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2-(5,6-Diphenyl-1,2,4-triazin-3-yl)aniline

The title compound, C(21)H(16)N(4), obtained under standard Suzuki cross-coupling conditions, is a model compound in the synthesis and biological activity evaluation of new aza-analogues of sildenafil containing a pyrazolo­[4,3-e][1,2,4]triazine system. An N—H⋯N intra­molecular hydrogen bond involvi...

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Detalles Bibliográficos
Autores principales: Mojzych, Mariusz, Karczmarzyk, Zbigniew, Fruziński, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588826/
https://www.ncbi.nlm.nih.gov/pubmed/23468791
http://dx.doi.org/10.1107/S1600536812044194
Descripción
Sumario:The title compound, C(21)H(16)N(4), obtained under standard Suzuki cross-coupling conditions, is a model compound in the synthesis and biological activity evaluation of new aza-analogues of sildenafil containing a pyrazolo­[4,3-e][1,2,4]triazine system. An N—H⋯N intra­molecular hydrogen bond involving the amino­benzene system and the 1,2,4-triazine moiety helps to establish a near coplanar orientation of the rings with a dihedral angle of 12.04 (4)°, which is believed to be necessary for the biological activity of sildenafil analogues. The 1,2,4-triazine ring is slightly distorted from planarity [r.m.s deviation = 0.0299 (11) Å] and forms dihedral angles of 58.60 (4) and 36.35 (3)° with the pendant phenyl rings. The crystal packing features bifurcated N—H⋯(N,N) hydrogen bonds linking screw-axis-related mol­ecules into chains parallel to the [010] direction and π–π inter­actions, with a centroid–centroid separation of 3.8722 (7) Å and a slippage of 1.412 (3) Å. The crystal studied was a nonmerohedral twin with a ratio of 0.707 (2):0293 (2).