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7-Carbamoyl-3-<2-<4-(2-methoxyphenyl)piperazin-1-yl>ethyl>-1-methyl-1H,3H-quinazoline-2,4-dione | 131068-19-4

中文名称
——
中文别名
——
英文名称
7-Carbamoyl-3-<2-<4-(2-methoxyphenyl)piperazin-1-yl>ethyl>-1-methyl-1H,3H-quinazoline-2,4-dione
英文别名
3-[2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl]-1-methyl-2,4-dioxoquinazoline-7-carboxamide
7-Carbamoyl-3-<2-<4-(2-methoxyphenyl)piperazin-1-yl>ethyl>-1-methyl-1H,3H-quinazoline-2,4-dione化学式
CAS
131068-19-4
化学式
C23H27N5O4
mdl
——
分子量
437.498
InChiKey
ALSGUUXTUTVOKV-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):
    0.63
  • 重原子数:
    32.0
  • 可旋转键数:
    6.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    102.8
  • 氢给体数:
    1.0
  • 氢受体数:
    8.0

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:
    (1R,8S,10R)-5-[2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl]-3-methyl-4,6-dioxo-11-oxa-3,5-diazatricyclo[6.2.1.02,7]undec-2(7)-ene-10-carbonitrile 、 (1S,8R,10R)-5-[2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl]-3-methyl-4,6-dioxo-11-oxa-3,5-diazatricyclo[6.2.1.02,7]undec-2(7)-ene-10-carbonitrile 生成 7-Carbamoyl-3-<2-<4-(2-methoxyphenyl)piperazin-1-yl>ethyl>-1-methyl-1H,3H-quinazoline-2,4-dione
    参考文献:
    名称:
    MCNALLY, JAMES J.;PRESS, JEFFREY B., J. ORG. CHEM., 56,(1991) N, C. 245-251
    摘要:
    DOI:
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文献信息

  • Investigations into a mild Diels-Alder approach to 6-substituted quinazoline-2,4-dione derivatives
    作者:James J. McNally、Jeffery B. Press
    DOI:10.1021/jo00001a046
    日期:1991.1
    Furo[3,4-d]pyrimidine-2,4-dione (2) has been reacted with a number of dienophiles to give the Diels-Alder adducts such as 3 and 4 under very mild reaction conditions. Methyl acrylate gives only two regioisomeric endo products which have been isolated and characterized. Other dienophiles give mixtures of endo and exo products as well as of regioisomers. The product ratios were determined by high field H-1 NMR analysis. These adducts are dehydrated by treatment with acid to form some novel quinazoline-2,4-dione derivatives.
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