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2-propylpentanoic acid 4-oxo-3,4-dihydroquinazolin-2-ylmethyl ester | 1260163-35-6

中文名称
——
中文别名
——
英文名称
2-propylpentanoic acid 4-oxo-3,4-dihydroquinazolin-2-ylmethyl ester
英文别名
(4-oxo-3H-quinazolin-2-yl)methyl 2-propylpentanoate
2-propylpentanoic acid 4-oxo-3,4-dihydroquinazolin-2-ylmethyl ester化学式
CAS
1260163-35-6
化学式
C17H22N2O3
mdl
——
分子量
302.373
InChiKey
DLHWDPWRVIRDAD-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):
    3.5
  • 重原子数:
    22
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    67.8
  • 氢给体数:
    1
  • 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:
    2-(bromomethyl)-4(3H)-quinazolinonesodium valproate乙醇 为溶剂, 反应 48.0h, 以52%的产率得到2-propylpentanoic acid 4-oxo-3,4-dihydroquinazolin-2-ylmethyl ester
    参考文献:
    名称:
    Design, synthesis, and anticonvulsant activity of novel quinazolinone analogues
    摘要:
    A number of 2-substituted and 2,3-disubstituted quinazolinone analogues have been synthesized. Their structures have been elucidated on the basis of elemental analyses and spectroscopic studies (IR, (1)H NMR, and MS). An evaluation of the anticonvulsant activity of the prepared compounds has indicated that some of them exhibit moderate to significant activity, compared to diazepam and phenobarbital standards.
    DOI:
    10.1007/s00044-010-9465-4
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文献信息

  • Design, synthesis, and anticonvulsant activity of novel quinazolinone analogues
    作者:Nagwa M. Abdel Gawad、Hanan Hanna Georgey、Riham M. Youssef、Nehad A. El Sayed
    DOI:10.1007/s00044-010-9465-4
    日期:2011.11
    A number of 2-substituted and 2,3-disubstituted quinazolinone analogues have been synthesized. Their structures have been elucidated on the basis of elemental analyses and spectroscopic studies (IR, (1)H NMR, and MS). An evaluation of the anticonvulsant activity of the prepared compounds has indicated that some of them exhibit moderate to significant activity, compared to diazepam and phenobarbital standards.
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