(3aR*,6R*,7aS*)-octahydro-6-hydroxy-3a-(3,4-dimethoxyphenyl)-1-methylindol-2-one | 21104-32-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: (3aR*,6R*,7aS*)-octahydro-6-hydroxy-3a-(3,4-dimethoxyphenyl)-1-methylindol-2-one
• 英文别名: (3aR*,6S*,7aS*)-octahydro-6-hydroxy-3a-(3,4-dimethoxyphenyl)-1-methylindol-2-one
• CAS: 21104-32-5；80516-00-3；129920-38-3
• 化学式: C₁₇H₂₃NO₄
• 分子量: 305.374
• InChiKey: IMBDOJCKOIEMIU-VUOSCMKMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.72
• 重原子数：
  22.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  59.0
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  (3aR*,6R*,7aS*)-octahydro-6-hydroxy-3a-(3,4-dimethoxyphenyl)-1-methylindol-2-one 在 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 三氯化铝 、 jones reagent 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 丙酮 为溶剂， 反应 2.17h， 生成 (+/-)-6-epimesembranol
  参考文献：
  名称：

  Radical cyclization of N-(cyclohex-2-enyl)-.alpha.,.alpha.-dichloroacetamides. Stereoselective syntheses of (.+-.)-mesembranol and (.+-.)-elwesine

  摘要：

  Stereoselective syntheses of the Sceletium alkaloid (+/-)-mesembranol (2) and the Amaryllidaceae alkaloid (+/-)-elwesine (3) have been achieved. A key step in the syntheses involves the Bu3SnH-mediated radical cyclization of the dichloroacetamides 34 and 46, which provides the cis-3a-aryloctahydroindolones 36 and 47, respectively. The amides 34 and 46 were prepared in a highly stereocontrolled manner from the corresponding 1-arylcyclohexenes 29 and 41 along the lines: 29 --> 30a --> 31 --> 32 --> 33 --> 34 and 41 --> 42a --> 44a --> 45a --> 46. Transformation of 36 into (+/-)-mesembranol was readily accomplished by reduction with diborane and subsequent removal of the O-benzyl protecting group by hydrogenolysis over Pd/C. On the other hand, debenzylation of 36 with Raney Ni afforded a mixture of the 6-alpha- and 6-beta-alcohols 39a and 39b, which was then reduced by alane to give a separable mixture of (+/-)-mesembranol and (+/-)-6-epimesembranol (40). Reduction of 47 with diborane followed by catalytic hydrogenolysis over Pd/C afforded the amino alcohol 50, which has already been converted into (+/-)-elwesine by Pictet-Spengler cyclization.

  DOI：

  10.1021/jo00001a021
• 作为产物：
  描述：

  4-(benzyloxy)-1-(3,4-dimethoxyphenyl)cyclohex-1-ene 在 Raney nickel (W-2) N-溴代丁二酰亚胺(NBS) 、 偶氮二异丁腈 、 水 、 三正丁基氢锡 、 三乙胺 作用下， 以 甲醇 、 乙醇 、 二氯甲烷 、 甲苯 、 乙腈 为溶剂， 反应 10.0h， 生成 (3aR*,6R*,7aS*)-octahydro-6-hydroxy-3a-(3,4-dimethoxyphenyl)-1-methylindol-2-one
  参考文献：
  名称：

  Radical cyclization of N-(cyclohex-2-enyl)-.alpha.,.alpha.-dichloroacetamides. Stereoselective syntheses of (.+-.)-mesembranol and (.+-.)-elwesine

  摘要：

  Stereoselective syntheses of the Sceletium alkaloid (+/-)-mesembranol (2) and the Amaryllidaceae alkaloid (+/-)-elwesine (3) have been achieved. A key step in the syntheses involves the Bu3SnH-mediated radical cyclization of the dichloroacetamides 34 and 46, which provides the cis-3a-aryloctahydroindolones 36 and 47, respectively. The amides 34 and 46 were prepared in a highly stereocontrolled manner from the corresponding 1-arylcyclohexenes 29 and 41 along the lines: 29 --> 30a --> 31 --> 32 --> 33 --> 34 and 41 --> 42a --> 44a --> 45a --> 46. Transformation of 36 into (+/-)-mesembranol was readily accomplished by reduction with diborane and subsequent removal of the O-benzyl protecting group by hydrogenolysis over Pd/C. On the other hand, debenzylation of 36 with Raney Ni afforded a mixture of the 6-alpha- and 6-beta-alcohols 39a and 39b, which was then reduced by alane to give a separable mixture of (+/-)-mesembranol and (+/-)-6-epimesembranol (40). Reduction of 47 with diborane followed by catalytic hydrogenolysis over Pd/C afforded the amino alcohol 50, which has already been converted into (+/-)-elwesine by Pictet-Spengler cyclization.

  DOI：

  10.1021/jo00001a021