| 摘要 |
Triazolopyrimidines of formula (I),in which the substituents are defined as follows:Lrepresents cyano, S(=O)Aor C(=O)A, wherein Astands for hydrogen, hydroxy, C-Calkyl, C-Calkylamino or di-( C-Calkyl)amino; Astands for C-Calkoxy, C-Chaloalkoxy or one of the groups named in A; and n stands for 0, 1 or 2;L, Lrepresent hydrogen or halogen; L, Lrepresent hydrogen, halogen or C-Calkyl;X represents halogen, cyano, C-Calkyl, C-Chaloalkyl, C-Calkoxy or C-Chaloalkoxy;Rrepresents C-Calkyl, C-Chaloalkyl, C-Ccycloalkyl, C-Chalocycloalkyl, C-Calkenyl, C-Calkadienyl, C-Chaloalkenyl, C-Ccycloalkenyl, C-Calkynyl, C-Chaloalkynyl or C-Ccycloalkynyl, 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;Rrepresents hydrogen or R;Rand Rcan 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 Rand/or Rcan 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. |
