2,2,2-trichloro-N-[(2R,3R,4R,5S,6R)-2-[[(2R,3S,4R,5R,6R)-6-[(Z)-4-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecoxy)but-2-enoxy]-3,4-bis(phenylmethoxy)-5-[(2,2,2-trichloroacetyl)amino]oxan-2-yl]methoxy]-6-(hydroxymethyl)-4,5-bis(phenylmethoxy)oxan-3-yl]acetamide

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,2,2-trichloro-N-[(2R,3R,4R,5S,6R)-2-[[(2R,3S,4R,5R,6R)-6-[(Z)-4-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecoxy)but-2-enoxy]-3,4-bis(phenylmethoxy)-5-[(2,2,2-trichloroacetyl)amino]oxan-2-yl]methoxy]-6-(hydroxymethyl)-4,5-bis(phenylmethoxy)oxan-3-yl]acetamide
• 化学式: C₇₂H₇₁Cl₆N₆O₂₁Pol
• 分子量: 1521.8
• InChiKey: WRGWSRNLGXIHPT-GWOIXOIESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  13.8
• 重原子数：
  96
• 可旋转键数：
  33
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  162
• 氢给体数：
  3
• 氢受体数：
  29

反应信息

• 作为反应物：
  描述：

  2,2,2-trichloro-N-[(2R,3R,4R,5S,6R)-2-[[(2R,3S,4R,5R,6R)-6-[(Z)-4-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecoxy)but-2-enoxy]-3,4-bis(phenylmethoxy)-5-[(2,2,2-trichloroacetyl)amino]oxan-2-yl]methoxy]-6-(hydroxymethyl)-4,5-bis(phenylmethoxy)oxan-3-yl]acetamide 在 palladium dichloride 作用下， 以 甲醇 为溶剂， 反应 8.0h， 以45.6 mg的产率得到
  参考文献：
  名称：

  Protecting-Group-Based Colorimetric Monitoring of Fluorous-Phase and Solid-Phase Synthesis of Oligoglucosamines

  摘要：

  A new hydroxyl protecting group, nitrophthalimidobutyric (NPB) acid, has been synthesized in one solvent-free step for colorimetric monitoring of reaction cycles upon its facile removal with hydrazine acetate in the solid-phase and fluorous-phase syntheses of antigenic oligoglucosamines associated with infectious Staphylococcus aureus. The NPB group serves as a convenient hydroxyl protecting group that is stable to the basic conditions required for the synthesis of the common trichloroacetimidate protecting groups, the strongly acidic conditions used in glycosylation reactions, as well as conditions commonly used to remove silicon-based protecting groups.

  DOI：

  10.1021/ol802229b
• 作为产物：
  描述：

  在 乙酸肼 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 0.08h， 以0.46 g的产率得到2,2,2-trichloro-N-[(2R,3R,4R,5S,6R)-2-[[(2R,3S,4R,5R,6R)-6-[(Z)-4-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecoxy)but-2-enoxy]-3,4-bis(phenylmethoxy)-5-[(2,2,2-trichloroacetyl)amino]oxan-2-yl]methoxy]-6-(hydroxymethyl)-4,5-bis(phenylmethoxy)oxan-3-yl]acetamide
  参考文献：
  名称：

  Protecting-Group-Based Colorimetric Monitoring of Fluorous-Phase and Solid-Phase Synthesis of Oligoglucosamines

  摘要：

  A new hydroxyl protecting group, nitrophthalimidobutyric (NPB) acid, has been synthesized in one solvent-free step for colorimetric monitoring of reaction cycles upon its facile removal with hydrazine acetate in the solid-phase and fluorous-phase syntheses of antigenic oligoglucosamines associated with infectious Staphylococcus aureus. The NPB group serves as a convenient hydroxyl protecting group that is stable to the basic conditions required for the synthesis of the common trichloroacetimidate protecting groups, the strongly acidic conditions used in glycosylation reactions, as well as conditions commonly used to remove silicon-based protecting groups.

  DOI：

  10.1021/ol802229b

文献信息

• Protecting-Group-Based Colorimetric Monitoring of Fluorous-Phase and Solid-Phase Synthesis of Oligoglucosamines
  作者：Kwang-Seuk Ko、Gisun Park、Yang Yu、Nicola L. Pohl

  DOI：10.1021/ol802229b

  日期：2008.12.4

  A new hydroxyl protecting group, nitrophthalimidobutyric (NPB) acid, has been synthesized in one solvent-free step for colorimetric monitoring of reaction cycles upon its facile removal with hydrazine acetate in the solid-phase and fluorous-phase syntheses of antigenic oligoglucosamines associated with infectious Staphylococcus aureus. The NPB group serves as a convenient hydroxyl protecting group that is stable to the basic conditions required for the synthesis of the common trichloroacetimidate protecting groups, the strongly acidic conditions used in glycosylation reactions, as well as conditions commonly used to remove silicon-based protecting groups.