4-azido-2-hydroxy-benzoic acid 4,4,7a-trimethyl-octahydro-inden-1-yl ester | 929038-60-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-azido-2-hydroxy-benzoic acid 4,4,7a-trimethyl-octahydro-inden-1-yl ester
• CAS: 929038-60-8
• 化学式: C₁₉H₂₅N₃O₃
• 分子量: 343.426
• InChiKey: XNKBSIOYXARSEF-BXWFABGCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.49
• 重原子数：
  25.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  95.29
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  4-azido-2-hydroxy-benzoic acid 4,4,7a-trimethyl-octahydro-inden-1-yl ester 在 caesium carbonate 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 、 N,N-二异丙基乙胺 、 三氟乙酸 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 8.5h， 生成 [(1S,3aS,7aS)-4,4,7a-trimethyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl] 2-[3-[5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]propoxy]-4-azidobenzoate
  参考文献：
  名称：

  Trifunctional norrisolide probes for the study of Golgi vesiculation

  摘要：

  Inspired by the effect of norrisolide on the Golgi complex, we synthesized norrisolide probes that contain: the perhydroindane core of the parent natural product for Golgi localization, a crosslinking unit (aryl azide or epoxide) for covalent binding to the target, and a tag (biotin or iodine) for subsequent target purification. We found that biotin-containing probes 14, 20 and 24 induced inefficient Golgi vesiculation. However, the iodinated probe 25 induced extensive and irreversible Golgi fragmentation. This probe can be used for the isolation of the cellular target of norrisolide. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.10.101
• 作为产物：
  描述：

  4-azidosalicylic acid 、 (+)-(1S,3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-ol 在 4-二甲氨基吡啶 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以77%的产率得到4-azido-2-hydroxy-benzoic acid 4,4,7a-trimethyl-octahydro-inden-1-yl ester
  参考文献：
  名称：

  Trifunctional norrisolide probes for the study of Golgi vesiculation

  摘要：

  Inspired by the effect of norrisolide on the Golgi complex, we synthesized norrisolide probes that contain: the perhydroindane core of the parent natural product for Golgi localization, a crosslinking unit (aryl azide or epoxide) for covalent binding to the target, and a tag (biotin or iodine) for subsequent target purification. We found that biotin-containing probes 14, 20 and 24 induced inefficient Golgi vesiculation. However, the iodinated probe 25 induced extensive and irreversible Golgi fragmentation. This probe can be used for the isolation of the cellular target of norrisolide. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.10.101