Antimykotische wirkstoffe. XXI. Aliphatisch und alicyclisch substituierte chlor-diallylamino-1l,3,5-triazine

By nucleophilic substitution of one chlorine atom in 2,4-dichloro-6-(diallylamino)-1,3,5-triazine(1) by amines 2a-g, the alkylamino and cycloalkylamino-chloro-(diallylamino)-1,3,5-triazines 3a-g are obtained. Typical spectroscopic singals of structure type 3 are the ir-band at 800 cm^μ caused by the 1,3,5-triazine ring, the four ¹ nmr signals between 4.1-6.1 ppm to be assigned to the allyl groups, and the mass s[ectrpscopic peak of the ring cation m/e 158. Representatives of compound class 3 exhibit marked antimycotic, trichomonacidal, and herbicidal activity.