EP2707373A1 - (thio)carbonylamidines bicycliques - Google Patents

(thio)carbonylamidines bicycliques

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Publication number
EP2707373A1
EP2707373A1 EP12719008.0A EP12719008A EP2707373A1 EP 2707373 A1 EP2707373 A1 EP 2707373A1 EP 12719008 A EP12719008 A EP 12719008A EP 2707373 A1 EP2707373 A1 EP 2707373A1
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EP
European Patent Office
Prior art keywords
spp
pyrid
alkyl
methyl
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.)
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Application number
EP12719008.0A
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German (de)
English (en)
Inventor
Peter Jeschke
Michael Schindler
Katharina WÖLFEL
Ulrich Ebbinghaus-Kintscher
Arnd Voerste
Olga Malsam
Peter Lösel
Ulrich Görgens
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Bayer Intellectual Property GmbH
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Bayer Intellectual Property GmbH
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Priority to EP12719008.0A priority Critical patent/EP2707373A1/fr
Publication of EP2707373A1 publication Critical patent/EP2707373A1/fr
Withdrawn legal-status Critical Current

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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
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems

Definitions

  • the invention relates to novel compounds, their preparation, and their use for controlling plant pests and pests which occur in the field of veterinary medicine.
  • Z is O or CH 2 ;
  • A is in each case optionally substituted aryl, hetaryl or heterocyclyl, in particular for thiazolyl or pyridyl, which in each case are optionally substituted by halogen (in particular chlorine) or C 1 -C 3 -alkyl (in particular methyl); and R ! , R 2 , R 3 and R 4 independently of one another are hydrogen or C 1 -C 3 -alkyl.
  • bicyclic enamino (thio) carbonyl compounds which are said to have a insecticidal activity are generally described in WO 2007/1 15647 A1.
  • I WO 2007/1 15647 Al compounds are described in detail in which the carbon atoms of the fused to the furanone 5-, 6- or 7-membered ring are only partially unsaturated. The document does not disclose compounds in which condensed rings are completely unsaturated.
  • the object of the present invention is therefore to provide compounds which have a biological activity, preferably insecticidal activity.
  • the He indians have found new bicyclic (thio) carbonylamidine, which have good biological activity and are otherwise beneficial.
  • Q is oxygen or sulfur; preferably Q is oxygen;
  • B is oxygen, sulfur, methylene, difluoromethylene, or optionally substituted nitrogen; preferably B is oxygen or methylene;
  • Y is a radical selected from a group consisting of hydrogen, cyano, halogen (eg., Fluorine, chlorine, bromine or iodine), Ci-Ce-alkoxy, Ci-Ce-Haliogenalkoxy, Ci-Ce-alkylthio , C 1 -C 6 -haloalkylthio, C 1 -C 6 -alkylsulfmyl, C 1 -C 6 -haloalkylsulfinyl, C 1 -C 6 -alkylsulfonyl and C 1 -C 6 -haloalkylsulfonyl, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl , C 1 -C 6 -haloalkenyl, C 1 -C 6 -alkynyl, C 2 -C 6 -haloalkynyl, nitro
  • R 1 is hydrogen or C 1 -C 6 -alkyl; preferably R 1 is hydrogen;
  • A is a hetaryl radical which is selected from a group consisting of pyrrolyl, pyrazolyl, imidazolyl, 1, 2,3-triazolyl, 1, 2,4-triazolyl, tetrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1, 2, 3-oxadiazolyl, 1, 2,4-oxadiazolyl, 1, 2,5-oxadiazolyl, 1, 3,4-oxadiazolyl, 1, 2,3-thiadiazolyl, 1, 2,4-thiadiazolyl, 1,2,5- Thiadiazolyl, 1, 3,4-thiadiazolyl, 1, 2,5-thiadiazolyl, Pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, wherein each of these Hetarylreste may be substituted with at least one substituent X, which is selected from a group consisting of fluorine, chlorine, bromine
  • A preferably represents thiazol-5-yl which is in the 2-position with fluorine, chlorine, bromine, iodine.
  • Ci-C 4 -alkyl or C 1 -C 4 -haloalkyl is substituted for isoxazol-5-yl in the 3-position with fluorine, chlorine, bromine, iodine, Ci-C 4 alkyl, C 1 -C 4 - Haloalkyl, ci
  • Fluorine, chlorine, bromine, iodine or Ci-C4 alkyl is substituted or is pyrid-3-vl in the 5-position by fluorine, chlorine, bromine, iodine, Ci-C 4 -Alkyi, Ci-C 4 haloalkyl, Ci-C 4 haloalkoxy, azido or cyano substituted and is substituted in the 6-position with fluorine, chlorine, bromine, iodine, Ci-C 4 alkyl, or C 1 -C 4 - haloalkyl; most preferably A is 6-chloro-pyrid-3-yl, 6-trifluoromethyl-pyrid-3-yl, 6-fluoro-pyrid-3-yl, 6-bromo-pyrid-3-yl, 1,2,5 Thiadiazol-3-yl, 5-
  • the double bonds may also be conjugated, forming an aromatic system.
  • the invention furthermore relates to bicyclic (thio) carbonylamidines having one of the formulas (I-a) to (Iq) in which R 1 , A, Y, B and (I) have the meanings given in this application:
  • Preferred according to the invention are bicyclic (thio) carbonylamidines of the formulas (I-a), (I-b), (I-c), (I-d) or (I-e) in which
  • R 1 is hydrogen or C 1 -C 6 -alkyl; R 1 is preferably hydrogen;
  • A is a hetaryl radical which is selected from a group consisting of pyrrolyl, pyrazolyl, imidazolyl, 1, 2,3-triazolyl, 1, 2,4-triazolyl, tetrazoiyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1, 2, 3-oxadiazolyl, 1, 2,4-oxadiazolyl, 1, 2,5-oxadiazolyl, 1, 3,4-oxadiazolyl, 1, 2,3-thiadiazolyl, 1, 2,4-thiadiazolyl, 1, 2,5- Thiadiazolyl, 1, 3, 4-thiadiazolyl, 1, 2,5-thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, wherein each of these hetaryl radicals may be substituted with at least one substituent X selected from a group consisting of fluorine, chlorine ,
  • Ci-C 4 alkyl or Ci-C 4 haloalkyl is substituted, pyrid-3-yl which is substituted in 6-position by fluorine, chlorine, bromine, iodine, Ci-C4-alkyl or C1-C4 haloalkyl, pyrimidine -5-yl in the 2-position with fluorine, chlorine, bromine.
  • Y is a radical which is selected from a group consisting of hydrogen, cyano, halogen (ie fluorine, chlorine, bromine or iodine), C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 6 haloalkylthio, Ci-C 6 -Alkylsulfmyl, Ci-Ce-haloalkylsulfinyl, Ci-C 6 - alkylsulfonyl, and Ci-Ce-haloalkylsulfonyl, Ci-Ce-alkyl, Ci-Ce-haloalkyl, C 2 -C 6 alkenyl,
  • Q is oxygen or sulfur; Q is preferably oxygen;
  • B is oxygen, sulfur, methylene, difluoromethylene, or optionally substituted nitrogen; B is preferably oxygen or methylene.
  • bicyclic (thio) carbonylamidines of the formulas (I-f) or (1-1) in which
  • R 1 is hydrogen or C 1 -C 6 alkyl; R 1 is preferably hydrogen;
  • A is a hetaryl radical which is selected from a group consisting of pyrrolyl, pyrazolyl, imidazolyl, 1, 2,3-triazolyl, 1, 2,4-triazolyl, tetrazolyl, oxazoiyl, isoxazolyl, thiazoiyl, isothiazolyl, 1, 2, 3-oxadiazolyl, 1, 2,4-oxadiazolyl, 1, 2,5-oxadiazolyl, 1, 3,4-oxadiazolyl, 1, 2,3-thiadiazolyl, 1, 2,4-thiadiazolyl, 1, 2,5- Thiadiazolyl, 1, 3,4-thiadiazolyl, 1, 2,5-thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, wherein each of these hetaryl radicals may be substituted with at least one substituent X selected from a group consisting of fluorine, chlorine
  • A is furthermore particularly preferably selected from a group consisting of 6-chloropyrid-3-yl, 6-trifluoromethylpyrid-3-yl, 6-fluoropyrid-3-yl. 6-Bromo-pyrid-3-yl, 1,2,5-thiadiazol-3-yl, 5-methylpyrazine-2-yl, 2-chloro-1,3-thiazol-5-yl, 2-methyl 1, 3-thiazol-5-yl, 2-methoxy-1,3-thiazole
  • 6-chloro-pyrid-3-yl, 5-difluoromethyl-6-bromo-pyrid-3-yl and 5-difluoromethyl-6-iodo-pyrid-3-yl; is a radical which is selected from a group consisting of hydrogen, cyano, halogen (ie fluorine, chlorine, bromine or iodine), Ci-Ce-alkoxy, Ci-Ce-haloalkoxy, Ci-Ce- alkylthio, C i- Ce-haloalkylthio, Ci-Ce-alkylsulfinyl, Ci-Ce-haloalkylsulfinyl, Ci-C 6 - alkylsulfonyl and Ci-Ce-haloalkylsulfonyl, Ci-Ce-alkyl, C 1 -Ce-haloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 haloalkeny
  • bicyclic (thio) carbonylamidines of the formulas (Ig), (Ih), (Ii), (Ij), (Ik), (Im), (In), (Io), (Ip) or (Iq) in which
  • R ' is hydrogen or C 1 -C 6 alkyl;
  • R ! is preferably hydrogen;
  • A is a hetaryl radical selected from a group consisting of pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1, 2,4-triazolyl, tetrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3 -Oxadiazolyl, 1, 2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1, 3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1, 2,4-thiadiazolyl, 1, 2,5-thiadiazolyl , 1, 3,4-thiadiazolyl, 1, 2,5-thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, wherein each of these hetaryl radicals may be substituted by at least one substituent X selected from a group consisting of fluorine, chlorine, Bro
  • Iodine, C 1 -C 4 - alkyl, Ci-C 4 haloalkyl, (YCYHalogenalkoxy, azido or cyano is substituted, and in the 6-position by fluorine, chlorine, bromine, iodine, Ci-C4-alkyl, or C 1 -C 4 A is furthermore particularly preferably selected from a group consisting of 6-chloropyrid-3-yl, 6-trifluoromethylpyrid-3-yl, 6-fluoropyrid-3-yl, 6-bromo pyrid-3-yl, 1,2,5-thiadiazol-3-yl, 5-methylpyrazine-2-yl, 2-chloro-1, 3-thiazol-5-yl, 2-methyl-1, 3 thiazol-5-yl, 2-methoxy-l, 3-thiazol-5-yl, 2-bromo-1,3-thiazol-5-yl, 3-trifluoromethyl-1,3-thiazol-5-yl, 3
  • Y is a radical selected from a group consisting of hydrogen, cyano, halogen (ie fluoro, chloro, bromo or iodo), Ci-Ce-alkoxy, Ci-Ce-haloalkoxy, Ci-Ce- alkylthio, C iC 6 haloalkylthio, Ci-C 6 -Alkylsulfmyl, Ci-C 6 haloalkylsulfinyl, Ci-C 6 - alkylsulphonyl and C i -Ce-haloalkylsulfonyl, Ci-Ce-alkyl, C i -Ce-haloalkyl, C 2 -C6- Alkenyl, C2-Ce-haloalkenyl, C2-Ce-alkynyl, C2-Ce-haloalkynyl, nitro, amino, Ci-Ce-alkylamino, di (Ci-Ce-alkyl
  • bicyclic (thio) carbonylamidines of the following formula (I-g-i),
  • Y is a radical selected from a group consisting of hydrogen, cyano, halogen (ie fluoro, chloro, bromo or iodo), C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C i -ce-haloalkylthio, Ci-Ce-Alkylsulfinyi, Ci-Ce-Halogenalkylsulfmyl, Ci-C 6 - alkylsulfonyl, and Ci -Ce-haloalkylsulfonyl, Ci-Ce-alkyl, C 1 -Ce-haloalkyl, C 2 -C 6 alkenyl, C 2 -C -haloalkenyl, C 2 -C 6 -alkynyl, C 2 -C 6 -haloalkynyl, nitro, amino, C 1 -C 6 -alkyla
  • A is heteraryl selected from a group consisting of 6-chloro-pyrid-3-yl, 6-trifluoromethyl-pyrid-3-yl, 6-fluoro-pyrid-3-yl, 6-bromo-pyrid-3-yl , 1,2,5-thiadiazol-3-yl, 5- Methyl-pyrazin-2-yl, 2-chloro, 3-thiazol-5-yl, 2-bromo-1,3-thiazol-5-yl, 2-methyl-1,3-thiazol-5-yl , 2-Methoxy-l, 3-thiazol-5-yl, 2-trifluoromethyl-1,3-thiazol-5-yl, 2-methyl et hy 1 - o ⁇ a /.
  • the bicyclic (thio) carbonylamidines according to the invention can be present as geometric and / or as optically active isomers or as starting compounds
  • stereoisomers are present in different compositions. These stereoisomers are, for example, enantiomers, diastereomers, atropisomers or geometric isomers.
  • the invention thus comprises pure stereoisomers as well as any mixtures of these isomers.
  • bicyclic (thio) carbonylamidines of the present invention may optionally be present in various poly-morphic forms or as a mixture of different polymorphic forms. Both the pure polymorphs and the polymorph mixtures are the subject of the invention and can be used according to the invention.
  • the bicyclic (thio) carbonylamidines of the formula (I) according to the invention can be prepared by customary methods known to those skilled in the art.
  • One possible production method is in
  • the invention also relates to a process for the preparation of bicyclic (thio) carbonylamidines of the formula (I) in which R.sup.1, Y.sup., (I ) and B have the abovementioned meanings, in particular those in connection with compounds of the substructure ( Ia), (Ib), (Ic), (Id) or (I- e), which comprises the reaction of a compound of the formula (IIa) and / or (IIb) (generally as a compound of the formula (II) designated),
  • R 1 , and A represents the compounds of the formula (I), (Ia), (Ib), (Ic), (Id) and (Ie), (If), (Ig), (Ih), (Ii) , (Ij), (Ik), (1-1), (Im), (In), (Io), (Ip), and (Iq) have meanings mentioned, and
  • LG is an optionally generated in-situ nucleofugic leaving group, in particular halogen, (chlorine, bromine, iodine), OTosyl, OMesyl, N-morpholino. in the presence of a diluent and optionally in the presence of a basic reaction auxiliary.
  • Suitable diluents (solvents) for carrying out the process according to the invention are all inert organic solvents.
  • Particularly suitable diluents according to the invention are, for example, homeopathic hydrocarbons, but especially chlorohydrocarbons, such as tetraethylene, tetrachloroethane, dichloropropane, methylene chloride, dichlorobutane, chloroform, carbon tetrachloride, trichloroethane, trichlorethylene , Pentachloroethane, difluorobenzene, 1, 2-dichloro ethane, chlorobenzene, bromobenzene, dichlorobenzene, chlorotoluene, trichlorobenzene; Alcohols such as methanol, ethanol, isopropanol, butanol; Ethers such as ethyl propyl ether, methyl tert-butyl ether, n-Butylet ago.
  • chlorohydrocarbons such as tetraethylene, tetrachloroethane, dichlor
  • Tributylamine N-methylmorpholine, pyridine and tetramethylenediamine; Nitrohydrocarbons such as nitromethane, nitro ethane, nitropropane, nitrobenzene, chloronitrobenzene, o-nitrotoluene; Nitriles such as acetonitrile, propionitrile, butyronitrile, isobutyronitrile, benzonitrile, m-chlorobenzonitrile and compounds such as tetrahydrothiophene dioxide and dimethyl sulfoxide, tetramethylene sulfoxide, dipropyl sulfoxide, benzylmethylsulfoxide, diisobutylsulfoxide, dibutylsulfoxide, diisoamylsulfoxide; Suifone such as dimethyl, diethyl, dipropyl, dibutyl, biphenyl.
  • Nitrohydrocarbons such as nitromethane, nitro
  • white spirits with components having boiling points in the range, for example, from 40 ° C. to 250 ° C., cymene, benzene fractions within a boiling interval from 70 ° C.
  • Preferred diluents for carrying out the process according to the invention are amides, formamide, N-methylformamide, NiV-dimethylformamide, IV, N-dipropylformamide, N, N-dibutylformamide, N-methylpyrrolidine, in particular N, N dimethyl formamide. Diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
  • Suitable acid binders are, for example, halides, hydroxides, hydrides, oxides and carbonates of lithium, sodium, potassium, magnesium, calcium and barium, in particular carbonates and halides of alkali metals, especially of sodium, potassium or cesium, or basic compounds such as Amidine bases or guanidine bases such as 7-methyl-l, 5,7-triaza-bicyclo (4.4.0) dec-5-ene (MTBD); Diazabicyclo (4.3.0) nonene (DBN), diazabicyclo (2.2.2) octane (DABCO), 1,8-diazabicyclo- (5.4.0) undecene (DBU), cyclohexyltetrabutyl-guanidine (CyTBG), Cy clob exyltetramethylguanidine (CyTMG), ⁇ , ⁇ , ⁇ , ⁇ -tetramethyl-1, 8-naphthalenediamine, pentamethylpiperidine, or tertiary
  • Preferred according to the invention are sodium carbonate, potassium carbonate, cesium carbonate, sodium halide (eg NaCl, NaF, Nal.NaBr), potassium baiogenide (KCl, KF, K l. KBr), cesium halide (CsCl, CsF, CsI, CsBr) and mixtures thereof. Particularly preferred is a mixture of cesium carbonate and cesium iodide.
  • sodium halide eg NaCl, NaF, Nal.NaBr
  • potassium baiogenide KCl, KF, K l. KBr
  • cesium halide CsCl, CsF, CsI, CsBr
  • Particularly preferred is a mixture of cesium carbonate and cesium iodide.
  • the reaction time is generally 10 minutes to 72 hours.
  • the implementation takes place at
  • It can be worked under normal pressure in principle. Preferably, one works at atmospheric pressure or at elevated pressure z. From about 2 to 15 bar and optionally under a protective gas atmosphere (eg nitrogen, helium or argon).
  • a protective gas atmosphere eg nitrogen, helium or argon.
  • the entire reaction mixture is concentrated, i. the solvent is removed (by distillation) and the reaction mixture is worked up in a customary manner (for example, aqueous).
  • the products obtained after working up can be purified in a customary manner by recrystallization, vacuum distillation or column chromatography (see also the Preparation Examples).
  • alkyl either alone or in combination with other B egri ffen, eig eispis example, haloalkyl, alkylthio, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, alkylamino, alkylcarbonylamino, alkylcarbonyl, or as a prefix "Alk” in combination with other terms such as, for example, alkoxy, haloalkoxy, alkoxycarbonyl, alkoxycarbonylamino, in the context of the present invention means a radical of a saturated, aliphatic hydrocarbon group with the corresponding number of carbon atoms, which may be branched or unbranched.
  • Ce-alkyl radicals are methyl, ethyl, n-propyl], isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-butyl Pentyl, isopentyl, neopentyl, tert-pentyl, 1-methylbutyl, 2-methylbutyl, 1-ethylpropyl, 1, 2-
  • Halogen is fluorine, chlorine, bromine or iodine.
  • halo-substituted radicals for example haloalkyl, are understood as meaning radicals which are mono- or polysubstituted to the maximum possible number of substituents.
  • the halogen atoms may be the same or different.
  • Halogen is fluorine, chlorine, bromine or iodine
  • examples of halogen-substituted radicals are chloromethyl, bromomethoxy, dichloromethylthio, trichloromethyl, fluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, trifluoromethyl, 2,2-difluoroethyl, difluoromethyl, trifluoromethoxy, difluoromethoxy.
  • C 1 -C 4 fluoroalkyl examples include CF 3 , CHF 2 , CH 2 F, CF 3 CF 2 , CH 2 CF 3 , CH 2 CHF 2 , CH 2 CH 2 F, CHFCF 3 , CHFCHF 2 , CHFCH 2 F, CHFCF 3 , CF 2 CF 3 , CF 2 CHF 2 , CF 2 CH 2 F, and CF 2 CF 3 .
  • heteroaryl refers to aromatic ring systems containing at least one heteroatom, such as e.g. Nitrogen, oxygen, or sulfur.
  • heteroaryls include pyrrole, pyrazole, imdida / o !. Triazole, tetrazole, oxazole, isoxazole, thiazole, isothiazole, oxadiazole, thiadiazole, pyridine, pyrimidine, pyridazine, and pyrazine ,.
  • the heteraryls may be substituted with suitable substituents.
  • Optionally substituted radicals may be monosubstituted or polysubstituted, wherein in a multiple substitution the substituents may be the same or different.
  • the compounds of the invention are suitable with good plant tolerance, favorable toxicity to warm-blooded animals and good environmental compatibility for the protection of plants and plant organs, to increase crop yields, improve the quality of the crop and to control animal pests, especially insects, arachnids, helminths, nematodes and mollusks, the in agriculture, horticulture, livestock, forests, gardens and recreational facilities, in the protection of materials and materials and in the hygiene sector. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
  • the above-mentioned pests include: pests from the strain: Arthropoda, especially from the genus Arachnida eg Acarus spp., Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Amphitetranychus viennensis, Argas Spp., Boophuus spp., Brevipalpus spp., Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssius, Dermal opliagoidces farinae, Dermacentor spp., Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp., Eriophyes spp , Halotydeus destructor, Hemitarsonemus spp.,
  • Anoplura e.g. Damalinia spp. Haematopinus spp. Linognathus spp., Pediculus spp., Ptirus pubis, Trichodectes spp.
  • Chironomus spp. Chironomus spp., Chrysomyia spp., Chrysops spp., Cochliomyia spp., Contarinia spp., Cordylobia anthropophaga, Culex spp. Culicoides spp., Culiseta spp., Cuterebra spp. Dacus oleae, Dasyneura spp. De!
  • ia spp. Dermaiobia 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., Phomia spp., Prodiplosis spp., Psila rosae , Rhagoletis spp., Sarcophaga spp., Simulium spp, Stomoxys spp., Tabanus spp., Tannia spp., Tetanops spp., Tipula spp.
  • Pentomidae Piesma quadrata, Piezodorus spp., Psallus spp., Pseudacysta persea, Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp ..
  • Mahanarva spp. Melanaphis sacchari, Metcalfiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., Nasonovia ribisnigri, Nephotettix spp., Niiaparvata lugens, Oncometo pia spp., Orthezia praelonga, Parabemisia myricae, Paratrioza spp., Parlatoria spp., Pemphigus spp., Peregrinus maidis, Phenacoccus spp.
  • Sogatella furcifera Sogatodes spp., Stictocephala festina, Tenalaphara malayensis, Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., Trialeurodes spp., Trioza spp., Typhlocyba spp., Unaspis spp., Viteus vitifolii, Zygina spp.
  • I lymenoptera From the order of the I lymenoptera, for example, Acromyrmex spp., Athalia spp., Atta spp., Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Solenopsis invicta, Tapinoma spp., Vespa spp.
  • Lepidoptera e.g. Acronicta major, Adoxophyes spp., Aedia leucomelas, Agrotis spp., Alabama spp., Amyelois transite IIa, Anarsia spp., Anticarsia spp., Argyroploce spp., Barathra brassicae, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp.
  • Cacoecia spp. Caloptilia theivora, Capua reticulana, Carpocapsa pomonella, Carposina niponensis, Cheimatobia brumata, Chilo spp., Choristoneura spp., Clysia ambiguella, Cnaphalocerus spp., Cnephasia spp. Conopomorpha spp., Conotrachelus spp., Copitarsia spp. Cydia spp., Dalaca noctuides, Diaphania spp., Diatraea saccharalis, Earias spp.
  • Mythimna separata Nymphula spp., Oiketicus spp., Oria spp., Orthaga spp., Ostrinia spp., Oulema oryzae, Panolis flammea, Parnara spp .. Pectinophora spp., Perileucoptera spp. Phthorimaea spp. Phyllocnistis citrella, Phyllonorycter Spp., Pieris spp.
  • Platynota stultana, Plodia interpunctella, Plusia spp., Plutella xylostella, Prays spp., Prodenia spp., Protoparce spp., Pseudaletia spp., Pseudoplusia includens, Pyrausta nubilalis, Rachiplusia nu, Schoenobius spp., Scirpophaga Spp., Ontario segetum, Sesamia spp., Sparganothis spp., Spodoptera spp., Stathmopoda spp., Stomopteryx subsecivella, Synanthedon spp., Tecia solanivora, Thermesia gemmatalis, Tinea pellionella, Tineola bisselliella, Tortrix spp., Trichophaga tapetzel la, Trichoplusia spp .. Tuta absoluta,
  • Zygentoma for example, Lepisma saccharina, Thermobia domestica. e.g. Lepisma saccharina, Thermobia domestica.
  • Pests from the strain Mollusca, especially from the bivalve class, e.g. Dreissena spp.
  • Cooperia spp. Dicrocoelium spp, Dictyocaulus filaria, Diphyllobothrium latum , Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosome spp, Strongyloides fuelleborni, Strongyloides stercoralis, Stronyloides spp.
  • Taenia saginata Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti.
  • Plant pests from the strain Nematoda, i. plant parasitic nematodes, especially Aphelenchoides spp., Bursaphelenchus spp., Ditylenchus spp., Globodera spp. Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Trichodorus spp., Tylenchulus semipenetrans, Xiphinema spp. Subphylum: protozoa
  • protozoa such as Eimeria
  • Eimeria protozoa
  • the compounds according to the invention can also be used to protect the plant against biotic stress factors and / or abiotic stress or to increase plant growth.
  • the compounds of the invention can be used to increase the plant's defense forces (pathogen defense in plants).
  • the compounds according to the invention can be used in combination with other agrochemically active substances, including all known insecticides, fungicides, herbicides or safeners.
  • the compounds of the invention can also be used in combination with agents or compounds of signal technology, which, for example, a better colonization with symbionts, such as rhizobia. Mycorrhiza and / or endophytic bacteria, takes place and / or there is an optimized nitrogen fixation.
  • the treatment of the plants and plant parts with the conditions according to the invention is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, spraying, sprinkling, evaporating, atomizing, atomizing, sprinkling, foaming, spreading, spreading, injecting, pouring, drip irrigation and propagation material, in particular at Seeds, further by dry pickling, wet pickling, slurry pickling, encrusting, single or multi-layer wrapping, etc. It is also possible to apply the active ingredients by the ultra-low-volume method or to inject the active substance or the active ingredient itself into the soil ,
  • a preferred direct treatment of the plants is foliar application, i. at least one compound of the invention is applied to the foliage, wherein the treatment frequency and the application rate is adjusted to the infestation pressure of the respective pest.
  • the compound according to the invention reaches the plants via the root system.
  • the treatment of the plants is then carried out by the action of the compound according to the invention on the habitat of the plant. This can be, for example, by drenching, mixing into the soil or the nutrient solution.
  • the location of the plant eg soil or hydroponic systems
  • a liquid form of the compound of the invention or the soil in which the plant grows with egg solid form of the compound of the invention (eg in the form of granules) treated (eg of the granules in the location of the plant).
  • this can also be done by dosing the invention in a solid form (e.g., as granules) into a flooded paddy field
  • 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 that 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 by Plant variety rights protectable or non-protectable plant varieties.
  • Plant parts are understood to mean all aboveground and subterranean parts and organs of plants such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes.
  • the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
  • wild-type or plant species and plant varieties obtained by conventional biological breeding methods such as crossing or protoplast fusion and parts thereof are treated.
  • transgenic plants and plant cultivars obtained by genetic engineering, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
  • the term "parts” or “parts of plants” or “parts of plants” has been explained above.Propes of the respective commercially available or in use plant varieties are particularly preferably treated according to the invention.PV plants are understood as meaning plants with new properties ("traits”) have been bred either by conventional breeding, by mutagenesis or by recombinant DNA techniques. These may be varieties, breeds, biotypes and genotypes.
  • suitable formulations and application forms prepared therefrom as pesticides and / or pesticides are, for. B. Drench, Drip and spray liquors comprising at least one of the compounds of the invention.
  • the use forms contain other crop protection agents and / or pesticides and / or the effect of improving adjuvants such as penetration enhancers, eg.
  • vegetative oils such as rapeseed oil, sunflower oil, mineral oils such as paraffin oils, alkyl esters of vegetal fatty acids such as rapeseed oil or S oj aölmethylester or alkanol alkoxylates and / or spreading agents such as alkyl siloxanes and / or salts, e.g.
  • organic or inorganic ammonium or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate and / or retention (ordering agents such as dioctylsulfosuccinate or hydroxypropyl-guar polymers and / or humectants such as glycerol and / or fertilizers such as ammonium, Potassium- or phosphorus-containing fertilizers.
  • Typical formulations are, for example, water-soluble liquids (SL), emulsion concentrates
  • EC emulsions in water
  • SC suspension concentrates
  • SE FS
  • OD water dispersible Granules
  • WG granules
  • CS capsule concentrates
  • the formulations contain, in addition to one or more active compounds according to the invention, further agrochemical active substances.
  • auxiliaries such as extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, antifreeze agents, biocides, thickeners and / or further auxiliaries, for example adjuvants.
  • An adjuvant in this context is a component that enhances the biological effect of the formulation without the component itself having a biological effect.
  • Examples of adjuvants are agents that promote retention, spreading behavior, adherence to the leaf surface, or penetration.
  • formulations are prepared in a known manner, e.g. by mixing the active ingredients with excipients such as extenders, solvents and / or solid carriers and / or other excipients such as surfactants.
  • excipients such as extenders, solvents and / or solid carriers and / or other excipients such as surfactants.
  • the preparation of the formulations is carried out either in suitable systems or before or during use.
  • Excipients which can be used are those which are suitable for shaping the formulation of the active ingredient or the application forms prepared from these formulations (such as, for example, usable crop protection agents such as fuel or brewing or seed dressing), such as certain physical, technical and chemical properties / or to confer biological properties.
  • polar and non-polar organic chemical liquids e.g. from the classes of aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), alcohols and polyols (which may also be substituted, etherified and / or esterified), ketones (such as acetone, cyclohexanone), Esters (including fats and oils) and (poly) ethers, simple and substituted amines, amides, lactams (such as alkylpyrrolidones) and lactones, sulfones and sulfoxides (such as dimethylsulfoxide).
  • aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
  • alcohols and polyols which may also be substituted, etherified and / or esterified
  • ketones such as ace
  • organic solvents can be used as auxiliary solvents.
  • liquid solvents are essentially in question: aromatics such as xylene, toluene or Alkyln aphth al in e, chlorinated aromatic or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatis che hydrocarbons such as cyclohexane or paraffins, eg petroleum fractions, mineral and vegetable Oils, alcohols such as butanol or glycol, and their ethers and esters, ketones such as acetone, Methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strong polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
  • aromatics such as xylene, toluene or Alkyln aphth al in e
  • Suitable solvents are, for example, aromatic hydrocarbons such as e.g. Xylene, toluene or alkylnaphthalenes, chlorinated aromatic or aliphatic hydrocarbons such as. Chlorobenzene, chloroethylene, or methylene chloride, aliphatic hydrocarbons, e.g. Cyclohexane, paraffins, petroleum fractions, mineral and vegetable oils, alcohols such as e.g. Methanol, ethanol, iso-propanol, butanol or glycol and their ethers and esters, ketones such as e.g.
  • suitable carriers are: e.g. Ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock flour, such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and / or solid fertilizers. Mixtures of such carriers can also be used.
  • suitable carriers for granules are: e.g.
  • liquefied gaseous diluents or solvents can be used.
  • Examples of emulsifying and / or foaming agents, dispersants or wetting agents having ionic or non-ionic properties or mixtures of these surfactants are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives (preferably alkyl taurates), phosphoric acid esters of polyethoxylated alcohols or phenols.
  • Fatty acid esters of polyols and derivatives of the compounds containing sulphates, sulphonates and phosphates for example alkylarylpolyglycol ethers, alkylsulphonates, alkylsulphates, arylsulphonates, protein hydrolysates, lignin-sulphite liquors and methylcellulose.
  • a surfactant is advantageous when one of the active ingredients and or one of the inert carriers is not soluble in water and when applied in water.
  • auxiliaries can in the formulations and the applications derived therefrom dyes such as inorganic pigments, such as iron oxide, titanium oxide, and blue organic dyes such as alizarin, azo and Metallphthalocyaninfarbstoffe and nutrient and trace nutrients such as salts of iron, manganese, boron, copper. Cobalt, molybdenum and zinc.
  • Stabilizers such as cold stabilizers, preservatives, antioxidants, solvents, or other agents which improve the chemical and / or physical stability, may furthermore be present. It may also contain foam-forming agents or defoamers.
  • formulations and the use forms derived therefrom may also contain, as additional auxiliaries, adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-like polymers such as gum arabic.
  • adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-like polymers such as gum arabic.
  • Polyvinyl alcohol, polyvinyl acetate and natural phospholipids such as cephalins and lecithins and synthetic phospholipids.
  • Other auxiliaries may be mineral and vegetable oils.
  • auxiliaries may be contained in the formulations and in the formulations derived therefrom.
  • additives are, for example, fragrances, protective colloids, biodiesel.
  • the active ingredients can be combined with any solid or liquid additive commonly used for formulation purposes.
  • Retention promoters are all those substances which reduce the dynamic surface tension, such as dioctyl sulfosuccinate, or which increase the viscoelasticity, such as hydroxypropyl guar polymers.
  • Suitable penetration promoters in the present context are all those substances which are usually used to improve the penetration of agrochemical active substances into plants.
  • Penetration promoters are in this context defined by the fact that they can penetrate from the (usually aqueous) application broth and / or from the spray coating into the cuticle of the plant and thereby increase the material mobility (mobility) of the active ingredients in the cuticle.
  • the method described in the literature can be used to determine this property.
  • Examples include alcohol alkoxylates such as Kokosfettethoxyiat (10) or Isotridecylethoxylat (12), fatty acid esters such as rapeseed oil or soy aölmethylester, fatty amine alkoxylates such as Tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate ,
  • the formulations preferably contain between 0.00000001 and 98 wt .-% of active ingredient or, more preferably between 0.01 and 95 wt .-% active ingredient, more preferably between 0.5 and 90 wt .-% active ingredient, based on the weight of Formulation.
  • the active substance content of the application forms (pesticides) prepared from the formulations can vary within wide ranges.
  • the active ingredient concentration of the application forms may usually be between 0.00000001 and 95% by weight of active compound, preferably between 0.00001 and 1% by weight, based on the weight of the application form.
  • the application is done in a custom forms adapted to the application.
  • compound of the formula (II) here the compound (IIa), 5,6,7,7a-tetrahydro-oxazolo [4,5-b] pyridin-2 (4H) -one and as a compound of the formula (III ) 2-chloro-5-chloromethylpyridine is used.
  • a diluent here DMF
  • suitable basic reaction auxiliaries here CS2CO3 and Csl
  • the compound of formula (Im) namely 4- (6-chloro-pyridin-3-ylmethyl) -5,6 , 7,7a-tetrahydro-oxazolo [4,5-b] pyridine-2 (4H) -one.
  • the compounds of formula (II) may, for. T. be obtained commercially or by literature methods.
  • the compounds of formula (III) may, for. T. be obtained commercially or by Literaturb known methods. General routes for the preparation of the compounds of formula (III) are shown in Reaction Scheme 6.
  • A-CH 3 > A-COOH ⁇ A-CH (R 1 ) -OH> A-CH (R 1 ) -LG
  • Known compounds of the formula (III) are, for example: 2-chloro-5-chloromethyl-1,3-thiazole (WO 98/32747 A1, EP 780384 A2), 2-bromo-5-bromomethyl-1,3-thiazole (EP 376279 A2), 5-bromomethyl-2-methyl-1,3-thiadiazole (WO 2010/132999 Al); 5-Bromomethyl-2-trichloromethyl-1, 3-thiazole (US Pat. No.
  • Methyl-substituted heterocycles can be converted, for example, by oxidation into corresponding heterocyclic carboxylic acids (A-COOH): see. for example, 3-thiophenecarboxylic acid (JP 03056478 A), 5-fluoro-6-bromo-nicotinic acid (F.L. Setliff, G.O. Rankin, J. Chem. Eng. Data 1972, 17,
  • heterocyclic carboxylic acids A-COOH
  • formyl-substituted heterocycles A-CHO
  • the latter can also be prepared from corresponding methylene groups.
  • halo heterocycles can be obtained using suitable halogenating agents known from the literature, examples of which are the syntheses of the halomethyl-substituted heterocycles, for example 2-chloro-5- (chloromethyl) -1, 3-thiazole (WO 97/23469 A1) or 5-bromomethyl-2-chloro-1,3-thiazole (WO 2005/082859 A1), 5-chloromethyl-2-methylpyrimidine (U. Eiermann et al., Chern At: 1990, 123 , 1885-9), 3-chloromethyl-5-bromo-6-chloro-pyridine or 3-bromo-5-iodo-6-chloro-pyridine (p. Agabu et al., J. Pestic. Be. 2005, 30, 409-413).
  • suitable halogenating agents known from the literature, examples of which are the syntheses of the halomethyl-substituted heterocycles, for example 2-chloro-5- (chloromethyl
  • Starting compounds (A-10) in which A is a 5,6-disubstituted 3-pyridinyl radical can also be obtained by known methods. Suitable and known starting compounds are, for example, 6-FIalogen-substituted 5-nitro-jss-picolines (A-5) which can be modified in accordance with known literature procedures (see Reaction Scheme 7). R cak oneshema 7
  • X. Y halogen, e.g. As fluorine, chlorine, bromine, iodine
  • LG halogen, O-mesyl, O-tosyl,
  • A-7 The oxidation of the methyl group in the 5,6-disubstituted ⁇ -picolines (A-7) can then be known to lead to the corresponding 5,6-disubstituted nicotinic acids (A-8): cf. 5-fluoro-6-chloronicotinic acid and 5-fluoro-6-bromo-nicotinic acid (Setliff F. L, Rankin G. (), J. Chem. Engineering Data 1972, 17, 515-516), 5-bromo- 6-fluoronicotinic acid (WO 2009/010488 A1), 5-bromo-6-chloronicotinic acid and 5-bromo-6-bromonicotinic acid (FL Setliff J. Chem. Engineering Data 1970, 15, 590-
  • halogenation of the methyl group in the 3-position may lead from (A-7) to the compounds (A-10) in which LG is halogen: cf. 3-bromomethyl-6-chloro-5-fluoropyridine or 3-bromomethyl-6-chloro-5-iodo-pyridine (Kagabu, S. et al., J. Pestic., Sci. 2005, 30, 409-413).
  • LG is halogen
  • nitro group may also be reduced at a later time in the reaction sequence.
  • Example 1-1 4- (6-trifluorometh-pyridine-3-methyl) -oxazolo [4,5-b-pyridie-2 (4H) -oe
  • Ci2H 8 ClN 3 O 2 261.6 ] II NMR (600 MHz, CD 3 CN) ⁇ 5.53 (s, 2H), 6.79 (t, IH), 7.21 (dd, IH), 7 , 40 (dd, III) .7.53 (dd, IH), 7.81 (dd, IH), 8.47 (m, III) ppm
  • Ci2H 7 BrClN 3 02 calculated: 340.5
  • the lydration was carried out according to the reaction before chrift (1st step / variant A) in a 600 ml vessel (material: Hastelloy) at room temperature (20 ° C) [time: about 48 hours, pressure: 10 bar] using : 15.6 g (141.6 mmol) of 2-amino-3-hydroxy-pyridine, 5.1 g of 5% rhodium-carbon catalyst, 300 ml of glacial acetic acid.
  • reaction mixture is concentrated in vacuo, the remaining residue is taken up in ethyl acetate and the organic phase is washed with water. After separation of the organic phase, this is dried over sodium sulfate, filtered and concentrated in vacuo. The remaining residue is purified by chromatography using medium-pressure chromatography (cyclohexane-acetone gradient).
  • Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
  • a suitable active compound To prepare a suitable active compound, it is mixed with 1 part by weight of active compound with the stated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Chinese cabbage latets (Brassica pekinensis) are sprayed with an active compound at the desired concentration and, after drying, are populated with larvae of the Mé err étal chaplain (Phaedon cochleariae).
  • Emulsifier 0.5 part by weight of alkylaryl polyglycol ether In order to prepare a suitable 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.
  • Chinese cabbage latets (Brassica pekinensis) infected by all stages of the Green Peach aphid (Myzus persicae) are sprayed with an active compound supply of the desired concentration.
  • Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
  • Bean leaf yolks Phaseolus vulgaris
  • Triticae Tricholine
  • CTECFE Ctenoccphalides felis oral
  • a suitable active compound For the preparation of a suitable active compound, it is mixed with 10 mg of active substance with 0.5 ml of dimethyl sulfoxide. Part of the concentrate is diluted with citrated bovine blood and the desired concentration is produced.
  • Approximately 20 fasting adult fleas (Ctenocephalides felis) are placed in a chamber sealed with gauze at the top and bottom.
  • a metal cylinder is placed on the chamber, the underside of which is sealed with parafilm.
  • the cylinder contains the blood-drug preparation, which can be absorbed by the fleas through the parathyroid membrane. After 2 days the kill is determined in%. 100% means that all fleas have been killed; 0% means that no flea has been killed.
  • Vessels containing horsemeat treated with the desired concentration of active compound are mated with about 20 Lucilla cuprina larvae.
  • Vessels containing the preparation of active compound of the desired concentration are filled with about 40 Cooperia curticei larvae.

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Abstract

L'invention concerne des (Thio)carbonylamidines bicycliques de la formule (I), dans laquelle Q, B. Y, R1, et A sont tels que définis dans la description, leur production, et leur utilisation pour lutter contre les végétaux nuisibles et les nuisibles que l'on rencontre dans le domaine de la médecine vétérinaire.
EP12719008.0A 2011-05-10 2012-05-07 (thio)carbonylamidines bicycliques Withdrawn EP2707373A1 (fr)

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EP12719008.0A EP2707373A1 (fr) 2011-05-10 2012-05-07 (thio)carbonylamidines bicycliques

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EP11165556 2011-05-10
PCT/EP2012/058340 WO2012152741A1 (fr) 2011-05-10 2012-05-07 (thio)carbonylamidines bicycliques
EP12719008.0A EP2707373A1 (fr) 2011-05-10 2012-05-07 (thio)carbonylamidines bicycliques

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150065501A1 (en) 2012-04-03 2015-03-05 Basf Se N-substituted hetero-bicyclic furanone derivatives for combating animal
WO2013150115A1 (fr) 2012-04-05 2013-10-10 Basf Se Composés hétéro-bicycliques et dérivés pour combattre les animaux nuisibles
JP6133907B2 (ja) 2013-01-31 2017-05-24 三井化学アグロ株式会社 縮合環ピリミジン化合物及びそれを含む有害生物防除剤
WO2020011808A1 (fr) 2018-07-13 2020-01-16 Syngenta Crop Protection Ag Composés hétéroaromatiques bicycliques à action pesticide
WO2020025658A1 (fr) 2018-08-03 2020-02-06 Syngenta Crop Protection Ag Composés hétéroaromatiques bicycliques à action pesticide
EP3833663A1 (fr) * 2018-08-07 2021-06-16 Syngenta Crop Protection AG Composés hétéroaromatiques bicycliques à action pesticide
WO2020030754A1 (fr) 2018-08-10 2020-02-13 Syngenta Crop Protection Ag Composés hétéroaromatiques bicycliques mésoioniques à action pesticide
WO2020035565A1 (fr) 2018-08-17 2020-02-20 Syngenta Crop Protection Ag Composés hétéroaromatiques bicycliques mésoioniques à action pesticide
WO2020120694A1 (fr) 2018-12-14 2020-06-18 Syngenta Participations Ag Composés hétéroaromatiques bicycliques à action pesticide
WO2021144354A1 (fr) 2020-01-15 2021-07-22 Syngenta Crop Protection Ag Composés hétéroaromatiques bicycliques à action pesticide

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH461489A (de) * 1965-03-26 1968-08-31 Geigy Ag J R Verfahren zur Herstellung von neuen Oxazolderivaten
CH452528A (de) 1965-04-30 1968-03-15 Geigy Ag J R Verfahren zur Herstellung von neuen Derivaten eines Pyrido-oxazins
CH536071A (de) 1970-06-26 1973-04-30 Agripat Sa Insektizides und akarizides Mittel
DE2045050A1 (en) 1970-09-11 1972-03-23 Dr Karl Thomae GmbH, 7950 Biberach 5-(2-amino-alkoxy-phenoxy-methyl)-3-alkyl-isoxazoles - useful as hypotensives and sedatives
BE788065A (fr) 1971-08-26 1973-02-26 Degussa Nouvelles aza-benzimidazoles et procede pour leur preparation
DE2439661A1 (de) 1973-08-21 1975-03-06 Ciba Geigy Ag Org. phosphorverbindungen, verfahren zu ihrer herstellung und ihre verwendung zur schaedlingsbekaempfung
FR2555583A1 (fr) 1983-11-29 1985-05-31 Irceba Derives du thiazole appartenant a la famille des (4-methyl-5-thiazolyl)-alcanols, procede de preparation et utilisation en therapeutique
DE3630046A1 (de) 1986-09-04 1988-03-17 Bayer Ag Verfahren zur herstellung von 5-chlormethylpyridinen
IL84944A (en) 1987-01-19 1992-02-16 Ici Plc Pharmaceutical compositions containing 1,2-dihydro-3h-indazolone derivatives,some new such compounds and their preparation
DE3856183T2 (de) 1987-08-01 1998-11-05 Takeda Chemical Industries Ltd Zwischenprodukte, ihre Herstellung und Verwendung zur Herstellung alpha-ungesättigter Amine
DE58908969D1 (de) 1988-12-16 1995-03-16 Bayer Ag Verfahren zur Herstellung von 2-Chlor-5-chlormethylpyridin.
IE960441L (en) 1988-12-27 1990-06-27 Takeda Chemical Industries Ltd Guanidine derivatives, their production and insecticides
DE3912964A1 (de) 1989-04-20 1990-10-25 Bayer Ag Verfahren zur herstellung von 2-chlor-5-chlormethyl-pyridin und neue zwischenprodukte
JP2926768B2 (ja) 1989-07-25 1999-07-28 日産化学工業株式会社 チオフェンカルボン酸類の製造方法
US5023265A (en) 1990-06-01 1991-06-11 Schering Corporation Substituted 1-H-pyrrolopyridine-3-carboxamides
JPH0713063B2 (ja) 1992-04-30 1995-02-15 日本バイエルアグロケム株式会社 新規ジアミン類
KR930023342A (ko) 1992-05-12 1993-12-18 비트 라우버, 토마스 케플러 2-클로로-5-클로로메틸- 피리딘의 제조방법
US5338856A (en) 1992-08-17 1994-08-16 Dowelanco 3,4-N,trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides
US5420270A (en) 1993-10-07 1995-05-30 G. D. Searle & Co. Aryl substituted dibenzoxazepine compounds, pharmaceutical compositions and methods of use
RU2136661C1 (ru) 1993-10-21 1999-09-10 Джи Ди Сирл энд Ко. Амидинопроизводные, их применение и фармацевтическая композиция
US5434181A (en) 1993-10-26 1995-07-18 Mitsui Toatsu Chemicals, Inc. Furanyl insecticide
US5618819A (en) 1994-07-07 1997-04-08 Adir Et Compagnie 1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one and oxazolo[4,5-b]pyridin-2-(3H)-one compounds
DE4429465A1 (de) 1994-08-19 1996-02-22 Bayer Ag Verfahren zur Herstellung von 2-Halogenpyridinaldehyden und neue 2-Halogenpyridinaldehyde
DE69632919T2 (de) 1995-12-21 2005-07-28 Syngenta Participations Ag Verfahren zur herstellung von 2-chlor-5-chloromethyl-thiazol
DE19548417A1 (de) 1995-12-22 1997-06-26 Bayer Ag Verfahren zur Herstellung von 2-Chlor-5-chlormethylthiazol
DE19605903A1 (de) 1996-02-17 1997-08-21 Basf Ag Pyridyl-phenyl- und -benzylether, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung
US5912364A (en) 1996-10-21 1999-06-15 Eastman Chemical Company Process for the preparation of 3-methyltetrahydrofuran
JP2001508452A (ja) 1997-01-22 2001-06-26 ノバルティス アクチェンゲゼルシャフト チアゾール誘導体の製造方法
CN1126742C (zh) 1997-02-03 2003-11-05 道农业科学公司 杀真菌化合物
AR029423A1 (es) 1999-12-21 2003-06-25 Sugen Inc Compuesto derivado de pirrolo-[pirimidin o piridin]-6-ona, metodo de preparacion de dichos compuestos, composiciones farmaceuticas que los comprenden, un metodo para regular, modular o inhibir la actividad de la proteina quinasa y un metodo de tratar o prevenir una enfermedad de mamiferos
DE10119423A1 (de) 2001-04-20 2002-10-24 Bayer Ag Neue insektizid wirkende Azole
JP3899373B2 (ja) 2002-02-14 2007-03-28 富士フイルム株式会社 核酸染色用色素
AP2114A (en) 2003-02-26 2010-03-04 Sugen Inc Aminoheteroaryl compounds as protein kinase inhibitors
CN1826334A (zh) 2003-03-18 2006-08-30 麦克公司 趋化因子受体活性的四氢吡喃基环戊基杂环酰胺调节剂
CN102311387A (zh) 2004-02-25 2012-01-11 伊莱利利公司 作为5-HT2C受体激动剂的6-取代的2,3,4,5-四氢-1H-苯并[d]氮杂䓬
CA2578075A1 (fr) 2004-08-26 2006-03-02 Pfizer Inc. Composes aminoheteroaryles en tant qu'inhibiteurs des proteines tyrosine kinases
US7541392B2 (en) 2004-09-14 2009-06-02 E.I. Du Pont De Nemours And Company Materials leading to improved dental composites and dental composites made therefrom
KR20070119655A (ko) 2005-02-28 2007-12-20 레노비스, 인크. 이온-채널 리간드로서의 아미드 유도체, 및 이를 사용한제약 조성물 및 방법
BRPI0611705A2 (pt) 2005-06-24 2016-11-16 Lilly Co Eli composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, uso de composto
AU2006261839B2 (en) 2005-06-28 2011-09-01 Merck Sharp & Dohme Corp. Niacin receptor agonists, compositions containing such compounds and methods of treatment
US7790726B2 (en) 2005-08-16 2010-09-07 Chemocentryx, Inc. Monocyclic and bicyclic compounds and methods of use
DE102006015456A1 (de) 2006-03-31 2007-10-04 Bayer Cropscience Ag Bicyclische Enamino(thio)carbonylverbindungen
DE102006015468A1 (de) 2006-03-31 2007-10-04 Bayer Cropscience Ag Substituierte Enaminocarbonylverbindungen
US8841334B2 (en) 2006-05-31 2014-09-23 Abbvie Inc. Compounds as cannabinoid receptor ligands and uses thereof
EP2044038B1 (fr) 2006-06-06 2014-07-02 Cornerstone Therapeutics Inc. Nouvelles pipérazines, compositions pharmaceutiques et procédés d'utilisation de celles-ci
EP2086324A2 (fr) 2006-11-02 2009-08-12 Merck & Co., Inc. Composés anti-hypercholestérolémique à substitution hétérocyclyle
UA98777C2 (en) 2006-11-20 2012-06-25 Эли Лилли Энд Компани Tetrahydrocyclopenta[b]indole compounds as androgen receptor modulators
WO2008073936A1 (fr) 2006-12-11 2008-06-19 Wyeth Derives de carboxamide utilises en tant que modulateurs des canaux ioniques
AR064416A1 (es) 2006-12-21 2009-04-01 Cancer Rec Tech Ltd Derivados de purina, piridina y pirimidina condensadas con heterociclos, moduladores de pka y/o pkb, composiciones farmaceuticas que los contienen, y usos para el tratamiento de enfermedades hiperproliferativas.
ATE490249T1 (de) 2007-02-19 2010-12-15 Glaxosmithkline Llc Purinderivate als immunmodulatoren
WO2008134035A1 (fr) 2007-04-27 2008-11-06 Panacos Pharmaceuticals, Inc. DÉRIVÉS D'AMIDE PYRIMIDINE ARYLMETHYL PIPERAZINE PYRAZOLO[1,5-α] À SUBSTITUTION ALPHA
MX2009014247A (es) 2007-07-16 2010-01-28 Novartis Ag Compuestos heterociclicos utiles como inhibidores de mk2.
AR069650A1 (es) 2007-12-14 2010-02-10 Actelion Pharmaceuticals Ltd Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano
BRPI0821115A8 (pt) 2007-12-18 2017-12-26 Actelion Pharmaceuticals Ltd Composto derivado de aminotriazol, medicamento, composição farmacêutica e uso do composto
EP2285807A1 (fr) 2008-05-09 2011-02-23 F. Hoffmann-La Roche AG Composés hétérocycliques antiviraux
WO2009139340A1 (fr) 2008-05-12 2009-11-19 武田薬品工業株式会社 Composé pyrazole
WO2010005692A2 (fr) 2008-06-16 2010-01-14 E. I. Du Pont De Nemours And Company Carbonyl-amidines cycliques insecticides
WO2010042642A1 (fr) 2008-10-08 2010-04-15 Amgen Inc. Agents modulateurs des récepteurs de calcium
EP2379564A1 (fr) 2008-12-19 2011-10-26 Schering Corporation Dérivés hétérocycliques bicycliques et leurs procédés d'utilisation
KR20110132564A (ko) 2009-02-11 2011-12-08 선오비온 파마슈티컬스 인코포레이티드 히스타민 ｈ3 역 작용제 및 길항제, 및 이의 사용 방법
AU2010250055A1 (en) 2009-02-27 2011-09-15 Vertex Pharmaceuticals Incorporated Tri-cyclic pyrazolopyridine kinase inhibitors
AR076601A1 (es) 2009-05-21 2011-06-22 Chlorion Pharma Inc Pirimidinas como agentes terapeuticos

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2012152741A1 *

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