(2S,3S)-3-azido-N-methoxy-N-methyl-2-phenylmethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]oxybutanamide | 947747-23-1

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (2S,3S)-3-azido-N-methoxy-N-methyl-2-phenylmethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]oxybutanamide
• CAS: 947747-23-1
• 化学式: C₄₇H₅₂N₄O₉
• 分子量: 816.951
• InChiKey: URGVEZADJXHSGF-QKQIRWKYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.4
• 重原子数：
  60
• 可旋转键数：
  23
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  109
• 氢给体数：
  0
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  (2S,3S)-3-azido-N-methoxy-N-methyl-2-phenylmethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]oxybutanamide 在 palladium dihydroxide sodium tetrahydroborate 、 正丁基锂 、 dimethyl sulfide borane 、 氢气 、 四丁基碘化铵 、 sodium hydride 、 (R)-(+)-tetrahydro-1-methyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole 作用下， 以 四氢呋喃 、 吡啶 、 甲醇 、 乙醇 、 氯仿 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 生成 (2S,3S,4R)-1-O-(α-D-galactopyranosyl)-2-(N-tetracosanoylamino)-1,3,4-nonanetriol
  参考文献：
  名称：

  Concise syntheses of immunostimulating glycolipids, α-galactosyl ceramides

  摘要：

  alpha-Galactosylceramides (alpha-GalCers) are well known as immunostimulating agents having therapeutic potential. To facilitate the synthesis of alpha-GalCers and their derivatives, a novel and convergent strategy was designed, which is expected to be versatile for the preparation of a variety of analogues in a diversity-oriented fashion. As an initial demonstration of our strategy, KRN7000 and OCH were synthesized in eight steps from a common intermediate, which is easily obtainable in a multi-gram scale. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.05.161
• 作为产物：
  描述：

  (2R,3R)-3-(benzyloxy)-4-(naphthalen-2-ylmethoxy)butane-1,2-diol 在 4-二甲氨基吡啶 、 sodium chlorite 、 sodium dihydrogenphosphate 、 sodium azide 、 N-甲基吲哚酮 、 四丙基高钌酸铵 、 2-甲基-2-丁烯 、 4-甲基苯磺酸吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 2,3-二氯-5,6-二氰基-1,4-苯醌 、 三氟甲烷磺酸甲酯 作用下， 以 吡啶 、 甲醇 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 、 乙腈 、 叔丁醇 为溶剂， 生成 (2S,3S)-3-azido-N-methoxy-N-methyl-2-phenylmethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]oxybutanamide
  参考文献：
  名称：

  Concise syntheses of immunostimulating glycolipids, α-galactosyl ceramides

  摘要：

  alpha-Galactosylceramides (alpha-GalCers) are well known as immunostimulating agents having therapeutic potential. To facilitate the synthesis of alpha-GalCers and their derivatives, a novel and convergent strategy was designed, which is expected to be versatile for the preparation of a variety of analogues in a diversity-oriented fashion. As an initial demonstration of our strategy, KRN7000 and OCH were synthesized in eight steps from a common intermediate, which is easily obtainable in a multi-gram scale. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.05.161