Abstract
The title compound, C28H19NO2, was synthesized by the reaction of 1,3-benzodioxole-5-carbaldehyde with naphthalen-2-amine catalyzed by thio-salicylic acid in acetic acid. The central dihydropyridine ring adopts a boat conformation. The two planar (r.m.s. deviations = 0.0158 and 0.0552 Å) bicyclic parts make a dihedral angle of 16.16 (5)° with respect to each other. The crystal packing is stabilized by inter-molecular N - H⋯O hydrogen bonds and C - H⋯π inter-actions.
Cite
CITATION STYLE
Jia, R., Peng, J., & Tu, S. (2010). 14-(1,3-Benzodioxol-5-yl)-7,14-dihydrodibenzo[a,j]acridine. Acta Crystallographica Section E: Structure Reports Online, 66(12). https://doi.org/10.1107/S1600536810044302
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