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
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
  • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
  • A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
  • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
  • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
  • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D249/12—Oxygen or sulfur atoms

Definitions

• the invention relates to new substituted arylsulfonylamino (thio) carbonyl-triazolin- (thi) one, several processes for their preparation and their use as
• Q 2 represents oxygen or sulfur
• R 1 stands for hydrogen, amino or for optionally substituted alkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkenyl, alkynyl or alkylidene amino
• R 2 stands for hydrogen or for optionally substituted alkyl, alkylcarbonyl, alkoxycarbonyl, alkylsulfonyl, alkenyl , or alkynyl, or together with R 1 represents optionally interrupted by oxygen and / or optionally substituted alkanediyl,
• R 3 represents hydrogen, cyano, nitro, halogen or optionally substituted alkyl, alkylcarbonyl or alkoxycarbonyl
• R 4 represents hydrogen, hydroxy, amino, alkylidene amino or an optionally substituted radical from the series alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkylamino, dialkylamino, cycloalkyl, cycloalkylalkyl, cycloalkylamino, aryl, arylalkyl
• R 3 represents hydrogen , Hydroxy, mercapto, amino, cyano, halogen or for an optionally substituted radical from the series alkyl, alkoxy, alkylthio, alkylamino, dialkylamino, alkenyl, alkynyl, alkenyloxy, alkynyloxy, alkenylthio, alkynylthio, alkenylamino, alkynylamino,
• Q 1 , Q 2 , R 4 and R 5 have the meaning given above and Z represents halogen, alkoxy, aralkoxy or aryloxy, with sulfonamides of the general formula (V)
• R 1 , R 2 and R 3 have the meaning given above, if appropriate in the presence of an acid acceptor and if appropriate in the presence of a diluent, or if
• Z represents halogen, alkoxy, aralkoxy or aryloxy, if appropriate in the presence of an acid acceptor and if appropriate in the presence of a diluent, or if
• R 1 , R 2 and R 3 have the meaning given above and X represents halogen, and metal (thio) cyanates of the general formula (VIII) MQ 2 CN (VIII) in which
• Q 2 has the meaning given above and M represents an alkali metal or alkaline earth metal equivalent, if appropriate in the presence of a reaction auxiliary and if appropriate in the presence of a diluent, and if appropriate the processes (a), (b), (c) or (d ) compounds of the formula (I) obtained converted into salts by customary methods.
• the new substituted arylsulfonylamino (thio) carbonyl-triazolinones of the general formula (I) are notable for strong herbicidal activity.
• the invention preferably relates to compounds of the formula (I) in which
• Q 1 represents oxygen or sulfur
• Q 2 represents oxygen or sulfur
• R 1 for hydrogen, amino, for each optionally substituted by cyano, halogen or C 1 -C 4 alkoxy-substituted alkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl, alkylthio, alkylsulfinyl or alkylsulfonyl each having 1 to 6 carbon atoms in the alkyl groups, or for each optionally alkenyl, alkynyl or alkylidene amino substituted by cyano or halogen, each having 2 to 6 carbon atoms,
• R 2 for hydrogen, for alkyl, alkylcarbonyl, alkoxycarbonyl or alkylsulfonyl, each optionally substituted by cyano, halogen or C 1 -C 4 -alkoxy, each having 1 to 6 carbon atoms in the alkyl groups, for alkenyl or alkynyl optionally substituted by cyano or halogen each has 2 to 6 carbon atoms, or together with R 1 represents alkanediyl having 2 to 6 carbon atoms which is optionally interrupted by oxygen and / or optionally substituted by halogen or C 1 -C 4 alkyl,
• R 3 represents hydrogen, cyano, nitro, halogen or alkyl, alkylcarbonyl or alkoxycarbonyl, each optionally substituted by halogen, each having 1 to 6 carbon atoms in the alkyl groups,
• R 4 for hydrogen, hydroxy, amino, C 1 -C 6 alkylidene amino, for optionally by fluorine, chlorine, bromine, cyano, C 1 -C 4 alkoxy, C 1 -C 4 alkylcarbonyl or C 1 -C 4 - Alkoxy-carbonyl substituted C 1 -C 6 alkyl, for each optionally substituted by fluorine, chlorine and / or bromine substituted C 2 -C 6 alkenyl or C 2 -C 6 alkynyl, for C 1 -C 6 alkyloxy or C 3 -C 6 - alkenyloxy, each for C 1 -C 6 alkylamino, di- (C 1 -C 4 alkyl) amino or C 1 -C 4 alkanoylamino optionally substituted by fluorine and / or chlorine, for each optionally by fluorine, chlorine, bromine and / or C 1 -C 4 alkyl-substituted C 3 -C 6
• R 5 for hydrogen, hydroxy, mercapto, amino, cyano, halogen, each optionally substituted by cyano, halogen or C 1 -C 4 alkoxy Alkyl, alkoxy, alkylthio, alkylamino or dialkylamino each having 1 to 6 carbon atoms in the alkyl groups, for alkenyl, alkynyl, alkenyloxy, alkynyloxy, alkenylthio, alkynylthio, alkenylamino or alkynylamino each having 2 to 6 carbon atoms each optionally substituted by cyano or halogen in each case optionally by cyano,
• the invention further preferably relates to sodium, potassium, magnesium, calcium, ammonium, C 1 -C 4 alkylammonium, di (C 1 -C 4 alkyl) ammonium, tri ( C 1 -C 4 alkyl) ammonium, tetra (C 1 -C 4 alkyl]) ammonium, tri (C 1 -C 4 alkyl) sulfonium, C 5 or C 6 Cycloalkylammonium and di (C 1 -C 2 alkyl) benzylammonium salts of compounds of formula (I) in which Q 1 , Q 2 , R 1 , R 2 , R 3 , R 4 and R have the meanings preferably given above.
• the invention relates in particular to compounds of the formula (I) in which
• Q 1 represents oxygen or sulfur
• Q 2 represents oxygen or sulfur
• R 1 for hydrogen, for each methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i- substituted by cyano, fluorine, methoxy or ethoxy Propoxy, acetyl, propionyl, n- or i-
• R 3 represents hydrogen, cyano, nitro, fluorine, chlorine, bromine or methyl, ethyl, n- or i-propyl which is optionally substituted by fluorine,
• R 4 for hydrogen, for each methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl optionally substituted by fluorine, chlorine, cyano, methoxy or ethoxy, for each optionally by fluorine, chlorine or bromine-substituted propenyl, butenyl, propynyl or butynyl, for methoxy,
• R 5 for hydrogen, hydroxyl, mercapto, amino, fluorine, chlorine, bromine, for methyl, ethyl, n- or i-propyl, n-, i-, s-, each optionally substituted by fluorine, chlorine, cyano, methoxy or ethoxy or t-butyl,
• Alkenyl or alkynyl, also in combinations with heteroatoms, such as in alkoxy, alkylthio or alkylamino, are straight-chain or branched, even if this is not expressly stated.
• Halogen generally represents fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine, in particular fluorine or chlorine.
• reaction sequence in process (b) according to the invention can be outlined using the following formula
• triazolin (thi) ones of the general formula (II) are known and / or can be prepared by processes known per se (cf. Arch. Pharm. 301 (1968), 827; loc. Cit. 307 (1974), 889; Bull. Soc. Chim. France 1962, 1365; loc. Cit. 1975, 1 191; Chem. Ber. 90 (1957), 909-921; loc. Cit. 98 (1965), 3025-3099; loc. Cit. 102 (1969), 755; J. Heterocycl. Chem. 15 (1978), 237-240; J. Indian Chem. Soc. 6 (1929), 565; Liebig Ann. Chem.
• EP-A 503 437 EP-A 505 819; EP-A 51 1 569; EP-A 513 621; DE-A 23 36 827; DE-A 38 39 206; DE-A 39 16 208; DE-A 39 16 930; DD-P 64 970; WO-A 93/04050).
• Formula (III) provides a general definition of the sulfonyliso (thio) cyanates to be used as starting materials in process (a) according to the invention for the preparation of compounds of the formula (I).
• Q 2 , R 1 , R 2 and R 3 preferably or in particular have those meanings which are preferred or particularly preferred for Q 2 in connection with the description of the compounds of the formula (I) according to the invention , R 1 , R 2 and R 3 were specified.
• the starting materials of the formula (III) are known and / or can be prepared by processes known per se (cf. EP 385 775, DE 43 22 067, production examples).
• Derivatives are generally defined by the formula (IV).
• Q 1 , Q 2 , R 4 and R 5 preferably or in particular have those meanings which have already been mentioned above in connection with the description of the compounds of Formula (I) has been indicated as preferred or as particularly preferred for Q 1 , Q 2 , R 4 and R 5 , Z preferably represents fluorine, chlorine, bromine, methoxy, ethoxy, benzyloxy, phenoxy, halogeno- or nitrophenoxy, especially for methoxy, phenoxy or 4-nitro-phenoxy.
• the starting materials of the formula (IV) are known and / or can be prepared by processes known per se (cf. EP 341 489, EP 422 469, EP 425 948, EP 431 291, EP 507 171, EP 534 266)
• Formula (I) sulfonic acid amide derivatives to be used as starting materials are generally defined by the formula (VI).
• Q 2 , R 1 , R 2 and R 3 preferably or in particular have those meanings which have already been mentioned above in connection with the description of the compounds of the formula (I) has been given as preferred or as particularly preferred for Q 2 , R 1 , R 2 and R 3 , Z preferably represents fluorine, chlorine, bromine, methoxy, ethoxy, benzyloxy or phenoxy, especially for methoxy or phenoxy
• Formula (I) sulfonic acid halides to be used as starting materials are by the formula (VII) generally defined
• R 1 , R 2 and R 3 preferably or in particular have those meanings which have already been mentioned above in connection with the description of the compounds of the formula (I) as preferred or as particularly preferred for R 1 , R 2 and R 3 have been specified
• X preferably represents fluorine, chlorine or bromine, in particular chlorine
• the starting materials of the formula (VII) are known and / or can be prepared by processes known per se
• These preferably include aliphatic and aromatic, optionally halogenated hydrocarbons such as pentane, hexane, heptane, cyclohexane, petroleum ether, gasoline, ligroin, benzene, toluene, xylene, methylene chloride, ethylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, ethers such as Diethyl and dibutyl ether, glycol dimethyl ether and diglycol dimethyl ether, tetrahydrofuran and dioxane, ketones such as acetone, methyl ethyl, methyl isopropyl and methyl isobutyl ketone, esters such as methyl acetate and ethyl acetate, nitriles such as acetonitrile and propio- nitrile, amides such as dimethylformamide, dimethylacet
• Suitable reaction auxiliaries or acid acceptors in the processes (a), (b), (c) and (d) according to the invention are all acid binders which can usually be used for such reactions.
• Alkali metal hydroxides such as sodium and potassium hydroxide, alkaline earth metal hydroxides are preferred such as calcium hydroxide, alkali carbonates and alcoholates such as sodium and potassium carbonate, sodium and potassium tert-butoxide, also basic nitrogen compounds such as trimethylamine, triethylamine, tripropylamine, t ⁇ butylamine, diisobutylamine, dicyclohexylamine, ethyldiisopropylamine, ethyldicyclohexylhexyl N-dimethylbenzylamine, N, N-dimethyl-an ⁇ l ⁇ n, py ⁇ din, 2-methyl, 3-
• temperatures between -20 ° C and + 100 ° C, preferably at temperatures between 0 ° C and + 80 ° C.
• Processes (a), (b), (c) and (d) according to the invention are generally carried out under atmospheric pressure. However, it is also possible to work under increased or reduced pressure.
• the starting materials required in each case are generally used in approximately equimolar amounts. However, it is also possible to use one of the respectively used
• salts can be prepared from the compounds of the general formula (I) according to the invention.
• Such salts are obtained in a simple manner by customary salt formation methods, for example by dissolving or dispersing a compound of the formula (I) in a suitable solvent, such as e.g. Methylene chloride, acetone, tert-butyl methyl ether or toluene, and addition of a suitable base.
• a suitable solvent such as e.g. Methylene chloride, acetone, tert-butyl methyl ether or toluene
• the salts can then be isolated - if appropriate after prolonged stirring - by concentration or suction.
• the active compounds according to the invention can be used as defoliants, desiccants, haulm killers and in particular as weed killers
• the active compounds according to the invention can be used, for example, in the following plants: Dicotyledonous weeds of the genera: Sinapis, Lepidium, Galium, Stellaria, Matricaria, Anthemis, Galinsoga, Chenopodium, Urtica, Senecio, Amaranthus, Portulaca, Xanthium, Convolvulus, Ipomoea, Polygonum, Sesbania, Ambrosia, Cirsium, Carduippum, Sonuanum , Rotala, Lindernia, Lamium, Veronica, Abutilon, Emex, Datura, Viola, Galeopsis, Papaver, Centaurea,
• Trifolium Ranunculus, Taraxacum.
• the use of the active compounds according to the invention is by no means restricted to these genera, but extends in the same way to other plants.
• the compounds are suitable for total weed control, e.g. on industrial and track systems and on paths and squares with and without tree cover.
• the compounds for weed control in permanent crops e.g. Forest, ornamental wood, fruit, wine, citrus, nut, banana, coffee, tea, rubber, oil palm, cocoa, berry fruit and hop plants, on ornamental and sports turf and pasture land and for selective purposes
• Weed control can be used in annual crops.
• the compounds of formula (I) according to the invention are particularly suitable for the selective control of monocotyledon and dicotyledon weeds in monocotyledon crops both in the pre-emergence and in the post-emergence process.
• the active ingredients can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, soluble powders, granules, suspension emulsion concentrates, active ingredient-impregnated natural and synthetic substances and very fine encapsulations in polymeric substances
• formulations are prepared in a known manner, for example by mixing the active ingredients with extenders, that is to say liquid solvents and / or solid carriers, optionally using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
• organic solvents can also be used as auxiliary solvents.
• Suitable liquid solvents are essentially aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chlorethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example 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
• Solid carrier materials that come into question are, for example, ammonium salts and natural rock powders such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock powders such as highly disperse silica, aluminum oxide and silicates B broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite as well as synthetic granules from inorganic and organic flours as well as granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stalks, as emulsifiers and / or foam-generating agents are possible
• B nonionic and anionic emulsifiers such as polyoxyethylene
• Fatty acid esters for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolyzates, as Dispersants come into question, for example lignin sulfite waste liquor and methyl cellulose
• Adhesives such as carboxymethyl cellulose, natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids, such as cephalins and lecithins and synthetic phospholipids, can be used in the formulations.
• Other additives can be mineral and vegetable oils
• Dyes such as inorganic pigments, e.g. iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper,
• Cobalt, molybdenum and zinc can be used
• the formulations generally contain between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%
• the active compounds according to the invention can also be used in a mixture with known herbicides for weed control, finished formulations or tank mixes being possible
• herbicides are suitable for the mixtures, for example anilides, such as, for example, diflufenican and propanil, arylcarboxylic acids, such as, for example, dichloropicolinic acid, dicamba and picloram; Aryloxy alkanoic acids, such as, for example, 2,4-D, 2,4-DB, 2,4-DP, fluroxypyr, MCPA, MCPP and tnclopyr, aryloxy-phenoxy-alkanoic acid esters, such as, for example, diclofop-methyl, fenoxaprop-ethyl, fluazifop butyl, haloxyfopmethyl and quizalofop-ethyl, azinones, such as, for example, chloridazon and norflurazon, carbamates, such as, for example, chlorpropham, desmedipham, phenmedipham and propham, chloroacetanilides, such as, for example, alachlor,
• Pendimethalin and trifluralin Diphenyl ethers, such as, for example, acifluorfen, bifenox, fluoroglycofen, fomesafen, halosafen, lactofen and oxyfluorfen, ureas, such as, for example, chlorotoluron, diuron, fluometuron, isoproturon, linuron and methabenzthiazuron, hydroxylamines, such as, for example, alloxydoxydimim, clethodim, alkoxydimim, clethodim , Imidazohnones such as imazethapyr, imazamethabenz, imazapyr and imazaqum, nitriles such as bromoxynil, dichlobemi and ioxynil, oxyacetamides such as mefenacet, sulfonylureas such as Amidosulfuron, bensulfuron-methyl
• Triazinones e.g. Hexazinone, metamitron and metribuzin
• Others such as Aminotriazole, Benfuresate, Bentazone, Cinmethylin, Clomazone, Clopyralid, Difenzoquat, Dithiopyr, Ethofumesate, Fluorochloridone, Glufosinate, Glyphosate, Isoxaben, Pyridate, Quinchlorac, Quinmerac, Sulphosate and Tridiphane.
• a mixture with other known active compounds such as fungicides, insecticides, acaricides, nematicides, bird repellants, plant nutrients and agents which improve soil structure, is also possible.
• Solutions, suspensions, emulsions, powders, pastes and granules are used. They are used in the usual way, e.g. by pouring, spraying, spraying, sprinkling.
• the active compounds according to the invention can be applied both before and after emergence of the plants. You can also sow before sowing
• the amount of active ingredient used can vary over a wide range. It essentially depends on the type of effect desired. In general, the application rates are between 1 g and 10 kg of active ingredient per hectare of soil, preferably between 5 g and 2 kg per ha.
• Step 1
• Emulsifier 1 part by weight of alkylaryl polyglycol ether
• active compound 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration. Seeds of the test plants are sown in normal soil. This soil is sprayed with the active ingredient preparation after 24 hours. The amount of water per unit area is expediently kept constant. The concentration of active substance in the preparation is irrelevant, the only decisive factor is the amount of active substance applied per unit area. After three weeks, the degree of damage to the plants is rated in%
• Production example 3 23, 49, 50, 60 and 68 with partially good compatibility with crop plants, such as Wheat and corn, strong activity against weeds (see Tables A-1 to A-5).
• Emulsifier 1 part by weight of alkylaryl polyglycol ether To produce a suitable preparation of active compound, mix 1
• Test plants with a height of 5-15 cm are sprayed with the active substance preparation, so that the respectively desired quantities of active substance are applied per unit area.
• the concentration of the spray mixture is chosen so that the respectively desired quantities of active substance are applied in 1000 l of water / ha.
• the degree of damage to the plants is rated in% damage compared to the development of the untreated control. Mean it.
• the compound according to the invention according to preparation example 71 shows a strong action against weeds (cf. Table B).
• Table B Post emergence test / greenhouse

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Dentistry (AREA)
• Pest Control & Pesticides (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Agronomy & Crop Science (AREA)
• General Health & Medical Sciences (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Plural Heterocyclic Compounds (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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• 1996
  • 1996-03-08 DE DE19609059A patent/DE19609059A1/de not_active Withdrawn
• 1997
  • 1997-02-24 KR KR1019980706965A patent/KR19990087530A/ko not_active Application Discontinuation
  • 1997-02-24 US US09/142,272 patent/US6200934B1/en not_active Expired - Fee Related
  • 1997-02-24 WO PCT/EP1997/000878 patent/WO1997032876A1/de not_active Application Discontinuation
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  • 1997-02-24 JP JP9531405A patent/JP2000506147A/ja active Pending
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  • 1997-02-24 CA CA002248285A patent/CA2248285A1/en not_active Abandoned
  • 1997-02-24 EP EP97906119A patent/EP0888342A1/de not_active Withdrawn
• 1999
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