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7,10-dimethoxy-2-benzyl-3,4,11,11a-tetrahydro-2H,6H-pyrazino[1,2-b]isoquinolin-1-one | 1609636-84-1

中文名称
——
中文别名
——
英文名称
7,10-dimethoxy-2-benzyl-3,4,11,11a-tetrahydro-2H,6H-pyrazino[1,2-b]isoquinolin-1-one
英文别名
——
7,10-dimethoxy-2-benzyl-3,4,11,11a-tetrahydro-2H,6H-pyrazino[1,2-b]isoquinolin-1-one化学式
CAS
1609636-84-1
化学式
C21H24N2O3
mdl
——
分子量
352.433
InChiKey
VQCMXPWMHKRPJX-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):
    2.47
  • 重原子数:
    26.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    42.01
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    7,10-dimethoxy-2-benzyl-3,4,11,11a-tetrahydro-2H,6H-pyrazino[1,2-b]isoquinolin-1-one三溴化硼硝酸 作用下, 以 二氯甲烷 为溶剂, 反应 2.25h, 以68%的产率得到2-benzyl-3,4,11,11a-tetrahydro-2H,6H-pyrazino[1,2-b]isoquinoline-1,7,10-trione
    参考文献:
    名称:
    Synthesis of Hexahydropyrazino[1,2-b]isoquinolines as Simplified Saframycin Analogues
    摘要:
    Various hexahydropyrazino[1,2-b]isoquinolines were synthesised as simplified saframycin analogues. Construction of this core proceeded through a tetrahydroisoquinoline synthesis followed by acylation/alkylation of the tetrahydroisoquinoline nitrogen and subsequent ring closure using various aliphatic and aromatic amines. The resulting piperazinones were reacted with LiAlH4 or LiAlH(OEt)(3) to synthesise further analogues.
    DOI:
    10.1055/s-0033-1340070
  • 作为产物:
    参考文献:
    名称:
    Synthesis of Hexahydropyrazino[1,2-b]isoquinolines as Simplified Saframycin Analogues
    摘要:
    Various hexahydropyrazino[1,2-b]isoquinolines were synthesised as simplified saframycin analogues. Construction of this core proceeded through a tetrahydroisoquinoline synthesis followed by acylation/alkylation of the tetrahydroisoquinoline nitrogen and subsequent ring closure using various aliphatic and aromatic amines. The resulting piperazinones were reacted with LiAlH4 or LiAlH(OEt)(3) to synthesise further analogues.
    DOI:
    10.1055/s-0033-1340070
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