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EP2587922A1 - Compositions insecticides améliorées contenant une carbonylamidine cyclique - Google Patents

Compositions insecticides améliorées contenant une carbonylamidine cyclique

Info

Publication number
EP2587922A1
EP2587922A1 EP11727191.6A EP11727191A EP2587922A1 EP 2587922 A1 EP2587922 A1 EP 2587922A1 EP 11727191 A EP11727191 A EP 11727191A EP 2587922 A1 EP2587922 A1 EP 2587922A1
Authority
EP
European Patent Office
Prior art keywords
methyl
pyridinyl
spp
oxazolone
chloro
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP11727191.6A
Other languages
German (de)
English (en)
Inventor
Peter Jeschke
Olga Malsam
Peter Lösel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer Intellectual Property GmbH
Original Assignee
Bayer Intellectual Property GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Intellectual Property GmbH filed Critical Bayer Intellectual Property GmbH
Priority to EP11727191.6A priority Critical patent/EP2587922A1/fr
Publication of EP2587922A1 publication Critical patent/EP2587922A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms

Definitions

  • the present invention relates to insecticidal compositions comprising at least one cyclic carbonylamidine and at least one activity modifier selected from ammonium or phosphonium salts and penetrants. It is known from WO 2010/005692 that certain cyclic carbonylamidines have biological activity and that they can be used to control insects. WO 2010/005692 also describes the preparation of such compounds. The effectiveness of these compounds is good, but not always fully satisfactory especially at low rates and concentrations. However, since the ecological and economic demands on modern plant treatment products are constantly increasing, for example as regards selectivity and application rate, and in addition, e.g. Problems with resistance can occur, there is the constant task of developing new plant treatment products that have advantages over the known at least in some areas.
  • the object of the present invention is therefore to provide an insecticidal composition which contains certain cyclic carbonyl amidines and which has an improved action or a widened activity spectrum compared with the known compositions.
  • WO 95/017817 describes that the effect of certain agrochemical active ingredients can be increased by adding surface-active agents (detergents) which contain various nitrogen-containing compounds, such as quaternary ammonium salts, betaines and amines.
  • surface-active agents such as quaternary ammonium salts, betaines and amines.
  • WO 95/017817 is concerned with providing optimized performance enhancers and describes that compositions comprising at least one nitrogen-containing salt and a chelating agent are particularly advantageous.
  • the nitrogen-containing salt is preferably a nitrogen-containing detergent.
  • nitrogen- or phosphorous-containing salts having longer alkyl and / or aryl substituents are also disclosed in EP-A-0 453 086, EP-A-0 664 081, FR-A-2 600 494, US 4,844,734B, US 5,462,912B, US 5,538,937B, US 20003 / 0224939A, US 2005 / 0009880A and / or US 2005 / 0096386A.
  • These salts have a permeabilizing effect or increase the solubility of the active ingredient; or they act as detergents.
  • US Pat. No. 2,848,476B proposes to use salts of sulfonic acids for enhancing the activity (increasing the activity).
  • the effect enhancement can be attributed to the fact that the acids used themselves have a paralyzing effect on insects.
  • the use of inorganic ammonium salts as formulation auxiliaries and enhancers in combination with certain herbicides is also known.
  • WO 92/16108 describes the use of ammonium sulfate as a formulation adjuvant in a granular formulation containing insecticidally active phosphoramidothioates.
  • WO 92/16108 describes that a certain amount of ammonium sulfate is necessary to ensure the chemical stability of granules containing phosphoramidothioates.
  • US Pat. No. 6,645,914 B and EP-A-0 036 106 describe the increase in activity for the herbicides glyphosate and phosphinothricin by adding ammonium sulfate
  • cyclic carbonylamidines of the formula (I) can be increased by the addition of at least one activity enhancer selected from among ammonium and / or phosphonium salts and penetrants.
  • the present invention thus provides a composition comprising at least one cyclic carbonylamidine of the formula (I)
  • Y is O, S, NR 5 or CR 3 R 4 ; preferably Y is CH 2 or O;
  • G is a saturated or unsaturated bond or is CR 3 R 4 ;
  • Z is O, S, CR 3 R 4 or NR 5 ; preferably Z is CH 2 ;
  • R 1 is hydrogen, C r C 3 alkoxy, C (0) R 6 or S0 2 R 7 , or one of the following radicals: C r C 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl, C 3 -C 4 cycloalkyl, C 4 -C 5 cycloalkylalkyl, C4 - C5 alkylcycloalkyl or benzyl, which are optionally substituted with 1 to 5 halogen atoms; is hydrogen or C 1 -C 2 -alkyl; R and R are independently hydrogen or methyl; R 5 is hydrogen, C 1 -C 2 alkyl or C 1 -C 2 haloalkyl; 2 alkyl or Ci-C 2 haloalkyl stands for Ci-C; 2 alkyl or Ci-C 2 haloalkyl stands for Ci-C; and
  • Q is a 5- or 6-membered unsaturated heterocyclic ring containing as ring atoms at least one nitrogen atom, and other ring atoms from the series carbon, oxygen and sulfur and optionally with 1 to 3 substituents selected from the group halogen, cyano, nitro, and Ci -C r alkyl, C 1 -C r alkoxy and C 1 -C 4 alkylthio, each of which is in turn optionally substituted with 1 to 5 fluorine atoms or chlorine atoms; or is 3-tetrahydrofuranyl; preferably Q is a heterocyclic ring selected from pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, pyrazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, isothiazolyl, imidazolyl, pyrrolyl, thiazolyl and triazolyl, optional
  • D is nitrogen or phosphorus; preferably D is nitrogen; is 1, 2, 3 or 4; preferably n stands for 1 or 2;
  • R 8 , R 9 , R 10 and R 11 are each independently hydrogen or optionally substituted Cp Cg-alkyl or mono- or polyunsaturated, optionally substituted C2-Cg-alkenyl, wherein the substituents can be selected from halogen, nitro and cyano ;
  • R 8 , R 9 , R 10 and R 11 are each independently of one another hydrogen or in each case optionally substituted C 1 -C 8 -alkyl, the substituents being selected from halogen, nitro and cyano; particularly preferably R 8 , R 9 , R 10 and R 11 are each independently hydrogen, methyl, ethyl, n-propyl, z o-propyl, n-butyl, where-butyl, sec-butyl or tert-butyl; most preferably R 8 , R 9 , R 10 and R 11 are each independently hydrogen, methyl or ethyl;
  • R 12 is an inorganic or organic anion;
  • R 12 is preferably hydrogencarbonate, tetraborate, fluoride, bromide, iodide, chloride, monohydrogenphosphate, dihydrogenphosphate, hydrogensulphate, tartrate, sulphate, nitrate, thiosulphate, thiocyanate, formate, lactate, acetate, propionate, butyrate, pentanoate, citrate or oxalate;
  • R 12 furthermore preferably represents carbonate, pentaborate, sulfite, benzoate, hydrogen oxalate, hydrogen citrate, methyl sulfate or the tetrafluoroborate;
  • R 12 particularly preferably represents lactate, sulfate, nitrate, thiosulphate, thiocyanate, citrate, oxalate, formate, monohydrogenphosphate or dihydrogenphosphate;
  • R 12 particularly preferably represents monohydrogenphosphate, dihydr
  • ammonium salts of the formula (II) are ammonium sulfate, ammonium lactate, ammonium nitrate, ammonium thiosulphate, ammonium thiocyanate, ammonium citrate, ammonium oxalate, ammonium formate, ammonium hydrogenphosphate, ammonium dihydrogenphosphate, ammonium carbonate, ammonium bicarbonate, ammonium onium phosphate, ammonium benzoate, ammonium hydrogen oxalate, ammonium hydrogen citrate, Ammonium acetate, tetramethylammonium sulfate,
  • Tetramethylammonium lactate Tetramethylammonium lactate, tetramethylammonium nitrate, tetramethylammonium thiosulfate, tetramethylammonium thiocyanate, tetramethylammonium citrate, tetramethylammonium oxalate, tetramethylammonium formate, tetramethylammonium hydrogenphosphate, tetramethylammonium dihydrogenphosphate, tetraethylammonium sulfate, tetraethylammonium lactate,
  • Tetraethylammonium citrate Tetraethylammonium oxalate, tetraethylammonium ammonium formate, tetraethylammonium hydrogenphosphate, and tetraethylammonium dihydrogenphosphate.
  • the invention relates in a first embodiment to a composition as defined above, in which at least one cyclic carbonylamidine of the formula (Ia) is present R 2 N ' ⁇
  • R 1 is hydrogen or C r C 3 alkoxy, Ci-C 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl, C 3 -C 4 - cycloalkyl, C 4 -C 5 cycloalkylalkyl or C 4 -C 5 alkylcycloalkyl optionally substituted with halogen; preferably R 1 is hydrogen, CH 2 -CF 3 , or is methyl, ethyl, n-, z o-propyl, or cyclopropyl, which are optionally substituted by halogen;
  • R 2 is hydrogen, methyl, or ethyl; preferably R 2 is hydrogen or methyl;
  • R 3 and R 4 independently of one another represent hydrogen or methyl
  • R 5 is hydrogen, C 1 -C 2 -alkyl or C 1 -C 2 -haloalkyl
  • Q is a 5- or 6-membered unsaturated heterocyclic ring containing as ring atoms at least one nitrogen atom, and other ring atoms from the series carbon, oxygen and sulfur and optionally with 1 to 3 substituents selected from the group halogen, cyano, nitro, and C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy and C 1 -C 4 -alkylthio are substituted, which in turn are each optionally substituted by 1 to 5 fluorine atoms or chlorine atoms; or is 3-tetrahydrofuranyl; preferably Q is a heterocyclic ring selected from pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, pyrazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, isothiazolyl, imidazolyl, pyrrolyl, thiazolyl
  • the invention relates to a composition as defined above, in which at least one cyclic carbonylamidine is selected, which is selected from the compounds (1-1) to (1-42)
  • the present invention furthermore relates to a composition as defined above which contains at least one cyclic carbonylamidine of the formula (I) in which
  • Y is CR 3 R 4
  • G is a saturated or unsaturated bond
  • Z is O or S, wherein the radicals R 1 to R 4 and Q have the meanings given above.
  • the present invention furthermore relates to a composition as defined above which contains at least one cyclic carbonylamidine of the formula (I) in which
  • the present invention furthermore relates to a composition as defined above which contains at least one cyclic carbonylamidine of the formula (I) in which Y is O, S, NR 5 or CR 3 R 4 , G is CR 3 R 4 , and Z is O, S, NR 5 or CR 3 R 4 , wherein the radicals R 1 to R 5 and Q are as above have given meanings.
  • the present invention furthermore relates to a composition as defined above which contains at least one cyclic carbonylamidine of the formula (I) in which
  • the present invention also provides the use of the effect enhancers of the invention, i. the ammonium and / or phosphonium salts according to the invention optionally in combination with the penetrants according to the invention, for enhancing the effect (increasing the activity) of the carbonylamidines according to the invention.
  • the effect enhancers of the invention i. the ammonium and / or phosphonium salts according to the invention optionally in combination with the penetrants according to the invention, for enhancing the effect (increasing the activity) of the carbonylamidines according to the invention.
  • the effect enhancers can be added to the application solution containing the active compounds according to the invention (Tankrmx / tank mix application) or incorporated into formulation comprising active ingredients according to the invention (formulated product).
  • the invention thus also relates to formulated insecticidal compositions and ready-to-use crop protection agents (for example spray liquors). Finally, the invention also relates to the use of the composition according to the invention and to agents for combating insect pests (plant pests) which occur in agriculture.
  • the active compounds according to the invention can be used in the compositions according to the invention in a wide concentration range.
  • the concentration of the active ingredients in the composition is usually 0.1-50% by weight.
  • ammonium or phosphonium salts of the formula (II) according to the invention can be used in the compositions according to the invention in a wide concentration range.
  • ammonium or phosphonium salts according to the invention are added in the composition in such a concentration that they are present in the ready-to-use plant protection agent (in the spray mixture or in a tank mix / T mixture application) in a concentration of 0.5 to 80 mmol / l, preferably 0, 75 to 37.5 mmol / l, particularly preferably 1.5 to 25 mmol / l.
  • the ammonium and / or phosphonium salt concentration in the formulation is chosen so that it lies after dilution of the formulation to the desired active ingredient concentration in the aforementioned ranges.
  • the concentration of the salt in the formulation is usually 1-50 wt .-%.
  • the composition according to the invention contains as an effect enhancer an inventive ammonium and / or phosphonium salt and a penetration promoter according to the invention (in particular alkanol alkoxylates of the formula (III) as defined herein and / or mineral or vegetable oils and their modifications).
  • Penetration promoters according to the invention are substances which are usually used to improve the penetration of agrochemical active substances into plants, in that they penetrate from the corresponding application form (in particular aqueous spray mixture) and / or from the spray coating into the cuticle of the plant and thereby increase the material mobility ( Mobility) of active ingredients in the cuticle.
  • the method described in the literature can be used to determine this property (Baur et al., 1997, Pesticide Science 51, 131-152).
  • Suitable penetrants according to the invention are also substances which promote the solubility of the compounds according to the invention in the spray coating. These include, for example, mineral or vegetable oils (vegetable oil, vegetable oil).
  • Suitable oils are all commonly used in agrochemical means mineral or vegetable - optionally modified - oils in question. Examples include sunflower oil, rapeseed oil, olive oil, castor oil, rapeseed oil, corn oil, cottonseed oil and soybean oil and their esters (preferably methyl or ethyl esters). Preferred oils are rapeseed oil, sunflower oil and their methyl or ethyl esters (e.g., rapeseed oil methyl ester).
  • Penetration promoters suitable according to the invention are also alkanol alkoxylates of the formula (III)
  • R is straight-chain or branched C 1 -C 20 -alkyl;
  • R is preferably butyl, where is-butyl, n-pentyl, z-pentyl, neopentyl, n-hexyl, iso-hexyl, n-octyl, z o-octyl, 2-ethyl-hexyl, nonyl, isononyl, Decyl, n-dodecyl, z o -dodecyl, lauryl, myristyl, z o -tridecyl, trimethyl-nonyl, palmityl, stearyl or eicosyl;
  • R is hydrogen, methyl, ethyl, n -propyl, z o -propyl, n -butyl, z o -butyl, tert -butyl, n -pentyl or n -hexyl;
  • AO is an ethylene oxide radical, a propylene oxide radical, a butylene oxide radical or mixtures of ethylene oxide and propylene oxide radicals or butylene oxide radicals; and
  • v is a number from 2 to 30.
  • Penetration enhancers suitable according to the invention are in particular alkanol alkoxylates of the formula (IIIa), (IIIb) or (never)
  • EO represents a grouping -CH 2 -CH 2 -O-; n is a number from 2 to 20; PO represents CH-CH-O-;
  • CH 3 p, q, r, and s each independently represent a number from 1 to 10.
  • R and R ' have the meanings given above; EO is CH 2 -CH 2 -O-; BO is -CH-CH-QH-O;
  • CH 3 p and q each independently, stand for a number from 1 to 10.
  • EO is CH 2 -CH 2 -O-; each of r and s independently represents a number from 1 to 10.
  • An example of an alkanol alkoxylate of the formula (III-c) is a 2-ethylhexyl alkoxylate of the formula (III-c-1)
  • CH 3 the numbers represent 8 and 6 averages.
  • An example of an alkanol alkoxylate of the formula (III-d) is a compound of the formula (III-d-1)
  • alkanol alkoxylates are generally defined by the above formulas. These substances are mixtures of substances of the specified type with different chain lengths. For the indices, therefore, average values are calculated, which can also differ from whole numbers.
  • alkanol alkoxylates of the formulas given are known and are partly available commercially or can be prepared by known methods (cf., WO 98/035553, WO 00/35278 and EP-A
  • the concentration of penetration promoter can be varied within a wide range in the compositions according to the invention.
  • a formulated plant protection product it is generally from 1 to 95% by weight, preferably at
  • the concentration is generally between 0.1 and 10 g / l, preferably between 0.5 and 5 g / l.
  • Pesticide promoter according to the test means that any compound which is suitable for use in the test for cuticle penetration according to Baur et al., 1997, Pesticide Science 51, 131- 152 acts as a penetration promoter.
  • compositions according to the invention may also contain further components, for example surfactants (nonionic or anionic) or dispersing aids or emulsifiers.
  • Suitable nonionic surfactants or dispersing agents are all substances of this type which can usually be used in agrochemical compositions. Preference is given to polyethylene oxide-polypropylene oxide block copolymers, polyethylene glycol ethers of linear alcohols, reaction products of fatty acids with ethylene oxide and / or propylene oxide, furthermore polyvinyl alcohol, polyvinylpyrrolidone, copolymers of polyvinyl alcohol and polyvinylpyrrolidone and copolymers of (meth) acrylic acid and (meth) acrylic acid esters, furthermore alkyl ethoxylates and alkylaryl ethoxylates which may optionally be phosphated and optionally neutralized with bases, sorbitol ethoxylates being mentioned by way of example, and also polyoxyalkyleneamine derivatives.
  • Suitable anionic surfactants are all substances of this type conventionally usable in agrochemical compositions. Preference is given to alkali metal and alkaline earth metal salts of alkylsulfonic acids or alkylarylsulfonic acids.
  • Another preferred group of anionic surfactants or dispersing aids are salts of polystyrenesulfonic acids which are sparingly soluble in vegetable oil, salts of polyvinylsulfonic acids, salts of Naphthalenesulfonic acid-formaldehyde condensation products, salts of condensation products of naphthalenesulfonic acid, phenolsulfonic acid and formaldehyde, and salts of lignosulfonic acid.
  • Suitable additives which may be present in the formulations according to the invention are emulsifiers, foam-inhibiting agents, preservatives, antioxidants, dyes and inert fillers.
  • Preferred emulsifiers are ethoxylated nonylphenols, reaction products of alkylphenols with ethylene oxide and / or propylene oxide, ethoxylated arylalkylphenols, furthermore ethoxylated and propoxylated arylalkylphenols, and sulfated or phosphated arylalkyl ethoxylates or ethoxypropoxylates, sorbitan derivatives such as polyethylene oxide sorbitan fatty acid esters and sorbitan - fatty acid esters, are exemplified.
  • composition according to the invention may contain, in addition to the cyclic carbonylamidines according to the invention, further active ingredients, including synergists, and fertilizers.
  • synergists are compounds that increase the effect of the active ingredients without the added synergist itself having to be active.
  • Active ingredients suitable according to the invention are, for example, the following insecticides, acaricides or nematicides:
  • (Inl) acetylcholinesterase (AChE) inhibitors such as, for example, carbamates, eg alanycarb, aldicarb, bendocarb, benfuracarb, butocarboxime, butoxycarboxime, carbaryl, carbofuran, carbosulfan, ethiophencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, Oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamates, trimethacarb, XMC and xylylcarb; or organophosphates, e.g.
  • carbamates eg alanycarb, aldicarb, bendocarb, benfuracarb, butocarboxime, butoxycarboxime, carbaryl, carbofuran, carbosulfan,
  • GABA-controlled chloride channel antagonists such as organochlorines, eg, chlordane and endosulfan (alpha); or fiproles (phenylpyrazoles), eg, ethiprole, fipronil, pyrafluprole and pyriprole.
  • (In3) sodium channel modulators / voltage dependent sodium channel blockers such as pyrethroids, e.g. Acrinathrin, allethrin (d-cis -trans, d-trans), bifenthrin, bioallethrin, bioallethrin-S-cyclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin (beta), cyhalothrin (gamma, lambda), cypermethrin (alpha, beta , theta, zeta), cyphenothrin [(lR) trans isomers], deltamethrin, dimefluthrin, empenthrin [(EZ) (lR) isomers], esfenvalerates, etofenprox, fenpropathrin, fenvalerates, flucythrinates, flumethrin, fluvalinates (tau), Half
  • nicotinergic acetylcholine receptor agonists such as neonicotinoids, e.g. Acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, thiamethoxam; or nicotine.
  • allosteric acetylcholine receptor modulators such as spinosyns, e.g. Spinetoram and spinosad.
  • (In6) chloride channel activators such as avermectins / milbemycins, e.g. Abamectin, Emamectin benzoate, Lepimectin and Milbemectin.
  • juvenile hormone analogs e.g. Hydroprene, kinoprene, methoprene; or fenoxycarb; Pyriproxyfen.
  • agents with unknown or nonspecific modes of action such as fumigants, e.g. Methyl bromide and other alkyl halides; or chloropicrin; sulfuryl fluoride; Borax; Tartar emetic.
  • (In10) mite growth inhibitors eg clofentezine, diflovidazine, hexythiazox, etoxazole.
  • Inl2 (Inl2) inhibitors of oxidative phosphorylation, ATP disruptors, such as diafenthiuron; or organotin compounds, eg azocyclotine, cyhexatin, fenbutatin oxide; or propargite; Tetradifon.
  • ATP disruptors such as diafenthiuron
  • organotin compounds eg azocyclotine, cyhexatin, fenbutatin oxide
  • propargite Tetradifon.
  • Nicotinergic acetylcholine receptor antagonists such as Bensultap, Cartap (hydrochloride), thiocylam, and thiosultap (-sodium).
  • inhibitors of chitin biosynthesis type 0, such as benzoylureas, e.g. Bistrifluron, chlorofluorazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron.
  • benzoylureas e.g. Bistrifluron, chlorofluorazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron.
  • ecdysone agonists / disruptors such as diacylhydrazines, e.g. Chromafenozide, Halofenozide, Methoxyfenozide and Tebufenozide.
  • Octopaminergic agonists such as amitraz.
  • (In20) complex III electron transport inhibitors such as hydramethylnone; acequinocyl; Fluacrypyrim.
  • (In21) complex I electron transport inhibitors for example from the group of the METI acaricides, e.g. Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad, Tolfenpyrad; or Rotenone (Derris).
  • METI acaricides e.g. Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad, Tolfenpyrad; or Rotenone (Derris).
  • (In23) inhibitors of acetyl-CoA carboxylase such as tetronic acid derivatives, e.g. B. Spirodiclofen and spiromesifen; or tetramic acid derivatives, e.g. Spirotetramat.
  • tetronic acid derivatives e.g. B. Spirodiclofen and spiromesifen
  • tetramic acid derivatives e.g. Spirotetramat.
  • ryanodine receptor effectors such as, for example, diamides, for example flubendiamide, chlorantraniliprole (rynaxypyr), cyanotraniliprole (cyazypyr) and 3-bromo-N- ⁇ 2-bromo-4-chloro-6 - [(1-cyclopropylethyl) carbamoyl] phenyl ⁇ 1- (3-chloro-2-yl) -1H-pyrazole-5-carboxamide (known from WO2005 / 077934) or methyl 2- [3,5-dibromo-2 - ( ⁇ [3-bromo -l- (3-chloropyridin-2-yl) -1H-pyrazol-5-yl] carbonyl ⁇ amino) benzoyl] -1,2-dimethylhydrazinecarboxylate (known from WO2007 /
  • Active ingredients which are suitable according to the invention are, for example, the following fungicides: (F1) inhibitors of ergosterol biosynthesis, for example aldimorph, azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazole, difenoconazole, diniconazole, dinomonazole M, dodemorph, dodemorph acetate, epoxiconazole, etaconazole, fenarimol, Fenbuconazole, fenhexamid, fenpropidin, fenpropimorph, fluquinconazole, flurprimidol, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imazalil, imazalil sulfate, imibenconazole, ipconazole, metconazole, myclobutanil, naft
  • F2 inhibitors of respiration such as bixafen, boscalid, carboxin, diflumetorim, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, furmecyclox, isopyrazam mixture of the syn-epimeric racemate 1RS, 4SR, 9RS and the anti- more highly enriched racemates 1RS, 4SR, 9SR, isopyrazam (anti-epimeric racemate), isopyrazam (anti-epimeric enantiomer 1R, 4S, 9S), isopyrazam (anti-epimeric enantiomer 1S, 4R, 9R), isopyrazam (syn-epimeric racemate 1RS , 4SR, 9RS), isopyrazam (syn-epimeric enantiomer 1R, 4S, 9R), isopyrazam (syn-epimeric enantiomer 1R, 4S,
  • (F4) inhibitors of mitosis and cell division such as benomyl, carbendazim, chlorfenazole, diethofencarb, ethaboxam, fluopicolide, fuberidazole, pencycuron, thiabendazole, thiophanate-methyl, thiophanate, zoxamide, 5-chloro-7- (4-methylpiperidine-1 - yl) -6- (2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidine and 3-chloro-5- (6-chloropyridin-3-yl) -6-methyl -4- (2,4,6-trifluorophenyl) -pyridazine.
  • (F5) Compounds with multisite activity, such as Bordeaux mixture, captafol, captan, chlorothalonil, copper preparations such as copper hydroxide, copper naphthenate, copper oxide, copper oxychloride, copper sulfate, dichlofluanid, dithianon, dodine, dodine free base, Ferbam, Fluorofolpet, Folpet, guazatine, guazatin acetate , Iminoctadine, iminoctadinal besylate, iminoctadine triacetate, mancopper, mancozeb, maneb, metiram, zinc metiram, copper oxine, propamidine, propineb, sulfur and sulfur preparations such as calcium polysulfide, thiram, tolylfluanid, zineb and ziram.
  • copper preparations such as copper hydroxide, copper naphthenate, copper oxide, copper oxychloride, copper sulfate, dichl
  • (F6) resistance inducers such as acibenzolar-S-methyl, isotianil, probenazole and tiadinil.
  • inhibitors of cell wall synthesis such as benthiavalicarb, dimethomorph, flumorph, iprovalicarb, mandipropamide, polyoxins, polyoxorim, validamycin A, and valifenalate.
  • inhibitors of lipid and membrane synthesis such as biphenyl, chloroneb, dicloran, edifenphos, etridiazole, iodocarb, Iprobenfos, isoprothiolane, propamocarb, propamocarb hydrochloride, prothiocarb, pyrazophos, quintozene, tecnazene and tolclofos-methyl.
  • (Fl 1) inhibitors of melanin biosynthesis such as carpropamide, diclocymet, fenoxanil, fthalide, pyroquilone and tricyclazole.
  • (Fl 2) Inhibitors of nucleic acid synthesis such as benalaxyl, benalaxyl-M (kiralaxyl), bupirimate, clozylacon, dimethirimol, ethirimol, furalaxyl, hymexazole, metalaxyl, metalaxyl-M (mefenoxam), ofurace, oxadixyl, oxolinic acid.
  • Signal transduction inhibitors such as, for example, chlozolinate, fenpiclonil, fludioxonil, iprodione, procymidone, quinoxyfen and vinclozolin.
  • Fl4 decouplers such as binapacryl, dinocap, ferimzone, fluazinam and meptyldinocap.
  • the above-mentioned active ingredients can form salts.
  • the active substances mentioned here with their "common name” are known and described, for example, in the Pesticide Handbook ("The Pesticide Manual” 14th Ed., British Crop Protection Council 2006) or searchable on the Internet (eg http://www.alanwood.net/pesticides ).
  • plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
  • Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant breeders' rights.
  • Plant parts are to be understood as meaning all aboveground and underground parts and organs of the plants, such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, as well as roots, tubers and rhizomes.
  • the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
  • the treatment according to the invention of the plants and plant parts with the composition according to the invention is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, for example by dipping, spraying, evaporating, atomizing, spreading, spreading, injecting and propagating material, in particular in the case of seed , further by single or multi-layer wrapping.
  • the composition according to the invention is suitable for the treatment of seed. Preference is given to mention the combinations according to the invention mentioned above as being preferred or particularly preferred.
  • the present invention therefore more particularly relates to a method of protecting seed and germinating plants from the infestation of plant pests by treating the seed with the composition of the invention.
  • the invention also relates to the use of the composition according to the invention for controlling plant pests, in which the composition is applied to seeds of conventional or transgenic plants.
  • the invention relates to seed which has been treated with the composition according to the invention for protection against plant pests.
  • plant pests are insects, arachnids, helminths, nematodes and molluscs found in agriculture, horticulture, forests, gardens and recreational facilities.
  • the compositions according to the invention are active against normally sensitive and resistant species as well as against all or individual stages of development. Plant pests include:
  • Pests from the strain Arthropoda, especially from the class Arachnida eg Acarus spp., Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa , Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssius, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp., Eriophyes spp., Halotydeus destructor, Hemitarsonemus spp.
  • Hyalomma spp. Ixodes spp., Latrodectus spp., Loxosceles spp., Metatetranychus spp., Nuphersa spp., Oligonychus spp., Ornithodorus spp., Ornithonyssus spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp.
  • Rhipicephalus spp. Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Stenotarsonemus spp., Tarsonemus spp., Tetranychus spp., Vaejovis spp., Vasates lycopersici.
  • Anoplura e.g. Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Ptirus pubis, Trichodectes spp.
  • Attagenus spp. Bruchidius obtectus, Bruchus spp., Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp., Chaetocnema spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Ctenicera spp., Curculio spp., Cryptorhynchus lapathi , Cylindrocopturus spp., Dermestes spp., Diabotica spp., Dichocrocis spp., Diloboderus spp., Epilachna spp., Epitrix spp., Faustinus spp., Gibbium psylloides, Hellula and alis, Heteronychus arator, Heteronyx spp., Hylamorpha elegans , Hy
  • Cochliomyia spp. Contarinia spp., Cordylobia anthropophaga, Culex spp., Culicoides spp., Culiseta spp., Cuterebra spp., Dacus oleae, Dasyneura spp., Delia spp., Dermatobia hominis, Drosophila spp., Echinocnemus spp., Fannia spp., Gasterophilus spp., Glossina spp., Haematopota spp., Hydrellia spp., Hylemyia spp., Hyppobosca spp., Hypoderma spp., Liriomyza spp.
  • Lucilla spp. Lutzomia spp., Mansonia spp., Musca spp., Nezara spp., Oestrus spp., Oscinella frit, Pegomyia spp., Phlebotomus spp., Phorbia spp., Phormia spp., Prodiplosis spp. Psila rosae, Rhagoletis spp., Sarcophaga spp., Simulium spp, Stomoxys spp., Tabanus spp., Tannia spp., Tetanops spp., Tipula spp.
  • Eusystus spp. Eurygaster spp., Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Monalonion atratum, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp.
  • Psallus spp. Pseudacysta persea, Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.
  • Dysaphis spp. Dysmicoccus spp., Empoasca spp., Eriosoma spp., Erythroneura spp., Euscelis bilobatus, Ferrisia spp., Geococcus coffeae, Hieroglyphus spp., Homalodisca coagulata, Hyalopterus arundinis, Icerya spp., Idiocerus sp p., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lepidosaphes spp., Lipaphis erysimi, Macrosiphum spp., Mahanarva spp., Melanaphis sacchari, Metcalfiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp.
  • Hymenoptera From the order of Hymenoptera, for example, Acromyrmex spp., Athalia spp., Atta spp., Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Solenopsis invicta, Tapinoma spp., Vespa spp.
  • Orthoptera for example, Acheta domesticus, Blatta orientalis, Blattella germanica, Dichroplus spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta spp., Pulex irritans, Schistocerca gregaria, Supella longipalpa.
  • Siphonaptera eg Ceratophyllus spp.
  • Ctenocephalides spp. Tunga penetrans
  • Xenopsylla cheopis From the order of Symphyla eg Scutigerella spp ..
  • Pests from the strain Mollusca, especially from the bivalve class, e.g. Dreissena spp.
  • Gastropoda e.g. Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp. Plant pests from the strain: Nematoda, i.
  • plant parasitic nematodes in particular Aphelenchoides spp., Bursaphelenchus spp., Ditylenchus spp., Globodera spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Trichodorus spp., Tylenchus semipenetrans, Xiphinema spp ..
  • Subphylum Protozoa Furthermore, protozoa, such as Eimeria, can be controlled.
  • One of the advantages of the present invention is that, because of the particular systemic properties of the composition of the invention, treatment of the seed with this composition protects not only the seed itself but also the resulting plants after emergence from pests. In this way, the immediate treatment of the culture at the time of sowing or shortly afterwards can be omitted.
  • a further advantage consists in the synergistic increase of the insecticidal activity of the composition according to the invention over the insecticidal single active substance, which goes beyond the expected effectiveness of the two individually applied active substances. This allows optimization of the amount of active ingredients used.
  • composition according to the invention can also be used on transgenic plants or on transgenic seed, whereby the plants resulting from this seed are capable of expressing a protein directed against pests.
  • certain pests can already be controlled by the expression of the insecticidal protein, for example, and additionally protected from damage by the agents according to the invention.
  • the composition of the invention is suitable for the protection of seed of any plant variety as mentioned above, which is used in agriculture, in the greenhouse, in forests or in horticulture.
  • compositions according to the invention are likewise suitable for the treatment of the seed of fruit plants and vegetables as already mentioned above. Of particular importance is the treatment of the seeds of maize, soya, cotton, wheat and canola or rapeseed.
  • Transgenic plants or seeds of transgenic plants generally contain at least one heterologous gene which controls the expression of a polypeptide having in particular insecticidal properties.
  • the heterologous genes in transgenic plants or in the seeds of transgenic plants can originate from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium.
  • the present invention is particularly useful for the treatment of transgenic plants or seeds containing at least one heterologous gene derived from Bacillus sp. and whose gene product shows activity against corn borer and / or corn rootworm. Most preferably, this is a heterologous gene derived from Bacillus thuringiensis.
  • the composition according to the invention is applied alone or in a suitable formulation to the seed of transgenic or conventional plants.
  • the seed is treated in a condition that is so stable that no damage occurs during the treatment.
  • the treatment of the seed can be done at any time between harvesting and sowing.
  • seed is used which has been separated from the plant and freed from flasks, shells, stems, hull, wool or pulp.
  • plants and their parts can be treated.
  • wild species or plant species obtained by conventional biological breeding methods such as crossing or protoplast fusion
  • plant varieties and their parts are treated (conventional plants).
  • transgenic plants and plant cultivars which may be obtained by genetic engineering, optionally in Combination with conventional methods were obtained (Genetically Modified Organisms) and their parts treated.
  • Plant varieties are understood as meaning plants having new traits which have been bred by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be varieties, biotypes and genotypes.
  • the preferred plants or plant varieties to be treated according to the invention to be treated include all plants which, as a result of the genetic engineering modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits").
  • traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to bottoms salt, increased flowering, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products , higher shelf life and / or workability of the harvested products.
  • Further and particularly emphasized examples of such properties are an increased defense of the plants against animal and microbial pests, as against insects, mites, phytopathogenic fungi, bacteria and / or viruses as well as an increased tolerance of the plants against certain herbicidal active substances.
  • transgenic plants are the important crops such as cereals (wheat, rice), corn, soybeans, potatoes, sugar beets, tomatoes, peas and other vegetables, cotton, tobacco, oilseed rape and fruit plants (with the fruits apples, pears, citrus fruits and Grapes), with special emphasis on maize, soya, potato, cotton, tobacco and oilseed rape.
  • Traits which are particularly emphasized are the increased defense of the plants against insects, arachnids, nematodes and snails by toxins produced in the plants, in particular those produced by the genetic material from Bacillus thuringiensis (eg by the genes CrylA (a) , CrylA (b), CrylA (c), CryllA, CrylllA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF and combinations thereof) in the plants (hereinafter "Bt plants”). Traits also highlight the increased resistance of plants to fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins.
  • SAR systemic acquired resistance
  • trastraits can also occur in combinations with one another in the transgenic plants.
  • Bt plants are maize varieties, cotton varieties, soya bean varieties and potato varieties which are sold under the trade names YIELD GARD ® (for example maize, cotton, soya beans), KnockOut ® (for example maize), StarLink ® (for example maize), Bollgard ® ( Cotton), Nucotn ® (cotton) and NewLeaf ® (potato).
  • herbicide-tolerant plants are maize varieties, cotton varieties and soybean varieties may be mentioned, under the trade names Roundup Ready ® (tolerance to glyphosate, for example maize, cotton, soya bean), Liberty Link ® (tolerance to phosphinotricin, for example oilseed rape), IMI ® (tolerance against imidazolinone) and STS® (tolerance to sulfonylureas eg corn).
  • Roundup Ready ® tolerance to glyphosate, for example maize, cotton, soya bean
  • Liberty Link ® tolerance to phosphinotricin, for example oilseed rape
  • IMI ® tolerance against imidazolinone
  • STS® tolerance to sulfonylureas eg corn
  • Clearfield ® varieties eg corn
  • treatment with the composition according to the invention may also result in superadditive ("synergistic") effects.
  • superadditive for example, reduced application rates and / or extensions of the spectrum of action and / or an increase in the effect of the substances and agents usable in the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering power facilitated harvest, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or machinability of the harvested products, which exceed the actual expected effects.
  • Example 1 foliar application Mvzus persicae / paprika
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • emulsifier-containing water 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • ammonium salts ammonium salts
  • Penetrations bankern rapeseed oil methyl ester 500 EW
  • Paprika plants (Capsicum annuum), which are heavily attacked by the green peach aphid ⁇ Myzus persicae), are treated by spraying with the preparation of active compound in the desired concentration. After 6 days the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • emulsifier-containing water 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • ammonium salts and penetration enhancers these are each added to the spray mixture in a concentration of 1000 ppm.
  • Cotton plants which are heavily affected by the cotton aphid ⁇ Aphis gossypii), are treated by spraying with the preparation of active compound in the desired concentration. After 6 days the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
  • Emulsifier 0.5 part by weight of alkylaryl polyglycol ether To prepare a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Cotton leaf discs (Gossypium hirsutum) infested with larvae of the white fly (Bemisia tabaci) are sprayed with an active compound preparation of the desired concentration. After 7 days, the effect is determined in%. 100% means that all white flies have been killed; 0% means that no white fly has been killed.

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

L'invention concerne au moins une carbonylamidine cyclique de la formule (I) dans laquelle Y, G, Z, Q, R1 et R2, sont tels que définis dans la description, et au moins un agent potentialisant sélectionné parmi des excipients et des sels d'ammonium ou de phosphonium de la formule (II) dans laquelle D, n, R8, R9, R10, R11 et R12 sont tels que définis dans la description.
EP11727191.6A 2010-06-29 2011-06-24 Compositions insecticides améliorées contenant une carbonylamidine cyclique Withdrawn EP2587922A1 (fr)

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PCT/EP2011/060629 WO2012000902A1 (fr) 2010-06-29 2011-06-24 Compositions insecticides améliorées contenant une carbonylamidine cyclique

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KR20130039331A (ko) 2013-04-19
WO2012000902A1 (fr) 2012-01-05
CN103079407A (zh) 2013-05-01
US20120004268A1 (en) 2012-01-05
JP2013529660A (ja) 2013-07-22
MX2013000193A (es) 2013-01-28
BR112012033694A2 (pt) 2015-09-15

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