Novel pseudopolymorph of the active metabolite of perindopril

The dimethyl sulfoxide hemisolvate of perindoprilat [systematic name: (1S)‐2‐((S)‐{1‐[(2S,3aS,7aS)‐2‐carboxyoctahydro‐1H‐indol‐1‐yl]‐1‐oxopropan‐2‐yl}azaniumyl)pentanoate dimethyl sulfoxide hemisolvate], C17H28N2O5·0.5C2H6OS, an active metabolite of perindopril, has been synthesized, structurally ch...

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Veröffentlicht in:Acta crystallographica. Section C, Crystal structure communications Crystal structure communications, 2012-09, Vol.68 (9), p.o341-o343
Hauptverfasser: Bojarska, Joanna, Maniukiewicz, Waldemar, Sieroń, Lesław, Fruziński, Andrzej, Kopczacki, Piotr, Walczyński, Krzysztof, Remko, Milan
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Sprache:eng
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Zusammenfassung:The dimethyl sulfoxide hemisolvate of perindoprilat [systematic name: (1S)‐2‐((S)‐{1‐[(2S,3aS,7aS)‐2‐carboxyoctahydro‐1H‐indol‐1‐yl]‐1‐oxopropan‐2‐yl}azaniumyl)pentanoate dimethyl sulfoxide hemisolvate], C17H28N2O5·0.5C2H6OS, an active metabolite of perindopril, has been synthesized, structurally characterized by single‐crystal X‐ray diffraction and compared with its ethanol disolvate analogue [Pascard et al. (1991). J. Med. Chem.34, 663–669]. Both compounds crystallize in the orthorhombic P212121 space group in the same zwitterionic form, with a protonated alanine N atom and an anionic carboxylate group at the n‐alkyl chain. The three structural units present in the unit cell (two zwitterions and the solvent molecule) are held together by a rich system of O—H...O, N—H...O and C—H...O hydrogen‐bond contacts.
ISSN:0108-2701
1600-5759
DOI:10.1107/S0108270112032349