2-[5-chloro-2-oxo-3-(2-oxoethyl)-1-((2-(trimethylsilyl)ethoxy)methyl)indolin-3-yl]acetonitrile | 1258864-70-8

• 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: 2-[5-chloro-2-oxo-3-(2-oxoethyl)-1-((2-(trimethylsilyl)ethoxy)methyl)indolin-3-yl]acetonitrile
• 英文别名: 2-[5-Chloro-2-oxo-3-(2-oxoethyl)-1-(2-trimethylsilylethoxymethyl)indol-3-yl]acetonitrile；2-[5-chloro-2-oxo-3-(2-oxoethyl)-1-(2-trimethylsilylethoxymethyl)indol-3-yl]acetonitrile
• CAS: 1258864-70-8
• 化学式: C₁₈H₂₃ClN₂O₃Si
• 分子量: 378.931
• InChiKey: KLBIIKGTSAKCNA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.74
• 重原子数：
  25
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  70.4
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-[5-chloro-2-oxo-3-(2-oxoethyl)-1-((2-(trimethylsilyl)ethoxy)methyl)indolin-3-yl]acetonitrile 在 sodium tetrahydroborate 、 cobalt(II) chloride hexahydrate 、 盐酸 、 sodium hydroxide 作用下， 以 甲醇 、 水 为溶剂， 反应 1.25h， 以55%的产率得到5-chloro-1-((2-(trimethylsilyl)ethoxy)methyl)spiro[indoline-3,4'-piperidin]-2-one
  参考文献：
  名称：

  Palladium-catalyzed domino Heck/cyanation: synthesis of 3-cyanomethyloxindoles and their conversion to spirooxoindoles

  摘要：

  3'-Alkyl-3-cyanomethyloxindoles, prepared by a palladium-catalyzed domino Heck/cyanation, were efficiently converted to spiropyrrolidinyl-, spiropiperidinyl- and spirocyclopropyl-oxindoles. The so-obtained spirooxindoles bearing three diversity points were further functionalized via selective N-acylation, N-alkylation, N-sulfonylation, SNAr reaction and Buchwald-Hartwig N-arylation reaction to reach diverse set of heterocycles. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.09.056
• 作为产物：
  描述：

  2-[3-((1,3-dioxolan-2-yl)methyl)-5-chloro-2-oxo-1-((2-(trimethylsilyl)ethoxy)methyl)indolin-3-yl]acetonitrile 在 盐酸 、 水 作用下， 以 四氢呋喃 为溶剂， 以53%的产率得到2-[5-chloro-2-oxo-3-(2-oxoethyl)-1-((2-(trimethylsilyl)ethoxy)methyl)indolin-3-yl]acetonitrile
  参考文献：
  名称：

  Palladium-catalyzed domino Heck/cyanation: synthesis of 3-cyanomethyloxindoles and their conversion to spirooxoindoles

  摘要：

  3'-Alkyl-3-cyanomethyloxindoles, prepared by a palladium-catalyzed domino Heck/cyanation, were efficiently converted to spiropyrrolidinyl-, spiropiperidinyl- and spirocyclopropyl-oxindoles. The so-obtained spirooxindoles bearing three diversity points were further functionalized via selective N-acylation, N-alkylation, N-sulfonylation, SNAr reaction and Buchwald-Hartwig N-arylation reaction to reach diverse set of heterocycles. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.09.056

文献信息

• Palladium-catalyzed domino Heck/cyanation: synthesis of 3-cyanomethyloxindoles and their conversion to spirooxoindoles
  作者：Stéphanie Jaegli、Jean-Pierre Vors、Luc Neuville、Jieping Zhu

  DOI：10.1016/j.tet.2010.09.056

  日期：2010.11

  3'-Alkyl-3-cyanomethyloxindoles, prepared by a palladium-catalyzed domino Heck/cyanation, were efficiently converted to spiropyrrolidinyl-, spiropiperidinyl- and spirocyclopropyl-oxindoles. The so-obtained spirooxindoles bearing three diversity points were further functionalized via selective N-acylation, N-alkylation, N-sulfonylation, SNAr reaction and Buchwald-Hartwig N-arylation reaction to reach diverse set of heterocycles. (C) 2010 Elsevier Ltd. All rights reserved.