CAS: 1813-94-1; Ethyl 2-(4-Fluorophenyl)-2-Oxoacetate

该化合物是一种氟化芳烃甘氧酸酯,广泛用作有机合成和制药应用中的关键中间体,其结构具有类似于氟联苯组的活性丙烯酸酯,能够进行多种变异,如凝结,循环和核生殖添加.氟代换会增强电子特性,影响目标反应中的回动性和选择性.该化合物在异性循环,农用化学品和生物活性分子的合成中特别宝贵.它具有较高的纯度(>98%)和在标准储存条件下的稳定性.其定义明确的再活动特征使得研究人员更愿意选择寻找通往氟化建筑块的有效途径.

结构式图片

欧盟法规

C&L通报

上下游产品

ethanol 2-(4-fluorophenyl)-2-oxoacetic acid oxalic acid diethyl ester 4-flourophenylmagnesium bromideCyclohexyl-(4-fluor-phenyl)-glykolsaeure-aethylester 2-(4-fluorophenyl)-2-oxoacetic acid ethyl α,α-difluoro-α-(p-fluorophenyl)acetate (S)-(+)-1-(4-fluorophenyl)-1,2-ethanediol

合成工艺路线路线简述

    📜对氟扁桃酸置于氯化亚砜,Caesium Carbonate,二甲基亚砜,三乙胺体系中,用 二氯甲烷,N,N-二甲基甲酰胺 用作溶剂,化学反应生成4-氟苯基乙醛酸乙酯
    参考文献:新型2-(3-苯基哌嗪-1-基)-嘧啶-4-酮作为糖原合酶激酶-3β抑制剂的发现
    标题:新型2-(3-苯基哌嗪-1-基)-嘧啶-4-酮作为糖原合酶激酶-3β抑制剂的发现
    摘要:我们在本文中描述了糖原合酶激酶(gsk)-3β抑制剂从含有2-苯基吗啉部分的有希望的化合物中进一步进化的结果.吗啉部分转化为哌嗪部分会产生有效的gsk-3β抑制剂.专注于苯基部分的sar研究表明,4-氟-2-甲氧基对gsk-3β具有有效的抑制活性.基于对接研究,已表明哌嗪部分的氮原子与gln185主链的氧原子之间存在新的氢键,与相应的苯吗啉类似物相比,这可能有助于增加活性.还讨论了苯基哌嗪部分的立体化学作用.
    Doi:10.1016/j.Bmcl.2017.06.078

    海关参考信息

    专利信息


    专利号:US-2025222120-A1
    优先权日:2024-01-09
    标题 :Synthesis of novel small molecule carm1 degraders, compounds formed thereby, and pharmaceutical compositions containing them
    发明人:TANG WEIPING; XU WEI; XIE HAIBO; BACABAC MEGAN
    权利人:WISCONSIN ALUMNI RES FOUND
    摘要:Provided herein are CARM1 PROTACs comprising a binding molecule of CARM1 with an optimized linker attached to an E3 ubiquitin ligase ligand that recruits the E3 ubiquitin ligase to CARM1. The PROTACs find use, e.g., for selectively targeted degradation of CARM1 protein in cancer cells. Also provided herein are compositions comprising the PROTACs, as well as methods of using the PROTACs.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Copper-Catalyzed Pummerer Type Reaction Of α -Thio Aryl/heteroarylacetates: Synthesis Of Aryl/heteroaryl α -Keto Esters
    作者:Pipas Saha,Sumit Kumar Ray,Vinod K. Singh |发布日期:2017.5
    摘要:A Copper Catalyzed Pummerer Type Reaction Of α-Thio Aryl/heteroarylacetates Is Described For The First Time. This Transformation Represents A New Route To Synthesize α-Keto Esters, Which Are Important Intermediates For Pharmaceuticals And Organic Synthesis. The Reaction Proceeds Via In Situ Generation Of A Thionium Ion That Undergoes Hydrolysis To Furnish α-Keto Esters In Synthetically Viable Yields

    合成参考文献


    摘要:De Wildeman, S.; Sereinig, N., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 177.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知