2-tert-Butoxycarbonylamino-2-difluoromethyl-hexanedioic acid 1-ethyl ester | 322474-16-8

• 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: 2-tert-Butoxycarbonylamino-2-difluoromethyl-hexanedioic acid 1-ethyl ester
• 英文别名: 5-(Difluoromethyl)-6-ethoxy-5-[(2-methylpropan-2-yl)oxycarbonylamino]-6-oxohexanoic acid
• CAS: 322474-16-8
• 化学式: C₁₄H₂₃F₂NO₆
• 分子量: 339.337
• InChiKey: ZQGWRKZXCGDYHJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  23
• 可旋转键数：
  11
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  102
• 氢给体数：
  2
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  2-tert-Butoxycarbonylamino-2-difluoromethyl-hexanedioic acid 1-ethyl ester 在 吡啶 、 ammonium hydroxide 、 N,N'-二环己基碳二亚胺 、 [双(三氟乙酰氧基)碘]苯 作用下， 以 甲醇 为溶剂， 生成 3-difluoromethyl-3-(tert-butoxycarbonylamino)piperidin-2-one
  参考文献：
  名称：

  First Synthesis of Totally Orthogonal Protected α-(Trifluoromethyl)- and α-(Difluoromethyl)arginines

  摘要：

  The first synthesis of a series of totally orthogonal protected racemic alpha-(trifluoromethyl)- and alpha-(difluoromethyl)arginines is described. The key steps of the synthesis are the mild guanidinylation procedure and the selective hydrogenation of a CC triple bond in the presence of a Cbz-group.

  DOI：

  10.1021/jo0009043
• 作为产物：
  描述：

  2-tert-Butoxycarbonylamino-2-difluoromethyl-hept-6-enoic acid ethyl ester 在 potassium permanganate 、 硫酸 作用下， 生成 2-tert-Butoxycarbonylamino-2-difluoromethyl-hexanedioic acid 1-ethyl ester
  参考文献：
  名称：

  First Synthesis of Totally Orthogonal Protected α-(Trifluoromethyl)- and α-(Difluoromethyl)arginines

  摘要：

  The first synthesis of a series of totally orthogonal protected racemic alpha-(trifluoromethyl)- and alpha-(difluoromethyl)arginines is described. The key steps of the synthesis are the mild guanidinylation procedure and the selective hydrogenation of a CC triple bond in the presence of a Cbz-group.

  DOI：

  10.1021/jo0009043

文献信息

• First Synthesis of Totally Orthogonal Protected α-(Trifluoromethyl)- and α-(Difluoromethyl)arginines
  作者：Maurizio Moroni、Beate Koksch、Sergey N. Osipov、Marcello Crucianelli、Massimo Frigerio、Pierfrancesco Bravo、Klaus Burger

  DOI：10.1021/jo0009043

  日期：2001.1.1

  The first synthesis of a series of totally orthogonal protected racemic alpha-(trifluoromethyl)- and alpha-(difluoromethyl)arginines is described. The key steps of the synthesis are the mild guanidinylation procedure and the selective hydrogenation of a CC triple bond in the presence of a Cbz-group.