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1-benzyl-4-(2-methoxyphenyl)-1H-benzo[b][1,4]diazepin-2(3H)-one | 1337994-19-0

中文名称
——
中文别名
——
英文名称
1-benzyl-4-(2-methoxyphenyl)-1H-benzo[b][1,4]diazepin-2(3H)-one
英文别名
——
1-benzyl-4-(2-methoxyphenyl)-1H-benzo[b][1,4]diazepin-2(3H)-one化学式
CAS
1337994-19-0
化学式
C23H20N2O2
mdl
——
分子量
356.424
InChiKey
FWTNZFMMGRTQKA-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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Enantioselective Synthesis of 4-Substituted 4,5-Dihydro-1H-[1,5]benzodiazepin-2(3H)-ones by the Lewis Base-Catalyzed Hydrosilylation
    摘要:
    Enantioselective synthesis of 4-substituted 4,5-dihydro-1H-[1,5]benzodiazepin-2(3H)-ones has been accomplished through chiral Lewis base-catalyzed hydrosilylation. The corresponding products were obtained in excellent yields (up to 99%) and enantioselectivities (up to 98%). The absolute configuration of product 3n has been determined as S by X-ray crystallographic analysis.
    DOI:
    10.1021/jo201334n
  • 作为产物:
    描述:
    4-(2-methoxyphenyl)-1,5-benzodiazepin-2-one 、 溴甲苯caesium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 生成 1-benzyl-4-(2-methoxyphenyl)-1H-benzo[b][1,4]diazepin-2(3H)-one
    参考文献:
    名称:
    Enantioselective Synthesis of 4-Substituted 4,5-Dihydro-1H-[1,5]benzodiazepin-2(3H)-ones by the Lewis Base-Catalyzed Hydrosilylation
    摘要:
    Enantioselective synthesis of 4-substituted 4,5-dihydro-1H-[1,5]benzodiazepin-2(3H)-ones has been accomplished through chiral Lewis base-catalyzed hydrosilylation. The corresponding products were obtained in excellent yields (up to 99%) and enantioselectivities (up to 98%). The absolute configuration of product 3n has been determined as S by X-ray crystallographic analysis.
    DOI:
    10.1021/jo201334n
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