WO2000047585A1 - Herbicides nouveaux derives de 3-hydroxy-4-aryle-5-pyrazoline en tant qu'herbicides - Google Patents

Herbicides nouveaux derives de 3-hydroxy-4-aryle-5-pyrazoline en tant qu'herbicides Download PDF

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WO2000047585A1
WO2000047585A1 PCT/EP1999/000898 EP9900898W WO0047585A1 WO 2000047585 A1 WO2000047585 A1 WO 2000047585A1 EP 9900898 W EP9900898 W EP 9900898W WO 0047585 A1 WO0047585 A1 WO 0047585A1
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alkyl
hydrogen
halogen
formula
substituted
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PCT/EP1999/000898
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English (en)
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Michel Mühlebach
Jutta Glock
Thomas Maetzke
André Stoller
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Novartis Ag
Novartis-Erfindungen Verwaltungsgesellschaft M.B.H.
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Priority to PCT/EP1999/000898 priority Critical patent/WO2000047585A1/fr
Priority to AU26233/99A priority patent/AU2623399A/en
Publication of WO2000047585A1 publication Critical patent/WO2000047585A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/08—Bridged systems

Definitions

  • the present invention relates to novel herbicidally active 3-hydroxy-4-aryl-5-oxopyrazoline derivatives, to processes for their preparation, to compositions which comprise these compounds and may additionally comprise safeners, and to the use of these compounds as herbicides for controlling weeds and grasses, in particular in crops of useful plants.
  • R ⁇ , R 2 and R 3 independently of one another are halogen, nitro, cyano, C C 4 alkyl, C 2 - C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 2 -C 6 haloalkenyl, C 3 -C 6 cycloalkyl, halogen- substituted C 3 -C 6 cycloalkyl, d-Cealkoxyalkyl, C C 6 alkylthioalkyl, hydroxyl, mercapto, C r C 6 alkoxy, C 3 -C 6 alkenyloxy, C 3 -C 6 alkynyloxy, CrC 4 alkylcarbonyl, C ⁇ -C 4 alkoxycarbonyl, C C 4 alkylthio, CrC 4 alkylsulfinyl, C C alkylsulfonyl, amino, C r C alkyiamino or di(C r
  • R25, 26, R27, R28, and R 29 independently of one another are hydrogen, halogen, C C alkyl or C C 4 haloalkyl where an alkylene ring, which together with the carbon atoms of the groups Z 1( Z 2 or Z 3 contains 2 to 6 carbon atoms and may be interrupted by oxygen, may either be fused or spiro-linked to the carbon atoms of the groups Z ⁇ , Z 2 or Z 3 , or where this alkylene ring bridges at least one ring atom of the groups Z ⁇ , Z 2 or Z 3 ;
  • G is hydrogen, -C(X ⁇ )-R 30 , -C(X 2 )-X 3 -R 3 ⁇ , -C(X 4 )-N(R 3 2)-R 33 , -SO 2 -R 3 , an alkali metal, alkaline earth metal, sulfonium or ammonium cation or -P(Xs)( 35)-R36;
  • Xi hal
  • halogen is to be understood as meaning fluorine, chlorine, bromine and iodine, preferably fluorine, chlorine and bromine.
  • the alkyl groups in the definitions of the substituents are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl or tert-butyl, and the isomeric pentyls and hexyls.
  • Suitable cycloalkyl substituents contain 3 to 6 carbon atoms and are, for example, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
  • Alkenyl is to be understood as meaning, for example, vinyl, allyl, methallyl, 1 -methylvinyl or but-2-en-1-yl.
  • Alkynyl is, for example, ethinyl, propargyl, but-2-in- 1-yl, 2-methylbutin-2-yl or but-3-in-2-yl.
  • Haloalkyl groups preferably have a chain length of 1 to 4 carbon atoms.
  • Haloalkyl is, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2- chloroethyl, pentafluoroethyl, 1 J-difiuoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl and 2,2,2-trichloroethyl; preferably trichloromethyl, difluorochloromethyl, difluoromethyl, trifluoromethyl and dichlorofluoromethyl.
  • Suitable haloalkenyls are alkenyl groups which are mono- or polysubstituted by halogen, halogen being fluorine, chlorine, bromine and iodine and in particular fluorine and chlorine, for example 2,2-difluoro-1 -methylvinyl, 3- fluoropropenyl, 3-chloropropenyl, 3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3- trichloropropenyl and 4,4,4-trifluorobut-2-en-1-yl.
  • halogen being fluorine, chlorine, bromine and iodine and in particular fluorine and chlorine, for example 2,2-difluoro-1 -methylvinyl, 3- fluoropropenyl, 3-chloropropenyl, 3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3- trichloropropenyl and 4,4,4-trifluor
  • Alkoxy groups preferably have a chain length of 1 to 6 carbon atoms.
  • Alkoxy is, for example, methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, isobutoxy, sec- butoxy and tert-butoxy, and the isomeric pentyloxy and hexyloxy radicals; preferably methoxy and ethoxy.
  • Alkylcarbonyl is preferably acetyl or propionyl.
  • Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n- butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferably methoxycarbonyl or ethoxycarbonyl.
  • Alkylthio groups preferably have a chain length of 1 to
  • Alkylthio is, for example, methylthio, ethylthio, propylthio, isopropylthio, n- butylthio, isobutylthio, sec-butylthio or tert-butylthio, preferably methylthio and ethylthio.
  • Alkylsulfinyl is, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, n- butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl, tert-butylsulfinyl; preferably methylsulfinyl and ethylsulfinyl.
  • Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl or tert-butyisulfonyl; preferably methylsulfonyl or ethylsulfonyl.
  • Alkylamino is, for example, methylamino, ethylamino, n-propylamino, isopropylamino or the isomeric butylamines.
  • Dialkylamino is, for example, dimethylamino, methylethylamino, diethylamino, n-propylmethylamino, dibutyiamino and diisopropylamino.
  • Alkoxyalkyl groups preferably have 1 to 6 carbon atoms.
  • Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl or isopropoxyethyl.
  • Alkylthioalkyl is, for example, methylthiomethyl, methylthioethyl, ethylthiomethyl, ethylthioethyl, n-propylthiomethyl, n-propylthioethyl, isopropylthiomethyl, isopropylthioethyl, butylthiomethyl, butylthioethyl or butylthiobutyl.
  • Phenyl may be substituted.
  • the substituents may be in the ortho, meta and/or para position. The substituents are preferably located in the positions ortho and para to the site where the ring is attached.
  • halogen, alkyl, cycloalkyl, alkoxy, alkylthio, alkylcarbonyl, alkylsulfonyl and (di)alkylamino radicals which may be present in the radicals R 3 , in particular -SO ⁇ M (G), are derived from the corresponding radicals mentioned above.
  • Preferred heterocyclyl radicals are those containing 1 or 2 heteroatoms, for example N, S or O. They are usually saturated.
  • Heteroaryl radicals are customarily aromatic heterocycles which preferably contain 1 to 3 heteroatoms, such as N, S and O.
  • heterocycles and heteroaromatics examples include: pyrrolidine, piperidine, pyran, dioxane, azetidine, oxetan, pyridine, pyrimidine, triazine, thiazole, thiadiazole, imidazole, oxazole, isoxazole and pyrazine, furan, morpholine, piperazine, pyrazole, benzoxazole, benzothiazole, quinoxaline and quinoline.
  • heterocycles and heteroaromatics may also be substituted, for example by halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, nitro, cyano, thioalkyl, alkylamino or phenyl.
  • the C 2 - C 20 alkenyl and alkynyl groups R 34 may be mono- or polyunsaturated. They preferably contain 2 to 12, in particular 2 to 6, carbon atoms.
  • suitable groups -SO 2 R 34 are given in the example below:
  • Alkali metal cations, alkaline earth metal cations or ammonium cations for the substituent G are, for example, the cations of sodium, potassium, magnesium, calcium and ammonium.
  • Preferred sulfonium cations are, in particular, trialkylsulfonium cations, where the alkyl radicals each preferably contain 1 to 4 carbon atoms.
  • the free valency on the left hand of the groups Z-i, Z 2 and Z 3 is linked to the 1 -position and the free valency on the right hand is linked to the 2-position of the pyrazoline ring.
  • R 4 and R 5 together are in particular a group
  • R28 and R g independently of one another are hydrogen, halogen, C ⁇ -C 4 alkyl or CrC haioalkyl, where an alkylene ring which, together with the carbon atoms of the groups Z , Z 2 and Z 3 , contains 3 to 6 carbon atoms may be fused or spiro-linked to the groups Z_, Z 2 and Z 3 .
  • R 4 and R 5 together form a group Z 2 .
  • R L R 2 and R 3 independently of one another are halogen, CrC 4 alkyl, C 2 -C 4 alkenyl, C 2 - C 4 alkynyl or d-C 6 -alkoxy.
  • R 2 is halogen, methyl, ethyl or ethinyl
  • R ⁇ and R 3 independently of one another are methyl, ethyl, isopropyl, vinyl, allyl, ethinyl, methoxy, ethoxy, bromine or chlorine.
  • G is the group -C(X ⁇ )-R 3 o or C(X 2 )-(X 3 )-R 31 in which X 1t X 2 and X 3 are, in particular, oxygen, and R 30 and R 31 independently of one another are preferably d- C 5 alkyl.
  • Another preferred group of compounds of the formula I is that where at least one ring atom of the groups Z Z 2 or Z 3 is bridged by an alkylene ring which, together with the carbon atoms of the groups Z ⁇ , Z 2 or Z 3 , contains 2 to 6 carbon atoms and may be interrupted by oxygen.
  • the invention also includes the salts which the compounds of the formula I can form with acids.
  • Suitable acids for forming the acid addition salts are both organic and inorganic acids. Examples of such acids are hydrochloric acid, hydrobromic acid, nitric acid, phosphoric acids, sulfuric acid, acetic acid, propionic acid, butyric acid, valeric acid, oxalic acid, malonic acid, fumaric acid, organic sulfonic acids, lactic acid, tartaric acid, citric acid and salicylic acid.
  • the salts of the compounds of the formula I with acidic hydrogen also include alkali metal salts, for example sodium salts and potassium salts; alkaline earth metal salts, for example calcium salts and magnesium salts; ammonium salts, i.e. unsubstituted ammonium salts and mono- or polysubstituted ammonium salts, and salts with other organic nitrogen bases.
  • suitable salt formers are alkali metal and alkaline earth metal hydroxides, in particular the hydroxides of lithium, sodium, potassium, magnesium or calcium, where those of sodium or potassium are particularly important.
  • amines which are suitable for forming ammonium salts are both ammonia and primary, secondary and tertiary CrCisalkylamines, d-C hydroxyalkylamines and C 2 - dalkoxyalkylamines, for example methylamine, ethylamine, n-propylamine, isopropylamine, the four isomeric butylamines, n-amylamine, isoamylamine, hexylamine, heptylamine, octylamine, nonylamine, decylamine, pentadecylamine, hexadecylamine, heptadecylamine, octadecylamine, methylethylamine, methylisopropylamine, methylhexylamine, methylnonylamine, methylpentadecylamine, methyloctadecylamine, ethylamine
  • the unsymmetrically substituted compounds of the formula I are generally obtained as racemates.
  • the stereoisomers can then be separated by known methods, such as fractional crystallization after salt formation with optically pure bases, acids or metal complexes, or else by chromatographic processes such as high pressure liquid chromatography (HPLC) on acetylcellulose, owing to their physicochemical properties.
  • HPLC high pressure liquid chromatography
  • the active compounds of the formula I are to be understood as meaning both the enriched and optically pure forms of the stereoisomers in question, and the racemates or diastereomers.
  • the compounds of the formula I may be present as geometrical and/or optical isomers and isomer mixtures, and also as tautomers and mixtures of tautomers. These compounds of the formula I likewise form part of the subject-matter of the present invention.
  • G is hydrogen may, for example, be present in the following tautomer equilibriums:
  • the compound of the formula I may be present as an isomer of the formula Id
  • Processes for preparing compounds which, with respect to the meaning of the substituents R and R 5 , are different from the compounds of the formula I according to the present invention are, for example, described in WO 96/21652.
  • the compounds of the formula I according to the present invention can be prepared by methods similar to the processes described in WO 96/21652.
  • the compounds of the formula II in which Ri, R 2 , R 3 , R 4 and R 5 are as defined under formula I and which are employed as starting materials for such processes can be prepared, for example, by reacting a compound of the formula III
  • R is CrCealkyl, d-C 6 haloalkyl, preferably methyl, ethyl or trichloroethyl, and Ri, R 2 and R 3 are as defined under formula I in an inert organic solvent, if appropriate in the presence of a base, with a compound of the formula IV or IVa
  • R 4 and R 5 are as defined under formula I.
  • Other preparation processes for compounds of the formula II are described, for example, in WO 92 16510 .
  • the compounds of the formula III are either known, or they can be prepared similarly to known processes. Processes for preparing compounds of the formula III and their reaction with hydrazines are described, for example, in WO 97/02243 .
  • Compounds of the formula III in which R is d-C 6 alkyl, CrC 6 haloalkyi, preferably methyl, ethyl or trichloroethyl, and R ( R 2 and R 3 are as defined under formula I can be prepared by methods known to the person skilled in the art.
  • compounds of the formula III in which R is CrC 6 alkyl, d- C 6 haloalkyl, preferably methyl, ethyl or trichloroethyl, and R 1 R 2 and R 3 independently of one another are d-C alkyl, C 2 -C alkenyl, C 2 -C 4 alkynyl
  • R 1 R 2 and R 3 independently of one another are d-C alkyl, C 2 -C alkenyl, C 2 -C 4 alkynyl
  • Stille J.K. Stille, Angew. Chem. 1986. 98, 504-519
  • Sonogashira K. Sonogashira et al., Tetrahedron Lett. 1975. 4467-4470
  • Suzuki N. Miyaura, A. Suzuki, Chem. Rev. 1995. 95, 2457-2483
  • Heck R.F. Heck, Org. React. 1982. 27, 345-390
  • the compounds of the formulae IV and IVa are either known, or they can be prepared by known processes. Processes for preparing compounds of the formula IV are described, for example, in WO 95/00521. These compounds can be prepared, for example, by heating a compound of the formula V
  • R 42 is hydrogen, C C 4 alkyl, CrC 6 alkoxy, C ⁇ -C 6 haloalkoxy, benzyloxy, preferably hydrogen, methyl, methoxy, ethoxy, trichloroethoxy, tert-butoxy or benzyloxy and R 4 and R 5 are as defined under formula I in the presence of a base or an acid in an inert solvent.
  • R 42 is hydrogen, C C 4 alkyl, d-C 6 alkoxy, C r C 6 haloalkoxy, benzyloxy, preferably hydrogen, methyl, methoxy, ethoxy, trichloroethoxy, tert-butoxy or benzyloxy in the presence of a base and an inert solvent with a compound of the formula VII
  • the free valencies of the groups Z ⁇ ,Z 2 and Z 3 are in each case attached to the group Y.
  • Compounds of the formula VI and VII are known, or they can be prepared by methods known to the person skilled in the art.
  • the end products of the formula I can be isolated in a customary manner by concentration and/or evaporation of the solvent and be purified by recrystallization or trituration of the solid residue in solvents in which they are not readily soluble, such as ethers, alkanes, aromatic hydrocarbons or chlorinated hydrocarbons, or by chromatography. Salts of compounds of the formula I can be prepared in a manner known per se. Such preparation methods are described, for example, in WO 96/21652.
  • the compounds of the formula I or compositions comprising them can be used according to the invention by all the application methods customary in agriculture, for example pre- emergence application, postemergence application and seed dressing, and various methods and techniques, for example controlled release of active compounds.
  • the active compound is absorbed in solution onto mineral granule carriers or polymerized granules (urea/formaldehyde) and dried. If appropriate, a coating which allows the active compound to be released in metered form over a certain period of time can additionally be applied (coated granules).
  • the compounds of the formula I can be employed as herbicides in unchanged form, i.e.
  • the formulations i.e. the compositions, formulations or preparations comprising the active compound of the formula I or at least one active compound of the formula I and as a rule one or more solid or liquid formulation auxiliaries, are prepared in a known manner, for example by intimate mixing and/or grinding of the active compounds with the formulation auxiliaries, for example solvents or solid carriers.
  • Surface-active compounds surfactants
  • solvents and solid carriers are given, for example, in WO 97/34485 on page 6.
  • suitable surface-active compounds are nonionic, cationic and/or anionic surfactants and surfactant mixtures having good emulsifying, dispersing and wetting properties.
  • anionic, nonionic and cationic surfactants examples include WO 97/34485 on pages 7 and 8.
  • compositions according to the invention containing a herbicidally effective amount of a compound of the formula I can be enhanced by addition of spray tank adjuvants.
  • adjuvants may be, for example: nonionic surfactants, mixtures of nonionic surfactants, mixtures of anionic surfactants with nonionic surfactants, cationic surfactants, organosilicon surfactants, mineral oil derivatives with and without surfactants, vegetable oil derivatives with and without addition of surfactants, alkylated derivatives of oils of vegetable or mineral origin with and without surfactants, fish oils and other oils of animal nature and their alkyl derivatives with and without surfactants, natural higher fatty acids, preferably having 8 to 28 carbon atoms, and their alkyl ester derivatives, organic acids which contain an aromatic ring system and one or more carboxylic esters, and their alkyl derivatives, furthermore suspensions of polymers of vinyl acetate or copolymers of vinyl acetate
  • Suitable nonionic surfactants are, for example, polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, saturated or unsaturated fatty acids and alkylphenols, preferably those which may contain 3 to 30 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon radical and 6 to 18 carbon atoms in the alkyl radical of the alkylphenols.
  • nonionic surfactants are the water-soluble polyethylene oxide adducts on polypropylene glycol, ethylenediaminopolypropylene glycol and alkylpolypropylene glycol preferably having 1 to 10 carbon atoms in the alkyl chain which preferably contain 20 to 250 ethylene glycol ether groups and 10 to 100 propylene glycol ether groups.
  • the abovementioned compounds generally contain 1 to 5 ethylene glycol units per propylene glycol unit.
  • nonionic surfactants which may be mentioned are nonylphenolpolyethoxyethanols, castor oil polyglycol ethers, polypropylene/polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethylene glycol and octylphenoxypolyethoxyethanol.
  • fatty esters of polyoxyethylene sorbitan for example polyoxyethylene sorbitan trioleate.
  • Preferred anionic surfactants are, in particular, alkyl sulfates, alkyl sulfonates, alkylaryl sulfonates, alkylated phosphoric acids and their ethoxylated derivatives.
  • the alkyl radicals usually contain 8 to 24 carbon atoms.
  • Preferred nonionic surfactants are known under the following trade names:
  • Polyoxyethylene cocoalkylamine for example AMIET 105 (Kao Co.)
  • polyoxyethylene oleyiamine for example AMIET ® 415 (Kao Co.)
  • nonylphenolpolyethoxyethanols for example polyoxyethylene stearylamine (for example AMIET ® 320 (Kao Co.))
  • N- polyethoxyethylamines for example GENAMIN ® (Hoechst AG)
  • N,N,N',N'- tetra(polyethoxypolypropoxyethyl)ethylene diamines for example TERRONIL ⁇ and TETRONIC ⁇ (BASF Wyandotte Corp.)
  • BRIJ ⁇ Alkylamine
  • ETHYLAN ® CD and ETHYLAN ® D Diamond Shamrock
  • GENAPOL ® C for example AMIET 105 (Kao Co.)
  • polyoxyethylene oleyiamine for example AMIET ® 415 (Kao Co.
  • the cationic surfactants are primarily quaternary ammonium salts which contain, as N- substituents, at least one alkyl radical having 8 to 22 C atoms and, as further substituents, lower nonhalogenated or halogenated alkyl, benzyl or lower hydroxyalkyl radicals.
  • the salts are preferably present as halides, methyl sulfates or ethyl sulfates, for example stearyltrimethylammonium chloride or benzyldi(2-chloroethyl)ethylammonium bromide.
  • the oils used are either of mineral or natural origin.
  • the natural oils may additionally be of animal or vegetable origin.
  • preference is given, in particular, to derivatives of beef tallow, but fish oils (for example sardine oil) and derivatives thereof are also used.
  • Vegetable oils are mainly seed oils of various origin. Examples of particularly preferred vegetable oils which may be mentioned are coconut, rapeseed or sunflower oils and derivatives thereof.
  • surfactants oils, in particlar vegetable oils, derivatives thereof such as alkylated fatty acids and mixtures thereof, for example with preferably anionic surfactants such as alkylated phosphoric acids, alkyl sulfates and alkyiaryl sulfonates and higher fatty acids which are customary in formulation and adjuvant technique and which can also be employed in the compositions according to the invention and spray tank solutions thereof are described, inter alia, in "Mc Cutcheon's Detergents and Emulsifiers Annual", MC Publishing Corp., Ridgewood New Jersey, 1998, Stache, H., "Tensid-Taschenbuch” [Surfactant handbook], Carl Hanser Verlag, Kunststoff/Vienna, 1990, M.
  • the herbicidal formulations as a rule comprise 0.1 to 99% by weight, in particular 0.1 to 95% by weight, of herbicide, 1 to 99.9% by weight, in particular 5 to 99.8% by weight, of a solid or liquid formulation auxiliary and 0 to 25% by weight, in particular 0.1 to 25% by weight, of a surfactant. While concentrated compositions are rather preferred as commercial goods, the end user as a rule uses dilute compositions.
  • compositions can also comprise further additives, such as stabilizers, for example epoxidized or non- epoxidized vegetable oils (epoxidized coconut oil, rapeseed oil or soya oil), defoamers, for example silicone oil, preservatives, viscosity regulators, binders, tackifiers and fertilizers or other active compounds.
  • stabilizers for example epoxidized or non- epoxidized vegetable oils (epoxidized coconut oil, rapeseed oil or soya oil)
  • defoamers for example silicone oil, preservatives, viscosity regulators, binders, tackifiers and fertilizers or other active compounds.
  • the herbicidally active compounds of the formula I are as a rule applied to the plants or their habitat, at application rates of 0.001 to 4 kg/ha, in particular 0.005 to 2 kg/ha.
  • the dosage required for the desired effect can be determined by tests. It depends on the nature of the effect, the development stage of the crop plant and the weed and on the application (location, time, process) and can, as a function of these parameters, vary within wide ranges.
  • the compounds of the formula I have herbicidal and growth-inhibiting properties, owing to which they can be used in crops of useful plants, in particular in cereals, cotton, soya, sugar beet, sugar cane, plantings, rapeseed, maize and rice, very particularly in maize and cereals, and for the non-selective control of weeds.
  • Crops include those which have been rendered tolerant towards herbicides or herbicide classes by conventional breeding methods or genetical engineering methods.
  • the weeds to be controlled can be both monocotyledonous and dicotyledonous weeds, for example Stellaria, Agrostis, Digitaria, Avena, Brachiaria, Phalaris, Setaria, Sinapis, Lolium, Solanum, Echinochioa, Scirpus, Monochoria, Sagittaria, Panicum, Bromus, Alopecurus, Sorghum halepense, Sorghum bicolor, Rottboellia, Cyperus, Abutilon, Sida, Xanthium, Amaranthus, Chenopodium, Ipomoea, Chrysanthemum, Galium, Viola, Matricharia, Papaver and Veronica.
  • the herbicidal composition according to the invention is particularly suitable for controlling Alopecurus, Avena, Agrostis, Setaria, Phalaris, Lolium, Panicum, Echinochloa, Brachiaria and Digitaria.
  • the present invention also relates to a selective herbicidal composition for controlling grasses and weeds in crops of useful plants, in particular in crops of maize and cereals, said composition comprising a herbicide of the formula I and a safener (antidote) and which protects the useful plants, but not the weeds, against the phytotoxic effect of the herbicide, and to the use of this composition for controlling weeds in crops of useful plants.
  • a selective-herbicidal composition which, in addition to customary inert formulation auxiliaries such as carriers, solvents and wetting agents, comprises, as active compound, a mixture of a) a herbicidally effective amount of a compound of the formula I
  • R 1 R 2 , R 3 , R 4 , R 5 and G are as defined above, and b) a herbicide-antagonistically effective amount of either a compound of the formula X
  • R 37 is hydrogen, d-C 8 alkyl or d-C 6 alkoxy- or C 3 -C 6 alkenyloxy-substituted d- C ⁇ alkyl; and X 6 is hydrogen or chlorine; or a compound of the formula XI
  • E is nitrogen or methine
  • R 38 is -CCI 3 , phenyl or halogen-substituted phenyl; R 39 and R 40 independently of one another are hydrogen or halogen; and R 4 ⁇ is d-dalkyl; or a compound of the formula XII
  • R ⁇ j and R 45 independently of one another are hydrogen or halogen and R 46 , R 47 and R 4 ⁇ independently of one another are d-C alkyl, or a compound of the formula XIII
  • R 51 and R 52 independently of one another are hydrogen, CrC 8 alkyl, C 3 -C 8 cycloalkyl,
  • R 53 is hydrogen or d-C alkyl
  • R 49 is hydrogen, halogen, cyano, trifluoromethyl, nitro, d-C 4 alkyl, d-C 4 alkoxy, d-
  • R g is hydrogen, halogen, cyano, nitro, d-C alkyl, CrC 4 haloalkyl, d-C 4 alkylthio, d- dalkylsulfinyl, CrC alkylsulfonyl, -COOR,, -CONR k R m , -COR n , -SO 2 NR k R m , -OSO 2 -C
  • R50 and R h independently of one another are hydrogen, halogen, d-C 4 alkyl, trifluoromethyl, d-C 6 alkoxy, C C 6 alkylthio or -COOR,;
  • R c is hydrogen, halogen, nitro, d-C 4 alkyi or methoxy
  • R d is hydrogen, halogen, nitro, d- dalkyl, d-C 4 alkoxy, C C 4 alkylthio, d-C 4 alkylsulfinyl, C C alkylsulfonyl, -COOR, or
  • R e is hydrogen, halogen, d-C 4 alkyl, -COOR,, trifluoromethyl or methoxy, or R d and R e together form a C 3 -C 4 alkyiene bridge;
  • Rp is hydrogen, halogen, d-dalkyl, -COOR,, trifluoromethyl or methoxy;
  • Rq is hydrogen, halogen, nitro, C C 4 alkyl, C r C alkoxy, d-C 4 alkylthio, d-C 4 alkylsulfinyl, C ⁇ -C 4 alkylsulfonyl,
  • Rr is hydrogen, halogen, C C 4 alkyl, -COOR,, trifluoromethyl or methoxy;
  • Rs is hydrogen, halogen, nitro, d-C 4 alkyl, C r C alkoxy, d-C 4 alkylthio, d-dalkylsulfinyl, C C 4 alkylsulfonyl,
  • Rt is hydrogen, halogen, C C 4 alkyl, -COOR,, trifluoromethyl or methoxy;
  • Ru is hydrogen, halogen, nitro, d-C 4 alkyl, d-C alkoxy, d-C alkylthio, C C 4 alkylsulfinyl, CrC alkylsulfonyl,
  • R f and Rv are hydrogen, halogen or C C 4 alkyl
  • R x and R y independently of one another are hydrogen, halogen, d-C alkyl, C C alkoxy, d-
  • R,, R k and R m independently of one another are hydrogen or d-C 4 alkyl; or
  • R k and R m together form a C 4 -C 6 alkylene bridge which may be interrupted by oxygen, NH or
  • R n is d-C alkyl, phenyl, or halogen-, C C 4 alkyl-, methoxy-, nitro- or trifluoromethyl- substituted phenyl;
  • R M is hydrogen, d-C 10 alkyl, CrC 4 alkoxy-C C alkyl, C C alkylthio-CrC 4 alkyl, di-d-
  • Cycycloalkylcarbonyl benzoyl which is unsubstituted or substituted up to three times on the phenyl ring by identical or different substituents selected from the group consisting of halogen, d-C 4 alkyl, halo-d-C 4 alkyl, halo-C ⁇ -C 4 alkoxy or d-C 4 alkoxy; or furoyl, thienyl; or d-C 4 alkyl which is substituted by phenyl, halophenyl, d-C alkylphenyl, d-C 4 alkoxyphenyl, halo-d-C alkylphenyl, halo-C ⁇ -C alkoxyphenyl, CrC 6 alkoxycarbonyl, d-C 4 alkoxy-Cr
  • C ⁇ -C alkylaminocarbonyl di-C ⁇ -C 4 alkylaminocarbonyl; or phenylaminocarbonyl which is unsubstituted or substituted up to three times on the phenyl by identical or different substituents selected from the group consisting of halogen, C C alkyl, halo-C C 4 alkyl, halo-d-C 4 alkoxy and d-C 4 alkoxy, or is monosubstituted by cyano or nitro, or dioxoian-2-yl which is unsubstituted or substituted by one or two d-C 4 alkyl radicals, or dioxan-2-yl which is unsubstituted or substituted by one or two d-C 4 alkyl radicals, or d-C 4 alkyl which is substituted by cyano, nitro, carboxyl or d-C 8 alkylthio-CrC 8 alkoxycarbonyI; or a compound
  • R 57 together are ;
  • Rse and R 59 independently of one another are hydrogen
  • R 6 o and R 6 ⁇ independently of one another are d-C alkyl, or R 6 oand R 6 ⁇ together are -(CH 2 ) 5 -;
  • R 62 is hydrogen, d-C 4 alkyl or
  • Res, Re 4 , Res, Ree, R ⁇ 7, Re ⁇ , Reg, R70, R71, R72, R73, R7 4 , R75, R76, R77 and R 78 independently of one another are hydrogen or d-C 4 alkyl; or a compound of the formula XV in which R 80 is hydrogen or chlorine and R 79 is cyano or trifluoromethyl, or a compound of the formula XVI
  • R 81 is hydrogen or methyl, or of the formula XVII
  • R 82 is hydrogen, C ⁇ -C 4 alkyl, C C 4 alkyl which is substituted by CrC 4 alkyl-X - or d- C 4 haloalkyi-X 2 -, CrC 4 haloalkyl, nitro, cyano, -COOR 85 , -NR 86 R 87 , -SO 2 NR 88 R 89 or
  • R 83 is hydrogen, halogen, d-C 4 alkyl, trifluoromethyl, C ⁇ -C 4 alkoxy or d-C haloalkoxy;
  • R 84 is hydrogen, halogen or d-C alkyl;
  • U, V, W1 and Z 4 independently of one another are oxygen, sulfur, C(R 92 )R 93 , carbonyl, NR 94 ,
  • R 102 is C 2 -C 4 alkenyl or C 2 -C 4 alkynyl; with the proviso that a) at least one of the ring members U, V, ⁇ N or Z, is carbonyl, and a ring member which is
  • H C C , this group being present only once; and b) two adjacent ring members U and V, V and Wi and Wi and t may not simultaneously be oxygen;
  • R 95 and R 96 independently of one another are hydrogen or d-C 8 alkyl; or
  • R 95 and R 96 together form a C 2 -C 6 alkylene group
  • AT is R 99 -Y or -NR 97 R 98 ;
  • X 2 is oxygen or -S(O) s ;
  • Y1 is oxygen or sulfur
  • R 99 is hydrogen, d-C 8 alkyl, d-C 8 haloalkyl, C ⁇ -C alkoxy-C ⁇ -C 8 alkyl, C 3 -C 6 alkenyloxy-Cr
  • R 85 is hydrogen or C C alkyl
  • R 86 is hydrogen, d-C 4 alkyl or C C 4 alkylcarbonyl
  • R 87 is hydrogen or d-C 4 alkyl
  • R 8 6 and R 87 together form a C 4 - or C 5 alkylene group
  • Res, R89, R90 and R 91 independently of one another are hydrogen or d-C 4 alkyl; or R 88 together with R 89 or Rgo together with R 9 ⁇ independently of one another are C 4 - or C 5 - alkylene, where a carbon atom may be replaced by oxygen or sulfur, or one or two carbon atoms may be replaced by -NR 10 o-;
  • R92, R100 and R 93 independently of one another are hydrogen or d-C 8 alkyl; or
  • R92 and R 93 together are C 2 -C 6 alkylene
  • R 94 is hydrogen or d-C 8 alkyl
  • R 97 is hydrogen, d-C 8 alkyl, phenyl, phenyl-d-C 8 alkyl, where the phenyl rings may be substituted by fluorine, chlorine, bromine, nitro, cyano, -OCH 3 , d-C 4 alkyl or CH 3 SO 2 -, d-
  • R 98 is hydrogen, C C 8 alkyl, C 3 -C 6 alkenyl or C 3 -C 6 alkynyl; or R 97 and R 98 together are C 4 - or C 5 -alkylene, where a carbon atom may be replaced by oxygen or sulfur, or one or two carbon atoms may be replaced by -NR 10 r;
  • R 1 0 1 is hydrogen or d-C 4 alkyl; r is 0 or 1 ; and s is 0, 1 or 2, or a compound of the formula XVIII
  • R 103 is hydrogen, CrC 6 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 alkenyl or C 3 -C 6 alkynyi; and RK M , R 1 05 and R 10 e independently of one another are hydrogen, C C 6 alkyl, C 3 -C 6 cycloalkyl or CrC 6 alkoxy, with the proviso that one of the substituents R ⁇ , R 1 05 and R 106 is different from hydrogen; a compound of the formula XIX
  • R 107 is halogen, CrC 4 alkyl, C C 4 haloalkyl, d-C 4 alkoxy, d- dhaloalkoxy, nitro, d-C 4 alkylthio, d-C alkylsulfonyl, d-C 4 alkoxycarbonyl or unsubstituted or substituted phenyl or phenoxy, R ⁇ 08 is hydrogen or d-C 4 alkyl, R 109 is hydrogen, d- C 4 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C ⁇ -C 4 haloalkyl, C 2 -C 6 haloalkenyl, C 2 - C 6 haloalky
  • Rm and Ru 2 independently of one another are cyano, hydrogen, d-C 4 alkyl, C 3 - C 6 cycloalkyl, C 2 -C 6 alkenyl, unsubstituted or substituted phenyl or heteroaryl;
  • Rn 9 and R 120 independently of one another are hydrogen, halogen or d- dhaloalkyl
  • R 121 is hydrogen, CrC 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl, C C haloalkyl, C 3 - C 6 cycloalkyl, a metal cation or an ammonium cation
  • Z 8 is N, CH, C-F or C-CI
  • W is a group of the formula in which R ⁇ 22 and R 123 independently of one another are hydrogen or d-C 4 alkyl and R ⁇ 24 and R 125 independently of one another are hydrogen or d-C alkyl; a compound of the formula XXIII
  • R ⁇ 26 is hydrogen, cyano, halogen, d-C alkyl, C 3 -C 6 cycloalkyl, d-C alkoxy, d-
  • R 127 is hydrogen, cyano, nitro, halogen, d-C alkyl, d-C 4 haloalkyl, d-C 4 alkoxy, d-
  • R 129 and R 130 independently of one another are hydrogen, d-C 4 alkyl, d- dhaloalkyl, d-C 4 alkoxy, mono-CrC 8 - or di-d-C 8 alkylamino, C 3 -C 6 cycloalkyl, d-dthioalkyl, phenyl or heteroaryl
  • R 131 has the meaning of R 129 and is additionally OH, NH 2 , halogen, di- C ⁇ -C 4 aminoalkyl, d-C 4 alkylthio, CrC 4 alkylsulfonyl or d-C 4 alkoxycarbonyl
  • R ⁇ 32 has the meaning of R 129 and is additionally cyano, nitro, carboxyl, d-C 4 alkoxycarbonyl, di-d- C 4 aminoalkyl, d-C 4 alkylthio, d-C aikylsulfonyl, SO 2 -OH, iso-d
  • R ⁇ is hydrogen, C alkyl, d-C haloalkyl, C 2 -C 4 alkenyl, C 2 -C alkynyl or d-C 4 alkoxy- CrC alkyl
  • R 135 is hydrogen, halogen, d-C alkyl, d-C 4 haloalkyl or C C 4 alkoxy
  • R 36 is hydrogen, halogen, d-C 4 alkyl, d-C haloalkyl or d-C 4 alkoxy, with the proviso that R ⁇ 35 and R 136 are not simultaneously hydrogen.
  • the selective-herbicidal composition according to the invention preferably comprises, as herbicide-antagonistically effective amount, either a compound of the formula X
  • R 37 is hydrogen, C C 8 alkyl or d-C 6 alkoxy- or C 3 -C 6 alkenyloxy-substituted d- C 8 alkyl; and X 6 is hydrogen or chlorine; or a compound of the formula XI
  • E is nitrogen or methine;
  • R 38 is -CCI 3 , phenyl or halogen-substituted phenyl;
  • R 39 and R 40 independently of one another are hydrogen or halogen; and
  • R 4 ⁇ is d-C 4 alkyl; or a compound of the formula XII
  • R t and R 45 independently of one another are hydrogen or halogen and R 46 , R 47 and R 48 independently of one another are d-C 4 alkyl.
  • compositions according to the invention comprise a safener selected from the group consisting of the formula Xa
  • the invention also relates to a method for the selective control of weeds in crops of useful plants which comprises treating the useful plants, their seeds or seedlings or the area on which they are cultivated jointly or separately with a herbicidally effective amount of the herbicide of the formula I and a herbicide-antagonistically effective amount of the safener of the formula X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII.
  • Crop plants which can be protected against the damaging effect of the abovementioned herbicides by the safeners of the formula X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII are, in particular, cereals, cotton, soya, sugarbeet, sugarcane, plantings, rapeseed, maize and rice, very particularly maize and cereals. Crops are to be understood as including those which have been rendered tolerant towards herbicides or classes of herbicides by conventional breeding methods or genetical engineering methods.
  • the weeds to be controlled can be both monocotyledonous and dicotyledonous weeds, for example the monocotyledonous weeds Avena, Agrostis, Phalaris, Lolium, Bromus, Alopecurus, Setaria, Digitaria Brachiaria, Echinochloa, Panicum, Sorghum hal./bic, Rottboellia, Cyperus, Brachiaria, Scirpus, Monochoria, Sagittaria, and Stellaria and the dicotyledonous weeds Sinapis, Chenopodium, Gaiium, Viola, Veronica, Matricaria, Papaver, Solanum, Abutilon, Sida, Xanthium, Amaranthus, Ipomoea and Chrysanthemum. Areas under cultivation are the areas on which the crop plants are already growing, or on which the seeds of these crop plants have been sown, and also the soils which are intended to be cultivated with these crop plants.
  • a safener of the formula X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII can be employed for pretreating the seeds of the crop plant (dressing of the seeds or the seedlings), or it can be worked into the soil before or after seeding. However, it can also be applied on its own or together with the herbicide after the plants have emerged. Thus, the treatment of the plants or the seeds with the safener can, in principle, be carried out independently of when the herbicide is applied. However, the plant can also be treated by simultaneous application of herbicide and safener (for example as tank mix). The application rate of safener to herbicide to be applied depends essentially on the type of application.
  • the ratio of herbicide to safener is as a rule from 100:1 to 1 :10, preferably from 20:1 to 1 :1.
  • 0.001 to 1.0 kg of safener/ha preferably 0.001 to 0.25 kg of safener/ha are applied in the field treatment.
  • the application rates of herbicide are as a rule between 0.001 and 2 kg/ha, but preferably between 0.005 to 0.5 kg/ha.
  • compositions according to the invention are suitable for all application methods which are customary in agriculture, for example pre-emergence application, postemergence application and seed dressing.
  • safener/kg of seed For seed dressing, generally 0.001 to 10 g of safener/kg of seed, preferably 0.05 to 2 g of safener/kg of seed, are applied. If the safener is applied in liquid form while swelling the seeds shortly before seeding, it is advantageous to employ safener solutions which comprise the active compound in a concentration of from 1 to 10000, preferably from 100 to 1000, ppm.
  • the safeners of the formula X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII or combinations of these safeners with the herbicides of the formula I are advantageously processed together with auxiliaries conventionally used in the art of formulation, for example to give emulsion concentrates, spreadable pastes, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granules or microcapsules.
  • formulations are described, for example, in WO 97/34485 on pages 9 to 13.
  • the formulations are prepared in a known manner, for example by intimate mixing and/or grinding of the active compounds with liquid or solid formulation auxiliaries, for example solvents or solid carriers.
  • Surface-active compounds (surfactants) can furthermore additionally be used during preparation of the formulations.
  • Solvents and solid carriers which are suitable for this purpose are mentioned, for example, in WO 97/34485 on page 6.
  • Suitable surface-active compounds are, depending on the nature of the active compound of the formula I to be formulated, nonionic, cationic and/or anionic surfactants and surfactant mixtures having good emulsifying, dispersing and wetting properties.
  • suitable anionic, nonionic and cationic surfactants are listed, for example, in WO 97/34485 on pages 7 and 8.
  • the herbicidal formulations as a rule comprise 0.1 to 99% by weight, in particular 0.1 to 95% by weight, of the active compound mixture of the compound of the formula I with the compounds of the formulae X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII, 1 to 99.9% by weight of a solid or liquid formulation auxiliary and 0 to 25% by weight, in particular 0.1 to 25% by weight, of a surfactant. While concentrated compositions are usually preferred as commercial goods, the end user as a rule uses dilute compositions.
  • compositions can also comprise further additives, such as stabilizers, for example epoxidized or non-epoxidized vegetable oils (epoxidized coconut oil, rapeseed oil or soya oil), defoamers, for example silicone oil, preservatives, viscosity regulators, binders, tackifiers and fertilizers or other active substances.
  • stabilizers for example epoxidized or non-epoxidized vegetable oils (epoxidized coconut oil, rapeseed oil or soya oil)
  • defoamers for example silicone oil, preservatives, viscosity regulators, binders, tackifiers and fertilizers or other active substances.
  • Seed dressing or the treatment of the germinated seedling are the naturally preferred application methods, since the treatment with active compound is completely directed at the target culture.
  • 1 to 1000 g of antidote, preferably 5 to 250 g of antidote, are employed per 100 kg of seed, but, depending on the method, which also permits the addition of other active compounds or micronutrients, it is possible to deviate above or below the stated limit concentrations (repeat dressing).
  • a liquid preparation of a mixture of antidote and herbicide (mutual ratio between 10:1 and 1:100) is employed, the application rate of herbicide being from 0.005 to 5.0 kg per hectare.
  • Such tank mixes are applied before or after seeding.
  • the active compound of the formula X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII is applied into the open seeded seed farrow as an emulsion concentrate, a wettable powder or as granules. After the seed farrow has been covered, the herbicide is applied in a customary manner by the pre-emergence method.
  • the active compound of the formula X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII is absorbed in solution onto mineral granule carriers or polymerized granules (urea/formaldehyde) and dried. If appropriate, a coating which allows the active compound to be released in metered form over a certain period of time can be applied (coated granules).
  • compositions according to the invention comprising a herbicidally effective amount of a compound of the formula I and a herbicide-antagonistically effective amount of a compound of the formula X, XI, XII, XIII, XIV, XV, XVI, XVII or XVIII can be increased by addition of spray tank adjuvants.
  • These adjuvants may be, for example, nonionic surfactants, mixtures of nonionic surfactants, mixtures of anionic surfactants with nonionic surfactants, cationic surfactants, organosiiicon surfactants, mineral oil derivatives with or without surfactants, vegetable oil derivatives with or without addition of surfactants, alkylated derivatives of oils of vegetable or mineral origin with or without surfactants, fish oils and other oils of animal nature and their alkyl derivatives with or without surfactants, natural higher fatty acids, preferably having 8 to 28 carbon atoms, and their alkyl ester derivatives, organic acids which contain an aromatic ring system and one or more carboxylic esters, and their alkyl derivatives, furthermore suspensions of polymers of vinyl acetate or copolymers of vinyl acetate/acrylic esters. Mixtures of individual adjuvants with one another and in combination with organic solvents may further increase the effect.
  • Suitable nonionic surfactants are, for example, polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, saturated or unsaturated fatty acids and alkylphenols, preferably those which may contain 3 to 30 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon radical and 6 to 18 carbon atoms in the alkyl radical of the alkylphenols.
  • nonionic surfactants are the water-soluble polyethylene oxide adducts on polypropylene glycol, ethylenediaminopolypropyiene glycol and alkylpolypropylene glycol preferably having 1 to 10 carbon atoms in the alkyl chain which preferably contain 20 to 250 ethylene glycol ether groups and 10 to 100 propylene glycol ether groups.
  • the abovementioned compounds generally contain 1 to 5 ethylene glycol units per propylene glycol unit.
  • nonionic surfactants which may be mentioned are nonyiphenoipolyethoxyethanols, castor oil polyglycol ethers, polypropylene/polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethylene glycol and octylphenoxypolyethoxyethanol.
  • fatty esters of polyoxyethylene sorbitan for example polyoxyethylene sorbitan trioleate.
  • Preferred anionic surfactants are, in particular, alkyl sulfates, alkyl sulfonates, alkylaryl sulfonates, alkylated phosphoric acids and their ethoxylated derivatives.
  • the alkyl radicals usually contain 8 to 24 carbon atoms.
  • Preferred nonionic surfactants are known under the following trade names:
  • Polyoxyethylene cocoalkylamine for example AMIET ® 105 (Kao Co.)
  • polyoxyethylene oleylamine for example AMIET ® 415 (Kao Co.)
  • nonylphenolpolyethoxyethanols for example polyoxyethylene stearylamine (for example AMIET ® 320 (Kao Co.))
  • N- polyethoxyethylamines for example GENAMIN ® (Hoechst AG)
  • N,N,N',N'- tetra(polyethoxypolypropoxyethyl)ethylene diamines for example TERRONIL ® and TETRONIC ⁇ (BASF Wyandotte Corp.)
  • BRIJ* Alkylamine
  • ETHYLAN ® CD and ETHYLAN* D Diamond Shamrock
  • GENAPOL ® C for example AMIET ® O, GENAPOL ® S and GENAPOL ® X080 (Hoechst AG)
  • the cationic surfactants are primarily quaternary ammonium salts which contain, as N- substituents, at least one alkyl radical having 8 to 22 C atoms and, as further substituents, lower nonhalogenated or halogenated alkyl, benzyl or lower hydroxyalkyl radicals.
  • the salts are preferably present as halides, methyl sulfates or ethyl sulfates, for example stearyltrimethylammonium chloride or benzyldi(2-chioroethyl)ethylammonium bromide.
  • the oils used are either of mineral or natural origin. The natural oils may additionally be of animal or vegetable origin.
  • Vegetable oils are mainly seed oils of various origin. Examples of particularly preferred vegetable oils which may be mentioned are coconut, rapeseed or sunflower oils and derivatives thereof.
  • surfactants oils, in particlar vegetable oils, derivatives thereof such as alkylated fatty acids and mixtures thereof, for example with preferably anionic surfactants such as alkylated phosphoric acids, alkyl sulfates and alkylaryl sulfonates and higher fatty acids which are customary in formulation and adjuvant technique and which can also be employed in the compositions according to the invention and spray tank solutions thereof are described, inter alia, in "Mc Cutcheon's Detergents and Emulsifiers Annual", MC Publishing Corp., Ridgewood New Jersey, 1998, Stache, H., Tensid-Taschenbuch” [Surfactant handbook], Carl Hanser Verlag, Kunststoff/Vienna, 1990, M. and J.
  • Emulsifiable concentrates active compound mixture: 1 to 90%, preferably 5 to 20% surface-active agent: 1 to 30%, preferably 10 to 20% liquid carrier: 5 to 94%, preferably 70 to 85%
  • Dusts active compound mixture: 0.1 to 10%, preferably 0.1 to 5% solid carrier: 99.9 to 90%, preferably 99.9 to 99%
  • Suspension concentrates active compound mixture: 5 to 75%, preferably 10 to 50% water: 94 to 24%, preferably 88 to 30% surface-active agent: 1 to 40%, preferably 2 to 30% Wettable powders: active compound mixture: 0.5 to 90%, preferably 1 to 80% surface-active agent: 0.5 to 20%, preferably 1 to 15% solid carrier material: 5 to 95%, preferably 15 to 90%
  • Granules active compound mixture: 0.1 to 30%, preferably 0.1 to 15% solid carrier: 99.5 to 70%, preferably 97 to 85%
  • Emulsion concentrates a) b) c) d)
  • Active compound mixture 5% 10% 25% 50%
  • Emulsions of any desired concentration can be prepared from such concentrates by dilution with water.
  • Active compound mixture 5% 10% 50% 90%
  • Wettable powders a) b) c) d)
  • Active compound mixture 5% 25% 50% 80%
  • the active compound is thoroughly mixed with the additives and ground well in a suitable mill. This gives spray powders which can be diluted with water to give suspensions of any desired concentration.
  • Active compound mixture 0.1% 5% 15%
  • the active compound is dissolved in methylene chloride, the solution is sprayed onto the carrier and the solvent is subsequently evaporated off under reduced pressure.
  • Active compound mixture 0.1 % 5% 15%
  • Inorg. carrier material 98.0% 92% 80%
  • the finely ground active compound is applied evenly to the carrier material moistened with polyethylene glycol. In this manner, dust-free coated granules are obtained.
  • the active compound is mixed with the additives, ground and moistened with water. This mixture is extruded and subsequently dried in a stream of air.
  • Ready-to-use dusts are obtained by mixing the active compound with the carriers and grinding the mixture in a suitable mill.
  • Active compound mixture 3% 10% 25% 50%
  • the finely ground active compound is intimately mixed with the additives. This gives a suspension concentrate, from which suspensions of any desired concentration can be prepared by dilution with water.
  • test plants Under greenhouse conditions, the test plants are grown in plastic pots until they have reached the 4-leaf-stage. In this stage, both the herbicide on its own and the mixtures of the herbicide with the test substances to be tested as safeners are applied to the test plants.
  • the application is carried out as an aqueous suspension of the test substances, prepared from a 25% wettable powder (Example F3, b)), using 500 I of water/ha. 3 weeks after the application, the phytotoxic effect of the herbicide on the crop plants, for example maize and cereals, is evaluated using a percentage scale. 100% means that the test plant has died, 0% means no phytotoxic effect.
  • test plants Under greenhouse conditions, the test plants are grown in plastic pots until they have reached the 4-leaf-stage. In this stage, both the herbicide on its own and the mixtures of the herbicide with the test substances to be tested as safeners are applied to the test plants.
  • the application is carried out as an aqueous suspension of the test substances, prepared from an emulsion concentrate (EC 100; Example F1) of the herbicides and an emulsion concentrate (EC 100; Example F1) of the safeners (exceptions: the safeners no. 10.05 and 20.17, which are employed as a 25% wettable powder (Example F3, b)).
  • 9 days after the application the phytotoxic effect of the herbicide on summer wheat and durum wheat is evaluated using a percentage scale (100%: test plant has died; 0%: no phytotoxic effect).
  • Table S2 Safening of the compound no. 1.032
  • test plants Under greenhouse conditions, the test plants are grown in plastic pots until they have reached the 4-leaf-stage. In this stage, both the herbicide on its own and the mixtures of the herbicide with the test substances to be tested as safeners are applied to the test plants.
  • the application is carried out as an aqueous suspension of the test substances, prepared from an emulsion concentrate (EC 100; Example F1 ) of the herbicides and an emulsion concentrate (EC 100; Example F1) of the safeners (exceptions: the safeners no. 10.05 and 20.17, which are employed as a 25% wettable powder (Example F3, b)).
  • 11 days after the application the phytotoxic effect of the herbicide on summer wheat and durum wheat is evaluated using a percentage scale (100%: test plant has died; 0%: no phytotoxic effect).
  • Table S3 Safening of the compound no. 1.025
  • test plants Under greenhouse conditions, the test plants are grown in plastic pots until they have reached the 4-leaf-stage. In this stage, both the herbicide on its own and the mixtures of the herbicide with the test substances to be tested as safeners are applied to the test plants.
  • the application is carried out as an aqueous suspension of the test substances, prepared from an emulsion concentrate (EC 100; Example F1) of the herbicides and an emulsion concentrate (EC 100; Example F1) of the safeners (exceptions: the safeners no. 10.05 and 20.17, which are employed as a 25% wettable powder (Example F3, b)).
  • 9 days after the application the phytotoxic effect of the herbicide on summer wheat and durum wheat is evaluated using a percentage scale (100%: test plant has died; 0%: no phytotoxic effect).
  • Table S4 Safening of the compound no. 1.007
  • a solution of 68.78 g (0.30 mol) of (2) in 140 ml of dimethylformamide is added dropwise for a period of 30 minutes to a suspension of 23.9 g (0.60 mol) of 60% sodium hydride in 500 ml of dimethylformamide which had been cooled to 5°C. Cooling is removed and the reaction mixture is stirred until it has reached a temperature of 20°C. The mixture is subsequently briefly heated to a temperature of from 30 to 40°C to bring the evolution of hydrogen to completion.
  • the reaction mixture is made alkaline and the aqueous phase (which contains the product) is washed twice with ethyl acetate.
  • the organic phase is reextracted twice using aqueous 1 N sodium hydroxide solution, the aqueous phases are combined, the remaining xylene is distilled off and the combined aquoeus phases are adjusted to pH 2-3 using 4N HCI with cooling.
  • the product which precipitates is transferred onto a suction filter, the filter cake is washed with water and briefly with hexane and is subsequently dried under reduced pressure at a temperature of 60°C over P 2 O 5 . This gives 34.6 g of (6) as a slightly beige solid of melting point 242-244°C (decomp.).
  • Example H6 At a temperature of from 20 to 25°C, 15.2 g of the compound (8) obtained according to Example H6 are hydrogenated with hydrogen over a palladium catalyst (using carbon as carrier, 7 g of 5% Pd/C) in 160 ml of tetrahydrofuran. After the hydrogenation has ended, the product is filtered through Hyflo, and the resulting filtrate is concentrated on a rotary evaporator. This gives 13.7 g of (9) in the form of yellow crystals of melting point 47 - 49°C.
  • Example H8 Example H8:
  • the starting material (12) is known from the literature: see, for example, K. Naemura et al., Tetrahedron Asymmetry 1993, 4, 911-918.
  • Emulsion concentrates a) b) c) d)
  • Emulsions of any desired concentration can be prepared from such concentrates by dilution with water.
  • the active compound is thoroughly mixed with the additives and ground well in a suitable mill. This gives spray powders which can be diluted with water to give suspensions of any desired concentration.
  • the active compound is dissolved in methylene chloride, the solution is sprayed onto the carrier and the solvent is subsequently evaporated off under reduced pressure.
  • Finely divided silica 0.9% 1 % 2%
  • Inorg. carrier material 98.0% 92% 80%
  • the active compound is mixed with the additives, ground and moistened with water. This mixture is extruded and subsequently dried in a stream of air.
  • Ready-to-use dusts are obtained by mixing the active compound with the carriers and grinding the mixture in a suitable mill.
  • the finely ground active compound is intimately mixed with the additives. This gives a suspension concentrate, from which suspensions of any desired concentration can be prepared by dilution with water.
  • Test plants Alopecurus (Alo), Avena (Ave), Lolium (Lol), Setaria (Set), Panicum (Pan), Sorghum (Sor), Digitaria (Dig), Echinocloa (Ech) and Brachiaria (Bra).
  • Test plants Alopecurus (Alo), Avena (Ave), Lolium (Lol), Setaria (Set), Panicum (Pan), Sorghum (Sor), Digitaria (Dig), Echinocloa (Ech) and Brachiaria (Bra).
  • Example B3 Herbicidal action of compounds of the present invention before emergence of the plants (pre-emergence action):
  • Monocotyledonous and dicotyledonous weeds are grown in standard soil in plastic pots. Directly after sowing, the test substances are applied (500 I of water/ha) as an aqueous suspension (prepared using a 25% wettable powder (Example F3, b)) or as an emulsion (prepared using a 25% emulsion concentrate (Example F1 , c)). The application rate is 500 g of active substance/ha.
  • Test plants Avena (Ave), Lolium (Lol), Setaria (Set).

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Abstract

La présente invention a trait à des composés de formule (I), où les substituants sont tels que définis dans la revendication 1, aptes à être utilisés an tant qu'herbicides, notamment en combinaison avec des composés herbicides ayant une activité antagoniste.
PCT/EP1999/000898 1999-02-11 1999-02-11 Herbicides nouveaux derives de 3-hydroxy-4-aryle-5-pyrazoline en tant qu'herbicides WO2000047585A1 (fr)

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PCT/EP1999/000898 WO2000047585A1 (fr) 1999-02-11 1999-02-11 Herbicides nouveaux derives de 3-hydroxy-4-aryle-5-pyrazoline en tant qu'herbicides
AU26233/99A AU2623399A (en) 1999-02-11 1999-02-11 3-hydroxy-4-aryl-5-pyrazoline derivatives as herbicides

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PCT/EP1999/000898 WO2000047585A1 (fr) 1999-02-11 1999-02-11 Herbicides nouveaux derives de 3-hydroxy-4-aryle-5-pyrazoline en tant qu'herbicides

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Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001017352A1 (fr) * 1999-09-07 2001-03-15 Syngenta Participations Ag Herbicide
WO2001017353A1 (fr) * 1999-09-07 2001-03-15 Syngenta Participations Ag Composition herbicide
WO2006029799A1 (fr) * 2004-09-16 2006-03-23 Bayer Cropscience Ag Cetoenols cycliques a substitution iode-phenol
JP2006519801A (ja) * 2003-03-13 2006-08-31 ビーエーエスエフ　アクチェンゲゼルシャフト ３−フェニルウラシル化合物に基づく除草剤混合物
WO2007073933A2 (fr) * 2005-12-27 2007-07-05 Syngenta Participations Ag Composition herbicide
JP2009527513A (ja) * 2006-02-21 2009-07-30 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト シクロアルキルフェニル置換環状ケトエノール
US7605111B2 (en) 1999-09-07 2009-10-20 Syngenta Crop Protection, Inc. Herbicides
US7915199B1 (en) 1999-09-07 2011-03-29 Syngenta Crop Protection, Inc. Herbicidal composition
US8754242B2 (en) 2007-08-08 2014-06-17 Syngenta Crop Protection Llc Herbicides
US8940913B2 (en) 2007-08-09 2015-01-27 Syngenta Crop Protection, Llc Herbicides
US8956999B2 (en) 2007-06-28 2015-02-17 Syngenta Limited Herbicides
WO2015032702A1 (fr) * 2013-09-06 2015-03-12 Syngenta Limited Dérivés de 2-halogéno-4-alcynylphénylpyrazolidinedione ou de pyrrolidinedione à activité herbicide
WO2015040114A1 (fr) * 2013-09-20 2015-03-26 Syngenta Limited Dérivés de 2-halogéno-4-alcynylphénylpyrazolidinedione ou de pyrrolidinedione ayant une activité herbicide
US9096560B2 (en) 2008-07-03 2015-08-04 Syngenta Limited 5-heterocyclylalkyl-3-hydroxy-2-phenylcyclopent-2-enones as herbicides
CN105814031A (zh) * 2013-12-19 2016-07-27 阿彻丹尼尔斯米德兰德公司 呋喃-2,5-二甲醇和(四氢呋喃-2,5-二基)二甲醇的磺酸酯及其衍生物
CN108017593A (zh) * 2017-12-06 2018-05-11 东南大学 一种简便高效的1-氧-4,5-二氮杂环庚烷合成方法
US10415307B2 (en) 2012-05-15 2019-09-17 Geigtech East Bay Llc Assembly for mounting shades
CN110526927A (zh) * 2018-05-25 2019-12-03 江苏中旗科技股份有限公司 一种唑啉草酯的制备方法
CN112159321A (zh) * 2015-06-22 2021-01-01 拜耳作物科学股份公司 新的炔基取代的3-苯基吡咯烷-2,4-二酮及其作为除草剂的用途
CN115894518A (zh) * 2022-11-09 2023-04-04 江西农业大学 一种唑啉草酯代谢物m3的合成方法

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0355599A1 (fr) * 1988-08-20 1990-02-28 Bayer Ag Aryl-3 pyrrolidinediones-2,4
EP0508126A1 (fr) * 1991-03-21 1992-10-14 Bayer Ag Dérivés de hydroxy-3-aryl-4-oxo-5-pyrazoline
DE4413669A1 (de) * 1993-07-05 1995-01-12 Bayer Ag Substituierte Aryl-ketoenolheterocyclen
WO1996011574A1 (fr) * 1994-10-17 1996-04-25 Novartis Ag Compositions herbicides
WO1996021652A1 (fr) * 1995-01-13 1996-07-18 Novartis Ag Derives 4-aryl- et 4-heteroaryl-5-oxo-pyrazoline possedant des proprietes pesticides
WO1996025395A1 (fr) * 1995-02-13 1996-08-22 Bayer Aktiengesellschaft 1,3-cetoenols heterocycliques substitues en 2-phenyle utilises sous forme d'herbicides et de pesticides

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0355599A1 (fr) * 1988-08-20 1990-02-28 Bayer Ag Aryl-3 pyrrolidinediones-2,4
EP0508126A1 (fr) * 1991-03-21 1992-10-14 Bayer Ag Dérivés de hydroxy-3-aryl-4-oxo-5-pyrazoline
DE4413669A1 (de) * 1993-07-05 1995-01-12 Bayer Ag Substituierte Aryl-ketoenolheterocyclen
WO1996011574A1 (fr) * 1994-10-17 1996-04-25 Novartis Ag Compositions herbicides
WO1996021652A1 (fr) * 1995-01-13 1996-07-18 Novartis Ag Derives 4-aryl- et 4-heteroaryl-5-oxo-pyrazoline possedant des proprietes pesticides
WO1996025395A1 (fr) * 1995-02-13 1996-08-22 Bayer Aktiengesellschaft 1,3-cetoenols heterocycliques substitues en 2-phenyle utilises sous forme d'herbicides et de pesticides

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Publication number Priority date Publication date Assignee Title
US7915199B1 (en) 1999-09-07 2011-03-29 Syngenta Crop Protection, Inc. Herbicidal composition
WO2001017353A1 (fr) * 1999-09-07 2001-03-15 Syngenta Participations Ag Composition herbicide
AU762436B2 (en) * 1999-09-07 2003-06-26 Syngenta Participations Ag Herbicide agent
US6962894B1 (en) 1999-09-07 2005-11-08 Syngenta Crop Protection, Inc. Herbicidal composition
WO2001017352A1 (fr) * 1999-09-07 2001-03-15 Syngenta Participations Ag Herbicide
US7605111B2 (en) 1999-09-07 2009-10-20 Syngenta Crop Protection, Inc. Herbicides
JP2006519801A (ja) * 2003-03-13 2006-08-31 ビーエーエスエフ　アクチェンゲゼルシャフト ３−フェニルウラシル化合物に基づく除草剤混合物
KR101202886B1 (ko) * 2003-03-13 2012-11-19 바스프 에스이 3-페닐우라실 기재 제초제 혼합물
JP4879732B2 (ja) * 2003-03-13 2012-02-22 ビーエーエスエフ ソシエタス・ヨーロピア ３−フェニルウラシル化合物に基づく除草剤混合物
WO2006029799A1 (fr) * 2004-09-16 2006-03-23 Bayer Cropscience Ag Cetoenols cycliques a substitution iode-phenol
US8629084B2 (en) 2004-09-16 2014-01-14 Bayer Cropscience Ag Iodine-phenyl-substituted cyclic cetoenols
JP2008513391A (ja) * 2004-09-16 2008-05-01 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト ヨード−フェニル置換された環状ケトエノール
JP2009524597A (ja) * 2005-12-27 2009-07-02 シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト 除草用組成物
WO2007073933A2 (fr) * 2005-12-27 2007-07-05 Syngenta Participations Ag Composition herbicide
CN101453894B (zh) * 2005-12-27 2012-08-08 先正达参股股份有限公司 除草组合物
WO2007073933A3 (fr) * 2005-12-27 2009-02-19 Syngenta Participations Ag Composition herbicide
US10952437B2 (en) 2005-12-27 2021-03-23 Syngenta Crop Protection Llc Herbicidal composition
EA018654B1 (ru) * 2005-12-27 2013-09-30 Зингента Партисипейшнс Аг Гербицидная композиция
JP2009527513A (ja) * 2006-02-21 2009-07-30 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト シクロアルキルフェニル置換環状ケトエノール
JP2013100310A (ja) * 2006-02-21 2013-05-23 Bayer Cropscience Ag シクロアルキルフェニル置換環状ケトエノール
US8956999B2 (en) 2007-06-28 2015-02-17 Syngenta Limited Herbicides
US8754242B2 (en) 2007-08-08 2014-06-17 Syngenta Crop Protection Llc Herbicides
US8940913B2 (en) 2007-08-09 2015-01-27 Syngenta Crop Protection, Llc Herbicides
US9096560B2 (en) 2008-07-03 2015-08-04 Syngenta Limited 5-heterocyclylalkyl-3-hydroxy-2-phenylcyclopent-2-enones as herbicides
US10822872B2 (en) 2012-05-15 2020-11-03 Geigtech East Bay Llc Shade bracket with concealed wiring
US10988982B2 (en) 2012-05-15 2021-04-27 Geigtech East Bay Llc Assembly for mounting shades
US10415307B2 (en) 2012-05-15 2019-09-17 Geigtech East Bay Llc Assembly for mounting shades
WO2015032702A1 (fr) * 2013-09-06 2015-03-12 Syngenta Limited Dérivés de 2-halogéno-4-alcynylphénylpyrazolidinedione ou de pyrrolidinedione à activité herbicide
WO2015040114A1 (fr) * 2013-09-20 2015-03-26 Syngenta Limited Dérivés de 2-halogéno-4-alcynylphénylpyrazolidinedione ou de pyrrolidinedione ayant une activité herbicide
US20160219881A1 (en) * 2013-09-20 2016-08-04 Syngenta Limited Herbicidally active 2-halogen-4-alkynyl-phenyl-pyrazolidine-dione or pyrrolidine-dione derivatives
CN105814031A (zh) * 2013-12-19 2016-07-27 阿彻丹尼尔斯米德兰德公司 呋喃-2,5-二甲醇和(四氢呋喃-2,5-二基)二甲醇的磺酸酯及其衍生物
CN112159321A (zh) * 2015-06-22 2021-01-01 拜耳作物科学股份公司 新的炔基取代的3-苯基吡咯烷-2,4-二酮及其作为除草剂的用途
CN108017593A (zh) * 2017-12-06 2018-05-11 东南大学 一种简便高效的1-氧-4,5-二氮杂环庚烷合成方法
CN108017593B (zh) * 2017-12-06 2021-05-11 东南大学 一种简便高效的1-氧-4,5-二氮杂环庚烷合成方法
CN110526927A (zh) * 2018-05-25 2019-12-03 江苏中旗科技股份有限公司 一种唑啉草酯的制备方法
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CN115894518A (zh) * 2022-11-09 2023-04-04 江西农业大学 一种唑啉草酯代谢物m3的合成方法
CN115894518B (zh) * 2022-11-09 2024-05-17 江西农业大学 一种唑啉草酯代谢物m3的合成方法

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