摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

7-chloro-4-(4-phenoxymethyl-[1,2,3]triazol-1-yl)-quinoline | 1261145-75-8

中文名称
——
中文别名
——
英文名称
7-chloro-4-(4-phenoxymethyl-[1,2,3]triazol-1-yl)-quinoline
英文别名
7-Chloro-4-[4-(phenoxymethyl)triazol-1-yl]quinoline
7-chloro-4-(4-phenoxymethyl-[1,2,3]triazol-1-yl)-quinoline化学式
CAS
1261145-75-8
化学式
C18H13ClN4O
mdl
——
分子量
336.78
InChiKey
LWVQHMDEAFGJND-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):
    3.7
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    52.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    苯基炔丙基醚4-叠氮基-7-氯喹啉 在 copper(II) sulfate 、 sodium ascorbate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 以69%的产率得到7-chloro-4-(4-phenoxymethyl-[1,2,3]triazol-1-yl)-quinoline
    参考文献:
    名称:
    Design, synthesis and in vitro antimalarial evaluation of triazole-linked chalcone and dienone hybrid compounds
    摘要:
    A targeted series of chalcone and dienone hybrid compounds containing aminoquinoline and nucleoside templates was synthesized and evaluated for in vitro antimalarial activity. The Cu(I)-catalyzed cycloaddition of azides and terminal alkynes was applied as the hybridization strategy. Several chalcone-chloroquinoline hybrid compounds were found to be notably active, with compound 8b the most active, exhibiting submicromolar IC50 values against the D10, Dd2 and W2 strains of Plasmodium falciparum. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.10.009
点击查看最新优质反应信息

文献信息

  • Design, synthesis and in vitro antimalarial evaluation of triazole-linked chalcone and dienone hybrid compounds
    作者:Eric M. Guantai、Kanyile Ncokazi、Timothy J. Egan、Jiri Gut、Philip J. Rosenthal、Peter J. Smith、Kelly Chibale
    DOI:10.1016/j.bmc.2010.10.009
    日期:2010.12
    A targeted series of chalcone and dienone hybrid compounds containing aminoquinoline and nucleoside templates was synthesized and evaluated for in vitro antimalarial activity. The Cu(I)-catalyzed cycloaddition of azides and terminal alkynes was applied as the hybridization strategy. Several chalcone-chloroquinoline hybrid compounds were found to be notably active, with compound 8b the most active, exhibiting submicromolar IC50 values against the D10, Dd2 and W2 strains of Plasmodium falciparum. (C) 2010 Elsevier Ltd. All rights reserved.
查看更多