benzyl (2R)-2-[(2S)-1-(4-methylphenyl)sulfonylazetidin-2-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate | 1178006-10-4

• 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: benzyl (2R)-2-[(2S)-1-(4-methylphenyl)sulfonylazetidin-2-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate
• CAS: 1178006-10-4
• 化学式: C₂₄H₃₀N₂O₆S
• 分子量: 474.578
• InChiKey: AZOZURVVJLFFDJ-LEWJYISDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  33
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  110
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  (2R)-2-[(2S)-1-(4-methylphenyl)sulfonylazetidin-2-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid 、 溴甲苯 在 caesium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 以90%的产率得到benzyl (2R)-2-[(2S)-1-(4-methylphenyl)sulfonylazetidin-2-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate
  参考文献：
  名称：

  Stereoselective synthesis of 2-azetidinylglycine and aminopyrrolidone derivatives from Garner’s aldehyde

  摘要：

  A new route to two hitherto unknown 2-azetidinylglycine derivatives and an aminopyrrolidone derivative has been developed which featured a diastereoselective conjugate addition of benzyl amine to an alpha,beta-unsaturated ester derived from Garner's aldehyde as the key step. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2009.04.010

文献信息

• Stereoselective synthesis of 2-azetidinylglycine and aminopyrrolidone derivatives from Garner’s aldehyde
  作者：Latibuddin Thander、Kaushik Sarkar、Shital K. Chattopadhyay

  DOI：10.1016/j.tetasy.2009.04.010

  日期：2009.6

  A new route to two hitherto unknown 2-azetidinylglycine derivatives and an aminopyrrolidone derivative has been developed which featured a diastereoselective conjugate addition of benzyl amine to an alpha,beta-unsaturated ester derived from Garner's aldehyde as the key step. (C) 2009 Elsevier Ltd. All rights reserved.