2-[(3R,5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-17-(2-methyl-1,3-dioxolan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]isoindole-1,3-dione | 1375488-80-4

• 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: 2-[(3R,5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-17-(2-methyl-1,3-dioxolan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]isoindole-1,3-dione
• CAS: 1375488-80-4
• 化学式: C₃₁H₄₁NO₄
• 分子量: 491.671
• InChiKey: RDBUMPZTKLQETG-YPTZQLMOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.6
• 重原子数：
  36
• 可旋转键数：
  2
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  55.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-[(3R,5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-17-(2-methyl-1,3-dioxolan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]isoindole-1,3-dione 在 盐酸 、 乙醇 、 水 、 sodium carbonate 、 一水合肼 作用下， 以 四氢呋喃 、 二氯甲烷 、 丙酮 为溶剂， 反应 0.25h， 生成 丝胶树碱
  参考文献：
  名称：

  A novel scalable and stereospecific synthesis of 3α- and 3β-amino-5α-androstan-17-ones and 3α- and 3β-amino-5α-pregnan-20-ones

  摘要：

  A novel scalable stereoselective synthesis of 3 alpha- and 3 beta-amino-5 alpha-androstan-17-ones and 3 alpha- and 3 beta-amino-5 alpha-pregnan-20-ones has been developed using phthalimide based Mitsunobu chemistry. In all four cases, the products were isolated as single diastereoisomers in high chemical yield and purity without the need for chromatography at any stage in their syntheses. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2012.03.124
• 作为产物：
  描述：

  别孕烯醇酮 在 偶氮二甲酸二异丙酯 、 对甲苯磺酸 、 三苯基膦 、 原甲酸三甲酯 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 2-[(3R,5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-17-(2-methyl-1,3-dioxolan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]isoindole-1,3-dione
  参考文献：
  名称：

  A novel scalable and stereospecific synthesis of 3α- and 3β-amino-5α-androstan-17-ones and 3α- and 3β-amino-5α-pregnan-20-ones

  摘要：

  A novel scalable stereoselective synthesis of 3 alpha- and 3 beta-amino-5 alpha-androstan-17-ones and 3 alpha- and 3 beta-amino-5 alpha-pregnan-20-ones has been developed using phthalimide based Mitsunobu chemistry. In all four cases, the products were isolated as single diastereoisomers in high chemical yield and purity without the need for chromatography at any stage in their syntheses. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2012.03.124

文献信息

• A novel scalable and stereospecific synthesis of 3α- and 3β-amino-5α-androstan-17-ones and 3α- and 3β-amino-5α-pregnan-20-ones
  作者：James R. Hitchin、Niall M. Hamilton、Allan M. Jordan、Amanda J. Lyons、Donald J. Ogilvie

  DOI：10.1016/j.tetlet.2012.03.124

  日期：2012.6

  A novel scalable stereoselective synthesis of 3 alpha- and 3 beta-amino-5 alpha-androstan-17-ones and 3 alpha- and 3 beta-amino-5 alpha-pregnan-20-ones has been developed using phthalimide based Mitsunobu chemistry. In all four cases, the products were isolated as single diastereoisomers in high chemical yield and purity without the need for chromatography at any stage in their syntheses. (C) 2012 Elsevier Ltd. All rights reserved.