1-carbamoyl-2-pyrazolines, composition containing them, and insecticidal and acaricidal method of using them

The present invention relates to 1-carbamoyl-3-phenyl-4-benzyl-.DELTA..sup.2 -pyrazolines, to the preparation thereof and to the use thereof in pest control.
The compounds of this invention are of formula I ##STR2## wherein R.sub.1 and R.sub.2 are each independently hydrogen, methyl halogen, trifluoromethyl, C.sub.1 -C.sub.4 haloalkoxy containing 1 to 7 halogen atoms or C.sub.1 -C.sub.4 haloalkylthio containing 1 to 7 halogen atoms;
R.sub.3 is hydrogen, halogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl containing 1 to 7 halogen atoms, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy containing 1 to 7 halogen atoms or alkoxycarbonyl containing 1 to 4 carbon atoms in the alkyl moiety;
R.sub.4 is hydrogen, halogen, C.sub.1 -C.sub.4 alkyl or trifluoromethyl;
R.sub.5 is hydrogen, halogen, C.sub.1 -C.sub.4 alkyl, trifluoromethyl or C.sub.1 -C.sub.4 alkoxy; and
R.sub.6 and R.sub.7 are each independently hydrogen, halogen or trifluoromethyl or R.sub.6 and R.sub.5 or R.sub.7 and R.sub.5 are methylenedioxy.
To be singled out for particular mention are those compounds of formula I, wherein R.sub.2, R.sub.4, R.sub.6 and R.sub.7 are hydrogen.
Preferred compounds of formula I are those wherein R.sub.1 is hydrogen, fluorine, chlorine or C.sub.1 -C.sub.3 haloalkoxy containing 1 to 7 fluorine or chlorine atoms;
R.sub.2 is hydrogen;
R.sub.3 is hydrogen, fluorine, chlorine, C.sub.1 -C.sub.3 alkoxy, C.sub.1 -C.sub.3 haloalkoxy containing 1 to 7 fluorine, chlorine or bromine atoms or isopropoxycarbonyl;
R.sub.4 is hydrogen, methyl or ethyl;
R.sub.5 is hydrogen, fluorine, chlorine, bromine, C.sub.1 -C.sub.3 alkyl, trifluoromethyl or C.sub.1 -C.sub.3 alkoxy;
R.sub.6 is hydrogen, fluorine in the 2- or 3-position or chlorine in the 2- or 3-position or R.sub.6 and R.sub.5 are a 3,4-methylenedioxy group; and
R.sub.7 is hydrogen or 6-chlorine.
Further preferred compounds of formula I are those wherein
R.sub.1 is hydrogen, fluorine, chlorine or methyl;
R.sub.2 is hydrogen;
R.sub.3 is fluorine, chlorine or trifluoromethoxy, difluorobromomethoxy or isopropoxycarbonyl;
R.sub.4 is hydrogen or 3-methyl;
R.sub.5 is hydrogen, fluorine, chlorine, bromine or methyl;
R.sub.6 is hydrogen or 3-chlorine; and
R.sub.7 is hydrogen;
as well as those of formula I, wherein
R.sub.1 is hydrogen, fluorine or chlorine;
R.sub.2, R.sub.4, R.sub.6 and R.sub.7 are hydrogen;
R.sub.3 is chlorine or trifluoromethoxy; and
R.sub.5 is fluorine or chlorine.
Depending on the number of carbon atoms indicated, within the scope of the present invention alkyl by itself or as moiety of another substituent will be understood as meaning straight chain or branched alkyl radicals, for example the following groups: methyl, ethyl, propyl, butyl, and the isomers thereof, e.g. isopropyl, isobutyl, tert-butyl, sec-butyl.
Haloalkyl within the scope of the present invention will be understood as meaning alkyl radicals such as methyl, ethyl, n-propyl, isopropyl and butyl etc., which are substituted by 1 to 7 different or identical halogen atoms. Said alkyl radicals may be perhalogenated alkyl radicals or alkyl radicals in which the hydrogen atoms are only partially substituted by halogen.
Halogen within the scope of the present invention will be understood as meaning fluorine, chlorine and bromine, with fluorine and chlorine being preferred.
The compounds of formula I can be prepared by processes analogous to known ones (q.v. e.g. German Offenlegungsschrift specifications Nos. 2 529 689 and 2 700 258 and European patent application No. 0 004 733).
Thus, for example, a compound of formula I can be obtained by reacting a compound of formula II ##STR3## with a compound of formula III ##STR4## in which formulae II and III the radicals R.sub.1 to R.sub.7 are as defined above for formula I.
The above process can preferably be carried out under normal pressure and in the presence of an organic solvent or diluent which is inert to the reactants. Suitable solvents or diluents are e.g. ethers and ethereal compounds such as diethyl ether, dipropyl ether, dibutyl ether, dioxane, dimethoxyethane and tetrahydrofuran; N,N-dialkylated carboxamides; aliphatic, aromatic and halogenated hydrocarbons, especially benzene, toluene, xylene, chloroform, methylene chloride, carbon tetrachloride and chlorobenzen; nitriles such as acetonitrile or propionitrile; dimethyl sulfoxide; and ketones such as acetone, methyl ethyl ketone, methyl ispropyl ketone and methyl isobutyl ketone. In general, the process can be carried out readily in the temperature range from -10.degree. to 100.degree. C., preferably from 10.degree. to 30.degree. C., e.g. at room temperature, optionally in the presence of a suitable aprotic, organic base, e.g. triethylamine, N-methylmorpholine or pyridine.
The starting materials of formulae II and III are known and can be prepared by processes analogous to known ones. The 3-phenyl-4-benzyl-.DELTA..sup.2 -pyrazolines of formula II can be obtained e.g. by reacting a corresponding .beta.-phenylpropiophenone of formula IV ##STR5## with formaldehyde, at elevated temperature and in the presence of a catalyst, and cyclising the resultant 1-phenyl-2-benzyl-prop-2-en-1-one of formula V ##STR6## by condensation with hydrazine (q.v. the above references to the literature).
The propiophenone of formula IV is obtainable by hydrogenating a corresponding benzylideneacetophenone of formula VI ##STR7## by a conventional method. In the above formulae IV to VI R.sub.1, R.sub.2, R.sub.5, R.sub.6 and R.sub.7 are as defined for formula I.
Substituted 1-carbamoyl-3-phenyl-.DELTA..sup.2 -pyrazolines having insecticidal properties are known from German Offenlegungsschrift specifications Nos. 2 529 689 and 2 700 258 and European patent application No. 0 004 733. Compared with these known compounds, the compounds of formula I of the present invention differ structurally in particular by the presence of a benzyl group in place of a phenyl radical in the 4-position of the .DELTA..sup.2 -pyrazoline ring.
Surprisingly, it has been found that the compounds of formula I of the present invention have excellent properties as pesticides while being well tolerated by plants and having low toxicity to warm-blooded animals. They are particularly suitable for controlling insects and representatives of the order Acarina that attack plants and animals.
In particular, the compounds of formula I are suitable for controlling insects of the orders: Lepidoptera, Coleoptera, Homoptera, Heteroptera, Diptera, Thysanoptera, Orthoptera, Anoplura, Siphonaptera, Mallophaga, Thysanura, Isoptera, Psocoptera and Hymenoptera, as well as representatives of the order Acarina of the families: Ixodidae, Argasidae, Tetranychidae and Dermanyssidae.
In addition to their action against flies, e.g. Musca domestica, and mosquito larvae, the compounds of formula I can also be used for controlling plant-destructive feeding insects in ornamentals and crops of useful plants, especially in cotton (e.g. against Spodoptera littoralis and Heliothis virescens) and in crops of fruit and vegetables (e.g. Laspeyresia pomonella, Leptinotarsa decemlineata and Epilachna varivestis). The compounds of formula I have a pronounced larvicidal action against insects, in particular against larvae and nymphs of noxious feeding insects. If compounds of formula I are ingested by adult insect stages with the feed, then a diminished oviposition and/or reduced hatching rate is observed in many insects, in particular in Coleoptera, e.g. Anthonomus grandis. The compounds of this invention are also suitable for controlling soil insects (e.g. Aulacophora femoralis, Chortophila brassicae, Diabrotica balteata, Pachnoda savigni and Scotia ypsilon). The compounds of formula I can also be used with great success against plant-destructive cicadas, especially in crops of rice, and have both systemic and contact action.
The compounds of formula I can also be used for controlling ectoparasites such as Lucilia sericata, in domestic animals and producive livestock, e.g. by treating animals, cowsheds, barns, stables etc., and pastures.
The good pesticidal activity of the compounds of formula I of the invention corresponds to a mortality of at least 50-60% of the above pests.
The activity of the compounds of formula I and of the compositions containing them can be substantially broadened and adapted to prevailing circumstances by addition of other insecticides and/or acaricides. Examples of suitable additives include: organophosphorus compounds, nitrophenols and derivatives thereof, formamidines, ureas, carbamates, pyrethroids, chlorinated hydrocarbons, and Bacillus thuringiensis preparations.
By the addition of compounds of formula I, the insecticidal activity of the known insecticide dimethyl-(Z)-1-methyl-2-methylcarbamoyl vinyl phosphate can be increased or activated.
The compounds of formula I are used in unmodified form, or preferably together with the adjuvants conventionally employed in the art of formulation, and are therefore formulated in known manner to emulsifiable concentrates, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granulates, and also encapsulations in e.g. polymer substances. As with the nature of the compositions, the methods of application such as spraying, atomising, dusting, scattering or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances.
The formulations, i.e. the compositions, preparations or mixtures containing the compound (active ingredient) of formula I or combinations thereof with other insecticides or acaricides, and, where appropriate, a solid or liquid adjuvant, are prepared in known manner, e.g. by homogeneously mxing and/or grinding the active ingredients with extenders, e.g. solvents, solid carriers and, in some cases, surface-active compounds (surfactants).
Suitable solvents are: aromatic hydrocarbons, preferably the fractions containing 8 to 12 carbon atoms, e.g. xylene mixtures or substituted naphthalenes, phthalates such as dibutyl phthalate or dioctyl phthalate, aliphatic hydrocarbons such as cyclohexane or paraffins, alcohols and glycols and their ethers and esters, such as ethanol, ethylene glycol, ethylene glycol monomethyl or monoethyl ether, ketones such as cyclohexanone, strongly polar solvents such as N-methyl-2-pyrrolidone, dimethyl sulfoxide or dimethylformamide, as well as vegetable oils or epoxidised vegetable oils such as epoxidised coconut oil or soybean oil; or water.
The solid carriers used e.g. for dusts and dispersible powders are normally natural mineral fillers such as calcite, talcum, kaolin, montmorillonite or attapulgite. In order to improve the physical properties it is also possible to add highly dispersed silicic acid or highly dispersed absorbent polymers. Suitable granulated adsorptive carriers are porous types, for example pumice, broken brick, sepiolite or bentonite; and suitable nonsorbent carriers are materials such as calcite or sand. In addition, a great number of pregranulated materials of inorganic or organic nature can be used, e.g. especially dolomite or pulverised plant residues.
Depending on the nature of the compound of formula I to be formulated, or of combinations thereof with other insecticides or acaricides, suitable surface-active compounds are nonionic, cationic and/or anionic surfacants having good emulsifying, dispersing and wetting properties. The term "surfactants" will also be understood as comprising mixtures of surfactants.
Suitable anionic surfactants can be both water-soluble soaps and water-soluble synthetic surface-active compounds.
Suitable soaps are the alkali metal salts, alkaline earth metal salts or unsubstituted or substituted ammonium salts of higher fatty acids (C.sub.10 -C.sub.22), e.g. the sodium or potassium salts of oleic or stearic acid, or of natural fatty acid mixtures which can be obtained, e.g. from coconut oil or tallow oil. Further suitable surfactants are also the fatty acid methyltaurin salts as well as modified and unmodified phospholipids.
More frequently, however, so-called synthetic surfactants are used, especially fatty sulfonates, fatty sulfates, sulfonated benzimidazole derivatives or alkylarylsulfonates.
The fatty sulfonates or sulfates are usually in the form of alkali metal salts, alkaline earth metal salts or unsubstituted or substituted ammonium salts and contain a C.sub.8 -C.sub.22 alkyl radical which also includes the alkyl moiety of acyl radicals, e.g. the sodium or calcium salt of lignosulfonic acid, of dodecylsulfate, or of a mixture of fatty alcohol sulfates obtained from natural fatty acids. These compounds also comprise the salts of sulfuric acid esters and sulfonic acids of fatty alcohol/ethylene oxide adducts. The sulfonated benzimidazole derivatives preferably contain 2 sulfonic acid groups and one fatty acid radical containing about 8 to 22 carbon atoms. Examples of alkylarylsulfonates are the sodium, calcium or triethanolamine salts of dodecylbenzenesulfonic acid, dibutylnaphthalenesulfonic acid, or of a naphthalenesulfonic acid/formaldehyde condensation product. Also suitable are corresponding phosphates, e.g. salts of the phosphoric acid ester of an adduct of p-nonylphenol with 4 to 14 moles of ethylene oxide.
Non-ionic surfactants are preferably polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, or saturated or unsaturated fatty acids and alkylphenols, said derivatives containing 3 to 30 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon moiety and 6 to 18 carbon atoms in the alkyl moiety of the alkylphenols.
Further suitable non-ionic surfactants are the water-soluble adducts of polyethylene oxide with polypropylene glycol, ethylenediaminopolypropylene glycol and alkylpolypropylene glycol containing 1 to 10 carbon atoms in the alkyl chain, which adducts contain 20 to 250 ethylene glycol ether groups and 10 to 100 propylene glycol ether groups. These compounds usually contain 1 to 5 ethylene glycol units per propylene glycol unit.
Representative examples of non-ionic surfactants are nonylphenolpolyethoxyethanols, castor oil polyglycol ethers, polypropylene/polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethylene glycol and octylphenoxypolyethoxyethanol. Fatty acid esters of polyoxyethylene sorbitan, e.g., polyoxyethylene sorbitan trioleate, are also suitable non-ionic surfactants.
Cationic sufactants are preferably quaternary ammonium salts which contain, as N-substituent, at least one C.sub.8 -C.sub.22 alkyl radical and, as further substituents, unsubstituted or halogenated lower alkyl, benzyl or hydroxy-lower alkyl radicals. The salts are preferably in the form of halides, methylsulfates, or ethylsulfates, e.g. stearyltrimethylammonium chloride or benzyldi(2-chloroethyl)ethylammonium bromide.
The surfactants customarily employed in the art of formulation are described e.g. in "McCutcheon's Detergents and Emulsifiers Annual", MC Publishing Corp. Ridgewood, N.J., 1979; Dr. Helmut Stache, "Tensid Taschenbuch" (Handbook of Surfactants), Carl Hanser Verlag, Munich/Vienna, 1981.
The pesticidal compositions of this invention usually contain 0.1 to 99%, preferably 0.1 to 95%, of a compound of formula I or combination thereof with other insecticides, or acaricides, 1 to 99.9% of a solid or liquid adjuvant, and 0 to 25%, preferably 0.1 to 20%, of a surfactant.
Whereas commercial products are preferably formulated as concentrates, the end user will normally employ dilute formulations of substantially lower concentration.
The compositions may also contain further ingredients, such as stabilisers, antifoams, viscosity regulators, binders, tackifiers as well as fertilisers or other active ingredients in order to obtain special effects.

EXAMPLE 1
(a) Preparation of 4,4'-difluoro-.beta.-phenylpropiophenone
A solution of 59.9 g of 4,4'-difluorobenzylideneacetophenone in 600 ml of tetrahydrofuran is hydrogenated in the presence of 6 g of Raney nickel. After removal of the catalyst, the reaction mixture is concentrated by rotary evaporation, affording the title compound of the formula ##STR8## as a crude product with a refractive index of n.sub.20.sup.D =1.5478.
(b) Preparation of 3-(4-fluorophenyl)-4-(4-fluorobenzyl)-.DELTA..sup.2 -pyrazoline
59.4 g of 4,4'-difluoro-.beta.-phenylpropiophenone, prepared in accordance with step (a), together with 39.2 g of dimethylamine hydrochloride and 14.4 g of paraformaldehyde are heated overnight under reflux. The reaction mixture is then concentrated by evaporation and the residue is taken up in 300 ml of water and is extracted with three 200 ml portions of ether. The combined ether extracts are washed twice with water and then twice with a saturated solution of NaCl, dried over Na.sub.2 SO.sub.4 and filtered. The filtrate is concentrated, affording 1-(4-fluorophenyl)-2-(4-fluorobenzyl)-prop-2-en-1-one of the formula ##STR9## as a crude product which is immediately reacted further. The crude product is dissolved in 140 ml of ethanol and a solution of 18.8 g of hydrazine hydrate in 70 ml of methanol is added dropwise to this ethanolic solution. When the addition is complete, the reaction mixture is heated under reflux for three hours, cooled and then concentrated by rotary evaporation. The resultant residue is taken up in ether and the ethereal solution is washed twice with water and then twice with a saturated solution of NaCl, dried over Na.sub.2 SO.sub.4 and filtered. The filtrate is concentrated by evaporation, thus affording the title compound of the formula ##STR10##
(c) Preparation of 1-(4-trifluoromethoxyphenylcarbamoyl)-3-(4-fluorophenyl)-4-(fluorobenzyl)-.DELTA..sup.2 -pyrazoline
A reaction vessel is charged with a solution of 20 g of 3-(4-fluorophenyl)-4-(4-fluorobenzyl)-.DELTA..sup.2 -pyrazoline, prepared in accordance with step (b), in 50 ml of ether. With ice cooling, 14.9 of 4-trifluoromethoxyphenylisocyanate are added dropwise to this solution. After one hour at room temperature, the precipitated product is isolated by filtration, washed with ether and dried. The resultant title compound of the formula ##STR11## ps has a melting point of 98.degree.-100.degree. C. (compound 1).
The following compounds of formula I are prepared by procedures analogous to those described above.
__________________________________________________________________________Com- Physicalpound R.sub.1 R.sub.2 R.sub.3 R.sub.4 R.sub.5 R.sub.6 R.sub.7 data__________________________________________________________________________2 H H H H 3,4--O--CH.sub.2 --O-- H m.p. 107-109.degree. C.3 H H H 3-CH.sub.3 3,4--O--CH.sub.2 --O-- H m.p. 121-123.degree. C.4 H H --CO--O--CH(CH.sub.3).sub.2 H 3,4--O--CH.sub.2 --O-- H viscous mass5 H H H H Cl H H m.p. 142-144.degree. C.6 H H H 3-CH.sub.3 Cl H H m.p. 134-135.degree. C.7 H H --O--CF.sub.3 H Cl H H m.p. 114-116.degree. C.8 H H --O--CBrF.sub.2 H Cl H H m.p. 109-111.degree. C.9 H H H H Br H H m.p. 150-152.degree. C.10 H H H 3-CH.sub.3 Br H H m.p. 132-135.degree. C.11 H H --O--CF.sub.3 H Br H H m.p. 128-129.degree. C.12 H H H H F H H m.p. 128-130.degree. C.13 H H --CO--O--CH(CH.sub.3).sub.2 H Cl H H m.p. 68-70.degree. C.14 H H H 3-CH.sub.3 F H H m.p. 129-131.degree. C.15 H H --O--CF.sub.3 H F H H m.p. 107-108.degree. C.16 H H H H --CH.sub.3 H H m.p. 128-130.degree. C.17 H H --CO--O--CH(CH.sub.3).sub.2 H --CH.sub.3 H H m.p. 67-69.degree. C.18 H H H 3-CH.sub.3 --CH.sub.3 H H m.p. 126-128.degree. C.19 H H --O--CF.sub.3 H --CH.sub.3 H H m.p. 134-136.degree. C.20 H H H H Cl 3-Cl H m.p. 129-131.degree. C.21 H H H 3-CH.sub.3 Cl 3-Cl H m.p. 134-136.degree. C.22 H H --O--CF.sub.3 H Cl 3-Cl H m.p. 118-120.degree. C.23 H H H H H 6-Cl 2-Cl m.p. 188-190.degree. C.24 H H H 3-CH.sub.3 H 6-Cl 2-Cl m.p. 178-180.degree. C.25 H H --O--CF.sub.3 H H 6-Cl 2-Cl m.p. 180-182.degree. C.26 Cl H H H Cl H H m.p. 133-135.degree. C.27 F H H H F H H m.p. 124-126.degree. C.28 F H H 3-CH.sub.3 F H H m.p. 96-98.degree. C.29 --CH.sub.3 H H H --CH.sub.3 H H m.p. 151-153.degree. C.30 --CH.sub.3 H H 3-CH.sub.3 --CH.sub.3 H H m.p. 130-132.degree. C.31 --CH.sub.3 H --O--CF.sub.3 H --CH.sub.3 H H m.p. 108-109.degree. C.32 --CH.sub.3 H H H Cl 3-Cl H m.p. 160-162.degree. C.33 --CH.sub.3 H H 3-CH.sub.3 Cl 3-Cl H viscous mass34 --CH.sub.3 H --O--CF.sub.3 H Cl 3-Cl H m.p. 143-145.degree. C.35 Cl H H H H H H m.p. 70-72.degree. C.36 Cl H H 3-CH.sub.3 H H H m.p. 104-106.degree. C.37 Cl H --O--CF.sub.3 H H H H m.p. 133-135.degree. C.38 Cl H H H F H H m.p. 126-128.degree. C.39 Cl H H 3-CH.sub.3 F H H m.p. 130-132.degree. C.40 Cl H --O--CF.sub.3 H F H H m.p. 141-142.degree. C.41 Cl H F H F H H m.p. 149-152.degree. C.42 Cl H H H H 2-Cl 6-Cl m.p. 144-146.degree. C.43 Cl H H 3-CH.sub.3 H 2-Cl 6-Cl m.p. 174-176.degree. C.44 Cl H --O--CF.sub.3 H H 2-Cl 6-Cl m.p. 192-193.degree. C.45 H 2-Cl H H Cl H H viscous mass46 H 2-Cl H 3-CH.sub.3 Cl H H m.p. 182-184.degree. C.47 H 2-Cl --O--CF.sub.3 H Cl H H viscous mass48 H 2-Cl F H Cl H H viscous mass49 H 2-Cl H H -- CH.sub.3 H H m.p. 141-143.degree. C.50 H 2-Cl --O--CF.sub.3 H --CH.sub.3 H H n.sub.20.sup.D = 1.569551 F H Cl H F H H m.p. 140-142.degree. C.52 F H F H F H H m.p. 127-130.degree. C.53 Cl H --O--CF.sub.3 H Cl H H m.p. 139-140.degree. C.54 Cl H Cl H Cl H H m.p. 64-68.degree. C.55 Cl H F H Cl H H m.p. 156-158.degree. C.56 F H --O--CF.sub.3 H H H H m.p. 106-107.degree. C.57 F H F H H H H m.p. 111-112.degree. C.58 F H Cl H H H H viscous mass59 F H H H Cl H H m.p. 123-125.degree. C.60 F H H 3-CH.sub.3 Cl H H m.p. 130-134.degree. C.61 F H --O--CF.sub.3 H Cl H H m.p. 148-150.degree. C.62 F H H 3-CF.sub.3 Cl H H viscous mass63 F H Cl H Cl H H m.p. 110-112.degree. C.64 F H F H Cl H H m.p. 125-127.degree. C.65 Cl H --CO--O--CH(CH.sub.3).sub.2 H Cl H H m.p. 86-88.degree. C.66 Cl H --OCF.sub.2 CHF.sub.2 H Cl H H m.p. 124-126.degree. C.67 F H --OCF.sub.2 CHF.sub.2 H F H H m.p. 134-136.degree. C.68 F H --CO--O--CH(CH.sub.3).sub.2 H F H H m.p. 65-68.degree. C.69 Cl H --CO--O--CH(CH.sub.3).sub.2 H F H H m.p. 74-76.degree. C.70 Cl H --OCF.sub.2 CHF.sub.2 H F H H m.p. 160-162.degree. C.71 F H --CO--O--CH(CH.sub.3).sub.2 H Cl H H m.p. 70-72.degree. C.72 F H --OCF.sub.2 CHF.sub.2 H Cl H H m.p. 145-147.degree. C.73 F H H 3-CF.sub.3 F H H m.p. 110-112.degree. C.74 F H --O--CH.sub.3 H F H H m.p. 106-111.degree. C.75 F H --CH.sub.3 H F H H m.p. 146-148.degree. C.76 F H H 3-Cl F H H m.p. 138-140.degree. C.77 F H --CF.sub.3 H F H H m.p. 189-191.degree. C.78 H H --CO--O--CH(CH.sub.3).sub.2 H 3,4--O--CH.sub.2 --O-- H viscous mass79 --O--CHF.sub.2 H --O--CF.sub.3 H F H H m.p. 99-100.degree. C.80 --O--CHF.sub.2 H F H F H H m.p. 147-148.degree. C.81 --O--CHF.sub.2 H Cl H F H H m.p. 134-136.degree. C.82 --O--CHF.sub.2 H H H F H H m.p. 109-111.degree. C.83 F H Cl 3-Cl F H H m.p. 195-196.degree. C.84 F H H 3-F F H H m.p. 121-122.degree. C.85 F H H 2-CF.sub.3 F H H m.p. 107-108.degree. C.86 F H Br H F H H m.p. 152-154.degree. C.87 F H H 2-F F H H m.p. 140-142.degree. C.__________________________________________________________________________
The following compounds of formula I can also be obtained in accordance with the procedures described above:
__________________________________________________________________________Compound R.sub.1 R.sub.2 R.sub.3 R.sub.4 R.sub.5 R.sub.6 R.sub.7__________________________________________________________________________88 Cl H Cl H F H H89 F H Cl H --CF.sub.3 H H90 F H --O--CF.sub.3 H --CF.sub.3 H H91 F H --CO--O--CH(CH.sub.3).sub.2 H --CF.sub.3 H H92 --O--CHF.sub.2 H Cl H Cl H H93 --O--CHF.sub.2 H Cl H CF.sub.3 H H94 --O--CHF.sub.2 H --O--CF.sub.3 H Cl H H95 --O--CHF.sub.2 H --O--CF.sub.3 H CF.sub.3 H H96 --O--CHF.sub.2 H --CO--O--CH(CH.sub.3).sub.2 H F H H97 --O--CHF.sub.2 H --CO--O--CH(CH.sub.3).sub.2 H Cl H H98 --O--CHF.sub.2 H --CO--O--CH(CH.sub.3).sub.2 H CF.sub.3 H H__________________________________________________________________________
EXAMPLE 2
Formulations for liquid active ingredients of formula I according to Example 1 or combinations thereof with other insecticides or acaricides (throughout, percentages are by weight)
______________________________________1. Emulsifiable concentrates (a) (b) (c)______________________________________active ingredient or active ingredient 25% 40% 50%combinationcalcium dodecylbenzenesulfonate 5% 8% 6%castor oil polyethylene glycol 5% -- --ether (36 moles of ethylene oxide)tributylphenol polyethylene glycol -- 12% 4%ether (30 moles of ethylene oxide)cyclohexane -- 15% 20%xylene mixture 65% 25% 20%______________________________________
Emulsions of any required concentration can be produced from such concentrates by dilution with water.
______________________________________2. Solutions (a) (b) (c) (d)______________________________________active ingredient or active 80% 10% 5% 95%ingredient combinationethylene glycol monomethyl ether 20% -- -- --polyethylene glycol 400 -- 70% -- --N--methyl-2-pyrrolidone -- 20% -- --expoxidised coconut oil -- -- 1% 5%ligroin (boiling range 160-190.degree.) -- -- 94% --______________________________________
These solutions are suitable for application in the form of microdrops.
______________________________________3. Granulates (a) (b)______________________________________active ingredient or active ingredient 5% 10%combinationkaolin 94% --highly dispersed silicic acid 1% --attapulgite -- 90%______________________________________
The active ingredient or active ingredient combination is dissolved in methylene chloride, the solution is sprayed onto the carrier, and the solvent is subsequently evaporated off in vacuo.
______________________________________4. Dusts (a) (b)______________________________________active ingredient or active ingredient 2% 5%combinationhighly dispersed silicic acid 1% 5%talcum 97% --kaolin -- 90%______________________________________
Ready for use dusts are obtained by intimately mixing the carriers with the active ingredient or active ingredient combination.
Formulations for solid active ingredients of formula I according to Example 1 or combinations thereof with other insecticides or acaricides (throughout, percentages are by weight)
______________________________________1. Wettable powders (a) (b) (c)______________________________________active ingredient or activeingredient combination 25% 50% 75%sodium lignosulfonate 5% 5% --sodium laurylsulfate 3% -- 5%sodium diisobutylnaphthalenesulfonate -- 6% 10%octylphenol polyethylene glycol ether(7-8 moles of ethylene oxide) -- 2% --highly dispersed silicic acid 5% 10% 10%kaolin 62% 27% --______________________________________
The active ingredient or active ingredient combination is thoroughly mixed with the adjuvants and the mixture is thoroughly ground in a suitable mill, affording wettable powders which can be diluted with water to give suspensions of any desired concentration.
______________________________________2. Emulsifiable concentrate______________________________________active ingredient or active ingredient combination 10%octylphenol polyethylene glycol ether 3%(4-5 moles of ethylene oxide)calcium dodecylbenzenesulfonate 3%castor oil polyglycol ether 4%(36 moles of ethylene oxide)cyclohexanone 30%xylene mixture 50%______________________________________
Emulsions of any required concentration can be obtained from this concentrate by dilution with water.
______________________________________3. Dusts (a) (b)______________________________________active ingredient or active 5% 8%ingredient combinationtalcum 95% --kaolin -- 92%______________________________________
Ready for use dusts are obtained by mixing the active ingredient or active ingredient combination with the carrier, and grinding the mixture in a suitable mill.
______________________________________4. Extruder granulate______________________________________active ingredient or active ingredient combination 10%sodium lignosulfonate 2%carboxymethylcellulose 1%kaolin 87%______________________________________
The active ingredient or active ingredient combination is mixed and ground with the adjuvants, and the mixture is subsequently moistened with water. The mixture is extruded, granulated and then dried in a stream of air.
______________________________________5. Coated granulate______________________________________active ingredient or active ingredient combination 3%polyethylene glycol 200 3%kaolin 94%______________________________________
The finely ground active ingredient or active ingredient combination is uniformly applied, in a mixer, to the kaolin moistened with polyethylene glycol. Non-dusty coated granulates are obtained in this manner.
______________________________________6. Suspension concentrate______________________________________active ingredient or active ingredient combination 40%ethylene glycol 10%nonylphenol polyethylene glycol ether 6%(15 moles of ethylene oxide)sodium lignosulfonate 10%carboxymethylcellulose 1%37% aqueous formaldehyde solution 0.2%silicone oil in the form of a 75% 0.8%aqueous emulsionwater 32%______________________________________
The finely ground active ingredient or active ingredient combination is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired concentration can be obtained by dilution with water.
EXAMPLE 3: Action against Musca domestica
50 g of freshly prepared nutrient substrate for maggots are charged into each of a number of beakers. A specific amount of an acetonic solution containing 1% by weight of the respective test compound is pipetted onto the nutrient substrate present in the beakers to give an acitve ingredient concentration of 800 ppm. The substrate is then thoroughly mixed and the acetone subsequently allowed to evaporate over a period of at least 20 hours.
Then 25 one-day-old maggots of Musca domestica are put into each of the beakers containing the treated nutrient substrate for testing with each active ingredient at the given concentration. After the maggots have pupated, the pupae are separated from the substrate by flushing them out with water and then deposited in containers closed with a perforated top.
Each batch of flushed out pupae is counted to determine the toxic effect of the test compound on the maggot development. A count is then made after 10 days of the number of flies which have hatched out of the pupae.
The compounds of formula I according to Example 1 exhibit good activity in this test.
EXAMPLE 4: Action against Aedes aegypti
A concentration of 800 ppm is obtained by pipetting a specific amount of an acetonic solution containing 0.1% by weight of the test compound onto the surface of 150 ml of water in a beaker. After the acetone has evaporated, 30 to 40 two-day-old larvae of Aedes aegypti are put into the beaker containing the test compound. Mortality counts are made after 1, 2 and 5 days.
In this test, the compounds of formula I according to Example 1 exhibit good activity against Aedes aegypti.
EXAMPLE 5: Insecticidal stomach poison action
Cotton plants about 25 cm high, in pots, are sprayed with aqueous emulsions containing the respective test compound in concentrations of 100, 200 and 400 ppm. After the spray coating has dried, the cotton plants are populated with Spodoptera littoralis and Heliothis virescens larvae in the L.sub.3 -stage. The test is carried out at 24.degree. C. and 60% relative humidity. The percentage mortality of the test insects is determined after 120 hours.
In this test, the compounds of the present invention effect 80 to 100% mortality at the following concentrations:
______________________________________ Active ingredientCom- concentrationpound Spodoptera Heliothis______________________________________13 400 ppm --15 400 ppm 400 ppm31 400 ppm --37 400 ppm 400 ppm40 400 ppm 200 ppm51 -- 100 ppm54 -- 400 ppm56 400 ppm 400 ppm______________________________________
EXAMPLE 6: Action against Anthonomus grandis (Adults)
Cotton plants in pots are sprayed with a wettable aqueous emulsion formulation containing 400 ppm of the test compound. After the spray coating has dried (about 11/2 hours), each plant is populated with 10 adult unsexed beetles (Anthonomus grandis). Plastic cylinders, covered at the top with gauze, are then slipped over the treated plants populated with the test insects to prevent the beetles from migrating from the plants. The treated plants are then kept at 25.degree. C. and about 60% relative humidity. Evaluation of the stomach poison action is made after 1, 2, 3 and 6 days on the basis of the percentage mortality of the beetles (percentage in dorsal position).
The surviving beetles are transferred to Anthonomus diat pellets and left for 3 days for oviposition. The beetles are then removed and the pellets with the egg deposits are incubated for 7 days at 28.degree. C. Evaluation of the reproduction inhibiting effect is made by determining the reduction in the number of deposited eggs, the number of larvae which have hatched from these eggs and the number of dead larvae in comparison with untreated controls.
At a concentration of 400 ppm, with respect to stomach poison action, compounds 1, 4, 13 and 15 and, with respect to reproduction inhibition, compounds 7, 8 18, 19, 20 and 22 according to Example 1 effect 80 to 100% mortality in comparison with untreated controls.
Example 7: Action against soil insects (Diabrotica balteata)
5 maize seedlings 1 to 3 cm in height and a filter paper disc are immersed in an aqueous solution of the test compound containing about 4% by volume of acetone. The immersed filter paper disc is placed on the bottom of a plastic beaker (contents 200 ml) and on it is then placed a dry filter paper disc together with the maize seedlings and 10 larvae of Diabrotica balteata in the L.sub.2 or L.sub.3 stage. The batch is kept at about 24.degree. C. and 40 to 60% relative humidity under daylight. Evaluation is made after 6 days in comparison with untreated controls.
At the following concentrations, the compounds of the present invention effect 80 to 100% mortality:
______________________________________Compound Active ingredient concentration______________________________________1 and 53 3 ppm11, 15 and 40 12.5 ppm7, 51, 56 and 61 50 ppm4, 37, 54 and 63 100 ppm58 200 ppm1 and 6 400 ppm______________________________________
EXAMPLE 8: Action against Laodelphax striatellus and Nilaparvata lugens (nymphs)
The test is carried out with growing plants. For this purpose 4 rice plants (thickness of stem 8 mm) about 20 cm in height are planted into each of a number of pots (diameter 8 cm). The plants in each pot are sprayed on a rotary table with 100 ml of an acetonic solution containing 400 ppm of the test compound. After the spray coating has dried, each plant is populated with 20 nymphs of the test organisms in the third stage. To prevent the cicadas from escaping, a glass cylinder is slipped over each of the plants and sealed with a gauze top. The nymphs are kept for 10 days on the treated plant until the next development stage has been reached. Evaluation of percentage mortality is made 1, 4 and 8 days after treatment.
The compounds of formula I according to Example 1 of the present invention exhibit good activity in this test.
Example 9: Action against Laodelphax striatellus and Nilaparvata lugens (ovicidal)
The test is carried out with growing plants. For this purpose 4 rice plants (thickness of stem 8 mm; height about 20 cm) are planted into each of a number of pots (diameter 8 cm).
The plants in each pot are sprayed on a rotary table with 100 ml of an acetonic solution containing 400 ppm of the test compound. After the spray coating has dried, each plant is populated with 3 adult females. To prevent the females from escaping, a glass cylinder is slipped over each of the plants and sealed with a gauze top. The females are left on the plant for 4 days for oviposition and are then removed.
About 8 days after the females have been placed on the plants, the young cicadas hatch from the eggs and a count is made. The percentage mortality is calculated by comparing the number of larvae which have hatched on the treated plants with the number which have hatched on the untreated control plants.
The compounds of formula I according to Example 1 exhibit good ovicidal activity in this test.

Number	Date	Country	Kind
5489/84	Nov 1984	CHX
4551/85	Oct 1985	CHX

Number	Name	Date
4174393	Van Dahlen et al.	Nov 1979
4439440	Van Hes et al.	Mar 1984
4540706	Ozawa et al.	Sep 1985

Number	Date	Country
0004733	Oct 1979	EPX
2529689	Jan 1976	DEX
2700258	Jul 1977	DEX

1-carbamoyl-2-pyrazolines, composition containing them, and insecticidal and acaricidal method of using them

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