ethyl 3-(3-bromo-4-fluorophenyl)acrylate | 1147334-61-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: ethyl 3-(3-bromo-4-fluorophenyl)acrylate
• 英文别名: ethyl 3-(3-bromo-4-fluorophenyl)prop-2-enoate
• CAS: 1147334-61-9
• 化学式: C₁₁H₁₀BrFO₂
• 分子量: 273.102
• InChiKey: UHENAOKTIVDSSB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  15
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  ethyl 3-(3-bromo-4-fluorophenyl)acrylate 在 tris-(dibenzylideneacetone)dipalladium(0) 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 sodium hydride 、 sodium t-butanolate 作用下， 以 paraffin oil (nujol) 、 二甲基亚砜 、 甲苯 为溶剂， 反应 4.0h， 生成 rac-ethyl 2-[3-(benzylamino)-4-fluorophenyl]-trans-cyclopropanecarboxylate
  参考文献：
  名称：

  SUBSTITUTED 3-PHENYLPROPIONIC ACIDS AND THE USE THEREOF

  摘要：

  本申请涉及新颖的3-苯丙酸衍生物，其制备方法，它们用于治疗和/或预防疾病的用途，以及它们用于制备治疗和/或预防疾病的药物的用途，特别是用于治疗和/或预防心血管疾病。

  公开号：

  US20110130445A1
• 作为产物：
  描述：

  3-溴-4-氟苯甲醇 、 ethoxycarbonylmethylenephosphorane 在 manganese dioxide silica gel 、 乙酸乙酯 作用下， 以 甲苯 为溶剂， 反应 17.0h， 生成 ethyl 3-(3-bromo-4-fluorophenyl)acrylate
  参考文献：
  名称：

  SUBSTITUTED 3-PHENYLPROPIONIC ACIDS AND THE USE THEREOF

  摘要：

  本申请涉及新型3-苯丙酸衍生物，其制备过程，其用于治疗和/或预防疾病以及其用于制备治疗和/或预防疾病的药物，特别是用于治疗和/或预防心血管疾病。

  公开号：

  US20140142069A1

文献信息

• Catalytic Enantioselective [2,3]-Rearrangements of Allylic Ammonium Ylides: A Mechanistic and Computational Study
  作者：Thomas H. West、Daniel M. Walden、James E. Taylor、Alexander C. Brueckner、Ryne C. Johnston、Paul Ha-Yeon Cheong、Guy C. Lloyd-Jones、Andrew D. Smith

  DOI：10.1021/jacs.6b11851

  日期：2017.3.29

  A mechanistic study of the isothiourea-catalyzed enantioselective [2,3]-rearrangement of allylic ammonium ylides is described. Reaction kinetic analyses using 19F NMR and density functional theory computations have elucidated a reaction profile and allowed identification of the catalyst resting state and turnover-rate limiting step. A catalytically relevant catalyst–substrate adduct has been observed

  描述了异硫脲催化的烯丙基铵叶立德的对映选择性 [2,3] 重排的机理研究。使用 19F NMR 和密度泛函理论计算的反应动力学分析阐明了反应曲线并允许识别催化剂静止状态和周转率限制步骤。已经观察到催化相关的催化剂 - 底物加合物，其组成通过 13C 和 15N 同位素标记明确阐明。同位素夹带表明观察到的催化剂-底物加合物是催化生产循环中真正的中间体。已经检查了 HOBt 作为添加剂对反应、催化剂静止状态和周转率限制步骤的影响。交叉实验已经探讨了催化循环中每个建议步骤的可逆性。计算也被用来阐明立体控制的起源，1,5-S···O 相互作用和催化剂立体定向基团提供了过渡结构刚性和对映选择性，同时偏爱阳离子-π 相互作用而不是 C-H···π负责非对映选择性。
• Substituted 3-phenylpropionic acids and the use thereof
  申请人：Bayer Intellectual Property GmbH

  公开号：US09018414B2

  公开（公告）日：2015-04-28

  The present application relates to novel 3-phenylpropionic acid derivatives, to processes for their preparation, to their use for the treatment and/or prevention of diseases and to their use for preparing medicaments for the treatment and/or prevention of diseases, in particular for the treatment and/or prevention of cardiovascular disorders.

  本申请涉及新型3-苯丙酸衍生物，其制备方法，用于治疗和/或预防疾病的用途以及用于制备治疗和/或预防疾病的药物的用途，特别是用于治疗和/或预防心血管疾病的用途。
• Enantioselective Sulfonium–Claisen Rearrangement with Cinnamyl Thioethers
  作者：Jiwon Jang、Youngjin Bae、Seunghoon Shin

  DOI：10.1021/acs.orglett.3c01244

  日期：2023.6.2

  Sulfonium–Claisen rearrangement leveraged by the gold-catalyzed formation of allyl sulfonium intermediates has enabled an exceptional level of regio- and enantiocontrol for the synthesis of skipped 1,4-dienes. However, the application of cinnamyl thioether derivatives to the sulfonium–Claisen rearrangement has been unsuccessful so far due to the extensive dissociation of the cinnamyl cation. By fine-tuning

  金催化形成烯丙基硫中间体所利用的硫 - 克莱森重排使跳过的 1,4-二烯合成具有特殊水平的区域和对映控制。然而，由于肉桂基阳离子的广泛解离，迄今为止，肉桂基硫醚衍生物在硫-克莱森重排中的应用一直没有成功。通过微调双膦配体，我们能够使肉桂基硫醚参与 [3,3]-σ 重排，以高度对映选择性的方式并以良好的产率提供所需的 1,4-二烯。所得产物可转化为具有乙烯基部分的光学活性 2-色满酮和 4 H-色烯。
• Structure Mechanism Insights and the Role of Nitric Oxide Donation Guide the Development of Oxadiazole-2-Oxides as Therapeutic Agents against Schistosomiasis
  作者：Ganesha Rai、Ahmed A. Sayed、Wendy A. Lea、Hans F. Luecke、Harinath Chakrapani、Stefanie Prast-Nielsen、Ajit Jadhav、William Leister、Min Shen、James Inglese、Christopher P. Austin、Larry Keefer、Elias S. J. Arnér、Anton Simeonov、David J. Maloney、David L. Williams、Craig J. Thomas

  DOI：10.1021/jm901021k

  日期：2009.10.22

  Schistosomiasis is a chronic parasitic disease affecting hundreds of millions of individuals worldwide. Current treatment depends on a single agent, praziquantel, raising concerns of emergence of resistant parasites. Here, we continue our explorations of an oxadiazole-2-oxide class of compounds we recently identified as inhibitors of thioredoxin glutathione reductase (TGR), a selenocysteine-containing flavoenzyme required by the parasite to maintain proper cellular redox balance. Through systematic evaluation of the core molecular structure of this chemotype, we define the essential pharmacophore, establish a link between the nitric oxide donation and TGR inhibition, determine the selectivity for this chemotype versus related reductase enzymes, and present evidence that these agents can be modified to possess appropriate drug metabolism and pharmacokinetic properties. The mechanistic link between exogenous NO donation and parasite injury is expanded and better defined. The results of these studies verify the utility of oxadiazole-2-oxides as novel inhibitors of TGR and as efficacious antischistosomal agents.
• Synthesis of oxadiazole-2-oxide analogues as potential antischistosomal agents
  作者：Ganesha Rai、Craig J. Thomas、William Leister、David J. Maloney

  DOI：10.1016/j.tetlet.2009.01.120

  日期：2009.4

  The synthesis of several 1,2,5-oxadiazole-2-oxide (Furoxan) analogues is described herein. These compounds were prepared in an effort to probe the SAR around the phenyl substituent and oxadiazole core for our studies toward thioredoxin-glutathione reductase (TGR) inhibition and antischistosomal activity. Published by Elsevier Ltd.