3-trimethylsilylethynylisoquinoline | 86521-11-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异喹啉及其衍生物
• 英文名称: 3-trimethylsilylethynylisoquinoline
• 英文别名: 3-((Trimethylsilyl)ethynyl)isoquinoline；2-isoquinolin-3-ylethynyl(trimethyl)silane
• CAS: 86521-11-1
• 化学式: C₁₄H₁₅NSi
• 分子量: 225.365
• InChiKey: DCTOSPSCGVALNI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.46
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  12.9
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3-trimethylsilylethynylisoquinoline 在 氢氧化钾 作用下， 以 甲醇 为溶剂， 反应 3.0h， 以60%的产率得到3-乙炔异喹啉
  参考文献：
  名称：

  A Facile Synthesis of Ethynyl-Substituted Six-MemberedN-Heteroaromatic Compounds

  摘要：

  DOI：

  10.1055/s-1983-30319
• 作为产物：
  描述：

  3-羟基异喹啉 在 copper(l) iodide 、 四(三苯基膦)钯 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 3-trimethylsilylethynylisoquinoline
  参考文献：
  名称：

  Ru(II) coordination compounds of N N bidentate chelators with 1,2,3 triazole and isoquinoline subunits: Synthesis, spectroscopy and antimicrobial properties

  摘要：

  Bidentate chelators 1 -(1-benzyl-1,2,3-triazol-4-yl)isoquinoline and 3-(1-benzyl-1,2,3-triazol-4-yl)isoquinoline were prepared from benzyl bromide and trimethylsilylethynylisoquinoline precursors using a tandem deprotection/substitution/CuAAC synthetic approach. Each chelator is capable of forming a stable 3:1 Ru(II) coordination compound, which forms as a geometric isomer mixture. These Ru(II) complexes possess unique MLCT absorbance signatures at 450/472 nm (1-isomer) and 367 nm (3-isomer) relative to their constituent chelating units. Minimum inhibitory concentration values as low as 0.4 mu M are observed for Ru(II) complexes against representative Gram-positive bacteria Bacillus subtilis and Staphylococcus epidermidis. Comparing the MIC values of these isoquinoline compounds with analogous 2-(1-benzyl-1,2,3-triazol-4-yl)pyridine compounds shows a 2.5- to 40-fold improvement in potency. This study establishes that increased hydrophobicity introduced at the central chelating units of Ru(II) coordination compounds can be a useful means by which to optimize antimicrobial activity that is complimentary to the variation of peripheral substituent identity at the chelator's N1 triazole position. (C) 2019 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2019.114259

文献信息

• SAKAMOTO, TAKAO;SHIRAIWA, MASAFUMI;KONDO, YOSHINORI;YAMANAKA, HIROSHI, SYNTHESIS, BRD, 1983, N 4, 312-314
  作者：SAKAMOTO, TAKAO、SHIRAIWA, MASAFUMI、KONDO, YOSHINORI、YAMANAKA, HIROSHI

  DOI：——

  日期：——
• A Facile Synthesis of Ethynyl-Substituted Six-Membered<i>N</i>-Heteroaromatic Compounds
  作者：Takao Sakamoto、Masafumi Shiraiwa、Yoshinori Kondo、Hiroshi Yamanaka

  DOI：10.1055/s-1983-30319

  日期：——
• Ru(II) coordination compounds of N N bidentate chelators with 1,2,3 triazole and isoquinoline subunits: Synthesis, spectroscopy and antimicrobial properties
  作者：Nicholas W. Kreofsky、Maxwell D. Dillenburg、Eric M. Villa、James T. Fletcher

  DOI：10.1016/j.poly.2019.114259

  日期：2020.2

  Bidentate chelators 1 -(1-benzyl-1,2,3-triazol-4-yl)isoquinoline and 3-(1-benzyl-1,2,3-triazol-4-yl)isoquinoline were prepared from benzyl bromide and trimethylsilylethynylisoquinoline precursors using a tandem deprotection/substitution/CuAAC synthetic approach. Each chelator is capable of forming a stable 3:1 Ru(II) coordination compound, which forms as a geometric isomer mixture. These Ru(II) complexes possess unique MLCT absorbance signatures at 450/472 nm (1-isomer) and 367 nm (3-isomer) relative to their constituent chelating units. Minimum inhibitory concentration values as low as 0.4 mu M are observed for Ru(II) complexes against representative Gram-positive bacteria Bacillus subtilis and Staphylococcus epidermidis. Comparing the MIC values of these isoquinoline compounds with analogous 2-(1-benzyl-1,2,3-triazol-4-yl)pyridine compounds shows a 2.5- to 40-fold improvement in potency. This study establishes that increased hydrophobicity introduced at the central chelating units of Ru(II) coordination compounds can be a useful means by which to optimize antimicrobial activity that is complimentary to the variation of peripheral substituent identity at the chelator's N1 triazole position. (C) 2019 Elsevier Ltd. All rights reserved.