dimethyl (4S)-1-(4-methoxycarbonylphenyl)-4-(phenylmethoxymethyl)imidazolidine-2,2-dicarboxylate | 1060729-45-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: dimethyl (4S)-1-(4-methoxycarbonylphenyl)-4-(phenylmethoxymethyl)imidazolidine-2,2-dicarboxylate
• CAS: 1060729-45-4
• 化学式: C₂₃H₂₆N₂O₇
• 分子量: 442.469
• InChiKey: GUMQMEMTUYVGAH-SFHVURJKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  32
• 可旋转键数：
  11
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  103
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  dimethyl (4S)-1-(4-methoxycarbonylphenyl)-4-(phenylmethoxymethyl)imidazolidine-2,2-dicarboxylate 在 palladium hydroxide on carbon 、 氢气 作用下， 以 乙酸乙酯 为溶剂， 以75%的产率得到C₁₆H₂₂N₂O₇
  参考文献：
  名称：

  Total Synthesis of (−)-Aplaminal

  摘要：

  The total synthesis and assignment of absolute configuration of (-)-aplaminal (1), a cytotoxic metabolite from a sea hare possessing a triazobicyclo[3.2.1]octane skeleton, has been achieved. The synthesis entailed condensation of a monoprotected diamine (3) with dimethyl 2-oxomalonate (4) to generate the imidazolidine core (2). Introduction of the third nitrogen via Mitsunobu activation and azide displacement, followed by reduction and lactam formation (AIMe(3)), furnished (-)-aplaminal (1). Overall, the synthesis entailed 9 steps and proceeded in 19% overall yield.

  DOI：

  10.1021/ol801794f
• 作为产物：
  描述：

  二甲基氧代丙二酸酯 、 methyl (S)-4-((3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)propyl)amino)benzoate 在 三氟乙酸 、 magnesium sulfate 作用下， 以 二氯甲烷 为溶剂， 反应 54.0h， 以70%的产率得到dimethyl (4S)-1-(4-methoxycarbonylphenyl)-4-(phenylmethoxymethyl)imidazolidine-2,2-dicarboxylate
  参考文献：
  名称：

  Total Synthesis of (−)-Aplaminal

  摘要：

  The total synthesis and assignment of absolute configuration of (-)-aplaminal (1), a cytotoxic metabolite from a sea hare possessing a triazobicyclo[3.2.1]octane skeleton, has been achieved. The synthesis entailed condensation of a monoprotected diamine (3) with dimethyl 2-oxomalonate (4) to generate the imidazolidine core (2). Introduction of the third nitrogen via Mitsunobu activation and azide displacement, followed by reduction and lactam formation (AIMe(3)), furnished (-)-aplaminal (1). Overall, the synthesis entailed 9 steps and proceeded in 19% overall yield.

  DOI：

  10.1021/ol801794f