ингибиторов bace, композиции и их применение |
| CA2871264A1 (en) | 2012-04-27 | 2013-10-31 | Eisai R&D Management Co., Ltd. | Method for producing 5-(difluoromethyl)pyrazine-2-carboxilic acid and production intermediate thereof |
| GB201212871D0 (en) | 2012-07-20 | 2012-09-05 | Eisai Ltd | Novel compounds |
| EP2912035A4 (en) | 2012-10-24 | 2016-06-15 | Shionogi & Co | DERIVATIVES OF DIHYDROOXAZINE OR OXAZEPINE HAVING BACE1 INHIBITING ACTIVITY |
| JP6223563B2 (ja) | 2013-10-14 | 2017-11-01 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 選択的に置換されたキノリン化合物 |
| CN105636945B (zh) | 2013-10-14 | 2017-11-17 | 卫材R&D管理有限公司 | 选择性取代的喹啉化合物 |
| US10047098B2 (en) | 2014-11-25 | 2018-08-14 | Merck Sharp & Dohme Corp. | C5-C6-oxacyclic fused iminopyrimidinone compounds as bace inhibitors, compositions, and their use |
| WO2016100184A1 (en) | 2014-12-16 | 2016-06-23 | Forum Pharmaceuticals, Inc. | Geminal substituted quinuclidine amide compounds as agonists of alpha-7 nicotinic acetylcholine receptors |
| MX2017016231A (es) | 2015-06-10 | 2018-11-29 | Axovant Sciences Gmbh | Compuestos de aminobencisoxazol como agonistas de receptores a7-nicotínicos de acetilcolina. |
| WO2017027600A1 (en) | 2015-08-12 | 2017-02-16 | Forum Pharmaceuticals, Inc. | GEMINAL SUBSTITUTED AMINOBENZISOXAZOLE COMPOUNDS AS AGONISTS OF α7-NICOTINIC ACETYLCHOLINE RECEPTORS |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006041404A1 (en) * | 2004-10-15 | 2006-04-20 | Astrazeneca Ab | Substituted amino-compounds and uses thereof |
| WO2006138264A2 (en) * | 2005-06-14 | 2006-12-28 | Schering Corporation | Aspartyl protease inhibitors |
| WO2008073365A1 (en) * | 2006-12-12 | 2008-06-19 | Schering Corporation | Aspartyl protease inhibitors |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US3227713A (en) | 1966-01-04 | Azine derivatives | ||
| US3235551A (en) | 1966-02-15 | Novel derivatives of | ||
| JPH0967355A (ja) | 1995-08-31 | 1997-03-11 | Tokyo Tanabe Co Ltd | チアジン誘導体、チアゾール誘導体及びそれらの製造方法 |
| CN1251671C (zh) | 2000-05-19 | 2006-04-19 | 武田药品工业株式会社 | β分泌酶抑制剂 |
| US6562783B2 (en) | 2001-05-30 | 2003-05-13 | Neurologic, Inc. | Phosphinylmethyl and phosphorylmethyl succinic and glutauric acid analogs as β-secretase inhibitors |
| BR0309875A (pt) | 2002-05-03 | 2007-04-10 | Israel Inst For Biolog Res Isr | métodos e composições para tratamento de distúrbios do sistema nervoso periférico e novos compostos úteis para isto |
| WO2004014843A1 (ja) | 2002-08-09 | 2004-02-19 | Takeda Chemical Industries, Ltd. | 置換アミノ化合物およびその用途 |
| WO2004037212A2 (en) | 2002-10-24 | 2004-05-06 | Sepracor, Inc. | Compositions comprising zopiclone derivatives and methods of making and using the same |
| JP2004149429A (ja) | 2002-10-29 | 2004-05-27 | Takeda Chem Ind Ltd | インドール化合物およびその用途 |
| CA2505098A1 (en) | 2002-11-12 | 2004-05-27 | Merck & Co., Inc. | Phenylcarboxamide beta-secretase inhibitors for the treatment of alzheimer's disease |
| US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| PT1699455E (pt) | 2003-12-15 | 2013-08-27 | Merck Sharp & Dohme | Inibidores de protease de aspartilo heterocíclicos |
| JP2007530696A (ja) | 2004-03-30 | 2007-11-01 | メルク エンド カムパニー インコーポレーテッド | アスパラギン酸プロテアーゼ阻害剤として有用な2−アミノチアゾール化合物 |
| PE20060664A1 (es) | 2004-09-15 | 2006-08-04 | Novartis Ag | Amidas biciclicas como inhibidores de cinasa |
| WO2006041405A1 (en) | 2004-10-15 | 2006-04-20 | Astrazeneca Ab | Substituted amino-pyrimidones and uses thereof |
| CA2594946A1 (en) | 2005-01-19 | 2006-07-27 | Merck & Co., Inc | Tertiary carbinamines having substituted heterocycles, which are active as inhibitors of beta-secretase, for the treatment of alzheimer's disease |
| US8211904B2 (en) | 2005-07-18 | 2012-07-03 | Merck, Sharp & Dohme Corp. | Spiropiperidine beta-secretase inhibitors for the treatment of alzheimer's disease |
| RU2416603C9 (ru) | 2005-10-25 | 2012-06-20 | Сионоги Энд Ко., Лтд. | Производные аминодигидротиазина |
| US20090099217A1 (en) | 2006-04-05 | 2009-04-16 | Astex Therapeutics Ltd. | 2-Aminopyrimidin-4-Ones And Their Use For Treating Or Preventing Alpha Beta-Related Pathologies |
| JP5117382B2 (ja) | 2006-05-31 | 2013-01-16 | 第一三共株式会社 | 7員環化合物の製造方法 |
| KR20090015967A (ko) | 2006-06-12 | 2009-02-12 | 쉐링 코포레이션 | 헤테로사이클릭 아스파르틸 프로테아제 억제제 |
| EP2151435A4 (en) | 2007-04-24 | 2011-09-14 | Shionogi & Co | PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF ALZHEIMER'S DISEASE |
| EP2147914B1 (en) | 2007-04-24 | 2014-06-04 | Shionogi&Co., Ltd. | Aminodihydrothiazine derivatives substituted with cyclic groups |
| PE20091236A1 (es) | 2007-11-22 | 2009-09-16 | Astrazeneca Ab | Derivados de pirimidina como immunomoduladores de tlr7 |
| RU2476431C2 (ru) | 2008-01-18 | 2013-02-27 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Конденсированное производное аминодигидротиазина |
| TWI431004B (zh) | 2008-05-02 | 2014-03-21 | Lilly Co Eli | Bace抑制劑 |
| EP2318416B1 (en) | 2008-07-28 | 2013-09-04 | Eisai R&D Management Co., Ltd. | Spiroaminodihydrothiazine derivatives |
| WO2010013302A1 (ja) | 2008-07-28 | 2010-02-04 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | スピロアミノジヒドロチアジン誘導体 |
| KR20110076965A (ko) | 2008-09-30 | 2011-07-06 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 신규한 축합 아미노 디하이드로티아진 유도체 |
| AR077277A1 (es) | 2009-07-09 | 2011-08-17 | Lilly Co Eli | Compuestos de biciclo (1,3)tiazin-2-amina formulacion farmaceutica que lo comprende y su uso para la manufactura de un medicamento util para el tratamiento de la enfermedad de alzheimer |
| GB0912777D0 (en) | 2009-07-22 | 2009-08-26 | Eisai London Res Lab Ltd | Fused aminodihydropyrimidone derivatives |
| GB0912778D0 (en) | 2009-07-22 | 2009-08-26 | Eisai London Res Lab Ltd | Fused aminodihydro-oxazine derivatives |
| JP2013530238A (ja) | 2010-07-01 | 2013-07-25 | アムジエン・インコーポレーテツド | Pi3k活性の阻害剤としての複素環化合物及びその使用 |
| GB201100181D0 (en) | 2011-01-06 | 2011-02-23 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
| GB201101139D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
| GB201101140D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
| US8426584B2 (en) | 2011-01-21 | 2013-04-23 | Eisai R&D Management Co., Ltd. | Methods and compounds useful in the synthesis of fused aminodihydrothiazine derivatives |
-
2009
- 2009-07-22 GB GB0912777A patent/GB0912777D0/en not_active Ceased
-
2010
- 2010-07-21 KR KR20127004626A patent/KR20120052343A/ko not_active Ceased
- 2010-07-21 CA CA2768881A patent/CA2768881A1/en not_active Abandoned
- 2010-07-21 US US13/386,199 patent/US9139594B2/en not_active Expired - Fee Related
- 2010-07-21 CN CN201080034140.0A patent/CN102574864B/zh not_active Expired - Fee Related
- 2010-07-21 JP JP2012521034A patent/JP5699146B2/ja not_active Expired - Fee Related
- 2010-07-21 EP EP20100734143 patent/EP2456771A1/en not_active Withdrawn
- 2010-07-21 AU AU2010275196A patent/AU2010275196B2/en not_active Ceased
- 2010-07-21 IN IN688DEN2012 patent/IN2012DN00688A/en unknown
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006041404A1 (en) * | 2004-10-15 | 2006-04-20 | Astrazeneca Ab | Substituted amino-compounds and uses thereof |
| WO2006138264A2 (en) * | 2005-06-14 | 2006-12-28 | Schering Corporation | Aspartyl protease inhibitors |
| CN101228163A (zh) * | 2005-06-14 | 2008-07-23 | 先灵公司 | 天冬氨酰蛋白酶抑制剂 |
| WO2008073365A1 (en) * | 2006-12-12 | 2008-06-19 | Schering Corporation | Aspartyl protease inhibitors |
Non-Patent Citations (1)
| Title |
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| Development of Strategies for the Preparation of Designed Solids. An Investigation of the 2-Amino-4(1 H)-pyrimidone Ring System for the Molecular Self-Assembly of Hydrogen Bonded a-and β-Network;Leticia M. Toledo,等;《Chem. Mater.》;19950930;第7卷(第9期);第1639-1647页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011009897A1 (en) | 2011-01-27 |
| AU2010275196B2 (en) | 2015-08-06 |
| CN102574864A (zh) | 2012-07-11 |
| JP5699146B2 (ja) | 2015-04-08 |
| AU2010275196A1 (en) | 2012-02-16 |
| JP2012533602A (ja) | 2012-12-27 |
| GB0912777D0 (en) | 2009-08-26 |
| US20120202828A1 (en) | 2012-08-09 |
| CA2768881A1 (en) | 2011-01-27 |
| KR20120052343A (ko) | 2012-05-23 |
| US9139594B2 (en) | 2015-09-22 |
| EP2456771A1 (en) | 2012-05-30 |
| IN2012DN00688A (https=) | 2015-06-19 |
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