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2-<4-(2-hydroxyethyl)-1-piperazinyl>-1-cycloheptanone | 89747-07-9

中文名称
——
中文别名
——
英文名称
2-<4-(2-hydroxyethyl)-1-piperazinyl>-1-cycloheptanone
英文别名
2-[4-(2-Hydroxyethyl)piperazin-1-yl]cycloheptan-1-one
2-<4-(2-hydroxyethyl)-1-piperazinyl>-1-cycloheptanone化学式
CAS
89747-07-9
化学式
C13H24N2O2
mdl
MFCD13155994
分子量
240.346
InChiKey
JPQDXHYQIOBCDX-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):
    0.6
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.923
  • 拓扑面积:
    43.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    4-(2-oxo-3,5,7-cycloheptatrien-1-yl)-1-piperazineethanol 在 palladium on activated charcoal 氢气 作用下, 以 甲醇 为溶剂, 反应 8.0h, 以13%的产率得到2-<4-(2-hydroxyethyl)-1-piperazinyl>-1-cycloheptanone
    参考文献:
    名称:
    Troponoids. 6. Troponylpiperazines: a new class of dopamine agonists
    摘要:
    A series of alkyltroponylpiperazine derivatives was synthesized and evaluated for dopaminergic activity in rats rendered hypokinetic by the bilateral injection of 6-hydroxydopamine (6-OHDA) into the anterolateral hypothalamus. Several members of the series were active, and a structure-activity relationship is presented. A few selected compounds were also evaluated with regard to their ability to induce contralateral rotational behavior in rats with a unilateral 6-OHDA-induced lesion of the nigrostriatal dopamine pathway. The compounds were compared to bromocriptine. The results indicate that dopaminergic activity is very sensitive to small changes in the troponylpiperazine moiety.
    DOI:
    10.1021/jm00373a012
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文献信息

  • Troponoids. 6. Troponylpiperazines: a new class of dopamine agonists
    作者:Jehan Bagli、T. Bogri、Katherine Voith
    DOI:10.1021/jm00373a012
    日期:1984.7
    A series of alkyltroponylpiperazine derivatives was synthesized and evaluated for dopaminergic activity in rats rendered hypokinetic by the bilateral injection of 6-hydroxydopamine (6-OHDA) into the anterolateral hypothalamus. Several members of the series were active, and a structure-activity relationship is presented. A few selected compounds were also evaluated with regard to their ability to induce contralateral rotational behavior in rats with a unilateral 6-OHDA-induced lesion of the nigrostriatal dopamine pathway. The compounds were compared to bromocriptine. The results indicate that dopaminergic activity is very sensitive to small changes in the troponylpiperazine moiety.
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