WO2011073143A1 - Substituted cyanobutyrates having herbicidal action - Google Patents

Substituted cyanobutyrates having herbicidal action Download PDF

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WO2011073143A1
WO2011073143A1 PCT/EP2010/069532 EP2010069532W WO2011073143A1 WO 2011073143 A1 WO2011073143 A1 WO 2011073143A1 EP 2010069532 W EP2010069532 W EP 2010069532W WO 2011073143 A1 WO2011073143 A1 WO 2011073143A1
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alkyl
formula
compound
methyl
group
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PCT/EP2010/069532
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French (fr)
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Dschun Song
Julia Major
Johannes Hutzler
Trevor William Newton
Andrea Vescovi
Robert Reinhard
Bernd Sievernich
Cyrill Zagar
Elmar Kibler
Ricarda Niggeweg
Toralf KÜHN
Matthias Witschel
William Karl Moberg
Liliana Parra Rapado
Tao QU
Frank Stelzer
Andree Van Der Kloet
Thomas Seitz
Thomas Ehrhardt
Klaus Kreuz
Klaus Grossmann
Anna Aleksandra Michrowska-Pianowska
Anja Simon
Richard Roger Evans
Eike Hupe
Klaus Reinhard
Matthias Bergtold
Susanne Noreen Evelyn Kolle
Stefan Tresch
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Basf Se
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    • C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
    • C07C255/41—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
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    • A01N43/20—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom three- or four-membered rings
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Abstract

Substituted cyanobutyrates of the formula I in which the variables are defined according to the description, processes and intermediates for preparing the compounds of the formula I and their N-oxides, their agriculturally suitable salts, compositions comprising them and their use as herbicides, and also a method for controlling unwanted vegetation.

Description

Substituted cyanobutyrates having herbicidal action Description The present invention relates to substituted cyanobutyrate compounds of the formula I
Figure imgf000003_0001
in which the variables have the following meaning:
R is halogen, cyano, nitro, Ci-C4-alkyl, Ci-C4-haloalkyl, C2-C6-alkenyl, C2-C6- alkynyl, Ci-C4-alkoxy, Ci-C4-alkylthio, Z-(tri-Ci-C4-alkyl)silyl;
R1 is hydrogen, Z-CN, Ci-Ce-alkyI, Z-C3-C6-cycloalkyl, Ci-C8-haloalkyl, Ci-C4-alkoxy- Ci-C4-alkyl, Ci-C4-alkylthio-Ci-C4-alkyl, C3-C8-alkenyl, Z-C3-C6-cycloalkenyl, C3- Cs-alkynyl, NR'R", Z-(tri-Ci-C4-alkyl)silyl, Z-N=C(Ra)2, Z-C(Ra)=NRa, Z-C(=T)-Ra, Z-P(=T)(Ra)2, Z-phenyl, a 3- to 7-membered monocyclic or 9- or 10-membered bicyclic saturated, unsaturated or aromatic heterocycle which contains 1 , 2, 3 or 4 heteroatoms selected from the group consisting of O, N and S, which may carry carbonyl or thiocarbonyl groups and which is attached via carbon or nitrogen, T is O or S;
Ra is hydrogen, TH, Ci-C8-alkyl, Ci-C4-haloalkyl, Z-C3-C6-cycloalkyl, C2-C8- alkenyl, Z-C5-C6-cycloalkenyl, C2-C8-alkynyl, Z-Ci-C6-alkoxy, Z-C1-C4- haloalkoxy, Z-C3-C8-alkenyloxy, Z-C3-C8-alkynyloxy, Z-Ci-C4-alkylthio, Z-
Ci-C4-haloalkylthio, Z-C3-C8-alkenylthio, Z-C3-C8-alkynylthio, NR'R", Ci- Ce-alkylsulfonyl, oxy-Ci-C3-alkyleneoxy, Z-BRV, Z-C(=T)-RA, Z-T-C(=T)- RA, Z-(tri-Ci-C4-alkyl)silyl, Z-phenyl, Z-phenoxy, Z-phenylamino or a 3- to 7-membered monocyclic or 9- or 10-membered bicyclic heterocycle which contains 1 , 2, 3 or 4 heteroatoms selected from the group consisting of O, N and S, where the cyclic groups are unsubstituted or may carry 1 , 2, 3 or 4 groups Rb and/or carbonyl or thiocarbonyl groups; R', R" independently of one another are hydrogen, Ci-C8-alkyl,
CrC4-haloalkyl, C3-C8-alkenyl, C3-C8-alkynyl,
Z-Cs-Cs-cycloalkyl, Z-Ci-C8-alkoxy, Z-Ci-C8-alkylthio, Z-Ci-C8- haloalkoxy, Z-Ci-C8-haloalkylthio, Z-C(=T)-RA, where RA is TH, Ci-C4-alkyl, Ci-C4-alkoxy or Ci-C4-alkylthio;
R' and R" together with the nitrogen atom to which they are attached may also form a 3- to 7-membered monocyclic or 9- or 10- membered bicyclic heterocycle which contains 1 , 2, 3 or 4 heteroatoms selected from the group consisting of O, N and S and which may carry carbonyl or thiocarbonyl groups;
Rb independently of one another are Z-CN, Z-TH, Z-NO2, Z-halogen, Ci-Ce-alkyl, Ci-C4-haloalkyl, C2-Ce-alkenyl, C2-Cs-alkynyl, Z-Ci-Cs-alkoxy, Z-Ci-C8-alkylthio, Z-Ci-C8-haloalkylthio, Z-Ci-C8- haloalkoxy, Z-C3-Cio-cycloalkyl, T-Z-C3-Cio-cycloalkyl,
Z-C(=T)-Ra, NR'R", Z-(tri-Ci-C4-alkyl)silyl , Z-phenyl and S(0)mRbb, where
Rbb is d-Ce-alkyl or Ci-C5-haloalkyl;
m is 0, 1 or 2;
Rb together with the group Rb attached to the adjacent carbon atom may also form a five- or six-membered saturated or partially or fully unsaturated ring which, in addition to carbon atoms, may contain 1 , 2 or 3 heteroatoms selected from the group consisting of O, N and S;
Z is a covalent bond or Ci-Cs-alkylene;
n is 0, 1 , 2, 3, 4 or 5;
R2,R3, R4 independently of one another are halogen, cyano, nitro, N=C=T, C1-C4- alkyl, Ci-C4-alkoxy, Ci-C4-alkylthio, S(0)mR b, NR'R'', Ci-C4-haloalkyl, Ci-C4- haloalkoxy, Ci-C4-haloalkylthio; where, if the index x is 2 or 3, the groups R4 may be identical or different;
x is 0, 1 , 2 or 3;
where in the groups R and R1 and their subsubstituents, the carbon chains and/or the cyclic groups may be partially or fully substituted by groups Ra and/or Rb, or an N-oxide or an agriculturally suitable salt thereof;
with the proviso that R2 and R3 are not both chlorine if the indices n and x are 0 and R1 is Ci-C4-alkyl or H; and
R2 and R3 are not both fluorine if the index n is 1 , the index x is 0 or 3 and R and R4 are fluorine and R1 is Ci-C4-alkyl.
Moreover, the invention relates to processes and intermediates for preparing the compounds of the formula I and the N-oxides thereof, the agriculturally usable salts thereof, to compositions comprising them and to their use as herbicides, i.e. for controlling harmful plants, and also to a method for controlling unwanted vegetation which comprises allowing a herbicidally effective amount of at least one compound of the formula I or of an agriculturally suitable salt thereof to act on plants, their seed and/or their habitat.
Further embodiments of the present invention can be found in the claims, the description and the examples. It is to be understood that the features mentioned above and those still to be illustrated below of the subject matter of the invention can be applied not only in the respective given combination but also in other combinations without leaving the scope of the invention.
EP-A 5 341 , EP-A 266 725, EP-A 270 830, J P 04/297 454, J P 04/297 455 and J P 05/058 979 disclose herbicidal cyanobutyrates; however, their herbicidal action especially at low application rates and/or their compatibility with crop plants leave scope for improvement. It is an object of the present invention to provide compounds having herbicidal action. To be provided are in particular active compounds having strong herbicidal action, in particular even at low application rates, whose compatibility with crop plants is sufficient for commercial application.
These and further objects are achieved by the compounds of the formula I defined at the outset and by their N-oxides and also their agriculturally suitable salts.
The compounds according to the invention can be prepared analogously to the synthesis routes described in the documents cited according to standard processes of organic chemistry, for example according to the following synthesis route:
Phenylacetonitrile derivatives of the formula II can be reacted with cinnamate derivatives of the formula III according to a Michael addition to give compounds of the formula I. mula I.
Figure imgf000005_0001
This reaction is usually carried out at temperatures of from -100°C to 150°C, preferably from -78°C to 50°C, in a solvent in the presence of a base and/or a catalyst [cf. J. Chem. Soc. (1945), p. 438].
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 (THF), nitriles, such as acetonitrile and propionitrile, ketones, such as acetone, methyl ethyl ketone, diethyl ketone and tert- butyl methyl ketone, alcohols, such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide and water, particularly preferably THF and methanol. It is also possible to use mixtures of the solvents mentioned.
Suitable bases are, in general, 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 also alkali metal bicarbonates, such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls, such as methyllithium, butyllithium and phenyllithium, alkylmagnesium halides, such as methylmagnesium chloride, and also alkali metal and alkaline earth metal alkoxides, such as sodium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide and dimethoxymagnesium, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, tributylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to potassium tert-butoxide, lithium bis(trimethylsilyl)amide and 7-methyl-1 ,5,7-triazabicyclo[4.4.0]dec-5-ene.
The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvents.
Suitable for use as acidic catalysts are inorganic acids, such as hydrofluoric acid, hydrochloric acid, hydrobromic acid, sulfuric acid and perchloric acid, Lewis acids, such as boron trifluoride, aluminum trichloride, iron(lll) chloride, tin(IV) chloride, titanium(IV) chloride, scandium(lll) triflate and zinc(ll) chloride, and also organic acids, such as formic acid, acetic acid, propionic acid, oxalic acid, toluenesulfonic acid,
benzenesulfonic acid, camphorsulfonic acid, citric acid and trifluoroacetic acid.
The acids are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.
Alternatively, the compounds of the formula I can also be obtained by
transesterification of other cyanobutyrates. This may take place by various methods, for example those described below: The transesterification can be carried out in the presence of molecular sieves in an alcohol R1-OH, if appropriate in an aprotic solvent. This reaction is usually carried out at temperatures of from 0°C to 180°C, preferably from 20°C to 80°C, in the presence of a Lewis or Bronsted acid or an enzyme [cf. J. Org. Chem. 2002, 67, 431].
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 THF, nitriles, such as acetonitrile and propionitrile, ketones, such as dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably the alcohol R1-OH. It is also possible to use mixtures of the solvents mentioned.
Alternatively, the transesterification may be carried out by acidic or basic hydrolysis of other cyanobutyrates (a), followed by reaction with an alcohol R1-OH. These reactions are usually carried out at temperatures of from 0°C to 120°C, preferably from 20°C to 50°C, in the presence of a base or an acid and/or a catalyst [cf. J. Am. Chem. Soc. 2007, 129 (43), 13321 ; J. Org. Chem. 1984, 49 (22), 4287.].
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 chloro- benzene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and THF, nitriles, such as acetonitrile and propionitrile, ketones, such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols, such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide and water, particularly preferably (a) water, THF; (b) R1-OH. It is also possible to use mixtures of the solvents mentioned.
Suitable bases are, in general, 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 also alkali metal bicarbonates, such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls, such as methyllithium, butyllithium and phenyllithium, alkylmagnesium halides, such as methylmagnesium chloride, and also alkali metal and alkaline earth metal alkoxides, such as sodium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide and dimethoxymagnesium, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, tributylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to lithium hydroxide.
The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvents.
Suitable for use as acids and acidic catalysts are inorganic acids, such as hydrofluoric acid, hydrochloric acid, hydrobromic acid, sulfuric acid and perchloric acid,
Lewis acids, such as boron trifluoride, aluminum trichloride, iron(lll) chloride, tin(IV) chloride, titanium(IV) chloride and zinc(ll) chloride, and also organic acids, such as formic acid, acetic acid, propionic acid, oxalic acid, toluenesulfonic acid,
benzenesulfonic acid, camphorsulfonic acid, citric acid and trifluoroacetic acid.
The acids are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent. The starting materials required for preparing the compounds I are known from the literature or can be prepared in accordance with the literature cited.
The reaction mixtures are worked up in a customary manner, for example by mixing with water, separating the phases and, if appropriate, chromatographic purification of the crude products. Some of the intermediates and end products are obtained in the form of colorless or slightly brownish viscous oils which are purified or freed from volatile components under reduced pressure and at moderately elevated temperature. If the intermediates and end products are obtained as solids, the purification can also be carried out by recrystallization or digestion.
If individual compounds I cannot be obtained by the routes described above, they can be prepared by derivatization of other compounds I.
If the synthesis yields mixtures of isomers, a separation is generally however not necessarily required since in some cases the individual isomers can be intercon verted during work-up for use or during application (for example under the action of light, acids or bases). Such conversions may also take place after application, for example in the case of the treatment of plants in the treated plant or in the harmful plant to be controlled. The organic moieties mentioned for the substituents of the compounds I according to the invention are collective terms for individual enumerations of the individual group members. All hydrocarbon chains, such as alkyl, haloalkyl, alkenyl, alkynyl, and the alkyl moieties and alkenyl moieties in alkoxy, haloalkoxy, alkylamino, dialkylamino, N-alkylsulfonylamino, alkenyloxy, alkynyloxy, alkoxyamino, alkylaminosulfonylamino, dialkylaminosulfonylamino, alkenylamino, alkynylamino, N-(alkenyl)-N-(alkyl)amino, N-(alkynyl)-N-(alkyl)amino, N-(alkoxy)-N-(alkyl)amino, N-(alkenyl)-N-(alkoxy)amino or N-(alkynyl)-N-(alkoxy)amino can be straight-chain or branched.
The prefix Cn-Cm- indicates the respective number of carbons of the hydrocarbon unit. Unless indicated otherwise, halogenated substituents preferably carry one to five identical or different halogen atoms, in particular fluorine atoms or chlorine atoms. The meaning halogen denotes in each case fluorine, chlorine, bromine or iodine. Examples of other meanings are:
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 carbon atoms, for example 1 or 2, 1 to 4 or 1 to 6 carbon atoms, for example Ci-Cs-alkyl, such as methyl, ethyl, propyl, 1 -methylethyl, butyl, 1 -methylpropyl, 2-methylpropyl, 1 ,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1 -ethylpropyl, hexyl, 1 ,1-dimethylpropyl, 1 ,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1 ,1 -dimethyl butyl, 1 ,2-dimethylbutyl, 1 ,3-dimethylbutyl, 2,2-dimethyl- butyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1 ,1 ,2-trimethyl- propyl, 1 ,2,2-trimethylpropyl, 1 -ethyl-1-methylpropyl, 1 -ethyl-2-methylpropyl. In one embodiment according to the invention, alkyl denotes small alkyl groups, such as
Ci-C4-alkyl. In another embodiment according to the invention, alkyl denotes relatively large alkyl groups, such as Cs-Ce-alkyl.
Haloalkyl: an alkyl radical as mentioned above, some or all of whose hydrogen atoms are substituted by halogen atoms, such as fluorine, chlorine, bromine and/or iodine, for example chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoro- methyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl,
2- fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2,2-trifluoro- ethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl,
2,2,2-trichloroethyl, pentafluoroethyl, 2-fluoropropyl, 3-fluoropropyl, 2,2-difluoropropyl, 2,3-difluoropropyl, 2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl,
3- bromopropyl, 3,3,3-trifluoropropyl, 3,3,3-trichloropropyl, 2,2,3,3,3-pentafluoropropyl, heptafluoropropyl, 1-(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl, 1-(bromomethyl)-2-bromoethyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl and nonafluorobutyl.
Cycloalkyl and the cycloalkyl moieties for example in cycloalkoxy or
cycloalkylcarbonyl: 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 the 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, for example 2 to 4, 2 to 6 or 3 to 6 carbon atoms, and a double bond in any position, for example 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- ethyl-1 -propenyl, 1 -ethyl-2-propenyl, 1 -hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1 -pentenyl, 2-methyl-1-pentenyl, 3-methyl-1 -pentenyl, 4-methyl-1- pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2- pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3- pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4- pentenyl, 1 ,1 -dimethyl-2-butenyl, 1 ,1 -dimethyl-3-butenyl, 1 ,2-dimethyl-1-butenyl, 1 ,2- dimethyl-2-butenyl, 1 ,2-dimethyl-3-butenyl, 1 ,3-dimethyl-1 -butenyl, 1 ,3-dimethyl-2- butenyl, 1 ,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1 -butenyl, 2,3- dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1 -butenyl, 3,3-dimethyl-2- butenyl, 1 -ethyl-1 -butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1 -butenyl,
2- ethyl-2-butenyl, 2-ethyl-3-butenyl, 1 ,1 ,2-trimethyl-2-propenyl, 1 -ethyl-1 -methyl-2- propenyl, 1 -ethyl-2-methyl-1 -propenyl, 1 -ethyl-2-methyl-2-propenyl. Cycloalkenyl: monocyclic monounsaturated hydrocarbon groups having 3 to 6, preferably 5 or 6, carbon ring members, such as cyclopenten-1-yl, cyclopenten-3-yl, cyclohexen-1-yl, cyclohexen-3-yl, cyclohexen-4-yl.
Alkynyl and the 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, for example 2 to 4, 2 to 6 or 3 to 6 carbon atoms, and a triple bond in any position, for example C2-C6-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, 1 -hexynyl,
2- hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1 -methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1 -pentynyl,
3- methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1 ,1-dimethyl-2-butynyl, 1 ,1-dimethyl-3-butynyl, 1 ,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1 - butynyl, 1 -ethyl-2-butynyl, 1 -ethyl-3-butynyl, 2-ethyl-3-butynyl, 1-ethyl-1 -methyl-2- propynyl.
Alkoxy: alkyl as defined above which is attached via an oxygen atom, for example methoxy, ethoxy, n-propoxy, 1 -methylethoxy, butoxy, 1-methylpropoxy, 2-methyl- propoxy or 1 ,1-dimethylethoxy, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methyl- butoxy, 1 ,1-dimethylpropoxy, 1 ,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1 -ethyl- propoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methyl- pentoxy, 1 ,1-dimethylbutoxy, 1 ,2-dimethylbutoxy, 1 ,3-dimethylbutoxy, 2,2-dimethyl- butoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1 -ethyl butoxy, 2-ethylbutoxy,
1 ,1 ,2-trimethylpropoxy, 1 ,2,2-trimethylpropoxy, 1 -ethyl-1 -methylpropoxy or 1 -ethyl-2- methylpropoxy.
Alkylene: divalent unbranched chains of 3 to 5 Chb groups, for example CH2, CH2CH2, CH2CH2CH2, CH2CH2CH2CH2 and CH2CH2CH2CH2CH2.
Oxyalkylene: divalent unbranched chains of 2 to 4 CH2 groups, where one valency is attached to the skeleton via an oxygen atom, for example OCH2CH2, OCH2CH2CH2
Figure imgf000010_0001
Oxyalkyleneoxy: divalent unbranched chains of 1 to 3 CH2 groups, where both valencies are attached to the skeleton via an oxygen atom, for example OCH2O, OCH2CH2O and OCH2CH2CH2O;
A 5- or 6-membered heterocycle: a cyclic group which has 5 or 6 ring atoms, 1 , 2, 3 or 4 ring atoms being heteroatoms selected from the group consisting of O, S and N, where the cyclic group is saturated, partially unsaturated or aromatic.
The compounds of the formula I contain two centers of chirality and may, depending on the substitution pattern, contain one or more further. Accordingly, the compounds according to the invention can be present as pure enantiomers or diastereomers or as enantiomer or diastereomer mixtures. The invention provides both the pure
enantiomers or diastereomers and their mixtures.
Figure imgf000011_0001
The compounds of the formula I may also be present in the form of the N-oxides and/or of their agriculturally useful salts, the type of salt generally not being important. Suitable salts are generally the salts of those cations or the acid addition salts of those acids whose cations and anions, respectively, have no adverse effect on the herbicidal activity of the compounds I.
Suitable cations are in particular ions of the alkali metals, preferably lithium, sodium or potassium, of the alkaline earth metals, preferably calcium or magnesium, and of the transition metals, preferably manganese, copper, zinc or iron. Another cation that may be used is ammonium, where, if desired, one to four hydrogen atoms may be replaced by Ci-C4-alkyl, hydroxy-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C4-alkyl, hydroxy-Ci-C4-alkoxy- Ci-C4-alkyl, phenyl or benzyl, preferably ammonium, dimethylammonium, diisopropyl- ammonium, tetramethylammonium, tetrabutylammonium, 2-(2-hydroxyeth-1-oxy)eth-1 - ylammonium, di(2-hydroxyeth-1 -yl)ammonium, trimethylbenzylammonium. Another suitable ammonium cation is the pyridine nitrogen atom of the formula I quaternized by alkylation or arylation. Also suitable are phosphonium ions, sulfonium ions, preferably tri(Ci-C4-alkyl)sulfonium, or sulfoxonium ions, preferably tri(Ci-C4-alkyl)sulfoxonium. Anions of suitable acid addition salts are primarily chloride, bromide, fluoride, hydrogensulfate, sulfate, dihydrogenphosphate, hydrogenphosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate and also the anions of Ci-C4-alkanoic acids, preferably formate, acetate, propionate, butyrate or trifluoroacetate. With respect to the variables, the particularly preferred embodiments of the intermediates correspond to those of the groups of the formula I.
In a particular embodiment, the variables of the compounds of the formula I have the following meanings, these meanings, both on their own and in combination with one another, being particular embodiments of the compounds of the formula I:
In one embodiment of the compounds of the formula I, the index n has a value from 0 to 3, preferably 0 or 1 , in particular Un a further embodiment, n is 0. If at least one group R is present, it is preferably located in positions 3, 4 and/or 5, in particular 3 or 4. If the index n has the value 2, the groups R are preferably located in positions 3,5 or 3,4. Embodiments of the group(s) R relate to halogen. Preferably, the group(s) R are selected, independently of one another, from the group consisting of fluorine, chlorine and bromine, in particular from the group consisting of chlorine and fluorine. Most preferably, the group(s) R relate to fluorine. Further embodiments of the group(s) R relate to cyano or nitro, in particular cyano.
In another embodiment, the group(s) R relate to fluorine or cyano.
In another embodiment, the index n has the value 1 and the group R is fluorine or cyano.
In a preferred embodiment the index n is 1 , 2 or 3. Particularly preferred
embodiments of group Rn include the following: 3-F; 3,4-F2; 3,5-F2; 3,4,5-F3; 3-F,4-CI; 3-CI.4-F; 4-CI; 4-F; 3-CN; 3-CI.
Preferred embodiments of group R1 relate to hydrogen, d-Cs-alkyl, cyano-Ci-C4- alkyl, C3-C6-alkenyl, C3-C6-alkynyl, C-i-Ce-haloalkyl, optionally substituted Z-phenyl or NR'RiLCi-C4-alkyl, where R' is hydrogen or Ci-C4-alkyl and R" is hydrogen, Ci-C4-alkyl or C(=0)-RA. Particularly preferred embodiments of group R1 relate to hydrogen, C1-C4- alkyl, cyanomethyl, allyl, propargyl, Ci-C4-haloalkyl comprising preferably 1 to 3 halogen atoms, phenyl or benzyl, which aromatic groups may be partially or fully substituted. Particularly preferred embodiments of R1 include the following: H, CH3, C2H5, CH2CN, CH2C≡ CH, CH2CH2F, CH2CHF2, CH2CF3, CH2OCH3. R1 is in particular selected from the group consisting of H and CH3.
Preferred embodiments of group R2 relate to halogen. More preferably, R2 is selected from the group consisting of fluorine, chlorine and bromine. More particularly preferably, R2 is chlorine. More particularly preferably, R2 is fluorine. More particularly preferably, R2 is bromine.
Preferred embodiments of group R3 relate to halogen. More preferably, R3 is selected from the group consisting of fluorine, chlorine and bromine. More particularly preferably, R3 is chlorine. More particularly preferably, R3 is fluorine. More particularly preferably, R3 is bromine.
Preferred embodiments of group (R4)x relate to halogen, cyano, nitro, Ci-C4-alkyl, Ci-C4-alkoxy, S(0)mR , NR'R", Ci-C4-haloalkyl and Ci-C4-haloalkoxy. Particularly preferred embodiments of group (R4)x relate to halogen, cyano, nitro, Ci-C4-alkyl, Ci-C4-alkoxy, Ci-C4-haloalkyl and Ci-C4-haloalkoxy. Especially preferred embodiments of group (R4)x are selected from the group consisting of halogen, OCH3, OCF3, OCHF2, CH3, NO2, CN, CHF2 and CF3. An even more preferred embodiment of group (R4)x relates to halogen. In particular, the group(s) (R4)x are selected, independently of one another, from the group consisting of fluorine, chlorine and bromine.
In one embodiment, the index x is 0. In a further embodiment, the index x is 1. If the index x is 1 , the group R4 is preferably located in the 3-position or 4-position. If x is 1 , the group R4 is more preferably located in the 4-position. In another embodiment, the group R4 is located in the 3-position.
In a further embodiment, the index x is 2; if x is 2, the groups R4 are preferably located in the 3,5-position.
In a further embodiment, the index x is 3.
More particularly preferably, R4 is fluorine.
More particularly preferably, R4 is chlorine.
More particularly preferably, R4 is bromine.
More particularly preferably, R4 is CF3.
More particularly preferably, R4 is OCF3.
More particularly preferably, R4 is OCHF2. In a preferred embodiment of the compounds I according to the invention, R2 and R3 are different, in particular if at least one group R2 and/or R3, preferably both, are halogen, such as CI and/or F.
Especially preferably, the combinations of R2, R3 and (R4)x are selected from the group consisting of: 2,6-F2-4-halo; 2,6-F2-4-OCF3; 2,6-F2-4-OCHF2; 2,6-F2-4-CF3; 2,6-F2-4-CHF2; 2,3,5,6-F4; 2,6-F2-3-halo; 2,6-F2-3-CH3 and 2,6-F2-3-OCH3.
In particular with a view to their use, preference is given to the compounds of the formula I compiled in the tables below. The groups mentioned for a substituent in the tables are furthermore per se, independently of the combination in which they are mentioned, a particularly preferred aspect of the substituent in question.
Table 1
Compounds of the formula I in which Rn is 3-CN and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A
Table 2
Compounds of the formula I in which Rn is 4-CI and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A
Table 3
Compounds of the formula I in which Rn is 3-F and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A Table 4
Compounds of the formula I in which Rn is 4-F and the combination of R1, R2 , R3 and (R4)x for a compound corresponds in each case to one row of table A Table 5
Compounds of the formula I in which Rn is 3,4-F2 and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A
Table 6
Compounds of the formula I in which Rn is 3,5-F2 and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A Table 7
Compounds of the formula I in which Rn is 3-CI,4-F and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A
Table 8
Compounds of the formula I in which Rn is 3-F,4-CI and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A
Table 9
Compounds of the formula I in which Rn is 3,4,5-F3 and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A
Table 10
Compounds of the formula I in which the index n is 0 and the combination of R1, R2, R3 and (R4)x for a compound corresponds in each case to one row of table A
Table A
Compounds of the fo
Figure imgf000014_0001
No. R1 R2 R3 (R4)x
A-1 H F F -
A-2 H F F 3-F
A-3 H F F 3-CI
A-4 H F F 3-Br
A-5 H F F 4-F
A-6 H F F 4-CI
A-7 H F F 4-Br
Figure imgf000015_0001
Figure imgf000016_0001
Figure imgf000017_0001
Figure imgf000018_0001
Figure imgf000019_0001
Figure imgf000020_0001
The compounds I and their agriculturally useful salts are suitable, both as isomer mixtures and in the form of the pure isomers, as herbicides. They are suitable as such or as an appropriately formulated composition. The herbicidal compositions comprising the compound I, in particular the preferred aspects thereof, control vegetation on non- crop areas very efficiently, especially at high rates of application. They act against broad-leaved weeds and weed grasses in crops such as wheat, rice, corn, soybeans and cotton without causing any significant damage to the crop plants. This effect is mainly observed at low rates of application.
Depending on the application method in question, the compounds I, in particular the preferred aspects thereof, or compositions comprising them can additionally be employed in a further number of crop plants for eliminating unwanted plants. Examples of suitable crops are the following:
Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis, Avena sativa, Beta vulgaris spec, altissima, Beta vulgaris spec, rapa, Brassica napus var. napus, Brassica napus var. napobrassica, Brassica rapa var. silvestris, Brassica oleracea, Brassica nigra, Camellia sinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon, Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vulgare, Humulus lupulus, Ipomoea batatas, Juglans regia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum, Malus spec, Manihot esculenta, Medicago sativa, Musa spec, Nicotiana tabacum (N.rustica), Olea europaea, Oryza sativa, Phaseolus lunatus, Phaseolus vulgaris, Picea abies, Pinus spec, Pistacia vera, Pisum sativum, Prunus avium, Prunus persica, Pyrus communis, Prunus armeniaca, Prunus cerasus, Prunus dulcis and Prunus domestica, Ribes sylvestre, Ricinus communis, Saccharum officinarum, Secale cereale, Sinapis alba, Solanum tuberosum, Sorghum bicolor (s. vulgare), Theobroma cacao, Trifolium pratense, Triticum aestivum, Triticale, Triticum durum, Vicia faba, Vitis vinifera, Zea mays. The term "crop plants" also includes plants which have been modified by breeding, mutagenesis or genetic engineering. Genetically modified plants are plants whose genetic material has been modified in a manner which does not occur under natural conditions by crossing, mutations or natural recombination (i.e. reassembly of the genetic information). Here, in general, one or more genes are integrated into the genetic material of the plant to improve the properties of the plant.
Accordingly, the term "crop plants" also includes plants which, by breeding and genetic engineering, have acquired tolerance to certain classes of herbicides, such as hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors, acetolactate synthase (ALS) inhibitors, such as, for example, sulfonylureas (EP-A 257 993, US 5,013,659) or imidazolinones (see, for example, US 6,222,100, WO 01/82685, WO 00/26390, WO 97/41218, WO 98/02526, WO 98/02527, WO 04/106529, WO 05/20673,
WO 03/14357, WO 03/13225, WO 03/14356, WO 04/16073), enolpyruvylshikimate 3- phosphate synthase (EPSPS) inhibitors, such as, for example, glyphosate (see, for example, WO 92/00377), glutamine synthetase (GS) inhibitors, such as, for example, glufosinate (see, for example, EP-A 242 236, EP-A 242 246), or oxynil herbicides (see, for example, US 5,559,024). Numerous crop plants, for example Clearfield® oilseed rape, tolerant to
imidazolinones, for example imazamox, have been generated with the aid of classic breeding methods (mutagenesis). Crop plants such as soybeans, cotton, corn, beet and oilseed rape, resistant to glyphosate or glufosinate, which are available under the tradenames RoundupReady® (glyphosate) and Liberty Link® (glufosinate) have been generated with the aid of genetic engineering methods.
Accordingly, the term "crop plants" also includes plants which, with the aid of genetic engineering, produce one or more toxins, for example those of the bacterial strain Bacillus ssp. Toxins which are produced by such genetically modified plants include, for example, insecticidal proteins of Bacillus spp., in particular B. thuringiensis, such as the endotoxins CrylAb, CrylAc, Cryl F, Cry1 Fa2, Cry2Ab, Cry3A, Cry3Bb1 , Cry9c, Cry34Ab1 or Cry35Ab1 ; or vegetative insecticidal proteins (VI Ps), for example VIP1 , VIP2, VIP3, or VIP3A; insecticidal proteins of nematode-colonizing bacteria, for example Photorhabdus spp. or Xenorhabdus spp.; toxins of animal organisms, for example wasp, spider or scorpion toxins; fungal toxins, for example from
Streptomycetes; plant lectins, for example from peas or barley; agglutinins; proteinase inhibitors, for example trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors, ribosome-inactivating proteins (RIPs), for example ricin, corn-RIP, abrin, luffin, saporin or bryodin; steroid-metabolizing enzymes, for example 3- hydroxysteroid oxidase, ecdysteroid-IDP glycosyl transferase, cholesterol oxidase, ecdysone inhibitors, or HMG-CoA reductase; ion channel blockers, for example inhibitors of sodium channels or calcium channels; juvenile hormone esterase;
receptors of the diuretic hormone (helicokinin receptors); stilbene synthase, bibenzyl synthase, chitinases and glucanases. In the plants, these toxins may also be produced as pretoxins, hybrid proteins or 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 disclosed 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 to the person skilled in the art and disclosed, for example, in the publications mentioned above. Numerous of the toxins mentioned above bestow, upon the plants by which they are produced, tolerance to pests from all taxonomic classes of arthropods, in particular to beetles (Coeleropta), dipterans (Diptera) and butterflies (Lepidoptera) and to nematodes (Nematoda).
Genetically modified plants which produce one or more genes coding for insecticidal toxins are described, for example, in the publications mentioned above, and some of them are commercially available, such as, for example, YieldGard® (corn varieties producing the toxin CrylAb), YieldGard® Plus (corn varieties which produce the toxins Cry1 Ab and Cry3Bb1), Starlink® (com varieties which produce the toxin Cry9c), Herculex® RW (corn varieties which produce the toxins Cry34Ab1 , Cry35Ab1 and the enzyme phosphinothricin-N-acetyltransferase [PAT]); NuCOTN® 33B (cotton varieties which produce the toxin CrylAc), Bollgard® I (cotton varieties which produce the toxin CrylAc), Bollgard® II (cotton varieties which produce the toxins CrylAc and Cry2Ab2); VIPCOT® (cotton varieties which produce a VIP toxin); NewLeaf® (potato varieties which produce the toxin Cry3A); Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Bt1 1 (for example Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France (corn varieties which produce the toxin CrylAb and the PAT enyzme), MIR604 from Syngenta Seeds SAS, France (corn varieties which produce a modified version of the toxin Cry3A, see WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium (corn varieties which produce the toxin Cry3Bb1 ), IPC 531 from Monsanto Europe S.A., Belgium (cotton varieties which produce a modified version of the toxin CrylAc) and 1507 from Pioneer Overseas Corporation, Belgium (corn varieties which produce the toxin Cry1 F and the PAT enzyme).
Accordingly, the term "crop plants" also includes plants which, with the aid of genetic engineering, produce one or more proteins which are more robust or have increased resistance to bacterial, viral or fungal pathogens, such as, for example, pathogenesis- related proteins (PR proteins, see EP 392 225), resistance proteins (for example potato varieties producing two resistance genes against Phytophthora infestans from the wild Mexican potato Solanum bulbocastanum) or T4 lysozyme (for example potato cultivars which, by producing this protein, are resistant to bacteria such as Erwinia amylvora).
Accordingly, the term "crop plants" also includes plants whose productivity has been improved with the aid of genetic engineering methods, for example by enhancing the potential yield (for example biomass, grain yield, starch, oil or protein content), tolerance to drought, salt or other limiting environmental factors or resistance to pests and fungal, bacterial and viral pathogens.
The term "crop plants" also includes plants whose ingredients have been modified with the aid of genetic engineering methods in particular for improving human or animal diet, for example by oil plants producing health-promoting long-chain omega 3 fatty acids or monounsaturated omega 9 fatty acids (for example Nexera® oilseed rape).
The term "crop plants" also includes plants which have been modified with the aid of genetic engineering methods for improving the production of raw materials, for example by increasing the amylopectin content of potatoes (Amflora® potato).
Furthermore, it has been found that 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, are suitable. In this regard, there have been found compositions for the desiccation and/or defoliation of plants, processes for preparing these compositions and methods for desiccating and/or defoliating plants using the compounds of the formula I.
As desiccants, the compounds of the formula I are particularly suitable for desiccating the above-ground parts of crop plants such as potato, oilseed rape, sunflower and soybean, but also cereals. This makes possible the fully mechanical harvesting of these important crop plants. Also of economic interest is to facilitate harvesting, which is made possible by concentrating within a certain period of time the dehiscence, or reduction of adhesion to the tree, in citrus fruit, olives and other species and varieties of pomaceous fruit, stone fruit and nuts. The same mechanism, i.e. the promotion of the development of abscission tissue between fruit part or leaf part and shoot part of the plants is also essential for the readily controllable defoliation of useful plants, in particular cotton.
Moreover, a shortening of the time interval in which the individual cotton plants mature leads to an increased fiber quality after harvesting. The compounds I, or the herbicidal compositions comprising the compounds I, can be used, for example, in the form of ready-to-spray aqueous solutions, powders, suspensions, also highly concentrated aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, materials for broadcasting, or granules, by means of spraying, atomizing, dusting, spreading, watering or treatment of the seed or mixing with the seed. The use forms depend on the intended purpose; in each case, they should ensure the finest possible distribution of the active ingredients according to the invention.
The herbicidal compositions comprise a herbicidally effective amount of at least one compound of the formula I or an agriculturally useful salt of I, and auxiliaries which are customary for the formulation of crop protection agents.
Examples of auxiliaries customary for the formulation of crop protection agents are inert auxiliaries, solid carriers, surfactants (such as dispersants, protective colloids, emulsifiers, wetting agents and tackifiers), organic and inorganic thickeners, bactericides, antifreeze agents, antifoams, optionally colorants and, for seed formulations, adhesives.
Examples of thickeners (i.e. compounds which impart to the formulation modified flow properties, i.e. high viscosity in the state of rest and low viscosity in motion) are polysaccharides, such as xanthan gum (Kelzan® from Kelco), hodopol® 23 (Rhone Poulenc) or Veegum® (from R.T. Vanderbilt), and also organic and inorganic sheet minerals, such as Attaclay® (from Engelhardt).
Examples of antifoams are 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 can be added for stabilizing the aqueous herbicidal formulation.
Examples of bactericides are bactericides based on diclorophen and benzyl alcohol hemiformal (Proxel® from ICI or Acticide® RS from Thor Chemie and Kathon® MK from Rohm & Haas), and also isothiazolinone derivates, such as alkylisothiazolinones and benzisothiazolinones (Acticide MBS from Thor Chemie).
Examples of antifreeze agents are ethylene glycol, propylene glycol, urea or glycerol.
Examples of colorants are both sparingly water-soluble pigments and water-soluble dyes. Examples which may be mentioned are the dyes known under the names Rhodamin B, C.I. Pigment Red 112 and C.I. Solvent Red 1 , and also 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 48:2, 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, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.
Examples of adhesives are polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose. Suitable inert auxiliaries are, for example, the following:
mineral oil fractions of medium to high boiling point, such as kerosene and diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butanol and cyclohexanol, ketones such as cyclohexanone or strongly polar solvents, for example amines such as N- methylpyrrolidone, and water.
Solid carriers are mineral earths such as silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate and magnesium oxide, ground synthetic materials, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate and ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders, or other solid carriers.
Suitable surfactants (adjuvants, wetting agents, tackifiers, dispersants and also emulsifiers) are the alkali metal salts, alkaline earth metal salts and ammonium salts of aromatic sulfonic acids, for example lignosulfonic acids (e.g. Borresperse®-types, Borregaard), phenolsulfonic acids, naphthalenesulfonic acids (Morwet types, Akzo Nobel) and dibutylnaphthalenesulfonic acid (Nekal® types, BASF SE), and of fatty acids, alkyl- and alkylarylsulfonates, alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols, and also of fatty alcohol glycol ethers, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctyl-, octyl- or nonylphenol, alkylphenyl or tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers or polyoxypropylene alkyl ethers, lauryl alcohol polyglycol ether acetate, sorbitol esters, lignosulfite waste liquors and proteins, denatured proteins, polysaccharides (e.g. methylcellulose), hydrophobically modified starches, polyvinyl alcohol (Mowiol types Clariant), polycarboxylates (BASF SE, Sokalan® types), polyalkoxylates, polyvinylamine (BASF SE, Lupamine® types), polyethyleneimine (BASF SE, Lupasol® types), polyvinylpyrrolidone and copolymers thereof.
Powders, materials for broadcasting and dusts can be prepared by mixing or grinding the active ingredients together with a solid carrier.
Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers.
Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water. To prepare emulsions, pastes or oil dispersions, the compounds of the formula I, either as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetting agent, tackifier, dispersant or emulsifier. Alternatively, it is also possible to prepare concentrates comprising active substance, wetting agent, tackifier, dispersant or emulsifier and, if desired, solvent or oil, which are suitable for dilution with water.
The concentrations of the compounds of the formula I in the ready-to-use preparations can be varied within wide ranges. In general, the formulations comprise from 0.001 to 98% by weight, preferably 0.01 to 95% by weight of at least one active compound. The active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
The compounds I of the invention can for example be formulated as follows:
1. Products for dilution with water
A Water-soluble concentrates
10 parts by weight of active compound are dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, wetters or other adjuvants are added. The active compound dissolves upon dilution with water. This gives a formulation with an active compound content of 10% by weight.
B Dispersible concentrates
20 parts by weight of active compound are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion. The active compound content is 20% by weight.
C Emulsifiable concentrates
15 parts by weight of active compound are dissolved in 75 parts by weight of an organic solvent (e.g. alkylaromatics) with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion. The formulation has an active compound content of 15% by weight.
D Emulsions
25 parts by weight of active compound are dissolved in 35 parts by weight of an organic solvent (e.g. alkylaromatics) with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifier (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion. The formulation has an active compound content of 25% by weight.
E Suspensions
In an agitated ball mill, 20 parts by weight of active compound are comminuted with addition of 10 parts by weight of dispersants and wetters and 70 parts by weight of water or an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound. The active compound content in the formulation is 20% by weight.
F Water-dispersible granules and water-soluble granules
50 parts by weight of active compound are ground finely with addition of 50 parts by weight of dispersants and wetters and made into water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound. The formulation has an active compound content of 50% by weight.
G Water-dispersible powders and water-soluble powders
75 parts by weight of active compound are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound. The active compound content of the formulation is 75% by weight.
H Gel formulations
In a ball mill, 20 parts by weight of active compound, 10 parts by weight of dispersant, 1 part by weight of gelling agent and 70 parts by weight of water or of an organic solvent are ground to give a fine suspension. Dilution with water gives a stable suspension with active compound content of 20% by weight.
2. Products to be applied undiluted
I Dusts
5 parts by weight of active compound are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dusting powder with an active compound content of 5% by weight.
J Granules (GR, FG, GG, MG)
0.5 parts by weight of active compound are ground finely and associated with 99.5 parts by weight of carriers. Current methods here are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted with an active compound content of 0.5% by weight.
K ULV solutions (UL)
10 parts by weight of active compound are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product to be applied undiluted with an active compound content of 10% by weight. The compounds I or the herbicidal compositions comprising them can be applied pre- or post-emergence, or together with the seed of a crop plant. It is also possible to apply the herbicidal compositions or active compounds by applying seed, pretreated with the herbicidal compositions or active compounds, of a crop plant. If the active compounds are less well tolerated by certain crop plants, application techniques may be used in which the herbicidal compositions are sprayed, with the aid of the spraying equipment, in such a way that as far as possible they do not come into contact with the leaves of the sensitive crop plants, while the active compounds reach the leaves of undesirable plants growing underneath, or the bare soil surface (post-directed, lay-by). I n a further em bodi ment, the compounds of the formula I or the herbicidal compositions can be applied by treating seed.
The treatment of seed comprises essentially all procedures familiar to the person skilled in the art (seed dressing, seed coating, seed dusting, seed soaking, seed film coating, seed multilayer coating, seed encrusting, seed dripping and seed pelleting) based on the compound s of the form ula I accordi ng to the invention or the compositions prepared therefrom. Here, the herbicidal compositions can be applied diluted or undiluted.
The term seed comprises seed of all types, such as, for example, corns, seeds, fruits, tubers, cuttings and similar forms. Here, preferably, the term seed describes corns and seeds.
The seed used can be seed of the useful plants mentioned above, but also the seed of transgenic plants or plants obtained by customary breeding methods.
The rates of application of active compound are from 0.001 to 3.0, preferably 0.01 to 1.0, kg/ha of active substance (a.s.), depending on the control target, the season, the target plants and the growth stage. To treat the seed, the compounds I are generally employed in amounts of from 0.001 to 10 kg per 100 kg of seed.
It may also be advantageous to use the compounds of the formula I in combination with safeners. Safeners are chemical compounds which prevent or reduce damage to useful plants without substantially affecting the herbicidal action of the compounds of the formula I on unwanted plants. They can be used both before sowing (for example in the treatment of seed, or on cuttings or seedlings) and before or after the emergence of the useful plant. The safeners and the compounds of the formula I can be used simultaneously or in succession. Suitable safeners are, for example, (quinolin-8- oxy)acetic acids, 1 -phenyl-5-haloalkyl-1 7-1 ,2,4-triazole-3-carboxylic acids, 1-phenyl- 4,5-dihydro-5-alkyl-1 H-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-benzamides, 1 ,8-naphthalic anhydride, 2-halo-4-(haloalkyl)-5-thiazole- carboxylic acids, phosphorothiolates and O-phenyl N-alkylcarbamates and their agriculturally useful salts and, provided that they have an acid function, their agriculturally useful derivatives, such as amides, esters and thioesters.
To broaden the activity spectrum and to obtain synergistic effects, the compounds of the formula I can be mixed and jointly applied with numerous representatives of other herbicidal or growth-regulating groups of active compounds or with safeners. Suitable mixing partners are, for example, 1 ,2,4-thiadiazoles, 1 ,3,4-thiadiazoles, amides, aminophosphoric acid and its derivatives, aminotriazoles, anilides, aryloxy/heteroaryl- oxyalkanoic acids and their derivatives, benzoic acid and its derivatives,
benzothiadiazinones, 2-(hetaroyl/aroyl)-1 ,3-cyclohexanediones, heteroaryl aryl ketones, benzylisoxazolidinones, meta-CF3-phenyl derivatives, carbamates, quinoline carboxylic acid and its derivatives, chloroacetanilides, cyclohexenone oxime ether derivates, diazines, dichloropropionic acid and its derivatives, dihydrobenzofurans, dihydrofuran-3-ones, dinitroanilines, dinitrophenols, diphenyl ethers, dipyridyls, halocarboxylic acids and their derivatives, ureas, 3-phenyluracils, imidazoles, imidazolinones, N-phenyl-3,4,5,6-tetrahydrophthalimides, oxadiazoles, oxiranes, phenols, aryloxy- and heteroaryloxyphenoxypropionic esters, phenylacetic acid and its derivatives, 2-phenylpropionic acid and its derivatives, pyrazoles, phenylpyrazoles, pyridazines, pyridinecarboxylic acid and its derivatives, pyrimidyl ethers, sulfonamides, sulfonylureas, triazines, triazinones, triazolinones, triazolecarboxamides, uracils and also phenylpyrazolines and isoxazolines and their derivatives.
Moreover, it may be useful to apply the compounds I alone or in combination with other herbicides or else also mixed with further crop protection agents, jointly, for example with compositions for controlling pests or phytopathogenic fungi or bacteria. Also of interest is the miscibility with mineral salt solutions which are employed for alleviating nutritional and trace element deficiencies. Other additives such as nonphytotoxic oils and oil concentrates may also be added.
Examples of herbicides which can be used in combination with the compounds of the formula I according to the present invention are:
b1 ) from the group of the lipid biosynthesis inhibitors:
alloxydim, alloxydim-sodium, butroxydim, clethodim, clodinafop, clodinafop- propargyl, cycloxydim, cyhalofop, cyhalofop-butyl, diclofop, diclofop-methyl, fenoxaprop, fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fluazifop, fluazifop- butyl, fluazifop-P, fluazifop-P-butyl, haloxyfop, haloxyfop-methyl, haloxyfop-P, haloxyfop-P-methyl, metamifop, pinoxaden, profoxydim, propaquizafop, quizalofop, quizalofop-ethyl, quizalofop-tefuryl, quizalofop-P, quizalofop-P-ethyl, quizalofop-P- tefuryl, sethoxydim, tepraloxydim, tralkoxydim, benfuresate, butylate, cycloate, dalapon, dimepiperate, EPTC, esprocarb, ethofumesate, flupropanate, molinate, orbencarb, pebulate, prosulfocarb, TCA, thiobencarb, tiocarbazil, triallate and vernolate;
b2) from the group of the ALS inhibitors:
amidosulfuron, azimsulfuron, bensulfuron, bensulfuron-methyl, bispyribac, bispyribac-sodium, chlorimuron, chlorimuron-ethyl, chlorsulfuron, cinosulfuron, cloransulam, cloransulam-methyl, cyclosulfamuron, diclosulam, ethametsulfuron, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron, florasulam, flucarbazone, flucarbazone-sodium, flucetosulfuron, flumetsulam, flupyrsulfuron, flupyrsulfuron- methyl-sodium, foramsulfuron, halosulfuron, halosulfuron-methyl, imazamethabenz, imazamethabenz-methyl, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron, iodosulfuron-methyl-sodium, mesosulfuron, metosulam, metsulfuron, metsulfuron-methyl, nicosulfuron, orthosulfamuron, oxasulfuron, penoxsulam, primisulfuron, primisulfuron-methyl, propoxycarbazone,
propoxycarbazone-sodium, prosulfuron, pyrazosulfuron, pyrazosulfuron-ethyl, pyribenzoxim, pyrimisulfan, pyriftalid, pyriminobac, pyriminobac-methyl, pyrithiobac, pyrithiobac-sodium, pyroxsulam, rimsulfuron, sulfometuron, sulfometuron-methyl, sulfosulfuron, thiencarbazone, thiencarbazone-methyl, thifensulfuron, thifensulfuron- methyl, triasulfuron, tribenuron, tribenuron-methyl, trifloxysulfuron, triflusulfuron, triflusulfuron-methyl and tritosulfuron;
b3) from the group of the photosynthesis inhibitors:
ametryn, amicarbazone, atrazine, bentazone, bentazone-sodium, bromacil, bromofenoxim, bromoxynil and its salts and esters, chlorobromuron, chloridazone, chlorotoluron, chloroxuron, cyanazine, desmedipham, desmetryn, dimefuron, dimethametryn, diquat, diquat-dibromide, diuron, fluometuron, hexazinone, ioxynil and its salts and esters, isoproturon, isouron, karbutilate, lenacil, linuron, metamitron, methabenzthiazuron, metobenzuron, metoxuron, metribuzin, monolinuron, neburon, paraquat, paraquat-dichloride, paraquat-dimetilsulfate, pentanochlor, phenmedipham, phenmedipham-ethyl, prometon, prometryn, propanil, propazine, pyridafol, pyridate, siduron, simazine, simetryn, tebuthiuron, terbacil, terbumeton, terbuthylazine, terbutryn, thidiazuron and trietazine;
b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:
acifluorfen, acifluorfen-sodium, azafenidin, bencarbazone, benzfendizone, bifenox, butafenacil, carfentrazone, carfentrazone-ethyl, chlomethoxyfen, cinidon-ethyl, fluazolate, flufenpyr, flufenpyr-ethyl, flumiclorac, flumiclorac-pentyl, flumioxazin, fluoroglycofen, fluoroglycofen-ethyl, fluthiacet, fluthiacet-methyl, fomesafen, halosafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone, profluazol, pyraclonil, pyraflufen, pyraflufen-ethyl, saflufenacil, sulfentrazone, thidiazimin, 2-chloro-5-[3,6- dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1 (2/-/)-pyrimidinyl]-4-fluoro-N-[(isopropyl)- methylsulfamoyl]benzamide (B-1 ; CAS 372137-35-4), ethyl [3-[2-chloro-4-fluoro-5-(1- methyl-6-trifluoromethyl-2,4-dioxo-1 ,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2- pyridyloxy]acetate (B-2; CAS 353292-31 -6), N-ethyl-3-(2,6-dichloro-4-trifluoro- methylphenoxy)-5-methyl-1 /-/-pyrazole-1 -carboxamide (B-3; CAS 452098-92-9), N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1 -/-pyrazole-1- carboxamide (B-4; CAS 915396-43-9), N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethyl- phenoxy)-5-methyl-1 /--pyrazole-1 -carboxamide (B-5; CAS 452099-05-7) and
N-tetrahydrofurfuryl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1 H- pyrazole-1 -carboxamide (B-6; CAS 452100-03-7);
b5) from the group of the bleacher herbicides: aclonifen, amitrol, beflubutamid, benzobicyclon, benzofenap, clomazone, diflufenican, fluridone, flurochloridone, flurtamone, isoxaflutole, mesotrione, norflurazon, picolinafen, pyrasulfutole, pyrazolynate, pyrazoxyfen, sulcotrione, tefuryltrione, tembotrione, topramezone, 4-hydroxy-3-[[2-[(2-methoxyethoxy)methyl]-6- (trifluoromethyl)-3-pyridyl]carbonyl]bicyclo[3.2.1 ]oct-3-en-2-one (B-7; CAS 352010-68- 5) and 4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)pyrimidine (B-8; CAS 180608-33-7);
b6) from the group of the EPSP synthase inhibitors:
glyphosate, glyphosate-isopropylammonium and glyphosate-trimesium (sulfosate); b7) from the group of the glutamine synthase inhibitors:
bilanaphos (bialaphos), bilanaphos-sodium, glufosinate and glufosinate-ammonium; b8) from the group of the DHP synthase inhibitors:
asulam;
b9) from the group of the mitose inhibitors:
amiprophos, amiprophos-methyl, benfluralin, butamiphos, butralin, carbetamide, chlorpropham, chlorthal, chlorthal-dimethyl, dinitramine, dithiopyr, ethalfluralin, fluchloralin, oryzalin, pendimethalin, prodiamine, propham, propyzamide, tebutam, thiazopyr and trifluralin;
b10) from the group of the VLCFA inhibitors:
acetochlor, alachlor, anilofos, butachlor, cafenstrole, dimethachlor, dimethanamid, dimethenamid-P, diphenamid, fentrazamide, flufenacet, mefenacet, metazachlor, metolachlor, metolachlor-S, naproanilide, napropamide, pethoxamid, piperophos, pretilachlor, propachlor, propisochlor, pyroxasulfone (KIH-485) and thenylchlor;
Compounds of the formula 2:
Figure imgf000031_0001
in which the variables have the following meanings:
Y is phenyl or 5- or 6-membered heteroaryl as defined at the outset, which radicals may be substituted by one to three groups Raa; R21,R22,R23,R24 are H, halogen or Ci-C4-alkyl; X is O or NH; N is 0 or 1.
Figure imgf000031_0002
where # denotes the bond to the skeleton of the molecule; and
R2i R22 R23 R24 a re H i F o r C H3; R25 js halogen, Ci-C4-alkyl or Ci-C4-haloalkyl; R26 is Ci-C4-alkyl; R27 is halogen, Ci-C4-alkoxy or Ci-C4-haloalkoxy; R28 is H, halogen, Ci-C4-alkyl, Ci-C4-haloalkyl or Ci-C4-haloalkoxy; M is 0, 1 , 2 or 3; X is oxygen; N is 0 or 1 .
Preferred compounds of the formula 2 have the following meanings:
Figure imgf000032_0001
R21 is H; R22,R23 are F; R24 is H or F; X is oxygen; N is 0 or 1 .
Particularly preferred compounds of the formula 2 are:
3-[5-(2,2-difluoroethoxy)-1-methyl-3-trifluoromethyl-1 H-pyrazol-4-ylmethane- sulfonyl]-4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole (2-1 ); 3-{[5-(2,2-difluoro- ethoxy)-1-methyl-3-trifluoromethyl-1 H-pyrazol-4-yl]fluoromethanesulfonyl}-5,5-dimethyl- 4,5-dihydroisoxazole (2-2); 4-(4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonyl- methyl)-2-methyl-5-trifluoromethyl-2H-[1 ,2,3]triazole (2-3); 4-[(5,5-dimethyl-4,5- dihydroisoxazole-3-sulfonyl)fluoromethyl]-2-methyl-5-trifluoromethyl-2H-[1 ,2,3]triazole (2-4); 4-(5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonylmethyl)-2-methyl-5-trifluoro- methyl-2H-[1 ,2,3]triazole (2-5); 3-{[5-(2,2-difluoroethoxy)-1 -methyl-3-trifluoromethyl-1 H- pyrazol-4-yl]difluoromethanesulfonyl}-5,5-dimethyl-4,5-dihydroisoxazole (2-6);
4-[(5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonyl)difluoromethyl]-2-methyl-5-trifluoro- methyl-2H-[1 ,2,3]triazole (2-7); 3-{[5-(2,2-difluoroethoxy)-1 -methyl-3-trifluoromethyl-1 H- pyrazol-4-yl]difluoromethanesulfonyl}-4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole (2-8); 4-[difluoro-(4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonyl)methyl]-2-methyl-5- trifluoromethyl-2H-[1 ,2,3]triazole (2-9);
b1 1 ) from the group of the cellulose biosynthesis inhibitors:
chlorthiamid, dichlobenil, flupoxam and isoxaben;
b12) from the group of the decoupler herbicides:
dinoseb, dinoterb and DNOC and its salts;
b13) from the group of the auxin herbicides:
2,4-D and its salts and esters, 2,4-DB and its salts and esters, aminopyralid and its salts such as aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, benazolin, benazolin-ethyl, chloramben and its salts and esters, domeprop, dopyralid and its salts and esters, dicamba and its salts and esters, dichlorprop and its salts and esters, dichlorprop-P and its salts and esters, fluroxypyr, fluroxypyr-butometyl, fluroxypyr- meptyl, MCPA and its salts and esters, MCPA-thioethyl, MCPB and its salts and esters, mecoprop and its salts and esters, mecoprop-P and its salts and esters, picloram and its salts and esters, quinclorac, quinmerac, TBA (2,3,6) and its salts and esters, triclopyr and its salts and esters, and 5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid (B-9; CAS 858956-08-8) and its salts and esters;
b14) from the group of the auxin transport inhibitors: diflufenzopyr, diflufenzopyr- sodium, naptalam and naptalam-sodium;
b15) from the group of the other herbicides: bromobutide, chlorflurenol, chlorflurenol- methyl, cinmethylin, cumyluron, dalapon, dazomet, difenzoquat, difenzoquat- metilsulfate, dimethipin, DSMA, dymron, endothal and its salts, etobenzanid, flamprop, flamprop-isopropyl, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flurenol, flurenol-butyl, flurprimidol, fosamine, fosamine-ammonium, indanofan, maleic hydrazide, mefluidide, metam, methyl azide, methyl bromide, methyl-dymron, methyl iodide, MSMA, oleic acid, oxaziclomefone, pelargonic acid, pyributicarb, quinoclamine, triaziflam, tridiphane 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, cyprosulfamide, dichlormid, dicyclonone, dietholate, fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen, mefenpyr, mephenate, naphthalic anhydride, oxabetrinil, 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; -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, The Compendium of Pesticide Common Names (http://www.alanwood.net/pesticides/); B. Hock, C. Fedtke, R. R. Schmidt, Herbizide [Herbicides], Georg Thieme Verlag, Stuttgart, 1995. Further herbicidally active compounds are known from WO 96/26202, WO 97/41 1 16, WO 97/41 117, WO
97/41 1 18, WO 01/83459 and WO 2008/074991 and from W. Kramer et al. (ed.) "Modern Crop Protection Compounds", Vol. 1 , Wiley VCH, 2007 and the literature quoted therein.
The compounds I and the compositions according to the invention may also have a plant-strengthening action. Accordingly, they are suitable for mobilizing the defense system of the plants against attack by unwanted microorganisms, such as harmful fungi, but also viruses and bacteria. Plant-strengthening (resistance-inducing) substances are to be understood as meaning, in the present context, those substances which are capable of stimulating the defense system of treated plants in such a way that, when subsequently inoculated by unwanted microorganisms, the treated plants display a substantial degree of resistance to these microorganisms.
The compounds I can be employed for protecting plants against attack by unwanted microorganisms within a certain period of time after the treatment. The period of time within which their protection is effected generally extends from 1 to 28 days, preferably from 1 to 14 days, after the treatment of the plants with the compounds I, or, after treatment of the seed, for up to 9 months after sowing.
The compounds I and the compositions according to the invention are also suitable for increasing the harvest yield.
Moreover, they have reduced toxicity and are tolerated well by the plants. Hereinbelow, the preparation of compounds of the formula I is illustrated by way of examples, without limiting the subject matter of the present invention to the examples shown. Synthesis examples
With appropriate modification of the starting materials, the procedures given in the synthesis examples below were used to obtain further compounds I. The compounds obtained in this manner are listed in the table that follows, together with physical data.
The products shown below were characterized by melting point determination, by NMR spectroscopy or by the mass ([m/z]) or retention time (RT; [min.]) determined by HPLC- MS spectrometry.
HPLC-MS = high performance liquid chromatography-coupled mass spectrometry; HPLC column:
RP-18 column (Chromolith Speed ROD from Merck KgaA, Germany), 50*4.6 mm; mobile phase: acetonitrile + 0.1 % trifluoroacetic acid (TFA)/water + 0.1 % TFA using a gradient from 5:95 to 100:0 over 5 minutes at 40°C, flow rate 1.8 ml/min.
MS: quadrupole electrospray ionization, 80 V (positive mode).
I . Preparation examples
Example 1 : Preparation of methyl 3-(4-chloro-2,6-difluorophenyl)-4-cyano-4- (4-fluorophenyl)butyrate [1-197]
At -78°C and under an atmosphere of protective gas (argon), 2.6 ml of a 1.0 M solution of lithium bis(trimethylsilyl)amide were added dropwise to a solution of 349 mg of (3-fluorophenyl)acetonitrile in 10 ml of THF. After 10 min, a solution of 500 mg of methyl 3-(2,6-difluorophenyl)acrylate in 10 ml of THF was added. After 2 h, the reaction solution was, at 20-25°C, diluted with CH2CI2 and washed successively with 2N HCI, sat. NaHCC>3 solution and sat. NaCI solution. After drying and removal of the solvent, the residue was purified on silica gel (10 g cartridge, cyclohexane:ethyl acetate 9:1-1 :1 ). This gave 873 mg of the title compound.
Example 2: Preparation of prop-2-ynyl 3-(4-chloro-2,6-difluorophenyl)-4-cyano-4- (4-fluorophenyl)butyrate [1-211 ]
12 mg of potassium phosphate were added to a solution of 200 mg of the ester from Ex. 1 in 3 ml of propargyl alcohol, and the mixture was stirred at 45°C. After 72 h, the reaction mixture was diluted with CH2CI2 and washed successively with water, 2N HCI, sat. NaHC03 solution and sat. NaCI solution. After drying and removal of the solvent, the residue was purified by preparative HPLC. This gave 76 mg of the title compound.
Table I: Compounds of the formula I:
Figure imgf000035_0001
I racemate isomer 1
Figure imgf000035_0002
Figure imgf000036_0001
Figure imgf000037_0001
Figure imgf000038_0001
phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
M+23
3.726 / 435
1-96 4-F CH3 F F 3-Br
M+23
1-97 - CH3 F F 3-Br 3.770 / 394
3.820 / 406
1-98 - CH3 F F 3-CF3
M+23
1-99 4-F 4-CI-C6H4 F F 3,5-F2
-100 4-F 2,4-CI2-C6H3 F F 3,5-F2
-101 4-F CH(CH3)CH2OCH3 F F 3,5-F2
-102 4-F [CH(CH3)]2NHCH3 F F 3,5-F2
-103 4-F CH(CH3)NHCH(CH3)2 F F 3,5-F2
-104 4-F CH(CH3)N(CH3)2 F F 3,5-F2
-105 4-F (S) CH(CH3)CON(CH3)2 F F 3,5-F2
CH3 r^^ NH
-106 4-F F F 3,5-F2 -107 4-F CH(CH3)COOH F F 3,5-F2
-108 4-F CH2N(CH3)COOCH3 F F 3,5-F2
-109 4-F CH2CH=CHCI F F 3,5-F2
3.847 / 404-1 10 3-CI.5-F CH3 F F 3,5-F2
(M+H)
3.803 / 384-1 1 1 3-CH3,5-F CH3 F F 3,5-F2
(M+H)-1 12 4-F C(CH3)2COOCH3 F F 3,5-F2
-1 13 4-F C(CH3)2CH2OCH3 F F 3,5-F2
-1 14 4-F C(CH3)2CH2SCH3 F F 3,5-F2
-1 15 4-F CH(CH3)CH2OCH=CH2 F F 3,5-F2
-1 16 4-F CH(CH3)CH(OCH3)2 F F 3,5-F2
-1 17 4-F C(CH3)CF3 F F 3,5-F2
-1 18 4-F C(CH3)CH2CH2CH3 F F 3,5-F2
-1 19 4-F (1 -CH3)-C5H8 F F 3,5-F2
-120 4-F CH(CH3)CH(CH3)2 F F 3,5-F2
-121 4-F C(CH3)2COOC2H5 F F 3,5-F2
-122 4-F C(CH3)2CH(CH3)2 F F 3,5-F2 -123 4-F F F 3,5-F2
# CH3
-124 4-F CH(CH3)CH(CH3)C2H5 F F 3,5-F2
-125 4-F CH2C≡ CH F F 3-Br 3.814 / 459
Figure imgf000040_0001
Figure imgf000041_0001
Figure imgf000042_0001
phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
3.722/447
I-207 4-F CH3 F CI 3-F,5-Br
M+1
3.616/338
I-208 4-F C(CH3)2C(OCH3)2CH3 F F 3,5-F2
M-161
4.174/338
I-209 4-F CH(CF3)2 F F 3,5-F2
M-167
1-210 4-F C(CH3)2CN F F 3,5-F2 3.766/422
1-211 4-F CH2C≡ CH F F 4-CI 3.845/391
4.145/491
1-212 4-F C(CH3)2C=CH2 F F 3,5-F2
M+68
3.620/429.5
1-213 4-F CH3 F Br 5-CI
M+H
1-214 4-F CH3 CI F 4-Br,5-F
1-215 4-F H CI F 5-CI 3.350 / 370
3.526/392
1-216 4-C≡ CH CH3 F F 3,5-F2
M+17
1-217 4-F CH3 F F 3-F,5-Br
3.356/415
1-218 4-F H F F 3-F,5-Br
M-1
3.817/456
1-219 4-F CH2C≡ CH F F 3-F,5-Br
M+2
I-220 4-CI H F F 3,5-F2
3,5-F2, 3.897/422
1-221 CH3 F F 3,5-F2
4-CI M+H
3.988/455
I -222 3,4,5-CI3 CH3 F F 3,5-F2
M+H
3,5-CI2, 4.003/419
I-223 4-F CH3 F F
4-F M-1
I -224 4-F CH2CH2OC2H5 F F 3,5-F2 3.587/427
3.922/466
I-225 3-CI.4-F CH3 F F 3-F,5-Br
M+2
I-226 4-F CH3 F F 4-SCH3 3.580 / 379
4.321 /665
I-227 4-F C(CH3)2OH F F 3,5-F2
M+311
I-228 4-F C(CF3)2COCH3 F F 3,5-F2
I-229 4-F 4-N02-C6H4 F F 3,5-F2 3.978/490
4.280 / 665
I-230 4-F 4-Br-C6H4 F F 3,5-F2
M+141
Figure imgf000044_0001
Figure imgf000045_0001
phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
4.077/419
1-285 3,4-Cb CH3 F F 4-CI
M+1
3.739/418
1-286 3-CI.4-F CH3 F F 4-CI
M+16
1-287 - CH3 F F 4-CI 3.710/349
3.977/401
1-288 3-CI.5-F CH3 F F 4-CI
M-1
1-289 3-CN CH3 F F 4-CI 3.492 / 374
1-290 3-F CH3 F F 4-CI 3.717/367
3.879 / 383
1-291 3-CI CH3 F F 4-CI
M-1
3.919/383
I-292 4-CI CH3 F F 4-CI
M-1
3.354/449
I-293 3-CN CH2CF2H F F 3,5-F2
M+Na
3.228/429
I-294 3-CN CH2OCH3 F F 3,5-F2
M+Na
I-295 2,3-F2 CH3 F F 4-CI 3.783 / 385
3.955/431
I-296 3-F.4-CI CH2OCH3 F F 4-CI
M-1
4.090/449
I-297 3,4-CI2 CH2OCH3 F F 4-CI
M+H
3.831 /416
I-298 3,4-F2 CH2OCH3 F F 4-CI
M+H
3.696/453
I-299 3-CI.4-F CH2OCH3 F F 4-CI
M+21
I-300 - CH2OCH3 F F 4-CI 3.721 / 379
3.967/431
1-301 3-F.5CI CH2OCH3 F F 4-CI
M-1
3.538/405
I-302 3-CN CH2OCH3 F F 4-CI
M+H
3.758/366
I-303 3-F CH2OCH3 F F 4-CI
M-33
3.896/413
I-304 3-CI CH2OCH3 F F 4-CI
M-1
3.899/413
I-305 4-CI CH2OCH3 F F 4-CI
M-1
I-306 4-Br H F F 3,5-F2 3.410/398 phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
M-18
3.951 /407
1-307 3-CI CH2CCH F F 4-CI
M-1
3.950/410
1-308 2,3-F2 CH2CCH F F 4-CI
M+H
3.754/447
1-309 3-CI.4-F CH2CCH F F 4-CI
M+21
3.625/399
1-310 3-CN CH2CCH F F 4-CI
M+H
1-311 3-F.4-CI CH2OCH3 F F - 3.694 / 398
3.666/402
1-312 4-CI CH2OCH3 F F - M+23
3.544 / 389
1-313 4-F CH2OCH3 CI F 3-F
M+23
3.865/420
1-314 4-F CH3 F F 3-F,4-CF3
M+H
3.703/495
1-315 4-F CH3 F Br 4-Br
M+23
3.491 /414
1-316 4-F CH2CH2OCH3 F F 3,5-F2
M+H
3.388/302
1-317 4-F CH3 F F - M-31
3.149/309
1-318 3-CN CH3 F F - M-31
3.454 / 320
1-319 3,4-F2 CH3 F F - M-32
3.562 / 338
I-320 3,4,5-F3 CH3 F F - M-31
CH3 3.459 /320
1-321 3,5-F2 F F - M-31
CH3 3.346/284
I-322 - F F - M-31
CH3 3.381 /302
I-323 3-F F F - M-31
2.913/320
I-324 4-F H F F - M+H
3.790/478
I-325 4-I CH3 F F 3,5-F2
M+H phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
3.741 /478
1-326 3-I CH3 F F 3,5-F2
M+H
2.706/327
1-327 3-CN H F F - M+H
2.993/338
1-328 3,4-F2 H F F - M+1
3.121 /356
1-329 3,4,5-F3 H F F - M+H
3.008/338
1-330 3,5-F2 H F F - M+1
2.879 / 302
1-331 - H F F - M+1
2.915/320
I-332 3-F H F F - M+1
3.468/352
I-333 4-F CH3 F F 3-F
M+H
3.476/460
I-334 4-F CH3 F F 4-I
M+H
2.917/355
I-335 4-F H F F 3-F
M+17
3.328/468
I-336 4-F H F F 4-I
M+Na
I-337 3,4-F2 CH3 F F 3-F 3.523 / 369
3.117/378
I-338 3,4-F2 H F F 3-F
M+Na
3.010/320
I-339 - H F F 3-F
M+H
3.292 / 356
I-340 - CH3 F F 3-F
M+Na
3.105/354
1-341 4-F H F F 4-CI
M+H
I-342 3,5-F2 CH3 F F 4-Br 3.804/430
3.482 / 388
I-343 3,4,5-F3 CH3 F F 3-F
M+H
3.609 / 382
I-344 3,5-F2 CH3 F F 3-F
M+Na
3.323/440
I-345 3,5-F2 H F F 3-Br
M+Na phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
1-346 3,4,5-F3 H F F 3-F 3.228/355
3.094 / 356
1-347 3,5-F2 H F F 3-F
M+H
3.633/401
1-348 4-F CH3 CI CI 3-F
M+17
3.391 /481
1-349 4-I H F F 3,5-F2
M+18
3.344/481
1-350 3-I H F F 3,5-F2
M+18
3.493/401
1-351 3,5-F2 CH3 CI CI 4-CI
M+17
I -352 3,4-F2 CH3 CI CI 4-CI 3.974/418
4.073/435
I-353 3,4,5-F3 CH3 CI CI 4-CI
M-1
I-354 3-CN CH3 CI CI 4-CI 3.661 /407
4.047-4.125/
I-355 4-CI CH3 CI CI 4-CI 418
M+H
3.852-3.916/
I-356 - CH3 CI CI 4-CI 384-382
M+2
3.934/402
I-357 4-F CH3 CI CI 4-CI
M+2
3.904/402
I-358 3-F CH3 CI CI 4-CI
M+2
3.081 /388
I-359 4-F H CI CI 3-F
M+18
3.088/359
I-360 3-CN CH3 F F 3-F
M+H
3.496/386
1-361 4-CI CH3 F F 3-F
M+H
2.684 / 367
I -362 3-CN H F F 3-F
M+Na
3.097 / 376
I-363 4-CI H F F 3-F
M+Na
3.323 / 374
I-364 3-F CH3 F F 3-F
M+Na
I-365 3-F H F F 3-F 2.921 /360
Figure imgf000050_0001
phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
3.549 / 522
1-385 4-F H Br Br 4-Br
M+H
3.591 /540
1-386 3,4-F2 H Br Br 4-Br
M+H
3.696/556
1-387 3,4,5-F3 H Br Br 4-Br
M+H
3.518/481
1-388 3-CN CH3 Br Br 4-F
M+H
3.755/478
1-389 - CH3 Br Br 4-F
M+Na
3.575/496
1-390 4-F CH3 Br Br 4-F
M+Na
3.042/467
1-391 3-CN H Br Br 4-F
M+H
3.262/440
I-392 - H Br Br 4-F
M+H
3.303/460
I-393 4-F H Br Br 4-F
M+H
3.511 /369
I-394 3.5-F-2 H CI CI 4-CI
M-37
3.433 / 386
I-395 3,4-F2 H CI CI 4-CI
M-18
3.525/406
I-396 3,4,5-F3 H CI CI 4-CI
M-22
I-397 3-F H CI CI 4-CI 3.437/386
3.656/421
I-398 4-CI H CI CI 4-CI
M+18
3.442 / 351
I-399 - H CI CI 4-CI
M-17
3.480 / 369
I-400 4-F H CI CI 4-CI
M-17
3.519/386
1-401 3,5-F2 CH3 F F 4-CI
M+H
I -402 4-F CH3 F Br - 3.546 / 394
3.546/413
I-403 4-F H F Br - M+Na
I -404 - CH3 F Br - 3.401 /376
I-405 3,4-F2 CH3 F Br - 3.603/435 phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
M+Na
1-406 - H F Br - 2.866/262
3.084/400
1-407 3,4-F2 H F Br - M+Na
3.496/429
1-408 3,4,5-F3 CH3 F Br - M-1
1-409 3,5-F2 CH3 F Br - 3.525/412
1-410 3,4,5-F H F Br - 3.106/416
3.064/400
1-411 3,5-F2 H F Br - M+2
3.102/354
1-412 3,5-F2 H F F 4-CI
M-17
3.962 /394
1-413 3-CN H CI CI 4-CI
M+1
3.428/383
1-414 3,4-F2 H F F 4-CI
M+Na
3.661 /302
1-415 - CH2CCH F F 3-F
M-55
3.577/332
1-416 - CH2OCH3 F F 3-F
M-31
3.611 /382
1-417 4-F CH2OCH3 F F 3-F
M+H
3.741 /394
1-418 3,4-F2 CH2CCH F F 3-F
M+1
3.672/400
1-419 3,4-F2 CH2OCH3 F F 3-F
M+H
3.456/383
I-420 3-CN CH2CCH F F 3-F
M+H
3.369/411
1-421 3-CN CH2OCH3 F F 3-F
M-23
3.673 / 320
I -422 3-F CH2CCH F F 3-F
M-55
3.603 / 350
I-423 3-F OCH2OCH3 F F 3-F
M-31
3.744 / 394
I -424 3,5-F2 CH2CCH F F 3-F
M+H
3.682/422
I-425 3,5-F2 OCH2OCH3 F F 3-F
M+Na phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
3.838/412
I-426 3,4,5-F3 CH2CCH F F 3-F
M+H
3.787/439
I-427 3,4,5-F3 OCH2OCH3 F F 3-F
M+Na
3.333 / 352
I-428 - H F F 4-Br
M-28
3.463 / 397
I-429 3,4-F2 H F F Br
M-19
3.106/426
I-430 3-CN H F F Br
M+21
3.362 / 381
1-431 3-F H F F 3-Br
M-17
3.557/457
I -432 3,4,5-F3 H F F 4-Br
M+Na
3.896/361
I-433 - CH2CCH F F 4-Br
M-51
3.973 / 397
I -434 3,4-F2 CH2CCH F F 4-Br
M-57
3.687/442
I-435 3-CN CH2CCH F F 4-Br
M-1
3.909 / 379
I-436 3-F CH2CCH F F 4-Br
M-57
3.971 /399
I-437 3,5-F2 CH2CCN F F 4-Br
M-55
3.917/429
I-438 3,5-F2 OCH2OCH3 F F 4-Br
M-31
4.057/471
I-439 3,4,5-F3 CH2CCN F F 4-Br
M-1
3.808/464
I-440 - CH3 F F 4-I
M+Na
1-441 - H F F 4-I 3.329/427
3.914/478
I -442 3,4-F2 CH3 F F 4-I
M+H
3.453/486
I-443 3,4-F2 H F F 4-I
M+Na
3.636/489
I -444 3-CN CH3 F F 4-I
M+Na
I-445 3-CN H F F 4-I 3.154/475 phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
M+Na
3.739/445
1-446 - CH2OCH3 F F 4-Br
M+21
3.823/483
1-447 3,4-F2 CH2OCH3 F F 4-Br
M+Na
3.523/470
1-448 3-CN CH2OCH3 F F 4-Br
M+21
3.756/465
1-449 3-F CH2OCH3 F F 4-Br
M-23
3.923/499
1-450 3,4,5-F3 CH2OCH3 F F 4-Br
M+23
3.822/482
1-451 3-F CH3 F F 4-I
M+Na
I -452 3-F H F F 4-I 3.362/445
I-453 3,4,5-F3 CH3 F F 4-I 3.989/518
3.577/491
I -454 3,5-F2 CH3 Br Br 4-F
M+H
3.864 / 796
I -455 3,5-F2 CH3 Br Br - M+Na
3.793/474
I-456 3,4-F2 CH3 Br Br - M+H
3.974/492
I -457 3,4,5-F3 CH3 Br Br - M+H
3.787/456
I-458 3-F CH3 Br Br - M+H
3.523/463
I-459 3-CN CH3 Br Br - M+H
3.806/456
I-460 4-F CH3 Br Br - M+H
3.706/460
1-461 - CH3 Br Br - M+Na
3.382/460
I -462 3,4-F2 CH3 Br Br - M+H
3.398/500
I-463 3,4,5-F3 H Br Br - M+Na
3.299/442
I -464 3-F H Br Br - M+H
I -465 3-CN H Br Br - 3.037/449 phys. data
No. Rn R1 R2 R3 (R4)x (HPLC:
RT[min]/m/z)
M+H
3.174/464
1-466 4-F H Br Br - M+Na
3.143/446
1-467 - H Br Br - M+Na
3.257/482
1-468 3,5-F2 H Br Br - M+Na
3.558/482
1-469 3,4,5-F3 H F F 4-1
M+H
3.893/478
1-470 3,5-F2 CH3 F F 4-1
M+H
3.437/486
1-471 3,5-F2 H F F 4-I
M+Na
I -472 3,5-F2 CH2CCH F F 4-I 3.882 / 501
4.047/413
I -473 4-F CH3 CI CI 4-Br
M-23
3.774/420
I -474 3-CN CH3 CI CI 4-Br
M-23
3.550 / 346
I -475 - CH2OCH3 F F - M+H
3.606 / 364
I-476 4-F CH2OCH3 F F - M+H
3.686 / 382
I-477 3,4-F2 CH2OCH3 F F - M+H
3.588 / 364
I-478 3-F CH2OCH3 F F - M+H
3.670 / 381
I-479 3,5-F2 CH2OCH3 F F - M+H
3.778/422
I-480 3,4,5-F3 CH2OCH3 F F - M+23
3.642/284
1-481 - CH2CCH F F - M-55
3.740 / 376
I -482 3,4-F2 CH2CCH F F - M+H
3.670 / 302
I -483 3-F CH2CCH F F - M-55
3.745 / 376
I-484 3,5-F2 CH2CCH F F - M+H
Figure imgf000056_0001
Unless indicated otherwise, the compounds are present as a racemate
# denotes the bond through which the group R1 is attached
Use examples
The herbicidal activity of the compounds of the formula I was demonstrated by the following greenhouse experiments:
The culture containers used were plastic flowerpots containing loamy sand with approximately 3.0% of humus as the substrate. The seeds of the test plants were sown separately for each species.
For the pre-emergence treatment, the active compounds, which had been suspended or emulsified in water, were applied directly after sowing by means of finely distributing nozzles. The containers were irrigated gently to promote germination and growth and subsequently covered with transparent plastic hoods until the plants had rooted. This cover caused uniform germination of the test plants, unless this has been impaired by the active compounds.
For the post-emergence treatment, the test plants were first grown to a height of 3 to
15 cm, depending on the plant habit, and then treated with the active compounds which had been suspended or emulsified in water. For this purpose, 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 prior to treatment.
Depending on the species, the plants were kept at 10 - 25°C or 20 - 35°C. The test period extended over 2 to 4 weeks. During this time, the plants were tended, and their response to the individual treatments was evaluated.
Evaluation was carried out using a scale from 0 to 100. 100 means no emergence of the plants, or complete destruction of at least the aerial moieties, and 0 means no damage, or normal course of growth. A good herbicidal activity is given at values of at least 70 and a very good herbicidal activity is given at values of at least 85.
The plants used in the greenhouse trials were of the following species: Bayer code Scientific name Common name
ALOMY Alopecurus myosuroides Blackgrass
AMARE Amaranthus retroflexus Carelessweed
AVE FA Avena fatua spring wild-oat
ECHCG Echinochloa crus-galli Cockspur
GALAP Galium aparine Goosegrass
LOLMU Lolium multiflorum Italian ryegrass
POLCO Fallopia convolvulus Bearbine
SETVI Setaria viridis Green foxtail
1 ) Applied by the post-emergence method at an application rate of 0.125 kg/ha, the active compounds 1-164, 1-178, I-300, I-303, 1-316, I-324, I-327, I-328, I-329, I-330, 1-331 , I-332, I-335, I-338, I-339, I-345, I-346, I-347, I-350, I-363, I-365 and I-369 showed very good herbicidal activity and the active compound I-336 showed good herbicidal activity against ALOMY. Applied by the post-emergence method at an application rate of 0.250 kg/ha, the active compounds I-295, I-307, I-308, I-309, 1-31 1 , 1-314, I-320, 1-321 , I-322, I-333, I-334, I-337, I-343, 1-361 and I-362 showed very good herbicidal activity against ALOMY.
2) Applied by the post-emergence method at an application rate of 0.125 kg/ha, the active compounds 1-186, I-233, I-243, I-303, I-324; I-327, I-328, I-329, I-330, I-407, 1-410, 1-471 and I-472 showed very good herbicidal activity against AMARE. Applied by the post-emergence method at an application rate of 0.250 kg/ha, the active compounds I-295, I-307, I-308, I-309, 1-311 , I-320, 1-321 , I-368, I-476, I-478, I-479, I-480, I-486 and I-487 showed very good herbicidal activity and the active compound I-322 showed good herbicidal activity against AMARE.
3) Applied by the post-emergence method at an application rate of 0.125 kg/ha, the active compounds I-2, I-7, I-8, I-9, 1-1 1 , 1-12, 1-14, 1-19, I-20, 1-21 , I-22, I-24, I-26, I-30, I-34, I-37, I-39, I-45, I-46, I-49, I-50, 1-51 , I-54, I-56, I-58, I-62, I-67, I-72, I-80, 1-81 , 1-91 , I-95, I-96, I-97, I-99, 1-100, 1-109, 1-1 10, 1-128, 1-131 , 1-135, 1-139, 1-140, 1-142, 1-143, 1-151 , 1-178, 1-193, 1-194, 1-195, 1-199, I-209, 1-21 1 , I-380 and I-403 showed very good herbicidal activity against AVEFA. Applied by the post-emergence method at an application rate of 0.250 kg/ha, the active compound I-370 showed very good herbicidal activity against AVEFA.
4) Applied by the post-emergence methd at an application rate of 0.125 kg/ha, the active compounds I-2, I-4, I-7, I-9, 1-1 1 , 1-12, 1-14, 1-19, I-20, 1-21 , I-22, I-24, I-26, I-27, I-30, I-34, I-37, I-39, I-45, I-46, I-48, I-49, I-50, 1-51 , I-52, I-56, I-62, I-67, I-80, 1-81 , I-99, 1-100, 1-109, 1-1 10, 1-135, 1-139, 1-140 and 1-151 showed very good and the active compound I-58 showed good herbicidal activity against ECHCG.
5) Applied by the post-emergence method at an application rate of 0.125 kg/ha, the active compounds 1-181 , 1-186, I-235 and I-243 showed very good herbicidal activity against GALAP.
6) Applied by the post-emergence method at an application rate of 0.250 kg/ha, the active compound 1-370 showed very good herbicidal activity against LOLMU.
7) Applied by the post-emergence method at an application rate of 0.125 kg/ha, the active compounds 1-181 , I-235, I-300, I-303, 1-316, I-324, I-327, I-328, I-329, I-330, I-332, I-335, I-336, I-338, I-339, I-345, I-346, I-347, I-363, I-365, I-369, 1-412, 1-414, 1-418, I-429, I-430, 1-431 , I-432, I-445, I-446, I-452, 1-471 and I-472 showed very good herbicidal activity against POLCO. Applied by the post-emergence method at an application rate of 0.250 kg/ha, the active compounds I-295, I-307, I-308, I-309, 1-31 1 , 1-314, I-320, 1-321 , I-322, I-333, I-334, I-337, I-343, 1-361 , I-362, I-368, 1-415, 1-416, 1-417, 1-419, I-420, 1-421 , I-422, I-423, I-424, I-425, I-426, I-427, I-433, I-434, I-435, I-437, I-438, I-440, I-444, I-447, I-448, I-449, I-450, I-470, I-476, I-478, I-479, I-480, I-486 and I-487 showed very good herbicidal activity against POLCO.
8) Applied by the post-emergence method at an application rate of 0.125 kg/ha, the active compounds I-2, I-4, I-7, I-8, I-9, 1-1 1 , 1-12, 1-14, 1-19, I-20, 1-21 , I-22, I-24, I-26, I-27, I-30, I-34, I-37, I-39, I-45, I-46, I-48, I-49, I-50, 1-51 , I-52, I-54, I-56, I-58, I-62, I-67, I-72, I-80, 1-81 , 1-91 , I-96, I-97, I-99, 1-100, 1-109, 1-1 10, 1-128, 1-131 , 1-135, 1-139, 1-140, 1-142, 1-143, 1-151 , 1-164, 1-193, 1-194, 1-195, 1-199, I-209, 1-21 1 , I-233, 1-331 , I-332, I-335, I-338, I-339, I-345, I-346, I-347, I-350, I-363, I-365, I-369, 1-412, 1-414, 1-418, I-445, I-446 and I-452 showed very good herbicidal activity and the compounds I-95, I-300, I-336 and I-430 showed good herbicidal activity against SETVI. Applied by the post-emergence method at an application rate of 0.250 kg/ha, the active compounds I-333, I-334, I-337, I-343, 1-361 , I-362, I-368, 1-415, 1-416, 1-417, 1-419, I-420, I-422, I-423, I-424, I-425, I-426, I-427, I-434, I-435, I-437, I-438, I-440, I-444, I-447, I-448, I-449, I-450, I-470, I-480, I-486 and I-487 showed very good herbicidal activity and the compound 1-421 showed good herbicidal activity against SETVI.

Claims

ims
A cyanobutyrate compound of the formula I
Figure imgf000059_0001
in which the variables have the following meaning:
R is halogen, cyano, nitro, Ci-C4-alkyl, Ci-C4-haloalkyl, C2-C6-alkenyl, C2-C6- alkynyl, CrC4-alkoxy, Ci-C4-alkylthio, Z-(tri-Ci-C4-alkyl)silyl;
R1 is hydrogen, Z-CN, Ci-C8-alkyl, Z-C3-C6-cycloalkyl, Ci-C8-haloalkyl, C1-C4- alkoxy-Ci-C4-alkyl, Ci-C4-alkylthio-Ci-C4-alkyl, C3-C8-alkenyl, Z-C3-C6- cycloalkenyl, C3-C8-alkynyl, NR'R", Z-(tri-Ci-C4-alkyl)silyl, Z-N=C(Ra)2,
Z-C(Ra)=NRa, Z-C(=T)-Ra, Z-P(=T)(Ra)2, Z-phenyl, a 3- to 7-membered monocyclic or 9- or 10-membered bicyclic saturated, unsaturated or aromatic heterocycle which contains 1 , 2, 3 or 4 heteroatoms selected from the group consisting of O, N and S, which may carry carbonyl or thiocarbonyl groups and which is attached via carbon or nitrogen,
T is O or S;
Ra is hydrogen, TH, d-Cs-alkyl, Ci-C4-haloalkyl, Z-C3-C6-cycloalkyl, C2-C3-alkenyl, Z-C5-Cs-cycloalkenyl, C2-C8-alkynyl, Z-Ci-C6-alkoxy, Z-Ci-C4-haloalkoxy, Z-C3-C8-alkenyloxy, Z-C3-Cs-alkynyloxy, Z-C1-C4- alkylthio, Z-Ci-C4-haloalkylthio, Z-C3-C8-alkenylthio, Z-C3-C8- alkynylthio, NR'R", Ci-C6-alkylsulfonyl, oxy-Ci-C3-alkyleneoxy, Z-BRb3® , Z-C(=T)-RA, Z-T-C(=T)-RA, Z-(tri-Ci-C4-alkyl)silyl, Z-phenyl, Z-phenoxy, Z-phenylamino or a 3- to 7-membered monocyclic or 9- or 10-membered bicyclic heterocycle which contains 1 , 2, 3 or 4 heteroatoms selected from the group consisting of O, N and S, where the cyclic groups are unsubstituted or may carry 1 , 2, 3 or 4 groups Rb and/or carbonyl or thiocarbonyl groups;
R', R" independently of one another are hydrogen, Ci-Ce-alkyl,
Ci-C4-haloalkyl, C3-C8-alkenyl, C3-C8-alkynyl, Z-C3-C6-cycloalkyl, Z-d-Ce-alkoxy, Z-Ci-C8-alkylthio, Z-Ci-C8-haloalkoxy, Z-Ci-C8- haloalkylthio, Z-C(=T)-RA, where RA is TH, Ci-C4-alkyl, C1-C4- alkoxy or Ci-C4-alkylthio;
R' and R" together with the nitrogen atom to which they are attached may also form a 3- to 7-membered monocyclic or 9- or 10-membered bicyclic heterocycle which contains 1 , 2, 3 or 4 heteroatoms selected from the group consisting of O, N and S and which may carry carbonyl or thiocarbonyl groups;
R independently of one another are Z-CN, Z-TH, Z-NO2,
Z-halogen, d.Cs-alkyl, Ci-C4-haloalkyl, C2-Cs-alkenyl, C2-C8- alkynyl, Z-Ci-Ce-alkoxy, Z-d-Cs-alkylthio, Z-d-Ce-haloalkylthio, Z-Ci-Ce-haloalkoxy, Z-C3-Cio-cycloalkyl, T-Z-C3-Cio-cycloalkyl, Z-C(=T)-Ra, NRiRii, Z-(tri-Ci-C4-alkyl)silyl, Z-phenyl and
S(0)mRbb, where Rbb is Ci-C8-alkyl or Ci-C6-haloalkyl;
m is 0, 1 or 2;
R together with the group R attached to the adjacent carbon atom may also form a five- or six-membered saturated or partially or fully unsaturated ring which, in addition to carbon atoms, may contain 1 , 2 or 3 heteroatoms selected from the group consisting of O, N and S; Z is a covalent bond or d-Ce-alkylene;
n is 0, 1 ,
2,
3,
4 or 5;
R2, R3, R4 independently of one another are halogen, cyano, nitro, N=C=T, Ci-C4-alkyl, Ci-C4-alkoxy, Ci-C4-alkylthio, S(0)mRb , N R'R", Ci-C -haloalkyl, Ci-C4-haloalkoxy, Ci-C4-haloalkylthio; where, if the index x is 2 or 3, the groups R4 may be identical or different;
x is 0, 1 , 2 or 3;
where in the groups R and R1 and their subsubstituents, the carbon chains and/or the cyclic groups may be partially or fully substituted by groups Ra and/or Rb,
or an N-oxide or an agriculturally suitable salt thereof;
with the proviso that R2 and R3 are not both chlorine if the indices n and x are 0 and R1 is Ci-C4-alkyl or H; and
R2 and R3 are not both fluorine if the index n is 1 the index x is 0 or 3 and R and R4 are fluorine and R1 is Ci-C4-alkyl.
The compound of the formula I according to claim 1 in which R2 and/or R3 are independently selected from the group consisting of fluorine, chlorine and bromine.
The compound of the formula I according to claim 1 or 2 in which the index x is 1 or 2.
The compound of the formula I according to any of claims 1 to 3 in which R2 is fluorine.
The compound of the formula I according to any of claims 1 to 4 in which R4 is located in the 4-position. The compound of the formula I according to any of claims 1 to 5 in which the combination of R2, R3 and (R4)x is selected from the group consisting of: 2,6-F2-4- halo; 2,6-F2-4-OCF3; 2,6-F2-4-OCHF2; 2,6-F2-4-CF3; 2,6-F2-4-CHF2; 2,3,
5,6-F4; 2,6-F2-3-halo; 2,6-F2-3-CH3 and 2,
6-F2-3-OCH3.
7. The compound of the formula I according to any of claims 1 to 6 in which the
index n is 0.
8. The compound of the formula I according to any of claims 1 to 6 in which R is chlorine, fluorine, cyano or nitro and the index n has the value 1 or 2.
9. The compound of the formula I according to any of claims 1 to 6 in which Rn is 3-F; 3,4-F2; 3,5-F2; 3,4,5-F3; 3-F.4-CI; 3-CI.4-F; 4-CI; 4-F, 3-CI or 3-CN.
10. The compound of the formula I according to any of claims 1 to 6 in which R is fluorine or cyano and the index n has the value 1 .
1 1. The compound of the formula I according to any of claims 1 to 10 in which R1 is H, CH3, C2H5, CH2CN, Ci-C2-haloalkyl, CH2OCH3 or CH2C≡ CH.
12. The compound of the formula I according to any of claims 1 to 10 in which R1 is H or CH3.
A process for preparing the compounds of the formula I according to any of claims 1 to 12 comprising enylacetonitrile derivatives of the formula II
Figure imgf000061_0001
with cinnamate derivatives of the formula
Figure imgf000061_0002
under basic conditions.
A composition comprising a herbicidally effective amount of at least one cyanobutyrate compound of the formula I or an agriculturally suitable salt thereof according to any of claims 1 to 12 and auxiliaries customary for formulating crop protection agents. A method for controlling unwanted vegetation which comprises allowing a herbicidally effective amount of at least one cyanobutyrate compound of the formula I or of an agriculturally suitable salt thereof according to any of claims to 12 to act on plants, their seed and/or their habitat.
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EP2474226A1 (en) * 2011-01-07 2012-07-11 Basf Se Herbicidally active composition comprising cyanobutyrates
WO2012126764A1 (en) * 2011-03-18 2012-09-27 Bayer Cropscience Ag Substituted 4-cyan-3-(2,6-difluorophenyl)-4-phenylbutanoates, method for the production thereof and use thereof as herbicides and plant growth regulators
WO2013010882A2 (en) 2011-07-15 2013-01-24 Bayer Intellectual Property Gmbh 2,3-diphenyl-valeronitrile derivatives, method for the production thereof and use thereof as herbicides and plant growth regulators
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EP2474226A1 (en) * 2011-01-07 2012-07-11 Basf Se Herbicidally active composition comprising cyanobutyrates
WO2012126764A1 (en) * 2011-03-18 2012-09-27 Bayer Cropscience Ag Substituted 4-cyan-3-(2,6-difluorophenyl)-4-phenylbutanoates, method for the production thereof and use thereof as herbicides and plant growth regulators
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WO2013010882A3 (en) * 2011-07-15 2013-04-11 Bayer Intellectual Property Gmbh 2,3-diphenyl-valeronitrile derivatives, method for the production thereof and use thereof as herbicides and plant growth regulators
CN103748075B (en) * 2011-07-15 2016-09-07 拜耳知识产权有限责任公司 2,3-diphenyl valeronitrile derivant, its preparation method and as herbicide and the purposes of plant growth regulator
JP2014520830A (en) * 2011-07-15 2014-08-25 バイエル・インテレクチユアル・プロパテイー・ゲー・エム・ベー・ハー 2,3-Diphenyl-valeronitrile derivatives, processes for their preparation and their use as herbicides and plant growth regulators
WO2013010882A2 (en) 2011-07-15 2013-01-24 Bayer Intellectual Property Gmbh 2,3-diphenyl-valeronitrile derivatives, method for the production thereof and use thereof as herbicides and plant growth regulators
US9084425B2 (en) 2011-07-15 2015-07-21 Bayer Intellectual Property Gmbh 2,3-diphenyl-valeronitrile derivatives, method for the production thereof and use thereof as herbicides and plant growth regulators
WO2013064462A1 (en) 2011-10-31 2013-05-10 Bayer Intellectual Property Gmbh Substituted 4-cyano-3-phenyl-4-(pyridin-3-yl)butanoates, processes for preparation thereof and use thereof as herbicides and plant growth regulators
US8975412B2 (en) 2011-10-31 2015-03-10 Bayer Intellectual Property Gmbh Substituted 4-cyano-3-phenyl-4-(pyridin-3-yl)butanoates, processes for preparation thereof and use thereof as herbicides and plant growth regulators
WO2013092500A1 (en) 2011-12-19 2013-06-27 Bayer Intellectual Property Gmbh Substituted 4-cyan-3-phenyl-4-(pyridine-3-yl)butanoates, processes for preparation thereof and use thereof as herbicides and plant growth regulators.
US9161537B2 (en) 2011-12-19 2015-10-20 Bayer Intellectual Property Gmbh Substituted 4-cyan-3-phenyl-4-(pyridine-3-yl)butanoates, processes for preparation thereof and use thereof as herbicides and plant growth regulators
US9661848B2 (en) 2012-12-21 2017-05-30 Bayer Cropscience Ag Substituted 4-cyan-3-(pyridyl)-4-phenylbutanoates, method for the production thereof and uses as herbicides and plant growth regulators
WO2014195253A1 (en) 2013-06-07 2014-12-11 Bayer Cropscience Ag Substituted 5-hydroxy-2,3-diphenylpentanonitrile derivatives, processes for their preparation and their use as herbicides and/or plant growth regulators
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WO2016001204A1 (en) 2014-07-04 2016-01-07 Bayer Cropscience Ag Substituted 5-hydroxy-2-heteroaryl-3-phenylpentanonitrile derivatives, processes for their preparation and their use as herbicides and/or plant growth regulators
US9957248B2 (en) 2014-07-04 2018-05-01 Bayer Cropscience Aktiengesellshaft Substituted 5-hydroxy-2-heteroaryl-3-phenylpentanonitrile derivatives, processes for their preparation and their use as herbicides and/or plant growth regulators
US10172350B2 (en) 2014-10-08 2019-01-08 Bayer Cropscience Aktiengesellschaft Substituted 5-hydroxy-2-phenyl-3-heteroaryl pentanenitrile derivatives, method for the production thereof and use thereof as herbicides and/or plant growth regulators
US11889833B2 (en) 2022-01-14 2024-02-06 Enko Chem, Inc. Protoporphyrinogen oxidase inhibitors

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