Insecticide and fungicide active agent combinations 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
EP2000029 A1 2008-12-10 [EP2000029] / 2008-12-10
申请号/申请日
2007EP-0011095 / 2007-06-06
发明人
;
申请人
BAYER CROPSCIENCE;
主分类号
IPC分类号
A01N-037/22A01N-043/22A01N-043/56A01N-047/02A01N-047/22A01N-047/24A01N-051/00A01N-061/00A01P-007/00
摘要
(EP2000029) Fungicidal, insecticidal and acaricidal active combination (Q) comprises a carboxamide compound of formula (I), and at least an active agent from e.g. acetylcholine-receptor-agonist/antagonist (II) (preferably chloronicotinyl/neonicotinoid); acetylcholinesterase inhibitor (III) (preferably carbamate or organophosphate); sodium-channel-modulator/stress dependent sodium-channel-blocker (IV) (preferably pyrethroid or oxadiazine) and acetylcholine-receptor-modulator (V) (preferably spinosyn).  Fungicidal, insecticidal and acaricidal active combination (Q) comprises a carboxamide compound of formula (I), and at least an active agent from: acetylcholine-receptor-agonist/antagonist (II) (preferably chloronicotinyl/neonicotinoid); acetylcholinesterase inhibitor (III) (preferably carbamate or organophosphate); sodium-channel-modulator/stress dependent sodium-channel-blocker (IV) (preferably pyrethroid or oxadiazine); acetylcholine-receptor-modulator (V) (preferably spinosyn); gamma -aminobutyric acid controlled chloride-channel-antagonist (VI) (preferably cyclodiene organochlorine or fipronil); chloride-channel-activator (VII) (preferably mectin); juvenile hormone mimetic (VIII); ecdysone agonist/disruptor (XI) (preferably diacylhydrazine); inhibitors of the chitin biosynthesis (X) (preferably benzoylurea); inhibitors of the oxidative phosphorylation (XI); adenosine triphosphate-disruptor (XII) (preferably organotin); decoupler of the oxidative phosphorylation through interruption of H-proton gradient (XIII) (preferably pyrrole or dinitrophenol); side-I-electron transport inhibitor (XIV) (preferably mitochondrial electron transport inhibitor); side-II-electron transport inhibitors (XV); side-III-electron transport inhibitor (XVI); microbial disruptor of the insects intestinal membrane (XVII); inhibitors of the fat synthesis (XVIII) (preferably tetronic acid or tetramic acid); carboxamide (XIX); inhibitors of magnesium-stimulator adenosine triphosphatase (XX); phthalamide (XXI); nereistoxin analogue (XXII); biological, hormone or pheromone (XXIII); an active agent with unknown or non-specific active mechanism (XXIV) (preferably gasing agent, selective antifeeding agent and mite growth inhibitor).  R : H or F; A : pyrazole moiety of formula (a), benzene moiety of formula (b), thiazole moiety of formula (c), thiophene moiety of formula (d), 2,3-dihydro-[1,4]oxathiane moiety of formula (e), pyridine moiety of formula (f), 1-methyl-1H-pyrrole unit of formula (g) or furan moiety of formula (h); R 2>1-3C-alkyl; R 1>, R 3>, R 5>, R 7>, R 1>0>H, halo, 1-3C-alkyl or 1-3C-haloalkyl with 1-7 F, Cl and/or Br; R 4>H, halo or 1-3C-alkyl; R 6>H, halo, 1-3C-alkyl, amino, mono- or di(1-3C-alkyl)amino; and R 8>, R 9>halo, 1-3C-alkyl or 1-3C-haloalkyl with 1-7 F, Cl and/or Br.  Independent claims are included for: (1) seeds, which are treated with (Q); and (2) the preparation of (Q) comprising mixing (Q) with diluting agent and/or surface active materials. [Image] [Image] [Image] ACTIVITY : Pesticide; Fungicide; Acaricide; Arthropodicide; Nematocide; Insecticide.  MECHANISM OF ACTION : None given.
机翻摘要
暂无翻译结果,您可以尝试点击头部的翻译按钮。
地址
代理人
代理机构
;
优先权号
2007EP-0011095 2007-06-06
主权利要求
(EP2000029)  Claims machine translated from German 1. Fungicides, insecticides and acaricidal Active Substance Combinations containing a Carboxamid of the general Formula (I) (Group of 1) in which R for Hydrogen or Fluorine stands, R (1) for Hydrogen, Halogen, C [1] - C [3] - Alkyl or C [1] - C [3] - Halogen Alkyl with 1 to 7 Fluorine, Chlorine and/or Bromine Atoms stands, A for one of the following Remains of A1 to A8 stands: R (2) for C [1] - C [3] - Alkyl stands, R (3) for Hydrogen, Halogen, C [1] - C [3] - Alkyl or C [1] - C [3] - Halogen Alkyl with 1 to 7 Fluorine, Chlorine and/or Bromine Atoms stands, R (4) for Hydrogen, Halogen or C [1] - C [3] - Alkyl stands, R (5) for Halogen, C [1] - C [3] - Alkyl or C [1] - C [3] - Halogen Alkyl with 1 to 7 Fluorine, Chlorine and/or Bromine Atoms stands, R (6) for Hydrogen, Halogen, C [1] - C [3] - Alkyl, Amino, Mono or Di (C [1] - C [3] - alkyl) amino stands, R (7) for Hydrogen, Halogen, C [1] - C [3] - Alkyl or C [1] - C [3] - Halogen Alkyl with 1 to 7 Fluorine, Chlorine and/or Bromine Atoms stands, R (8) for Halogen, C [1] - C [3] - Alkyl or C [1] - C [3] - Halogen Alkyl with 1 to 7 Fluorine, Chlorine and/or Bromine Atoms stands, R (9) for Halogen, C [1] - C [3] - Alkyl or C [1] - C [3] - Halogen Alkyl with 1 to 7 Fluorine, Chlorine and/or Bromine Atoms stands, R (10) for Hydrogen, Halogen, C [1] - C [3] - Alkyl or C [1] - C [3] - Halogen Alkyl with 1 to 7 Fluorine, Chlorine and/or Bromine Atoms stands, and at least one Active Substance, which from the following Groups (2) to (24) is selected: Group (2) acetyl choline receptor agonist/ANTAGONISt (Chloronicotinyle/Neonicotinoide prefers);  Group (3) Acetylcholinesterase (AChE) Inhibiters (prefers Carbamate and Organophosphates);  Group (4) sodium channel modulators/Voltage-dependant sodium channel blockers (Pyrethroide and Oxadiazine prefers);  Group (5) acetyl choline receptor modulators (Spinosyne prefers);  Group (6) GABA steered chloride channel antagonist (cyclodiene Organochlorine and Fiprole prefers);  Group (7) chloride channel activators (Mectine prefers);  Group (8) Juvenilhormon Mimetika;  Group (9) Ecdysonagonisten/disruptoren (Diacylhydrazine prefers);  Group (10) Inhibiters of the Chitinbiosynthese (Benzoyihamstoffe prefers);  Group (of 11) Inhibiters of the oxidative Phosphorylation, ATP Disruptoren (Organotine prefers);  Group (of 12) Entkoppler of the oxidative Phoshorylierung by Interruption of the H-Protongradienten (Pyrrole and Dinitrophenole prefers);  Group (of 13) side I Elektronentransportinhibitoren (METI's) prefers;  Group (of 14) side ii-electron transport inhibiters;  Group (of 15) side iii-electron transport inhibiters;  Group (of 16) Mikrobielle Disruptoren of the Insect Intestine Diaphragm;  Group (of 17) Inhibiters of the Fat Synthesis (Tetronsauren and Tetramsauren prefers);  Group (of 18) Carboxamide;  Group (of 19) Oktopaminerge Agonists;  Group (of 20) Inhibiters of the Magnesium-stimulated ATPase;  Group (of 21) Phthalamide;  Group (22) Nereistoxin similar ones;  Group (of 23) Biologika, Hormones or Pheromones;  Group (of 24) Active Substances with unknown or not specific Effect Mechanisms (prefers Aeration Means, selective eating Retardants and Mite growth inhibiters). 2. Active Substance Combinations in accordance with claim 1 containing a Carboxamid of the general Formula (I) in accordance with claim 1 (Group of 1), in which R (1) for Hydrogen, Fluorine, Chlorine, Methyl, Ethyl, n, ISO Propyl, Mono Fluorine Methyl, Difluormethyl, Tri Fluorine Methyl, Mono Chlorine Methyl, Dichlormethyl or Tri Chlorine Methyl stands, A for one of the following Remains of A1 to A5 stands: R (2) for Methyl, Ethyl, n or ISO Propyl stands, R (3) for Iodine, Methyl, Difluormethyl or Tri Fluorine Methyl stands, R (4) for Hydrogen, Fluorine, Chlorine or Methyl stands, R (5) for Chlorine, Bromine, Iodine, Methyl, Difluormethyl or Tri Fluorine Methyl stands, R (6) for Hydrogen, Chlorine, Methyl, Amino or Dimethylamino stands, R (7) for Methyl, Difluormethyl or Tri Fluorine Methyl stands, R (8) for Bromine or Methyl stands, R (9) for Methyl or Tri Fluorine Methyl stands. 3. Active Substance Combinations in accordance with claim 1, whereby the Active Substances of the Groups (2) to (24) from the following List is selected: (2.1) Chloronicotinyle/Neonicotinoide (Acetamiprid, Clothianidin, Dinotefuran, Imidacloprid, Nitenpyram, Nithiazine, Thiacloprid, Thiamethoxam prefers);  (2.2) Nicotine, Bensultap, Cartap;  (3.1) Carbamate (Alanycarb, Aldicarb, Aldoxycarb, Allyxycarb, Aminocarb, Bendiocarb, Benfuracarb, Bufencarb, Butacarb, Butocarboxim, Butoxycarboxim, Carbaryl prefers, Carbofuran, Carbosulfan, Chloethocarb, Dimetilan, Ethiofencarb, Fenobucarb, Fenothiocarb, Formetanate, Furathiocarb, Isoprocarb, Metam Sodium, Methiocarb, Methomyl, Metolcarb, Oxamyl, Phosphocarb, Pirimicarb, Promecarb, Propoxur, Thiodicarb, Thiofanox, Triazamate, Trimethacarb, XMC, Xylylcarb);  (3.2) Organophosphates (Acephate, Azamethiphos, Azinphos (- methyl, - ethyl) prefers, Bromophos Ethyl, Bromfenvinfos (- methyl), Butathiofos, Cadusafos, Carbophenothion, Chlorethoxyfos, Chlorfenvinphos, Chlormephos, Chlorpyrifos (- methyl/ethyl), Coumaphos, Cyanofenphos, Cyanophos, Chlorfenvinphos, Demeton S methyl, Demeton S methylsulphon, dia.  LIFO, Diazinon, Dichlofenthion, Dichlorvos/DDVP, Dicrotophos, Di-Methoate, Dimethylvinphos, Dioxabenzofos, Disulfoton, EPN, Ethion, Ethoprophos, Etrimfos, Famphur, Fenamiphos, Fenitrothion, Fensulfothion, Fenthion, Flupyrazofos, Fonofos, Formothion, Fosmethilan, Fosthiazate, Heptenophos, Iodofenphos, Iprobenfos, Isazofos, Isofenphos, Isopropyl of O-Salicylate, Isoxathion, Malathion, Mecarbam, Methacrifos, Methamidophos, Methidathion, MEV Information, Monocrotophos, Naled, Omethoate, Oxydemeton Methyl, Parathion (- methyl/ethyl), Phenthoate, Phorate, Phosalone, Phosmet, Phosphamidon, Phosphocarb, Phoxim, Pirimiphos (- methyl/ethyl), Profenofos, Propaphos, Propetamphos, Prothiofos, Prothoate, Pyraclofos, Pyridaphenthion, Pyridathion, Quinalphos, Sebufos, Sulfotep, Sulprofos, Tebupirimfos, Temephos, Terbufos, Tetrachlorvinphos, Thiometon, Triazophos, Triclorfon, Vamidothion);  (4.1) Pyrethroide [Acrinathrin, Allethrin (of D-cis-trans, D-trans prefers), beta Cyfluthrin, Bifenthrin, Bioallethrin, Bioallethrin S cyclopentyl isomer, Bioethanomethrin, Biopermethrin, Bioresmethrin, Chlovaporthrin, Cis Cypermethrin, Cis Resmethrin, Cis Permethrin, Clocythrin, Cycloprothrin, Cyfluthrin, Cyhalothrin, Cypermethrin (alpha, beta, theta, zeta), Cyphenothrin, DDT, Deltamethrin, Empenthrin (1R-isomer), Esfenvalerate, Etofenprox, Fenfluthrin, Fenpropathrin, Fenpyrithrin, Fenvalerate, Flubrocythrinate, Flucythrinate, Flufenprox, Flumethrin, Fluvalinate, Fubfenprox, gamma Cyhalothrin, Imiprothrin, Kadethrin, Lambda Cyhalothrin, Metofluthrin, Permethrin (cis, trans), Phenothrin (1R-trans isomer), Prallethrin, Profluthrin, Protrifenbute, Pyresmethrin, Resmethrin, RU 15525, Silafluofen, rope Fluvalinate, Tefluthrin, Terallethrm, Tetramethrin (1R-isomer), Tralocythrin, Tralomethrin, Transfluthrin, ZXI 8901, Pyrethrins (pyrethrum)];  (4.2) Oxadiazine (Indoxacarb prefers);  (5.1) Spinosyne (Spinosad prefers);  (6.1) Cyclodiene Organochlorine (Camphechlor, Chlordane, Endosulfan, gamma HCH, HCH, Heptachlor, Lindane, Methoxychlor prefers);  (6.2) Fiprole (Acetoprole, Ethiprole, Fipronil, Vaniliprole prefers);  (7.1) Mectine (Abamectin, Avermectin, Emamectin, Emamectin Benzoate, Ivermectin, Milbemectin, Milbemycin prefers);  (8) Juvenilhormon Mimetika (Diofenolan, Epofenonane, Fenoxycarb, Hydroprene, Kinoprene, Methoprene, Pyriproxifen, Triprene prefers);  (9.1) Diacylhydrazine (Chromafenozide, Halofenozide, Methoxyfenozide, Tebufenozide prefers);  (10.1) Benzoylharnstoffe (Bistrifluron, Chlofluazuron, Diflubenzuron, Fluazuron, Flucycloxuron, Flufenoxuron, Hexaflumuron, Lufenuron, Novaluron, Noviflumuron, Penfluron, Teflubenzuron prefers, Triflumuron);  (10.2) Buprofezin;  (10.3) Cyromazine;  (11.1) Diafenthiuron;  (11.2) Organotine (Azocyclotin, Cyhexatin, Fenbutatin Oxides prefers);  (12.1) Pyrrole (Chlorfenapyr prefers);  (12.2) Dinitrophenole (Binapacyrl, Dinobuton, Dinocap, DNOC prefers);  (13.1) METI's (Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad, Tolfenpyrad prefers);  (13.2) Hydramethylnone;  (13.3) Dicofol;  (14.1.1) Rotenone;  (15.1) Acequinocyl, Fluacrypyrim;  (16.1) Bacillus of thuringiensis trunks;  (17.1) Tetronsauren (Spirodiclofen, Spiromesifen prefers);  (17.2) Tetramsauren {prefers 3 (2,5-Dimethylphenyl) - 8-methoxy-2-oxo-1-azaspiro [4.5] dec-3-en-4-yl ethyl of carbonates};  (18.1.1) Flonicamid;  (19.1.1) Amitraz;  (20.1.1) Propargite;  (21.1.1) N (2) - [1,1-Dimethyl-2 (methyl sulphonyl) ethyl] - 3-iod-N (1) - [2 methyl 4 [1,2,2,2-tetrafluor-1 (tri fluorine methyl) ethyl] phenyl] - 1,2-benzenedicarboxamide;  (22) Thiocyclam hydraulictowards oxalates, Thiosultap Sodium;  (23) Azadirachtin, Bacillus spec., Beauveria spec., Codlemone, Metarrhizium spec., Paecilomyces spec., Thuringiensin, Verticillium spec.;  (24.1) Aeration Means (Aluminum of phosphide, Methyl of bromide, Sulfuryl of fluorides prefers);  (24.2) Selective eating Retardants (Cryolite, Flonicamid, Pymetrozine prefers);  (24.3) Mite growth inhibiters (Clofentezine, Etoxazole, Hexythiazox prefers);  (24.4) Amidoflumet, Benclothiaz, Benzoximate, Bifenazate, Bromopropylate, Buprofezin, Chinomethionat, Chlordimeform, Chlorobenzilate, Chloropicrin, Clothiazoben, Cycloprene, Cyflumetofen, Dicyclanil, Fenoxacrim, Fentrifanil, Flubenzimine, Flufenerim, Flutenzin, Gossyplure, Hydramethylnone, Japonilure, Metoxadiazone, Petroleum, Piperonyl butoxide, Potassium of oleates, Pyrafluprole, Pyridalyl, Pyriprole, Sulfluramid, Tetradifon, Tetrasul, Triarathene, Verbutin, furthermore the Connection 3-Methyl-phenyl-propylcarbamat (Tsumacide Z), which Connection 3 (5-Chlor-3-pyridinyl) - 8 (2,2,2-trifluorethyl) - 8-azabicyclo [3.2.1] octan-3-carbonitril, as well as Preparations, which insecticide Mushrooms or Viruses contain effective Plant Extracts, Nematoden. 4. Active Substance Combinations in accordance with one of the claims 1 to 3, whereby the Active Substances of the Groups (2) to (24) from the following List is selected: (2.1.1) Clothianidin (2.1.2) Imidacloprid (2.1.3) Thiacloprid (2.1.4) Thiamethoxam (2.1.5) Acetamiprid (2.1.6) Dinotefuran (2.1.7) Nitenpyram (3.1.1) Methiocarb (3.1.2) Thicdicarb (3.1.3) Ethiofencarb (3.1.4) Aldicarb (3.1.5) Propoxur (3.2.1) Azinphos Methyl (3.2.2) Azinphos Ethyl (3.2.3) Phoxim (3.2.4) Prothiophos (4.1.1) Beta Cyfluthrin (4.1.2) Cyfluthrin (4.1.3) Deltamethrin (4.1.4) Rope Fluvalinate (4.1.5) Eflusilanate (4.2.1) Indoxacarb (5.1.1) Spinosad (6.1.1) Endosulfan (6.2.1) Fipronil (6.2.2) Ethiprole (7.1.1) Emamectin Benzoate (8.1.1) Pyriproxifen (9.1.1) Methoxyfenozide (10.1.1) Triflumuron (10.1.2) Flufenoxuron (13.1.1) Tebufenpyrad (13.2.1) Hydramethylone (14.1.1) Rotenone (17.1.1) Spirodiclofen (17.1.2) Spiromesifen (17.2.1) 3 (2,5-Dimethylphenyl) - 8-methoxy-2-oxo-1-azaspiro [4.5] dec-3-en-4-yl ethyl of carbonates (18.1.1) Flonicamid (19.1.1) Amitraz (20.1.1) Propargite (21.1.1) N (2) - [1,1-Dimethyl-2 (methyl sulphonyl) ethyl] - 3-iod-N (1) - [2 methyl 4 [1,2,2,2-tetrafluor-1 (tri fluorine methyl) ethyl] phenyl] - 1,2-benzenedicarboxamide 5. Active Substance Combinations in accordance with one of the claims 1 to 4 containing the Carboxamid (1-1) 5-Fluor-1,3-dimethyl N - [2 (3-methylbutyl) - 1H - pyrazol-4-carboxamid (Group of 1). 6. Active Substance Combinations in accordance with one of the claims 1 to 4 containing the Carboxamid (1-2) 3 (Difluormethyl) - N - [2 (3,3-dimethylbutyl) - 4-fluorphenyl] - 1-methyl 1H - pyrazol-4-carboxamid (Group of 1). 7. Wirkstoffkombuiationen in accordance with one of the claims 1 to 4 containing the Carboxamid (1-3) 3 (Difluormethyl) - N - [2 (3,3-dimethylbutyl) phenyl] - 1-methy 1H - pyrazol-4-carboxamid (Group of 1). 8. Active Substance Combinations in accordance with one of the claims 1 to 4 containing the Carboxamid (1-4) N - [2 (3,3-Dimethylbutyl) phenyl] - 2 (tri fluorine methyl) benzamid (Group of 1). 9. Active Substance Combinations in accordance with one of the claims 1 to 4 containing the Carboxamid (1-5) N - [2 (3,3-Dimethylbutyl) - 4-fluorphenyl] - 2 methyl 4 (tri fluorine methyl) - 1,3-thiazol-5-carboxamid (Group of 1). 10. Active Substance Combinations in accordance with one of the claims 1 to 4 containing the Carboxamid (1-6) N - [2 (3,3-Dimethylbutyl) phenyl] - 3-methylthiophen-2-carboxamid (Group of 1). 12. Use of Active Substance Combinations in accordance with one the claims 1 to 10 to Fight against unwanted animal Parasits as well as unwanted phytopathogenen Mushrooms. 13. Use of Active Substance Combinations in accordance with one of the claims 1 to 10 for the Treatment of Seeds. 14. Use of Active Substance Combinations in accordance with one of the claims 1 to 10 for the Treatment of transgenen Plants. 15. Use of Active Substance Combinations in accordance with one of the claims 1 to 10 Plants transgener for the Treatment of Seeds. 16. Seeds, which were treated with an Active Substance Combination in accordance with one of the claims 1 to 10. 17. Procedure for Fighting against unwanted animal Parasits as well as unwanted phytopathogenen Mushrooms, by the fact characterized that one yields for Active Substance Combinations in accordance with one of the claims 1 to 10 on the unwanted phytopathogenen Mushrooms and/or their Habitat and/or Seeds. 18. Procedure for Manufacturing fungicides, insecticides and acaricidal Means, by the fact characterized that one mixes Active Substance Combinations in accordance with one of the claims 1 to 10 with Stretching Means and/or surface-active Materials. 19. Procedure for the Protection of Seed Goods from unwanted animal Parasits as well as unwanted phytopathogenen Mushrooms comprehensively the Treatment of the Seeds with an Active Substance Combination in accordance with one of the claims 1 to 10.
法律状态
(EP2000029) LEGAL DETAILS FOR EP2000029  Actual or expected expiration date=2009-05-21    Legal state=DEAD    Status=REVOKED     Event publication date=2007-06-06  Event code=EP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=EP EP07011095  Application date=2007-06-06  Standardized application number=2007EP-0011095     Event publication date=2008-12-10  Event code=EP/A1  Event type=Examination events  Application published with search report  Publication country=EP  Publication number=EP2000029  Publication stage Code=A1  Publication date=2008-12-10  Standardized publication number=EP2000029     Event publication date=2008-12-10  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR    Event publication date=2008-12-10  Event code=EP/AX  Event indicator=Pos  Event type=Designated states  Extension of the European patent to Request for extension of the european patent to AL BA HR MK RS    Event publication date=2009-08-19  Event code=EP/AKX  Event indicator=Pos  Event type=Designated states  Event type=Payment or non-payment notifications  Event type=Examination events  Payment of designation fees Zahlung von benennungsgebuehren    Event publication date=2009-09-30  Event code=EP/18R  Event indicator=Neg  Event type=Event indicating Not In Force  Refused  Effective date of the event=2009-05-21  MEMBER STATE LEGAL DETAILS FOR DE  Actual or expected expiration date=2009-10-01    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=DE     Event publication date=2009-10-01  Event code=EP/REG  Event code=DE/8566  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Designated states  Reference to a national code Designated country de not longer valid Vertragsstaat de nicht mehr benannt Corresponding cc:  Designated or member state=DE
专利类型码
A1
国别省市代码
若您需要申请原文,请登录。

最新评论

暂无评论。

登录后可以发表评论

意见反馈
返回顶部