1-(3-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acetylene | 1380434-10-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: 1-(3-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acetylene
• 英文别名: 1,2,3-Trimethoxy-5-(3-methoxy-phenylethynyl)-benzene；1,2,3-trimethoxy-5-[2-(3-methoxyphenyl)ethynyl]benzene
• CAS: 1380434-10-5
• 化学式: C₁₈H₁₈O₄
• 分子量: 298.339
• InChiKey: WMUKONWOCCOVJI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.12
• 重原子数：
  22.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  36.92
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  1-(3-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acetylene 在 potassium permanganate 、 碳酸氢钠 、 magnesium sulfate 作用下， 以 水 、 丙酮 为溶剂， 反应 24.0h， 以83%的产率得到1-(3-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethandione
  参考文献：
  名称：

  Synthesis of Highly Functionalized 9,10-Phenanthrenequinones by Oxidative Coupling Using MoCl₅

  摘要：

  The strong oxidative power of molybdenum pentachloride gives rise to an efficient oxidative C-C bond formation of benzil derivatives to the corresponding 9,10-phenanthrenequinones. A highly complementary method to previous approaches was developed. The required derivatives are accessible in a modular fashion and in excellent yields. By this approach the orchid-derived natural product cypripediquinone A was synthesized for the first time.

  DOI：

  10.1021/ol300948u
• 作为产物：
  描述：

  5-碘-1,2,3-三甲氧基苯 、 3-乙炔基苯甲醚 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 16.0h， 以83%的产率得到1-(3-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acetylene
  参考文献：
  名称：

  Synthesis of Highly Functionalized 9,10-Phenanthrenequinones by Oxidative Coupling Using MoCl₅

  摘要：

  The strong oxidative power of molybdenum pentachloride gives rise to an efficient oxidative C-C bond formation of benzil derivatives to the corresponding 9,10-phenanthrenequinones. A highly complementary method to previous approaches was developed. The required derivatives are accessible in a modular fashion and in excellent yields. By this approach the orchid-derived natural product cypripediquinone A was synthesized for the first time.

  DOI：

  10.1021/ol300948u

文献信息

• Diaryl-substituted ortho-carboranes as a new class of hypoxia inducible factor-1α inhibitors
  作者：Hiroyuki Nakamura、Lisa Tasaki、Daisuke Kanoh、Shinichi Sato、Hyun Seung Ban

  DOI：10.1039/c3dt52828f

  日期：——

  Diaryl-substituted ortho-carboranes 1 were synthesized from the corresponding alkynes by decaborane coupling under microwave-irradiated conditions with a combination of N,N-dimethylaniline and chlorobenzene. Among the compounds synthesized, 1a and 1d exhibited significant inhibition of hypoxia-induced HIF-1 transcriptional activity. Both compounds similarly suppressed hypoxia-induced HIF-1α accumulation in a concentration-dependent manner without affecting HIF-1α mRNA expression.

  二芳基取代邻位碳硼烷1通过在微波辐照条件下，结合N,N-二甲基苯胺和氯苯，利用癸硼烷与相应炔烃的耦合反应合成。在合成的化合物中，1a和1d表现出显著抑制缺氧诱导的HIF-1转录活性。这两种化合物均以浓度依赖性方式相似地抑制缺氧诱导的HIF-1α积累，而不影响HIF-1α mRNA表达。
• Efficient synthesis of quinoxalines with hypervalent iodine as a catalyst
  作者：Chung-Yu Chen、Wan-Ping Hu、Mei-Chun Liu、Pi-Cheng Yan、Jeh-Jeng Wang、Mei-Ing Chung

  DOI：10.1016/j.tet.2013.09.027

  日期：2013.11

  Various biologically important quinoxalines were efficiently synthesized in excellent yields via one-pot reaction between 1,2-diaminobenzenes and internal alkynes. The method utilizes inexpensive and readily available hypervalent iodine source, such as (diacetoxyiodo)benzene (PhI(OAc)(2)) and proved to be a better alternative as compared to expensive transition metal catalysts. Quinoxaline 4i [(2-phenyl-3-(3,4,5-trimethoxy phenyl)quinoxaline)] was evaluated for leukemia cancer cell lines and turned out to be a good candidate. (C) 2013 Elsevier Ltd. All rights reserved.
• Metal-Free, Acid-Promoted Synthesis of Imidazole Derivatives via a Multicomponent Reaction
  作者：Chung-Yu Chen、Wan-Ping Hu、Pi-Cheng Yan、Gopal Chandru Senadi、Jeh-Jeng Wang

  DOI：10.1021/ol402892z

  日期：2013.12.20

  An expedient and metal-free synthetic route has been developed for the construction of tri- and tetrasubstituted imidazole derivatives via acid promoted multicomponent reaction methodology. The reaction proceeded smoothly with a range of functionalities to produce the imidazole scaffolds in good to excellent yields.