Solid-State Stereochemistry of (−)-Scopolamine Hydrobromide Sesquihydrate, a New Polymorph of the Anticholinergic Drug

Abstract

The solid-state structure of (−)-scopolamine hydrobromide sesquihydrate was determined by single-crystal X-ray diffraction analysis at low temperature. (Nr, Cα-S)-(−)-Scopolamine hydrobromide sesquihydrate gives crystals belonging to the tetragonal space groupP43212, and at 180 K:a= 11.870(4),c= 26.193(3) Å,V= 3691(1) Å3,Z= 8,R(F)= 0.062, andRw(F) = 0.059. Thermogravimetric analysis afforded a total weight loss of ∼6%, consistent with a loss of 1.5 molecules of water and in accord with the sesquihydrate stoichiometry found by single-crystal X-ray crystallography. The unit cell dimensions, molecular structure, basic packing arrangement [minus the full water molecule], and the crystal system are all the same as that of theP41212 hemihydrate from [R(F) = 0.09] reported earlier by Pauling and Petcher. This suggests that the previously reported “hemihydrate” description of the structure should be reconsidered. In addition to partial dehydration of the sesquihydrate crystal, non-observance of the eight water molecules might have arisen from their relatively large thermal motions at ambient temperature coupled with a lack of sufficient data versus the number of variable parameters. The phenyl ring syn-to-oxirane arrangement in the sesquihydrate form is the same as that in the corresponding crystalline methyliodide quaternary ammonium salt and in (−)-(Ns, Cα-S)-hyoscyamine [atropine] hydrobromide, but differs from the elongated anti-to-oxirane arrangement in anhydrous (Nr, Cα-S)-(−)-scopolamine hydrobromide. TheUnited States Pharmacopoeia XXII Official Monographslist the trihydrate form for scopolamine hydrobromide, and states a maximum permissible 13% weight loss after drying at 105 °C for 3 h, although no lower limits for weight loss are given. Because the melting point range, specific rotation, and IR spectrum are all performed on predried anhydrous samples, the theoretical weight loss from anhydrous, hemihydrate, sesquihydrate, and trihydrate polymorphs all fall within the permissible limit.