(2S)-2-乙基-1-[(1R)-2-甲氧基-1-苯基乙基]氮丙啶 | 514168-46-8

• 分子结构分类: 有机化合物 - 有机氮化合物
• 中文名称: (2S)-2-乙基-1-[(1R)-2-甲氧基-1-苯基乙基]氮丙啶
• 英文名称: (S)-2-Ethyl-1-((R)-2-methoxy-1-phenyl-ethyl)-aziridine
• 英文别名: Aziridine, 2-ethyl-1-[(1R)-2-methoxy-1-phenylethyl]-, (2S)-(9CI)；(2S)-2-ethyl-1-[(1R)-2-methoxy-1-phenylethyl]aziridine
• CAS: 514168-46-8
• 化学式: C₁₃H₁₉NO
• 分子量: 205.3
• InChiKey: RYVJPLDAEFFOTE-RFHHWMCGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  12.2
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2933990090

反应信息

• 作为反应物：
  描述：

  (2S)-2-乙基-1-[(1R)-2-甲氧基-1-苯基乙基]氮丙啶 在 platinum(IV) oxide 氢气 作用下， 生成 (1R,1'R)-N-(2'-methoxy-1'-phenylethyl)-1-methylpropylamine
  参考文献：
  名称：

  Facile Asymmetric Synthesis of Aziridine Derivatives via the Diastereoselective Reaction of Chiral Imines with Dimethylsulfonium Methylide

  摘要：

  A simple method for the synthesis of chiral 2-substituted aziridine derivatives is described. The reaction pathway consists of the diastereoselective addition of dimethylsulfonium methylide to chiral imines derived from (R)-phenylglycinol and various aldehydes.

  DOI：

  10.3987/com-02-s(m)32
• 作为产物：
  描述：

  (R)-(-)-2-甲氧基-1-苯乙胺 在 六甲基磷酰三胺 、 正丁基锂 、 magnesium sulfate 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 为溶剂， 生成 (2S)-2-乙基-1-[(1R)-2-甲氧基-1-苯基乙基]氮丙啶
  参考文献：
  名称：

  Facile Asymmetric Synthesis of Aziridine Derivatives via the Diastereoselective Reaction of Chiral Imines with Dimethylsulfonium Methylide

  摘要：

  A simple method for the synthesis of chiral 2-substituted aziridine derivatives is described. The reaction pathway consists of the diastereoselective addition of dimethylsulfonium methylide to chiral imines derived from (R)-phenylglycinol and various aldehydes.

  DOI：

  10.3987/com-02-s(m)32

文献信息

• Regio- and Stereoselective Ring-Opening Reaction of Chiral Aziridines: A Facile Synthesis of Chiral β-Amino Alcohols
  作者：Kimio Higashiyama、Masataka Matsumura、Hiroshi Kojima、Takayasu Yamauchi

  DOI：10.3987/com-08-11537

  日期：——

  The reaction of chiral 2-alkylsubstituted aziridines (1a-d) with acetic acid afforded beta-amino alcohols with an (S)-chiral center at the beta position (with respect to oxygen). In contrast, a reaction of the same chiral aziridines with acetyl chloride followed by treatment with water gave beta-amino alcohols that have an (S)-chiral center at the alpha position. In addition, the reaction of the same chiral aziridines with benzyl bromide followed by treatment with 2% sulfuric acid gave the beta-amino alcohols with an (R)-chiral center at the alpha position. Thus, we could control the regioselectivity and stereoselectivity of the ring-opening reaction of chiral aziridines (1a-d).
• Facile Asymmetric Synthesis of Aziridine Derivatives via the Diastereoselective Reaction of Chiral Imines with Dimethylsulfonium Methylide
  作者：Kimio Higashiyama、Masataka Matsumura、Ayako Shiogama、Takayasu Yamauchi、Sigeru Ohmiya

  DOI：10.3987/com-02-s(m)32

  日期：——

  A simple method for the synthesis of chiral 2-substituted aziridine derivatives is described. The reaction pathway consists of the diastereoselective addition of dimethylsulfonium methylide to chiral imines derived from (R)-phenylglycinol and various aldehydes.