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2-(2,4,6-Trimethylanilino)ethyl imidazole-1-carboxylate | 1371582-11-4

中文名称
——
中文别名
——
英文名称
2-(2,4,6-Trimethylanilino)ethyl imidazole-1-carboxylate
英文别名
——
2-(2,4,6-Trimethylanilino)ethyl imidazole-1-carboxylate化学式
CAS
1371582-11-4
化学式
C15H19N3O2
mdl
——
分子量
273.335
InChiKey
LXYAMJUOIPMRCD-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):
    3.1
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    56.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2-(2,4,6-Trimethylanilino)ethyl imidazole-1-carboxylate吡啶盐酸盐 作用下, 以 乙腈 为溶剂, 反应 9.0h, 以0.09 g的产率得到N-(2,4,6-trimethylphenyl)oxazolidin-2-one
    参考文献:
    名称:
    Dual Brønsted Acid/Nucleophilic Activation of Carbonylimidazole Derivatives
    摘要:
    Carbonylimidazole derivatives have been found to be highly active acylation reagents for esterification and amidation in the presence of pyridinium salts. These reactions are thought to involve both Bronsted acid and nucleophilic catalysis. This mode of activation has been applied to the synthesis of difficult to access oxazolidinones, as well as esters and amides. Finally, the use of pyridinium salts has been shown to accelerate the esterification of carboxylic acids with imidazole carbamates.
    DOI:
    10.1021/ol300339q
  • 作为产物:
    参考文献:
    名称:
    Dual Brønsted Acid/Nucleophilic Activation of Carbonylimidazole Derivatives
    摘要:
    Carbonylimidazole derivatives have been found to be highly active acylation reagents for esterification and amidation in the presence of pyridinium salts. These reactions are thought to involve both Bronsted acid and nucleophilic catalysis. This mode of activation has been applied to the synthesis of difficult to access oxazolidinones, as well as esters and amides. Finally, the use of pyridinium salts has been shown to accelerate the esterification of carboxylic acids with imidazole carbamates.
    DOI:
    10.1021/ol300339q
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