| abstract |
This invention relates to heterocyclic compounds. The goal is to identify more active compounds. The process is carried out by a two-step synthesis, from M- (4-chlorophenyl) -2- (benzo-2.1.3-thiadiazole-4-sulfonyl) amino} 5-chlorobenzoic acid, which is converted into the acid chloride, followed by treatment of the resulting product 4- chloroaniline in dichloroethane in the presence of triethylamine. A new drug at a dose of 100 mg / kg in a group dacha with fodder in a hemogenic farm, bunostomosis, nematodirosis. haberthioe and trichocephalosis showed 100% efficacy. 4 tab. w ё |