Publication Date:
1992-04-01
Description:
C20H28NS+.Cl−, 2-(diethylamino)ethyl 1,1-diphenylethyl sulfide hydrochloride (thiodeacylaprophen hydrochloride), Mr = 349.9, orthorhombic, P212121, a = 8.933 (2), b = 11.710 (3), c = 18.934 (4) Å, V= 1980.6 (7) Å3, Z = 4, Dx = 1.173 g cm−3, Cu Kα = 1.54178 Å, μ = 26.70 cm−1, F(000) = 752, room temperature, final R = 4.1% for 1417 reflections with mid F_o mid 〉 3 sigma (F). Thiodeacylaprophen crystallized as a tertiary amine hydrochloride salt. The S—C—C—N+ segment adopts a trans configuration as does one of the Cphenyl—C—S—C segments. A comparison of the structure of thiodeacylaprophen with the crystal structures of potent antimuscarinic agents suggests that the relatively weak antimuscarinic activity of thiodeacylaprophen compared to atropine and aprophen may be substantially due to the short intramolecular ScdotsN+ distance of 4.106 (6) Å. Other contributing structural factors may include the direction of the N+—H bond and restricted accessibility of the sulfur atom for interatomic interactions.
Print ISSN:
0108-7681
Electronic ISSN:
1600-5740
Topics:
Chemistry and Pharmacology
,
Geosciences
,
Physics
Permalink