(2S,3R,4aS,5S,8aR)-1-(tert-butyloxycarbonyl)-2-methyl-3-hydroxy-5-[(1E,3E)-7,7-(ethylenedioxy)octadien-1-yl]decahydroquinoline | 910030-47-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉类
• 英文名称: (2S,3R,4aS,5S,8aR)-1-(tert-butyloxycarbonyl)-2-methyl-3-hydroxy-5-[(1E,3E)-7,7-(ethylenedioxy)octadien-1-yl]decahydroquinoline
• 英文别名: tert-butyl (2S,3R,4aS,5S,8aR)-3-hydroxy-2-methyl-5-[(1E,3E)-6-(2-methyl-1,3-dioxolan-2-yl)hexa-1,3-dienyl]-3,4,4a,5,6,7,8,8a-octahydro-2H-quinoline-1-carboxylate
• CAS: 910030-47-6
• 化学式: C₂₅H₄₁NO₅
• 分子量: 435.604
• InChiKey: FBXVIPPULMJQQZ-HETLYRTPSA-N

物化性质

• 沸点：
  534.1±50.0 °C(Predicted)
• 密度：
  1.094±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  31
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  68.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (2S,3R,4aS,5S,8aR)-1-(tert-butyloxycarbonyl)-2-methyl-3-hydroxy-5-[(1E,3E)-7,7-(ethylenedioxy)octadien-1-yl]decahydroquinoline 在 4-二甲氨基吡啶 、 sodium tetrahydroborate 、 三氟化硼乙醚 、 碳酸氢钠 、 戴斯-马丁氧化剂 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 13.1h， 生成 lepadin C
  参考文献：
  名称：

  Facile Entry to Substituted Decahydroquinoline Alkaloids. Total Synthesis of Lepadins A−E and H

  摘要：

  Condensation of a L-alanine derived delta-bromo-beta-silyloxy-propylamine with 1,3-cyclohexadione followed by alkylative cyclization produces a bicyclic enone. Diastereoselective Pt/C-catalyzed hydrogenation of this enone in HOAc provides a 5-oxo-cis-fused decahydroquinoline. Wittig olefination of this decahydroquinoline and subsequent epimerization of the resulting 5-formyl intermediate gives rise to a 5-beta-formyl decahydroquinoline exclusively. In a parallel procedure, Peterson reaction of this decahydroquinoline and subsequent hydrogenation of the generated 5-exo-olefin provides a decahydroquinoline with a 5-alpha-substituent predominantly. For these two diastereoselective processes, using the intermediates without N-protection as the substrates is essential because the corresponding N-Boc intermediates give poor diastereoselectivity. The intermediate with beta-form side chain is further converted into lepadins A-C via carbon chain elongation, while the intermediate with alpha-form side chain is transformed into lepadins D, E, and H and corresponding 5'-epimers via connection with two sulfones generated from two Sharpless epoxidation products. By comparison of the rotations and NMR data, the stereochemistry of lepadins D, E, and H is assigned as 2S, 3R, 4aS, 5S, 8aR, 5'R.

  DOI：

  10.1021/jo061070c
• 作为产物：
  描述：

  6-甲基-5-庚烯-2-酮 在 咪唑 、 四溴化碳 、 四丁基氟化铵 、 4-甲基苯磺酸吡啶 、 双(三甲基硅烷基)氨基钾 、 二异丁基氢化铝 、 potassium carbonate 、 臭氧 、 三苯基膦 作用下， 以 四氢呋喃 、 乙二醇二甲醚 、 乙腈 、 苯 为溶剂， 反应 114.5h， 生成 (2S,3R,4aS,5S,8aR)-1-(tert-butyloxycarbonyl)-2-methyl-3-hydroxy-5-[(1E,3E)-7,7-(ethylenedioxy)octadien-1-yl]decahydroquinoline
  参考文献：
  名称：

  Facile Entry to Substituted Decahydroquinoline Alkaloids. Total Synthesis of Lepadins A−E and H

  摘要：

  Condensation of a L-alanine derived delta-bromo-beta-silyloxy-propylamine with 1,3-cyclohexadione followed by alkylative cyclization produces a bicyclic enone. Diastereoselective Pt/C-catalyzed hydrogenation of this enone in HOAc provides a 5-oxo-cis-fused decahydroquinoline. Wittig olefination of this decahydroquinoline and subsequent epimerization of the resulting 5-formyl intermediate gives rise to a 5-beta-formyl decahydroquinoline exclusively. In a parallel procedure, Peterson reaction of this decahydroquinoline and subsequent hydrogenation of the generated 5-exo-olefin provides a decahydroquinoline with a 5-alpha-substituent predominantly. For these two diastereoselective processes, using the intermediates without N-protection as the substrates is essential because the corresponding N-Boc intermediates give poor diastereoselectivity. The intermediate with beta-form side chain is further converted into lepadins A-C via carbon chain elongation, while the intermediate with alpha-form side chain is transformed into lepadins D, E, and H and corresponding 5'-epimers via connection with two sulfones generated from two Sharpless epoxidation products. By comparison of the rotations and NMR data, the stereochemistry of lepadins D, E, and H is assigned as 2S, 3R, 4aS, 5S, 8aR, 5'R.

  DOI：

  10.1021/jo061070c