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6-N-phenyl-2-piperidin-1-yl-4-N-pyrimidin-5-ylpyrimidine-4,6-diamine | 1191936-86-3

中文名称
——
中文别名
——
英文名称
6-N-phenyl-2-piperidin-1-yl-4-N-pyrimidin-5-ylpyrimidine-4,6-diamine
英文别名
——
6-N-phenyl-2-piperidin-1-yl-4-N-pyrimidin-5-ylpyrimidine-4,6-diamine化学式
CAS
1191936-86-3
化学式
C19H21N7
mdl
——
分子量
347.423
InChiKey
FRQJRVHXIHMDQL-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):
    3.5
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    78.9
  • 氢给体数:
    2
  • 氢受体数:
    7

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:
    5-溴嘧啶N-phenyl-2-(piperidin-1-yl)pyrimidine-4,6-diaminetris-(dibenzylideneacetone)dipalladium(0)caesium carbonate2-二环己基磷-2,4,6-三异丙基联苯 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以87%的产率得到6-N-phenyl-2-piperidin-1-yl-4-N-pyrimidin-5-ylpyrimidine-4,6-diamine
    参考文献:
    名称:
    A practical strategy for the synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines
    摘要:
    Starting from commercially available 4-amino-2,6-dichloropyrimidine, a practical four steps synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines was developed. This strategy could introduce a diverse set of secondary amines and arylamines to displace the 2- and 4-chloro groups. The products of this route are otherwise difficult to access. In addition, 6-amino arylation was carried out to demonstrate the reactivity and utility of 2-dialkylamino-4-arylamino-6-aminopyrimidines as building blocks for assembling interesting aminopyrimidine molecules. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.07.154
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文献信息

  • A practical strategy for the synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines
    作者:Chaomin Li、Andrew Rosenau
    DOI:10.1016/j.tetlet.2009.07.154
    日期:2009.10
    Starting from commercially available 4-amino-2,6-dichloropyrimidine, a practical four steps synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines was developed. This strategy could introduce a diverse set of secondary amines and arylamines to displace the 2- and 4-chloro groups. The products of this route are otherwise difficult to access. In addition, 6-amino arylation was carried out to demonstrate the reactivity and utility of 2-dialkylamino-4-arylamino-6-aminopyrimidines as building blocks for assembling interesting aminopyrimidine molecules. (C) 2009 Elsevier Ltd. All rights reserved.
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