6-phenyl-7-amino-triazolopyrimidines, methods for the production thereof, the use thereof for controlling pathogenic fungi, and agents containing the same

The present invention relates to 6-phenyl-7-aminotriazolopyrimidines of the formula I, in which the substituents are as defined below: R is hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl,haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle, which comprises one to four heteroatoms from the group consisting of O, N and S, R is alkyl, haloalkyl,cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which comprises one to four heteroatoms from the group consisting of O, N and S, R ,R ,R ,R ,R are hydrogen or one of the groups mentioned under R , and R with R , R with R , R with R may in each case together, with formation of carbonyl groups, also be oxygen and, with formation of spiro groups, form a C2-C5-alkylene, or alkenylene or alkynylene chain which may be interrupted by one to three heteroatoms from the group consisting of O, N and S; p is zero or 1; L is halogen, alkyl, haloalkyl, alkoxy, cyano, nitro, amino, alkylamino, di-alkylamino, alkylcarbonylamino, C(O)-R, S(O)n-R; n is zero, 1 or 2; m is 1, 2, 3, 4 or 5; X is halogen, cyano, alkyl, alkoxy, alkenyloxy, alkynyloxy or haloalkoxy, Y is oxygen or sulfur; X is hydrogen, alkyl, haloalkyl, cycloalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, cycloalkylcarbonyl, alkenyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl, cycloalkoxycarbonyl, cycloalkenyloxycarbonyl, alkylsulfinyl,alkylthio, alkylsulfonyl, phenyl, naphthyl, a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which comprises one to four heteroatoms from the group consisting of O, N and S.