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ethyl 6-aminobenzimidazo[2,1-a]isoquinoline-5-carboxylate | 1301148-77-5

中文名称
——
中文别名
——
英文名称
ethyl 6-aminobenzimidazo[2,1-a]isoquinoline-5-carboxylate
英文别名
Ethyl 6-aminobenzimidazolo[2,1-a]isoquinoline-5-carboxylate
ethyl 6-aminobenzimidazo[2,1-a]isoquinoline-5-carboxylate化学式
CAS
1301148-77-5
化学式
C18H15N3O2
mdl
——
分子量
305.336
InChiKey
RTPZTIMUYUZGPU-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):
    4.9
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    69.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2-(2-溴苯基)苯并咪唑氰乙酸乙酯copper(l) iodidepotassium carbonate六氢吡啶-alpha-羧酸 作用下, 以 二甲基亚砜 为溶剂, 反应 12.0h, 以81%的产率得到ethyl 6-aminobenzimidazo[2,1-a]isoquinoline-5-carboxylate
    参考文献:
    名称:
    Copper-Catalyzed Cascade Synthesis of Alkyl 6-Aminobenzimidazo[2,1-a]isoquinoline-5-carboxylates
    摘要:
    A convenient and efficient copper-catalyzed cascade method has been developed for synthesis of benzimidazoisoquinoline derivatives via reactions of readily available substituted 2-(2-halophenyObenzoimidazoles with alkyl cyanoacetates under mild condition, and the corresponding alkyl 6-aminobenzimidazo[2,1-a]isoquinoline-5-carboxylates were obtained in good to excellent yields. The novel method provides diverse and useful poly N-heterocyclic compounds for combinatorial chemistry and medicinal chemistry.
    DOI:
    10.1021/jo200508q
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文献信息

  • Copper-Catalyzed Cascade Synthesis of Alkyl 6-Aminobenzimidazo[2,1-<i>a</i>]isoquinoline-5-carboxylates
    作者:Juyou Lu、Hua Fu
    DOI:10.1021/jo200508q
    日期:2011.6.3
    A convenient and efficient copper-catalyzed cascade method has been developed for synthesis of benzimidazoisoquinoline derivatives via reactions of readily available substituted 2-(2-halophenyObenzoimidazoles with alkyl cyanoacetates under mild condition, and the corresponding alkyl 6-aminobenzimidazo[2,1-a]isoquinoline-5-carboxylates were obtained in good to excellent yields. The novel method provides diverse and useful poly N-heterocyclic compounds for combinatorial chemistry and medicinal chemistry.
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