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N-[(2-甲基-1,5-二苯基吡咯-3-基)甲基]苯胺 | 146204-79-7

中文名称
N-[(2-甲基-1,5-二苯基吡咯-3-基)甲基]苯胺
中文别名
——
英文名称
(2-Methyl-1,5-diphenyl-1H-pyrrol-3-ylmethyl)-phenyl-amine
英文别名
1H-Pyrrole-3-methanamine, 2-methyl-N,1,5-triphenyl-;N-[(2-methyl-1,5-diphenylpyrrol-3-yl)methyl]aniline
N-[(2-甲基-1,5-二苯基吡咯-3-基)甲基]苯胺化学式
CAS
146204-79-7
化学式
C24H22N2
mdl
——
分子量
338.452
InChiKey
GPYQUJMPXOYJMV-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):
    5.9
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    17
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    Trimethyl-(2-methyl-1,5-diphenyl-1H-pyrrol-3-ylmethyl)-ammonium; iodide苯胺二甲基亚砜 为溶剂, 反应 4.0h, 以35%的产率得到N-[(2-甲基-1,5-二苯基吡咯-3-基)甲基]苯胺
    参考文献:
    名称:
    Studies on anti-Candida agents with a pyrrole moiety. Synthesis and microbiological activity of some 3-aminomethyl-1,5-diaryl-2-methyl-pyrrole derivatives
    摘要:
    The synthesis and anti-Candida activity of some 3-aminomethyl-1,5-diaryl-2-methyl-pyrrole derivatives are reported. Some derivatives show a rather strong anti-Candida activity. On the basis of experimental results, microbiological activity of 1,5-diarylpyrroles appears to be mainly related to aminic nitrogen lone pair availability of C3 substituent of the pyrrole nucleus. The C5 and N1 substituents play an important role in modulating biological activity. Some structure-activity relationships are proposed.
    DOI:
    10.1016/0223-5234(92)90090-n
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文献信息

  • Studies on anti-Candida agents with a pyrrole moiety. Synthesis and microbiological activity of some 3-aminomethyl-1,5-diaryl-2-methyl-pyrrole derivatives
    作者:F Cerreto、A Villa、A Retico、M Scalzo
    DOI:10.1016/0223-5234(92)90090-n
    日期:1992.10
    The synthesis and anti-Candida activity of some 3-aminomethyl-1,5-diaryl-2-methyl-pyrrole derivatives are reported. Some derivatives show a rather strong anti-Candida activity. On the basis of experimental results, microbiological activity of 1,5-diarylpyrroles appears to be mainly related to aminic nitrogen lone pair availability of C3 substituent of the pyrrole nucleus. The C5 and N1 substituents play an important role in modulating biological activity. Some structure-activity relationships are proposed.
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