(4S)-4-(4-diazo-3-oxobutyl)-3-methyl-2,2-bis(trifluoromethyl)-1,3-oxazolidin-5-one | 261943-26-4

• 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: (4S)-4-(4-diazo-3-oxobutyl)-3-methyl-2,2-bis(trifluoromethyl)-1,3-oxazolidin-5-one
• CAS: 261943-26-4
• 化学式: C₁₀H₉F₆N₃O₃
• 分子量: 333.19
• InChiKey: PLIGZZLJYNPMLE-LURJTMIESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  48.6
• 氢给体数：
  0
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  (4S)-4-(4-diazo-3-oxobutyl)-3-methyl-2,2-bis(trifluoromethyl)-1,3-oxazolidin-5-one 在 氢溴酸 作用下， 以 四氢呋喃 为溶剂， 以81%的产率得到(4S)-4-(4-bromo-3-oxobutyl)-3-methyl-2,2-bis(trifluoromethyl)-1,3-oxazolidin-5-one
  参考文献：
  名称：

  A New Approach toN-Methylaspartic,N-Methylglutamic, andN-Methyl-α-aminoadipic Acid Derivatives

  摘要：

  N-Methylaspartic acid derivatives and its homologues are obtained by a stereoconservative one-pot procedure from hexafluoroacetone-protected aspartic and glutamic acid, 2a and 2b, respectively. alpha-Aminoadipic acid (5c) and its derivative 6c are accessible from the corresponding glutamic acid derivative 9b by a Wolff rearrangement. A variety of homochiral N-methylamino acids, 5 and 12, and their derivatives, 6 and 8-11, become readily available by the new synthetic concept.

  DOI：

  10.1002/(sici)1099-0690(200001)2000:1<199::aid-ejoc199>3.0.co;2-8
• 作为产物：
  描述：

  重氮甲烷 、 3-[(4S)-3-methyl-5-oxo-2,2-bis(trifluoromethyl)-1,3-oxazolidin-4-yl]propionyl chloride 以 乙醚 为溶剂， 反应 1.5h， 以85%的产率得到(4S)-4-(4-diazo-3-oxobutyl)-3-methyl-2,2-bis(trifluoromethyl)-1,3-oxazolidin-5-one
  参考文献：
  名称：

  A New Approach toN-Methylaspartic,N-Methylglutamic, andN-Methyl-α-aminoadipic Acid Derivatives

  摘要：

  N-Methylaspartic acid derivatives and its homologues are obtained by a stereoconservative one-pot procedure from hexafluoroacetone-protected aspartic and glutamic acid, 2a and 2b, respectively. alpha-Aminoadipic acid (5c) and its derivative 6c are accessible from the corresponding glutamic acid derivative 9b by a Wolff rearrangement. A variety of homochiral N-methylamino acids, 5 and 12, and their derivatives, 6 and 8-11, become readily available by the new synthetic concept.

  DOI：

  10.1002/(sici)1099-0690(200001)2000:1<199::aid-ejoc199>3.0.co;2-8