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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2021, том 31, выпуск 6, страницы 821–823 (Mi mendc1054)

Эта публикация цитируется в 3 статьях

Communications

Regioselective synthesis of novel imidazo[1,5-b]pyridazine derivatives from diaminoimidazoles and α-acylacrylonitriles

D. Yu. Vandysheva, E. A. Koshelevaa, V. A. Polikarchuka, D. A. Mangushevaa, G. Denisovb, Kh. S. Shikhalieva

a Voronezh State University, Voronezh, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation


Аннотация: The heterocyclization of 1,2-diamino-4H-phenylimidazole with α-acylacrylonitriles affords cleanly 7-amino-2-R-5- phenylimidazo[1,5-b]pyridazine-3-carbonitriles. The strating α-acylacrylonitriles can be generated in situ from 3-oxo-3-(het)arylpropanenitriles and triethylorthoformate or dimethylformamide dimethyl acetal, and the products can be prepared in one pot.

Ключевые слова: imidazo[1,5-b]pyridazine, 1,2-diamino-4H-phenylimidazole, nitrogen heterocycles, regioselectivity, multicomponent reactions.

Язык публикации: английский

DOI: 10.1016/j.mencom.2021.11.017



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