2-cyclopropyl-oct-7-en-3-ynoic acid benzylamide | 1206892-57-0

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 2-cyclopropyl-oct-7-en-3-ynoic acid benzylamide
• 英文别名: N-benzyl-2-cyclopropyloct-7-en-3-ynamide
• CAS: 1206892-57-0
• 化学式: C₁₈H₂₁NO
• 分子量: 267.371
• InChiKey: DEUAXOZPUKXPRB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  20
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  甲醇 、 2-cyclopropyl-oct-7-en-3-ynoic acid benzylamide 在 N-碘代丁二酰亚胺 作用下， 以 丙酮 为溶剂， 以70%的产率得到1-benzyl-5-but-3-enyl-3-cyclopropyl-4-iodo-5-methoxy-1,5-dihydro-pyrrol-2-one
  参考文献：
  名称：

  Unusual Approach to Branched 3-Alkynylamides and to 1,5-Dihydropyrrol-2-ones

  摘要：

  Rare carboxamide branched alkynes such as 11a can be readily obtained by reaction of the electrophilic 4-alkylidene isoxazolinones with isocycanides followed by nitrosative cleavage of the heterocyclic ring. N-lodosuccinimide induced ring closure in the presence of a nucleophile results in the formation of new iodopyrrolinones such as 16c.

  DOI：

  10.1021/ol902472r
• 作为产物：
  描述：

  N-benzyl-2-(3-but-3-enyl-5-oxo-4,5-dihydro-isoxazol-4-yl)-2-cyclopropyl-acetamide 在 iron(II) sulfate 、 溶剂黄146 、 sodium nitrite 作用下， 以 水 为溶剂， 以60%的产率得到2-cyclopropyl-oct-7-en-3-ynoic acid benzylamide
  参考文献：
  名称：

  Unusual Approach to Branched 3-Alkynylamides and to 1,5-Dihydropyrrol-2-ones

  摘要：

  Rare carboxamide branched alkynes such as 11a can be readily obtained by reaction of the electrophilic 4-alkylidene isoxazolinones with isocycanides followed by nitrosative cleavage of the heterocyclic ring. N-lodosuccinimide induced ring closure in the presence of a nucleophile results in the formation of new iodopyrrolinones such as 16c.

  DOI：

  10.1021/ol902472r

文献信息

• Unusual Approach to Branched 3-Alkynylamides and to 1,5-Dihydropyrrol-2-ones
  作者：Igor Dias-Jurberg、Fabien Gagosz、Samir Z. Zard

  DOI：10.1021/ol902472r

  日期：2010.2.5

  Rare carboxamide branched alkynes such as 11a can be readily obtained by reaction of the electrophilic 4-alkylidene isoxazolinones with isocycanides followed by nitrosative cleavage of the heterocyclic ring. N-lodosuccinimide induced ring closure in the presence of a nucleophile results in the formation of new iodopyrrolinones such as 16c.