GB2219794A - Plant growth regulating and fungicidal pyrimidine derivatives - Google Patents

Abstract

Pyrimidine derivatives useful as plant growth regulating agents and fungicides have the formula (I): <IMAGE> wherein Y is an optionally substituted secondary or tertiary alkyl group containing from 3 to 7 carbon atoms or an optionally substituted cycloalkyl or alkylcycloalkyl group containing from 3 to 7 carbon atoms; R<1 > is hydrogen or a lower alkyl group; A is an optionally substituted aryl group; and R<2> is hydrogen, an alkyl group containing from 1 to 4 carbon atoms or an alkenyl or alkynyl group containing from 2 to 4 carbon atoms, or are agrochemically acceptable salts or metal complexes thereof or, when R<2> is hydrogen, esters thereof. They can be incorporated into agrochemical compositions.

Description

PYRIMIDINE DERIVATIVES This invention relates to pyrimidine derivatives useful as plant growth regulating agents and fungicides, to processes for preparing them, to compositions containing them and to methods of regulating plant growth and combating fungal diseases in plants using them.

According to the present invention there is provided a pyrimidine derivative having the general formula (I)

and stereoisomers thereof, wherein Y is an optionally substituted secondary or tertiary alkyl group containing from 3 to 7 carbon atoms or an optionally substituted cycloalkyl or alkylcycloalkyl group containing from 3 to 7 carbon atoms; R1 is hydrogen or a lower alkyl group; A is an optionally substituted aryl group; and R2 is hydrogen, an alkyl group containing from 1 to 4 carbon atoms, an alkenyl group containing from 2 to 4 carbon atoms or an alkynyl group containing form 2 to 4 carbon atoms; and agrochemically acceptable salts and metal complexes of the compounds of formula (I) and esters (acylates) of compounds of formula (I) wherein R2 is hydrogen.

The compounds of the invention contain one or more chiral centres. Such compounds are generally obtained in the form of racemic mixtures. However, these and other mixtures can be separated into the individual isomers by methods known in the art, and this invention embraces such isomers.

Preferred optional substituents in the group Y are halogen, especially chlorine or fluorine.

Y is preferably a group which in its unsubstituted form has the structure:

wherein R3, R4 and R5, which may be the same or different, are separately hydrogen or an alkyl group, provided that no more than one of R3, R4 and R5 is hydrogen, or wherein R3 and R4, together with the carbon atom joining them, form a cycloalkyl ring and R5 is hydrogen or an alkyl group, the total number of carbon atoms in the group (II) being from 3 to 7.

Especially preferred groups Y are isopropyl, t-butyl, l,1-dimethylpropyl (t-pentyl), cyclopropyl or 1-methylcyclopropyl, each of which may be optionally halo-substituted.

It is preferred that Y is unsubstituted.

R1 is preferably hydrogen or methyl.

R2 is preferably hydrogen or methyl. Hydrogen is especially preferred.

As examples of optional substituents which may be present in the aryl group, A there may be mentioned one or more substituents selected from halogen, for example chlorine, bromine or fluorine; alkyl, for example lower alkyl and especially methyl; alkoxy, for example lower alkoxy and especially methoxy; haloalkyl, for example lower haloalkyl and especially trifluoromethyl; nitro; and cyano. The term "lower" as applied to the above groups indicates that the group contains from 1 to 6, and preferably from 1 to 4 carbon atoms. A is preferably optionally substituted phenyl.

Thus as specific examples of the group A there may be mentioned phenyl, o-, m- and p-chlorophenyl; o-, m- and pfluorophenyl; dichlorophenyl (for example 2,4-dichlorophenyl); difluorophenyl (for example 2,4-difluorophenyl); o-, m- and p-methylphenyl; o-, m- and p-trifluoromethylphenyl; o-, m- and p-methoxyphenyl; chloronitrophenyl (for example 3-nitro-4-chlorophenyl); o-, m- and p-methoxyphenyl; and o-, m- and p-nitrophenyl.

The present invention includes salts and metal complexes of the compounds of formula (I) and esters (acylates) of compounds of formula (I) wherein R2is hydrogen. As examples of esters there may be mentioned for example acetates or benzoates. As examples of salts there may be mentioned for example toluene sulphonate salts, dodecylbenzene sulphonate salts, hydrochloride salts, hydrobromide salts and orthophosphate salts.

Without limitation of the generality of the above statement, the present invention also includes any compound which breaks down in agrochemical use to a compound of formula (I).

Examples of the compounds of the invention are presented in Table I in which the values for A and-R1, in the formula (III) below are as indicated.

TABLE I

COMPOUND MELTING 1 NO R A POINT OC COMMENTS 1 H 4-chlorophenyl 139-141 2 H 2,4-dichlorophenyl 153-155 3 H phenyl 83-85 4 H 3-chlorophenyl 114-116 5 H 4-methylphenyl 100-102 6 H 4-fluorophenyl 106-109 7 CB phenyl 158-162 a 3 (a) 2::1 mixture of diastereoisomers Also specifically embraced by the present disclosure are compounds wherein R1 and A take the values listed in Table I and Y, rather that being isopropyl as in Table 1 takes the specific values t-butyl, l,l-dimethylpropyl, cyclopropyl and l-methylcyclopropyl respectively.

Compounds of general formula (I) above wherein R2 is hydrogen and Y, A and R1 are as defined may be prepared by reacting a compound of general formula (IV)

with an organometallic compound which may be represented by the general formula (V) A - (CHR1) - M (V) where M is a suitable metal, for example lithium, magnesium, titanium or zirconium.

The reaction conveniently takes place in a solvent such as diethylether, tetrahydrofuran or dichloromethane at -800C to +800C in an inert atmosphere. The product is obtained by quenching with a proton donor. When M is magnesium, the organometallic compound is more specifically R1-ng-halogen. When M is titanium, the organometallic compound is more specifically R1 Rl-Ti(Oalkyl)3.When N is zirconium, the organometallic compound is more specifically R1-Zr(O alkyl)3. 2 The compounds of general formula (I) wherein R is hydrogen may also be prepared by reacting a ketone of general formula (VI), wherein A and R1 are as defined with an organometallic compound which may be represented by the general formula (VII) wherein M is a suitable metal, for example lithium and Y is as defined above:

The reaction preferably takes place in a suitable solvent such as diethyl ether or tetrahydrofuran at a temperature of from -1200C to +800C and in an inert atmosphere. The product is obtained by quenching with a suitable proton donor.

The ketones of the general formula (IV) may be prepared by the method described in United States Patent No 4,713,456 or by alkylation of a lower alkyl ketone homologue.

The ketones of general formula (VI) may be prepared using standard methods set out in the literature.

The ethers (wherein R2 is alkyl) and esters (acylates) of the invention may be made from the corresponding hydroxy compound by reaction with the appropriate halide, acid chloride or acid anhydride in the presence of a suitable base.

The plant growth regulating effects of the compounds are manifested as, for example, by a stunting or dwarfing effect on the vegetative growth of woody and herbaceous mono- and di-cotyledonous plants. Such stunting or dwarfing may be useful, for example, in peanuts, cereals such as wheat and barley, oil seed rape, field beans, sunflowers, potatoes and soya bean where reduction in stem height, with or without further advantageous effects such as stem strengthening, thickening and shortening, internode shortening, increased buttress root formation and more erect stem and leaf orientation, may reduce the risk of lodging and may also permit increased amounts of fertiliser to be applied. The stunting of woody species is useful in controlling the growth of undergrowth under power lines etc.Compounds which induce stunting or dwarfing may also be useful in modifying the stem growth of sugar cane thereby increasing the concentration of sugar in the cane at harvest; in sugar cane, the flowering and ripening may be controllable by applying the compounds. Stunting of peanuts can assist in harvesting.

Growth retardation of grasses can help maintenance of grass swards. Examples of suitable grasses are Stenotaphrum secundatum (St. Augustine grass), Cynosurus cristatus, Lolium multiflorum and perenne, Agrostis tenuis, Cynodon dactylon (Bermuda grass), Dactylis glomerata, Festuca spp. (eg, Festuca rubra) and Poa spp.

(eg, Poa pratense). The compounds may stunt grasses without significant phytotoxic effects and without deleteriously affecting the appearance (particularly the colour) of the grass; this makes such compounds attractive for use on ornamental lawns and on grass verges. They may also have an effect on flower head emergence in, for example,grasses. The compounds can also stunt weed species present in the grasses; examples of such weed species are sedges (eg, Cyperus spp.) and dicotyledonous weeds (eg, daisy, plantain, knotweed, speedwell, thistle, docks and ragwort). The growth of non-crop vegetation (eg, weeds or cover vegetation) can be retarded thus assisting in the maintenance of plantation and field crops. In fruit orchards, particularly orchards subject to soil erosion, the presence of grass cover is important. However excessive grass growth requires substantial maintenance.

The compounds of the invention could be useful in this situation as they could restrict growth without killing the plants which would lead to soil erosion; at the same time the degree of competition for nutrients and water by the grass would be reduced and this could result in an increased yield of fruit. In some cases, one grass species may be stunted more than another grass species; this selectivity could be useful, for example, for improving the quality of a sward by preferential suppression of the growth of undesirable species.

The dwarfing may also be useful in miniaturising ornamental, household, garden and nursery plants (eg, poinsettias, chrysanthemums, carnations, tulips and daffodils).

As indicated above, the compounds can also be used to stunt woody species. This property can be used to control hedgerows or to shape or reduce the need for pruning, of fruit trees (eg, apples, pears, cherries, peaches, vines etc).

The plant growth regulating effect may (as implied above) manifest itself in an increase in crop yield; or in an ability in orchards and other crops to increase fruit set, pod set and grain set. Some coniferous trees are not significantly stunted by the compounds so the compounds could be useful in controlling undesirable vegetation in conifer nurseries.

In the potato, vine control in the field and inhibition of sprouting in the store may be possible.

In addition the compounds may be useful as absicision agents resulting in thinning of fruit on the tree and an increase in fruit quality.

Other plant growth regulating effects caused by the compounds include alteration of leaf angle and changes in leaf morphology (both of which may permit increased light interception and utilisation) and promotion of tillering in monocotyledonous plants. Improved light interception is of value in all major world crops, eg, wheat, barley, rice, maize, soya, sugarbeet, potatoes, plantation crops and orchard crops. The leaf angle effect may be useful for example in altering the leaf orientation of, for example, potato crops thereby letting more light into the crops and inducing an increase in photosynthesis and tuber weight. By increasing tillering in monocotyledonous crops (eg, rice), the number of flowering shoots per unit area may be increased thereby increasing the overall grain yield of such crops.In addition better control and modification of hierarchical relationships is possible both in vegetative and reproductive stages of monocotyledonous and dicotyledonous plant growth, especially in cereals such as wheat, barley, rice and maize, whereby the number of flowering shoots per unit area may be increased and the size distribution of grains within the ear may be modified in such a way as to increase yield. In the treatment of rice plants, or rice crops the invention compounds can be applied, eg, as granules or a granular formulation, for example as slow release granules, to nursery boxes, paddy water and other like cultivation loci and media.In grass swards, especially amenity grass, an increase in tillering could lead to a denser sward which may result in increased resilience in wear; and to increased yields and better quality of forage grass, eg, improved digestability and palatability.

The treatment of plants with the compounds can lead.

to the leaves developing a darker green colour. In dicotyledonous plants such as soyabean and cotton, there may be promotion of sideshooting.

The compounds may inhibit, or at least delay, the flowering of sugar beet (and thereby may increase sugar yield) or otherwise modify the flowering patterns in many other crops. They may also reduce the size of sugar beet without reducing significantly the sugar yield thereby enabling an increase in planting density to be made.

Similarly in other root crops (eg, turnip, swede, mangold, parsnip, beetroot, yam and cassava) it may be possible to increase the planting density. The compounds could be useful in restricting the vegetative growth of cotton thereby leading to an increase in cotton yield. Crop yields may also be increased by improvement of the harvest index (ie. the harvested yield as a proportion of the total dry matter produced) by altering dry matter partitioning. This applies to all the aforementioned root, pod, cereal, tree, plantation and orchard crops.

The compounds may be useful in rendering plants resistant to stress since the compounds can delay the emergence of plants grown from seed, shorten stem height and delay flowering; these properties could be useful in preventing frost damage in countries where there is significant snow cover in the winter since then the treated plants would remain below snow cover during the cold weather. Further the compounds may cause drought or cold resistance in certain plants.

When applied as seed treatments at low rates the compounds can have a growth stimulating effect on plants.

It is to be understood that not all the compounds of the present invention will necessarily show all the above mentioned plant growth regulating effects. Thus whilst there may be advantages in compounds which have a broad spectrum of plant growth regulating effects- against a wide range of species, compounds having a high specific activity with respect to a particular species and/or plant growth regulating effect may also be of great benefit.

In carrying out the plant growth regulating method of the invention, the amount of compound to be applied to regulate the growth of plants will depend upon a number of factors, for example the particular compound selected for use, and the identity of the plant species whose growth is to be regulated. However, in general an application rate of 0.1 to 15, preferably 0.1 to 5, kg per hectare is used.

With the use of biodegradable polymeric slow release granules rates of 1 to 10g per hectare are feasible; whilst electrodynamic spraying techniques may also deploy lower rates of application. However, on certain plants even application rates within these ranges may give undesired phytotoxic effects. Routine tests may be necessary to determine the best rate of application of a specific compound for any specific purpose for which it is suitable.

The compounds may also be active fungicide and may be used to control one or more of the following pathogens Pyricularia oryzae on rice.

Puccinia recondita, Puccinia striiformis and other rust on wheat, Puccinia hordei, Puccinia striiformis and other rusts on barley, and rusts on other hosts, e.g. coffee, pears, apples, peanuts, vegetables and ornamental plants.

Erysiphe graminis (powdery mildew) on barley and wheat and other powdery mildews on various hosts such as Sphaerotheca macularis on hops, Sphaerotheca fuliginea on cucurbits (e.g. cucumber), Podosphaera leucotricha on apple and Uncinula necator on vines.

Helminthosporium spp., Rhynchosporium spp., Septoria spp., Pseudocercosporella herepotrichoides and Gaeumannomyces graminis on cereals.

Cercospora arachidicola and Cercosporidium personata on peanuts and other Cercospora species on other hosts, for example, sugar beet, bananas, soya beans and rice.

Botrytis cinerea (grey mould) on tomatoes, strawberries, vegetables, vines and other hosts.

Alternaria species on vegetables (e.g. cucumber), oil seed rape, apples, tomatoes and other hosts.

Venturia inaequalis (scab) on apples.

plasmopara viticola on vines.

Other downy mildews such as Bremia lactucae on lettuce, Peronospora spp. on soya beans, tobacco, onions and other hosts and Pseudoperonospora humuli on hops and Pseudoperonospora cubensis on cucurbits Phytophthora infestans on potatoes and tomatoes and other Phytophthora spp. on vegetables, strawberries, avocado, pepper, ornamentals, tobacco, cocoa and other hosts.

Thanaterphorus cucumeris on rice and other Rhizoctonia species on various host such as wheat and barley, vegetables, cotton and turf.

Some of the compounds show a broad range of activities against fungi in vitro. They may also have activity against various post-harvest diseases on fruit (e.g. Penicillium digitatum and Italicum and Trichoderma virile on oranges, Gloesporium musarum and bananas and Botrytis cinerea on grapes).

Further some of the compounds may be active as seed dressings against Fusarium spp., Septoria spp., Tilletia spp., (bunt, a seed borne disease of wheat), Ustilago spp., Helminthosporium spp. on cereals, Rhizoctonia solani on cotton and Pyricularia oryzae on rice.

The compounds may be used as such for plant growth regulating purposes or as fungicides but are more conveniently formulated into compositions for such usage.

The invention thus provides a plant growth regulating or fungicidal composition comprising a compound of general formula (I) as hereinbefore defined, or a salt or metal complex thereof; and, optionally, a carrier or diluent.

The invention also provides a method of regulating plant growth or of fungicidal treatment, which comprises applying to the plant, to seed of a plant or to the locus of a plant or seed, a compound, or a salt or metal complex thereof, as hereinbefore defined, or a composition combining the same.

The compounds, salts, metal complexes, ethers and esters can be applied in a number of ways, for example they can be applied, formulated or unformulated, directly to the foliage of a plant, or they can be applied also to bushes and trees, to seeds or to other medium in which plants, bushes or trees are growing or are to be planted, or they can be sprayed on, dusted on or applied as a cream or paste formulation, or they can be applied as a vapour; or as slow release granules. Application can be to any part of the plant, bush or tree, for example to the foliage, stems, branches or roots, or to soil surrounding the roots, or to the seed before it is planted; or to the soil generally, to paddy water or to hydroponic culture systems. The invention compounds may also be injected into plants or trees and they may also be sprayed onto vegetation using electrodynamic spraying techniques.

The term "plant" as used herein includes seedlings, bushes and trees.

The compounds are preferably used for agricultural and horticultural purposes in the form of a composition.

The type of composition used in any instance will depend upon the particular purpose envisaged.

The compositions may be in the form of dusting powders or granules comprising the active ingredient and a solid diluent or carrier, for example fillers such as kaolin, bentonite, kieselguhr, dolomite, calcium carbonate, talc, powdered magnesia, Fuller's earth gypsum, Hewitt's earth, diatomaceous earth and China clay. Such granules can be pre-formed granules suitable for application to the soil without further treatment. These granules can be made either by impregnating pellets of filler with the active ingredient or by pelleting a mixture of the active ingredient and powdered filler.

Compositions for dressing seed, for example, may comprise an agent (for example a mineral oil) for assisting the adhesion of the composition to the seed; alternatively the active ingredient can be formulated for seed dressing purposes using an organic solvent (for example Nmethylpyrrolidone or dimethylformamide).

The compositions may also be in the form of dispersible powders, granules or grains comprising a wetting agent to facilitate the dispersion in liquids of the powder or grains which may contain also fillers and suspending agents.

The aqueous dispersions or emulsions may be prepared by dissolving the active ingredient(s) in an organic solvent optionally containing wetting, dispersing or emulsifying agent(s) and then adding the mixture to water which may also contain wetting, dispersing or emulsifying agent(s). Suitable organic solvents are ethylene dichloride, isopropyl alcohol, propylene glycol, diacetone alcohol, toluene, kerosene, methylnaphthalene, the xylenes, trichloroethylene, furfuryl alcohol, tetrahydrofurfuryl alcohol, and glycol ethers (eg, 2ethoxyethanol and 2-butoxyethanol).

The compositions to be used as sprays may also be in the form of aerosols wherein the formulation is held in a container under pressure in the presence of a propellant, eg, fluorotrichloromethane or dichlorodjfluoromethane.

The compounds can be mixed in the dry state with a pyrotechnic mixture to form a composition suitable for generating in enclosed spaces a smoke containing the compounds.

Alternatively, the compounds may be used in a microencapsulated form. They may also be formulated in biodegradable polymeric formulations to obtain a slow, controlled release of the active substance.

By including suitable additives, for example additives for improving the distribution, adhesive power and resistance to rain on treated surfaces, the different compositions can be better adapted for various utilities.

The compounds can be used as mixtures with fertilisers (eg, nitrogen-, potassium- or phosphoruscontaining fertilisers). Compositions comprising only granules of fertiliser incorporating, for example coated with, the compound are preferred. Such granules suitably contain up to 25% by weight of the compound. The invention therefore also provides a fertiliser composition comprising the compound of general formula (I) or a salt or metal complex thereof.

The compositions may also be in the form of liquid preparations for use as dips or sprays which are generally aqueous dispersions or emulsions containing the active ingredient in the presence of one or more surfactants eg, wetting agent(s), dispersing agent(s), emulsifying agent(s) or suspending agent(s); or which are spray formulations of the kind suitable for use in electrodynamic spraying techniques. The foregoing agents can be cationic, anionic or non-ionic agents. Suitable cationic agents are quaternary ammonium compounds, for example cetyltrimethylammonium bromide.

Suitable anionic agents are soaps, salts of aliphatic monoesters of sulphuric acid (for example sodium lauryl sulphate), and salts of sulphonated aromatic compounds (for example sodium dodecylbenzenesulphonate, sodium, calcium or ammonium lignosulphonate, butylnaphthalene sulphonate, and a mixture of sodium diisopropyl- and triisopropyl-naphthalene sulphonates).

Suitable non-ionic agents are the condensation products of ethylene oxide with fatty alcohols such as oleyl or cetyl alcohol, or with alkyl phenols such as octyl- or nonyl-phenol and octylcresol. Other non-ionic agents are the partial esters derived from long chain fatty acids and hexitol anhydrides, the condensation products of the said partial esters with ethylene oxide, and the lecithins. Suitable suspending agents are hydrophilic colloids (for example polyvinylpyrrolidone and sodium carboxymethylcellulose), and the vegetable gums (for example gum acacia and gum tragacanth).

The compositions for use as aqueous dispersions or emulsions are generally supplied in the form of a concentrate containing a high proportion of the active ingredient(s), and the concentrate is to be diluted with water before use. These concentrates often should be able to withstand storage for prolonged periods and after such storage be capable of dilution with water in order to form aqueous preparations which remain homogeneous for a sufficient time to enable them to be applied by conventional and electrodynamic spray equipment. The concentrates may conveniently contain up to 95%, suitably 10-85%, for example 25-60%, by weight of the active ingredient(s).These concentrates suitably contain organic acids (eg, alkaryl or aryl sulphonic acids such as xylenesulphonic acid or dodecyl benzenesulphonic acid) since the presence of such acids can increase the solubility of the active ingredient(s) in the polar solvents often used in the concentrates. The concentrates suitably contain also a high proportion of surfactants so that sufficiently stable emulsions in water can be obtained. After dilution to form aqueous preparations, such preparations may contain varying amounts of the active ingredient(s) depending upon the intended purpose, but an aqueous preparation containing 0.0005% to 10%, or 0.01% to 10%, by weight of active ingredient(s) may be used.

The compositions of this invention can comprise also one or more additional compound(s) having biological activity, eg, compounds having similar or complementary fungicidal or plant growth activity or compounds having plant growth regulating, herbicidal or insecticidal activity.

The additional fungicidal compound can be, for example, one which is capable of combating ear diseases of cereals (eg,wheat) such as Septoria, Gibberella and Helminthosporium spp., seed and soil borne diseases and downy and powdery mildews on grapes and powdery mildew and scab on apple etc. Examples of suitable additional fungicidal compound are imazalil, benomyl, carbendazim, thiophanate-methyl, captafol, captan, sulphur, triforine, dodemorph, tridemorph, pyrazophos, furalaxyl, ethirimol, tecnazene, dimethirimol, bupirimate, chlorothalonil, vinclozolin, procymidone, iprodione, metalaxyl, forsetylaluminium, carboxin, oxycarboxin, fenarimol, nuarimol, fenfuram, methfuroxan, nitrotal-isopropyl, triadimefon, thiabendazole, etridiazole, triadimenol, biloxazol, dithianon, binapacryl, quinomethionate, guazatine, dodine fentin acetate, fentin hydroxide, dinocap, folpet, dichlofluanid, ditalimphos, kitazin, cycloheximide, dichlobutrazol, a dithiocarbamate, a copper compound, a mercury compound, l-(2-cyano-2-methoxyiminoacetyl)-3-ethyl urea, fenaponil, ofurace, propiconazole, etaconazole and fenpropemorph and fenpropidine.

The compounds of general formula (I) can be mixed with soil, peat or other rooting media for the protection of plants against seed-borne, soil-borne or foliar fungal diseases.

Suitable additional insecticides are Pirimor, Croneton, dimeth- oate, Metasystox, pyrethroid insecticides and formothion.

The other, additional, plant growth regulating compound can be one which controls weeds or seedhead formation, improves the level or longevity df the plant growth regulating activity of the compounds of general formula (I), selectively controls the growth of the less desirable plants (eg, grasses) or causes the compound of general formula (I) to act faster or slower as a plant growth regulating agent. Some of these other agents will also be herbicides.

Examples of suitable plant growth regulating compounds, which can display synergy in admixture, or use, with the invention compounds are the gibberellins (eg, GA3, GA4 or GA7), the auxins (eg, indoleacetic acid, indolebutyric acid, naphthoxyacetic acid or naphthylacetic acid), the cytokinins (eg, kinetin, diphenylurea, benzimidazole, benzyladenine or benzylaminopurine), phenoxyacetic acids (eg, 2,4-D or MCPA), substituted benzoic acids (eg, triiodobenzoic acid), morphactins (eg, chlorfluorecol), maleic hydrazide, glyphosate, glyphosine, long chain fatty alcohols and acids, dikegulac, fluoridamid, mefluidide, substituted quaternary ammonium and phosphonium compounds (eg, chlormequat* chlorphonium or mepiquat chloride*), ethephon, carbetamide, methyl-3,6dichloroanisate, daminozide*, asulam, abscisic acid, isopyrimol, 1-(4-chlorophenyl)-4,6-dimethyl-2-oxo-l,2- dihydropyridine-3-carboxylic acid, hydroxybenzonitriles (eg, bromoxynil), difenzoquat*, benzoylprop-ethyl 3,6dichloropicolinic acid, fenpentezol, triapenthanol, flurpirimidol, paclobutrazol, tetcyclacis and tecnazene.

Synergy will be most likely to occur with those of the foregoing which are quaternary ammonium compounds and with those marked with an asterisk.

For certain applications, for example in the injection of the compounds of the invention into trees or plants, it is desirable that the compounds have a relatively high solubility in water, for example a solubility in excess of 30 parts per million. The compounds may alternatively be injected into the tree in the form of an organic solution, for example a solution in a lower alcohol.

For certain applications it is also desirable that the compound has a low persistency in soil to prevent carry-over to adjacent crops or even crops planted subsequently in the same soil. Preferably the compound for use in such applications has a half life in the soil of less than 20 weeks.

The invention is illustrated by the following Examples in which all parts and percentages are by weight unless otherwise stated EXAMPLE 1 This Example illustrates the preparation of 2-methyl3-hydroxy-3-(pyrimidin-5-yl)-4-(4-chlorophenyl)-butane (Compound No 1 of Table 1).

A Grignard reagent was prepared by reacting in a dry vessel and under nitrogen 4-chlorobenzyl chloride (2.36g, 0.015 moles), magnesium turnings (0.45g, 0.019 g atoms) and a crystal of iodine in dry diethylether (30ml). The mixture was cooled to 50C and a solution of 2-methyl-3-(pyrimidin-5-yl)-propan-3-one (2.0g, 0.013 moles), prepared using the methods described in United States Patent No 4,713,456, in ether was gradually added dropwise with stirring. The resulting suspension was stirred at 200C for 3 hours and then left overnight.

Aqueous ammonium chloride was added and the ether layer was separated and the aqueous layer extracted once more with ether. The combined organic layers were washed with water and then brine and dried over anhydrous magnesium sulphate. Concentration in vacuo left a pale yellow oil which was purified by chromatography over silica with dichloromethane followed by dichloromethane/ether (in a 2:1 ratio) as eluents. The desired product was obtained as a cream solid (0.80'g) having a melting point of 139-1410C.

EXAMPLE 2 This Example illustrates the preparation of 2-methyl3-hydroxy-3-(pyrimidin-5-yl)-4-(2,4-dichlorophenyl)-butane (Compound No 2 of Table 1).

Compound No 2 of Table 1 was prepared using the general method of Example 1, but with 2,4-dichlorobenzyl chloride as starting material. The product was a pale cream solid having a melting point of 153-1550C.

EXAMPLE 3 This Example illustrates the preparation of 2-methyl 3-hydroxy-3-(pyrimidin-5-yl )-4-phenyl-butane (Compound No 3 of Table 1).

Compound No 3 of Table 1 was prepared using the general method of Example 1, but with benzyl chloride as starting material. The product was a cream solid having a melting point of 83-85 C.

EXAMPLE 4 This Example illustrates the preparation of 2-methyl3-hydroxy-3-(pyrimidin-5-yl)-4-(3-chlorophenyl)-butane (Compound No 4 of Table 1).

Compound No 4 of Table 1 was prepared using the general method of Example 1, but with 3-chlorobenzyl chloride as starting material. The product was a cream solid having a melting point of 114-1160C.

EXAMPLE 5 This Example illustrates the preparation of 2-methyl3-hydroxy-3-(pyrimidin-5-yl)-4-(4-methylphenyl)-butane (Compound No 5 of Table 1).

Compound No 5 of Table 1 was prepared using the general method of Example 1, but with 4-methylbenzyl chloride as starting material. The product was a pale cream solid having a melting point of 100-1020C.

EXAMPLE 6 This Example illustrates the preparation of 2-methyl3-hydroxy-3-(pyrimidin-5-yl)-4-(4-fluorophenyl)-butane (Compound No 6 of Table 1).

Compound No 6 of Table 1 was prepared using the general method of Example 1, but with 4-fluorobenzyl chloride as starting material. The product was a pale yellow solid having a melting point of 106-1090C.

EXAMPLE 7 This Example illustrates the preparation of 2,4-dimethyl-3-hydroxy-3-(pyrimidin-5-yl)-4-phenyl-butane (Compound No 7 of Table 1).

Compound No 7 of Table 1 was prepared using the general method of Example 1, but with l-chloro-l-phenyl-ethane as starting material. The product was a pale cream solid having a melting point of 158-1620C. It was found to be a mixture of diasterioisomers having a ratio RS,SR:RR,SS of 2:1.

EXAMPLE 8 Compound Nos. 1 to 7 in Table I were tested for plant growth regulator activity against three species for various growth effects relevant to plant growth regulation.

Methodology The plant species used in this screen are presented in Table II with the leaf stage at which they were sprayed.

Each chemical was applied at 4000 ppm (4 kg/ha in a 1000 1/aha field volume) using a tracksprayer and a SS8004E (Teejet) nozzle. After spray the plants were grown in a glasshouse with 250C day/220C night temperatures and supplementary lighting was supplied when necessary (from mercury vapour lamps), to provide a 16 hour photoperiod.

The exception to this were the temperate cereals, wheat and barley which grown in 160C day/130C night temperatures.

After 2-6 weeks in the glasshouse, depending on the time of year, the plants were visually assessed for morphological characteristics. Formulation blanks were used as controls to assess the plants. The results are in Table III.

TABLE II PLANT MATERIAL USED FOR WHOLE PLANT SCREEN

Species Code Variety Growth Stage No.Plants Compost at'treatment per 3" pot Type Barley BR Atem 1-1.5 leaves 4 JIP* Wheat WW Timmo 1-1.5 leaves 4 JIP Tomato TO Ailsa Craig 2-2.5 leaves 1 JIP JIP* ^ John Innes Potting Compost.

TABLE III

COMPOUND BR WW NO.

R GA TI RGATI 2 3 1 1 1 1 4 1 11 5 22 22 21 13 6 21 2 21 3 7 TABLE III (continued)

COMPOUND TO NO.

RG A TI 1 1 G A T I 2 4 5 1 1 6 1 7 Key R w Retardation G = Greening effect A - Apical damage T - Tillering or side shooting I s Interligular or internodal length reduction All effects are scored visually on a 1-3 basis where 1 = 10-30% 2 = 31-60% 3 = 61-100% The manner in which the compounds of the present invention may be formulated into compositions suitable for application is shown generally in the following indicative illustrations numbered as Examples 9 to 18.

EXAMPLE 9 An emulsifiable concentrate is made up by mixing the following ingredients, and stirring the mixture until all the constituents are dissolved.

Compound of Table I 10% Calcium dodecylbenzenesulphonate 5% "SYNPERONIC" NP13 5% "Aromasol1, H 80% EXAMPLE 10 A composition in the form of grains readily dispersible in a liquid, e.g.. water, is prepared by grinding together the first three ingredients in the presence of added water and then mixing in the sodium acetate. The resultant mixture is dried and passed through a British Standard mesh sieve, size 44-100, to obtain the desired size of grains.

Compound of Table I 50% "Dispersol" T 25% "SYNPERONIC" NP5 1.5% Sodium acetate 23.5% EXAMPLE 11 The following ingredients are ground together to produce a powder formulation readily dispersible in liquids.

Compound of Table I 45% "Dispersol" T 5% "SYNPERONIC" NX 0.5% "Cellofas" B600 2% China clay GTY powder 47.5% EXAMPLE 12 The active ingredient is dissolved in acetone and the resultant liquid is sprayed on to the granules of attapulgite clay. The solvent is then allowed to evaporate to produce a granular composition.

Compound of Table I 5% Attapulgite granules 95% EXAMPLE 13 A composition suitable for use as a seed dressing is prepared by mixing the three ingredients.

Compound of Table I 50% Mineral oil 2% China clay 48% EXAMPLE 14 A dusting powder is prepared by mixing the active ingredient with talc.

Compound of Table I 5% Talc 95% EXAMPLE 15 A flowable formulation is prepared by bead-milling the constituents set out below and then forming an aqueous suspension of the ground mixture with water.

Compound of Table I 40% "Dispersol" T 4% "SYNPERONIC" NP5 1% Water 55% EXAMPLE 16 A dispersible powder formulation is made by mixing together the ingredients set out below and then grinding the mixture until all are thoroughly mixed.

Compound of Table I- 25% "Aerosol" OT/B 2% "Dispersol" A.C. 5% China clay 28% Silica 40% EXAMPLE 17 This Example illustrates the preparation of a dispersible powder formulation. The ingredients are mixed and the mixture then ground in a comminution mill.

Compound of Table I 25% "PERMINAL" BX 1% "Dispersol" T 5% Polyvinylpyrrolidone 10% Silica 25% China clay 34% EXAMPLE 18 The ingredients set out below are formulated into dispersible powder by mixing then grinding the ingredients.

Compound of Table I 25% "Aerosol" OT/B , 2% "Dispersol" A 5% China clay 68% There now follows an explanation of the compositions or substances represented by the various Trade Marks and Trade Names mentioned above.

"SYNPERONIC" NP13 : a condensate of nonyl phenol (1 mole) with ethylene oxide (13 moles).

"AROMASOL" H : a solvent mixture of alkyl benzenes.

"DISPERSOL" T AND AC : a mixture of sodium sulphate and a condensate of formaldehyde with sodium naphthalene sulphonate.

"SYNPERONIC" NP5 a condensate of nonyl phenol (1 mole) with naphthalene oxide (5.5 moles).

CELLOFAS B600 : a sodium carboxymethyl cellulose thickener

Claims (11)

1. CLAIMS 1. A pyrimidine derivative having the general formula (I)

   and stereoisomers thereof, wherein Y is an optionally substituted secondary or tertiary alkyl group containing from 3 to 7 carbon atoms or an optionally substituted cycloalkyl or alkylcycloalkyl group containing from 3 to 7 carbon atoms; R1 is hydrogen or a lower alkyl group; A is an optionally substituted aryl group; and R2 is hydrogen, an alkyl group containing from 1 to 4 carbon atoms, an alkenyl group containing from 2 to 4 carbon atoms or an alkynyl group containing form 2 to 4 carbon atoms; and agrochemically acceptable salts and metal complexes of the compounds of formula (I) and esters (acylates) of compounds of formula (I) wherein R2 is hydrogen.
2. 2. A pyrimidine derivative according to claim 1 wherein Y is a group which in its unsubstituted form has the structure:

   wherein R3, R4 and R5, which may be the same or different, are separately hydrogen or an alkyl group, provided that no more than one of R3, R4 and R5 is hydrogen, or wherein R3 and R4, together with the carbon atom joining them, form a cycloalkyl ring and R5 is hydrogen or an alkyl group, the total number of carbon atoms in the group (II) being from 3 to 7.
3. 3. A pyrimidine derivative according to claim 1 wherein Y is isopropyl, t-butyl, 1,1-dimethylpropyl, cyclopropyl or 1-methylcyclopropyl, each of which may be optionally halo-substituted
4. 4. A pyrimidine derivative according to any of the preceding claims wherein R1 is hydrogen or methyl.
5. 5. A pyrimidine derivative according to any of the preceding claims wherein R2 is hydrogen or methyl.
6. 6. A pyrimidine derivative according to any of the preceding claims wherein A is phenyl optionally substituted with one or more substituents selected from halogen, lower alkyl, lower alkoxy, lower haloalkyl, nitro and cyano.
7. 7. A pyrimidine derivative according to claim 6 wherein A is phenyl; o-, m- or p-chlorophenyl; o-, m- or p fluorophenyl; 2,4-dichlorophenyl; 2,4-difluorophenyl; o-, m- or p-methylphenyl; o-, m- or p-trifluoromethylphenyl; o-, m- or p-methoxyphenyl; 3-nitro-4-chlorophenyl; o-, m- or p-methoxyphenyl; or o-, m- or p-nitrophenyl.
8. 8. A plant growth regulating composition comprising-a plant growth regulating amount of a pyrimidine derivative according to claim 1 and an agrochemically acceptable carrier or diluent.
9. 9. A method of regulating plant growth which comprises applying to the plant, to the seed of the plant or to the locus of the plant or seed, a plant growth regulating amount of a pyrimidine derivative according to claim 1.
10. 10. A fungicidal composition comprising a fungicidally effective amount of a pyrimidine derivative according to claim 1 and an agrochemically acceptable carrier or diluent.
11. 11. A method of combating fungi which comprises applying to the plant, to the seed of the plant or to the locus of the plant or seed, a fungicidally effective amount of a pyrimidine derivative according to claim 1.