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N-[3,5-bis(3-chlorophenyl)pyridin-2-yl]pyridinium aminide | 1011793-83-1

中文名称
——
中文别名
——
英文名称
N-[3,5-bis(3-chlorophenyl)pyridin-2-yl]pyridinium aminide
英文别名
N-[3,5-bis(3-chlorophenyl)pyridin-2-yl](pyridinium)amide
N-[3,5-bis(3-chlorophenyl)pyridin-2-yl]pyridinium aminide化学式
CAS
1011793-83-1
化学式
C22H15Cl2N3
mdl
——
分子量
392.287
InChiKey
ZWFYMBLZCHZYEU-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Pyridinium N-heteroarylaminides: synthesis of N-heteroarylpolyamines
    摘要:
    The synthesis of a set of new N-heteroarylpolyamines is reported. A multiple and regioselective alkylation on the exo nitrogen of pyridinium N-(heteroaryl)aminides with several polybromo compounds, followed by a clean N-N bond reduction of the corresponding pyridinium salts, provides an easy and general method to obtain the title compounds. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.09.079
  • 作为产物:
    描述:
    3-氯苯硼酸N-(3',5'-dibromopyrid-2'-yl)pyridinium aminide四(三苯基膦)钯 caesium carbonate 作用下, 以 乙醇甲苯 为溶剂, 反应 8.0h, 以78%的产率得到N-[3,5-bis(3-chlorophenyl)pyridin-2-yl]pyridinium aminide
    参考文献:
    名称:
    Suzuki reaction on pyridinium N-haloheteroarylaminides: regioselective synthesis of 3,5-disubstituted 2-aminopyrazines
    摘要:
    An extensive study of Suzuki-Miyaura cross-coupling processes on N-pyridinium bromoazinyl aminides has been performed. Mono- and disubstitution on 5- and 3,5-bromo derivatives produced the corresponding aryl derivatives. In the disubstituted compounds regioselective substitution at the 3-position occurred, vicinal to the aminide nitrogen, and this was more evident in pyrazine derivatives. The commonly used strategy involving N-alkylation and reduction of the N-N bond gave rise to a series of 2-alkylamino-3,5-disubstituted-pyrazines. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.11.057
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