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1,2-bis(4-bromophenyl)-6,7-dihydro-3-methoxy-6,6-dimethyl-1H-indol-4(5H)-one | 1436868-36-8

中文名称
——
中文别名
——
英文名称
1,2-bis(4-bromophenyl)-6,7-dihydro-3-methoxy-6,6-dimethyl-1H-indol-4(5H)-one
英文别名
1,2-Bis(4-bromophenyl)-3-methoxy-6,6-dimethyl-5,7-dihydroindol-4-one;1,2-bis(4-bromophenyl)-3-methoxy-6,6-dimethyl-5,7-dihydroindol-4-one
1,2-bis(4-bromophenyl)-6,7-dihydro-3-methoxy-6,6-dimethyl-1H-indol-4(5H)-one化学式
CAS
1436868-36-8
化学式
C23H21Br2NO2
mdl
——
分子量
503.233
InChiKey
OTZWEYLQFXXWSU-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):
    6.3
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    31.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    3-(4-溴苯胺基)-5,5-二甲基环己-2-烯-1-酮甲醇4-溴苯基水合乙二醛对甲苯磺酸 作用下, 反应 0.37h, 以81%的产率得到1,2-bis(4-bromophenyl)-6,7-dihydro-3-methoxy-6,6-dimethyl-1H-indol-4(5H)-one
    参考文献:
    名称:
    Three-component synthesis of poly-substituted tetrahydroindoles through p-TsOH promoted alkoxylation
    摘要:
    Concise and efficient three-component domino reactions to highly substituted tetrahydroindole derivatives promoted by p-TsOH have been developed under microwave irradiation condition. The direct C3-alkoxylation of indole framework was achieved in a one-pot operation. The reaction proceeds at fast rates and can be finished within 30 mm, which makes workup convenient to give good chemical yields. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.04.029
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文献信息

  • Three-component synthesis of poly-substituted tetrahydroindoles through p-TsOH promoted alkoxylation
    作者:Qing-Qing Shi、Li-Ping Fu、Yu Shi、Hua-Qin Ding、Jing-Hua Luo、Bo Jiang、Shu-Jiang Tu
    DOI:10.1016/j.tetlet.2013.04.029
    日期:2013.6
    Concise and efficient three-component domino reactions to highly substituted tetrahydroindole derivatives promoted by p-TsOH have been developed under microwave irradiation condition. The direct C3-alkoxylation of indole framework was achieved in a one-pot operation. The reaction proceeds at fast rates and can be finished within 30 mm, which makes workup convenient to give good chemical yields. (C) 2013 Elsevier Ltd. All rights reserved.
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