EP2376465A1 - Dérivés de 4-amino-1,2,3- benzoxathiazine comme pesticides - Google Patents

Dérivés de 4-amino-1,2,3- benzoxathiazine comme pesticides

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Publication number
EP2376465A1
EP2376465A1 EP09767967A EP09767967A EP2376465A1 EP 2376465 A1 EP2376465 A1 EP 2376465A1 EP 09767967 A EP09767967 A EP 09767967A EP 09767967 A EP09767967 A EP 09767967A EP 2376465 A1 EP2376465 A1 EP 2376465A1
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EP
European Patent Office
Prior art keywords
alkyl
alkoxy
spp
cycloalkyl
hetaryl
Prior art date
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Application number
EP09767967A
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German (de)
English (en)
Inventor
Bernd Alig
Klaus-Helmut Müller
Eva-Maria Franken
Ulrich Görgens
Arnd Voerste
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Bayer CropScience AG
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Bayer CropScience AG
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Priority to EP09767967A priority Critical patent/EP2376465A1/fr
Publication of EP2376465A1 publication Critical patent/EP2376465A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D291/00—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
    • C07D291/08—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
    • 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
    • A01N43/88—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 six-membered rings with three ring hetero atoms
    • 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
    • C07D419/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
    • C07D419/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D419/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Definitions

  • the present invention relates to novel pesticides, to a plurality of processes for their preparation and to their use as active substances, in particular their use as insecticides and / or acaricides.
  • 4-Amino-l, 2,3-benzoxathiazine derivatives are partially described in the literature.
  • 4-Amino-1,2,3-benzoxathiazine-2,2-dioxide (CAS Registry No .: 129661-85-4) is described in Heterocycles, Vol. 31, no. 4, 577-579 (1990) and 4-amino-5-methoxy-N- (2-methyl-2-phenylpropyl) -l, 2,3-benzoxathiazine-2,2-dioxide (CAS registry No. : 929022-83-3) in WO 2007/030582.
  • An insecticidal, acaricidal or nematicidal activity is reported in both publications.
  • the object of the present invention is to provide amino-benzoxathiazine derivatives which are useful as insecticides and / or acaricides, in particular with a satisfactory insecticidal and / or acaricidal activity against animal pests, with a broad spectrum against animal pests, with a high selectivity and good compatibility in crops, as well as those in combination with other agents to improve the effectiveness especially against difficult to control insects and spider mites, can be used.
  • R 1 , R 2 , R 3 and R 4 are independently selected from the group consisting of
  • radicals may be unsubstituted or one, two or more radicals from the group
  • R 5 is selected from the group consisting of hydrogen, (C r C 6 alkyl) carbonyl, (C r C 6 -
  • radicals may be unsubstituted or one, two or more radicals from the group Halogen, cyano, C r C 6 alkyl, C 3 -C 8 cycloalkyl, C, -C 4 alkoxy, C 4 alkylthio, C 1 -C 4 - alkylsulfinyl, C r C 4 alkylsulfonyl, C r C 4 haloalkyl, C, -C 4 -haloalkoxy, C 1 -C 4 - haloalkylthio, (C r C 4 alkyl) amino, di- (Ci -C 4 alkyl) amino, aryl and hetaryl may carry;
  • R 6 is selected from the group consisting of hydrogen, (Ci-C 6 alkyl) carbonyl, (C 1 -C 6 - alkoxy) carbonyl, (C, -C 6 alkylthio) carbonyl, (C r C 6 - Alkyl) thiocarbonyl, (C 1 -C 6 -
  • radicals may be unsubstituted or one, two or more radicals from the group
  • R 5 , R 6 together are not phenylbutyl and hydrogen if R 1 is methoxy;
  • radicals R 1 , R 2 , R 3 , R 4 are not simultaneously hydrogen, if R 5 and R 6 are hydrogen;
  • R 7 is selected from the group consisting of C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 6 -alkoxy, C] -C 6 -haloalkyl, C r C 6 -haloalkoxy, aryl , Hetaryl,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C, -C 6 alkyl, C 3 6 cycloalkyl, C, -C 6 alkoxy, C r C 6 haloalkyl, C 1 -C 6 -C - may bear haloalkoxy;
  • R 7 ' is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 cycloalkyl, QC ö alkoxy, Q-C ⁇ -haloalkyl, CRQ-haloalkoxy, aryl, hetaryl,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C r C 6 alkyl, C 3 -C 6 cycloalkyl, C r C 6 alkoxy, dC 6 haloalkyl, C r C 6 - may bear haloalkoxy;
  • the compounds of formula (I) may optionally be present in different polymorphic forms or as a mixture of different polymorphic forms. Both the pure polymorphs and the polymorph mixtures are the subject of the invention and can be used according to the invention.
  • the compounds of formula (I) optionally comprise diastereomers or enantiomers.
  • the inventive 4-amino-l, 2,3-benzoxathiazine are generally defined by the formula (I).
  • Preferred radical definitions of the above and below formulas are given below. These definitions apply equally to the end products of formula (I) as well as to all intermediates.
  • a first embodiment of the present invention comprises compounds of the general formula (I) in which
  • R 1 , R 2 , R 3 and R 4 are independently preferably selected from the group consisting of
  • radicals R 1 , R 2 , R 3 and R 4 are not simultaneously hydrogen, if R 5 and R 6 are hydrogen;
  • R 1 , R 2 , R 3 and R 4 are more preferably independently selected from the group consisting of hydrogen, halogen, cyano, C r C 3 alkyl, C r C 3 haloalkyl, QC 3 - alkoxy, C r C 2 -haloalkoxy, Ci-C 4 -alkoxy-C r C 4 alkyl, QC 4 alkoxycarbonyl, O-
  • Acetyl as well as optionally substituted by Ci-C 6 alkyl substituted aryloxy, hetaryloxy,
  • radicals R 1 , R 2 , R 3 and R 4 are not simultaneously hydrogen, if R 5 and R 6 are hydrogen;
  • R 1 , R 2 , R 3 and R 4 independently of one another are very particularly preferably selected from the group consisting of hydrogen, methoxy, ethoxy, cyano, fluorine, chlorine, methyl, ethyl, bromine, trifluoromethyl, OCHF 2 , OCF 3 and OCClF 2 , imidazolyl, methyl-benzyloxy,
  • radicals R 1 , R 2 , R 3 and R 4 are not simultaneously hydrogen, if R 5 and R 6 are hydrogen;
  • R 1 , R 2 , R 3 and R 4 independently of one another are more preferably selected from the group consisting of hydrogen, methoxy, ethoxy, fluorine, chlorine, bromine, methyl, trifluoromethyl, OCHF 2 ,
  • radicals R 1 , R 2 , R 3 and R 4 are not simultaneously hydrogen, if R 5 and R 6 are hydrogen.
  • a second embodiment of the present invention comprises compounds of the general formula (I) in which
  • R 5 is preferably selected from the group consisting of hydrogen, (C 1 -C 6 - alkyl) carbonyl, (Ci-C 6 alkoxy) carbonyl, (Ci-C 6 alkylthio) carbonyl, (C r C 6 - alkyl) thiocarbonyl, (dC 6 alkoxy) thiocarbonyl, (Ci-C 6 alkylthio) thiocarbonyl, C 1 -C 6 -
  • R 5 is particularly preferably selected from the group consisting of hydrogen, (C 1 -C 3 - alkyl) carbonyl, (C r C 3 alkoxy) carbonyl, C 1 -C 4 -alkyl, C, -C 4 alkoxy , QQ-haloalkyl, dC 4 -haloalkoxy, aryl-C, -C 2 -alkyl, hetaryl-QQ-alkyl, (C 1 -C 4 -)
  • R 5 is very particularly preferably selected from the group consisting of hydrogen, methyl, ethyl, isopropyl, methoxycarbonyl, ethoxycarbonyl, acetyl and trifluoroacetyl,
  • R 5 is particularly preferably hydrogen, methyl
  • R 7 is preferably selected from the group consisting of C 1 -C 4 -alkyl, C 3 -C 4 cycloalkyl, C 1 -C 4 -alkoxy, Ci-C 4 haloalkyl, C 1 -C 4 haloalkoxy, Phenyl, pyridyl, thiophene, furan, where these radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C, -C 4 alkyl, C 3 -C 4 cycloalkyl, Ci-C 4 -alkoxy, Ci-C 4 haloalkyl, C, -C 4 - may bear haloalkoxy;
  • R 7 is particularly preferably selected from the group consisting of C r C 4 alkyl, C 3 -C 4 - cycloalkyl, C 1 -C 4 -alkoxy, Ci-C 4 haloalkyl, C r C 4 -haloalkoxy, phenyl , Pyridyl,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C, -C 4 alkyl, C 3 -C 4 cycloalkyl, C, -C 4 alkoxy, C, -C 4 haloalkyl, C 1 -C 4 - may bear haloalkoxy;
  • R 7 ' is preferably selected from the group consisting of hydrogen, Ci-C 4 alkyl, C 3 -C 4 - cycloalkyl, C 1 -C 4 -alkoxy, QC-haloalkyl, dC 4 -haloalkoxy, phenyl, pyridyl,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C r C 4 alkyl, C 3 -C 4 cycloalkyl, C, -C 4 alkoxy, C, -C 4 haloalkyl, C 1 -C 4 - may bear haloalkoxy;
  • R 7 ' is particularly preferably selected from the group consisting of hydrogen, C 1 -C 4 - alkyl, C 3 -C 4 cycloalkyl, C r C 4 alkoxy, C, -C 4 haloalkyl, C r C 4 Haloalkoxy, phenyl, pyridyl,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C r C 4 alkyl, C 3 -C 4 cycloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 - may bear haloalkoxy;
  • X is preferred and particularly preferably represents O.
  • a third embodiment of the present invention comprises compounds of the general formula (I) in which
  • R 6 is preferably selected from the group consisting of hydrogen, (C 1 -C 6 - alkyl) carbonyl, (Ci-C 6 alkoxy) carbonyl, (C r C 6 alkylthio) carbonyl, (C 1 -C 6 -
  • R 6 is very particularly preferably selected from the group consisting of hydrogen, methyl, ethyl, isopropyl, methoxycarbonyl, ethoxycarbonyl, acetyl and trifluoroacetyl;
  • R 6 is particularly preferably hydrogen.
  • R 7 is preferably selected from the group consisting of Ci-C 4 -alkyl, C 3 -C 4 cycloalkyl, Ci-C 4 alkoxy, Ci-C 4 haloalkyl, C] -C 4 -haloalkoxy, phenyl, Pyridyl, thiophene, furan,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C r C 4 alkyl, C 3 -C 4 cycloalkyl, C r C 4 alkoxy, Ci-C 4 haloalkyl, C 1 -C 4 - may bear haloalkoxy;
  • R 7 is particularly preferably selected from the group consisting of C r C 4 alkyl, C 3 -C 4 - cycloalkyl, Ci-C 4 alkoxy, Ci-C 4 haloalkyl, C r C 4 -haloalkoxy, phenyl, pyridyl,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C 1 -C 4 -alkyl, C 3 -C 4 cycloalkyl, C, -C 4 alkoxy, C, -C 4 haloalkyl, C 1 -C 4 - may bear haloalkoxy;
  • R 7 ' is preferably selected from the group consisting of hydrogen, C] -C 4 alkyl, C 3 -C 4 - cycloalkyl, Ci-C 4 alkoxy, Ci-C4-haloalkyl, Ci-C4-haloalkoxy , Phenyl, pyridyl, thiophene, furan,
  • radicals may be unsubstituted or one, two or more radicals from the group
  • Halogen, cyano, nitro, C, -C 4 alkyl, C 3 -C 4 cycloalkyl, C r C 4 alkoxy, C, -C 4 haloalkyl, C 1 -C 4 - may bear haloalkoxy;
  • R 7 ' is particularly preferably selected from the group consisting of hydrogen, C 1 -C 4 - alkyl, C 3 -C 4 cycloalkyl, C r C 4 alkoxy, C, -C 4 haloalkyl, C r C 4 -haloalkoxy,
  • radicals may be unsubstituted or one, two or more radicals from the group Halogen, cyano, nitro, C, -C 4 alkyl, C 3 -C 4 cycloalkyl, C r C 4 alkoxy, QQ haloalkyl, C 1 -C 4 - may bear haloalkoxy;
  • X is preferred and particularly preferably represents O.
  • the present invention preferably also the lithium, sodium, potassium, magnesium, calcium, ammonium, Ci-C 4 -alkyl-ammonium, di (Ci-C 4 -alkyl) -ammonium, tri -
  • the compounds of the general formula (I) can furthermore, if appropriate, be prepared by addition of a suitable inorganic or organic acid, such as, for example, HCl, HBr, H 2 SO 4 or HNO 3 , but also oxalic acid or sulfonic acids to a basic group, such as.
  • a suitable inorganic or organic acid such as, for example, HCl, HBr, H 2 SO 4 or HNO 3
  • oxalic acid or sulfonic acids to a basic group, such as.
  • amino or alkylamino salts.
  • Suitable substituents which are present in deprotonated form such as, for example, sulfonic acids or carboxylic acids, can form internal salts with groups which can themselves be protonated, such as amino groups. Salts may also be formed by reacting with suitable substituents, such as.
  • salts are, for example, metal salts, in particular alkali metal salts or alkaline earth metal salts, in particular sodium and potassium salts, or else ammonium salts, salts with organic amines or quaternary (quaternary) ammonium salts with cations of the formula [NRR 1 R 11 R '"] +, where R to R each independently represent an organic radical, especially alkyl, aryl, aralkyl or alkylaryl.
  • radicals alkyl, alkoxy, haloalkyl, alkoxyalkyl, alkenyl, alkynyl, haloalkoxy, alkylamino, dialkylamino, alkylthio and haloalkylthio as well as the corresponding unsaturated and / or substituted radicals in the Carbon skeleton in each case be straight-chain or branched.
  • these radicals are the lower carbon skeletons, for example having 1 to 6 C atoms, in particular 1 to 4 C atoms, or in unsaturated groups having 2 to 6 C atoms, in particular 2 to 4 C atoms , prefers.
  • Alkyl radicals including in the composite meanings such as alkoxy, haloalkyl, etc., mean, for example, methyl, ethyl, propyls such as n- or i-propyl, butyls such as n-, iso- or tert-butyl, pentyls such as n-pentyl, iso- Pentyl or neo-pentyl, hexyls such as n-hexyl, i-hexyl, 3-methylpentyl, 2,2-dimethylbutyl or 2,3-dimethylbutyl, heptyls, such as n-heptyl, 1-methylhexy or 1,4-dimethylpentyl; Alkenyl and alkynyl radicals have the meaning of the possible unsaturated radicals corresponding to the alkyl radicals; wherein at least one double bond or triple bond, preferably a double bond or triple bond is included.
  • Alkenyl is, for example, vinyl, AHyI, 1-methylprop-2-en-1-yl, 2-methylprop-2-en-1-yl, but-2-en-1-yl, but-3-ene-1 -yl, 1-methylbut-3-en-1-yl and 1-methylbut-2-en-1-yl;
  • Alkynyl means, for example, ethynyl, propargyl, but-2-yn-1-yl, but-3-yn-1-yl and 1-methyl-but-3-yn-1-yl.
  • haloalkyl groups and haloalkyl groups of haloalkoxy, haloalkylthio, haloalkenyl, haloalkynyl and the like are mentioned. are indicated in these residues, the lower carbon skeletons, z. B. with 1 to 6 carbon atoms or 2 to 6, in particular 1 to 4 carbon atoms or preferably 2 to 4 carbon atoms, and the corresponding unsaturated and / or substituted radicals in the carbon scaffold each straight-chain or branched. Examples are difluoromethyl, 2,2,2-trifluoroethyl, trifluoroallyl, 1-chloroprop-1-yl-3-yl.
  • halo is used according to the invention synonymously with "halogen”.
  • Halogen is fluorine, chlorine, bromine or iodine.
  • Haloalkoxy is, for example, OCF 3 , OCHF 2 , OCH 2 F, CF 3 CF 2 O, OCH 2 CF 3 and OCH 2 CH 2 Cl; the same applies to haloalkenyl and other halogen-substituted radicals.
  • the present compounds of the general formula (I) may optionally have a chiral carbon atom. Corresponding chiral carbon atoms can occur in particular in the substituent R 5 and R 6 .
  • these substituents may have both an (R) and an (S) configuration.
  • the present invention encompasses compounds of the general formula (I) having both (S) and (R) configuration at the respective chiral carbon atoms, that is, that the present invention covers the compounds of the general formula (I), in each of which carbon atoms are independently
  • Another object of the present invention are methods for preparing corresponding compounds of general formula (I) and / or salts thereof.
  • the compounds of the general formula (I) are prepared by reacting 2-cyano-phenyloxysulfonamides of the general formula (II) in which R 1 , R 2 , R 3 and R 4 denote the having the abovementioned meaning, cyclized in the presence of ultrasound-pretreated baker's yeast to 4-amino-l, 2,3-benzoxathiazine derivatives of the general formula (I),
  • the compounds of the general formula (I) are prepared by reacting 2-cyano-phenols of the general formula (III) in which R 1 , R 2 , R 3 and R 4 denote the Having the abovementioned meaning, according to known methods (see Chemical Reports 105 (9), 2791-9 (1972)) with chlorosulfonyl isocyanate to 2-cyano-phenyloxysulfonamiden the general formula (II) and these without further isolation under the reaction conditions to 4 Cyclized -mino-l, 2,3-benzoxathiazine derivatives of general formula (I),
  • the compounds of the general formula (I) are prepared by reacting 2-amidino-phenols of the general formula (IV) in which R 1 , R 2 , R 3 , R 4 , R 5 and R 6 have the abovementioned meaning, with a sulfonyl derivative of the general formula (V), where X and Y is a leaving group such as halogen, pyrazole, triazole or imidazole, cf. WO 2007/030582:
  • Sulfonyl derivatives of the general formula (V) are known (see Journal of Inorganic and General Chemistry 629 (7-8), 1300-1307 (2003)) or commercially available (l, l'-sulfonyl-bis-lH-l , 2,4-triazoles: Florida Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, PO Box 117200, Gainesville, FL, 32611-7200, USA; 1,1'-sulfonyldiimidazoles: Sigma-Aldrich, PO Box 14508, St. Louis, MO, 63178, USA).
  • the compounds of the general formula (Ia) are prepared by reacting 2-amidino-phenols of the general formula (IVa) in which R 2 , R 3 , R 4 , R 5 and R 6 have the abovementioned meaning and R 1 for fluorine is reacted with a sulfonyl derivative of the formula (Va):
  • Suitable alkylating agents are all customary reagents such as, for example, alkyl halides, alkenyl halides, alkynyl halides, benzyl halides or their sulfonic acid esters. Examples which may be mentioned are methyl iodide, allyl bromide, propargyl bromide, benzyl bromide, dimethyl sulfate, methyl trifluoromethanesulfonate.
  • Suitable acylating agents are all customary reagents such as, for example, (thio) -carboxylic acid halides, or (thio) -carboxylic acid anhydrides. Examples which may be mentioned are acetyl chloride, cyclopropyl chloride, dimethylcarbamoyl chloride, ethyl chloroformate, chloroformic acid thiomethyl ester, nicotinic acid chloride,
  • Trifluoroacetic anhydride Trifluoroacetic anhydride.
  • Suitable sulfonylating reagents are sulfonyl halides and sulfonyl anhydrides. Examples which may be mentioned are trifluoromethanesulfonic anhydride, methanesulfonyl chloride, para-toluenesulfonyl chloride.
  • R 6 is a monosubstituted amino (thio) carbonyl radical
  • the compounds of the general formula (I) are prepared by reacting 4-amino-1, 2 , 3-benzoxathiazine derivatives of general formula (Ib) or (Ic) in which R 1 , R 2 , R 3 , R 4 , R 5 , R 7 , X have the abovementioned meaning, with iso (thio) cyanates of the general formula (VIII) is reacted:
  • inert solvents are used in each case.
  • inert solvents are solvents which are inert under the particular reaction conditions, ie. in particular do not react with the starting materials, but need not be inert under any reaction conditions.
  • organic solvents examples include aromatic or aliphatic solvents, such as benzene, toluene, xylene, mesitylene, hexane, heptane, octane, cyclohexane; aliphatic and aromatic halohydrocarbons, such as methylene chloride, dichloroethane, chloroform, carbon tetrachloride, chlorobenzene, dichlorobenzene, ethers, such as diethyl ether, dibutyl ether, diisobutyl ether, methyl tert-butyl ether, isopropyl ethyl ether, diisopropyl ether, tetrahydrofuran, and dioxane; also dimethylsulfoxide, and acid amide derivatives, such as N, N-dimethylformamide, N, N-dimethylacetamide and N-methyl-2-pyrrolidone
  • toluene particularly preferred are toluene, xylene, dichlorobenzene, chlorobenzene, acetonitrile, acetone, butyronitrile or ethyl acetate.
  • the present invention is not limited to the solvents exemplified above.
  • the reaction temperature at which the reactions according to the above embodiments can be carried out can vary widely. Corresponding temperatures are mentioned in the respective embodiments of the reactions. In addition, the reactions at a temperature of 0 to 160 0 C, preferably 20 to 120 0 C, are performed.
  • the reactions of the present invention are generally carried out under normal pressure. However, it is also possible to work under elevated pressure or reduced pressure, generally between 0.1 bar and 10 bar.
  • the processes for the preparation of the 4-amino-l, 2,3-benzoxathiazine derivatives of the general formula (I) according to the invention are optionally carried out in the presence of a basic or acidic reaction auxiliary or cleavage reagent.
  • customary inorganic or organic bases are suitable. These include, for example, alkali metal or alkaline earth metal hydrides, hydroxides,
  • amides, alcoholates, acetates, carbonates or bicarbonates such as, for example, lithium, sodium, potassium or calcium hydride, lithium, sodium or potassium amide, sodium or potassium methoxide, sodium or potassium ethylate, sodium or potassium propylate ,
  • Acid reaction auxiliaries are all customary inorganic or organic acids. These include, for example, mineral acids such as sulfuric acid H 2 SO 4 , phosphoric acid H 3 PO 4 or hydrochloric acid HCl or organic acids such as formic acid, acetic acid or trifluoroacetic acid.
  • the active compounds according to the invention are suitable for plant tolerance, favorable warm-blood toxicity and good environmental compatibility for the protection of plants and plant organs, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs which are found in agriculture, horticulture, livestock, forests, gardens and recreational facilities, in the protection of materials and materials and in the hygiene sector. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
  • the above mentioned pests include:
  • Anoplura eg Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Trichodectes spp.
  • Arachnida eg Acarus siro, Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Argas spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa, Chorioptes spp., Dermanyssus gallinae, Eotetranychus spp.
  • Epitrimerus pyri Eutetranychus spp., Eriophyes spp., Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Oligonychus spp., Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp , Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Stenotarsonemus spp., Tarsonemus spp., Tetranychus spp., Vasates lycopersici.
  • Ceuthorhynchus spp. Ceuthorhynchus spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Curculio spp., Cryptorhynchus lapathi, Dermestes spp., Diabrotica spp., Epilachna spp., Faustinus cubae, Gibbium psylloides, Heteronychus arator, Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypothenemus spp., Lachnosterna consanguinea, Leptinotarsa decemlineata, Lissorhoptrus oryzophilus, Lixus spp., Lyctus spp., Meligethes aeneus, Melolontha melolontha, Migdolus spp., Mono
  • helminths e.g. Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma brazihensis, Ancylostoma spp., Asca ⁇ s lubiccoides, Ascans spp., Brugia malayi, Brugia timo ⁇ , Bunostomum spp., Chabertia spp., Clonorchis spp., Coope ⁇ a spp., Dicrocoehum spp., Dictyocaulus fila ⁇ a, Diphylloboth ⁇ um latum, Dracunculus medmensis, Echinococcus granulosus, Echinococcus multilocula ⁇ s, Enterobius vermicula ⁇ s, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus
  • protozoa such as Eimena
  • Eimena can be controlled.
  • Hehopeltis spp. Horcias nobilellus, Leptoco ⁇ sa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Mi ⁇ dae, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus se ⁇ atus, Pseudacysta persea, Rhodmus spp. Sahlbergella singulas, Scotmophora spp., Stepharmis nashi, Tibraca spp., T ⁇ atoma spp.
  • Hymenoptera e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.
  • Lepidoptera e.g. Acronicta major, Aedia leucomelas, Agrotis spp., Alabama argillacea, Anticarsia spp., Barathra brassicae, Bucculatrix thurberiella, Bupalus piniarius,
  • Cacoecia podana Capua reticulana, Carpocapsa pomonella, Cheimatobia brumata, Chilo spp.,
  • Heliothis spp. Hofmannophila pseudospretella, Homona magnanima, Hyponomeuta padella, Lophygma spp., Lithocolletis blancardella, Lithophane antennata, Loxagrotis albicosta, Lymantria spp., Malacosoma neustria, Mamestra brassicae, Mocis repanda, Mythimna separata, Oria spp.
  • Plutella xylostella Prodenia spp., Pseudaletia spp., Pseudoplusia includens, Pyrausta nubilalis,
  • Orthoptera e.g. Acheta domesticus, Blatta orientalis, Blattella germanica, Gryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana, Schistocerca gregaria.
  • siphonaptera e.g. Ceratophyllus spp., Xenopsylla cheopis.
  • Symphyla eg Scutigerella immaculata.
  • Thysanoptera eg Basothrips biformis, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni, Thrips spp.
  • Thysanura e.g. Lepisma saccharina.
  • the plant parasitic nematodes include e.g. Anguina spp., Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera spp., Heliocotylenchus spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Rotylenchus spp. Trichodorus spp., Tylenchorhynchus spp., Tylenchulus spp., Tylenchulus semipenetrans, Xiphinema spp.
  • Anguina spp. Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera
  • the effectiveness of the compounds of the formula (I) can be increased by the addition of ammonium and phosphonium salts.
  • the ammonium and phosphonium salts are defined by formula (DC)
  • D is nitrogen or phosphorus
  • D is preferably nitrogen
  • R 8 , R 9 , R 10 , and R 11 independently of one another represent hydrogen or in each case optionally substituted C 1 -C 8 -alkyl or mono- or polyunsaturated, optionally substituted C 1 -C 6 -alkylene, where the substituents are halogen, nitro and cyano can be selected
  • R 8 , R 9 , R 10 , and R 11 preferably independently of one another represent hydrogen or in each case optionally substituted C 1 -C 4 -alkyl, where the substituents can be selected from halogen, nitro and cyano,
  • R 8 , R 9 , R 10 , and R 11 more preferably independently of one another represent hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl or t-butyl, R 8 , R 9 , R 10 , and R 11 very particularly preferably represent hydrogen,
  • n 1, 2, 3 or 4
  • n is preferably 1 or 2
  • R 12 is an inorganic or organic anion
  • R 12 is preferably hydrogencarbonate, tetraborate, fluo ⁇ d, bromide, iodide, chlo ⁇ d, monohydrogenphosphate, dihydrogenphosphate, hydrogensulphate, tartrate, sulphate, nitrate, thiosulphate, thiocyanate, formate, lactate, acetate, propionate, butyrate, pentanoate, citrate or oxalate,
  • R 12 is particularly preferred for lactate, sulfate, monohydrogen phosphate, dihydrogen phosphate, nitrate, thiosulfate, thiocyanate, citrate, oxalate or formate.
  • R 12 very particularly preferably represents sulfate.
  • the ammonium and phosphomium salts of the formula (DC) can be used in a wide concentration range for increasing the effect of crop protection agents containing compounds of the formula (I).
  • the ammonium or phosphomium salts are used in the ready-to-use crop protection agent in a concentration of 0.5 to 80 mmol / l, preferably 0.75 to 37.5 mmol / l, particularly preferably 1.5 to 25 mmol / l.
  • the ammonium and / or phosphomium salt concentration in the formulation is selected to be, after dilution of the formulation, to the desired drug concentration in these indicated general, preferred or more preferred ranges.
  • the concentration of the salt in the formulation is usually 1-50 wt .-%.
  • a penetration promoter is added to the crop protection agents to increase the effect. Even in these cases, an increase in activity can be observed.
  • the present invention thus also relates to the use of penetration promoters, as well as the use of a combination of penetration enhancers and ammonium and / or phosphomium salts to increase the efficacy of crop protection agents containing aka ⁇ zid / insecticidal compounds of formula (I) as an active ingredient.
  • the subject matter of the invention is the use of these agents for controlling harmful insects.
  • all substances which are customarily used to improve the penetration of agrochemical active substances into plants are suitable as penetration promoters.
  • Penetration promoters are in this context defined by the fact that they can penetrate from the aqueous spray mixture and / or from the spray coating in the cuticle of the plant and thereby increase the material mobility (mobility) of active ingredients in the cuticle.
  • the method described in the literature can be used to determine this property.
  • Suitable penetration promoters are, for example, alkanol alkoxylates.
  • Penetration promoters according to the invention are alkanol alkoxylates of the formula
  • R is straight-chain or branched alkyl having 4 to 20 carbon atoms
  • R 1 is hydrogen, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl or n-hexyl,
  • AO stands for an ethylene oxide radical, a propylene oxide radical, a butylene oxide radical or mixtures of ethylene oxide and propylene oxide radicals or butylene oxide radicals and
  • v stands for numbers from 2 to 30.
  • a preferred group of penetration enhancers are alkanol alkoxylates of the formula
  • n stands for numbers from 2 to 20.
  • Another preferred group of penetration enhancers are alkanol alkoxylates of the formula
  • EO stands for -CH 2 -CH 2 -O-
  • q stands for numbers from 1 to 10.
  • Another preferred group of penetration promoters are alkanol alkoxylates of the formula
  • EO stands for -CH 2 -CH 2 -O-
  • s stands for numbers from 1 to 10.
  • Another preferred group of penetration enhancers are alkanol alkoxylates of the formula
  • q stands for numbers from 1 to 10.
  • Penetrationsf ⁇ rdere ⁇ i are alkanol alkoxylates of the formula
  • EO is CH 2 -CH 2 -O-
  • s stands for numbers from 1 to 10.
  • Another preferred group of penetration promoters are alkanol alkoxylates of the formula
  • u stands for numbers from 6 to 17.
  • R is preferably butyl, isobutyl, n-pentyl, i-pentyl, neopentyl, n-hexyl, i-hexyl, n-octyl, i-octyl, 2-ethylhexyl, nonyl, i-nonyl, decyl, n Dodecyl, i-dodecyl, lauryl, myristyl, i-tridecyl, trimethyl-nonyl, palmityl, stearyl or eicosyl.
  • alkanol alkoxylate of the formula (X-c) is 2-ethyl-hexyl alkoxylate of the formula
  • EO stands for -CH 2 -CH 2 -O-
  • the numbers 8 and 6 represent average values called.
  • EO is CH 2 -CH 2 -O-
  • the numbers 10, 6 and 2 represent average values called.
  • alkanol alkoxylates of the formula (X-f) are compounds of this formula in which
  • u stands for the average 8.4.
  • alkanol alkoxylates are generally defined by the above formulas. These substances are mixtures of substances of the specified type with different chain lengths. For the indices, therefore, average values are calculated, which can also differ from whole numbers.
  • alkanol alkoxylates of the formulas given are known and are partly available commercially or can be prepared by known methods (compare WO 98/35 553, WO 00/35 278 and EP-A 0 681 865).
  • Suitable penetration promoters are substances which promote the solubility of the compounds of the formula (I) in the spray coating. These include, for example, mineral or vegetable oils. Suitable oils are all mineral or vegetable, optionally modified, oils which can usually be used in agrochemical compositions. Examples include sunflower oil, rapeseed oil, olive oil, castor oil, rapeseed oil, corn kernel oil, cottonseed oil and soybean oil or the esters of said oils. Rape oil, sunflower oil and their methyl or ethyl esters are preferred.
  • the concentration of penetration promoter can be varied within a wide range. In the case of a formulated crop protection agent, it is generally from 1 to 95% by weight, preferably from 1 to 55% by weight, more preferably from 15 to 40% by weight. In the ready-to-use agents (spray liquors), the concentration is generally between 0.1 and 10 g / l, preferably between 0.5 and 5 g / l.
  • 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, or as microbicides, for example as fungicides, antimycotics, bactericides, Vi ⁇ zide (including agents against viroids) or as Agents against MLO (Mycoplasma-hke-organism) and RLO (Rickettsia-hke-organism) are used. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
  • the active compounds can be converted into the customary formulations, such as solutions, emulsions, spray powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, scattering granules, suspension-emulsion concentrates, active substance-impregnated natural substances, active substance-impregnated synthetic Substances, fertilizers and superfine encapsulations in polymeric substances.
  • customary formulations such as solutions, emulsions, spray powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, scattering granules, suspension-emulsion concentrates, active substance-impregnated natural substances, active substance-impregnated synthetic Substances, fertilizers and superfine encapsulations in polymeric substances.
  • formulations are prepared in a known manner, e.g. by mixing the active compounds with extenders, ie liquid solvents and / or solid carriers, if appropriate using surface-active agents, ie emulsifiers and / or dispersants and / or foam-forming agents.
  • extenders ie liquid solvents and / or solid carriers
  • surface-active agents ie emulsifiers and / or dispersants and / or foam-forming agents.
  • Excipients which can be used are those which are suitable for imparting special properties to the composition itself and / or preparations derived therefrom (for example spray liquor, seed dressing), such as certain technical properties and / or specific biological properties.
  • Typical auxiliaries are: extenders, solvents and carriers.
  • Suitable extenders include, for example, water, polar and non-polar organic chemical liquids, for example 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 the ketones (such as acetone, cyclohexanone), esters (also fats and oils) and (poly) ethers, the simple and substituted wet nurse, amides, Lactams (such as N-alkyl pyrrolidones) and lactones, sulfones and sulfoxides (such as dimethyl sulfoxide).
  • aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
  • alcohols and polyols which may also be substituted, etherified and / or
  • Suitable liquid solvents are essentially: aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, e.g. 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 dimethyl sulfoxide, and water.
  • Suitable solid carriers are:
  • ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulite, montmorillonite or diatomaceous earth
  • ground synthetic minerals such as fumed silica, alumina and silicates, as solid carriers for granules
  • ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulite, montmorillonite or diatomaceous earth
  • ground synthetic minerals such as fumed silica, alumina and silicates, as solid carriers for granules
  • fumed silica, alumina and silicates as solid carriers for granules
  • crushed 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 paper, sawdust, coconut shells, corncobs and tobacco stalks
  • suitable emulsifiers and / or foam formers are: e
  • nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates and protein hydrolysates;
  • suitable dispersants are non-ionic and / or ionic substances, e.g.
  • Adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-type polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins and synthetic phospholipids may be used in the formulations.
  • Dyes such as inorganic pigments such as iron oxide, titanium oxide, ferrocyan blue and organic dyes such as Aliza ⁇ n-, azo and Metallphthalocyaninfarbstoffe and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used.
  • additives may be fragrances, mineral or vegetable optionally modified oils, waxes and nutrients (also 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.
  • the formulations generally contain between 0.01 and 98% by weight of active ingredient, preferably between 0.5 and 90%.
  • the active ingredient may be used in its commercial formulations as well as m the formulations prepared from these formulations in admixture with other active ingredients such as insecticides, attractants, Ste ⁇ lantien, bactericides, Aca ⁇ ziden, nematodes, fungicides, growth regulators, herbicides, safeners, fertilizers, semiochemicals or with agents for Improvement of plant properties are present.
  • active ingredients such as insecticides, attractants, Ste ⁇ lantien, bactericides, Aca ⁇ ziden, nematodes, fungicides, growth regulators, herbicides, safeners, fertilizers, semiochemicals or with agents for Improvement of plant properties are present.
  • the active compounds according to the invention can furthermore be present when used as insecticides in their commercially available formulations and in the forms of use prepared from these formulations in admixture with synergists.
  • Synergists are compounds that increase the effect of the active ingredients without the added synergist itself having to be active.
  • the active compounds according to the invention may furthermore, when used as insecticides in their commercial formulations and in the forms of use prepared from these formulations, be present in mixtures with inhibitors which reduce degradation of the active ingredient after application in the environment of the plant, on the surface of plant parts or in plant tissues ,
  • the active substance content of the application forms prepared from the commercial formulations can vary widely.
  • the active ingredient concentration of the use forms may be from 0.00000001 up to 95% by weight of active compound, preferably between 0.00001 and 1% by weight.
  • plants and parts of plants can be treated.
  • plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
  • Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant breeders' rights.
  • Plant parts are to be understood as meaning all aboveground and underground parts and organs of the plants, such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, as well as roots, tubers and rhizomes.
  • the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
  • the treatment according to the invention of the plants and plant parts with the active ingredients 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, evaporating, nebulizing, spreading, brushing, injecting, casting and in propagating material, in particular in seeds, further by single or multi-layer wrapping.
  • plants and their parts can be treated.
  • wild-type or plant species obtained by conventional biological breeding methods such as crossing or protoplast fusion
  • plant cultivars and their parts 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 terms "parts” or “parts of plants” or “plant parts” have been explained above.
  • Plant varieties are understood as meaning plants having new traits which have been bred by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be varieties, biotypes and genotypes.
  • the treatment according to the invention may also give rise to superadditive ("synergistic") effects.
  • superadditive for example, reduced application rates and / or extensions of the spectrum of action and / or an increase in the Effect of the substances and compositions which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to water or soil salt content, 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 harvested products possible, which go beyond the expected effects actually.
  • the preferred plants or plant varieties to be treated according to the invention to be treated include all plants which, as a result of the genetic engineering modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits").
  • traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to bottoms salt, increased flowering, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products , higher shelf life and / or workability of the harvested products.
  • Further and particularly emphasized examples of such properties are an increased defense of the plants against animal and microbial pests, as against insects, mites, phytopathogenic fungi, bacteria and / or viruses as well as an increased tolerance of the plants to certain herbicidal active substances.
  • transgenic plants are the important crops, such as cereals (wheat, rice), maize, soya, potatoes, sugar beets, tomatoes, peas and other vegetables, cotton, tobacco, oilseed rape, and fruit plants (with the fruits apples, pears, Citrus fruits and grapes), with special emphasis on maize, soya, potato, cotton, tobacco and oilseed rape.
  • Bt plants are the increased defense of the plants against insects, arachnids, nematodes and snails by toxins produced in the plants, in particular those which are produced by the genetic material from Bacillus thuringiensis (eg by the genes Cry ⁇ A (a) , Cry ⁇ A (b), Cry ⁇ A (c), CryllA, CryllLA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF, and combinations thereof) in the plants (hereinafter "Bt plants”).
  • Bacillus thuringiensis eg by the genes Cry ⁇ A (a) , Cry ⁇ A (b), Cry ⁇ A (c), CryllA, CryllLA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF, and combinations thereof
  • Traits also highlight the increased resistance of plants to fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins. Traits which are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT" gene). The genes which confer the desired properties (“traits”) can also occur in combinations with one another in the transgenic plants.
  • SAR systemic acquired resistance
  • PAT phosphinotricin
  • Bt plants maize varieties, cotton varieties, soybean varieties and potato varieties are mentioned, which are under the trade names YIELD GARD® (eg corn, cotton, soy), KnockOut® (eg corn), StarLink® (eg corn), Bollgard® (cotton), Nucotn® (cotton) and NewLeaf® (potato).
  • YIELD GARD® eg corn, cotton, soy
  • KnockOut® eg corn
  • StarLink® eg corn
  • Bollgard® cotton
  • Nucotn® cotton
  • NewLeaf® potato
  • herbicide-tolerant plants are maize varieties, cotton varieties and soybean varieties, which are sold under the trade names Roundup Ready® (tolerance to glyphosate eg corn, cotton, soy), Liberty Link® (tolerance to phosphinotricin, eg rapeseed), IMI® (tolerance against imidazolinone) and STS® (tolerance to sulfonylureas eg corn).
  • Roundup Ready® tolerance to glyphosate eg corn, cotton, soy
  • Liberty Link® tolerance to phosphinotricin, eg rapeseed
  • IMI® tolerance against imidazolinone
  • STS® tolerance to sulfonylureas eg corn
  • Clearfield® varieties eg corn
  • the plants listed can be treated particularly advantageously according to the invention with the compounds of general formula I or the Wirkstoffrnischungen invention.
  • the preferred ranges given above for the active compounds or mixtures also apply to the treatment of these plants.
  • Particularly emphasized is the plant treatment with the compounds or mixtures specifically mentioned in the present text.
  • the active compounds of the invention not only act against plant, hygiene and storage pests, but also in the veterinary sector against animal parasites (ecto- and endoparasites) such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitizing fly larvae, lice , Hair pieces, featherlings and fleas.
  • animal parasites ecto- and endoparasites
  • ticks ecto- and endoparasites
  • leather ticks such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitizing fly larvae, lice , Hair pieces, featherlings and fleas.
  • flies stinging and licking
  • Anoplurida e.g. Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.
  • Trimenopon spp. Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp.
  • Nematocerina and Brachycerina eg Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp.
  • Atylotus spp. Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia spp., Sarcophaga spp., Oestrus spp., Hypoderma spp., Gasterophilus spp., Hippobosca spp., Lipoptena spp., Melophagus spp. From the order of the siphon adapter eg Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp
  • heteropterid e.g. Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp.
  • Actinedida Prostigmata
  • Acaridida e.g. Acarapis spp., Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp , Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp.
  • the active compounds of the formula (I) according to the invention are also suitable for controlling arthropods which are farm animals, such as e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as e.g. Dogs, cats, caged birds, aquarium fish and so-called experimental animals, such. Hamsters, guinea pigs, rats and mice.
  • arthropods are farm animals, such as e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as e.g. Dogs, cats, caged birds, aquarium fish and so-called experimental animals, such. Hamsters, guinea pigs, rats and mice.
  • the application of the active compounds according to the invention takes place in the veterinary sector and in animal husbandry in a known manner by enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories, by parenteral administration, as by injections (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.), implants, by nasal application, by dermal application in the form of, for example, diving or bathing (dipping), spraying, pouring (pour-on and spot-on ), washing, powdering and with the aid of active substance-containing moldings, such as collars, ear tags, tail marks, limb bands, holsters, marking devices, etc.
  • enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories
  • parenteral administration as by injections (intr
  • the active compounds of the formula (I) can be used as formulations (for example powders, emulsions, flowable agents) which contain the active ingredients in an amount of from 1 to 80% by weight, directly or apply after 100 to 10,000 times dilution or use as a chemical bath.
  • formulations for example powders, emulsions, flowable agents
  • the compounds according to the invention exhibit a high insecticidal activity against insects which destroy industrial materials.
  • insects By way of example and preferably without limiting however, the following insects are mentioned:
  • Hymenoptera such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus, Urocerus augur;
  • Termites such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis, Coptotermes formosanus;
  • Non-living materials such as preferably plastics, adhesives, glues, papers and cardboard, leather, wood, wood processing products and paints.
  • the ready-to-use agents may optionally contain further insecticides and optionally one or more fungicides.
  • the compounds according to the invention can be used to protect against fouling of objects, in particular hulls, sieves, nets, structures, quay systems and signal systems, which come into contact with seawater or brackish water.
  • the compounds according to the invention can be used alone or in combinations with other active substances as antifouling agents.
  • the active compounds are also suitable for controlling animal pests in household, hygiene and storage protection, in particular of insects, arachnids and mites, which in enclosed spaces, such as homes, factories, offices, vehicle cabs, etc. occur. They can be used to control these pests, alone or in combination with other active ingredients and adjuvants in household insecticide products. They are effective against sensitive and resistant species and against all stages of development. These pests include:
  • Acarina e.g. Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, Ornithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi, Neutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides forinae.
  • Opiliones e.g. Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.
  • Zygentoma e.g. Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus.
  • Psocoptera eg Lepinatus spp.
  • Liposcelis spp. From the order of Coleoptera, for example, Anthrenus spp., Attagenus spp., Dermestes spp., Latheticus oryzae, Necrobia spp., Ptinus spp., Rhizopertha dominica, Sitophilus granarius, Sitophilus oryzae, Sitophilus zeamais, Stegobium paniceum.
  • Diptera e.g. Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp., Sarcophaga carnaria, Simulium spp., Stomoxys Calcitrans, Tipula paludosa.
  • Lepidoptera e.g. Achroia grisella, Galleria mellonella, Plodia inte ⁇ unctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella.
  • Ctenocephalides canis Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis.
  • Hymenoptera e.g. Camponotus herculeanus, Lasius fuliginosus, Lasius niger, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitum.
  • Heteroptera e.g. Cimex hemipterus, Cimex lectularius, Rhodinus prolixus, Triatoma infestans.
  • Application is in aerosols, non-pressurized sprays, e.g. Pump and atomizer sprays, misting machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller driven evaporators, energyless or passive evaporation systems, moth papers, moth cakes and moth gels, as granules or dusts, in litter or bait stations.
  • Pump and atomizer sprays misting machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller driven evaporators, energyless or passive evaporation systems, moth papers, moth cakes and moth gels, as granules or dusts, in litter or bait stations.
  • 2-Cyanophenols are known in some cases and can be prepared by processes known per se (compare US 2006/0052374, WO 1997/037967, WO 2007/089646).
  • Amidino-phenols of the general formula (IV) are partly commercially available or can be prepared by known methods [cf. EP626372, WO 1997/49404, WO 2003/047517, US 5863929, Journal of Medicinal Chemistry (2001), 44 (21), 3424-3439), Bulletin de la Societe Chimique de France (1958), 185-187].
  • R ! 3 is hydrogen, C 1 -C 6 -alkyl, aryl, is preferred and particularly preferably hydrogen, C, -C 4 alkyl, phenyl;
  • Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Chinese cabbage leaf discs (Brassica pekinensis) infested with all stages of the green peach aphid (Myzus persicae) are sprayed with an active compound preparation of the desired concentration.
  • the effect is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
  • active compound For the preparation of a suitable preparation of active compound, 2 parts by weight of active compound are mixed with the stated amount of solvent. A portion of the concentrate is diluted with citrated bovine blood and the desired concentration produced.
  • fasting adult fleas (Ctenocephalides felis) are placed in a chamber sealed with gauze at the top and bottom.
  • a metal cylinder is placed on the chamber, the underside of which is sealed with parafilm.
  • the cylinder contains the blood-drug preparation that can be absorbed by the fleas through the parafilm membrane.
  • the kill is determined in%. 100% means that all fleas have been killed; 0% means that no flea has been killed.
  • Boophilus microplus test (BOOPMI injection)
  • the drug solution is injected into the abdomen (Boophilus microplus), the animals are transferred to trays and stored in an air-conditioned room. The effect control takes place on storage of fertile eggs.
  • the effect is determined in%. 100% means that no ticks have laid fertile eggs.

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  • Organic Chemistry (AREA)
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Abstract

La présente invention concerne de nouveaux dérivés de benzoathiazine de la formule (I) dans laquelle R1, R2, R3, R4, R5 et R6 ont les significations indiquées dans la description, plusieurs procédés pour leur production et leur utilisation comme insecticide et/ou acaricide en combinaison avec d'autres agents tels que des promoteurs de pénétration et/ou des sels d'ammonium ou de phosphonium.
EP09767967A 2008-12-15 2009-12-02 Dérivés de 4-amino-1,2,3- benzoxathiazine comme pesticides Withdrawn EP2376465A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP09767967A EP2376465A1 (fr) 2008-12-15 2009-12-02 Dérivés de 4-amino-1,2,3- benzoxathiazine comme pesticides

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08171681A EP2196461A1 (fr) 2008-12-15 2008-12-15 Dérivés de 4-Amino-1,2,3-benzoxathiazines comme pesticides
EP09767967A EP2376465A1 (fr) 2008-12-15 2009-12-02 Dérivés de 4-amino-1,2,3- benzoxathiazine comme pesticides
PCT/EP2009/008581 WO2010072310A1 (fr) 2008-12-15 2009-12-02 Dérivés de 4-amino-1,2,3- benzoxathiazine comme pesticides

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EP2376465A1 true EP2376465A1 (fr) 2011-10-19

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EP09767967A Withdrawn EP2376465A1 (fr) 2008-12-15 2009-12-02 Dérivés de 4-amino-1,2,3- benzoxathiazine comme pesticides

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US (1) US8173641B2 (fr)
EP (2) EP2196461A1 (fr)
JP (1) JP2012512141A (fr)
KR (1) KR20110095417A (fr)
CN (1) CN102317271A (fr)
BR (1) BRPI0922927A2 (fr)
MX (1) MX2011006143A (fr)
WO (1) WO2010072310A1 (fr)

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KR20130039331A (ko) * 2010-06-29 2013-04-19 바이엘 인텔렉쳐 프로퍼티 게엠베하 사이클릭 카보닐아미딘을 포함하는 개량된 살충성 조성물
KR20190120155A (ko) * 2017-02-27 2019-10-23 시드 리서치 인스티튜트 컴퍼니, 리미티드 항진균 조성물

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2842476A (en) 1953-04-23 1958-07-08 Mclaughlin Gormley King Co Insecticidal compositions
US3317523A (en) * 1965-03-29 1967-05-02 Upjohn Co 4-substituted-1, 2, 3-benzoxathiazine 2, 2 dioxides
US3780030A (en) * 1971-10-29 1973-12-18 Dow Chemical Co 1,2,3-benzoxathiazin-4(3h)-one 2-oxides and their preparation
DE3008186A1 (de) 1980-03-04 1981-10-15 Hoechst Ag, 6000 Frankfurt Synergistische kombinationen von phosphinothricin
DE3339344A1 (de) * 1983-10-29 1985-05-09 Hoechst Ag, 6230 Frankfurt Substituierte 2,3,dihydro-1,4,3-benzoxathiazin-4,4-dioxide, verfahren zu ihrer herstellung und verwendung als herbizide
JPS638302A (ja) 1986-06-27 1988-01-14 Kao Corp 殺生剤用効力増強剤
JPH0618761B2 (ja) 1986-07-14 1994-03-16 花王株式会社 粒状農薬の製造方法
DE3869167D1 (de) * 1987-03-27 1992-04-23 Kumiai Chemical Industry Co Phenyltriazol-derivate und insectizid.
US4960767A (en) 1988-08-01 1990-10-02 Hoechst-Roussel Pharmaceuticals Inc. Isoxazolobenzoxazepines
JPH0747523B2 (ja) 1990-04-16 1995-05-24 花王株式会社 殺生剤効力増強剤
US5352674A (en) 1991-03-25 1994-10-04 Valent U.S.A. Chemically stable granules containing insecticidal phosphoroamidothioates
US5462912A (en) 1991-10-09 1995-10-31 Kao Corporation Agricultural chemical composition enhancer comprising quaternary di(polyoxyalkylene) ammonium alkyl sulfates
MY111077A (en) 1992-11-13 1999-08-30 Kao Corp Agricultural chemical composition
GB9310965D0 (en) 1993-05-27 1993-07-14 Ucb Sa 2-hydroxy-3-(1h-imidazol-4-yl)alkyl)benzenecarboximidamides
CN1112846C (zh) 1993-12-28 2003-07-02 花王株式会社 农药增效剂组合物和农药组合物
DE4401542A1 (de) 1994-01-20 1995-07-27 Hoechst Schering Agrevo Gmbh Synergistische Kombinationen von Ammoniumsalzen
DE4416303A1 (de) 1994-05-09 1995-11-16 Bayer Ag Schaumarmes Netzmittel und seine Verwendung
DE69733649T2 (de) 1996-04-09 2006-05-18 NPS Pharmaceuticals, Inc., Salt Lake City Calcylitische verbindungen
CA2258915A1 (fr) 1996-06-25 1997-12-31 Michael Robert Wiley Agents anticoagulants
GB9703054D0 (en) 1997-02-14 1997-04-02 Ici Plc Agrochemical surfactant compositions
DE19857963A1 (de) 1998-12-16 2000-06-21 Bayer Ag Agrochemische Formulierungen
TW200303309A (en) 2001-12-04 2003-09-01 Bristol Myers Squibb Co Novel n-[4-(1h-imidazol-1-yl)-2-fluorophenyl]-3-trifluoromethyl)-1h-pyrazole-5-carboxamides as factor Xa inhibitors
DE10201075A1 (de) 2002-01-14 2003-07-24 Basf Ag Verfahren und Vorrichtung zur Untersuchung des Weissanlaufens
US6645914B1 (en) 2002-05-01 2003-11-11 Ndsu-Research Foundation Surfactant-ammonium sulfate adjuvant composition for enhancing efficacy of herbicides
WO2003101197A1 (fr) 2002-05-31 2003-12-11 Cjb Industries, Inc. Additif pour pesticides
US7132448B2 (en) 2002-09-12 2006-11-07 The Hartz Mountain Corporation High concentration topical insecticide containing insect growth regulator
US6984662B2 (en) 2003-11-03 2006-01-10 The Hartz Mountain Corporation High concentration topical insecticide containing insect growth regulator
EP1747206A1 (fr) 2004-04-29 2007-01-31 Abbott Laboratories Analogues d'amino-tétrazoles et méthodes d'utilisation
EP1922311A2 (fr) 2005-09-09 2008-05-21 Brystol-Myers Squibb Company Inhibiteurs d'ikur acycliques
DE102005059467A1 (de) 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
DE102005059469A1 (de) 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
DE102005059470A1 (de) * 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
DE102005059468A1 (de) * 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
DE102005059466A1 (de) * 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
CN101415685B (zh) 2006-01-31 2011-08-24 阿雷生物药品公司 激酶抑制剂及其使用方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2010072310A1 *

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CN102317271A (zh) 2012-01-11
JP2012512141A (ja) 2012-05-31
EP2196461A1 (fr) 2010-06-16
US20110118240A2 (en) 2011-05-19
US8173641B2 (en) 2012-05-08
US20100267703A1 (en) 2010-10-21
WO2010072310A1 (fr) 2010-07-01
KR20110095417A (ko) 2011-08-24
MX2011006143A (es) 2011-06-27
BRPI0922927A2 (pt) 2015-08-25

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