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10-(4-methoxyphenyl)-1-oxo-3,4,9,10-tetrahydro-1H-benzo[b]furo[3,4-e][1,4]diazepine-6-carboxylic acid | 1313371-06-0

中文名称
——
中文别名
——
英文名称
10-(4-methoxyphenyl)-1-oxo-3,4,9,10-tetrahydro-1H-benzo[b]furo[3,4-e][1,4]diazepine-6-carboxylic acid
英文别名
4-(4-Methoxyphenyl)-3-oxo-1,4,5,10-tetrahydrofuro[3,4-c][1,5]benzodiazepine-8-carboxylic acid;4-(4-methoxyphenyl)-3-oxo-1,4,5,10-tetrahydrofuro[3,4-c][1,5]benzodiazepine-8-carboxylic acid
10-(4-methoxyphenyl)-1-oxo-3,4,9,10-tetrahydro-1H-benzo[b]furo[3,4-e][1,4]diazepine-6-carboxylic acid化学式
CAS
1313371-06-0
化学式
C19H16N2O5
mdl
——
分子量
352.346
InChiKey
XDUXEBQVQZMENV-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):
    2.2
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    96.9
  • 氢给体数:
    3
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    4-羟乙酰乙酸内酯4-甲氧基苯甲醛3,4-二氨基苯甲酸溶剂黄146 作用下, 以 为溶剂, 反应 0.75h, 以81%的产率得到10-(4-methoxyphenyl)-1-oxo-3,4,9,10-tetrahydro-1H-benzo[b]furo[3,4-e][1,4]diazepine-6-carboxylic acid
    参考文献:
    名称:
    Microwave-assisted multi-component reaction in water leading to highly regioselective formation of benzo[f]azulen-1-ones
    摘要:
    Microwave-assisted three-component reaction has been established for the regioselective synthesis of benzo[f]azulen-1-ones. The reaction was performed in aqueous media under microwave irradiation by using readily available and inexpensive starting materials. A total of 38 examples were examined to show a broad substrate scope and good overall yields (70-89%). The present new synthesis shows attractive green chemistry characteristics, such as the use of water as reaction media, concise one-pot conditions, short reaction periods (7-24 min), easy work-up/purification, and reduced waste production without the use of any strong acids or metal promoters. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.05.002
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