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4-(cyclohexyloxy)quinazoline | 1156333-28-6

中文名称
——
中文别名
——
英文名称
4-(cyclohexyloxy)quinazoline
英文别名
4-cyclohexyloxyquinazoline
4-(cyclohexyloxy)quinazoline化学式
CAS
1156333-28-6
化学式
C14H16N2O
mdl
——
分子量
228.294
InChiKey
QNXOLVQGDILPJV-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):
    3.8
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    35
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    4-羟基喹唑啉环己醇 在 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 caesium carbonate 作用下, 以 四氢呋喃 为溶剂, 反应 8.83h, 以77%的产率得到4-(cyclohexyloxy)quinazoline
    参考文献:
    名称:
    One-Pot Etherification of Purine Nucleosides and Pyrimidines
    摘要:
    A one-pot synthesis of ethers derived from inosine, guanosine, 2'-deoxyguanosine, and pyrimidinones is described Exposure of the heterocycle to 1H-benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and Cs2CO3 produces a reactive intermediate, which is converted to the desired ether by subsequent addition of an appropriate alcohol or phenol and Cs2CO3. Although rapid formation of HMPA from BOP can occur in the presence of an alcohol and base, as demonstrated by the reaction with methanol, under appropriate conditions these heteroaryl ethers can be efficiently synthesized
    DOI:
    10.1021/ol101655h
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文献信息

  • One-Pot Etherification of Purine Nucleosides and Pyrimidines
    作者:Hari Prasad Kokatla、Mahesh K. Lakshman
    DOI:10.1021/ol101655h
    日期:2010.10.15
    A one-pot synthesis of ethers derived from inosine, guanosine, 2'-deoxyguanosine, and pyrimidinones is described Exposure of the heterocycle to 1H-benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and Cs2CO3 produces a reactive intermediate, which is converted to the desired ether by subsequent addition of an appropriate alcohol or phenol and Cs2CO3. Although rapid formation of HMPA from BOP can occur in the presence of an alcohol and base, as demonstrated by the reaction with methanol, under appropriate conditions these heteroaryl ethers can be efficiently synthesized
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