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N'-[4,6-bis(4-pyrazol-1-ylphenylamino)-1,3,5-triazin-2-yl]-N-[4,6-bis(1-phenylpyrazol-4-ylamino)-1,3,5-triazin-2-yl]-4-aminobenzylamine | 1207194-73-7

中文名称
——
中文别名
——
英文名称
N'-[4,6-bis(4-pyrazol-1-ylphenylamino)-1,3,5-triazin-2-yl]-N-[4,6-bis(1-phenylpyrazol-4-ylamino)-1,3,5-triazin-2-yl]-4-aminobenzylamine
英文别名
6-N-[4-[[[4,6-bis[(1-phenylpyrazol-4-yl)imino]-1,3,5-triazinan-2-ylidene]amino]methyl]phenyl]-2-N,4-N-bis(4-pyrazol-1-ylphenyl)-1,3,5-triazine-2,4,6-triamine
N'-[4,6-bis(4-pyrazol-1-ylphenylamino)-1,3,5-triazin-2-yl]-N-[4,6-bis(1-phenylpyrazol-4-ylamino)-1,3,5-triazin-2-yl]-4-aminobenzylamine化学式
CAS
1207194-73-7
化学式
C49H40N20
mdl
——
分子量
908.991
InChiKey
AMBGBRLSRYCFBV-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    9.1
  • 重原子数:
    69
  • 可旋转键数:
    17
  • 环数:
    11.0
  • sp3杂化的碳原子比例:
    0.02
  • 拓扑面积:
    221
  • 氢给体数:
    6
  • 氢受体数:
    16

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    N-(4-aminobenzyl)-N',N''-bis-(1-phenyl-1H-pyrazol-4-yl)-[1,3,5]triazine-2,4,6-triamine6-chloro-N,N'-bis-(4-pyrazol-1-yl-phenyl)-[1,3,5]triazine-2,4-diamineN,N-二异丙基乙胺 作用下, 以 二甲基亚砜 为溶剂, 反应 0.17h, 以92%的产率得到N'-[4,6-bis(4-pyrazol-1-ylphenylamino)-1,3,5-triazin-2-yl]-N-[4,6-bis(1-phenylpyrazol-4-ylamino)-1,3,5-triazin-2-yl]-4-aminobenzylamine
    参考文献:
    名称:
    Microwave-assisted synthesis of pyrazolyl bistriazines
    摘要:
    Reaction of 6-chloro-N,N '-bispyrazolyl-[1,3,5]triazine-2,4-diamines with 4-aminobenzylamine under microwave irradiation produces bistriazines in excellent yields. The use of a diamine bearing amino groups with different reactivities allowed the reaction to be carried out in two steps and selectively gave monotriazines, bistriazines with identical substituents and differently substituted bistriazines. The structures of these new compounds have been studied by NMR spectroscopy, mass spectrometry and in one case by X-ray crystallogrphy. These new bistriazines have promising applications in supramolecular chemistry based on hydrogen bonds and/or complexation with metals. The presence of a rigid linker can be used for the efficient preparation of extended supramolecular polymers with interesting fluorescence properties by complexation with cyanuric and barbituric acid derivatives. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.11.028
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文献信息

  • Microwave-assisted synthesis of pyrazolyl bistriazines
    作者:Mónica Moral、Amparo Ruiz、Andrés Moreno、Angel Díaz-Ortiz、Isabel López-Solera、Antonio de la Hoz、Ana Sánchez-Migallón
    DOI:10.1016/j.tet.2009.11.028
    日期:2010.1
    Reaction of 6-chloro-N,N '-bispyrazolyl-[1,3,5]triazine-2,4-diamines with 4-aminobenzylamine under microwave irradiation produces bistriazines in excellent yields. The use of a diamine bearing amino groups with different reactivities allowed the reaction to be carried out in two steps and selectively gave monotriazines, bistriazines with identical substituents and differently substituted bistriazines. The structures of these new compounds have been studied by NMR spectroscopy, mass spectrometry and in one case by X-ray crystallogrphy. These new bistriazines have promising applications in supramolecular chemistry based on hydrogen bonds and/or complexation with metals. The presence of a rigid linker can be used for the efficient preparation of extended supramolecular polymers with interesting fluorescence properties by complexation with cyanuric and barbituric acid derivatives. (C) 2009 Elsevier Ltd. All rights reserved.
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