Abstract:
The present invention relates to pyrimidin-4-ylmethyl-sulfonamides of formula (I) wherein Ra, n, R, A, Y and Het are as defined in the claims and to the N-oxides, and salts thereof and their use for combating harmful fungi, and also to compositions and seed comprising at least one such compound. The invention also relates to a process for preparing these compounds.
Abstract:
The present invention relates to novel pyridylmethyl-sulfonamide compounds of formula (I) where: n is 0 to 4; m is 0 to 4; R1 is halogen, CN, NO2, OH, SH, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, etc.; and/or two radicals R1 together form a fused ring; R2 is H, C1-C4-alkyl, C1-C4-haloalkyl, C2-C4-alkenyl, C2-C4-alkynyl, C3-C8-cycloalkyl, C1-C4-alkyl-C3-C8-cycloalkyl or benzyl; R3 is halogen, CN, NO2, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C4-haloalkoxy; Y is -O-, C1-C4-alkane- diyl, -O-CH2-, -CH2-O-, -C(NOR')-, -S-, -S(=0)-, -Sf=O)2- or -N(R')-; and the N-oxides, and salts thereof and their use for combating phytopathogenic harmful fungi, and also to compositions and seed comprising at least one such compound.
Abstract:
Azolopyrimidines of the formula (I), wherein the symbols have the meanings provided in the description, are suited to fight plant pathogenic fungi.
Abstract:
The invention relates to 2-(2-pyridyl)-5-phenyl-6-aminopyrimidines of formula I, wherein the substitutes and the index have the following meaning: R1 represents halogen, hydroxy, hyano, hxo, nitro, amino, mercapto, alkyl, halogenalkyl, alkenyl, alkinyl, cycloalkyl, alkoxy, halogenalkoxy, carboxyl, alkoxycarbonyl, carbamoyl, alkylaminocarbonyl, dialkylamincarbonyl, morpholinocarbonyl, pyrrolidinocarbonyl, alkylcarbonylamino, alkylamino, dialkylamino, alkylthio, alkylsulfinyl, alkylsulfonyl, hydroxysulfonyl, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl; m = 0 or 1 - 4; R2 represents hydrogen, halogen, cyano, alkyl, halogenalkyl or alkoxy; R3, R4 represents hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, alkinyl, halogenalkinyl or cycloalkinyl, R3 and R4 together with the nitrogen atom to which they are connected, form a five or six-membered ring which is interrupted by an atom from the group O, N or S and/or can be substituted according to the description; R5 represents halogen, alkyl or halogenalkyl; R6 represents hydrogen or one of the known groups in R5; R7, R8 represent hydrogen, halogen, alkyl or halogenalkyl; R9 represents hydrogen, halogen, hydroxy, cyano, alkyl, alkoxy, cycloalkoxy, halogenalkoxy, alkoxycarbonyl or alkylaminocarbonyl. The invention also relates to a method and intermediate product for the production of said compound in addition to the use thereof for combating undesirable plants.
Abstract:
The invention relates to 2-(pyridin-2-yl)-pyrimidines of formula (I) and their use in the control of parasitic fungi and to herbicides that contain said compounds as an effective ingredient thereof. In formula (I), Q represents a condensed, saturated five-, six- or seven-membered carbocycle or five-, six- or seven-membered heterocycle which, in addition to the carbon ring members, has one or two heteroatoms selected from oxygen and sulfur as the ring members, the carbocycle and the heterocycle being unsubstituted or having 1, 2, 3 or 4 C1-C4 alkyl groups as the substituents; R1 represents hydrogen, OH, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy or halogen; R2 represents hydrogen, NO2, halogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 halogenalkyl or C1-C6 halogenalkoxy; R3 represents hydrogen, halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl or C1-C4 halogenalkoxy; R4 has phenyl, 5-membered heteroaryl which has 1, 2, 3 or 4 nitrogen atoms or 1 heteroatom selected from oxygen and sulfur and optionally 1, 2 or 3 nitrogen atoms as the ring atoms, or 6-membered hetaryl, which has 1, 2, 3 or 4 nitrogen atoms as the ring members, wherein phenyl, 5- and 6-membered hetaryl may have 1, 2, 3 or 4 substituents Ra.
Abstract:
The invention relates to 5-methyl-6-phenyl-triazolopyrimidinyl amines of formula (I) wherein the substituents have the designations cited in the description. The invention also relates to methods for producing said compounds, to agents containing the same, and to the use thereof for controlling plant pathogenic fungi.
Abstract:
The invention relates to 6-(2-halogen-4-alcoxyphenyl)-triazolopyrimidine of formula (I), wherein substituents have the following significance: R1 is alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalcenyl, cycloalkenyl, halogenocycloalkenyl, alkynyl, halogenoalkynyl, cycloalkynyl, halogencycloalkynyl or phenyl, naphthyl or a type of heterocycle having from 5 to 6 saturated, partially saturated or aromatic chains containing one or four heteroatoms of a O, N and S group; R2 is hydrogen or one of groups mentioned in R1, R1 and R2 can also form together with a nitrogen atom to which they are linked a 5 or 6-links heterocycle or a heteroaryl which is linked by N and can contain from one to three other heteroatoms of the O, N and S group in the form of a ring link; R3 is alkyl, halogenalkyl, alcenyl, halogenalcenyl, alcynyl, halogenoalkynyl, phenylalkyl, mono or dialcoxyalkyl; R1, R2 and/or R3 can be substituted according to a description; L is hydrogen, fluoride or chlorine; x is cyano, alkyl, alkoxy, alkenyloxy, halogenalkoxy or halogenalkenyloxy;. A method for producing said compounds, the agents containing said compounds and the use thereof against phytopathogenic harmful fungus are also disclosed.