azintamide

The commonly used industrial method is as follows: using 3,6-dichloropyridazine (2) as the starting material, after thiol substitution and acidification, it is condensed with N,N-diethylchloroacetamide to obtain 1. The extraction process using benzene is eliminated in the synthesis process, with a total yield of 40.5% and a purity of over 99.0%. This method has a simple route, readily available raw materials, and is suitable for large-scale production. Figure 2 Synthetic route of azintamide

Azintamide,Bristhar Laboratorios

ChEBI: Azintamide is an aryl sulfide.

7.3 parts of 3-chloro-6-mercaptopyridazine are neutralised with 20 parts of 10% caustic soda solution, diluted with 60 parts of 50% ethanol, and heated to 60°C. 7.5 parts of chloroacetic acid diethyl amide dissolved in 20 parts of ethanol are added to this solution over a period of 10 min and the resulting mixture is heated to 60°C for 30 min. The reaction solution is then cooled, the resulting crystallisate is removed by suction, and the filtrate is extracted with ethyl acetate. The solvent is removed by evaporation and the concentration residue is combined with the crystallisate. After two recrystallisations from benzene, 11 parts of 3-chloro-pyridazine-6-mercaptoacetic acid diethyl amide, having a melting point of from 139° to 140°C are yielded.

Choleretic