3-(3-(1H-imidazol-1-yl)propyl)-5-methyl-5-(naphthalen-1-yl)imidazolidine-2,4-dione | 883753-97-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: 3-(3-(1H-imidazol-1-yl)propyl)-5-methyl-5-(naphthalen-1-yl)imidazolidine-2,4-dione
• 英文别名: 3-(3-imidazol-1-ylpropyl)-5-methyl-5-naphthalen-1-ylimidazolidine-2,4-dione
• CAS: 883753-97-7
• 化学式: C₂₀H₂₀N₄O₂
• 分子量: 348.404
• InChiKey: VESCLSDOPNDLRS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  26
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  67.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-(3-(1H-imidazol-1-yl)propyl)-5-methyl-5-(naphthalen-1-yl)imidazolidine-2,4-dione 、 间苯氧基溴化苄 在 sodium hydride 作用下， 生成 3-(3-imidazol-1-yl-propyl)-5-methyl-5-naphthalen-1-yl-1-(3-phenoxy-benzyl)-imidazolidin-2,4-dione
  参考文献：
  名称：

  Hydantoin derivatives as non-peptidic inhibitors of Ras farnesyl transferase

  摘要：

  1, 3,5,5-Tetrasubstituted 2,4-imidazolinedione (hydantoin) derivatives were evaluated as Ftase inhibitors. Potent Ftase inhibitors without thiol or peptide were obtained in three steps. (C) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.12.074
• 作为产物：
  描述：

  methyl 3-(imidazol-1-yl)propionate 在 lithium aluminium tetrahydride 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 生成 3-(3-(1H-imidazol-1-yl)propyl)-5-methyl-5-(naphthalen-1-yl)imidazolidine-2,4-dione
  参考文献：
  名称：

  Hydantoin derivatives as non-peptidic inhibitors of Ras farnesyl transferase

  摘要：

  1, 3,5,5-Tetrasubstituted 2,4-imidazolinedione (hydantoin) derivatives were evaluated as Ftase inhibitors. Potent Ftase inhibitors without thiol or peptide were obtained in three steps. (C) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.12.074

文献信息

• Hydantoin derivatives as non-peptidic inhibitors of Ras farnesyl transferase
  作者：Jinho Lee、Jonghyun Kim、Jong Sung Koh、Hyun-Ho Chung、Kyoung-Hee Kim

  DOI：10.1016/j.bmcl.2005.12.074

  日期：2006.4

  1, 3,5,5-Tetrasubstituted 2,4-imidazolinedione (hydantoin) derivatives were evaluated as Ftase inhibitors. Potent Ftase inhibitors without thiol or peptide were obtained in three steps. (C) 2006 Elsevier Ltd. All rights reserved.