Abstract
In the title compound, C18H22BrN3OS, the piperidine ring adopts a chair conformation. The mean plane of the thiazole ring forms dihedral angles of 23.97 (10) and 75.82 (10)° with the mean planes of its adjacent benzene and piperidine rings, respectively. An intramolecular N—H⋯N hydrogen bond generates an S(7) ring motif in the molecule. In the crystal, no significant intermoelcular hydrogen bonds are observed, but a weak π–π interaction with a centroid–centroid distance of 3.8855 (13) Å occurs.
Highlights
In the title compound, C18H22BrN3OS, the piperidine ring adopts a chair conformation
For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986)
H atoms treated by a mixture of independent and constrained refinement
Summary
El-Subbagh,b Tze Shyang Chiac and Hoong-Kun Func*‡. Key indicators: single-crystal X-ray study; T = 100 K; mean (C–C) = 0.003 A; R factor = 0.042; wR factor = 0.114; data-to-parameter ratio = 22.7. C18H22BrN3OS, the piperidine ring adopts a chair conformation. The mean plane of the thiazole ring forms dihedral angles of 23.97 (10) and 75.82 (10) with the mean planes of its adjacent benzene and piperidine rings, respectively. An intramolecular N—HÁ Á ÁN hydrogen bond generates an S(7) ring motif in the molecule. No significant intermoelcular hydrogen bonds are observed, but a weak – interaction with a centroid–centroid distance of 3.8855 (13) Aoccurs. See: Cremer & Pople (1975). See: El-Subbagh et al (1999). For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986)
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