EP1324996A2 - Substituierte arylketone - Google Patents

Substituierte arylketone

Info

Publication number
EP1324996A2
EP1324996A2 EP01903626A EP01903626A EP1324996A2 EP 1324996 A2 EP1324996 A2 EP 1324996A2 EP 01903626 A EP01903626 A EP 01903626A EP 01903626 A EP01903626 A EP 01903626A EP 1324996 A2 EP1324996 A2 EP 1324996A2
Authority
EP
European Patent Office
Prior art keywords
cyano
chlorine
fluorine
optionally substituted
ethoxy
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Withdrawn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
EP01903626A
Other languages
German (de)
English (en)
French (fr)
Inventor
Otto Schallner
Stefan Lehr
Hans-Georg Schwarz
Klaus-Helmut Müller
Dorothee Hoischen
Mark Wilhelm Drewes
Peter Dahmen
Dieter Feucht
Rolf Pontzen
Akihiko Yanagi
Shinichi Narabu
Toshio Goto
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
Bayer CropScience KK
Original Assignee
Bayer CropScience AG
Bayer CropScience KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE10039723A external-priority patent/DE10039723A1/de
Application filed by Bayer CropScience AG, Bayer CropScience KK filed Critical Bayer CropScience AG
Publication of EP1324996A2 publication Critical patent/EP1324996A2/de
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • 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
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D249/12—Oxygen or sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04—Five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • the invention relates to new substituted aryl ketones, ner processes for their preparation and their use as herbicides.
  • n the numbers 0, 1 or 2
  • A represents alkanediyl (alkylene)
  • R represents one of the groupings below
  • n the numbers 0 to 6
  • R stands for halogen or for optionally substituted alkyl, alkylthio or aryl, or - if m stands for 2 - optionally also together with a second radical R 5 stands for alkanediyl (alkylene),
  • R for hydroxyl, formyloxy, halogen, or for each optionally substituted alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylcarbonyloxy, alkoxycarbonyloxy, alkylaminocarbonyloxy, alkylsulfonyloxy, alkenyloxy, alkynyloxy, aryloxy, arylthio, arylsulfmyl, arylsulfonyl, arylcarbonylalkyl, arylcarbonylalkyl, arylcarbonylalkylyl , Arylsulfonyloxy, arylalkoxy, arylalkylthio, arylalkylsulfmyl or arylalkylsulfonyl,
  • R 7 represents hydrogen, cyano, carbamoyl, thiocarbamoyl, halogen, or optionally substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkoxycarbonyl or cycloalkyl,
  • R represents hydrogen or alkyl which is optionally substituted
  • R 9 represents hydroxyl, formyloxy, or optionally substituted alkoxy, alkylcarbonyloxy, alkoxycarbonyloxy, alkylaminocarbonyloxy, alkylsulfonyloxy, alkenyloxy, alkynyloxy, arylalkoxy, arylcarbonyloxy, arylcarbonylalkoxy or arylsulfonyloxy,
  • R 10 represents hydrogen, cyano, carbamoyl, thiocarbamoyl, halogen, or represents optionally substituted alkyl, alkylcarbonyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulfinyl or alkylsulfonyl,
  • R 11 stands for hydrogen or for optionally substituted alkyl or cycloalkyl
  • R, 12 represents hydrogen or represents optionally substituted alkyl or cycloalkyl
  • R represents hydrogen, cyano, carbamoyl, halogen, or optionally substituted alkyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulfinyl or alkylsulfonyl,
  • R represents hydrogen, nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, halogen, or optionally substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl,
  • R stands for nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, halogen, or for optionally substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl, and R represents an optionally substituted 4- to 12-membered, saturated or unsaturated, monocyclic or bicyclic, heterocyclic grouping which has 1 to 4 heteroatoms (up to 4 nitrogen atoms and optionally - alternatively or additively - one or two oxygen atoms or one or two sulfur atoms , or one or two SO groups or one or two
  • hydrocarbon chains such as alkyl or alkanediyl - also in combination with heteroatoms, such as in alkoxy - are each straight-chain or branched.
  • the compounds of the general formula (I) according to the invention optionally contain one or more asymmetrically substituted carbon atoms and can therefore be present in various enantiomeric (R- and S-configured forms) or diastereomeric forms.
  • the invention relates both to the various possible individual enantiomeric or stereoisomeric forms of the compounds of the general formula (I) and to the mixtures of these stereoisomers
  • n is preferably the number 0 or 1 m preferably represents the numbers 0, 1, 2, 3 or 4.
  • A preferably represents alkanediyl (alkylene) having 1 to 6 carbon atoms.
  • R 1 preferably represents one of the groupings below
  • R preferably represents hydrogen, nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, halogen, or each optionally by cyano, halogen, C 1 -C 4 -alkoxy, C r C 4 -alkylthio, C 1 -C 4 -alkylsulfinyl or C r C 4 alkyl sulfonyl substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl each having 1 to 6 carbon atoms in the alkyl groups.
  • R 3 preferably represents nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen-, C1-C4 alkoxy, C r C 4 - alkylthio, C r C 4 - alkylsulfinyl or C r C 4 - Alkylsulfonyl substituted alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl each having 1 to 6 carbon atoms in the alkyl groups.
  • R 4 preferably represents one of the heterocyclic groupings below
  • Q oxygen or sulfur
  • R 14 for hydrogen, hydroxy, mercapto, cyano, halogen, for each alkyl optionally substituted by cyano, halogen, Cj-C ⁇ alkoxy, C * -C4-alkylthio, C1-C4-alkylsulfinyl or C1-C4-alkylsulfonyl, Alkylcarbonyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulfinyl or alkylsulfonyl, each having up to 6 carbon atoms in the alkyl groups, for each alkylamino or dialkylamino optionally substituted by halogen, each having up to 6 carbon atoms in the alkyl groups, for alkenyl, alkynyl optionally substituted by halogen, Alkenyloxy, alkenylthio or alkenylamino, each having up to 6 carbon atoms in the alkenyl or alkynyl groups
  • R 15 for hydrogen, hydroxy, arnino, alkylidene amino with up to 4 carbon atoms, for each optionally substituted by halogen or C * [-C4-alkoxy substituted alkyl, alkoxy, alkylamino, dialkylamino or alkanoylamino each with up to 6 carbon atoms in the alkyl groups, for each optionally substituted by halogen alkenyl, alkynyl or alkenyloxy each having up to 6 carbon atoms in the alkenyl or alkynyl groups, for each optionally substituted by halogen cycloalkyl, cycloalkylalkyl or cycloalkylamino each having 3 to 6 carbon atoms in the cycloalkyl groups and optionally up to 3 carbon atoms in the alkyl part, or for phenyl or benzyl which is in each case optionally substituted by halogen, C1-C4-alkyl or C1-C4-
  • R 5 preferably represents halogen, alkyl or alkylthio, each optionally substituted by cyano, halogen or C 1 -C 4 alkoxy, each having 1 to 6 carbon atoms, optionally halogen, C 1 -C 4 alkyl or CrC 4 alkoxy substituted phenyl, or optionally - in the event that m is 2 - together with a second radical R 5 for alkanediyl
  • R 6 preferably represents hydroxyl, formyloxy, or alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylcarbonyloxy, alkoxycarbonyloxy, alkylaminocarbonyloxy or alkylsulfonyloxy each having 1 to 6 carbon atoms in each case optionally substituted by cyano, halogen or C 1 -C 4 -alkoxy the alkyl groups, for alkenyloxy or alkynyloxy each optionally substituted by cyano or halogen, each having 2 to 6 carbon atoms, or for in each case optionally by nitro, cyano, halogen, C 1 -C 4 -alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 - Alkoxy or -C 4 -
  • R 7 preferably represents hydrogen, cyano, carbamoyl, thiocarbamoyl, halogen, in each case alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl or alkoxycarbonyl optionally substituted by cyano, halogen or - - alkoxy, each having 1 to 6 carbon atoms in the alkyl groups, or for optionally substituted by cyano, halogen or -CC 4 alkyl cycloalkyl having 3 to 6 carbon atoms.
  • R 8 preferably represents hydrogen, each alkyl having 1 to 6 carbon atoms optionally substituted by cyano, halogen or Cr alkoxy, and each optionally substituted by cyano or halogen Alkenyl or alkynyl each having 2 to 6 carbon atoms, each optionally by cyano, halogen or C- .
  • R 9 preferably represents hydroxyl, formyloxy, each optionally through
  • R 10 preferably represents hydrogen, cyano, carbamoyl, thiocarbamoyl,
  • Halogen or for each optionally by cyano, halogen or C 1 -C 4 -
  • R 11 preferably represents hydrogen, represents optionally cyano-, halogen or Cj-C 4 - alkoxy-substituted alkyl having 1 to 6 carbon atoms or represents optionally cyano-, halogen or C ⁇ -C 4 alkyl
  • R 12 preferably represents hydrogen, alkyl optionally substituted by cyano, halogen or -C 4 -alkoxy having 1 to 6 carbon atoms or cycloalkyl optionally substituted by cyano, halogen or C 1 -C 4 -alkyl having 3 to 6 carbon atoms.
  • R preferably represents hydrogen, cyano, carbamoyl, halogen, or alkyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulfinyl or alkylsulfonyl, each of which has 1 to 6 carbon atoms in the alkyl groups and is optionally substituted by cyano, halogen or - -alkoxy.
  • n particularly preferably represents the numbers 0, 1, 2 or 3.
  • Butane-l, 3-diyl or butane-1,4-diyl (tetramethylene).
  • R 2 particularly preferably represents hydrogen, nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, iodine, or, if appropriate, in each case by fluorine and or chlorine, methoxy, ethoxy, n- or i-propoxy,
  • R 3 particularly preferably represents nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, each optionally by fluorine and / or chlorine, methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, n- or i-propylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl or ethylsulfonyl substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, each optionally with fluorine and / or chlorine, methoxy, ethoxy, n- or i-propoxy substituted methoxy, ethoxy, n- or i-propoxy, for each methylthio, ethylthio optionally substituted by fluor
  • R 4 particularly preferably represents one of the heterocyclic groupings below
  • R 5 particularly preferably represents fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, which are each optionally substituted by cyano, fluorine, chlorine, methoxy or ethoxy, Methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, for phenyl optionally substituted by fluorine, chlorine, methyl or methoxy, or optionally also - for the case that m is 2 - together with a second radical R 5 for ethane-1,2-diyl (dimethylene), propane-l, 3-diyl (trimethylene) or butane-1,4-diyl (tetramethylene).
  • a second radical R 5 for ethane-1,2-diyl (dimethylene), propane-
  • R particularly preferably represents hydroxy, formyloxy, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, each optionally substituted by cyano, fluorine, chlorine, methoxy or ethoxy , n- or i-Propylthio, n-, i-, s- or t-butylthio, methylsulfinyl, ethylsulfinyl, n- or i-propylsulfinyl, methylsulfonyl, ethylsulfonyl, n- or i-propylsulfonyl, acetyloxy, propionyloxy, n- or i-butyroyloxy, methoxycarbonyloxy, ethoxycarbonyloxy, n- or i-propoxycarbony
  • Phenylmethylsulfinyl or phenylmethylsulfonyl is a group consisting of:
  • R particularly preferably stands for hydrogen, cyano, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, for methyl, ethyl, n- or i-, each optionally substituted by cyano, fluorine, chlorine, methoxy or ethoxy.
  • R 8 particularly preferably represents hydrogen, in each case methyl optionally substituted by cyano, fluorine, chlorine, bromine, methoxy or ethoxy,
  • R 9 particularly preferably represents hydroxyl, formyloxy, methoxy, ethoxy, n- or i-propoxy, n-, i-, in each case optionally substituted by cyano, fluorine, chlorine, bromine, methoxy, ethoxy, n- or i-propoxy, s- or t-butoxy, acetyloxy, propionyloxy, n- or i-butyroyloxy, methoxycarbonyloxy,
  • R 10 particularly preferably represents hydrogen, cyano, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, or methyl, ethyl, n- which is optionally substituted by cyano, fluorine, chlorine, bromine, methoxy, ethoxy, n- or i-propoxy.
  • R 11 particularly preferably represents hydrogen, in each case optionally through
  • R particularly preferably represents hydrogen, in each case methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl which is optionally substituted by cyano, fluorine, chlorine, bromine, methoxy or ethoxy, or in each case cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl optionally substituted by cyano, fluorine, chlorine, bromine, methyl or ethyl.
  • R particularly preferably represents hydrogen, cyano, carbamoyl, fluorine, chlorine, bromine, or methyl, ethyl, n- or i-propyl, n-, i-, in each case optionally substituted by cyano, fluorine, chlorine, bromine, methoxy or ethoxy.
  • s- or t-butyl methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methoxycarbonyl, ethoxycarbonyl, n- or i-propoxycarbonyl, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylsulfinyl, ethylsulfinyl, n- or i-propylsulfinyl, methylsulfonyl, ethylsulfonyl, n- or i-propylsulfonyl.
  • R 15 particularly preferably represents hydrogen, hydroxyl, amino, methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, methoxy, ethoxy, each optionally substituted by fluorine and / or chlorine, methoxy or ethoxy , n- or i-propoxy, methylamino, ethylamino or dimethylamino, for ethenyl, propenyl optionally substituted by fluorine and / or chlorine,
  • Ethynyl, propynyl or propenyloxy for each cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, optionally substituted by fluorine and or chlorine, or for each optionally by fluorine, chlorine, methyl, ethyl, n- or i -Propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-
  • n very particularly preferably represents the numbers 0, 1 or 2.
  • R very particularly preferably represents hydrogen, nitro, cyano, fluorine, chlorine,
  • R very particularly preferably represents nitro, cyano, fluorine, chlorine, bromine, iodine,
  • R 5 very particularly preferably represents methyl, ethyl, n- or i-propyl, methylthio, ethylthio, n- or i-propylthio, optionally substituted by fluorine or chlorine, in each case for phenyl, or, if appropriate, in the case where m is 2 stands - together with a second radical R 5 for ethane-1,2-diyl (dimethylene), propane-1,3-diyl (trimethylene) or butane-1,4-diyl (tetramethylene).
  • R very particularly preferably represents hydroxyl, formyloxy, methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, n- or i-propylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl, each optionally substituted by fluorine, chlorine, methoxy or ethoxy, Ethylsulfonyl, acetyloxy, propionyloxy, n- or i-butyroyloxy, methoxycarbonyloxy, ethoxycarbonyloxy, n- or i-propoxycarbonyloxy, methylaminocarbonyloxy, ethylaminocarbonyloxy, n- or i-propylaminocarbonyloxy, methylsulfonyloxy, ethyl- or sulfonyloxy, Propylsulfonyloxy
  • R 7 very particularly preferably represents hydrogen, cyano, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, methoxy, ethoxy, n- or i-propoxy which are each optionally substituted by fluorine, chlorine, methoxy or ethoxy , Methylthio, ethylthio, n- or i-propylthio, methylsulfinyl, ethylsulfinyl, n- or i-propylsulfinyl, methylsulfonyl, ethylsulfonyl, n- or i-propylsulfonyl, methoxycarbonyl, ethoxycarbonyl, n- or i-propoxycarbonyl.
  • R very particularly preferably represents hydrogen, represents in each case optionally substituted * by cyano, fluorine, chlorine, methoxy or ethoxy-substituted methyl, ethyl, n- or i-propyl, represents in each case optionally fluorine- or chlorine-substituted propenyl or propynyl, represents optionally fluorine- , Chlorine, bromine, methyl or ethyl substituted cyclopropyl, or for each optionally substituted by fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, trifluoromethyl, methoxy, ethoxy, n- or i-propoxy, difluoromethoxy or trifluoromethoxy Phenyl or benzyl.
  • R 9 very particularly preferably represents hydroxy, formyloxy, methoxy, ethoxy, n- or i-propoxy, acetyloxy, propionyloxy, n, each optionally substituted by cyano, fluorine, chlorine, bromine, methoxy, ethoxy, n- or i-propoxy - or i-butyroyloxy, methoxycarbonyloxy, ethoxycarbonyloxy, n- or i-propoxycarbonyloxy, methylaminocarbonyloxy, ethylaminocarbonyloxy, n- or i-propylaminocarbonyloxy, methylsulfonyloxy, ethylsulfonyloxy, n- or i-propylsulfonyloxy or for propenyloxy, or for phenylmethoxy, benzoyloxy, benzoylmethoxy or phenylsulfonyloxy each optional
  • R 10 very particularly preferably represents hydrogen, cyano, fluorine, chlorine, bromine, or methyl, ethyl, n- or i-propyl, acetyl, which are each optionally substituted by fluorine, chlorine, methoxy, ethoxy, n- or i-propoxy, Propionyl, n- or i-butyroyl, methoxy, ethoxy, n- or i-propoxy, methoxycarbonyl, ethoxycarbonyl, n- or i-propoxycarbonyl, methylthio, ethylthio, n- or i-propylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl or ethylsulfonyl.
  • R 11 very particularly preferably represents hydrogen, in each case methyl, ethyl optionally substituted by fluorine, chlorine, bromine, methoxy or ethoxy, n- or i-propyl, or for cyclopropyl optionally substituted by fluorine, chlorine, bromine, methyl or ethyl.
  • R 12 very particularly preferably represents hydrogen, in each case methyl, ethyl, n- or i-propyl which is optionally substituted by fluorine, chlorine, methoxy or ethoxy, or cyclopropyl which is optionally substituted by fluorine, chlorine, bromine, methyl or ethyl.
  • R very particularly preferably represents hydrogen, cyano, fluorine, chlorine, bromine, or each optionally by fluorine, chlorine, bromine, methoxy or
  • R 14 very particularly preferably represents hydrogen, hydroxy, mercapto, cyano, fluorine, chlorine, bromine, iodine, in each case optionally by fluorine, chlorine, methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, n- or i -Propyl- thio, methylsulfinyl, ethylsulfinyl, n- or i-propylsulfinyl, methylsulfonyl,
  • Chlorine methyl, ethyl, n- or i-propyl, methoxy, ethoxy, n- or i-propoxy substituted phenyl, phenyloxy, phenylthio, phenylamino, benzyl, benzyloxy, benzylthio or benzylamino, or - in the event that two adjacent radicals R 14 and R 14 are on a double bond - together with the neighboring radical R 14 also for a benzo group.
  • R 15 very particularly preferably represents hydrogen, hydroxyl, amino, methyl, ethyl, n- or i-propyl, methoxy, ethoxy, n- or i-propoxy, methylamino, each optionally substituted by fluorine and / or chlorine, methoxy or ethoxy , Ethylamino or Dimethylamino, for propenyl or propynyl, for each optionally substituted by fluorine and / or chlorine
  • n, A, R 1 , R 2 , R 3 and R 4 each have the most preferable meaning.
  • the invention also sodium, potassium, magnesium, calcium, ammonium, C ⁇ -C alkyl ammonium-4, di- (C 1 -C 4 -alkyl) -ammonium, tri- (C 1 -C 4 - alkyl) -ammonium, tetra- (C ⁇ -C 4 -alkyl) -ammonium, tri- (C 1 -C 4 alkyl) -sulfonium-, C 5 - or C 6 cycloalkyl-ammonium and di- - (C 1 -C 2 -alkyl) -benzyl-ammonium salts of compounds of the formula (I), in which preferably n, A, R 1 , R 2 , R 3 and R 4 are those preferred above, particularly preferred or have very particularly preferably given meanings.
  • the new substituted aryl ketones of the general formula (I) are notable for their strong and selective herbicidal activity.
  • R 1 has the meaning given above
  • R 2 , R 3 , R 4 and R n have the meaning given above,
  • n, A, R 2 , R 3 and R 4 preferably have those meanings which are already preferred above, particularly preferred or very particularly preferred in connection with the description of the compounds of the general formula (I) according to the invention for n, A, R 2 , R 3 and R 4 have been specified.
  • Esters especially the methyl esters and ethyl esters - if one
  • n, A, R and R have the meaning given above and
  • X 1 represents halogen (in particular fluorine, chlorine or bromine) or alkylsulfonyloxy (in particular methylsulfonyloxy or ethylsulfonyloxy),
  • esters especially the methyl esters
  • an acid acceptor e.g. Potassium carbonate
  • a diluent e.g. Acetone, butanone, acetonitrile, N, N-dimethylformamide or dimethyl sulfoxide
  • esters especially the methyl esters and ethyl esters -
  • a and R 4 have the meaning given above,
  • condensation aids e.g. Azodicarboxylic acid diethyl ester and triphenylphosphine
  • a diluent e.g. Tetrahydrofuran
  • esters especially the methyl esters and ethyl esters -
  • a and R 4 have the meaning given above and
  • X 2 represents halogen (in particular fluorine, chlorine or bromine), alkylsulfonyloxy (in particular methylsulfonyloxy or ethylsulfonyloxy) or arylsulfonyloxy (in particular p-tolylsulfonyloxy),
  • an acid acceptor e.g. Potassium carbonate or triethylamine
  • a diluent e.g. Acetone, butanone, acetonitrile, N, N-dimethylformamide or dimethyl sulfoxide
  • Formula (III) provides a general definition of the compounds to be used further as starting materials in process (a) according to the invention for the preparation of compounds of the general formula (I).
  • R 1 preferably has the meaning which has already been given above in connection with the description of the compounds of the general formula (I) according to the invention as preferred, particularly preferred or very particularly preferred for R 1 .
  • the starting materials of the general formula (III) are known organic compounds.
  • Formula (Ia) provides a general definition of substituted benzoyl ketones to be used as starting materials.
  • n, A, R 2 , R 3 , R 4 and R 11 preferably have those meanings which are preferred, particularly preferred or already in connection with the description of the compounds of the general formula (I) according to the invention have very particularly preferably been given for n, A, R 2 , R 3 , R 4 and R u .
  • the starting materials of the general formula (Ia) are new compounds according to the invention; they can be prepared by process (a) according to the invention.
  • Process (a) according to the invention for the preparation of the new substituted aryl ketones of the general formula (I) is optionally carried out using a dehydrating agent.
  • a dehydrating agent The usual chemicals suitable for binding water can be considered.
  • Dicyclohexylcarbodiimide and carbonyl-bis-imidazole are mentioned as examples.
  • Dicyclohexylcarbodiimide is mentioned as a particularly suitable dehydrating agent.
  • Process (a) according to the invention for the preparation of the new substituted aryl ketones of the general formula (I) is optionally carried out using one or more reaction auxiliaries.
  • Examples include sodium cyanide, potassium cyanide, acetone cyanohydrin, 2-cyano-2- (trimethylsilyloxy) propane and trimethylsilyl cyanide. Trimethylsilyl cyanide is mentioned as a particularly suitable further reaction auxiliary.
  • Process (a) according to the invention for the preparation of the new substituted aryl ketones of the general formula (I) is optionally carried out using a further reaction auxiliary.
  • Basic organic nitrogen compounds such as, for example, trimethylamine, triethylamine, tripropylamine, tributylamine, ethyldiisopropylamine, N, N-dimethylcyclohexylamine, dicyclohexylamine, ethyldicyclohexylamine, N, N-, generally come as further reaction auxiliaries for the process according to the invention.
  • DABCO 1,4-diazabicyclo [2,2,2] octane
  • DBU 1,8-diazabicyclo [5,4,0] -undec-7-ene
  • Process (b) according to the invention for the preparation of the compounds of the formula (I) is optionally carried out using orthoformic acid esters or N, N-dimethylformamide acetals. These compounds preferably contain alkyl groups with 1 to 4 carbon atoms, especially methyl or ethyl.
  • (I) is optionally carried out using cyano formic acid esters. These compounds preferably contain alkyl groups with 1 to 4 carbon atoms, especially methyl or ethyl. Examples include methyl cyano formate and ethyl cyano formate.
  • the process (b) according to the invention for the preparation of the compounds of the formula (I) is optionally carried out using (carbon disulfide and) alkylating agents. These compounds preferably contain alkyl groups with 1 to 4 carbon atoms, especially methyl or ethyl.
  • Examples include methyl chloride, methyl bromide, methyl iodide, dimethyl sulfate, ethyl chloride, ethyl bromide, ethyl iodide and diethyl sulfate.
  • Process (b) according to the invention for the preparation of the compounds of the formula (I) are carried out using hydroxylamine or an acid adduct thereof.
  • Hydroxylamine hydrochloride is mentioned as the preferred acid adduct.
  • diluents are particularly suitable as diluents for carrying out processes (a) and (b) according to the invention.
  • diluents include in particular aliphatic, alicyclic or aromatic, optionally halogenated hydrocarbons, such as, for example, gasoline, benzene, toluene, xylene, chlorobenzene, dichlorobenzene, petroleum ether, hexane, cyclohexane, dichloromethane, chloroform, carbon tetrachloride; Ethers, such as diethyl ether, diisopropyl ether,
  • Dioxane, tetrahydrofuran or ethylene glycol dimethyl or diethyl ether Dioxane, tetrahydrofuran or ethylene glycol dimethyl or diethyl ether; Ketones, such as acetone, butanone or methyl isobutyl ketone; Nitriles, such as acetonitrile, propionitrile or butyronitrile; Amides such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methylformanilide, N-methylpyrrolidone or hexamethylphosphoric acid triamide; Esters such as methyl acetate or ethyl acetate, sulfoxides such as
  • Dimethyl sulfoxide alcohols such as methanol, ethanol, n- or i-propanol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether.
  • reaction temperatures can be carried out when the inventive compounds
  • Processes (a) and (b) can be varied over a wide range. In general one works at temperatures between 0 ° C and 150 ° C, preferably between 10 ° C and 120 ° C.
  • Processes (a) and (b) according to the invention are generally carried out under atmospheric pressure. However, it is also possible to carry out the processes according to the invention under elevated or reduced pressure - generally between 0.1 bar and 10 bar.
  • the starting materials are generally used in approximately equimolar amounts. However, it is also possible to use one of the components in a larger excess.
  • the reaction is generally carried out in a suitable diluent and the reaction mixture is generally stirred at the required temperature for several hours. Working up is carried out according to customary methods (cf. the production examples).
  • the compounds of the formulas (IV), (V), (VI), (VII) and (VIII) to be used as starting materials in the process according to the invention for the preparation of the compounds of the general formula (II) are known organic compounds.
  • the active compounds according to the invention can be used as defoliants, desiccants, haulm killers and in particular as weed killers. Weeds in the broadest sense are all plants that grow in places where they are undesirable. Whether the substances according to the invention act as total or selective herbicides depends essentially on the amount used.
  • the active compounds according to the invention can e.g. can be used in the following plants:
  • the active compounds according to the invention are suitable for combating total weeds, e.g. on industrial and track systems and on paths and squares with and without tree cover.
  • the active compounds according to the invention for weed control in permanent crops e.g. Forest, ornamental wood, fruit, wine, citrus, nut, banana, coffee, tea, rubber, oil palm,
  • the compounds of formula (I) according to the invention show strong herbicidal activity and a broad spectrum of activity when used on the soil and on above-ground parts of plants. To a certain extent, they are also suitable for the selective control of monocotyledon and dicotyledon weeds in monocotyledon and dicotyledon crops, both in the pre-emergence and in the post-emergence process.
  • the active compounds according to the invention can be used in certain concentrations or
  • Application rates can also be used to control animal pests and fungal or bacterial plant diseases. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active compounds.
  • plants and parts of plants can be treated.
  • Plants are understood here to mean all plants and plant populations, such as desired and undesirable wild plants or crop plants (including naturally occurring crop plants).
  • Cultivated 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 cultivars which can or cannot be protected by plant breeders' rights.
  • Plant parts are to be understood to mean all above-ground and underground parts and organs of the plants, such as sprout, leaf, flower and root, by way of example
  • Leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds as well as roots, tubers and rhizomes are listed.
  • the plant parts also include crops and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
  • the treatment of the plants and parts of plants with the active compounds according to the invention is carried out directly or by acting on their surroundings, living space or storage space according to the customary treatment methods, for example by dipping, spraying, evaporating, atomizing, scattering, spreading and using propagation material, in particular seeds. continue by wrapping one or more layers.
  • the active ingredients can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, soluble powders, granules, suspension emulsion concentrates, active ingredient-impregnated natural and synthetic substances and very fine encapsulations in polymers
  • formulations are prepared in a known manner, e.g. B. by mixing the active ingredients with extenders, ie liquid solvents and / or solid carriers, optionally using surface-active agents
  • Agents ie emulsifiers and or dispersants and / or foam-generating agents.
  • organic solvents can also be used as auxiliary solvents.
  • auxiliary solvents e.g. organic solvents
  • aromatics such as xylene, toluene, or alkylnaphthalenes
  • chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chlorethylenes or methylene chloride
  • aliphatic hydrocarbons such as cyclohexane or paraffins, e.g. Petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol as well as their ethers and esters, ketones such as
  • Possible solid carriers are: for example ammonium salts and natural rock powders, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillo ' nit or diatomaceous earth and synthetic rock powders, such as highly disperse Silicic acid, aluminum oxide and silicates are suitable as solid carriers for granules: e.g.
  • suitable emulsifiers and / or foam-generating agents are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolyzates; Possible dispersants are: eg lignin sulfite waste liquor and methyl cellulose.
  • Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins and synthetic phospholipids can be used in the formulations. Further,
  • Additives can be mineral and vegetable oils.
  • 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 trace nutrients such as salts of iron, manganese, boron, copper, cobalt,
  • Molybdenum and zinc can be used.
  • the formulations generally contain between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%.
  • the active compounds according to the invention can also be used in a mixture with known herbicides and / or with substances which improve crop tolerance ("safeners") for weed control, ready-to-use formulations or tank mixes being possible. Mixtures are also possible possible with weed control agents which contain one or more known herbicides and a safener.
  • Known herbicides are suitable for the mixtures, for example
  • Acetochlor Acifluorfen (-sodium), Aclonifen, Alachlor, Alloxydim (-sodium), Ametryne, Amicarbazone, Amidochlor, Amidosulfuron, Anilofos, Asulam, Atrazine,
  • Fluridone Fluroxypyr (-butoxypropyl, -meptyl), Flurprimidol, Flurtamone, Fluothiacet (-methyl), Fluthiamide, Fomesafen, Foramsulfuron, Glufosinate (-ammonium), Glyphosate (-isopropylammonium), Halosafen, Haloxy- ethyloxy-( -P-methyl), hexazinones, imazamethabenz (-methyl), imazamethapyr, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron
  • Insecticides Insecticides, acaricides, nematicides, bird repellants, plant nutrients and soil structure improvers are possible.
  • Solutions, suspensions, emulsions, powders, pastes and granules are used. They are used in the customary manner, for example by watering, spraying, spraying or scattering.
  • the active compounds according to the invention can be applied both before and after emergence of the plants. They can also be worked into the soil before sowing.
  • the amount of active ingredient used can vary over a wide range. It essentially depends on the type of effect desired. In general, the application rates are between 1 g and 10 kg of active ingredient per hectare of soil, preferably between 5 g and 5 kg per ha.
  • reaction solution is washed successively with IN hydrochloric acid and saturated sodium chloride solution, dries over magnesium sulfate and removes the solvent in a water jet vacuum.
  • the residue is dissolved in 30 ml of acetonitrile and successively with gentle cooling with 0.28 g (3.3 mmol) of 2-hydroxy-2-methyl-propionitrile and 1.4 g
  • the calibration was carried out with unbranched alkan-2-ones (with 3 to 16 carbon atoms) whose logP values are known (determination of the logP values using the
  • R has one of the meanings given in the table below.
  • connection listed in Table 2 as an example (11-35) can be produced, for example, as follows:
  • connection listed in Table 2 as an example (11-61) can be produced, for example, as follows:
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.
  • Seeds of the test plants are sown in normal soil. After 24 hours, the soil is sprayed with the active ingredient preparation in such a way that the desired amount of active ingredient is applied per unit area.
  • the concentration of active ingredient in the spray liquor is chosen so that the desired amount of active ingredient is applied in 1000 liters of water per hectare.
  • Example B the compounds according to Preparation Example 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 and 11 show, with largely good tolerance to crop plants, such as maize, a strong action against weeds.
  • Example B the compounds according to Preparation Example 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 and 11 show, with largely good tolerance to crop plants, such as maize, a strong action against weeds.
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.
  • Test plants which have a height of 5-15 cm are sprayed with the active substance preparation in such a way that the desired amounts of active substance are applied per unit area.
  • the concentration of the spray liquor is chosen so that in
  • the degree of damage to the plants is rated in% damage compared to the development of the untreated control.
  • the compounds according to Preparation Example 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 13 show with good tolerance to crop plants, such as e.g. Corn, strong against weeds.

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Environmental Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Plant Pathology (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Pyrrole Compounds (AREA)
EP01903626A 2000-01-17 2001-01-05 Substituierte arylketone Withdrawn EP1324996A2 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DE10001588 2000-01-17
DE10001588 2000-01-17
DE10039723 2000-08-14
DE10039723A DE10039723A1 (de) 2000-01-17 2000-08-14 Substituierte Arylketone
PCT/EP2001/000092 WO2001053275A2 (de) 2000-01-17 2001-01-05 Substituierte arylketone

Publications (1)

Publication Number Publication Date
EP1324996A2 true EP1324996A2 (de) 2003-07-09

Family

ID=26003876

Family Applications (1)

Application Number Title Priority Date Filing Date
EP01903626A Withdrawn EP1324996A2 (de) 2000-01-17 2001-01-05 Substituierte arylketone

Country Status (11)

Country Link
US (2) US6864219B2 (es)
EP (1) EP1324996A2 (es)
JP (1) JP2004504266A (es)
CN (1) CN1509285A (es)
AU (1) AU784813B2 (es)
BR (1) BR0107624A (es)
CA (1) CA2397387A1 (es)
MX (1) MXPA02006966A (es)
PL (1) PL362683A1 (es)
RU (1) RU2299879C2 (es)
WO (1) WO2001053275A2 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7842727B2 (en) 2001-03-27 2010-11-30 Errant Gene Therapeutics, Llc Histone deacetylase inhibitors
US7214831B2 (en) * 2002-05-22 2007-05-08 Errant Gene Therapeutics, Llc Histone deacetylase inhibitors based on alpha-chalcogenmethylcarbonyl compounds
US7057057B2 (en) 2002-05-22 2006-06-06 Errant Gene Therapeutics, Llc Histone deacetylase inhibitors based on alpha-ketoepoxide compounds
DE10142333A1 (de) * 2001-08-30 2003-03-20 Bayer Cropscience Ag Herbizide Mischungen auf Basis von substituierten Arylketonen
DE10144529A1 (de) * 2001-09-11 2003-03-27 Bayer Cropscience Gmbh 3-Aminocarbonyl substituierte Benzoylcyclohexandione
DE10209645A1 (de) * 2002-03-05 2003-09-18 Bayer Cropscience Ag Substituierte Arylketone
DE10215723A1 (de) 2002-04-10 2003-10-30 Bayer Cropscience Gmbh 3-Keto oder 3-Oximether substituierte Benzoylcyclohexandione
JP5209194B2 (ja) * 2006-10-13 2013-06-12 バイエル・クロップサイエンス・アーゲー ベンゾイルピラゾール類及び除草剤
PL2461688T3 (pl) * 2009-08-07 2017-08-31 Dow Agrosciences Llc Kompozycje szkodnikobójcze
DK2848612T3 (da) * 2012-05-08 2017-11-06 Ishihara Sangyo Kaisha Fremgangsmåde til fremstilling af en substitueret benzoesyreforbindelse
CN112430220B (zh) * 2019-08-26 2023-12-08 东莞市东阳光农药研发有限公司 取代的苯甲酰类化合物及其应用

Family Cites Families (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5006158A (en) 1984-12-20 1991-04-09 Ici Americas Inc. Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones
US4946981A (en) 1982-03-25 1990-08-07 Ici Americas Inc. Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones
US5085688A (en) 1982-03-25 1992-02-04 Ici Americas Inc. Certain 2-(2-chloro-3-alkoxy-4-substituted benzoyl)-5-methyl-5-1,3-cyclohexanediones as herbicides
US4780127A (en) 1982-03-25 1988-10-25 Stauffer Chemical Company Certain 2-(substituted benzoyl)-1,3-cyclohexanediones and their use as herbicides
US4816066A (en) 1983-09-16 1989-03-28 Stauffer Chemical Company Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones
US4806146A (en) 1984-12-20 1989-02-21 Stauffer Chemical Company Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones
JPS63258463A (ja) 1987-04-14 1988-10-25 Kumiai Chem Ind Co Ltd ２−フエノキシピリミジン誘導体及び除草剤
JPS63264584A (ja) * 1987-04-20 1988-11-01 Aguro Kanesho Kk 除草剤組成物
EP0319075B1 (en) 1987-11-28 1994-07-20 Nippon Soda Co., Ltd. Cyclohexenone derivatives
US4986845A (en) * 1988-07-15 1991-01-22 Nissan Chemical Industries Ltd. Pyrazole derivatives and herbicides containing them
US5656573A (en) 1989-09-11 1997-08-12 Rhone-Poulenc Agriculture Ltd. Herbicidal 4-substituted isoxazoles
US5747424A (en) 1989-09-11 1998-05-05 Rhone-Poulenc Agriculture Ltd. Herbicidal 4-substituted isoxazol
US5650533A (en) 1989-09-11 1997-07-22 Rhone-Poulenc Agriculture Ltd. Intermediates to herbicidal 4-substituted isoxazoles
US5804532A (en) * 1991-01-25 1998-09-08 Rhone-Poulenc Agriculture Limited Herbicidal 2-cyano-1,3-diones
JPH04327578A (ja) * 1991-04-30 1992-11-17 Mitsubishi Petrochem Co Ltd フェノキシメチルピリミジン誘導体およびそれを有効成分とする除草剤
GB9116834D0 (en) 1991-08-05 1991-09-18 Rhone Poulenc Agriculture Compositions of new matter
JP3252232B2 (ja) * 1992-06-29 2002-02-04 コニカ株式会社 ハロゲン化銀写真感光材料
GB9302049D0 (en) 1993-02-03 1993-03-24 Rhone Poulenc Agriculture Compositions of new matter
GB9302072D0 (en) * 1993-02-03 1993-03-24 Rhone Poulenc Agriculture New compositions of matter
JPH06256113A (ja) * 1993-03-01 1994-09-13 Mitsubishi Petrochem Co Ltd 除草剤組成物
JPH06271562A (ja) * 1993-03-23 1994-09-27 Hokko Chem Ind Co Ltd シクロヘキサンジオン誘導体および除草剤
JPH06321932A (ja) * 1993-05-07 1994-11-22 Hokko Chem Ind Co Ltd シクロヘキサンジオン誘導体および除草剤
CA2117413C (en) 1993-07-30 2006-11-21 Neil Geach Herbicidal isoxazole-4-yl-methanone derivatives
JPH07206808A (ja) * 1994-01-17 1995-08-08 Hokko Chem Ind Co Ltd シクロヘキサンジオン誘導体および除草剤
NZ292683A (en) 1994-08-25 1998-07-28 Merrell Pharma Inc Piperidine derivatives
GB9420390D0 (en) 1994-10-10 1994-11-23 Nycomed Salutar Inc Liposomal agents
MX9706382A (es) 1995-02-24 1997-11-29 Basf Ag Derivados de benzoilo.
CA2211534C (en) 1995-02-24 2004-10-26 Basf Aktiengesellschaft Isoxazolyl-benzoyl derivatives
JPH11500721A (ja) 1995-02-24 1999-01-19 ビーエーエスエフ アクチェンゲゼルシャフト フェニルジケトン誘導体
TR199600329A2 (tr) * 1995-05-05 1997-03-21 Hoffmann La Roche Seker alkollerin yeni sülfürik asit esterleri.
AU1593497A (en) 1996-01-26 1997-08-20 Rhone-Poulenc Agriculture Limited Isoxazole and 2-cyano-1,3-diones derivatives and their use as herbicides
US5948917A (en) 1996-03-26 1999-09-07 Nippon Soda Co., Ltd. 3-(isoxazol-5-yl)-substituted benzoic acid derivative and method for production thereof
AU2405897A (en) 1996-04-26 1997-11-19 Nippon Soda Co., Ltd. Novel heterocycle-substituted benzene derivatives and herbicides
CA2252543C (en) 1996-04-26 2003-01-14 Nippon Soda Co., Ltd. Benzene derivatives substituted by heterocycles and herbicides
AU1670997A (en) 1996-04-26 1997-11-19 Nippon Soda Co., Ltd. Novel benzene derivatives substituted by heterocycles and herbicides
AU1670797A (en) 1996-04-26 1997-11-19 Nippon Soda Co., Ltd. Benzene derivatives substituted by heterocycles and herbicides
US6297198B1 (en) 1996-05-14 2001-10-02 Syngenta Participations Ag Isoxazole derivatives and their use as herbicides
AU2977397A (en) * 1996-05-30 1998-01-05 Hokko Chemical Industry Co. Ltd. Cyclohexanedione derivatives and herbicidal compositions
CA2257196A1 (en) 1996-06-06 1997-12-11 Morris Padgett Rorer Herbicidal pyridinyl and pyrazolylphenyl ketones
WO1998028981A1 (fr) 1996-12-27 1998-07-09 Nippon Soda Co., Ltd. Composition herbicide
JP2001508075A (ja) 1997-01-17 2001-06-19 ビーエーエスエフ アクチェンゲゼルシャフト 硫黄含有２−クロロ−３−（４，５−ジヒドロ−３−イソキサゾリル）−安息香酸の製造法
US6165944A (en) 1997-01-17 2000-12-26 Basf Aktiengesellschaft 4-(3-heterocyclyl-1-benzoyl) pyrazoles and their use as herbicides
ES2318868T3 (es) 1997-01-17 2009-05-01 Basf Se Derivados del benzoilo sustituidos por 3-heterociclilo.
AU7427298A (en) * 1997-03-14 1998-10-12 Novartis Ag Novel herbicides
AU8863798A (en) 1997-07-18 1999-02-10 Rhone-Poulenc Agriculture Limited 4-benzoyl-isoxazole- and -pyrazole derivatives and 2-cyano 1,3-dione derivativesas herbicides
AU9156198A (en) * 1997-08-07 1999-03-01 Basf Aktiengesellschaft 2-benzoyl-cyclohexane-1,3-diones
JP2001514172A (ja) 1997-08-07 2001-09-11 ビーエーエスエフ アクチェンゲゼルシャフト 置換４−ベンゾイルピラゾール
CA2298462C (en) 1997-08-07 2008-02-12 Basf Aktiengesellschaft 2-benzoyl-cyclohexane-1,3-dione as herbicides
US5863865A (en) 1997-10-28 1999-01-26 Zeneca Limited Herbicidal 4-benzoylisoxazoles derivatives
EP1054865A1 (en) * 1998-02-10 2000-11-29 AstraZeneca UK Limited Farnesyl transferase inhibitors
IL137540A0 (en) * 1998-02-25 2001-07-24 Genetics Inst Inhibitors of phospholipase a2
IL139169A0 (en) * 1998-05-05 2001-11-25 Hoffmann La Roche Pyrazole derivatives as p-38 map kinase inhibitors
EP1077972A1 (en) * 1998-05-22 2001-02-28 Dow AgroSciences LLC 1-alkyl-4-[(3-oxetanyl-)benzoyl]-5-hydroxypyrazole compounds and their use as herbicides
PE20001566A1 (es) * 1999-03-26 2001-02-05 Ucb Sa Piperazinas 1,4-sustituidas, piperidinas 1,4-sustituidas y 4-alquilidenilpiperidinas 1-sustituidas
EP1176958B1 (en) 1999-05-05 2004-07-28 Merck & Co., Inc. Novel catechols as antimicrobial agents
ES2165274B1 (es) 1999-06-04 2003-04-01 Almirall Prodesfarma Sa Nuevos derivados de indolilpiperidina como agentes antihistaminicos y antialergicos.
EP1189612A4 (en) * 1999-06-30 2005-02-16 Daiichi Seiyaku Co VLA-4 INHIBITORY COMPOUNDS
AU6597100A (en) * 1999-08-19 2001-03-19 Ishihara Sangyo Kaisha Ltd. Triketone compounds, process for producing the same and herbicides containing the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0153275A3 *

Also Published As

Publication number Publication date
US6864219B2 (en) 2005-03-08
AU784813B2 (en) 2006-06-29
WO2001053275A3 (de) 2003-04-17
AU3166601A (en) 2001-07-31
PL362683A1 (en) 2004-11-02
US20030153465A1 (en) 2003-08-14
CA2397387A1 (en) 2001-07-26
RU2299879C2 (ru) 2007-05-27
US20050009704A1 (en) 2005-01-13
WO2001053275A2 (de) 2001-07-26
CN1509285A (zh) 2004-06-30
RU2002122392A (ru) 2004-01-10
MXPA02006966A (es) 2003-01-28
JP2004504266A (ja) 2004-02-12
BR0107624A (pt) 2002-11-12

Similar Documents

Publication Publication Date Title
WO2000005221A1 (de) Substituierte benzoylcyclohexandione
EP1165547B1 (de) Substituierte benzoylpyrazole als herbizide
DE19920791A1 (de) Substituierte Benzoylisoxazole
EP1181280A1 (de) Substituierte benzoylketone, verfahren zu ihrer herstellung und ihre verwendung als herbizide
EP1263738B1 (de) Substituierte benzoylcyclohexenone
EP1324996A2 (de) Substituierte arylketone
WO2002090336A1 (de) Substituierte arylketone
WO2001090102A2 (de) 6-heterocyclyl-3-oxo-3,4-dihydro-chinoxaline
WO2001047894A1 (de) Substituierte benzoylcyclohexandione als herbizide
WO2001010861A2 (de) Substituierte heterocyclyl-2h-chromene
EP1480944A2 (de) Substituierte arylketone
DE10039723A1 (de) Substituierte Arylketone
DE19921732A1 (de) Substituierte Benzoylcyclohexandione
WO2001023367A1 (de) Substituierte arylketone
EP1395565A1 (de) Herbizidwirksame substituierte benzoylpyrazole
DE10051981A1 (de) Substituierte Phenyluracile
WO2003070696A2 (de) Substituierte arylketone
WO2002010155A1 (de) Substituierte arylketone und ihre verwendung als herbizide
WO2002020487A1 (de) Substituierte 1-aryl-pyridin-2-(thi)one
DE10028687A1 (de) Substituierte Benzoylcyclohexenone
WO2001068616A1 (de) Substituierte 1-aryl-cyclopropylmethylamino-1,3,5-triazine
EP1501360A1 (de) 2,6 substituierte pyridin-3-carbonyl derivate als pflanzenschutzmittel mit herbizider wirkung
DE10055499A1 (de) 6-Heterocyclyl-3-oxo-3,4-dihydro-chinoxaline

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

17P Request for examination filed

Effective date: 20031017

17Q First examination report despatched

Effective date: 20040415

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20080801