2-[5-(1-Hydroxy-1-thiophen-2-ylethyl)thiophen-2-yl]ethyl 4-methylbenzenesulfonate | 219737-10-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-[5-(1-Hydroxy-1-thiophen-2-ylethyl)thiophen-2-yl]ethyl 4-methylbenzenesulfonate
• CAS: 219737-10-7
• 化学式: C₁₉H₂₀O₄S₃
• 分子量: 408.563
• InChiKey: JBMRYDBBROAIKN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  26
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  129
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2-[5-(1-Hydroxy-1-thiophen-2-ylethyl)thiophen-2-yl]ethyl 4-methylbenzenesulfonate 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 生成
  参考文献：
  名称：

  Excellent acceleration of the Diels-Alder reaction by microwave irradiation for the synthesis of new fluorine-substituted ligands of NMDA receptor

  摘要：

  A series of 6,11-ethanobenzo[b]quinolizinium derivatives was synthesized through the Diels-Alder reaction between azoniaanthracne and the corresponding 1,1-disubstituted olefin. After a systematic investigation for achieving rapid synthesis, it was found that the reaction is accelerated in polar media such as H2O and trifluoroethanol. In particular, excellent acceleration was effected by microwave irradiation. The new fluorine-substituted ligands thus obtained exhibited potential affinity toward NMDA receptors. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00541-1
• 作为产物：
  描述：

  2-噻吩乙醇 在 正丁基锂 、 TEA 作用下， 以 二氯甲烷 为溶剂， 生成 2-[5-(1-Hydroxy-1-thiophen-2-ylethyl)thiophen-2-yl]ethyl 4-methylbenzenesulfonate
  参考文献：
  名称：

  Excellent acceleration of the Diels-Alder reaction by microwave irradiation for the synthesis of new fluorine-substituted ligands of NMDA receptor

  摘要：

  A series of 6,11-ethanobenzo[b]quinolizinium derivatives was synthesized through the Diels-Alder reaction between azoniaanthracne and the corresponding 1,1-disubstituted olefin. After a systematic investigation for achieving rapid synthesis, it was found that the reaction is accelerated in polar media such as H2O and trifluoroethanol. In particular, excellent acceleration was effected by microwave irradiation. The new fluorine-substituted ligands thus obtained exhibited potential affinity toward NMDA receptors. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00541-1

文献信息

• Excellent acceleration of the Diels-Alder reaction by microwave irradiation for the synthesis of new fluorine-substituted ligands of NMDA receptor
  作者：Shigeki Sasaki、Nobuyasu Ishibashi、Tshuneo Kuwamura、Hiromi Sano、Masaki Matoba、Tohru Nisikawa、Minoru Maeda

  DOI：10.1016/s0960-894x(98)00541-1

  日期：1998.11

  A series of 6,11-ethanobenzo[b]quinolizinium derivatives was synthesized through the Diels-Alder reaction between azoniaanthracne and the corresponding 1,1-disubstituted olefin. After a systematic investigation for achieving rapid synthesis, it was found that the reaction is accelerated in polar media such as H2O and trifluoroethanol. In particular, excellent acceleration was effected by microwave irradiation. The new fluorine-substituted ligands thus obtained exhibited potential affinity toward NMDA receptors. (C) 1998 Elsevier Science Ltd. All rights reserved.