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N,N,N'-tris[(6-bromo-2,2'-bipyridine-5'-yl)methyl]-N'-(t-butyloxycarbonylmethyl)ethylenediamine | 439614-48-9

中文名称
——
中文别名
——
英文名称
N,N,N'-tris[(6-bromo-2,2'-bipyridine-5'-yl)methyl]-N'-(t-butyloxycarbonylmethyl)ethylenediamine
英文别名
Tert-butyl 2-[2-[bis[[6-(6-bromopyridin-2-yl)pyridin-3-yl]methyl]amino]ethyl-[[6-(6-bromopyridin-2-yl)pyridin-3-yl]methyl]amino]acetate
N,N,N'-tris[(6-bromo-2,2'-bipyridine-5'-yl)methyl]-N'-(t-butyloxycarbonylmethyl)ethylenediamine化学式
CAS
439614-48-9
化学式
C41H39Br3N8O2
mdl
——
分子量
915.525
InChiKey
HEUBRGSVAWEBEE-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):
    7.4
  • 重原子数:
    54
  • 可旋转键数:
    16
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    110
  • 氢给体数:
    0
  • 氢受体数:
    10

上下游信息

  • 下游产品
    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:
    N,N,N'-tris[(6-bromo-2,2'-bipyridine-5'-yl)methyl]-N'-(t-butyloxycarbonylmethyl)ethylenediamine 在 bis-triphenylphosphine-palladium(II) chloride sodium hydroxide三乙胺 作用下, 以 甲醇 为溶剂, 80.0 ℃ 、101.33 kPa 条件下, 反应 1.0h, 生成 N,N,N'-tris[(6-carboxy-2,2'-bipyridine-5'-yl)methyl]-N'-(carboxymethyl)ethylenediamine
    参考文献:
    名称:
    5‘-Substituted-6-carboxylic-2,2‘-bipyridine Acid:  A Pivotal Architecton for Building Preorganized Ligands
    摘要:
    A set of ligands bearing 6-bromo-2,2'-bipyridine pendant arms attached in the 5'-position are described. Trans formation of the bromo to an ester was performed by a carboethoxylation reaction promoted by low-valent Pd(0), while saponification followed by acidification gave the acids. The introduction of an appended function 3-nitrobenzyl, benzamidomethyl, and tert-butylacetyl opens the way to further functionalize these scaffolds for potential labeling of biological material. The synthetic protocols represent a valuable approach to the rational design of ligands bearing oxophilic and anionic sidearms.
    DOI:
    10.1021/jo0200015
  • 作为产物:
    描述:
    (2-氨基乙基氨基)乙酸叔丁酯 、 6-bromo-5'-bromomethyl-2,2'-bipyridine 在 sodium carbonate 作用下, 以 乙腈 为溶剂, 反应 22.0h, 以85%的产率得到N,N,N'-tris[(6-bromo-2,2'-bipyridine-5'-yl)methyl]-N'-(t-butyloxycarbonylmethyl)ethylenediamine
    参考文献:
    名称:
    5‘-Substituted-6-carboxylic-2,2‘-bipyridine Acid:  A Pivotal Architecton for Building Preorganized Ligands
    摘要:
    A set of ligands bearing 6-bromo-2,2'-bipyridine pendant arms attached in the 5'-position are described. Trans formation of the bromo to an ester was performed by a carboethoxylation reaction promoted by low-valent Pd(0), while saponification followed by acidification gave the acids. The introduction of an appended function 3-nitrobenzyl, benzamidomethyl, and tert-butylacetyl opens the way to further functionalize these scaffolds for potential labeling of biological material. The synthetic protocols represent a valuable approach to the rational design of ligands bearing oxophilic and anionic sidearms.
    DOI:
    10.1021/jo0200015
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文献信息

  • 5‘-Substituted-6-carboxylic-2,2‘-bipyridine Acid:  A Pivotal Architecton for Building Preorganized Ligands
    作者:Loïc J. Charbonnière、Nicolas Weibel、Raymond F. Ziessel
    DOI:10.1021/jo0200015
    日期:2002.5.1
    A set of ligands bearing 6-bromo-2,2'-bipyridine pendant arms attached in the 5'-position are described. Trans formation of the bromo to an ester was performed by a carboethoxylation reaction promoted by low-valent Pd(0), while saponification followed by acidification gave the acids. The introduction of an appended function 3-nitrobenzyl, benzamidomethyl, and tert-butylacetyl opens the way to further functionalize these scaffolds for potential labeling of biological material. The synthetic protocols represent a valuable approach to the rational design of ligands bearing oxophilic and anionic sidearms.
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