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4-(1,3-di(quinolin-2-yl)propan-2-yl)benzonitrile | 1446451-56-4

中文名称
——
中文别名
——
英文名称
4-(1,3-di(quinolin-2-yl)propan-2-yl)benzonitrile
英文别名
4-[1,3-Di(quinolin-2-yl)propan-2-yl]benzonitrile;4-[1,3-di(quinolin-2-yl)propan-2-yl]benzonitrile
4-(1,3-di(quinolin-2-yl)propan-2-yl)benzonitrile化学式
CAS
1446451-56-4
化学式
C28H21N3
mdl
——
分子量
399.495
InChiKey
FGPOHHKFCUOBHX-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):
    6.2
  • 重原子数:
    31
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    49.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-甲基喹啉4-氰基苯甲醛对甲苯磺酸 作用下, 以 对二甲苯 为溶剂, 反应 24.0h, 以85%的产率得到4-(1,3-di(quinolin-2-yl)propan-2-yl)benzonitrile
    参考文献:
    名称:
    Brønsted acid catalyzed synthesis of 1,3-di(2-quinolyl)propane derivatives via tandem C(sp3)–H functionalization
    摘要:
    A novel protocol for Bronsted acid catalyzed reaction of 2-methyl azaarenes and aromatic aldehyde to give 1,3-di(2-quinolyl)propane derivatives through tandem C(sp(3))-H bond functionalization has been developed. This approach provides a new access to a variety of 1,3-di(2-quinolyl)propane derivatives, which are potentially of great importance in pharmaceuticals and ligand fields. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.05.135
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文献信息

  • Brønsted acid catalyzed synthesis of 1,3-di(2-quinolyl)propane derivatives via tandem C(sp3)–H functionalization
    作者:Jia-jia Jin、Dong-chao Wang、Hong-ying Niu、Shan Wu、Gui-rong Qu、Zhong-bo Zhang、Hai-ming Guo
    DOI:10.1016/j.tet.2013.05.135
    日期:2013.8
    A novel protocol for Bronsted acid catalyzed reaction of 2-methyl azaarenes and aromatic aldehyde to give 1,3-di(2-quinolyl)propane derivatives through tandem C(sp(3))-H bond functionalization has been developed. This approach provides a new access to a variety of 1,3-di(2-quinolyl)propane derivatives, which are potentially of great importance in pharmaceuticals and ligand fields. (C) 2013 Elsevier Ltd. All rights reserved.
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