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N,N-diphenyl-4-(piperidin-1-yl)-6-(1H-pyrrol-1-yl)-1,3,5-triazin-2-amine | 633279-23-9

中文名称
——
中文别名
——
英文名称
N,N-diphenyl-4-(piperidin-1-yl)-6-(1H-pyrrol-1-yl)-1,3,5-triazin-2-amine
英文别名
N,N-diphenyl-4-piperidin-1-yl-6-pyrrol-1-yl-1,3,5-triazin-2-amine
N,N-diphenyl-4-(piperidin-1-yl)-6-(1H-pyrrol-1-yl)-1,3,5-triazin-2-amine化学式
CAS
633279-23-9
化学式
C24H24N6
mdl
MFCD03820536
分子量
396.495
InChiKey
XWLPICNXGCHJHJ-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):
    5.6
  • 重原子数:
    30
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    50.1
  • 氢给体数:
    0
  • 氢受体数:
    5

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:
    2,5-二甲氧基四氢呋喃[1,3,5]Triazine-2,4-diamine, N,N-diphenyl-6-(piperidin-1-yl)- 在 phosphorus pentoxide 作用下, 以 甲苯 为溶剂, 以77%的产率得到N,N-diphenyl-4-(piperidin-1-yl)-6-(1H-pyrrol-1-yl)-1,3,5-triazin-2-amine
    参考文献:
    名称:
    三嗪类。8. 4,6-二取代的2-(1H-吡咯基)-1,3,5-三嗪的合成及一些反应
    摘要:
    We have studied the reaction of 2,5-dimethoxytetrahydrofuran with 4,6-disubstituted 2-amino-1,3,5-triazines with the aim of obtaining novel coupled polyheterocyclic systems with potential bioactivity. Reaction conditions were optimized. A series of novel 4,6-disubstituted 2-(1H-1-pyrrolyl)-sym-triazines was obtained. It was found that the product yields depended on the nature of the substituent in the 4 and 6 positions of the triazine ring and on the reaction conditions.
    DOI:
    10.1007/s10593-008-0050-4
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文献信息

  • sym-triazines. 8. Synthesis and some reactions of 4,6-disubstituted 2-(1H-pyrrolyl)-1,3,5-triazines
    作者:A. A. Chesnyuk、S. N. Mikhailichenko、V. N. Zaplishnyi、L. D. Konyushkin、S. I. Firgang
    DOI:10.1007/s10593-008-0050-4
    日期:2008.3
    We have studied the reaction of 2,5-dimethoxytetrahydrofuran with 4,6-disubstituted 2-amino-1,3,5-triazines with the aim of obtaining novel coupled polyheterocyclic systems with potential bioactivity. Reaction conditions were optimized. A series of novel 4,6-disubstituted 2-(1H-1-pyrrolyl)-sym-triazines was obtained. It was found that the product yields depended on the nature of the substituent in the 4 and 6 positions of the triazine ring and on the reaction conditions.
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