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2'-amino-4-bromo-1'-(4-methoxyphenyl)-7',7'-dimethyl-2,5'-dioxo-5',6',7',8'-tetrahydro-1'H-spiro[indoline-3,4'-quinoline]-3'-carbonitrile | 1146746-58-8

中文名称
——
中文别名
——
英文名称
2'-amino-4-bromo-1'-(4-methoxyphenyl)-7',7'-dimethyl-2,5'-dioxo-5',6',7',8'-tetrahydro-1'H-spiro[indoline-3,4'-quinoline]-3'-carbonitrile
英文别名
2'-amino-4-bromo-1'-(4-methoxyphenyl)-7',7'-dimethyl-2,5'-dioxospiro[1H-indole-3,4'-6,8-dihydroquinoline]-3'-carbonitrile
2'-amino-4-bromo-1'-(4-methoxyphenyl)-7',7'-dimethyl-2,5'-dioxo-5',6',7',8'-tetrahydro-1'H-spiro[indoline-3,4'-quinoline]-3'-carbonitrile化学式
CAS
1146746-58-8
化学式
C26H23BrN4O3
mdl
——
分子量
519.398
InChiKey
YVIOKTKLTAESHR-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):
    3.9
  • 重原子数:
    34
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    108
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    4-溴靛红3-[(4-甲氧苯基)氨基]-5,5-二甲基-1-环己-2-烯酮丙二腈乙醇 为溶剂, 反应 0.17h, 以67%的产率得到2'-amino-4-bromo-1'-(4-methoxyphenyl)-7',7'-dimethyl-2,5'-dioxo-5',6',7',8'-tetrahydro-1'H-spiro[indoline-3,4'-quinoline]-3'-carbonitrile
    参考文献:
    名称:
    Microwave-Assisted Synthesis of New Spiro[indoline-3,4′-quinoline] Derivatives via a One-Pot Multicomponent Reaction
    摘要:
    A simple and efficient synthesis of spiro[indoline-3,4'-quinoline] derivatives by a one-pot reaction of isatin, malononitrile, and enaminone under microwave irradiation was investigated. This protocol has the advantages of short reaction time, high yields of products, broad substrate scope, and easy workup procedure.
    DOI:
    10.1080/00397910802527714
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文献信息

  • Microwave-Assisted Synthesis of New Spiro[indoline-3,4′-quinoline] Derivatives via a One-Pot Multicomponent Reaction
    作者:Song-Lei Zhu、Kai Zhao、Xiao-Ming Su、Shun-Jun Ji
    DOI:10.1080/00397910802527714
    日期:2009.3.25
    A simple and efficient synthesis of spiro[indoline-3,4'-quinoline] derivatives by a one-pot reaction of isatin, malononitrile, and enaminone under microwave irradiation was investigated. This protocol has the advantages of short reaction time, high yields of products, broad substrate scope, and easy workup procedure.
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