2-羟基-4-甲氧基-N,N-二甲基苯甲酰胺 | 1019388-59-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 2-羟基-4-甲氧基-N,N-二甲基苯甲酰胺
• 英文名称: 2-hydroxy-4-methoxy-N,N-dimethylbenzamide
• CAS: 1019388-59-0
• 化学式: C₁₀H₁₃NO₃
• mdl: MFCD11131092
• 分子量: 195.218
• InChiKey: VDBASNFFIGCEOD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  49.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-羟基-4-甲氧基-N,N-二甲基苯甲酰胺 在 4-二甲氨基吡啶 四甲基乙二胺 、 叔丁基锂 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 正戊烷 为溶剂， 反应 14.0h， 生成 2-(tert-butyldimethylsilyloxy)-6-formyl-N,N,4-trimethylbenzamide
  参考文献：
  名称：

  Total Syntheses of 2,2‘-epi-Cytoskyrin A, Rugulosin, and the Alleged Structure of Rugulin

  摘要：

  The total syntheses of 2,2'-epi-cytoskyrin A, rugulosin, and the alleged structure of rugulin are described. These naturally occurring bisanthraquinones and their relatives are characterized by novel molecular architectures at the core, at which lies a more or less complete, cage-like structural motif termed "skyrane". The strategies developed for their total synthesis feature a cascade sequence called the "cytoskyrin cascade" and deliver these molecules in short order and in a stereoselective manner.

  DOI：

  10.1021/ja0685708
• 作为产物：
  描述：

  4-甲氧基水杨酸 在 N,N-二甲基甲酰胺 草酰氯 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 10.0h， 生成 2-羟基-4-甲氧基-N,N-二甲基苯甲酰胺
  参考文献：
  名称：

  Total Syntheses of 2,2‘-epi-Cytoskyrin A, Rugulosin, and the Alleged Structure of Rugulin

  摘要：

  The total syntheses of 2,2'-epi-cytoskyrin A, rugulosin, and the alleged structure of rugulin are described. These naturally occurring bisanthraquinones and their relatives are characterized by novel molecular architectures at the core, at which lies a more or less complete, cage-like structural motif termed "skyrane". The strategies developed for their total synthesis feature a cascade sequence called the "cytoskyrin cascade" and deliver these molecules in short order and in a stereoselective manner.

  DOI：

  10.1021/ja0685708

文献信息

• Rhoda‐Electrocatalyzed Bimetallic C−H Oxygenation by Weak <i>O</i> ‐Coordination
  作者：Xuefeng Tan、Leonardo Massignan、Xiaoyan Hou、Johanna Frey、João C. A. Oliveira、Masoom Nasiha Hussain、Lutz Ackermann

  DOI：10.1002/anie.202017359

  日期：2021.6.7

  Rhodium-electrocatalyzed arene C−H oxygenation by weakly O-coordinating amides and ketones have been established by bimetallic electrocatalysis. Likewise, diverse dihydrooxazinones were selectively accessed by the judicious choice of current, enabling twofold C−H functionalization. Detailed mechanistic studies by experiment, mass spectroscopy and cyclovoltammetric analysis provided support for an unprecedented

  通过双金属电催化建立了弱O配位酰胺和酮的铑电催化芳烃 C−H 氧化反应。同样，通过明智的电流选择，可以选择性地获得多种二氢恶嗪酮，从而实现双重 C−H 官能化。通过实验、质谱和循环伏安分析进行的详细机理研究为双金属铑催化歧管前所未有的电氧化诱导的 C−H 活化提供了支持。
• Synthesis and in vitro evaluation of fluorinated diphenyloxide derivatives and sulfur analogs as serotonin transporter ligands
  作者：Sylvie Mavel、Nathalie Meheux、Denis Guilloteau、Patrick Emond

  DOI：10.1016/j.bmc.2009.10.062

  日期：2010.1

  several neurodegenerative and psychiatric disorders; radiopharmaceuticals to image the SERT by PET would be valuable in studying these diseases. To this end we synthesized diphenyloxide derivatives and sulfide analogs, as new tracers, incorporating a fluorine or oxyalkyl fluorinated group on 4′ or 5′-position on phenyl ring B. Three of these exhibited good to high in vitro affinity (7 < Ki < 8 nM) and

  由于5-羟色胺转运蛋白（SERT）参与了多种神经退行性疾病和精神疾病。用PET对SERT成像的放射性药物在研究这些疾病中将是有价值的。为此，我们合成了二苯醚衍生物和硫化物类似物，作为新的示踪剂，在苯环B的4'或5'位置掺入了氟或氧烷基氟代基团。其中三个具有良好的体外亲和力（7 <  K i  <8 nM）和相对于其他单胺转运蛋白的SERT选择性。
• Total Syntheses of 2,2‘-<i>epi</i>-Cytoskyrin A, Rugulosin, and the Alleged Structure of Rugulin
  作者：K. C. Nicolaou、Yee Hwee Lim、Jared L. Piper、Charles D. Papageorgiou

  DOI：10.1021/ja0685708

  日期：2007.4.1

  The total syntheses of 2,2'-epi-cytoskyrin A, rugulosin, and the alleged structure of rugulin are described. These naturally occurring bisanthraquinones and their relatives are characterized by novel molecular architectures at the core, at which lies a more or less complete, cage-like structural motif termed "skyrane". The strategies developed for their total synthesis feature a cascade sequence called the "cytoskyrin cascade" and deliver these molecules in short order and in a stereoselective manner.