4-(5-chloro-1-methyl-1H-indol-4-yl)morpholine | 1444747-20-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 4-(5-chloro-1-methyl-1H-indol-4-yl)morpholine
• 英文别名: 4-(5-Chloro-1-methylindol-4-yl)morpholine
• CAS: 1444747-20-9
• 化学式: C₁₃H₁₅ClN₂O
• 分子量: 250.728
• InChiKey: CCTDDNSDCUZBPI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  17
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  17.4
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  n-氯吗啉 、 1-methyl-4-(trimethylsilyl)-1H-indol-5-yl trifluoromethanesulfonate 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 24.0h， 生成 4-(4-chloro-1-methyl-1H-indol-5-yl)morpholine 、 4-(5-chloro-1-methyl-1H-indol-4-yl)morpholine
  参考文献：
  名称：

  Synthesis of ortho-Haloaminoarenes by Aryne Insertion of Nitrogen–Halide Bonds

  摘要：

  A rapid and general access to ortho-haloaminoarenes has been developed by aryne insertion into N-chloramine, N-bromoamine, and N-iodoamine bonds via two complementary protocols harnessing fluoride-promoted 1,2-elimination of ortho-trimethylsilyl aryltriflates. Typically, electron-deficient N-chloramines effectively react with aryne intermediates generated at elevated temperature with CsF, while less stable N-haloamines are found more efficient under milder, TBAF-mediated aryne formation at room temperature. Both protocols demonstrate a good level of regioselectivity and functional group tolerance. Efforts to elucidate the mechanism of NX insertion are also discussed. The practical value of this transformation is highlighted by rapid synthesis of novel analogues of the antipsychotic cariprazine.

  DOI：

  10.1021/jo502541t

文献信息

• Insertion of Arynes into <i>N</i>-Halo Bonds: A Direct Approach to <i>o</i>-Haloaminoarenes
  作者：Charles E. Hendrick、Stacey L. McDonald、Qiu Wang

  DOI：10.1021/ol401518c

  日期：2013.7.5

  A new approach to access o-haloaminoarenes has been achieved by insertion of arynes into a nitrogen-halide bond (N-X). This transition-metal-free transformation displays a broad substrate scope of arynes, good compatibility with functional groups, and high regioselectivity. Representative transformations of the o-haloaminoarenes are described to highlight their utility for rapid access to diversely functionalized a minoarene derivatives.