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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⋯Cl, C—H⋯Cl, C—H⋯S and C—H⋯π inter­actions

✍ Scribed by Suresh, J. ;Kumar, R. Suresh ;Perumal, S. ;Natarajan, S.

Publisher
International Union of Crystallography
Year
2007
Tongue
English
Weight
231 KB
Volume
63
Category
Article
ISSN
1600-5368

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✦ Synopsis

In the title molecule, C 26 H 23 Cl 2 NO 3 S, the tetrahydropyridine ring adopts a half-chair conformation. Intramolecular O-HÁ Á ÁO hydrogen bonding generates an S(6) ring motif. Intermolecular N-HÁ Á ÁCl, C-HÁ Á ÁCl and C-HÁ Á ÁS hydrogen bonding generates primary graph-set motifs C(8), C(11) and C(6), respectively. No significantinteractions exist in the crystal structure.

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