摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-[2-(4-hydroxyphenyl)-4-oxo-(1,3-thiazolidin-3-yl)]{4-[2-(4-methylphenyl)-4-oxo-(3-hydroquinazolin-3-yl)]phenyl}carboxamide | 1316838-83-1

中文名称
——
中文别名
——
英文名称
N-[2-(4-hydroxyphenyl)-4-oxo-(1,3-thiazolidin-3-yl)]{4-[2-(4-methylphenyl)-4-oxo-(3-hydroquinazolin-3-yl)]phenyl}carboxamide
英文别名
N-[2-(4-hydroxyphenyl)-4-oxo(1,3-thiazolidin-3-yl)] {4-[2-(4-methylphenyl)-4-oxo(3-hydroquinazolin-3-yl)]phenyl}carboxamide;N-[2-(4-hydroxyphenyl)-4-oxo-1,3-thiazolidin-3-yl]-4-[2-(4-methylphenyl)-4-oxoquinazolin-3-yl]benzamide
N-[2-(4-hydroxyphenyl)-4-oxo-(1,3-thiazolidin-3-yl)]{4-[2-(4-methylphenyl)-4-oxo-(3-hydroquinazolin-3-yl)]phenyl}carboxamide化学式
CAS
1316838-83-1
化学式
C31H24N4O4S
mdl
——
分子量
548.622
InChiKey
JPTNXLIMARHTFT-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):
    5.1
  • 重原子数:
    40
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    128
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-[2-(4-hydroxyphenyl)-4-oxo-(1,3-thiazolidin-3-yl)]{4-[2-(4-methylphenyl)-4-oxo-(3-hydroquinazolin-3-yl)]phenyl}carboxamide苯甲醛sodium methylate 作用下, 以 1,4-二氧六环 为溶剂, 反应 8.0h, 以68%的产率得到N-{5-[(phenyl)methylene]-2-(4-hydroxyphenyl)-4-oxo-(1,3-thiazolidin-3-yl)}{4-[2-(4-methylphenyl)-4-oxo-(3-hydroquinazolin-3-yl)] phenyl}carboxamide
    参考文献:
    名称:
    A clubbed quinazolinone and 4-thiazolidinone as potential antimicrobial agents
    摘要:
    A series of N-{5-[(2-chlorophenyl)methylene]-2-(4-hydroxyphenyl]-4-oxo(1,3-thiazolidin-3-yl)}{4-[2-(4-methylphenyl)-4-oxo(3-hydroquinazolin-3-yl)]phenyl}carboxamides (6a-n) have been synthesized. All the synthesized compounds were screened for in vitro antibacterial and antifungal activities on Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Staphylococcus pyogenes, Candida albicans, Aspergillus niger, and Aspergillus clavatus. The structures of the compounds were elucidated by IR, H-1 NMR, C-13 NMR, and Mass spectra.
    DOI:
    10.1007/s00044-011-9674-5
  • 作为产物:
    描述:
    ethyl 4-[2-(4-methylphenyl)-4-oxo-3-hydroquinazolin-3-yl]benzoate 在 作用下, 以 1,4-二氧六环甲醇 为溶剂, 反应 17.0h, 生成 N-[2-(4-hydroxyphenyl)-4-oxo-(1,3-thiazolidin-3-yl)]{4-[2-(4-methylphenyl)-4-oxo-(3-hydroquinazolin-3-yl)]phenyl}carboxamide
    参考文献:
    名称:
    A clubbed quinazolinone and 4-thiazolidinone as potential antimicrobial agents
    摘要:
    A series of N-{5-[(2-chlorophenyl)methylene]-2-(4-hydroxyphenyl]-4-oxo(1,3-thiazolidin-3-yl)}{4-[2-(4-methylphenyl)-4-oxo(3-hydroquinazolin-3-yl)]phenyl}carboxamides (6a-n) have been synthesized. All the synthesized compounds were screened for in vitro antibacterial and antifungal activities on Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Staphylococcus pyogenes, Candida albicans, Aspergillus niger, and Aspergillus clavatus. The structures of the compounds were elucidated by IR, H-1 NMR, C-13 NMR, and Mass spectra.
    DOI:
    10.1007/s00044-011-9674-5
点击查看最新优质反应信息