(S)-2-(2-chloro-5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)ethanol | 1211961-17-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: (S)-2-(2-chloro-5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)ethanol
• 英文别名: 2-[2-chloro-5-[(2S)-1-methylpyrrolidin-2-yl]pyridin-3-yl]ethanol
• CAS: 1211961-17-9
• 化学式: C₁₂H₁₇ClN₂O
• 分子量: 240.733
• InChiKey: ZZXZBUCATMPSFG-NSHDSACASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.58
• 拓扑面积：
  36.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (S)-2-(2-chloro-5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)ethanol 在 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 以99%的产率得到(S)-5-(1-methylpyrrolidin-2-yl)-2,3-dihydrofuro[2,3-b]pyridine
  参考文献：
  名称：

  Synthesis of Fused-Ring Nicotine Derivatives from (S)-Nicotine

  摘要：

  The synthesis of novel fused-ring bicyclic (4-6) and tricyclic(7-10) nicotine derivatives from natural (S)-nicotine are described. Enantiopure bicyclic dioxino, dihydrofuo, and dihydropyranol nicotine derivatives as well as tricylic benzofuro and benzopyran derivatives were synthesized from simple alkoxy or halonicotine intermediates. Attempts to synthesize furonicotines (11, 12) resulted in formation of the furonicotine dimers 42 and 49.

  DOI：

  10.1021/jo9026929
• 作为产物：
  描述：

  (S)-2-(2-chloro-5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)ethyl benzoate 在 水 、 sodium hydroxide 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 1.0h， 以71%的产率得到(S)-2-(2-chloro-5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)ethanol
  参考文献：
  名称：

  Synthesis of Fused-Ring Nicotine Derivatives from (S)-Nicotine

  摘要：

  The synthesis of novel fused-ring bicyclic (4-6) and tricyclic(7-10) nicotine derivatives from natural (S)-nicotine are described. Enantiopure bicyclic dioxino, dihydrofuo, and dihydropyranol nicotine derivatives as well as tricylic benzofuro and benzopyran derivatives were synthesized from simple alkoxy or halonicotine intermediates. Attempts to synthesize furonicotines (11, 12) resulted in formation of the furonicotine dimers 42 and 49.

  DOI：

  10.1021/jo9026929