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3-[1-(tert-butoxycarbonyl)-2-methyl-1H-indol-3-yl]-N-butyl-4-(2-methyl-1-benzothiophen-3-yl)maleimide | 894428-76-3

中文名称
——
中文别名
——
英文名称
3-[1-(tert-butoxycarbonyl)-2-methyl-1H-indol-3-yl]-N-butyl-4-(2-methyl-1-benzothiophen-3-yl)maleimide
英文别名
Tert-butyl 3-[1-butyl-4-(2-methyl-1-benzothiophen-3-yl)-2,5-dioxopyrrol-3-yl]-2-methylindole-1-carboxylate;tert-butyl 3-[1-butyl-4-(2-methyl-1-benzothiophen-3-yl)-2,5-dioxopyrrol-3-yl]-2-methylindole-1-carboxylate
3-[1-(tert-butoxycarbonyl)-2-methyl-1H-indol-3-yl]-N-butyl-4-(2-methyl-1-benzothiophen-3-yl)maleimide化学式
CAS
894428-76-3
化学式
C31H32N2O4S
mdl
——
分子量
528.672
InChiKey
QFURUXKJDCLSHS-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):
    7.2
  • 重原子数:
    38
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    96.8
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    3-[1-(tert-butoxycarbonyl)-2-methyl-1H-indol-3-yl]-N-butyl-4-(2-methyl-1-benzothiophen-3-yl)maleimide正丁胺 作用下, 反应 4.0h, 以80%的产率得到N-butyl-3-(2-methyl-1-benzothiophen-3-yl)-4-(2-methyl-1H-indol-3-yl)maleimide
    参考文献:
    名称:
    A convenient synthesis of 3,4-diaryl(hetaryl)-substituted maleimides and maleic anhydrides
    摘要:
    A convenient procedure has been developed for the synthesis of 3,4-diaryl(or hetaryl)maleimides by cross coupling of N-substituted 3,4-dibromomaleimides with aryl(hetaryl)boronic acids in the presence of Pd(Ph3P)(4) and CsF The reaction ensures high yields of the products and requires relatively small amount of the catalyst; it can be performed on an enlarged scale. The resulting maleimides are readily converted into the corresponding maleic anhydrides.
    DOI:
    10.1134/s1070428006100162
  • 作为产物:
    参考文献:
    名称:
    A convenient synthesis of 3,4-diaryl(hetaryl)-substituted maleimides and maleic anhydrides
    摘要:
    A convenient procedure has been developed for the synthesis of 3,4-diaryl(or hetaryl)maleimides by cross coupling of N-substituted 3,4-dibromomaleimides with aryl(hetaryl)boronic acids in the presence of Pd(Ph3P)(4) and CsF The reaction ensures high yields of the products and requires relatively small amount of the catalyst; it can be performed on an enlarged scale. The resulting maleimides are readily converted into the corresponding maleic anhydrides.
    DOI:
    10.1134/s1070428006100162
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文献信息

  • Thermally irreversible organic photochromic compounds for optical memory
    作者:V. A. Barachevsky、Yu. P. Strokach、Yu. A. Puankov、M. M. Krayushkin
    DOI:10.1002/poc.1191
    日期:2007.11
    some photochromic compounds (58 diarylethenes and 9 fulgimides), the results of our spectral and kinetic studies are presented. Aiming at targeted synthesis of new photochromic compounds, the structure – photochromic behavior relationship (SPBR) for the synthesized compounds has been analyzed. The perspectives for application of these compounds in development of recording media for use in optical memory
    对于某些光致变色化合物(58个双芳硫醚和9个全黄酰亚胺),我们给出了光谱和动力学研究的结果。为了有针对性地合成新的光致变色化合物,已经分析了合成化合物的结构-光致变色行为关系(SPBR)。概述了这些化合物在开发用于光学存储设备的记录介质中的应用前景。版权所有©2007 John Wiley&Sons,Ltd.
  • A convenient synthesis of 3,4-diaryl(hetaryl)-substituted maleimides and maleic anhydrides
    作者:S. V. Shorunov、M. M. Krayushkin、F. M. Stoyanovich、M. Irie
    DOI:10.1134/s1070428006100162
    日期:2006.10
    A convenient procedure has been developed for the synthesis of 3,4-diaryl(or hetaryl)maleimides by cross coupling of N-substituted 3,4-dibromomaleimides with aryl(hetaryl)boronic acids in the presence of Pd(Ph3P)(4) and CsF The reaction ensures high yields of the products and requires relatively small amount of the catalyst; it can be performed on an enlarged scale. The resulting maleimides are readily converted into the corresponding maleic anhydrides.
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