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2-benzyl-4-chloro-2,5-diazabicyclo<2.2.2>octan-3-one | 139268-34-1

中文名称
——
中文别名
——
英文名称
2-benzyl-4-chloro-2,5-diazabicyclo<2.2.2>octan-3-one
英文别名
2-Benzyl-4-chloro-2,5-diazabicyclo[2.2.2]octan-3-one
2-benzyl-4-chloro-2,5-diazabicyclo<2.2.2>octan-3-one化学式
CAS
139268-34-1
化学式
C13H15ClN2O
mdl
——
分子量
250.728
InChiKey
TVVNTFISNSGYSB-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:
    17
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2-Benzyl-4,6-dichloro-2,5-diaza-bicyclo[2.2.2]oct-5-en-3-one 在 palladium on activated charcoal 三乙烯二胺氢气 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以71%的产率得到2-benzyl-4-chloro-2,5-diazabicyclo<2.2.2>octan-3-one
    参考文献:
    名称:
    Cycloadducts of ethene with 2(1H)-pyrazinones functionalisation and reduction to 2,5-diazabicyclo[2.2.2]octan-3-ones.
    摘要:
    The title compounds 4 were prepared via Diels-Alder reaction of 3,5-dichloro-2(1H)-pyrazinones 1 with ethene, followed by catalytic reduction of the iminochloride group generated in the cycloadducts 2. Substitution of the iminochloride group with various nucleophiles afforded the 6-functionalised analogues of 2. Their reduction can lead to 6-substituted derivatives of compounds 4. One example is given.
    DOI:
    10.1016/s0040-4020(01)96215-5
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文献信息

  • Cycloadducts of ethene with 2(1H)-pyrazinones functionalisation and reduction to 2,5-diazabicyclo[2.2.2]octan-3-ones.
    作者:Patrick K. Loosen、Masoumeh F. Khorasani、Suzanne M. Toppet、Georges J. Hoornaert
    DOI:10.1016/s0040-4020(01)96215-5
    日期:1991.11
    The title compounds 4 were prepared via Diels-Alder reaction of 3,5-dichloro-2(1H)-pyrazinones 1 with ethene, followed by catalytic reduction of the iminochloride group generated in the cycloadducts 2. Substitution of the iminochloride group with various nucleophiles afforded the 6-functionalised analogues of 2. Their reduction can lead to 6-substituted derivatives of compounds 4. One example is given.
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