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[C-alkylpiperazines. XII. Synthesis and diuretic activity of compounds structurally related to clopamide]
L Landriani1, D Barlocco, G Cignarella
1Istituto Chimico Farmaceutico e Tossicologico, Università di Milano.
Abstract:
The synthesis and diuretic activity were reported of a series of N1-(4-chloro-3-sulfamoylbenzamide)-N4-alkylpiperazines, 2-methyl- and cis-2,6-dimethyl substituted, structurally related to clopamide, as well as of two N4-alkyl-N1-(4-chloro-3-sulfamoylbenzoyl)-2-methyl-1,2,3, 4-tetrahydroquinoxalines. In the piperazine series the presence of methyl group in position 2 and 6 of the piperazinic ring was found to increase the diuretic potency of the C-unmethylated compound.