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Synthesis and crystal structures of three new benzotriazolylpropanamides

The base-catalyzed Michael addition of 2-methyl­acryl­amide to benzotriazole afforded 3-(1H-benzotriazol-1-yl)-2-methyl­propanamide, C(10)H(12)N(4)O (1), in 32% yield in addition to small amounts of isomeric 3-(2H-benzotriazol-2-yl)-2-methyl­propanamide, C(10)H(12)N(4)O (2). In a similar manner, 3-(...

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Detalles Bibliográficos
Autores principales: Amenta, Donna S., Liebing, Phil, Biero, Julia E., Sherman, Robert J., Gilje, John W., Edelmann, Frank T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458315/
https://www.ncbi.nlm.nih.gov/pubmed/28638650
http://dx.doi.org/10.1107/S2056989017007472
Descripción
Sumario:The base-catalyzed Michael addition of 2-methyl­acryl­amide to benzotriazole afforded 3-(1H-benzotriazol-1-yl)-2-methyl­propanamide, C(10)H(12)N(4)O (1), in 32% yield in addition to small amounts of isomeric 3-(2H-benzotriazol-2-yl)-2-methyl­propanamide, C(10)H(12)N(4)O (2). In a similar manner, 3-(1H-benzotriazol-1-yl)-N,N-di­methyl­propanamide, C(11)H(14)N(4)O (3), was prepared from benzotriazole and N,N-di­methyl­acryl­amide. All three products have been structurally characterized by single-crystal X-ray diffraction. The crystal structures of 1 and 2 comprise infinite arrays formed by N—H⋯O and N—H⋯N bridges, as well as π–π inter­actions, while the mol­ecules of 3 are aggregated to simple π-dimers in the crystal.