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4-Furoyl-2,3,4,5,6,7-hexa­hydro-r-2,c-7-di­phenyl-1H-1,4-diazepin-5-one: supramolecular aggregation through C—H⋯O interactions

✍ Scribed by Thamotharan, S. ;Parthasarathi, V. ;Muthukumar, M. ;Thanikasalam, K. ;Jeyaraman, R. ;Linden, Anthony

Publisher
International Union of Crystallography
Year
2003
Tongue
English
Weight
316 KB
Volume
59
Category
Article
ISSN
1600-5368

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✦ Synopsis

In the title compound, C 22 H 20 N 2 O 3 , the phenyl substituents adopt equatorial orientations. The seven-membered heterocyclic ring adopts a distorted chair conformation. In the solid state, the symmetry-related molecules are linked by intermolecular CÐHÁ Á ÁO hydrogen bonds to form a supramolecular aggregation.

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