Abstract:
Substituted sulphonyl ureas have the general formula (I), in which n and m equal 0 or 1 and the substituents have the following meaning: R1 is hydrogen, alkyl, alkenyl or alkinyl; R2 is halogen or trifluoromethyl, when m equals 0 or, when m equals 1, R2 is alkyl, alkenyl or alkinyl, and when X stands for O or S and m equals 1, trifluoromethyl or chlorodifluoromethyl; X is O, S or N-R4, whereas R4 is hydrogen or alkyl; R3 is hydrogen, halogen, alkyl, halogenalkyl, alkoxy or halogenalkoxy; A is NO¿2?, NH2, OH, CN, SCN, S(O)oR?5, SO¿2NR?6R7, ER7¿, whereas E stands for O, S or NR9, the groups (a), (b) possibly substituted C¿1?-C4-alkyl or C2-C4-alkenyl; R?5¿ is a possibly substituted alkyl group, a possibly substituted cycloalkyl group, an alkenyl group or an alkinyl group; R6 is hydrogen, an alkoxy group, an alkyl group, or represents together with R7 a C4-C6-alkylene chain, wherein a methylene group may be substituted by an oxygen atom or a C1-C4-alkylimino group; R7 is a possibly substituted alkyl, alkenyl or alkinyl group, a cycloalkyl group and may also represent, when E = NR9, methyl sulphone, trifluoromethyl sulphone, ethylsulphone, possibly halogen-substituted acetyl, dimethylcarbamoyl, dimethylsulphamoyl; o equals 0, 1 or 2; p, q equal 0 and/or 1 (when p = 0, q = 0); R8 is hydrogen or halogen; R9 is hydrogen, methyl, ethyl; R10 is alkyl, halogenalkyl, alkoxyalkyl, alkenyl, cycloalkyl, halogenalkenyl or, when p = 1 and q = 0, it may also be alkylamino or dialkylamino. Also disclosed are their environmentally compatible salts, a process and intermediates for producing the compounds having the formula (I) and their use as herbicides.
Abstract:
Ovaj se izum odnosi na monoklinski 2-kloro-N-(4'-klorobifenil-2-yl)nikotinamid formule I, tališta na 147 - 148°C, kao i na postupak njegovog pripravljanja.
Abstract:
The invention concerns a method for producing 2-halogen-pyridine-carboxylic acid amides of primary aromatic monoamines I which include, in ortho position relative to the amino group, a different hydrogen substituent, by reacting 2-halogen-pyridine-carboxylic acid chloride II with the aromatic monoamine I. The inventive method is characterized in that it consists in carrying out the reaction in a solvent mixture consisting of at least an organic solvent non-miscible with water, the mixture containing or not containing less than 10 mole %, relative to the 2-halogen-pyridine-carboxylic acid chloride II, a base different from I and II.
Abstract:
Monoclinic boscalide (2-chloro-N-(4'-chloro-2-biphenylyl)-nicotinamide) crystal modification (modification II) with a m. pt. of 147-148[deg]C, is new. An independent claim is also included for a preparation of modification II. ACTIVITY : Herbicide. No agricultural data is given. MECHANISM OF ACTION : None given.
Abstract:
Monoclinic boscalide (2-chloro-N-(4'-chloro-2-biphenylyl)-nicotinamide) crystal modification (modification II) with a m. pt. of 147-148[deg]C, is new. An independent claim is also included for a preparation of modification II. ACTIVITY : Herbicide. No agricultural data is given. MECHANISM OF ACTION : None given.
Abstract:
Monoclinic boscalide (2-chloro-N-(4'-chloro-2-biphenylyl)-nicotinamide) crystal modification (modification II) with a m. pt. of 147-148[deg]C, is new. An independent claim is also included for a preparation of modification II. ACTIVITY : Herbicide. No agricultural data is given. MECHANISM OF ACTION : None given.