High-temperature catalytic synthesis of quinolino[1,2-a]benzimid azole and some of its transformations

The possibility of synthesis of quinoline[1,2-a]benzimidazole from aniline and quinoline on a dehydrogenating mark K-16 catalyst at 560-580°C was demonstrated. It was established that in the nitration of quinolino[1,2-a]benzimidazole, a 10-nitro-derivative is formed, whereas in the reaction with ADCE, tetramethoxycarbonylquinolino[1,2-a]pyrido[2′,1′-b]benzimidazole is formed. ©1996 Plenum Publishing Corporation.

Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
4
Language
English
Pages
459-461
Status
Published
Department
-
Number
-
Volume
32
Year
1996
Organizations
  • 1 Russian University of Peoples' Friendship, Moscow 117923, Russian Federation
Keywords
-
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/848/