N-(4-morpholinobenzylidene)aniline | 62441-70-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 恶嗪烷类
• 英文名称: N-(4-morpholinobenzylidene)aniline
• 英文别名: N-(4-morpholin-4-yl-benzylidene)-aniline；1-(4-morpholin-4-ylphenyl)-N-phenylmethanimine
• CAS: 62441-70-7
• 化学式: C₁₇H₁₈N₂O
• 分子量: 266.343
• InChiKey: PFBYGEGREFBQBL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  24.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-(4-morpholinobenzylidene)aniline 在 吡啶 、 苯硫酚 作用下， 以 丙酮 为溶剂， 生成 6-(4-morpholin-4-yl-phenyl)-1-phenyl-[1,3,5]triazinane-2,4-dione
  参考文献：
  名称：

  Suschitzky,H. et al., Journal of the Chemical Society. Perkin transactions I, 1977, p. 47 - 52

  摘要：

  DOI：
• 作为产物：
  描述：

  苯胺 、 4-(4-吗啉)苯甲醛 在 magnesium sulfate 作用下， 以 二氯甲烷 为溶剂， 以99 %的产率得到N-(4-morpholinobenzylidene)aniline
  参考文献：
  名称：

  10.1002/chem.202401034

  摘要：

  AbstractSyntheses of (partially) aromatic nitrogen heterocycles increasingly rely on transition‐metal catalyzed C−C‐ and C−N‐cross‐coupling reactions. Here we describe a different approach to the synthesis of indolines by a domino C(sp3)−H activation, 1,2‐addition, and defluorinative SNAr‐cyclization sequence to provide the target 1,2‐diarylindolines (1,2‐diaryl‐2,3‐dihydroindoles) from ortho‐fluorinated methyl‐arenes and N‐aryl imines (benzylidene anilines) in a cyclocondensation that is mediated by potassium hexamethyldisilazide (KHMDS) as base exclusively. This transition‐metal‐free process via C−H and C−F bond activation provides a one‐step entry into a wide array of indoline scaffolds (43 examples, up to 96 % yield). This privileged substructure is common in natural products and pharmaceuticals alike, and cannot be accessed by traditional condensation reactions.

  DOI：

  10.1002/chem.202401034

文献信息

• Solvent-Switched Benzylic Methylene Functionalization: Addition, Ring-Opening, Cyclization, and Unexpected Cleavage of C–O and C–C Bonds
  作者：Deng Yuan Li、Xue Song Shang、Guo Rong Chen、Pei Nian Liu

  DOI：10.1021/ol401470y

  日期：2013.8.2

  been achieved using imines as reagents and potassium tert-butoxide as the catalyst. Depending on the solvent used, the reaction proceeds by two pathways. In THF, an addition/elimination reaction of exo-cyclic enol ethers with imines provides dihydroisobenzofuran derivatives in good yield. In DMSO, an addition/ring-opening/cyclization cascade reaction occurs with unexpected cleavage of C–O and C–C bonds

  使用亚胺作为试剂并使用叔丁醇钾作为催化剂，可以实现环外烯醇醚的分子间苄基亚甲基官能化。根据所使用的溶剂，反应通过两个途径进行。在THF中，的加成/消除反应外切-环烯醇醚与亚胺提供以良好的收率二氢异苯并呋喃衍生物。在DMSO中，加成/开环/环化级联反应会发生意外的C–O和C–C键断裂，从而在环境反应条件下以高收率提供异喹啉-1（2 H）-一产品。
• Transition Metal-Free Cascade Reactions of Alkynols to Afford Isoquinolin-1(2<i>H</i>)-one and Dihydroisobenzofuran Derivatives
  作者：Deng Yuan Li、Ke Ji Shi、Xiao Feng Mao、Guo Rong Chen、Pei Nian Liu

  DOI：10.1021/jo5006312

  日期：2014.5.16

  Transition metal-free cascade reactions of alkynols with imines have been achieved using potassium tert-butoxide as catalyst. Switching the reaction solvent gives two kinds of products in good yield: isoquinolin-1(2H)-one derivatives and dihydroisobenzofuran derivatives. This approach was used to generate the natural product 8-oxypseudopalmatine in a two-step procedure from commercially available starting materials. Additionally, multicomponent reactions of alkynols, aldehydes, and amines were also successfully achieved to afford isoquinolin-1(2H)-one derivatives.
• Suschitzky,H. et al., Journal of the Chemical Society. Perkin transactions I, 1977, p. 47 - 52
  作者：Suschitzky,H. et al.

  DOI：——

  日期：——
• 10.1002/chem.202401034
  作者：Weindl, Christian、Hintermann, Lukas

  DOI：10.1002/chem.202401034

  日期：——

  AbstractSyntheses of (partially) aromatic nitrogen heterocycles increasingly rely on transition‐metal catalyzed C−C‐ and C−N‐cross‐coupling reactions. Here we describe a different approach to the synthesis of indolines by a domino C(sp3)−H activation, 1,2‐addition, and defluorinative SNAr‐cyclization sequence to provide the target 1,2‐diarylindolines (1,2‐diaryl‐2,3‐dihydroindoles) from ortho‐fluorinated methyl‐arenes and N‐aryl imines (benzylidene anilines) in a cyclocondensation that is mediated by potassium hexamethyldisilazide (KHMDS) as base exclusively. This transition‐metal‐free process via C−H and C−F bond activation provides a one‐step entry into a wide array of indoline scaffolds (43 examples, up to 96 % yield). This privileged substructure is common in natural products and pharmaceuticals alike, and cannot be accessed by traditional condensation reactions.