tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbo benzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl)amino)-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl)carbamate | 1602531-11-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbo benzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl)amino)-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl)carbamate
• CAS: 1602531-11-2
• 化学式: C₃₇H₄₈N₆O₁₀
• 分子量: 736.822
• InChiKey: JESHGLHTXFTXDT-CEAIMUJHSA-N

物化性质

• 沸点：
  1026.2±65.0 °C(predicted)
• 密度：
  1.36±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

反应信息

• 作为反应物：
  描述：

  tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbo benzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl)amino)-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl)carbamate 在 1,4-环己二烯 、 palladium 10% on activated carbon 作用下， 以 溶剂黄146 为溶剂， 反应 14.0h， 生成
  参考文献：
  名称：

  Rigid spiroethers targeting the decoding center of the bacterial ribosome

  摘要：

  Continuing our efforts towards understanding the principles governing ribosomal recognition and function, we have synthesized and evaluated a series of diversely functionalized 5,6-, 6,6- and 7,6- spiroethers. These compounds successfully mimic natural aminoglycosides regarding their binding to the decoding center of the bacterial ribosome. Their potential to inhibit prokaryotic protein production in vitro along with their antibacterial potencies have also been examined. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2013.12.068
• 作为产物：
  描述：

  N-Boc-L-组氨酸 、 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 N,N-二异丙基乙胺 作用下， 以 氘代四氢呋喃 为溶剂， 反应 12.0h， 以41%的产率得到tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbo benzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl)amino)-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl)carbamate
  参考文献：
  名称：

  Rigid spiroethers targeting the decoding center of the bacterial ribosome

  摘要：

  Continuing our efforts towards understanding the principles governing ribosomal recognition and function, we have synthesized and evaluated a series of diversely functionalized 5,6-, 6,6- and 7,6- spiroethers. These compounds successfully mimic natural aminoglycosides regarding their binding to the decoding center of the bacterial ribosome. Their potential to inhibit prokaryotic protein production in vitro along with their antibacterial potencies have also been examined. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2013.12.068