A novel method for the synthesis of pyrimido[1,2-a]benzimidazoles

[Figure not available: see fulltext.] Condensation of 1,2-diaminobenzimidazole with N-arylitaconimides was studied. It was found that 2-(10-amino-N-aryl-2-oxo-2,3,4,10-tetrahydropyrimido[1,2-a]benzimidazol-3-yl)acetamides were formed in the course of this reaction upon brief heating to reflux of the reagent mixture in 2-propanol in the presence of catalytic amounts of acetic acid. © 2016, Springer Science+Business Media New York.

Авторы
Vandyshev D.Y.1 , Shikhaliev K.S.1 , Kokonova A.V.1 , Potapov A.Y.1 , Kolpakova M.G.1 , Sabynin A.L.1 , Zubkov F.I. 2
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
7
Язык
Английский
Страницы
493-497
Статус
Опубликовано
Том
52
Год
2016
Организации
  • 1 Voronezh State University, 1 Universitetskaya Sq., Voronezh, 394006, Russian Federation
  • 2 People’s Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
Ключевые слова
1,2-diaminobenzimidazole; methypyrrolidine-2,5-dione; N-arylitaconimides; polynucleophiles; pyrimido[1,2-a]benzimidazole
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