3-乙酰基-6-氯吲哚 | 184151-47-1

• 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
• 中文名称: 3-乙酰基-6-氯吲哚
• 英文名称: 1-(6-chloro-1H-indol-3-yl)ethan-1-one
• 英文别名: 1-(6-chloro-1H-indol-3-yl)ethanone
• CAS: 184151-47-1
• 化学式: C₁₀H₈ClNO
• mdl: MFCD11212227
• 分子量: 193.633
• InChiKey: KQLYMFKKPNNGQR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  32.9
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3-乙酰基-6-氯吲哚 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 生成 6-chloro-3-ethyl-1H-indole
  参考文献：
  名称：

  Discovery of a novel indole series of EP1 receptor antagonists by scaffold hopping

  摘要：

  We describe the medicinal chemistry approach that generated a novel indole series of EP1 receptor antagonists. The SAR of this new template was evaluated and culminated in the identification of compound 12g which demonstrated in vivo efficacy in a preclinical model of inflammatory pain. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.03.018
• 作为产物：
  描述：

  6-氯吲哚 、 乙酰氯 在 四氯化锡 作用下， 以 甲苯 为溶剂， 反应 12.17h， 生成 3-乙酰基-6-氯吲哚
  参考文献：
  名称：

  铑（III）催化的区域选择性直接C4烷基化和吲哚的C2环化反应：直接获得吲哚并吡啶酮

  摘要：

  通过使用可变的重氮酯开发了Rh III催化的吲哚衍生物的位点C4烷基化和C2环化。对重氮酯反应性的微调可以控制区域选择性，具有宽范围和官能团耐受性。已经建立了一种简单的方法来提供吲哚并吡啶酮支架。

  DOI：

  10.1002/ejoc.201701755

文献信息

• Towards the syntheses of<i>N</i>-H and<i>N</i>-alkylated derivatives of meridianins
  作者：Bernard Corbel、FrançOis Michaud、Laurent Meijer、Gaëlle Simon、Hélène Couthon-Gourves、Jean-Pierre Haelters、Nelly Kervarec

  DOI：10.1002/jhet.5570440407

  日期：2007.7

  Novel N-H and N-alkylated derivatives of meridianins have been synthesized as potential antitumor agents by a two-step conversion of N-tosyl-3-acetylindoles or N-alkyl-3-acetylindoles to the corresponding enaminones using DMF-DMA, with or without added pyrrolidine. Further cyclization with guanidine gave the corresponding 2-aminopyrimidines. The structures of the compounds, thus obtained, were proved

  通过使用DMF-DMA将N-甲苯磺酰基-3-乙酰基吲哚或N-烷基-3-乙酰基吲哚经两步转化为相应的烯胺酮，合成了经络胺的新型N- H和N-烷基化衍生物作为潜在的抗肿瘤药。或不添加吡咯烷。用胍进一步环化得到相应的2-氨基嘧啶。由此获得的化合物的结构通过1 H和13 C NMR光谱，NOE实验和X射线分析证明。
• Regiocontrolled direct C4 and C2-methyl thiolation of indoles under rhodium-catalyzed mild conditions
  作者：Saurabh Maity、Ujjwal Karmakar、Rajarshi Samanta

  DOI：10.1039/c7cc07086a

  日期：——

  Rh(III)catalyzed general strategy was developed for the site selective remote C4 (sp2) and C2 (sp3)-methyl thiolation of indole core keeping the oxime directing group at the C3 position. The transformation was accomplished under mild conditions with wide scope and functional group tolerance. The directing group can easily be removed after operation. Methyl substitution at the C2 position of indole core

  一种直接的Rh（III）催化的一般策略是针对吲哚核的位点选择性远程C4（sp 2）和C2（sp 3）-甲基硫醇化而开发的，将肟导向基团保持在C3位置。该转化是在温和条件下完成的，具有宽范围和官能团耐受性。引导组可以在操作后轻松移除。吲哚核的C2位置处的甲基取代导致C2（sp 3）-甲基硫醇化。
• A radical addition and cyclization relay promoted by Mn(OAc)3⋅2H2O: Synthesis of 1,2-oxaphospholoindoles and mechanistic study
  作者：Meng-Meng Xu、Lu-Yao Kou、Xiao-Guang Bao、Xiao-Ping Xu、Shun-Jun Ji

  DOI：10.1016/j.cclet.2021.02.001

  日期：2021.6

  Novel and efficient Mn(OAc)3⋅2H2O promoted radical addition-[4 + 1] cyclization relay of 3-indolymethanols and phosphites was disclosed, which afforded 1,2-oxaphospholoindole derivatives in moderate to good yields. Based on the experimental and computational studies, a mechanism involving radical addition and intramolecular cyclization cascade was proposed.

  新型高效的 Mn(OAc) 3 ⋅2H 2 O 促进了 3-吲哚甲醇和亚磷酸酯的自由基加成-[4 + 1] 环化中继，以中等至良好的产率提供了 1,2-氧杂磷并吲哚衍生物。基于实验和计算研究，提出了一种涉及自由基加成和分子内环化级联的机制。
• C4-arylation and domino C4-arylation/3,2-carbonyl migration of indoles by tuning Pd catalytic modes: Pd(<scp>i</scp>)–Pd(<scp>ii</scp>) catalysis <i>vs.</i> Pd(<scp>ii</scp>) catalysis
  作者：Yaohang Cheng、Shijie Yu、Yuhang He、Guanghui An、Guangming Li、Zhenyu Yang

  DOI：10.1039/d0sc05409g

  日期：——

  have been developed. The former route enables C4-arylation in a highly efficient and mild manner and the latter route provides an alternative straightforward protocol for synthesis of C2/C4 disubstituted indoles. The mechanism studies imply that the different reaction pathways were tuned by the distinct acid additives, which led to either the Pd(I)–Pd(II) pathway or Pd(II) catalysis.

  吲哚的高效 C4-芳基化和多米诺 C4-芳基化/3,2-羰基迁移已经开发出来。前一种路线能够以高效且温和的方式实现C4-芳基化，后一种路线为合成C2/C4二取代吲哚提供了一种替代的简单方案。机理研究表明不同的反应途径是通过不同的酸添加剂调节的，从而导致 Pd()–Pd( II ) 途径或 Pd( II ) 催化。
• Rh(III)-Catalyzed [5 + 1] Annulation of Indole-enaminones with Diazo Compounds To Form Highly Functionalized Carbazoles
  作者：Zhidong Jiang、Jianhui Zhou、Haoran Zhu、Hong Liu、Yu Zhou

  DOI：10.1021/acs.orglett.1c01341

  日期：2021.6.4

  A novel Rh(III)-catalyzed C–H activation/annulation cascade of indole-enaminones with diazo compounds was reported to construct diversely functionalized carbazole frameworks. The most notable characteristic is that this transformation could smoothly furnish a novel [5 + 1] cyclization product with good to excellent yields (up to 95%), accompanied by the thorough removal of acetyl and N,N-dimethyl groups

  据报道，一种新型 Rh(III) 催化的吲哚-烯胺酮与重氮化合物的 C-H 活化/环化级联可构建多种功能化的咔唑框架。最显着的特点是这种转化可以顺利地提供一种新的 [5 + 1] 环化产物，收率从高到高（高达 95%），同时彻底去除了两种底物的乙酰基和N , N-二甲基基团。目标产物，而不是通常预期的 [4 + 2] 环化产物。