
合成工艺路线路线简述
- 120-92-3 = 83507-33-9 [标题:Reaction Conditions
标题:Aza-Tricyclic Substance P Antagonists
作者:Lowe,John A. Iii; Et Al
参考文献:Journal Of Medicinal Chemistry 日期:1994 卷标:37(18) 页码:2831-40]
778581-74-1 = 83507-33-9
反应条件:1.1 Solvents: Trifluoroacetic Acid; Overnight,Rt1.2 Reagents: Sodium Bicarbonate Solvents: Water; Ph 8,Rt
标题:An Approach To Azabicyclo[n.3.1]Alkanes By Double Mannich Reaction
作者:Mityuk,Andrey P.; Et Al
参考文献:Synthesis 日期:2010 卷标:(3) 页码:493-497]
120-92-3 + 104247-86-1 = 83507-33-9
反应条件:1.1 Reagents: Chlorotrimethylsilane Solvents: Acetonitrile; Rt; 15 Min,Rt1.2 Rt; 24 H,Rt1.3 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Reflux; Cooled1.4 Reagents: Sodium Hydroxide; Ph 10
标题:5,6-Membered Cnn Palladium Pincer Complexes Of 3-Benzyl-8-Dimethylamino -3-Azabicyclo[3.2.1]Octane And 3-Benzyl-9-Dimethylamino-3-Azabicyclo[3.3.1]Nonane
作者:Bulygina,Ludmila A.; Et Al
参考文献:Journal Of Organometallic Chemistry 日期:2019 卷标:887 页码:64-70]
= 83507-33-9
反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol; 1.5 H,Rt; 48 H,Rt2.1 Reagents: Chlorotrimethylsilane Solvents: Acetonitrile; 96 H,Rt2.2 Reagents: Sodium Bicarbonate Solvents: Water; Rt3.1 Solvents: Trifluoroacetic Acid; Overnight,Rt3.2 Reagents: Sodium Bicarbonate Solvents: Water; Ph 8,Rt
标题:An Approach To Azabicyclo[n.3.1]Alkanes By Double Mannich Reaction
作者:Mityuk,Andrey P.; Et Al
参考文献:Synthesis 日期:2010 卷标:(3) 页码:493-497
3-Benzyl-8,8-Dimethoxy-3-Azabicyclo[3.2.1]octane置于三氟乙酸体系中,用3.3 G的收率获得产物3-苄基-3-氮杂双环[3.2.1]辛-8-酮
参考文献:An Approach To Azabicyclo[n.3.1]Alkanes By Double Mannich Reaction
标题:An Approach To Azabicyclo[n.3.1]Alkanes By Double Mannich Reaction
摘要:研究人员探索了以 N,N-双(甲氧基甲基)苄胺为原料,由三甲基氯硅烷促进的酮类化合物双曼尼希环化反应.结果表明,底物的结构对反应结果有很大影响.通过这种方法可以获得氮杂双环[n.3.1]烷烃衍生物(n = 2-5),而且产率很高.
DOI:10.1055/s-0029-1217137
海关参考信息
- 2902300000-甲苯
2912110000-甲醛
2912120000-乙醛
2914110000-丙酮 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-12275709-B2
优先权日:2018-12-27
标 题 :Process for the preparation of exo-tert-butyl N-(3-azabicyclo[3.2.1]octan-8-yl)carbamate
发明人:CHEN WEICHUN; ZHANG GUOCAI
权利人:HOFFMANN LA ROCHE
摘要:The present invention relates to a process for the preparation of a compound (I) or pharmaceutically acceptable salt thereof, which is useful as the key intermediate for the synthesis of compounds for prophylaxis and treatment of a disease associated with the deposition of β-amyloid in the brain, in particular Alzheimer's disease, and other diseases such as cerebral amyloid angiopathy, hereditary cerebral hemorrhage with amyloidosis, Dutch-type (HCHWA-D), multi-infarct dementia, dementia pugilistica and Down syndrome.
专利号:US-2005192265-A1
优先权日:2003-03-20
标 题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds
发明人:THOMPSON RICHARD C; WILKIE STEPHEN; STACK DOUGLAS R; VANMETER ELDON E; SHI QING; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; HENRY STEVEN S; MCDANIEL STACEY L; STUCKY RUSSELL D; PORTER WARREN J
摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions that include a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.
专利号:US-6906056-B2
优先权日:1998-06-22
标 题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
发明人:THOMPSON RICHARD C; WILKIE STEPHEN; STACK DOUGLAS R; VANMETER ELDON E; SHI QING; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; HENRY STEVEN S; MCDANIEL STACEY L; STUCKY RUSSELL D; PORTER WARREN J
权利人:LILLY CO ELI
摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions that include a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.
专利号:US-2012172350-A1
优先权日:2009-09-11
标题 :Histamine h3 inverse agonists and antagonists and methods of use thereof
发明人:CHYTIL MILAN; ENGEL SHARON R; FANG QUN KEVIN
权利人:CHYTIL MILAN; ENGEL SHARON R; FANG QUN KEVIN; SUNOVION PHARMACEUTICALS INC
摘要:Provided herein are fused imidazolyl compounds, methods of synthesis, and methods of use thereof. The compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, including, e.g., neurological disorders and metabolic disorders. Compounds provided herein inhibit the activity of histamine H3 receptors and modulate the release of various neurotransmitters, such as, e.g., histamine, acetylcholine, norepinephrine, and dopamine (e.g. at the synapse). Pharmaceutical compositions containing the compounds and their methods of use are also provided herein.
专利号:CN-116240194-B
优先权日:2021-12-08
标 题 :Limonene epoxy hydrolase mutant and catalytic synthesis of chiral oxygen/nitrogen-heterocyclic compound thereof
专利号:CN-116240194-A
优先权日:2021-12-08
标 题 :Limonene Epoxyhydrolase Mutants and Their Catalytic Synthesis of Chiral Oxygen/Nitrogen-Heterocyclic Compounds