Investigation of the reaction of N-acetylindoxyl with substituted anilines. Synthesis of derivatives of indolo[3,2-b]quinolines

被引：0
|
作者：
Tugusheva N.Z. [1 ]
Ryabova S.Yu.
Solov'eva N.P. [2 ]
Anisimova O.S. [2 ]
Granik V.G. [1 ]
机构：
[1] nIOPIK State Science Center of the Russian Federation
[2] Center for the Chemistry of Medicinal Materials, All-Russia Scientific Chemical-Pharmaceutical Research Institute
来源：
Chemistry of Heterocyclic Compounds | 2001年 / 37卷 / 7期
关键词：
Acetylindoxyl; Aniline; Indoloquinoline; Quinazoline; Quinoxaline;
D O I：
10.1023/A:1012459810266
中图分类号：
学科分类号：
摘要：
1-Acetyl-2,3-dihydrospiro[indolo-3, 2′-(1′,2′,3′, 4′-tetrahydroquinazolin-4′-one) was obtained from the reaction with anthranilamide, and 3-(2′-acetylaminophenyl)quinoxalin-2-one from the reaction with o-phenylenediamine, along with the normal products of the condensation of N-acetylindoxyl with substituted anilines. Derivatives of indolo[3,2-b]quinoline were synthesized from the obtained condensation products.
引用
收藏
页码：885 / 893
页数：8
相关论文
共 50 条
  • [31] Facile synthesis of 3-substituted thieno[3,2-b]furan derivatives
    Hergue, Noemie
    Mallet, Charlotte
    Touvron, Julia
    Allain, Magali
    Leriche, Philippe
    Frere, Pierre
    TETRAHEDRON LETTERS, 2008, 49 (15) : 2425 - 2428
  • [32] Indolo[3,2-b]carbazole derivatives as hole transporting materials for electrophotography
    Velasco, Dolores
    Jankauskas, Vygintas
    Stumbraite, Jolanta
    Grazulevicius, Juons V.
    Getautis, Vytautas
    SYNTHETIC METALS, 2009, 159 (7-8) : 654 - 658
  • [33] SYNTHESIS AND ANTITUMOR-ACTIVITY OF FUSED QUINOLINE DERIVATIVES .2. NOVEL 4-HYDROXYINDOLO[3,2-B]QUINOLINES AND 7-HYDROXYINDOLO[3,2-B]QUINOLINES
    YAMATO, M
    TAKEUCHI, Y
    CHANG, MR
    HASHIGAKI, K
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1992, 40 (02) : 528 - 530
  • [34] SYNTHESIS AND ANTITUMOR-ACTIVITY OF FUSED QUINOLINE DERIVATIVES .3. NOVEL N-GLYCOSYLAMINOINDOLO[3,2-B]QUINOLINES
    TAKEUCHI, Y
    CHANG, MR
    HASHIGAKI, K
    TASHIRO, T
    TSURUO, T
    TSUKAGOSHI, S
    YAMATO, M
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1992, 40 (06) : 1481 - 1485
  • [35] Synthesis and DNA binding profile of N-mono- and N,N′-disubstituted indolo[3,2-b]carbazoles
    Panesar, Harmanpreet Kaur
    Solano, Jennifer
    Minehan, Thomas G.
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2015, 13 (10) : 2879 - 2883
  • [36] Revisiting Indolo[3,2-b]carbazole: Synthesis, Structures, Properties, and Applications
    Zhao, Mengna
    Zhang, Binghao
    Miao, Qian
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (24) : 9678 - 9683
  • [37] Synthesis, characterization and printing application of alkylated indolo[3,2-b]carbazoles
    Bintinger, Johannes
    Yang, Shyuan
    Fruhmann, Philipp
    Holzer, Brigitte
    Stoeger, Berthold
    Svirkova, Anastasiya
    Marchetti-Deschmann, Martina
    Horkel, Ernst
    Hametner, Christian
    Froehlich, Johannes
    Kymissis, Ioannis
    Mikula, Hannes
    SYNTHETIC METALS, 2017, 228 : 9 - 17
  • [38] Synthesis of N-Mannich bases of 10H-indolo [3,2-b] quinoxalines
    Sridhar, SK
    Roosewelt, C
    Leonard, JT
    Anbalagan, N
    INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY, 2002, 12 (02) : 157 - 158
  • [39] Theoretical Study on the Carrier Transport Properties of Indolo[3,2-b]carbazole Derivatives
    Wang Guang-Yu
    Duan Yu-Ai
    Geng Yun
    Zhang Bing
    Tang Xiao-Dan
    Wu Shui-Xing
    Hao Li-Zhu
    Su Zhong-Min
    CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2013, 34 (06): : 1490 - 1496
  • [40] Four new bipolar Indolo [3,2-b] carbazole derivatives for blue OLEDs
    Yang, Hongyan
    Li, Yanmei
    Zhao, Yuling
    Yu, Shupei
    Ma, Hailin
    Qian, Long
    Wang, Ruidong
    Yu, Tianzhi
    Su, Wenming
    DYES AND PIGMENTS, 2021, 187
12345