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6-(4-chlorophenyl)-2-[(4-methylpiperazin-1-yl)methyl]-4,5-dihydropyridazin-3(2H)-one | 1229037-49-3

中文名称
——
中文别名
——
英文名称
6-(4-chlorophenyl)-2-[(4-methylpiperazin-1-yl)methyl]-4,5-dihydropyridazin-3(2H)-one
英文别名
6-(4-Chlorophenyl)-2-[(4-methylpiperazin-1-yl)methyl]-4,5-dihydropyridazin-3-one
6-(4-chlorophenyl)-2-[(4-methylpiperazin-1-yl)methyl]-4,5-dihydropyridazin-3(2H)-one化学式
CAS
1229037-49-3
化学式
C16H21ClN4O
mdl
——
分子量
320.822
InChiKey
IWYKMDUPIZGXOY-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):
    1.7
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    39.2
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    N-甲基哌嗪聚合甲醛2,3,4,5-四氢-6(4-氯苯基)-3(2H-)-吡嗪酮乙醇 为溶剂, 反应 24.0h, 以66%的产率得到6-(4-chlorophenyl)-2-[(4-methylpiperazin-1-yl)methyl]-4,5-dihydropyridazin-3(2H)-one
    参考文献:
    名称:
    Synthesis, characterization and antihypertensive activity of pyridazinone derivatives
    摘要:
    Some 6-(substituted-phenyl)-2-(substitutedmethyl)-4,5-dihydropyridazin-3(2H)-one derivatives were synthesized by reacting 6-substituted-phenyl-4,5-dihydropyridazin-3(2H)-one with cyclic secondary amine under Mannich reaction conditions. The final compounds (15-70) were evaluated for antihypertensive activities by non-invasive method using Tail Cuff method. The compounds 16, 19, 24, 30, 39, 42 and 45 showed good antihypertensive activity.
    DOI:
    10.1016/j.ejmech.2010.02.003
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文献信息

  • Synthesis, characterization and antihypertensive activity of pyridazinone derivatives
    作者:Anees A. Siddiqui、Ravinesh Mishra、Mohammad Shaharyar
    DOI:10.1016/j.ejmech.2010.02.003
    日期:2010.6
    Some 6-(substituted-phenyl)-2-(substitutedmethyl)-4,5-dihydropyridazin-3(2H)-one derivatives were synthesized by reacting 6-substituted-phenyl-4,5-dihydropyridazin-3(2H)-one with cyclic secondary amine under Mannich reaction conditions. The final compounds (15-70) were evaluated for antihypertensive activities by non-invasive method using Tail Cuff method. The compounds 16, 19, 24, 30, 39, 42 and 45 showed good antihypertensive activity.
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