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methyl 4-(tetrahydrofuran-2-ylmethyl)-4H-1,4-benzoxazine-2-carboxylate | 1332878-74-6

中文名称
——
中文别名
——
英文名称
methyl 4-(tetrahydrofuran-2-ylmethyl)-4H-1,4-benzoxazine-2-carboxylate
英文别名
Methyl 4-(oxolan-2-ylmethyl)-1,4-benzoxazine-2-carboxylate;methyl 4-(oxolan-2-ylmethyl)-1,4-benzoxazine-2-carboxylate
methyl 4-(tetrahydrofuran-2-ylmethyl)-4H-1,4-benzoxazine-2-carboxylate化学式
CAS
1332878-74-6
化学式
C15H17NO4
mdl
——
分子量
275.304
InChiKey
DOOCUKLJVPSQLB-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):
    2.3
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    48
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    methyl 2-(2-bromophenoxy)-3-(((tetrahydrofuran-2-yl)methyl)amino)acrylate 在 potassium phosphatecopper(l) iodide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 以594 mg的产率得到methyl 4-(tetrahydrofuran-2-ylmethyl)-4H-1,4-benzoxazine-2-carboxylate
    参考文献:
    名称:
    A general synthesis of N-substituted 1,4-benzoxazine- and 1,4-benzothiazine-2-carboxylates via copper-catalyzed intramolecular amination of arylbromides
    摘要:
    Starting from ortho-bromosubstituted phenoxyacetates or (phenythio)acetates and primary amines, various N-substituted 4H-1,4-benzoxazine- and 4H-1,4-benzothiazine-2-carboxylates were synthesized in moderate to high yields by using a Cu(I)-catalyzed Ullmann-type cyclization as a key step. The method is simple to operate, tolerates many functional groups and does not require any additives. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.06.081
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文献信息

  • A general synthesis of N-substituted 1,4-benzoxazine- and 1,4-benzothiazine-2-carboxylates via copper-catalyzed intramolecular amination of arylbromides
    作者:Ferdinand Melkonyan、Artiom Topolyan、Alexander Karchava、Marina Yurovskaya
    DOI:10.1016/j.tet.2011.06.081
    日期:2011.9
    Starting from ortho-bromosubstituted phenoxyacetates or (phenythio)acetates and primary amines, various N-substituted 4H-1,4-benzoxazine- and 4H-1,4-benzothiazine-2-carboxylates were synthesized in moderate to high yields by using a Cu(I)-catalyzed Ullmann-type cyclization as a key step. The method is simple to operate, tolerates many functional groups and does not require any additives. (C) 2011 Elsevier Ltd. All rights reserved.
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