N-(4-Aethoxy-phenyl)-acrylamid | 2918-94-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(4-Aethoxy-phenyl)-acrylamid
• 英文别名: N-Acryloyl-4-aethoxy-anilin；N-(4-ethoxyphenyl)prop-2-enamide
• CAS: 2918-94-7
• 化学式: C₁₁H₁₃NO₂
• 分子量: 191.23
• InChiKey: MAYFLXGHTBAUNU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  14
• 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：
  38.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-(4-Aethoxy-phenyl)-acrylamid 在 亚硝酸特丁酯 作用下， 以 乙腈 为溶剂， 反应 6.0h， 以66%的产率得到(E)-N-(4-ethoxyphenyl)-3-nitroacrylamide
  参考文献：
  名称：

  苯胺和丙烯酰胺的有效硝化亚硝酸叔丁酯

  摘要：

  硝基化合物是合成有机化学和化学工业中的重要中间体。在此，以TBN（亚硝酸叔丁酯）为硝化试剂，开发了铜催化[10% Cu(NO3)(2)3H(2)O]硝化苯胺的高效硝化反应，得到相应的硝基取代芳烃产物。良好的产量。TBN 的使用还导致丙烯酰胺在室温下选择性硝化以仅提供硝化产物的 (E) 异构体。该程序对一系列具有广泛官能团的苯胺和丙烯酰胺具有良好的耐受性。该合成方法具有原料廉价、反应条件温和、反应速度快、收率高等优点。机理研究表明，一个硝基自由基，

  DOI：

  10.1002/ejoc.201403510
• 作为产物：
  描述：

  对乙氧基苯胺 、 丙烯酰氯 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 N-(4-Aethoxy-phenyl)-acrylamid
  参考文献：
  名称：

  基于无氧化剂 α,β-酰胺（三氟甲基）磺酰化反应的 AgSCF3 自由基加成

  摘要：

  (三氟甲基)磺酰胺是天然产物和药物分子中常见的一类重要的有机化合物。在这里，我们报道了使用（三氟甲基）硫化银（I）作为β-酰胺化合物的自由基（三氟甲基）磺酰化试剂的（三氟甲基）磺酰化反应。该反应不需要化学计量的氧化剂或额外的过渡金属催化剂，并且可以通过添加常见的有机酸来实现。该方法具有优异的适用性，可以容纳多种官能团，包括酯基、酰基，甚至溴基或碘基。杂环α,β-酰胺也可以很容易地转化为相应的产品。该反应也为氘代(三氟甲基)磺酰胺的合成提供了新的方法。

  DOI：

  10.1055/s-0043-1763759

文献信息

• Design, synthesis, antiviral and cytostatic evaluation of novel isoxazolidine nucleotide analogues with a carbamoyl linker
  作者：Kamil Kokosza、Jan Balzarini、Dorota G. Piotrowska

  DOI：10.1016/j.bmc.2013.01.007

  日期：2013.3

  phorylnitrone and N-arylacrylamides in good yields. cis- and trans-isoxazolidine phosphonates obtained herein were evaluated for activity against a broad range of DNA and RNA viruses. None of the compounds were endowed with antiviral activity at subtoxic concentrations. Isoxazolidines having phenyl substituted with halogen (Ar = 2-F-C6H4; 3-Br-C6H4; and 4-Br-C6H4) have been found to inhibit proliferation

  5-芳基氨基甲酰基-2-甲基异恶唑烷-3-基-3-膦酸酯已经由N-甲基-C-二乙氧基磷酰基硝酮和N-芳基丙烯酰胺以良好收率合成。评估了本文获得的顺式和反式异恶唑烷膦酸盐对广泛的 DNA 和 RNA 病毒的活性。没有一种化合物在亚毒性浓度下具有抗病毒活性。已发现具有被卤素取代的苯基的异恶唑烷（Ar = 2-FC 6 H 4；3-Br-C 6 H 4；和 4-Br-C 6 H 4）可抑制 L1210、CEM 和 HeLa 细胞的增殖带集成电路50在 100–170 μM 范围内。
• 一类含酰胺和甲氧苯结构的FXa抑制剂、制备 方法及其用途
  申请人：佛山市赛维斯医药科技有限公司

  公开号：CN104610258B

  公开（公告）日：2016-03-30

  本发明涉及与静脉血栓性疾病相关的药物领域。具体而言，本发明涉及一类含酰胺和甲氧苯结构的FXa抑制剂、其制备方法、以及在制备抗静脉血栓性疾病药物中的应用。其中，R选自C1-C3的烷基。
• Rubber composition useful for tires
  申请人：SUMITOMO CHEMICAL COMPANY, LIMITED

  公开号：EP0409565A1

  公开（公告）日：1991-01-23

  A rubber composition comprising a natural and/or synthetic rubber, a filler and an acrylamide compound represented by the formula of X-NHCH=CH₂ wherein X is an aliphatic or alicyclic group, phenyl or phenoxyphenyl, in which said aliphatic or alicyclic group may contain halogen or oxygen in the group, said phenyl may be substituted once or twice by halogen, hydroxy, alkyl of 1 to 8 carbon atoms, alkoxy of 1 to 8 carbon atoms, nitro, cyano, carboxy or alkoxycarbonyl, and said phenoxyphenyl is represented by the formula of wherein Q¹ and Q² independently of one another are each hydrogen, alkyl of 1 to 8 carbon atoms, cyclohexyl, phenyl, halogen, hydroxy or amino. This rubber composition is increased in its loss factor, and is useful for tires and tread parts. The resulting tires prepared from the rubber composition are improved in their gripping performance.

  一种橡胶组合物，由天然和/或合成橡胶、填料和丙烯酰胺化合物组成，丙烯酰胺化合物的分子式为 X-NHCH=CH₂ 其中 X 为脂肪族或脂环族基团、苯基或苯氧基苯基，其中所述脂肪族或脂环族基团中可含有卤素或氧，所述苯基可被卤素、羟基、1 至 8 个碳原子的烷基、1 至 8 个碳原子的烷氧基、硝基、氰基、羧基或烷氧基羰基取代一次或两次，所述苯氧基苯基由以下式子表示 其中 Q¹ 和 Q² 各自独立地为氢、1 至 8 个碳原子的烷基、环己基、苯基、卤素、羟基或氨基。这种橡胶组合物的损耗因子增加，适用于轮胎和胎面部件。用该橡胶组合物制备的轮胎抓地性能得到改善。
• 1-2-(Pyridinyl)piperazine derivatives with antianaphylactic, antibronchospastic and mast cell stabilizing activities
  作者：Alberto Catto、Gianni Motta、Alberto Tajana、Pietro Cazzulani、Dante Nardi、Amedeo Leonardi

  DOI：10.1021/jm00384a002

  日期：1987.1

  New 1-(2-pyridinyl)piperazine derivatives were synthesized and tested as inhibitors of the reaginic passive cutaneous anaphylaxis in the rat (PCA), of the histamine-induced bronchospasm in the guinea pig, and of the rat mesenteric mast cell degranulation induced by compound 48/80. On the basis of test results, a series of N-(substituted phenyl)-omega-[4-(2-pyridinyl)-1-piperazinyl]alkanamides was prepared. The nature of substituents at the anilide ring strongly influenced mast cell stabilizing activity, whereas it was less determining in the case of the other two tests. No clear correlation between the most common physicochemical parameters (pi, sigma, Vw volume) of substituents and activity could be detected. With regard to the position of substituents at the anilide ring, the rank order of potency, in the PCA and bronchoconstriction tests, was para greater than meta greater than ortho. Introduction of substituents in the 1-(2-pyridinyl)piperazinyl moiety of the N-(substituted phenyl)propanamide derivatives hardly affected activity, or the effect was deleterious. Some of the new compounds exhibited a simultaneous remarkable activity in all the three assays employed.
• Anti-hepatitis B virus and anti-cancer activities of novel isoflavone analogs
  作者：Yikai Zhang、Hanyu Zhong、Zhiliang Lv、Mingfeng Zhang、Tao Zhang、Qisheng Li、Ke Li

  DOI：10.1016/j.ejmech.2012.09.017

  日期：2013.4

  We have synthesized a series of novel isoflavone analogs and evaluated their anti-HBV and anti-cancer activities in vitro. The bioassays showed that the majority of the resultant compounds exerted inhibitory effects on HBsAg and HBeAg levels, HBV DNA replication, as well as the growth of four human cancer cell lines to various extents, which supported the rationale of the design. In particular, compound 8f showed the highest activity against HBV infection and HBV-related liver cancer. Compound 71 (IC50 = 0.47 mu M) also exerted remarkable inhibitory effect on the growth lung cancer cell line A-549. (C) 2012 Elsevier Masson SAS. All rights reserved.

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