DERIVATIVES OF 5-FLUORPYRIMIDINONE, ITS USES, COMPOSITION AND METHOD FOR CONTROL OR PREVENTION OF FU

专利摘要:
5-fluorpyrimidinone derivatives, their uses, composition and method for controlling or preventing fungal attack in a plant The present invention relates to the field of 5-fluorpyrimidinones and their derivatives and their use as fungicides.
公开号:BR112012002828B1
申请号:R112012002828-6
申请日:2010-08-05
公开日:2019-05-28
发明作者:Timothy Boebel；Kristy Bryan；Peter Johnson；Beth Lorsbach；Kevin Meyer；W. Owen；Michael Sullenberger；Jeffery Webster；Chenglin Yao；Timothy P. Martin
申请人:Adama Makhteshim Ltd.；
IPC主号:

专利说明:

Invention Patent Descriptive Report for 5-FLUORPYRIMIDINONE DERIVATIVES, THEIR USES, COMPOSITION AND METHOD FOR THE CONTROL OR PREVENTION OF FUNGAL ATTACK IN A PLANT.
Cross Reference to Related Orders [001] This application claims the benefit of US Series Interim Patent Application No. 61 / 232,177 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 important fungi. Generally, no single fungicide is useful in all situations. Consequently, research continues to produce fungicides that can perform better, that are easier to use, and that are more economical.
[003] US Patent 3,368,938 (dated February 13, 1968) disclosed the use of 5-fluorocytosine to combat fungi. Examples of other research efforts regarding different synthesis and use of fluorocytosines and related compounds are as follows: Chiacchio et al. Enantioselective syntheses and cytotoxicity of N, ONucleosides, J. Med. Chem., 46 (17), pages 3696-3702 (2003) revealed enantiomers of 4'-aza-2 ', 3'-didesoxynucleosides and that (5'S) -
5-fluoro-1-isoxazolidin-5-yl-1H-pyrimidin-2,4-dione is a good inducer of apoptosis in lymphoid and monocytoid cells. Robins et al. A Direct Synthesis of 5-Fluorocytosine and its Nucleosides Using Trifluoromethyl Hypofluorite, J. Chem. Soc. Chem. Commun., Pages 18-19 (1972) revealed a direct method for synthesizing 5-fluorocytosine to make antineoplastic and antiviral agent 5-fuorocytosine arabinoside. Lewis et al. Synthesis and activity of anti-human cytomegalovirus in vitro (HCMV) of certain alkenyl-substituted cytosines and 5
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2/73 halocytosines, J. Het. Chem., 32 (5), pages 1513-1515 (1995) evaluated eight cytokocytosines for in vitro activity against cells infected with Anti-Human Cytomegalovirus (HCMV) in AIDS patients. Kulikowski et al. Methylation and tautomerism of nucleosides from
5-fluorocytosine and its analogs, Nuc. Acids, 4, page S9 (1978) revealed the synthesis of substituted N-methyl derivatives of 5-fluorocytosine 1 for antitumor and antiviral activities. U.S. Patent 4,845,081 (July 4, 1989) disclosed new aminomethyl derivatives, which increase the topical distribution of pharmaceutical products.
[004] The present invention relates to 5 fluoropyrimidinone compounds and their use as fungicides. The compounds of the present invention can offer protection against ascomycetes, basidiomycetes, deuteromycetes and oomycetes.
[005] An embodiment of the present invention can include compounds of Formula I:
Formula I [006] in which [007] R ¹ is:
[008] H;
[009] C-rCe alkyl optionally substituted with 1-3 R ⁴ ;
[0010] C-rCe alkenyl optionally substituted with 1-3 R ⁴ ;
[0011] C ₃ -C ₆ alkynyl optionally substituted with 1-3 R ⁴ ;
[0012] phenyl or benzyl wherein each of phenyl and 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
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3/73 of fused rings 5-6, or with a system of fused rings 6-6 each containing 1-3 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1 -3 R ⁵ ;
[0013] - (CHR ⁶ ) mOR ⁷ ;
[0014] - (CHR ⁶ ) _m N (R ⁹ ) R ¹⁰ ;
[0015] -C (= O) R ⁸ ;
[0016] -C (= S) R ⁸ ;
[0017] -S (O) 2R ⁸ ;
[0018] -C (= O) OR ⁸ ;
[0019] -C (= S) OR ⁸ ;
[0020] - (CHR ⁶ ) mN (R ⁹ ) R ¹⁰ ;
[0021] -C (= O) N (R ⁹ ) R ¹⁰ ; or [0022] -C (= S) N (R ⁹ ) R ¹⁰ ;
[0023] where m is an integer 1-4;
[0024] R ² is:
[0025] H; or [0026] C1-C6 alkyl optionally substituted with R ⁴ ;
[0027] alternatively R ¹ and R ² can be taken together to form:
[0028] = CR ^p N (R ¹² ) R ¹³ ;
[0029] R ³ is:
[0030] C ₁ -C ₆ alkyl optionally substituted with 1-3 R ⁴ , C ₁ -C ₆ haloalkyl, C1-C6 hydroxyalkyl, C2-C6 alkoxyalkyl, C2-C6 haloalkoxyalkyl, C2-C6 alkenyl optionally substituted with R ¹⁴ , C2-C6 haloalkenyl, C3-C6 alkynyl, phenyl or benzyl where each of phenyl and 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 fused ring system 5-6, or with a fused ring system 6-6 each containing 1-3 heteroatoms where each ring can be
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4/73 optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
[0031] - (CHR ⁶ ) mOR ⁷ ;
[0032] - (CHR ⁶ ) _m SR ⁸ ; or [0033] - (CHR ⁶ ) _m N (R ⁹ ) R ¹⁰ ;
[0034] R ⁴ is independently halogen, C1-C6 alkyl, C1-C4 haloalkyl, C ₁ -C ₄ alkoxy, C ₁ -C ₄ haloalkoxy, C ₁ -C ₄ alkylthio, C ₁ -C ₄ haloalkylthio, amino, halothio , C ₁ -C ₃ alkylamino, C ₂ -C ₆ alkoxycarbonyl, C ₂ -C ₆ alkylcarbonyl, C ₂ -C ₆ alkylaminocarbonyl, hydroxyl, C ₃ -C ₆ [0035] trialkylsilyl, phenyl optionally substituted with 1-3 R ⁵ , or with a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ ;
[0036] R ⁵ is independently halogen, C ₁ -C ₆ alkyl, C ₁ -C ₆ haloalkyl, C ₁ -C ₆ alkoxy, C ₁ -C ₆ haloalkoxy, C ₁ -C ₆ alkylthio, C ₁ -C ₆ haloalkylthio halogen, amino, C ₁ -C ₆ alkylamino, C ₂ -C ₆ dialkylamino, C ₂ -C ₆ alkoxycarbonyl, C ₂ -C ₆ alkylcarbonyl, C ₁ -C ₆ alkylsulfonyl, nitro, hydroxyl, or cyano;
[0037] R ⁶ is H, C ₁ -C ₆ alkyl, C ₁ -C ₆ alkoxy, C ₁ -C ₆ alkoxycarbonyl, phenyl or benzyl where each of phenyl and benzyl can be optionally substituted with 1-3 R ⁵ ;
[0038] R ⁷ is H, C ₁ -C ₈ alkyl, C ₂ -C ₆ alkenyl, C ₃ -C ₆ alkynyl, C ₁ -C ₆ haloalkyl, C ₁ -C ₆ alkoxyalkyl, C ₂ -C ₆ trialkylsilyl, C ₂ -C ₆ trialkylsilylalkyl C ₂ -C ₆ alkylcarbonyl, C ₁ -C ₆ alkoxycarbonyl, phenyl or benzyl where each of phenyl and benzyl can be optionally substituted with 13 R ⁵ , or with a saturated ring system or 5- or 6-membered unsaturated, or with a 5-6 fused ring system, or with a 6-6 fused ring system each containing 1-3 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
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5/73 [0039] R ⁸ is H, C ₁ -C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₃ -C ₆ alkynyl, C ₁ -C ₆ haloalkyl, C ₁ -C ₆ alkoxyalkyl, phenyl or benzyl in that each of phenyl and benzyl can optionally be 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 fused rings 6-6 each containing 1-3 heteroatoms each ring optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
[0040] R ⁹ is H, C ₁ -C ₆ alkyl, C ₁ -C ₆ haloalkyl, C ₁ -C ₆ alkoxyalkyl, C ₂ C ₆ alkylcarbonyl, phenyl or benzyl where each of the phenyl and benzyl can be 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 fused ring system
6-6 each containing 1-3 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
[0041] R ¹⁰ is H, C ₁ -C ₆ alkyl, C ₁ -C ₆ haloalkyl, C ₁ -C ₆ alkoxyalkyl, C2-C6 alkylcarbonyl, or benzyl, where benzyl can be optionally substituted with 1-3 R ⁵ ;
[0042] alternatively R and R can be taken together to form a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ ;
[0043] R ¹¹ is H or C ₁ -C ₄ alkyl;
[0044] R ¹² is H, cyano, hydroxyl, C1-C4 alkyl, C1-C6 alkoxy, C2-C6, alkylcarbonyl, phenyl or benzyl where each of the phenyl and 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 heteroatoms where each ring can be
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6/73 optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl 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 containing 1-3 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ ;
[0046] R ¹³ is H, C ₁ -C ₄ alkyl, C ₁ -C ₆ alkoxy, C ₂ -C ₆ , alkylcarbonyl, phenyl or benzyl where each of the phenyl and 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 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ , biphenyl or naphthyl optionally substituted with 1-3 R ⁵ ;
[0047] and [0048] alternatively R ¹² and R ¹³ can be taken together to form a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms where each ring can be optionally substituted with 1-3 R ⁵ .
[0049] R is phenyl or benzyl in which each of phenyl and benzyl can be optionally substituted with 1-3 R ⁵ .
[0050] Another embodiment of the present invention may include a fungicidal composition for the control or prevention against fungal attack comprising the compounds described below and a phytologically acceptable carrier material.
[0051] Yet another embodiment of the present invention may include a method for controlling or preventing fungal 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 fungus, to a plant, to an area adjacent to
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7/73 plant, or to a seed adapted to produce the plant.
[0052] The term alkyl refers to a branched, unbranched, or cyclic carbon chain, including methyl, ethyl, propyl, butyl, isopropyl, isobutyl, tertiary butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl among others.
[0053] The term alkenyl refers to a branched, unbranched, or cyclic carbon chain containing one or more double bonds including ethylene, propenyl, butenyl, isopropenyl, isobutenyl, cyclohexenyl, among others.
[0054] The term alkynyl refers to a branched or unbranched carbon chain containing one or more triple bonds including propynyl, butynyl among others.
[0055] As used throughout this report, the term 'R' refers to the group consisting of C ₂ -8 alkyl, C3-8 alkenyl or C3-8 alkynyl, unless otherwise specified.
[0056] The term alkoxy refers to a substituent -OR.
[0057] The term alkoxycarbonyl refers to a substituent -C (O) OR.
[0058] The term alkylcarbonyl refers to a substituent -C (O) -R. [0059] The term alkylsulfonyl refers to a substituent -SO ₂ -R.
[0060] The term haloalkylsulfonyl refers to an SO ₂ -R substituent in which R is totally or partially substituted with Cl, F, I, or Br or any combination thereof.
[0061] The term alkylthio refers to a substituent -S-R.
[0062] The term haloalkylthio refers to an alkylthio, which is substituted with Cl, F, I, or Br or any combination thereof.
[0063] The term halothio refers to a sulfur substituted with three or five substituents F.
[0064] The term alkylaminocarbonyl refers to a C (O) -N (H) -R substituent.
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8/73 [0065] The term dialkylaminocarbonyl refers to a C (O) -NR2 substituent.
[0066] The term alkylcycloalkylamino refers to a cycloalkylamino substituent that is substituted with an alkyl group.
[0067] The term trialkylsilyl refers to -SiR ₃ .
[0068] The term cyan refers to a substituent -C = N.
[0069] The term hydroxyl refers to a substituent -OH.
[0070] The term amino refers to a substituent -NH ₂ .
[0071] The term alkylamino refers to a substituent -N (H) -R.
[0072] The term dialkylamino refers to a substituent -NR ₂ .
[0073] The term trialkylsilylalkyl refers to a substituent -SiR ₃ in an alkyl.
[0074] The term alkoxyalkoxy refers to -O (CH ₂ ) _n O (CH ₂ ) _m CH ₃ where n is an integer from 1-3 and is 0-2.
[0075] The term alkoxyalkyl refers to an alkoxy substitution on an alkyl.
[0076] The term haloalkoxyalkyl refers to an alkoxy substitution on an alkyl that is totally or partially substituted with Cl, F, Br, or I, or any combination thereof.
[0077] The term hydroxyalkyl refers to an alkyl that is substituted with a hydroxyl group.
[0078] The term haloalkoxy refers to a substituent -OR-X, where X is Cl, F, Br, or I, or any combination thereof.
[0079] The term haloalkyl refers to an alkyl, which is substituted with Cl, F, I, or Br or any combination thereof.
[0080] The term haloalkenyl refers to an alkenyl, which is substituted with Cl, F, I, or Br or any combination thereof.
[0081] The term haloalkynyl refers to an alkynyl that is substituted with Cl, F, I, or Br or any combination thereof.
[0082] The term halogen or halo refers to one or more atoms
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9/73 halogen, defined as F, Cl, Br, and I.
[0083] The term hydroxycarbonyl refers to a substituent -C (O) OH.
[0084] The term nitro refers to a substituent -NO ₂ .
[0085] Throughout this report, any reference to compounds of Formula I should be considered to also include 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, among others. In addition, compounds of Formula I can include tautomeric forms.
[0086] Certain compounds disclosed 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 disclosed in the present invention show the design of only one geometric shape for the sake of clarity, but are intended to represent all geometric and tautomeric shapes of the molecule.
[0087] Those skilled in the art also understand that additional substitutions are permissible, unless otherwise noted, as long as the chemical bonding and deformation energy rules are satisfied and the product still exhibits fungicidal activity.
[0088] Another embodiment of the present invention is the use of a compound of Formula I for the protection of a plant against attack by a phytopathogenic organism or for the treatment of a plant infested by a phytopathogenic organism, comprising the application of a compound of Formula I, or a composition comprising the compound to the soil, to a plant, to a part of a plant, to the foliage, and / or to the seeds.
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In addition, another embodiment of the present invention is a composition useful for protecting a plant from attack by a phytopathogenic organism and / or for treating a plant infested by a phytopathogenic organism comprising a compound of Formula I and a carrier material phytologically acceptable.
[0090] Additional aspects and advantages of the present invention will become apparent to those skilled in the art upon consideration of the detailed description below of the illustrative modalities exemplifying the best embodiment of the invention as now perceived.
Detailed Description of the Invention [0091] The compounds of the present invention can be applied by any of several known techniques, either as the compounds or as formulations comprising the compounds. For example, the compounds can be applied to the roots, seeds or foliage 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, sprinkles, wetting powders, flowable concentrates, or emulsifiable concentrates.
[0092] Preferably, the compounds of the present invention 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 other liquids, for application, or formulations can be of a powder or granular type, which can be applied without further treatment. Formulations can be prepared according to procedures that are conventional in the agricultural chemistry literature.
[0093] The present invention contemplates all vehicles by means of which one or more of the compounds can be formulated to dis
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11/73 distribution 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-suspendable, or emulsifiable formulations that are solid, commonly known as wetting powders; or liquids, usually known as emulsifiable concentrates, aqueous suspensions, or suspension concentrates. As will be easily understood, it is possible to use any material to which these compounds can be added, as long as it produces the desired utility without significantly interfering with the activity of these compounds as antifungal agents.
[0094] Humectable 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 carrier and surfactants. The concentration of the compound in the wettable powder can vary from about 10 percent to about 90 weight percent based on the total weight of the wettable powder, more preferably from about 25 weight percent to about 75 weight percent. In the preparation of formulations in the form of wettable powder, the compounds can be mixed with any finely divided solid, such as propylene, talc, chalk, plaster, Fuller earth, bentonite, atapulgite, starch, casein, gluten, montmorillonite clay, earth diatoms, purified silicates, among others. In such operations, the finely divided carrier and surfactant are typically mixed with the compounds and ground.
[0095] Emulsifiable concentrates of the compounds of Formula I may comprise 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 carrier, which is either a water-miscible solvent or a mixture of organic solvents.
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12/73 water-immiscible cos, 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 aromatics, especially the high boiling point naphthalene and olefinic portions of oil such as heavy aromatic naphtha. Other organic solvents can also be used, including terpenic solvents, rosin derivatives, aliphatic ketones, such as cyclohexanone, and complex alcohols, such as 2-ethoxyethanol.
[0096] Emulsifiers that can be advantageously employed in this invention can be easily 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 non-ionic emulsifiers useful in the preparation of emulsifiable 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 alkyl phenols and esters carboxylics 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 polyglycol sulfated ethers and appropriate salts of polyglycol phosphate ether.
[0097] Representative organic liquids that can be employed in the preparation of the emulsifiable concentrates of the room temperature compounds of the present invention are aromatic liquids such as xylene, propyl benzene fractions; or mixed naphthalenic 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 the
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13/73 methyl methylene glycol ether among others. Mixtures of two or more organic liquids can also be used in the preparation of the emulsifiable concentrate. Organic liquids include xylene, and propyl benzene fractions, with xylene being more preferred in some cases. Surfactant 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.
Aqueous suspensions comprise suspensions of one or more water-insoluble Formula I compounds, dispersed in an aqueous vehicle at 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 comprised of water and surfactants selected from the same types 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.
[0099] It is generally more effective to grind and mix at the same time by preparing the aqueous mixture and homogenizing it in equipment such as a sand mill, a ball mill, or a piston-type homogenizer.
Aqueous emulsions comprise emulsions of one or more water insoluble pesticide active ingredients emulsified in an aqueous vehicle at a 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
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14/73 it must be dissolved in a suitable water-immiscible solvent before preparing the aqueous emulsion. Emulsions are prepared by emulsifying the liquid pesticide active ingredient or a water-immiscible solution of the same in an aqueous medium typically with the inclusion of surfactants that assist in the formation and stabilization of the emulsion described above. This is usually done with the help of vigorous mixing provided by high shear mixers or homogenizers.
[00101] 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 granular formulation of the compounds, dispersed in an inert carrier that consists entirely or largely of coarsely divided inert material such as atapulgite , bentonite, diatomite, clay or similar cheap substance. Such formulations are usually prepared by dissolving the compounds in a suitable solvent and applying the solution to a granular carrier that has previously been reduced to the appropriate particle size, in the range of about 0.5 to about 3 mm. A suitable solvent is a solvent in which the compound is substantially or completely soluble. Such formulations can also be prepared by making a mass or paste from the carrier and the compound and solvent, and grinding and drying to obtain the desired granular particle.
[00102] Sprinkles containing the compounds of Formula I can be prepared by intimately mixing one or more of the compounds in powder form with a powdery agricultural vehicle, such as, for example, kaolin type clay, ground volcanic rock, among others. Pits can suitably contain from about 1 to about 10 weight percent of the compounds, based on the total weight of the starch.
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15/73 [00103] The formulations may additionally contain adjuvant surfactants to improve the deposition, wetting and penetration of the compounds in the target culture 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 typically decay 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.
[00104] Suitable adjuvant surfactants include, but are not limited to, ethoxylated nonyl phenols, ethoxylated synthetic or natural 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 US Patent Application Series No. 11 / 495,228, the report of which is expressly incorporated herein by reference.
[00105] Formulations can optionally include combinations that contain other pesticidal compounds. Such additional pesticidal compounds may be fungicides, insecticides, herbicides, nematicides, miticides, arthropodicides, bactericides or combinations thereof which are compatible with the compounds of the present invention in the medium selected for application, and not antagonistic to the activity of the present compounds. Therefore, in such embodiments, the other pesticidal compound is used as a supplementary toxic agent for the same or different pesticide use. The combined Formula I compounds and the pesticidal compound can generally be present in a weight ratio of 1: 100 to 100: 1.
[00106] The compounds of the present invention can also be combined with other fungicides to form fungicidal mixtures and
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16/73 synergistic mixtures thereof. The fungicidal compounds of the present invention are generally applied in conjunction with one or more other fungicides to control a wider variety of undesirable diseases. When used in conjunction with other fungicides, the compounds now claimed can be formulated with the other fungicides, mixed in tank with the other fungicides or applied sequentially with the other fungicides. Such other fungicides may include 2- (thiocyanatomethylthio) -benzothiazole, 2-phenylphenol sulfate, 8-hydroxyquinoline, ametoctradine, amisulbrom, antimycin, Ampelomyces quisqualis, azaconazole, azoxystrobin, Bacillus subtilis, Bacillusyl, benilxyl, bylxyl, bylxyl, bylylyl, benzoyl benzylaminobenzene sulfonate salt (BABS), bicarbonates, biphenyl, bismertiazole, bitertanol, bixafen, blasticidin-S, borax, Bordeaux mixture, boscalid, bromuconazole, bupyrimide, calcium polysulfide, captafol, carmine, carbendazim, carbendazim, carbendazim, carbendazim, carbendazim clazafenone, chloroneb, chlorotalonil, clozolinate, Coniothyrium minitans, copper hydroxide, copper octanoate, copper oxychloride, copper sulfate, copper sulphate (tribasic), cuprous oxide, ciazofamide, ciflufenamide, cymoxanil, cyproxacil, cyproconzol, cyproconzol, , ethylenebis- (dithiocarbamate) diamone, diclofluanide, dichlorophene, diclocymet, diclomezine, dichloran, diethofencarb, diphenoconazole, difenz oquat ion, diflumetorim, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinobuton, dinocap, diphenylamine, ditianon, dodemorph, dodemorph acetate, dodine, dodine free base, edifenphos, enestrobin, epoxiconamidone, iamoxyamine, ethoxyzazam, ethoxyzazam, ethoxyzazone , fenarimol, fenbuconazole, fenfuram, fenexamide, fenoxanil, fenpiclonil, fenpropidina, fenpropimorph, fenpyazamine, fentina, fentina acetate, fentina hydroxide, ferbam, ferinzone, fruazinam, fludioxonil, flumorph, flu fluololimide , flusulfamide, flutianil, flutolanil, flutriafol, flu
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17/73 xapyroxad, folpet, formaldehyde, fosetyl, fosetyl-aluminum, fuberidazole, furalaxyl, furametpyr, guazatin, guazatin acetate, GY-81, hexachlorobenzene, hexaconazole, hymexazole, imazalil, imazaladine sulphate, imibenazoline, imibenconol, imibenconazole , iminoctadine tris (albesylate), iodocarb, ipconazole, ipfenpyrazolone, iprobenfos, iprodione, iprovalicarb, isoprothiolan, isopyrazam, isothianyl, kasugamycin, hydrated kasugamycin hydrochloride, mehmetin, mannipin, mandarin, manipin, mandarin, laminar, , meptyl-dinocap, mercuric chloride, mercuric oxide, mercuric chloride, metalaxyl, mefenoxam, metalaxyl-M, metam, metam- ammonium, metampotassic, metam-sodium, metconazole, methasulfocarb, methyl iodide, methyl isothiocyanate, methyl methionine, methylamine metrafenone, mildiomycin, myclobutanil, nabam, nitrotal-isopropyl, nuarimol, octyline, ofurace, oleic acid (fatty acids), orisastrobin, oxadixyl, oxine-copper, fu oxpoconazole marate, oxycarboxine, pefurazoate, penconazole, pencycuron, penflufen, pentachlorophenol, pentachlorophenyl laurate, penthiopyrad, phenylmercury acetate, phosphonic acid, phthalide, picoxystrobin, polyoxin bicarbonate, polyoxin, potassium, polyoxin, hydroxy , prochloraz, procimidone, propamocarb, propamocarb hydrochloride, propiconazole, propineb, proquinazide, protioconazole, piraclostrobin, pyrametostrobin, piraoxystrin, pyrazophos, pyribencarb, pyributicarb, pyrifenox, pyrifenone, pyrimethoxy, pyrimetiline, pyrimetiline, pyrimethanine, pyrimethanone silkxane, siltiofam, simeconazole, sodium 2-phenylphenoxide, sodium bicarbonate, sodium pentachlorophenoxide, spiroxamine, sulfur, SYP-Z071, SYP-Z048, tar oils, tebuconazole, tebufloquine, tecnazene, tetraconazole, tiablazide, tiablazide, thiabendazole methyl, thiram, thiadinyl, tolclofos-methyl, tolylfluanide, triadimefo n, triadimenol, triazoxide, tricyclazole, tridemorph, trifloxystrobin, triflumizole, triforin, triticonazole, validamycin, valifenalPetition 870180003263, from 15/01/2018, p. 26/96
18/73 to, valifenal, vinclozoline, zineb, ziram, zoxamide, Candida oleophila, Fusarium oxysporum, Gliocladium spp., Phlebiopsis gigantea, Streptomyces griseoviridis, Trichoderma spp., (R, S) -N- (3,5-dichlorophenil) -2 (methoxymethyl) -succinimide, 1,2-dichloropropane, 1,3-dichloro-1,1,3,3tetrafluoroacetone hydrated, 1-chloro-2,4-dinitronaphthalene, 1-chloro-2-nitropropane, 2- (2- heptadecyl-2-imidazolin-1-yl) ethanol, 2,3-dihydro-5-phenyl-1,4-dithine 1,1,4,4-tetraoxide, 2-methoxyethylmercury acetate, 2-methoxyethylmercury chloride, silicate 2-methoxyethylmercury, 3- (4-chlorophenyl) -5-methylrodanine, 4- (2-nitroprop-1-enyl) phenyl thiocyanate, ampropylphos, anilazine, azithiram, barium polysulfide, Bayer 32394, benodanil, benquinox, bentaluron, benzoinone; benzamacryl-isobutyl, benzamorf, binapacryl, bis (methylmercury) sulphate, bis (tributyltin) oxide, butiobate, mixed copper zinc cadmium chromate sulphate, carbamorph, ECSC, clobentiazone, chloramphoromethane, chlorfenazol, chloramide cypendazole, cyprofuram, decafentina, diclona, diclozolina, diclobutrazol, dimetirimol, dinocton, dinosulfon, dinoterbon, dipiritiona, ditalimfos, dodicina, drazoxolon, EBP, ESBP, etaconazol, etem, ethirim, phenaminosulfan, phenaminosulfan, phenaminosulfan, phenaminosulfan, phenaminosulfan, fenaminosulfan, same, fluotrimazole, furcarbanil, furconazole, furconazol-cis, furmeciclox, furofanato, gliodina, griseofulvina, halacrinato, Hercules 3944, hexiltiofos, ICIA0858, isopamphos, isovaledione, meben, mecarzhid, methoxymethyl, methoxamine, methoxamine mucochloric, myclozoline, N-3,5-dichlorophenyl-succinimide, N-3-nitrophenylitaconimide, natamycin, N-ethylmercury-4toluenesulfonanilide, bis (d nickel imethyldithiocarbamate), OCH, phenylmercury dimethyldithiocarbamate, phenylmercury nitrate, phosdiphen, picolinamide UK-2A and derivatives thereof, prothiocarb; prothiocarb hydrochloride, pyracarbolide, pyridinitrile, pyroxychlor, pyroxyfur, quinacetol; quinacetol sulfate, quinazamide, quinconazole, rabenzazole, salicylani
Petition 870180003263, of 01/15/2018, p. 27/96
19/73 lida, SSF-109, sultropen, weaoram, thiadifluoride, thicyofen, thiochlorfenphim, thiophanate, thioquinox, tioxymid, triamiphos, triarimol, triazbutyl, triclamide, urbacida, zarilamida, and any combinations thereof. [00107] Additionally, the compounds of the present invention can be combined with other pesticides, including insecticides, nematicides, miticides, arthropodicides, bactericides or combinations thereof that are compatible with the compounds of the present invention in the medium selected for application, and not antagonistic to activity of the present compounds to form pesticidal mixtures and synergistic mixtures thereof. The fungicidal compounds of the present invention can be applied in conjunction with one or more other pesticides to control a wider variety of undesirable pests. When used in conjunction with other pesticides, the compounds now claimed can be formulated with the other pesticides, mixed in tank with the other pesticides or applied sequentially with the other pesticides. Typical insecticides include, but are not limited to: antibiotic insecticides such as alosamidine and thuringensin; macrocyclic lactone-based insecticides such as spinosad and spinetoram; avermectin-based insecticides such as abamectin, doramectin, emamectin, eprinomectin, ivermectin and selamectin; milbemycin-based insecticides such as lepimectin, milbemectin, milbemycin oxime and moxidectin; arsenic insecticides such as calcium arsenate, copper acetoarsenite, copper arsenate, lead arsenate, potassium arsenite and sodium arsenite; botanical insecticides such as anabasin, azadiractin, Jlimonene, nicotine, pyrethrins, cinerines, cinerin I, cinerin II, jasmine I, jasmine II, pyrethrin I, pyrethrin II, quassia, rotenone, ryania and sabadilla; carbamate-based insecticides such as bendiocarb and carbaryl; benzofuranyl methylcarbamate insecticides such as benfuracarb, carbofuran, carbosulfan, decarbofuran and furatiocarb; insecticides
Petition 870180003263, of 01/15/2018, p. 28/96
20/73 dimethylcarbamate base such as dimitan, dimethylan, hyquincarb and pyrimicarb; carbamate oxime insecticides such as alanycarb, aldicarb, aldoxycarb, butocarboxy, butoxycarboxy, methomyl, nitrilacarb, oxamyl, tazimcarb, thiocarboxime, thiodicarb and thiofanox; insecticides based on phenyl methylcarbamate such as allyxycarb, aminocarb, bufencarb, butacarb, carbanolate, cloethocarb, dicresyl, dioxacarb, EMPC, ethiofencarb, fenethacarb, fenobucarb, isoprocarb, methiocarb, metolcarb, metolcarb, propolcar, xylylcarb; desiccant insecticides such as boric acid, diatomaceous earth and silica gel; diamide-based insecticides such as chlorantraniliprol, cyantraniliprol and flubendiamide; dinitrophenol-based insecticides such as dinex, dinoprop, dinosam and DNOC; fluorine-based insecticides such as barium hexafluorsilicate, cryolite, sodium fluoride, sodium hexafluorsilicate and sulfluramid; formamidine-based insecticides such as amitraz, chlordimeform, formethanate and formpamnate; smoking insecticides such as acrylonitrile, carbon disulfide, carbon tetrachloride, chloroform, chloropicrine, paradichlorobenzene, 1,2-dichloropropane, ethyl formate, ethylene dibromide, ethylene dichloride, ethylene oxide, hydrogen cyanide, iodomethane, bromine methyl, methylchloroform, methylene chloride, naphthalene, phosphine, sulfuryl fluoride and tetrachloroethane; inorganic insecticides such as borax, calcium polysulfide, copper oleate, mercury chloride, potassium thiocyanate and sodium thiocyanate; inhibitors of chitin synthesis such as bistrifluron, buprofezin, chlorfluazuron, ciromazine, diflubenzuron, flucicloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron and triflum; juvenile hormone mimetics such as epophenonane, phenoxycarb, hydroprene, quinoprene, methoprene, pyriproxifene and triprene; youth hormones such as youth hormone I, youth hormone II and youth hormone III; antagonists of molting hormones such as
Petition 870180003263, of 01/15/2018, p. 29/96
21/73 chromafenozide, halofenozide, methoxyfenozide and tebufenozide; molting hormones such as a-ecdysone and ecdysterone; seedling inhibitors such as diophenolan; precocenes such as precocene I, precocene II and precocene III; growth regulators for unclassified insects such as dicyclanil; nereistoxin analog insecticides such as bensultap, cartap, thiocyclam and thiosultap; nicotinoid insecticides such as flonicamide; nitroguanidine-based insecticides such as clothianidin, dinotefuran, imidacloprid and tiamethoxam; nitromethylene-based insecticides such as nitenpyram and nitiazine; pyridylmethylamine-based insecticides such as acetamiprid, imidacloprid, nitenpyram and tiacloprid; organochlorine-based insecticides such as bromoDDT, camphechlor, DDT, pp'-DDT, ethyl-DDD, HCH, gamma-HCH, lindane, methoxychlor, pentachlorophenol and TDE; cyclodiene-based insecticides such as aldrin, bromocyclen, chlorbicyclen, chlordane, chlordecone, dieldrin, dilor, endosulfan, alpha-endosulfan, endrin, HEOD, heptachlor, HHDN, isobenzan, isodrin, kelevan and mirex; organophosphate-based insecticides such as bromfenvinfos, chlorfenvinphos, crotoxyphos, dichlorvos, dicrotophos, dimethylvinphos, phospirate, heptenophos, methocrotophos, mevinphos, monocrotophos, naled, naphthalophos, prophethos, phospho and phosphoidon; organothiophosphate-based insecticides such as dioxabenzofos, fosmethilan and fentoate; aliphatic organothiophosphate-based insecticides such as acetion, amiton, cadusaphos, chlorethoxyphos, chlormephos, demephion, demephion-O, demephion-S, demeton, demeton-O, demeton-S, demeton-methyl, demeton-O-methyl, demeton- S-methyl, demeton-S-methylsulphon, disulfoton, etion, ethoprophos, IPSP, isothioate, malathion, methacrifos, oxydemeton-methyl, oxydeprofos, oxydisulfoton, phorate, sulfotep, terbufos and tiometon; insecticides based on aliphatic organothiophosphate amide such as amidithion, cyantoate, dimetoate, methyl ethoate, formothion, mecarbam, ometoate, protoate, sofamide and vamidothion; insecticides
Petition 870180003263, of 01/15/2018, p. 30/96
22/73 organothiophosphate oxime base such as chlorphoxim, phoxim and phoximmethyl; heterocyclic organothiophosphate-based insecticides such as azamethiphos, coumaphos, coumitoate, dioxathion, endothion, menazon, morphothion, fosalone, pyraclofos, pyridaphenthion and quinothion; benzothiopyran insecticides based on organothiophosphate such as dithicrophos and thicrophos; benzothriazine organothiophosphate insecticides such as azinphos-ethyl and azinphos-methyl; insecticides based on isoindole organothiophosphate such as dialiphos and phosmet; insecticides based on isoxazole organothiophosphate such as isoxathion and zolaprofos; pyrazolpyrimidine organothiophosphate insecticides such as chlorprazophos and pyrazophos; pyridine organothiophosphate-based insecticides such as chlorpyrifos and chlorpyrifos-methyl; pyrimidine organothiophosphate-based insecticides such as butathione, diazinon, etrimphos, lirimphos, pyrimiphos-ethyl, pyrimiphos-methyl, primidophos, pyrimitate and tebupirimphos; insecticides based on quinoxaline organothiophosphate such as quinalphos and quinalphos-methyl; insecticides based on thiadiazole organothiophosphate such as athidathion, lythidathion, methidathion and prothidathion; triazole organothiophosphate-based insecticides such as isazophos and triazophos; insecticides based on phenyl organothiophosphate such as nitrogen, bromophos, bromophos-ethyl, carbophenothion, chlortiophos, cyanophos, citioate, dicapthon, dichlofenthion, etaphos, famphur, fenchlorphos, fenitrothion fensulfothion, ethyphos, , parathion-methyl, phenkapton, phosnichlor, profenofos, prothiofos, sulprofos, temephos, trichlormetaphos-3 and triphenofos; phosphonate-based insecticides such as butonate and trichlorfon; phosphonothioate-based insecticides such as mecarphon; insecticides based on phenyl ethylphosphonothioate such as phonophos and trichloronat; insecticides based on phenyl phenylphosphonothioate such as cyanophenphos, EPN and leptophos; phosphoramidate-based insecticides such as crufomato, fenamiphos, fosthietan, mephosfolan, phosfolan and pyrimeta
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23/73 phos; phosphoramidothioate insecticides such as acephate, isocarbophos, isofenphos, isofenphos-methyl, methamidophos and propetamphos; phosphorodiamide-based insecticides such as dimefox, mazidox, mipafox and schradan; oxadiazine-based insecticides such as indoxacarb; oxadiazoline-based insecticides such as methoxyzazone; phthalimide-based insecticides such as dialiphos, phosmet and tetramethrin; pyrazole insecticides such as tebufenpyrad, tolefenpyrad; phenylpyrazole-based insecticides such as acetoprol, etiprol, fipronil, pirafluprol, pyriprol and vaniliprol; pyrethroid ester-based insecticides such as acrinatrin, alethrin, bioalethrin, bartrin, bifentrin, bioethanometrine, cyclethrin, cycloprotrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, gamma-cyhalothrin, lambda-cyhalothrin, cypermethrin, beta-methyrethrin, beta-methytrine, beta-methymethrin, beta-methytrine, beta-metherine -cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, dimeflutrin, dimethrin, empentrine, fenflutrin, phenpiritrin, fenpropatrin, fenvalerate, esfenvalerate, flucitrinaate, fluvalinate, tau-fluvalinate, methetrine, transmethrin, transmethrin, meetrine, imetrine, , pralethrin, proflutrin, pyresmethrin, resmethrin, bioresmethrin, cymethrin, teflutrin, teralethrin, tetramethrin, tetramethylflutrin, tralometrine and transflutrin; pyrethroid ether insecticides such as etofenprox, flufenprox, halfenprox, protrifenbute and silafluofen; pyrimidinamine-based insecticides such as flufenerin and pyrimidifene; pyrrole-based insecticides such as chlorfenapyr; tetramic acid-based insecticides such as spirotetramat; tetronic acid-based insecticides such as spiromesifen; thiourea insecticides such as diafenthiuron; urea-based insecticides such as flucofuron and sulcofuron; and unclassified insecticides such as closantel, copper naphthenate, crotamiton, EXD, phenazaflor, fenoxacrim, hydrametilnon, isoprothiolan, malonoben, metaflumizone, nifluridide, plifenate, pyridaben, pyridalyl, pyrifluquinazon, rafoxanide, rafoxanide and rafoxanide
Petition 870180003263, of 01/15/2018, p. 32/96
24/73 any combinations thereof.
[00108] Additionally, 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 application, and not antagonistic of the activity of the present compounds to form pesticidal mixtures and synergistic mixtures thereof. The fungicidal compounds of the present invention can be applied in conjunction with one or more herbicides to control a wide variety of undesirable plants. When used in conjunction with herbicides, the compounds now claimed can be formulated with the herbicides, mixed in tank with the herbicides or applied sequentially with the herbicides. Typical herbicides include, but are not limited to: amide herbicides herbicides such as allidochlor, beflubutamide, benzadox, benzipram, bromobutide, cafenstrol, CDEA, cyprazole, dimethenamide, dimethenamide-P, diphenamide, epronaz, etnipromide, fienazide, fennazide, fennrazide halosafen, isocarbamide, isoxaben, napropamide, naptalam, petoxamide, propizamide, quinonamide and tebutam; anilide-based herbicides such as chloranocryl, cisanilide, clomeprop, cypromid, diflufenican, etobenzanide, fenasulam, flufenacet, flufenican, mefenacet, mefluidide, metamifop, monalide, naproanilide, pentanochlor, picolinefen; arylalanine-based herbicides such as benzoylprop, flamprop and flamprop-M; chloroacetanilide herbicides such as acetochlor, alachlor, butachlor, butenachlor, delachlor, diethatyl, dimethachlor, metazachlor, metolachlor, S-metolachlor, pretilachlor, propachlor, propisochlor, prynachlor, terbuchlor, thenylchlor and xylach; sulfonanilide-based herbicides such as benzofluorine, perfluidone, pyrimisulfan and profluazole; sulfonamide based herbicides such as asulam, carbasulam, fenasulam and oryzalin; thioamide-based herbicides such as chlortiamide; antibiotic herbicides such as bilanafos; herbicides
Petition 870180003263, of 01/15/2018, p. 33/96
25/73 benzoic acid based such as chloramben, dicamba, 2,3,6-TBA and tricamba; herbicides based on pyrimidinyloxobenzoic acid such as bispyribac and pyriminobac; pyrimidinylthiobenzoic acid herbicides such as pyritiobac; phthalic acid-based herbicides such as chlorthal; 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; benzoylcyclohexanedione based herbicides such as mesotrione, sulcotrione, tefuriltrione and tembotrione; benzofuranyl alkylsulfonate herbicides such as benfuresate and etofumesate; benzothiazole herbicides such as benzazoline; carbamate-based herbicides such as asulam, carboxazole chlorprocarb, dichlormate, fenasulam, karbutilate and terbucarb; carbanylate herbicides such as barban, BCPC, carbasulam, carbetamide, CEPC, chlorbufam, chlorpropham, CPPC, desmedipham, phenisopham, phenmedipham, phenmedipham-ethyl, propham and swep; herbicides based on cyclohexene oxime such as alloxydim, butroxydim, clethodim, cloproxydim, cycloxydim, profoxydim, setoxidim, tepraloxydim and tralcoxidim; cyclopropylisoxazole herbicides such as isoxaclortol and isoxaflutole; dicarboximide-based herbicides such as cinidon-ethyl, flumezin, flumichlorac, flumioxazin and flumipropyn; dinitroaniline-based herbicides such as benfluralin, butralin, dinitramine, etalfluralin, flucloraline, isopropalin, metallopraline, nitralin, oryzaline, pendimethalin, prodiamine, profluralin and trifluralin; dinitrophenol-based herbicides such as dinofenate, dinoprop, dinosam, dinoseb, dinoterb, DNOC, ethinophene and medinoterb; diphenyl ether herbicides such as ethoxyfen; nitrophenyl ether herbicides such as acifluorfen, aclonifen, bifenox, clomethoxyfen, chlornitrofen, etnipromide, fluordifene, fluorglicofene, fluornitrofeno, fomesa
Petition 870180003263, of 01/15/2018, p. 34/96
26/73 hay, furyloxifene, halosaphen, lactophen, nitrophene, nitrofluorphene and oxyfluorfen; dithiocarbamate-based herbicides such as dazomet and metam; halogenated aliphatic herbicides such as alorac, chloropon, dalapon, flupropanate, hexachloroacetone, iodomethane, methyl bromide, monochloroacetic acid, SMA and TCA; imidazolinone herbicides such as imazamethabenz, imazamox, imazapic, imazapyr, imazaquin and imazethapyr; inorganic herbicides such as ammonium sulfamate, borax, calcium chlorate, copper sulfate, ferrous sulfate, potassium azide, potassium cyanate, sodium azide, sodium chlorate and sulfuric acid; nitritoe-based herbicides such as bromobonyl, bromoxynil, chloroxynil, dichlobenyl, iodobonyl, ioxynil and pyraclonil; organophosphorus-based herbicides such as amiprofos-methyl, anilophos, bensulide, bilanafos, butamiphos, 2,4-DEP, DMPA, EBEP, phosamine, glufosinate, glufosinate-P, glyphosate and piperophos; phenoxy-herbicides such as bromophenoxy, clomeprop, 2,4-DEB, 2,4-DEP, diphenopentene, disul, erbon, etnipromide, phenteracol and triphosphate; oxadiazoline-based herbicides such as metazol, oxadiargyl, oxadiazon; oxazole-based 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 2,4,5TB; phenoxypropionic herbicides such as cloprop, 4-CPP, dichlorprop, dichlorprop-P, 3,4-DP, fenoprop, mecoprop and mecoprop-P; aryloxyphenoxypropionic herbicides such as chlorazifop, clodinafop, clofop, cyhalofop, diclofop, fenoxaprop, fenoxaprop-P, fentiaprop, fluazifop, fluazifop-P, haloxyfop, haloxyfop-P, isoxapyrifop, metamifop, quamifop, tram phenylenediamine-based herbicides such as dinitramine and prodiamine; pyrazole-based herbicides such as pyrosulfone; benzoylpyrazole based herbicides such as benzofenap, pirasulfotol, pyrazolinate, pyrazoxifene, and topramezone; phenylpyrazole-based herbicides such as fluazolate, nipyraclo
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27/73 hay, pioxadene and piraflufene; pyridazine-based herbicides such as credazine, pyridafol and pyridate; pyridazinone-based herbicides such as brompyrazon, chloridazon, dimidazon, flufenpyr, metflurazon, norflurazon, oxapyrazon and pydanon; pyridine-based herbicides such as aminopyralid, cliodinate, clopyralid, dithiopyr, fluroxypyr, haloxidine, picloram, picolinafen, pyriclor, tiazopyr and triclopyr; pyrimidinediamine-based herbicides such as iprymidam and thioclorin; quaternary ammonium herbicides such as cyperquat, diethamquat, difenzoquat, diquat, morfamquat and paraquat; thiocarbamate based herbicides such as butylate, cyclate, dialate, EPTC, esprocarb, etiolate, isopolynate, metiobencarb, molinate, orbencarb, pebulate, prosulfocarb, pyributicarb, sulfalate, thiobencarb, thiocarbazil, trialate and vernol; thiocarbonate herbicides such as dimexane, EXD and proxan; thiourea-based herbicides such as methiuron; triazine-based herbicides such as dipropetrin, indaziflam, triaziflam and trihydroxythriazine; chlorotriazine-based herbicides such as atrazine, chlorazine, cyanazine, cyprazine, eglinazine, ipazine, mesoprazine, prociazine, proglinazine, propazine, sebutilazine, simazine, terbutilazine and trietazine; methoxythriazine herbicides such as atraton, methometon, prometon, secbumeton, simeton and terbumeton; methyltiotriazine herbicides such as ametrine, aziprotrin, cyanatrin, desmethrin, dimethmetrine, methoprotrin, promethrin, symmetrine and terbutrin; triazinone-based herbicides such as ametridione, amibuzine, hexazinone, isomethiozine, metamitron and metribuzin; triazole-based herbicides such as amitrol, cafenstrol, epronaz and flupoxam; triazolone-based herbicides such as amicarbazone, bencarbazone, carfentrazone, flucarbazone, ipfencarbazone, propoxycarbazone, sulfentrazone and thiencarbazone-methyl; triazolopyrimidine-based herbicides such as cloransulam, diclosulam, florasulam, flumetsulam, metosulam, penoxsulam and pyroxsulam; uracil-based herbicides such as
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28/73 by benzfendizone, bromacil, butafenacil, flupropacil, isocil, lenacil, saflufenacil and terbacil; urea-based herbicides such as benzthiazuron, cumyluron, cycluron, dichloralurea, diflufenzopyr, isonoruron, isouron, methabenzthiazuron, monisouron and noruron; phenylurea-based herbicides such as anisuron, buturon, chlorbromuron, chloreturon, chlorotoluron, chloroxuron, daimuron, diphenoxuron, dimefuron, diuron, fenuron, fluometuron, fluothiuron, isoproturon, linuron, methiuron, methiuron, methiuron, methiuron, methiuron, methiuron, methiuron, , neburon, parafluron, phenobenzuron, siduron, tetrafluron and thidiazuron; pirimidinilsulfonilureia herbicides such as amidosulfuron, azimsulfuron, bensulfuron, chlorimuron, cyclosulfamuron, ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron, foramsulfuron, halosulfuron, imazosulfuron, mesosulfuron, metazosulfuron, nicosulfuron, orthosulfamuron, oxasulfuron, primisulfuron, propyrisulfuron, pyrazosulfuron, rimsulfuron, sulfometuron , sulfosulfuron and trifloxysulfuron; triazinylsulfonylurea based herbicides such as chlorsulfuron, cinosulfuron, ethametsulfuron, iodosulfuron, metsulfuron, prosulfuron, thifensulfuron, triasulfuron, tribenuron, triflusulfuron and tritosulfuron; thiadiazolylurea-based herbicides such as buthiuron, ethidimuron, tebuthiuron, tiazafluron and thidiazuron; and unclassified herbicides such as acrolein, allyl alcohol, aminocyclopyrachlor, azafenidin, bentazone, benzobicyclon, bicyclopyrone, butidazole, calcium cyanamide, cambendichlor, chlorfenac, chlorfenprop, chlorflurazol, chlorflurenol, cinmetiline, clomzone, clomazone, clomazone , dimepiperate, endothal, fluormidine, fluridone, flurochloridone, flurtamone, flutiacet, indanofan, methyl isothiocyanate, OCH, oxaziclomefone, pentachlorophenol, pentoxazone, phenylmercury acetate, prosulfalin, pyribenzoximilin, pyribenzoximilin, pyribenzoximilin, pyribenzoxim, quinine , tripropindan and tritac.
[00109] Another embodiment of the present invention relates to a
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29/73 method for the control or prevention against fungal attack. This method involves applying to the soil, plant, roots, foliage, seed or fungus site, or to a location where infestation is to be prevented (for example, by application 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, and still presenting low phytotoxicity. The compounds can be useful in a protective and / or eradicating manner.
[00110] We 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 advantages may include, but are not limited to, improving the health of a plant; increased yield of a plant (for example, increased biomass and / or increased content of valuable ingredients); increasing the vigor of a plant (for example, improved plant growth and / or greener leaves); improving the quality of a plant (for example increased content or composition of certain ingredients); and increased tolerance to abiotic and / or biotic plant stress.
[00111] It will be understood by those skilled in the art that the effectiveness of the compound for the above fungi establishes the general utility of the compounds as fungicides.
[00112] The compounds have broad limits of activity against fungal pathogens.
[00113] Exemplary pathogens may include, but are not limited to, wheat leaf rust (Septoria tritici, also known as Mycosphaerella graminicola), apple scab (Venturia inaequalis), and beet leaf rust (Cercospora beticola) ), peanut leaf rust (Cercospora arachidicola and Cercosporidium personatum) and other crops, and black sigatoka from
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30/73 banana (Mycosphaerella fijiensis). The exact amount of active material to be applied is dependent not only on the specific active material being applied, but also on the particular desired action, the fungal species to be controlled, and the growth stage of the same, as well as on the part of the plant or other product to be contacted with the compound. Therefore, not all compounds, and formulations containing them, can be equally effective at similar concentrations or against the same fungal species.
[00114] The compounds are effective in use with plants in an inhibitory amount of diseases and phytologically acceptable. The term disease-inhibiting and phytologically acceptable amount refers to an amount of a compound that eliminates or inhibits the plant disease for which control is desired, but is not significantly toxic to the plant. This amount will generally range from about 0.1 to about 1000 ppm (parts per million), with 1 to 500 ppm being preferred. The exact amount required of a compound varies with the fungal disease to be controlled, the type of formulation used, the method of application, the particular plant species, the climatic conditions, among others. A suitable application rate typically ranges from about 0.01 to 0.45 grams per square meter, g / m ² (about 0.10 to about 4 pounds / acre).
[00115] Any desired range or value given in this report can be expanded or changed without losing the effects sought, as should be evident to the expert in the technique to understand the teachings of this invention.
[00116] The compounds of Formula I can be made using well-known chemical procedures. Intermediates not specifically mentioned in this report are either commercially available, or can be made by routes disclosed in the chemical literature, or can be easily synthesized from mate
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31/73 commercial departure rials using traditional procedures.
[00117] The following examples are presented to illustrate the various aspects of the compounds of the present invention and are not to be construed as limiting the claims.
Example 1: Preparation of 5-fluorine-1-morpholin-4-ylmethyl-4 - [(morpholin-4ylmethylDamino] - 1H-pyrimidin-2-one (1)

[00118] This material was prepared in the manner described in Int. J. Pharm. 1987, 35, 243-252. To a mixture of paraformaldehyde (240 milligrams (mg), 8 millimols (mmol) of monomer) in dichloromethane (CH ₂ CI ₂ ; 20 ml_) in a 25 milliliter (ml_) bottle with screw cap was added morpholine (697 mg , 8 mmols). The reaction mixture was stirred on an orbital shaker for one night at room temperature. 4-Amino-5-fluorpirimidin-2-ol * (250 mg, 2 mmol) was added, and the resulting heterogeneous mixture was stirred at room temperature for 48 hours. The reaction mixture was evaporated to dryness and the residue was treated with ether (Et ₂ O) to give a white solid, which was filtered and dried to give the title compound (381 mg, 65%): mp 156-1 δδΌ ; ¹ H NMR (300 MHz, CDCI ₃ ) δ 7.46 (d, J = 2.5 Hz, 1H), 5.69 (br t, 1H), 4.53 (s, 2H), 4.46 ( d, J = 2.6 Hz, 2H), 3.72 (m, 8H), 2.64 (m, 8H); IR (ATR) 3483 (br), 3293 (br), 1680 (s), 1639 (s), 1574 (s), 1521 (s) cm ^-1 .
[00119] * 4-Amino-5-fluorpirimidin-2-ol can be purchased commercially.
Example 2: Preparation of 5-fluorine-1- (4-methylpiperazin-1-ylmethyl) -4 - [(4methylpiperazin-1-ylmethyl) -amino] -1 H-pyrimidin-2-one (2)
ΌΗ
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32/73 [00120] This material was prepared in the manner described in Int. J. Pharm. 1987, 35, 243-252. To a mixture of paraformaldehyde (240 mg, 8 mmols of monomer) in CH ₂ CI ₂ (20 ml) in a 25 ml flask with screw cap was added N-methylpiperazine (813 mg, 8 mmols). The reaction mixture was stirred on an orbital shaker for one night at room temperature. 4-Amino-5-fluorpirimidin-2-ol (250 mg, 2 mmol) was added and the resulting heterogeneous mixture was stirred at room temperature for 48 hours. The reaction mixture was evaporated to dryness and the residue was treated with Et ₂ O to give a beige solid, which was filtered and dried to give the title compound (247 mg, 31%): mp 165-166X3; ¹ H NMR (300 MHz, CDCI ₃ ) δ 7.45 (d, J = 2.5 Hz, 1H), 5.62 (brt, 1H), 4.55 (s, 2H), 4.5 (d , J = 2.6 Hz, 2H), 2.69 (m, 8H), 2.44 (br, 8H), 2.38 (s, 6H); IR (ATR) 3465 (br), 1679 (s), 1646 (s), 1574 (s), 1522 (s) cm ^-1 .
[00121] Compound 3 in Table I was synthesized in the same manner as in Example 2.
Example 3: Preparation of N '- [5-fluoro-1- (4-fluorbenzyl) -2-oxo-1,2-dihydro-pyrimidin-4-yl] -N, N-dimethylformamidine (4)
[00122] To an 8 ml flask with screw cap were added Ν, Ν-dimethylformamide (DMF; 1.5 ml_), N '- (5-fluoro-2-hydroxypyrimidin4-yl) -N, N-dimethylformamidine ( 100 mg, 0.54 mmol), anhydrous potassium carbonate (K ₂ CO ₃ ; 138 mg, 1.0 mmol), and 4-fluorbenzyl bromide (113 mg, 0.60 mmol). The mixture was stirred and heated to 70Ό for 2 hours and then at room temperature for another 16 hours. The crude reaction mixture was filtered and placed directly on a reverse phase chromatography column. After elution, the title compound was isolated as a white solid (30 mg, 20%): mp 134-136X3;
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33/73 ¹ H NMR (300 ΜΗζ, CDCI ₃ ) δ 8.68 (s, 1 Η), 8.07 (d, J = 2.5 Hz, 1H), 7.49-7.43 (m, 2H), 7.10-7.01 (m, 2H), 5.33 (s, 2H), 3.20 (s, 3H), 3.18 (s, 3H);
[00123] ESIMS m / z 293 ([M + H] ⁺ ).
[00124] Compounds 5-7 in Table I were synthesized in the same manner as in Example 3.
Example 4: Preparation of N- (5-fluor-1-methyl-2-oxo-1,2-dihydropyrimidin-4-yl) -4-methyl-benzamide (8)
[00125] To N- (5-fluor-2-hydroxypyrimidin-4-yl) -4-methylbenzamide (200 mg, 0.81 mmol) in DMF (5 ml) was added K ₂ CO ₃ (224 mg, 1, 6 mmol), and iodomethane (230 mg, 1.6 mmol). The mixture was stirred and heated to 60Ό for 30 minutes and then was stirred for 16 hours at room temperature. The mixture was distributed between ethyl acetate (EtOAc) and water (H ₂ O). The organic phase was dried over magnesium sulfate (MgSO ₄ ), filtered and evaporated. The crude material was purified by reverse phase chromatography to give the title compound as a white solid (17 mg, 8%): mp 229-230Ό; ¹ H NMR (300 MHz, CDCI ₃ ) δ 13.2 (br s, 1H), 8.23-8.15 (br m, 2H), 7.42-7.37 (br m, 1H), 7 , 30-7.25 (br m, 2H), 3.45 (s, 3H), 2.44 (s, 3H); ESIMS m / z 262 ([M + H] ⁺ ), m / z 260 ([MH] ').
Example 5: Preparation of N- (5-fluor-1-methyl-2-oxo-1,2-dihydropyrimidin-4-yl) -N-methyl-C-phenylmethanesulfonamide (9)
1. GHj.CN. BSA
3. K ₃ CCç, CH., 1, DMF
4. NaH
[00126] 4-Amino-5-fluorpirimidin-2-ol (2 grams (g), 15.5 mmols) was stirred in acetonitrile (CH ₃ CN; 80 ml) at 50 °. The hot mixture was
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34/73 N, O-bis (trimethylsilyl) acetamide (BSA; 9.4 g, 46.3 mmoles) was added, and stirring and heating continued for 1.5 hours. Phenylmethanesulfonyl chloride (3.2 g, 16.8 mmols) was added. After 2 hours, the reaction mixture was cooled to room temperature and distributed between CH ₃ CN and brine. The organic phase was dried over MgSO ₄ , filtered, and evaporated and placed directly on a silica gel column which was eluted (gradient, 0 to 100% EtOAc in petroleum ether). Combination of the fractions containing the main UV absorbing portion of the produced mixture gave a white solid that was used without further purification. To a portion of this material (100 mg) were added DMF (3 ml), K ₂ CO ₃ (100 mg), and iodomethane (100 mg), and the mixture was stirred at 60 ° C for 1 hour. The reaction mixture was cooled to room temperature and an excess of sodium hydride (NaH; 60% dispersion in mineral oil) was added. The entire mixture was stirred for 30 minutes and then heated to 45 ° C for
2.5 hours. The crude mixture was filtered and purified by reverse phase chromatography followed by normal phase chromatography (gradient, 30 to 100% EtOAc in petroleum ether) for the title compound as a white solid (28 mg, 27%): mp 159 -160Ό; ¹ H NMR (300 MHz,
CDCI ₃ ) δ 7.6 (m, 1H), 7.42-7.41 (m, 2H), 7.38-7.36 (m, 3H), 4.8 (s, 2H),
3.5 (s, 3H), 2.82 (s, 3H); ESIMS m / z 312 ([M + H] ⁺ ), m / z 310 ([MH] ').
Example 6: Preparation of iso-butyl ester of (5-fluor-1-methyl-2oxo-1,2-dihydropyrimidin-4-yl) carbamic acid (10) and iso-butyl acid ester (5-fluorine -l -methyl-2-oxo-1,2-dihydropyrimidin-4-yl) methylcarbamic acid (11)
[00127] 4-Amino-5-fluorpirimidin-2-ol (0.5 g, 3.9 mmols) and isobutyl chloroform (0.58 g, 4.2 mmols) were stirred in pyridine (5 ml) at
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60Ό for 1.5 hours. The crude mixture was distributed between EtOAc and 1 N hydrochloric acid (HCl). The organic phase was dried over MgSO ₄ , filtered and evaporated. The residue was precipitated from ethyl alcohol (EtOH) to give a white solid which was used without further purification. A portion of this material (100 mg), K ₂ CO ₃ (125 mg), and iodomethane (125 mg) was added to the DMF (3 ml), and the mixture was stirred at 60 ° C for 1 hour. The mixture was cooled to room temperature and an excess of NaH (60% dispersion in mineral oil) was added. The entire mixture was stirred for 30 minutes and then heated to 45Ό for 2 hours. The crude mixture was filtered and purified by reverse phase chromatography to give the title compounds.
[00128] The (5-fluoro-1-methyl-2-oxo-1,2-dihydropyrimidin-4-yl) carbamic acid iso-butyl ester was isolated as a white solid (16 mg): mp 126-128Ό; ¹ H NMR (300 MHz, CDCI ₃ ) δ 12.2 (br s, 1H), 7.32 (br s, 1H), 3.98 (d, J = 6.6 Hz, 2H), 3.4 (s, 3H), 2.02 (sept, J = 6.6 Hz, 1H), 1.01 (d, J = 6.6 Hz, 6H); ESIMS m / z 244 ([M + H] ⁺ ), m / z 242 ([MH] -).
[00129] The methylcarbamic acid (5-fluor-1-methyl-2-oxo-1,2-dihydropyrimidin-4-yl) iso-butyl ester was isolated as a clear colorless oil (22 mg): ¹ H NMR ( 300 MHz, CDCI3) δ 7.52 (d, J = 5.5 Hz, 1H), 4.02 (d, J = 6.8 Hz, 2H), 3.55 (s, 3H), 3.40 (s, 3H), 1.99 (sept, J = 6.8 Hz, 1H), 0.95 (d, J = 6.8 Hz, 6H); ¹³ C NMR (150 MHz, CDCI3) δ 158.24, 158.17, 154.7,154.1, 140.5, 138.8, 134.0, 133.7, 73.6, 38.6, 34, 9, 27.9, 19.2; ESIMS m / z 258 ([M + H] ⁺ ).
Example 7: Preparation of 2,2-dimethylpropionic acid 4- (dimethylamino-methyleneamino) -5-fluor-2-oxo-2H-pyrimidin-1-ylmethyl ester
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36/73 [00130] To the DMF (3 mL) were added N '- (5-fluor-2hydroxypyrimidin-4-yl) -N, N-dimethylformamidine (100 mg, 0.54 mmol), cesium carbonate (196 mg , 0.6 mmol), and chloromethyl pivalate (90 mg, 0.6 mmol), and the mixture was stirred at room temperature for 16 hours. The mixture was distributed between EtOAc and H ₂ O. The organic phase was dried over MgSO ₄ , filtered, and evaporated. To the resulting crude oil, Et ₂ O (3.5 ml) was added and a precipitate formed which was collected by filtration. The title compound was isolated as a white solid (37 mg, 23%): mp 193-194Ό; ¹ H NMR (300 MHz, DMSO-J ₆ ) δ 8.67 (s, 1H), 8.07 (d, J = 6.3 Hz, 1H), 5.60 (s, 2H), 3.22 (s, 3H), 3.09 (s, 3H), 1.11 (s, 9H); ESIMS m / z 299 ([M + H] ⁺ ).
[00131] Compound 13 in Table I was synthesized in the same manner as in Example 7.
Example 8: Preparation of 4-amino-1- (benzyloxymethyl) -5-fluorpirimidin2 (1H) -one (14) and 1- (benzyloxymethyl) -4- (benzyloxymethylamino) -5fluorpirimidin-2 (1H) -one (15) [00132] A 25 mL Schlenk flask was filled with 4 amino-5- fluorpirimidin-2-ol (500 mg, 3.87 mmols), CH ₃ CN (10 mL), and BSA (1.42 mL, 5 , 81 mmols). The resulting white suspension was then heated to 65 °. After 90 minutes, the clear, color solution was cooled to room temperature and benzyl chloromethyl ether (1.07 mL, 7.72 mmol) was added, giving a cloudy white suspension. After stirring for 2 hours at room temperature, the reaction mixture was concentrated in vacuo to give a white residue which was purified by reverse phase column chromatography giving 4-amino1- (benzyloxymethyl) -5-fluorpirimidin-2 (1H) - one (14; 433 mg, 45%) as a white solid: mp 213-217Ό; ¹ H NMR (400 MHz, CDCI ₃ ) δ 7.98 (d,
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J = 6.5 Hz, 1H), 7.81 (br s, 1H), 7.56 (br s, 1H), 7.24-7.36 (m, 5H), 5.11 (s, 2H ), 4.54 (s, 2H); IR 3302 (s), 3082 (s), 2939 (w), 2869 (w), 1688 (s), 1619 (s), 1522 (s), 1468 (m), 1333 (m), 1131 (w) , 1054 (m) cm ^-1 ; ESIMS m / z 250 ([M + H] ⁺ ).
[00133] 1 - (Benzyloxymethyl) -4- (benzyloxymethylamino) -5-fluorpirimidin2 (1H) -one (15; 16.5 mg, 1.2%) was obtained as a by-product in the form of a colorless oil in the synthesis of 14: ¹ H NMR (400 MHz, CDCI ₃ ) δ 8.85 (t, J = 5.8 Hz, 1H), 8.08 (d, J = 6.6 Hz, 1H), 7.22-7 , 39 (m, 10H), 5.15 (s, 2H), 4.87 (d, J = 5.8 Hz, 2H), 4.56 (s, 2H), 4.54 (s, 2H) ; IR 3248 (w), 3062 (w), 3031 (w), 1683 (s), 1644 (m), 1569 (m), 1520 (s), 1454 (w), 1357 (w), 1328 (m) , 1189 (w), 1069 (m) cm ^-1 ; ESIMS m / z 370 ([M + H] ⁺ ).
[00134] Compounds 16-23 in Table I were synthesized in the same manner as in Example 8.
Example 9: Preparation of N '- (5-fluoro-1-methylsulfanylmethyl-2-oxo-1,2-dihydropyrimidin-4-yl) -N, N-dimethylformamidine (24)

A 250 ml_ round-bottom flask was charged with N '- (5-fluor-2-hydroxypyrimidin-4-yl) -N, N-dimethylformamidine (1.00 g, 5.43 mmols) and DMF ( 55 ml_) giving a white suspension. Solid potassium ter-butoxide (1.07 g, 9.53 mmols) was added, and the resulting pale yellow suspension was allowed to stir in an atmosphere of nitrogen at room temperature for 20 minutes. Chloromethyl sulfide (682 microliters (μΙ_), 8.14 mmols) was then added, and the mixture was heated at 60 ° C for 21 hours. The crude reaction mixture was concentrated in vacuo at 55 ° C to give an off-white residue which was purified by reverse phase column chromatography giving N- (5-fluor-1methylsulfanylmethyl-2-oxo-1,2-dihydropyrimidin-4 -il) -N, Ndimethylformamidine (36 mg, 25%) as a pale yellow solid: mp
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132-136Ό; ¹ H NMR (400 ΜΗζ, CDCI ₃ ) δ 8.68 (s, 1 Η), 8.20 (d, J = 3.2 Hz, 1H), 5.40 (s, 2H), 3.19 ( s, 3H), 3.07 (s, 3H), 2.20 (s, 3H); IR 2960 (w), 2926 (w), 1640 (s), 1582 (s), 1447 (s), 1382 (m), 1319 (m), 1269 (m), 1108 (m), 1051 (m) cm '¹; ESIMS m / z 267 ([M + Na] ⁺ ).
Example 10: Preparation of 4-amino-5-fluoro-1- (4-methylbenzyl) -pyrimidin2 (1H) -one (25)
DVF-DMA. DMF

3. ZnCl _lr EtOH, rstiuM [00136] Step 1: To a magnetically stirred solution of 4 amino-5- fluorpirimidin-2-ol (4.00 g, 31.0 mmols) in DMF (100 ml_) was added Ν, Ν -dimethylformamide dimethyl acetal (DMF-D MA; 4.00 g, 34.0 mmols). The mixture was stirred at room temperature for 72 hours, diluted with Et ₂ O (200 ml), and filtered. The solid product was washed with heptane to give (E) -N '- (5-fluor-2-oxo-1,2-dihydropyrimidin-4-yl) N, N-dimethylformimidamide (5.23 g, 92% ) as a white solid: mp 240-243Ό; ¹ H NMR (300 MHz, DMSO-J ₆ ) δ 10.7 (br s, 1H), 8.59 (s, 1H), 7.7 (d, J = 5.6 Hz, 1H), 3, 18 (s, 3H), 3.06 (s, 3H); ESIMS m / z 185 ([M + H] ⁺ ), m / z 183 ([MH] ').
[00137] Step 2: K ₂ CO ₃ powder (325 mesh; 2.03 g, 14.7 mmols) was added to a mixture of the product from Step 1 (1.35 g, 7.35 mmols) and a- bromo-p-xylene (1.36 g, 7.35 mmols) in DMF (20 ml), in an atmosphere of N ₂ , at room temperature. The resulting white paste was heated to 80 ° C. After stirring at 80 ° C for 2 hours, the reaction mixture was cooled, diluted with EtOAc (150 ml) and the solution was washed with e H ₂ O (4 x 50 ml) and saturated NaCl (satd) (1 x 50 ml_). The organic phase was dried (Na ₂ SO ₄ ), filtered and concentrated in vacuo to give 1.01 g of a light yellow solid. The crude material was dissolved in an EtOAc / CH ₂ CI ₂ mixture and treated with Celite (3 g). The solven
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39/73 te was removed in vacuo and the residue was purified by normal phase chromatography (gradient, 0 to 100% EtOAc / hexanes) to remove the isomeric O-alkylated product. The column was then eluted with 90% CH ₂ Cl ₂ /10% CH ₃ OH to obtain the desired N-alkylated product, N '[5-fluoro-1- (4-methylbenzyl) -2-oxo-1, 2-dihydropyrimidin-4-yl] -N, Ndimethylforamidine (0.688 g, 32%) as a white solid: mp 178179 ° C; ¹ H NMR (300 MHz, CDCl ₃ ) δ 8.82 (s, 1H), 7.22-7.15 (m, 4H), 4.97 (s, 2H), 3.18 (s, 3H) , 3.17 (s, 3H), 2.34 (s, 3H); ESIMS m / z 289 ([M + H] ⁺ ).
[00138] Step 3: Zinc chloride (1.24 g, 9.12 mmol) was added to a mixture of formamidine produced in Step 2 (0.656 g, 2.28 mmol) in absolute EtOH (10 mL). The resulting mixture was heated to reflux in an N2 atmosphere. The mixture gradually became a light yellow solution. After refluxing for 90 minutes, a precipitate formed, and after 2 hours, the reaction mixture was allowed to cool to room temperature and was concentrated in vacuo. The residue was treated with CH2Cl2 (75 mL, freely cloudy in appearance) and washed with H2O (25 mL). As soon as H2O was added, a white precipitate formed on the two layers in the separating funnel. The solid was removed by vacuum filtration. The solid was washed with H2O followed by Et2O. After air drying overnight, the white solid (0.58 g) was treated with 1: 1 CH ₂ Cl ₂ / MeOH (-70 ml) and heated to reflux (cloudy mixture). The mixture was filtered and the filtrate was concentrated in vacuo. The residual solid was pasted with hexanes / Et ₂ O (-3: 1) and isolated by vacuum filtration, air-dried and then dried in a vacuum oven (70-80 ° C) to give N '- (5 -fluor-2hydroxypyrimidin-4-yl) -N, N-dimethylformamidine (0.417 g, 78%) as a white powder: mp 291-293 ° C dec; ¹ H NMR (300 MHz, DMSO-J ₆ ) δ 8.03 (d, J = 6.9 Hz, 1H), 7.62 (br s, 1H), 7.40 (br s, 1H), 7 , 17 (d, J = 7.8 Hz, 2H), 7.12 (d, J = 8.1 Hz, 2H), 4.73 (s, 2H), 2.25 (s, 3H); ¹³ C NMR (150
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MHz, DMSO-J ₆ ) δ 158.2, 154.8, 137.3, 136.3 (d, J = 240 Hz), 135.3, 131.1 (d, J = 30.6 Hz), 129.7, 128.3, 51.8, 21.3; ESIMS m / z 234 ([M + H] ⁺ ), m / z 232 ([MH]); IR 3298 (m, br), 3100 (m, br), 1685 (s), 1619 (s), 1518 (s), 1447 (m), 1383 (m), 1343 (w), 1120 (w), 776 (w) cm ^-1 .
Example 11: Preparation of 4-amino-5-fluorine-1- (4-iodobutyl) -1Hpirimidin-2-one (26)
OH
2.
[00139] To a suspension of 4-amino-5-fluorpirimidin-2-ol (0.50 g,
3.87 mmols) in acetonitrile (CH ₃ CN; 20 ml_) BSA (1.58 g, 7.75 mmols) was added, and the mixture was heated to 70Ό for 1 hour resulting in a clear solution. After cooling to room temperature, 1,4-diiodobutane (1.2 g, 3.87 mmols) was added, and the mixture was stirred for 16 hours at room temperature and then at 70 ° C for 3 hours . The solvent was evaporated and the residue was purified by normal phase chromatography (24 g SiO ₂ ; gradient, 0 to 15% MeOH / CH ₂ CI ₂ ) to give an orange oil. The oil was dissolved in EtOAc and the solution was slowly cooled. The resulting solid was collected by filtration, washed with additional EtOAc, and dried to give 4 amino-5- fluoro-1- (4-iodobutyl) -1H-pyrimidin-2-one (0.52 g, 43%) as a solid brown: mp 181-184Ό; ¹ H NMR (400 MHz, DMSO-J ₆ ) δ 8.56 (s, 2H), 8.25 (d, J = 6.7 Hz, 1H), 3.70 (t, J = 6.7 Hz , 2H), 3.29 (t, J = 6.7
Hz, 2H), 1.73 (m, 4H); ESIMS m / z 312 ([M + H] ⁺ ).
Example 12: Preparation of 4-amino-5-fluor-1- (4- [1,2,4] triazol-1-yl-butyl) 1H-pyrimidin-2-one (27)
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41/73 [00140] To a mixture of 1,2,4-triazole (0.044 g, 0.64 mmol), potassium butoxide (KO'Bu; 0.072 g, 0.64 mmol), and 18-crown-6 (18C6; 0.008 g, 0.03 mmol) in CH ₃ CN (3.5 ml_) 4-amino-5-fluoro-1- (4-iodobutyl) -1H-pyrimidin-2-one (0.10 g, 0.32 mmol), and the mixture was heated to 70Ό and stirred for 16 hours. The resulting homogeneous solution was concentrated in vacuo to give the crude product as a white solid. Purification by reverse phase chromatography (13 g C18; gradient, 0 to 20% CH ₃ CN / water) gave 4-amino-5-fluor-1- (4 [1,2,4] triazol-1-yl-butyl ) -1 H-pyrimidin-2-one (0.023 g, 28%) as a white solid: mp 197-200Ό; ¹ H NMR (400 MHz, DMSO-J ₆ ) δ 8.50 (s, 1H), 7.94 (m, 2H), 7.56 (s, 1H), 7.35 (s, 1H), 4 , 19 (t, J = 6.9 Hz, 2H), 3.61 (t, J = 7.0 Hz, 2H), 1.73 (m, 2H), 1.51 (m, 2H); ESIMS m / z 253 ([M + H] ⁺ ), m / z 251 ([MH] ').
Example 13: Preparation of 4-amino-5-fluoro-1-methylpyrimidin-2 (1H) -one £ 28)
KjOOL · ,, 1 Ú -ατΎίη 6
Mflãn.Mft. dm [00141] A 25 ml_ flask with screw cap was charged with 4-amino-5-fluorpirimidin-2-ol (151.0 mg, 1.17 mmol), K ₂ CO ₃ (289.2 mg, 2 , 09 mmol), 18C6 (278.6 mg, 0.901 mmol) and anhydrous DMF (10 ml). Methyl methanesulfonate (0.0814 ml, 0.961 mmol) was added, and the resulting mixture was stirred on a rotary shaker at 85 ° C for 21 hours. After cooling to room temperature, the crude material was concentrated in vacuo and purified by reverse phase column chromatography to give 4-amino-5-fluorine-1-methylpyrimidin-2 (1H) -one (61.9 mg, 37%) as a beige solid: mp 195Ό (dec); ¹ H NMR (400 MHz, DMSO-J ₆ ) δ 7.94 (d, J = 6.8 Hz, 1H), 7.52 (s, 1H), 7.32 (s, 1H), 3.18 (s, 3H); ESIMS m / z 144 ([M + H] ⁺ .
[00142] Compounds 29-33 were prepared in the same way
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42/73 than in Example 13.
Example 14: Preparation of (E) -N '- (1-ethyl-5-fluor-2-oxo-1,2-dihydropyrimidin-4-yl) -N, N-dimethylformimidamide (34) [00143] 25 ml_ with screw cap was loaded with (E) -N '- (5-fluoro-2-hydroxypyrimidin-4-yl) -N, N-dimethylformimidamide (99.5 mg, 0.540 mmol), DMF (2 ml_) , and NaH (60% dispersion in mineral oil; 24.5 mg, 0.613 mmol) and was stirred on a rotary shaker at 50Ό for 40 minutes. After cooling to room temperature, carbon disulfide (0.036 ml, 0.599 mmol) was added, and the reaction mixture was stirred on a rotary shaker at room temperature for 90 minutes. At this point, iodoethane (0.052 ml, 0.650 mmol) was added, and the reaction mixture was further stirred at room temperature for 3.5 hours, after which the crude mixture was concentrated in vacuo. The crude material by purified by normal phase chromatography (gradient, 0 to 30% MeOH / CH ₂ CI ₂ ) to give (E) -N '- (1-ethyl-5-fluor-2oxo-1,2-di- hydropyrimidin-4-yl) -N, N-dimethylformimidamide (105 mg, 67%) as a white solid: mp 157-160Ό; ¹ H NMR (400 MHz, DMSO-J ₆ ) δ 8.62 (s, 1H), 8.09 (d, J = 6.2 Hz, 1H), 3.70 (q, J = 7.1 Hz , 2H), 3.20 (s, 3H), 3.07 (s, 3H), 1.18 (t, J = 7.1 Hz, 3H); ESIMS m / z213 ([M + H] ⁺ .
[00144] Compounds 35 and 36 were prepared in the manner described in Example 14.
Example 15: Preparation of 1- (ethoxymethyl) -5-fluorine-4- (2-fluorobenzylamino) -pyrimidin-2 (1 H) -one (37) [00145] A 25 ml flask with a screw cap was filled with
5-fluorine-4- (2-fluorobenzylamino) pyrimidin-2-ol (49.7 mg, 0.210 mmol),
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CH ₃ CN (1 mL), and BSA (0.054 mL, 0.0221 mmol), and the mixture was stirred on a 65Ό rotary shaker for 30 minutes. After cooling to room temperature, (chloromethoxy) ethane (0.022 mL, 0.237 mmol) was added, and the resulting mixture was stirred on a rotary shaker at room temperature for 16 hours. The crude reaction mixture was concentrated in vacuo and was purified by normal phase chromatography (gradient, 0 to 25% MeOH / CH ₂ CI ₂ ) to give 1- (ethoxymethyl) -5 fluorine-4- (2-fluorobenzylamino) -pyrimidin- 2 (1H) -one (55.0 mg, 89%) as a yellow oil: ¹ H NMR (400 MHz, DMSO-J ₆ ) δ 8.60 (t, J = 5.8 Hz, 1H), 8 , 05-7.95 (m, 1H), 7.40-7.26 (m, 2H), 7.26-7.10 (m, 2H), 5.01 (s, 2H), 4.59 (d, J = 5.9 Hz, 2H), 3.49 (q, J = 7.0 Hz, 2H), 1.09 (dd, J = 9.0, 5.0 Hz, 3H); ESIMS m / z 296 ([M + H] ⁺ ), m / z 294 ([MH] ').
Example 16: Preparation of 5-fluorine-4 - ((2-fluorobenzyl) (methyl) amino) -1- (4methylbenzyl) pyrimidin-2 (1 H) -one (38)
1. DUF, NnH
2. Mal [00146] A 25 mL flask with screw cap was loaded with NaH (60% dispersion in mineral oil; 20.5 mg, 0.513 mmol) and DMF (2.5 mL). 5-fluorine-N- (2-fluorbenzyl) -2- (4-methylbenzyloxy) pyrimidin-4-amine (149 mg, 0.436 mmol) was added, and the mixture was allowed to stir at room temperature. After 10 minutes, iodomethane (0.033 mL, 0.530 mmol) was added, and the resulting mixture was allowed to stir at room temperature for an additional 28 hours. At this point, the crude reaction mixture was concentrated in vacuo and purified by normal phase chromatography (gradient, 0 to 40% EtOAc / Hexanes) to give 5-fluor-4 ((2-fluorbenzyl) (methyl) amino) -1- (4-methylbenzyl) pyrimidin-2 (1H) -one (119.7 mg, 77%) as a colorless oil: ¹ H NMR (400 MHz, DMSO-J6) δ 8.16 (d, J = 9.5 Hz, 1H), 7.45-7.06 (m, 8H), 4.83 (s, 2H), 4.79 (s, 2H), 3.13 (d, J = 3.3 Hz, 3H ), 2.27 (s, 3H); ¹³ C NMR (101 MHz, DMSO-J6) δ 160.1 (d, J = 244.4 Hz), 154.9 (d, J = 7.1 Hz), 152.9, 136.8, 136, 2 (d, J
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44/73 = 243.2 Ηζ), 134.2, 132.8 (d, J = 37.3 Hz), 129.2 (d, J = 8.2 Hz), 129.0, 128.7, 127.8, 124.6 (d, J = 3.4 Hz), 124.0 (d, J = 14.5 Hz), 115.3 (d, J = 21.0 Hz), 51.0, 47.7, 37.2 (d, J = 8.3 Hz), 20.6; ESIMS m / z 356 ([M + H] ⁺ ).
Example 17: Preparation of 4-amino-5-fluor-1- (thiophen-3-yl) pyrimidin2 (1H) -one (39)
THE
P ^, ΝμΙ · £ Ο ₃ digl / mn
hhfOMa. ÍAük c
pyridinfl.
IHQl.
H

[00147] A) To a solution of phosphorus pentasulfide (102.6 g, 0.46 mol) in diglyme (1 L) was added 5-fluorpirimidine-2,4 (1H, 3H) -dione (30 g, 0 , 23 mol). Solid sodium acid carbonate (NaHCO ₃ ; 77.3 g, 1.04 mol) was added at a rate determined by the release of carbon dioxide. The reaction mixture was stirred overnight at 110 ° C. The yellow mixture was cooled and poured into 1 L of cold water. The precipitated solid product was isolated by filtration and purified by normal phase chromatography (gradient, 10 to 50% EtOAc / petroleum ether) to give 5-fluoro-4-thioxo-3,4-dihydropyrimidin-2 (1H ) -one (13.4 g, 40%) as a yellow solid: mp 254-255 ° C; ¹ H NMR (301 MHz, DMSO-J ₆ ) δ 7.81 (d, J = 4.0 Hz, 1H); ESIMS m / z 145 ([MH]).
[00148] B) This material was prepared by the procedure described in Tetrahedron 1985, 41, 5289-5293. To a solution of 5-fluor-4tioxo-3,4-dihydropyrimidin-2 (1H) -one (12.4 g, 84.9 mmol) and sodium methoxide (4.54 g, 84.9 mmol) in MeOH (100 ml) was added in
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45/73 drops allyl bromide (10.27 g, 84.9 mmol) at room temperature. The reaction mixture was stirred overnight at room temperature. After removing the solvent, the residue was purified by normal phase chromatography (gradient, 10 to 33% EtOAc / hexane), to give A (allylio) -5-fluorpirimidin-2 (1H) -one (6 g, 38% ) as a white solid: mp 150-152 ° C; ¹ H NMR (301 MHz, DMSO-J ₆ ) δ 11.60 (s, 1H), 8.00 (d, J = 4.5 Hz, 1H), 5.90 (ddt, J = 16.8, 10.0, 6.8 Hz, 1H), 5.34 (dd, J = 16.9, 1.4 Hz, 1H), 5.15 (dd, J = 10.0, 0.7 Hz, 1H ), 3.83 (d, J = 6.8 Hz, 2H); ESIMS m / z 187 ([M + H] ⁺ ).
[00149] C) This material was prepared by the procedure described in J. Org. Chem. 2006, 71, 9183-9190. To a stirred suspension of dry Cu (OAc) ₂ (1.02 g, 5.64 mmols), A- (allyl) -5-fluoro-pyrimidin-2 (1H) one (700 mg, 3.76 mmols), thiophen-3-ylboronic acid (962 mg, 7.52 mmols), and activated molecular sieves of 3 A (2 g) in dry CH ₂ Cl ₂ (30 ml) were added pyridine (595 mg, 7.52 mmols) to the room temperature. The mixture was stirred for 24 hours at room temperature in the presence of air. The reaction mixture was diluted with CH2Cl2 (30 ml), filtered through a pad of Celite, and washed with water (50 ml) in the presence of ethylene diaminetetraacetic acid (EDTA; 700 mg, 2.4 mmols). The colorless organic phase was dried over MgSO ₄ and was concentrated in vacuo. The residue was purified by normal phase chromatography (isocratic, 2: 1 petroleum ether: EtOAc) to give 4- (allyl) -5-fluoro1- (thiophen-3-yl) pyrimidin-2 (1H) -one (290 mg, 29%) as a yellow solid: mp 125-127 ° C; ¹ H NMR (301 MHz, DMSO-J ₆ ) δ 8.52-8.35 (m, 1H), 7.81 (s, 1H), 7.69-7.55 (m, 1H), 7, 32 (d, J = 3.5 Hz, 1H), 6.05-5.81 (m, 1H), 5.36 (d, J = 16.9 Hz, 1H), 5.18 (d, J = 9.8 Hz, 1H), 3.89 (d, J = 6.4 Hz, 2H); ESIMS m / z 269 ([M + H] ⁺ ).
[00150] D) This material was prepared by the procedure described in J. Org. Chem. 2006, 71, 9183-9190. 4- (Aliltio) -5-fluoro-1- (thiophen-3yl) pyrimidin-2 (1H) -one (330 mg, 1.23 mmol) was dissolved in a solution
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46/73 tion of ammonia in methanol (7 N, 5 ml). The resulting mixture was stirred overnight at 100 ° C in a pressure vessel. After removing the solvent, the residue was purified by preparatory thin layer chromatography to give 4-amino-5-fluor-1- (thiophen-3-yl) pyrimidin-2 (1H) -one (177 mg, 68%) as a yellow solid: mp 228-229 ° C; ¹ H NMR (300 MHz, DMSO-J ₆ ) δ 8.11 (d, J = 6.9 Hz, 1H), 7.89 (s, 1H), 7.65 (d, J = 1.9 Hz , 2H), 7.56 (dd, J = 5.1, 3.3 Hz, 1H), 7.29 (dd, J = 5.1, 1.0 Hz, 1H); ESIMS m / z 212 ([M + H] ⁺ ).
[00151] Compounds 40-55 were prepared in the manner described in Example 17.
Example 18: Preparation of (E) -N '- (5-fluor-2-oxo-1- (thiophen-3-yl) -1,2-dihydropyrimidin-4-yl) -N, N-dimethylformimidamide (56) [00152] 4-Amino-5-fluor-1- (thiophen-3-yl) pyrimidin-2 (1H) -one (140 mg, 0.66 mmol) was dissolved in DMF-DMA (5 ml). The reaction mixture was stirred at reflux for one night. The residual DMF-DMA was removed in vacuo, and the residue was purified by preparative thin layer chromatography to give (E) -N '- (5-fluorine-2-oxo-1- (thiophen-3-yl) -1 , 2-dihydropyrimidin-4-yl) -N, N-dimethylformimidamide (75 mg, 43%) as a yellow solid: mp 211-213Ό; ¹ H NMR (300 MHz, DMSO-J ₆ ) δ 8.73 (s, 1H), 8.22 (d, J = 6.4 Hz, 1H), 7.75 (dd, J = 3.2, 1.4 Hz, 1H), 7.60 (dd, J = 5.2, 3.2 Hz, 1H), 7.34 (dd, J = 5.2, 1.4 Hz, 1H), 3, 26 (s, 3H), 3.13 (s, 2H);
[00153] ESIMS m / z 267 ([M + H] ⁺ ).
[00154] Compounds 57-64 were prepared in the manner described in Example 18.
Example 19: Preparation of 5-fluorine-4- (2-fluorobenzylamino) -1- (thiophen-3yl) pyrimidin-2 (1H) -one (65)
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Α7Π3
[00155] To a solution of 4- (allyl) -5-fluor-1- (thiophen-3-yl) pyrimidin2 (1H) -one (140 mg, 0.66 mmol) in MeOH (1 ml) was added ( 2fluorfenyl) methanamine (50 mg, 0.186 mmol). The reaction mixture was heated at 100 ° C for 30 minutes in a microwave. After cooling, the mixture was purified by preparative thin layer chromatography to give 5-fluorine-4- (2-fluorobenzylamino) -1- (thiophen-3-yl) pyrimidin2 (1H) -one (41 mg, 20%) as a white solid: mp 75-78X2; ¹ H NMR (300 MHz, DMSO-J ₆ ) δ 8.70 (s, 1H), 8.16 (d, J = 7.0 Hz, 1H), 7.66 (dd,
J = 3.2, 1.4 Hz, 1H), 7.57 (dd, J = 5.2, 3.2 Hz, 1H), 7.43-7.13 (m, 5H), 4.63 (d, J = 5.5 Hz, 2H); ESIMS m / z 320 ([M + H] ⁺ ).
[00156] Compounds 66-73 were prepared in the manner described in Example 19.
Example 20: Preparation of 4-amino-1- (cyclopropylmethyl) -5fluorpirimidin-2 (1H) -one (74)

[00157] To a solution of (bromomethyl) cyclopropane (1.0 g, 7.4 mmols) in DMF (20 ml), molecular sieves (~ 2 g) were added, and the resulting mixture was stirred at room temperature. After 1 hour, 4-amino-5-fluorpirimidin-2-ol (1.9 g, 14.8 mmols) and K ₂ CO ₃ (5.1 g, 37 mmols) were added, and the reaction mixture was heated at 90 ° C for 12 hours. After cooling to room temperature, the crude reaction mixture was filtered through a Büchner funnel, and the solid residue was washed with EtOAc. The collected filtrate was concentrated in vacuo to give a residue which was purified by normal phase chromatography (isocratic, 5% MeOH / EtOAc). Subsequent to recrystallization from methyl tert-butyl ether, 4-amino-1- (cyclopropylmethyl) -5
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48/73 fluorpirimidin-2 (1 H) -one (1.12 g, 83%) was isolated as a white solid: mp 224-226Ό; ¹ H NMR (400 MHz, methanol-d ₄ ) δ 7.86 (d, J = 6.2 Hz, 1H), 3.61 (d, J = 7.2 Hz, 2H), 1.24 (ddd , J = 12.8, 7.6, 4.8 Hz, 1H), 0.65-0.50 (m, 2H), 0.39 (q, J = 4.8 Hz, 2H); ESIMS m / z 184 ([M ₊ H] ⁺ ).
[00158] Compounds 75-79 were prepared in the manner described in Example 20.
Example 21: Preparation of ethyl 1 - (cyclopropylmethyl) -5-fluor-2-oxo-1,2dihydropyrimidin-4-ylcarbamate (80) [00159] 4-Amino-1- (cyclopropylmethyl) -5-fluorpirimidin-2 (1 H) -one (200 mg, 1.09 mmol) was dissolved in CH ₂ CI ₂ (0.90 ml) and pyridine (172.4 mg, 2.18 mmols) at room temperature and then the mixture was cooled to -20Ό. Ethyl chloroformate (166 mg, 1.53 mmol) was then added to the reaction mixture in drops, with the reaction temperature being maintained between -20 and -5Ό. After the addition was complete, the reaction was allowed to warm up slowly to room temperature and stirred for 2 hours. The reaction mixture was filtered, and the solids were rinsed with EtOAc (15 ml x 3). The filtrate was concentrated in vacuo, and purified by preparative thin layer chromatography, to give ethyl 1- (cyclopropylmethyl) -5-fluorine-2-oxo-1,2-dihydropyrimidin-4ylcarbamate (70 mg, 30%) as a pale yellow solid: mp 9092Ό; ¹ H NMR (400 MHz, methanol-d ₄ ) δ 8.20 (s, 1H), 4.26 (q, J = 7.1 Hz, 2H), 3.70 (d, J = 7.2 Hz , 2H), 1.24-1.36 (m, 4H), 0.65-0.57 (m, 2H), 0.46-0.39 (m, 2H); ESIMS m / z 256 ([M + H] ⁺ ).
[00160] Compounds 81-84 were prepared in the manner described in Example 21.
Example 22: Preparation of 1- (2-chlorophenyl) -3- (1- (cyclopropylmethyl) -5fluor-2-oxo-1,2-dihydropyrimidin-4-yl) urea (85)
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[00161] To a stirred solution of 4-amino-1- (cyclopropylmethyl) -5fluorpirimidin-2 (1H) -one (150 mg, 0.819 mmol) in dry CH ₃ CN (7.5 ml_) at room temperature and in a nitrogen atmosphere was added 2-chlorophenylisocyanate (138.3 mg, 0.90 mmol). After stirring for 1 hour, the crude reaction mixture was filtered, and the solids were rinsed with CH ₃ CN (10 ml). The collected filtrate was then concentrated in vacuo and dried in high vacuum to give 1- (2-chlorophenyl) -3- (1 (cyclopropylmethyl) -5-fluor-2-oxo-1,2-dihydropyrimidiη-4-yl ) urea (160 mg, 58%) as an off-white solid: mp 197-199Ό; ¹ H NMR (400 MHz, methanol-d ₄ ) δ 8.26 (d, J = 6.0 Hz, 1H), 8.21 (dd, J = 8.3, 1.5 Hz, 1H), 7 , 47 (dd, J = 8.0, 1.4 Hz, 1H), 7.35-7.28 (m, 1H), 7.13 (td, J = 7.8,
1.5 Hz, 1H), 3.74 (d, J = 7.3 Hz, 2H), 1.32 (m, 1H), 0.69-0.58 (m, 2H), 0.50- 0.38 (m, 2H); ESIMS m / z 337 ([M + H] ⁺ ).
[00162] Compounds 86-93 were prepared in the manner described in Example 22.
Example 23: Preparation of N- (5-fluoro-2-oxo-1 - ((tetrahydrofuran-2iDmethyl) -1, 2-dihydropyrimidin-4-yl) thiophene-2-carboxamide (94)
[00163] This material was prepared by the procedure described in J. Org. Chem. 2005, 70, 7459-7467. To a solution of 4-amino-5fluor-1 - ((tetrahydrofuran-2-yl) methyl) pyrimidin-2 (1H) -one (200 mg, 0.94 mmol) in dry THF (1 ml) at temperature 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide (EDC; 180 mg, 0.94 mmol) and 1H-benzo [d] [1,2,3] triazole-1-ol (HOBt; 139 mg, 1.03 mmol). After stirring for 10 minutes, thiophene-2-carboxylic acid (145 mg, 1.13 mmol) was added, and the resulting solution was allowed to stir at temperature
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50/73 environment for 12 hours. The reaction mixture was concentrated in vacuo, quenched with a saturated aqueous solution of NaHCO ₃ (10 ml), and extracted with EtOAc (25 ml x 3). The combined extracts were washed with a saturated aqueous solution of sodium chloride (NaCl), dried over Na ₂ SO ₄ , filtered and concentrated by rotary evaporation. Purification by normal phase chromatography (gradient, 0 to 2% MeOH / CH ₂ CI ₂ ) gave 4-amino-5-fluorine-1 - ((tetrahydrofuran-2yl) methyl) pyrimidin-2 (1 H) -one (60 mg, 20%) as a white solid: mp 168 - 170 °; ¹ H NMR (400 MHz, CDCI ₃ ) δ 12.96 (s, 1H), 7.96 (d, J = 3.7 Hz, 1H), 7.63 (d, J = 5.7 Hz, 1H ), 7.60 (d, J = 4.9 Hz, 1H), 7,167.11 (m, 1H), 4.20-4.08 (m, 2H), 3.89 (dd, J = 15, 1, 6.9 Hz, 1H), 3.80 (dd, J = 14.5, 7.5 Hz, 1H), 3.57 (dd, J = 14.4, 7.7 Hz, 1H), 2.10 (dt, J = 12.8, 6.7 Hz, 1H), 1.99-1.87 (m, 2H), 0.88 (m, 1H); ESIMS m / z 324 ([M + H] ⁺ ).
[00164] Compounds 95-101 were prepared in the manner described in Example 23.
Example 24: Preparation of 5-fluorine-1 - ((tetrahydrofuran-2-yl) methyl) -4 (thiophen-2-ylmethylamino) pyrimidin-2 (1 H) -one (102) [00165] This material was prepared by the procedure described in J. Org. Chem. 2005, 70, 7459-7467. To a solution of 4-amino-5fluor-1 - ((tetrahydrofuran-2-yl) methyl) pyrimidin-2 (1H) -one (160 mg, 0.495 mmol) in THF (4 ml) at room temperature was added in BSA drops (0.61 ml_, 2.47 mmols). After the addition was complete, the borane-N, N-diisopropylethylamine complex (DIPEA-BH ₃ ; 0.90 ml_, 4.95 ml_) was added in drops, and the resulting solution was stirred at room temperature for 15 minutes. . The reaction mixture was quenched by the addition of MeOH (20 ml), and the mixture was concentrated in vacuo. The resulting mixture was dissolved in a 1: 1 (v: v) mixture of ammonia
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51/73 to 17% in methanol: 28% ammonia in water (135 mL) and heated to 50Ό for 13 hours. After cooling to room temperature, the mixture was extracted with chloroform (CHCI ₃ ; 100 ml x 2). The combined extracts were washed with an aqueous NaCl solution, dried over Na ₂ SO ₄ , filtered, and concentrated in vacuo. Purification by preparative thin layer chromatography gave 5-fluorine-1 - ((tetrahydrofuran-2-yl) methyl) -4- (thiophen-2-ylmethylamino) pyrimidin-2 (1H) -one (40 mg, 26%) as a gummy white solid: ¹ H NMR (400 MHz, na-d ₆ ) δ 7.69 (d, J = 6.7 Hz, 1H), 7.52 (s, 1H), 7.32 (dd, J = 5.1, 1.2 Hz,
1H), 7.08 (dd, J = 3.4, 0.9 Hz, 1H), 6.95 (dd, J = 5.1, 3.5 Hz, 1H), 4.85 (d, J = 6.0 Hz, 2H), 4.12 (ddd, J = 14.6, 7.1, 3.2 Hz, 1H), 4.00 (dd, J =
13.6, 2.8 Hz, 1H), 3.83 (dt, J = 8.1.6.7 Hz, 1H), 3.72-3.64 (m, 1H), 3.56 (dd , J = 13.6, 7.7 Hz, 1H), 2.02-1.93 (m, 1H), 1.86 (ddd, J = 11.0, 8.1,
1.6 Hz, 2H), 1.67-1.54 (m, 1H); IR (thin film) 3222, 3125, 3068, 2950, 2875, 1673, 1623, 1586, 1556, 1508, 1368, 1329, 1186, 1139, 1065, 906 cm ^-1 ; ESIMS m / z 310 ([M + H] ⁺ ).
[00166] Compounds 103 and 104 were prepared in the manner described in Example 24.
Example 25: Preparation of 5-fluorine-4- (2-fluorobenzylamino) -1-isobutylpyrimidin-2 (1H) -one (105)
AND
C [00167] A) To a solution of 5-fluorpyrimidine-2,4 (1H, 3H) -dione (5.0 g, 38 mmols) and 1,8-diazabicyclo [5.4.0] undec-7 -ene (DBU; 6.4 g, 42 mmols) in dry CH ₃ CN (150 mL) at room temperature and in a
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52/73 nitrogen atmosphere was added in 1-bromo-2-methylpropane drops (5.3 g, 38 mmols). The reaction was then heated to reflux for 18 hours. After cooling to room temperature, the solvent was removed in vacuo. The crude residue was purified by normal phase chromatography (gradient, 0 to 20% EtOAc / petroleum ether), giving 5-fluorine-1-isobutylpyrimidine-2,4 (1H, 3H) -dione (2.5 g, 35%) as a white solid: mp 173-174 ° C; ¹ H NMR (400 MHz, CDCl ₃ ) δ 8.61 (s, 1H), 7.21 (d, J = 5.5 Hz, 1H), 3.53 (d, J = 7.5 Hz, 2H ), 2,132.01 (m, 1H), 0.98 (d, J = 6.7 Hz, 6H); ESIMS m / z 185 ([MH] ^- ).
[00168] B) Phosphoryl trichloride (3.3 g, 21 mmol) was added to a solution of 1,2,4-triazole (6.7 g, 97 mmol) in CH3CN (53 mL) in a nitrogen atmosphere at room temperature. The mixture was cooled to 0 ° C, and thereafter triethylamine (Et ₃ N; 9.5 g, 92 mmols) was added in drops followed by the addition of a solution of 5 fluorine-1-isobutylpyrimidine-2.4 (1H, 3H ) -dione (2.0 g, 11 mmols) in CH 3 CN (30 ml). After stirring for 1 hour at room temperature, Et3N (3.6 g, 36 mmols) and then water (5 ml, 280 mmols) were added, and the reaction mixture was stirred for another 10 minutes. The crude reaction mixture was then concentrated in vacuo. Recrystallization from EtOAc / petroleum ether gave 5-fluor-1-isobutyl-4- (1H-1,2,4triazol-1-yl) pyrimidin-2 (1H) -one (1.9 g, 74%) as an off-white crystalline solid: mp 150-153 ° C; ¹ H NMR (400 MHz, CDCl ₃ ) δ 9.26 (s, 1H), 8.23 (s, 1H), 7.84 (d, J = 5.7 Hz, 1H), 3.79 (d , J = 7.4 Hz, 2H), 2.28 (dt, J = 13.7, 6.9 Hz, 1H), 1.02 (d, J = 6.7 Hz, 6H); ESIMS m / z 238 ([M + H] ⁺ ).
[00169] C) A solution of 5-fluor-1-isobutyl-4- (1H-1,2,4-triazol-1yl) pyrimidin-2 (1H) -one (500 mg, 2.1 mmol) and 2 -fluorbenzylamine (313 mg, 2.5 mmols) in dry 1,4-dioxane (10 mL) was heated to reflux for 1 hour in a nitrogen atmosphere. After cooling to room temperature, the reaction mixture was concentrated in vacuo.
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Recrystallization from EtOAc / methyl tert-butyl ether gave 5-fluoro-4- (2-fluorobenzylamino) -1-isobutylpyrimidin-2 (1H) -one (545 mg, 89%) as an off-white solid: mp 118-119X2; ¹ H NMR (400 MHz, CDCI ₃ ) δ 7.45 (td, J = 7.6, 1.7 Hz, 1H), 7.35-7.28 (m, 2H), 7.13 (ddd, J = 21.9, 13.9, 7.3 Hz, 3H), 5.58 (s, 1H), 4.81 (d, J = 5.4 Hz, 2H), 3.56 (d, J = 7.5 Hz, 2H), 2.16 (dt, J = 13.6, 6.8 Hz, 1H), 0.95 (d, J = 6.7 Hz, 6H); ESIMS m / z 295 ([M + H] ⁺ ).
[00170] Compounds 106-110 were prepared in the manner described for Example 25.
TABLE I: Related Compounds and Characterization Data
Cmpd Structure Appearance mp (‘'O MS Ti NMR ^a | Ô, SOlvéilt) 3 ch ₃ ^h wliite solid 157-187dec (CDCh) 7.47 (<], J = 6-1 m, 111), 591fs, 1H), 4.45 (s,211), 4.38 (d,. / = 5.2 Hz, 211), 2.36(5, 121b 5 ClCHj yclJow niJESIMS nt / z 343 f | M + H] ⁺ ) (CDCLj) 8.81 (si, 111), 7.40 (d, J =2.3 Πζ, 111) .7.37(d, ./ = 8.2Hz, Hl),7.33 (d, 7 = 5.6 Hz,IH), 7 22 (dd, J =8.2.2.3 Hz, UI), 5.06 (s, 2H), 3.18(s, 611) 6 9 ^ no h ₃ cn white solid 186-188 LSLV1S nt / z275 OM + llf) (CDCb) 8.85 is, 111), 7.41-7.31 (m, 511.), 7.24 (d, J =5.5 Hz, 111), 5.04 (s, 211), 3.22 <s, 111), 3.21 (s, 311)
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Cmptl StriJCtuH! Appeti rance mp CC) ΊΙΝΜΚ * (δ, solvent) 7 CIL ^f Xa CH, while solkl 178-179 (C1X Ij) 8.85 (s, FSIMSi / z 1H), 7.26-7.17 (m, 289 511). 4.99 (s, 211). (| M + 1I] ⁺ ) 3.21 (3.611), 2.37 (s, 311} 13 The η, ο-ν _λ CH, whire solid 109-111 (600 MHz, DMSOrfí) 8 65 (s, 111),8.04 (d, J = 6.2 llz,JiSIMSui / t 111), 5.58 (3.211),285 3.20 (s, 311), 3.07([Μ + 1Ϊ1 *) (s, 311), 2.27 ((, / =7.3 Hz, 211), 1.53-1.46 (m, 2H), 0.83 items. 7 = 7.3 llz, 3H) 16 H _J C '°' ^V ^ O H, NN ^ O while solid 160-163 (DMSO-i / r.) 7.97 (d. 7 = 6.6 Hz. III), F.STMSwi 7.83 ís, 11T), 7.58 218 (.s, 111), 5.03 (s, Í [M + HJ ^T ) 2H ), 3.65-3.53 (m, 2H), 3.46-3.38 (m, 211), 3.22 (s, 3H) 17 H, C CH, 3 ^1. í J h ₃ c ' ^{S | s} ^ o ^F y ^ J h ^ AA off-whitfsolid 187-192 (DMS (W ₆ ) δ 7.96 (d. 7 = 6.6 Hz, 111), .......... 7.80 is, 111), 7.57 ^{, S [} ^^ ( _S , 111). 4.99 (s, ([M + IID 2H), 3.51 (dd. 7 = - ^{1 1} '20.2, 12.Ξ Hz, 211), 0.85 (t, 7 = 7.9 Hz, 2H), -0.03 (s. 911 ). IS ch ₃ H-jAíAo off-whitcsoli <l 166-170 (DMSO- / _f ) 7-98 (d, 7 = 6.5 Hz, III), 7.85 (s, 1H), 7.62 FSlMSm / z (s. ΊΗ), 5.01 (s, 272 211), 3.44 (L, 7 = (ΙΜ + 11Γ) 6.4 llz, 2H), 1.47 Cm, 211), 1.24 (m, 1011), 0.86 (1.7 = 5.Ó Hz, 311) 19 ^G, n ₀ h ₂ AAj while 240-245 (DMS (j-4 _P1 ) 8.09 Çd. 7 = 6.6 llz, 111), FSIMS »Á 7.97 (s.lH), 7.72 270 (s, 111), 7.36 (d, 7 = ([M + HJQ 8.8 Hz , 2H), 7. () 7 (d. 7 = 8.9 Hz, 211), 5 58 (s, 211)
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Cmpd Stmcturc Appearance mp CO ΊΙ NMK ^a (δ, solverit) 20 ^F y ^ N ' <''CH _J η, νΑΑο white solid 150-154 (DMSO-Λ) 7.97(s, ΠΙ), 7.81 (d, 7 =6.3 Hz, 111), 7.72ESIMS m / z (s, 1H), 5.84 (s,260 lH), 4.15 (dd. J =(ΙΜ + 11Γ) 13.7,6.811 /, 211),3.59 (dd, 7 = 13 3,6.4 Hz, 211), 1.28-1.04 (in, 6H) 21 0 whité stsliti 210-214 (DMSO-rf _r ,) 7.99 (m, 7 ~ 6.7 Hz, ruue / 2H), 7.72 (s, JH), ,, _n 5, .75 Cs, 211). 2.30 .... „. ₊ , (t, 7 = 7.2 Hz. 211), ([M + HJ) 1.68-1.39 (m, 2H), 0.86 Çt, 7 = 7.4 Hz, 3ii) 22 AA ^H s ^c ch ₃ H NN ^ O white solid 259-264 (DMSO-íW 7.99 ESIMS m / z (d, 7 = 6.7 Hz, 1H), 244 7.97 (s, IH), 7.71 (| M + 1I] ⁺ ) (s. 111), 5.54 (s, 211 ), 1.12 Cs, 911) 23 CH, OAuZrAo '·' · ^ H.N ^ N ^ O white solid 162-166 (DMSO-4;) 8.08 (d, 7 = 7.DIL ·. III),7.95 Cs, 111), 7.69ESIMS m / z (s, 111), 6.72 (q, 7 = 246 5.2 llz, 111), 4.12(IM + Hf) (q, 7 = 70 Hz, 2H),1.55 (d, 7 = 6.1 Hz, 311), 1.20 íl, 7 =7.1 Hz. 3H) 29 Yr ^cH 'H ^ N ^ N ^ O white solid 279 dec (DMSO-ifc) 7.98 .i 01, 7 = 6.8 llz, 1111, LSEMS ^ z _{7 57fs | H) 7 3} g (s, 1 H), 3.63 (q. 7 = ^{u 1} 7.1 llz, 2H), 1.14 (1.7 = 7.1 llz, 311) 30 Ay ° ' ^ch = hjAUo white Solid 168-189 (DMSO-dc,) 7-93 (d, 7 = 3.3 Hz, 1Π), 7.31 ($, 2H), 7.19 ESIMS m / z (d. 7 = 8.6 Hz, 2Π), 264 6.90-6.82 (ni, 2H), (| M + J1 | ⁴ ) 4.28 0, 7 = 6.9 Hz, 211). 3.72 (s, 311), 2.89 (1.7 = 6.9 Hz, 211) 31 Γϊ ^α white solid 252—254 (l) MSOU ₆₎ 7.97 (d 3.5Πζ = 7, III) rcivoe / -. 7:46 (s, 211), 7.39- ₇ .34 _{(m, 21I) 734.} A11 '} 7.28 (m, 211), 4.34 ^{(| x 1 + 111 1} (L, 7 = 6 7 Hz, 211), 2.97 ((, 7 = 6.7 Hz, 2H)
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Cmptl StnjCÍUH! Appwi rance mp CC) ΊΙΝΜΚ * (δ, solvent) 32pale ycllow solid 255 dec (IJMSO-íÁ) 7.92 (d, 7 = 32Hz, 1Π). 7.27 (3,211), 4.1 () (dd. J = 10.5,6.7 Hz. IH), 4.02 (dd, 7 = 10.5, 8.0 1 Iz, VSIMS ^ 'lllU ^ -3.69 (m, 211), 3.63 (dd, 7 = ,,,,, 15.0, 7.8 Hz, 1H), ^{(| M + 11 |)} 3.47 (dd, J = 8.6, 5.6 Ilz, 111), 2.59 (dt, 7 = 14.1,7.2 Ilz, Kl), 1.97 (did, J = 13.8.8.2,5.6 Hz. 111), 1.65-1.53 (ni, 1H) 33 FΚ, Ν ^ Ν ^ Ο F beige snlid 256-254 (HMS (jd ₆ ) 8.04 (d. 7 = 6 6 llz, 111), ESIMS il '7.74 (s, 111), 7.50 256 (s, 111), 7.35-7.20 (1Μ + 1ΙΓ) (ηι, 21Γ) , 7.06 (td. 7 = 8.5, 1.8 Hz, III), 4.82 (s, 2H) 35 ^h = s ^ XCCX 1 CH, whíie solid 196-20Ü (DMSO-íW 8.64(s. 111), 8.24 (d. 7 =ESIMS «See 6.211 / .111), 7.48-311 7.35 (m, 21T), 7.23-([M + II] · ') 7.13 (m, III), 4.85Cs, 2H), 3.21 (s,3H), 3.08 (s, 3H) 36 ^H A ^ _N -à _N A _n 0 ch ₃ white solid 196-199 (l.) MSO-d _É ) 8.67 (s, 1H). 8.05 (d, 7 =. 6.2 Hz, 111), 4.48 ESIMS ($, 2H), 4.14 (q, 7 = 7.1 Ilz. 211), 3.22 * ^{1X1 + 111 1} Cü, 3H>, 3.10 (S, 3H), 1-20 (L, 7 = 7.1 Hz. II) 41) ^ Ύ ^Ο ' ^GH 3 white solid 244. 8-245.6 (l) MS (MO 7.98 (d, 7 = 6.7 Ilz, 111), i-ervit / - 7.80 (5,110,7.57 ^, Sis ^ ís, 1H). 7.00 (in. d + lll ⁺ ) 2H), 6.89 (dd, 7 = (IM + lll) 8.6, 2.3 Hz. 111), 3.79 (s. 311), 3.76 (s, 3H) 41 ^f 'Y ^ n' ^ ch ₃ whiie solid 213.5-214.4 (DMSO-df.) 8.28 (d, .1 = 7.1 Ilz, 111), ....... 8.01 (s, 111), 7.77 ^LS1 s (s, 1H). 7.18 (dd, J avi + JlP) = 15.4, 10.3 Hz, ^{u 1} ) III), 5.27 id, J = 16.2 Hz, 111), 4.78 (d, J = 8.0 Hz. 1H)
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Ctnpd Structurc Appcarancc rnp m MS '11 XMR ^J (S »sulvent) 42 HjN ^ N ^ O οίΓ-whiic soJid 233-235 liSlMS ^:206 ΠΜ + ΠΓ) (DMSO-rfí.) 8.05(dd, 7 = 6.8, 1.7 Ilz, 111), 7.86 (s, 111), 7.62 (s, III}, 7.51-7.31 (ni, 511) 43 KN ^ N ^ O ofl-white sdid 225-227 ESIMS m / ’220 ([M + 1T] *) (E> MS <M) 8.00(d, 7 = 6.7 Hz, III),7.83 (s, 111), 7.59 (s, 111), 7.25 0, 411), 2.34 (s, 3H) 44 rr ° ^ h _; rZ ^x rAo brnwn solid 230-232 esims ml / ’236 ([M + 1T1Ó (IJMSO-fr,) 7.99 (d. 7 = 6.71 Iz, 1H), 7.8'1 (s, 111), 7.57(s. IH), 7.29 (d. J =8.8 Hz, 211), 6.98 (d. 7 = 8.8 Hz, 2H), 3.78 (s, 7 = 8 6 Hz,3H) 45 j ^ y ^cl η, ΛΛο off-white sclid 255-257 ESIMS tiVz240 OM + llfl (DMSO-Jr,) 8.07(d. 7 = 6.3 Hz, III),7.93 (s, IH), 7.68 (s, I1T), 7.51 (dd, 7 = 8.6.1.0 Hz. 211).7.43 (dd, 7 = 8.7,1.1 Hz, 21Γ) 46 η ₂ ν · %% pale bwwn s <> Jid 175—178 ESIMS m / z231 ([Μ + 1Ι] *) (HMSO-de) 816 (d, 7 = 6.9 Hz, 1H), 7.98-7.94 (m, IH), 7.86-7.82 (ni, IH), 7.82-7.76 (ni, IH}, 7.67 (d, 7 = S.OJIz.1H) 47 ^f y ^ _n XXo ^> Λ Λ H NNO off-whiie soJid 275-279 ESIMS ιιι / ζ250([Μ + 1ΙΓ) (TJMSOVj 7.96 (d, 7 = 6.7 Hz, IH),7.82 (s, IH), 7.57 (s, IH). 6.99 (d. 7 =2.1 Hz, HI), 6.96 (d, 7 = 8.2 Hz, III),6.82 fdd, 7 = 8.3,2.1 Ilz, 111), 6.08(s, 211} 4 « F jOhxSAo yelluw snlid 256-258 ESIMS πΛ 232 (| M + J1 | ⁴ ) (DMSO ^) S8.42(d. 7 = 7.2 Hz, IH),8.04 (8, 111), 7.82(s, 1H), 7.66 (d, 7 =15.0 Hz, JH), 7.44 (d, 7 = 7.9 Hz, 211), 7.36 (1.7 = 7.6 Hz,211), 7.26 (dd, 7 =10.5.4.0 Hz, 111),681 id, 7 = 15-0Hz, IH)
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Cmpd Structure Λρρ ea rance mp CO Ίινμκ ¹ * (δ, solvent) 49 KlAtAo skip brown yciJitl 212-214 (IÍMSO-íM 8.24 (d, J = 7-2 Πζ, 1113, 7.92 (s, 111), 7.69 (s, 1H), 7.31 (ni, ESIMS mÇ 2H), 7 22 (dd, J = 246 14.9, 7.1 Hz, 311), (| xM + ll | ⁴ ) 7 03 ((1 (1.7 = 14 5, 1.6 Hz, 11 D, 5.95 (dl, 7 = 14.5.7.3 Hz, 1H). 3.45 (d .7 = 7.1 Hz, 2ED 50 f xy ^cH3 Η) ΑΛ ofl-whilesciJicl 244.4-245.7 (BMSO-7 ₆ ) 8.14 (d, 7 = 6.8 Hz, 1113, ESIMS m / z 8.04-7.92 (ηι, 3H), 284 7.75 (s. 7 = 7.8IL ·, (| M + J1 | ⁴ ) 111 ) .7.69 ((1.7 = 8.4 Hz, 211), 3.26 (s, 3H). 51 F0 whire solid 190.6-192.7 (DMSOW _tl ) 7.75 (d. 7 = 6.6I1Z, 111), rouc, 7.62 (3,110,7.41 ^EM ™ * (s, 1TI), 5.66 (,, 7 = ([M ₊ nn 3.7 Hz. 1H), 2.15 ^{1 1} (D, 7 = 36.9 Hz, 411), 1.6t) (dt, J = 10 5.50 Hz, 411} 52 rnAAo yell «w solid 211.2—213.0 (DMSO-d _f ,) 7.97 (d, ./= 6.5 Hz, 1113, ESIMS m / z 7.83 (s. IH). 7.60 232 (s, IHJ, 7.45-7.24 (| M + 1I] ⁺ ) (m , 5H). 5.86 (d. 7 = 09 117.111), 5 37 (d, 7 = 0.9 Hz, 1113 53 η ₂ νΆΑο whitc solid 152.8-153.4 (DMSO-Je) 8.17 (d, 7 = 7.1 Ilz. 111), 7.85 (s. IH), 7.62 (s, IH), 6.88 (d. J = ESIMS m / z 14.5 Hz, 110.5 74 198 ( dt, 7 = 14.3, 7.1 (IM + HJ ⁴ ) Hz., 1Hj, 2.06 (q, ./ = 7.1 Hz. 2H), 1.48-1.31 (ni, 2H), 0.89 item, 7 = 7.3 Hz, 310 54 iar ^{the 'Ch3} hjAnAd ydJvW solid 263.3-265.1 (CLEOO 8.20 ((1.7 = 6.7 Hz, 1111.7 55 (dd. 7 = 14.8, 1.9 ESIMS m / j Hz, 1H). 7.40 (d. J 262 = 87 117.211), (| M + 11 | ⁴ ) 6-94-6.87 (ni, 211), 6.68 (d. 7 = 14.7 Hz, 1T 0.3 80 (s, 310
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Cmpd Stmcture Appea rance mp (C) ΊΙ NMR (δ, solvent) 55 • _r ./ white solid 272.8-274.2 (DMSO-íÜ8.17ESIMS «Λ (d. 3 = 6.7 IIz, III),256 8.00-7.85 (111,511),([Μ + ΙΙΓ) 7.65 (s, III), 7.61-7.49 (111, 3H) 57 fV ° ' ^{CMa F} Y ^ _N AtA ₀ -cH ₅ ycJJow solid 196.1-198 0 (DMSO-ífc) 8-72 (s, 1II), 8.09 (d, J = 6.2 Hz, 11D, 7.071'SIMSw / i 7.02 (m, II 11.7.00 321 (s, 111), 6.94 (dd, / (| M + 1I] ⁺ ) = 8.5, 2.3 IIz, III), 3.80 (s, 311), 3.77 fs, 311), 3.25 (s, 3H), 3.13 Cs, 311) 5 « ^F y ^{H 'C'} -IA / ^GH 1 1 4ac ycllow solid 179.6-181.3 (DMSOWe.) 8 69 (d, 3 = 17.4 Hz, 1U). 8.37 (d, J = 6.6 Hz. 111), 7.21ESIMS íddd, J = 22.7,211 11.3, 6 8 Hz, III),(IM + Hf) 5.41 dd, 3 = 16.2Hz, JH) .4.89 (11, J = 9.2 IIz, 1111.3.25 (s, 311). 3.11 (¢ 1.3 = 11.5 Hz, 3H) 59 f jCT ^{ch3 H} ' ^C ' iZ% - Ao ^CH S whiie solid 284.6-186.9 (DMSO-d _c ,) 8.75 (s, IH), 8 .23 (d, 3 = rcrvrc / 6.3 Hz, 1H), 8.01 (d, 3 = 8-6 Hz, 2H), 7.74 (d.3 = 8.6 Hz, ([M + HJ) 211), 3.27 (s, 311), 3.26 (s, 311), 3.14 (s, 3H) 60 F N — N- ^ ^λ 'H, CO white solid 173.2-174.4 (DMSO-J _s ) 8.63 (s, IH), 7.87 (tl, 3 = 6-OIIz, 111), 5.72 ESIMS 'Vz (s. 111), 3.21 (s, 265 3Η), 3.08 (5,311), ( | M + H] Ú 2.18 (d. 3 = 37.4 Hz.411), 1.62 (dd, 3 = 29.1.4.7 Hz, 411) 61 ^F y ^ Íc _H , *% ^Λ ΑΑ> ch ₃ ycllow solid 147 .ΟΙ 47.0 (DMSO-iW 8.69 (s, JH), 8.08 (d, 3 = renie / 6.0 Hz, 111), 7.40- ^s 7.27 (m, 5111,5.92 (| M + H | ⁺ ) (d, 3 = 1- 2 IIz, III), tl.vi + Jil j _{5 44 (d} 3 = 1.1 Hz., 111), 3.23 (s, 311), 3.12 (5,311)
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Cmpd Structurc Appea rance mp C ’€) Ίινμκ ¹ * (δ, solvent) 62 ^kc 'n ^ nAAu CH, whiie siilid 144.7-146.3 (CD, OD) 8 72 (s, 110. 8.06 (d, 7 =6.0 Hz, 1H), 6.96 (dd, 7 = 14.3,1.6ESIMS(ΙΜ + ΗΓ) 111). 3.27 (5.311).([M + H]) 3.21 (5,310,2.18(ddd, 7 = 14.7,7.3,], 4 Hz. 2H), 1.59-1.44 (m. 211), 0.98 (C. 7 = 7.4 Hz, 310 63 HCt ^ rAtAc. CH _g YdJuw solid 264.3-265.3 DMSCWi) 8.72 (s, 111) .8.44 (d, 7 = 6.8 Hz, 111), 7.56 (dd, 7 = 14.9, 18 ESIMS wt Hz, 111), 7.40 (d, 7 317 = 8.7 Hz, 2111, 6.93 (| Μ + Π] ⁺ ) (d, 7 = 8.7 IIz, 2Π). 6.86 (d. 7 = 14.9 Hz, 1T 0.3.76 (s, 3II), 3.25 (s, 311), 3.12 (s, 3H ) 64 CHj ydlow snlid 222.4—224.4 (DMSO4) 8.74 (s, HO. 8.27 (d. 7 = ESIMS wl 6 2 Hz, 111), R.04- 311 7.90 (111, 4H), 7.65- (| M + HJ ⁺ ) 7.49 (m, 3H ), 3.25 (s, 310.3.13 (s, 311) Mwhite solid 206.3-207.9 (D MS <} - </ ;,) 8 .60 (t, 7 = 6.0 Hz .. 1H), 8.03 (d, 7 = 68 Hz, 110, 7.43-7.29 (m, ESIMS 211), 7 26- 7.16 (m. „7 7 = 12.8, 5.9 Hz, (ΊΜ + 1ΙΓ) 210.7.03-6 97 (m, ^{u 1} '211), 6.90 (dd, 7 = 8.5.2.0 Hz, 1H), 4.63 (d , 7 = 5.7 Hz, 210.3.79 (s, 311), 3.75 (5,311) 67 q ^ AA white- solid 168.6-169 1 (DMSO - </ _f ,) 8.81 fs, 110.8.32 (d, 7 = 7.3 Hz, 111), 7.34 (dd, 7 = 14.4.6.6 ESIMS ut / z IIz, 21T), 7.27-7.09 264 (m. 211), 5.31) (dd, ([Μ + 11Γ) 7 = 16.1.1.5 Hz, IH). 4.80 (dd, 7 = 9.2, 1.5 Hz, 1H), 4.62 (d, 7 = 5.8 IIz, 210
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Cmpd Stmcture Appea rance mp (C) Ίΐ NMK '(δ, solventiVOÇ while solid 231.6-233.1 (CD, O1J) 8.11 - 8 00 (111, 211), 7.94 (d, J = 6.3Ik, III), rcrvre / 7.76-7.66 (m, _2H) , ₇ . _{47 (U =} ^J ₄ 6.9 Hz, 111). 7.37- (IM + HJ) 7.25 (m, 1H1, 7.20 -7.04 (in.211), 4.78 (s, 2H), 3.16 (s, 3H) 69 FQ- ° tyr ^F whire solid 151.5-152.6 (l) MSO-4>'45 (t, 2 = 5.7 Hz, IH), 7.80 (d, 2 = 6.7 lk,, 111), 737-7.10 ^LSI ^ ^S / ^{H /;} ^, 411), 5.68 0, 1H). 4.57 (d, 2 = ^{11 1} '5.8 Ik, 211), 2.15 (d, 2 = 33.7 Hz, 411), 1.75-1.47 (m, 411} 70 F U ^H while solid 138.9-140 2 (DMSO-A) 8.63 (t, 2 = 5.91IZ, 111), 8.02 (d, J = 6.611 /, rcrvrc / - 111), 7.46-7.25 (m, 7H), 7.25- _m , 7.12 (m 211), 5.89 (IM + HI) _{(dJ = 0OT (zJlr)} 5.39 (d, 2 = 0.9 Ik, 1H), 4.62 (d, 2 = 5.8 Hz, 2H) 71while oil(DMSO-4) «.68 (t, 2 = 5.7 Hz, 111), 8.22 (d, 2 = 7.21 k, III), 739-7.23 (m, 2 = 7.51k, 211), 7.23-7.05 011.2 = r ^ rv.re / 15.2, 8.1 Hz, 2H), W (d, 2 = 14.4 lk, lll), 5.76 (dt.2 ¹¹ 1 ^J = 14.4, 7.2 Hz, 111). 4.60 (d. 2 = 5.8 Ik. 211), 2.06 (dd. 2 = 143.7.1 Hz, 211), 1.48-1 29 (πι, 211), 0.89 (t, J = 7.31k, 3H)
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Cmpd Slructuro Appcarancc mp m IIXMR ^J {5, solveat) 72 cç « ycJJow solid 196.8-198.5 (CD.OD) 8.18 (d, 7 = 6.8 Hz. 1111,7.56(dd, 7 = 14.8, 2.0 Hz, 1H), 7.50-7.36 (m, 3H), 7.35-7.24ESIMS i; 7; (ηι. III), 7.14 (dd,370 7 = 7.6.6.4 Hz,([Μ + 11Γ1 111), 7.10-7.03 (m,2H), 6.90 (d, J = 8.8 Hz, 2H), 6.68(d, 7 = 14.7 Hz, 111), 4.76 (s, 211), 3.80 (s, 311) 73 q-AA whire solid 207.5-209.0 (DMSOO 8.768.60 (m, 110.8.21 rcruc, (d. 7 = 6 8 Hz, 1H), ^{Ι Μ} ^ '8.01-7.87 (m, 4H), (ΙΜ4ΠΓ) 7.64-7.47 (^ 311), ^{u 1} '7.10-7.45 (m, 410, 4.65 (d, 7 = 6.2 1 Iz, 2H) 75 ^F -y ^x 'N'^> p ^> N brown solid 229.2-231.3 (CD OD) 8 .58 (d, 7 = 2.011 / .1111.8.49 (dd, 7 = 4.9, 1.5 ESlMSni / ϊ Jlz, lll), 7.98 íd,. / 221 = 6.2 Hz, 111), (IM + llf) 7.90-7.82 (ηι. 1H), 7.44 (dd, 7 = 7.9, 4.9 Hz, ÍH), 4.9 «(s. 2H) 76 hAA offi-whitc solid 179.2-181.1 (IJMSO-aU 7.83 (d, 7 = 6 8 Hz, 1H), 7.58 (s, 111), 7.37 (s, 110.4.08-3.98 ES1MS tit / z magnet,) I1), 3.84-3.71 214 (m, 2H), 3.63 (dd, (| M + H] ⁺ ) 7 = 14.3, 7.3 Hz, 1H), 3.5 (1 (dd, ./ = 13.5,7.8 Hz. 111), 1.98-1.72 (m, 3H) , 1.61-1.43 (ni. UI) 77 ^F 'y ^ N' ^ Y ' ^GH5 H ₂ nA | A ₀ CH ₃ wbirc solid 140-142.8 (DMSO-dr,) 8.57 (d, 7 = 6 8 Hz, 1H),ESLV1S rtt / z 8.15 (s, 111), 7.98186 (s, 110. 4.06 (d. 7 =(ΊΜ + 1ΙΓ) 7.4 Hz. 211), 2.72-2.54 (m, 110, 1.47 (d. 7 = 6 6 Hz, 611) 78 h ₂ no ofi-white solid 207.3-208.2 (CI.X ‘0) 7.56 (d, 7= 5.3 Hz.] H), 3 99ESIMSzíi / z -3.91 (m, 211),202 3.68 - 3.62 fni,(ΊΜ + 1ΙΓ) 211), 3.48 (q, J =7.0 Hz, 20). 1.17(1.7 = 7.0 Hz, 310
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Cmpd Structurc Appea rance mp f '€) Ίινμκ ¹ * (δ, solvent) 79 h ₂ iAiAo ofí-white MoJicl 128 5-130.6 ESTMS m / i (jCD OD) 7.52 (d, J 190 = 5.8 11 /, 111), 4.59 µM + H [*). (s, 2H). 2.21 <s, I8H IMH-H1) 3H) Kl o ^F Y ^ '''% Ç7 solid ofl-whitc 228-230 (CD, OD) 8.22 (s, 111), 7.54-7.25 (m,ESTMS m / z 511), 5.26 (s, 211),318 3.71 (d, 7 = 6.4 Hz,(ΙΜ + ΤΙΓ), 211), 1.30 (s, III),0.68-0.53 (ni, 211). 0.50-0.33 (m. 21Γ) 82 αιχχ> dog ò ofT-whiteSCllld 159-161 (CD.OD) 8.72 (d, J = 4.9 11 /, 111), ¹¹ 7.52-7.41 (ni, 4EI), rctvtc / - 7.36-7.31 (ni, 2H), 7.28-7.23 (ηι, 4H), ( ΙΜ + Η1 ⁺ 1 W (d, ./ = 7.3 Hz. (| M ₊ HJ) _2IT ), 1.41-1.33 (m, 111), 0.71-0.63 (m, 2H), 0.53-0.45 (m, 211) 83 ο ^ρ Ύ ^ ν '' V ⁵³ n ³ H gnm(CIWD) 8 62 (d, J = 1.6 Hz, III), 8.51 (dd. J = 4.9.1.3 IIz, 111), 8-29 (d. / ESIMS πι / z = 5.3 11 /, 111), 7.90 293 (d, J = 7.8 Hz, 1H), (| M + 1I] ⁺ ) 7.45 (dd, 7 = 8.0, 4 9 Hz, 1H), 5-06 (s, 211), 4.25 (q / = 7.1 Ilz, 211), 1.32 (1,. / = 7.1 IIz, 311) 84 o ^f -> ^ n '^'s' ^CH3 HC ^ lA (A hAo ^J H ofl-whiic solicl 137.1-138.8 (Accept-dg) 8.18 (s, 111), 8.00 (d. ./= ¹ 7.2 Πζ. 1H), 4.64 ESIMS m / z (d, J = 6.3 IIz, 211). 260ÍIM-1ID 4.37 (q, 7 = 7.1 Hz, 2H), 2.23 (d, 7 = 4.4 Hz, 311), 1.35 (1, 7 = 7.1 Hz, 3H) H6 ^ Y ^CI O ^F V ^ N ^ 5 ' ^CH = HH velluw snlid 181.8-183.5 (('[). <} □) 8.28 (d, 7= 5.9 11 /, lm. 8.22(dd, 7 = 8.3.1-4ESIMS n-Jz Hz, 111), 7.47 (tid,343 ./= 8.0, 1.4 IIz,([Μ + 11Γ) 1H), 7.35-7.27 (m,IH), 7.17-7.09 (m,111), 4.98 (s, 211),2.23 (s, 3H)
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Htnpd StnjCÍUH! Appea rance mp CC) NMι NMir (6, solvent) «7 H H ofl-wliitcsolid 113.0-114.9 (DMSO) 9.87 (s, 1TT), 9.38 (s, III}, 04 (.0.7 = 5.911 /, 1H), 3.56 Cd, 7 = / 7.2 Hz, 2H), 3-21 ^FSI ^ '^W; (d, 7 = 5.8 Hz. 211), ÍIM + Hlh 15S-1-41 011, ([M + H]) 211), 1.40-1.09 (m, 5H), 0.88 0.7 = 6 8 Hz, 3H ), 0.56 -0.41 (m, 2H), 0.41-0.29 Or. 2111 8 « wxvII Ί ofi-whitesolid 205.6-207.5 (CD ₃ OD) 8.25 (d. 7 = 6.0 Hz, 111). 7.53 (d, 7 = 8.4 Hz, 211), .......... 7.16 Cd, J = 8.3 Hz, '211), 3.75 (d, 7 = 7.3 Hz, 210.2.32 ^{1 IJ} (s, 311). 1.37-1.26 (m, 111), 0.67-0.59 Cm. 211), 0.45 0j, J = 4.7 Hz, 211) 89 Ο ^Ρ 'γ ^ίΓ ' Ν '^ τ < ^{5! Ι} Ν off-whitc solid 146.0—147.6 (DMSO-e / e,) 9.96 (s, 111), 9.33 (1.7 =5.4 Hz. 111), 8.59 (d, J = 1.7 Hz, 111).8.51 <s, 111), 8.50 (s, III), 7 76 (d, 7 =ESIMS m / z. 8.0 Hz, 1H), 7.38334 (dd, 7 = 7.6,4.9(| M + II] “), Ilz, 111), 4.93 (s,1H). 3.20 (dd, 7 =12.7, 6.7 Hz, 211),1.55-1.38 Çni, 2H), 1.29 OJd, J = 8 7, 5.4 Hz, 411), 0.87(I, J = 6.7 Hz, 311) 90 Η H oil-whiicsolid 178.2-180 (CD3OD) 8.66 (d, 7 = 1.7 Hz, Hl). 8.52 (dd, 7 = 4.9, 1.6Hz, 111) .8.37 (d. 7 = 5.9 Hz, 111),ESIMS m / z 7.96-7.90 Çni, 1H), 354 (| Μ + Ι1Γ '7.51 (d, 7 = 8 511 /,211), 7.47 (dd, 7 = 8.2.5.2 Hz, 111),7.1.5 (d, 7 = 8 .311 /, 2H), 5.11 (s, 2H}.2.32 (s. 3H)
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Ctnpd Slmcturc Appca rance mp CO ΊΙ NMR (δ, solvent) 91 αχχχοΗ H ofi-whiicsolid 210.5-212.3 (DMSCi-ds) 12.29 (s, 1H). 10.59 (s, III), 8.64 (m, 211), 8.52 (d, J = 4.8 Hz. / 1H), 8 31 (dd, J = ESIMSiw '; _ ₄ 8.3, 1.2 Hz. 111), yixi + m ⁺ i 7-83-7.77 (ill, 1H), ([M + HJ) 7.52 (dd, / = 8.0, 1.2 Hz, 1H), 7,437.31 (m, 2H), 7.12 (ui, / = 7.9.1.5 Hz, 111), 4.98 (s, 2H) 92 —- 'aAnAAüΗ H off-whitc solid 100.2-101.8 (CDjOD) 8.43 (d, / = 74117, 111), 4 62 (s, 211), 3.37 (t, J = / 7.0 Hz, 211), 2.22 JiSlMSí »/:,, 301 (IVI-ΙΙΓ) ( ^s > 7-5.7 Hz, .ill), ^{11 H} 161 id ./= 14.1. 7.1 Hz. 211), 1.44-1.32 (m, 411), 0.94 (t, / = 7.0 Hz, 3H) 93 ^HaC V% O off-white solid 188.8-190.2 (C11 ₃ OD) 8.27 (d, / = 5.9 Hz, 111) .7 53 1'SMSw / i (d, 3 = 8.4 Hz. 211), 323 7.16 (d. 3 = 8.2 Hz. (| Μ + 1Ι | Ί 211), 5-00 (s, 211), 2.32 (s, 3H). 2.24 (s, 311) 95 A H AV, CNN ^ O ³ H pale yellow gum(CDCl ₃ ) 7.76 Cd, / = 5.5 Hz, IH), 4.30 (dd, 3 = 13.8.2.1 Hz, 111), 4.18 (dd. / = 14.8, 7.6 Hz, 1H), 3 87 id, / =. 15.2.6.9 11 /, 111). ^L SLV1S uí / z _{3 7S íd (J y = u 4} 7.6 Hz, 10.3-57 ^{11 1 J} (dd.J = 13.8.7.9 llz, 111) .2.65 (s, 311), 2.20-2.06 (m , 111), 2.01-1 85 (m, 211), 1.58 (ddd, .1 = 16.1, 12.5, 8.0 Hz, 1H)
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Ctnpd Structurc Appcarancc rnp m IIXMR ^J (5, solvent) 96 F 0 white solid 119.8-121.9 (DMSO-dn) 11.22 Is, 11T), 8.38 Is, III), 7.70 (s, III}, 7.63 (dd, J = 13.0, 6.4 Hz, IH), 7.33. (1 ../ = 7.6 Hz, 211 ), ESIMS 'P 4.11 (5,111), 3.96 (ΙΜ + ΙΙΓ) ( _S , III), 3.80 (dd, 7 ” ^{1, T} = 14.8.6.9 Hz, IH), 3.74-3.59 (m, 211), 2.02 -1.91 (ni, 111), 1.91-1.75 (m, 211), 1.63-1.51 (m, IH) 97 o ^F y ^ N ^x Y ^CH = vMA ^c ' ^! * H wbite solid 134.5-136.5 (í)) (1,) 7.72 (s, 111.). 7.43 (d.} = ESIMS íh / z 4.6 Hz, JH), 3.63 228 (d. 7 = 7.4 Ilz, 3H), t | M + H ] ⁺ ) 2.67 (s, 311), 2.29-2.212 (m, 1H), 0.98 (d, 7 = 6.7 Hz, 6Π) 98 f oA ^ jAAo while solid 161.3-163 (DMSO-7 _s ) 11.20 is, 111), 8.49 (s,, IH), 7.80-7.54 (ni, ^L X ' ^S / ^ 211), 7.33 (1.7 = (ΙΜ + ΠΓ) ^ Hz, 211), 3.62 ^{u 1} (d, 7 = 6.5 Hz, 2H), 2.08 (s, 111), 0.87 (d, 7 = 6.7 Hz, 6H) 99 ^ch = pale yellow solid 125.6-127.5 (COCh) 12.85 (s, 1H), 7.97 (dd. 7 = 3.8, 1.2Hz, JH), 7.61 (dd.7 = 4.9./ - 12 Hz, IH). 7.33ESIMS (d, 7 = 5.4 Hz, 111),([Μ + Π1 *) 7-W <U = 4.9,3.8 Hz, IH), 3.57 (d. 7 = 7.5 Hz, 211),2.19-2.04 (ni, IH), 0.99 (d, 7 = 6.7 JIz.6ΤΓ) 100 _o Fy- ^ OxzCH, </ Α ^Λ ° oli-while solid 109-110.4 ((39 (-10 8.00-7.93(m, LH), 7.60 (dd, 7 = 4.8, 0.8 Hz, 111) .7.56 (d, 7 =ESIMS μΛ 5.6 Hz, 111), 7.13312 (dd, 7 = 4.7.4.0(LM + TIJ ’), Hz, 11T), 3.98-3 901, 211), 3.70-3.63 (ni, 2H), 3.51 (q, 7 = 7,011 / .211). 1.19 (t, J = 7.0 Hz, 311)
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Cmpd Stmcturc Appeti rance mp (’C) ΊΙ NMK (δ, solvent) 101 off-whitc sclid 116.8-117.8 (CDCh) 8.20 (Ld, 2 = 78, 16 11 /, 1 II). 8.02 (1, 2 = 7.6 Hz, 1H), 7.69 (d, J = 55 Hz, 1H), 7 55 / (dd, 2 = 13.1,5.9 ESIMS Hz. 111) .7.32-7.24 _M ; (m, III), 7.18 (dd, ^{U 11} ./ = 11.7.8.3 Hz, LH), 4.05-3.97 (m, 211), 3.74-3.66 (m, 211). 3.5Ü (q, J = 7.0 Hz, 2H), 1.19 (t, J = 7.0 Hz, 311) 103 KC ^ N ^ N ^ O ³ H hrown gum(AccUiuc-t / j) 7.61 (d, 2 = 6-9 Hz. 1H), 7.05-6.84 (111, III). 4.15-4.06 (in, 1H), 3 97 (dd, 2 = 13 7, 3.2 Hz, 111), 3.83 (dd, J = 14.9.6.7 ESIMS i / i; Hz, 111), 3.68 (dd, 242 2 = 14.8.6.9 Hz, (| M + 1I1 ⁺ ) 1H), 3.51 (ddd, 2 = 20.0, 13.7.7.3 Hz, 311), 2.03-1.93 (m, 1H), 1.92-1.78 (m, 2H) , 1.60 (dd, J = 12.1, 8.1 Hz, 111), 1.20 (t, J = 7.2 Ilz, 3H) 104 F gnm(Acctoue-i / f,) 7.70 (d,. / = 6.7 Ilz, 111), 7.53-7.42 (m, 2 = 6.9 Hz. 2Hi, 7.377.27 (111, 111), 7.217Ό6 (m, 2111.4.75 (d, 2 = 5.7 Ilz, 211), cross, 4.11 (qd, / = 7.1, ^1Μ ^ ^Λ 3.2 Ilz. 1H), 3.99 _Π Μ ₊ 1ΙΓ) ^ -2 = 13.6. 3.2 ^{u 1} 'Hz, 111), 3.88-3.79 (m, 111), 3.69 (dd, .1 = 14.9.6.9 Hz. III), 3.55 (dd, .1 = 13.6.7.8 Hz, 1H), 2.03-1.93 (m, 1H), 1.92-1.8 () (ni, 2H), 1.67-1.53 (m, 111)
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Cmpd Structure Apputrance mp C'C) ΊΙ NMR “(6, solvent) 1ÍK> γΜ ^CH · ILO-whiresolid 88.8-91.7 (Cl) Cli) 7.30-7.25 (m. 211), 7.19 01.7 = 5.8 Hz, 111), 7.08 (d, 7 = 3.1 Hz, IH), ev 6 6 (dd, 7 = 5.1, 3.5 IIz. ll 1), 4.91 0Μ + Η1Ί (d./=4.9 llz, 2H), QM + HJ) 3.57 ₌ 7.5 jfc 2H), 2.17 (dl, 7 = 13-6.6-8 Hz. IH), 0.96 ( d, 7 = 6.7 llz, 611) 107 η / ΆΑ) ^{CH3 3} H brown gum(CDCLj} 7.14 (d, 7 = 5.9 llz. 1) 1),. 3.65-3.50 (m, 411), ^L SLVS ^ 2.16 (dl, 7 = 13.7, (ΙΜ + 1ΙΓ) 6.9 Hz, HO, 1.27 ^UH ((, 7 = 7.3112.311), 0.94 (d, 7 = 6.7 llz , 611) 108 htAA) ¹ H brown fiolid 63—65 (Acctonc-dr,) 7.61(d. 7 = 6.8 Hz, III), 6.99 (s, IH), 3.85JiSIMSíiiC (1.7 = 52 Hz, 211),230 3.62 ((, / = 5.2 Hz,MIC + Hf) 2) [), 3-54-3.42 (m,411). 1.20 (1.7 =7.2 Hz, 310, 1.12 (1.7 = 7.0 Hz, 3H) 109 F A.CK U ^H hrown gum(Acclone-ί / β) 7.69(d. 7 = 6.7 Hz, IH), 7.48 (1.7 = 7.0 Hz, 111), 7.37-7.27 (m,111) .7.20-7.05 (m,ESIMS i) i /; 2Π), 4.75 (d,.! =310 5.5 Hz, 2H), 3.88Í [M + Hf) (dd, 7 = 11.8,6.6Hz, 211), 3.61 (dd. 7 = 12.7, 7.7 Hz, 211), 3.54-3.41 (m,211), 118-1.05 (m, 3Π) 110gum(Acetont-ík) 7.68 (d. 7 = 6.7 llz, III), 7.57 (s, 1) 1), 7.32 (dd, 7 = 5.1, 1.2 Hz. 111). 7.12-7.04 liSIMS ^ 20R '.5.1.3.5 Hz, .... _lir , HI) .4.85 (d, / = ([M + HD 5.9HX, 211X3.88 (t, 7 = 5.2 Hz, 211), 3.63 0.7 = 5.2 Hz, 2H), 3.47 (q, J = 7.0 Hz, 2H), 1.12 (l, .1 = 7.0 Hz, 311)
Captions in the table above:
cmpd = compound; structure = structure; appearance = aspect; mp = mp .; solvent = solvent; white solid = white solid; yellow oil = yellow oil; off-white solid = off-white solid; white = white; pale yellow solid = pale yellow solid; beige solid = beige solid; brown solid = brown solid; pale brown solid = pale brown solid; white oil = white oil; gum = gum; pale yellow gum = pale yellow gum; brown gum = brown gum
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Example 26 Evaluation of Fungicidal Activity: wheat leaf rust (Mycosphaerella gramainicola; anamorph: Septoria tritici; Baver SEPTTR code) [00171] Wheat plants (variety Yuma) were grown from seeds in a greenhouse at 50% mineral soil / 50% Metro mix without soil until the first leaf has fully emerged, with 7-10 seedlings per pot. These plants were inoculated with an aqueous spore suspension of Septoria tritici either before or after fungicide treatments. After inoculation, the plants were kept in 100% relative humidity (one day in a humid dark chamber followed by two to three days in a clear moist chamber) to allow the spores to germinate and infect the leaf. The leaves were then transferred to a greenhouse for the disease to develop.
[00172] The following table shows the activity of typical compounds of the present invention 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, and then converting the severity into a percentage of control based on the level of disease of the inoculated and untreated plants.
[00173] In all cases in Table II, the rating scale is as follows:
% Disease Control Rating 76-100 Λ 51-75 B 26-50 Ç 0-25 D Not Tested AND
Captions in the table above:
% disease control =% disease control; rating = classification; not tested = not tested.
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Table II: Protective activity in one day (1DP) and curative activity in three days (3DC) of the compounds in SEPTTR at 100 ppm
((mpd SEPTTR100 PPM IDP SEPTTR100 PPM 3DC 1 Λ THE 2 Λ THE J THE THE 4 Ç 11 5 D 11 6 11 11 7 D D s (' D 9 (' 11 10 Ç R 11 (’ I) 12 THE THE
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Cmpd SEPTTtt100 1’1’MIDF SEPTTIt100PPM3DC 13 Λ THE 14 D IJ 15 D D 16 D 1.1 17 B THE 18 (’ B 19 Ç D 2" D 1.1 21 THE THE 22 THE THE 23 THE THE 24 Λ THE 25 D D 26 D Ç 27 D 1.1 28 B THE 29 B THE 30 D THE 31 D THE 32 THE THE 33 D B 34 THE THE 35 R R 36 B Ç 37 D D 38 D 11 39 D THE 40 D 1.1 41 THE THE 42 AND AND 43 (’ 1.1 44 AND AND 45 AND H 46 D D 47 (’ 1.1 48 AND AND 49 AND AND 50 AND AND 51 AND AND 52 AND AND 53 AND AND 54 AND AND 55 AND AND 56 (’ B 57 D 11 58 THE THE 59 AND AND 60 AND AND
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Cmpd SEPTTR100PPMIDP SEPTTR100PPM jix: 61 AND AND 62 AND AND 63 AND AND 64 AND AND 65 D D 66 D D 67 D B 68 AND AND 69 AND AND 70 AND AND 71 AND AND 72 AND AND 73 AND AND 74 Λ R 75 (’ THE 76 D B 77 Ç D 78 AND AND 79 AND AND 80 D B 81 (' THE 82 Ç Ç «3 Ç ç 84 AND AND 85 D D 86 Ç Ç 87 D B 88 D B 89 D Ç 90 D D 91 D 1.) 92 THE THE 93 D R 94 ü D 95 D B 96 D Ç 97 (' Ç 98 D D 99 13 THE 100 AND AND 101 AND AND 102 AND AND 103 AND AND 104 AND AND 105 D Ç 106 Ç Ç 107 D ç 108 AND AND
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Cmpd SEPTTR 101) PPMIDE SEPTTR 101) PPM 3I> CAND AND 110 AND AND
Captions in the table above: cmpd = compound.
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权利要求:
Claims (14)
[1]
1. Compound, characterized by the fact that it presents the Formula (I): VA 1 R ²
Formula (I) in which
R ¹ is:
H;
Ci-Ce alkyl, optionally substituted with 1-3 R ⁴ ;
benzyl, with benzyl being optionally substituted with 1-3 R ⁵ , piperazine or morpholine, with piperazine being optionally substituted with 1-3 R ⁵ ;
- (CHR ⁶ ) _m OR ⁷ ;
-C (= O) R ⁸ ;
-S (O) ₂ R ⁸ ;
-C (= O) OR ⁸ ; or
-C (= O) N (R ⁹ ) R ¹⁰ ;
where m is an integer 1-4;
R ² is:
H; or
Ci-Ce alkyl;
alternatively, R ¹ and R ² can be taken together to form = CR ¹¹ N (R ¹² ) R ¹³ ;
R ³ is:
Ci-Ce alkyl, optionally substituted with 1-3 R ⁴ , Ci-Ce haloalkyl, C2-C6 alkenyl, optionally substituted with R ¹⁴ , phenyl or benzyl, each of which between phenyl and benzyl can be
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[2]
2/5 optionally substituted with 1-3 R ⁵ , piperazine, morpholine, cyclohexene, thiophene or benzodioxol, piperazine being optionally substituted with 1-3 R ⁵ , naphthyl;
- (CHR ⁶ ) mOR ⁷ ; or
- (CHR ⁶ ) m N (R ⁹ ) R ¹⁰ ;
R ⁴ is independently halogen, C1-C6 alkyl, C1-C4 haloalkyl, C1-C4 alkylthio, phenyl optionally substituted with 1-3 R ⁵ , thiophene, triazole, tetrahydrofuran or pyridine;
R ⁵ is independently halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkylsulfonyl or cyano;
R ⁶ is H, C1-C6 alkyl or C1-C6 alkoxycarbonyl;
R ⁷ is C1-C8 alkyl, C1-C6 alkoxyalkyl, C2-C6 trialkylsilyl, C2C6 alkylcarbonyl, phenyl or benzyl, each of which between phenyl and benzyl can be optionally substituted with 1-3 R ⁵ ;
R ⁸ is C1-C6 alkyl, phenyl or benzyl, each of phenyl and benzyl being optionally substituted with 1-3 R ⁵ , or thiophene;
R ⁹ is H, C1-C6 alkyl or phenyl, with phenyl optionally being substituted with 1-3 R ⁵ ;
R ¹⁰ is H or C1-C6 alkyl;
R ¹¹ is H;
R ¹² is C1-C4 alkyl,
R ¹³ is C1-C4 alkyl; and
R ¹⁴ is phenyl or benzyl, each of phenyl and benzyl being optionally substituted with 1-3 R ⁵ ;
with the proviso that said compound does not represent a compound, in which R ¹ , R ² and R ³ are each CH3; R ¹ and R ² are both H, and R ³ is -CH = CH2, -CH2CH = CHCH2CH3, -CH2CH = C (CH3) 2, -CH3, (CH2) 2CO2Et, - (CH2) 2CO2Me, -CH2CO2Et, hydrochloride -CH2CONEt2, 2 (chloromethyl) benzyl or -CH (O ⁱ Pr) (CH2OC (O) (CH2) 2CH3); or R ¹ is H, and R ²
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[3]
3/5 and R ³ are both -CH3.
2. Compound, according to claim 1, characterized by the fact that it is selected from the group consisting of:
J e
3. Composition for the control of a fungal pathogen, characterized by the fact that it comprises a compound, such as
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[4]
4/5 defined in claim 1 or 2, and a phytologically acceptable carrier material, selected from the group consisting of: profillite, talc, chalk, plaster, Fuller earth, bentonite, attapulgite, starch, casein, gluten, montmorillonite clays, diatomaceous earth, purified silicates, aromatic organic solvents, terpenic solvents, aliphatic ketones, complex alcohols, polyalkylene glycol ethers, alkyl and aryl phenol condensation products, aliphatic alcohols, aliphatic amines or fatty acids with ethylene oxide, propylene oxides, propylene oxides carboxylics solubilized with polyol or polyoxyalkylene, quaternary ammonium compounds, fatty amine salts, oil-soluble salts of alkylaryl sulfonic acids, oil-soluble salts or sulphated polyglycol ethers, phosphate polyglycolic ether salts, aromatic organic liquids, substituted aromatic organic liquids , bentonite, diatomite, clay, kaolin clay o, ground volcanic rock, ethoxylated nonyl phenols, ethoxylated synthetic or natural alcohols, salts of sulfosuccinic esters or acids, ethoxylated organosilicones, ethoxylated grease amine, and mixtures of surfactants with mineral or vegetable oils.
4. Composition according to claim 3, characterized by the fact that the fungal pathogen is apple scab (Venturia inaequalis), wheat leaf rust (Septoria tritici), beet leaf rust (Cercospora beticola ), peanut leaf rust (Cercospora arachidicola and Cercosporidium personatum), or banana black sigatoka (Mycosphaerella fijiensis).
[5]
5. Composition according to claim 3 or 4, characterized by the fact that the fungal pathogen is wheat leaf rust (Septoria tritici).
[6]
6. Method for controlling or preventing fungal attack on a plant, characterized by the fact that it comprises the steps of:
apply a fungicidally effective amount of the compound
Petition 870180136224, of 10/01/2018, p. 7/12
5/5 of Formula (I), as defined in claim 1 or 2, to at least one plant, to an area adjacent to the plant, to the soil adapted to support the plant's development, to a plant root, to the plant's foliage , and a seed adapted to produce the plant.
[7]
7. Method according to claim 6, characterized in that the concentration of the compound of Formula (I) is from 0.1 to 1000 ppm.
[8]
8. Method according to claim 6 or 7, characterized in that the concentration of the compound of Formula (I) is from 1 to 500 ppm.
[9]
Method according to any one of claims 6 to 8, characterized in that the compound of Formula (I) is applied at a concentration of 0.01 to 0.45 g per square meter.
[10]
Method according to any one of claims 6 to 9, characterized in that it further comprises applying an adjuvant surfactant.
[11]
11. Method according to claim 10, characterized by the fact that the adjuvant surfactant is selected from nonyl ethoxylated phenols, synthetic or natural ethoxylated alcohols, salts of sulfosuccinic esters or acids, ethoxylated organosilicones, ethoxylated fatty amines and mixtures of surfactants with ethoxylates mineral or vegetable oils.
[12]
12. Use of a compound of Formula (I), as defined in claim 1 or 2, characterized by the fact that it is for controlling or preventing fungal attack on a plant.
[13]
13. Compound of Formula (I) according to claim 1 or 2, characterized by the fact that it is for use as a fungicide.
[14]
14. Use of a compound of Formula (I), as defined in claim 1 or 2, characterized by the fact that it is for the preparation of a composition for the control or prevention of a fungal pathogen in a plant.

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法律状态:
2016-05-31| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|

---

2016-11-08| B07D| Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]|

---

2017-08-08| B07G| Grant request does not fulfill article 229-c lpi (prior consent of anvisa) [chapter 7.7 patent gazette]|

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2017-08-15| B25A| Requested transfer of rights approved|Owner name: ADAMA MAKHTESHIM LTD. (IL) |

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2017-10-17| B07A| Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]|

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2018-03-20| B06G| Technical and formal requirements: other requirements [chapter 6.7 patent gazette]|

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2018-05-15| B07A| Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]|

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2018-09-25| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|

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

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2019-04-09| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|

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2019-05-28| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|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 |

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2021-06-08| B21F| Lapse acc. art. 78, item iv - on non-payment of the annual fees in time|Free format text: REFERENTE A 11A ANUIDADE. |

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2021-09-28| B24J| Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12)|Free format text: EM VIRTUDE DA EXTINCAO PUBLICADA NA RPI 2631 DE 08-06-2021 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDA A EXTINCAO DA PATENTE E SEUS CERTIFICADOS, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |

优先权:

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申请号 | 申请日 | 专利标题

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US23217709P| true| 2009-08-07|2009-08-07|

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US61/232,177|2009-08-07|

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PCT/US2010/044579|WO2011017540A1|2009-08-07|2010-08-05|5-fluoropyrimidinone derivatives|

---