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N-(tert-butyl)-4H-benzo[e][1,3]oxazin-2-amine | 1427469-14-4

中文名称
——
中文别名
——
英文名称
N-(tert-butyl)-4H-benzo[e][1,3]oxazin-2-amine
英文别名
N-tert-butyl-4H-1,3-benzoxazin-2-amine
N-(tert-butyl)-4H-benzo[e][1,3]oxazin-2-amine化学式
CAS
1427469-14-4
化学式
C12H16N2O
mdl
——
分子量
204.272
InChiKey
ATBQSUAGYGLQCT-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):
    2.1
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    33.6
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    异氰酸叔丁酯(氨基甲基)-苯酚四(三苯基膦)钯 作用下, 以 1,4-二氧六环 为溶剂, 反应 2.0h, 以93%的产率得到N-(tert-butyl)-4H-benzo[e][1,3]oxazin-2-amine
    参考文献:
    名称:
    Synthesis of 2-Aminobenzoxazoles and 3-Aminobenzoxazines via Palladium-Catalyzed Aerobic Oxidation of o-Aminophenols with Isocyanides
    摘要:
    A Pd-catalyzed aerobic oxidation of o-aminophenols and isocyanides for the synthesis of 2-aminobenzoxazoles and 3-aminobenzoxazines has been achieved in an air atmosphere. The procedure constructs 2-aminobenzoxazoles and 3-aminobenzoxazines with moderate to excellent yields and a broad substrate scope. Apart from experimental simplicity, this methodology has the advantages of mild reaction conditions and easily accessible starting materials. Furthermore, the utility of this method has also been successfully applied to the synthesis of other types of useful nitrogen heterocycles.
    DOI:
    10.1021/jo400002f
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文献信息

  • Synthesis of 2-Aminobenzoxazoles and 3-Aminobenzoxazines via Palladium-Catalyzed Aerobic Oxidation of <i>o</i>-Aminophenols with Isocyanides
    作者:Bifu Liu、Meizhou Yin、Hanling Gao、Wanqing Wu、Huanfeng Jiang
    DOI:10.1021/jo400002f
    日期:2013.4.5
    A Pd-catalyzed aerobic oxidation of o-aminophenols and isocyanides for the synthesis of 2-aminobenzoxazoles and 3-aminobenzoxazines has been achieved in an air atmosphere. The procedure constructs 2-aminobenzoxazoles and 3-aminobenzoxazines with moderate to excellent yields and a broad substrate scope. Apart from experimental simplicity, this methodology has the advantages of mild reaction conditions and easily accessible starting materials. Furthermore, the utility of this method has also been successfully applied to the synthesis of other types of useful nitrogen heterocycles.
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