7α-(Benzyloxy)-3ξ-<5,10-bis(tert-butoxycarbonyl)-1,5,10-triazadecyl>-24ξ-<(tert-butyldimethylsilyl)oxy>-cholestane | 166896-86-2

• 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: 7α-(Benzyloxy)-3ξ-<5,10-bis(tert-butoxycarbonyl)-1,5,10-triazadecyl>-24ξ-<(tert-butyldimethylsilyl)oxy>-cholestane
• 英文别名: tert-butyl N-[3-[[(5R,7R,8R,9S,10S,13R,14S,17R)-17-[(2R)-5-[tert-butyl(dimethyl)silyl]oxy-6-methylheptan-2-yl]-10,13-dimethyl-7-phenylmethoxy-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]amino]propyl]-N-[4-[(2-methylpropan-2-yl)oxycarbonylamino]butyl]carbamate
• CAS: 166896-86-2
• 化学式: C₅₇H₁₀₁N₃O₆Si
• 分子量: 952.531
• InChiKey: LMYFWNJOVZPLIE-JJZZFPBYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  14.19
• 重原子数：
  67
• 可旋转键数：
  25
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  98.4
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  7α-(Benzyloxy)-3ξ-<5,10-bis(tert-butoxycarbonyl)-1,5,10-triazadecyl>-24ξ-<(tert-butyldimethylsilyl)oxy>-cholestane 在 palladium on activated charcoal 吡啶 、 盐酸 、 pyridine-SO3 complex 、 氢气 、 三氟乙酸 作用下， 以 乙醇 、 氯仿 为溶剂， 25.0~40.0 ℃ 、379.21 kPa 条件下， 反应 26.25h， 生成 24ξ-Squalamine
  参考文献：
  名称：

  Synthesis of 24.xi.-Squalamine, an Anti-Infective Steroidal Polyamine

  摘要：

  Squalamine (1) is a novel steroidal polyamine which exhibits broad spectrum anti-infective activity. It inhibits the growth of bacteria, both Gram positive and Gram negative, and fungi. The synthesis of 24 xi-squalamine was accomplished in 17 steps from 3 beta-hydroxy-5-cholenic acid. The stereospecific introduction of the 7 alpha-hydroxyl group was achieved by allylic oxidation followed by hydrogenation of the Delta(5) olefin and reduction of the 7-keto group with K-selectride. The polyamine side chain was introduced via reductive amination of an appropriately functionalized 3-keto steroid with a suitably protected spermidine utilizing sodium cyanoborohydride as the reducing agent. The required 24-sulfate was introduced by selective sulfation of the 7 alpha,24 xi-diol with sulfur trioxide-pyridine complex.

  DOI：

  10.1021/jo00121a033
• 作为产物：
  描述：

  3β-(tetrahydro-2H-pyran-2-yloxy)chol-5-en-24-ol 在 platinum(IV) oxide 咪唑 、 3,5-二甲基吡唑 、 chromium(VI) oxide 、 草酰氯 、 3 A molecular sieve 、 四丁基氟化铵 、 氢气 、 dipyridine chromium trioxide 、 sodium hydride 、 sodium cyanoborohydride 、 potassium tri-sec-butyl-borohydride 、 二甲基亚砜 、 N,N-二异丙基乙胺 、 magnesium bromide 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 、 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 反应 79.0h， 生成 7α-(Benzyloxy)-3ξ-<5,10-bis(tert-butoxycarbonyl)-1,5,10-triazadecyl>-24ξ-<(tert-butyldimethylsilyl)oxy>-cholestane
  参考文献：
  名称：

  Synthesis of 24.xi.-Squalamine, an Anti-Infective Steroidal Polyamine

  摘要：

  Squalamine (1) is a novel steroidal polyamine which exhibits broad spectrum anti-infective activity. It inhibits the growth of bacteria, both Gram positive and Gram negative, and fungi. The synthesis of 24 xi-squalamine was accomplished in 17 steps from 3 beta-hydroxy-5-cholenic acid. The stereospecific introduction of the 7 alpha-hydroxyl group was achieved by allylic oxidation followed by hydrogenation of the Delta(5) olefin and reduction of the 7-keto group with K-selectride. The polyamine side chain was introduced via reductive amination of an appropriately functionalized 3-keto steroid with a suitably protected spermidine utilizing sodium cyanoborohydride as the reducing agent. The required 24-sulfate was introduced by selective sulfation of the 7 alpha,24 xi-diol with sulfur trioxide-pyridine complex.

  DOI：

  10.1021/jo00121a033

文献信息

• Synthesis of 24.xi.-Squalamine, an Anti-Infective Steroidal Polyamine
  作者：Anthony D. Pechulis、Frank H. Bellevue、Christopher L. Cioffi、Sean G. Trapp、John P. Fojtik、Anthony A. McKitty、William A. Kinney、Leah L. Frye

  DOI：10.1021/jo00121a033

  日期：1995.8

  Squalamine (1) is a novel steroidal polyamine which exhibits broad spectrum anti-infective activity. It inhibits the growth of bacteria, both Gram positive and Gram negative, and fungi. The synthesis of 24 xi-squalamine was accomplished in 17 steps from 3 beta-hydroxy-5-cholenic acid. The stereospecific introduction of the 7 alpha-hydroxyl group was achieved by allylic oxidation followed by hydrogenation of the Delta(5) olefin and reduction of the 7-keto group with K-selectride. The polyamine side chain was introduced via reductive amination of an appropriately functionalized 3-keto steroid with a suitably protected spermidine utilizing sodium cyanoborohydride as the reducing agent. The required 24-sulfate was introduced by selective sulfation of the 7 alpha,24 xi-diol with sulfur trioxide-pyridine complex.