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4-Acetyl-3-chloro-6-phenylpyridazine

中文名称
——
中文别名
——
英文名称
4-Acetyl-3-chloro-6-phenylpyridazine
英文别名
1-(3-Chloro-6-phenylpyridazin-4-yl)ethanone;1-(3-chloro-6-phenylpyridazin-4-yl)ethanone
4-Acetyl-3-chloro-6-phenylpyridazine化学式
CAS
——
化学式
C12H9ClN2O
mdl
——
分子量
232.669
InChiKey
ADZZJXRUOGRQHI-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):
    2.2
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    42.8
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 作为反应物:
    描述:
    4-Acetyl-3-chloro-6-phenylpyridazine溶剂黄146 作用下, 以92%的产率得到4-acetyl-6-phenylpyridazin-3(2H)-one
    参考文献:
    名称:
    A new two-step procedure for functionalized-3(2H)-pyridazinones through homolytic substitution of 3-chloropyridazines.
    摘要:
    The homolytic substitution of protonated 3-chloro-6-methylpyridazine 1a, followed by hydrolysis with AcOH affords 4- or 4,5-functionalized pyridazinones 3a-c. Less reactivity is found for 3-chloro-6-phenylpyridazine 1b. Hypotheses about these different behaviour patterns are proposed and discussed.
    DOI:
    10.1016/s0040-4039(00)79259-8
  • 作为产物:
    描述:
    叔丁基过氧化氢3-氯-6-苯基哒嗪乙醛硫酸双氧水 、 iron(II) sulfate 作用下, 以 丙酮 为溶剂, 反应 0.08h, 以24%的产率得到4-Acetyl-3-chloro-6-phenylpyridazine
    参考文献:
    名称:
    A new two-step procedure for functionalized-3(2H)-pyridazinones through homolytic substitution of 3-chloropyridazines.
    摘要:
    The homolytic substitution of protonated 3-chloro-6-methylpyridazine 1a, followed by hydrolysis with AcOH affords 4- or 4,5-functionalized pyridazinones 3a-c. Less reactivity is found for 3-chloro-6-phenylpyridazine 1b. Hypotheses about these different behaviour patterns are proposed and discussed.
    DOI:
    10.1016/s0040-4039(00)79259-8
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文献信息

  • [EN] PYRAZOLOPYRIDAZINE DERIVATIVES, PROCESS FOR PREPARATION AND USE FOR THE INHIBITION OF GSK-3<br/>[FR] DERIVES DE PYRAZOLOPYRIDAZINE, LEUR PROCEDE DE PREPARATION ET LEUR UTILISATION POUR L'INHIBITION DE GSK-3
    申请人:GLAXO GROUP LTD
    公开号:WO2003080616A1
    公开(公告)日:2003-10-02
    Certain compounds of formula (I) or a salt thereof and/or a solvate thereof, wherein, R1, R2 and R3 are as defined in the specification, processes for the preparation of such compounds, a pharmaceutical composition comprising such compounds and the use of such compounds in medicine.
  • A new two-step procedure for functionalized-3(2H)-pyridazinones through homolytic substitution of 3-chloropyridazines.
    作者:Vittorio Dal Piaz、Maria Paola Giovannoni、Giovanna Ciciani
    DOI:10.1016/s0040-4039(00)79259-8
    日期:1993.6
    The homolytic substitution of protonated 3-chloro-6-methylpyridazine 1a, followed by hydrolysis with AcOH affords 4- or 4,5-functionalized pyridazinones 3a-c. Less reactivity is found for 3-chloro-6-phenylpyridazine 1b. Hypotheses about these different behaviour patterns are proposed and discussed.
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