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4'-dehydro-cholest-4-eno[3,4-e]piperazin-6-one | 1104455-73-3

中文名称
——
中文别名
——
英文名称
4'-dehydro-cholest-4-eno[3,4-e]piperazin-6-one
英文别名
(1R,2S,5R,6R,9S,10S)-1,5-dimethyl-6-[(2R)-6-methylheptan-2-yl]-15,18-diazapentacyclo[11.8.0.02,10.05,9.014,19]henicosa-13,18-dien-12-one
4'-dehydro-cholest-4-eno[3,4-e]piperazin-6-one化学式
CAS
1104455-73-3
化学式
C29H46N2O
mdl
——
分子量
438.697
InChiKey
UWWCMGSLLIWXLG-TXRYXPRMSA-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):
    7.5
  • 重原子数:
    32
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    41.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-胆甾烯-3-酮乙二胺aluminum oxide 作用下, 以90%的产率得到4'-dehydro-cholest-4-eno[3,4-e]piperazin-6-one
    参考文献:
    名称:
    Microwave promoted one-pot synthesis of novel A-ring fused steroidal dehydropiperazines
    摘要:
    The preparation of ring-A fused steroidal dehydropiperazine at the 3,4-position is herein described. The novel steroidal dehydropiperazines were prepared from the annulation reaction of ethylenediamine with 3-keto-4-en steroids in a one-pot reaction under microwave irradiation. The key step involves base catalysed aerial oxidation of the C-6 methylene group followed by cyclocondensation of ethylenediamine via Michael addition reaction. (C) 2008 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2008.01.005
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文献信息

  • Microwave promoted one-pot synthesis of novel A-ring fused steroidal dehydropiperazines
    作者:Moyurima Borthakur、Madan G. Barthakur、Romesh C. Boruah
    DOI:10.1016/j.steroids.2008.01.005
    日期:2008.5
    The preparation of ring-A fused steroidal dehydropiperazine at the 3,4-position is herein described. The novel steroidal dehydropiperazines were prepared from the annulation reaction of ethylenediamine with 3-keto-4-en steroids in a one-pot reaction under microwave irradiation. The key step involves base catalysed aerial oxidation of the C-6 methylene group followed by cyclocondensation of ethylenediamine via Michael addition reaction. (C) 2008 Elsevier Inc. All rights reserved.
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