(5S,7R,8S,9S,10R)-8,9,10-trihydroxy-7-(hydroxymethyl)-3-(2-naphthalenyl)-6-oxa-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide | 1357160-52-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (5S,7R,8S,9S,10R)-8,9,10-trihydroxy-7-(hydroxymethyl)-3-(2-naphthalenyl)-6-oxa-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide
• 英文别名: (5S,7R,8S,9S,10R)-7-(hydroxymethyl)-3-naphthalen-2-yl-2,2-dioxo-6-oxa-2lambda6-thia-1,3-diazaspiro[4.5]decane-8,9,10-triol；(5S,7R,8S,9S,10R)-7-(hydroxymethyl)-3-naphthalen-2-yl-2,2-dioxo-6-oxa-2λ6-thia-1,3-diazaspiro[4.5]decane-8,9,10-triol
• CAS: 1357160-52-1
• 化学式: C₁₇H₂₀N₂O₇S
• 分子量: 396.421
• InChiKey: PFJHTPDSTDWLHJ-UUAJXVIYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.5
• 重原子数：
  27
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  148
• 氢给体数：
  5
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  (5S,7R,8R,9S,10R)-8,9,10-tribenzyloxy-7-(benzyloxymethyl)-N-(2-naphthalenyl)-6-oxa-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide 在 甲醇 、 palladium dichloride 作用下， 反应 10.0h， 生成 (5S,7R,8S,9S,10R)-8,9,10-trihydroxy-7-(hydroxymethyl)-3-(2-naphthalenyl)-6-oxa-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide 、 (5S,7R,8R,9S,10R)-8,9,10-trihydroxy-7-(hydroxymethyl)-3-(5,6,7,8-tetrahydronaphthalen-2-yl)amino-6-oxa-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide
  参考文献：
  名称：

  Synthesis of N-aryl spiro-sulfamides as potential glycogen phosphorylase inhibitors

  摘要：

  A new C-glucosylated spiro-sulfamide has been prepared and evaluated toward glycogen phosphorylase inhibition. The synthesis was carried out successfully by nucleophilic displacement of 1-O-tosyl or 1-deoxy-1-iodo-alpha-D-gluco-hept-2-ulopyranose tetra-O-benzylated derivative using aryl amines. followed by the formation of the corresponding cyclic sulfamide. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.12.049