1. Supramolecular interactions in cocrystals of benzoic acid derivatives with selective COX-2 inhibitor etoricoxib.
- Author
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Ma YH, Yang K, Qian YL, Hong WP, Zhang KY, Tao ZW, Meng H, and Ma WJ
- Abstract
The structures of three 1:1 cocrystal forms of etoricoxib {ETR; systematic name: 5-chloro-2-(6-methylpyridin-3-yl)-3-[4-(methylsulfonyl)phenyl]pyridine, C
18 H15 ClN2 O2 S} have been synthesized and characterized by single-crystal X-ray diffraction; these are etoricoxib-benzoic acid (1/1), C18 H15 ClN2 O2 S·C7 H6 O2 (ETR-Bz), etoricoxib-4-fluorobenzoic acid (1/1), C18 H15 ClN2 O2 S·C7 H5 FO2 (ETR-PFB), and etoricoxib-4-nitrobenzoic acid (1/1), C18 H15 ClN2 O2 S·C7 H5 NO4 (ETR-PNB). Powder X-ray diffraction and thermal differential scanning calorimetry-thermogravimetry (DSC-TG) techniques were also used to characterize these multicomponent systems. Due to the influence of the corresponding acids, ETR shows different conformations. Furthermore, the energetic contributions of the supramolecular motifs have been established by energy framework studies of the stabilizing interaction forces and are consistent with the thermal stability of the cocrystals.- Published
- 2024
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