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Hydro­chloro­thia­zide N , N ‐dimethyl­acetamide disolvate
Author(s) -
Johnston Andrea,
Kennedy Alan R.,
Florence Alastair J.
Publication year - 2006
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536806022859
Subject(s) - dimethylacetamide , hydrochlorothiazide , chemistry , benzothiadiazine , solvent , medicinal chemistry , molecule , sulfonamide , hydrogen bond , stereochemistry , organic chemistry , medicine , blood pressure
Hydro­chloro­thia­zide forms a 1:2 solvate with N , N ‐dimethyl­acetamide (systematic name: 6‐chloro‐3,4‐dihydro‐2 H ‐1,2,4‐benzothia­diazine‐7‐sulfonamide 1,1‐dioxide dimethyl­acet­amide disolvate), C 7 H 8 ClN 3 O 4 S 2 ·2C 4 H 9 NO. The compound crystallizes with one hydro­chorothia­zide and two disordered solvent mol­ecules in the asymmetric unit, with a hydrogen‐bonding network comprising four N—H⋯O contacts.

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