6β-Methoxy-18,20α-epoxy-3α,5-cyclo-5α-pregnan-18-one | 143947-67-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: 6β-Methoxy-18,20α-epoxy-3α,5-cyclo-5α-pregnan-18-one
• CAS: 143947-67-5
• 化学式: C₂₂H₃₂O₃
• 分子量: 344.494
• InChiKey: QGPCJVWNPABPRD-FBUZIXHUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  25.0
• 可旋转键数：
  1.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.95
• 拓扑面积：
  35.53
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为产物：
  描述：

  6β-Methoxy-18,20α-epoxy-3α,5-cyclo-5α-pregnan-18-ol 在 碘 、 mercury(II) oxide 作用下， 以 吡啶 、 丙酮 为溶剂， 反应 4.0h， 以25%的产率得到6β-Methoxy-18,20α-epoxy-3α,5-cyclo-5α-pregnan-18-one
  参考文献：
  名称：

  Photoinduced molecular transformations. Part 131. Synthesis of 18-norsteroids, deoxofukujusonorone and the related steroids, based on a selective β-scission of alkoxyl radicals as the key step

  摘要：

  A new transformation of steroids into 18-norsteroids under mild conditions is described. The key step was a regioselective beta-scission of the alkoxyl radicals generated by photolysis of the hypoiodite of 18-hydroxy-18,20-alpha-epoxy steroids, prepared by photolysis of steroidal 20-alpha-ol nitrites followed by deoximation of the resulting 18-hydroxyimino-20-alpha-hydroxy steroid with sodium nitrite and acetic acid. 3-beta-Hydroxypregn-5-en-20-one (pregnenolone) was thus transformed into 3-beta-hydroxy-18-norpregna-5,13-dien-20-one (12-deoxofukujusonorone) in 10 steps.

  DOI：

  10.1039/p19920001837