N,N-Bis(benzotriazol-1-ylmethyl)ethanamine | 111184-78-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并三唑类
• 英文名称: N,N-Bis(benzotriazol-1-ylmethyl)ethanamine
• 英文别名: Bis(1H-1,2,3-benzotriazol-1-ylmethyl)(ethyl)amine
• CAS: 111184-78-2
• 化学式: C₁₆H₁₇N₇
• 分子量: 307.358
• InChiKey: XJIGWGCVPDLMEN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  23
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  64.7
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  N,N-Bis(benzotriazol-1-ylmethyl)ethanamine 、 N-乙烯基吡咯烷酮 以66%的产率得到
  参考文献：
  名称：

  Katritzky Alan R., Rachwal Stanislaw, Rachwal Bogumila, J. Org. Chem, 59 (1994) N 18, S 5206-5214

  摘要：

  DOI：
• 作为产物：
  描述：

  1H-苯并三唑-1-甲醇 、 乙胺 以 乙醇 、 溶剂黄146 为溶剂， 反应 0.03h， 以84%的产率得到N,N-Bis(benzotriazol-1-ylmethyl)ethanamine
  参考文献：
  名称：

  Katritzky, Alan R.; Rachwal, Stanislaw; Rachwal, Bogumila, Journal of the Chemical Society. Perkin transactions I, 1987, p. 799 - 804

  摘要：

  DOI：

文献信息

• Additions of 1-(.alpha.-Aminoalkyl)benzotriazoles to N-Vinylamines and N-Vinylamides. A Novel and Versatile Method for the Preparation of Unsymmetrically Substituted 1,3-Diamines
  作者：Alan R. Katritzky、Stanislaw Rachwal、Bogumila Rachwal

  DOI：10.1021/jo00097a023

  日期：1994.9

  Additions of N,N-dialkyl-1H-benzotriazole-1-methanamines 1 to 9-vinylcarbazole followed by reduction of the adducts with lithium aluminum hydride gave the corresponding 9-(3-(dialkylamino)propyl)carbazoles 8 in good yield. Treatment of the adducts with Grignard reagents gave products 9 with an alkyl or aryl group at the C-1 atom of the propylene linkage. Use of alpha-phenyl-N,N-dialkyl-1H-benzotriazole-1-methanamine (14) in the addition led to the C-3 phenyl substituted products 15-18. Similar additions to N-vinyl-N-methylacetamide or 1-vinyl-2-pyrrolidinone followed by reduction of the adducts gave unsymmetrically substituted 1,3-propanediamines. Triamine 36 was obtained by condensation of ethylamine with formaldehyde and benzotriazole, addition of the product to 1-vinylpyrrolidinone, and reduction of the adduct with lithium aluminum hydride. 1,3-Propanediamine used in this process gave hexahydropyrimidine 39 while 1,6-hexanediamine gave hexamine 42.
• Katritzky Alan R., Rachwal Stanislaw, Rachwal Bogumila, J. Org. Chem, 59 (1994) N 18, S 5206-5214
  作者：Katritzky Alan R., Rachwal Stanislaw, Rachwal Bogumila

  DOI：——

  日期：——
• KATRITZKY A. R.; RACHWAL S.; RACHWAL B., J. CHEM. SOC. PERKIN TRANS.,(1987) N 4, 799-804
  作者：KATRITZKY A. R.、 RACHWAL S.、 RACHWAL B.

  DOI：——

  日期：——
• Katritzky, Alan R.; Rachwal, Stanislaw; Rachwal, Bogumila, Journal of the Chemical Society. Perkin transactions I, 1987, p. 799 - 804
  作者：Katritzky, Alan R.、Rachwal, Stanislaw、Rachwal, Bogumila

  DOI：——

  日期：——