Derivatives of n1-sulfonyl-5-fluoropyrimidinone, composition for controlling a fungal pathogen, and

专利摘要:
n1-sulfonyl-5-fluoropyrimidinone derivatives this disclosure relates to the field of n1-sulfonyl-5-fluoropyrimidinones and their derivatives and the use of these compounds as fungicides.
公开号:BR112012002830B1
申请号:R112012002830-8
申请日:2010-08-05
公开日:2019-05-28
发明作者:Timothy Boebel；Kristy Bryan；Beth Lorsbach；Timothy Martin；W. Owen；Mark Pobanz；Scott Thornburgh；Jeffery Webster；Chenglin Yao
申请人:Adama Makhteshim Ltd.；
IPC主号:

专利说明:

Invention Patent Descriptive Report for M-SULFONYL-5-FLUOROPIRI-MIDINONE DERIVATIVES, COMPOSITION FOR THE CONTROL OF A FUNGAL PATHOGEN, AND METHOD FOR THE CONTROL OR PREVENTION OF FUNGAL ATTACK ON A PLANT.
Cross Reference to Related Orders [001] This order claims the benefit of US Provisional Patent Application Serial No. 61 / 232,204 filed on August 7, 2009.
Background and Summary of the Invention [002] Fungicides are compounds, of natural or synthetic origin, that act to protect and / or cure plants against damage caused by agriculturally relevant fungi. Generally, no single fungicide is useful in all situations. Consequently, research is underway to produce fungicides that can perform better, are easier to use, and cost less.
[003] The current description refers to N1-sulfonyl-5 fluoropyrimidinone compounds and their use as a fungicide. The compounds of the present description can offer protection against ascomycetes, basidiomycetes, deuteromycetes and oomycetes.
[004] One embodiment of the present description can include compounds of Formula I:
R ²
Formula I [005] where R ¹ is:
[006] H;
[007] C1-C6 alkyl optionally substituted with 1-3 R ⁴ ;
[008] C1-C6 alkenyl optionally substituted with 1-3 R ⁴ ;
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2/49 [009] C3-C6 alkynyl optionally substituted with 1-3 R ⁴ ;
phenyl or benzyl, each of phenyl or benzyl can optionally be replaced with 1-3 R ⁵ , or with a 5- or 6-element saturated or unsaturated ring system, or with a 5-6 fused ring system, or with a system of 6-6 fused rings each containing 1-3 heteroatoms, each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
- (CHR ⁶ ) mOR ⁷ ;
-C (= O) R ⁸ ;
-C (= S) R ⁸ ;
-C (= O) OR ⁸ ;
-C (= S) OR ⁸ ;
-S (O) 2R ⁸ ;
- (CHR ⁶ ) m N (R ⁹ ) R ¹⁰ ;
-C (= O) N (R ⁹ ) R ¹⁰ ; or -C (= S) N (R ⁹ ) R ¹⁰ ;
where m is an integer of 1-3;
[0010] R ² is:
[0011] H; or [0012] C1-C6 alkyl optionally substituted with R ⁴ ;
alternatively, R ¹ and R ² can be taken together to form = CR ¹¹ N (R ¹² ) R ¹³ ;
[0013] R ³ is -S (O) 2R ¹⁴ ;
[0014] R ⁴ is independently halogen, C1-C6 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 haloalkylthio, amino, halo, C1-C3 alkylamino, C2- C6 alkoxycarbonyl, C2-C6 alkylcarbonyl, C2-C6 alkylaminocarbonyl, hydroxyl, or C3-C6 trialkylsilyl;
[0015] R ⁵ is independently halogen, C1-C6 alkyl, C1-C6 ha
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3/49 loalkyl, Ci-Ce alkoxy, Ci-Ce haloalkoxy, Ci-Ce alkylthio, Ci-Ce haloalkylthio, halothio, amino, Ci-Ce alkylamino, C ₂ -Ce dialkylamino, C ₂ -Ce alkoxycarbonyl, Ci-Ce alkylsulfonyl or C2-Ce alkylcarbonyl, nitro, hydroxyl, or cyano;
[OOie] R ^e is H, Ci-Ce alkyl, Ci-Ce alkoxy, phenyl or benzyl, each of benzyl or phenyl being optionally substituted with i-3 R ⁵ ;
[00i7] R ⁷ is H, Ci-Ce alkyl, C2-Ce alkenyl, C3-Ce alkynyl, Ci-Ce haloalkyl, Ci-Ce alkoxyalkyl, C2-Ce alkylcarbonyl, phenyl or benzyl, each of which is phenyl or benzyl can optionally be replaced with i-3 R ⁵ , or with a saturated or unsaturated ring system of 5 or e elements, or with a system of 5-e fused rings, or with a system of e-fused rings each containing i-3 heteroatoms, each ring being optionally substituted with i3 R ⁵ , biphenyl or naphthyl optionally substituted with i-3 R ⁵ ;
[00i8] R ⁸ is H, Ci-Ce alkyl, C2-Ce alkenyl, C3-Ce alkynyl, Ci-Ce haloalkyl, Ci-Ce alkoxyalkyl, phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with i-3 R ⁵ , or with a system of saturated or unsaturated ring of 5 or e elements, or with a system of 5-e fused rings, or system of e and fused rings each containing i-3 hetero atoms, each of which ring can be optionally substituted with i-3 R ⁵ , biphenyl or naphthyl optionally substituted with i-3 R ⁵ ;
[00i9] R ⁹ is H, Ci-Ce alkyl, Ci-Ce haloalkyl, Ci-Ce alkoxyalkyl,
C2-Ce alkylcarbonyl, phenyl or benzyl, each of phenyl or benzyl can optionally be substituted with i-3 R ⁵ , or with a saturated or unsaturated ring system of 5 or e elements, or with a system of 5 -e fused rings, or with a fused ring system and each containing i-3 heteroatoms, each ring can optionally be replaced with i-3 R ⁵ , biphenyl or naphthyl
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4/49 optionally substituted with 1-3 R ⁵ ;
[0020] R ¹⁰ is H, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl,
C2-C6 alkylcarbonyl, or benzyl, with benzyl optionally being substituted with 1-3 R ⁵ ;
Alternatively, R ⁹ and R ¹⁰ can be taken together to form a 5- or 6-element saturated or unsaturated ring system containing 1-3 heteroatoms, each ring optionally being substituted with 1-3 R ⁵ ;
[0022] R ¹¹ is H or C1-C4 alkyl;
[0023] R ¹² is H, cyano, hydroxyl, C1-C4 alkyl, C1-C6 alkoxy, C2-C6, alkylcarbonyl, phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with 1-3 R ⁵ ;
Alternatively, R ¹¹ and R ¹² can be taken together to form a 5- or 6-element saturated or unsaturated ring system containing 1-3 hetero atoms, each ring being optionally substituted with 1-3 R ⁵ ;
[0025] R ¹³ is H, C1-C4 alkyl, C1-C6 alkoxy, C2-C6, alkylcarbonyl, phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with 1-3 R ⁵ ;
Alternatively R ¹² and R ¹³ can be taken together to form a 5- or 6-element saturated or unsaturated ring system containing 1-3 hetero atoms, each ring optionally being substituted with 1-3 R ⁵ ; and [0027] R ¹⁴ is C1-C6 alkyl, C1-C6 haloalkyl, amino, C1-C6 alkylamino, C2-C6 dialkylamino, a phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with 1-3 R ⁵ , 4- (3-chloro-5- (tri-fluoro-methyl) pyridin-2-yloxy) -3-methylphenyl, 4- (3-chloro-5- (tri-fluoro-methyl) pyridin-2-yloxy) -2 -methylphenyl, or a 5- or 6-element saturated or unsaturated ring containing 1-3 heteroatoms, each ring optionally substituted with 1-3 R ⁵ .
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5/49 [0028] Another embodiment of the present description may include a fungicidal composition for the control or prevention of fungal attack comprising the compounds described below and a phytologically acceptable support material.
[0029] Yet another embodiment of the present description may include a method for controlling or preventing fungi attack on a plant, the method including the steps of applying a fungicidally effective amount of one or more of the compounds described below, to at least , one of the fungi, the plant, an area adjacent to the plant, and the seeds adapted to produce the plant.
[0030] The term alkyl refers to a branched carbon chain, unbranched, or cyclic, including methyl, ethyl, propyl, butyl, isopropyl, isobutyl, tertiary butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like.
[0031] The term alkenyl refers to a branched carbon chain, unbranched or cyclic, containing one or more double bonds, including ethylene, propenyl, butenyl, isopropenyl, isobutenyl, cyclohexenyl, and the like.
[0032] The term alkynyl refers to a branched or unbranched carbon chain, containing one or more triple bonds, including propynyl, butynyl and the like.
[0033] As used throughout this specification, the term 'R' refers to the group consisting of C2-8 alkyl, C3-8 alkenyl or C3-8 alkynyl, unless otherwise indicated.
[0034] The term alkoxy refers to a substituent -OR.
[0035] The term alkoxycarbonyl refers to a substituent -C (O) OR.
[0036] The term alkylcarbonyl refers to a substituent -C (O) -R. [0037] The term alkylsulfonyl refers to a substituent -SO2-R.
[0038] The term haloalkylsulfonyl refers to a substituent Petition 870180056292, of 29/06/2018, p. 12/76
6/49
SO2-R where R is replaced entirely or partially with Cl, F, I, or Br or any combination thereof.
[0039] The term alkylthio refers to a substituent -S-R.
[0040] The term halothelium refers to a sulfur substituted with three or five substituents of F.
[0041] The term haloalkylthio refers to an alkylthio, which is substituted with Cl, F, I, or Br or any combination thereof.
[0042] The term alkylaminocarbonyl refers to a C (O) -N (H) -R substituent.
[0043] The term dialkylaminocarbonyl refers to a substituent -C (O) -NR2.
[0044] The term alkylcycloalkylamino refers to a cycloalkylamino substituent that is substituted with an alkyl group.
[0045] The term trialkylsilyl refers to -SiR3.
[0046] The term cyan refers to a substituent -C ^ N.
[0047] The term hydroxyl refers to a substituent -OH.
[0048] The term amino refers to a substituent -NH2.
[0049] The term alkylamino refers to a substituent -N (H) -R.
[0050] The term dialkylamino refers to a substituent -NR2.
[0051] The term alkoxyalkoxy refers to - O (CH2) nO (CH2) mCH3 where n is 1-3 and m is 0-2.
[0052] The term alkoxyalkyl refers to an alkoxy substitution on an alkyl.
[0053] The term haloalkoxyalkyl refers to an alkoxy substitution on an alkyl which is substituted totally or partially with Cl, F, Br, or I, or any combination thereof.
[0054] The term hydroxyalkyl refers to an alkyl which is replaced with a hydroxyl group.
[0055] The term haloalkoxy refers to a substituent of -OR-X, where X is Cl, F, Br, or I, or any combination thereof.
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7/49 [0056] The term haloalkyl refers to an alkyl, which is replaced with Cl, F, I, or Br or any combination thereof.
[0057] The term haloalkenyl refers to an alkenyl, which is replaced with Cl, F, I, or Br or any combination thereof.
[0058] The term haloalkynyl refers to an alkynyl which is substituted with Cl, F, I, or Br or any combination thereof.
[0059] The term halogen or halo refers to one or more halogen atoms, defined as F, Cl, Br, and I.
[0060] The term hydroxycarbonyl refers to a C (O) -OH substituent.
[0061] The term nitro refers to a -NO2 substituent.
[0062] The term aryl refers to a cyclic aromatic substituent consisting of hydrogen and carbon.
[0063] Throughout the description, reference to the compounds of Formula I is read as well as including optical isomers and salts of Formula I, and hydrates thereof. Specifically, when Formula I contains a branched chain alkyl group, it is understood that such compounds include optical isomers and racemates thereof. Exemplary salts include: hydrochloride, hydrobromide, iodhydrate, and the like. In addition, compounds of Formula I can include tautomeric forms.
[0064] Certain compounds described in this document may exist as one or more isomers. It will be noted by those skilled in the art that one isomer may be more active than the others. The structures described in this description are drawn in only one geometric shape for clarity, but are intended to represent all the geometric and tautomeric shapes of the molecule.
[0065] It is also understood by those skilled in the art that additional substitution is allowed, unless otherwise indicated, provided that the chemical bonding and deformation energy rules are satisfied and the product still has fungicidal activity.
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8/49 [0066] Another modality of the present description is the use of a compound of Formula I, for the protection of a plant against the attack of a phytopathogenic organism or the treatment of a plant infested by a phytopathogenic organism, which includes the application of a compound of Formula I, or a composition comprising the compound for the soil, a plant, a part of a plant, leaf, and / or seeds.
[0067] Furthermore, another embodiment of the present description is a composition useful for protecting a plant against attack by a phytopathogenic organism and / or treating a plant infested by a phytopathogenic organism comprising a compound of formula I and a support material phytologically acceptable.
[0068] Additional features and advantages of the present invention will become apparent to those skilled in the art considering the following detailed description of the illustrative modalities exemplifying the best way to carry out the invention as currently perceived.
Detailed Description of Description [0069] The compounds of the present description can be applied by any of a variety of known techniques, either as the compounds or as formulations comprising the compounds. For example, the compounds can be applied to the roots, seeds or leaves of plants to control various fungi, without impairing the commercial value of the plants. The materials can be applied in the form of any of the types of formulation generally used, for example, as solutions, dust, humidifiable powders, fluid concentrates or emulsifying concentrates.
[0070] Preferably, the compounds of the present description are applied in the form of a formulation, comprising one or more of the compounds of Formula I, with a phytologically acceptable carrier. Concentrated formulations can be dispersed in water or
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9/49 other liquids, for application, or formulations can be dust or granular, which can then be applied without further treatment. The formulations can be prepared according to procedures that are conventional in the art of agricultural chemicals. [0071] This description covers all vehicles through which one or more of the compounds can be formulated for delivery and use as a fungicide. Typically, formulations are applied as aqueous suspensions or emulsions. Such suspensions or emulsions can be produced from water-soluble, water-suspended formulations, or emulsifiers that are solid, generally known as wetting powders; or liquids, usually known as emulsifying concentrates, aqueous suspensions, or suspension concentrates. As will be readily noted, any material to which these compounds can be added can be used, as long as it produces the desired utility without significant interference with the activity of these compounds as antifungal agents.
[0072] Wetting powders, which can be compacted to form water-dispersible granules, comprise an intimate mixture of one or more of the compounds of Formula I, an inert vehicle and surfactants. The concentration of the compound in the wettable powders can be from about 10 percent, to about 90 percent by weight based on the total weight of the wettable powder, more preferably about 25 percent by weight to about 75 percent by weight. In the preparation of wetted powder formulations, the compounds can be composed of any finely divided solids, such as profilite, talc, chalk, plaster, Fuller earth, bentonite, atapulgite, starch, casein, gluten, montmorillonite clays, diatomaceous earth, purified silicates or similar. In such operations, a finely divided vehicle and surfactants are usually mixed with the compound (s) and ground (s).
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Emulsifying concentrates of the compounds of Formula I may include a convenient concentration, such as from about 10 weight percent to about 50 weight percent of the compound, in a suitable liquid, based on the total weight of the concentrate. The compounds can be dissolved in an inert vehicle, which is either a water-miscible solvent or a mixture of water-immiscible organic solvents, and emulsifiers. The concentrates can be diluted with water and oil to form spray mixtures in the form of oil-in-water emulsions. Useful organic solvents include portions of aromatic oil, especially high-boiling naphthalene and olefin, such as heavy aromatic naphtha. Other organic solvents, too, can be used, for example, terpenic solvents, including rosin derivatives, aliphatic ketones, such as cyclohexanone, and complex alcohols, such as 2ethoxyethanol.
[0074] Emulsifiers which can be advantageously employed here at present can be readily determined by those skilled in the art and include various nonionic, anionic, cationic and amphoteric emulsifiers, or a mixture of two or more emulsifiers. Examples of nonionic emulsifiers useful in the preparation of emulsifying concentrates include polyalkylene glycol ethers and condensation products of alkyl and aryl phenols, aliphatic alcohols, aliphatic amines or fatty acids with ethylene oxide, propylene oxides, such as ethoxylated phenols alkyl and carboxylic esters solubilized with polyol or polyoxyalkylene. Cationic emulsifiers include quaternary ammonium compounds and fatty amine salts. Anionic emulsifiers include the oil-soluble salts (e.g., calcium) of alkylaryl sulfonic acids, oil-soluble salts or sulfated polyglycol ethers and appropriate salts of phosphate polyglycol ether.
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Representative organic liquids that can be used in the preparation of the emulsifying concentrates of the compounds of the present invention are aromatic liquids, such as xylene, propyl benzene fractions; or mixed naphthalene fractions, mineral oils, substituted aromatic organic liquids, such as dioctyl phthalate, kerosene; dialkyl amides of various fatty acids, particularly the dimethyl amides of fatty glycols and glycol derivatives such as n-butyl ether, ethyl ether or diethylene glycol methyl ether and triethylene glycol methyl ether and the like. Mixtures of two or more organic liquids can also be used in the preparation of the emulsifiable concentrate. Organic liquids include xylene, propyl benzene fractions, with xylene being the most preferred in some cases. Surface active dispersing agents are typically employed in liquid formulations and in an amount of 0.1 to 20 weight percent based on the combined weight of the dispersing agent with one or more of the compounds. The formulations can also contain other compatible additives, for example, plant growth regulators and other biologically active compounds used in agriculture.
[0076] Aqueous suspensions comprise suspensions of one or more water-insoluble compounds of Formula I, dispersed in an aqueous vehicle in a concentration in the range of about 5 to about 50 weight percent, based on the total weight of the aqueous suspension. The suspensions are prepared by finely grinding one or more of the compounds, and vigorously mixing the ground material in a vehicle composed of water and surfactants chosen from the same type discussed above. Other components, such as inorganic salts and synthetic or natural gums, can also be added to increase the density and viscosity of the aqueous vehicle. It is often more effective to grind and mix at the same time, preparing the mixture
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12/49 aqueous and homogenizing it in an implement such as a sand mill, ball mill, or piston-type homogenizer.
[0077] Aqueous emulsions comprise emulsions of one or more water-insoluble pesticide active ingredients in an aqueous vehicle in concentration typically in the range of about 5 to about 50 weight percent, based on the total weight of the aqueous emulsion. If the pesticide-active ingredient is a solid, it must be dissolved in a suitable water-immiscible solvent before preparing the aqueous emulsion. Emulsions are prepared by emulsifying the pesticide-active liquid ingredient or water-immiscible solution thereof in an aqueous medium typically with the inclusion of surfactants that aid in the formation and stabilization of the emulsion as described above. This is usually done with the aid of a vigorous mixture provided by high shear mixers or homogenizers.
[0078] The compounds of Formula I can also be applied as granular formulations, which are particularly useful for soil applications. Granular formulations generally contain from about 0.5 to about 10 weight percent, based on the total weight of the granulated formulation of the compound (s), dispersed in an inert vehicle that consists entirely or largely of inert material roughly divided as low cost atapulgite, bentonite, diatomite, clay or similar substance. Such formulations are generally prepared by dissolving the compounds in a suitable solvent and applying them to a granular carrier that has been preformed for the appropriate particle size, in the range of about 0.5 to about 3 mm. A suitable solvent is a solvent with the compound being substantially or completely soluble. Such formulations can also be prepared by making a mass or paste of the vehicle and the compound and solvent, and crushing and drying to obtain the
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13/49 desired granular particle.
[0079] Powders containing the compounds of Formula I can be prepared by intimately mixing one or more of the compounds in powder form with a suitable powdered agricultural vehicle, such as, for example, kaolin clay, ground volcanic rock, and the like. Powder can conveniently contain from about 1 to about 10 weight percent of the compounds, based on the total weight of the powder.
[0080] The formulations may additionally contain adjuvant surfactants to increase the deposition, moistening and penetration of the compounds in the target grain and organism. These adjuvant surfactants can optionally be used as a component of the formulation or as a tank mixture. The amount of adjuvant surfactant will normally vary from 0.01 to 1.0 percent by volume, based on a volume of water spray, preferably 0.05 to 0.5 percent by volume. Suitable adjuvant surfactants include, but are not limited to ethoxylated nonyl phenols, synthetic or natural ethoxylated alcohols, salts of sulfosuccinic esters or acids, ethoxylated organosilicones, ethoxylated fatty amines and mixtures of surfactants with mineral or vegetable oils. The formulations may also include oil-in-water emulsions, such as those described in U.S. Patent Application Serial No. 11 / 495,228, the description of which is expressly incorporated herein by reference.
[0081] Formulations may optionally include combinations that contain other pesticidal compounds. Such additional pesticidal compounds may be fungicides, insecticides, herbicides, nematicides, acaricides, arthropodicides, bactericides or combinations thereof, which are compatible with the compounds of the present invention in the medium selected for the application, and not antagonistic to the activity of the compounds present. Thus, in such modalities, the other pesticidal compound is used as an additional toxic agent for the same
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14/49 or for a different pesticide use. The compounds of Formula I and the pesticidal compound in the combination can generally be present in a weight ratio of 1: 100 to 100: 1.
[0082] The compounds of the present description can also be combined with other fungicides to form mixtures of fungicides and synergistic mixtures thereof. The fungicidal compounds of the present description are often applied in conjunction with one or more other fungicides to control a wider variety of disease as undesirable. When used in conjunction with other fungicide (s), the compounds currently claimed can be formulated with the other fungicide (s), mixed in tank with the other fungicide (s) ) or applied sequentially with the other fungicide (s). Such other fungicides may include 2 (thiocyanatomethylthio) -benzothiazole, 2-phenylphenol, 8-hydroxyquinoline sulphate, ametoctradin, amisulbrom, antimycin, Ampelomyces quisqualis, azaconazole, azoxystrobin, Bacillus subtilis, benzoil, benzoil, subtilis, benzoil, bilexyl, benzoil, bilexyl, benzoil, bile; benzylaminobenzene sulfonate salt (BABS), bicarbonates, biphenyl, bismertiazole, bitertanol, bixafen, blasticidin-S, borax, Bordeaux mixture, boscalide, bromuconazole, bupirimate, calcium polysulfide, captafol, carmine, carmine, carbendazim, carbendazim clazafenone, chloroneb, chlorothalonil, clozolinate, Coniothyrium minitans, copper hydroxide, copper octanoate, copper oxychloride, copper sulphate, copper sulphate (tribasic), cuprous oxide, ciazofamide, ciflufenamide, cymoxanil, cyproxin, cyproconzol, cyproconzol, , ethylenebis- (dithiocarbamate) diamonium, diclofluanide, dichlorophen, diclocimet, diclomezine, dichloran, dietofencarb, diphenoconazole, ion and difenzoquat, diflumetorim, dimetomorph, dimoxystrobin, diniconazole, diniconazole-M, dinobuton, dinocape, diphenylamine, dithianone, dodemorf, dodemorf acetate, dodine, free base dodine, edifenfos, enestrobin, epoxy
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15/49 nazole, etaboxam, ethoxyquin, etridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fenfuram, fenhexamide, phenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fenpyrazamine, phentin, phentin, fluentin, phentin, hydrofinamide , flumorf, fluopicolide, fluopiram, fluoroimide, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianyl, flutolanyl, flutriafol, fluxpyroxad, leaflet, formaldehyde, fosetil, fosetil-aluminum, fuberidazole, furalaxil, acetaminophen, furametpirate, acetaminophen , hexachlorobenzene, hexaconazole, himexazole, imazalil, imazalyl sulfate, imibenconazole, iminoctadine, iminoctadine triacetate, iminoctadine tris (albesylate), iodocarb, ipconazole, ipfenpyrazine, iprobyvan, iprobenazine, iprobenazine of casugamycin hydrochloride, cresoxime-methyl, mancopper, mancozeb, mandipropamide, manebe, mepanipyrim, mepronil, mercury chloride, mercury oxide, mercury chloride, metalaxyl, mefenoxam, meptil-dinocape, metalaxyl-M, metam, metameamonium, metam potassium, metam sodium, metconazole, metasulfocarb, methyl iodide, methyl isothiocyanate, methyminostram, methyminostram, metrafenone, mildiomicin, miclobutanil, nabam, nitrotal-isopropyl, nuarimol, octilinone, ofurace, oleic acid (fatty acids), orisastrobin, oxadixyl, copper oxine, oxpoconazole fumarate, oxicarboxin, pefurazoate, pentconenacol, pentconazole, pencloracol, pencloracol, pencentol, pentconazole laurate, pentiopyrad, phenylmercury acetate, phosphonic acid, phthalide, picoxystrobin, polyoxin B, polyoxins, polyoxorin, potassium bicarbonate, potassium sulfate hydroxyquinoline, probenazole, prochloraz, procymidone, propamocarb, propamazine, propamazole, propamecarbine, propamazoline, propamecarbine, propamazol, , piraclostrobin, pirametostrobin, piraoxystrobin, pyrazophos, pyribencarb, pyributicarb, pirifenox, pyrimethanil, pyriophenone, piroquilon, quinoclamine, quinoxyphen, quintozene, Reynoutria sachalinensis extract, silkxane, siltiofam,
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16/49 simeconazole, 2-phenylphenoxide sodium, sodium bicarbonate, sodium pentachlorophenoxide, spiroxamine, sulfur, SYP-Z071, SYP-Z048, tar oils, tebuconazole, tebufloquin, tecnazene, tetraconazole, tiabendazole, tiabendazide, thiabofamide , take away, thiadinyl, tolclofos-methyl, tolylfluanide, triadimefon, triadimenol, triazoxide, tricyclazole, tridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, validamicin, valifenalate, valifenal, oxoxylamide, zinc, zinc, zeolide, zinc, zinc, zinc spp., Phlebiopsis gigantea, Streptomyces griseoviridis, Trichoderma spp., (RS) -M- (3,5-dichlorophenyl) -2 (methoxymethyl) -succinimide, 1,2-dichloropropane, 1,3-dichlorohydrate1, 1, 3,3-tetrafluoro-acetone, 1-chloro-2,4-dinitronaphthalene, 1-chloro-2-nitropropane, 2- (2-heptadecyl-2-imidazolin-1-yl) ethanol, 2,3-dihydro-5-phenyl -1,4-dithiine 1,1,4,4-tetraoxide, 2-methoxyethylmercury acetate, 2-methoxyethylmercury chloride, 2-methoxyethyl silicate mercury, 3- (4-chlorophenyl) -5-methylrhodanine, 4- (2-nitroprop-1-enyl) phenyl thiocyanate, ampropylphos, anilazine, azitiram, barium polysulfide, Bayer 32394, benodanil, benquinox, bentaluron, benzamacril; benzamacryl-isobutyl, benzamorf, binapacril, bis (methylmercury) sulfate, bis (tributyltin) oxide, butiobate, cadmium, copper sulfate, zinc chromate calcium, carbamorf, ECSC, clobentiazone, chloraniformetan, chlorfenazole, chloroquine, chloroquine, chloroquine cipendazole, ciprofuram, decafentin, diclone, diclozoline, diclobutrazol, dimethyrimol, dinocton, dinosulfon, dinoterbon, dipyrithione, ditalymphos, dodicine, drazoxolon, EBP, ESBP, etaconazole, Etem, etirim, fenaminos, fenaminos, 5 fluotrimazole, furcarbanila, furconazol, furconazol-cis, furmeciclox, furofanato, gliodine, griseofulvina, halacrinato, Hercules 3944, hexiltiofos, ICIA0858, isopamfos, isovaledione, mebenil, mecarbinzid, methoxymethyl, methoxymethyl, methoxyzoxide , N-3,5-dichlorophenyl-succinimide, N-3-nitrophenylite-conimide, in
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17/49 tamicin, N-ethylmercurium-4-toluenesulfonanilide, nickel bis (dimethyldithiocarbamate), OCH, phenylmercury dimethyldithiocarbamate, phenylmercury nitrate, phosdiphen, picolinamide UK-2A and its derivatives, protiocarb; protiocarb hydrochloride, piracarbolide, pyridinitrile, pyroxychlor, piroxifur, quinacetol; quinacetol sulfate, quinazamid, quinconazole, rabenzazole, salicylanilide, SSF-109, sultropen, tecoram, thiadifluor, ticiofen, thioclorphenphen, thiophanate, thioquinox, thioximid, triamiphos, triarimol, triazbutil, triazbutil and triclamide.
[0083] In addition, the compounds of the present invention can be combined with other pesticides, including insecticides, nematicides, acaricides, arthropodicides, bactericides, or combinations thereof that are compatible with the compounds of the present invention in the medium selected for the application, and not antagonistic to the activity of the present compounds to form mixtures of pesticides and synergistic mixtures thereof. The fungicidal compounds of the present description can be applied in conjunction with one or more other pesticides to control a wider variety of desirable pests. When used in conjunction with other pesticides, the compounds currently claimed can be formulated with the other pesticide (s), mixed in tank with the other pesticide or applied sequentially with the other pesticide (s) ( s). Typical insecticides include, but are not limited to: antibiotic insecticides, such as allosamidin thuringiensin; macrocyclic lactone insecticides such as spinosad and spinetoram; avermectin insecticides, such as abamectin, doramectin, emamectin, eprinomectin, ivermectin and selamectin; milbemycin insecticides such as lepimectin, milbemectin, milbemycin oxime and moxidectin, arsenic insecticides such as calcium arsenate, copper acetoarsenite, copper arsenate, lead arsenite, potassium arsenate and sodium arsenite; botanical insecticides such as ana
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18/49 basin, azadiractin, d-limonene, nicotine, pyrethrins, cinerines, cinerin I, cinerin II, jasmine I, jasmine II, pyrethrin I, pyrethrin II, kassia, rotenone, riania and sabadilla; carbamate insecticides, such as bendiocarb and carbaryl; benzofuranyl methylcarbamate insecticides such as benfuracarb, carbofuran, carbosulfan, decarbofuran and furatiocarb; dimethylcarbamate insecticides dimitan, dimethylan, hiquincarb and pirimicarb; carbamate oxime insecticides, such as alanicarb, aldicarb, aldoxicarb, butocarboxy, butoxycarboxy, metomyl, nitrilacarb, oxamil, tazimcarb, thiocarboxy, thiodicarb and thiophanox; insecticides phenyl methylcarbamate such as alixicarb, aminocarb, bufencarb, butacarb, carbanolate, cloetocarb, dicresil, dioxacarb, EMPC, etiofencarb, fenethacarb, fenobucarb, isoprocarb, metiocarb, metolcarb, propharcarbate, propylcarbate, propylcarbate, prophylaxis, desiccant insecticides, such as boric acid, diatomaceous earth and silica gel; diamide insecticides such as cyantraniliprole, chlorantraniliprole and flubendiamide; dinitrophenol insecticides such as dinex, dinoprop, dinosam and DNOC; fluorine insecticides, such as barium hexafluorosilicate, cryolite, sodium fluoride, hexafluorosilicate and sulfluramide; formamidine insecticides, such as amitraz, chlordimeform, formethanate and formparanate; fumigating insecticides such as acrylonitrile, carbon disulfide, carbon tetrachloride, chloroform, chloropicrin, paradichlorobenzene, 1,2-dichloropropane, ethyl formate, ethyl dibromide, ethylene dichloride, ethylene oxide, hydrogen cyanide, iodomethane, bromine , methylchloroform, methylene chloride, naphthalene, phosphine, sulfuryl fluoride and tetrachloroethane; insecticides such as inorganics, such as borax, calcium polysulfide, copper oleate, mercury chloride, potassium thiocyanate and sodium thiocyanate; inhibitors of chitin synthesis, such as bistrifluron, buprofezin, chlorfluazuron, cyromazine, diflubenzuron, flucicloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron and triflum; mimi
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19/49 cos of juvenile hormone such as epophenonan, phenoxycarb, hydroprene, quinoprene, methoprene, pyriproxifem and triprene; juvenile hormones, such as juvenile hormone I, juvenile hormone II and juvenile hormone III; molting hormone agonists such as chromafenozide, halofenozide, methoxyfenozide and tebufenozide; molting hormones, such as aecdysone and ecdysterone; seedling inhibitors, such as diofenolan; precocenes such as precocene I, precocene II and precocene III; non-classified insect growth regulators, such as dicyclanil; nereistoxin-like insecticides, such as bensultape, cartape, tiocyclam and thiosultape; nicotinoid insecticides like flonicamid; nitroguanidine insecticides such as clothianidin, dinotefuran, imidacloprid and thiamethoxam; nitromethylene insecticides such as nitenpiram and nitiazine; pyridylmethyl-amine insecticides such as acetamipride, imidacloprid, nitenpiram and tiaclopride; organochlorine insecticides such as bromo-DDT, campheclor, DDT, pp'-DDT, ethyl-DDD, HCH, gamma-HCH, lindane, methoxychlor, pentachlorophenol and TDE; cyclodiene insecticides such as aldrin, bromocyclen, clorbicyclen, chlordane, chlordecone, dieldrin, dilor, endosulfan, alfaendosulfan, endrin, HEOD, heptachlor, HHDN, isobenzan, isodrine, kelevan and mirex; organophosphate insecticides, such as bromfenvinfos, chlorfenvinfos, crotoxifos, dichlorvos, dichrotofos, dimethilvinfos, phospirato, heptenofós, metocrotofós, mevinfós, monocrotofós, nalede, naphthalofós, phosphamidon, propafós, Tepós; organothiophosphoric insecticides such as dioxabenzophos, fosmethylan and fentoate; aliphatic organothiophosphoric insecticides, such as acetion, amiton, cadusaphos, chlorethoxyphos, chlormphes, demefion, demefion-O, demefion-S, demeton, demetonO, demeton-S, demeton-methyl, demeton-O-methyl, demeton-S-methyl, demeton-S-methylsulfon, disulfoton, etion, etoprofos, IPSP, isothioate, malation, methacrifos, oxidemeton-methyl, oxideprofos, oxidisulfoton, phorate, sulfotepe, terbufos and tiometon; organothiophosphoric insecticides aliphatic amide such as amidition, cyantoate, dimetoate, methyl etoate, formotion,
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20/49 mecarbame, ometoate, protoate, sofamide and vamidotion; oxime organothiophosphoric insecticides, such as chlorfoxime, foxime and methyloxime; heterocyclic organothiophosphoric insecticides such as azametiphos, coumafos, coumitoate, dioxation, endotion, menazon, morphotion, fosalone, piraclofos, pyridafention and quinotion; benzothiopyran organothiophosphate insecticides such as dichrophos and ticrophos; benzothriazine organothiophosphoric insecticides such as ethyl azymphs and methyl azymphs; organothiophosphate isoindole insecticides such as dialiphos and phosmet; organoxyphosphate isoxazole insecticides such as isoxation and zolaprofos; pyrazolopyrimidine organothiophosphoric insecticides such as chlorprazophos and pyrazophos; pyridine organothiophosphoric insecticides such as chlorpyrifos and methylchlorpyrifos; pyrimidine organothiophosphoric insecticides such as butathione, diazinon, etrimphos, lirimphos, ethyl-pyrimiphos, methyl-pyrimiphos, primidophos, pyrimitate and tebupirimphos; quinoxaline organothiophosphoric insecticides such as quinalphos and methylquinalphos; organiadiophosphoric insecticides thiadiazole as atidation, litidation, metidation and protidation; organothiophosphoric triazole insecticides such as isazophos and triazophos; organothiophosphoric phenyl insecticides such as nitrogen, bromophos, ethyl-bromophos, carbofenotion, chlortiofos, cyanophos, cytioate, dicapton, diclofention, etafos, famfur, fenclorfos, fensulfotion fenitrotiom, fentiom, methyl-fosion, methyl-fention paration, fencapton, fosniclor, profenofos, protiofos, sulprofos, temefos, triclormetafos-3 e triphenofos; phosphonate insecticides such as butonate and trichlorfon; phosphonothioate insecticides such as mecarfon; phenyl ethylphosphonothioate insecticides such as phonophos and trichloronat; phenylphosphonothioate phenyl insecticides such as cyanophenphos, EPN and leptophos; phosphoramidate insecticides such as crufomato, fenamiphos, fostietan, mefosfolan, phosfolan and pyrimetafos; phosphoramidothioate insecticides, such as acephate, isocarbophones, isophenphos, methyl isophenphos, metamidophos and propetamphos; phosphorodiamide insecticides such as dimefox, mazidox, mipafox and schradan; oxadiazine insecticides like indoxacar
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21/49 be; oxadiazoline insecticides such as methoxyzazone; phthalimide insecticides such as dialiphos, phosmet and tetramethrin; pyrazole insecticides such as tebufenpirad, tolefenpirad; phenylpyrazole insecticides such as acetoprol, etiprol, fipronil, pirafluprol, pyriprol and vaniliprol; pyrethroid ester insecticides such as acrinatrin, alethrin, bioalethrin, bartrin, bifentrin, bioethanometrine, cyclethrin, cycloprotrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, gammathelin, lambda-cyhalothrin, cypermethrin, alpha-cypermethrin, betipermethrin, ketamine, ketamine cyphenothrin, deltamethrin, dimeflutrin, dimethrin, empentrin, fenflutrin, fenpiritrin, fempropatrin, fenvalerate, sphenophernine, flucitrinate, fluvalinate, taufluvalinate, furetrin, imiprotrin, meperflutrin, methetrethin, transmethrone, methetrethin, permethrin, transmethrone bioresmethrin, cyismetrine, teflutrin, teralethrin, tetramethrin, tetramethylflutrine, tralometrine and transflutrin; pyrethroid ether insecticides, such as etofenprox ether, flufenprox, halfenprox, protrifenbute and silafluofen; pyrimidinamine insecticides such as flufenerin and pyrimidifen; pyrrole insecticides such as chlorfenapyr; tetramic acid insecticides such as spirotetramate; tetronic acid insecticides such as spiromesifen; thiourea insecticides such as diafentiuron; urea insecticides such as flucofuron and sulcofuron; and insecticides not classified as closantel, copper naphthenate, crotamiton, EXD, fenazaflor, fenoxacrim, hydramethylnon, isoprothiolan, malonoben, metaflumizone, nifluridide, plifenate, pyridaben, pyridalil, pyrifluquinazone, rafoxanide and troxoxide; .
[0084] Furthermore, the compounds of the present invention can be combined with herbicides that are compatible with the compounds of the present invention in the medium selected for the application, and not antagonistic to the activity of the compounds present to form pesticidal mixtures and synergistic mixtures thereof. The fungicidal compounds of the present description can be applied together with a
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22/49 or more herbicides to control a wide variety of plants as desirable. When used in conjunction with herbicides, the compounds currently claimed can be formulated with the herbicide (s), mixed in tank with the herbicide (s) or applied sequentially with the herbicide (s). Typical herbicides include, but are not limited to: amide herbicides, such as alidochlor, beflubutamide, benzadox, benzipram, bromobutide, cafenstrol, CDEA, cyprazole, dimethenamide, dimethenamid-P, diphenamid, epronaz, etnipromid, fenphenamide, fentrazide, fentrazide, fentrazide, fentrazide, fentrazide , isocarbamid, isoxaben, napropamide, naptalam, petoxamide, propizamide, quinonamid and tebutam; anilide herbicides such as chloranocril, cisanilide, clomeprop, cipromid, diflufenicão, etobenzanid, fenasulam, flufenacet, flufenican, mefenacet, mefluidide, metamifop, monalide, naproanilide, pentanochlor, picolinefen and propanil; arylalanine herbicides such as benzolprop, flamprop and flamprop-M; chloroacetanilide herbicides such as acetochlor, alachlor, butachlor, butenachlor, delachlor, diethyl, dimetachlor, metazachlor, metolachlor, S-metolachlor, pretylachlor, propachlor, propisochlor, prinachlor, terbuclor, tenilchlor and xylachlor; sulfonanilide herbicides such as benzofluor, perfluidone, pyrimisulfan and profluazole; sulfonamide herbicides, such as asulam, carbasulam, fenasulam and orizalin; thioamide herbicides such as chlortiamid; antibiotic herbicides, such as bilanafos; benzoic acid herbicides such as chloramben, dicamba, 2,3,6-TBA and tricamba; pyrimidinyloxybenzoic acid herbicides such as bispiribac and piriminobac; pyrimidinylthiobenzoic acid herbicides such as piritiobac; phthalic acid herbicides, such as chlortal; picolinic acid herbicides, such as aminopyralide, clopyralide and picloram; quinolinecarboxylic acid herbicides such as quinclorac and quinmerac; arsenic herbicides such as cacodylic acid, CMA, DSMA, hexaflurate, MAA, MAMA, MSMA, potassium arsenite and sodium arsenite; benzolcyclohexanedione herbicides such as mesotrione, sulcotrione, tefuriltrione and tembotrione; benzofuranyl herbicides al
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23/49 kylsulfonate as benfuresate and etofumesate; benzothiazole herbicides such as benzazolin; carbamate herbicides such as asulam, chlorprocarb carboxazole, dichlormat, fenasulam, karbutilate and terbucarb; carbanylate herbicides such as barbana, BCPC, carbasulam, carbetamide, CEPC, chlorinate, chlorprofam, CPPC, desmedipham, fenisofam, fenemedipham, ethyl fenemedipham, profame and swep; cyclohexene oxime herbicides, such as aloxidim, butroxidim, cletodim, cloproxidim, cycloxidim, profoxidim, setoxidim, tepraloxidim and tralcoxidim; cyclopropylisoxazole herbicides such as isoxaclortol and isoxaflutol; dicarboximide herbicides such as ethyl-cinidon, flumezin, flumiclorac, flumioxazin and flumipropin; dinitroaniline herbicides such as benfluralin, butralin, dinitramine, etalfluralin, flucloraline, isopropalin, metallopraline, nitralin, oryzine, pendimethalin, prodiamine, profluralin and trifluralin; dinitrophenol herbicides such as dinofenate, dinoprop, dinosam, dinosebe, dinoterb, DNOC, ethinophen and medinoterb; diphenyl ether herbicides such as ethoxyfen; nitrophenyl ether herbicides such as acifluorfen, aclonifen, bifenox, clomethoxyfen, chlornitrofen, etnipromid, fluorodifen, fluoroglycophen, fluoronitrofen, fomesafen, furyloxifen, halosafen, lactofen, nitrofen, nitrofluorfen and oxif; dithiocarbamate herbicides such as dazomet and metam; aliphatic halogenated herbicides, such as alorac, chloropon, dalapon, flupropanate, hexachloroacetone, iodomethane, methyl bromide, monochloroacetic acid, SMA and TCA; imidazolinone herbicides, such as imazametabenze, imazamox, imazapic, imazapyr, imazaquin and imazetapyr; non-organic herbicides such as ammonium sulfamate, borax, calcium chloride, copper sulfate, ferrous sulfate, potassium azide, potassium cyanate, sodium azide, sodium chloride and sulfuric acid; nitrile herbicides such as bromobonyl, bromoxynil, chloroxynil, dichlobenyl, iodobonyl, ioxynil and pyraclonil; organophosphate herbicides, such as amiprofosmethyl, anilophos, bensulide, bilanafos, butamiphos, 2,4-DEP, DMPA, EBEP, phosamine, glufosinate, glufosinate-P, glyphosate and piperophos; her
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24/49 phenoxy bicides such as bromophenoxy, clomeprop, 2,4-DEB, 2,4-DEP, diphenopenten, disul, erbon, etnipromid, phenteracol and trifopsime; oxadiazoline herbicides such as metazol, oxadiargyl, oxadiazon; oxazole herbicides such as phenoxysulfone; phenoxyacetic herbicides such as 4-CPA, 2,4-D,
3,4-DA, MCPA, MCPA-thioethyl and 2,4,5-T; phenoxybutyric herbicides such as 4-CPB, 2,4-DB, 3,4-DB, MCPB and 2,4,5-TB; phenoxypropionic herbicides such as cloprop, 4-CPP, dichlorprope, dichlorprope-P, 3,4-DP, fenoprope, mecoprope and mecoprope-P; aryloxyphenoxypropionic herbicides such as chlorazifop, clodinafop, clofop, cihalofop, diclofop, fenoxaprop, fenoxaprop-P, fentiaprop, fluazifop, fluazifop-P, haloxifop, haloxifop-P, isoxapirifop, metamifop, pquizopop, truffle phenylenediamine herbicides such as dinitramine and prodiamine; pyrazole herbicides such as pyrosulfone; benzolpyrazole herbicides such as benzofenap, pyrasulfotole, pyrazolinate, pyrazoxifen and topramezone; phenylpyrazole herbicides such as fluazolate, nipyraclofen, pioxaden and piraflufen; pyridazine herbicides such as credazine, pyridafol and pyridate; pyridazinone herbicides such as brompirazon, chloridazon, dimidazon, flufenpir, metflurazon, norflurazon, oxapirazon and pidanon; pyridine herbicides, such as aminopyralide, cliodinate, clopyralide, dithiopir, fluroxypyr, haloxidine, picloram, picolinafen, pyrichlor, thiazopyr and triclopyr; pyrimidinediamine herbicides such as iprimidam and thioclorim; quaternary ammonium herbicides such as ciperquat, dietamquat, difenzoquat, diquat, paraquat and morfamquat; thiocarbamate herbicides such as butylate, cyclate, di-alate, EPTC, sprocarb, etiolate, isopolynate, methiobencarb, molinate, orbencarb, pebulate, prosulfocarb, pyributicarb, sulfalate, thiobencarb, thiocarbazil, tri-alate and vernolate; thiocarbonate herbicides such as dimexane, EXD and proxan; thiourea herbicides such as methuron; triazine herbicides such as dipropetrin, indaziflam, triaziflam and trihydroxythriazine; chlorotriazine herbicides such as atrazine, chlorazine, cyanazine, cyprazine, eglinazine, ipazine, mesoprazine, prociazine, proglinazine, propazine,
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Sebuthylazine, simazine, terbuthylazine and trietazine; methoxythriazine herbicides such as atraton, metometon, prometon, secbumeton, simeton and terbumeton; methyltiotriazine herbicides such as ametrin, aziprotrine, cyanatrin, desmetrin, dimetametrin, metoprotrine, prometrin, simetrin and terbutrin; triazinone herbicides such as ametridione, amibuzin, hexazinone, isomethiozine, metamitron and metribuzin; triazole herbicides such as amitrol, cafenstrole, epronaz and flupoxam; triazolone herbicides such as amicarbazone, bencarbazone, carfentrazone, flucarbazone, ipfencarbazone, propoxycarbazone, sulfentrazone and methyl-thencarbazone; triazolopyrimidine herbicides such as cloransulam, diclosulam, florasulam, flumetsulam, metosulam, penoxsulam and pyroxsulam; uracil herbicides such as benzfendizone, bromacil, butafenacil, flupropacil, isocil, lenacil, saflufenacil and terbacil; urea herbicides such as benztiazuron, cumiluron, cycluron, dichloralurea, diflufenzopyr, isonoruron, isouron, metabenztiazuron, monisouron and noruron; phenylurea herbicides such as anisuron, buturon, clorbromuron, chloreturon, chlorotoluron, chloroxuron, daimuron, diphenoxuron, dimefuron, diuron, fenuron, fluometuron, fluotiuron, isoproturon, linuron, metiuron, metildimon, metildimon, metoburon, metoburon, metoburon, metoburon, , phenobenzuron, siduron, tetrafluron and tidiazuron; herbicides pirimidinilsulfonilureia as amidosulfuron, azimsulfuron, bensulfuron, chlorimuron, cyclosulfamuron, etoxissulfuron, flazassulfuron, flucetossulfuron, flupirsulfuron, foramsulfuron, halossulfuron, imazossulfuron, mesossulfuron, metazossulfuron, nicosulfuron, ortossulfamuron, oxassulfuron, primisulfuron, propirissulfuron, pyrazosulfuron, rimsulfuron, sulfometuron, sulfossulfuron and trifloxissulfuron ; triazinylsulfonylurea herbicides such as chlorsulfuron, cinosulfuron, etametsulfuron, iodosulfuron, metsulfuron, prosulfuron, tifensulfuron, triasulfuron, tribenuron, triflussulfuron and tritosulfuron; thiadiazolylurea herbicides such as butiuron, etidimuron, tebutiuron, thiazafluron and tidiazuron and unclassified herbicides, such as acrolein, alcohol
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26/49 allylic cool, aminocyclopyrachlor, azafenidin, bentazone, benzobicyclon, bicyclopyrone, butidazole, calcium cyanamide, cambendichlor, chlorphenac, chlorphenprop, chlorflurazole, chlorflurenol, cinmetilin, clomazone, CPMF, dichloride, dichloride, dichloride, dichloride, dichloride , fluridone, flurochloridone, flurtamone, flutiacet, indanofan, methyl isothiocyanate, OCH, oxaziclomefone, pentachlorophenol, pentoxazone, phenylmercurium acetate, prosulfalin, pyribenzoxim, pyriftalid, quinoclamine, rhodetanil, trulgitine, trulgitine, trulgitine, trulginine, trulginine, trulginine, trulgine
[0085] Another embodiment of the present description is a method for the control or prevention of fungal attack. This method comprises applying to the soil, plant, roots, leaves, seed or locus of the fungus, or to a place where the infestation is to be prevented (for example, applying to cereal plants), a fungicidally effective amount of one or more of the compounds of Formula I. The compounds are suitable for the treatment of various plants at fungicidal levels, while exhibiting low phytotoxicity. The compounds can be useful both in a protective and / or eradicating form.
[0086] It has been found that the compounds have a significant fungicidal effect, particularly for agricultural use. Many of the compounds are particularly effective for use with agricultural crops and vegetables. Additional benefits may include, but are not limited to, improving the health of a plant, improving the yield of a plant (for example, increased biomass and / or higher content of valuable ingredients), improving the vigor of a plant (for example , improve plant growth and / or greener leaves); improve the quality of a plant (for example, improved the content or composition of certain ingredients), and improve the tolerance to abiotic and / or biotic stress of the plant.
[0087] It will be understood by those in the art that effectiveness
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27/49 of the compound for the preceding fungi establishes the general utility of the compounds as fungicides.
[0088] The compounds have broad ranges of activity against fungal pathogens. Exemplary pathogens may include, but are not limited to, wheat leaf spot (Septoria tritici, also known as Mycosphaerella graminicola), apple scab (Venturia inaequalis), and beet Cercospora leaf spots (Cercospora beticola), peanut leaf spots (Cercospora arachidicola and Cercosporidium personatum) and other crops, and black banana sigatoka (Mycosphaerella fujiensis). The exact amount of active material to be applied depends not only on the specific active material to be applied, but also on the specific action desired, the species of fungi to be controlled, and their growth stage, as well as the part of the plant or another product to be contacted with the compound. Thus, all compounds and formulations containing the same, may not be equally effective at similar concentrations or against the same species of fungi.
[0089] The compounds are effective in use with plants in a disease-inhibiting and phytologically acceptable amount. The term disease-inhibiting and phytologically acceptable amount refers to an amount of a compound that kills or inhibits the plant disease for which control is desired, but is not significantly toxic to the plant. This amount will generally be about 0.1 to about 1000 ppm (parts per million), with 1 to 500 ppm being preferred. The exact amount needed for a compound varies with the fungal disease to be controlled, the type of formulation employed, the method of application, the plant species in particular, the climatic conditions, and so on. The appropriate application rate is generally in the range of about 0.10 to about 4 pounds / acre (about 0.01 to 0.45 grams per square meter, g / m ² ).
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28/49 [0090] Any desired range or value given here can be extended or changed without losing the desired effects, as is apparent to a person qualified to understand the teachings here in this document.
[0091] The compounds of Formula I can be made using known chemical procedures. Intermediates not specifically mentioned in the present description are either commercially available, can be made by routes described in the chemical literature, or can be readily synthesized from commercial raw materials using standard procedures.
[0092] The following examples are presented to illustrate the various aspects of the compounds of the present description and are not to be construed as limiting the claims.
Example 1: Preparation of A '- (1-benzenesulfonyl-5-fluoro-2-oxo-1,2dihydro-pyrimidin-4-yl) -M, M-dimethylformamidine (1)

pyridine
[0093] To an 8 ml flask with screw cap, pyridine (2 ml), M '- (5-fluoro-2-hydroxy-pyrimidin-4-yl) -M, Mdimethylformamidine (100 mg, 0.54 mmol), and benzenesulfonyl chloride (106 mg, 0.60 mmol), and the mixture was stirred at room temperature for 24 hours (h). The crude mixture was partitioned between ethyl acetate (EtOAc) and aqueous saturated sodium bicarbonate (aqueous saturated NaHCO3), and the organic phase was dried over magnesium sulfate (MgSO4), filtered and evaporated to produce 153 mg of crude material. Reverse phase chromatography gave the title product as a white solid (33 mg, 19%): mp 203-204 ° C; ¹ H NMR (300 MHz, CDCl3) δ 8.77 (s, 1H), 8.16-8.11 (m, 3H), 7.72-7.65 (m, 1H) 7.60-7, 53 (m, 2H), 3.24 (s, 3H), 3.23 (s, 3H); ESIMS m / z 325 ([M + H] ⁺ ).
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Example 2: Preparation of N '- [1- (4-chloro-benzenesulfonyl) -5-fluoro-2oxo-1,2-dihydro-pyrimidin-4-yl] -N, N-dimethylformamidine (2)
Et ₃ N, CH ₂ Cl ₂
[0094] Dichloromethane (CH2Cb; 10 mL), N '- (5-fluoro-2-hydroxy-pyrimidin4-yl) -N, N-dimethylformamidine (250 mg, 1 , 36 mmol), and triethylamine (Et3N,
300 mg, 3 mmols). To this mixture, 4-chlorobenzenesulfonyl chloride (315 mg, 1.5 mmol) was added, and the resulting mixture was stirred at room temperature for 3 hours. The crude reaction mixture was partitioned between CH2Cl2 and brine, dried over MgSÜ4, filtered, and evaporated. The residue was purified by reverse phase chromatography to yield the title compound as a white solid (321 mg, 66%): mp 207-210 ° C; ¹ H NMR (300 MHz, CDCh) δ 8.75 (s, 1H), 8.088.02 (m, 3H), 7.53-7.47 (m, 2H), 3.23 (s, 3H), 3.21 (s, 3H); ESIMS m / z 360 ([M + H] ⁺ ).
[0095] Compounds 3-7 in Table I were synthesized as in Example 2.
Example 3: Preparation of 4-amino-1- (4-chloro-benzenesulfonyl) -5fluoro-1H-pyrimidin-2-one (8; Method A)
1. ch ₃ cn, bsa

[0096] For 4-amino-5-fluoro-pyrimidin-2-ol * (1.0 g, 7.75 mmol) in acetonitrile (CH3CN; 40 mL), bis-N, Otrimethylsilylacetamide (BSA; 5.7 mL, 23.3 mmols) and the mixture was heated to 70 ° C for 1 hour resulting in a clear solution. After cooling to room temperature, 4-chlorobenzene sulfonyl chloride (1.8 g,
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8.5 mmols) was added, and the mixture was stirred for 24 hours. The solvent was evaporated and the residue was partitioned between EtOAc and brine. The organic phase was dried over MgSO4, filtered, and evaporated to yield the crude product as a white solid (1.3 g). Recrystallization from EtOAc and heptane provided the title product as a white solid (0.96 g, 41%): mp 174-178 ° C; ¹ H NMR (300 MHz, CDCb) δ 8.5 (br s, 1H), 8.08 (d, J = 5.9 Hz, 1H), 8.04-7.98 (m, 2H), 7 , 55-7.49 (m, 2H), 5.9 (br s, 1H); ESIMS m / z 304 ([M + H] ⁺ ).
* 4-Amino-5-fluoro-pyrimidin-2-ol can be purchased commercially.
[0097] Compounds 9-23 in Table I were synthesized as in
Example 3.
Example 4: Preparation of 4-amino-1- (4-chloro-benzenesulfonyl) -5fluoro-1H-pyrimidin-2-one (8; Method B)
N HCl, dioxane
[0098] Dioxane (9 mL), 1 N aqueous hydrochloric acid (HCl; 1 mL), and M '- [1- (4-chloro-benzenesulfonyl) -5-fluoro-) were added to an 8-ml screw cap. 2-oxo-1,2-dihydro-pyrimidin-4-yl] -M, Mdimethylformam-midine (269 mg, 0.75 mmol). The mixture was stirred at room temperature for 16 h, evaporated under a flow of nitrogen, and partitioned between EtOAc and aqueous saturated NaHCO3. The organic phase was dried over MgSO4, filtered, and evaporated to yield the title product as a white solid (196 mg, 86%): mp 174-178 ° C; ¹ H NMR (300 MHz, CDCb) δ 8.5 (br s, 1H), 8.08 (d, J = 5.9 Hz, 1H), 8.047.98 (m, 2H), 7.55-7 , 49 (m, 2H), 5.9 (br s, 1H); ESIMS m / z 304 ([M + H] ⁺ ).
Compounds 24-27 in Table I were synthesized as in
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Example 4.
Example 5: Preparation of M '- [5-fluoro-1- (1-methyl-1H-imidazol-4sulfonyl) -2-oxo-1,2-dihydro-pyrimidin-4-yl] -M, M- dimethylformamidine (28)
DMF-DMA, DMF
[0099] 4-Amino-5-fluoro-1- (1-methyl-1 H-imidazole-4-sulfonyl) -1 H-pyrimidin-2-one was added to an 8 ml screw cap. mg, 0.3 mmol), Μ, Μ-dimethylformamide (DMF; 3 mL), and dimethylacetal dimethylformamide (DMF-DMA; 70 mg, 0.6 mmol). The mixture was stirred at room temperature for 16 h, diluted with Et2O and filtered to yield the title product as a light yellow solid (68 mg, 69%): mp 228-232 ° C dec; ¹ H NMR (300 MHz, DMSO-cfe) δ 8.67 (s, 1H), 8.25-8.21 (m, 2H), 7.82 (s, 1H), 3.73 (s, 3H ), 3.24 (s, 3H), 3.13 (s, 3H); ESIMS m / z 329 ([M + H] ⁺ ).
Compounds 29-32 in Table I were synthesized as in Example 5.
Example 6: Preparation of M- (1-benzenesulfonyl-5-fluoro-2-oxo-1,2dihydro-pyrimidin-4-yl) -benzamide (33)

[00100] 4-amino-1-benzenesulfonyl-5-fluoro-1H-pyrimidin-2-one (200 mg, 0.74 mmol), CH2Cl2 (5 mL) was added to an 8 mL screw cap. Et3N (200 mg, 1.98 mmol), and benzol chloride (114 mg, 0.82 mmol). The mixture was stirred at room temperature for 2.5 hours, evaporated under a flow of nitrogen, and partitioned between EtOAc and H2O. The organic phase was dried over MgSO4, filtered, and
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Compounds 34-37 in Table I were synthesized as in
Example 6.
Example 7: Preparation of 4-chloro-V- [1- (4-chlorobenzenesulphonyl) -5fluoro-2-oxo-1,2-dihydropyrimidin-4-yl] benzamidamide (38) [00101] For a suspension of 4-chloro-V- (5-fluoro-2-oxo-1,2-dihydropyrimid-4-yl) benzamide (0.10 g, 0.37 mmol) in CH ₂ Cl ₂ (4 mL) was added Et3N (0.08 g, 0.82 mmol) and 4-chlorobenzenesulfonyl chloride (0.087 g, 0.41 mmol) at 0 ° C, and the resulting mixture was warmed to room temperature and stirred for 3 h. The reaction was diluted with CH2Cl2 (10 ml) and washed with brine. The phases were separated and the organic phase was dried over sodium sulfate (Na ₂ SO4), filtered, and concentrated to an amber oil (0.295 g). Purification by normal phase chromatography (12 g SiO2; gradient, 0 to 35% EtOAc / hexanes) provided 4-chloro-V- [1- (4chlorobenzenesulfonyl) -5-fluoro-2-oxo-1,2-dihydropyrimidin -4yl] benzamide (0.025 g, 26%) as a white solid: mp 169-172 ° C; ¹ H NMR (300 MHz, CDCls) δ 12.59 (s, 1H), 8.29-8.15 (m, 3H), 8.05 (d, J = 8.8 Hz, 2H), 7, 59 (d, J = 8.7 Hz, 2H), 7.42 (d, J = 8.6 Hz, 2H);
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ESIMS m / z 442 ([M + H] ⁺ ), 440 ([MH] -).
Compound 39 in Table I was synthesized as in Example 7.
Example 8: Preparation of 1- (1-benzenesulfonyl-5-fluoro-2-oxo-1,2dihydropyrimidin-4-yl) -3-phenylurea (40)
OH
NCO [00102] A) To a suspension of 4-amino-5-fluoropyrimidin-2-ol (0.200 g, 1.5 mmol) in anhydrous DMF (3 mL), phenylisocyanate (0.251 g, 2.1 mmol) was added and the mixture was stirred at 23 ° C for 1 hour and then at 60 ° C for 16 hours. The reaction mixture was cooled to room temperature, and the residual solid was collected by filtration. The filter cake was washed with diethyl ether (Et2O) and dried in a vacuum oven at 40 ° C for 3 hours to give 1- (5-fluoro-2-hydroxypyrimidin-4-yl) -3-phenylurea as a white solid ( 0.210 g, 55%), which was used immediately in the next step.
[00103] B) To a suspension of 1- (5-fluoro-2-hydroxypyrimidin-4yl) -3-phenylurea (0.200 g, 0.8 mmol) in anhydrous CH3CN (4 mL) was added BSA (0.487 g, 2 , 4 mmol), and the mixture was heated to 70 ° C and stirred for 1 hour. The resulting solution was cooled to room temperature, treated with benzenesulfonyl chloride (0.156 g, 0.9 mmol), and the mixture was stirred for 12 hours. The solvent was evaporated, and the residue was partitioned between EtOAc and brine. The organic phase was dried over MgSO4, filtered, and concentrated to give the crude product as a white solid. Recrystallization from EtOAc and heptane provided 1 - (1-benzenesulfonyl-5-fluoro-2-oxo-1,2-dihydropyrimi-din-4-yl) -3phenylurea as a white solid (0.100 g, 32%): mp 210-214 ° C; ¹ H NMR (400 MHz, DMSO-cfe) δ 11.26 (dd, J = 3.7, 1.1 Hz, 1H), 10.87 (m, 1H), 8.65 (m, 1H), 8.10 (d, J = 7.5 Hz, 2H), 7.85 (t, J = 7.5 Hz, 1H),
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7.71 (m, 2H), 7.45 (m, 2H), 7.34 (m, 2H), 7.10 (m, 1H); ESIMS m / z 389 ([M + H] ⁺ ).
Compounds 41-43 in Table I were synthesized as in
Example 8.
Example 9: Preparation of (1-benzenesulfonyl-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl) -3-phenylthiourea (44)
1. NaH

HH [00104] To a suspension of 4-amino-1-benzenesulfonyl-5fluoro-1H-pyrimidin-2-one (0.20 g, 0.74 mmol) in anhydrous tetrahydrofuran (THF; 3 mL) was added sodium hydrate (NaH; 0.044 g of 60% by weight of suspension in mineral oil, 1.11 mmol) at 0 ° C. After the evolution of gas decreased, the mixture was transferred via cannula to a cold mixture of phenyl isothiocyanate (1.0 g, 7.4 mmols) in anhydrous THF (5 mL) and stirred for 6 hours. The reaction mixture was diluted with EtOAc (25 ml), and the resulting solution was washed with saturated aqueous ammonium chloride (NH ₄ Cl; 15 ml) and brine (15 ml). The organic phase was dried over Na2SO4, filtered, and the solvent evaporated. The residue was purified by methanol (MeOH) and Et2O precipitation to give (1-benzenesulfonyl-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl) -3-phenylthiourea as a light yellow solid (0.025 g , 8%): mp 205208 ° C; ¹ H NMR (400 MHz, DMSO-cfe) δ 11.26 (dd, J = 3.7, 1.1 Hz, 1H),
10.87 (m, 1H), 8.65 (m, 1H), 8.10 (d, J = 7.5 Hz, 2H), 7.85 (t, J = 7.5 Hz, 1H), 7.71 (m, 2H), 7.45 (m, 2H), 7.34 (m, 2H), 7.10 (m, 1H); ESIMS m / z 405 ([M + H] ⁺ ).
Compounds 45 and 46 in Table I were synthesized as in Example 9.
Example 10: Preparation of phenyl ester of (1-benzenesulfonyl5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl) carbamic acid (47)
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1. NaH
2.

H [00105] To a suspension of 4-amino-1-benzenesulfonyl-5fluoro-1H-pyrimidin-2-one (0.20 g, 0.74 mmol) in anhydrous THF (3 mL) was added NaH (0.044 g of 60% by weight of suspension in mineral oil, 1.11 mmol) at 0 ° C. After the evolution of gas decreased, the mixture was transferred via cannula to a cold mixture of diphenyl carbonate (1.5 g, 7.4 mmols) in anhydrous THF (5 mL) and stirred for 6 hours. The reaction was diluted with EtOAc (25 ml) and the resulting solution was washed with saturated aqueous NH4Cl (15 ml) and brine (15 ml). The organic phase was dried over Na2SO4, filtered, and the solvent evaporated. The residue was purified by precipitation of MeOH and Et2O to give carbamic acid (1-benzenesulfonyl-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl) phenyl ester as a light brown solid (0.070 g, 24 %): mp 182-185 ° C; ¹ H NMR (400 MHz, DMSO- ^ 6) δ 7.95 (m, 2H),
7.87 (d, J = 7.0 Hz, 1H), 7.71 (d, J = 7.5 Hz, 1H), 7.61 (t, J = 7.7 Hz, 2H), 7, 33 (t, J = 7.9 Hz, 2H), 7.15 (d, J = 7.3 Hz, 1H), 7.06 (d, J = 7.6 Hz, 2H); ESIMS m / z 390 ([M + H] ⁺ ), 388 ([MH] ^- ).
Compounds 48-50 in Table I were synthesized as in Example 10.
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TABLE I: Compound Data and Related Characterization
Comp Structure MS Federal Police. (° C) Appearance ¹ NMR * (δ, CDCla) 3 ^O S ' ^CH 3 ^f tt ° / = Ν ^ Ν ^ Θ H3C-N CH3 ESIMS m / z 263 ([M +] ⁺ ) 133-134 Crystalline solidWhite 8.8 (s, 1), 7.81 (d, 1), 3.6 (s, 3), 3.23 (s, 3),3.21 (s, 3) 4 VA / = ^^ Θ H3C-NC3 ESIMS m / z 340 ([M +] ⁺ ) 199-203 white solid 8.73 (s, 1), 8.09 (d, J = 5.6 z, 1), 7.98 (d, J =8.4 z, 2), 7.32 (d, J = 8.4 z, 2), 3.21 (s, 3),3.20 (s, 3), 2.42 (s, 3) 5 F * sn ° “3 / = ^^ ° H ₃ CN ^CH 3 ESIMS m / z 356 ([M +] ⁺ ) 188-190 white solid 8.67 (s, 1), 8.04 (d, J = 5.6 z, 1), 7.99 (d, J =9.2 z, 2), 6.92 (d, J = 9.2 z, 2), 3.81 (s, 3),3.16 (s, 6) 6 ° /.C ₃ ΥΥ'Θ ³ / = ^^ ° 3C-N C3 ESIMS m / z 291 ([M +] ⁺ ) 144-145 yellow solidorange 8.83 (s, 1), 7.84 (d, J = 5.6 z, 1), 3.84-3.77 (m, 2), 3.25 (s, 3), 3.24 (s, 3), 1.91 - 1.74 (m, 2), 1.04 (t, J = 7.6 z, 3)
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Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 7 on ^S H3C-N CH3 ESIMS m / z 331 ([M + H] ⁺ ) 205-207 Brown solid 8.79 (s, 1H), 8.09-8.06 (m, 1H), 8.04 (d, J = 5.6Hz, 1H), 7.77-7.74 (m, 1H), 7.15-7.11 (m, 1H),3.23 (s, 6H) 9 _F o _s / Q> Yfo ^S H ₂ N ^ N ^ O ESIMS m / z 275 ([M + H] ⁺ ) 187-189 white solid (DMSO-cfe) 8.59 (br s, 1H), 8.33-8.24 (br s and d,2H), 8.21-8.18 (m, 1H), 8.00-7.96 (m, 1H), 7.29-7.24 (m, 1H) 10 ⁰ CH ₃ H ₂ NN ^ O ESIMS m / z 236 ([M + H] ⁺ ) 144-146 white solid (DMSO-cfe) 8.58 (br s, 1H), 8.28 (br s, 1H), 8.01 (d, J = 6.6 Hz, 1H), 3.88-3.82 (m , 2H), 1.74-1.63 (m, 2H), 0.97 (t, J = 7.4 Hz, 3H) 11 N = 0 A ' ^CH 3 XÁ H ₂ NN ^ O ESIMS m / z 274 ([M + H] ⁺ ) 235-237 white solid (DMSO-cfe) 8.48 (br s, 1H), 8.23 (d, J = 6.6 Hz,1H), 8.21 (br s, 1H), 8.20 (s, 1H), 7.84 (s, 1H),3.74 (s, 3H) 12 Yx ^s o ° o h ₂ n N ^ O ESIMS m / z 284 ([M + H] ⁺ ) 172-174 white solid (DMSO-cfe) 8.57 (br s, 1H), 8.25 (br s, 1H), 7.65 (d, J = 6.6 Hz, 1H), 7.41-7.35 (m , 3H), 7.30-7.26 (m, 2H), 5.20 (s, 2H)
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Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 13 ΥΎ'0 Η, Λ ESIMS m / z 339 ([M + H] ⁺ ) 229-230 white solid (DMSO-cfe) 8.56 (br s, 2H), 8.30 (d, J = 6.3 Hz,1H), 8.17 (d, J = 8.6 Hz, 1H), 7.95 (d, J = 2.0 Hz,1H), 7.74 (dd, J = 8.6, 2.0 Hz, 1H) 14 ^F TT ^S ° HjN ^ N ^ O ESIMS m / z 338 ([M + H] ⁺ ) 202-204 white solid (DMSO-cfe) 8.66 (br s, 1H), 8.37 (br s, 1H), 8.33(d, J = 6.6 Hz, 1H), 8.25 (d, J = 8.5 Hz, 2H), 8.06(d, J = 8.5 Hz, 2H) 15 Ch ₃ o £ T ^S 'O Υχ'ο h ₂ nno ESIMS m / z 348 ([M + H] ⁺ ) 220-223 white solid (DMSO-cfe + CD3CO2D) 8.30 (d, J = 6.6 Hz, 1H),8.27-8.23 (m, 2H), 8.19-8.15 (m, 2H), 3.3 (s, 3H) 16 . // // _F rx ° h ₂ nn ^ o ESIMS m / z 295 ([M + H] ⁺ ) 210 white solid (DMSO-cfe) 8.67 (br s, 1H), 8.38 (br s, 1H), 8.30 (d, J = 6.6 Hz, 1H), 8.22-8.13 (m , 4H)
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Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 17 Cl. ·, Ώ ' ESIMS m / z 338 ([M + H] ⁺ ) 206-207 white solid (DMSO-cfe) 8.65 (br s, 1H), 8.36 (br s, 1H), 8.28 (d, J = 2 Hz, 1H), 8.26 (d, J = 6.6 Hz, 1H), 8.01 (dd, J = 8.6, 2 Hz, 1H), 7.96 (d, J = 8.6 Hz, 1H) 18 ^Cl Vil o · AJ h ₂ nno ESIMS m / z 338 ([M + H] ⁺ ) 209-212 solid cream (DMSO-d6) 8.76 (s, 1H), 8.46 (s, 1H), 8.33 (d, J =6.4 Hz, 1H), 7.70 (m, 3H) 19 O ^N o 11 A · As Br H ₂ NN ^ O ESIMS ESIMS m / z 361 ([M + H] ⁺ ) 156-159 white solid (DMSO-cfe) 8.63 (s, 1H), 8.31 (s, 1H), 7.72 (d, J =6.4 Hz, 1H), 7.63 (d, J = 8.4 Hz, 2H), 7.26 (d, J =8.3 Hz, 2H), 5.23 (s, 2H) 20 The AA _s ^^ Cl ^ NN H ₂ O ESIMS m / z 318 ([M + H] ⁺ ) 168-170 white solid (DMSO-d6) 8.63 (s, 1H), 8.32 (s, 1H), 7.72 (d, J =6.5 Hz, 1H), 7.49 (d, J = 8.5 Hz, 2H), 7.33 (d, J =8.5 Hz, 2H), 5.25 (s, 2H) 21 O, Y ^ n / ^ OYI A ^ As CH, h ₂ nn ^ o ³ ESIMS m / z 298 ([M + H] ⁺ ) 164-166 white solid (DMSO-d6) 8.60 (s, 1H), 8.28 (s, 1H), 7.68 (d, J =6.5 Hz, 1H), 7.19 (d, J = 3.0 Hz, 4H), 5.17 (s, 2H),2.29 (s, 3H)
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Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 22 ^F ^ N ^{; SCI} ^ | Af Η, ΑΑο CH3 ESIMS m / z 480 ([M + H] ⁺ )white solid 9.12 (s, 1H), 8.26-8.20 (m, 1H), 8.07 (d, J = 6.5 Hz, 1H), 8.05-7.99 (m, 2H) , 7.96 (dd, J = 8.6, 2.2Hz, 1H), 7.31-7.23 (m, 1H), 6.21 (s, 1H), 2.26 (s, 3H) 23 ° ° C ^H 3 L ^f ESIMS m / z 481 ([M + 2H] ⁺ ), 477 ([M-2H] -) 132 dec white solid (DMS ° -fe) 9.26 (s, 1H), 8.29 (d, J = 8.8 Hz, 2H),8.11 (d, J = 5.8 Hz, 1H), 8.03 (d, J = 2.0 Hz, 1H),7.22 (dd, J = 8.8, 2.3 Hz, 1H), 7.12 (d, J = 2.1 Hz, 1H), 6.24 (s, 1H), 2.51 (s , 3H) 24 h ₂ u ^> u ^ o ESIMS m / z 270 ([M + H] ⁺ ) 195-196 white solid (CD3CN) 8.17 (d, J = 6.3 Hz, 1H), 8.05-8.00 (m, 2H), 7.80-7.73 (m, 1H), 7.66-7 , 60 (m, 2H), 6.86 (br s, 1H), 6.62 (br s, 1H) 25 ^ / ^CH 3 ° 'XJ h ^ n ^ o ESIMS m / z 284 ([M + H] ⁺ ) 208-210 white solid 8.18 (d, J = 6.3 Hz, 1H), 7.96-7.90 (m, 2H), 7.48-7.43 (m, 2H), 6.95 (br s, 1H), 6.64 (br s, 1H), 2.48 (s, 3H)
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Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 26 I ^ V ° ch3 o 1 II ³ Vn HN ^ N ^ O ESIMS m / z 300 ([M + H] ⁺ ) 182.5 white solid 8.40 (br s, 1H), 8.11 (d, J = 5.9 Hz, 1H), 8.04-7.98 (m, 2H), 7.02-6.96 (m, 2H ), 5.77 (br s, 1H), 3.88 (s, 3H) 27 O A - ^CH 3 ^F yY ^s % H ₂ N ESIMS m / z 208 ([M + H] ⁺ ) 181-184 white solid (CDaCN) 7.91 (d, J = 6.3 Hz, 1H), 7.2 (br s, 1H),6.7 (br s, 1H), 3.54 (s, 3H) 29 F Cl ^H 3C h ₃ co Cl ESIMS m / z 393 ([M + H] ⁺ ) 207-211 Light yellow solid (DMSO-ck) δ 8.73 (d, J = 0.6 Hz, 1H), 8.34 (d, J =5.9 Hz, 1H), 7.72 (m, 3H), 3.28 (s, 3H), 3.17 (d, J = 0.8 Hz, 3H) 30 O TVo U / = N ^ N ^ VO ^H 3c-N CH3 ESIMS m / z 339 ([M + H] ⁺ ) 152-154 white solid (DMSO-ck) 8.82 (s, 1H), 7.68 (d, J = 6.0 Hz, 1H),7.39 (m, 3H), 7.31 (dd, J = 6.6, 2.9 Hz, 2H), 5.26 (s, 2H), 3.31 (s, 3H), 3.15 (s, 3H)
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Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 31 O T ^ i 0 IA XC xC Cl / = NNO ^H 3 ^ N CH3 ESIMS m / z 373 ([M + H] ⁺ ) 140-143 white solid (DMSO-d6) 8.71 (s, 1H), 8.45 (d, J = 1.7 Hz, 1H),7.52 (d, J = 1.2 Hz, 4H), 5.23 (s, 2H), 3.24 (s, 3H),3.13 (s, 3H) 32 The N / aAX. NO ³ H3C-N CH3 ESIMS m / z 353 ([M + H] ⁺ ) 150-152 white solid (DMSO-d6) 8.71 (s, 1H), 8.44 (d, J = 1.9 Hz, 1H), 7.37 (d, J = 7.8 Hz, 2H), 7.22 ( d, J = 7.9 Hz, 2H), 5.14 (s, 2H), 3.24 (s, 3H), 3.13 (s, 3H), 2.31 (s, 3H) 34 rr ^Cl o L ü O V-n '% H ₃ ANANA ³ H ESIMS m / z 346 ([M + H] ⁺ ), 344 ([MH] ^- ) 159-162 tan solid 8.27 (d, J = 5.5 Hz, 1H), 8.07 (d, J = 8.7 Hz, 2H),7.80 (s, 1H), 7.57 (d, J = 8.7 Hz, 2H), 2.62 (s, 3H) 35 A ¥ ^Cl o JU o S ^ n '% Η3Μ-ΛΛ0 H ESIMS m / z 360 ([M + H] ⁺ ), 358 ([MH] ^- ) 148-154 dec Yellow solid (DMSO-cfe) 10.83 (s, 1H), 8.61 (d, J = 6.0 Hz, 1H),8.10 (d, J = 8.6 Hz, 2H), 7.79 (d, J = 8.6 Hz, 2H),2.63 (q, J = 7.3 Hz, 2H), 1.01 (t, J = 7.3 Hz, 3H)
42/49
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Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 36 ° ^ ^Cl ESIMS m / z 388 ([M + H] ⁺ ), 386 ([MH] ^- ) 129-132 Light yellow solid 8.16 (d, J = 5.5 Hz, 1H), 8.04 (d, J = 8.8 Hz, 2H),7.56 (d, J = 8.9 Hz, 2H), 1.24 (s, 9H) 37 . ° xr ^Cl ESIMS m / z 408 ([M + H] ⁺ ), 406 ([MH] ^- ) 156-159 white solid 12.64 (s, 1H), 8.25 (d, J = 7.6 Hz, 2H), 8.18 (d, J =5.5 Hz, 1H), 8.05 (m, 2H), 7.58 (m, 3H), 7.46 (t, J = 7.6 Hz, 2H) 39 rr ^C ° .. XJ O ^f Y ^ n ' ^s o „Α ^Λ · ESIMS m / z 422 ([M + H] ⁺ ), 420 ([MH] ^- ) 156-158 Brown solid 12.50 (s, 1H), 8.15 (m, 3H), 8.05 (d, J = 8.7 Hz,2H), 7.59 (d, J = 8.7 Hz, 2H), 7.25 (d, J = 6.9 Hz,2H), 2.42 (s, 3H) 41 f H> = ° / = H / ¼ / ^N_ $ AV ^Cl Ó ° ° ESIMS m / z 423 ([M + H] ⁺ ) 211-214 Pale yellow solid (DMSO-cfe) 11.26 (s, 1H), 10.90 (s, 1H), 8.64 (d, J = 5.6 Hz, 1H), 8.11 (d, J = 8.6 Hz, 2H), 7.81 (d, J = 8.7 Hz, 2H), 7.45 (d, J = 7.6 Hz, 2H), 7.35 (t, J = 7.3 Hz, 2H), 7.11 (s, 1H)
43/49
Petition 870180056292, of 06/29/2018, p. 50/76
Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 42 F Cl, M Ή o M / = <O O ClW ESIMS m / z 457 ([M + H] ⁺ ) 205-210 white solid (DMSO-cfe) 11.19 (s, 1H), 11.02 (s, 1H), 8.72 (s,1H), 7.76 (m, 3H), 7.47 (d, J = 8.4 Hz, 2H), 7.34 (t, J = 7.5 Hz, 2H), 7.10 (m, 1H) 43 F O ^{O 0} ESIMS m / z 419 ([M + H] ⁺ ) 185-191 white solid45 F h ₃ c H / ⁰ / = ⁰ A ^SO ESIMS m / z 435 ([M + H] ⁺ ) 190-195 Light brown solid (DMSO-cfe) 11.31 (s, 1H), 10.84 (s, 1H), 8.62 (s, 1H), 8.03 (d, J = 8.8 Hz, 2H), 7, 44 (s, 2H), 7.35 (s, 2H), 7.21 (d, J = 8.7 Hz, 2H), 7.10 (s, 1H), 3.89 (s, 3H) 46 F H / ' ⁰ H / ^N A 1 ^N ^ o S' A ^SO ESIMS m / z 411 ([M + H] ⁺ ) 182-185 Pale yellow solid (DMSO-cfe) 11.28 (s, 1H), 10.87 (s, 1H), 8.61 (s,1H), 8.29 (dd, J = 5.0, 1.4 Hz, 1H), 8.08 (d, J = 2.7Hz, 1H), 7.46 (m, 2H), 7.34 (m, 4H)
44/49
Petition 870180056292, of 06/29/2018, p. 51/76
Comp Structure MS Federal Police. (° C) Appearance ¹ H NMR * (δ, CDCla) 48 ^O % ^N O '-' oo ESIMS m / z 424 ([M + H] ⁺ ) 192-195 Pale yellow solid (DMSO-cfe) 7.97 (m, 2H), 7.85 (m, 1H), 7.69 (m,2H), 7.34 (dd, J = 10.9, 5.0 Hz, 2H), 7.15 (t, J = 7.3 Hz, 1H), 7.06 (m, 2H) 49 MO ^^ ^CH 3 OO ESIMS m / z 420 ([M + H] ⁺ ), 418 ([MH] -) 138-142 Pale yellow solid (DMSO-cfe) δ 7.89 (m, 2H), 7.84 (d, J = 7.1 Hz,1H), 7.33 (t, J = 7.9 Hz, 2H), 7.13 (m, 3H), 7.06 (dd, J = 7.6, 0.9 Hz, 2H), 3, 85 (s, 3H) 50 / = F ClN-S— (ΟMM O MO O Cl ESIMS m / z 458 ([M + H] ⁺ ) 199-203 Pale yellow solid (DMSO-cfe) 8.10 (m, 1H), 7.89 (m, 1H), 7.80 (d, J = 7.0 Hz, 1H), 7.35 (t, J = 7.9 Hz, 3H), 7.21 (dd, J = 4.9, 3.9 Hz, 1H), 7.15 (dd, J = 11.5, 4.2 Hz, 1H), 7.07 (m , 2H) * All ¹ H NMR spectra were recorded on CDCI3 at 300 or 400 MHz unless otherwise noted.
45/49
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46/49
Example 11: Evaluation of fungicidal activity: Wheat leaf spot (Mycosphaerella graminicola; anamorph: Septoria tritici; Bayer SEPTTR code) [00106] Wheat plants (variety Yuma) were grown from seeds in a 50% Metro mix greenhouse mineral soil / 50% without soil until the first leaf has fully emerged, with 710 seedlings per pot. These plants were inoculated with an aqueous spore suspension of Septoria tritici both before and after fungicidal treatments. After inoculation, the plants were kept in 100% relative humidity (one day in a dark dew chamber followed by two or three days in a lighted dew chamber) to allow the spores to germinate and infect the leaf. The plants were then transferred to a greenhouse for the disease to develop.
[00107] The following table shows the activity of typical compounds of the present description when evaluated in these experiments. The effectiveness of the test compounds in controlling the disease was determined by assessing the severity of the disease in the treated plants, then converting the severity to a control percentage based on the disease level of inoculated, untreated plants.
In each case of Table II the rating scale is as follows:
% Disease control Classification 76-100 THE 51-75 B 26-50 Ç 0-25 D Not tested AND
TABLE II: Activity of Compounds in SEPTTR at 100 ppm Protector in one day (1DP) and Dressing in three days (3DC)
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Comp SEPTTR 100 PPM 1DP SEPTTR 100 PPM 3DC 1 THE THE 2 THE THE 3 THE THE 4 THE THE 5 THE THE 6 THE THE 7 THE THE 8 THE THE 9 THE THE 10 THE THE 11 Ç Ç 12 THE THE 13 THE THE 14 THE THE 15 B THE 16 B THE 17 THE THE 18 THE THE 19 THE THE 20 AND AND 21 AND AND 22 THE THE 23 THE THE
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Comp SEPTTR 100 PPM 1DP SEPTTR 100 PPM 3DC 24 THE THE 25 THE THE 26 THE THE 27 THE THE 28 Ç B 29 THE THE 30 AND AND 31 AND AND 32 AND AND 33 THE Ç 34 THE THE 35 THE THE 36 THE THE 37 THE Ç 38 THE D 39 D THE 40 D Ç 41 AND AND 42 D Ç 43 D Ç 44 D Ç 45 Ç B 46 D Ç 47 B THE
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49/49
Comp SEPTTR 100 PPM 1DP SEPTTR 100 PPM 3DC 48 AND AND 49 D THE 50 THE THE
Petition 870180056292, of 06/29/2018, p. 56/76

权利要求:
Claims (16)
[1]
1/14
claims1. Compound, characterized by the fact that it presents the Formula I: , Vn ' ^{R3 r} ' A% 1 r ²
Formula I in which
R ¹ is:
H;
C 1 -C 6 alkyl optionally substituted with 1-3 R ⁴ ;
C2-C6 alkenyl optionally substituted with 1-3 R ⁴ ;
C3-C6 alkynyl optionally substituted with 1-3 R ⁴ ;
phenyl or benzyl, each of the phenyl or benzyl can optionally be replaced with 1-3 R ⁵ , or with a 5- or 6-membered saturated or unsaturated ring system, or with a 5-6 fused ring system, or with a system of 6-6 fused rings each containing 1-3 heteroatoms, each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
- (CHR ⁶ ) mOR ⁷ ;
-C (= O) R ⁸ ;
-C (= S) R ⁸ ;
-C (= O) OR ⁸ ;
-C (= S) OR ⁸ ;
- (CHR ⁶ ) m N (R ⁹ ) R ¹⁰ ;
-C (= O) N (R ⁹ ) R ¹⁰ ; or
-C (= S) N (R ⁹ ) R ¹⁰ ;
where m is an integer 1-3;
R ² is:
Petition 870180056292, of 06/29/2018, p. 57/76
[2]
2/14
H; or
Ci-Ce alkyl optionally substituted with R ⁴ ;
alternatively R ¹ and R ² can be taken together to form = CR ¹¹ N (R ¹² ) R ¹³ ;
R ³ is -S (O) 2R ¹⁴ ;
R ⁴ is independently halogen, C1-C6 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 haloalkylthio, amino, halothio, C1-C3 alkylamino, C2-C6 alkoxycarbonyl, C2-C6 alkylcarbonyl, C2-C6 alkylaminocarbonyl, hydroxyl, or C3-C6 trialkylsilyl;
R ⁵ is independently halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 haloalkylthio, halothio, amino, C1-C6 alkylamino, C2-C6 dialkylamino, C2-C6 alkoxycarbonyl, C1-C6 alkylsulfonyl, C2-C6 alkylcarbonyl, nitro, hydroxyl, or cyano;
R ⁶ is H, C1-C6 alkyl, C1-C6 alkoxy, phenyl or benzyl, each of benzyl or phenyl being optionally substituted with 1-3 R ⁵ ;
R ⁷ is H, C1-C6 alkyl, C2-C6 alkenyl, C3-C6 alkynyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl, C2-C6 alkylcarbonyl, phenyl or benzyl, each of which may be phenyl or benzyl optionally replaced with 1-3 R ⁵ , or with a 5- or 6-membered saturated or unsaturated ring system, or with a 5-6 fused ring system, or with a 6-6 fused ring system each containing 1-3 heteroatoms, each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
R ⁸ is H, C1-C6 alkyl, C2-C6 alkenyl, C3-C6 alkynyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl, phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with 1- 3 R ⁵ , or with a 5 or 6 mem saturated or unsaturated ring system
Petition 870180056292, of 06/29/2018, p. 58/76
[3]
3/14 bros, or with 5-6 fused ring system, or 6-6 fused ring system each containing 1-3 heteroatoms, each ring can optionally be replaced with 1-3 R ⁵ , biphenyl or naphthyl optionally replaced with 1-3 R ⁵ ;
R ^{9 is} H, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl, C2-C6 alkylcarbonyl, phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with 1-3 R ⁵ , or with a 5- or 6-membered saturated or unsaturated ring system, or with a 5-6 fused ring system, or with a 6-6 fused ring system each containing 1-3 hetero atoms, with each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
R ¹⁰ is H, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl, C2-C6 alkylcarbonyl, or benzyl, with benzyl being optionally substituted with 1-3 R ⁵ ;
alternatively R ⁹ and R ¹⁰ can be taken together to form a 5- or 6-membered saturated or unsaturated ring system containing 1-3 heteroatoms, each ring optionally being substituted with 1-3 R ⁵ ;
R ¹¹ is H or C1-C4 alkyl;
R ^{12 is} H, cyano, hydroxyl, C1-C4 alkyl, C1-C6 alkoxy, C2-C6 alkylcarbonyl, phenyl or benzyl, each of phenyl or benzyl being optionally substituted with 1-3 R ⁵ ;
alternatively R ¹¹ and R ¹² can be taken together to form a 5- or 6-membered saturated or unsaturated ring system containing 1-3 heteroatoms, each ring optionally being substituted with 1-3 R ⁵ ;
R ¹³ is H, C1-C4 alkyl, C1-C6 alkoxy, C2-C6 alkylcarbonyl, phenyl or benzyl, with each of phenyl or benzyl being optionally substituted with 1-3 R ⁵ ;
Petition 870180056292, of 06/29/2018, p. 59/76
[4]
4/14
Alternatively, R ¹² and R ¹³ can be taken together to form a 5- or 6-membered saturated or unsaturated ring system containing 1-3 heteroatoms, each ring optionally being substituted with 1-3 R ^{2 3 4 5} ; and
R ¹⁴ is Ci-Ce alkyl, Ci-Ce haloalkyl, amino, Ci-Ce alkylamino, C2-C6 dialkylamino, phenyl or benzyl, each of which phenyl or 0 benzyl can be optionally substituted with 1-3 R ⁵ , 4 (3-chloro-5- (tri-fluoro-methyl) pyridin-2-yloxy) -3-methylphenyl, 4- (3-chloro-5- (trifluor-methyl) pyridin-2-yloxy) -2-methylphenyl , or a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms, each ring being optionally substituted with 1-3 R ⁵ ;
with the proviso that if R ¹ and R ² are both H, then R ¹⁴
2. Compound according to claim 1, characterized by the fact that R ¹ is selected from the group consisting of H, C (= O) R ⁸ , -C (= O) OR ⁸ , -C (= O) N (R ⁹ ) R ¹⁰ and -C (= S) N (R ⁹ ) R ¹⁰ .
Compound according to claim 1 or 2, characterized in that R ⁸ is C- | -C ₆ alkyl or phenyl, the phenyl being optionally substituted with 1-3 R ⁵ .
Compound according to claim 1 or 2, characterized by the fact that R ⁹ is phenyl, and R ¹⁰ is H.
[5]
Compound according to any one of claims 1 to 4, characterized by the fact that R ² is H.
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5/14
[6]
6. Compound according to claim 1, characterized by the fact that R ¹ and R ² are taken together to form = CR ¹¹ N (R ¹² ) R ¹³ .
[7]
7. A compound according to claim 6, characterized by the fact that R ¹¹ is H, and R ¹² and R ¹³ are each, independently, C1-C4 alkyl.
[8]
A compound according to any one of claims 1 to 7, characterized in that R ¹⁴ is selected from the group consisting of C1-C6 alkyl, 4- (3-chloro-5- (tri-fluoro-methyl) pyridin -2-yloxy) -3methylphenyl, 4- (3-chloro-5- (tri-fluoro-methyl) pyridin-2-yloxy) -2-methylphenyl, phenyl or benzyl, each of which may be phenyl or benzyl optionally substituted with 1-3 R ⁵ , or a saturated or unsaturated ring, with 5 or 6 members, containing 1-3 heteroatoms, each ring being optionally substituted with 1-3 R ⁵ .
[9]
Compound according to claim 3 or 8, characterized in that R ⁵ is independently selected from the group consisting of halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1C6 alkoxy, C1-C6 alkylsulfonyl, ecyan.
[10]
10. Compound according to claim 1, characterized by the fact that it is selected from the group consisting of:
Petition 870180056292, of 06/29/2018, p. 61/76
6/14
J J
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7/14
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8/14
Petition 870180056292, of 06/29/2018, p. 64/76
9/14
J
[11]
11. Compound according to claim 1, characterized by the fact that it is selected from the group consisting of:
Petition 870180056292, of 06/29/2018, p. 65/76
10/14
[12]
12. Composition for the control of a fungal pathogen, characterized by the fact that it comprises a compound of Formula II
Formula II
Petition 870180056292, of 06/29/2018, p. 66/76
11/14 in which
R ¹ is:
H;
C ₁ -C ₆ alkyl optionally substituted with 1-3 R ⁴ ; C ² -C ⁶ alkenyl optionally substituted with 1-3 R ⁴ ; C ₃ -C ₆ alkynyl optionally substituted with 1-3 R ⁴ ;
phenyl or benzyl, each of the phenyl or benzyl can optionally be replaced with 1-3 R ⁵ , or with a 5- or 6-membered saturated or unsaturated ring system, or with a 5-6 fused ring system, or with a system of 6-6 fused rings each containing 1-3 heteroatoms, each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
- (CHR ⁶ ) mOR ⁷ ;
-C (= O) R ⁸ ;
-C (= S) R ⁸ ;
-C (= O) OR ⁸ ;
-C (= S) OR ⁸ ;
-S (O) 2R ⁸ ;
- (CHR ⁶ ) m N (R ⁹ ) R ¹⁰ ;
-C (= O) N (R ⁹ ) R ¹⁰ ; or
-C (= S) N (R ⁹ ) R ¹⁰ ;
where m is an integer 1-3;
R ² is:
H; or
C1-C6 alkyl optionally substituted with R ⁴ ;
alternatively, R ¹ and R ² can be taken together to form = CR ¹¹ N (R ¹² ) R ¹³ ;
R ³ is -S (O) 2R ¹⁴ ;
Petition 870180056292, of 06/29/2018, p. 67/76
12/14
R ⁴ is independently halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 haloalkylthio, amino, halothio, C1-C3 alkylamino, C2-C6 alkoxycarbonyl, C2-C6 alkylcarbonyl, C2-C6 alkylaminocarbonyl, hydroxyl, or C3-C6 trialkylsilyl;
R ⁵ is independently halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 haloalkylthio, halothio, amino, C1-C6 alkylamino, C2-C6 dialkylamino, C2-C6 alkoxycarbonyl, C1-C6 alkylsulfonyl, C2-C6 alkylcarbonyl, nitro, hydroxyl, or cyano;
R ⁶ is H, C1-C6 alkyl, C1-C6 alkoxy, phenyl or benzyl, each of benzyl or phenyl being optionally substituted with 1-3 R ⁵ ;
R ⁷ is H, C1-C6 alkyl, C2-C6 alkenyl, C3-C6 alkynyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl, C2-C6 alkylcarbonyl, phenyl or benzyl, each of which may be phenyl or benzyl optionally replaced with 1-3 R ⁵ , or with a 5- or 6-membered saturated or unsaturated ring system, or with a 5-6 fused ring system, or with a 6-6 fused ring system each containing 1-3 heteroatoms, each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
R ⁸ is H, C1-C6 alkyl, C2-C6 alkenyl, C3-C6 alkynyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl, phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with 1- 3 R ⁵ , either with a 5- or 6-membered saturated or unsaturated ring system, or with a 5-6 fused ring system, or with a 6-6 fused ring system each containing 1-3 hetero atoms, each ring being able to optionally be substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
R ⁹ is H, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl,
Petition 870180056292, of 06/29/2018, p. 68/76
[13]
13/14
C2-C6 alkylcarbonyl, phenyl or benzyl, each of the phenyl or benzyl can be optionally substituted with 1-3 R ⁵ , or with a 5- or 6-membered saturated or unsaturated ring system, or with 5- 6 fused rings, or with 6-6 fused rings each containing 1-3 heteroatoms, each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
R ¹⁰ is H, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxyalkyl, C2-C6 alkylcarbonyl, or benzyl, with benzyl being optionally substituted with 1-3 R ⁵ ;
alternatively, R ⁹ and R ¹⁰ can be taken together to form a 5- or 6-membered saturated or unsaturated ring system containing 1-3 heteroatoms, each ring optionally being substituted with 1-3 R ⁵ ;
R ¹¹ is H or C1-C4 alkyl;
R ¹² is H, cyano, hydroxyl, C1-C4 alkyl, C1-C6 alkoxy, C2-C6 alkylcarbonyl, phenyl or benzyl, each of phenyl or benzyl being optionally substituted with 1-3 R ⁵ ;
alternatively, R ¹¹ and R ¹² can be taken together to form a 5- or 6-membered saturated or unsaturated ring system containing 1-3 heteroatoms, each ring optionally being substituted with 1-3 R ⁵ ;
R ¹³ is H, C1-C4 alkyl, C1-C6 alkoxy, C2-C6 alkylcarbonyl, phenyl or benzyl, with each of phenyl or benzyl being optionally substituted with 1-3 R ⁵ ;
alternatively, R ¹² and R ¹³ can be taken together to form a 5- or 6-membered saturated or unsaturated ring system containing 1-3 heteroatoms, each ring optionally being substituted with 1-3 R ⁵ ; and
R ¹⁴ is C1-C6 alkyl, C1-C6 haloalkyl, amino, C1-C6 alkyl
Petition 870180056292, of 06/29/2018, p. 69/76
[14]
14/14 mino, C2-C6 dialkylamino, phenyl or benzyl, each of which phenyl or benzyl can be optionally substituted with 1-3 R ⁵ , 4 (3-chloro-5- (tri-fluorine-methyl) pyridin-2-yloxy) -3-methylphenyl, 4- (3-chloro-5- (trifluoromethyl) pyridin-2-yloxy) -2-methylphenyl, or a 5- or 6-membered saturated or unsaturated ring containing 1- 3 heteroatoms, with each ring optionally substituted with 1-3 R ⁵ ; and a phytologically acceptable vehicle material.
13. Composition according to claim 12, characterized by the fact that the fungal pathogen is apple Sarana (Venturia inaequalis), Wheat Leaf Macha (Septoria tritici), Beet Leaf Stain (Cercospora beticola), Stain Peanut Leaf (Cercospora arachidicola and Cercosporidium personatum) or Black Banana Sigatoka (Mycosphaerella fijiensis).
14. Composition according to claim 12 or 13, characterized by the fact that it also comprises an adjuvant surfactant.
[15]
15. Method for controlling or preventing fungi attack on a plant, characterized by the fact that it comprises the steps of applying a fungicidally effective amount of at least one compound of Formula II, as defined in claim 12, to at least one plant, an area adjacent to the plant, the soil adapted to support the growth of the plant, the root of the plant, the plant's foliage, and a seed adapted to produce the plant.
[16]
16. Method, according to claim 15, characterized by the fact that it also comprises applying an adjuvant surfactant.

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法律状态:
2017-12-12| B25A| Requested transfer of rights approved|Owner name: ADAMA MAKHTESHIM LTD. (IL) |

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2018-04-03| B07A| Technical examination (opinion): publication of technical examination (opinion)|

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2018-09-11| B06G| Technical and formal requirements: other requirements|

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2018-10-02| B06I| Technical and formal requirements: publication cancelled|Free format text: ANULADA A PUBLICACAO CODIGO 6.7 NA RPI NO 2488 DE 11/09/2018 POR TER SIDO INDEVIDA. |

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2019-01-15| B25G| Requested change of headquarter approved|Owner name: ADAMA MAKHTESHIM LTD. (IL) |

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2019-04-02| B15K| Others concerning applications: alteration of classification|Free format text: A CLASSIFICACAO ANTERIOR ERA: C07D 339/02 Ipc: C07D 239/47 (1980.01), C07D 401/12 (1974.07), C07D |

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2019-04-09| B09A| Decision: intention to grant|

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2019-05-28| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 05/08/2010, OBSERVADAS AS CONDICOES LEGAIS. (CO) 20 (VINTE) ANOS CONTADOS A PARTIR DE 05/08/2010, OBSERVADAS AS CONDICOES LEGAIS |

优先权:

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申请号 | 申请日 | 专利标题

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US23220409P| true| 2009-08-07|2009-08-07|

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US61/232,204|2009-08-07|

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PCT/US2010/044592|WO2011017547A1|2009-08-07|2010-08-05|N1-sulfonyl-5-fluoropyrimidinone derivatives|

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