| 152610-74-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 菲及其衍生物
• CAS: 152610-74-7
• 化学式: C₂₇H₃₆N₂O₄
• 分子量: 452.594
• InChiKey: BNIUSDKOHBJDSD-ADKPUPEHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.79
• 重原子数：
  33.0
• 可旋转键数：
  3.0
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  74.95
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  在 氢氧化钾 、 碳酸氢钠 作用下， 以 N,N-二甲基甲酰胺 、 二乙二醇 为溶剂， 反应 21.25h， 生成 7β-buprenorphine
  参考文献：
  名称：

  Studies on the synthesis of β-thevinone derivatives

  摘要：

  The reactions of beta-thevinone and beta-dihydrothevinone with tert.-butylmagnesium chloride and n-propylmagnesium bromide were investigated. Further chemical transformations (N-demethylation, N-alkylation, O-demethylation) of the tertiary alcohols afforded the known beta-buprenorphine and the hitherto unknown beta-etorphine and beta-dihydroetorphine. The by-products of these reactions were also isolated, their structures identified, and the mode of their formation was explained. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00551-1
• 作为产物：
  描述：

  溴化氰 、 2-((4R,4aS,6S,7R,7aR,12bS)-7,9-dimethoxy-3-methyl-1,2,3,4,5,6,7,7a-octahydro-4a,7-ethano-4,12-methanobenzofuro[3,2-e]isoquinolin-6-yl)-3,3-dimethylbutan-2-ol 以 二氯甲烷 为溶剂， 反应 24.0h， 以90%的产率得到
  参考文献：
  名称：

  Studies on the synthesis of β-thevinone derivatives

  摘要：

  The reactions of beta-thevinone and beta-dihydrothevinone with tert.-butylmagnesium chloride and n-propylmagnesium bromide were investigated. Further chemical transformations (N-demethylation, N-alkylation, O-demethylation) of the tertiary alcohols afforded the known beta-buprenorphine and the hitherto unknown beta-etorphine and beta-dihydroetorphine. The by-products of these reactions were also isolated, their structures identified, and the mode of their formation was explained. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00551-1