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6,6'-[(3β,5β)-cholane-3,24-diyldi(oxy)]bis[N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)pyridin-2-amine] | 1224736-85-9

中文名称
——
中文别名
——
英文名称
6,6'-[(3β,5β)-cholane-3,24-diyldi(oxy)]bis[N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)pyridin-2-amine]
英文别名
——
6,6'-[(3β,5β)-cholane-3,24-diyldi(oxy)]bis[N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)pyridin-2-amine]化学式
CAS
1224736-85-9
化学式
C54H92N6O8
mdl
——
分子量
953.36
InChiKey
XMKNDJIGYHHZES-NOXUELQSSA-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):
    8.78
  • 重原子数:
    68.0
  • 可旋转键数:
    36.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    175.72
  • 氢给体数:
    4.0
  • 氢受体数:
    14.0

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

  • 作为反应物:
    描述:
    1-氯蒽醌6,6'-[(3β,5β)-cholane-3,24-diyldi(oxy)]bis[N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)pyridin-2-amine]caesium carbonateR-(+)-1,1'-联萘-2,2'-双二苯膦 、 bis(dibenzylideneacetone)-palladium(0) 作用下, 以 1,4-二氧六环 为溶剂, 反应 24.0h, 以53%的产率得到1-{[3-(2-{2-[3-({6-([(3β,5β)-24-{[6-({3-[2-(2-{3-[(9,10-dioxo-9,10-dihydroanthracen-1-yl)amino]propoxy}ethoxy)ethoxy]propyl}amino)pyridin-2-yl]oxy}cholan-3-yl]oxy)pyridin-2-yl}amino)propoxy]ethoxy}ethoxy)propyl]amino}-9,10-dihydroanthracene-9,10-dione
    参考文献:
    名称:
    Palladium-catalyzed amination in the synthesis and modification of acyclic oxadiamino cholane derivatives
    摘要:
    Palladium-catalyzed reactions of 24-(haloaryloxy)cholanes and 3,24-bis(haloaryloxy)cholanes with excess oxadiamines gave the corresponding mono- and bis(oxadiamino)-substituted cholanes which were subjected to palladium-catalyzed arylation with 1,3-dibromobenzene, 2,6-dibromopyridine, 1,8-dichloroanthracene, 9-bromoanthracene, 1-chloroanthracene, and 1-chloroanthraquinone. The results of these reactions were found to strongly depend on the haloarene nature. The arylation with 1,3-dibromobenzene and 2,6-dibromopyridine led to the formation of new macrocyclic compounds containing one cholane, one arene, and two oxadiamine fragments.
    DOI:
    10.1134/s1070428009120021
  • 作为产物:
    描述:
    4,7,10-三氧-1,13-十三烷二胺3,24-bis(6-chloropyridin-2-yloxy)-3α,5β-cholaneR-(+)-1,1'-联萘-2,2'-双二苯膦 、 bis(dibenzylideneacetone)-palladium(0)sodium t-butanolate 作用下, 以 1,4-二氧六环 为溶剂, 反应 4.0h, 以54%的产率得到6,6'-[(3β,5β)-cholane-3,24-diyldi(oxy)]bis[N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)pyridin-2-amine]
    参考文献:
    名称:
    Palladium-catalyzed amination in the synthesis and modification of acyclic oxadiamino cholane derivatives
    摘要:
    Palladium-catalyzed reactions of 24-(haloaryloxy)cholanes and 3,24-bis(haloaryloxy)cholanes with excess oxadiamines gave the corresponding mono- and bis(oxadiamino)-substituted cholanes which were subjected to palladium-catalyzed arylation with 1,3-dibromobenzene, 2,6-dibromopyridine, 1,8-dichloroanthracene, 9-bromoanthracene, 1-chloroanthracene, and 1-chloroanthraquinone. The results of these reactions were found to strongly depend on the haloarene nature. The arylation with 1,3-dibromobenzene and 2,6-dibromopyridine led to the formation of new macrocyclic compounds containing one cholane, one arene, and two oxadiamine fragments.
    DOI:
    10.1134/s1070428009120021
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