4-amino-5-cyclopropanoylveratrole | 905809-88-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-amino-5-cyclopropanoylveratrole
• 英文别名: (2-Amino-4,5-dimethoxyphenyl)(cyclopropyl)methanone；(2-amino-4,5-dimethoxyphenyl)-cyclopropylmethanone
• CAS: 905809-88-3
• 化学式: C₁₂H₁₅NO₃
• mdl: MFCD08685715
• 分子量: 221.256
• InChiKey: TXVKKFFJUVDLIM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  61.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (4-甲氧基-苯氧基)-乙酰氯 、 4-amino-5-cyclopropanoylveratrole 在 sodium hydroxide 作用下， 以 1,4-二氧六环 、 水 为溶剂， 以85%的产率得到N-[2-(cyclopropylcarbonyl)-4,5-dimethoxyphenyl]-2-(4-methoxyphenoxy)acetamide
  参考文献：
  名称：

  Synthesis of cyclopropyl-substituted 4H-3,1-benzoxazines from 2-amino-phenyl cyclopropyl ketones and 2-cyclopropanoylaminoacylbenzenes

  摘要：

  2- and 4-cyclopropyl- and 2,4-dicyclopropyl-substituted 4H-3,1-benzoxazines were synthesized by the intramolecular acid catalyzed heterocyclization of ortho-acylamino-substituted benzyl alcohols, obtained from 2-aminophenyl cyclopropyl ketones and 2-cyclopropanoylaminoacylbenzenes.

  DOI：

  10.1007/s10593-009-0251-5
• 作为产物：
  描述：

  5-cyclopropanoyl-4-nitroveratrole 在 水 、 铁粉 作用下， 以 苯 为溶剂， 以67%的产率得到4-amino-5-cyclopropanoylveratrole
  参考文献：
  名称：

  Synthesis of cyclopropyl-substituted 4H-3,1-benzoxazines from 2-amino-phenyl cyclopropyl ketones and 2-cyclopropanoylaminoacylbenzenes

  摘要：

  2- and 4-cyclopropyl- and 2,4-dicyclopropyl-substituted 4H-3,1-benzoxazines were synthesized by the intramolecular acid catalyzed heterocyclization of ortho-acylamino-substituted benzyl alcohols, obtained from 2-aminophenyl cyclopropyl ketones and 2-cyclopropanoylaminoacylbenzenes.

  DOI：

  10.1007/s10593-009-0251-5

文献信息

• Synthesis of quinolin-2-ones by an intramolecular Knoevenagel condensation and by tandem Michael–Knoevenagel heterocyclization
  作者：S. S. Mochalov、M. I. Chasanov、A. N. Fedotov、N. S. Zefirov

  DOI：10.1007/s10593-011-0881-2

  日期：2011.12

  The synthesis of 2-(N-R-amino)- and 2-(N-vinylcarbonylamino)acylbenzenes has been carried out and their heterocyclization into quinolin-2-ones under the action of sodium ethylate has been studied.
• Synthesis of cyclopropyl-substituted 4H-3,1-benzoxazines from 2-amino-phenyl cyclopropyl ketones and 2-cyclopropanoylaminoacylbenzenes
  作者：S. S. Mochalov、M. I. Khasanov、N. S. Zefirov

  DOI：10.1007/s10593-009-0251-5

  日期：2009.2

  2- and 4-cyclopropyl- and 2,4-dicyclopropyl-substituted 4H-3,1-benzoxazines were synthesized by the intramolecular acid catalyzed heterocyclization of ortho-acylamino-substituted benzyl alcohols, obtained from 2-aminophenyl cyclopropyl ketones and 2-cyclopropanoylaminoacylbenzenes.