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8-methyl-10-phenylpyridazino<3,4-e>quinolino<1,2-b>-as-triazinium-9-ide | 146746-15-8

中文名称
——
中文别名
——
英文名称
8-methyl-10-phenylpyridazino<3,4-e>quinolino<1,2-b>-as-triazinium-9-ide
英文别名
8-methyl-10-phenylpyridazino[3,4-e]quinolino[1,2-b]-as-triazinium-9-ide
8-methyl-10-phenylpyridazino<3,4-e>quinolino<1,2-b>-as-triazinium-9-ide化学式
CAS
146746-15-8
化学式
C20H15N5
mdl
——
分子量
325.373
InChiKey
BDJJLGXADFAQBG-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):
    3.61
  • 重原子数:
    25.0
  • 可旋转键数:
    1.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    47.22
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    trimethyloxonium hexafluorophosphate 、 8-methyl-10-phenylpyridazino<3,4-e>quinolino<1,2-b>-as-triazinium-9-ide二氯甲烷 为溶剂, 反应 24.0h, 以24%的产率得到8,12-dimethyl-10-phenylpyridazino<3,4-e>quinolino<1,2-b>-as-triazinium hexafluorophosphate
    参考文献:
    名称:
    Synthesis and ring transformation of novel tetracyclic fused as-triazines
    摘要:
    Eight new tetracyclic fused as-triazines (4 - 6, 8, 11 - 13, and 15) have been synthesized by conversion and subsequent ring transformation of 1,2-diaminoisoquinolinium (2) and -quinolinium salts (9) with 4-benzoyl-5-phenylfuran-2,3-dione (1). Selective alkylations of the new products revealed that these reactions are governed mainly by the electronic density of the lone pairs as well as by steric effects.
    DOI:
    10.1007/bf00808281
  • 作为产物:
    参考文献:
    名称:
    Synthesis and ring transformation of novel tetracyclic fused as-triazines
    摘要:
    Eight new tetracyclic fused as-triazines (4 - 6, 8, 11 - 13, and 15) have been synthesized by conversion and subsequent ring transformation of 1,2-diaminoisoquinolinium (2) and -quinolinium salts (9) with 4-benzoyl-5-phenylfuran-2,3-dione (1). Selective alkylations of the new products revealed that these reactions are governed mainly by the electronic density of the lone pairs as well as by steric effects.
    DOI:
    10.1007/bf00808281
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