Two Novel Potential Anticonvulsant Salts of 5-Amino-2-Sulfonamide-1,3,4-Thiadiazole

Abstract

Two crystal structures of sulfonamide salts were studied by X-Ray diffraction. The compound C2H5N4O2S2 +·H2O·Cl− (I), (Hats·H2O·Cl, Hats = protonated 5-amino-2-sulfonamide-1,3,4-thiadiazole) crystallizes in orthorhombic space group, P212121, with unit cell parameters a = 10.047(4), b = 5.186(2), c = 16.766(6) A and the compound C2H5N4O2S2 +·CH3O3S− (II), crystallizes in monoclinic space group, Cc, with unit cell parameters a = 5.378(3), b = 19.707(6), c = 10.014(5) A, beta = 99.97(1)°. The molecules in compound I are arranged in a helix of alternating water and Hats molecules. Helixes are interconnected by hydrogen bonds provided by Cl− ions and one ring with a graph set R 6 4 (12) is determined. The crystal structure of compound II presents mesylate and Hats molecules bonded by two hydrogen bond determining a ring with a graph set R 2 2 (8). Two substituted sulfonamide salts were obtained, the hydrochloride is monohydrate and develops a helix arrangement of alternating water/sulfonamide molecules, meanwhile the mesylate is bonded to sulfonamide molecule determining a ring, with a graph set R 2 2 (8).