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2-methoxy-3-(3-(pyrrolidin-1-yl)propoxy)-quinazolino[3,4-a]thieno[3,2-d]pyrimidin-8-one | 1204579-59-8

中文名称
——
中文别名
——
英文名称
2-methoxy-3-(3-(pyrrolidin-1-yl)propoxy)-quinazolino[3,4-a]thieno[3,2-d]pyrimidin-8-one
英文别名
5-Methoxy-4-(3-pyrrolidin-1-ylpropoxy)-13-thia-8,10,17-triazatetracyclo[8.7.0.02,7.012,16]heptadeca-1(17),2,4,6,8,12(16),14-heptaen-11-one
2-methoxy-3-(3-(pyrrolidin-1-yl)propoxy)-quinazolino[3,4-a]thieno[3,2-d]pyrimidin-8-one化学式
CAS
1204579-59-8
化学式
C21H22N4O3S
mdl
——
分子量
410.497
InChiKey
CRSWLQXTEDTEFU-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):
    2.9
  • 重原子数:
    29
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    95
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    四氢吡咯 、 3-methoxy-2-(3-chloropropoxy)-quinazolino[3,4-a]thieno[3,2-d]pyrimidin-8-one 在 potassium carbonate 、 potassium iodide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.5h, 生成 2-methoxy-3-(3-(pyrrolidin-1-yl)propoxy)-quinazolino[3,4-a]thieno[3,2-d]pyrimidin-8-one
    参考文献:
    名称:
    Design, Synthesis, Docking and Antitumor Activity of Quinazolino [3, 4-a] thieno [3, 2-d] pyrimidin-8-one Derivatives
    摘要:
    Several novel quinazolino [3, 4‐a] thieno [3, 2‐d] pyrimidin‐8‐one derivatives were synthesized. All of the compounds were determined against MiaPaCa2 and DU145 cells in vitro, and the crystal structures of analog 8 and 20 in the active site of the EGFR complexes were presented. The entire compounds had been identified by 1HNMR, 13CNMR, IR, MS and EA.
    DOI:
    10.1111/j.1747-0285.2010.01008.x
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文献信息

  • Design, Synthesis, Docking and Antitumor Activity of Quinazolino [3, 4-a] thieno [3, 2-d] pyrimidin-8-one Derivatives
    作者:Youguang Zheng、Xiaoqing Wu、Bai Xue、Mingdong Li、Min Ji
    DOI:10.1111/j.1747-0285.2010.01008.x
    日期:——
    Several novel quinazolino [3, 4‐a] thieno [3, 2‐d] pyrimidin‐8‐one derivatives were synthesized. All of the compounds were determined against MiaPaCa2 and DU145 cells in vitro, and the crystal structures of analog 8 and 20 in the active site of the EGFR complexes were presented. The entire compounds had been identified by 1HNMR, 13CNMR, IR, MS and EA.
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