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A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines

An efficient approach to the synthesis of novel 2,3-diaryl-3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines via a base-catalyzed intramolecular cyclization of 2-arylmethylthio-N-arylidene-1H-benzo[d]imidazol-1-amines has been developed. The use of alkali is critical for the annulation of t...

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Hoofdauteurs: Pobedinskaya, D. Y., Побединская, Д. Ю., Demidov, O. P., Демидов, О. П.
Formaat: Статья
Taal:English
Gepubliceerd in: Taylor and Francis Ltd. 2024
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Online toegang:https://dspace.ncfu.ru/handle/123456789/29403
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spelling ir-123456789-294032024-12-13T11:41:07Z A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines Pobedinskaya, D. Y. Побединская, Д. Ю. Demidov, O. P. Демидов, О. П. 1,3,4-thiadiazine 2-benzylthio-1H-benzimidazole Annulation Benzimidazole Benzonitrile Intramolecular cyclization An efficient approach to the synthesis of novel 2,3-diaryl-3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines via a base-catalyzed intramolecular cyclization of 2-arylmethylthio-N-arylidene-1H-benzo[d]imidazol-1-amines has been developed. The use of alkali is critical for the annulation of the thiadiazine ring. In the absence of strong bases, the starting compounds undergo deamination with elimination of benzonitrile and formation of 2-arylmethylthiobenzimidazoles. 2024-12-13T11:40:05Z 2024-12-13T11:40:05Z 2024 Статья Khodykina E., Pobedinskaya D., Borodkina I., Astakhov A., Demidov O., Metelitsa A., Chernyshev V., Kolodina A. A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines // Journal of Sulfur Chemistry. - 2024. - 45 (6). - pp. 917 - 940. - DOI: 10.1080/17415993.2024.2394627 https://dspace.ncfu.ru/handle/123456789/29403 en Journal of Sulfur Chemistry application/pdf application/pdf Taylor and Francis Ltd.
institution СКФУ
collection Репозиторий
language English
topic 1,3,4-thiadiazine
2-benzylthio-1H-benzimidazole
Annulation
Benzimidazole
Benzonitrile
Intramolecular cyclization
spellingShingle 1,3,4-thiadiazine
2-benzylthio-1H-benzimidazole
Annulation
Benzimidazole
Benzonitrile
Intramolecular cyclization
Pobedinskaya, D. Y.
Побединская, Д. Ю.
Demidov, O. P.
Демидов, О. П.
A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines
description An efficient approach to the synthesis of novel 2,3-diaryl-3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines via a base-catalyzed intramolecular cyclization of 2-arylmethylthio-N-arylidene-1H-benzo[d]imidazol-1-amines has been developed. The use of alkali is critical for the annulation of the thiadiazine ring. In the absence of strong bases, the starting compounds undergo deamination with elimination of benzonitrile and formation of 2-arylmethylthiobenzimidazoles.
format Статья
author Pobedinskaya, D. Y.
Побединская, Д. Ю.
Demidov, O. P.
Демидов, О. П.
author_facet Pobedinskaya, D. Y.
Побединская, Д. Ю.
Demidov, O. P.
Демидов, О. П.
author_sort Pobedinskaya, D. Y.
title A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines
title_short A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines
title_full A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines
title_fullStr A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines
title_full_unstemmed A facile approach to the synthesis of 3,4-dihydro-2H-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines
title_sort facile approach to the synthesis of 3,4-dihydro-2h-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines
publisher Taylor and Francis Ltd.
publishDate 2024
url https://dspace.ncfu.ru/handle/123456789/29403
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