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2-(3,6-Diphenyl-2,5-dihydropyridazin-4-yl)-1h-benzimidazole | 1083198-24-6

中文名称
——
中文别名
——
英文名称
2-(3,6-Diphenyl-2,5-dihydropyridazin-4-yl)-1h-benzimidazole
英文别名
2-(3,6-diphenyl-1,4-dihydropyridazin-5-yl)-1H-benzimidazole
2-(3,6-Diphenyl-2,5-dihydropyridazin-4-yl)-1h-benzimidazole化学式
CAS
1083198-24-6
化学式
C23H18N4
mdl
——
分子量
350.423
InChiKey
NLRSLLVHOAWANM-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):
    4.6
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    53.1
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-(3,6-Diphenyl-2,5-dihydropyridazin-4-yl)-1h-benzimidazole溶剂黄146 作用下, 反应 1.0h, 以95%的产率得到2-[(3,5-diphenylpyrazol-4-yl)methyl]-1H-benzimidazole
    参考文献:
    名称:
    Recyclization of 2-(3,6-diaryl-2,5-dihydropyridazin-4-yl)-1H-benzimidazoles to 2-[(3,5-diarylpyrazol-4-yl)methyl]-1H-benzimidazoles
    摘要:
    2-(3,6-Diaryl-2,5-dihydropyridazin-4-yl)-1H-benzimidazoles undergo a previously unknown type of recyclization of the pyridazine ring to a pyrazole to give 2-[(3,5-diarylpyrazol-4-yl)methyl]-1H-benzimidazoles. It is suggested that the mechanism of this conversion, which includes formation of a secondary enhydrazine group in the diazine ring and its subsequent contraction, occurs after the intramolecular formation and opening of a cyclopropane ring.
    DOI:
    10.1007/s10593-008-0108-3
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文献信息

  • Recyclization of 2-(3,6-diaryl-2,5-dihydropyridazin-4-yl)-1H-benzimidazoles to 2-[(3,5-diarylpyrazol-4-yl)methyl]-1H-benzimidazoles
    作者:I. B. Dzvinchuk、A. N. Chernega、M. O. Lozinskii、A. A. Tolmachev
    DOI:10.1007/s10593-008-0108-3
    日期:2008.6
    2-(3,6-Diaryl-2,5-dihydropyridazin-4-yl)-1H-benzimidazoles undergo a previously unknown type of recyclization of the pyridazine ring to a pyrazole to give 2-[(3,5-diarylpyrazol-4-yl)methyl]-1H-benzimidazoles. It is suggested that the mechanism of this conversion, which includes formation of a secondary enhydrazine group in the diazine ring and its subsequent contraction, occurs after the intramolecular formation and opening of a cyclopropane ring.
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