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Ethyl 2,6-bis(4-chlorophenyl)-4-hydroxy-5-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate: supramolecular aggregation through N-H center dot center dot center dot Cl, C-H center dot center dot center dot Cl, C-H center dot center dot center dot S and C-H center dot center dot center dot pi interactions
Journal article

Ethyl 2,6-bis(4-chlorophenyl)-4-hydroxy-5-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate: supramolecular aggregation through N-H center dot center dot center dot Cl, C-H center dot center dot center dot Cl, C-H center dot center dot center dot S and C-H center dot center dot center dot pi interactions

J. Suresh, R. Suresh Kumar, S. Perumal and S. Natarajan
Acta crystallographica. Section E, Structure reports online, Vol.63, pp.O777-O779
01/02/2007
DOI: https://doi.org/10.1107/S1600536807001237

Abstract

Crystallography Physical Sciences Science & Technology
In the title molecule, C26H23Cl2NO3S, the tetrahydropyridine ring adopts a half-chair conformation. Intramolecular O-H center dot center dot center dot O hydrogen bonding generates an S(6) ring motif. Intermolecular N-H center dot center dot center dot Cl, C-H center dot center dot center dot Cl and C-H center dot center dot center dot S hydrogen bonding generates primary graph-set motifs C(8), C(11) and C(6), respectively. No significant pi-pi interactions exist in the crystal structure.

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