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1-(but-3-ynyl)-2-(quinolin-2-ylethynyl)pyridinium trifluoromethanesulfonate | 1229283-68-4

中文名称
——
中文别名
——
英文名称
1-(but-3-ynyl)-2-(quinolin-2-ylethynyl)pyridinium trifluoromethanesulfonate
英文别名
——
1-(but-3-ynyl)-2-(quinolin-2-ylethynyl)pyridinium trifluoromethanesulfonate化学式
CAS
1229283-68-4
化学式
CF3O3S*C20H15N2
mdl
——
分子量
432.423
InChiKey
NQQOIWJBACLMNU-UHFFFAOYSA-M
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):
    3.0
  • 重原子数:
    30.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    73.97
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    1-(but-3-ynyl)-2-(quinolin-2-ylethynyl)pyridinium trifluoromethanesulfonate 、 pent-4-yn-1-yl trifluoromethanesulfonate 以 二氯甲烷 为溶剂, 反应 48.0h, 以53%的产率得到2-((1-(but-3-ynyl)pyridinium-2-yl)ethynyl)-1-(pent-4-ynyl)-quinolinium trifluoromethanesulfonate
    参考文献:
    名称:
    Highly modular assembly of cationic helical scaffolds: rapid synthesis of diverse helquats via differential quaternization
    摘要:
    A protocol for rapid and highly modular assembly of a diverse set of helquats is described. From a common bis-isoquinoline precursor, two successive distinct pyridine-type nitrogen quaternizations followed by rhodium-catalyzed [2+2+2] cycloaddition afford non-symmetric [7]helquats. This route allows for straightforward molecular editing of cationic helical skeletons as exemplified by the synthesis of 15 different [5]-, [6]-, and [7]helquats. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.03.007
  • 作为产物:
    描述:
    but-3-yn-1-yl trifluoromethanesulfonate2-(pyridine-2-ylethynyl)quinoline甲苯 为溶剂, 反应 25.0h, 以75%的产率得到1-(but-3-ynyl)-2-(quinolin-2-ylethynyl)pyridinium trifluoromethanesulfonate
    参考文献:
    名称:
    Highly modular assembly of cationic helical scaffolds: rapid synthesis of diverse helquats via differential quaternization
    摘要:
    A protocol for rapid and highly modular assembly of a diverse set of helquats is described. From a common bis-isoquinoline precursor, two successive distinct pyridine-type nitrogen quaternizations followed by rhodium-catalyzed [2+2+2] cycloaddition afford non-symmetric [7]helquats. This route allows for straightforward molecular editing of cationic helical skeletons as exemplified by the synthesis of 15 different [5]-, [6]-, and [7]helquats. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.03.007
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