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Crystal structure of a 2:1 piroxicam–gentisic acid co-crystal featuring neutral and zwitterionic piroxicam molecules
A new 2:1 co-crystal of piroxicam and gentisic acid [systematic name: 4-hydroxy-1,1-dioxo-N-(pyridin-2-yl)-2H-1λ(6),2-benzothiazine-3-carboxamide–2-(4-oxido-1,1-dioxo-2H-1λ(6),2-benzothiazine-3-amido)pyridin-1-ium–2,5-dihydroxybenzoic acid, 2C(15)H(13)N(3)O(4)S·C(7)H(6)O(4)] has been synthes...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137592/ https://www.ncbi.nlm.nih.gov/pubmed/27980814 http://dx.doi.org/10.1107/S2056989016017321 |
Sumario: | A new 2:1 co-crystal of piroxicam and gentisic acid [systematic name: 4-hydroxy-1,1-dioxo-N-(pyridin-2-yl)-2H-1λ(6),2-benzothiazine-3-carboxamide–2-(4-oxido-1,1-dioxo-2H-1λ(6),2-benzothiazine-3-amido)pyridin-1-ium–2,5-dihydroxybenzoic acid, 2C(15)H(13)N(3)O(4)S·C(7)H(6)O(4)] has been synthesized using a microfluidic platform and initially identified using Raman spectroscopy. In the co-crystal, one piroxicam molecule is in its neutral form and an intramolecular O—H⋯O hydrogen bond is observed. The other piroxicam molecule is zwitterionic (proton transfer from the OH group to the pyridine N atom) and two intramolecular N—H⋯O hydrogen bonds occur. The gentisic acid molecule shows whole-molecule disorder over two sets of sites in a 0.809 (2):0.191 (2) ratio. In the crystal, extensive hydrogen bonding between the components forms layers propagating in the ab plane. |
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