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6-([1,1'-biphenyl]-2-yl)-9-isopropyl-9H-purine | 1284287-14-4

中文名称
——
中文别名
——
英文名称
6-([1,1'-biphenyl]-2-yl)-9-isopropyl-9H-purine
英文别名
6-(2-Phenylphenyl)-9-propan-2-ylpurine;6-(2-phenylphenyl)-9-propan-2-ylpurine
6-([1,1'-biphenyl]-2-yl)-9-isopropyl-9H-purine化学式
CAS
1284287-14-4
化学式
C20H18N4
mdl
——
分子量
314.39
InChiKey
JMLQABVVVGDKIG-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):
    4
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    43.6
  • 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:
    碘苯9-isopropyl-6-phenyl-9H-purinesilver(I) acetate 、 palladium diacetate 、 溶剂黄146 作用下, 反应 48.0h, 以93%的产率得到6-([1,1'-biphenyl]-2-yl)-9-isopropyl-9H-purine
    参考文献:
    名称:
    Pd(II)-Catalyzed Ortho Arylation of 6-Arylpurines with Aryl Iodides via Purine-Directed C−H Activation: A New Strategy for Modification of 6-Arylpurine Derivatives
    摘要:
    Purine is utilized as a new directing group for the Pd-catalyzed monoarylation of 6-arylpurines with simple aryl iodides via C H bond activation in good yields, providing a complementary tool for the modification of 6-arylpurines (nucleosides). Most importantly, purine can be used as a building block for nucleoside derivatives, and the use of purine as a directing group helps avoid additional synthetic steps.
    DOI:
    10.1021/ol200405w
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文献信息

  • Pd(II)-Catalyzed <i>Ortho</i> Arylation of 6-Arylpurines with Aryl Iodides via Purine-Directed C−H Activation: A New Strategy for Modification of 6-Arylpurine Derivatives
    作者:Hai-Ming Guo、Li-Li Jiang、Hong-Ying Niu、Wei-Hao Rao、Lei Liang、Run-Ze Mao、De-Yang Li、Gui-Rong Qu
    DOI:10.1021/ol200405w
    日期:2011.4.15
    Purine is utilized as a new directing group for the Pd-catalyzed monoarylation of 6-arylpurines with simple aryl iodides via C H bond activation in good yields, providing a complementary tool for the modification of 6-arylpurines (nucleosides). Most importantly, purine can be used as a building block for nucleoside derivatives, and the use of purine as a directing group helps avoid additional synthetic steps.
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