Abstract
Condensation of quinaldine with seven kinds of aromatic primary amines in the presence of sulfur was carried out at an elevated temperature. With the exception of p-phenetidine and p-isopropoxyaniline, which yielded only the corresponding thioanilides, these amines gave N-(2-quinolinecarbothionoyl) anilines and also 2-(2-quinolyl) benzothiazoles, without much difference in the yield. The results of microbiological screening will be reported elsewhere in due course.
