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2-pyrimidinyl triflate | 154447-06-0

中文名称
——
中文别名
——
英文名称
2-pyrimidinyl triflate
英文别名
Pyrimidin-2-yl trifluoromethanesulfonate
2-pyrimidinyl triflate化学式
CAS
154447-06-0
化学式
C5H3F3N2O3S
mdl
——
分子量
228.152
InChiKey
UWYUSZSXDUOBOA-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

物化性质

  • 沸点:
    260.0±50.0 °C(Predicted)
  • 密度:
    1.661±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    77.5
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    (E)-1-phenyl-(2-tributylstannyl)ethene2-pyrimidinyl triflate四(三苯基膦)钯lithium chloride 作用下, 以 1,4-二氧六环 为溶剂, 反应 3.0h, 以57%的产率得到2-[(E)-2-苯基乙烯基]嘧啶
    参考文献:
    名称:
    Synthesis of Pyrimidinyl Triflates and Palladium-catalyzed Coupling with Organotion and Organozic Reagents
    摘要:
    Pyrimidinyl triflates have been synthesized from pyrimidinones using triflic anhydride in the presence of triethylamine. The triflates, in the pyrimidine electrophilic positions, are versatile intermediates for substitution reactions. Carbon substituents are readily introduced in any position by Pd-catalyzed coupling reactions between pyrimidinyl triflates and aryl- or alkenyltin or with the corresponding organozinc reagents. Organozinc reagents are generally more reactive in coupling reaction and will effect the introduction of alkyl substituents.
    DOI:
    10.3987/com-93-s39
  • 作为产物:
    描述:
    三氟甲磺酸酐2-羟基嘧啶 在 TEA 作用下, 以 二氯甲烷 为溶剂, 以36%的产率得到2-pyrimidinyl triflate
    参考文献:
    名称:
    Synthesis of Pyrimidinyl Triflates and Palladium-catalyzed Coupling with Organotion and Organozic Reagents
    摘要:
    Pyrimidinyl triflates have been synthesized from pyrimidinones using triflic anhydride in the presence of triethylamine. The triflates, in the pyrimidine electrophilic positions, are versatile intermediates for substitution reactions. Carbon substituents are readily introduced in any position by Pd-catalyzed coupling reactions between pyrimidinyl triflates and aryl- or alkenyltin or with the corresponding organozinc reagents. Organozinc reagents are generally more reactive in coupling reaction and will effect the introduction of alkyl substituents.
    DOI:
    10.3987/com-93-s39
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文献信息

  • Synthesis of Pyrimidinyl Triflates and Palladium-catalyzed Coupling with Organotion and Organozic Reagents
    作者:Jessie Sandosham、Kjell Undheim
    DOI:10.3987/com-93-s39
    日期:——
    Pyrimidinyl triflates have been synthesized from pyrimidinones using triflic anhydride in the presence of triethylamine. The triflates, in the pyrimidine electrophilic positions, are versatile intermediates for substitution reactions. Carbon substituents are readily introduced in any position by Pd-catalyzed coupling reactions between pyrimidinyl triflates and aryl- or alkenyltin or with the corresponding organozinc reagents. Organozinc reagents are generally more reactive in coupling reaction and will effect the introduction of alkyl substituents.
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