tert-butyl-[[3-[2-[tert-butyl(dimethyl)silyl]oxyethyl]-1H-indol-5-yl]oxy]-dimethylsilane | 876743-45-2

• 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: tert-butyl-[[3-[2-[tert-butyl(dimethyl)silyl]oxyethyl]-1H-indol-5-yl]oxy]-dimethylsilane
• CAS: 876743-45-2
• 化学式: C₂₂H₃₉NO₂Si₂
• 分子量: 405.728
• InChiKey: XRPUYBNGIIBTBF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.12
• 重原子数：
  27
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  34.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  tert-butyl-[[3-[2-[tert-butyl(dimethyl)silyl]oxyethyl]-1H-indol-5-yl]oxy]-dimethylsilane 在 cerium(III) chloride 、 2-碘苯甲酸 作用下， 以 二甲基亚砜 、 乙腈 为溶剂， 反应 11.0h， 生成 2-[5-[tert-butyl(dimethyl)silyl]oxy-1H-indol-3-yl]acetaldehyde
  参考文献：
  名称：

  Chemical synthesis and structural elucidation of a new serotonin metabolite: (4R)-2-[(5′-hydroxy-1′H-indol-3′-yl)methyl]thiazolidine-4-carboxylic acid

  摘要：

  A new serotonin (5-hydroxytryptamine) metabolite, (4R)-2-[(5'-hydroxy-1'H-indol-3'-yl)methyl]thiazolidine-4-carboxylic acid (5'-HITCA),. was synthesized in 30% overall yield. The key step involved oxidation of protected 5-hydroxytryptophol using IBX followed by spontaneous cyclization with L-cysteine. The stereochemistry of condensation product thiazolidine-4-carboxylic acid was studied using NMR spectroscopy techniques. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2005.11.153
• 作为产物：
  描述：

  5-羟基吲哚-3-乙醇 、 叔丁基二甲基氯硅烷 在 咪唑 作用下， 以 四氢呋喃 为溶剂， 以100%的产率得到tert-butyl-[[3-[2-[tert-butyl(dimethyl)silyl]oxyethyl]-1H-indol-5-yl]oxy]-dimethylsilane
  参考文献：
  名称：

  Chemical synthesis and structural elucidation of a new serotonin metabolite: (4R)-2-[(5′-hydroxy-1′H-indol-3′-yl)methyl]thiazolidine-4-carboxylic acid

  摘要：

  A new serotonin (5-hydroxytryptamine) metabolite, (4R)-2-[(5'-hydroxy-1'H-indol-3'-yl)methyl]thiazolidine-4-carboxylic acid (5'-HITCA),. was synthesized in 30% overall yield. The key step involved oxidation of protected 5-hydroxytryptophol using IBX followed by spontaneous cyclization with L-cysteine. The stereochemistry of condensation product thiazolidine-4-carboxylic acid was studied using NMR spectroscopy techniques. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2005.11.153

文献信息

• Chemical synthesis and structural elucidation of a new serotonin metabolite: (4R)-2-[(5′-hydroxy-1′H-indol-3′-yl)methyl]thiazolidine-4-carboxylic acid
  作者：Chunyang Jin、Jason P. Burgess、Madathil B. Gopinathan、George A. Brine

  DOI：10.1016/j.tetlet.2005.11.153

  日期：2006.2

  A new serotonin (5-hydroxytryptamine) metabolite, (4R)-2-[(5'-hydroxy-1'H-indol-3'-yl)methyl]thiazolidine-4-carboxylic acid (5'-HITCA),. was synthesized in 30% overall yield. The key step involved oxidation of protected 5-hydroxytryptophol using IBX followed by spontaneous cyclization with L-cysteine. The stereochemistry of condensation product thiazolidine-4-carboxylic acid was studied using NMR spectroscopy techniques. (c) 2005 Elsevier Ltd. All rights reserved.