WO1995000521A1 - Herbicidal thiadiazabicyclodecanes - Google Patents
Herbicidal thiadiazabicyclodecanes Download PDFInfo
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- WO1995000521A1 WO1995000521A1 PCT/EP1994/001893 EP9401893W WO9500521A1 WO 1995000521 A1 WO1995000521 A1 WO 1995000521A1 EP 9401893 W EP9401893 W EP 9401893W WO 9500521 A1 WO9500521 A1 WO 9500521A1
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- alkyl
- formula
- haloalkyl
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- cycloalkyl
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- 0 CC*CCC1C(C[C@@](CC2)C3C2C3C)CC1 Chemical compound CC*CCC1C(C[C@@](CC2)C3C2C3C)CC1 0.000 description 3
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/02—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 2
Definitions
- the present invention relates to novel, herbicidally active thiadiazabicyclodecanes, to processes for the preparation thereof, to compositions comprising those compounds as active ingredients, and to the use thereof in controlling weeds, especially selectively in crops of useful plants, such as cereals, maize, soybeans, rape, rice and cotton.
- Z is oxygen or sulfur
- R is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl,
- W is a group of formula W 1 to W 10
- R 1 , R 22 , R 23 , R 24 , R 27 , R 30 , R 33 , R 37 , R 38 and R 41 are each independently of the others hydrogen or halogen;
- R 2 is cyano, nitro, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkoxy or C 1 -C 4 haloalkyl;
- A is hydrogen, cyano, nitro, -COR 3 , -X 3 R 4 , -COR 8 , ,
- a 1 is cyano or -COR 16 ;
- R 4 , R 42 and R 43 are hydrogen, C 1 -C 10 alkyl, C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 1 -C 4 alkylthioC 1 -C 4 alkyl, di-C 1 -C 4 alkylamino-C 1 -C 4 alkyl, C 1 -C 8 haloalkyl, C 2 -C 8 alkenyl, C 2 -C 8 - haloalkenyl, C 3 -C 8 alkynyl, C 3 -C 7 cycloalkyl, oxetan-3-yl, halo-C 3 -C 7 cycloalkyl, C 1 -C 8 alkylcarbonyl, allylcarbonyl, C 3 -C 7 cycloalkylcarbonyl, benzoyl that is unsubstituted or substituted at the phenyl ring by up to three identical or different substituents selected from halogen
- R 5 is hydrogen, C 1 -C 10 alkyl, C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 2 -C 8 haloalkyl, C 1 -C 10 alkylthio-C 1 -C 4 alkyl, di-C 1 -C 4 alkylamino-C 1 -C 4 alkyl, cyano-C 1 -C 8 alkyl, C 3 -C 8 alkenyl, C 3 -C 8 haloalkenyl, C 3 -C 8 alkynyl, C 3 -C 7 cycloalkyl, oxetan-3-yl, C 3 -C 7 cycloalkyl- C 1 -C 4 alkyl, halo-C 3 -C 7 cycloalkyl, or is benzyl that is unsubstituted or substituted at the phenyl ring by up to three identical or different substituents selected from halogen, C 1 -
- R 20 and R 21 are each independently of the other hydrogen, C 1 -C 4 alkyl or fluorine;
- R 6 , R 26 , R 28 , R 32 , R 34 , R 39 , R 40 , R 46 , R 47 , R 49 , R 50 and R 51 are each independently of the others hydrogen or C 1 -C 4 alkyl;
- R 7 and R 48 are each independently of the other hydrogen, C 1 -C 6 alkyl, C 3 -C 8 alkenyl,
- R 8 is hydrogen or C 1 -C 4 alkyl
- R 44 and R 45 are each independently of the other hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or C 1 -C 4 alkoxy-C 1 -C 4 alkyl;
- R 9 and R 10 are each independently of the other C 1 -C 4 alkyl, C 2 -C 4 haloalkyl or C 2 -C 8 - alkoxyalkyl; or
- R 9 and R 10 together are an ethano, a propano or a cyclohexane-1,2-diyl bridge, it being possible for those groups to be either unsubstituted or substituted by one or two radicals from the group C 1 -C 4 alkyl, C 1 -C 4 haloalkyl and C 1 -C 4 hydroxyalkyl;
- R 11 is hydrogen, C 1 -C 5 alkyl or C 3 -C 7 alkenyl
- R 12 is C 1 -C 8 alkyl
- R 13 is hydrogen, C 1 -C 5 alkyl, benzyl, C 1 -C 4 haloalkyl, C 3 -C 8 alkenyl or C 3 -C 8 alkynyl;
- R 14 is C 1 -C 6 alkyl, C 1 -C 5 haloalkyl or di-C 1 -C 4 alkylamino;
- R 15 is hydrogen, fluorine, chlorine, bromine, C 1 -C 4 alkyl or trifluoromethyl
- R 16 is chlorine, -X 5 -R 17 , amino, C 1 -C 4 alkylamino, di-C 1 -C 4 alkylamino, C 2 -C 4 haloalkylamino, di-C 2 -C 4 haloalkylamino, C 1 -C 4 alkoxyalkylamino, di-C 1 -C 4 alkoxyalkylamino, C 3 -C 4 alkenylamino, diallylamino, -N-pyrrolidino, -N-piperidino,
- R 17 is hydrogen, C 1 -C 10 alkyl, C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 2 -C 8 haloalkyl, C 1 -C 10 alkylthio-C 1 -C 4 alkyl, di-C 1 -C 4 alkylamino-C 1 -C 4 alkyl, cyano-C 1 -C 8 alkyl, C 3 -C 8 alkenyl, C 3 -C 8 haloalkenyl, C 3 -C 8 alkynyl, C 3 -C 7 cycloalkyl, C 3 -C 7 cycloalkyl-C 1 -C 4 alkyl, halo-C 3 -C 7 cycloalkyl, or is benzyl that is unsubstituted or substituted at the phenyl ring by up to three identical or different substituents selected from halogen, C 1 -C 4 - alkyl, C 1
- n 0, 1, 2, 3 or 4;
- t 0, 1, 2, 3 or 4;
- R 18 is C 1 -C 4 alkyl
- R 19 is hydrogen, C 1 -C 6 alkyl, C 2 -C 4 alkenyl or C 2 -C 6 alkynyl; halo-substituted C 1 -C 6 - alkyl, C 2 -C 4 alkenyl or C 3 -C 6 alkynyl; C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 1 -C 4 alkoxy-C 1 -C 2 - alkoxy-C 1 -C 2 alkyl, 1-phenylpropen-3-yl, cyano- or C 3 -C 6 cycloalkyl-substituted C 1 -C 6 alkyl; carboxy-C 1 -C 4 alkyl, C 1 -C 6 alkoxycarbonyl-C 1 -C 4 alkyl, C 2 -C 6 haloalkoxycarbonyl-C 1 -C 4 alkyl, C 1 -C 4 alkoxy-C 1 -
- R 25 , R 29 , R 31 , R 35 and R 36 are each independently of the others hydrogen, C 1 -C 4 alkyl, C 1 -C 6 haloalkyl, C 3 -C 8 alkenyl, C 3 -C 8 haloalkenyl, C 3 -C 8 alkynyl, C 1 -C 4 alkoxy- C 1 -C 8 alkyl, cyano-C 1 -C 4 alkyl, C 1 -C 8 alkoxycarbonyl-C 1 -C 4 alkyl, C 3 -C 7 cycloalkyl, C 3 -C 7 cycloalkyl-C 1 -C 4 alkyl, benzyl, C 1 -C 4 alkyl substituted by -N-morpholino, -N-thiomorpholino or by -N-piperazino, di-C 1 -C 4 alkylamino-C 1 -C 4 alkyl, C 1 -C 4
- halogen is to be understood as being fluorine, chlorine, bromine and iodine, preferably fluorine, chlorine and bromine.
- Suitable alkyl groups are straight-chained or branched alkyl groups, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, ten-butyl, and the various isomeric pentyl, hexyl, heptyl, octyl, nonyl and decyl radicals.
- Suitable as haloalkyl are alkyl groups mono- or poly-substituted, especially mono- to trisubstituted, by halogen, halogen being individually bromine or iodine and especially fluorine or chlorine, for example fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl and 2,2,2-trichloroethyl; preferably difluorochloromethyl, trifluoromethyl, dichlorofluoromethyl and trichloromethyl.
- Alkoxy is, for example, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy; preferably methoxy, ethoxy and isopropoxy.
- Haloalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy and 2,2,2-trichloroethoxy; preferably difluoromethoxy, trifluoromethoxy and 2-chloroethoxy.
- Alkylthio is, for example, methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio, tert-butylthio or isomeric pentylthio, preferably methylthio and ethylthio.
- Alkenyl is to be understood as being straight-chained or branched alkenyl, such as vinyl, allyl, methallyl, 1-methylvinyl, but-2-en-1-yl, pentenyl, 2-hexenyl or 3-heptenyl; the same applies also to the alkenyl moiety of alkenyloxy, alkenylthio and alkenylamino groups. Preference is given to alkenyl radicals having a chain length of from 2 to 4 carbon atoms.
- alkynyl radicals in the definitions of the substituents may be straight-chained or branched, such as ethynyl, propargyl, 3-butynyl, 1 -methylpropargyl, 1 -pentynyl or 2-hexynyl; the same applies also to the alkynyl moiety of alkynyloxy and alkynylthio groups. Preference is given to ethynyl, propargyl and 1 -methylpropargyl.
- Cycloalkyl is, for example, cyclopropyl, dimethylcyclopropyl, cyclobutyl, cyclopentyl, methylcyclopentyl, cyclohexyl or cycloheptyl, but preferably cyclopropyl, cyclopentyl and cyclohexyl.
- Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl or n-butoxycarbonyl, preferably methoxycarbonyl and ethoxycarbonyl.
- Alkoxyalkyl is, for example, methoxymethyl, ethoxymethyl, propoxymethyl, methoxyethyl, ethoxyethyl, propoxyethyl, methoxypropyl, ethoxypropyl or propoxypropyl.
- Alkylthioalkyl is, for example, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl or isopropylthioethyl.
- Alkylamino is, for example, methylamino, ethylamino and isomeric propyl- and butylamino.
- Cyanoalkyl is, for example, cyanomethyl, cyanoethyl or cyanopropyl.
- Halocycloalkyl is, for example, 2,2-dichlorocyclopropyl or pentachlorocyclohexyl.
- Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl or butylsulfonyl, preferably methyl- and ethyl-sulfonyl.
- Phenyl also as part of a substituent such as phenoxy, phenylthio, phenoxycarbonyl, phenylaminocarbonyl, benzyl or benzoyl, may generally be unsubstituted or substituted. In the latter case, the substituents may be in the ortho-, meta- and/or para-position. Preferred substituent positions are the ortho- and para-positions to the ring-linkage position.
- Preferred substituents are halogen atoms.
- alkoxyalkoxycarbonylalkyl alkylthioalkoxycarbonyl, haloalkoxycarbonylalkyl, alkoxyalkoxyalkyl, cycloalkylalkyl, cycloalkylalkoxycarbonylalkyl and alkoxyalkylamino, may have the same definitions as those above.
- the salts of compounds of formula I having acidic hydrogen are, for example, alkali metal salts, such as sodium and potassium salts;
- alkaline earth metal salts such as calcium and magnesium salts
- ammonium salts i.e. unsubstituted ammonium salts and mono- or poly-substituted ammonium salts, such as triethylammonium and methylammonium salts
- salts with other organic bases such as calcium and magnesium salts
- ammonium salts i.e. unsubstituted ammonium salts and mono- or poly-substituted ammonium salts, such as triethylammonium and methylammonium salts
- amines suitable for salt formation are primary, secondary and tertiary aliphatic and aromatic amines, such as methylamine, ethylamine, n-propylamine, isopropylamine, the four isomeric butylamines, n-amylamine, isoamylamine, hexylamine, heptylamine, octylamine, nonylamine, decylamine, pentadecylamine, hexadecylamine, heptadecylamine, octadecylamine, methyl-ethylamine, methyl-isopropylamine, methylhexylamine, methyl-nonylamine, methyl-pentadecylamine, methyl-octadecylamine, ethyl-butylamine, ethyl-heptylamine, ethyl-octylamine, he
- asymmetric carbon atom may be present in compounds of formula I, for example in ester and ether derivatives having substituted aliphatic and alicyclic groups, means that the compounds may occur both in the form of optically active individual isomers and in the form of racemic mixtures.
- R 4 is C 1 -C 4 alkyl substituted by C 1 -C 6 alkoxycarbonyl.
- R 1 and R 2 are halogen; R 1 is especially fluorine and R 2 is especially chlorine.
- the preferred compounds likewise include those of formula Ib
- R 19 is C 1 -C 4 alkyl, C 3 - or C 4 -alkenyl, C 3 - or C 4 -haloalkenyl, C 3 -C 6 alkynyl, C 1 -C 4 - alkoxy-C 1 -C 4 alkyl, cyano-C 1 -C 4 alkyl, C 1 -C 6 alkoxycarbonyl-C 1 -C 4 alkyl, C 3 -C 6 - cycloalkyl, C 3 -C 6 cycloalkyl-C 1 -C 4 alkyl, benzyl, di-C 1 -C 4 alkylamino-C 1 -C 4 alkyl, C 1 -C 4 alkylaminocarbonyl-C 1 -C 4 alkyl, di-C 1 -C 4 alkylaminocarbonyl-C 1 -C 4 alkyl, C 1 -C 4 alkoxycarbonyl or C 1 -C 4 alky
- R 19 is C 1 -C 3 alkyl, C 1 -C 3 alkoxycarbonyl-C 1 - or -C 2 -alkyl or C 3 - or C 4 -alkynyl;
- R 22 is hydrogen or fluorine
- R 50 is hydrogen
- n 2 is 0 or 1.
- reaction of an isothiocyanate of formula II with a compound of formula III is advantageously carried out in an inert organic solvent at temperatures of from -5°C to the boiling temperature of the solvent, especially from 0 to +50°C, preferably at room temperature.
- suitable solvents for that reaction are toluene, xylenes, ethyl acetate and acetonitrile.
- reaction of a compound of formula IN with a compound of formula N is advantageously carried out in an inert organic solvent at low temperatures, preferably at from 0 to +50°C, especially at from 0 to +15°C.
- bases suitable for that reaction are pyridine, triethylamine and ⁇ , ⁇ -dimethylaniline.
- Suitable solvents are, for example, 1,2-dichloroethane, dichloromethane and toluene.
- formulae VI, Via and VIb are each an unbranched aliphatic pentane chain having a hydroxy group (VI) or an R 0 SO 2 O group (VIb) or bromine (VIa) bonded to each of its terminal carbon atoms C 1 and C 5 .
- the radical R can be linked 0, 1 , 2, 3 or 4 times to all of the 5 carbon atoms of the n-pentane chain, where appropriate also geminally.
- the isothiocyanates of formula II are known or can be prepared analogously to known processes. Such compounds are described, for example, in EP-A-0304920,
- EP-A-0238 711 EP-A-0409 025, EP-A-0 373461, EP-A-0 311 135 and
- any of the methods of application customary in agriculture such as preemergence application, postemergence application and seed dressing, as well as various methods and techniques, such as the controlled release of active ingredient
- the compound is applied in solution to mineral granule carriers or polymerised granules (urea/formaldehyde) and dried.
- a coating coated granules which allows the active ingredient to be released in metered amounts over a specific period.
- the compounds of formula I can be used in unmodified form, i.e. as obtained during synthesis, but are preferably formulated in customary manner together with the adjuvants conventionally employed in formulation technology, e.g. into emulsifiable concentrates, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granules and microcapsules.
- the methods of application such as spraying, atomising, dusting, wetting, scattering or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances.
- compositions, preparations or mixtures comprising the compound (active ingredient) of formula I or at least one compound of formula I and, where appropriate, one or more solid or liquid adjuvants, are prepared in known manner, e.g. by homogeneously mixing and/or grinding the active ingredients with the adjuvants, e.g. solvents or solid carriers.
- adjuvants e.g. solvents or solid carriers.
- Surface-active compounds surfactants may additionally be used in the preparation of the formulations.
- Suitable solvents are: aromatic hydrocarbons, preferably the fractions containing 8 to 12 carbon atoms, such as mixtures of alkylbenzenes, e.g. xylene mixtures or alkylated naphthalenes; aliphatic and cycloaliphatic hydrocarbons such as paraffins, cyclohexane or tetrahydronaphthalene; alcohols, such as ethanol, propanol or butanol; glycols and their ethers and esters, such as propylene glycol or dipropylene glycol ether, ketones such as cyclohexanone, isophorone or diacetone alcohol, strongly polar solvents such as
- N-methyl-2-pyrrolidone dimethyl sulfoxide or water
- vegetable oils and their esters such as rape oil, castor oil or soybean oil
- silicone oils such as rape oil, castor oil or soybean oil
- the solid carriers used e.g. for dusts and dispersible powders are normally natural mineral fillers, such as calcite, talcum, kaolin, montmorillonite or attapulgite.
- Suitable granulated adsorptive carriers are porous types, for example pumice, broken brick, sepiolite or bentonite; and suitable non-sorbent carriers are, for example, calcite or sand.
- a great number of pregranulated materials of inorganic or organic nature can be used, such as especially dolomite or pulverised plant residues.
- suitable surface-active compounds are non-ionic, cationic and/or anionic surfactants having good emulsifying, dispersing and wetting properties.
- surfactants will also be understood as comprising mixtures of surfactants.
- Suitable soaps are the alkali metal salts, alkaline earth metal salts or unsubstituted or substituted ammonium salts of higher fatty acids (C 10 -C 22 ), e.g. the sodium or potassium salts of oleic or stearic acid, or of natural fatty acid mixtures which can be obtained e.g. from coconut oil or tallow oil; mention may also be made of fatty acid methyltaurin salts.
- fatty alcohol sulfonates especially fatty alcohol sulfonates, fatty alcohol sulfates, sulfonated benzimidazole derivatives or alkylarylsulfonates.
- the fatty alcohol sulfonates or sulfates are usually in the form of alkali metal salts, alkaline earth metal salts or unsubstituted or substituted ammonium salts and contain a C 8 -C 22 alkyl radical, which also includes the alkyl moiety of acyl radicals, for example the sodium or calcium salt of lignosulfonic acid, of dodecyl sulfate or of a mixture of fatty alcohol sulfates obtained from natural fatty acids.
- These compounds also comprise the salts of sulfated and sulfonated fatty alcohol/ethylene oxide adducts.
- the sulfonated benzimidazole derivatives preferably contain 2 sulfonic acid groups and one fatty acid radical containing 8 to 22 carbon atoms.
- alkylarylsulfonates are the sodium, calcium or triethanolamine salts of dodecylbenzenesulfonic acid, dibutylnaphthalenesulfonic acid or of a condensate of naphthalenesulfonic acid and formaldehyde.
- corresponding phosphates e.g. salts of the phosphoric acid ester of an adduct of p-nonylphenol with 4 to 14 mol of ethylene oxide, or phospholipids.
- Non-ionic surfactants are preferably polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, saturated or unsaturated fatty acids and alkylphenols, it being possible for said derivatives to contain 3 to 30 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon moiety and 6 to 18 carbon atoms in the alkyl moiety of the alkylphenols.
- non-ionic surfactants are water-soluble adducts of polyethylene oxide with polypropylene glycol, ethylenediaminopolypropylene glycol and alkylpolypropylene glycol containing 1 to 10 carbon atoms in the alkyl chain, which adducts contain 20 to 250 ethylene glycol ether groups and 10 to 100 propylene glycol ether groups. These compounds usually contain 1 to 5 ethylene glycol units per propylene glycol unit
- non-ionic surfactants are nonylphenol polyethoxyethanols, castor oil polyglycol ethers, polypropylene/polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethylene glycol and octylphenoxypolyethoxyethanol.
- Fatty acid esters of polyoxyethylene sorbitan e.g. polyoxyethylene sorbitan trioleate, are also suitable non-ionic surfactants.
- Cationic surfactants are preferably quaternary ammonium salts which contain, as
- the salts are preferably in the form of halides, methyl sulfates or ethyl sulfates, for example stearyltrimethylammonium chloride or benzyldi(2-chloroethyl)ethylammonium bromide.
- the herbicidal compositions usually comprise 0.1 to 99 %, preferably 0.1 to 95 %, of a compound of formula 1, 1 to 99 % of a solid or liquid adjuvant, and 0 to 25 %, preferably 0.1 to 25 %, of a surfactant
- compositions may also comprise further ingredients such as stabilisers, e.g. vegetable oils and epoxidised vegetable oils (epoxidised coconut oil, rape oil or soybean oil), anti-foams, e.g. silicone oil, preservatives, viscosity regulators, binders and tackifiers, as well as fertilisers or other active ingredients for obtaining special effects.
- stabilisers e.g. vegetable oils and epoxidised vegetable oils (epoxidised coconut oil, rape oil or soybean oil)
- anti-foams e.g. silicone oil
- preservatives e.g. silicone oil
- viscosity regulators e.g. binders and tackifiers
- fertilisers or other active ingredients for obtaining special effects.
- Preferred formulations have especially the following composition (throughout, percentages are by weight)
- Emulsifiable concentrates are:
- active ingredient 1 to 90%, preferably 5 to 50%
- surfactant 5 to 30%, preferably 10 to 20%
- liquid carrier 15 to 94%, preferably 70 to 85%
- active ingredient 0.1 to 50%, preferably 0.1 to 1%
- solid carrier 99.9 to 90%, preferably 99.9 to 99%
- active ingredient 5 to 75%, preferably 10 to 50%
- active ingredient 0.5 to 90%, preferably 1 to 80%
- surfactant 0.5 to 20%, preferably 1 to 15%
- solid carrier 5 to 95%, preferably 15 to 90%
- active ingredient 0.1 to 30%, preferably 0.1 to 15%
- solid carrier 99.5 to 70%, preferably 97 to 85%
- the compounds of formula I are generally used successfully at rates of application of from 0.001 to 2 kg/ha, especially from 0.005 to 1 kg/ha.
- concentration required to achieve the desired effect can be determined by experiment It is dependent upon the type of action, the stage of development of the crop plant and of the weed, and also upon the application (place, time, method) and, in dependence on those parameters, can vary within wide limits.
- the compounds of formula I are distinguished by growth-inhibiting and herbicidal properties that make them outstandingly suitable for use in crops of useful plants, especially in cereals, maize, rape, soybeans, rice and cotton.
- Crops are also to be understood as being those which have been rendered tolerant to herbicides or classes of herbicide by conventional methods of breeding or by genetic techniques.
- Example P1 Preparation of 3-trifluoromethyl-1,5-pentanediol (intermediate)
- reaction mixture is then stirred for 16 hours at that temperature, then poured onto ice-water and filtered to yield 4.4 g of the desired 1,2-dicarboxylic acid di-tert-butyl5-trifluoromethyl-1,2-diazacycloheptane having a melting point of 98-100°C.
- Emulsifiable concentrates a) b) c) d) a compound of Tables 1-16 5% 10% 25% 50% calcium dodecylbenzene- 6% 8% 6% 8%sulfonate
- Emulsions of any desired concentration can be produced from such concentrates by dilution with water.
- Wettable powders a) b) c) d) a compound of Tables 1-16 5 % 25 % 50 % 80 % sodium lignosulfonate 4 % - 3 % - sodium lauryl sulfate 2 % 3 % - 4 % sodium diisobutylnaphthalene - 6 % 5 % 6 % sulfonate
- the active ingredient is thoroughly mixed with the adjuvants and the mixture is thoroughly ground in a suitable mill, affording wettable powders which can be diluted with water to give suspensions of the desired concentration.
- the active ingredient is dissolved in methylene chloride, the solution is sprayed onto the carrier, and the solvent is subsequently evaporated off in vacuo.
- the active ingredient is mixed and ground with the adjuvants, and the mixture is moistened with water.
- the mixture is extruded and then dried in a stream of air.
- Ready-for-use dusts are obtained by mixing the active ingredient with the carriers and grinding the mixture in a suitable mill.
- the finely ground active ingredient is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired concentration can be obtained by dilution with water.
- Monocotyledonous and dicotyledonous test plants are sown in plastic pots containing standard soil and, immediately after sowing, are sprayed with an aqueous suspension of the test compounds, prepared from a 25 % wettable powder formulation (Formulation example F3 b)), corresponding to a rate of application of 2 kg of active ingredient/hectare (5001 of water/ha).
- Test plants Avena, Lolium, Setaria, Sinapis, Solanum, Stellaria.
- Monocotyledonous and dicotyledonous test plants are raised in a greenhouse in plastic pots containing standard soil and in the 4- to 6-leaf stage are sprayed with an aqueous suspension of the test compounds of formula I, prepared from a 25 % wettable powder formulation (Formulation example F3 b)), corresponding to a rate of application of 2 kg of active ingredient/hectare (5001 of water/ha).
- Test plants Avena, Lolium, Setaria, Sinapis, Solanum, Stellaria
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Abstract
Description
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP94918863A EP0705267B1 (en) | 1993-06-23 | 1994-06-10 | Herbicidal thiadiazabicyclodecanes |
DE69404995T DE69404995T2 (en) | 1993-06-23 | 1994-06-10 | HERBICIDE THIADIAZABICYCLODEKANE |
JP7502388A JPH09500373A (en) | 1993-06-23 | 1994-06-10 | Herbicidal thiadia zabicyclodecane |
BR9406971A BR9406971A (en) | 1993-06-23 | 1994-06-10 | Thiadiazabicyclodecanes herbicides |
US08/569,071 US5817602A (en) | 1993-06-23 | 1994-06-10 | Herbicidal thiadiazabicyclodecanes |
AU70002/94A AU7000294A (en) | 1993-06-23 | 1994-06-10 | Herbicidal thiadiazabicyclodecanes |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1888/93-6 | 1993-06-23 | ||
CH188893 | 1993-06-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1995000521A1 true WO1995000521A1 (en) | 1995-01-05 |
Family
ID=4220951
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1994/001893 WO1995000521A1 (en) | 1993-06-23 | 1994-06-10 | Herbicidal thiadiazabicyclodecanes |
Country Status (9)
Country | Link |
---|---|
US (1) | US5817602A (en) |
EP (1) | EP0705267B1 (en) |
JP (1) | JPH09500373A (en) |
AU (1) | AU7000294A (en) |
BR (1) | BR9406971A (en) |
CA (1) | CA2165196A1 (en) |
DE (1) | DE69404995T2 (en) |
ES (1) | ES2107233T3 (en) |
WO (1) | WO1995000521A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995021174A1 (en) * | 1994-02-04 | 1995-08-10 | Ciba-Geigy Ag | Phenylimino-thiadiazabicycloalkane derivatives, processes and intermediates for their preparation and their use as herbicides |
WO2000019416A2 (en) | 1998-09-29 | 2000-04-06 | Tdk Electronics Corporation | Removable media recording station for the medical industry |
US6060432A (en) * | 1995-10-25 | 2000-05-09 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
WO2002024709A2 (en) * | 2000-09-22 | 2002-03-28 | Syngenta Participations Ag | Bicycloderivatives as herbicides |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0238711A1 (en) * | 1986-03-25 | 1987-09-30 | Kumiai Chemical Industry Co., Ltd. | Thiadiazabicyclononane derivatives, processes for their production and herbizidal compositions |
EP0273417A1 (en) * | 1986-12-24 | 1988-07-06 | Kumiai Chemical Industry Co., Ltd. | Thiadiazabicyclononane derivatives and herbicidal compositions |
EP0304920A2 (en) * | 1987-08-28 | 1989-03-01 | Nissan Chemical Industries Ltd. | Condensed heterocyclic derivatives, process for their production and herbicides |
US4885023A (en) * | 1986-12-24 | 1989-12-05 | Kumiai Chemical Industry Co., Ltd. | Thiadiazabicyclononane derivatives and herbicidal compositions |
JPH05213970A (en) * | 1992-02-03 | 1993-08-24 | Kumiai Chem Ind Co Ltd | Condensed heterocyclic ring derivative and herbicide |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59212472A (en) * | 1983-05-16 | 1984-12-01 | Sumitomo Chem Co Ltd | 4,5,6,7-tetrahydro-2h-isoindole-1,3-dione derivative, its production and herbicide containing the same as active constituent |
-
1994
- 1994-06-10 EP EP94918863A patent/EP0705267B1/en not_active Expired - Lifetime
- 1994-06-10 CA CA002165196A patent/CA2165196A1/en not_active Abandoned
- 1994-06-10 JP JP7502388A patent/JPH09500373A/en active Pending
- 1994-06-10 AU AU70002/94A patent/AU7000294A/en not_active Abandoned
- 1994-06-10 US US08/569,071 patent/US5817602A/en not_active Expired - Fee Related
- 1994-06-10 BR BR9406971A patent/BR9406971A/en not_active Application Discontinuation
- 1994-06-10 WO PCT/EP1994/001893 patent/WO1995000521A1/en active IP Right Grant
- 1994-06-10 DE DE69404995T patent/DE69404995T2/en not_active Expired - Fee Related
- 1994-06-10 ES ES94918863T patent/ES2107233T3/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0238711A1 (en) * | 1986-03-25 | 1987-09-30 | Kumiai Chemical Industry Co., Ltd. | Thiadiazabicyclononane derivatives, processes for their production and herbizidal compositions |
EP0273417A1 (en) * | 1986-12-24 | 1988-07-06 | Kumiai Chemical Industry Co., Ltd. | Thiadiazabicyclononane derivatives and herbicidal compositions |
US4885023A (en) * | 1986-12-24 | 1989-12-05 | Kumiai Chemical Industry Co., Ltd. | Thiadiazabicyclononane derivatives and herbicidal compositions |
EP0304920A2 (en) * | 1987-08-28 | 1989-03-01 | Nissan Chemical Industries Ltd. | Condensed heterocyclic derivatives, process for their production and herbicides |
JPH05213970A (en) * | 1992-02-03 | 1993-08-24 | Kumiai Chem Ind Co Ltd | Condensed heterocyclic ring derivative and herbicide |
Non-Patent Citations (3)
Title |
---|
C.G. OVERBERGER ET AL, THE JOURNAL OF ORGANIC CHEMISTRY, vol. 46, no. 2, 16 January 1981 (1981-01-16), pages 442 - 446 * |
CHEMICAL ABSTRACTS, vol. 120, no. 1, 3 January 1994, Columbus, Ohio, US; abstract no. 2802h, page 333; column R; * |
CHEMICAL ABSTRACTS, vol. 86, no. 5, 31 January 1977, Columbus, Ohio, US; abstract no. 29859y, page 375; column L; * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995021174A1 (en) * | 1994-02-04 | 1995-08-10 | Ciba-Geigy Ag | Phenylimino-thiadiazabicycloalkane derivatives, processes and intermediates for their preparation and their use as herbicides |
US6060432A (en) * | 1995-10-25 | 2000-05-09 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
WO2000019416A2 (en) | 1998-09-29 | 2000-04-06 | Tdk Electronics Corporation | Removable media recording station for the medical industry |
WO2002024709A2 (en) * | 2000-09-22 | 2002-03-28 | Syngenta Participations Ag | Bicycloderivatives as herbicides |
WO2002024709A3 (en) * | 2000-09-22 | 2002-06-27 | Syngenta Participations Ag | Bicycloderivatives as herbicides |
Also Published As
Publication number | Publication date |
---|---|
US5817602A (en) | 1998-10-06 |
CA2165196A1 (en) | 1995-01-05 |
ES2107233T3 (en) | 1997-11-16 |
BR9406971A (en) | 1996-03-26 |
DE69404995T2 (en) | 1998-01-15 |
DE69404995D1 (en) | 1997-09-18 |
AU7000294A (en) | 1995-01-17 |
EP0705267A1 (en) | 1996-04-10 |
JPH09500373A (en) | 1997-01-14 |
EP0705267B1 (en) | 1997-08-13 |
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