(4bR,8aS,9R,10R)-10-(ethylthio)-3,4-dihydroxy-7-methoxy-11-methyl-9,10-dihydro-5H-9,4b-(epiminoethano)phenanthren-6(8aH)-one | 1361940-29-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 菲及其衍生物
• 英文名称: (4bR,8aS,9R,10R)-10-(ethylthio)-3,4-dihydroxy-7-methoxy-11-methyl-9,10-dihydro-5H-9,4b-(epiminoethano)phenanthren-6(8aH)-one
• CAS: 1361940-29-5
• 化学式: C₂₀H₂₅NO₄S
• 分子量: 375.489
• InChiKey: PASGRNJFILYDSC-URGABHJQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.97
• 重原子数：
  26.0
• 可旋转键数：
  3.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  70.0
• 氢给体数：
  2.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  盐酸青藤碱 在 碘苯二乙酸 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 1.0h， 生成 (4bR,8aS,9R,10R)-10-(ethylthio)-3,4-dihydroxy-7-methoxy-11-methyl-9,10-dihydro-5H-9,4b-(epiminoethano)phenanthren-6(8aH)-one
  参考文献：
  名称：

  Regio- and stereoselective C10β–H functionalization of sinomenine: an access to more potent immunomodulating derivatives

  摘要：

  Regio- and stereoselective C-10 beta-H functionalization of sinomenine, an economically available natural immunomodulating alkaloid, has been studied, developed and successfully applied to the synthesis of new immunosuppressive sinomenine derivatives in a protecting-free fashion. Regioselective oxidation of sinomenine with (diacetoxylodo)benzene (DIB) in water provided a single stable benzoquinone derivative 4, and subsequent 1,6-conjugated addition of 4 with alcohols, amines, and thiols afforded a new series of C-10 beta-H functionalized sinomenine derivatives stereoselectively. Some derivatives with a newly introduced 10 beta-bezenesulfanyl substituent exhibited much higher TNF-alpha inhibitory potency than their natural parent sinomenine. This work opens a convenient access to novel sinomenine derivatives with medicinal interests. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2012.01.009