The solid-state structures of (-)-scopolamine free base, (-)-scopolamine methobromide, (-)-scopolamine hydrobromide trihydrate, and of the pseudopolymorphic forms of (-)-scopolamine hydrochloride anhydrate and 1.66hydrate
R. Glaser et al., The solid-state structures of (-)-scopolamine free base, (-)-scopolamine methobromide, (-)-scopolamine hydrobromide trihydrate, and of the pseudopolymorphic forms of (-)-scopolamine hydrochloride anhydrate and 1.66hydrate, CAN J CHEM, 78(2), 2000, pp. 212-223
Citations number
29
Categorie Soggetti
Chemistry
Journal title
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE
(-)-Scopolamine hydrochloride anhydrate gives crystals belonging to the ort
horhombic space group P2(1)2(1)2(1) and at 293(2) K: a = 7.097(2), b = 10.6
86(2), c = 22.623(2) Angstrom, V = 1715.7(6) Angstrom(3), Z = 4, R(F) = 0.0
39, and R-w(F) = 0.053. (-)-Scopolamine hydrochloride 1.66hydrate yields cr
ystals belonging to the tetragonal space group P4(3)2(1)2 and at 293(2) K:
a = b = 11.843(6), c = 26.211(4) +, V = 3676(3) Angstrom(3), Z = 8, R(F) =
0.047, and R-w(F-2) = 0.135. (-)-Scopolamine methobromide affords crystals
belonging to the orthorhombic space group P2(1)2(1)2(1) and at 293(2) K: a
= 7.0403(8), b = 10.926(2), c = 23.364(5) +, V = 1797.2(6) Angstrom(3), Z =
4, R(F) = 0.039, and R-w(F) = 0.052. The two hydrochloride pseudopolymorph
s were isostructural to the corresponding two hydrobromide analogues. Both
hydrohalide hydrated crystals have a water molecule occupying a general pos
ition of symmetry, and another water molecule occupying a special position
of C-2-rotation symmetry. The hydrated hydrochloride salt also had an addit
ional 0.322(17) partial occupancy water molecule (absent in the hydrobromid
e sesquihydrate) occupying another special position of C-2-rotation symmetr
y, i.e., the extra water molecule occupied the special position in statisti
cally ca. one-third of the unit-cells to give a total hydrate stoichiometry
of 1.66 molecules of water. While the two hydrohalide anhydrates exhibited
extended tropate ester conformations (phenyl-ring antiperiplanar to oxiran
e moiety) vs. compact conformations (phenyl-ring near the scopine underside
) for the two hydrated hydrohalides, all four displayed other common struct
ural features: axial N-methyl stereochemistry, antiperiplanar methylol oxyg
en/aromatic C(ipso) relationships, and phenyl-ring eclipsing of the C(alpha
)-H bond. The CPMAS C-13 NMR spectrum of (-)-scopolamine hydrobromide "trih
ydrate" shows it to be a conglomerate of (-)-scopolamine hydrobromide sesqu
ihydrate plus two or more hydrated species (three ca. equal intensity carbo
nyl signals at 5.0 kHz spin-rate). High-speed rotor spinning (e.g., ca. 10
kHz and higher) causes a temperature-induced phase-transition to yield only
the sesquihydrate form. The same transformation was noted with a 18 K roto
r-temperature increase and an invariant 5.0 kHz spin-rate. The sesquihydrat
e spectrum remained after spin-rate decrease to 5.0 kHz, but the three comp
onent mixture 5.0 kHz spectrum was regenerated after three weeks sample sto
rage within the capped rotor. The (-)-scopolamine free base crystalline mel
t CPMAS spectrum also shows a mixture of at least three hydrated species.