EP2437605A1 - Pyridopyrazines substituées à action herbicide - Google Patents
Pyridopyrazines substituées à action herbicideInfo
- Publication number
- EP2437605A1 EP2437605A1 EP10724420A EP10724420A EP2437605A1 EP 2437605 A1 EP2437605 A1 EP 2437605A1 EP 10724420 A EP10724420 A EP 10724420A EP 10724420 A EP10724420 A EP 10724420A EP 2437605 A1 EP2437605 A1 EP 2437605A1
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- European Patent Office
- Prior art keywords
- formula
- alkyl
- compounds
- methyl
- haloalkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—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
Definitions
- the present invention relates to substituted pyrazines of the formula I.
- variables have the following meaning R 1 OR A , S (O) n -R A or OS (O) n -R A ;
- R A is hydrogen, C 1 -C 4 -alkyl, ZC 3 -C 6 -cycloalkyl, C 1 -C 4 -haloalkyl, C 2 -C 6 -alkenyl, ZC 3 -C 6 -cycloalkenyl, C 2 -C 6 Alkynyl, Z- (tri-C 1 -C 4 -alkyl) silyl,
- R a is hydrogen, OH, Ci-C 8 -alkyl, C 4 haloalkyl, ZC 3 -C 6 cycloalkyl, C 2 -C 8 -alkenyl-Al, ZC 5 -C 6 cycloalkenyl, C 2 -C 8 -alkynyl, Z-Ci-C 6 -alkoxy, Z-Ci-C 4 -haloalkoxy, ZC 3 -C 8 -alkenyloxy, ZC 3 -C 8 -alkynyloxy, NR 1 R ", d-Ce-alkylsulfonyl, Z- (tri-Ci-C 4 alkyl) silyl, Z-phenyl, Z-phenoxy-phenylamino Z and 5- or 6-membered monocyclic or 9- or
- R 1 and R may also together with the N-atom to which they are attached form a 5- or 6-membered monocyclic or 9- or 10-membered bicyclic heterocycle containing 1, 2, 3 or
- n 0, 1 or 2;
- R 2 is phenyl, naphthyl or and 5- or 6-membered monocyclic or 9- or 10-membered bicyclic aromatic heterocycle containing 1, 2, 3 or 4 heteroatoms selected from O, N and S, wherein the cyclic groups unsubstituted or by 1 , 2, 3 or 4 groups R b are substituted, means;
- R b is independently Z-CN, Z-OH, Z-NO 2,
- R b1 , R b2 is one of the groups mentioned for R b ;
- R b , R b1 , R b2 can also independently together with the bonded to the adjacent carbon atom group R b , R b1 or R b2 form a five- or six-membered saturated, partially or fully unsaturated ring, which in addition to carbon , 2 or 3 heteroatoms selected from O, N and S may contain;
- X is O, S or NR 3;
- R 3 is hydrogen, Ci-C 6 alkyl, Ci-C 4 haloalkyl, C 2 -C 6 alkenyl, C 3 -C 6 kinyl Al,
- R a2 is C 1 -C 6 -alkyl, C 1 -C 4 -haloalkyl, Z-C 1 -C 6 -alkoxy, Z-C 1 -C 4 -haloalkoxy and
- NR 1 R " in groups R A , R 2 , R 3 and their sub-substituents, the carbon chains and / or the cyclic groups may be partially or completely substituted by groups R a , and also their N-oxides and agriculturally suitable salts; with the proviso that R 1 does not represent 0R A or OS (O) n -R A when X is O.
- the invention relates to processes and intermediates for the preparation of the pyrazines of the formula I and their N-oxides, their agriculturally useful salts, as well as active ingredient combinations containing them, agents containing them and their use as herbicides, i. for controlling harmful plants, and a method for controlling undesired plant growth, which comprises allowing a herbicidally effective amount of at least one pyrazine compound of the formula I or a agriculturally useful salt of I to act on plants, their seeds and / or their habitat.
- herbicidal pyrazines are described, their herbicidal activity at low application rates, or compatibility with crops remains in need of improvement.
- An object of the present invention is to provide compounds having herbicidal activity.
- active ingredients should be made available which have a high herbicidal action, in particular even at low application rates, and their compatibility with crop plants for commercial exploitation is sufficient.
- the compounds according to the invention can be prepared by standard methods of organic chemistry, for example according to the following synthesis route:
- This reaction is usually carried out at temperatures of -78 0 C to 12O 0 C, preferably -2O 0 C to 5O 0 C, in an inert organic solvent in the presence of a base (see Greene's Protective Groups in Organic Synthesis, Wiley).
- Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and dimethyl sulfoxide, dimethylformamide (DMF) and dimethylacetamide, particularly preferably halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene ,
- Bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, Alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate, and alkali metal hydrogen carbonate.
- alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide
- alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide
- alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium
- bonates such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyllithium and phenyllithium, alkylmagnesium halides such as methylmagnesium chloride, and alkali metal and alkaline earth metal alkoxides such as sodium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide and dimethoxy magnesium, as well as organic bases, eg tertiary Amines such as trimethylamine, triethylamine, tributylamine, di-isopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration. Preference is given to alkali metal and alkaline earth metal hydrides, particularly preferably sodium hydride.
- the bases are generally used in catalytic amounts, but they can
- the starting materials are generally reacted with one another in equimolar amounts.
- Suitable solvents are water, alcohols such as methanol, ethanol, iso-propanol, aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and Chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and dimethyl sulfoxide, DMF and dimethylacetamide, particularly preferably halogenated hydrocarbons such Methylene chloride
- Bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, Alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate, and alkali metal hydrogencarbonates such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyl lithium and phenyl lithium, alkylmagnesium halides such as methylmagnesium chloride and also alkali metal and alkaline earth metal alcoholates.
- alkali metal and alkaline earth metal hydroxides such as lithium hydro
- te as sodium methoxide, sodium, potassium, potassium tert-butoxide and Dimethoxymagnesium
- organic bases for example tertiary amines such as trimethylamine, triethylamine, tributylamine, di-isopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration.
- tertiary amines such as trimethylamine, triethylamine, tributylamine, di-isopropylethylamine and N-methylpiperidine
- pyridine substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration.
- alkali metal and alkaline earth metal hydroxides particularly preferably lithium hydroxide.
- the bases are generally used in catalytic amounts, but they can also be used e
- Suitable leaving groups L 1 are generally those groups which increase the electrophilicity of the carbonyl group, for example O-alkyl, O-aryl, halides, activated esters or aldehydes (such as, for example, Weinreb amide), in particular pentafluorophenoxy.
- This reaction is usually carried out at temperatures of -78 0 C to 12O 0 C, preferably -2O 0 C to 5O 0 C, in an inert organic solvent in the presence of a base such as. Triethylamine (see J. Agric and Food Chem., 1994, 42 (4), 1019-1025), a catalyst such as e.g. B. Dicyclohexylcarbodiimide (see Egyptian Journal of Chemistry 1994, 37 (3), 273-282) or other known coupling reagents.
- a base such as. Triethylamine (see J. Agric and Food Chem., 1994, 42 (4), 1019-1025)
- a catalyst such as e.g. B. Dicyclohexylcarbodiimide (see Egyptian Journal of Chemistry 1994, 37 (3), 273-282) or other known coupling reagents.
- Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and dimethyl sulfoxide, DMF and dimethylacetamide, more preferably methylene chloride and toluene. Mixtures of the solvents mentioned can also be used.
- Bases generally include inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcite oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, Alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate, and alkali metal hydrogencarbonates such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyl lithium and phenyl lithium, alkylmagnesium halides such as methylmagnesium chloride and also alkali metal and alkaline earth metal alcoholates.
- alkali metal and alkaline earth metal hydroxides such as
- tertiary amines such as trisodium methylamine, triethylamine, tributylamine, di-isopropylethylamine and N-methylpiperidine
- pyridine substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration.
- alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate, calcium carbonate, cesium carbonate and rubidium carbonate.
- the bases are generally used in catalytic amounts, but they can also be used equimolar, in excess or optionally as a solvent.
- the starting materials are generally reacted with one another in equimolar amounts.
- agent HL 1 are alcohols, optionally subst. Phenols, N, O-dialkylhydroxylamine, in particular pentafluorophenol or N, O-dimethylhydroxylamine in question.
- the compounds of formula VI are with acetic acid derivatives of the formula VII to the
- This reaction is usually carried out at temperatures of from -78 ° C to 120 0 C, preferably from -20 0 C to 50 0 C, in an inert organic solvent in the presence of a base or a Lewis acid or a catalyst [cf.. Bioorganic & Medicinal Chemistry (2004) Vol. 12 (6), 1357-1366].
- Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and also dimethyl sulfoxide, DMF and dimethylacetamide, particularly preferably acetonitrile and DMF. Mixtures of the solvents mentioned can also be used.
- Bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, Alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate, calcium carbonate, cesium carbonate and rubidium carbonate, and alkali metal hydrogencarbonates such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyllithium and phenyllithium, alkylmagnesium halides such as methylmagnesium chloride and alkali metal and alkaline earth metal alcoholates such as sodium methoxide,
- the bases are generally used in catalytic amounts, but they can also be used equimolar, in excess or optionally as a solvent.
- the starting materials are generally reacted with one another in equimolar amounts.
- the compounds of the formula IX can be liberated by cleaving the protective group from the compounds of the formula VIII.
- the reaction conditions depend on the nature of the protecting group SG; the splitting off of a possibly subst. Benzyl group succeeds z. B. with trifluoroacetic acid at temperatures of -78 ° C to 100 0 C, preferably -20 0 C to 50 0 C, in an inert organic solvent [cf. Greene's Protective Groups in Organic Synthesis, Wiley].
- the compounds of formula IX and their precursors can exist in two tautomeric forms.
- the invention relates to both tautomers. For the sake of clarity, only one tautomer is mentioned in the description.
- the compounds of the formula IX can be converted by cyclization into compounds of the formula I.
- the cyclization succeeds z. B. with ges. Brine and an organic solvent at temperatures from -30 ° C to 150 ° C, preferably 30 ° to 100 ° C.
- This reaction is usually carried out at temperatures of -78 ° C to 120 0 C, preferably -20 0 C to 50 ° C.
- Suitable solvents are water, alcohols such as methanol, ethanol, iso-propanol, aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and Chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, and dimethyl sulfoxide, DMF and dimethylacetamide, particularly preferably halogenated hydrocarbons such Methylene chloride
- the sulfurization of the compounds of formula X is carried out under known conditions with a Schwefelungsagenz [S], it is usually carried out at temperatures of 0 0 C to 180 0 C, preferably 20 ° C to 140 ° C, in an inert organi ⁇
- Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons such as toluene, o-, m- and p-XyIoI, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane , Anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, and dimethyl sulfoxide, particularly preferably toluene and tetrahydrofuran. It is also possible to use mixtures of the solvents mentioned.
- Suitable sulfurizing agents are, for example, phosphorus pentasulfide or La wesson's reagent.
- the compounds of the formula I in which R 1 represents a group bonded via S can be obtained, for example, via a reaction sequence according to Newman-Kwart starting from chlorothiocarbonyl compounds [cf.: J. Org. Chem., Vol. 59 (21), p 6318-21 (1994)].
- the reaction mixtures are worked up in a customary manner, for example by mixing with water, separating the phases and optionally chromatographic purification of the crude products.
- Some of the intermediate and end products are in the form of colorless or slightly brownish, viscous oils which are freed from volatile constituents under reduced pressure and at a moderately elevated temperature. If the intermediate and end products are obtained as solids, the purification can also be carried out by recrystallization or trituration.
- the organic molecular moieties mentioned for the substituents of the compounds according to the invention are collective terms for individual listings of the individual group members.
- halogenated substituents preferably carry one to five identical or different halogen atoms, in particular fluorine atoms or chlorine atoms.
- halogen in each case represents fluorine, chlorine, bromine or iodine. Furthermore, for example:
- Alkyl and the alkyl moieties for example, in alkoxy, alkylamino, dialkylamino, N-alkylsulfonylamino, alkylaminosulfonylamino, dialkylaminosulfonylamino, N- (alkenyl) -N- (alkyl) -amino, N- (alkynyl) -N- (alkyl) -amino, N- (Alkoxy) -N- (alkyl) -amino: saturated, straight-chain or branched hydrocarbon radicals having one or more C atoms, for example 1 to 2, 1 to 4, or 1 to 6 carbon atoms, for example C 1 -C 6 -alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1, 1-dimethylethyl, pentyl, 1-methylbutyl, 2-methyl
- alkyl is small alkyl groups such as C 1 -C 4 -alkyl. In another embodiment of the invention, alkyl is greater alkyl groups such as Cs-C ⁇ -alkyl.
- Haloalkyl also referred to as haloalkyl: an alkyl radical as mentioned above whose hydrogen atoms are partially or fully substituted by halogen atoms such as fluorine, chlorine, bromine and / or iodine, for example chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl , Dichlorofluoro-methyl, chlorodifluoromethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-di-fluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluor
- Cycloalkyl and the cycloalkyl moieties for example in cycloalkoxy or cycloalkyl carbonyl: monocyclic saturated hydrocarbon groups having three or more carbon atoms, for example 3 to 6 carbon ring members such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
- Alkenyl and alkenyl moieties for example, in alkenylamino, alkenyloxy, N- (alkenyl) -N- (alkyl) -amino, N- (alkenyl) -N- (alkoxy) -amino: monounsaturated, straight-chain or branched hydrocarbon radicals having two or more carbon atoms. Atoms, z. B.
- C2-C6 alkenyl such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl , 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4 Pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2 -Butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1, 1-dimethyl-2-propenyl, 1, 2-dimethyl-1-propenyl, 1 , 2-dimethyl-2-propenyl, 1 , 2-dimethyl-2
- Cycloalkenyl monocyclic, monounsaturated hydrocarbon groups having 3 to 6, preferably 5 to 6 carbon ring members, such as cyclopenten-1-yl, cyclopentene-3-yl, cyclohexen-1-yl, cyclohexen-3-yl, cyclohexen-4-yl ,
- Alkynyl and alkynyl moieties for example in alkynyloxy, alkynylamino, N- (alkynyl) -N- (alkyl) -amino or N- (alkynyl) -N- (alkoxy) -amino: straight-chain or branched hydrocarbon groups having two or more carbon atoms , z. B. 2 to 4, 2 to 6, or 3 to 6 carbon atoms and a triple bond in any position, for.
- C 2 -C 6 -alkynyl such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1, 1-dimethyl-2-propynyl, 1-ethyl 2-propynyl,
- Alkoxy alkyl, as defined above, which is bonded via an oxygen atom: z.
- 5- or 6-membered heterocycle a cyclic group having 5 or 6 ring atoms wherein 1, 2, 3 or 4 ring atoms are heteroatoms selected from O, S and N, the cyclic group being saturated, partially unsaturated or aromatic is.
- the compounds of the formula I may contain one or more further chiral centers.
- the compounds according to the invention can therefore be present as pure enantiomers or diastereomers or as mixtures of enantiomers or diastereomers.
- the invention relates to both the pure enantiomers or diastereomers and mixtures thereof.
- the compounds of the formula I can also be present in the form of the N-oxides and / or their agriculturally useful salts, the type of salt generally not being important.
- the salts of those cations or the acid addition salts of those acids come into consideration whose cations, or anions, do not adversely affect the herbicidal activity of the compounds I.
- the cations used are, in particular, ions of the alkali metals, preferably lithium, sodium or potassium, the alkaline earth metals, preferably calcium or magnesium, and the transition metals, preferably manganese, copper, zinc or iron.
- ammonium can be used as cation, whereby here optionally one to four hydrogen atoms by C 1 -C 4 -alkyl, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, hydroxy-C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, phenyl or benzyl may be replaced, preferably ammonium, dimethylammonium, diisopropylammonium, tetramethylammonium, tetrabutylammonium, 2- (2-hydroxyeth-1-oxy) eth-1 -ylammonium, di (2-hydroxyeth-1-yl) ammoni
- ammonium cation is the pyridine nitrogen atom of the formula I quaternized by alkylation or arylation.
- Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate and the anions of Ci-C4-alkanoic acids, preferably formate, acetate, propionate, Butyrate or trifluoroacetate.
- variables of the compounds of the formula I have the following meanings, these being considered both individually and in combination with one another in particular embodiments of the compounds of the formula I:
- R 1 is OR A. In a further preferred embodiment of the invention, R 1 is S (O) n -R A , where n is preferably 0 or 2, in particular 0.
- Benzoyl such as C (O) C 6 H 5 ,
- R A is H, Ci-C ⁇ -alkyl, optionally substituted. Phenyl, di-C 1 -C 6 -alkylaminocarbonyl, C 1 -C 6 -alkylcarbonyl or benzoyl. With particular preference R A is H or C 1 -C 6 -alkylcarbonyl.
- R A is a 5- or 6-membered heterocycle optionally substituted by R b as defined above, which is preferably either 1, 2, 3 or 4 nitrogen atoms or 1 oxygen or 1 sulfur atom and optionally 1 or 2 has nitrogen atoms as ring members and which is unsubstituted or may have 1 or 2 substituents selected from R b .
- N for example: Heteroaromatic groups: pyridazin-3-yl, pyridazin-4-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, pyrazine-2-yl, 2-furyl, 3-furyl, 2-thienyl , 3-Thienyl, pyrazol-1-yl, pyrazol-3-yl, pyrazol-4-yl, isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl, isothiazol-3-yl, isothiazole-4 -yl, isothiazol-5-yl, imidazol-1-yl, imidazol-2-yl, imidazol-4-yl, oxazol-2-yl, oxazol-4-yl, oxazol-5-yl
- R A is a C-bonded heteroaromatic group such as pyrazol-3-yl, imidazol-5-yl, oxazol-2-yl, thiazol-2-yl, thiazol-4-yl, thiazole-5 yl, pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidine-5-yl, pyridazin-4-yl, pyrazine-2-yl yl, [1 H] -tetrazol-5-yl and [2H] -tetrazol-5-yl, where the heterocycles 1 or 2 mentioned here by way of example from R b may have selected substituents.
- Preferred groups R b are in particular F, Cl, CN, NO 2 , CH 3 , C 2 H 5 , OCH 3 , OC 2 H 5 , OCHF 2 ,
- R 2 is phenyl which is unsubstituted or partially or completely substituted by groups R b .
- Particularly preferred are those compounds in which a group R b is in the ortho position.
- Such compounds of the formula I are described by the formula I.A .:
- R 5 and R 6 are groups R b , as defined above, preferably halogen, NO 2 , C 1 -C 4 -alkyl, C 1 -C 2 -haloalkyl and C 1 -C 4 -alkoxy.
- a group R 6 is preferably in position 5.
- X is S. In another embodiment, X is NR 3 . Both groups R 3 may be the same or different.
- Phenyl such as C 6 H 5 , 4 -CH 3 -C 6 H 4 , 4-FC 6 H 4 or S (O) n -R N , wherein R N is C 1 -C 6 -haloalkyl, such as CH 2 CF. 3, CH 2 CHF. 2
- R 3 is not hydrogen.
- R 3 is preferably C 1 -C 6 -haloalkyl, such as CH 2 CF 3 or CH 2 CHF 2 .
- Another embodiment relates to compounds of the formula I in which R b1 and R b2 are each hydrogen.
- Another embodiment relates to the N-oxides of the compounds of the formula I.
- a further embodiment relates to salts of the compounds of the formula I, especially those obtainable by quaternization of at least one pyrazine nitrogen atom, which can preferably be effected by alkylation or arylation of the compounds of the formula I. Accordingly, preferred salts of the compounds are the N-alkyl, in particular the N-methyl or N-phenyl salts.
- R 3 ⁇ is preferred.
- the groups mentioned in the tables for a substituent are also considered individually, regardless of the combination in which they are mentioned, a particularly preferred embodiment of the substituent in question.
- the compounds I and their agriculturally useful salts are suitable - both as mixtures of isomers and in the form of pure isomers - as herbicides. They are suitable as such or as appropriately formulated agent.
- the compounds I in particular the preferred embodiments thereof, or agents containing them can be used in a further number of crop plants for the removal of undesirable plants.
- the following cultures may be considered:
- crops also includes those that have been modified by breeding, mutagenesis or genetic engineering methods.
- Genetically engineered plants are plants whose genetic material has been altered in a way that does not occur under natural conditions by crossing, mutations or natural recombination (i.e., rearrangement of genetic information).
- one or more genes are integrated into the genome of the plant in order to improve the properties of the plant.
- crops thus also encompasses plants which by breeding and genetic engineering measures tolerance to certain herbicide classes, such as hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors, acetolactate synthase (ALS) inhibitors, such as. Sulfonylureas (EP-A 257 993, US Pat. No. 5,013,659) or imidazolinones (see, for example, US Pat. No.
- certain herbicide classes such as hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors, acetolactate synthase (ALS) inhibitors, such as. Sulfonylureas (EP-A 257 993, US Pat. No. 5,013,659) or imidazolinones (see, for example, US Pat. No.
- EPSPS enolpyruvylshikimate-3-phosphate synthase
- Glyphosate see, for example, WO 92/00377), glutamine synthetase (GS) inhibitors, such as, for example, Glufosinate (see eg EP-A 242 236, EP-A 242 246) or oxynil herbicides (see eg US 5,559,024).
- GS glutamine synthetase
- crops thus also includes plants that use genetic engineering measures one or more toxins, eg. As those from the bacterial strain Bacillus ssp., Produce.
- Toxins produced by such genetically engineered plants include e.g. Insecticidal proteins of Bacillus spp., In particular B. thuringiensis such as the endotoxins CrylAb, CrylAc, CrylF, Cry1Fe2, Cry2Ab, Cry3A, Cry3Bb1, Cry9c, Cry34Ab1 or Cry35Ab1; or vegetative insecticidal proteins (VIPs), e.g.
- VIPs vegetative insecticidal proteins
- VIP1, VIP2, VIP3, or VIP3A insecticidal proteins of nematode-colonizing bacteria, e.g. B. Photorhabdus spp. or Xenorhabdus spp .; Toxins from animal organisms, eg. B. Wepsen, spider or scorpion toxins; fungal toxins, e.g. B. from streptomycetes; herbal lectins, e.g. From pea or barley; agglutinins; Proteinase inhibitors, e.g. Trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors; Ribosome Inactivating Proteins (RIPs), e.g. Ricin, corn RIP, abrin, luffin, saporin or bryodin; Steroid metabolizing
- RIPs Ribosome Inactivating Proteins
- Enzymes e.g. 3-hydroxysteroid oxidase, ecdysteroid IDP glycosyltransferase, cholesterol oxidase, ecdysone inhibitors or HMG-CoA reductase; ion channel blockers, z. B. inhibitors of sodium or calcium channels; Juvenile hormone esterase; Receptors for the diuretic hormone (helicokinin receptors); Stilbene synthase, bibenzyl synthase, chitinases and glucanases. These toxins can also be produced in the plants as proteoxins, hybrid proteins, truncated or otherwise modified proteins.
- Hybrid proteins are characterized by a novel combination of different protein domains (see, for example, WO 2002/015701). Further examples of such toxins or genetically modified plants which produce these toxins are described in EP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427 529, EP-A 451 878, WO 03/018810 and WO 03/052073. The methods for producing these genetically modified plants are known in the art and z. As set forth in the publications mentioned above.
- YieldGard ® (corn cultivars producing the toxin CrylAb), YieldGard ® Plus (corn cultivars producing the toxins CrylAb and Cry3Bb1), StarLink ® (corn cultivars producing the toxin Cry9c), Herculex ® RW (corn cultivars toxins which Cry34Ab1, Cry35Ab1 and the enzyme
- Agrisure ® CB and Bt176 from Syngenta Seeds SAS, France corn varieties which produce the toxin CrylAb and the PAT enzyme
- MIR604 from Syngenta Seeds SAS, France
- MON 863 from Monsanto Europe SA, Belgium
- IPC 531 from Monsanto Europe SA, Belgium
- cottons producing a modified version of the toxin CrylAc 1507 from Pioneer Overseas Corporation, Belgium (maize varieties producing the toxin Cryl F and the PAT enzyme).
- crops thus also includes plants that produce by genetic engineering measures one or more proteins that cause increased resistance or resistance to bacterial, viral or fungal pathogens, such as. B. so-called pathogenesis-related proteins (PR proteins, see EP-A 392 225), resistance proteins (eg, potato varieties that produce two resistance genes against Phytophthora infestans from the Mexican wild potato Solanum bulbocastanum) or T4 lysozyme (z. Potato varieties resistant to bacteria such as Erwinia amylvora by the production of this protein).
- PR proteins pathogenesis-related proteins
- resistance proteins eg, potato varieties that produce two resistance genes against Phytophthora infestans from the Mexican wild potato Solanum bulbocastanum
- T4 lysozyme z. Potato varieties resistant to bacteria such as Erwinia amylvora by the production of this protein.
- crops thus also includes plants whose productivity has been improved by means of genetic engineering methods by z. For example, the productivity (eg biomass, grain yield, starch
- crops also includes plants whose ingredients have been modified in particular to improve the human or animal diet using genetic engineering methods by z.
- oil plants can produce health-promoting long-chain omega-3 fatty acids or monounsaturated omega-9 fatty acids (eg Nexera ® oilseed rape).
- crops also includes plants that have been modified for the improved production of raw materials by means of genetic engineering methods by z.
- the amylopectin content of potatoes (Amflora ® potato) was increased.
- the compounds of the formula I are also suitable for the defoliation and / or desiccation of plant parts, for which crop plants such as cotton, potato, oilseed rape, sunflower, soybean or field beans, in particular cotton, come into consideration.
- compositions for the desiccation and / or defoliation of plants, processes for the preparation of these agents and methods for the desiccation and / or defoliation of plants with the compounds of formula I have been found.
- Desiccants are the compounds of formula I in particular for dehydration of the aerial parts of crop plants such as potato, oilseed rape, sunflower and soybean but also cereals. This enables a completely mechanical harvesting of these important crops.
- the compounds I or the herbicidal compositions containing them can, for example, in the form of directly sprayable aqueous solutions, powders, suspensions, even high-percentage aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, scattering agents or granules by spraying, atomizing , Dusting, scattering, pouring or treatment of the seed or mixing with the seed.
- the application form depending on the intended use; In any case, they should ensure the finest possible distribution of the active compounds according to the invention.
- the herbicidal compositions contain a herbicidally effective amount of at least one compound of the formula I or an agriculturally useful salt of I and auxiliaries customary for the formulation of pesticides.
- auxiliaries include auxiliaries, solid carriers, surface-active substances (such as dispersants protective colloids, emulsifiers, wetting agents and adhesives), organic and inorganic thickeners, bactericides, antifreeze agents, defoamers, if necessary, dyes and for seed formulations adhesives ,
- thickeners ie, compounds which impart modified flowability to the formulation, ie, high-level at low viscosity and low viscosity in the agitated state
- polysaccharides such as xanthan gum (Kelzan® from Kelco), Rhodopol® 23 (Rhone Poulenc) or Veegum ® (RT Vanderbilt) and organic and inorganic layer minerals such as Attaclay® (Engelhardt).
- antifoams examples include silicone emulsions (such as, for example, Silikon® SRE, Wacker or Rhodorsil® from Rhodia), long-chain alcohols, fatty acids, salts of fatty acids, organofluorine compounds and mixtures thereof.
- Bactericides may be added to stabilize the aqueous herbicidal formulation.
- bactericides are bactericides based on diclorophene and benzyl alcohol hemiformal (Proxel® from ICI or Acticide® RS from Thor Chemie and Kathon® MK from Rohm & Haas) and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones (Acticide MBS der Fa. Thor Chemie)
- antifreeze agents are ethylene glycol, propylene glycol, urea or glycerol.
- colorants are both water-insoluble pigments and water-soluble dyes. Examples which may be mentioned under the names rhodamine B, Cl. Pigment Red 112 and Cl. Solvent Red 1 known dyes, and pigment blue 15: 4, pigment blue 15: 3, pigment blue 15: 2, pigment blue 15: 1, pigment blue 80, pigment yellow 1, pigment yellow 13, pigment red 1 12, pigment red 48: 1, pigment red 48: 1, pigment red 57: 1, pigment red 53: 1, pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, aeid red 51, aeid red 52, aeid red 14, aeid blue 9, aeid yellow 23, basic red 10, basic red 108.
- adhesives are polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol and
- Suitable inert additives are, for example, mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, alkylated benzenes or their derivatives, Alcohols such as methanol, ethanol, propanol, butanol, cyclohexanol, ketones such as cyclohexanone or strongly polar solvents, eg. As amines such as N-methylpyrrolidone or water.
- Solid carriers are mineral soils such as silicic acids, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, Ureas and vegetable products such as cereal flour, tree bark, wood and nutshell flour, cellulose powder or other solid carriers.
- surface-active substances adjuvants, wetting, adhesion, dispersing and emulsifying agents
- the alkali, alkaline earth, ammonium salts of aromatic sulfonic acids e.g.
- Ligninsulfon Acid eg Borrespers types, Borregaard
- phenolsulfonic acids naphthalene sulfonic acids
- naphthalene sulfonic acids Methoxylated isooctyl-, octyl
- polyethylenimine BASF SE, Lupasol types
- polyvinylpyrrolidone and copolymers thereof.
- Powders, dispersants and dusts may be prepared by mixing or co-grinding the active substances with a solid carrier.
- Granules, e.g. Coating, impregnation and homogeneous granules can by
- Binding of the active ingredients to solid carriers are produced.
- Aqueous application forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water.
- the compounds of the formula I or Ia as such or dissolved in an oil or solvent, can be homogenized in water by means of wetting agents, tackifiers, dispersants or emulsifiers.
- concentrates consisting of active substance, wetting, adhesion, dispersing or emulsifying agent and possibly solvent or oil, which are suitable for dilution with water.
- concentrations of the compounds of the formula I in the ready-to-use formulations can be varied within wide limits.
- the formulations generally contain from 0.001 to 98% by weight, preferably from 0.01 to 95% by weight, at least of an active substance.
- the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
- the compounds I according to the invention can be formulated, for example, as follows:
- active compound 20 parts by weight are dissolved in 70 parts by weight of cyclohexanone with the addition of 10 parts by weight of a dispersant, e.g. Polyvinylpyrrolidone dissolved. Dilution in water gives a dispersion.
- a dispersant e.g. Polyvinylpyrrolidone dissolved. Dilution in water gives a dispersion.
- the active ingredient content is 20% by weight
- active compound 15 parts by weight of active compound are dissolved in 75 parts by weight of an organic solvent (for example alkylaromatics) with the addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution in water results in an emulsion.
- the formulation has 15% by weight active ingredient content.
- active compound 25 parts by weight of active compound are dissolved in 35 parts by weight of an organic solvent (for example alkylaromatics) with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
- organic solvent for example alkylaromatics
- calcium dodecylbenzenesulfonate and castor oil ethoxylate in each case 5 parts by weight.
- This mixture is added to water by means of an emulsifying machine (e.g., Ultraturax) in 30 parts by weight and made into a homogeneous emulsion. Dilution in water results in an emulsion.
- the formulation has an active ingredient content of 25% by weight.
- active compound 20 parts by weight of active compound are comminuted with the addition of 10 parts by weight dispersing and wetting agents and 70 parts by weight of water or an organic solvent in a stirred ball mill to a fine active substance suspension. Dilution in water results in a stable suspension of the active ingredient.
- the active ingredient content in the formulation is 20% by weight.
- Water-dispersible and water-soluble granules 50 parts by weight of active compound are finely ground with the addition of 50 parts by weight of dispersing and wetting agents and prepared by means of industrial equipment (for example extrusion, spray tower, fluidized bed) as water-dispersible or water-soluble granules. Dilution in water results in a stable dispersion or solution of the active ingredient.
- the formulation has an active ingredient content of 50% by weight.
- active compound 75 parts by weight of active compound are ground with the addition of 25 parts by weight of dispersing and wetting agents and silica gel in a rotor-Strator mill. In the dilution In water gives a stable dispersion or solution of the active ingredient.
- the active ingredient content of the formulation is 75% by weight.
- 0.5 parts by weight of active compound are finely ground and combined with 99.5 parts by weight of carrier substances. Common processes are extrusion, spray drying or fluidized bed. This gives a granulate for direct application with 0.5 wt .-% active ingredient content.
- the application of the compounds I or the herbicidal compositions containing them can take place in the pre-emergence, post-emergence or together with the seed of a crop. It is also possible to apply the herbicidal compositions or active ingredients characterized in that with the herbicidal agents or active ingredients pretreated seed of a crop plant is applied. If the active ingredients are less compatible with certain crops, then application techniques may be employed whereby the herbicidal agents are sprayed by the sprayers so as not to hit the leaves of the sensitive crops as far as possible, while the active ingredients affect the leaves underneath growing undesirable plants or the uncovered floor surface (post-directed, lay-by).
- the application of the compounds of the formula I or of the herbicidal compositions can be carried out by treating seed.
- seed dressing seed coating, seed dusting, seed soaking, seed film coating, seed multilayer coating, seed encrusting, seed dripping, and seed pelleting
- seed dressing seed dressing, seed coating, seed dusting, seed soaking, seed film coating, seed multilayer coating, seed encrusting, seed dripping, and seed pelleting
- seed film coating seed multilayer coating
- seed encrusting seed dripping
- seed pelleting seed pelleting
- seed includes seeds of all kinds, such as grains, seeds, fruits, tubers, cuttings and similar forms.
- seed preferably describes grains and seeds here.
- Seeds of the abovementioned crops but also the seeds of transgenic or obtained by conventional breeding methods plants can be used as seeds.
- the application rates of active ingredient are 0.001 to 3.0, preferably 0.01 to 1.0 kg / ha of active substance (a. S.).
- the compounds I are usually used in amounts of 0.001 to 10 kg per 100 kg of seed.
- Safeners are chemical compounds that prevent or reduce damage to crops without significantly affecting the herbicidal activity of the compounds of formula I on undesirable plants. They can be used both before sowing (for example in seed treatments, cuttings or seedlings) as well as in the pre- or post-emergence of the crop. The safeners and the compounds of formula I can be used simultaneously or sequentially.
- Suitable safeners are, for example, (quinoline- ⁇ -oxy) acetic acids, 1-phenyl-5-haloalkyl-1H-1, 2,4-triazole-3-carboxylic acids, 1-phenyl-4,5-dihydro-5 alkyl-1H-pyrazole-3,5-dicarboxylic acids, 4,5-dihydro-5,5-diaryl-3-isoxazolecarboxylic acids, dichloroacetamides, alpha-oximinophenylacetonitriles, acetophenone oximes, 4,6-dihalo-2-phenylpyrimidines, N- [ [4- (aminocarbonyl) phenyl] sulfonyl] -2-benzoic acid amides, 1,8-naphthalic anhydride, 2-halo-4- (haloalkyl) -5-thiazolecarboxylic acids, phosphorothiolates and N-alkyl-O-phenylcarba
- the compounds of formula I can be mixed with numerous representatives of other herbicidal or growth-regulating active ingredient groups or with safeners and applied together.
- Glyphosate, glyphosate isopropylammonium and glyphosate trimesium sulfosate
- Y is phenyl or 5- or 6-membered heteroaryl, as defined above, which may be substituted by one to three groups R aa ;
- R 21 , R 22 , R 23 , R 24 are H, halogen, or C 1 -C 4 -alkyl;
- X is O or NH;
- n 0 or 1. 2 have in particular the following meanings:
- R where # is the bond to the molecular skeleton; and 5 R 21 , R 22 , R 23 , R 24 are H, Cl, F or CH 3 ; R 25 is halogen, C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl; R 26 is C 1 -C 4 -alkyl; R 27 is halogen, C 1 -C 4 -alkoxy or C 1 -C 4 -haloalkoxy; R 28 is H, halogen, CrC 4 - alkyl, Ci-C 4 haloalkyl or Ci-C4-haloalkoxy; m is 0, 1, 2 or 3; X oxygen; n 0 or 1.
- Particularly preferred compounds of the formula 2 are:
- MSMA oleic acid, oxaziclomefon, pelargonic acid, pyributicarb, quinoclamin, triaziflam, tridiphan and 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol (B-10; CAS 499223-49-3 ) and its salts and esters.
- Examples of preferred safeners C are Benoxacor, Cloquintocet, Cyometrinil, Cyprusulfamide, Dichlormid, Dicyclonon, Dietholate, Fenchlorazole, Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen, Mefenpyr, Mephenate, Naphthalic Anhydride, Oxabetrinile, 4- (Dichloroacetyl ) -1-oxa-4-azaspiro [4.5] decane (B-1 1, MON4660, CAS 71526-07-3) and 2,2,5-trimethyl-3- (dichloroacetyl) -1,3-oxazolidine (B -12; R-29148, CAS 52836-31-4).
- the active compounds of groups b1) to b15) and the safeners C are known herbicides and safeners, see, for example, US Pat. B. The Compendium of Pesticide Common Names (http://www.alanwood.net/pesticides/); B. Hock, C. Fedtke, RR Schmidt, herbicides, Georg Thieme Verlag, Stuttgart 1995. Further herbicidal active compounds are known from WO 96/26202, WO 97/411 16, WO 97/41 117, WO 97/411 18, WO 01 / 83459 and WO 2008/074991 and W. Krämer et al. (ed.) "Modern Crop Protection Compounds", Vol.
- compositions in the form of a crop protection agent formulated as a 1-component composition comprising a combination of active substances comprising at least one pyridine compound of the formula I and at least one further active ingredient, preferably selected from the active substances of groups b1 to b15, and at least one solid or liquid carrier and / or one or more surface-active substances and, if desired, one or more further auxiliaries customary for crop protection agents.
- the invention also relates to compositions in the form of a plant protection composition formulated as a 2-component composition
- a 2-component composition comprising a first component containing at least one pyridine compound of the formula I, a solid or liquid carrier and / or one or more surface-active substances, and a second component containing at least one further active ingredient selected from the active substances of groups b1 to b15, a solid or liquid carrier and / or one or more surface-active substances, wherein in addition both components may also contain further adjuvants customary for crop protection agents.
- the weight ratio of the active compounds A: B is generally in the range from 1: 1000 to 1000: 1, preferably in the range from 1: 500 to 500: 1, in particular in the range of 1: 250 to 250: 1 and particularly preferably in the range of 1: 75 to 75: 1.
- the weight ratio of the active compounds A: C is generally in the range from 1: 1000 to 1000: 1, preferably in the range from 1: 500 to 500: 1, in particular in the range of 1: 250 to 250: 1 and particularly preferably in the range of 1: 75 to 75: 1.
- the relative proportions by weight of the components A: B are generally in the range from 1: 1000 to 1000: 1, preferably in the range from 1: 500 to 500: 1, in particular in the range from 1: 250 to 250: 1 and more preferably in the range from 1: 75 to 75: 1,
- the weight ratio of component A: C is generally in the range of 1: 1000 to 1000: 1, preferably in the range of 1: 500 to 500: 1, in particular in the range of 1: 250 to 250: 1 and more preferably in the range of 1: 75 to 75: 1
- the weight ratio of the components B: C is generally in the range from 1: 1000 to 1000: 1, preferably in the range from 1: 500 to 500: 1, in particular in the range from 1: 250 to 250: 1 and particularly preferably in the range from 1: 75 to 75: 1st
- the weight ratio of components A + B to component C is preferably in the range from 1: 500 to 500: 1, in
- compositions according to the invention containing in each case an individualized compound of the formula I and a mixture of partner, or a mixture partner combination are given in Table B below.
- a further embodiment of the invention relates to the compositions B-1 to B-1235 listed in Table B, wherein in each case one row of Table B corresponds to a herbicidal composition comprising an individualized in the present specification compounds of formula I (component 1) and the further active ingredient from groups b1) to b15) and / or safener C (component 2) respectively indicated in the relevant line.
- the active ingredients in the described compositions are each preferably present in synergistically effective amounts.
- the compounds I and the compositions according to the invention may also have a plant-strengthening effect. They are therefore suitable for mobilizing plant-own defenses against infestation by undesirable microorganisms, such as harmful fungi, but also viruses and bacteria.
- plant-strengthening (resistance-inducing) substances are to be understood as meaning those substances which are capable of stimulating the defense system of treated plants in such a way that they develop extensive resistance to these microorganisms during subsequent inoculation with undesired microorganisms.
- the compounds I can be used to protect plants against attack by undesired microorganisms within a certain period of time after the treatment. The period within which protection is provided generally extends from 1 to 28 days, preferably 1 to 14 days after treatment of the plants with the compounds I or after treatment of the seed, up to 9 months after sowing.
- the compounds I and the compositions according to the invention are also suitable for increasing crop yield.
- Step 1 3- (4-methoxy-benzyloxy) -pyridine-2-carbonklaremethylester
- a solution of 15.2 g of 3-hydroxy-pyridin-2-methylester in 200 ml DMF was added 4g NaH and 30 min at 20-25 0 C stirred.
- 15.4 g of para-methoxybenzyl chloride was added.
- the mixture was stirred at 40 ° C. for about 15 hours and then poured into water. After extraction with ethyl acetate, phase separation and washing of the combined organic phases with water and sat. NaCl solution, then drying and removal of the solvent, the residue was subjected to column chromatography. 20 g of the title compound were obtained as a yellow oil.
- Step 2 3- (4-Methoxy-benzyloxy) -pyridine-2-carboxylic acid
- a solution of 7g of the ester of Step 1 and 2.2g of LiOH in 60ml of methanol and 40ml of water was stirred at 20-25 ° C for approximately 15h. touched. Then, 100 ml of water and 7 ml of acetic acid were added. The mixture was extracted with ethyl acetate. The combined organic phases were dried and freed from the solvent. 5 g of the title compound were obtained as a yellowish solid.
- Step 3 3- (4-Methoxy-benzyloxy) -pyridine-2-carboxylic acid pentafluorophenyl ester
- Step 4 Methyl 3- [3- (4-methoxy-benzyloxy) -pyridin-2-yl] -3-oxo-2- (2-trifluoromethyl-phenyl) -propionate
- Step 5 3- (3-Hydroxy-pyridin-2-yl) -3-oxo-2- (2-trifluoromethyl-phenyl) -propionic acid methyl ester
- Step 6 8-Hydroxy-7- (2-trifluoromethyl-phenyl) -pyrano [2,3-b] pyrazine-6-one 350 mg of Step 5 was dissolved in 7 ml of DMSO / sat. Saline solution dissolved. The mixture was stirred at 100 0 C for 2 h. Subsequently, the reaction solution was diluted with 70 ml of 2N HCl and extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate. After removal of the solvent in vacuo and purification by prep. HPLC gave 83 mg of the title compound.
- the culture vessels used were plastic pots with loamy sand with about 3.0% humus as substrate.
- the seeds of the test plants were sown separately by species.
- the active ingredients suspended or emulsified in water were applied directly after sowing by means of finely distributing nozzles.
- the jars were lightly rained to promote germination and growth and then covered with clear plastic hoods until the plants had grown. This cover causes a uniform germination of the test plants, if it was not affected by the active ingredients.
- test plants were, depending on the growth habit, first grown to a height of from 3 to 15 cm and then treated with the active ingredients suspended or emulsified in water.
- the test plants were either sown directly and grown in the same containers or they were first grown separately as seedlings and transplanted into the test containers a few days before the treatment.
- the plants were kept species-specific at temperatures of 10 - 25 ° C and 20 - 35 ° C, respectively.
- the trial period lasted for 2 to 4 weeks. During this time, the plants were cared for, and their response to each treatment was evaluated.
- the rating was based on a scale from 0 to 100. 100 means no emergence of the plants or complete destruction of at least the above-ground parts and 0 none
- a good herbicidal activity is at Wer- at least 70 and a very good herbicidal activity is given at values of at least 85.
- the plants used in the greenhouse experiments are composed of the following species:
- Example 1 The active ingredient from Example 1 showed at a rate of 3.0 kg / ha in the pre-emergence against SETIT a very good herbicidal activity.
- Example 2 The active ingredient from Example 1 showed at a rate of 3.0 kg / ha postemergence against ABUTH, AVEFA, or SETFA a very good herbicidal activity.
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Abstract
L'invention concerne des pyrazines substituées de formule (I), dans laquelle les variables sont telles que définies dans la description, leurs sels appropriés en agriculture, des procédés et produits intermédiaires pour la préparation des pyrazines de formule (I), des agents contenant lesdites pyrazines et leur utilisation comme herbicides, c.-à-d dans la lutte contre les adventices, ainsi qu'un procédé de lutte contre la croissance indésirable de plantes, qui consiste à faire agir une quantité à action herbicide d'au moins un composé de pyrazine de formule (I) sur des plantes, leurs semences et/ou dans leur habitat.
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EP10724420A EP2437605A1 (fr) | 2009-06-05 | 2010-05-31 | Pyridopyrazines substituées à action herbicide |
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PCT/EP2010/057523 WO2010139658A1 (fr) | 2009-06-05 | 2010-05-31 | Pyridopyrazines substituées à action herbicide |
EP10724420A EP2437605A1 (fr) | 2009-06-05 | 2010-05-31 | Pyridopyrazines substituées à action herbicide |
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EP (2) | EP2437605A1 (fr) |
JP (1) | JP2012528821A (fr) |
CN (1) | CN102459277A (fr) |
AR (1) | AR076986A1 (fr) |
BR (1) | BRPI1008214A2 (fr) |
TW (1) | TW201102001A (fr) |
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EP2550277A1 (fr) * | 2010-03-23 | 2013-01-30 | Basf Se | Pyridazines substituées à action herbicide |
US8575068B2 (en) | 2010-03-23 | 2013-11-05 | Basf Se | Pyrazinothiazines having herbicidal action |
CN102906096A (zh) | 2010-03-23 | 2013-01-30 | 巴斯夫欧洲公司 | 具有除草作用的吡啶类 |
AU2011231819A1 (en) | 2010-03-23 | 2012-10-18 | Basf Se | Pyridothiazines having herbicidal action |
AR081526A1 (es) | 2010-03-23 | 2012-10-03 | Basf Se | Piridazinas sustituidas que tienen accion herbicida |
BR112013011750A8 (pt) * | 2010-11-12 | 2017-07-11 | Syngenta Ltd | Compostos herbicidas |
BR112015012645A2 (pt) | 2012-12-18 | 2018-10-23 | Basf Se | métodos para produção, molécula e constructo de ácido nucleico, vetor, polipeptídeo, núcleo de célula vegetal, planta transgênica, processo, composição, uso do ácido nucleico e método para controlar ervas daninhas |
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ES2046167T3 (es) | 1985-12-13 | 1994-02-01 | American Cyanamid Company | Procedimiento para la preparacion de composiciones herbicidas de (2-imidazolin-2-il)-heteropiridina condensadas. |
DE4131029A1 (de) * | 1991-09-18 | 1993-07-29 | Basf Ag | Substituierte pyrido (2,3-d) pyrimidine als antidots |
US5563280A (en) * | 1994-07-25 | 1996-10-08 | American Cyanamid Co. | 4-Phenoxycoumarins as herbicidal agents |
US5801183A (en) | 1995-01-27 | 1998-09-01 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon | Aza and aza (N-oxy) analogs of glycine/NMDA receptor antagonists |
BR0313743A (pt) | 2002-08-23 | 2005-07-05 | Chiron Corp | Benzimidazol quinolinonas e usos destas |
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WO2005010000A2 (fr) | 2003-07-18 | 2005-02-03 | Basf Aktiengesellschaft | Composes de 3-arylpyridine arylcondenses et leur utilisation pour lutter contre des champignons pathogenes |
GB0614471D0 (en) * | 2006-07-20 | 2006-08-30 | Syngenta Ltd | Herbicidal Compounds |
GB0624760D0 (en) * | 2006-12-12 | 2007-01-17 | Syngenta Ltd | Herbicidal compounds |
GB0800855D0 (en) | 2008-01-17 | 2008-02-27 | Syngenta Ltd | Herbicidal compounds |
GB0800856D0 (en) | 2008-01-17 | 2008-02-27 | Syngenta Ltd | Herbicidal compounds |
GB0816880D0 (en) * | 2008-09-15 | 2008-10-22 | Syngenta Ltd | Improvements in or relating to organic compounds |
WO2010049269A1 (fr) * | 2008-10-29 | 2010-05-06 | Basf Se | Pyridines substituées à action herbicide |
EP2550277A1 (fr) * | 2010-03-23 | 2013-01-30 | Basf Se | Pyridazines substituées à action herbicide |
-
2010
- 2010-05-31 WO PCT/EP2010/057523 patent/WO2010139658A1/fr active Application Filing
- 2010-05-31 US US13/375,516 patent/US8841298B2/en not_active Expired - Fee Related
- 2010-05-31 BR BRPI1008214-0A patent/BRPI1008214A2/pt not_active IP Right Cessation
- 2010-05-31 JP JP2012513578A patent/JP2012528821A/ja not_active Ceased
- 2010-05-31 CN CN2010800246497A patent/CN102459277A/zh active Pending
- 2010-05-31 US US13/375,508 patent/US20120071322A1/en not_active Abandoned
- 2010-05-31 EP EP10724420A patent/EP2437605A1/fr not_active Withdrawn
- 2010-05-31 WO PCT/EP2010/057522 patent/WO2010139657A1/fr active Application Filing
- 2010-05-31 EP EP10724419A patent/EP2438071A1/fr not_active Withdrawn
- 2010-06-04 UY UY32692A patent/UY32692A/es unknown
- 2010-06-04 AR ARP100101988 patent/AR076986A1/es unknown
- 2010-06-04 TW TW99118233A patent/TW201102001A/zh unknown
Non-Patent Citations (1)
Title |
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See references of WO2010139658A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2010139657A1 (fr) | 2010-12-09 |
EP2438071A1 (fr) | 2012-04-11 |
BRPI1008214A2 (pt) | 2015-08-25 |
US8841298B2 (en) | 2014-09-23 |
TW201102001A (en) | 2011-01-16 |
US20120077678A1 (en) | 2012-03-29 |
CN102459277A (zh) | 2012-05-16 |
US20120071322A1 (en) | 2012-03-22 |
UY32692A (es) | 2010-11-30 |
JP2012528821A (ja) | 2012-11-15 |
WO2010139658A1 (fr) | 2010-12-09 |
AR076986A1 (es) | 2011-07-20 |
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