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3-butyl-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydroquinazolin-4(1H)-one | 1350915-73-9

中文名称
——
中文别名
——
英文名称
3-butyl-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydroquinazolin-4(1H)-one
英文别名
3-Butyl-2-(4-hydroxy-3-methoxyphenyl)-1,2-dihydroquinazolin-4-one;3-butyl-2-(4-hydroxy-3-methoxyphenyl)-1,2-dihydroquinazolin-4-one
3-butyl-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydroquinazolin-4(1H)-one化学式
CAS
1350915-73-9
化学式
C19H22N2O3
mdl
——
分子量
326.395
InChiKey
DXEUVBJUXCMWMN-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):
    3.6
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    61.8
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    香草醛2-氨基-n-丁基苯甲酰胺对甲苯磺酸 作用下, 以 甲苯 为溶剂, 反应 4.0h, 以78%的产率得到3-butyl-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydroquinazolin-4(1H)-one
    参考文献:
    名称:
    Design, synthesis and in vitro PDE4 inhibition activity of certain quinazolinone derivatives for treatment of asthma
    摘要:
    In this study, a novel series of quinazolinone derivatives analogue to nitraquazone structure were synthesized. The compounds tested for their inhibitory activity against phosphodiesterase 4B revealed that compound 6d shows promising inhibitory activity comparable to that of Rolipram, whereas compounds 6a and 6c exhibited moderate inhibitory activity.
    DOI:
    10.1007/s00044-011-9846-3
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文献信息

  • Design, synthesis and in vitro PDE4 inhibition activity of certain quinazolinone derivatives for treatment of asthma
    作者:Afaf K. Elansary、Hanan H. Kadry、Eman M. Ahmed、Amr Sayed Motawi Sonousi
    DOI:10.1007/s00044-011-9846-3
    日期:2012.11
    In this study, a novel series of quinazolinone derivatives analogue to nitraquazone structure were synthesized. The compounds tested for their inhibitory activity against phosphodiesterase 4B revealed that compound 6d shows promising inhibitory activity comparable to that of Rolipram, whereas compounds 6a and 6c exhibited moderate inhibitory activity.
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