Abstract
In the title compound, C16H22Cl2N2O2, the substituted piperidine ring adopts a chair conformation with both substituents in equatorial positions. In the crystal, N—H⋯O and C—H⋯O hydrogen bonds connect molecules into ribbons along the a-axis direction.
Highlights
Bruker Kappa APEXII DUO CCD diffractometerH-atom parameters constrained a Institute of Chemistry, University of The Punjab, Qaid-i-Azam Campus, Lahore
In the title compound, C16H22Cl2N2O2, the substituted piperidine ring adopts a chair conformation with both substituents in equatorial positions
During our search to find new synthetic novel multivalent ligands for the treatment of pain and depression, the title compound was synthesized as an intermediate
Summary
H-atom parameters constrained a Institute of Chemistry, University of The Punjab, Qaid-i-Azam Campus, Lahore. 54590, Pakistan, and bDepartment of Chemistry and Biochemistry, 1306 E University. R factor = 0.034; wR factor = 0.079; data-to-parameter ratio = 65.3. Symmetry code: (i) x þ 12; y þ 32; z þ 1. C16H22Cl2N2O2, the substituted piperidine ring adopts a chair conformation with both substituents in equatorial positions. N—H O and C—H O hydrogen bonds connect molecules into ribbons along the a-axis direction
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