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2-methyl-4-naphthalen-2-yl-2-phenyl-6-thiophen-3-yl-2H-1,3-oxazine | 1202553-56-7

中文名称
——
中文别名
——
英文名称
2-methyl-4-naphthalen-2-yl-2-phenyl-6-thiophen-3-yl-2H-1,3-oxazine
英文别名
2-Methyl-4-naphthalen-2-yl-2-phenyl-6-thiophen-3-yl-1,3-oxazine;2-methyl-4-naphthalen-2-yl-2-phenyl-6-thiophen-3-yl-1,3-oxazine
2-methyl-4-naphthalen-2-yl-2-phenyl-6-thiophen-3-yl-2H-1,3-oxazine化学式
CAS
1202553-56-7
化学式
C25H19NOS
mdl
——
分子量
381.498
InChiKey
SXQMJTMBQAVUST-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):
    6.1
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    49.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    1-Naphthalen-2-yl-3-thiophen-3-ylprop-2-yn-1-one(S)-2-叠氮基-2-苯基乙醇三丁基膦 作用下, 以 甲苯 为溶剂, 反应 14.0h, 以87%的产率得到2-methyl-4-naphthalen-2-yl-2-phenyl-6-thiophen-3-yl-2H-1,3-oxazine
    参考文献:
    名称:
    A Phosphine-Mediated Construction of 1,4-Oxazepines and 1,3-Oxazines
    摘要:
    A simple and efficient method for constructing 1,4-oxazepines and 1,3-oxazines was developed with use of a phosphine-mediated tandem reaction of ynones with 2-azido alcohols. The method offers a promising route to synthetically useful as well as biologically active heterocycles under mild conditions and may be exploited for the preparation of interesting chiral ligands.
    DOI:
    10.1021/ol9024309
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文献信息

  • A Phosphine-Mediated Construction of 1,4-Oxazepines and 1,3-Oxazines
    作者:Céline François-Endelmond、Thomas Carlin、Pierre Thuery、Olivier Loreau、Frédéric Taran
    DOI:10.1021/ol9024309
    日期:2010.1.1
    A simple and efficient method for constructing 1,4-oxazepines and 1,3-oxazines was developed with use of a phosphine-mediated tandem reaction of ynones with 2-azido alcohols. The method offers a promising route to synthetically useful as well as biologically active heterocycles under mild conditions and may be exploited for the preparation of interesting chiral ligands.
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