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4-phenyl-N-(pyrazin-2-yl)pyrimidin-2-amine | 1236002-86-0

中文名称
——
中文别名
——
英文名称
4-phenyl-N-(pyrazin-2-yl)pyrimidin-2-amine
英文别名
4-phenyl-N-pyrazin-2-ylpyrimidin-2-amine
4-phenyl-N-(pyrazin-2-yl)pyrimidin-2-amine化学式
CAS
1236002-86-0
化学式
C14H11N5
mdl
——
分子量
249.275
InChiKey
WSCXOWGEZGKKRN-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):
    1.9
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    氨基吡嗪4-苯基-2-氯嘧啶potassium phosphatetris-(dibenzylideneacetone)dipalladium(0)4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下, 以 1,4-二氧六环 为溶剂, 反应 6.0h, 以45%的产率得到4-phenyl-N-(pyrazin-2-yl)pyrimidin-2-amine
    参考文献:
    名称:
    Convenient preparation of 4-aryl-2-(heteroarylamino)pyrimidines and 4-anilino-2-(heteroarylamino)pyrimidines
    摘要:
    4-Aryl-2-anilinopyrimidines and 2,4-dianilinopyrimidines are privileged structures found in many drug-like molecules and biologically active compounds. A method for the quick assembly of novel 4-aryl- and 4-anilino-2-(heteroarylamino)pyrimidines via Buchwald-Hartwig N-arylations at elevated temperatures under sealed tube conditions is reported. This method's convenience and practicality is demonstrated through the preparation of several novel non-nucleoside reverse transcriptase inhibitor (NNRTI) analogues. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.04.062
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文献信息

  • Convenient preparation of 4-aryl-2-(heteroarylamino)pyrimidines and 4-anilino-2-(heteroarylamino)pyrimidines
    作者:Brian I. Bliss、Feryan Ahmed、Subashree Iyer、Weimin Lin、Joel Walker、He Zhao
    DOI:10.1016/j.tetlet.2010.04.062
    日期:2010.6
    4-Aryl-2-anilinopyrimidines and 2,4-dianilinopyrimidines are privileged structures found in many drug-like molecules and biologically active compounds. A method for the quick assembly of novel 4-aryl- and 4-anilino-2-(heteroarylamino)pyrimidines via Buchwald-Hartwig N-arylations at elevated temperatures under sealed tube conditions is reported. This method's convenience and practicality is demonstrated through the preparation of several novel non-nucleoside reverse transcriptase inhibitor (NNRTI) analogues. (C) 2010 Elsevier Ltd. All rights reserved.
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