EP3227283A1 - Bicyclische verbindungen als schädlingsbekämpfungsmittel - Google Patents

Bicyclische verbindungen als schädlingsbekämpfungsmittel

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Publication number
EP3227283A1
EP3227283A1 EP15801853.1A EP15801853A EP3227283A1 EP 3227283 A1 EP3227283 A1 EP 3227283A1 EP 15801853 A EP15801853 A EP 15801853A EP 3227283 A1 EP3227283 A1 EP 3227283A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
alkoxy
radical
optionally substituted
substituted
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Withdrawn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
EP15801853.1A
Other languages
German (de)
English (en)
French (fr)
Inventor
Thomas Bretschneider
Silvia Cerezo-Galvez
Arnd Voerste
Reiner Fischer
Martin FÜSSLEIN
Alexander ARLT
Peter Jeschke
Kerstin Ilg
Ulrich Görgens
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 CropScience AG
Original Assignee
Bayer CropScience AG
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Filing date
Publication date
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of EP3227283A1 publication Critical patent/EP3227283A1/de
Withdrawn legal-status Critical Current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
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • 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
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • 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
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • 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
    • A01N43/80—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 1,2
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A61P33/14—Ectoparasiticides, e.g. scabicides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Definitions

  • the present application relates to novel bicyclic compounds, agents containing these compounds, their use for combating animal pests and methods and intermediates for their preparation.
  • WO 2012/102387 Al heterocyclic compounds are described, which can be used in particular as insecticides and acaricides.
  • the object of the present invention was to provide compounds which broaden the spectrum of pesticides from various aspects.
  • B is a radical from the group consisting of hydrogen, halogen, cyano, nitro, alkyl, haloalkyl, alkoxy, haloalkoxy and in each case optionally substituted cycloalkyl and cycloalkenyl,
  • R 1 is a radical from the series hydrogen, alkyl, alkoxy and cyano
  • R 2 a) is a B radical from the series
  • dashed line represents the bond to the carbon atom of the bicycle of the formula (I), or R 2 f) represents a radical of the formula wherein the dashed line represents the bond to the carbon atom of the bicycle of formula (I), or
  • R 2 g) is optionally substituted phenyl, wherein is hydrogen or a radical from the series halogen, nitro, amino, cyano, alkylamino, haloalkylamino, dialkylamino, alkyl, haloalkyl, optionally substituted and optionally interrupted by one or more heteroatoms saturated or unsaturated cycloalkyl, cycloalkylalkyl, alkoxy, haloalkoxy, alkoxyalkyl, halogenated Alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, bis (alkoxy) alkyl,
  • R 8 is where the dotted line represents the bond to the B residues
  • X is oxygen or sulfur
  • X 1 is a radical selected from among hydrogen, halogen, cyano, nitro, alkyl, haloalkyl,
  • X 2 is oxygen, sulfur, NR 5 or NOH
  • L is oxygen or sulfur
  • R is NR 18 R 19 or represents a respectively optionally substituted radical from the series alkyl, alkenyl, alkynyl, alkoxyalkyl, alkyl-S-alkyl, alkyl-S (0) -alkyl, alkyl-S (0) 2 alkyl, R 18 -CO-alkyl, NR 18 R 19 is -CO-alkyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, cycloalkenylalkyl, heterocyclyl, heterocyclylalkyl, phenyl, phenylalkyl, hetaryl and hetarylalkyl,
  • R 3 is hydrogen or alkyl
  • R 4 is a radical from the group consisting of hydrogen, alkyl, haloalkyl, cyanoalkyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, aryl, arylalkyl and hetarylalkyl
  • R 5 is a radical from the group consisting of hydrogen, alkyl, haloalkyl, cyanoalkyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkylthioalkyl, aryl, arylalkyl and hetarylalkyl, or
  • R 3 and R 4 together with the nitrogen atom to which they are attached form a ring which may contain one or more further nitrogen, oxygen and sulfur heteroatoms, or
  • R 3 and R 5 together with the nitrogen atoms to which they are attached form a ring
  • R 6 is hydrogen or alkyl
  • R 7 is a radical selected from hydrogen, alkyl, haloalkyl, cyanoalkyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxy, haloalkoxy, alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkylthioalkyl, aryl, arylalkyl and hetarylalkyl, or
  • R 6 and R 7 together with the nitrogen atom to which they are attached form a ring which may contain one or more further nitrogen, oxygen and sulfur heteroatoms,
  • R 8 is a radical from the group consisting of hydrogen, alkyl, haloalkyl, cyanoalkyl, alkoxy, haloalkoxy, alkenyl, alkoxyalkyl, in each case optionally halogen-substituted alkylcarbonyl and alkylsulfonyl, optionally halogen-substituted alkoxycarbonyl and optionally by halogen, alkyl, alkoxy, haloalkyl and cyano is substituted cycloalkylcarbonyl, or represents a cation or an optionally substituted by alkyl or arylalkyl ammonium ion,
  • R 9 is a radical from the series in each case optionally substituted alkyl, alkenyl and alkynyl, in each case optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl, in which the rings at least one heteroatom selected from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen each optionally substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group,
  • R and R in the radicals (Cl) and (Fl) may also together with the NS (0) n group to which they are attached form a saturated or unsaturated and optionally substituted 4- to 8-membered ring, the or a plurality of further heteroatoms from the group consisting of sulfur, oxygen (where oxygen atoms are not allowed to be immediately adjacent) and nitrogen and / or at least one carbonyl group, R is hydrogen or alkyl,
  • R 8 and R 10 in the radicals (C-2) and (F-2) may also together with the N atoms to which they are bonded represent a saturated or unsaturated and optionally substituted 4- to 8-membered ring, the at least one further heteroatom from the series sulfur, oxygen (oxygen atoms may not be immediately adjacent) and contain nitrogen and / or at least one carbonyl group,
  • R and R in the radicals (C-2) and (F-2) may also together with the NS (0) n group to which they are attached form a saturated or unsaturated and optionally substituted 4- to 8-membered ring which may contain one or more further heteroatoms from the group consisting of sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one carbonyl group,
  • R U is an optionally substituted radical from the series alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkyloxy, cycloalkenyloxy, cycloalkylalkoxy, alkylthio, alkenylthio, phenoxy, phenylthio, benzyloxy, benzylthio, heteroaryloxy, heteroarylthio, heteroarylalkoxy and heteroarylalkylthio stands,
  • R represents an optionally substituted radical from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkyloxy, cycloalkenyloxy, cycloalkylalkoxy, alkylthio, alkenylthio, phenoxy, phenylthio, benzyloxy, benzylthio, heteroaryloxy, heteroarylthio, heteroarylalkoxy and heteroarylalkylthio .
  • R and R in the radicals (C-3) and (F-3) may also together with the phosphorus atom to which they are attached form a saturated or unsaturated and optionally substituted 5- to 7-membered ring, one or two Heteroatoms from the series oxygen (oxygen atoms may not be immediately adjacent) and may contain sulfur,
  • R is an optionally substituted radical from the series alkyl, alkenyl, alkynyl, phenyl and phenylalkyl,
  • R is an optionally substituted radical from the series alkyl, alkenyl, alkynyl, phenyl and phenylalkyl,
  • R 15 is a radical from the series each optionally substituted alkyl, alkenyl and alkynyl, each optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl, in which the rings at least one heteroatom selected from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen may be included, respectively substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group,
  • R 8 and R 15 in the radicals (C-6) and (F-6) also together with the NS (0) n group to which they are attached, a saturated or unsaturated and optionally substituted 4- to 8-membered ring can form one or more other heteroatoms from the series sulfur,
  • Oxygen (where oxygen atoms are not immediately adjacent) and may contain nitrogen and / or at least one carbonyl group, a radical selected from the group consisting of hydrogen, each optionally substituted alkyl, alkoxy, alkenyl and alkynyl, respectively optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl, in in which each of the rings is at least one heteroatom selected from the group consisting of sulfur, oxygen (where oxygen atoms are not immediately adjacent) and nitrogen, optionally substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group,
  • R “ and R 16 in the radicals (C-7) and (F-7) together with the N-atom to which they are attached can form a saturated or unsaturated and optionally substituted 4- to 8-membered ring, the one or more other heteroatoms from the series sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one carbonyl group, a radical from the series each optionally substituted alkyl, alkoxy, alkenyl and alkynyl, respectively optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl in which the rings may contain at least one heteroatom selected from sulfur, oxygen (where oxygen atoms are not immediately adjacent) and nitrogen, each optionally substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group R 8 and R 17 in the radicals (C-8) and (F-8) also together with the NC (X) group to which they are attached may form a saturated or
  • R 19 is a radical selected from the group consisting of hydrogen, an alkali metal or alkaline earth metal ion or an optionally monosubstituted to trisubstituted by C 1 -C 4 -alkyl-substituted ammonium ion or an optionally halogen or cyano-substituted radical from the series consisting of alkyl, alkoxy, Alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl and alkylsulfonylalkyl,
  • Y 3 is a radical from the group consisting of hydrogen, halogen, cyano, alkyl, cycloalkyl, haloalkyl, alkoxy, haloalkoxy and NR 20 R 21 ,
  • W is a radical from the series O, S, SO and SO2,
  • R 22 is a radical from the group consisting of hydrogen, alkyl, haloalkyl, cyanoalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkoxy, haloalkoxy, optionally halogen-substituted alkoxyalkyl, optionally halogen-substituted bis (alkoxy) alkyl, optionally halogen-substituted alkylsulfanylalkyl, alkylcarbonylalkyl optionally substituted by halogen, optionally alkyl substituted by halogen, alkylsulphonylalkyl optionally substituted by halogen, dialkylaminosulphanylalkyl, dialkylaminosulphinylalkyl, dialkylaminosulphonylalkyl, optionally halogen-substituted alkoxycarbonyl, optionally halogen-substituted alkoxycarbon
  • alkyl is a radical selected from among hydrogen, halogen, cyano, nitro, amino, hydroxy and in each case optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, alkylcarbonyloxy, alkenylcarbonyloxy, alkynylcarbonyloxy, cycloalkylcarbonyloxy, alkoxycarbonyloxy , Alkylsulfonyloxy, alkylamino, alkenylamino, alkynylamino, cycloalkylamino, alkylthio, haloalkylthio, alkenylthio, alkynylthio, cycloalkylthio, alkylsulfinyl, alkylsulfonyl, alkylcarbonyl, alkoxyiminoalky
  • R is a radical selected from the group consisting of hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylsulfanyl, haloalkylsulfanyl, alkylsulfinyl, Haloalkylsulfinyl, alkylsulfonyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, cyanoalkyl, and compounds of the formula (I) in which A is the A radical (Aa)
  • G 1 is N or CB 1 ,
  • B 1 is a radical from the series consisting of hydrogen, halogen, cyano, nitro, alkyl, haloalkyl, alkoxy, haloalkoxy and in each case optionally substituted cycloalkyl and cycloalkenyl,
  • B 2 is a radical from the series consisting of hydrogen, halogen, cyano, nitro, alkyl, haloalkyl, alkoxy, haloalkoxy and in each case optionally substituted cycloalkyl and cycloalkenyl,
  • T oxygen or a pair of electrons
  • R 1 is a radical selected from the group consisting of hydrogen, alkyl, alkoxy and cyano,
  • the dashed line represents the bond to the carbon atom of the bicyclic compound of the formula (I) in which hydrogen or a radical from the series halogen, nitro, amino, cyano, alkylamino, haloalkylamino, dialkylamino, alkyl, haloalkyl, optionally substituted and optionally saturated or unsaturated cycloalkyl, cycloalkylalkyl, alkoxy, haloalkoxy, alkoxyalkyl, halogenated alkoxyalkyl, alkylthioalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylthioalkyl interrupted by one or more heteroatoms,
  • the dashed line denotes the bond to the carbon atom of the bicyclic compound of the formula (I)
  • wonn is a radical from the series halogen, nitro, amino, cyano, alkylamino, haloalkylamino, dialkylamino, optionally substituted and optionally interrupted by one or more heteroatoms saturated or unsaturated cycloalkyl, cycloalkylalkyl, haloalkoxy, alkoxyalkyl, halogenated alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, haloalkylthioalkyl, haloalkylsulfinylalkyl, haloalkylsulfonylalkyl, bis (alkoxy) alkyl, bis (haloalkoxy) alkyl, alkoxy (alkylsulfanyl) alkyl,
  • R 2 c is a radical of the formula
  • R f is a radical of the formula in which the dashed line denotes the bond to the carbon atom of the bicyclic compound of the formula (I),
  • X is oxygen or sulfur
  • X 2 is oxygen, sulfur or NOH
  • L is oxygen or sulfur
  • R 4 is a radical from the group consisting of hydrogen, alkyl, haloalkyl, cyanoalkyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, aryl, arylalkyl and hetarylalkyl, or
  • R 3 and R 4 together with the nitrogen atom to which they are attached form a ring which may contain one or more further nitrogen, oxygen and sulfur heteroatoms,
  • R 6 is hydrogen or alkyl
  • R 7 is a radical selected from hydrogen, alkyl, haloalkyl, cyanoalkyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxy, haloalkoxy, alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkylthioalkyl, aryl, arylalkyl and hetarylalkyl, or
  • R 6 and R 7 together with the nitrogen atom to which they are attached form a ring which may contain one or more further nitrogen, oxygen and sulfur heteroatoms,
  • R 8 is a radical from the group consisting of hydrogen, alkyl, haloalkyl, cyanoalkyl, alkoxy, haloalkoxy, alkenyl, alkoxyalkyl, in each case optionally halogen-substituted alkylcarbonyl and alkylsulfonyl, optionally halogen-substituted alkoxycarbonyl and optionally by halogen, alkyl, alkoxy, haloalkyl and cyano substituted Is cycloalkylcarbonyl, or is a cation or an optionally substituted by alkyl or arylalkyl ammonium ion,
  • R 9 is a radical from the series in each case optionally substituted alkyl, alkenyl and alkynyl, in each case optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl, in which the rings at least one heteroatom selected from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen each optionally substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group,
  • R 10 is hydrogen or alkyl
  • R and R in the radicals (C-2) and (F-2) may also together with the NS (0) n group to which they are attached form a saturated or unsaturated and optionally substituted 4- to 8-membered ring which may contain one or more other heteroatoms from the group consisting of sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one carbonyl group, each of an optionally substituted radical from the series alkyl, alkenyl, alkynyl, alkoxy, Alkenyloxy, alkynyloxy, cycloalkyl, cycloalkyloxy, cycloalkenyloxy, cycloalkylalkoxy, alkylthio, alkenylthio, phenoxy, phenylthio, benzyloxy, benzylthio, heteroaryloxy, heteroarylthio, heteroarylalkoxy and heteroarylalkylthio, represents an optionally substituted radical from the series alkyl
  • R and R in the radicals (C-3) and (F-3) may also together with the phosphorus atom to which they are attached form a saturated or unsaturated and optionally substituted 5- to 7-membered ring, one or two Heteroatoms from the series oxygen (where
  • Oxygen atoms may not be immediately adjacent) and may contain sulfur, R is an optionally substituted radical from the series alkyl, alkenyl, alkynyl, phenyl and phenylalkyl,
  • R is an optionally substituted radical from the series alkyl, alkenyl, alkynyl, phenyl and phenylalkyl,
  • R 15 is a radical from the series each optionally substituted alkyl, alkenyl and alkynyl, each optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl, in which the rings at least one heteroatom selected from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen each optionally substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group,
  • R 8 and R 15 in the radicals (C-6) and (F-6) also together with the NS (0) n group to which they are attached, a saturated or unsaturated and optionally substituted 4- to 8-membered ring which may contain one or more further heteroatoms selected from the group consisting of sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one carbonyl group,
  • R 16 is a radical from the group consisting of hydrogen, in each case optionally substituted alkyl, alkoxy, alkenyl and alkynyl, in each case optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl, in which the rings are at least one heteroatom selected from the group consisting of sulfur, oxygen (oxygen atoms not being directly adjacent may each contain) and nitrogen, each optionally substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group,
  • R 8 and R 16 in the radicals (C-7) and (F-7) together with the N-atom to which they are attached can form a saturated or unsaturated and optionally substituted 4- to 8-membered ring, which may contain one or more further heteroatoms from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one carbonyl group,
  • R 17 is a radical from the series in each case optionally substituted alkyl, alkoxy, alkenyl and alkynyl, in each case optionally substituted cycloalkyl, cycloalkylalkyl and cycloalkenyl, in which the rings are at least one heteroatom from the series sulfur, oxygen (oxygen atoms may not be immediately adjacent) and each may contain nitrogen, each optionally substituted aryl, heteroaryl, arylalkyl and heteroarylalkyl and an optionally substituted amino group, R 8 and R 17 in the radicals (C-8) and (F-8) together with the NC (X) group to which they are attached form a saturated or unsaturated and optionally substituted 4- to 8-membered ring can contain one or more further heteroatoms from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one carbonyl group, and in the case that R 2 is one of the radicals listed under f) .
  • R 22 is a radical from the group consisting of hydrogen, alkyl, haloalkyl, cyanoalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkoxy, haloalkoxy, optionally halogen-substituted alkoxyalkyl, optionally halogen-substituted bis (alkoxy) alkyl, optionally halogen-substituted alkylsulfanylalkyl, optionally substituted by halogen alkylsulfinylalkyl, optionally substituted by halogen alkylsulfinylalkyl, optionally substituted by halogen alkylsulfinylalkyl, optionally substituted by halogen alkylsulfonylalkyl, dialkylaminosulfanylalkyl, dialkylaminosulfinylalkyl, dialkylaminosulfonyl
  • R 18 is a radical selected from the group consisting of hydrogen, hydroxy, in each case optionally substituted alkyl, alkoxy, alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, alkylcarbonyl, alkoxycarbonyl, alkenyl and alkynyl, in each case optionally substituted cycloalkyl, cycloalkylalkyl, cycloalkenyl and cycloalkenylalkyl, in which the rings at least one
  • R 20 is a radical selected from among hydrogen, halogen, cyano, nitro, amino, hydroxy and in each case optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, alkylcarbonyloxy, alkenylcarbonyloxy,
  • R 23 is a radical from the series consisting of hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, alkylthioalkyl, alkenylthioalkyl, cyanoalkyl and alkoxyalkyl or, if R 2 is one of the radicals listed under f) stands,
  • R 22 and R 23 together with the nitrogen atom to which they are attached form a ring which may contain one or more other nitrogen, oxygen and sulfur heteroatoms, and
  • R is hydrogen or an optionally substituted radical from the series alkyl, alkenyl, alkynyl, phenyl and phenylalkyl and
  • R is hydrogen or an optionally substituted radical from the group consisting of alkyl, alkenyl, alkynyl, phenyl and phenylalkyl,
  • R 27 is hydrogen or alkyl and R 26 is a radical selected from the group consisting of hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylsulfanyl, haloalkylsulfanyl, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl and Cyanoalkyl stands.
  • the dashed line denotes the bond to the carbon atom of the bicyclic compound of the formula (I) in which, for hydrogen or a radical from the series, halogen, nitro, amino, cyano, C 1 -C 4 -alkylamino, halogeno-C 1 -C 4 -alkylamino , di (Ci-C4-alkyl) amino, Ci-C4-alkyl, halo-Ci-C4- alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkenyl, C3-C6 cycloalkyl C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy,
  • C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl, ⁇ - ⁇ A-hydroxyimino-C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkoxy-imino-C 1 -C 4 -alkoxycarbonyl -C-C 4 alkyl, C (X 2) NR 3 R 4, NR 6 R 7, C 1 -C4- alkylthio, Ci-C 4 -Alkylsulfmyl, Ci-C 4 alkylsulfonyl, Ci-C4-haloalkylthio , C1-C4 haloalkylsulfinyl, Ci-C4-haloalkylsulfonyl, the heterocyclyl
  • the dashed line denotes the bond to the B radicals, a radical selected from the group consisting of hydrogen, halogen, C 1 -C 6 -alkyl and C 1 -C 6 -haloalkyl, X is oxygen or sulfur,
  • X 1 is a radical from the series consisting of hydrogen, halogen, cyano, nitro, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy,
  • X 2 is oxygen, sulfur, NR 5 or NOH
  • n is 1 or 2
  • R for NR 18 R 19 or for any given by halogen, oxygen (leads to C 0) or cyano substituted Ci-Ce-alkyl, C 3 -C 6 alkenyl, Cs-Ce-alkynyl, Ci-C 6 alkoxy -C-C 4 alkyl, Ci-C 6 - alkyl-S-Ci-C4-alkyl, Ci-C 6 alkyl-S (0) -C C-4 alkyl, Ci-C 6 alkyl S (0) 2- Ci-C 4 -alkyl, for R 18 -CO-Ci-C 4 -alkyl, for NR 18 R 19 -CO-Ci-C 4 -alkyl, optionally optionally once or twice by
  • R 4 is a radical selected from hydrogen, Ci-C 4 alkyl, halo-Ci-C4-alkyl, cyano-Ci-C 4 alkyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl , C 3 -C 6 cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C4-alkyl, Ci- C 4 alkoxycarbonyl, Ci-C 4 alkoxycarbonyl-Ci-C 4 alkyl , C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, aryl, aryl-C 1 -C 4 -alkyl and hetaryl-C 1 -C 4 -alkyl, R 5 is a radical from the series consisting of hydrogen, C 1 -C 4 Alkyl, halo-C 1 -C 4 -alkyl, cyano-C
  • R 3 and R 4 together with the nitrogen atom to which they are attached, form a 4- to 7-membered ring containing one or two further nitrogen, oxygen and sulfur heteroatoms (where oxygen and sulfur atoms are not immediately adjacent may contain)
  • R 6 is hydrogen or C 1 -C 4 -alkyl
  • R 7 is a radical from the group consisting of hydrogen, C 1 -C 4 -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 3 -C 4 cycloalkyl-Ci-C4-alkyl, Ci-C 4 alkoxy, halogen-Ci-C 4 - alkoxy, Ci-C4-alkoxy-Ci-C4-alkyl, Ci-C4-alkoxycarbonyl, Ci-C4 alkoxycarbonyl-Ci-C4-alkyl, Ci-C4-alkylthio-Ci-C 4 alkyl, aryl, aryl-Ci-C4-alkyl or hetaryl-Ci-C4 -alkyl, or
  • R 6 and R 7 together with the nitrogen atom to which they are attached, form a 4- to 7-membered ring containing one or two further nitrogen, oxygen and sulfur heteroatoms (with oxygen and sulfur atoms not being immediately adjacent may contain)
  • R 8 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 2 -C 6 -alkenyl, ci C6-alkoxy-Ci-C6-alkyl, in each case optionally substituted by halogen Ci-Cö-alkylcarbonyl and Ci-Cö-alkylsulfonyl, optionally substituted by halogen Ci-C6-alkoxycarbonyl and optionally by halogen, Ci-Cö-alkyl, Ci-C6 Alkoxy, C 1 -C 6 -haloalkyl and cyano-substituted C 3 -C 6 -cycloalkylcarbonyl, or represents a cation or an ammonium ion which
  • R 9 is a radical from the series in each case optionally substituted by halogen, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -haloalkylsulfinyl, C 1 -C 4 -alkyl -Cö-alkylsulfonyl and C 1 -C 6 -haloalkylsulfonyl-substituted C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl and C 2 -C 6 -alkynyl, each optionally substituted by halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkyl -
  • C6-cycloalkyl-Ci-C6-alkyl and C3-C6-cycloalkenyl in which a ring member by a heteroatom selected from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen may be replaced (and in particular for
  • R 8 and R 9 in the radical (Cl) and in the radical (Fl) can also be used together with the NS (0) n group to which they are attached, a saturated or unsaturated and optionally halogen, C 1 -C 6 -alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy substituted 5- to 7-membered ring forming one or two heteroatoms selected from sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one and preferably a carbonyl group may contain, in particular R 8 and R 9 together with the NS (0) n group to which they are attached, a radical from the series
  • a radical from the series in each case optionally substituted by methyl, cyano, carbamoyl-substituted Ci-Cö-alkyl, C2-C6-alkenyl and C2-C6-alkynyl each optionally substituted by methyl, trifluoromethyl, halogen, cyano or carbamoyl substituted C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C 2 -alkyl and C3-C6-cycloalkenyl, in which the rings at least one heteroatom selected from the group sulfur , Oxygen (oxygen atoms may not be immediately adjacent) and nitrogen, each optionally substituted by Ci-C i-alkyl, C1-C4-haloalkyl, Ci-C i-alkoxy, Ci-C i -haloalkoxy, Ci-C i alkylthio,
  • R 8 and R 15 in the radical (C-6) together with the NS (0) n group to which they are attached can form a saturated or unsaturated and optionally substituted 4- to 8-membered ring, the one or two further heteroatoms from the series sulfur, oxygen (oxygen and sulfur atoms may not be immediately adjacent) and contain nitrogen and / or at least one carbonyl group, a radical from the series hydrogen, in each case optionally by methyl, cyano, carbamoyl or carboxyl substituted C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 2 -C 4 -alkenyl and C 2 -C 4 -alkynyl, each optionally substituted by halogen, cyano, nitro, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -alkyl cycloalkyl, Ci-Ce-alkoxy, Ci-Ce-halo
  • R is a radical from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxyl, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 2 -C -alkenyl, C 2 -C 6 Alkynyl, Cs-Ce-cycloalkyl (which is optionally substituted by halogen, cyano, Ci-C i-alkyl and C3-C6-cycloalkyl), C3-C6-cycloalkyl-Ci-C6-alkyl, Ci-C6-alkoxy, C 1 -C 6 -haloalkoxy, C 3 -C 6 -alkenyloxy, C 3 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 6 -alkylcarbonyloxy, C 2 hal
  • R 21 is a radical from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl Ci-Ce-alkyl, cyano-Ci-Ce-alkyl, Ci-C 6 - alkylcarbonyl, C 2 -C 6 alkenylcarbonyl, Ci-C6-haloalkylcarbonyl, C 2 -C6-
  • R 23 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, C 1 -C 6 -alkoxy, C 2 -C 6 -alkoxy alkenyloxy, C2-C6 alkynyloxy, C3-C6-cycloalkyloxy, Ci-C4-alkylthio-Ci-C4-alkyl, C2-C4-alkenylthio Ci- C4-alkyl, cyano-Ci-C4- alkyl, Ci-C4- Alkoxy-Ci-C 4 -alkyl, or, in the case that R 2 is one of the radicals mentioned under c) or f)
  • R 22 and R 23 together with the nitrogen atom to which they are attached form a saturated ring which may contain one or two further nitrogen, oxygen and sulfur heteroatoms, and
  • R 24 is hydrogen or a radical optionally substituted by halogen or cyano radical from the series Ci-C 4 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, phenyl and phenyl-Ci-C 2 alkyl stands, R is hydrogen or a radical optionally substituted by halogen or cyano radical from the series Ci-C 4 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, phenyl and phenyl-Ci-C 2 alkyl .
  • R 27 is hydrogen or C i-alkyl
  • R 26 is a radical from the group of hydrogen, Ci-C / i-alkyl, Ci-C i-haloalkyl, C 2 -C 4 alkenyl, C 2 - C 4 alkynyl, C 3 -C 6 cycloalkyl, C3- C 6 cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C 2 alkyl, Ci-C 6 - alkylsulfanyl, Ci-C6-Halogenalkylsulfanyl Ci-C6-alkylsulfinyl, Ci-C6-haloalkylsulfinyl, Ci- Ce-alkylsulfonyl, Ci-C4-alkylthio-Ci-C 2 alkyl, Ci-C 4 -Alkylsulfmyl-Ci-C 2 alkyl, C 1 -C4- alkylsulphonyl-Ci-C
  • G 1 is N or CB 1 ,
  • B 1 is a radical selected from the group consisting of hydrogen, halogen, C 1 -C 6 -alkyl and C 1 -C 4 -haloalkyl,
  • B 2 is a radical selected from the group consisting of hydrogen, halogen, C 1 -C 6 -alkyl and C 1 -C 4 -haloalkyl,
  • T oxygen or a pair of electrons
  • R 1 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl and C 1 -C 6 -alkoxy,
  • R 2 c is a radical of the formula
  • R 2 d is a radical of the formula
  • R 2 e for an F radical from the series (F-8), (F-10) and (F-11) wherein the dashed line represents the bond to the carbon atom of the bicycle of formula (I), or
  • R 2 f is a radical of the formula in which the dashed line denotes the bond to the carbon atom of the bicyclic compound of the formula (I),
  • X is oxygen or sulfur
  • X 2 is oxygen, sulfur or NOH
  • n is 1 or 2
  • R 3 is hydrogen or C 1 -C 6 -alkyl
  • R 4 is a radical from the group consisting of hydrogen, C 1 -C -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 6 -alkyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl , C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, aryl, aryl
  • Ci-C 4 -alkyl and hetaryl-Ci-C 4 -alkyl or
  • R 3 and R 4 together with the nitrogen atom to which they are attached, form a 4- to 7-membered ring containing one or two further nitrogen, oxygen and sulfur heteroatoms (where oxygen and sulfur atoms are not immediately adjacent may contain)
  • R 6 is hydrogen or C 1 -C 4 -alkyl
  • R 7 is a radical from the group consisting of hydrogen, C 1 -C -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 3 -C 4 cycloalkyl-Ci-C4-alkyl, Ci-C 4 alkoxy, halogen-Ci-C 4 - alkoxy, Ci-C4-alkoxy-Ci-C4-alkyl, Ci-C 4 - alkoxycarbonyl, Ci-C 4 alkoxycarbonyl-Ci-C4-alkyl, Ci-C alkylthio-Ci-C alkyl, aryl, aryl-C alkyl or hetaryl-Ci-C -alkyl, or
  • R 6 and R 7 together with the nitrogen atom to which they are attached, form a 4- to 7-membered ring containing one or two further nitrogen, oxygen and sulfur heteroatoms (with oxygen and sulfur atoms not being immediately adjacent may contain)
  • R 8 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 2 -C 6 -alkenyl, ci C6-alkoxy-Ci-C6-alkyl, in each case optionally substituted by halogen Ci-Cö-alkylcarbonyl and Ci-Cö-alkylsulfonyl, optionally substituted by halogen Ci-C6-alkoxycarbonyl and optionally by halogen, Ci-Cö-alkyl, Ci-C6 Alkoxy, C 1 -C 6 -haloalkyl and cyano-substituted C 3 -C 6 -cycloalkylcarbonyl, or represents a cation or an ammonium ion which
  • R 9 is a radical from the series in each case optionally substituted by halogen, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -haloalkylsulfinyl, C 1 -C 4 -alkyl -Cö-alkylsulfonyl and C 1 -C 6 -haloalkylsulfonyl-substituted C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl and C 2 -C 6 -alkynyl, each optionally substituted by halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkyl -
  • C6-cycloalkyl-Ci-C6-alkyl and C3-C6-cycloalkenyl in which a ring member by a heteroatom selected from the group sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen may be replaced (and in particular for
  • R 15 is a radical from the series each optionally substituted by methyl, cyano, carbamoyl, substituted C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl and C 2 -C 6 -alkynyl, each optionally substituted by methyl, trifluoromethyl, halogen, cyano or carbamoyl C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkyl-C 1 -C 2 -alkyl and C 3 -C 6 -cycloalkenyl in which the rings may contain at least one heteroatom selected from the group consisting of sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen in each case optionally by C 1 -C -alkyl, C 1 -C 4 -haloalkyl, C 1 -C -alkoxy, C 1 -C -haloalkoxy, C 1 -C 4 -alkylthio
  • R 8 and R 15 in the radical (C-6) together with the NS (0) n group to which they are attached can form a saturated or unsaturated and optionally substituted 4- to 8-membered ring, the one or two further heteroatoms from the series sulfur, oxygen (where oxygen and sulfur atoms may not be immediately adjacent) and contain nitrogen and / or at least one carbonyl group,
  • R 16 is a radical from the series hydrogen, in each case optionally substituted by methyl, cyano, carbamoyl or carboxyl-substituted C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 2 -C 4 -alkenyl and C 2 -C 4 -alkynyl, in each case optionally by halogen, Cyano, nitro, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -alkoxy, C 1 -C 4 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio, C 1 -C 6 -cycloalkyl Alkylsulfinyl, Ci-C6-haloalkylsulfinyl, Ci-C6-alkyls
  • R 2 is one of the radicals listed under f
  • a radical is selected from hydrogen, Ci-COE-alkyl, C 2 -C 6 haloalkyl, cyano-Ci-C6-alkyl, C 2 -C 4 alkenyl, C 2 -C i-haloalkenyl, C 2 -C 4 alkynyl, C 2 C 4 -haloalkynyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl optionally substituted by halogen, optionally bis-C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl substituted by halogen alkyl, optionally halogen-substit
  • Haloalkylsulfonyl amino, C 1 -C 6 -alkylamino, di- (C 1 -C 6 -alkyl) -amino, C 1 -C 6 -alkylcarbonylamino, C 1 -C 6 -alkoxycarbonylamino, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -alkyl-, haloalkoxy-Ci-Ce-alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, Cs-Ce-cycloalkyl-Ci-Ce-alkyl, Ci-C 6 - alkylcarbonyl, CI-C ⁇ - alkoxycarbonyl or Aminocarbonyl substituted hetaryl-C 1 -C 6 -alkyl, and, in the case where R 2 is one of the radicals listed under c),
  • X 1 is a radical from the series consisting of hydrogen, halogen, cyano, nitro, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy,
  • Y 3 is a radical selected from hydrogen, halogen, cyano, Ci-COE-alkyl, Ci-C6-haloalkyl, C3-Ce-cycloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, and NR 20 R 21 stands,
  • W is a radical from the series S, SO and SO2,
  • R 18 is a radical from the series consisting of hydrogen, hydroxyl, in each case optionally monosubstituted or polysubstituted by halogen or mono- or disubstituted by cyano, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkoxy-C 1 -C 4 - alkyl, Ci-C 6 alkyl-S-Ci-C4-alkyl, Ci-C 6 alkyl-S (0) -C C-4 alkyl, Ci-C 6 - alkyl-S (0) 2 - Ci-C4-alkyl, Ci-C6 alkylcarbonyl, Ci-C 6 alkoxycarbonyl, C 3 -C 6 cycloalkyl, C 3 -C 6 - cycloalkenyl, C3-C6-cycloalkyl-Ci-C3-alkyl, C3 C6-cycloalkenyl-C
  • R 19 represents hydrogen, an alkali or alkaline earth metal ion or an optionally monosubstituted to cis-C 4 -alkyl-substituted ammonium ion or an optionally mono- or polysubstituted by halogen or mono- or di-cyano-substituted radical from the series Ci-C 4 alkyl, Ci-C 4 alkoxy, Ci-C4-alkoxy-Ci-C4-alkyl, Ci-C4-alkyl-S-Ci-C4-alkyl, C1-C4 alkyl-S (0 ) -Ci-C 4 -alkyl and Ci-C 4 -alkyl-S (0) 2 -Ci-C 4 -alkyl, in the case that R 2 is one of the radicals listed under f)
  • R 22 also for one of the E radicals (E-1) to (E-11)
  • R is a radical from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxyl, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 2 -C -alkenyl, C 2 -C 6 Alkynyl, Cs-Ce-cycloalkyl (which is optionally substituted by halogen, cyano, Ci-C i-alkyl and C3-C6-cycloalkyl), C3-C6-cycloalkyl-Ci-C6-alkyl, Ci-C6-alkoxy, C 1 -C 6 -haloalkoxy, C 3 -C 6 -alkenyloxy, C 3 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 6 -alkylcarbonyloxy, C 2 -
  • R 21 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl Ci-Ce-alkyl, cyano-Ci-C 6 alkyl, C 6 - alkylcarbonyl, C 2 -C 6 alkenylcarbonyl, Ci-C6-haloalkylcarbonyl, C 2 -C6-
  • R 23 is a radical from the group of hydrogen, Ci-COE-alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C3-C6 cycloalkyl, C3-C6-cycloalkenyl, Ci-C6-alkoxy, C2- C 6 -alkenyloxy, C 2 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, C 2 -C 4 -alkenylthio-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 4 -alkoxy-C 1 -C 4 -alkyl, or, if R 2 is one of the radicals listed under f),
  • R 24 is hydrogen or a radical optionally substituted by halogen or cyano radical from the series Ci-C 4 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, phenyl and phenyl-Ci-C 2 alkyl stands,
  • R 25 is hydrogen or in each case optionally substituted by halogen or cyano radical from the series Ci-C 4 alkyl, C 2 -Ce-alkenyl, C 2 -C 6 -alkynyl, phenyl and phenyl-Ci-C 2 alkyl,
  • R 27 is hydrogen or C 1 -C 4 -alkyl
  • R 26 is a radical from the group of hydrogen, Ci-C 4 alkyl, Ci-C 4 haloalkyl, C 2 -C 4 alkenyl, C 2 - C 4 alkynyl, C 3 -C 6 cycloalkyl, C3- C 6 cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C 2 alkyl, Ci-C 6 - alkylsulfanyl, Ci-C6-Halogenalkylsulfanyl Ci-C6-alkylsulfinyl, Ci-C6-haloalkylsulfinyl, Ci- Ce-alkylsulfonyl, Ci-C4-alkylthio-Ci-C 2 alkyl, Ci-C 4 -Alkylsulfmyl-Ci-C 2 alkyl, C 1 -C4- alkylsulphonyl-Ci-C 2 alkyl,
  • B 2 is a radical selected from the group consisting of hydrogen, halogen, C 1 -C 6 -alkyl and C 1 -C -haloalkyl, Q is sulfur, R 1 is a radical selected from the group consisting of hydrogen, C 1 -C -alkyl and carbonyl.
  • C i-alkoxy, R 2 a) is a B radical from the series
  • R 2 c is a radical of the formula
  • R 23 is where the dashed line represents the bond to the carbon atom of the bicycle of formula (I), or e) for an F radical from the series (Fl), (F-8) and (F-10)
  • R 2 g is a radical of the formula in which the dashed line denotes the bond to the carbon atom of the bicyclic compound of the formula (I),
  • halogen is hydrogen or a radical from the series halogen, nitro, amino, cyano, C 1 -C 4 -alkylamino, halogeno-C 1 -C 4 -alkylamino, di (C 1 -C 4 -alkyl) amino, C 1 -C 4 -alkyl, halogen C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, halogeno-C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, halogenated C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, bis (C 1 -C 4 -alkyl) 4 -alkoxy) -Ci-C 4 -alkyl, bis (halo-C 1 -C 4 -alkoxy) C 1 -C 4 -alkyl, C 1 -C 4 -al
  • X I is a radical from the series consisting of hydrogen, fluorine, chlorine, bromine, iodine, cyano, nitro, C 1 -C 4 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -cycloalkyl, C 1 -C 4 -alkoxy and C 1 -C 4 -alkyl -C 4 haloalkoxy,
  • X 2 is oxygen, sulfur, NR 5 or NOH, n is 2,
  • R 3 is C 1 -C 4 -alkyl, a radical selected from the group consisting of hydrogen, C 1 -C -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 3 - C 6 -cycloalkyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl and C 1 -C 4 -alkyl 4- alkylthio-C 1 -C 4 -alkyl,
  • R 5 is a radical from the group of hydrogen, Ci-C 4 alkyl, halo-Ci-C4-alkyl, cyano-Ci-C 4 alkyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl , C 3 -C 6 cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C4-alkyl, Ci- C 4 alkoxycarbonyl, Ci-C 4 alkoxycarbonyl-Ci-C 4 alkyl and C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl,
  • R 6 is hydrogen or C 1 -C 4 -alkyl
  • R 7 is a radical from the group consisting of hydrogen, C 1 -C 4 -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 1 -C 4 -alkoxy, halogen -C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkylthio-Ci- -C 4 alkyl, aryl-Ci-C 4 - alkyl is or hetaryl-Ci-C4 alkyl, or
  • R 8 is a radical from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 2 -C 6 Alkenyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, in each case optionally halogen-substituted C 1 -C 6 -alkylcarbonyl and C 1 -C 6 -alkylsulfonyl, optionally C 1 -C 4 -alkoxycarbonyl which is substituted by halogen and optionally by halogen, C 1
  • R represents a radical from the series in each case optionally substituted by halogen, Ci-C4 alkoxy, C1-C4 haloalkoxy, Ci-C4-alkylthio, Ci-C4-haloalkylthio, Ci-C4 alkylsulfinyl, C1-C4 haloalkylsulfinyl, Ci-C4-alkylsulfonyl and Ci-C4-haloalkylsulfonyl-substituted C 1 -C 4 - alkyl, C 2 -C 4 alkenyl and C 2 -C 4 alkynyl each optionally substituted by halogen, Ci-C 4 - Alkyl,
  • R 8 and R 9 in the radical (Cl) and in the radical (Fl) can also be used together with the NS (0) n group to which they are attached, a saturated or unsaturated and optionally halogen, CI-C ⁇ -alkyl, Ci -Cö-haloalkyl, Ci-C 6 alkoxy, Ci-C6-haloalkoxy substituted 5- to 7-membered ring forming one or two heteroatoms selected from sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one and preferably contain exactly one carbonyl group, in particular R 8 and R 9 may together with the NS (0) n group to which they are attached, stand for a residue from the series
  • R 15 is a radical from the series each optionally substituted by methyl Ci-Cö-alkyl, C 2 -C 6 -alkenyl and C 2 -C 6 -alkynyl and each optionally substituted by methyl, halogen, cyano or carbamoyl substituted C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C2-alkyl and C3-C6-cycloalkenyl,
  • R 8 and R 15 in the radical (C-6) together with the NS (0) n group to which they are attached can form a saturated or unsaturated and optionally substituted 4- to 8-membered ring, the one or two further heteroatoms from the series sulfur, oxygen (where Oxygen and sulfur atoms may not be immediately adjacent) and may contain nitrogen and / or at least one carbonyl group, a radical from the series in each case optionally substituted by halogen, Ci-C i-alkoxy, C1-C4-haloalkoxy, Ci-C4-alkylthio , C 1 -C 4 -haloalkylthio, C 1 -C 4 -alkylsulfinyl, C 1 -C 4 -halogenoalkylsulfinyl, C 1 -C 4 -alkylsulfonyl and C 1 -C 4 -haloalkylsulfonyl-substituted C 1 -C 4
  • E-49 E-51 is, or, in the case that R 2 is one of the radicals listed under d)
  • R 23 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, C 1 -C 6 Alkoxy, C 2 -C 6 -alkenyloxy, C 2 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, C 2 -C 4 -alkenylthio-C 1 -C 4 -alkyl, cyano-ci- C 4 -alkyl and C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, or, in the case where R 2 is one of the radicals listed under c) or f),
  • R 27 is hydrogen or C 1 -C 4 -alkyl
  • R 26 is a radical from the group of hydrogen, Ci-C4-alkyl, Ci-C4-haloalkyl, C 2 -C 4 alkenyl, C 2 - C 4 alkynyl, C 3 -C 6 cycloalkyl, C 3 -C 6 - cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C 2 alkyl, C 1 -C4-
  • G 1 is N or CB 1 ,
  • B 1 is a radical selected from hydrogen, halogen, Ci-COE-alkyl and Ci-C i-haloalkyl
  • B 2 is a radical selected from hydrogen, halogen, Ci-COE-alkyl and Ci-C / i- Haloalkyl is
  • T oxygen or a pair of electrons
  • R 1 is a radical selected from the group consisting of hydrogen, C 1 -C -alkyl and C 1 -C -alkoxy,
  • R 2 d is a radical of the formula
  • X 2 is oxygen, sulfur or NOH, n is 2,
  • R 3 is C 1 -C 4 -alkyl
  • R 4 is a radical selected from the group consisting of hydrogen, C 1 -C -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 6 -alkyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl , C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl and C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, R 6 represents hydrogen or C 1 -C 4 -alkyl,
  • R 7 is a radical from the group consisting of hydrogen, C 1 -C 4 -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 1 -C 4 -alkoxy, halogen -C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkylthio-Ci- -C 4 alkyl, aryl-Ci-C 4 - alkyl or hetaryl-Ci-C 4 -alkyl, or R 6 and R 7 together with the nitrogen atom to which they are attached, a 4- to 7-membered ring
  • R 8 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 2 -C 6 -alkenyl, ci C6-alkoxy-Ci-C6-alkyl, in each case optionally substituted by halogen Ci-Cö-alkylcarbonyl and Ci-Cö-alkylsulfonyl, optionally substituted by halogen Ci-C6-alkoxycarbonyl and optionally by halogen, Ci-Cö-alkyl, Ci-C6 Alkoxy, Ci-C6-haloalkyl and cyano substituted C3-C6-cycloalkylcarbonyl, or represents a cation or an optionally substituted by Ci-Cö-alkyl or ary
  • R 8 and R 15 in the radical (C-6) together with the NS (0) n group to which they are attached form a saturated or unsaturated and optionally substituted 4- to 8-membered ring may contain one or two further heteroatoms selected from the group consisting of sulfur, oxygen (oxygen and sulfur atoms may not be immediately adjacent) and nitrogen and / or at least one carbonyl group; C 1 alkoxy, C 1 -C 4 haloalkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkylthio, C 1 -C 4 -alkylsulfinyl, C 1 -C 4 -haloalkylsulfinyl, C 1 -C 4 -alkylsulfonyl and C 1 -C 4 -haloalkylsulfonyl-substituted C 1 - C 4 -C 4 -alkyl, C 2 -C 4 -alkenyl
  • R 19 is hydrogen, an alkali or alkaline earth metal ion, an optionally monosubstituted to fourfold substituted by Ci-C 4 alkyl ammonium ion or a each optionally mono- or polysubstituted by halogen or mono- or cyano-double-substituted radical from the series Ci- C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 2 -alkyl, C 1 -C 4 -alkyl-S-C 1 -C 2 -alkyl, C 1 -C 4 -alkyl-S ( 0) -CC-C 2 -alkyl and C 1 -C 4 -alkyl-S (O) 2 -C 1 -C 2 -alkyl, or
  • R 23 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, C 1 -C 6 -alkoxy, C 2 -C 4 -cycloalkyl C 6 alkenyloxy, C 2 -C 6 alkynyloxy, C 3 -C 6 cycloalkyloxy, C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, C 2 -C 4 -alkenylthio-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl and C 1 -C 4 -alkyl C4-alkoxy-Ci-C 4 alkyl, or, when R 2 is one of the radicals listed under f
  • R 22 and R 23 may also together with the nitrogen atom to which they are attached form a saturated four- to six-membered ring which may contain another heteroatom from the series consisting of nitrogen, oxygen and sulfur,
  • R 27 is hydrogen or C 1 -C 4 -alkyl
  • R 26 is a radical from the group of hydrogen, Ci-C4-alkyl, Ci-C4-haloalkyl, C 2 -C 4 alkenyl, C 2 - C 4 alkynyl, C 3 -C 6 cycloalkyl, C 3 -C 6 - Cycloalkyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 2 -alkyl, C 1 -C 4 -alkylsulfanyl, C 1 -C 4 -haloalkylsulfanyl, C 1 -C 4 -alkylsulfinyl, C 1 -C 4 -haloalkylsulfinyl, C 4 alkylsulfonyl, Ci-C4-alkylthio-Ci-C 2 alkyl, Ci-C 4 -Alkylsulfmyl-Ci-C 2 alkyl, C 1 -C
  • R 1 is hydrogen
  • R 2 c is a radical of the formula
  • the dashed line represents the bond to the carbon atom of the bicycle of the formula (I), or f) a radical of the formula wherein the dotted line represents the bond to the carbon atom of the bicycle of the formula (I), or g) a radical of the formula in which the dashed line denotes the bond to the carbon atom of the bicyclic compound of the formula (I),
  • G 2 is hydrogen or a radical selected from halogen, nitro, amino, cyano, C 1 -C 4 -alkylamino, halogeno C 1 -C 4 -alkylamino, di (C 1 -C 4 -alkyl) amino, C 1 -C 4 -alkyl, halogen -C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, halogeno-C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, halogenated C 1 -C 4 -alkoxy-C 1 -C 4 -alkoxy alkyl, bis-C 4 -C (Ci-C 4 alkoxy) alkyl, bis-C 4 -C (halo-Ci-C4-alkoxy) alkyl, Ci-C4 alkoxy (Ci- C4 -alkylsulfanyl)
  • the dashed line represents the bond to the B-radicals, a radical from the series hydrogen, halogen, Ci-C 4 - alkyl and Ci-C 4 haloalkyl, represents oxygen, a radical from the series Is hydrogen, fluoro, chloro, bromo, cyano, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy and trifluoromethoxy, is oxygen, sulfur, NR 5 or NOH, is 2, NR 18 R 19 or any one of them once, twice, three times, four times or five times by fluorine, chlorine or mono- or disubstituted by cyano radical from the series Ci- C 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl, C 2 -alkoxy-Ci-C 2 alkyl, and Ci-C2 alkyl-S-Ci-C 2 - alkyl, Ci-C2 alkyl, Ci
  • R 3 is C 1 -C 4 -alkyl
  • R 4 is a radical from the series consisting of hydrogen, C 1 -C -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C3-C6 cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C4-alkyl, Ci- C 4 alkoxycarbonyl, Ci-C 4 Alkoxycarbonyl-C 1 -C 4 -alkyl and C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl,
  • R 5 is a radical from the group of hydrogen, Ci-C 4 alkyl, halo-Ci-C4-alkyl, cyano-Ci-C 4 alkyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl , C 3 -C 6 cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C4-alkyl, Ci- C 4 alkoxycarbonyl, Ci-C 4 alkoxycarbonyl-Ci-C 4 alkyl and C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl,
  • R 6 is hydrogen or C 1 -C 4 -alkyl
  • R 7 is a radical from the group consisting of hydrogen, C 1 -C 4 -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 1 -C 4 -alkoxy, halogen -C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkylthio-Ci- -C 4 alkyl, aryl-Ci-C 4 - alkyl is or hetaryl-Ci-C4 alkyl, or
  • R 6 and R 7 together with the nitrogen atom to which they are attached, form a 4- to 7-membered ring containing one or two further nitrogen, oxygen and sulfur heteroatoms (with oxygen and sulfur atoms not being immediately adjacent may contain)
  • R 8 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 2 -C 6 -alkenyl, ci C6-alkoxy-Ci-C6-alkyl, in each case optionally substituted by halogen Ci-Cö-alkylcarbonyl and Ci-Cö-alkylsulfonyl, optionally substituted by halogen Ci-C6-alkoxycarbonyl and optionally by halogen, Ci-Cö-alkyl, Ci-C6 alkoxy, Ci-C6-haloalkyl and cyano substituted C3-C6 cycloalkylcarbonyl group, or an optionally a cation or CI-C ⁇ - represents alkyl or
  • R represents a radical from the series in each case optionally substituted by halogen, Ci-C4 alkoxy, C1-C4 haloalkoxy, Ci-C4-alkylthio, Ci-C4-haloalkylthio, Ci-C4 alkylsulfinyl, C1-C4 Haloalkylsulfinyl, C 1 -C 4 -alkylsulfonyl and C 1 -C 4 -haloalkylsulfonyl-substituted C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl and C 2 -C 4 -alkynyl, each optionally substituted by halogen, C 1 -C 4 -alkyl, C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, substituted C 3 -C 6 -cycloalkyl, C 3 -C 6
  • R 8 and R 9 in the radical (Cl) and in the radical (Fl) can also be used together with the NS (0) n group to which they are attached, a saturated or unsaturated and optionally halogen, CI-C ⁇ -alkyl, Ci -Cö-haloalkyl, Ci-C 6 alkoxy, Ci-C6-haloalkoxy substituted 5- to 7-membered ring forming one or two heteroatoms selected from sulfur, oxygen (oxygen atoms may not be immediately adjacent) and nitrogen and / or at least one and preferably a carbonyl group may contain, in particular R 8 and R 9 may together with the NS (0) n group to which they are attached, stand for a residue from the series
  • R 27 is hydrogen or methyl and R 26 is a radical from the group consisting of hydrogen, methyl, 2,2,2-trifluoroethyl, 2,2-difluoroethyl, propenyl, propargyl, cyclopropyl, cyclopropylmethyl, methoxymethyl, methylsulfanyl, trifluoromethylsulfanyl, ethylsulfanyl, Trifluoroethylsulfanyl, methylsulfinyl,
  • G 1 is N or CB 1 ,
  • B 1 is a radical from the series hydrogen and fluorine
  • T oxygen or an electron pair
  • Q is sulfur
  • R 1 is hydrogen
  • G 2 is a radical from the group consisting of halogen, nitro, amino, cyano, C 1 -C 4 -alkylamino, halogeno C 1 -C 4 -alkylamino, di (C 1 -C 4 -alkyl) amino, halogeno C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, halogenated C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, bis (C 1 -C 4 -alkoxy) C 1 -C 4 -alkyl, bis (halogen-C 1 -C 4 -alkoxy) -C-C 4 alkyl, Ci-C4-alkoxy- (Ci-C4-alkylsulfanyl) -C-C 4 alkyl, Ci-C4-alkoxy- (Ci-C 4 - alkylsulfanyl
  • G 2 is also one of the following C radicals
  • R is where the dotted line represents the bond to the carbon atom of the bicyclic moiety of formula (I), or
  • X is oxygen
  • X 2 is oxygen
  • sulfur NOH
  • n 2
  • R 3 is C 1 -C 4 -alkyl
  • R 4 is a radical selected from the group consisting of hydrogen, C 1 -C -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 6 -alkyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl , C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkyl and C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl,
  • R 5 is a radical from the group of hydrogen, Ci-C 4 alkyl, halo-Ci-C4-alkyl, cyano-Ci-C 4 alkyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl , C 3 -C 6 cycloalkyl-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C4-alkyl, Ci- C 4 alkoxycarbonyl, Ci-C 4 alkoxycarbonyl-Ci-C 4 alkyl and C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl,
  • R 6 is hydrogen or C 1 -C 4 -alkyl
  • R 7 is a radical from the series consisting of hydrogen, C 1 -C 4 -alkyl, halogeno-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 2 -C 4 -alkyl, C 4 -alkynyl, C 1 -C 4 -alkoxy, halogeno-C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxycarbonyl, C 1 -C 4 -alkoxycarbonyl-C 1 -C 4 -alkoxy C 4 alkyl, Ci-C4-alkylthio-Ci-C 4 alkyl, aryl-Ci-C 4 - alkyl is or hetaryl-Ci-C4 alkyl, or
  • R 6 and R 7 together with the nitrogen atom to which they are attached, form a 4- to 7-membered ring containing one or two further nitrogen, oxygen and sulfur heteroatoms
  • R 8 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, cyano-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 2 -C 6 -alkenyl, ci C6-alkoxy-Ci-C6-alkyl, in each case optionally substituted by halogen Ci-Cö-alkylcarbonyl and Ci-Cö-alkylsulfonyl, optionally substituted by halogen Ci-C6-alkoxycarbonyl and optionally by
  • Ci-Cö-alkyl, Ci-C6-Alkoxy, Ci-C6-haloalkyl and Cyano substituted C3-C6-Cycloalkylcarbonyl stands, or for a cation or an optionally by Ci-Cö-alkyl or Aryl-Ci-Cö-alkyl substituted ammonium ion is, 1 ⁇
  • - 106 - is a radical from the series in each case optionally substituted by halogen, Ci-C i-alkoxy, C1-C4-haloalkoxy, Ci-C4-alkylthio, Ci-C4-haloalkylthio, Ci-C4-alkylsulfinyl, C1-C4-haloalkylsulfinyl , C 1 -C 4 -alkylsulfonyl and C 1 -C 4 -haloalkylsulfonyl-substituted C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl and C 2 -C 4 -alkynyl, each optionally substituted by halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkyl, Haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkoxy-sub
  • Alkyl a radical selected from the group consisting of hydrogen, hydroxyl, in each case optionally mono-, di-, tri-, tetra- or quintuple by fluorine, chlorine or mono- or di-cyano-substituted C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkyl-S-C 1 -C 2 -alkyl, C 1 -C 4 -alkyl-S (0) -CC-C 2 -alkyl, C 1 -C 4 -alkyl -C 4 alkyl-S (0) 2 -C-C 2 alkyl, Ci-C 4 alkylcarbonyl, C 1 -C4- alkoxycarbonyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C3-al
  • R is NR R, or for an in each case optionally monosubstituted, disubstituted, trisubstituted, tetrasubstituted or pentasubstituted by fluorine, chlorine or mono- or disubstituted by cyano radical from the series Ci- C 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl, Ci-C 2 alkoxy-Ci-C 2 alkyl, and Ci-C2 alkyl-S-Ci-C 2 - alkyl, Ci-C2 alkyl-S (0) -ci- C 2 -alkyl, C 1 -C 2 -alkyl-S (0) 2 -C 1 -C 2 -alkyl, for R 18 -CO-C 1 -C 2 -alkyl, for NR 18 R 19 -CO-C 1 -C 2 alkyl, optionally mono- or disubstituted by Ci-
  • X 1 is a radical from the series consisting of hydrogen, fluorine, chlorine, bromine, cyano, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy and trifluoromethoxy,
  • W is a radical from the series S, SO and S0 2 ,
  • Y 3 is a radical from the series consisting of hydrogen, fluorine, chlorine, bromine, cyano, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy and trifluoromethoxy, or
  • R 23 is a radical selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, C 1 -C 6 -alkoxy, C 2 -C 6 -alkoxy Alkenyloxy, C 2 -C 6 -alkynyloxy, C 3 -C 6 -cycloalkyloxy, C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, C 2 -C 4 -alkenylthio-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, C 1 -C 4 Alkoxy-Ci-C 4 -alkyl, or, if R 2 is one of the radicals listed under f)
  • R 22 and R 23 are also taken together with the nitrogen atom to which they are attached, for pyrrolidinyl, piperidinyl, morpholinyl, thiomorpholinyl, thiomorpholinyl-1-oxide, thiomorpholinyl-1,1-dioxide, piperazinyl, 1-methylpiperazinyl or 2-oxo l-methylpiperazinyl, R 27 is hydrogen or methyl and
  • R 26 is a radical from the group consisting of hydrogen, methyl, 2,2,2-trifluoroethyl, 2,2-difluoroethyl, propenyl, propargyl, cyclopropyl, cyclopropylmethyl, methoxymethyl, methylsulfanyl, trifluoromethylsulfanyl, ethylsulfanyl, trifluoroethylsulfanyl, methylsulfinyl,
  • Preferred Range (4) A preferred group of compounds of the formula (I) are those in which
  • G 1 stands for CB 1 ,
  • B 1 is hydrogen or fluorine
  • B 2 is hydrogen
  • T stands for a pair of electrons
  • Q stands for sulfur
  • R 1 is hydrogen
  • the dashed line represents the bond to the carbon atom of the bicycle of the formula (I), or f) a radical of the formula wherein the dotted line represents the bond to the carbon atom of the bicycle of the formula (I), or g) a radical of the formula in which the dashed line denotes the bond to the carbon atom of the bicyclic compound of the formula (I),
  • G 2 is hydrogen or a radical from the series Ci-C i-alkyl, halo-Ci-C i-alkyl and pyrimidyl,
  • G 3 is a radical selected from the group consisting of hydrogen, halogen and C 1 -C 1 -alkyl,
  • X I is a radical selected from the group consisting of hydrogen, fluorine, chlorine, bromine, methyl and ethyl,
  • R represents optionally mono-, di-, tri-, tetra- or quintuply fluorine-, chlorine-substituted Ci-C / i-alkyl
  • W is a radical from the series S, SO and SO2
  • R 23 is hydrogen or C 1 -C 6 -alkyl, or
  • R 22 and R 23 together with the nitrogen atom to which they are attached represent morpholinyl.
  • G 1 is N or CB 1 ,
  • B 1 is a radical selected from the group consisting of hydrogen and fluorine
  • B 2 is hydrogen
  • T stands for a pair of electrons
  • R 1 is hydrogen
  • G 2 is hydrogen or a radical from the series Ci-C i-alkyl, halo-Ci-C i-alkyl, Ci-C i-alkoxy, halo-Ci-C i-alkoxy, Ci-C4-alkylthio-Ci C4-alkyl, halogenated Ci-C4-alkylthio-Ci-C4-alkyl, Ci-C 4 alkylthio, Ci-C 4 -Alkylsulfmyl, Ci-C 4 alkylsulfonyl, Ci-C4-haloalkylthio, C1-C4 haloalkylsulfinyl , Ci-C4-haloalkylsulfonyl, or
  • R 2 c) is a radical of the formula
  • R is wherein the dotted line represents the bond to the carbon atom of the bicyclic moiety of formula (I), is oxygen, the D moiety
  • R is optionally substituted once, twice, three times, four times or five times by fluorine, chlorine or mono- or disubstituted cyano-substituted GC i-alkyl,
  • X 1 is hydrogen, methyl or fluorine,
  • W is a radical from the series S, SO and SO 2
  • Y 3 is hydrogen or methyl
  • R 23 is a radical from the series hydrogen and Ci-Cö-alkyl.
  • Cation an alkali metal ion selected from the series lithium, sodium, potassium, rubidium, cesium, preferably from the series lithium, sodium, potassium or a
  • Alkaline earth ion selected from the series beryllium, magnesium, calcium, strontium, barium, preferably from the series magnesium, calcium,
  • Halogen selected from the group fluorine, chlorine, bromine and iodine, preferably in turn from the series fluorine, chlorine and bromine, aryl (also part of a larger unit such as arylalkyl) selected from the series phenyl, naphthyl, anthryl, phenanthrenyl and stands again preferred for phenyl,
  • Hetaryl (equivalent to heteroaryl, also as part of a larger unit such as hetarylalkyl) selected from the series furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1, 2,4-triazolyl, oxazolyl, isoxazolyl , Thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-thiadiazolyl, 1, 2,4 Thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5- Thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1, 2,4-triazinyl, 1,3,5-triazinyl, benzof
  • Heterocyclyl a saturated 4-, 5- or 6-membered ring containing 1 or 2 nitrogen atoms and / or an oxygen atom and / or a sulfur atom, for example azetidinyl, azolidinyl, azinanyl, oxetanyl, oxolanyl, oxanyl, dioxanyl, thiethanyl, thiolanyl, thianyl , Tetrahydrofuryl, piperazinyl, morpholinyl.
  • the combination of which forms the preferred range (2) unless otherwise stated,
  • Alkaline earth ion selected from the series beryllium, magnesium, calcium, strontium, barium, preferably from the series magnesium, calcium,
  • Halogen selected from the group fluorine, chlorine, bromine and iodine, preferably again from the series fluorine, chlorine and bromine,
  • Aryl also as part of a larger unit, such as arylalkyl selected from the group phenyl, naphthyl, anthryl, phenanthrenyl and in turn preferably represents phenyl, hetaryl (equivalent to heteroaryl, also as part of a larger unit, such as hetarylalkyl) selected from of the series pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1, 2,4-triazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1, 2, 4-triazinyl, 1,3,5-triazinyl,
  • Heterocyclyl selected from azetidinyl, azolidinyl, azinanyl, oxetanyl, oxolanyl, oxanyl, dioxanyl, thiethanyl, thiolanyl, thianyl, tetrahydrofuryl, piperazinyl, morpholinyl.
  • Hetaryl (synonymous with heteroaryl, as part of a larger unit, such as hetarylalkyl) for a radical from the series pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, thiazolyl and pyrazolyl.
  • Halogen for fluorine, chlorine, bromine and iodine preferably again fluorine, chlorine and bromine.
  • Halogen is fluorine, chlorine, bromine or iodine, in particular fluorine, chlorine or bromine.
  • Saturated or unsaturated hydrocarbon radicals such as alkyl or alkenyl
  • heteroatoms e.g. in alkoxy, as far as possible, in each case straight-chain or branched.
  • optionally substituted radicals may be monosubstituted or polysubstituted, with multiple substituents the substituents being the same or different.
  • (A-a) is an electron pair, the remainder is as a pyridine derivative of the formula
  • (A-a) is oxygen, the remainder is a pyridine-N-oxide derivative of the formula
  • a preferred embodiment of the invention relates to compounds of the formula (I) in which A represents the radical of the formula (Aa)
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which A is pyridin-3-yl.
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which A is 5-fluoropyridin-3-yl.
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which A is pyrimidin-5-yl.
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which A is pyridazin-4-yl.
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 has the meanings listed under a).
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 has the meanings listed under b).
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 has the meanings listed under c).
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 has the meanings listed under d).
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 has the meanings listed under e).
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 has the meanings listed under f).
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 has the meanings listed under g).
  • a further preferred embodiment of the invention relates to compounds of the formula (I) in which R 2 is the radical (D-2)
  • radical definitions or explanations given above apply to the end products (also for the compounds of the formulas (IA) to (IP) listed below and correspondingly to the starting materials and intermediates.) These radical definitions can be used among one another, ie also between the respective Preferred areas, can be combined arbitrarily.
  • the invention relates to compounds of the formula (I-C)
  • the invention relates to compounds of the formula (ID)
  • the invention relates to compounds of the formula (I-E)
  • the invention relates to compounds of the formula (I-F)
  • the invention relates to compounds of the formula (I-G)
  • the invention relates to compounds of the formula (I-H)
  • the invention relates to compounds of the formula (II)
  • the invention relates to compounds of the formula (IJ)
  • the invention relates to compounds of the formula (IK)
  • the invention relates to compounds of the formula (III) _
  • the invention relates to compounds of the formula (I-N)
  • the invention relates to compounds of the formula (I-O)
  • the invention relates to compounds of the formula (IP)
  • the compounds of the formula (I) and their acid addition salts and metal salt complexes have good activity, in particular for combating animal pests, which include arthropods and in particular insects.
  • Suitable salts of the compounds of the general formula (I) may be customary non-toxic salts, ie salts with corresponding bases and salts with added acids.
  • salts with inorganic bases such as alkali metal salts, for example sodium, potassium or cesium salts, alkaline earth metal salts, for example calcium or magnesium salts, ammonium salts, salts with organic bases and with inorganic amines, for example triethylammonium, dicyclohexylammonium, ⁇ , ⁇ '- Dibenzylethylenediammonium, pyridinium, picolinium or ethanolammonium salts, salts with inorganic acids, for example hydrochlorides, hydrobromides, dihydrosulfates, trihydrosulfates, or phosphates, salts with organic carboxylic acids or organic sulfonic acid, for example formates, acetates, trifluoroacetates, maleates, tartrates, methanesul
  • the compounds of the formula (I) may also be present in different compositions as stereoisomers, ie as geometric and / or optical isomers or mixtures of isomers. Both the pure stereoisomers and any mixtures of these isomers are the subject of this invention, although in general only compounds of the formula (I) are mentioned here.
  • the invention therefore relates to both the pure enantiomers and diastereomers, as well as their mixtures for controlling animal pests, which include arthropods and in particular insects.
  • optically active stereoisomeric forms of the compounds of the formula (I) and salts thereof are used according to the invention.
  • the substituted anilines of the formula (Al-I) with activated carboxylic acids (for example as the carboxylic acid chloride or its hydrochloride) of the formula (AI-II) in the presence of basic reaction auxiliaries in a first reaction step to compounds of formula (AI -III ) are implemented. These are then by sulfur donors such. B. Lawesson's reagent to compounds of formula (AI -IV) thionated. In a third reaction step, these can then be cyclized in the presence of a suitable base, for example potassium carbonate, to give the compounds of the formula (I).
  • a suitable base for example potassium carbonate
  • Method A - Step 1 The compounds of the formula (Al-I) are known in some cases and are commercially available or can be prepared by methods known in principle (for example for R 1 HH, R 2 BrBr 4 -bromo-2 fluoraniline (see GB 2 065 654 A).
  • Suitable condensing agents are all condensing agents customarily used for such amidation reactions. Examples which may be mentioned are acid halide formers such as phosgene, phosphorus trichloride, oxalyl chloride or thionyl chloride; Carbodiimides such as NN-dicyclohexylcarbodiimide (DCC) and 1- (3-dimethylaminopropyl) -3-ethyl-carbodiimide (EDCI), or other conventional condensing agents such as phosphorus pentoxide, polyphosphoric acid, NN-carbonyldiimidazole, 2-chloropyridine 1-methiodide (Mukaiyamas reagent ), 2-ethoxy-N-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), triphenylphosphine / carbon tetrachloride, bromotripyrrolidino-phosphonium hexafluorophosphat
  • Suitable acid acceptors are all customary inorganic or organic bases, for example triethylamine, diisopropylethylamine, N-methylmorpholine or N, N-dimethylaminopyridine. If appropriate, process A according to the invention is carried out in the presence of a suitable reaction auxiliary, for example N, N-dimethylformamide or N, N-dimethylaminopyridine.
  • Suitable solvents or diluents are all inert organic solvents, for example aliphatic or aromatic hydrocarbons (such as petroleum ether, toluene), halogenated hydrocarbons (such as chlorotoluene, dichloromethane, chloroform, 1, 2-dichloroethane), ethers (such as diethyl ether, dioxane, tetrahydrofuran , 1, 2-dimethoxyethane), esters (such as ethyl acetate or methyl ester), nitrohydrocarbons (such as nitromethane, nitroethane, nitrobenzene), nitriles (such as acetonitrile, benzonitrile), amides (such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methylformanilide , N-methylpyrrolidone, hexamethylphosphoric triamide) and dimethyl sulfoxide or water or
  • LG COOR
  • R alkyl, aryl
  • chloroformates can be used, such.
  • diethylacetyl chloride, trimethylacetyl chloride and the like can be used therefor.
  • Method A - Step 2 The amide function of the carboxylic acid amides of type (AI-III) can be achieved by suitable sulfurization reagents, e.g. Lawesson's reagent or phosphorus (V) sulfide, with heating in a suitable solvent, e.g. As toluene or anisole, are converted into a thioamide function, whereby compounds of the type (AI -IV) are formed [cp. z. WO2013 / 33901 for 5-bromo-N- (2,6-difluorophenyl) -pyridine-3-carbothioamide]. Partial cyclization to the type of compound (I) can already take place in this type of reaction.
  • suitable sulfurization reagents e.g. Lawesson's reagent or phosphorus (V) sulfide
  • a suitable solvent e.g. As toluene or anisole
  • the compounds of the formula (I) can be prepared by methods known from the literature (cf., for example, WO2013 / 33901 for 2- (5-bromopyridin-3-yl) -4-fluoro-1, 3 benzothiazole)) by heating in a suitable solvent, e.g. For example, toluene or DMF, in the presence of a base such as. As sodium hydride or potassium carbonate, in the thiazoles of the formula (I) convert.
  • brominated benzothiazoles can be prepared with in situ generated substituted arylboronic acids or aryl boronic acid pinacol esters in the presence of coupling catalysts, such as tetrakis (triphenylphosphine) palladium (0) or 1,1'-bis (diphenylphosphino) ferrocene] dichloro-palladium (II), in the presence of a base such.
  • coupling catalysts such as tetrakis (triphenylphosphine) palladium (0) or 1,1'-bis (diphenylphosphino) ferrocene] dichloro-palladium (II)
  • a base such as sodium carbonate, in an inert organic solvent or diluent, for.
  • arylation As dioxane in combination with water, arylation (Method B), whereby carbon-linked compounds of the type (I-b) [cf.
  • the compounds of the formula (I-a) can first be converted by methods known from the literature into compounds of the type (I-h) which are then subsequently reacted with halogen-activated and optionally, further substituted heterocycles according to Reaction Scheme II (Method F) [cf. T. Ishiyama et al, J. Org. Chem., 1995, 60, 7508-7510; WO 2010/151601] continue to react in an inert organic solvent or diluent to give carbon-bonded compounds of the type (I-i).
  • Suitable coupling catalysts are palladium catalysts such as [1,1'-bis (diphenylphosphino) ferrocene] dichloropalladium (II)] or tetrakis (triphenylphosphine) palladium (O).
  • palladium catalysts such as [1,1'-bis (diphenylphosphino) ferrocene] dichloropalladium (II)] or tetrakis (triphenylphosphine) palladium (O).
  • the basic reaction auxiliaries for carrying out the processes according to Reaction Scheme II are preferably carbonates of sodium or potassium.
  • the solvents used are preferably nitriles, such as acetonitrile, benzonitrile, in particular acetonitrile, or ethers, such as diethyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane, in particular 1,2-dimethoxyethane in combination with water.
  • nitriles such as acetonitrile, benzonitrile, in particular acetonitrile
  • ethers such as diethyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane, in particular 1,2-dimethoxyethane in combination with water.
  • Method C By means of catalysis by suitable coupling catalysts, such as tris (dibenzylideneacetone) dipalladium (O) using suitable ligands, for.
  • suitable coupling catalysts such as tris (dibenzylideneacetone) dipalladium (O) using suitable ligands, for.
  • B. 2,2'-bis (diphenylphosphino) -l, l'binaphthyl (BINAP), and a base such as sodium tert-butoxide can be brominated benzothiazoles of the formula (Ia) in an inert organic solution or Diluents with optionally substituted aliphatic primary or secondary amines to give compounds of the type (Ic) or (Id) [cf. z.
  • Suitable solvents or diluents are all inert organic solvents, for example aliphatic or aromatic hydrocarbons. Preference is given to using aromatic hydrocarbons (for example toluene).
  • Method D With optionally substituted anilines, brominated benzothiazoles of the formula (I-a) react in an inert organic solvent or diluent to give the arylamino compounds of the formula (I-e) [cf. also Application Example 18]), preferably with catalysis by coupling catalysts such as palladium (II) diacetate in the presence of a base, for. B.
  • Suitable solvents or diluents are all inert organic solvents, for example aliphatic or aromatic hydrocarbons. Preference is given to using aromatic hydrocarbons (for example toluene).
  • Method E Heterocyclic amines, such as optionally substituted imidazoles, pyrazoles or triazoles, can be prepared on the basis of the method E shown in Reaction Scheme II [cf. WO 2008/130368] preferably in the presence of suitable catalysts such as copper (I) iodide, in the presence of basic ligands, for.
  • Suitable solvents or diluents are all inert organic solvents, for example aliphatic or aromatic hydrocarbons. Preference is given to using aromatic hydrocarbons (for example toluene), but also more polar solvents such as DMF.
  • Method G - Step 1 Compounds of the formula (I) in which R 2 is halogen, for example bromine or iodine, can be prepared by methods known from the literature using carbon monoxide and an alcohol, eg. As ethanol, with catalysis by suitable metal compounds such as (1,1'-bis (diphenylphosphino) ferrocene) palladium (II) dichloride, and in the presence of bases such as triethylamine, in suitable solvents such. B. the alcohol itself, THF and / or DMF, to the corresponding carboxylic acid esters (Ij) are reacted [see.
  • suitable metal compounds such as (1,1'-bis (diphenylphosphino) ferrocene) palladium (II) dichloride
  • bases such as triethylamine
  • Method G - Step 2 The compounds of the formula (I-j) can be prepared by means of suitable bases, such. As aqueous lithium hydroxide or sodium hydroxide solution, in suitable solvents or diluents, such as. As dioxane or THF, to compounds of formula (I-k) are reacted with free acid function.
  • suitable bases such as aqueous lithium hydroxide or sodium hydroxide solution
  • suitable solvents or diluents such as.
  • dioxane or THF to compounds of formula (I-k) are reacted with free acid function.
  • Method G - Steps 3 and 4 Compounds of the formula (I) in which R 2 is a radical from the series (Cl) to (C-9) (Type Im) or for CX-NR 22 R 23 (Type In)
  • R 2 is a radical from the series (Cl) to (C-9) (Type Im) or for CX-NR 22 R 23 (Type In)
  • compounds of formula (I) in which R 2 is a carboxyl group (type Ik) after appropriate activation (ie LG represents an optionally in situ generated nucleofuge leaving group "Leaving Group") can be prepared by well-known methods to be produced [cf. Method A, step 1].
  • Compounds of the formula (I) in which R 2 is a group of the formula -NR 23 -C (X) -R 22 can, for example, be prepared from compounds of the formula (I) in which R 2 is a group of the formula -NHR 23 , by N-acylation reaction using activated compounds of the formula LG-C (X) - R 22 , wherein LG is an optionally in situ generated nucleofuge leaving group, can be obtained.
  • LG Leaving group, z. B. halogen
  • Method III For example, compounds of the formula (I-o) can be obtained by Curtius degradation, as described in Houben-Weyl, Methods of Organic Chemistry, Volume XI / 1 (Georg Thieme Verlag Stuttgart), page 865.
  • the compounds of the formula (I-k) can react, for example, with diphenylphosphoryl azide (DPPA) in the presence of tert-butanol directly to compounds of the formula (I-o).
  • DPPA diphenylphosphoryl azide
  • the compounds of the formulas (Ip) can be obtained by N-alkylation in a first reaction step, N-deblocking (ie cleavage of the Boc group) in a second reaction step and subsequent N-acylation in a third reaction step receive.
  • the compounds of the formula (Iq) can be prepared by N-deblocking (ie cleavage of the Boc group) in a first reaction step and subsequent N-acylation in a second reaction step.
  • acidic or basic reaction auxiliaries can be used according to the literature procedure for the removal of the protective group.
  • carbamate-type protecting groups preference is given to using acidic reaction auxiliaries.
  • tert-butylcarbamate protective group for example, mixtures of mineral acids such as hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, phosphoric acid or of organic acids such as benzoic acid, formic acid, acetic acid, trifluoroacetic acid, methanesulfonic acid, Benzenesulfonic acid or toluenesulfonic acid in a suitable diluent such as water and / or an organic solvent such as tetrahydrofuran, dioxane, dichloromethane, chloroform, ethyl acetate, ethanol or methanol.
  • suitable diluent such as water and / or an organic solvent
  • the compounds of the types Ip or Iq can also be prepared from compounds synthesized according to method A by the method H2 described below:
  • RM reducing agent, z. Fe, Zn, Sn (II), sodium cyanoborohydride, hydrogen on Pd / C, etc.
  • LG Leaving group, e.g. B. Halogen or OH Method H2: Compounds prepared according to Method A in which R 2 is nitro (Ir) can be converted into the corresponding amino compounds (Is) by reduction of the nitro group by methods known from the literature (cf., for example, WO2009 / 14674 AI, 2009 for reduction by Fe (0); US2005 / 197331 AI, 2005 for reduction by Sn (II) C12; WO2007 / 86800 AI, 2007 for reduction by sodium cyanoborohydride).
  • Compounds of the formula (I) in which W is SO (sulfoxides) or SO 2 (sulfones) can be prepared by oxidation by literature methods from compounds of the formula (I) in which W is S (thioethers), for example by an oxidizing agent in a suitable solvent or diluent.
  • Suitable oxidizing agents are, for example, dilute nitric acid, hydrogen peroxide, Oxone® and peroxycarboxylic acids, such as wefa-chloroperbenzoic acid.
  • Suitable solvents or diluents are inert organic solvents, typically acetonitrile and halogenated solvents such as dichloromethane, chloroform or dichloroethane, and water and alcohols such as methanol for the reaction with Oxone®.
  • suitable anilines R'-NF or boronic acids R 1 -B (OH) 2 in which W is SO or SO 2 , according to method D D approaching. D.
  • Enantiomerically enriched sulfoxides can be prepared by a variety of methods as described by GE O'Mahony et al in ARKIVOC (Gainesville, FL, United states), 2011, 1, 1-110: metal-catalyzed asymmetric oxidations of thioethers, for example, with titanium or vanadium as the most commonly used catalyst sources, in the form of Ti (0'Pr4) or VO (acac) 2, together with a chiral ligand and an oxidizing agent such as tert-butyl hydrogen peroxide (TBHP), 2-phenylpropan-2-yl hydroperoxide (CHP ) or hydrogen peroxide; non-metal catalyzed asymmetric oxidations by using chiral oxidants or chiral catalysts; electrochemical or biological asymmetric oxidation as well as kinetic resolution of sulfoxides and nucleophilic displacement (according to Andersen's method).
  • TBHP tert-butyl hydrogen per
  • the enantiomers can also be obtained from the racemate, for example by preparative separation by means of a chiral HPLC. With the production methods described above, it is also possible to prepare those compounds in Table 1 which do not fall under the formula (I).
  • the compounds of the formula (I) can be present as geometrical and / or as optically active isomers or corresponding isomer mixtures 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.
  • the invention also relates to methods for controlling animal pests, in which compounds of the formula (I) are allowed to act on animal pests and / or their habitat. Preference is given to the control of animal pests in agriculture and forestry and in the protection of materials. Excluded therefor are preferably methods for the surgical or therapeutic treatment of the human or animal body and diagnostic methods that are performed on the human or animal body.
  • the invention further relates to the use of the compounds of the formula (I) as pesticides, in particular pesticides.
  • pest control always includes the term pesticides.
  • the compounds of the formula (I) are suitable for plant protection, favorable warm-blooded toxicity and good environmental compatibility for the protection of plants and plant organs from biotic and abiotic stress factors, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, Arachnids, helminths, nematodes and molluscs found in agriculture, horticulture, livestock, aquaculture, forestry, gardens and recreation, storage and materials protection and hygiene. They can preferably be used as pesticides. 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 of the genus Arthropoda in particular of the class Arachnida eg Acarus spp., Eg Acarus siro, Aceria kuko, Aceria sheldoni, Aculops spp., Aculus spp., Eg Aculus fockeui, Aculus badendali, Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., Eg Brevipalpus phoenicis, Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp., Eg Eotetranychus hi
  • Aulacorthum solani Bemisia tabaci, Blastopsylla occidentalis, Boreioglycaspis melaleucae, Brachycaudus helichrysi, Brachycolus spp., Brevicoryne brassicae, Cacopsylla spp.
  • Euphyllura spp., Euscelis bilobatus, Ferrisia spp., Geococcus coffeae, Glycaspis spp., Heteropsylla cubana, Heteropsylla spinulosa, Homalodisca coagulata, Hyalopterus arundinis, Hyalopterus pruni, Icerya spp., Eg Icerya purchasi, Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Eg Lecanium corni ( Parthenolecanium corni), Lepidosaphes spp., Eg Lepidosaphes ulmi, Lipaphis erysimi, Lycorma americanula, Macrosiphum spp., eg Macrosiphum euphorbiae, Macrosiphum lilii, Macrosi
  • Pemphigus spp. Eg Pemphigus bursarius, Pemphigus populivenae, Peregrinus maidis, Phenacoccus spp., Eg Phenacoccus madeirensis, Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., Eg Phylloxera devastatrix, Phylloxera notabilis, Pinnaspis aspidistrae, Planococcus spp., Eg Planococcus citri, Prosopidopsylla flava, Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., Eg Pseudococcus calceolariae, Pseudococcus comstocki, Pseudococcus longispinus, Pseudococcus maritimus, Pseu
  • Pseudaletia unipuncta Pseudoplusia includens, Pyrausta nubilalis, Rachiplusia nu, Schoenobius spp., eg Schoenobius bipunctifer, Scirpophaga spp., eg Scirpophaga innotata, Ontario segetum, Sesamia spp., eg Sesamia infe Spartoptera spp., Spodoptera spp., Spodoptera frugiperda, Spodoptera praefica, Stathmopoda spp., Stomopteryx subsecivella, Synanthedon spp., Tecia solanivora, Thermesia gemmatalis, Tinea cloacella, Tinea pellionella, Tineola bisselliella, Tortrix spp., Trichophaga tapetzella, Trichoplusia spp.,
  • Ctenolepisma spp. Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica; from the class of Symphyla eg Scutigerella spp., eg Scutigerella immaculata;
  • Pests of the Mollusca strain in particular of the bivalve class, e.g. Dreissena spp .; and from the class of Gastropoda e.g. Arion spp., E.g. Arion ater rufus, Biomphalaria spp., Bulinus spp., Deroceras spp., E.g. Deroceras laeve, Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp .;
  • Animal and human parasites from the strains of Platyhelminthes and Nematoda e.g. Aelurostrongylus spp., Amidostomum spp., Ancylostoma spp, Angiostrongylus spp., Anisakis spp., Anoplocephala spp., Ascaris spp., Ascaridia spp., Baylisascaris spp., Brugia spp., Bunostomum spp., Capillaria spp., Chabertia spp.
  • Clonorchis spp. Cooperia spp., Crenosoma spp., Cyathostoma spp., Dicrocoelium spp., Dictyocaulus spp., Diphyllobothrium spp., Dipylidium spp., Dirofilaria spp., Dracunculus spp., Echinococcus spp., Echinostoma spp., Enterobius spp., Eucoleus spp., Fasciola spp., Fascioloides spp., Fasciolopsis spp., Filaroides spp., Gongylonema spp., Gyrodactylus spp., Habronema spp., Haemonchus spp., Heligmosomoides spp., Heterakis spp., Hymenolepis spp.
  • Hyostrongylus spp. Litomosoides spp., Loa spp., Metastrongylus spp., Metorchis spp., Mesocestoides spp., Moniezia spp., Muellerius spp., Necator spp., Nematodirus spp., Nippostrongylus spp., Oesophagostomum spp., Ollulanus spp., Onchocerca spp, Opisthorchis spp., Oslerus spp., Ostertagia spp., Oxyuris spp., Paracapillaria sp Paraglia spp., Paragonimus spp., Paramphistomum spp., Paranoplocephala spp., Parascaris spp., Passalurus spp., Protostrongylus spp., Schistosoma s
  • Strongyloides spp. Strongylus spp., Syngamus spp., Taenia spp., Teladorsagia spp., Thelazia spp., Toxascaris spp., Toxocara spp., Trichinella spp., Trichobilharzia spp., Trichostrongylus spp., Trichuris spp., Uncinaria spp., Wuchereria spp .;
  • Plant pests from the Nematoda strain ie plant parasitic nematodes, in particular Aglenchus spp., Eg Aglenchus agricola, Anguina spp., Eg Anguina tritici, Aphelenchoides spp., Eg Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimus spp., Eg Belonolaimus gracilis, Belonolaimus longicaudatus, Belonolaimus nortoni, Bursaphelenchus spp., Eg Bursaphelenchus cocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus, Cacopaurus spp., Eg Cacopaurus pestis, Criconemella spp., eg Criconemella curvata, Criconemella onoensis, Criconemella omat
  • the compounds of the formula (I) may optionally also be used in certain concentrations or application rates as herbicides, safeners, growth regulators or agents for improving plant properties, as microbicides or gametocides, for example as fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as a remedy for MLO (Mycoplasma-like-organism) and RLO (Rickettsia-like-organism). If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
  • the present invention further relates to formulations and application forms prepared therefrom as pesticides such.
  • B. drench, drip and spray liquors comprising at least one compound of formula (I).
  • the use forms contain other pesticides and / or the effect of improving adjuvants such as Penetrationsforderer, z.
  • vegetative oils such as rapeseed oil, sunflower oil, mineral oils such as paraffin oils, alkyl esters of vegetable fatty acids such as rapeseed oil or soybean oil or alkanol alkoxylates and / or spreading agents such as alkyl siloxanes and / or salts such as organic or inorganic ammonium or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate and / or retention-demanding agents such as.
  • dioctylsulfosuccinate or hydroxypropyl guar polymers and / or humectants such as glycerol and / or fertilizers such as ammonium, potassium or phosphorus-containing fertilizer.
  • Typical formulations are, for example, water-soluble liquids (SL), emulsion concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS). ;
  • SL water-soluble liquids
  • EC emulsion concentrates
  • EW emulsions in water
  • SC suspension concentrates
  • SC SE, SE, FS, OD
  • WG water-dispersible granules
  • GR granules
  • CS capsule concentrates
  • the formulations contain, in addition to one or more compounds of the formula (I), further agrochemical active substances.
  • adjuvants such as extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, antifreeze agents, biocides, thickeners and / or further adjuvants such as 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.
  • 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 compounds of the formula (I) with auxiliaries, such as, for example, extenders, solvents and / or solid carriers and / or further auxiliaries, for example surface-active substances.
  • auxiliaries such as, for example, extenders, solvents and / or solid carriers and / or further auxiliaries, for example surface-active substances.
  • 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 the formulation of the compounds of the formula (I) or the use forms prepared from these formulations (such as, for example, ready-to-use pesticides such as spray liquors or seed dressings), such as certain physical, technical and / or biological properties To give 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 N-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
  • organic solvents can also be used as auxiliary solvents.
  • Suitable liquid solvents are essentially: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic Hydrocarbons such as chlorobenzenes, chloroethylene or methylene chloride, aliphatic 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, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
  • Suitable solvents are, for example, aromatic hydrocarbons, e.g. Xylene, toluene or alkylnaphthalenes, chlorinated aromatic or aliphatic hydrocarbons, e.g. 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. Acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strong polar solvents such as dimethyl sulfoxide and water.
  • aromatic hydrocarbons e.g. Xylene, toluene or alkylnaphthalenes
  • chlorinated aromatic or aliphatic hydrocarbons e
  • Suitable carriers are, in particular: 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.
  • Cracked and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, paper, coconut shells, corn cobs and tobacco stems.
  • 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 alkyltaurates), 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, alkyl sulphates , Arylsulfonates, protein hydrolys
  • dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • inorganic pigments e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • Stabilizers such as cold stabilizers, preservatives, antioxidants, light stabilizers or other chemical and / or physical stability-improving agents may also be present. It may also contain foam-forming agents or defoamers.
  • the formulations and the use forms derived therefrom may also contain, as additional auxiliaries, adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-containing 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.
  • further auxiliaries may be present in the formulations and in the use forms derived therefrom.
  • Such additives are, for example, fragrances, protective colloids, binders, adhesives, thickeners, thixotropic substances, penetration promoters, retention promoters, stabilizers, sequestrants, complexing agents, humectants, spreading agents.
  • the compounds of formula (I) may 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 dioctylsulfosuccinate or increase the visco-elasticity such as hydroxypropyl guar polymers.
  • Penetration promoters in the present context include 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 coconut oil ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters such as rapeseed oil or soybean oil, fatty amine alkoxylates such as for example Tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate.
  • alcohol alkoxylates such as coconut oil ethoxylate (10) or isotridecyl ethoxylate (12)
  • fatty acid esters such as rapeseed oil or soybean oil
  • fatty amine alkoxylates such as for example 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 the compound of formula (I), more preferably between 0.01 and 95 wt .-% of the compound of formula (I), most preferably between 0.5 and 90% by weight of the compound of formula (I), based on the weight of the formulation.
  • the content of the compound of the formula (I) in the forms of application prepared from the formulations (in particular pesticides) can vary within wide ranges.
  • the concentration of the compound of the formula (I) in the use forms may usually be between 0.00000001 and 95% by weight of the compound of the formula (I), preferably between 0.00001 and 1% by weight, based on the weight of the application form , lie.
  • the application is done in a custom forms adapted to the application.
  • the compounds of formula (I) may also be used in admixture with one or more suitable fungicides, bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficials, herbicides, fertilizers, avian repellents, phytotonics, sterilants, safeners, semiochemicals and / or plant growth regulators be, for example to widen the spectrum of action, to extend the duration of action, to increase the speed of action, to prevent re-exposure or to prevent the development of resistance.
  • suitable fungicides bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficials, herbicides, fertilizers, avian repellents, phytotonics, sterilants, safeners, semiochemicals and / or plant growth regulators
  • suitable fungicides bactericides, acaricides, molluscicides, ne
  • the compounds of the formula (I) may be present in admixture with other active substances or semiochemicals such as attractants and / or avian repellents and / or plant activators and / or growth regulators and / or fertilizers.
  • the compounds of the formula (I) can be used in mixtures with agents for improving plant properties such as, for example, growth, yield and quality of the crop.
  • the compounds of the formula (I) are present in formulations or in the formulations prepared from these formulations in admixture with other compounds, preferably those as described below. If one of the following compounds can occur in different tautomeric forms, these forms are also included, even if they were not explicitly mentioned in each case.
  • Insecticides / Acaricides / Nematicides The active substances mentioned here with their "common name” are known and described, for example, in the Pesticide Handbook ("The Pesticide Manual” 16th ed., British Crop Protection Council 2012) or searchable on the Internet (eg http: // www. alanwood.net/pesticides).
  • Acetylcholinesterase (AChE) inhibitors such as carbamates, e.g. Alanycarb, Aldicarb, Bendiocarb, Benfuracarb, Butocarboxime, Butoxycarboxime, Carbaryl, Carbofuran, Carbosulfan, Ethiofencarb, Fenobucarb, Formetanate, Furathiocarb, Isoprocarb, Methiocarb, Methomyl, Metolcarb, Oxamyl, Pirimicarb, Propoxur, Thiodicarb, Thiofanox, Triazamate, Trimethacarb, XMC and Xylylcarb or organophosphates, eg Acephate, Azamethiphos, Azinophos-ethyl, Azinophos-methyl, Cadusafos, Chloroethoxyfos, Chlorfenvinphos, Chlormephos, Chlorpyrifos,
  • GABA-controlled chloride channel antagonists such as cyclodiene organochlorines, e.g. Chlordanes and endosulfan or phenylpyrazoles (fiproles), e.g. Ethiprole and fipronil.
  • sodium channel modulators / voltage dependent sodium channel blockers such as pyrethroids, e.g. Acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin,
  • Bioallethrin S-cyclopentenyl isomer bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(lR) trans isomers], deltamethrin, empenthrin [(EZ) (lR) isomers], esfenvalerates, etofenprox, fenpropathrin, fenvalerates, flucythrinates, flumethrin, tau-fluvalinates, halfenprox, imiprothrin, kadethrin, permethrin, phen
  • nicotinergic acetylcholine receptor (nAChR) agonists such as neonicotinoids, eg acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam or nicotine or sulfoxaflor or flupyradifurone.
  • nAChR nicotinergic acetylcholine receptor
  • nicotinergic acetylcholine receptor (nAChR) allosteric activators such as spinosines, e.g. Spinetoram and spinosad.
  • chloride channel activators such as avermectins / milbemycins, e.g. Abamectin, Emamectin benzoate, Lepimectin and Milbemectin.
  • Juvenile hormone mimics such as juvenile hormone analogs, e.g. Hydroprene, Kinoprene and Methoprene or Fenoxycarb or Pyriproxyfen.
  • Juvenile hormone mimics such as juvenile hormone analogs, e.g. Hydroprene, Kinoprene and Methoprene or Fenoxycarb or Pyriproxyfen.
  • agents with unknown or non-specific mechanisms of action such as
  • Alkyl halides e.g. Methyl bromide and other alkyl halides; or chloropicrin or sulfuryl fluoride or borax or tartar emetic.
  • mite growth inhibitors e.g. Clofentezine, hexythiazox and diflovidazine or etoxazole.
  • Insect intestinal membrane microbial disruptors e.g. Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis and BT plant proteins: CrylAb, CrylAc, CrylFa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, Cry34 / 35Abl.
  • oxidative phosphorylation inhibitors such as diafenthiuron or organotin compounds, e.g. Azocyclotin, Cyhexatin and fenbutatin oxide or propargite or
  • Nicotinergic acetylcholine receptor antagonists such as Bensultap, Cartap hydrochloride, Thiocyclam and Thiosultap sodium.
  • Type 0 inhibitors of chitin biosynthesis such as bistrifluron, chlorofluorazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron.
  • inhibitors of chitin biosynthesis type 1, such as buprofezin.
  • Moulting inhibitors especially in dipterans, ie tails), such as Cyromazine.
  • ecdysone receptor agonists such as chromafenozides, halofenozides, methoxyfenozides, and tebufenozides.
  • Octopaminergic agonists such as amitraz.
  • Complex III electron transport inhibitors such as, for example, hydramethylnone or acequinocyl or fluacrypyrim.
  • (21) complex I electron transport inhibitors for example, METI acaricides, e.g. Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad and Tolfenpyrad or Rotenone (Derris).
  • METI acaricides e.g. Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad and Tolfenpyrad or Rotenone (Derris).
  • (22) voltage dependent sodium channel blockers e.g. Indoxacarb or metaflumizone.
  • complex IV electron transport inhibitors such as phosphines, e.g. Aluminum phosphide, calcium phosphide, phosphine and zinc phosphide or cyanide.
  • Complex II electron transport inhibitors such as cyenopyrafen and cyflumetofen.
  • ryanodine receptor effectors such as diamides, e.g. Chlorantraniliprole, Cyantraniliprole and Flubendiamide.
  • drugs with unknown or ambiguous mechanism of action such as afidopyropene, afoxolaner, azadirachtin, benclothiaz, benzoximate, bifenazate, bromopropylate, quinomethionate, cryolites, cyclaniliprole, cycloxapride, cyhalodiamide dicloromezotiaz, dicofol, diflovidazine, flometoquine, fluensulfone, flufenerim, flufenoxystrobin, flufiprole, Flaxxafon, Fluopyram, Fluralaner, Fufenozide, Guadipyr, Heptafluthrin, Imidaclothiz, Iprodione, Meperfluthrin, Paichongding, Pyflubumide, Pyralidyl, Pyrifluquinazone, Pyriminostrobin, Tetramethylfluthrin
  • All listed fungicidal mixing partners of classes (1) to (15) can optionally form salts with corresponding bases or acids, provided that suitable functional groups are present. Furthermore tautomeric forms are also included for the listed five-membered hybrids of classes (1) to (15), provided that tautomerism is possible.
  • inhibitors of ergosterol biosynthesis for example (1.01) aldimorph, (1.02) azaconazole, (1.03) bitertanol, (1.04) bromuconazole, (1.05) cyproconazole, (1.06) diclobutrazole, (1.07) difenoconazole, (1.08) diniconazole, (1.09 ) Dinemonazole-M, (1.10) dodemorph, (1.11) dodemorphoacetate, (1.12) epoxiconazole, (1.13) etaconazole, (1.14) fenarimol, (1.15) fenbuconazole, (1.16) fenhexamid, (1.17) fenpropidin, (1.18) fenpropimorph, (1.19) fluquinconazole, (1.20) flurprimidol, (1.21) flusilazole, (1.22) flutriafol, (1.23) furconazole, (1.24) furconazole-cis,
  • inhibitors of mitosis and cell division for example (4.01) benomyl, (4.02) carbendazim, (4.03) chlorfenazole, (4.04) diethofencarb, (4.05) ethaboxam, (4.06) fluopicolide, (4.07) fuberidazole, (4.08) pencycuron, (4.09) thiabendazole, (4.10) thiophanate-methyl, (4.11) thiophanate, (4.12) zoxamide, (4.13) 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2A (4.14) 3-
  • inhibitors of amino acid and / or protein biosynthesis for example (7.01) andoprim, (7.02) blasticidin-S, (7.03) cyprodinil, (7.04) kasugamycin, (7.05) kasugamycin hydrochloride hydrate, (7.06) Mepanipyrim, (7.07) pyrimethanil, (7.08) 3- (5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl) quinoline, (7.09) oxytetracycline, (7.10) streptomycin.
  • inhibitors of ATP production for example (8.01) fentin acetate, (8.02) fentin chloride, (8.03) fentin hydroxide, (8.04) silthiofam.
  • inhibitors of cell wall synthesis for example (9.01) benthi- avalicarb, (9.02) dimethomorph, (9.03) flumorph, (9.04) iprovalicarb, (9.05) mandipropamide, (9.06) polyoxines, (9.07) polyoxorim, (9.08) validamycin A, ( 9.09) Valifenalate, (9.10) Polyoxin B, (9.11) (2E) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop -2-en-1-one, (9.12) (2Z) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4
  • inhibitors of lipid and membrane synthesis for example (10.01) biphenyl, (10.02) chloroneb, (10.03) diclorane, (10.04) edifenphos, (10.05) etridiazole, (10.06) iodocarb, (10.07) Iprobenfos, (10.08) isoprothiolane , (10.09) Propamocarb, (10.10) Propamocarb hydrochloride, (10.11) Prothiocarb, (10.12) Pyrazophos, (10.13) Quintozene, (10.14) Tecnazene, (10.15) Tolclofos-methyl.
  • inhibitors of melanin biosynthesis for example (11.01) carpropamide, (11.02) diclocymet, (1.03) fenoxanil, (11.04) phthalide, (11.05) pyroquilone, (11.06) tricyclazole, (11.07) 2,2,2-trifluoroethyl
  • inhibitors of signal mediation for example (13.01) chlozolinate, (13.02) fenpiclonil, (13.03) fludioxonil, (13.04) iprodione, (13.05) procymidone, (13.06) quinoxyfen, (13.07) vinclozoline, (13.08) proquinazide.
  • the compounds of formula (I) may be combined with biological pesticides.
  • biological pesticides include, in particular, bacteria, fungi, yeasts, plant extracts, and those products formed by microorganisms, including proteins and secondary metabolites.
  • Biological pesticides include bacteria such as spore-forming bacteria, root-colonizing bacteria and bacteria that act as biological insecticides, fungicides or nematicides.
  • Bacillus amyloliquefaciens strain FZB42 (DSM 231179), or Bacillus cereus, in particular B. cereus strain CNCM 1-1562 or Bacillus firmus, strain 1-1582 (Accession number CNCM 1-1582) or Bacillus pumilus, especially strain GB34 (Accession no. ATCC 700814) and strain QST2808 (Accession No. NRRL B-30087), or Bacillus subtilis, especially strain GB03 (Accession No. ATCC SD-1397), or Bacillus subtilis strain QST713 (Accession No. NRRL B-21661) or Bacillus subtilis Strain OST 30002 (Accession No.
  • NRRL B-50421 Bacillus thuringiensis, in particular B. thuringiensis subspecies israelensis (serotype H-14), strain AM65-52 (Accession No. ATCC 1276), or B. thuringiensis subsp. aizawai, in particular strain ABTS-1857 (SD-1372), or B. thuringiensis subsp. kurstaki strain HD-1, or B. thuringiensis subsp. tenebrionis strain NB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp.
  • fungi and yeasts which can be used as biological pesticides are:
  • Beauveria bassiana especially strain ATCC 74040, coniothyrium minitans, in particular strain CON / M / 91-8 (Accession No. DSM-9660), Lecanicillium spp., In particular strain HRO LEC 12, Lecanicillium lecanii, (formerly known as Verticillium lecanii), in particular strain KV01, Metarhizium anisopliae, in particular strain F52 (DSM3884 / ATCC 90448), Metschnikowia fructicola, in particular strain NRRL Y-30752, Paecilomyces fumosoroseus (new: Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka 97 (Accesion No.
  • Paecilomyces lilacinus in particular P. lilacinus strain 251 (AGAL 89/030550), Talaromyces flavus, in particular strain VI 17b, Trichoderma atroviride, in particular strain SCI (Accession Number CBS 122089), Trichoderma harzianum, in particular T. harzianum rifai T39. (Accession Number CNCM 1-952).
  • viruses that can be used or used as biological pesticides are: Adoxophyes orana (Apple peel winder) Granulosis virus (GV), Cydia pomonella (codling moth) Granulosis virus (GV), Helicoverpa armigera (cotton bollworm) Nuclear polyhedrosis virus (NPV), Spodoptera exigua (mNPV), Spodoptera frugiperda (armyworm) mNPV, Spodoptera littoralis (African Cotton worm) NPV. It also includes bacteria and fungi that are added as 'inoculant' plants or parts of plants or plant organs and promote by their special properties, plant growth and plant health. Examples are:
  • Agrobacterium spp. Azorhizobium caulinodans, Azospirillum spp., Azotobacter spp., Bradyrhizobium spp., Burkholderia spp., In particular Burkholderia cepacia (formerly known as Pseudomonas cepacia), Gigaspora spp., Or Gigaspora monosporum, Glomus spp., Laccaria spp.
  • plant extracts and those products formed by microorganisms, including proteins and secondary metabolites, which can be used as biological pesticides are:
  • the compounds of the formula (I) can be combined with safeners, for example Benoxacor, Cloquintocet (-mexyl), Cyometrinil, Cyprosulfamide, Dichlormid, Fenchlorazole (-ethyl), Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen (-ethyl), Mefenpyr (-diethyl), naphthalic anhydride, oxabetrinil, 2-methoxy-N - ( ⁇ 4 - [(methylcarbamoyl) amino] phenyl ⁇ sulfonyl) benzamide (CAS 129531-12-0), 4- (dichloroacetyl) -l-oxa 4-azaspiro [4.5] decane (CAS 71526-07-3), 2,2,5-trimethyl-3- (dichloroacetyl) -l, 3-oxazolidine (CAS 52836-31-4). Plants and plant
  • plants are understood as meaning all plants and plant populations, such as desired and undesired ones Wild plants or crops (including naturally occurring crops), for example cereals (wheat, rice, triticale, barley, rye, oats), corn, soybean, potato, sugar beets, sugar cane, tomatoes, peas and other vegetables, cotton, tobacco, rapeseed, and Fruit plants (with the fruits apples, pears, citrus fruits and grapes).
  • 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 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.
  • the treatment according to the invention of the plants and plant parts with the compounds of the formula (I) is carried out directly or by acting on their environment, habitat or storage room according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, nebulizing, spreading, spreading, indexing and in the case of nutrient material, in particular in the case of seeds, by further single or multi-layered sheathing.
  • plants and their parts can be treated according to the invention.
  • 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.
  • the preferred plants or plant cultivars to be treated according to the invention which are to be treated include all plants which, as a result of the gene-technological modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits"). Examples of such properties are better plant growth, increased Tolerance to high or low temperatures, increased tolerance to dryness or to water or soil salinity, increased flowering efficiency, easier harvest, 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 harvest products.
  • Such properties are an increased resistance of the plants against animal and microbial pests, such as insects, arachnids, nematodes, mites, snails, caused for example by toxins formed in the plants, in particular those caused 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 their combinations) are produced in the plants, also an increased resistance of the plants against Phytopathogenic fungi, bacteria and / or viruses, eg by systemically acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins, and increased tolerance of the plants against certain herbicidal active ingredients, such as imidazolinones, sulfonylureas, glyphosate or phosphinotric
  • transgenic plants are the important crops such as cereals (wheat, rice, triticale, barley, rye, oats), corn, soy, potato, sugar beets, sugarcane, 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 corn, soy, wheat, rice, potato, cotton, sugar cane, tobacco and oilseed rape. Traits that are particularly emphasized are the increased resistance of the plants to insects, arachnids, nematodes and snails.
  • the treatment of the plants and plant parts with the compounds of formula (I) 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, atomising, atomizing, sprinkling, foaming, brushing, spreading, injecting, pouring, drip irrigation and propagating material, in particular in the case of seeds further by dry pickling, wet pickling, slurry pickling, encrusting, single or multi-layer coating, etc. It is also possible to dispense the compounds of formula (I) by the ultra-low-volume method or the use form or the compound of formula ( I) inject myself into the soil.
  • a preferred direct treatment of the plants is foliar application, ie compounds of the formula (I) are applied to the foliage, wherein the treatment frequency and the application rate should be adjusted to the infestation pressure of the respective pest.
  • the compounds of the formula (I) also enter the plants via the root system. The treatment of the plants is then carried out by the action of the compounds of formula (I) on the habitat of the plant.
  • the present invention therefore more particularly relates to a method of protecting seed and germinating plants from attack by pests by treating the seed with one of the compounds of formula (I).
  • the method according to the invention for the protection of seeds and germinating plants from infestation by pests further comprises a method in which the seed is treated simultaneously in one operation or sequentially with a compound of formula (I) and mixing partner. It also also includes a method in which the seed is treated at different times with a compound of formula (I) and mixing partner.
  • the invention also relates to the use of the compounds of the formula (I) for the treatment of seed for the protection of the seed and the resulting plant from animal pests. Furthermore, the invention relates to seed which has been treated for protection against animal pests with a compound of formula (I). The invention also relates to seed treated at the same time with a compound of formula (I) and mixing partner. The invention further relates to seed which has been treated at different times with a compound of formula (I) and mixing partner. In the case of seed which has been treated at different times with a compound of formula (I) and mixing partner, the individual substances may be contained in different layers on the seed. In this case, the layers which comprise a compound of the formula (I) and mixture partners may optionally be separated by an intermediate layer. The invention also relates to seed in which a compound of the formula (I) and mixing partner are applied as a constituent of a coating or as a further layer or further layers in addition to a coating.
  • the invention relates to seed which, after treatment with a compound of the formula (I), is subjected to a film coating process in order to avoid dust abrasion on the seed.
  • a compound of the formula (I) acts systemically is that the treatment of the seed protects not only the seed itself, but also the resulting plants after emergence from animal pests. In this way, the immediate treatment of the culture at the time of sowing or shortly afterwards can be omitted.
  • Another advantage is the fact that by treating the seed with a compound of formula (I) germination and emergence of the treated seed can be promoted.
  • Compounds of formula (I) may also be used in combination with signal technology agents whereby better colonization with symbionts such as rhizobia, mycorrhiza and / or endophytic bacteria or fungi takes place and / or optimized nitrogen fixation occurs.
  • symbionts such as rhizobia, mycorrhiza and / or endophytic bacteria or fungi takes place and / or optimized nitrogen fixation occurs.
  • the compounds of the formula (I) are suitable for the protection of seed of any plant variety used in agriculture, in the greenhouse, in forests or in horticulture.
  • these are seeds of cereals (eg wheat, barley, rye, millet and oats), corn, cotton, soy, rice, potatoes, sunflower, coffee, tobacco, canola, rape, turnip (eg Sugar beet and fodder beet), peanut, vegetables (eg tomato, cucumber, bean, cabbage, onions and lettuce), fruit plants, turf and ornamental plants.
  • cereals eg wheat, barley, rye and oats
  • corn, soya, cotton, canola, oilseed rape and rice are examples of seeds of cereals (eg wheat, barley, rye and oats), corn, soya, cotton, canola, oilseed rape and rice.
  • transgenic seed with a compound of the formula (I) is also of particular importance.
  • the heterologous genes in transgenic seed can be derived from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium.
  • the present invention is particularly useful for the treatment of transgenic seed containing at least one heterologous gene derived from Bacillus sp. comes.
  • the compound of the formula (I) is applied to the seed.
  • the seed is treated in a state where it 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.
  • seed may be used that has been harvested, cleaned and dried to a moisture content that is storable.
  • seed can also be used, which after drying, for example, was treated with water and then dried again, for example priming.
  • the compounds of the formula (I) are generally applied to the seed in the form of a suitable formulation.
  • suitable formulations and methods for seed treatment are known to those skilled in the art.
  • the compounds of the formula (I) can be converted into the customary seed dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other seed coating compositions, and also ULV formulations.
  • formulations are prepared in a known manner by mixing compounds of formula (I) with conventional additives, such as conventional extenders and solution or Diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and also water.
  • conventional additives such as conventional extenders and solution or Diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and also water.
  • Dyes which may be present in the seed dressing formulations which can be used according to the invention are all dyes customary for such purposes. Both water-insoluble pigments and water-soluble dyes are useful in this case. Examples which may be mentioned under the names rhodamine B, C.I. Pigment Red 112 and C.I. Solvent Red 1 known dyes.
  • Suitable wetting agents which may be present in the seed dressing formulations which can be used according to the invention are all wetting-promoting substances customary for the formulation of agrochemical active compounds.
  • Preferably used are alkylnaphthalene sulfonates, such as diisopropyl or diisobutyl naphthalene sulfonates.
  • Suitable dispersants and / or emulsifiers which may be present in the seed dressing formulations which can be used according to the invention are all nonionic, anionic and cationic dispersants customary for the formulation of agrochemical active compounds. Preference is given to using nonionic or anionic dispersants or mixtures of nonionic or anionic dispersants.
  • Particularly suitable nonionic dispersants are, in particular, ethylene oxide-propylene oxide, block polymers, alkylphenol polyglycol ethers and tri-stryrylphenol polyglycol ethers and their phosphated or sulfated derivatives.
  • Suitable anionic dispersants are in particular lignosulfonates, polyacrylic acid salts and arylsulfonate-formaldehyde condensates.
  • Defoamers which may be present in the seed-dressing formulations which can be used according to the invention are all foam-inhibiting substances customary for the formulation of agrochemical active compounds.
  • Preferably usable are silicone defoamers and magnesium stearate.
  • Preservatives which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions. Examples include dichlorophen and Benzylalkoholhemiformal.
  • Suitable secondary thickeners which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions. Preference is given to cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and finely divided silica.
  • Suitable adhesives which may be present in the seed dressing formulations which can be used according to the invention are all customary binders which can be used in pickling agents.
  • polyvinylpyrrolidone polyvinyl acetate, polyvinyl alcohol and Tylose.
  • the gibberellins are known (see R. Wegler "Chemie der convinced- und Swdlingsbekungsstoff", Vol. 2, Springer Verlag, 1970, pp. 401-412).
  • the seed dressing formulations which can be used according to the invention can be used either directly or after prior dilution with water for the treatment of seed of various kinds.
  • the concentrates or the preparations obtainable therefrom by dilution with water can be used for dressing the seeds of cereals such as wheat, barley, rye, oats and triticale, as well as the seeds of corn, rice, rape, peas, beans, cotton, sunflowers , Soy and beets or vegetable seed of various nature.
  • the seed dressing formulations which can be used according to the invention or their dilute application forms can also be used for pickling seeds of transgenic plants.
  • the pickling is done by placing the seed in a batch or continuous mixer, adding either desired amount of seed dressing formulations, either as such or after prior dilution with water, and until the formulation is evenly distributed mix the seed.
  • a drying process follows.
  • the application rate of the seed dressing formulations which can be used according to the invention can be varied within a relatively wide range. It depends on the particular content of the compounds of the formula (I) in the formulations and on the seed.
  • the application rates for the compound of the formula (I) are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 15 g per kilogram of seed.
  • the compounds of formula (I) are active against animal parasites, in particular ectoparasites or endoparasites.
  • animal parasites in particular ectoparasites or endoparasites.
  • endoparasite includes in particular helminths and protozoa such as coccidia.
  • Ectoparasites are typically and preferably arthropods, especially insects and acarids.
  • the compounds of formula (I) which have a favorable toxicity to warm-blooded animals, are suitable for the control of parasites used in animal breeding and livestock in livestock, breeding animals, zoo animals, laboratory animals, experimental animals and pets occur. They are effective against all or individual stages of parasite development.
  • Farm animals include, for example, mammals such as sheep, goats, horses, donkeys, camels, buffaloes, rabbits, reindeer, fallow deer, and especially cattle and pigs; Poultry such as turkeys, ducks, geese and, in particular, chickens; Fish and shellfish, e.g. in aquaculture and also insects like bees.
  • the domestic animals include, for example, mammals such as hamsters, guinea pigs, rats, mice, chinchillas, ferrets, and especially dogs, cats, caged birds, reptiles, amphibians and aquarium fish.
  • the compounds of formula (I) are administered to mammals.
  • the compounds of the formula (I) are administered to birds, namely caged birds and in particular poultry.
  • control means that the compounds of formula (I) effectively reduce the incidence of the particular parasite in an animal infected with such parasites to a harmless extent can. More specifically, “combating” in the present context means that the compound of formula (I) can kill the respective parasite, prevent its growth or prevent its replication.
  • the arthropods include: from the order Anoplurida, for example Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp .; from the order Mallophagida and the suborders Amblycerina and Ischnocerina, for example Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp .; from the order Diptera and the suborders Nematocerina and Brachycerina, for example Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp.,
  • arthropods include:
  • Metastigmata From the subclass Akari (Acarina) and the order Metastigmata, for example from the family Argasidae, such as Argas spp., Omithodorus spp., Otobius spp., From the family Ixodidae, such as Ixodes spp., Amblyomma spp., Rhipicephalus (Boophilus) spp. Dermacentor spp., Haemophysalis spp., Hyalomma spp., Rhipicephalus spp.
  • Argasidae such as Argas spp., Omithodorus spp., Otobius spp.
  • Ixodidae such as Ixodes spp., Amblyomma spp., Rhipicephalus (Boophilus) spp. Dermacentor spp., Haemophysalis spp.,
  • Parasitic protozoa include:
  • Mastigophora such as Trypanosomatidae, for example Trypanosoma b. brucei, T.b. gambiense, T.b. rhodesiense, T. congolense, T. cruzi, T. evansi, T. equinum, T. lewisi, T. percae, T. simiae, T. vivax, Leishmania brasiliensis, L. donovani, L. tropica, such as Trichomonadidae, for example Giardia lamblia, G. canis;
  • Sarcomastigophora such as Entamoebidae, for example Entamoeba histolytica, Hartmanellidae, for example Acanthamoeba sp., Harmanella sp .; Apicomplexa (Sporozoa), such as Eimeridae, for example Eimeria acervulina, E. adenoides, E. alabamensis, E. anatis, E. anserina, E. arloingi, E. ashata, E. auburnensis, E. bovis, E. brunetti, E canis,
  • Toxoplasmadidae for example Toxoplasma gondii, Hammondia heydornii, Neospora caninum, Besnoitia besnoitii; such as Sarcocystidae, for example Sarcocystis bovicanis, S. bovihominis, S. ovicanis, S. ovifelis, S. neurona, S. spec., S. suihominis, such as Leucozoidae, for example Leucocytozoon simondi, such as Plasmodiidae, for example Plasmodium berghei, P. falciparum, P. malariae, P.
  • P.vivax P.spec, such as piroplasmea, for example Babesia argentina, B.bovis, B.canis, B.spec, Theileriaparva, Theileria spec, such as Adeleina, for example Hepatozoon canis, H. spec.
  • Pathogenic endoparasites which are helminths, include flatworms (e.g., Monogenea, Cestodes, and Trematodes), roundworms, Acanthocephala, and Pentastoma. These include:
  • Monogenea e.g., Gyrodactylus spp., Dactylogyrus spp., Polystoma spp .; Cestodes: from the order Pseudophyllidea, for example: Diphyllobothrium spp., Spirometra spp., Schistocephalus spp., Ligula spp., Bothridium spp., Diplogonoporus spp .; from the order Cyclophyllida for example: Mesocestoides spp., Anoplocephala spp., Paranoplocephala spp., Moniezia spp., Thysanosoma spp., Thysaniezia spp., Avitellina spp., Stilesia spp., Cittotaenia spp., Andyra spp., Bertiella spp.
  • Taenia spp. Echinococcus spp., Hydatigera spp., Davainea spp., Raillietina spp., Hymenolepis spp., Echinolepis spp., Echinocotyle spp., Diorchis spp., Dipylidium spp., Joyeuxiella spp., Diplopylidium spp .;
  • Trematodes from the genus Digenea, for example: Diplostomum spp., Posthodiplostomum spp., Schistosoma spp., Trichobilharzia spp., Ornithobilharzia spp., Austrobilharzia spp., Gigantobilharzia spp., Leucochloridium spp., Brachylaima spp., Echinostoma spp., Echinoparyphium spp., Echinochasmus spp., Hypoderaeum spp., Fasciola spp., Fascioloides spp., Fasciolopsis spp., Cyclocoelum spp., Typhlocoelum spp., Paramphistomum spp., Calicophoron spp., Cotylophoron spp., Gigantocotyle
  • Roundworms Trichinellida for example: Trichuris spp., Capillaria spp., Paracapillaria spp., Eucoleus spp., Trichomosoides spp., Trichinella spp .; from the order Tylenchida for example: Micronema spp., Strongyloides spp .; from the order Rhabditida, for example: Strongylus spp., Triodontophorus spp., Oesophagodontus spp., Trichonema spp., Gyalocephalus spp., Cylindropharynx spp., Poteriostomum spp., Cyclococercus spp., Cylicostephanus spp., Oesophagostomum spp., Chabertia spp.
  • Stephanurus spp. Ancylostoma spp., Uncinaria spp., Necator spp., Bunostomum spp., Globocephalus spp., Syngamus spp., Cyathostoma spp., Metastrongylus spp., Dictyocaulus spp., Muellerius spp., Protostrongylus spp., Neostrongylus spp., Cystocaulus spp., Pneumostrongylus spp., Spicocaulus spp., Elaphostrongylus spp.
  • Parelaphostrongylus spp. Crenosoma spp., Paracrenosoma spp., Oslerus spp., Angiostrongylus spp., Aelurostrongylus spp., Filaroides spp., Parafilaroides spp., Trichostrongylus spp., Haemonchus spp., Ostertagia spp., Teladorsagia spp., Marshallagia spp , Cooperia spp., Nippostrongylus spp., Heligmosomoides spp., Nematodirus spp., Hyostrongylus spp., Obeliscoides spp., Amidostomum spp., Ollulanus spp .; from the order Spirurida for example: Oxyuris spp., Enterobius spp., Passalurus spp., Syphacia s
  • Acanthocephala from the order Oligacanthorhynchida, for example: Macracanthorhynchus spp., Prosthenorchis spp .; from the order Polymorphida for example: Filicollis spp .; from the order Moniliformida for example: Moniliformis spp .; from the order Echinorhynchida for example Acanthocephalus spp., Echinorhynchus spp., Leptorhynchoides spp .;
  • Pentastoma from the order Porocephalida for example Linguatula spp ..
  • the compounds of the formula (I) are administered by methods well known in the art, such as enteral, parenteral, dermal or nasal in the form of suitable preparations.
  • the administration can be prophylactic or therapeutic.
  • one embodiment of the present invention relates to the use of a compound of formula (I) as a medicament.
  • Another aspect relates to the use of a compound of formula (I) as an antiendoparasitic agent, in particular as a helminthicide or antiprotozoal agent.
  • Compounds of the formula (I) are suitable for use as antiendoparasitic agents, in particular as a helminthicide or antiprotozoal agents, for example in animal breeding, animal husbandry, in stables and in the hygiene sector.
  • a further aspect in turn relates to the use of a compound of the formula (I) as an antiectica, in particular an arthropodicide such as an insecticide or an acaricide.
  • Another aspect relates to the use of a compound of the formula (I) as anticancer drug, in particular an arthropodicide such as an insecticide or acaricide, for example in animal husbandry, in animal husbandry, in stables or in the hygiene sector.
  • a vector in the context of the present invention is an arthropod, in particular an insect or arachnid, which is able to attack pathogens such.
  • pathogens such as viruses, worms, protozoa and bacteria from a reservoir (plant, animal, human, etc.) to a host to transfer.
  • the pathogens may be transferred to a host either mechanically (e.g., trachoma by non-stabbing flies) on a host, or after injection (e.g., malaria parasites by mosquitoes).
  • Examples of vectors and their transmitted diseases or pathogens are:
  • Anopheles malaria, filariasis
  • - Aedes yellow fever, dengue fever, filariasis, other viral diseases
  • - Simulia transmission of worms, in particular Onchocerca volvulus
  • flies sleeping sickness (trypanosomiasis); Cholera, other bacterial diseases;
  • Ticks Borellioses such as Borrelia duttoni, tick-borne encephalitis, Q fever (Coxiella burnetii), Babesia (Babesia canis canis).
  • vectors in the context of the present invention are insects such as aphids, flies, cicadas or thrips, which can transmit plant viruses to plants.
  • Other vectors that can transmit plant viruses are spider mites, lice, beetles and nematodes.
  • vectors for the purposes of the present invention are insects and arachnids such as mosquitoes, in particular of the genera Aedes, Anopheles, for example A. gambiae, A. arabiensis, A. funestus, A. dirus (malaria) and culex, lice, fleas, flies, mites and ticks that can transmit pathogens to animals and / or humans.
  • insects and arachnids such as mosquitoes, in particular of the genera Aedes, Anopheles, for example A. gambiae, A. arabiensis, A. funestus, A. dirus (malaria) and culex, lice, fleas, flies, mites and ticks that can transmit pathogens to animals and / or humans.
  • Compounds of formula (I) are suitable for use in the prevention of disease or pathogens transmitted by vectors.
  • another aspect of the present invention is the use of compounds of formula (I) for vector control, e.g. in agriculture, horticulture, forests, gardens and recreational facilities, as well as in the supply and protection of materials.
  • the compounds of formula (I) are useful for protecting engineering materials against attack or destruction by insects, e.g. from the order Coleoptera, Hymenoptera, Isoptera, Lepidoptera, Psocoptera and Zygentoma.
  • the compounds of the formula (I) are used together with at least one further insecticide and / or at least one fungicide.
  • the compounds of formula (I) are present as a ready-to-use pest control agent, that is, it can be applied to the corresponding material without further changes.
  • insecticides or as fungicides in particular the above-mentioned in question are present as a ready-to-use pest control agent, that is, it can be applied to the corresponding material without further changes.
  • the compounds of the formula (I) can be used to protect against the growth of objects, in particular hulls, sieves, nets, structures, quays and signal systems, which come into contact with seawater or brackish water.
  • the compounds of the formula (I) can be used alone or in combination with other active substances as antifouling agents.
  • the compounds of the formula (I) are suitable for controlling animal pests in the hygiene sector.
  • the invention can be used in household, hygiene and storage protection, especially for controlling insects, arachnids and mites, in closed Rooms, such as homes, factories, offices, vehicle cabs occur.
  • the compounds of formula (I) are used alone or in combination with other active ingredients and / or excipients.
  • they are used in household insecticide products.
  • the compounds of formula (I) are active against sensitive and resistant species and against all stages of development.
  • pests of the class Arachnida from the orders Scorpiones, Araneae and Opiliones, from the classes Chilopoda and Diplopoda, from the class Insecta the order Blattodea, from the orders Coleoptera, Dermaptera, Diptera, Heteroptera, Hymenoptera, Isoptera, Lepidoptera, Phthiraptera, Psocoptera, Saltatoria or Orthoptera, Siphonaptera and Zygentoma and from the class Malacostraca the order Isopoda.
  • Application is for example in aerosols, non-pressurized sprays, e.g. Pump and atomizer sprays, fog machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller-driven evaporators, energy-less or passive evaporation systems, moth papers, moth cushions and moth gels, as granules or dusts, in litter or bait stations.
  • Pump and atomizer sprays e.g. Pump and atomizer sprays, fog machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller-driven evaporators, energy-less or passive evaporation systems, moth papers, moth cushions and moth gels, as granules or dusts, in litter or bait stations.
  • the 1H NMR data of selected examples are noted in terms of 1H NMR peak lists. For each signal peak, first the ⁇ value in ppm and then the signal intensity in round brackets are listed. The ⁇ -value signal intensity number pairs of different signal peaks are listed separated by semicolons.
  • the peak list of an example therefore has the form: ⁇ (intensity ⁇ ; 82 (intensity 2);; ⁇ ; (intensity ⁇ ;; ⁇ ⁇ (intensity n ))
  • the intensity of sharp signals correlates with the height of the signals in a printed example of an NMR Spectrum in cm and shows the true ratios of the signal intensities For broad signals, several peaks or the center of the signal and their relative intensity compared to the most intense signal in the spectrum can be shown.
  • the lists of 1H NMR peaks are similar to the classical 1H NMR prints and thus usually contain all the peaks listed in a classical NMR interpretation. In addition, they can, like classical 1H-NMR prints solvent signals, signals of stereoisomers of the target compounds, which are also the subject of the invention, and / or show peaks of impurities.
  • the peaks of stereoisomers of the target compounds and / or peaks of impurities usually have on average a lower intensity than the peaks of the target compounds (for example with a purity of> 90%). Such stereoisomers and / or impurities may be typical of the particular preparation process. Their peaks can thus help to detect the reproduction of our manufacturing process by "by-product fingerprints.”
  • An expert calculating the peaks of the target compounds by known methods can isolate the peaks of the target compounds as needed, using additional intensity filters, if necessary. This isolation would be similar to peak picking in classical 1H NMR interpretation.

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  • Organic Chemistry (AREA)
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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
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  • Dentistry (AREA)
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  • Plant Pathology (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
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  • Agricultural Chemicals And Associated Chemicals (AREA)
EP15801853.1A 2014-12-02 2015-11-30 Bicyclische verbindungen als schädlingsbekämpfungsmittel Withdrawn EP3227283A1 (de)

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KR102536024B1 (ko) 2015-03-12 2023-05-24 에프엠씨 코포레이션 헤테로환-치환 이환 아졸 살충제
WO2016164200A1 (en) 2015-04-09 2016-10-13 E I Du Pont De Nemours And Company Bicyclic pyrazole pesticides
MX2019003136A (es) * 2016-09-19 2019-07-18 Bayer Cropscience Ag Derivados de pirazolo [1,5-a]piridina y su uso como pesticidas.
EP4013766B1 (en) * 2019-08-14 2025-01-22 Metro International Biotech, LLC Compounds and compositions for differential modulation of nicotinamide adenine dinucleotide
WO2025202955A1 (en) 2024-03-28 2025-10-02 Pi Industries Ltd. Fused bicyclic compounds and their use as pest control agents

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CA1019748A (en) * 1972-06-02 1977-10-25 Venkatachala L. Narayanan Isothiocyanobenzoxazoles
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PE20010830A1 (es) * 2000-01-28 2001-09-06 Syngenta Ltd Derivados de azol insecticidas o fungicidas y composiciones que los comprenden
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JP5369854B2 (ja) * 2008-04-21 2013-12-18 住友化学株式会社 有害節足動物防除組成物および縮合複素環化合物
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