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

3-[(Z)-4-(4-Chloro-phenyl)-6-p-tolyl-pyrimidin-2-ylimino]-1,3-dihydro-indol-2-one | 251983-19-4

中文名称
——
中文别名
——
英文名称
3-[(Z)-4-(4-Chloro-phenyl)-6-p-tolyl-pyrimidin-2-ylimino]-1,3-dihydro-indol-2-one
英文别名
(3Z)-3-[4-(4-chlorophenyl)-6-(p-tolyl)pyrimidin-2-yl]iminoindolin-2-one;(3Z)-3-[4-(4-chlorophenyl)-6-(4-methylphenyl)pyrimidin-2-yl]imino-1H-indol-2-one
3-[(Z)-4-(4-Chloro-phenyl)-6-p-tolyl-pyrimidin-2-ylimino]-1,3-dihydro-indol-2-one化学式
CAS
251983-19-4
化学式
C25H17ClN4O
mdl
——
分子量
424.889
InChiKey
SKONOXXPWHDJBQ-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):
    5.5
  • 重原子数:
    31
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    67.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    吗啉聚合甲醛3-[(Z)-4-(4-Chloro-phenyl)-6-p-tolyl-pyrimidin-2-ylimino]-1,3-dihydro-indol-2-one四氢呋喃 为溶剂, 以47%的产率得到(3Z)-3-[4-(4-chlorophenyl)-6-(p-tolyl)pyrimidin-2-yl]imino-1-(morpholinomethyl)indolin-2-one
    参考文献:
    名称:
    Syrltllesis and Alltituberculous activity of N-Mannich bases of 3-[4-(4 chloropheny1)-6-(4-methylphesyl) pyrimidin-2-yl] iminoisatin derivatives
    摘要:
    结核病正在全球范围内复苏。
    DOI:
    10.3797/scipharm.aut-02-05
  • 作为产物:
    描述:
    靛红4-(4-chlorophenyl)-6-(4-methylphenyl)-2-aminopyrimidine乙醇溶剂黄146 为溶剂, 以72%的产率得到3-[(Z)-4-(4-Chloro-phenyl)-6-p-tolyl-pyrimidin-2-ylimino]-1,3-dihydro-indol-2-one
    参考文献:
    名称:
    Syrltllesis and Alltituberculous activity of N-Mannich bases of 3-[4-(4 chloropheny1)-6-(4-methylphesyl) pyrimidin-2-yl] iminoisatin derivatives
    摘要:
    结核病正在全球范围内复苏。
    DOI:
    10.3797/scipharm.aut-02-05
点击查看最新优质反应信息

文献信息

  • Synthesis and antimicrobial activity of Schiff and Mannich bases of isatin and its derivatives with pyrimidine
    作者:S.N Pandeya、D Sriram、G Nath、E De Clercq
    DOI:10.1016/s0014-827x(99)00075-0
    日期:1999.9
    Isatin and its derivatives have been reacted with 4-(4'-chlorophenyl)-6-(4"-methyl phenyl)-2-aminopyrimidine to form Schiff bases and the N-Mannich bases of these compounds were synthesized by reacting them with formaldehyde and several secondary amines. Investigation of antimicrobial activity of the compounds was made by the agar dilution method against 28 pathogenic bacteria, eight pathogenic fungi and anti-HIV activity against replication of HIV-I (III B) in MT-4 cells. The compounds are significantly active against bacteria and fungi. (C) 1999 Elsevier Science S.A. All rights reserved.
  • Syrltllesis and Alltituberculous activity of N-Mannich bases of 3-[4-(4 chloropheny1)-6-(4-methylphesyl) pyrimidin-2-yl] iminoisatin derivatives
    作者:Sriram D.、Yogeeswari P.、Pandeya S.N.、Ananthan S.
    DOI:10.3797/scipharm.aut-02-05
    日期:——

    Tuberculosis is making a worldwide resurgence [...]

    结核病正在全球范围内复苏。
查看更多