CAS: 885693-20-9; Tert-Butyl 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)-5,6-Dihydropyridine-1(2H)-Carboxylate

该化合物是一种多用途的丙烯酯衍生物,通常用于铃木-米亚乌拉的交叉组合反应.二丁基碳氢化合物(Boc)保护组可增强稳定性,便利处理和储存,而四氢丙烯剑架则为进一步功能化提供了灵活性.双丙烯二酰胺在温和条件下确保了丙烯或乙烯的高效再活性,使其在制药和农用化学合成中具有价值.其晶状固态和高纯度(>95%)确保复杂转化中的再生性.这一化合物对于构建热循环框架的C-C联系特别有用,有助于生物活性分子和先进材料的开发.

结构式图片

相似化合物

1451153-83-5 1643573-74-3 2101498-93-3

欧盟法规

C&L通报

上下游产品

5-trifluoromethanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester bis(pinacol)diborane 3-oxo-piperidine-1-carboxylic acid tert-butyl ester 1-tert-butoxycarbonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acid3-[(S)-1-(2,6-dichloro-3-fluorophenyl)ethyl]-5-(1,2,5,6-tetrahydropyridin-3-yl)-1H-pyrrolo[2,3-b]pyridine 1-(6-(1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidin-3-yl)pyridin-2-yl)-3-phenylurea tert-butyl 3-(6-(3-phenylureido)pyridin-2-yl)piperidine-1-carboxylate

合成工艺路线路线简述

  • 24424-99-5 + 2101498-93-3 = 885693-20-9
    反应条件:1.1 Reagents: Triethylamine Solvents: Dichloromethane; Rt; 12 H,Rt
    标题:Gem-Difluorocyclopropanation Of Alkenyl Trifluoroborates With The Cf3Sime3-Nai System
    作者:Hryshchuk,Oleksandr V.; Varenyk,Anatolii O.; Yurov,Yevhen; Kuchkovska,Yuliya O.; Tymtsunik,Andriy V.; Et Al
    参考文献:European Journal Of Organic Chemistry 日期:2020 卷标:2020(15) 页码:2217-2224]

    2489456-27-9 = 885693-20-9
    反应条件:1.1 Solvents: Dichloromethane; 1 H,Reflux; Reflux -> Rt1.2 Catalysts: Grubbs Second Generation Catalyst; Rt; Overnight,Rt
    标题:Multigram Synthesis Of Heterabicyclo[n.1.0]Alkan-1-Yl Trifluoroborates
    作者:Kleban,Ihor; Krokhmaliuk,Yevhen; Reut,Sofiia; Shuvakin,Serhii; Pendyukh,Vyacheslav V.; Et Al
    参考文献:European Journal Of Organic Chemistry 日期:2021 卷标:2021(47) 页码:6551-6560]

    73183-34-3 + 180691-65-0 = 885693-20-9
    反应条件:1.1 Reagents: Potassium Acetate Catalysts: 1,1-Bis(Diphenylphosphino)Ferrocene,[1,1′-Bis(Diphenylphosphino)Ferrocene]Dichloropalladium Solvents: 1,4-Dioxane; 16 H,80 °C
    标题:[1,2,4]Triazolo[1,5-A]Pyrimidine Phosphodiesterase 2A Inhibitors: Structure And Free-Energy Perturbation-Guided Exploration
    作者:Tresadern,Gary; Velter,Ingrid; Trabanco,Andres A.; Van Den Keybus,Frans; Macdonald,Gregor J.; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2020 卷标:63(21) 页码:12887-12910
3-(((三氟甲基)磺酰基)氧基)-5,6-二氢吡啶-1(2H)-羧酸叔丁酯 反应生成 1-Boc-3,6-二氢-2H-吡啶-5-硼酸频哪醇酯
参考文献:Anti-Amyloid Compounds Containing Benzofurazan
标题:Anti-Amyloid Compounds Containing Benzofurazan
摘要:一般来说,除了其他事项外,还提供了式i的化合物:其中r11例如为4-(吡咯烷-1-基)哌啶-1-基,N-甲基-3-(吡咯烷-1-基)丙-1-胺,N1,N1,N3-三甲基丙烷-1,3-二胺,N,N-二甲基哌啶-4-胺,3-(吡咯烷-1-基甲基)氮杂环丁烷-1-基,3-(吡咯烷-1-基甲酮)氮杂环丁烷-1-基或3-(吗啉-1-基甲基)氮杂环丁烷-1-基;r13例如为可选择性地被一个或多个取代基取代的苯基;而r12和r14各自独立地为氢或烷基.还提供了治疗方法.

海关参考信息

专利信息


专利号:US-2022363662-A1
优先权日:2021-04-20
标题 :Compounds as lxr agonists
发明人:PUJALA BRAHMAM; SATHE BALAJI DASHRATH; DANODIA ABHINANDAN; GUPTA ASHU; SONI SANJEEV; KUMAR VIVEK; ANSARI AMANTULLAH; KHAN FARHA; SARKAR ARINDAM; PAYGHAN PAVAN V
权利人:INTEGRAL BIOSCIENCES PRIVATED LTD
摘要:The present invention generally discloses compounds having LXR (the liver X receptor) agonistic activity, to the use of such compounds in the treatment of various disorders such as proliferative disorders, Alzheimer's disease, inflammatory diseases, and diseases characterized by defects in cholesterol and lipid metabolism. Specifically, the present invention discloses compound of formula (IA) which exhibit LXR agonist activity, specifically to LXRβ. The invention also discloses method of synthesis of said compounds, method of using said compounds, pharmaceutical compositions comprising said compounds and method of using thereof.

专利号:US-9839642-B2
优先权日:2014-05-09
标 题:Beta-tetrazolyl-propionic acids as metallo-beta-lactamase inhibitors
发明人:TANG HAIFENG; YANG SHU-WEI; MANDAL MIHIR; SU JING; LI GUOQING; PAN WEIDONG; TANG HAIQUN; DEJESUS REYNALDA; PAN JIANPING; HAGMANN WILLIAM; DING FA-XIANG; XIAO LI; PASTERNAK ALEXANDER; HUANG YUHUA; DONG SHUZHI; YANG DEXI
权利人:MERCK SHARP & DOHME
摘要:The present invention relates to compounds of formula I that are metallo-β-lactamase inhibitors, the synthesis of such compounds, and the use of such compounds for use with β-lactam antibiotics for overcoming resistance.

专利号:US-10227344-B2
优先权日:2016-06-24
标题 :CK2 inhibitors, compositions and methods thereof
发明人:WEBBER STEPHEN E; TAO XUELIANG; BRIN ELENA
权利人:POLARIS PHARMACEUTICALS INC
摘要:The present invention provides synthesis, pharmaceutically acceptable formulations and uses of compounds in accordance with Formula (I), or a stereoisomer, a tautomer or a pharmaceutically acceptable salt thereof. n nFor Formula (I) compounds R 1 , R 2 , R 3 , Ar and Z are as defined in the specification. The inventive Formula (I) compounds are inhibitors of CK2 and find utility in any number of therapeutic applications, including but not limited to treatment of proliferative disorders such as cancer, inflammation and immunological disorders.

专利号:US-8592448-B2
优先权日:2008-11-20
标题:Substituted pyrrolo[2,3-b]-pyridines and -pyrazines
发明人:CHEN XIN; JIN MELZHONG; KLEINBERG ANDREW; LI AN-HU; MULVIHILL MARK J; STEINIG ARNO G; WANG JING
权利人:CHEN XIN; JIN MELZHONG; KLEINBERG ANDREW; LI AN-HU; MULVIHILL MARK J; STEINIG ARNO G; WANG JING; OSI PHARMACEUTICALS LLC
摘要:Compounds of Formula I, as shown below and defined herein: (I) pharmaceutically acceptable salts, synthesis, intermediates, formulations, and methods of disease treatment therewith, including cancers mediated at least in part by Ron and/or Met.
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合成参考文献

合成方法参考DOI号:10.1002/ej°C.202000346
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