3-[2-(4-Methoxyphenyl)ethyl]imidazole-4-carbaldehyde | 635754-89-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 3-[2-(4-Methoxyphenyl)ethyl]imidazole-4-carbaldehyde
• CAS: 635754-89-1
• 化学式: C₁₃H₁₄N₂O₂
• 分子量: 230.266
• InChiKey: JGPKFBBBEFINPE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  17
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  44.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-[2-(4-Methoxyphenyl)ethyl]imidazole-4-carbaldehyde 、 在 三乙酰氧基硼氢化钠 作用下， 以 二氯甲烷 为溶剂， 反应 12.0h， 生成
  参考文献：
  名称：

  Parallel liquid synthesis of N,N′-Disubstituted 3-amino azepin-2-ones as potent and specific farnesyl transferase inhibitors

  摘要：

  A rapid structure-activity study was performed by parallel liquid synthesis on N,N'-disubstitution of 3-amino azepin-2-one to afford potent and specific farnesyl transferase inhibitors with low nM enzymatic and cellular activities. The activities of the selected compounds were validated in vivo, and compounds 41a and 44a presented significant antitumour activity. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(03)00218-9
• 作为产物：
  描述：

  2-(4-甲氧苯基)乙胺 在 双氧水 、 三氧化硫吡啶 、 溶剂黄146 、 二甲基亚砜 、 丙酸 、 三乙胺 作用下， 以 水 、 乙腈 为溶剂， 反应 8.0h， 生成 3-[2-(4-Methoxyphenyl)ethyl]imidazole-4-carbaldehyde
  参考文献：
  名称：

  Parallel liquid synthesis of N,N′-Disubstituted 3-amino azepin-2-ones as potent and specific farnesyl transferase inhibitors

  摘要：

  A rapid structure-activity study was performed by parallel liquid synthesis on N,N'-disubstitution of 3-amino azepin-2-one to afford potent and specific farnesyl transferase inhibitors with low nM enzymatic and cellular activities. The activities of the selected compounds were validated in vivo, and compounds 41a and 44a presented significant antitumour activity. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(03)00218-9

文献信息

• Parallel liquid synthesis of N,N′-Disubstituted 3-amino azepin-2-ones as potent and specific farnesyl transferase inhibitors
  作者：Thierry Le Diguarher、Jean-Claude Ortuno、Gilbert Dorey、David Shanks、Nicolas Guilbaud、Alain Pierré、Jean-Luc Fauchère、John A. Hickman、Gordon C. Tucker、Patrick J. Casara

  DOI：10.1016/s0968-0896(03)00218-9

  日期：2003.7

  A rapid structure-activity study was performed by parallel liquid synthesis on N,N'-disubstitution of 3-amino azepin-2-one to afford potent and specific farnesyl transferase inhibitors with low nM enzymatic and cellular activities. The activities of the selected compounds were validated in vivo, and compounds 41a and 44a presented significant antitumour activity. (C) 2003 Elsevier Science Ltd. All rights reserved.