Crystal structure of tert-butyl 4-[4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl]piperazine-1-carboxylate

Abstract

The title sterically congested piperazine derivative, C20H27FN2O2, was prepared using a modified Bruylants approach. A search of the Cambridge Structural Database identified 51 compounds possessing an N-tert-butyl piperazine substructure. Of these only 14 were asymmetrically substituted on the piperazine ring and none with a synthetically useful second nitrogen. Given the novel chemistry generating a pharmacologically useful core, determination of the crystal structure for this compound was necessary. The piperazine ring is present in a chair conformation with di-equatorial substitution. Of the two N atoms, one is sp 3 hybridized while the other is sp 2 hybridized. Intermolecular interactions resulting from the crystal packing patterns were investigated using Hirshfeld surface analysis and fingerprint analysis. Directional weak hydrogen-bond-like interactions (C—H...O) and C—H...π interactions with the dispersion interactions as the major source of attraction are present in the crystal packing.

Crystal structure of 4-bromo-N-(propylcarbamoyl)benzenesulfonamide

“…The intermolecular distance between H10CÁ Á ÁO1 is 2.61 A ˚; C10Á Á ÁO1 is 4.028 A ˚with an angle of 173.7 between C10-H10CÁ Á ÁO1. The distances and angles of the C-HÁ Á ÁO-type hydrogen bond observed in the present structure are within the reported ranges (Desiraju, 1991;Gumireddy et al, 2021). Overall, the atoms involved in hydrogen bonding for bromopropamide are identical to those in the crystal structure for its analogue chlorpropamide (CSD refcode: BEDMIG10; Drebushchak et al, 2009).…”