The invention relates to triazolopyrimidines of formula (I), in which the
substituents are defined as follows: L.sup.1 represents cyano,
S(.dbd.O).sub.nA.sup.1 or C(.dbd.O)A.sup.2, wherein A.sup.1 stands for
hydrogen, hydroxy, alkyl, alkylamino or dialkylamino; A.sup.2 stands for
C.sub.1 C.sub.8 alkoxy, C.sub.1 C.sub.6 haloalkoxy or one of the groups
named in A.sup.1; and n stands for 0, 1 or 2; L.sup.2, L.sup.3 represent
hydrogen or halogen; L.sup.4, L.sup.5 represent hydrogen, halogen or
alkyl; X represents halogen, cyano, alkyl, haloalkyl, alkoxy or
haloalkoxy; R.sup.1 represents alkyl, haloalkyl, cycloalkyl,
halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, alkynyl,
haloalkynyl or cycloalkynyl, phenyl, naphthyl, or a five to ten-membered
saturated, partially unsaturated or aromatic heterocyclus containing
between one and four heteroatoms from the group containing O, N or S;
R.sup.2 represents hydrogen or R.sup.1; R.sup.1 and R.sup.2 can form,
together with the nitrogen atom to which they are bonded, a five or
six-membered ring, which can be interrupted and/or substituted by an atom
from the group O, N and S; whereby R.sup.1 and/or R.sup.2 can be
substituted in accordance with the description. The invention also
relates to methods and intermediate products for producing said
compounds, to agents containing the latter and to the use of said
compounds for combating harmful fungi. ##STR00001##