WO2014048827A1 - Herbizid wirksame 3-phenylisoxazolinderivate - Google Patents

Herbizid wirksame 3-phenylisoxazolinderivate Download PDF

Info

Publication number
WO2014048827A1
WO2014048827A1 PCT/EP2013/069453 EP2013069453W WO2014048827A1 WO 2014048827 A1 WO2014048827 A1 WO 2014048827A1 EP 2013069453 W EP2013069453 W EP 2013069453W WO 2014048827 A1 WO2014048827 A1 WO 2014048827A1
Authority
WO
WIPO (PCT)
Prior art keywords
methyl
phenyl
cyano
fluorine
chlorine
Prior art date
Application number
PCT/EP2013/069453
Other languages
German (de)
English (en)
French (fr)
Inventor
Birgit Kuhn
Lothar Willms
Thomas Frenzel
Klaus Bernhard HAAF
Stephen David Lindell
Hansjörg Dietrich
Dirk Schmutzler
Elmar Gatzweiler
Christopher Hugh Rosinger
Original Assignee
Bayer Cropscience Ag
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 to US14/430,018 priority Critical patent/US9585392B2/en
Priority to MX2015003538A priority patent/MX378312B/es
Priority to DK13766930.5T priority patent/DK2900645T3/da
Priority to ES13766930T priority patent/ES2747483T3/es
Priority to CN201380061304.2A priority patent/CN104812739B/zh
Priority to JP2015532405A priority patent/JP6472382B2/ja
Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag
Priority to BR112015006573-2A priority patent/BR112015006573B1/pt
Priority to EP13766930.5A priority patent/EP2900645B1/de
Priority to IN1315DEN2015 priority patent/IN2015DN01315A/en
Priority to KR1020157010148A priority patent/KR101977920B1/ko
Publication of WO2014048827A1 publication Critical patent/WO2014048827A1/de
Priority to IL23768515A priority patent/IL237685B/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member

Definitions

  • the invention relates to the technical field of herbicides, in particular that of herbicides for the selective control of weeds and weeds in
  • WO1999 / 05130 A1 discloses herbicidally active 3-phenylisoxazolines which are present in the 5-position i.a. are substituted by a hydroxy and trifluoromethyl group.
  • WO2005 / 021516 A1, WO1995 / 014680 A1, WO2008 / 035315 A1, WO2005 / 051931 A1 and WO2005 / 021515 A1 describe, inter alia, in each case 3-phenylisoxazoline-5-carboxylic acids, esters and aldehydes which on the phenyl ring in 3- and 4-position are substituted by alkoxy radicals. These compounds are used as precursors to
  • Khimicheskaya (1996), (2), 426-429 mentions the compound methyl 3- (3,5-di-tert-butyl-4-hydroxyphenyl) -5-methyl-4,5-dihydro-1,2-oxazole -5-carboxylate.
  • 1326815-55-7 3- (3-Bromophenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid
  • 1326814-80-5 3- (5-bromo-2-fluorophenyl ) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid
  • 1326814-71 -4 Ethyl 3- (3-chlorophenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate, 1326810-45-0: 3- (3,4-dichlorophenyl ) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid, 1326815-81 -9: 3- (2,5-dichlorophenyl) -5-methyl-4,5-dihydro-1, 2-oxazole-5-carboxylic acid, 1326813-44-8: 3- (4-chloro-3-nitrophenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid,
  • 1326810-73-4 3- (3,4-difluorophenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid, 132681 1 -86-2: 3- (2.5- Difluorophenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid, 132681 1 -50-0: 3- (2,3-difluorophenyl) -5-methyl-4,5-dihydro- 1, 2-oxazole-5-carboxylic acid, 1326813-45-9: 3- (4-fluoro-3-methoxyphenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid,
  • 1326813-55-1 3- (2,5-dimethylphenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid, 1326815-05-7: 5-methyl-3- (3 -nitrophenyl) -4,5-dihydro-1,2-oxazole-5-carboxylic acid, 1326812-83-2: 5-methyl-3- [3- (trifluoromethyl) phenyl] -4,5-dihydro-1,2 oxazole-5-carboxylic acid,
  • 3-phenylisoxazoline derivatives are particularly well suited for this purpose.
  • An object of the present invention are 3-phenylisoxazoline derivatives or their salts of the formula (I)
  • R 1 and R 2 are each independently hydrogen, fluorine, chlorine, bromine, iodine, cyano, or by in each case m radicals from the group consisting of fluorine, chlorine, bromine, iodine and cyano substituted (Ci-C 4 ) alkyl or (C 1 -C 4 ) -alkoxy, or
  • R 1 and R 2 together with the carbon atom to which they are attached form a saturated, partially or completely unsaturated tri-, tetra- or
  • R 3 is fluorine, chlorine, cyano, (Ci-C 3 ) -alkylcarbonyloxy or S (0) "R 5 , or by in each case m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano, (Ci-C 4 ) -alkoxy and hydroxy-substituted (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl, (C 2 -C 6 ) -alkenyl or (C 2 -C 6 ) -alkynyl, or (C 1 -C 6) -alkylcarbonyl, (C 2 -C 6) -alkenylcarbonyl or (C 3 -C 6) -substituted by in each case m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano and (C 1 -C 6) -
  • R 6 is hydrogen or R 5 ;
  • R 7 denotes hydrogen or (C 1 -C 6) -alkyl, (C 3 -C 6) -cycloalkyl, (C 2 -C 4) -alkyl substituted by in each case m radicals consisting of fluorine, chlorine, bromine, cyano and (C 1 -C 4) -alkoxy C) alkenyl or (C 2 -C) alkynyl;
  • R 8 is R 7 ;
  • W * represents COOH, COOY, CN or CHO
  • Y is represented by m radicals from the group consisting of fluoro, chloro, bromo, cyano, hydroxy and COO- (Ci-C8) alkyl substituted (Ci-C8) -alkyl, which is represented by n heteroatoms selected from the group consisting of oxygen, sulfur and nitrogen is interrupted, or
  • m radicals from the group consisting of fluorine, chlorine, bromine iodine, cyano and (Ci-C) -alkoxy-substituted (Ci-C) alkyl, (C 3 -C 5 ) -cycloalkyl, (C 2 -C ) - Alkenyl, (C 2 -C 4 ) -alkynyl, (C 1 -C 4 ) -alkoxy, (C 2 -C 4 ) -alkenyloxy, (C 2 -C 4 ) -alkynyloxy or (C 1 -C 4 ) -alkylcarbonyl;
  • Methyl 3- (3,5-di-tert-butyl-4-hydroxyphenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate and ethyl 3- (3-chlorophenyl) - 5-methyl-4,5-dihydro-1, 2-oxazole-5-carboxylate are excluded.
  • Alkyl denotes saturated, straight-chain or branched hydrocarbon radicals with the number of carbon atoms indicated in each case, e.g. C 1 -C 6 -alkyl, such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1, 1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2, 2-dimethylpropyl, 1-ethylpropyl, hexyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1, 1-dimethylbutyl, 1, 2 Dimethylbutyl, 1, 3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl,
  • Alkyl substituted by halogen means straight-chain or branched alkyl groups, in which groups some or all of the hydrogen atoms may be replaced by halogen atoms, e.g. Ci-C2-haloalkyl such as chloromethyl,
  • Alkenyl denotes unsaturated, straight-chain or branched hydrocarbon radicals having in each case the number of carbon atoms and a double bond in any desired position, for example C 2 -C 6 -alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2 Butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-2-butenyl
  • Alkynyl means straight-chain or branched hydrocarbon radicals having in each case the number of carbon atoms and a triple bond in any desired position, e.g. C 2 -C 6 -alkynyl, such as ethynyl, 1-propynyl, 2-propynyl (or
  • Alkoxy means saturated, straight-chain or branched alkoxy radicals with the number of carbon atoms given in each case, for example C 1 -C 6 -alkoxy, such as methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy, 1, 1-dimethylethoxy , Pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1, 1-dimethylpropoxy, 1, 2-dimethylpropoxy, 1-methylpentoxy, 2-methylpentoxy , 3-methylpentoxy, 4-methylpentoxy, 1, 1-dimethylbutoxy, 1, 2-dimethylbutoxy, 1, 3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1 Ethylbutoxy, 2-ethylbutoxy, 1, 1, 2-trimethylpropoxy, 1, 2,2-trimethylpropoxy, 1-eth
  • Alkoxy substituted by halogen means straight-chain or branched alkoxy radicals having in each case the number of carbon atoms, in which groups the hydrogen atoms may be partially or completely replaced by halogen atoms as mentioned above, for example C 1 -C 2 -haloalkoxy, such as chloromethoxy,
  • the compounds of formula (I) may, depending on the nature and linkage of
  • Stereoisomers exist as stereoisomers. For example, if one or more asymmetrically substituted carbon atoms and / or sulfoxides are present, enantiomers and diastereomers may occur. Stereoisomers can be prepared from the mixtures obtained in the preparation by conventional separation methods,
  • stereoisomers can be selectively prepared by using stereoselective reactions using optically active sources and / or adjuvants.
  • the invention also relates to all stereoisomers and mixtures thereof which are of the formula (I), but not specifically defined. However, in the following, for the sake of simplicity, compounds of the formula (I) will always be mentioned, although both the pure ones
  • the compounds of formula (I) bear hydroxy, carboxy or other acid
  • these compounds can be reacted with bases to salts.
  • bases are, for example, hydroxides,
  • R 3 represents (Ci-C 6) -alkyl, (Ci-C) alkoxy (Ci-C) alkyl, (C2-C6) alkenyl, (C 2 -C 6) - alkynyl, (C2- C 6) alkynyl, halo (Ci-C 6) alkyl or halo (C 2 -C 6) alkenyl;
  • R 5 is substituted by m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano and hydroxy-substituted (Ci-Ce) -alkyl or (C3-C6) -cycloalkyl;
  • R 6 is hydrogen or R 5 ;
  • R 7 represents hydrogen or (Ci-C6) -alkyl, (C3-C-6) -cycloalkyl (C .alpha.-C6) -alkyl substituted by in each case m radicals consisting of fluorine, chlorine, bromine, cyano and (Ci-C2) -alkoxy; 2 -C) alkenyl or (C 2 -C) alkynyl;
  • R 8 is R 7 ;
  • W * is COOH or COOY
  • Y is substituted by m radicals from the group consisting of fluorine, chlorine, bromine, cyano, hydroxy and COO- (Ci-C 4 ) alkyl substituted (Ci-CeJ-alkyl, which is interrupted by n oxygen atoms, or
  • m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano, and (Ci-C) alkoxy-substituted (Ci-C) alkyl, (C 3 -C 5) cycloalkyl, (C 2 - C) alkenyl, (C 2 -C 4 ) -alkynyl, (C 1 -C 4 ) -alkoxy, (C 2 -C 4 ) -alkenyloxy, (C 2 -C 4 ) -alkynyloxy or (C 1 -C 4 ) -alkylcarbonyl;
  • X 3 and X 4 are not simultaneously substituted or unsubstituted alkoxy, b) the compounds in which R 3 is methyl and W * is COOH, X 5 is not hydrogen, and
  • R 1 and R 2 are each hydrogen
  • R 3 is (Ci-C) alkyl, (Ci-C) alkoxy (Ci-C) -alkyl, vinyl, (C 2 -C) alkynyl, halogeno (Ci-C 4 ) alkyl or halogen - (C 2 -C 4 ) alkenyl;
  • R 5 is methyl or ethyl;
  • R 6 is hydrogen or R 5 ;
  • R 7 represents hydrogen or (Ci-Ce) -alkyl substituted by in each case m radicals from the group consisting of fluorine and chlorine;
  • R 8 is R 7 ;
  • W * is COOH or COOY
  • Y is represented by m radicals from the group consisting of fluoro, chloro, bromo, cyano, hydroxy and COO- (Ci-C 4 ) alkyl substituted (Ci-C6) -alkyl, which is interrupted by n oxygen atoms, or
  • X 2 , X 4 and X 6 independently of one another are each hydrogen, fluorine or chlorine, or in each case by m radicals from the group consisting of fluoro, chloro, cyano and (Ci-C) alkoxy substituted (Ci-C) alkyl or (Ci-C) alkoxy;
  • X 3 is fluorine, chlorine, bromine, cyano
  • X 5 is hydrogen, fluorine, chlorine, bromine, cyano,
  • n 0, 1 or 2; with the proviso that
  • X 3 and X 4 are not simultaneously substituted or unsubstituted alkoxy, b) the compounds in which R 3 is methyl and W * is COOH, X 5 is not hydrogen, and
  • R 3 is (Ci-C) alkyl, (Ci-C) alkoxy (Ci-C) -alkyl, vinyl, (C 2 -C) alkynyl, halogeno (Ci-C 4 ) alkyl or halogen - (C 2 -C 4 ) alkenyl;
  • R 5 is methyl or ethyl
  • R 6 is hydrogen or R 5 ;
  • R 7 represents hydrogen or (Ci-Ce) -alkyl substituted by in each case m radicals from the group consisting of fluorine and chlorine;
  • R 8 is R 7 ;
  • W * is COOH or COOY;
  • Y is represented by m radicals from the group consisting of fluoro, chloro, bromo, cyano, hydroxy and COO- (Ci-C 4 ) alkyl substituted (Ci-C6) -alkyl, which is interrupted by n oxygen atoms, or
  • X 2 , X 4 and X 6 independently of one another are each hydrogen, fluorine or chlorine,
  • X 3 is fluorine, chlorine, bromine, cyano
  • X 5 is fluorine, chlorine, bromine, cyano
  • n 0, 1 or 2; with the proviso that
  • X 3 and X 4 are not simultaneously substituted or unsubstituted alkoxy, b) the compounds in which R 3 is methyl and W * is COOH, X 5 is not hydrogen, and
  • Methyl 3- (3,5-di-tert-butyl-4-hydroxyphenyl) -5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate and ethyl 3- (3-chlorophenyl) - 5-methyl-4,5-dihydro-1, 2-oxazole-5-carboxylate are excluded.
  • the compounds described in the above-mentioned documents not only have a pharmacological action, but surprisingly also a herbicidal action. Moreover, they are outstandingly suitable as intermediates for the preparation of herbicidally active 3-phenylisoxazoline-5-carboxamides and 3-phenylisoxazoline-5-thioamides.
  • Another object of the present invention is therefore the use of 3-phenyl-isoxazolin derivatives of the formula (Ia) as herbicides.
  • Another object of the present invention is therefore the use of 3-phenyl-isoxazolin derivatives of the formula (Ia) as intermediates for the preparation of herbicidally active 3-phenylisoxazoline-5-carboxamides and 3-phenylisoxazoline-5-thioamides.
  • R 1 and R 2 are each independently hydrogen, fluorine, chlorine, bromine, iodine, cyano, or by in each case m radicals from the group consisting of fluorine, chlorine, bromine, iodine and cyano substituted (Ci-C 4 ) alkyl or (C 1 -C 4 ) -alkoxy, or
  • R 1 and R 2 together with the carbon atom to which they are attached form a saturated, partially or completely unsaturated tri-, tetra- or
  • R 3 is fluorine, chlorine, cyano, (C 1 -C 3 ) -alkylcarbonyloxy or S (O) "R 5 , or substituted in each case by m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano, (Ci-C 4) alkoxy and hydroxy (Ci-C6) alkyl, (C3-C6) cycloalkyl, (C 2 -C 6) -alkenyl or (C2-C6) alkynyl,
  • R 5 is substituted by m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano and hydroxy-substituted (Ci-Ce) -alkyl or (C3-C6) -cycloalkyl;
  • R 6 is hydrogen or R 5 ;
  • R 7 denotes hydrogen or (C 1 -C 6) -alkyl, (C 3 -C 6) -cycloalkyl, (C 2 -C 4) -alkyl substituted by in each case m radicals consisting of fluorine, chlorine, bromine, cyano and (C 1 -C 4) -alkoxy C) alkenyl or (C 2 -C) alkynyl;
  • R 8 is R 7 ;
  • W * represents COOH, COOY, CN or CHO
  • Y is represented by m radicals from the group consisting of fluorine, chlorine, bromine, cyano, hydroxy and COO (Ci-C8) alkyl substituted (Ci-C8) alkyl, which is represented by n heteroatoms selected from the group consisting of oxygen, sulfur and nitrogen is interrupted, or
  • X 2 , X 4 and X 6 are each independently hydrogen, fluorine, chlorine, bromine, iodine, cyano, nitro, or in each case by m radicals from the group consisting of fluorine, chlorine, bromine iodine, cyano and (Ci-C) -alkoxy-substituted (Ci-C) alkyl, (C 3 -C 5 ) -cycloalkyl, (C 2 -C ) - alkenyl, (C 2 -C 4 ) -alkynyl, (C 1 -C 4 ) -alkoxy, (C 2 -C 4 ) -alkenyloxy, (C 2 -C 4 ) -alkynyloxy or (C 1 -C 4 ) -alkylcarbonyl;
  • X 5 is hydrogen, fluorine, chlorine, bromine, iodine, hydroxy, cyano, nitro, SF 5 , CONR 8 SO 2 R 5 , CONR 6 R 8 , COR 6 , CO 2 R 8 , CONR 6 R 8 , C (R 6 ) NOR 8 , NR 6 COR 8 ,
  • R 1 and R 2 are each hydrogen
  • R 3 represents (Ci-C 6) -alkyl, (Ci-C) alkoxy (Ci-C) alkyl, (C2-C6) alkenyl, (C 2 -C 6) - alkynyl, halo ( C 1 -C 6) -alkyl or halo (C 2 -C 6) -alkenyl;
  • R 5 is substituted by m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano and hydroxy-substituted (Ci-Ce) -alkyl or (C3-C6) -cycloalkyl;
  • R 6 is hydrogen or R 5 ;
  • R 7 denotes hydrogen or (C 1 -C 6) -alkyl, (C 3 -C 6) -cycloalkyl, (C 2 -C 4) -alkyl substituted by in each case m radicals consisting of fluorine, chlorine, bromine, cyano and (C 1 -C 4) -alkoxy C) alkenyl or (C 2 -C) alkynyl;
  • R 8 is R 7 ;
  • W * is COOH or COOY
  • Y is represented by m radicals from the group consisting of fluorine, chlorine, bromine, cyano, hydroxy and COO- (Ci-C 4 ) alkyl substituted (Ci-C6) -alkyl, which is interrupted by n oxygen atoms, or
  • X 2 , X 4 and X 6 each independently of one another denote hydrogen, fluorine, chlorine, bromine iodine, cyano, nitro,
  • m radicals from the group consisting of fluorine, chlorine, bromine, iodine, cyano, and (Ci-C) alkoxy-substituted (Ci-C) alkyl, (C 3 -C 5) cycloalkyl, (C 2 - C) alkenyl, (C 2 -C 4 ) -alkynyl, (C 1 -C 4 ) -alkoxy, (C 2 -C 4 ) -alkenyloxy, (C 2 -C 4 ) -alkynyloxy or (C 1 -C 4 ) -alkylcarbonyl;
  • X 5 is hydrogen, fluorine, chlorine, bromine, iodine, hydroxy, cyano, nitro, SF 5 , CONR 8 SO 2 R 5 , CONR 6 R 8 , COR 6 , CO 2 R 8 , CONR 6 R 8 , C (R 6 ) NOR 8 , NR 6 COR 8 ,
  • R 1 and R 2 are each hydrogen
  • R 3 is (Ci-C) alkyl, (Ci-C) alkoxy (Ci-C) alkyl, vinyl, (C 2 -C) alkynyl, halogeno (Ci-C 6 ) alkyl or halogen - (C 2 -C 6 ) alkenyl;
  • R 5 is methyl or ethyl
  • R 6 is hydrogen or R 5 ;
  • R 7 represents hydrogen or (Ci-Ce) -alkyl substituted by in each case m radicals from the group consisting of fluorine and chlorine;
  • R 8 is R 7 ;
  • W * is COOH or COOY
  • Y is represented by m radicals from the group consisting of fluorine, chlorine, bromine, cyano, hydroxy and COO- (Ci-C 4 ) alkyl substituted (Ci-C6) -alkyl, which is interrupted by n oxygen atoms, or
  • Methoxycarbonylbenzyl 3,5-difluorobenzyl, 3,4-difluorobenzyl, 2,6-difluorobenzyl, 5-methylpyridin-3-ylmethyl, tetrahydrofuran-3yl and butan-1 -ol-4-yl;
  • X 2 , X 4 and X 6 independently of one another are each hydrogen, fluorine or chlorine,
  • X 5 is hydrogen, fluorine, chlorine, bromine, cyano,
  • n 0, 1 or 2.
  • herbicides and intermediates are 3-phenylisoxazoline derivatives of the formula (Ia) in which R 1 and R 2 are each hydrogen;
  • R 3 is (Ci-C) alkyl, (Ci-C) alkoxy (Ci-C) alkyl, vinyl, (C 2 -C) alkynyl, halogeno (Ci-C 6 ) alkyl or halogen - (C 2 -C 6 ) alkenyl;
  • R 5 is methyl or ethyl;
  • R 6 is hydrogen or R 5 ;
  • R 7 represents hydrogen or (Ci-Ce) -alkyl substituted by in each case m radicals from the group consisting of fluorine and chlorine;
  • R 8 is R 7 ;
  • W * is COOH or COOY;
  • Y is represented by m radicals from the group consisting of fluorine, chlorine, bromine, cyano, hydroxy and COO- (Ci-C 4 ) alkyl substituted (Ci-C6) -alkyl, which is interrupted by n oxygen atoms, or
  • X 2 , X 4 and X 6 independently of one another are each hydrogen, fluorine or chlorine,
  • X 3 is fluorine, chlorine, bromine, cyano
  • X 5 is hydrogen, fluorine, chlorine, bromine, cyano,
  • (X) n is the substituents X 2 , X 3 , X 4 , X 5 and X 6 .
  • Such 1, 3-dipolar cycloadditions of nitrile oxides with suitable dipolarophiles are described, for example, in reviews: 1,3 dipolar cycloaddition Chemistry, Padwa (Editor), Wiley, New York, 1984; Kanemasa and Tsuge,
  • the cycloadditions can be carried out in a one-pot reaction without isolation of the
  • Acid halides with the respective alcohol or by coupling the respective pressure be prepared with coupling reagents.
  • methyl 2-bromomethylacrylate can be reacted under basic conditions with alcohols to form methyl 2-alkoxymethyl acrylates, which then react with chloroximes via the nitrile oxides to give 3-phenyl-5-methoxymethylisoxazolines.
  • Various 2-alkylacrylic acid esters can be obtained starting from methyl 2-bromo-methylacrylate, for example by reaction with metal-organic
  • Reagents are produced. Such methods are described, for example, in Metzger, Albrecht; Piller, Fabian M .; Ankle, Paul; Chemical Communications, 2008, 44, p. 5824-5826 and also known from WO2006 / 33551.
  • the present invention therefore also provides a method for controlling unwanted plants or for regulating the growth of plants, preferably in plant crops, wherein one or more of the present invention
  • Compound (s) on the plants e.g., weeds such as mono- or dicotyledons
  • the compounds of the invention may be e.g. in pre-sowing (possibly also by incorporation into the soil), pre-emergence or Nachauflaufmaschine be applied.
  • some representatives of the monocotyledonous and dicotyledonous weed flora can be mentioned, which can be controlled by the compounds according to the invention, without the intention of limiting them to certain species.
  • the compounds according to the invention are applied to the surface of the earth prior to germination, either the emergence of the weed seedlings is completely prevented or the weeds grow up to the cotyledon stage, but then stop their growth and finally die after three to four weeks
  • Ipomoea Lactuca, Linum, Lycopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia, or monocotyledonous cultures of the genera Allium, Pineapple, Asparagus, Avena,
  • Crops such as agricultural crops or ornamental plantings.
  • the compounds of the invention (depending on their respective structure and the applied application rate) have excellent
  • the active compounds can also be used for controlling harmful plants in crops of known or yet to be developed genetically modified plants.
  • the transgenic plants are usually characterized by particular advantageous properties, for example by resistance to certain pesticides, especially certain herbicides, resistance to plant diseases or pathogens of plant diseases such as certain insects or microorganisms such as fungi, bacteria or viruses.
  • Other special special traits for example by resistance to certain pesticides, especially certain herbicides, resistance to plant diseases or pathogens of plant diseases such as certain insects or microorganisms such as fungi, bacteria or viruses.
  • Properties relate to e.g. the crop in terms of quantity, quality, shelf life, composition and special ingredients.
  • transgenic plants with increased starch content or altered quality of the starch or those with other fatty acid composition of the crop are known. More special
  • Properties may be in tolerance or resistance to abiotic stressors, e.g. Heat, cold, drought, salt and ultraviolet radiation are present.
  • abiotic stressors e.g. Heat, cold, drought, salt and ultraviolet radiation are present.
  • the compounds of the formula (I) according to the invention or their salts in economically important transgenic crops of useful and ornamental plants, for example cereals such as wheat, barley, rye, oats, millet, rice, manioc and maize or also cultures of sugar beet , Cotton, soy, rapeseed, potato, tomato, pea and other vegetables.
  • cereals such as wheat, barley, rye, oats, millet, rice, manioc and maize or also cultures of sugar beet , Cotton, soy, rapeseed, potato, tomato, pea and other vegetables.
  • Crop crops are used, which are resistant to the phytotoxic effects of herbicides or have been made genetically resistant. Conventional ways of producing new plants that have modified properties compared to previously occurring plants exist
  • transgenic crops which are resistant to certain glufosinate-type herbicides (cf., for example, EP 0242236 A, EP 0242246 A) or glyphosate (WO 92/000377 A) or the sulfonylureas (EP 0257993 A, US Pat. No. 5,013,659) or to combinations or mixtures of these herbicides "Gene stacking" are resistant, such as transgenic crops such as corn or soybean with the trade name or the name Optimum TM GAT TM (Glyphosate ALS Tolerant).
  • Transgenic crops such as cotton, with the ability to produce Bacillus thuringiensis toxins (Bt toxins), which make the plants resistant to certain pests (EP 0142924 A, EP 0193259 A).
  • Bacillus thuringiensis toxins Bacillus thuringiensis toxins
  • transgenic crops that are pharmaceutically or diagnostically important
  • transgenic crops characterized by a combination of eg the above-mentioned new properties ("gene stacking")
  • gene stacking Numerous molecular biology techniques that can be used to produce novel transgenic plants with altered properties are known in principle; See, for example, I. Potrykus and G. Spangenberg (eds.) Gene Transfer to Plants, Springer Lab Manual (1995), Springer Verlag Berlin, Heidelberg, or Christou, "Trends in Plant Science” 1 (1996) 423-431).
  • nucleic acid molecules can be used in any genetic manipulations.
  • nucleic acid molecules can be used in any genetic manipulations.
  • Plasmids are introduced which allow mutagenesis or a sequence change by recombination of DNA sequences.
  • Base exchanges are made, partial sequences removed or natural or synthetic sequences added.
  • For the connection of the DNA fragments with one another adapters or linkers can be attached to the fragments, see e.g. Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2nd Ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY; or Winnacker "Genes and Clones", VCH Weinheim 2nd edition 1996
  • the production of plant cells having a reduced activity of a gene product can be achieved, for example, by the expression of at least one
  • DNA molecules may be used which comprise the entire coding sequence of a gene product, including any flanking sequences that may be present, as well as DNA molecules which comprise only parts of the coding sequence, which parts must be long enough to be present in the cells to cause an antisense effect. It is also possible to use DNA sequences which have a high degree of homology to the coding sequences of a gene product, but are not completely identical.
  • the synthesized protein may be located in any compartment of the plant cell.
  • the coding region can be linked to DNA sequences that ensure localization in a particular compartment.
  • sequences are the See, for example, Braun et al., EMBO J. 1 1 (1992), 3219-3227, Wolter et al., Proc Natl Acad, U.S.A. 85 (1988), 846-850, Sonnewald et al. , Plant J. 1 (1991), 95-106).
  • Expression of the nucleic acid molecules can also be found in the
  • Organelles of the plant cells take place.
  • the transgenic plant cells can be whole by known techniques
  • transgenic plants are regenerated.
  • the transgenic plants may, in principle, be plants of any plant species, that is, both monocotyledonous and dicotyledonous plants.
  • Cultures are used, which against growths, such. 2,4 D, dicamba or against herbicides containing essential plant enzymes, e.g. Acetolactate synthases (ALS), EPSP synthases, glutamine synthases (GS) or Hydoxyphenylpyruvat Dioxygenases (HPPD) inhibit or resistant to herbicides from the group of sulfonylureas, the glyphosate, glufosinate or Benzoylisoxazole and analogues, or against any combination of these agents resistant.
  • ALS Acetolactate synthases
  • EPSP synthases e.g., EPSP synthases
  • G glutamine synthases
  • HPPD Hydoxyphenylpyruvat Dioxygenases
  • the compounds according to the invention can particularly preferably be used in transgenic crop plants which are resistant to a combination of glyphosates and glufosinates, glyphosates and sulfonylureas or imidazolinones. Very particular preference may be given to the compounds according to the invention in
  • transgenic crops such as maize or soybean with the trade name or the name Optimum TM GATTM (Glyphosate ALS Tolerant).
  • Optimum TM GATTM Glyphosate ALS Tolerant
  • Harmful plants often have effects that are specific for application in the particular transgenic culture, such as altered or specially extended weed spectrum that can be controlled
  • the invention therefore also relates to the use of the compounds of the formula (I) according to the invention and of the compounds of the formula (Ia) as herbicides for controlling harmful plants in transgenic crop plants.
  • the compounds of the invention may be in the form of wettable powders
  • Granules are used in the usual preparations.
  • the invention therefore also relates to herbicidal and plant growth-regulating agents which contain the compounds according to the invention.
  • the compounds according to the invention can be formulated in various ways, depending on which biological and / or chemical-physical parameters are predetermined. Possible formulation options are, for example: wettable powder (WP), water-soluble powders (SP), water-soluble concentrates,
  • EC emulsifiable concentrates
  • EW emulsions
  • Water-in-oil emulsions sprayable solutions, suspension concentrates (SC), oil- or water-based dispersions, oil-miscible solutions, capsule suspensions (CS), dusts (DP), mordants, granules for litter and soil application, granules (GR) in the form of micro, spray, elevator and adsorption granules, water-dispersible granules (WG), water-soluble granules (SG),
  • the necessary formulation auxiliaries such as inert materials, surfactants, solvents and other additives are also known and are, for example
  • Injectable powders are preparations which are uniformly dispersible in water and contain surfactants of the ionic and / or nonionic type (wetting agent, dispersing agent) in addition to the active ingredient, apart from a diluent or inert substance.
  • polyoxyethylated alkylphenols polyoxethylated fatty alcohols, polyoxethylated fatty amines, fatty alcohol polyglycol ether sulfates, alkanesulfonates, alkylbenzenesulfonates, sodium lignosulfonate,
  • the herbicidal active compounds are finely ground, for example, in customary apparatus such as hammer mills, blower mills and air-jet mills and mixed simultaneously or subsequently with the formulation auxiliaries.
  • Emulsifiable concentrates are made by dissolving the active ingredient in one
  • organic solvents e.g. Butanol, cyclohexanone, dimethylformamide, xylene or higher-boiling aromatics or hydrocarbons or mixtures of organic solvents with the addition of one or more surfactants of ionic and / or nonionic type (emulsifiers).
  • emulsifiers which may be used are: alkylarylsulfonic acid calcium salts, such as
  • Ca-dodecylbenzenesulfonate or nonionic emulsifiers such as fatty acid polyglycol esters, alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide-ethylene oxide condensation products, alkyl polyethers, sorbitan esters such as Sorbitan fatty acid esters or polyoxethylenesorbitan esters such as
  • Dusts are obtained by milling the active ingredient with finely divided solids, e.g. Talc, natural clays such as kaolin, bentonite and pyrophyllite, or diatomaceous earth.
  • finely divided solids e.g. Talc, natural clays such as kaolin, bentonite and pyrophyllite, or diatomaceous earth.
  • Suspension concentrates may be water or oil based. They can be prepared, for example, by wet grinding using commercially available bead mills and, if appropriate, addition of surfactants, as described, for example, in US Pat. upstairs with the others
  • Emulsions e.g. Oil-in-water emulsions (EW) can be prepared, for example, by means of stirrers, colloid mills and / or static mixers using aqueous organic solvents and optionally surfactants, as described e.g. listed above for the other formulation types.
  • EW Oil-in-water emulsions
  • Granules can be prepared either by spraying the active ingredient on adsorptive, granulated inert material or by applying
  • Active substance concentrates by means of adhesives, e.g. Polyvinyl alcohol, polyacrylic acid sodium or mineral oils, on the surface of carriers such as sand, kaolinites or granulated inert material. It is also possible to granulate suitable active ingredients in the manner customary for the production of fertilizer granules, if desired in admixture with fertilizers.
  • adhesives e.g. Polyvinyl alcohol, polyacrylic acid sodium or mineral oils
  • carriers such as sand, kaolinites or granulated inert material. It is also possible to granulate suitable active ingredients in the manner customary for the production of fertilizer granules, if desired in admixture with fertilizers.
  • Water-dispersible granules are generally prepared by the usual methods such as spray drying, fluidized bed granulation, plate granulation, mixing with high-speed mixers and extrusion without solid inert material.
  • spray drying fluidized bed granulation
  • plate granulation mixing with high-speed mixers and extrusion without solid inert material.
  • the agrochemical preparations generally contain from 0.1 to 99% by weight, in particular from 0.1 to 95% by weight, of compounds according to the invention.
  • the active ingredient concentration is e.g. about 10 to 90 wt .-%, the balance to 100 wt .-% consists of conventional formulation ingredients.
  • the active ingredient concentration may be about 1 to 90, preferably 5 to 80,% by weight.
  • Dust-like formulations contain 1 to 30 wt .-% of active ingredient, preferably usually 5 to 20 wt .-% of active ingredient, sprayable solutions contain about 0.05 to 80, preferably 2 to 50 wt .-% active ingredient.
  • the active ingredient content depends, in part, on whether the active compound is liquid or solid and which granulation auxiliaries,
  • the content of active ingredient is, for example, between 1 and 95% by weight, preferably between 10 and 80% by weight.
  • the active substance formulations mentioned optionally contain the customary adhesive, wetting, dispersing, emulsifying, penetrating, preserving,
  • Mixture formulations or in the tank mix are, for example, known active substances which are based on an inhibition of, for example, acetolactate synthase, acetyl-CoA carboxylase, cellulose synthase, enolpyruvylshikimate-3-phosphate synthase,
  • Glutamine synthetase, p-hydroxyphenylpyruvate dioxygenase, phytoene desaturase, photosystem I, photosystem II, protoporphyrinogen oxidase can be used, e.g. from Weed Research 26 (1986) 441-445 or "The Pesticide Manual", 15th edition, The British Crop Protection Council and the Royal Soc. of Chemistry, 2009 and cited therein. As known herbicides or
  • Plant growth regulators with the compounds of the invention may, for example, be mentioned (the compounds are denoted either by the "common name” according to the International Organization for Standardization (ISO) or by the chemical name or by the code number) and always include all forms of use such as acids, salts , Esters and isomers such as stereoisomers and optical isomers.
  • ISO International Organization for Standardization
  • the formulations present in commercial form are optionally diluted in a customary manner, e.g. for wettable powders, emulsifiable concentrates, dispersions and water-dispersible granules by means of water. Dusty preparations, ground or spreading granules and sprayable
  • the type of herbicide used u.a. varies the required application rate of the compounds of formula (I). It can vary within wide limits, e.g. between 0.001 and 1.0 kg / ha or more of active substance, but is preferably between 0.005 and 750 g / ha.
  • the agents of the invention may additionally contain other ingredients, e.g. surfactants.
  • Surface-active substances are emulsifying and / or foam-forming agents, dispersants or wetting agents having ionic or non-ionic properties or mixtures of these
  • surfactants in question examples thereof are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or
  • Naphthalenesulphonic acid polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives
  • alkyl taurates phosphoric acid esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols, and derivatives of the compounds containing sulphates, sulphonates and phosphates, for example alkylarylpolyglycol ethers, alkylsulphonates, alkylsulphates, arylsulphonates, protein hydrolysates, lignin-sulphite liquors and methylcellulose.
  • a surfactant is necessary when one of the active ingredients and / or one of the inert carriers is not soluble in water and when applied in water.
  • the content of surfactants is between 5 and 40 percent by weight of the composition according to the invention.
  • Dyes such as inorganic pigments such as 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.
  • additional components may also be included, e.g. protective colloids, binders, adhesives, thickeners, thixotropic substances,
  • the active ingredients can be mixed with any solid or liquid additive used for
  • the agents and formulations according to the invention contain between 0.05 and 99% by weight, 0.01 and 98% by weight, preferably between 0.1 and 95% by weight, particularly preferably between 0.5 and 90%.
  • Active ingredient most preferably between 10 and 70 weight percent.
  • the active compounds or compositions according to the invention can be used as such or as a function of their respective physical and / or chemical properties in the form of their formulations or those prepared therefrom
  • Use forms such as aerosols, capsule suspensions, cold spray concentrates, hot mist concentrates, encapsulated granules, fine granules, flowable concentrates for the treatment of seeds, ready-to-use solutions, dustable powders, emulsifiable concentrates, oil-in-water emulsions, water-in-oil emulsions, macrogranules , Microgranules, oil-dispersible powders, oil-miscible flowable concentrates, oil-miscible liquids, foams, pastes, pesticide-coated seeds, suspension concentrates, suspension-emulsion concentrates, soluble concentrates, suspensions, wettable powders, soluble powders, dusts and granules, water-soluble granules or tablets, water-soluble powders for seed treatment, wettable powders, active substance-impregnated natural and synthetic substances as well as microencapsulations in polymeric substances and in seed coating compositions, as well as ULV cold and warm mist
  • compositions mentioned can be prepared in a manner known per se, for example by mixing the active compounds with at least one customary extender, solvent or diluent, emulsifier, dispersing and / or binding or fixing agent, wetting agent, water repellent, optionally siccatives and UV stabilizers, and optionally dyes and pigments, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and other processing aids.
  • the compositions according to the invention comprise not only formulations which are already ready for use and which can be applied to the plant or the seed with a suitable apparatus, but also commercial concentrates which have to be diluted with water before use.
  • the active compounds according to the invention can be prepared as such or in their (commercially available) formulations as well as in those from these formulations
  • Insecticides Insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth regulators, herbicides, fertilizers, safeners or
  • Habitat or storage space according to the usual treatment methods, e.g. by dipping, (spraying), (spraying), sprinkling, evaporating, atomizing, misting, (ver) spreading, foaming, brushing, spreading, pouring
  • 1,156 g (6.08 mmol) of 3,5-dichlorobenzaldehyde oxime are mixed with 0.950 g (7.30 mmol) of methyl 2- (methoxymethyl) acrylate, 0.853 g (6.39 mmol) of N-chlorosuccinimide and 0.923 g (9.13 mmol) of triethylamine in 47.5 g Cyclized dimethylformamide.
  • Solvent is diluted with water, the aqueous phase washed with dichloromethane, then acidified the water phase with dilute hydrochloric acid and washed again with dichloromethane. The last dichloromethane phase is dried. This gives 100 mg (100%) of the above acid as a colorless oil.
  • NMR peak lists the NMR data of selected examples are recorded in the form of NMR peak lists, with the ⁇ value in ppm and then the signal intensity separated by a space for each signal peak.
  • the ⁇ value - signal intensity - number pairs of different signal peaks are determined by
  • D1, D2 denote diastereomers of a pair of diastereomers which are present as racemates of two enantiomers.
  • Table 1 .1 Compounds according to the invention of the general formula (I) in which W * is COOH, R 1 is hydrogen, and aryl is the radical

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
PCT/EP2013/069453 2012-09-25 2013-09-19 Herbizid wirksame 3-phenylisoxazolinderivate WO2014048827A1 (de)

Priority Applications (11)

Application Number Priority Date Filing Date Title
MX2015003538A MX378312B (es) 2012-09-25 2013-09-19 Derivados de 3-fenilisoxazolina con accion herbicida.
DK13766930.5T DK2900645T3 (da) 2012-09-25 2013-09-19 Herbicidt aktive 3-phenylisoxazolinderivater
ES13766930T ES2747483T3 (es) 2012-09-25 2013-09-19 Derivados de 3-fenilisoxazolina con acción herbicida
CN201380061304.2A CN104812739B (zh) 2012-09-25 2013-09-19 具有除草作用的3‑苯基异噁唑啉衍生物
JP2015532405A JP6472382B2 (ja) 2012-09-25 2013-09-19 除草効果を有する３−フェニルイソオキサゾリン誘導体
US14/430,018 US9585392B2 (en) 2012-09-25 2013-09-19 3-phenylisoxazolin derivatives with herbicidal action
BR112015006573-2A BR112015006573B1 (pt) 2012-09-25 2013-09-19 derivados de 3-fenilisoxazolina, compoisições herbicidas, seus usos, e método para controle de plantas indesejáveis
EP13766930.5A EP2900645B1 (de) 2012-09-25 2013-09-19 Herbizid wirksame 3-phenylisoxazolinderivate
IN1315DEN2015 IN2015DN01315A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) 2012-09-25 2013-09-19
KR1020157010148A KR101977920B1 (ko) 2012-09-25 2013-09-19 제초 작용을 가지는 3-페닐이속사졸린 유도체
IL23768515A IL237685B (en) 2012-09-25 2015-03-12 History of 3-phenylisoxazoline with herbicidal activity

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP12185768.4 2012-09-25
EP12185768 2012-09-25

Publications (1)

Publication Number Publication Date
WO2014048827A1 true WO2014048827A1 (de) 2014-04-03

Family

ID=47044811

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2013/069453 WO2014048827A1 (de) 2012-09-25 2013-09-19 Herbizid wirksame 3-phenylisoxazolinderivate

Country Status (13)

Country Link
US (1) US9585392B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
EP (1) EP2900645B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
JP (1) JP6472382B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
KR (1) KR101977920B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
CN (1) CN104812739B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
BR (1) BR112015006573B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
DK (1) DK2900645T3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
ES (1) ES2747483T3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
IL (1) IL237685B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
IN (1) IN2015DN01315A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
MX (1) MX378312B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
TW (1) TWI598344B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
WO (1) WO2014048827A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105198824A (zh) * 2015-10-09 2015-12-30 苏州大学 一种二氢异噁唑啉化合物及其制备方法和应用
WO2018228985A1 (de) 2017-06-13 2018-12-20 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von tetrahydro- und dihydrofurancarbonsäuren und -estern
WO2018228986A1 (de) 2017-06-13 2018-12-20 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von tetrahydro- und dihydrofurancarbonsäureamiden
WO2019034602A1 (de) 2017-08-17 2019-02-21 Bayer Aktiengesellschaft Herbizid wirksame 3-phenyl-5-trifluormethylisoxazolin-5-carboxamide von cyclopentylcarbonsäuren und -estern
WO2019145245A1 (de) 2018-01-25 2019-08-01 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von cyclopentenylcarbonsäurederivaten
US10550111B2 (en) 2014-12-16 2020-02-04 Shenyang Sinochem Agrochemicals R&D Co., Ltd. Pyrimidine urea compound containing isoxazolines and use thereof
WO2020182723A1 (de) 2019-03-12 2020-09-17 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von s-haltigen cyclopentenylcarbonsäureestern
WO2021209268A1 (en) 2020-04-14 2021-10-21 Basf Se Beta-lactams and their use as herbicides
WO2021224040A1 (en) 2020-05-05 2021-11-11 Basf Se Condensed isoxazoline derivatives and their use as herbicides
WO2022069553A1 (de) 2020-10-01 2022-04-07 Bayer Aktiengesellschaft Benzaldehydoxime und verfahren zu deren herstellung
WO2022112072A1 (en) * 2020-11-24 2022-06-02 Syngenta Crop Protection Ag Herbicidal compounds
WO2022189190A1 (en) 2021-03-09 2022-09-15 Basf Se Malonamides and their use as herbicides
WO2023099641A1 (de) * 2021-12-03 2023-06-08 Bayer Aktiengesellschaft Verfahren zur herstellung von isoxazolin-5,5-vinylcarbonsäure-derivaten
US11889833B2 (en) 2022-01-14 2024-02-06 Enko Chem, Inc. Protoporphyrinogen oxidase inhibitors

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112015006560A2 (pt) 2012-09-25 2017-07-04 Bayer Cropscience Ag 3-heteroaril-isoxazolina-5-carboxamidas e 3-heteroaril-isoxazolina-5-tioamidas com atividade herbicida e fungicida
BR112015006696A2 (pt) 2012-09-25 2017-07-04 Bayer Cropscience Ag 3-fenilisoxazolina-5-carboxamidas 5-oxi-substituídas e 3-fenilisoxazolina-5-tioamidas 5-oxi-substituídas herbicidas e fungicidas
CN112745269B (zh) * 2019-10-29 2023-01-24 沈阳中化农药化工研发有限公司 一种苯基异恶唑啉类化合物及其用途
CN114436834A (zh) * 2021-12-16 2022-05-06 江苏阿尔法药业股份有限公司 一种利用连续流微通道反应器合成瑞舒伐他汀钙中间体的方法

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0174685A2 (en) * 1984-09-14 1986-03-19 Shell Internationale Researchmaatschappij B.V. Ether herbicides
WO1992003053A1 (de) * 1990-08-17 1992-03-05 Hoechst Aktiengesellschaft Isoxazoline oder isothiazoline enthaltende pflanzschützende mittel und neue isoxazoline und isothiazoline
WO1995014680A1 (en) * 1993-11-26 1995-06-01 Pfizer Inc. 3-aryl-2-isoxazolines as antiinflammatory agents
WO1999005130A1 (de) * 1997-07-23 1999-02-04 Basf Aktiengesellschaft Substituierte 3-phenylisoxazoline
WO2005021515A2 (en) * 2003-08-29 2005-03-10 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type-iv
WO2005021516A1 (en) * 2003-08-27 2005-03-10 Lg Life Sciences Ltd. Caspase inhibitors containing isoxazoline ring
WO2005051931A2 (en) * 2003-11-26 2005-06-09 Ranbaxy Laboratories Limited Phosphodiesterase inhibitors
WO2008035315A2 (en) * 2006-09-22 2008-03-27 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type-iv

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8422701D0 (en) * 1984-09-07 1984-10-10 Shell Int Research Ether herbicides
JPS62103070A (ja) * 1985-10-29 1987-05-13 Mitsui Toatsu Chem Inc イソオキサゾリン誘導体および植物生長調節剤
DE3541722A1 (de) * 1985-11-26 1987-05-27 Basf Ag Chinolinderivate und ihre verwendung zur bekaempfung von unerwuenschtem pflanzenwachstum
US4956006A (en) * 1988-12-27 1990-09-11 Ici Americas Inc. Substituted 1-phenyl pyrrolidones and their use as herbicides
NZ274244A (en) * 1993-11-26 1997-09-22 Pfizer Isoxazoline derivatives and medicaments
US5939418A (en) * 1995-12-21 1999-08-17 The Dupont Merck Pharmaceutical Company Isoxazoline, isothiazoline and pyrazoline factor Xa inhibitors
RU2237664C2 (ru) * 1999-08-10 2004-10-10 Кумиай Кемикал Индастри Ко., Лтд. Изоксазолиновые производные и гербициды, содержащие их в качестве активных ингредиентов
JP2005112840A (ja) * 2003-09-16 2005-04-28 Nissan Chem Ind Ltd 新規ピラゾールスルホニルウレア化合物および除草剤
EP2691379B1 (de) 2011-03-31 2016-11-02 Bayer Intellectual Property GmbH Herbizid und fungizid wirksame 3-phenylisoxazolin-5-carboxamide und 3- phenylisoxazolin-5-thioamide
BR112015006696A2 (pt) 2012-09-25 2017-07-04 Bayer Cropscience Ag 3-fenilisoxazolina-5-carboxamidas 5-oxi-substituídas e 3-fenilisoxazolina-5-tioamidas 5-oxi-substituídas herbicidas e fungicidas
BR112015006560A2 (pt) 2012-09-25 2017-07-04 Bayer Cropscience Ag 3-heteroaril-isoxazolina-5-carboxamidas e 3-heteroaril-isoxazolina-5-tioamidas com atividade herbicida e fungicida

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0174685A2 (en) * 1984-09-14 1986-03-19 Shell Internationale Researchmaatschappij B.V. Ether herbicides
WO1992003053A1 (de) * 1990-08-17 1992-03-05 Hoechst Aktiengesellschaft Isoxazoline oder isothiazoline enthaltende pflanzschützende mittel und neue isoxazoline und isothiazoline
WO1995014680A1 (en) * 1993-11-26 1995-06-01 Pfizer Inc. 3-aryl-2-isoxazolines as antiinflammatory agents
WO1999005130A1 (de) * 1997-07-23 1999-02-04 Basf Aktiengesellschaft Substituierte 3-phenylisoxazoline
WO2005021516A1 (en) * 2003-08-27 2005-03-10 Lg Life Sciences Ltd. Caspase inhibitors containing isoxazoline ring
WO2005021515A2 (en) * 2003-08-29 2005-03-10 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type-iv
WO2005051931A2 (en) * 2003-11-26 2005-06-09 Ranbaxy Laboratories Limited Phosphodiesterase inhibitors
WO2008035315A2 (en) * 2006-09-22 2008-03-27 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type-iv

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
GUCMA MIROSLAW ET AL: "Synthesis and fungicidal activity of substituted isoxazolecarboxamides", vol. 2010, no. 1-4, 1 January 2011 (2011-01-01), pages 21 - 31, XP008159982, ISSN: 0208-8703, Retrieved from the Internet <URL:http://www.wydawnictwa.ipo.waw.pl/pestycydy/Pestycydy1-4-2010/Gucma.pdf> *
NAGARAJAN ET AL: "Synthesis of some isoxazolines and evaluation of carbon-13 NMR substituent parameters for 5-methyl substitution", INDIAN JOURNAL OF CHEMISTRY : IJC, COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH, IN, vol. 32B, no. 9, 1 January 1993 (1993-01-01), pages 938 - 941, XP009167082, ISSN: 0019-5103 *
PRIYA B S ET AL: "DELTA.2-Isoxazoline derivatives as antimicrobials", HETEROCYCLIC COMMUNICATIONS, FREUND PUBLISHING HOUSE, TEL AVIV, vol. 12, no. 1, 1 January 2006 (2006-01-01), pages 35 - 42, XP009140872, ISSN: 0793-0283 *
QUAN M L ET AL: "Design and Synthesis of Isoxazoline Derivatives as Factor Xa Inhibitors", JOURNAL OF MEDICINAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY, US, vol. 42, no. 15, 1 January 1999 (1999-01-01), pages 2760 - 2773, XP002213660, ISSN: 0022-2623, DOI: 10.1021/JM980406A *

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10550111B2 (en) 2014-12-16 2020-02-04 Shenyang Sinochem Agrochemicals R&D Co., Ltd. Pyrimidine urea compound containing isoxazolines and use thereof
CN105198824A (zh) * 2015-10-09 2015-12-30 苏州大学 一种二氢异噁唑啉化合物及其制备方法和应用
WO2018228985A1 (de) 2017-06-13 2018-12-20 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von tetrahydro- und dihydrofurancarbonsäuren und -estern
WO2018228986A1 (de) 2017-06-13 2018-12-20 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von tetrahydro- und dihydrofurancarbonsäureamiden
US11613522B2 (en) 2017-06-13 2023-03-28 Bayer Aktiengesellschaft Herbicidally active 3-phenylisoxazoline-5-carboxamides of tetrahydro- and dihydrofurancarboxamides
US11597724B2 (en) 2017-06-13 2023-03-07 Bayer Aktiengesellschaft Herbicidally active 3-phenylisoxazoline-5-carboxamides of tetrahydro and dihydrofuran carboxylic acids and esters
WO2019034602A1 (de) 2017-08-17 2019-02-21 Bayer Aktiengesellschaft Herbizid wirksame 3-phenyl-5-trifluormethylisoxazolin-5-carboxamide von cyclopentylcarbonsäuren und -estern
WO2019145245A1 (de) 2018-01-25 2019-08-01 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von cyclopentenylcarbonsäurederivaten
US12319664B2 (en) 2018-01-25 2025-06-03 Bayer Aktiengesellschaft Herbicidally active 3-phenylisoxazoline-5-carboxamides of cyclopentenylcarboxylic acid derivatives
WO2020182723A1 (de) 2019-03-12 2020-09-17 Bayer Aktiengesellschaft Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von s-haltigen cyclopentenylcarbonsäureestern
US12185723B2 (en) 2019-03-12 2025-01-07 Bayer Aktiengesellschaft Herbicidally active 3-phenylisoxazoline-5-carboxamides of s-containing cyclopentenylcarboxylic esters
US12389910B2 (en) 2020-04-14 2025-08-19 Basf Se Beta-lactams and their use as herbicides
WO2021209268A1 (en) 2020-04-14 2021-10-21 Basf Se Beta-lactams and their use as herbicides
WO2021224040A1 (en) 2020-05-05 2021-11-11 Basf Se Condensed isoxazoline derivatives and their use as herbicides
WO2022069553A1 (de) 2020-10-01 2022-04-07 Bayer Aktiengesellschaft Benzaldehydoxime und verfahren zu deren herstellung
WO2022112072A1 (en) * 2020-11-24 2022-06-02 Syngenta Crop Protection Ag Herbicidal compounds
WO2022189190A1 (en) 2021-03-09 2022-09-15 Basf Se Malonamides and their use as herbicides
WO2023099641A1 (de) * 2021-12-03 2023-06-08 Bayer Aktiengesellschaft Verfahren zur herstellung von isoxazolin-5,5-vinylcarbonsäure-derivaten
US11889833B2 (en) 2022-01-14 2024-02-06 Enko Chem, Inc. Protoporphyrinogen oxidase inhibitors
US12302900B2 (en) 2022-01-14 2025-05-20 Enko Chem, Inc. Protoporphyrinogen oxidase inhibitors

Also Published As

Publication number Publication date
US20150245615A1 (en) 2015-09-03
TW201418231A (zh) 2014-05-16
CN104812739A (zh) 2015-07-29
US9585392B2 (en) 2017-03-07
IL237685A0 (en) 2015-05-31
TWI598344B (zh) 2017-09-11
DK2900645T3 (da) 2019-10-14
MX378312B (es) 2025-03-10
MX2015003538A (es) 2015-10-12
IN2015DN01315A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) 2015-07-03
JP6472382B2 (ja) 2019-02-20
BR112015006573B1 (pt) 2020-11-03
EP2900645B1 (de) 2019-08-21
BR112015006573A2 (pt) 2017-07-04
CN104812739B (zh) 2017-12-12
ES2747483T3 (es) 2020-03-10
KR20150063445A (ko) 2015-06-09
EP2900645A1 (de) 2015-08-05
JP2015530397A (ja) 2015-10-15
IL237685B (en) 2019-11-28
KR101977920B1 (ko) 2019-05-13

Similar Documents

Publication Publication Date Title
WO2014048827A1 (de) Herbizid wirksame 3-phenylisoxazolinderivate
EP2379508B1 (de) Herbizid und insektizid wirksame 4-phenylsubstituierte pyridazinone
EP3356334A1 (de) Acylierte n-(1,2,5-oxadiazol-3-yl)-, n-(1,3,4-oxadiazol-2-yl)-, n-(tetrazol-5-yl)- und n-(triazol-5-yl)-arylcarbonsäureamide und ihre verwendung als herbizide
WO2017144402A1 (de) N-(5-halogen-1,3,4-oxadiazol-2-yl)arylcarbonsäureamide und ihre verwendung als herbizide
EP2855437B1 (de) N-(tetrazol-5-yl)- und n-(triazol-5-yl)arylcarbonsäurethioamide und ihre verwendung als herbizide
WO2014086746A1 (de) N-(isoxazol-3-yl)-arylcarbonsäureamide und ihre verwendung als herbizide
WO2014086734A1 (de) N-(oxazol-2-yl)-arylcarbonsäureamide und ihre verwendung als herbizide
WO2014053473A1 (de) 1,2,4-triazin-3,5-dion-6-carboxamide und ihre verwendung als herbizide
EP2831084B1 (de) Herbizid und insektizid wirksame thiazolopyridinone
EP3145917A1 (de) 5-(hetero)aryl-pyridazinone und ihre verwendung als herbizide
CN106470979A (zh) 除草活性的芳基羧酸酰胺
EP2844650B1 (de) 6-pyridon-2-carbamoyl-azole und ihre verwendung als herbizide
WO2017005567A1 (de) Herbizid wirksame n-(tetrazol-5-yl)- und n-(triazol-5-yl)arylcarboxamid-derivate
EP3068773A1 (de) Pyridazinon-derivate und ihre verwendung als herbizide
WO2019025540A1 (de) 3-acyl-benzamide und ihre verwendung als herbizide
WO2015007632A1 (de) Uracil-5-carboxamide und ihre verwendung als herbizide
WO2015007662A1 (de) Azin-2-on-3-carboxamide und ihre verwendung als herbizide
WO2015007633A1 (de) 6-azinon-2-carbonyl-derivate und ihre verwendung als herbizide
EP2882732B1 (de) Herbizid wirksame 6&#39;-phenyl-2,2&#39;-bipyridin-3-carbonsäure-derivate
WO2017220467A1 (de) 3-amino-1,2,4-triazinderivate und deren verwendung zur bekämpfung unerwünschten pflanzenwachstums
WO2015177108A1 (de) 2-(hetero)aryl-pyridazinone und ihre verwendung als herbizide

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13766930

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2013766930

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 237685

Country of ref document: IL

WWE Wipo information: entry into national phase

Ref document number: MX/A/2015/003538

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 14430018

Country of ref document: US

ENP Entry into the national phase

Ref document number: 2015532405

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112015006573

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 20157010148

Country of ref document: KR

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 112015006573

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20150324