WO2015059088A1 - Substituierte chinoxalin-derivate als schädlingsbekämpfungsmittel - Google Patents
Substituierte chinoxalin-derivate als schädlingsbekämpfungsmittel Download PDFInfo
- Publication number
- WO2015059088A1 WO2015059088A1 PCT/EP2014/072432 EP2014072432W WO2015059088A1 WO 2015059088 A1 WO2015059088 A1 WO 2015059088A1 EP 2014072432 W EP2014072432 W EP 2014072432W WO 2015059088 A1 WO2015059088 A1 WO 2015059088A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- spp
- alkyl
- alkoxy
- formula
- compounds
- Prior art date
Links
- RCTNRLFRRSPLMV-UHFFFAOYSA-N FC(c(cc1)ccc1-c1nc(cc(c(O2)c3)OC2(F)F)c3nc1)(F)F Chemical compound FC(c(cc1)ccc1-c1nc(cc(c(O2)c3)OC2(F)F)c3nc1)(F)F RCTNRLFRRSPLMV-UHFFFAOYSA-N 0.000 description 1
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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/50—Ketonic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
Definitions
- the present invention relates to novel substituted 2- (Het) aryl-quinoxaline derivatives of the formula (I), their use as acaricides and / or insecticides for controlling animal pests and processes and intermediates for their preparation.
- the compounds of the formula (I) are also suitable as nematicides against plant-damaging pests and / or anthelminthics against endoparasites in humans and animals.
- DD 262790 discloses the use of 2-aryl- and 2-hetaryl-quinoxalines as acaricides.
- Japanese Patent Application JP 2004346016 discloses trifluoromethyl-substituted quinoxalines as pesticides.
- DD 258165 discloses the use of 2-hetaryl quinoxalines as algicides and herbicides.
- WO 2013/19112 discloses heterocyclic compounds and their insecticidal activity.
- the object of the present invention is therefore to provide corresponding substituted 2- (Het) aryl-quinoxaline derivatives which are used as insecticides and / or acaricides with a satisfactory insecticidal and / or acaricidal activity against animal pests, in particular at lower application rates, with a high selectivity and improved compatibility in crops can be used. Furthermore, the object of the present invention to provide corresponding substituted 2- (Het) aryl-quinoxaline derivatives which can be used as nematicides and / or anthelmintics.
- Y 1 and Y 2 are each independently N or N + -0 " , in each case optionally monosubstituted or polysubstituted, identically or differently substituted aryl or hetaryl, where (in the case of hetaryl) optionally at least one carbonyl group may be present and / or where as substituents in question: cyano, carboxyl, halogen, nitro, acetyl , Hydroxy, amino, SCN, SF 5 , tri (C 1 -C 6 ) alkylsilyl, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) haloalkyl, (C 1 -C 6 ) cyanoalkyl, (C 1 -C 6 ) hydroxyalkyl, hydroxycarbonyl - (Ci-C4) alkoxy, (Ci- C 6) alkoxycarbonyl (Ci-C 4) alkyl, (Ci-C 6) alkoxy
- alkoxycarbonyl (C 1 -C 7) haloalkoxycarbonyl, aminocarbonyl, (C 1 -C 7) -alkylaminocarbonyl, di- (C 1 -C 7) -alkylaminocarbonyl, (C 2 -C 7) alkenylaminocarbonyl, di (C 2 -C 7) -alkenylaminocarbonyl, (C 3 -C 8) cycloalkylaminocarbonyl, (C 1 -C 6) alkylsulfonylamino, (C 1 -C 6) -alkylamino, aminosulfonyl,
- Aminothiocarbonyl (Ci-C6) alkylaminothiocarbonyl, di (Ci-C6) alkylaminothiocarbonyl, (C3- C8) cycloalkylamino, (Ci-C6) alkylsulfonylamino, in each case optionally substituted by halogen, (Ci- C6) alkyl, (Ci-C 6) haloalkyl, (Ci-C 6) alkylthio, (Ci-C 6) alkoxy or (Ci-C 6) haloalkoxy-substituted phenyl, pyridyl or phenoxy, where the combination of R 1 to the quinoxaline derivative can take place only via a carbon atom,
- R 3, R 4, R 5 and R 6 are each independently hydrogen, cyano, carboxy, halogen, nitro, acetyl, hydroxy, amino, SCN, tri- (Ci-C 6) alkylsilyl, (Ci-C 6) alkyl, (C 1 -C 6 ) haloalkyl, Ce) cyanoalkyl, (Ci-C6) hydroxyalkyl, hydroxycarbonyl (Ci-C4) alkoxy, (Ci-Ce) alkoxycarbonyl (Ci-C 4) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) haloalkenyl, (C 2 - C 6) cyanoalkenyl, (C 2 -C 6) alkynyl, (C 2 -C 6) haloalkynyl, (C 2 -C 6 ) cyano
- Form a 6-membered ring which may optionally contain one or two heteroatoms from the series O or S (where the heteroatoms may not be immediately adjacent) and / or optionally at least one carbonyl group,
- R 8 and R 9 are each independently hydrogen, (Ci-Ce) alkyl, (Ci-Ce) haloalkyl, (C 3 -C 8 ) cycloalkyl, (Ci-C 6 ) alkylthio, (Ci-C 6 ) alkylsulfinyl or (Ci -C 6 ) alkylsulfonyl.
- the compounds according to the invention can be present as geometrical and / or as optically active isomers or corresponding isomer mixtures in different compositions.
- These stereoisomers are, for example, enantiomers, diastereomers, atropisomers or geometric isomers.
- the invention thus comprises pure stereoisomers as well as any mixtures of these isomers.
- the compounds of the formula (I) can be present in the case where R 3, unlike R 6 and R 4 other than R 5, both as mixtures and in the form of their pure isomers (regioisomers). Mixtures can be optionally separated by physical methods, for example by chromatographic methods.
- the compounds of the formula (I) have very good activity as pesticides, preferably as insecticides and / or acaricides, moreover, as a rule, are very well tolerated by plants, in particular with respect to crop plants.
- the compounds of the formula (I) have a very good activity as nematicides and / or anthelmintics.
- Y 1 and Y 2 are each independently preferably represents N or N + -0 ", R 1 preferably represents in each case optionally monosubstituted or polysubstituted by identical or different substituents from the series or hetaryl Q to Q-69:
- At least one carbonyl group may be present (does not apply to phenyl) and / or being suitable as substituents in each case: cyano, halogen, nitro, acetyl, amino, (Ci-C 3 ) alkyl, (Ci-C 3) haloalkyl, (Ci-C 3) cyanoalkyl, (Ci-C 3) hydroxyalkyl, hydroxycarbonyl (Ci-C 3) alkoxy, (Ci-C 3) alkoxycarbonyl (Ci-C 3) alkyl , (C 1 -C 3 ) alkoxy- (ci) C 3) alkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (C 2 -C 3) cyanoalkenyl, (C 2 -C 3) alkynyl, (C 2 - C 3) hal
- R 3 , R 4 , R 5 and R 6 are each independently preferably hydrogen, halogen, cyano, (C 1 -C 3 ) alkyl, (C 1 -C 3 ) haloalkyl, (C 1 -C 3 ) cyanoalkyl, (C 1 -C 4) 3) hydroxyalkyl, hydroxycarbonyl (Ci- C3) alkoxy, (Ci-C 3) alkoxycarbonyl (Ci-C 3) alkyl, (Ci-C 3) alkoxy (Ci-C 3) alkyl, (C 2 -C 3 ) alkenyl, (C 2 -C 3 ) haloalkenyl, (C 2 -C 3 ) cyanoalkenyl, (C 2 -C 3 ) alkynyl, (C 2 -C 3 ) haloalkynyl, (C 2 -C 3 ) cyanoalkynyl , (Ci-C
- R 8 and R 9 independently of one another preferably represent hydrogen, (Ci-C3) alkyl, (C3-Ce) cycloalkyl, (Ci- C3) haloalkyl, (Ci-C 3) alkylsulfinyl or (Ci-C 3) alkylsulfonyl.
- Y 1 and Y 2 independently of one another particularly preferably represent N or N + -0 " ,
- R 1 particularly preferably in each case optionally monosubstituted or disubstituted by identical or different substituents phenyl or hetaryl from the series Ql, Q-22, Q-36, Q-37, Q-41, Q-44, Q-45, Q- 51, Q-64, Q-66, Q-67, wherein substituents in each case are: cyano, halogen, (Ci-C3) alkyl, (Ci- C3) haloalkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (Ci-C 3) alkoxy, (Ci-C 3) haloalkoxy, (Ci-C 3) alkylsulfinyl, (Ci-C 3) haloalkylsulfinyl, (Ci-C 3) alkylsulfonyl, ( ci
- R 2 particularly preferably represents hydrogen, cyano, halogen, (Ci-C 3) alkyl, (Ci-C 3) haloalkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (C 2 - C 3) -alkynyl, (C 2 -C 3) haloalkynyl, (Ci-C 3) alkoxy, (Ci-C 3) haloalkoxy, (Ci-C 3) alkylsulfinyl, (Ci-C 3) haloalkylsulfinyl, (Ci-C 3 ) alkylsulfonyl, (Ci-C 3 ) haloalkylsulfonyl or for each optionally mono- or di-substituted by identical or different substituents phenyl or hetaryl from the series Ql, Q-22, Q-36, Q-37, Q
- R 3, R 4, R 5 and R 6 independently of one another particularly preferably represent hydrogen, cyano, halogen, (Ci-C 3) alkyl, (Ci-C 3) haloalkyl, (C 2 -C 3) alkenyl, (C 2 -C 3 ) haloalkenyl, (C 2 -C 3 ) alkynyl, (C 2 - C 3) haloalkynyl, (Ci-C 3) alkoxy, (Ci-C 3) haloalkoxy, (Ci-C 3) alkylsulfinyl, (Ci- C3) haloalkylsulfinyl, (Ci-C 3) alkylsulfonyl, (Ci-C 3 ) Halogenalkylsulfonyl, with the proviso that R 3 , R 4 , R 5 and R 6 are not simultaneously hydrogen, or
- R 3 and R 4 , or R 4 and R 5 , or R 5 and R 6 together form particularly preferably with the atoms to which they are attached, a saturated, optionally substituted by fluorine, chlorine or (Ci-C 3 ) alkyl 5-membered ring optionally containing one or two oxygen atoms (the heteroatoms must not be immediately adjacent).
- Y 1 and Y 2 independently of one another very particularly preferably represent N or N + -0 " ,
- R 1 very particularly preferably represents in each case optionally monosubstituted or disubstituted by identical or different substituents phenyl or hetaryl from the series series Ql, Q-22, Q-36, Q-37, Q-41, Q-45, Q-51.
- Q-64 being suitable substituents: methyl, ethyl, chlorine, fluorine, cyano, difluoromethyl, trifluoromethyl, SCH 3 , SOCH 3 , S0 2 CH 3 , SC 2 H 5 , SOC 2 H 5 , S0 2 C 2 H 5 , methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy,
- R 2 very particularly preferably represents hydrogen, fluorine, chlorine, bromine, methyl, ethyl, difluoromethyl, trifluoromethyl, in each case optionally chlorine-substituted phenyl or hetaryl from the series Q-41,
- R 3 very particularly preferably represents hydrogen
- R 4 very particularly preferably represents hydrogen, chlorine, fluorine, cyano, SO 2 CH 3 , SO 2 C 2 Hs, trifluoromethyl, difluoromethyl, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy,
- R 5 very particularly preferably represents hydrogen, chlorine, fluorine, cyano, SO 2 CH 3 , SO 2 C 2 Hs, trifluoromethyl, difluoromethyl, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy,
- R 6 is very particularly preferably hydrogen, with the proviso that R 3 , R 4 , R 5 and R 6 are not simultaneously hydrogen, or
- R 3 and R 4 , or R 4 and R 5 , or R 5 and R 6 form very particularly preferred the following 5-membered ring optionally substituted once or twice by fluorine.
- Y 1 and Y 2 are each highlighted for N,
- R 1 stands for each optionally simply methyl-substituted hetaryl from the series Ql or Q-22,
- phenyl optionally substituted once or twice (variously) by methyl, ethyl, chloro, fluoro, trifluoromethyl, SCH 3 , SC 2 H 5 , SOC 2 H 5 , SO 2 CH 3 , SO 2 C 2 H 5 ,
- R 2 stands for hydrogen, chlorine, methyl, for hetaryl from the series Q-41 or for optionally monosubstituted chlorine, phenyl,
- R 3 is hydrogen
- R 4 stands for hydrogen, chlorine, cyano or trifluoromethyl
- R 5 stands for hydrogen, chlorine, trifluoromethyl or SO 2 CH 3 or R 4 and R 5 stand together highlighted for -O-CF 2 -O-
- R 6 stands highlighted for hydrogen, with the proviso that R 3 , R 4 , R 5 and R 6 are not simultaneously hydrogen.
- N stands out for N
- Y 2 also stands for N + -O "
- R 2 also stands for optionally mono- or disubstituted (differently) by trifluoromethyl, fluorine or methyl-substituted phenyl or optionally hetaryl substituted by methyl-substituted from the series Q- 64 R 2 is also hydrogen,
- R 3 is also hydrogen
- R 4 is also hydrogen or trifluoromethyl
- R 5 is also hydrogen or trifluoromethyl or R 4 and R 5 together are also -O-CF 2 -O-,
- R 6 is also hydrogen, with the proviso that R 3 , R 4 , R 5 and R 6 are not simultaneously hydrogen.
- the invention relates to compounds of the formula (IB)
- the invention relates to compounds of the formula (IC)
- the invention relates to compounds of the formula (ID)
- the invention relates to compounds of the formula (I-E)
- the invention relates to compounds of the formula (IG) In a further preferred Aus inditch of the formula (IH)
- R 10 preferably represents cyano, halogen, nitro, acetyl, amino, (C 1 -C 3) -alkyl, (C 1 -C 3) -haloalkyl, (C 1 -C 3) -cycloalkyl, (C 1 -C 3) -hydroxyalkyl, hydroxycarbonyl- (C 1 -C 3) alkoxy, (Ci-C3) alkoxycarbonyl (Ci-C 3) alkyl, (Ci-C 3) alkoxy (Ci-C 3) alkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) haloalkenyl, (C 2 - C 3) cyanoalkenyl, (C 2 -C 3) alkynyl, (C 2 -C 3) haloalkynyl, (C 2 -C 3) cyanoalkynyl, (Ci-C 3) alkoxy, (Ci
- R 10 particularly preferably represents cyano, halogen, (Ci-C 3) alkyl, (Ci-C 3) haloalkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (Ci-C 3) alkoxy, (Ci-C 3) haloalkoxy, (Ci-C 3) alkylsulfinyl, (Ci- C3) haloalkylsulfinyl, (Ci-C 3) alkylsulfonyl, (Ci-C 3) haloalkylsulfonyl, (Ci-C 3) alkylthio, n stands for 0 or 1, m stands for 0, 1 or 2,
- R 10 very particularly preferably represents methyl, ethyl, chlorine, fluorine, cyano, difluoromethyl, trifluoromethyl, SCH 3 , SOCH 3 , SO 2 CH 3 , SC 2 H 5, SOC 2 H 5, SO 2 C 2 H 5, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy , n is 0 or 1, m is 0, 1 or 2,
- R 10 is methyl, ethyl, chlorine, fluorine, trifluoromethyl, SCH 3 , SO 2 CH 3 , SC 2 H 5 , SOC 2 H 5 , SO 2 C 2 H 5 , methoxy or ethoxy, n is 0 or 1, m is 0, 1 or 2.
- R 2 , R 3 , R 4 , R 5 , R 6 , R 10 and n have the following meanings: preferably represents hydrogen, cyano, halogen, nitro, acetyl, amino, tri- (Ci-C3) alkylsilyl, cyclo (C 3 -C 6) alkyl, (Ci-C 3) alkyl, (Ci-C 3) haloalkyl, (Ci-C 3) cyanoalkyl, (Ci-C 3) hydroxyalkyl, hydroxycarbonyl (Ci-C 3) alkoxy, (Ci-C 3) alkoxycarbonyl (Ci-C 3) alkyl, (Ci-C 3) alkoxy - (Ci- C3) alkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (C 2 -C 3) cyanoalkenyl, (C 2 -C 3)
- R 3 , R 4 , R 5 and R 6 are each independently preferably hydrogen, halogen, cyano, (C 1 -C 3 ) alkyl, (C 1 -C 3 ) haloalkyl, (C 1 -C 3 ) cyanoalkyl, (C 1 -C 4) 3) hydroxyalkyl, hydroxycarbonyl (Ci- C3) alkoxy, (Ci-C 3) alkoxycarbonyl (Ci-C 3) alkyl, (Ci-C 3) alkoxy (Ci-C 3) alkyl, (C 2 -C 3 ) alkenyl, (C 2 -C 3 ) haloalkenyl, (C 2 -C 3 ) cyanoalkenyl, (C 2 -C 3 ) alkynyl, (C 2 -C 3 ) haloalkynyl, (C 2 -C 3 ) cyanoalkynyl , (Ci-C
- R 8 and R 9 independently of one another preferably represent hydrogen, (Ci-C3) alkyl, (C3-Ce) cycloalkyl, (Ci- C3) haloalkyl, (Ci-C 3) alkylsulfinyl or (Ci-C 3) alkylsulfonyl,
- R 10 preferably represents cyano, halogen, nitro, acetyl, amino, (C 1 -C 3) -alkyl, (C 1 -C 3) -haloalkyl, (C 1 -C 3) -cycloalkyl, (C 1 -C 3) -hydroxyalkyl, hydroxycarbonyl- (C 1 -C 3) alkoxy, (Ci-C 3) alkoxycarbonyl (Ci-C 3) alkyl, (Ci-C 3) alkoxy (Ci-C 3) alkyl, (C 2 -C 3) alkenyl, (C 2 -C 3 ) haloalkenyl, (C 2 - C 3) cyanoalkenyl, (C 2 -C 3) alkynyl, (C 2 -C 3) haloalkynyl, (C 2 -C 3) cyanoalkynyl, (Ci-C 3) alkoxy, (
- R 2 particularly preferably represents hydrogen, cyano, halogen, (Ci-C 3) alkyl, (Ci-C 3) haloalkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (C 2 - C 3) -alkynyl, (C 2 -C 3) haloalkynyl, (Ci-C 3) alkoxy, (Ci-C 3) haloalkoxy, (Ci-C 3) alkylsulfinyl, (Ci-C 3) haloalkylsulfinyl, (Ci-C 3 ) alkylsulfonyl, (Ci-C 3 ) haloalkylsulfonyl or for each optionally mono- or di-substituted by identical or different substituents phenyl or hetaryl from the series Ql, Q-22, Q-36, Q-37, Q
- R 3, R 4, R 5 and R 6 independently of one another particularly preferably represent hydrogen, cyano, halogen, (Ci-C 3) alkyl, (Ci-C 3) haloalkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (C 2 -C 3) alkynyl, (C 2 - C 3) haloalkynyl, (Ci-C 3) alkoxy, (Ci-C 3) haloalkoxy, (Ci-C 3) alkylsulfinyl, ( Ci- C 3) haloalkylsulfinyl, (Ci-C 3) alkylsulfonyl, (Ci-C 3) haloalkylsulfonyl, with the proviso that R 3, R 4, R 5 and R 6 are not simultaneously hydrogen, or
- R 3 and R 4 , or R 4 and R 5 , or R 5 and R 6 together form particularly preferably with the atoms to which they are attached, a saturated, optionally substituted by fluorine, chlorine or (Ci-C 3 ) alkyl 5-membered ring optionally containing one or two oxygen atoms (where the heteroatoms must not be immediately adjacent),
- R 10 particularly preferably represents cyano, halogen, (Ci-C 3) alkyl, (Ci-C 3) haloalkyl, (C 2 -C 3) alkenyl, (C 2 -C 3) -haloalkenyl, (Ci-C 3) alkoxy, (Ci-C 3) haloalkoxy, (Ci-C 3) alkylsulfinyl, (Ci- C3) haloalkylsulfinyl, (Ci-C 3) alkylsulfonyl, (Ci-C 3) haloalkylsulfonyl, (Ci-C 3) alkylthio, n stands for 0 or 1.
- R 2 very particularly preferably represents hydrogen, fluorine, chlorine, bromine, methyl, ethyl, difluoromethyl, trifluoromethyl, in each case optionally chlorine-substituted phenyl or hetaryl from the series Q-41,
- R 3 very particularly preferably represents hydrogen
- R 4 very particularly preferably represents hydrogen, chlorine, fluorine, cyano, SO 2 CH 3 , SO 2 C 2 Hs, trifluoromethyl, difluoromethyl, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy,
- R 5 very particularly preferably represents hydrogen, chlorine, fluorine, cyano, SO 2 CH 3 , SO 2 C 2 Hs, trifluoromethyl, difluoromethyl, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy,
- R 6 is very particularly preferably hydrogen, with the proviso that R 3 , R 4 , R 5 and R 6 are not simultaneously hydrogen, or
- R 3 and R 4 , or R 4 and R 5 , or R 5 and R 6 form very particularly preferred the following 5-membered ring optionally substituted once or twice by fluorine,
- R 10 very particularly preferably represents methyl, ethyl, chlorine, fluorine, cyano, difluoromethyl, trifluoromethyl, SCH 3 , SOCH 3 , SO 2 CH 3 , SC 2 H 5 , SOC 2 H 5 , SO 2 C 2 H 5 , methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy, n is 0 or 1.
- R 2 stands for hydrogen, chlorine, methyl, for hetaryl from the series Q-41 or for optionally monosubstituted chlorine, phenyl,
- R 3 stands for hydrogen
- R 4 stands for hydrogen, fluorine, chlorine, cyano or trifluoromethyl
- R 5 is hydrogen, fluorine, chlorine, trifluoromethyl or SO 2 CH 3, or
- R 4 and R 5 together are highlighted as -O-CF 2 -O-,
- R 6 is hydrogen, with the proviso that R 3 , R 4 , R 5 and R 6 are not simultaneously hydrogen,
- R 10 is methyl, ethyl, chloro, fluoro, trifluoromethyl, SCH 3 , SO 2 CH 3 , SC 2 H 5 , SOC 2 H 5 , SO 2 C 2 H 5 , methoxy or ethoxy, (especially methyl, ethyl, chloro or methoxy), n is 0 or 1.
- the compounds of the formula (I) according to the invention can be obtained by the processes illustrated in the following schemes: Method A
- R 1 , R 2 , R 3 , R 4 , R 5 and R 6 have the meanings described above and Hal is halogen.
- the compounds of the formula (Ia) can be prepared analogously to the process described in the patent application DD 0151753 by the reaction of benzene-1,2-diamines of the formula (II) with 2-halo-1- (het) aryl-ethanones of the formula (III) are produced. Further examples of this process are published in J. Org. Chem., 1966, 31 (3), 803-806, Pharmacie 40 (1985), 384-387, Bull. Soc. Chim. Fr., (1950) 753-757, Helv. Chim.
- Benzene-1,2-diamines of the formula (II) are either commercially available or can be prepared by known methods, for example analogously to J. Org. Chem., 1969, 384 or J. Med. Chem. 1981, 24 (1), 93-101.
- 2-Halogen-l- (Het) aryl-ethanones of the formula (III) are either commercially available or can be prepared by known methods, for example analogously to those described in Helv. Chim. Acta, 1955, 38, 1289-1291, Pharmacia 40 (1985), 384-387, WO 2009/114552 or DD 0151753.
- the reaction of the benzene-1,2-diamine of the formula (II) with 2-halo-1- (het) aryl-ethanones of the formula (III) can be carried out in bulk or in a solvent, preferably the reaction is carried out in a solvent , which is selected from conventional, inert in the prevailing reaction conditions solvents.
- a solvent which is selected from conventional, inert in the prevailing reaction conditions solvents.
- aliphatic alcohols such as, for example, methanol, ethanol, n-propanol or isopropanol
- Ethers such as diisopropyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane
- Nitriles such as acetonitrile or propionitrile.
- the reaction is preferably carried out in the presence of a base.
- Suitable bases are inorganic bases which are commonly used in such reactions.
- bases are used which are selected by way of example from the group consisting of acetates, phosphates, carbonates and bicarbonates of alkali or alkaline earth metals. Particularly preferred are sodium acetate, sodium phosphate, potassium phosphate, cesium carbonate, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate.
- the reaction can be carried out in vacuo, at atmospheric pressure or under overpressure and at temperatures of 0 ° C to 180 ° C, preferably the reaction is carried out at atmospheric pressure and temperatures of 20 to 110 ° C.
- benzene-1,2-diamines of the formula (II) are reacted with glyoxals of the formula (IV).
- glyoxals of the formula (IV) This is a special case of the general synthesis of quinoxalines in which benzene-1,2-diamines of formula (II) are reacted with ⁇ -dicarbonyl compounds.
- Glyoxals of formula (IV) are either commercially available or can be prepared by known methods, e.g. By methods described in Bull. Soc. Chim. Fr., (1950) 753-757, J.Med.Chem. 1979, 22 (6), 687-694, J. of Chem. And Eng. Data, 1973, 18 (1), 102-104, Current Chemistry Letters 2012, 1 (3), 139-146 or US 6649768.
- asymmetrical benzene-1,2-diamines of the formula (II) are used, a mixture of the regioisomeric quinoxalines of the formula (Ib) is optionally obtained. These can be with the usual ones be separated by chromatographic methods.
- the implementation takes place z.
- the reaction of the benzene-1,2-diamines of the formula (II) with glyoxals of the formula (IV) can be carried out in bulk or in a solvent, preferably the reaction is carried out in a solvent which is selected from the usual, under the prevailing reaction conditions inert solvents.
- aliphatic alcohols such as, for example, methanol, ethanol, n-propanol or isopropanol; Ethers such as diisopropyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane; Nitriles, such as acetonitrile or propionitrile; polar, aprotic solvents such as N, N-dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and mixtures of these solvents.
- Ethers such as diisopropyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane
- Nitriles such as acetonitrile or propionitrile
- polar, aprotic solvents such as N, N-dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and mixtures of these solvents.
- the reaction can be carried out in vacuo, at atmospheric pressure or under overpressure and at temperatures of 0 ° C to 180 ° C, preferably the reaction is carried out at atmospheric pressure and temperatures of 20 to 110 ° C.
- R 7 is hydrogen or (C 1 -C 6) alkyl (preferably hydrogen or (C 1 -C 4 -alkyl, particularly preferably hydrogen or methyl),
- M ' is hydrogen or (Ci-Ce) alkyl (preferably hydrogen or (Ci-C-OAlkyl, particularly preferably hydrogen, methyl or trifluoromethyl),
- M " is hydrogen, (Ci-C 6 ) alkyl or (C 3 -C 8 ) cycloalkyl (preferably hydrogen, (Ci-C 4 ) alkyl or (C3-Ce) cycloalkyl, particularly preferably hydrogen or methyl),
- M stands for M ' or M " G is hydrogen, (C 1 -C 6 ) alkyl, (C 2 -C 6 ) alkenyl or aryl (preferably hydrogen, (C 1 -C 4 ) alkyl, (C 2 -C 4 ) alkenyl or phenyl, particularly preferably hydrogen) or B (OG) 2 together form a 5- or 6-membered cycle (preferably a 5-membered cycle,
- benzene-1,2-diamines of the formula (II) are reacted with alkylhydroxy (alkoxy) acetates of the formula (V) to give the quinoxaline-2 (1H) -ones of the formula (Via).
- Carbonyl compounds of the formula (IX) are commercially available.
- the reactions of the benzene-1,2-diamines of the formula (II) with alkylhydroxy (alkoxy) acetates of the formula (V) or with carbonyl compounds of the formula (IX) can be carried out in bulk or in a solvent, preferably the reaction is carried out in a solvent which is selected from conventional, inert in the prevailing reaction conditions solvents.
- aliphatic alcohols such as, for example, methanol, ethanol or isopropanol
- Ethers such as diisopropyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane
- Nitriles like for example, acetonitrile or propionitrile
- amides such as N, N-dimethylformamide (DMF), ⁇ , ⁇ -dimethylacetamide or N-methylpyrrolidone; or mixtures of these with water and pure water or 1,2-dichloroethane.
- the reaction can be carried out in vacuo, at atmospheric pressure or under excess pressure and at temperatures of -20 to 180 ° C, preferably the reaction is carried out at atmospheric pressure and temperatures of 30 to 130 ° C.
- the quinoxaline-2 (1H) -ones of the formula (VIa) obtained in step (a) are reacted with a halogenating agent according to the invention to give the quinoxalines of the formula (VII).
- Suitable halogenating agents are, for example, PCI3, POCl3, PCI5, POBr3, PBrs, thionyl chloride or N-halosuccinimides or mixtures of these reagents.
- POCl 3 is used as the halogenating agent.
- WO 95/42463, WO 2008/141065, WO 2008/148867, WO 2011/022439, Ree. Trav. Chim. Pays-Bas, 1972, 91, 850-860, J. Med. Chem., 1981, 24 (1), 93-101, J. Heterocyclic Chem. 33, 447 (1996) and Tetrahedron Lett., 1999, 40, 7477 these synthesis variants are described.
- step (b) the halogenations according to step (b) were carried out with the aid of tetraalkylammonium iodides, tetraalkylammonium bromides and tetraalkylammonium chlorides in the presence of P 2 O 5 . This method is described in Tetrahedron Lett., 2001, 42, 4849-4851.
- the compounds of the formula (Via) are partly new, partly commercially available.
- the reaction of the compounds of formula (V) with the halogenating agent may be carried out in bulk or in a solvent, preferably the reaction is carried out in a solvent selected from conventional solvents which are inert under the prevailing reaction conditions.
- aromatic hydrocarbons such as benzene, toluene, xylene or decalin; halogenated hydrocarbons such as chlorobenzene, dichlorobenzene, dichloromethane or chloroform.
- the reaction is preferably carried out in the presence of a base.
- bases are organic and inorganic bases commonly used in such reactions.
- bases are used which are selected by way of example from the group consisting of acetates, phosphates, Carbonates and bicarbonates of alkali or alkaline earth metals. Particularly preferred are sodium acetate, sodium phosphate, potassium phosphate, cesium carbonate, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate.
- tertiary amines such as trimethylamine, triethylamine, tributylamine, triethylamine hydrochloride, N-ethyldiisopropylamine and pyridine are preferred.
- the reaction can be carried out in vacuo, under normal pressure or under overpressure and at temperatures of 0 ° C to 180 ° C, preferably the reaction is carried out at atmospheric pressure and temperatures of 30 to 130 ° C.
- Step c) The quinoxalines of the formula (VII) obtained in step (b) are reacted with a boron compound of the formula (Villa).
- the reaction preferably in the presence of a catalyst, if appropriate in the presence of a base in an organic solvent or in a mixture of a solvent with water at ambient temperature or elevated temperatures, leads to the quinoxalines of the formula (Ic) according to the invention.
- a catalyst if appropriate in the presence of a base in an organic solvent or in a mixture of a solvent with water at ambient temperature or elevated temperatures.
- WO 2008/148867 discloses analogous couplings with (morpholine) -arylboronic acids or corresponding aryl-1,3,2-dioxaborolanes in the presence of palladium catalysts. Further examples can be found in WO 2008/141065, WO 2009/073497, WO 2011/028947, WO 2012/045196, WO 2012/119046, J. Org. Chem. 1995, 60, 7508-7510, J. Med. Chem. 2005, 48 (21), 6632-6642 or in J. Am. Chem. Soc. 2007, 129 (11), 3358-3366.
- Boron derivatives of the formula (Villa) are either commercially available or can be prepared by known methods, e.g. As cited in J. Org. Chem., 1995, 60, 7508-7510, WO 2011/143495, WO2011 / 022439 or WO 2004/01913.
- the catalysts used in the reactions of the halo-quinoxalines are preferably salts or complexes of palladium, copper or nickel.
- Suitable palladium catalysts are, for example, palladium (II) acetate,
- ligands for example 2,2'-bis (diphenylphosphino) -l, 1 '-binaphthyl, 9,9-dimethyl-4,5-bis (diphenylphosphino) xanthene or 1, 1' bis (diphenylphosphino) -f errocene.
- Suitable copper salts include, for example, cuprous iodide, cuprous chloride, cuprous oxide, cupric triflate, cupric acetate, cupric triflate, often in the presence a ligand, for example diamine ligands such as N, N'-dimethylethylenediamine, ⁇ , ⁇ -dimethylethylenediamine or trans-N, N'-dimethyl-l, 2-cyclohexanediamine.
- a ligand for example diamine ligands such as N, N'-dimethylethylenediamine, ⁇ , ⁇ -dimethylethylenediamine or trans-N, N'-dimethyl-l, 2-cyclohexanediamine.
- Suitable nickel catalysts are, for example, nickel (II) acetylacetonate alone or in combination with the abovementioned phosphorus ligands or nickel (II) acetylacetonate with imidazolium carbene ligands.
- the catalyst is usually employed in a substoichiometric amount, preferably from 0.001 to 0.8 equivalents and particularly preferably from 0.01 to 0.5 equivalents, based on the quinoxalines of the formula (VII) used.
- the reaction of the quinoxalines of the formula (VII) with a boronic acid is preferably carried out in a solvent which is selected from conventional solvents which are inert under the prevailing reaction conditions.
- a solvent which is selected from conventional solvents which are inert under the prevailing reaction conditions.
- ethers such as, for example, dioxane, tetrahydrofuran, diethyl ether or 1,2-dimethoxyethane
- aromatic hydrocarbons such as benzene, toluene or xylene
- aliphatic alcohols such as methanol, ethanol or isopropanol
- Nitriles such as acetonitrile or propionitrile
- polar, aprotic solvents such as ⁇ , ⁇ -dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and mixtures of these solvents with water.
- the reaction is preferably carried out in the presence of a base.
- Suitable bases are inorganic bases, in particular acetates, phosphates, carbonates and bicarbonates of alkali or alkaline earth metals. Particularly preferred are sodium acetate, sodium phosphate, potassium phosphate, cesium carbonate, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate.
- the inorganic bases can also be used as aqueous solutions.
- the reaction can be carried out in vacuo, under normal pressure or under overpressure and at temperatures from 0 ° C to 200 ° C, preferably the reaction is carried out at atmospheric pressure and temperatures of 40 to 150 ° C, optionally under an inert gas atmosphere.
- boronic acid instead of the boronic acid, other boron compounds such as potassium trifluoroborates, boronic acid esters and other organometallic compounds such as stannanes, silanes or bismuthans may be used.
- boron compounds such as potassium trifluoroborates, boronic acid esters and other organometallic compounds such as stannanes, silanes or bismuthans may be used.
- Suitable organotin compounds are corresponding trimethylstannyl or tributylstannyl compounds, such as. As described in dWO 20111/22815 or WO 2011/022439.
- Step a) In an embodiment according to the invention, benzene-1,2-diamines of the formula (II) are reacted with carbonyl compounds of the formula (X) to give the quinoxaline-2 (1H) -ones of the formula (VIb).
- Carbonyl compounds of the formula (X) are commercially available or can be prepared by known methods, for example analogously to Synth. Commun. Chem. 1981, 211, Tetrahedron Lett., 2002, 43, 5361-5365, DE 2824407, JP 52027745 or EP-A-512352.
- quinoxalines of the formula (Id) are obtained from quinoxalines of the formula (XI) and a boron compound of the formula (Villa), analogously to the procedure as in process A, step c).
- the preparation of the 1,2-bis-halo-quinoxalines of the formula (XI) is carried out in analogy to processes from US 5514680, J. Med. Chem. 1981, 24 (1), 93-101 or J. Heterocycl. Chem. 2009, 46, 317-319 by the reaction of 1,4-dihydroquinoxaline-2,3-diones with suitable halogenating agents, for example POCl3 or thionyl chloride.
- step (b) or step (c) The quinoxalines of the formula (Id) according to the invention obtained in step (b) or step (c) are described in an analogous embodiment as in process A, step c) by reacting with a boron compound of the formula (VIIIb) to give the quinoxalines of the formula ( Ia) implemented.
- the quinoxalines of the formula (Ia) obtained in the processes A to D can be converted by reaction with oxidizing agents into the corresponding N-oxides of the general structure (I).
- the reaction is carried out in analogy to J. Chem. Soc. 479 (1938), J. of Chem. And Eng. Data, 1973, 18 (1), 102-104, Synlett 2001, (1), 73-73, WO 2008/015423, J. Org. Chem. 1977, 1869-1871, Chem. Pharm. Bull. 1974, 22 , 2097-2100 or J. Chem. Research (S), 1986, 16-17.
- Suitable solvents are dichloromethane, trichloromethane, methanol, formic acid, acetic acid or trifluoroacetic acid.
- a 35% aqueous solution of hydrogen peroxide in acetic acid is preferably used.
- the reaction can be carried out at atmospheric pressure or under pressure and at temperatures of 0 ° C to 60 ° C, preferably, the reaction is carried out at atmospheric pressure and temperatures of 40 to 50 ° C.
- the invention also relates to methods for controlling animal pests, in which compounds of the formula (I) are allowed to act on animal pests and / or their habitat. Preference is given to the control of animal pests in agriculture and forestry and in the Material protection carried out. Excluded therefor are preferably methods for the surgical or therapeutic treatment of the human or animal body and diagnostic methods that are performed on the human or animal body.
- the invention further relates to the use of the compounds of the formula (I) as pesticides, in particular pesticides.
- pest control always includes the term pesticides.
- the compounds of the formula (I) are suitable for plant protection, favorable warm-blooded toxicity and good environmental compatibility for the protection of plants and plant organs from biotic and abiotic stress factors, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, Arachnids, helminths, nematodes and molluscs found in agriculture, horticulture, livestock, aquaculture, forestry, gardens and recreation, storage and materials protection and hygiene. They can preferably be used as pesticides. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
- the above mentioned pests include:
- Pests of the genus Arthropoda in particular of the class Arachnida eg Acarus spp., Eg Acarus siro, Aceria kuko, Aceria sheldoni, Aculops spp., Aculus spp., Eg Aculus fockeui, Aculus badendali, Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., Eg Brevipalpus phoenicis, Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp., Eg Eotetranychus hi
- Euscelis bilobatus, Ferrisia spp., Geococcus coffeae, Glycaspis spp., Heteropsylla cubana, Heteropsylla spinulosa, Homalodisca coagulata, Hyalopterus arundinis, Hyalopterus pruni, Icerya spp., Eg Icerya purchasi, Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp eg Lecanium corni ( Parthenolecanium corni), Lepidosaphes spp., eg Lepidosaphes ulmi, Lipaphis erysimi, Lycorma americanula, Macrosiphum spp., eg Macrosiphum euphorbiae, Macrosiphum lilii, Macrosiphum rosae, Macro
- Pemphigus spp. Eg Pemphigus bursarius, Pemphigus populivenae, Peregrinus maidis, Phenacoccus spp., Eg Phenacoccus madeirensis, Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., Eg Phylloxera devastatrix, Phylloxera notabilis, Pinnaspis aspidistrae, Planococcus spp., Eg Planococcus citri, Prosopidopsylla flava, Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., Eg Pseudococcus calceolariae, Pseudococcus comstocki, Pseudococcus longispinus, Pseudococcus maritimus, Pseu
- Ctenolepisma spp. Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica; from the class of Symphyla eg Scutigerella spp., eg Scutigerella immaculata;
- Pests of the Mollusca strain in particular of the bivalve class, e.g. Dreissena spp .; and from the class of Gastropoda e.g. Arion spp., E.g. Arion ater rufus, Biomphalaria spp., Bulinus spp., Deroceras spp., E.g. Deroceras laeve, Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp .; Animal and human parasites from the strains of Platyhelminthes and Nematoda, e.g.
- Aelurostrongylus spp. Amidostomum spp., Ancylostoma spp, Angiostrongylus spp., Anisakis spp., Anoplocephala spp., Ascaris spp., Ascaridia spp., Baylisascaris spp., Brugia spp., Bunostomum spp., Capillaria spp., Chabertia spp.
- Clonorchis spp. Cooperia spp., Crenosoma spp., Cyathostoma spp., Dicrocoelium spp., Dictyocaulus spp., Diphyllobothrium spp., Dipylidium spp., Dirofilaria spp., Dracunculus spp., Echinococcus spp., Echinostoma spp., Enterobius spp., Eucoleus spp., Fasciola spp., Fascioloides spp., Fasciolopsis spp., Filaroides spp., Gongylonema spp., Gyrodactylus spp., Habronema spp., Haemonchus spp., Heligmosomoides spp., Heterakis spp., Hymenolepis spp.
- Hyostrongylus spp. Litomosoides spp., Loa spp., Metastrongylus spp., Metorchis spp., Mesocestoides spp., Moniezia spp., Muellerius spp., Necator spp., Nematodirus spp., Nippostrongylus spp., Oesophagostomum spp., Ollulanus spp., Onchocerca spp, Opisthorchis spp., Oslerus spp., Ostertagia spp., Oxyuris spp., Paracapillaria sp Paraglia spp., Paragonimus spp., Paramphistomum spp., Paranoplocephala spp., Parascaris spp., Passalurus spp., Protostrongylus spp., Schistosoma s
- Strongyloides spp. Strongylus spp., Syngamus spp., Taenia spp., Teladorsagia spp., Thelazia spp., Toxascaris spp., Toxocara spp., Trichinella spp., Trichobilharzia spp., Trichostrongylus spp., Trichuris spp., Uncinaria spp., Wuchereria spp .;
- Plant pests from the Nematoda strain ie plant parasitic nematodes, in particular Aglenchus spp., Eg Aglenchus agricola, Anguina spp., Eg Anguina tritici, Aphelenchoides spp., Eg Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimus spp., Eg Belonolaimus gracilis, Belonolaimus longicaudatus, Belonolaimus nortoni, Bursaphelenchus spp., Eg Bursaphelenchus cocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus, Cacopaurus spp., Eg Cacopaurus pestis, Criconemella spp., Eg Criconemella curvata, Criconemella onoensis, Criconemella ornata
- the order of coccidia can be determined, e.g. Eimeria spp. fight.
- nematodes in the present context includes all species of the strain Nematoda and in particular species, the plants or fungi (for example species of the order Aphelenchida, Meloidogyne, Tylenchida and others) or even humans and animals (for example species of the orders Trichinellida, Tylenchida, Rhabditina and Spirurida) or causing damage to these animals as well as other parasitic helminths.
- the plants or fungi for example species of the order Aphelenchida, Meloidogyne, Tylenchida and others
- humans and animals for example species of the orders Trichinellida, Tylenchida, Rhabditina and Spirurida
- a nematocide in crop protection has the ability to control nematodes.
- controlling nematodes means killing the nematodes or preventing or aggravating their development or growth or preventing or hindering their penetration into or their sucking on the plant tissue.
- the effectiveness of the compounds is compared by mortality, bile formation, cyst formation, nematode density per soil volume, nematode density per root, number of nematode eggs per soil volume, mobility (mobility) of the nematodes between a plant treated with the compound of formula (I), plant part or the treated soil and an untreated plant, plant part or untreated soil (100%).
- a reduction of 25-50% compared to an untreated plant, plant part or untreated Soil more preferably a reduction of 51-79%, and most preferably complete kill or complete prevention of development and growth of the nematodes by a reduction of 80-100%.
- Control of nematodes as described herein also includes control of nematode proliferation (development of cysts and / or eggs).
- Compounds of formula (I) may also be used to keep the plants or animals healthy and may be used for curative, preventive or systemic control of nematode control.
- Methods are known to those skilled in the art, such as mortality, bile formation, cyst formation, nematode density per volume of soil, nematode density per root, number of nematode eggs per soil volume, mobility (motility) of the nematodes.
- the use of a compound of the formula (I) can maintain the plant in a healthy state and also involves a reduction in the damage caused by nematodes and an increase in the amount of harvest.
- nematodes refers to plant nematodes, which includes all nematodes that damage plants, plant nematodes include plant parasitic nematodes and soil-borne nematodes, and plant parasitic nematodes include ectoparasites such as Xiphinema spp., Longidorus spp., And Trichodorus semi-parasites such as Tylenchulus spp; migratory endoparasites such as Pratylenchus spp., Radopholus spp., and Scutellonema spp; localized parasites such as Heterodera spp., Globodera spp., and Meloidogyne spp., and stalk and leaf endoparasites such as Ditylenchus spp., Aphelenchoides Specially harmful root parasitic nematodes are, for example, cyst-forming nematodes of the genera Heteroder
- Meloidogyne incognita acrita Meloidogyne javanica, Meloidogyne kikuyensis, Meloidogyne minor, Meloidogyne naasi, Meloidogyne paranaensis, Meloidogyne thamesi and the localized parasites Meloidogyne spp., Meloinema spp., Nacobbus aberrans, Neotylen chus vigissi, Paraphelenchus pseudoparietinus, Paratrichodorus allius, Paratrichodorus lobatus, Paratrichodorus minor, Paratrichodorus nanus, Paratrichodorus porosus, Paratrichodorus teres and Paratrichodorus spp., Paratylenchus hamatus, Paratylenchus minutus, Paratylenchus projectus and Paratylench
- Trichodorus spp. Subanguina radiciola, Tetylenchus nicotianae, Trichodorus cylindricus Trichodorus minor Trichodorus primitivus Trichodorus proximus Trichodorus similis Trichodorus sparsus and ectoparasites Trichodorus spp., Tylenchorhynchus agri, Tylenchorhynchus brassicae, Tylenchorhynchus clarus, Tylenchorhynchus claytoni, Tylenchorhynchus digitatus, Tylenchorhynchus ebriensis, Tylenchorhynchus maximus, Tylenchorhynchus nudus, Tylenchorhynchus vulgaris and Tylenchorhynchus spp., Tylenchulus semipenetrans and the semiparasites Tylenchulus spp., Xiphinema americanum, Xiphinema
- nematodes that can be used to control a compound of formula (I) include nematodes of the genus Meloidogyne, such as the Southern Root-Knot Nematode (Meloidogyne incognita), the Javanese Root-Knot Nematode (Meloidogyne javanica, the Northern Root-Knot Nematode (Meloidogyne hapla) and the Peanut Root-Knot Nematode (Meloidogyne arenaria); Nematodes of the genus Ditylenchus such as the potato scabies (Ditylenchus destructor) and the cane and stemlets (Ditylenchus dipsaci); Nematodes of the genus Pratylenchus such as the Cob root lesion Nematode (Pratylenchus penetrans), the Chrysanthemum Root-Lesion nematode (Pratylenchus fallax), the coffee
- plants for the protection of which a compound of the formula (I) can be used include plants such as cereals (for example, rice, barley, wheat, rye, oats, corn, and the like), beans (soybean, azuki bean, bean, fat Bean, peas, peanuts and the like), fruit trees / fruits (apples, citrus, pears, grapes, peaches, Japanese apricots, cherries, walnuts, almonds, bananas, strawberries and the like), vegetables (cabbage, tomato, spinach, broccoli, lettuce , Onion, tubeworm, pepper and the like), root crops (carrot, potato, sweet potato, radish, lotus root, rutabaga and the like), plants for industrial raw materials (cotton, hemp, paper mulberry, mitsumata, rape, turnip, hops, sugar cane, sugar beet, Olive, gum, palm, coffee, tobacco, tea and the like), cucurbits (squash, cucumber, watermelon, melon and
- the compounds of the formula (I) are particularly suitable for controlling nematodes of coffee, in particular Pratylenchus brachyurus, Pratylenchus coffeae, Meloidogyne exigua, Meloidogyne incognita, Meloidogyne coffeicola, Helicotylenchus spp. and from Meloidogyne paranaensis, Rotylenchus spp., Xiphinema spp., Tylenchorhynchus spp. and Scutellonema spp.
- the compounds of formula (I) are particularly suitable for controlling potato nematodes, in particular Pratylenchus brachyurus, Pratylenchus pratensis, Pratylenchus scribneri, Pratylenchus penetrans, Pratylenchus coffeae, Ditylenchus dipsaci and Pratylenchus alleni, Pratylenchus andinus, Pratylenchus cerealis, Pratylenchus crenatus, Pratylenchus hexincisus, Pratylenchus loosi, Pratylenchus neglectus, Pratylenchus teres, Pratylenchus thornei, Pratylenchus vulnus, Belonolaimus longicaudatus, Trichodorus cylindricus, Trichodorus primitivus, Trichodorus proximus, Trichodorus similis, Trichodorus sparsus, Paratrichodor
- the compounds of the formula (I) are particularly suitable for controlling tomato nematodes, in particular Meloidogyne arenaria, Meloidogyne hapla, Meloidogyne javanica, Meloidogyne incognita, Pratylenchus penetrans and Pratylenchus brachyurus, Pratylenchus coffeae, Pratylenchus scribneri, Pratylenchus vulnus, Paratrichodorus minor , Meloidogyne exigua, Nacobbus aberrans, Globodera solanacearum, Dolichodorus heterocephalus and Rotylenchulus reniformis.
- the compounds of the formula (I) are particularly suitable for controlling nematodes of cucurbits, in particular Meloidogyne arenaria, Meloidogyne hapla, Meloidogyne javanica, Meloidogyne incognita, Rotylenchulus reniformis and Pratylenchus thornei.
- the compounds of the formula (I) are particularly suitable for controlling cotton nematodes, in particular Belonolaimus longicaudatus, Meloidogyne incognita, Hoplolaimus columbus, Hoplolaimus galeatus and Rotylenchulus reniformis.
- the compounds of the formula (I) are particularly suitable for controlling nematodes of maize, in particular Belonolaimus longicaudatus, Paratrichodorus minor and Pratylenchus brachyurus, Pratylenchus delattrei, Pratylenchus hexincisus, Pratylenchus penetrans, Pratylenchus zeae, (Belonolaimus gracilis), Belonolaimus nortoni, Longidorus breviannulatus, Meloidogyne arenaria, graminis Meloidogyne arenaria thamesi, Meloidogyne, Meloidogyne incognita, Meloidogyne incognita acrita, Meloidogyne javanica, Meloidogyne naasi, Heterodera avenae, Heterodera oryzae, Heter
- the compounds of the formula (I) are particularly suitable for combating soybean nematodes, in particular Pratylenchus brachyurus, Pratylenchus pratensis, Pratylenchus penetrans, Pratylenchus scribneri, Belonolaimus longicaudatus, Heterodera glycines, Hoplolaimus columbus and Pratylenchus coffeae, Pratylenchus hexincisus, Pratylenchus neglectus.
- Pratylenchus crenatus Pratylenchus alleni
- Pratylenchus agilis Pratylenchus zeae
- Pratylenchus vulnus (Belonolaimus gracilis), Meloidogyne arenaria, Meloidogyne incognita, Meloidogyne javanica, Meloidogyne hapla, Hoplolaimus columbus, Hoplolaimus galeatus and Rotylenchulus reniformis.
- the compounds of the formula (I) are particularly suitable for controlling nematodes of the tobacco, in particular Meloidogyne incognita, Meloidogyne javanica and Pratylenchus brachyurus, Pratylenchus pratensis, Pratylenchus hexincisus, Pratylenchus penetrans, Pratylenchus neglectus, Pratylenchus crenatus, Pratylenchus thornei, Pratylenchus vulnus Pratylenchus zeae, Longidorus elongatu, Paratrichodorus lobatus, Trichodorus spp., Meloidogyne arenaria, Meloidogyne hapla, Globodera tabacum, Globodera solanacearum, Globodera virginiae, Ditylenchus dipsaci, Rotylenchus spp., Helicotylenchus spp.,
- the compounds of the formula (I) are particularly suitable for controlling citrus nematodes, in particular Pratylenchus coffeae and Pratylenchus brachyurus, Pratylenchus vulnus, Belonolaimus longicaudatus, Paratrichodorus minor, Paratrichodorus porosus, Trichodorus, Meloidogyne incognita, Meloidogyne incognita acrita, Meloidogyne javanica , Rotylenchus macrodoratus, Xiphinema americanum, Xiphinema brevicolle, Xiphinema index, Criconemella spp., Hemicriconemoides, Radopholus similis and Radopholus citrophilus, Hemicycliophora arenaria, Hemicycliophora nudata and Tylenchulus semipenetrans.
- the compounds of the formula (I) are particularly suitable for the control of banana nematodes, in particular Pratylenchus coffeae, Radopholus similis and Pratylenchus giibbicaudatus, Pratylenchus loosi, Meloidogyne spp., Helicotylenchus multicinctus, Helicotylenchus dihystera and Rotylenchulus spp.
- the compounds of the formula (I) are particularly suitable for controlling nematodes of the pineapple, in particular Pratylenchus zeae, Pratylenchus pratensis, Pratylenchus brachyurus, Pratylenchus goodeyi., Meloidogyne spp., Rotylenchulus reniformis and Longidorus elongatus, Longidorus laevicapitatus, Trichodorus primitivus, Trichodorus minor, Heterodera spp., Ditylenchus myceliophagus, Hoplolaimus californicus, Hoplolaimus pararobustus, Hoplolaimus indicus, Helicotylenchus dihystera, Helicotylenchus nannus, Helicotylenchus multicinctus, Helicotylenchus erythrine, Xiphinema dimorphicaudatum, Radopholus similis
- the compounds of the formula (I) are particularly suitable for combating nematodes of grapes, in particular Pratylenchus vulnus, Meloidogyne arenaria, Meloidogyne incognita, Meloidogyne javanica, Xiphinema americanum, Xiphinema index and Pratylenchus pratensis, Pratylenchus scribneri, Pratylenchus neglectus, Pratylenchus brachyurus , Pratylenchus thornei and Tylenchulus semipenetrans.
- Pratylenchus vulnus Meloidogyne arenaria, Meloidogyne incognita, Meloidogyne javanica, Xiphinema americanum, Xiphinema index and Pratylenchus pratensis, Pratylenchus scribneri, Pratylenchus neglectus
- the compounds of the formula (I) are particularly suitable for controlling nematodes of tree crops - pome fruit, in particular Pratylenchus penetrans and Pratylenchus vulnus, Longidorus elongatus, Meloidogyne incognita and Meloidogyne hapla.
- the compounds of the formula (I) are particularly suitable for controlling nematodes of tree crops - stone fruits, in particular Pratylenchus penetrans, Pratylenchus vulnus, Meloidogyne arenaria, Meloidogyne hapla, Meloidogyne javanica, Meloidogyne incognita, Criconemella xenoplax and Pratylenchus brachyurus, Pratylenchus coffeae.
- Pratylenchus scribneri Pratylenchus zeae, Belonolaimus longicaudatus, Helicotylenchus dihystera, Xiphinema americanum, Criconemella curvata, Tylenchorhynchus claytoni, Paratylenchus hamatus, Paratylenchus projectus, Scutellonema brachyurum and Hoplolaimus galeatus.
- the compounds of the formula (I) are particularly suitable for controlling nematodes in tree crops, sugarcane and rice, in particular Trichodorus spp., Criconemella spp. and from Pratylenchus spp.
- nematodes refers to nematodes that harm humans or animals.
- Trichinellida for example: Trichuris spp., Capillaria spp., Paracapillaria spp., Eucoleus spp., Trichomosoides spp., Trichinella spp. From the order of Tylenchida for example: Micronema spp., Strongyloides spp.
- Strongylus spp. Triodontophorus spp., Oesophagodontus spp., Trichonema spp., Gyalocephalus spp., Cylindropharynx spp., Poteriostomum spp., Cyclococercus spp., Cylicostephanus spp., Oesophagostomum spp., Chabertia spp , Stephanurus spp., Ancylostoma spp., Uncinaria spp., Necator spp., Bunostomum spp., Globocephalus spp., Syngamus spp., Cyathostoma spp., Metastrongylus spp., Dictyocaulus spp., Muellerius spp., Protostrongylus spp.
- Neostrongylus spp. Cystocaulus spp., Pneumostrongylus spp., Spicocaulus spp., Elaphostrongylus spp. Parelaphostrongylus spp., Crenosoma spp., Paracrenosoma spp., Oslerus spp., Angiostrongylus spp., Aelurostrongylus spp., Filaroides spp., Parafilaroides spp., Trichostrongylus spp., Haemonchus spp., Ostertagia spp., Teladorsagia spp., Marshallagia spp , Cooperia spp., Nippostrongylus spp., Heligmosomoides spp., Nematodirus spp., Hyostrongylus spp., Obeliscoides spp., Amidostomum spp., O
- the present invention also relates to the use of the compounds of formula (I) as anthelmintic drugs.
- helminths count Platyhelmintha (eg Monogenea, Cestodes and Trematodes), Acanthocephala and Pentastoma. The following helminths are to be mentioned as preferred:
- Monogenea e.g., Gyrodactylus spp., Dactylogyrus spp., Polystoma spp.
- Cestodes from the order of Pseudophyllidea for example: Diphyllobothrium spp., Spirometra spp., Schistocephalus spp., Ligula spp., Bothridium spp., Diplogonoporus spp.
- Trematodes from the class of Digenea for example: Diplostomum spp., Posthodiplostomum spp., Schistosoma spp., Trichobilharzia spp., Ornithobilharzia spp., Austrobilharzia spp., Gigantobilharzia spp., Leucochloridium spp., Brachylaima spp., Echinostoma spp.
- Echinoparyphium spp. Echinochasmus spp., Hypoderaeum spp., Fasciola spp., Fascioloides spp., Fasciolopsis spp., Cyclocoelum spp., Typhlocoelum spp., Paramphistomum spp., Calicophoron spp., Cotylophoron spp., Gigantocotyle spp., Fischoederius spp , Gastrothylacus spp., Notocotylus spp., Catatropis spp., Plagiorchis spp., Prosthogonimus spp., Dicrocoehum spp., Eurytrema spp., Troglotrema spp., Paragonimus spp., Collyriclum spp., Nanophyetus spp., Opisthorchis
- Acanthocephala from the order of Oligacanthorhynchida, for example: Macracanthorhynchus spp., Prosthenorchis spp .; from the order of Polymorphida for example: Filicollis spp .; from the order of Moniliformida for example: Moniliformis spp.,
- Echinorhynchida for example Acanthocephalus spp., Echinorhynchus spp., Leptorhynchoides spp.
- Pentastoma from the order of the Porocephalida for example Linguatula spp.
- the compounds of formula (I) are administered in a known manner directly or enterally, parenterally, dermally or nasally in the form of suitable forms of application.
- the administration can be prophylactic or therapeutic.
- the compounds of the formula (I) may optionally also be used in certain concentrations or application rates as herbicides, safeners, growth regulators or agents for improving the Plant properties, as microbicides or gametocides, for example as fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as agents against MLO (Mycoplasma -like-organism) and RLO (Rickettsia-like organism) can be used. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients. formulations
- the present invention further relates to formulations and application forms prepared therefrom as pesticides such.
- B. drench, drip and spray liquors comprising at least one compound of formula (I).
- the uses include other pesticides and / or effect-improving adjuvants such as penetration enhancers, e.g.
- vegetative oils such as rapeseed oil, sunflower oil, mineral oils such as paraffin oils, alkyl esters of vegetal fatty acids such as rapeseed oil or soybean oil methyl ester or alkanol alkoxylates and / or spreading agents such as alkyl siloxanes and / or salts, e.g.
- organic or inorganic ammonium or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate and / or retention-promoting agents such.
- Typical formulations are, for example, water-soluble liquids (SL), emulsion concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS). ;
- SL water-soluble liquids
- EC emulsion concentrates
- EW emulsions in water
- SC suspension concentrates
- SC SE, SE, FS, OD
- WG water-dispersible granules
- GR granules
- capsule concentrates CS
- the formulations contain, in addition to one or more compounds of the formula (I), further agrochemical active substances.
- auxiliaries such as extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, antifreeze agents, biocides, thickeners and / or further auxiliaries, for example adjuvants.
- An adjuvant in this context is a component that enhances the biological effect of the formulation without the component itself having a biological effect.
- adjuvants are agents that promote retention, spreading behavior, adherence to the leaf surface, or penetration.
- These formulations are prepared in a known manner, for example by mixing the compounds of formula (I) with excipients such as extenders, solvents and / or solid carriers and / or other excipients such as surfactants.
- Excipients which can be used are those which are suitable for the formulation of the compounds of the formula (I) or the use forms prepared from these formulations (such as, for example, ready-to-use pesticides such as spray liquors or seed dressings), such as certain physical, technical and / or biological properties To give properties.
- polar and non-polar organic chemical liquids e.g. from the classes of aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), alcohols and polyols (which may also be substituted, etherified and / or esterified), ketones (such as acetone, cyclohexanone), Esters (including fats and oils) and (poly) ethers, simple and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, sulfones and sulfoxides (such as dimethylsulfoxide).
- aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
- alcohols and polyols which may also be substituted, etherified and / or esterified
- ketones such as
- Suitable liquid solvents are essentially: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, e.g.
- Petroleum fractions mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
- alcohols such as butanol or glycol and their ethers and esters
- ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone
- strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
- Suitable solvents are, for example, aromatic hydrocarbons, e.g. Xylene, toluene or alkylnaphthalenes, chlorinated aromatic or aliphatic hydrocarbons, e.g. Chlorobenzene, chloroethylene, or methylene chloride, aliphatic hydrocarbons, e.g. Cyclohexane, paraffins, petroleum fractions, mineral and vegetable oils, alcohols such as e.g. Methanol, ethanol, iso-propanol, butanol or glycol and their ethers and esters, ketones such as e.g. Acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strong polar solvents such as dimethyl sulfoxide and water.
- aromatic hydrocarbons e.g. Xylene, toluene or alkylnaphthalenes
- chlorinated aromatic or aliphatic hydrocarbons e
- Suitable carriers are in particular: for example, ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock flour, such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and / or solid fertilizers. Mixtures of such carriers can also be used.
- Suitable carriers for granules are: eg broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, paper, coconut shells, corn cobs and tobacco stems.
- liquefied gaseous diluents or solvents can be used.
- Examples of emulsifying and / or foaming agents, dispersants or wetting agents having ionic or non-ionic properties or mixtures of these surfactants are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives (preferably 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, eg Alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates, protein hydroly
- dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
- inorganic pigments e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
- Stabilizers such as cold stabilizers, preservatives, antioxidants, light stabilizers or other chemical and / or physical stability-improving agents may also be present. It may also contain foam-forming agents or defoamers.
- formulations and the use forms derived therefrom may also contain, as additional auxiliaries, adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-form polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate and natural ones Phospholipids such as cephalins and lecithins and synthetic phospholipids.
- additional auxiliaries may be mineral and vegetable oils.
- auxiliaries may be present in the formulations and in the use forms derived therefrom.
- additives are, for example, fragrances, protective colloids, binders, adhesives, thickeners, thixotropic substances, penetration promoters, retention promoters, stabilizers, sequestrants, complexing agents, humectants, spreading agents.
- the compounds of formula (I) may be combined with any solid or liquid additive commonly used for formulation purposes.
- retention promoters are all those substances which reduce the dynamic surface tension such as dioctylsulfosuccinate or increase the visco-elasticity such as hydroxypropyl guar polymers.
- Penetration promoters are in this context defined by the fact that they can penetrate from the (usually aqueous) application broth and / or from the spray coating into the cuticle of the plant and thereby increase the material mobility (mobility) of the active ingredients in the cuticle.
- the method described in the literature can be used to determine this property.
- Examples include alcohol alkoxylates such as coconut oil ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters such as rapeseed oil or soybean oil, fatty amine alkoxylates such as tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate ,
- the formulations preferably contain between 0.00000001 and 98 wt .-% of the compound of formula (I), more preferably between 0.01 and 95 wt .-% of the compound of formula (I), most preferably between 0.5 and 90% by weight of the compound of formula (I), based on the weight of the formulation.
- the content of the compound of the formula (I) in the forms of application prepared from the formulations (in particular pesticides) can vary within wide ranges.
- the concentration of the compound of the formula (I) in the use forms may usually be between 0.00000001 and 95% by weight of the compound of the formula (I), preferably between 0.00001 and 1% by weight, based on the weight of the application form , lie.
- the application is done in a custom forms adapted to the application. mixtures
- the compounds of formula (I) may also be used in admixture with one or more suitable fungicides, bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficials, herbicides, fertilizers, avian repellents, phytotonics, sterilants, safeners, semiochemicals and / or plant growth regulators be, for example to widen the spectrum of action, to extend the duration of action, to increase the speed of action, to prevent re-exposure or to prevent the development of resistance.
- suitable fungicides bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficials, herbicides, fertilizers, avian repellents, phytotonics, sterilants, safeners, semiochemicals and / or plant growth regulators
- suitable fungicides bactericides, acaricides, molluscicides, ne
- the compounds of the formula (I) may be present in admixture with other active substances or semiochemicals such as attractants and / or avian repellents and / or plant activators and / or growth regulators and / or fertilizers.
- the compounds of the formula (I) can be used in mixtures with agents for improving plant properties such as, for example, growth, yield and quality of the crop.
- the compounds of the formula (I) are present in formulations or in the formulations prepared from these formulations in admixture with other compounds, preferably those as described below.
- Insecticides / Acaricides / Nematicides The active substances mentioned here with their "common name” are known and described, for example, in the Pesticide Handbook ("The Pesticide Manual” 16th ed., British Crop Protection Council 2012) or searchable on the Internet (eg http: // www. alanwood.net/pesticides).
- acetylcholinesterase (AChE) inhibitors such as carbamates, eg alanycarb, aldicarb, bendocarb, benfuracarb, butocarboxime, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, Pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC and xylylcarb or organophosphates, eg, acephates, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chloroethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyr
- GABA-controlled chloride channel antagonists such as cyclodiene organochlorines, e.g. Chlordanes and endosulfan or phenylpyrazoles (fiproles), e.g. Ethiprole and fipronil.
- sodium channel modulators / voltage dependent sodium channel blockers such as pyrethroids, e.g. Acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha- Cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(lR) trans isomers], deltamethrin, empenthrin [(EZ) (lR) isomers], e
- nicotinergic acetylcholine receptor (nAChR) agonists such as neonicotinoids, e.g. Acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam or nicotine or sulfoxaflor.
- nicotinergic acetylcholine receptor (nAChR) allosteric activators such as spinosines, e.g. Spinetoram and spinosad.
- chloride channel activators such as avermectins / milbemycins, e.g. Abamectin, emamectin benzoate, lepimectin and milbemectin.
- Juvenile hormone mimics such as juvenile hormone analogs, e.g. Hydroprene, Kinoprene and Methoprene or Fenoxycarb or Pyriproxyfen.
- agents with unknown or non-specific mechanisms of action such as Alkyl halides, eg methyl bromide and other alkyl halides; or chloropicrin or sulfuryl fluoride or borax or tartar emetic.
- mite growth inhibitors e.g. Clofentezine, hexythiazox and diflovidazine or etoxazole.
- Insect intestinal membrane microbial disruptors e.g. Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis and BT plant proteins: CrylAb, CrylAc, CrylFa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, Cry34 / 35Abl.
- oxidative phosphorylation inhibitors such as diafenthiuron or organotin compounds, e.g. Azocyclotin, Cyhexatin and fenbutatin oxide or propargite or
- Nicotinergic acetylcholine receptor antagonists such as Bensultap, Cartap hydrochloride, thiocyclam and thiosultap sodium.
- Type 0 inhibitors of chitin biosynthesis such as bistrifluron, chlorofluorazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron.
- inhibitors of chitin biosynthesis type 1, such as buprofezin.
- Anti-skinning agents especially in dipterans, i.e., two-toed, such as Cyromazine.
- ecdysone receptor agonists such as chromafenozides, halofenozides, methoxyfenozides, and tebufenozides.
- Octopaminergic agonists such as amitraz.
- (21) complex I electron transport inhibitors for example METI acaricides, eg fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad and tolfenpyrad or rotenone (Derris).
- (23) inhibitors of acetyl-CoA carboxylase such as tetronic and tetramic acid derivatives, e.g. Spirodiclofen, spiromesifen and spirotetramat.
- complex IV electron transport inhibitors such as phosphines, e.g. Aluminum phosphide, calcium phosphide, phosphine and zinc phosphide or cyanide.
- ryanodine receptor effectors such as diamides, e.g. Chlorantraniliprole, Cyantraniliprole and Flubendiamide, other active substances such as Afidopyropen, Azadirachtin, Benclothiaz, Benzoximate, Bifenazate, Bromopropylate, Chinomethionat, Cryolite,
- inhibitors of ergosterol biosynthesis such as (1.1) aldimorph, (1.2) azaconazole, (1.3) bitertanol, (1.4) bromuconazole, (1.5) cyproconazole, (1.6) diclobutrazole, (1.7) difenoconazole, (1.8) diniconazole , (1.9) Diniconazole-M, (1.10) dodemorph, (1.11) dodemorph acetate, (1.12) epoxiconazole, (1.13) etaconazole, (1.14) fenarimol, (1.15) fenbuconazole, (1.16) fenhexamide, (1.17) fenpropidine, ( 1.18) fenpropimorph, (1.19) fluquinconazole, (1.20) flurprimidol, (1.21) flusilazole, (1.22) flutriafol, (1.23) furconazole, (1.24) furconazole cis, (1.21)
- inhibitors of respiration such as (2.1) bixafen, (2.2) boscalid, (2.3) carboxin, (2.4) diflumetorim, (2.5) fenfuram, (2.6) fluopyram, (2.7) flutolanil, ( 2.8) Fluxapyroxad, (2.9) Furametpyr, (2.10) Furmecyclox, (2.11) Isopyrazam Mixture of the syn-epimeric racemate 1RS, 4SR, 9RS and the anti-empimidal racemate 1RS, 4SR, 9SR, (2.12) isopyrazam (anti- epimeric racemate ), (2.13) isopyrazam (anti-epimeric enantiomer 1R, 4S, 9S), (2.14) isopyrazam (anti- epimeric enantiomer 1S, 4R, 9R), (2.15) isopyrazam (syn-epimeric racemate 1RS, 4SR, 9RS),
- inhibitors of mitosis and cell division such as (4.1) benomyl, (4.2) carbendazim, (4.3) chlorfenazole, (4.4) diethofencarb, (4.5) ethaboxam, (4.6) fluopicolide, (4.7) fuberidazole, (4.8) pencycuron .
- resistance inducers such as (6.1) acibenzolar-S-methyl, (6.2) isotianil, (6.3) probenazole, (6.4) tiadinil, and (6.5) laminarin.
- inhibitors of amino acid and protein biosynthesis such as (7.1), (7.2) blasticidin-S, (7.3) cyprodinil, (7.4) kasugamycin, (7.5) kasugamycin hydrochloride hydrate, (7.6) mepanipyrim, (7.7) Pyrimethanil, (7.8) 3- (5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl) quinoline and (7.9) oxytetracycline and (7.10) streptomycin.
- inhibitors of ATP production such as (8.1) fentin acetate, (8.2) fentin chloride, (8.3) fentin hydroxide and (8.4) silthiofam.
- inhibitors of cell wall synthesis such as (9.1) benthia-valicarb, (9.2) dimethomorph, (9.3) flumorph, (9.4) iprovalicarb, (9.5) mandipropamide, (9.6) polyoxins, (9.7) polyoxorim, (9.8) validamycin A, (9.9) Valifenalate and (9.10) Polyoxin B.
- Inhibitors of lipid and membrane synthesis such as (10.1) biphenyl, (10.2) Chlorneb,
- inhibitors of melanin biosynthesis such as (11.1) carpropamide, (11.2) diclocymet, (11.3) fenoxanil, (11.4) fthalide, (11.5) pyroquilone, (11.6) tricyclazole, and (11.7) 2,2,2 Trifluoroethyl ⁇ 3-methyl-1 - [(4-methylbenzoyl) amino] butan-2-yl ⁇ carbamate.
- inhibitors of nucleic acid synthesis such as (12.1) benalaxyl, (12.2) benalaxyl-M (kiralaxyl), (12.3) bupirimate, (12.4) clozylacon, (12.5) dimethirimol, (12.6) ethirimol, (12.7) furalaxyl, ( 12.8) Hymexazole, (12.9) Metalaxyl, (12.10) Metalaxyl-M (mefenoxam), (12.11) Ofurace, (12.12) Oxadixyl, (12.13) Oxolinic acid and (12.14) Octhilinone.
- Signal transduction inhibitors such as (13.1) chlozolinate, (13.2) fenpiclonil, (13.3) fludioxonil, (13.4) iprodione, (13.5) procymidone, (13.6) quinoxyfen, (13.7) vinclozoline, and (13.8) proquinazide.
- decouplers such as (14.1) binapacryl, (14.2) dinocap, (14.3) ferimzone, (14.4) fluazinam, and (14.5) meptyldinocap.
- the compounds of formula (I) may be combined with biological pesticides.
- Biological pesticides include, in particular, bacteria, fungi, yeasts, plant extracts, and those products formed by microorganisms, including proteins and secondary metabolites.
- Biological pesticides include bacteria such as spore-forming bacteria, root-colonizing bacteria and bacteria that act as biological insecticides, fungicides or nematicides.
- Bacillus amyloliquefaciens strain FZB42 (DSM 231179), or Bacillus cereus, in particular B. cereus strain CNCM 1-1562 or Bacillus firmus, strain 1-1582 (Accession number CNCM 1-1582) or Bacillus pumilus, especially strain GB34 (Accession no. ATCC 700814) and strain QST2808 (Accession No. NRRL B-30087), or Bacillus subtilis, especially strain GB03 (Accession No. ATCC SD-1397), or Bacillus subtilis strain QST713 (Accession No. NRRL B-21661) or Bacillus subtilis Strain OST 30002 (Accession No.
- fungi and yeasts which can be used as biological pesticides are:
- Beauveria bassiana especially strain ATCC 74040, coniothyrium minitans, in particular strain CON / M / 91-8 (Accession No. DSM-9660), Lecanicillium spp., In particular strain HRO LEC 12, Lecanicillium lecanii, (formerly known as Verticillium lecanii), especially strain KV01, Metarhizium anisopliae, in particular strain F52 (DSM3884 / ATCC 90448), Metschnikowia fructicola, in particular strain NRRL Y-30752, Paecilomyces fumosoroseus (new: Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka 97 (Accesion No.
- Paecilomyces lilacinus in particular P. lilacinus strain 251 (AGAL 89/030550), Talaromyces flavus, in particular strain VI 17b, Trichoderma atroviride, in particular strain SCI (Accession Number CBS 122089), Trichoderma harzianum, in particular T. harzianum rifai T39. (Accession Number CNCM 1-952).
- viruses that can be used or used as biological pesticides are:
- Adoxophyes orana Apple peel winder
- Granulosis virus GV
- Cydia pomonella codling moth
- Granulosis virus GV
- Helicoverpa armigera cotton capsule worm
- Nuclear polyhedrosis virus NPV
- Spodoptera exigua mNPV Spodoptera frugiperda (armyworm) mNPV
- Spodoptera littoralis African cotton worm
- bacteria and fungi that are added as 'inoculant' plants or parts of plants or plant organs and promote by their special properties, plant growth and plant health. Examples are:
- Agrobacterium spp. Azorhizobium caulinodans, Azospirillum spp., Azotobacter spp., Bradyrhizobium spp., Burkholderia spp., In particular Burkholderia cepacia (formerly known as Pseudomonas cepacia), Gigaspora spp., Or Gigaspora monosporum, Glomus spp., Laccaria spp.
- plant extracts and those products formed by microorganisms, including proteins and secondary metabolites, which can be used as biological pesticides are:
- the compounds of the formula (I) can be combined with safeners, for example Benoxacor, Cloquintocet (-mexyl), Cyometrinil, Cyprosulfamide, Dichlormid, Fenchlorazole (-ethyl), Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen (-ethyl), Mefenpyr (-diethyl), naphthalic anhydride, oxabetrinil, 2-methoxy-N - ( ⁇ 4 - [(methylcarbamoyl) amino] phenyl ⁇ sulfonyl) benzamide (CAS 129531-12-0), 4- (dichloroacetyl) -l-oxa 4-azaspiro [4.5] decane (CAS 71526-07-3), 2,2,5-trimethyl-3- (dichloroacetyl) -l, 3-oxazolidine (CAS 52836-31-4).
- Plants are understood to mean all plants and plant populations, such as desirable and unwanted wild plants or crops (including naturally occurring crops), for example cereals (wheat, rice, triticale, barley, rye, oats), corn, soybeans, potatoes, sugar beets, sugarcane, tomatoes , Peas and other vegetables, cotton, tobacco, oilseed rape, as well as fruit plants (with the fruits apples, pears, citrus fruits and grapes).
- Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant breeders' rights.
- Plant parts are understood to mean all aboveground and subterranean parts and organs of plants such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes.
- the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
- the treatment according to the invention of the plants and plant parts with the compounds of the formula (I) is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, evaporating, atomizing, spreading, brushing, injecting and in propagating material, in particular in seeds, further by single or multilayer coating.
- plants and their parts can be treated according to the invention.
- wild-type or plant species and plant varieties obtained by conventional biological breeding methods such as crossing or protoplast fusion and parts thereof are treated.
- transgenic plants and plant varieties which may be obtained by genetic engineering, optionally in combination with conventional Methods were obtained (Genetically Modified Organisms) and their parts treated.
- the term "parts” or “parts of plants” or “parts of plants” has been explained above.Propes of the respective commercially available or in use plant varieties are particularly preferably treated according to the invention.PV plants are understood as meaning plants with new properties ("traits”) have been bred either by conventional breeding, by mutagenesis or by recombinant DNA techniques. These may be varieties, breeds, biotypes and genotypes.
- the preferred plants or plant varieties to be treated according to the invention to be treated include all plants which, as a result of the genetic engineering modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits").
- traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to bottoms salt, increased flowering, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products , higher shelf life and / or workability of the harvested products.
- Further and particularly emphasized examples of such properties are an increased resistance of the plants to animal and microbial pests, such as insects, arachnids, nematodes, mites, snails, causes e.g.
- toxins produced in the plants in particular those produced by the genetic material from Bacillus thuringiensis (eg by the genes CrylA (a), CrylA (b), CrylA (c), CryllA, CrylllA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF as well as their combinations) are produced in the plants, furthermore an increased ability to repel the plants against phytopathogenic fungi, bacteria and / or viruses, eg Systemically acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins, and increased tolerance of the plants to certain herbicidal active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT" gene ).
- SAR Systemically acquired resistance
- PAT phosphinotricin
- transgenic plants are the important crops such as cereals (wheat, rice, triticale, barley, rye, oats), corn, soy, potato, sugar beets, sugarcane, tomatoes, peas and other vegetables, cotton, tobacco, oilseed rape, and fruit plants (with the fruits apples, pears, citrus fruits and grapes), with special emphasis on corn, soy, wheat, rice, potato, cotton, sugar cane, tobacco and oilseed rape. Traits that are particularly emphasized are the increased resistance of the plants to insects, arachnids, nematodes and snails.
- Plant protection - types of treatment The treatment of the plants and plant parts with the compounds of formula (I) is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, for example by dipping, (spraying) spraying (spraying), sprinkling, evaporation , Spraying, misting, sprinkling, foaming, brushing, spreading, injecting, pouring, drip irrigation and, in the case of propagating material, in particular seed, further by dry pickling, wet pickling, slurry pickling, encrusting, single or multi-layer coating, etc It is also possible to apply the compounds of the formula (I) by the ultra-low-volume method or to inject the use form or the compound of the formula (I) itself into the soil.
- a preferred direct treatment of the plants is foliar application, ie compounds of the formula (I) are applied to the foliage, wherein the treatment frequency and the application rate should be adjusted to the infestation pressure of the respective pest.
- the compounds of the formula (I) also enter the plants via the root system.
- the treatment of the plants is then carried out by the action of the compounds of formula (I) on the habitat of the plant.
- This may be, for example, by drenching, mixing into the soil or the nutrient solution, i. the location of the plant (e.g., soil or hydroponic systems) is soaked in a liquid form of the compounds of formula (I), or by the soil application, i. the compounds of formula (I) are incorporated in solid form (e.g., in the form of granules) at the plant site.
- this may also be by metered addition of the compound of formula (I) in a solid form (e.g., as granules) into a flooded paddy field.
- seed treatment methods should also include the intrinsic insecticidal or nematicidal properties of pest-resistant transgenic plants to provide optimal protection of the seed Seeds and the germinating plant with a minimum effort to reach pesticides.
- the present invention therefore more particularly relates to a method of protecting seed and germinating plants from attack by pests by treating the seed with one of the compounds of formula (I).
- the method according to the invention for the protection of seeds and germinating plants from infestation by pests further comprises a method in which the seed is treated simultaneously in one operation or sequentially with a compound of formula (I) and mixing partner. It also also includes a method in which the seed is treated at different times with a compound of formula (I) and mixing partner.
- the invention also relates to the use of the compounds of the formula (I) for the treatment of seed for the protection of the seed and the resulting plant from animal pests.
- the invention relates to seed which has been treated for protection against animal pests with a compound of formula (I).
- the invention also relates to seed treated at the same time with a compound of formula (I) and mixing partner.
- the invention further relates to seed which has been treated at different times with a compound of formula (I) and mixing partner.
- the individual substances may be contained in different layers on the seed.
- the layers which comprise a compound of the formula (I) and mixture partners may optionally be separated by an intermediate layer.
- the invention also relates to seed in which a compound of the formula (I) and mixing partner are applied as a constituent of a coating or as a further layer or further layers in addition to a coating.
- the invention relates to seed which, after treatment with a compound of the formula (I), is subjected to a film coating process in order to avoid dust abrasion on the seed.
- a compound of the formula (I) acts systemically is that the treatment of the seed protects not only the seed itself, but also the resulting plants after emergence from animal pests. In this way, the immediate treatment of the culture at the time of sowing or shortly afterwards can be omitted.
- Another advantage is the fact that by treating the seed with a compound of formula (I) germination and emergence of the treated seed can be promoted. Likewise, it is considered to be advantageous that compounds of the formula (I) can also be used in particular in the case of transgenic seed.
- Compounds of formula (I) may also be used in combination with signal technology agents whereby better colonization with symbionts such as rhizobia, mycorrhiza and / or endophytic bacteria or fungi takes place and / or optimized nitrogen fixation occurs.
- symbionts such as rhizobia, mycorrhiza and / or endophytic bacteria or fungi takes place and / or optimized nitrogen fixation occurs.
- the compounds of the formula (I) are suitable for the protection of seed of any plant variety used in agriculture, in the greenhouse, in forests or in horticulture.
- these are seeds of cereals (eg wheat, barley, rye, millet and oats), corn, cotton, soy, rice, potatoes, sunflower, coffee, tobacco, canola, rape, turnip (eg Sugar beet and fodder beet), peanut, vegetables (eg tomato, cucumber, bean, cabbage, onions and lettuce), fruit plants, turf and ornamental plants.
- cereals eg wheat, barley, rye and oats
- corn, soya, cotton, canola, oilseed rape and rice are examples of seeds of cereals (eg wheat, barley, rye and oats), corn, soya, cotton, canola, oilseed rape and rice.
- transgenic seed with a compound of the formula (I) is also of particular importance.
- the heterologous genes in transgenic seed can be derived from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium.
- the present invention is particularly useful for the treatment of transgenic seed containing at least one heterologous gene derived from Bacillus sp. comes. Most preferably, this is a heterologous gene derived from Bacillus thuringiensis.
- the compound of the formula (I) is applied to the seed.
- the seed is treated in a state where it is so stable that no damage occurs during the treatment.
- the treatment of the seed can be done at any time between harvesting and sowing.
- seed is used which has been separated from the plant and freed from flasks, shells, stems, hull, wool or pulp.
- seed may be used that has been harvested, cleaned and dried to a moisture content that is storable.
- seed can also be used, which after drying, for example, was treated with water and then dried again, for example priming.
- the compounds of the formula (I) are generally applied to the seed in the form of a suitable formulation.
- suitable formulations and methods for seed treatment are known to those skilled in the art.
- the compounds of the formula (I) can be converted into the customary seed dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other seed coating compositions, and also ULV formulations.
- formulations are prepared in a known manner by mixing compounds of formula (I) with conventional additives, such as conventional extenders and solvents or diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and also water.
- conventional additives such as conventional extenders and solvents or diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and also water.
- Dyes which may be present in the seed-dressing formulations which can be used according to the invention are all dyes customary for such purposes. Both water-insoluble pigments and water-soluble dyes are useful in this case. Examples which may be mentioned under the names rhodamine B, C.I. Pigment Red 112 and C.I. Solvent Red 1 known dyes.
- Suitable wetting agents which may be present in the seed dressing formulations which can be used according to the invention are all wetting-promoting substances customary for the formulation of agrochemical active compounds.
- Preferably used are alkylnaphthalene sulfonates, such as diisopropyl or diisobutyl naphthalene sulfonates.
- Suitable dispersants and / or emulsifiers which may be present in the seed dressing formulations which can be used according to the invention are all nonionic, anionic and cationic dispersants customary for the formulation of agrochemical active compounds. Preference is given to using nonionic or anionic dispersants or mixtures of nonionic or anionic dispersants.
- Particularly suitable nonionic dispersants are, in particular, ethylene oxide-propylene oxide, block polymers, alkylphenol polyglycol ethers and tri-stryrylphenol polyglycol ethers and their phosphated or sulfated derivatives.
- Suitable anionic dispersants are in particular lignosulfonates, polyacrylic acid salts and arylsulfonate-formaldehyde condensates.
- Defoamers which may be present in the seed-dressing formulations which can be used according to the invention are all foam-inhibiting substances customary for the formulation of agrochemical active compounds.
- Defoamers which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions. Examples include dichlorophen and Benzylalkoholhemiformal.
- Suitable secondary thickeners which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions. Preference is given to cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and finely divided silica.
- Suitable adhesives which may be present in the seed dressing formulations which can be used according to the invention are all customary binders which can be used in pickling agents.
- Preferably mentioned are polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and Tylose.
- the gibberellins are known (see R. Wegler "Chemie der convinced- und Swdlingsbekungsstoff", Vol. 2, Springer Verlag, 1970, pp. 401-412).
- the seed dressing formulations which can be used according to the invention can be used either directly or after prior dilution with water for the treatment of seed of various kinds.
- the concentrates or the preparations obtainable therefrom by dilution with water can be used for dressing the seeds of cereals such as wheat, barley, rye, oats and triticale, as well as the seeds of corn, rice, rape, peas, beans, cotton , Sunflower, soy and beet or vegetable seed of various nature.
- the seed dressing formulations which can be used according to the invention or their dilute application forms can also be used for pickling seeds of transgenic plants.
- the pickling is done by placing the seed in a batch or continuous mixer, adding either desired amount of seed dressing formulations, either as such or after prior dilution with water, and until the formulation is evenly distributed mix the seed.
- a drying process follows.
- the application rate of the seed dressing formulations which can be used according to the invention can be varied within a relatively wide range. It depends on the particular content of the compounds of the formula (I) in the formulations and on the seed.
- the application rates for the compound of the formula (I) are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 15 g per kilogram of seed.
- the compounds of formula (I) are active against animal parasites, in particular ectoparasites or endoparasites.
- animal parasites in particular ectoparasites or endoparasites.
- endoparasite includes in particular helminths and protozoa such as coccidia.
- Ectoparasites are typically and preferably arthropods, especially insects and acarids.
- the compounds of formula (I) which are of low toxicity to warm-blooded animals are useful in the control of parasites found in livestock and livestock in livestock, breeding animals, zoo animals, laboratory animals, experimental animals and domestic animals. They are effective against all or individual stages of parasite development.
- Farm animals include, for example, mammals such as sheep, goats, horses, donkeys, camels, buffaloes, rabbits, reindeer, fallow deer, and especially cattle and pigs; Poultry such as turkeys, ducks, geese and, in particular, chickens; Fish and shellfish, e.g. in aquaculture and also insects like bees.
- the pets include, for example, mammals such as hamsters, guinea pigs, rats, mice, chinchillas, ferrets, and especially dogs, cats, caged birds, reptiles, amphibians, and aquarium fish.
- mammals such as hamsters, guinea pigs, rats, mice, chinchillas, ferrets, and especially dogs, cats, caged birds, reptiles, amphibians, and aquarium fish.
- the compounds of formula (I) are administered to mammals.
- the compounds of the formula (I) are administered to birds, namely domestic birds and in particular poultry.
- control means that the compounds of formula (I) effectively reduce the incidence of the particular parasite in an animal infected with such parasites to a harmless extent can.
- combating in the present context means that the compound of formula (I) can kill the respective parasite, prevent its growth or prevent its replication.
- the arthropods include: from the order Anoplurida, for example Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp .; from the order Mallophagida and the suborders Amblycerina and Ischnocerina, for example Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp .; from the order Diptera and the suborders Nematocerina and Brachycerina, for example Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp.,
- arthropods include:
- Metastigmata From the subclass Akari (Acarina) and the order Metastigmata, for example from the family Argasidae, such as Argas spp., Ornithodorus spp., Otobius spp., From the family Ixodidae, such as Ixodes spp., Amblyomma spp., Rhipicephalus (Boophilus) spp. Dermacentor spp., Haemophysalis spp., Hyalomma spp., Rhipicephalus spp.
- Argasidae such as Argas spp., Ornithodorus spp., Otobius spp.
- Ixodidae such as Ixodes spp., Amblyomma spp., Rhipicephalus (Boophilus) spp. Dermacentor spp., Haemophysalis spp
- Mastigophora such as Trypanosomatidae, for example Trypanosoma b. brucei, T.b. gambiense, T.b. rhodesiense, T. congolense, T. cruzi, T. evansi, T. equinum, T. lewisi, T. percae, T. simiae, T. vivax, Leishmania brasiliensis, L. donovani, L. tropica, such as Trichomonadidae, for example Giardia lamblia, G. canis.
- Trypanosomatidae for example Trypanosoma b. brucei, T.b. gambiense, T.b. rhodesiense, T. congolense, T. cruzi, T. evansi, T. equinum, T. lewisi, T. percae, T. simiae, T. vivax
- Sarcomastigophora such as Entamoebidae, for example Entamoeba histolytica, Hartmanellidae, for example Acanthamoeba sp., Harmanella sp.
- Apicomplexa such as Eimeridae, for example Eimeria acervulina, E. adenoides, E. alabamensis, E. anatis, E. anserina, E. arloingi, E. ashata, E. auburnensis, E. bovis, E. brunetti, E canis, E. chinchillae, E. clupearum, E. columbae, E. contorta, E. crandalis, E. debliecki, E. dispersa, E. ellipsoidales, E. falciformis,
- parvum such as Toxoplasmadidae, for example Toxoplasma gondii, Hammondia heydornii, Neospora caninum, Besnoitia besnoitii; like Sarcocystidae, for example Sarcocystis bovicanis,
- S. bovihominis S. ovicanis, S. ovifelis, S. neurona, S. spec., S. suihominis, such as Leucozoidae, for example
- Leucocytozoon simondi such as Plasmodiidae, for example Plasmodium berghei, P. falciparum, P. malariae, P. ovale, P. vivax, P. spec.
- Piroplasmea for example Babesia argentina, B. bovis, B. canis, B. spec .
- Theileria parva Theileria spec, as Adeleina, for example Hepatozoon canis, H. spec.
- Pathogenic endoparasites which are helminths, include flatworms (e.g., Monogenea, Cestodes, and Trematodes), roundworms, Acanthocephala, and Pentastoma.
- Other helminths include: Monogenea: e.g., Gyrodactylus spp., Dactylogyrus spp., Polystoma spp.
- Cestodes from the order Pseudophyllidea for example: Diphyllobothrium spp., Spirometra spp., Schistocephalus spp., Ligula spp., Bothridium spp., Diplogonoporus spp.
- Taenia spp. Echinococcus spp., Hydatigera spp., Davainea spp., Raillietina spp., Hymenolepis spp., Echinolepis spp., Echinocotyle spp., Diorchis spp., Dipylidium spp., Joyeuxiella spp., Diplopylidium spp.
- Trematodes from the genus Digenea, for example: Diplostomum spp., Posthodiplostomum spp., Schistosoma spp., Trichobilharzia spp., Ornithobilharzia spp., Austrobilharzia spp., Gigantobilharzia spp., Leucochloridium spp., Brachylaima spp., Echinostoma spp., Echinoparyphium spp., Echinochasmus spp., Hypoderaeum spp., Fasciola spp., Fasciolides spp., Fasciolopsis spp., Cyclocoelum spp., Typhlocoelum spp., Paramphistomum spp., Calicophoron spp., Cotylophoron spp., Gigantocoty
- Roundworms Trichinellida for example: Trichuris spp., Capillaria spp., Trichomosoides spp., Trichinella spp.
- Stephanurus spp. Ancylostoma spp., Uncinaria spp., Bunostomum spp., Globocephalus spp., Syngamus spp., Cyathostoma spp., Metastrongylus spp., Dictyocaulus spp., Muellerius spp., Protostrongylus spp., Neostrongylus spp., Cystocaulus spp., Pneumostrongylus spp., Spicocaulus spp., Elaphostrongylus spp.
- Parelaphostrongylus spp. Crenosoma spp., Paracrenosoma spp., Angiostrongylus spp., Aelurostrongylus spp., Filaroides spp., Parafilaroides spp., Trichostrongylus spp., Haemonchus spp., Ostertagia spp., Marshallagia spp., Cooperia spp., Nematodirus spp , Hyostrongylus spp., Obeliscoides spp., Amidostomum spp., Ollulanus spp.
- Acanthocephala from the order Oligacanthorhynchida eg: Macracanthorhynchus spp., Prosthenorchis spp .; from the order Polymorphida for example: Filicollis spp .; from the order Moniliformida for example: Moniliformis spp., From the order Echinorhynchida for example Acanthocephalus spp., Echinorhynchus spp., Leptorhynchoides spp.
- Pentastoma from the order Porocephalida for example Linguatula spp.
- the compounds of the formula (I) are administered by methods well known in the art, such as enteral, parenteral, dermal or nasal in the form of suitable preparations.
- the administration can be prophylactic or therapeutic.
- one embodiment of the present invention relates to the use of a compound of formula (I) as a medicament.
- Another aspect relates to the use of a compound of formula (I) as an antiendoparasitic agent, in particular as a helminthicide or antiprotozoal agent.
- Compounds of the formula (I) are suitable for use as antiendoparasitic agents, in particular as a helminthicide or antiprotozoal agents, for example in animal breeding, animal husbandry, in stables and in the hygiene sector.
- a further aspect in turn relates to the use of a compound of the formula (I) as an antiectica, in particular an arthropodicide such as an insecticide or an acaricide.
- Another aspect relates to the use of a compound of the formula (I) as an antiectica, in particular an arthropodicide such as an insecticide or acaricide
- an arthropodicide such as an insecticide or acaricide
- Anthelmintic Mixing Partners By way of example, the following anthelmintic mixing partners may be mentioned:
- Anthelmintic agents including trematicide and cestocide agents: from the class of macrocyclic lactones, e.g. Such as: abamectin, doramectin, emamectin, eprinomectin, ivermectin, milbemycin, moxidectin, nemadectin, selamectin; from the class of benzimidazoles and sample zimidazoles, e.g.
- albendazole albendazole, albendazole sulfoxide, cambendazole, cyclobendazole, febantel, fenbendazole, flubendazole, mebendazole, netobimine, oxfendazole, oxibendazole, parbendazole, thiabendazole, thiophanate, triclabendazole; from the class of cyclooctadepsipeptides, e.g. B: emodepside, PF1022; from the class of aminoacetonitrile derivatives, e.g. For example: Monepantel; from the class of tetrahydropyrimidines, e.g.
- B . Morantel, Pyrantel, Oxantel; from the class of imidazothiazoles, e.g. B .: butamisole, levamisole, tetramisole; from the class of salicylanilides, e.g. For example: bromoxanide, breadanide, clioxanide, closantel, niclosamide, oxyclozanide, rafoxanide, tribromomalan; from the class of Paraherquamide, z.
- B . Derquantel, paraherquamide; from the class of aminophenylamidines, e.g.
- amidantel deacylated amide shell (dAMD), tribendimidine
- organophosphates e.g. B .: Coumaphos, Crufomat, Dichlorvos, Haloxon, Naphthalofos, Trichlorfon
- substituted phenols e.g. Bithionol, disophenol, hexachlorophene, nicolofolan, meniclopholan, nitroxynil
- piperazinones e.g. B .: praziquantel, epsiprantel; from other diverse classes, eg.
- amoscanate bephenium, bunamidine, clonazepam, clorsulone, diamfenetide, dichlorophen, diethylcarbamazine, emetin, hetolin, hycanthone, lucanthone, miracil, mirasan, niclosamide, niridazole, nitroxynil, nitroscanate, oltipraz, omphalotin, oxamniquine, paromomycin, piperazine, resorantel ,
- a vector in the context of the present invention is an arthropod, in particular an insect or arachnid, which is able to attack pathogens such.
- pathogens such as viruses, worms, protozoa and bacteria from a reservoir (plant, animal, human, etc.) to a host to transfer.
- the pathogens may be transferred to a host either mechanically (e.g., trachoma by non-stabbing flies) on a host, or after injection (e.g., malaria parasites by mosquitoes).
- vectors and their transmitted diseases or pathogens are: 1) mosquitoes
- Anopheles malaria, filariasis
- - Culex Japanese encephalitis, filariasis, other viral diseases, transmission of worms
- - Aedes yellow fever, dengue fever, filariasis, other viral diseases
- Ticks Borellioses such as Borrelia duttoni, tick-borne encephalitis, Q fever (Coxiella burnetii), Babesia (Babesia canis canis).
- vectors in the context of the present invention are insects such as aphids, flies, cicadas or thrips, which can transmit plant viruses to plants.
- Other vectors that can transmit plant viruses are spider mites, lice, beetles and nematodes.
- vectors for the purposes of the present invention are insects and arachnids such as mosquitoes, in particular of the genera Aedes, Anopheles, e.g. A. gambiae, A. arabiensis, A. funestus, A. dirus (malaria) and Culex, lice, fleas, flies, mites and ticks that can transmit pathogens to animals and / or humans.
- insects and arachnids such as mosquitoes, in particular of the genera Aedes, Anopheles, e.g. A. gambiae, A. arabiensis, A. funestus, A. dirus (malaria) and Culex, lice, fleas, flies, mites and ticks that can transmit pathogens to animals and / or humans.
- Compounds of formula (I) are suitable for use in the prevention of disease or pathogens transmitted by vectors.
- another aspect of the present invention is the use of compounds of formula (I) for vector control, e.g. in agriculture, horticulture, forests, gardens and recreational facilities, as well as in the protection of materials and materials.
- the compounds of formula (I) are useful for protecting engineering materials against attack or destruction by insects, e.g. from the order Coleoptera, Hymenoptera, Isoptera, Lepidoptera, Psocoptera and Zygentoma.
- non-living materials such as, preferably, plastics, adhesives, glues, papers and cartons, leather, wood, Woodworking products and paints.
- non-living materials such as, preferably, plastics, adhesives, glues, papers and cartons, leather, wood, Woodworking products and paints.
- the application of the invention for the protection of wood is particularly preferred.
- the compounds of the formula (I) are used together with at least one further insecticide and / or at least one fungicide.
- the compounds of formula (I) are present as a ready-to-use pest control agent, that is, it can be applied to the corresponding material without further changes.
- further insecticides or as fungicides in particular the above-mentioned in question are particularly useful.
- the compounds of the formula (I) can be used to protect against the growth of objects, in particular hulls, sieves, nets, structures, quays and signal systems, which come into contact with seawater or brackish water.
- the compounds of the formula (I) can be used alone or in combination with other active substances as antifouling agents.
- the compounds of formula (I) are useful in the control of animal pests in the hygiene sector.
- the invention can be used in household, hygiene and storage protection, especially for controlling insects, arachnids and mites, which occur in enclosed spaces, such as apartments, factories, offices, vehicle cabins.
- the compounds of formula (I) are used alone or in combination with other active ingredients and / or excipients.
- they are used in household insecticide products.
- the compounds of formula (I) are active against sensitive and resistant species and against all stages of development.
- pests of the class Arachnida from the orders Scorpiones, Araneae and Opiliones, from the classes Chilopoda and Diplopoda, from the class Insecta the order Blattodea, from the orders Coleoptera, Dermaptera, Diptera, Heteroptera, Hymenoptera, Isoptera, Lepidoptera, Phthiraptera, Psocoptera, Saltatoria or Orthoptera, Siphonaptera and Zygentoma and from the class Malacostraca the order Isopoda.
- the application is carried out, for example, in aerosols, pressureless sprays, eg spray and atomizer sprays, fog machines, foggers, foams, gels, evaporator products with evaporator plates of cellulose or plastic, liquid evaporators, gel and membrane evaporators, propeller driven evaporators, energy-less or passive evaporation systems, moth papers .
- Moth sacs and moth gels as granules or dusts, in straw baits or bait stations.
- Injection volume 1 g of isomer mixture are taken up in 21 ml of acetonitrile / 35 ml of water / 7 ml of THF and after filtration on Chromasil 100 C18 7 ⁇ 250 * 50 mm 32/68 acetonitrile / water isocratic, flow: 100 ml / min, separated.
- the dashed line indicates the binding to the quinoxaline derivative.
- logP (HCOOH) logP [a] logP (neutral)
- the calibration is carried out with un branched alkan-2-ones (with 3 to 16 carbon atoms) whose logP values are known (determination of the logP values by means of the retention times by linear interpolation between two consecutive alkanones).
- the lambda-maX values were determined on the basis of the UV spectra from 200 nm to 400 nm in the maxima of the chromatographic signals.
- NMR data of selected examples are listed in classical form ( ⁇ values, number of H atoms, multiplet splitting).
- the compounds of the formula (VI) can be obtained, for example the following compounds of the formula (VI):
- the compounds of the formula (VII) can be obtained, for example the following compounds of the formula (VII):
- Boophilus microplus test (BOOPMI injection)
- the drug solution is injected into the abdomen (Boophilus microplus), the animals are transferred to trays and stored in an air-conditioned room.
- the effect control takes place after 7 days on storage of fertile eggs. Eggs whose fertility is not visible from the outside are stored in the climatic cabinet for about 42 days until larval hatching. An effect of 100% means that none of the ticks have laid fertile eggs, 0% means that all eggs are fertile.
- Haemonchus contortus - test (HAEMCO)
- Solvent dimethylsulfoxide To prepare a suitable preparation of active compound, 10 mg of active compound are mixed with 0.5 ml of dimethyl sulfoxide and the concentrate is diluted with "Ringer's solution" to the desired concentration.
- Vessels containing the preparation of active compound of the desired concentration are filled with approximately 40 larvae of the red gastric worm (Haemonchus contortus).
- the kill is determined in%. 100% means that all larvae have been killed; 0% means that none of the larvae have been killed.
- the following compounds of the preparation examples show an effect of 80% at an application rate of 20 ppm: 1-4, 1-32
- Vessels containing the preparation of active compound of the desired concentration are filled with about 40 nematode larvae (Cooperia curticei).
- Nippostrongylus brasiliensis test (NIPOBR) Test procedure for in vitro experiments with Nippostrongylus brasiliensis
- the incubation of the worms (both sexes) is carried out in 1.0 ml of medium, which is also used for the determination of acetylcholinesterase activity.
- the compounds are dissolved in DMSO and added to the incubation medium so that final concentrations of 10 and 1 ⁇ g / ml, respectively, were present.
- the controls only contain DMSO.
- the incubation takes place at 37 ° C and 5% C0 2 .
- the enzyme determination is carried out with an aliquot of the medium.
- the AChE to be measured cleaves the substrate acetylthiocholine iodide (in the present case as the iodide salt) into the products acetate and thiocholine.
- thiocholine forms a yellow dye (thionitrobenzoate) with dithiomethrobenzoic acid (DTNB, Ellman's reagent).
- the classification of efficacy is in the categories 84% (60-84% inhibition) and 100% (> 84-100% inhibition).
- Vessels are filled with sand, drug solution, an egg larvae suspension of the southern root gallbladder (Meloidogyne incognita) and lettuce seeds.
- the lettuce seeds germinate and the plantlets develop.
- the galls develop at the roots.
- the nematicidal activity is determined on the basis of bile formation in%. 100% means that no bile was found; 0% means that the number of bile on the treated plants corresponds to the untreated control. In this test, z.
- the following compounds of the Preparation Examples Effect of 90% at a rate of 20 ppm: 1-7, 1-74
- Phaedon cochleariae - spray test PHAECO
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Chinese cabbage leaf discs (Brassica pekinensis) are sprayed with a preparation of active compound of the desired concentration and, after drying, are populated with larvae of the horseradish leaf beetle (Phaedon cochleariae).
- the effect is determined in%. 100% means that all beetle larvae have been killed; 0% means that no beetle larvae have been killed. In this test, z.
- the following compounds of the Preparation Examples have an effect of 83% at a rate of 500 g / ha: 1-15, 1-36
- SPODFR Spodoptera frugiperda - spray test
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Maize leaf discs (Zea mays) are sprayed with an active compound preparation of the desired concentration and, after drying, are infested with caterpillars of the armyworm (Spodoptera frugiperda). After 7 days, the effect is determined in%. 100% means that all caterpillars have been killed; 0% means that no caterpillar has been killed.
- dimethylformamide emulsifier 1.5 parts by weight of dimethylformamide emulsifier: 0.5 part by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Bean leaf discs Phaseolus vulgaris infected by all stages of the common spider mite (Tetranychus urticae) are sprayed with an active compound preparation of the desired concentration.
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether To prepare a suitable preparation of active compound, 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Chinese cabbage leaf discs (Brassica pekinensis) infested with all stages of the green peach aphid (Myzus persicae) are sprayed with an active compound preparation of the desired concentration.
- Emulsifier alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is dissolved with the stated parts by weight of solvent and filled with water containing an emulsifier concentration of 1000 ppm until reaching the desired concentration.
- dilute with emulsifier-containing water When necessary addition of ammonium salts or / and penetration promoters they are added in each case in a concentration of 1000 ppm of the preparation solution.
- Cotton plants (Gossypium hirsutum), which are heavily affected by the cotton aphid ⁇ Aphis gossypii), are sprayed with an active compound preparation of the desired concentration.
- Emulsifier alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is dissolved with the stated parts by weight of solvent and filled with water containing an emulsifier concentration of 1000 ppm until reaching the desired concentration.
- emulsifier concentration 1000 ppm until reaching the desired concentration.
- dilute with emulsifier-containing water dilute with ammonium salts or / and penetration promoters they are added in each case in a concentration of 1000 ppm of the preparation solution.
- Cotton plants (Gossypium hirsutum) infested with larvae of the white fly (Bemisia tabaci) are sprayed with an active compound preparation of the desired concentration.
- Example the following compounds of the preparation examples effect of 90% at a rate of lOOppm: 1-15 In this test, for. Example, the following compounds of the preparation examples effect of 96% at a rate of lOOppm: 1-26
- Nilaparvata lugens - spray test solvent 7 parts by weight of dimethylformamide
- Emulsifier alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is dissolved with the stated parts by weight of solvent and filled with water containing an emulsifier concentration of 1000 ppm until reaching the desired concentration.
- emulsifier concentration 1000 ppm until reaching the desired concentration.
- dilute with emulsifier-containing water dilute with ammonium salts or / and penetration promoters they are added in each case in a concentration of 1000 ppm of the preparation solution.
- Rice plants (Oryza sativa) are sprayed with an active compound preparation of the desired concentration and then populated with larvae of the rice leafhopper (Nilaparvata lugens). After 7 days, the effect is determined in%. 100% means that all rice cicadas have been killed; 0% means that no rice cicadas have been killed.
- Emulsifier alkylaryl polyglycol ether To prepare a suitable preparation of active compound, 1 part by weight of active compound is dissolved with the stated parts by weight of solvent and filled with water which contains an emulsifier concentration of 1000 ppm until the desired concentration is reached. To prepare further test concentrations, dilute with emulsifier-containing water.
- Rice plants (Oryza sativa) are sprayed with an active compound preparation of the desired concentration and then populated with larvae of the rice leafhopper (Nilaparvata lugens).
- Emulsifier alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is dissolved with the stated parts by weight of solvent and filled with water containing an emulsifier concentration of 1000 ppm until reaching the desired concentration.
- emulsifier concentration 1000 ppm until reaching the desired concentration.
- dilute with emulsifier-containing water dilute with ammonium salts or / and penetration promoters (rapeseed oil methyl ester), these are pipetted in a concentration of in each case lOOOppm after dilution of the finished preparation solution.
- Rice plants (Oryza sativa, var. Balilla) are treated by spraying with the preparation of active compound in the desired concentration and then populated with larvae of the rice leafhopper ⁇ Nephotettix cincticeps).
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15/029,533 US9936700B2 (en) | 2013-10-23 | 2014-10-20 | Substituted quinoxaline derivatives as pest control agent |
JP2016525575A JP6472444B2 (ja) | 2013-10-23 | 2014-10-20 | 有害生物防除剤としての置換されているキノキサリン誘導体 |
CN201480070423.9A CN105873914B (zh) | 2013-10-23 | 2014-10-20 | 作为害虫防治剂的取代的喹喔啉衍生物 |
EP14786882.2A EP3060557A1 (de) | 2013-10-23 | 2014-10-20 | Substituierte chinoxalin-derivate als schädlingsbekämpfungsmittel |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13189894.2 | 2013-10-23 | ||
EP13189894 | 2013-10-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2015059088A1 true WO2015059088A1 (de) | 2015-04-30 |
Family
ID=49447488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2014/072432 WO2015059088A1 (de) | 2013-10-23 | 2014-10-20 | Substituierte chinoxalin-derivate als schädlingsbekämpfungsmittel |
Country Status (5)
Country | Link |
---|---|
US (1) | US9936700B2 (de) |
EP (1) | EP3060557A1 (de) |
JP (1) | JP6472444B2 (de) |
CN (1) | CN105873914B (de) |
WO (1) | WO2015059088A1 (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20170117079A (ko) | 2015-02-12 | 2017-10-20 | 닛산 가가쿠 고교 가부시키 가이샤 | 축합 복소 고리 화합물 및 유해 생물 방제제 |
KR20180116303A (ko) | 2016-03-10 | 2018-10-24 | 닛산 가가쿠 가부시키가이샤 | 축합 복소 고리 화합물 및 유해 생물 방제제 |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7013213B2 (ja) * | 2017-05-26 | 2022-01-31 | 日本化薬株式会社 | ピラジン化合物 |
MX2019015895A (es) * | 2017-06-30 | 2020-02-07 | Bayer Animal Health Gmbh | Nuevos derivados de azaquinolina. |
JP2019019124A (ja) * | 2017-07-19 | 2019-02-07 | 日本化薬株式会社 | ピラジン化合物 |
JP6924677B2 (ja) * | 2017-11-22 | 2021-08-25 | 日本化薬株式会社 | ピラジン化合物 |
CN111423388B (zh) * | 2020-04-29 | 2022-02-15 | 浙江工业大学 | 一种7-甲氧基-3-苯基喹喔啉-2(1h)-酮衍生物及其制备方法与应用 |
CN112778272B (zh) * | 2021-02-02 | 2022-03-29 | 华南理工大学 | 一种2,2′-联氮杂芳环类双齿配体及其制备方法和应用 |
Citations (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5227745B2 (de) | 1972-03-30 | 1977-07-22 | ||
DE2824407A1 (de) | 1978-06-03 | 1979-12-13 | Bayer Ag | Verfahren zur herstellung von arylglyoxylsaeuren |
DD151753A1 (de) | 1980-06-27 | 1981-11-04 | Gerhard Dr Rer Nat D Sarodnick | Verfahren zur herstellung von 2-pyridyl-chinoxalinen |
DD258165A1 (de) | 1987-03-05 | 1988-07-13 | Fahlberg List Veb | Algizide und herbizide mittel, die 2-hetaryl-chinoxaline enthalten |
DD262790A1 (de) | 1987-08-06 | 1988-12-14 | Fahlberg List Veb | Akarizide mittel |
EP0512352A2 (de) | 1991-05-09 | 1992-11-11 | F. Hoffmann-La Roche Ag | Substituierte Carbonsäurederivate |
US5514680A (en) | 1992-06-22 | 1996-05-07 | The State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University | Glycine receptor antagonists and the use thereof |
WO1999042463A1 (en) | 1998-02-23 | 1999-08-26 | Warner-Lambert Company | Substituted quinoxaline derivatives as interleukin-8 receptor antagonists |
WO2003076415A1 (en) | 2002-03-12 | 2003-09-18 | Sumitomo Chemical Company, Limited | Pyrimidine compounds and their use as pesticides |
US6649768B1 (en) | 2002-12-04 | 2003-11-18 | Sumika Fine Chemicals Co., Ltd. | Production methods of imidazole compound and salt thereof and intermediates therefor |
WO2003106457A1 (en) | 2002-06-14 | 2003-12-24 | Syngenta Limited | Spiroindolinepiperidine derivatives |
WO2004001913A1 (en) | 2002-06-25 | 2003-12-31 | Jae-Ha Lee | Electric outlet with rotatable receptacles |
WO2004099160A1 (en) | 2003-05-12 | 2004-11-18 | Sumitomo Chemical Company, Limited | Pyrimidine compounds and pests controlling composition containing the same |
JP2004346016A (ja) | 2003-05-22 | 2004-12-09 | Otsuka Chemical Co Ltd | トリフルオロメチルキノキサリン化合物、その製造方法、及び有害生物防除剤 |
WO2005077934A1 (ja) | 2004-02-18 | 2005-08-25 | Ishihara Sangyo Kaisha, Ltd. | アントラニルアミド系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
WO2005085216A1 (ja) | 2004-03-05 | 2005-09-15 | Nissan Chemical Industries, Ltd. | イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤 |
US20050256000A1 (en) | 2004-05-12 | 2005-11-17 | Bayer Cropscience Gmbh | Quinoxalin-2-one derivatives, compositions which protect useful plants and comprise these derivatives, and processes for their preparation and their use |
WO2006003494A2 (en) | 2004-06-28 | 2006-01-12 | Syngenta Participations Ag | Piperidine derivatives and their use as insecticides, acaricides, molluscicides or nematicides |
WO2006043635A1 (ja) | 2004-10-20 | 2006-04-27 | Kumiai Chemical Industry Co., Ltd. | 3-トリアゾリルフェニルスルフィド誘導体及びそれを有効成分として含有する殺虫・殺ダニ・殺線虫剤 |
WO2008015423A1 (en) | 2006-08-01 | 2008-02-07 | Sentinel Oncology Limited | Quinoline and quinoxaline n-oxides as chk-1 inhibitors |
WO2008134969A1 (fr) | 2007-04-30 | 2008-11-13 | Sinochem Corporation | Composés benzamides et leurs applications |
WO2008141065A1 (en) | 2007-05-10 | 2008-11-20 | Smithkline Beecham Corporation | Quinoxaline derivatives as p13 kinase inhibitors |
WO2008148867A2 (en) | 2007-06-08 | 2008-12-11 | Novartis Ag | Quinoxaline derivatives as inhibitors of the tyrosine kinase activity of janus kinases |
WO2009002809A2 (en) | 2007-06-26 | 2008-12-31 | E. I. Du Pont De Nemours And Company | Naphthalene isoxazoline invertebrate pest control agents |
CN101337940A (zh) | 2008-08-12 | 2009-01-07 | 国家农药创制工程技术研究中心 | 具杀虫活性的含氮杂环二氯烯丙醚类化合物 |
WO2009021083A1 (en) * | 2007-08-09 | 2009-02-12 | Smithkline Beecham Corporation | Quinoxaline derivatives as pi3 kinase inhibitors |
WO2009049851A1 (en) | 2007-10-15 | 2009-04-23 | Syngenta Participations Ag | Spiroheterocyclic pyrrolidine dione derivatives useful as pesticides |
WO2009073497A2 (en) | 2007-11-30 | 2009-06-11 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
WO2009080250A2 (en) | 2007-12-24 | 2009-07-02 | Syngenta Participations Ag | Insecticidal compounds |
WO2009099929A1 (en) | 2008-02-06 | 2009-08-13 | E. I. Du Pont De Nemours And Company | Mesoionic pesticides |
WO2009114552A1 (en) | 2008-03-10 | 2009-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Heteroaryl compounds, compositions, and methods of use in cancer treatment |
WO2010060231A1 (zh) | 2008-11-25 | 2010-06-03 | Qin Zhaohai | 硝基缩氨基胍类化合物及其制备方法与其作为杀虫剂的应用 |
WO2010069502A2 (de) | 2008-12-18 | 2010-06-24 | Bayer Cropscience Ag | Tetrazolsubstituierte anthranilsäureamide als pestizide |
WO2010069266A1 (zh) | 2008-12-19 | 2010-06-24 | 华东理工大学 | 二醛构建的具有杀虫活性的含氮或氧杂环化合物及其制备方法 |
WO2010129500A2 (en) | 2009-05-04 | 2010-11-11 | E. I. Du Pont De Nemours And Company | Nematocidal sulfonamides |
WO2011022439A1 (en) | 2009-08-17 | 2011-02-24 | Intellikine, Inc. | Heterocyclic compounds and uses thereof |
WO2011028947A2 (en) | 2009-09-03 | 2011-03-10 | Bioenergenix | Heterocyclic compounds for the inhibition of pask |
CN102057925A (zh) | 2011-01-21 | 2011-05-18 | 陕西上格之路生物科学有限公司 | 一种含噻虫酰胺和生物源类杀虫剂的杀虫组合物 |
WO2011122815A2 (en) | 2010-03-29 | 2011-10-06 | Dong-A Pharm.Co.,Ltd. | Novel quinoxaline derivatives |
WO2011143495A1 (en) | 2010-05-13 | 2011-11-17 | Amgen Inc. | Heteroaryloxyheterocyclyl compounds as pde10 inhibitors |
WO2012029672A1 (ja) | 2010-08-31 | 2012-03-08 | Meiji Seikaファルマ株式会社 | 有害生物防除剤 |
WO2012034472A1 (zh) | 2010-09-13 | 2012-03-22 | 中化蓝天集团有限公司 | 一种含氰基的邻苯二甲酰胺类化合物、制备方法和作为农用化学品杀虫剂的用途 |
WO2012045196A1 (en) | 2010-10-09 | 2012-04-12 | Abbott Laboratories | Phosphoglycerate kinase inhibitors |
WO2012119046A2 (en) | 2011-03-02 | 2012-09-07 | Bioenergenix | Heterocyclic compounds for the inhibition of pask |
WO2013019112A1 (en) | 2011-08-01 | 2013-02-07 | Koninklijke Douwe Egberts B.V. | Process for the production of a liquid coffee concentrate |
JP2013246249A (ja) * | 2012-05-24 | 2013-12-09 | Ricoh Co Ltd | エレクトロクロミック化合物、エレクトロクロミック組成物、及び表示素子 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63275569A (ja) * | 1987-05-07 | 1988-11-14 | Nissan Chem Ind Ltd | ピリダジノン誘導体および害虫防除剤 |
US5480883A (en) | 1991-05-10 | 1996-01-02 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
FR2688782A1 (fr) | 1992-03-19 | 1993-09-24 | Essilor Int | Nouveaux chromenes heterocycliques et leur utilisation dans le domaine de l'optique ophtalmique. |
JPWO2003062234A1 (ja) * | 2002-01-23 | 2005-05-19 | 山之内製薬株式会社 | キノキサリン化合物 |
US6541633B1 (en) | 2002-07-10 | 2003-04-01 | The United States Of America As Represented By The Secretary Of The Air Force | Bis-(ortho-aminophenol)-carboxylic acid AB2 monomer |
US8377639B2 (en) * | 2009-06-26 | 2013-02-19 | University Of Massachusetts | Compounds for modulating RNA binding proteins and uses therefor |
BR112014030147B1 (pt) | 2012-06-22 | 2019-10-15 | Sumitomo Chemical Company, Limited | Compostos heterocíclicos fundidos, composição e método para controlar pestes |
-
2014
- 2014-10-20 JP JP2016525575A patent/JP6472444B2/ja not_active Expired - Fee Related
- 2014-10-20 EP EP14786882.2A patent/EP3060557A1/de not_active Withdrawn
- 2014-10-20 WO PCT/EP2014/072432 patent/WO2015059088A1/de active Application Filing
- 2014-10-20 US US15/029,533 patent/US9936700B2/en not_active Expired - Fee Related
- 2014-10-20 CN CN201480070423.9A patent/CN105873914B/zh not_active Expired - Fee Related
Patent Citations (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5227745B2 (de) | 1972-03-30 | 1977-07-22 | ||
DE2824407A1 (de) | 1978-06-03 | 1979-12-13 | Bayer Ag | Verfahren zur herstellung von arylglyoxylsaeuren |
DD151753A1 (de) | 1980-06-27 | 1981-11-04 | Gerhard Dr Rer Nat D Sarodnick | Verfahren zur herstellung von 2-pyridyl-chinoxalinen |
DD258165A1 (de) | 1987-03-05 | 1988-07-13 | Fahlberg List Veb | Algizide und herbizide mittel, die 2-hetaryl-chinoxaline enthalten |
DD262790A1 (de) | 1987-08-06 | 1988-12-14 | Fahlberg List Veb | Akarizide mittel |
EP0512352A2 (de) | 1991-05-09 | 1992-11-11 | F. Hoffmann-La Roche Ag | Substituierte Carbonsäurederivate |
US5514680A (en) | 1992-06-22 | 1996-05-07 | The State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University | Glycine receptor antagonists and the use thereof |
WO1999042463A1 (en) | 1998-02-23 | 1999-08-26 | Warner-Lambert Company | Substituted quinoxaline derivatives as interleukin-8 receptor antagonists |
WO2003076415A1 (en) | 2002-03-12 | 2003-09-18 | Sumitomo Chemical Company, Limited | Pyrimidine compounds and their use as pesticides |
WO2003106457A1 (en) | 2002-06-14 | 2003-12-24 | Syngenta Limited | Spiroindolinepiperidine derivatives |
WO2004001913A1 (en) | 2002-06-25 | 2003-12-31 | Jae-Ha Lee | Electric outlet with rotatable receptacles |
US6649768B1 (en) | 2002-12-04 | 2003-11-18 | Sumika Fine Chemicals Co., Ltd. | Production methods of imidazole compound and salt thereof and intermediates therefor |
WO2004099160A1 (en) | 2003-05-12 | 2004-11-18 | Sumitomo Chemical Company, Limited | Pyrimidine compounds and pests controlling composition containing the same |
JP2004346016A (ja) | 2003-05-22 | 2004-12-09 | Otsuka Chemical Co Ltd | トリフルオロメチルキノキサリン化合物、その製造方法、及び有害生物防除剤 |
WO2005077934A1 (ja) | 2004-02-18 | 2005-08-25 | Ishihara Sangyo Kaisha, Ltd. | アントラニルアミド系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
WO2005085216A1 (ja) | 2004-03-05 | 2005-09-15 | Nissan Chemical Industries, Ltd. | イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤 |
US20050256000A1 (en) | 2004-05-12 | 2005-11-17 | Bayer Cropscience Gmbh | Quinoxalin-2-one derivatives, compositions which protect useful plants and comprise these derivatives, and processes for their preparation and their use |
WO2006003494A2 (en) | 2004-06-28 | 2006-01-12 | Syngenta Participations Ag | Piperidine derivatives and their use as insecticides, acaricides, molluscicides or nematicides |
WO2006043635A1 (ja) | 2004-10-20 | 2006-04-27 | Kumiai Chemical Industry Co., Ltd. | 3-トリアゾリルフェニルスルフィド誘導体及びそれを有効成分として含有する殺虫・殺ダニ・殺線虫剤 |
WO2008015423A1 (en) | 2006-08-01 | 2008-02-07 | Sentinel Oncology Limited | Quinoline and quinoxaline n-oxides as chk-1 inhibitors |
WO2008134969A1 (fr) | 2007-04-30 | 2008-11-13 | Sinochem Corporation | Composés benzamides et leurs applications |
WO2008141065A1 (en) | 2007-05-10 | 2008-11-20 | Smithkline Beecham Corporation | Quinoxaline derivatives as p13 kinase inhibitors |
WO2008148867A2 (en) | 2007-06-08 | 2008-12-11 | Novartis Ag | Quinoxaline derivatives as inhibitors of the tyrosine kinase activity of janus kinases |
WO2009002809A2 (en) | 2007-06-26 | 2008-12-31 | E. I. Du Pont De Nemours And Company | Naphthalene isoxazoline invertebrate pest control agents |
WO2009021083A1 (en) * | 2007-08-09 | 2009-02-12 | Smithkline Beecham Corporation | Quinoxaline derivatives as pi3 kinase inhibitors |
WO2009049851A1 (en) | 2007-10-15 | 2009-04-23 | Syngenta Participations Ag | Spiroheterocyclic pyrrolidine dione derivatives useful as pesticides |
WO2009073497A2 (en) | 2007-11-30 | 2009-06-11 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
WO2009080250A2 (en) | 2007-12-24 | 2009-07-02 | Syngenta Participations Ag | Insecticidal compounds |
WO2009099929A1 (en) | 2008-02-06 | 2009-08-13 | E. I. Du Pont De Nemours And Company | Mesoionic pesticides |
WO2009114552A1 (en) | 2008-03-10 | 2009-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Heteroaryl compounds, compositions, and methods of use in cancer treatment |
CN101337940A (zh) | 2008-08-12 | 2009-01-07 | 国家农药创制工程技术研究中心 | 具杀虫活性的含氮杂环二氯烯丙醚类化合物 |
WO2010060231A1 (zh) | 2008-11-25 | 2010-06-03 | Qin Zhaohai | 硝基缩氨基胍类化合物及其制备方法与其作为杀虫剂的应用 |
WO2010069502A2 (de) | 2008-12-18 | 2010-06-24 | Bayer Cropscience Ag | Tetrazolsubstituierte anthranilsäureamide als pestizide |
WO2010069266A1 (zh) | 2008-12-19 | 2010-06-24 | 华东理工大学 | 二醛构建的具有杀虫活性的含氮或氧杂环化合物及其制备方法 |
WO2010129500A2 (en) | 2009-05-04 | 2010-11-11 | E. I. Du Pont De Nemours And Company | Nematocidal sulfonamides |
WO2011022439A1 (en) | 2009-08-17 | 2011-02-24 | Intellikine, Inc. | Heterocyclic compounds and uses thereof |
WO2011028947A2 (en) | 2009-09-03 | 2011-03-10 | Bioenergenix | Heterocyclic compounds for the inhibition of pask |
WO2011122815A2 (en) | 2010-03-29 | 2011-10-06 | Dong-A Pharm.Co.,Ltd. | Novel quinoxaline derivatives |
WO2011143495A1 (en) | 2010-05-13 | 2011-11-17 | Amgen Inc. | Heteroaryloxyheterocyclyl compounds as pde10 inhibitors |
WO2012029672A1 (ja) | 2010-08-31 | 2012-03-08 | Meiji Seikaファルマ株式会社 | 有害生物防除剤 |
WO2012034472A1 (zh) | 2010-09-13 | 2012-03-22 | 中化蓝天集团有限公司 | 一种含氰基的邻苯二甲酰胺类化合物、制备方法和作为农用化学品杀虫剂的用途 |
WO2012045196A1 (en) | 2010-10-09 | 2012-04-12 | Abbott Laboratories | Phosphoglycerate kinase inhibitors |
CN102057925A (zh) | 2011-01-21 | 2011-05-18 | 陕西上格之路生物科学有限公司 | 一种含噻虫酰胺和生物源类杀虫剂的杀虫组合物 |
WO2012119046A2 (en) | 2011-03-02 | 2012-09-07 | Bioenergenix | Heterocyclic compounds for the inhibition of pask |
WO2013019112A1 (en) | 2011-08-01 | 2013-02-07 | Koninklijke Douwe Egberts B.V. | Process for the production of a liquid coffee concentrate |
JP2013246249A (ja) * | 2012-05-24 | 2013-12-09 | Ricoh Co Ltd | エレクトロクロミック化合物、エレクトロクロミック組成物、及び表示素子 |
Non-Patent Citations (54)
Title |
---|
"Pesticide Specifications, Manual on development and use of FAO and WHO specifications for pesticides, FAO Plant Production and Protection Papers", 2004, FAO/WHO JOINT MEETING ON PESTICIDE SPECIFICATIONS |
"The Pesticide Manual", 2012, BRITISH CROP PROTECTION COUNCIL |
ANALOGIE ZU DEN IN CURRENT CHEMISTRY LETTERS, vol. 1, no. 3, 2012, pages 139 - 146 |
ANGEW. CHEM. INT. ED., vol. 51, 2012, pages 2667 - 2672 |
BAUR ET AL., PESTICIDE SCIENCE, vol. 51, 1997, pages 131 - 152 |
BEISPIEL ANALOG SYNTH. COMMUN., vol. 38, no. 24, 2008, pages 4434 - 444 |
BULL. KOREAN CHEM. SOC., vol. 32, no. 10, 2011, pages 3720 |
BULL. KOREAN CHEM. SOC., vol. 33, no. 8, 2012, pages 2581 |
BULL. SOC. CHIM. FR., 1950, pages 753 - 757 |
CHEM. BER., vol. 87, 1954, pages 1062 |
CHEM. BER., vol. 90, 1957, pages 2604 |
CHEM. PHARM. BULL., vol. 22, 1974, pages 2097 - 2100 |
CURRENT CHEMISTRY LETTERS, vol. 1, no. 3, 2012, pages 139 - 146 |
HELV. CHIM. ACTA, vol. 35, 1952, pages 2301 - 2314 |
HELV. CHIM. ACTA, vol. 38, 1955, pages 1289 - 1291 |
HELV. CHIM. ACTA, vol. 93, 2010, pages 1216 - 1220 |
J. AM. CHEM. SOC., vol. 129, no. 11, 2007, pages 3358 - 3366 |
J. CHEM. RESEARCH (S), 1986, pages 16 - 17 |
J. CHEM. RESEARCH (S, 1986, pages 16 - 17 |
J. CHEM. SOC., vol. 479, 1938 |
J. CHIN. CHEM. SOC., vol. 56, no. 4, 2009, pages 683 - 687 |
J. HETEROCYCL. CHEM., vol. 24, 1987, pages 1771 |
J. HETEROCYCL. CHEM., vol. 46, 2009, pages 317 - 319 |
J. HETEROCYCLIC CHEM., vol. 29, 1976, pages 129 |
J. HETEROCYCLIC CHEM., vol. 29, 1992, pages 129 |
J. HETEROCYCLIC CHEM., vol. 33, 1996, pages 447 |
J. MED. CHEM., vol. 22, no. 6, 1979, pages 687 - 694 |
J. MED. CHEM., vol. 24, no. 1, 1981, pages 93 - 101 |
J. MED. CHEM., vol. 48, no. 21, 2005, pages 6632 - 6642 |
J. MED. CHEM., vol. 53, 2010, pages 1128 |
J. OF CHEM. AND ENG. DATA, vol. 18, no. 1, 1973, pages 102 - 104 |
J. ORG. CHEM., 1969, pages 384 |
J. ORG. CHEM., 1977, pages 1869 - 1871 |
J. ORG. CHEM., vol. 211, 1981 |
J. ORG. CHEM., vol. 31, no. 3, 1966, pages 803 - 806 |
J. ORG. CHEM., vol. 60, 1995, pages 7508 - 7510 |
ORGANIC LETT., vol. 16, 2011, pages 4374 - 4377 |
PHARMAZIE, vol. 40, 1985, pages 384 - 387 |
PIERRE KOCH ET AL: "Pyridinylquinoxalines and Pyridinylpyridopyrazines as Lead Compounds for Novel p38[alpha] Mitogen-Activated Protein Kinase Inhibitors", JOURNAL OF MEDICINAL CHEMISTRY, vol. 53, no. 3, 11 February 2010 (2010-02-11), pages 1128 - 1137, XP055153418, ISSN: 0022-2623, DOI: 10.1021/jm901392x * |
R. WEGLER: "Chemie der Pflanzenschutz- und Schädlingsbekämpfungsmittel", vol. 2, 1970, SPRINGER VERLAG, pages: 401 - 412 |
REC. TRAV. CHIM. PAYS-BAS, vol. 91, 1972, pages 850 - 860 |
SHILU FAN ET AL: "Pd-Catalyzed Direct Cross-Coupling of Electron-Deficient Polyfluoroarenes with Heteroaromatic Tosylates", ORGANIC LETTERS, vol. 13, no. 16, 19 August 2011 (2011-08-19), pages 4374 - 4377, XP055153413, ISSN: 1523-7060, DOI: 10.1021/ol201706t * |
SYNLETT, 2001, pages 73 - 73 |
SYNTH. COMMUN., vol. 25, no. 15, 1995, pages 2319 - 26 |
SYNTH. COMMUN., vol. 42, 2012, pages 236 - 245 |
TETRAHEDRON LETT., vol. 40, 1999, pages 7477 |
TETRAHEDRON LETT., vol. 42, 2001, pages 4849 - 4851 |
TETRAHEDRON LETT., vol. 43, 2002, pages 5361 - 5365 |
TETRAHEDRON LETT., vol. 46, 2005, pages 6345 |
TETRAHEDRON LETT., vol. 46, 2005, pages 7183 |
TETRAHEDRON LETT., vol. 48, 2007, pages 5371 |
TETRAHEDRON LETT., vol. 49, 2008 |
TETRAHEDRON LETT., vol. 52, 2011, pages 2862 |
TETRAHEDRON, vol. 64, 2008, pages 8676 - 8684 |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20170117079A (ko) | 2015-02-12 | 2017-10-20 | 닛산 가가쿠 고교 가부시키 가이샤 | 축합 복소 고리 화합물 및 유해 생물 방제제 |
US10464950B2 (en) | 2015-02-12 | 2019-11-05 | Nissan Chemical Corporation | Condensed heterocyclic compounds and pesticides |
US10882869B2 (en) | 2015-02-12 | 2021-01-05 | Nissan Chemical Corporation | Condensed heterocyclic compounds and pesticides |
KR20180116303A (ko) | 2016-03-10 | 2018-10-24 | 닛산 가가쿠 가부시키가이샤 | 축합 복소 고리 화합물 및 유해 생물 방제제 |
US10544163B2 (en) | 2016-03-10 | 2020-01-28 | Nissan Chemical Corporation | Condensed heterocyclic compounds and pesticides |
US10640518B2 (en) | 2016-03-10 | 2020-05-05 | Nissan Chemical Corporation | Condensed heterocyclic compounds and pesticides |
US10759815B2 (en) | 2016-03-10 | 2020-09-01 | Nissan Chemical Corporation | Condensed heterocyclic compounds and pesticides |
Also Published As
Publication number | Publication date |
---|---|
CN105873914B (zh) | 2018-10-19 |
JP6472444B2 (ja) | 2019-02-20 |
EP3060557A1 (de) | 2016-08-31 |
JP2016536302A (ja) | 2016-11-24 |
CN105873914A (zh) | 2016-08-17 |
US9936700B2 (en) | 2018-04-10 |
US20160227779A1 (en) | 2016-08-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3484877B1 (de) | Bicyclische verbindungen als schädlingsbekämpfungsmittel | |
EP3331870B1 (de) | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel | |
EP3253210B1 (de) | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlings-bekämpfungsmittel | |
EP3280716B1 (de) | Imidazo[1,2-a]pyridin-2-yl-derivate als schädlingsbekämpfungsmittel und deren zwischenprodukte | |
EP3356362B1 (de) | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel | |
EP3227288B1 (de) | Bicyclische verbindungen als schädlingsbekämpfungsmittel | |
EP3253757A1 (de) | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel | |
EP3256462B1 (de) | Substituierte 2-thioimidazolyl-carboxamide als schädlingsbekämpfungsmittel | |
EP3107912A1 (de) | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel | |
EP3227274B1 (de) | Bicyclische verbindungen als schädlingsbekämpfungsmittel | |
EP3227302B1 (de) | Bicyclische verbindungen als schädlingsbekämpfungsmittel | |
EP3319943A1 (de) | Stickstoffhaltige heterocyclen als schädlingsbekämpfungsmittel | |
EP3083570B1 (de) | Sechsgliedrige c-n-verknüpfte arylsulfid- und arylsulfoxid- derivate als schädlingsbekämpfungsmittel | |
US9936700B2 (en) | Substituted quinoxaline derivatives as pest control agent | |
EP3152216B1 (de) | Bicyclische verbindungen als schädlingsbekämpfungsmittel | |
EP3116868B1 (de) | Heterocylische verbindungen als schädlingsbekämpfungsmittel | |
WO2016091857A1 (de) | Fünfgliedrige c-n-verknüpfte arylsulfid- und arylsulfoxid-derivate als schädlingsbekämpfungsmittel | |
WO2015132313A1 (de) | Heterocyclische verbindungen als schädlingsbekämpfungsmittel | |
EP3126335B1 (de) | N-(1-(hetero)aryl-1h-pyrazol-4-yl)-(hetero)arylamid- derivate und ihre verwendung als schädlingsbekämpfungsmittel | |
EP3191458B1 (de) | Arylsulfid- und arylsulfoxid-derivate mit c-c verknüpften uracilen als schädlingsbekämpfungsmittel | |
WO2015107133A1 (de) | Chinolinderivate als insektizide und akarizide | |
WO2015169718A1 (de) | Arylsulfid- und arylsulfoxid-derivate mit c-c verknüpften (aza)uracilen als schädlingsbekämpfungsmittel |
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: 14786882 Country of ref document: EP Kind code of ref document: A1 |
|
REEP | Request for entry into the european phase |
Ref document number: 2014786882 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2014786882 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 15029533 Country of ref document: US |
|
ENP | Entry into the national phase |
Ref document number: 2016525575 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: 112016008749 Country of ref document: BR |
|
ENP | Entry into the national phase |
Ref document number: 112016008749 Country of ref document: BR Kind code of ref document: A2 Effective date: 20160419 |