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2,3-Diethylbenzo[g]quinoxaline
The title compound, C(16)H(16)N(2), was synthesized by dispersing 3,4-hexanedione in a methanol–water solution containing the acid catalyst NH(4)HF(2), then adding 1,2-diaminonaphthalene. The fused-ring system of the title compound is close to planar (r.m.s. deviation = 0.028 Å); one of the penda...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462215/ https://www.ncbi.nlm.nih.gov/pubmed/36338306 http://dx.doi.org/10.1107/S241431462000454X |
Sumario: | The title compound, C(16)H(16)N(2), was synthesized by dispersing 3,4-hexanedione in a methanol–water solution containing the acid catalyst NH(4)HF(2), then adding 1,2-diaminonaphthalene. The fused-ring system of the title compound is close to planar (r.m.s. deviation = 0.028 Å); one of the pendant methyl C atoms lies close to the ring plane [deviation = 0.071 (2) Å; N—C—C—C = −0.27 (18)°] whereas the other is significantly displaced [–1.7136 (18) Å; 91.64 (16)°]. The molecules pack in space group I [Image: see text] in a distinctive criss-cross motif supported by numerous aromatic π–π stacking interactions [shortest centroid–centroid separation = 3.5805 (6) Å]. [Image: see text] |
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