International Union of Crystallography, Acta Crystallographica Section E: Crystallographic Communications, 6(73), p. 880-885, 2017
DOI: 10.1107/s2056989017007472
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The base-catalyzed Michael addition of 2-methylacrylamide to benzotriazole afforded 3-(1H-benzotriazol-1-yl)-2-methylpropanamide, C10H12N4O (1), in 32% yield in addition to small amounts of isomeric 3-(2H-benzotriazol-2-yl)-2-methylpropanamide, C10H12N4O (2). In a similar manner, 3-(1H-benzotriazol-1-yl)-N,N-dimethylpropanamide, C11H14N4O (3), was prepared from benzotriazole andN,N-dimethylacrylamide. All three products have been structurally characterized by single-crystal X-ray diffraction. The crystal structures of1and2comprise infinite arrays formed by N—H...O and N—H...N bridges, as well as π–π interactions, while the molecules of3are aggregated to simple π-dimers in the crystal.