GB2189786A - Aromatic or heterocyclic amide derivatives - Google Patents

Abstract

A compound of the general formula IX <IMAGE> or a tautomer thereof where: R<1> is an aryl or substituted aryl radical or a heterocyclyl or substituted heterocyclyl radical; R<2> is an alkynyl radical or substituted alkynyl radical; R<6> is C1-6 alkyl; and X is oxygen or sulphur. The compounds may be used as intermediates in the production of the biologically active amide derivatives described in specification no 2152927.

Description

SPECIFICATION Biologically active amide derivatives This invention relates to substituted benzamide derivatives useful as herbicides and fungicides, to processes of combatting weeds and fungal infestations and to herbicidal and fungicidal compositions.

Substituted benzamide derivatives have previously been proposed for use as herbicides and fungicides, and for example, the compounds disclosed in European patent applications, publication numbers 59536, 61836 and 76030, may be mentioned.

We have now found that a certain, related, class of compounds possess an appreciably longer persistence of effect against certain fungicidal diseases of plants.

According to the present invention therefore there are provided amide derivatives of the general formula (I):

FORMULA I wherein R1 is an optionally substituted aryl or heterocyclyl radical; R2 is an optionally substituted alkynyl radical; Xis oxygen or sulphur; and E is CN, CONH2 or 0SNH2.

When R1 is an optionally substituted aryl group it may be a phenyl or naphthyl radical. Examples of substituents which may be present include C1-C4 alkyl, fluorine, chlorine, bromine, iodine, C1-C4 alkoxy, methylenedioxy and ethylenedioxy, C1-C4 alkylthio, C1-C4 haloalkyl (eg. CF3) nitro and cyano. There may be from one to three or more substituents which may be the same or different. When R1 is a substituted phenyl radical the substituents are preferably in the 3,4 or 5 positions. When a methylenedioxy or ethylenedioxy substituent is present, it preferably is attached to the 3 and 4 positions of the phenyl ring. A halogen substituent (eg. CI or Br) may also be present in the 4-or 5-position, or both, in such compounds.

When R1 is an optionally substituted heterocyclyl radical, it may for example be a furyl, benzfuryl, thienyl, pyridyl, thiazolyl, or benzthiazolyl radical. Examples of substituents which may be present include those listed above for the case when R1 is a substituted phenyl radical. There may be from one to three or more substituents which may be the same or different.

R2 may be an optionally substituted C3C7 alkynyl group. Examples of substituents which may be present include C1-C4 alkyl, and chlorine, bromine or iodine.

The structural formula (I) given above is believed to be the one which best represent the structure of the compounds. For some compounds within the scope of the formula (I) it may be possible for tautomeric forms of the compound to exist, in which a hydrogen atom is transposed to another part of the molecule and the chemical bonds between the atoms of the molecule are consequently rearranged. Thus it is possible for the molecule to exist in the alternative form (all):

FORMULA II The structural formula (I) is intended to represent and include such tautomeric forms, insofar as they may exist.The structural formula (I) is also intended to include any physically distinguishable modifications of the compounds which may arise, for example, from different ways in which the molecules are arranged in a crystal lattice, or from the inability of parts of the molecules to rotate freely in relation to other parts, or from geometrical and or optical isomerism, or from intramolecular or intermolecular bonding, or otherwise.

Particular examples of compounds according to the invention are listed in Table I below: TABLE I

COMPOUND R1 XR E Route Melting NO Point C 1 4-Cl.C6H4 OCH2C#CH CONH2 A 124-126 2 4-Cl.C6H4 OCH2C#CH CN A 84-87 3 4-Br.C6H4 OCH2C#CH CONH2 A 130-132 4 4-Br.C6H4 OCH2C#CH CN A 96-98 5 4-CH3O.C6H4 OCH2C#CH CONH2 A 6 4-CH3O.C6H4 OCH2C#CH CN A 7 4-CH3.C6H4 OCH2C#CH CONH2 A 8 4-CH3.C6H4 OCH2C#CH CN A 9 4-CN.C6H4 OCH2#CH CONH2 A 10 4-CN.C6H4 OCH2C#CH CN A 11 4-Cl.C6H4 OCH2C#CCH3 CONH2 A 131-134 12 4-Cl.C6H4 OCH2C#CCH3 CN A 92-93 13 4-Cl.C6H4 OC(CH3)2C#CH CONH2 A 14 4-Cl.C6H4 OC(CH3)2C#CH CN A 143-145 15 4-Cl.C6H4 OCH2C#CI CONH2 A 16 4-Cl.C6H4 OCH2C#CI CN A 17 4-Cl.C6H4 OCH2C#CBr CONH2 A 18 4-Cl.C6H4 OCH2C#CBr CN A 19 4-Br.C6H4 OCH2C#CH CSNH2 E 145-146 20 4-Cl.C6H4 OCH2C#CH CSNH2 E 21 4-CH3.C6H4 OCH2C#CH CSNH2 E 22 4-Cl.C6H4 OCH(CH3)C#CH CN D 80-81 23 4-CF3.C6H4 OCH2C#CH CN A 24 4-NO2.C6H4 OCH2C#CH CN A 25 4-C2H5.C6H4 OCH2C#CH CN A 26 4-C2H5O.C6H4 OCH2C#CH CN A 27 2-Cl-5-pyridyl OCH2C#CH CN D 110-112 28 2-naphthyl OCH2C#CH CN A 29 2-Cl-5-thienyl OCH2C#CH CN A 30 2-Br-5-furyl OCH2C#CH CN A 31 4-Cl.C6H4 SCH2C#CH CN D The invention further provides processes for preparing compounds of formula (I) above.Thus the compounds may be prepared, for example, by the process of Scheme A below: Scheme A (a) R1COCI+NH2CH2CNoR1CONHCH2CN (111)

Br (b) (llI)+brominating agenteRaCONHCHCONH2 (IV) XR2 (c) (IV)+R2XH4R1CONHCH CONH2 (V) (d) (V)+dehydrating agentR1CONH-CH CN (Vl) The process outlined in Scheme A begins with step (a), in which an acid chloride R1COCI is reacted with aminoacetonitrile by a conventional procedure to obtain the acylaminoacetonitrile derivative (III). This is then reacted in step (b) with a brominating agent (for example bromine in glacial acetic acid) to give the brominated derivative (IV).This bromination procedure also simultaneously hydrates the cyano group to a carbamoyl group -CON H2, and necessitates treatment with a dehydrating agent at a later stage to convert the carbamoyl group back into a cyano group. It may be possible to avoid the undesired conversion of the cyano group to carbamoyl by use of a different solvent or brominating agent and thereby shorten the process by making step (d) unnecessary.

In step (c),the bromo compound (IV) is reacted with an appropriate alcohol orthiol, of formula R2XH to obtain the carbamoyl compound (V). Preferably the reaction is carried out in a solvent; the solvent should be an aprotic solvent to avoid reaction of the solvent with the bromo-compound (IV). Preferably an acid acceptor is present in at least a stoichiometric proportion. Examples of acid acceptors include tertiary amines, for example triethylamine and pyridine. The reaction takes place readily even at ambient temperatures but may be accelerated if desired by heating for example to 1 00 C or above.

The intermediate compounds of formula IV and V are novel and constitute a further aspect of the present invention.

The final step (d) of Scheme A is the treatment of the carbamoyl compound (V) with a dehydrating agent to convert it to the corresponding cyano compound. The dehydrating agent may be, for example, a bi-molar amount of p-toluene sulphonyl chloride in pyridine as solvent and acid acceptor, or another dehydrating agent, for example phosphorus oxychloride-dimethylformamide. The reaction with p-toluenesulphonyl chloride proceeds readily at ambient temperature. Scheme A has been described in terms of brominated compounds; however, the scheme could equally be carried out using a chlorinating agent (eg. gaseous chlorine) in place of a brominating agent, to produce the chlorinated compound corresponding to compound (IV); this could then be used in step (c) in place of compound (IV). This route cannot be used where R1 is readily attacked by elemental bromine or chlorine.

A further process for making compounds of the invention is outlined in Scheme B, wherein R6 is C1--Cs alkyl: Scheme B (a) R1CONH2+HCO-0O2R6R1CONH-CH(OH)CO2R6 (Vll) (b) (Vll)+SOCI2oR1CONHCH(Cl)CO2R6 (veil)

(d) (IX)+NH3e(V) In step (a) of Scheme B, an amide R'CONH2 is condensed with a glyoxylic ester HCOCO2R6 to give the hydroxy intermediate (VII). The group R6 is an ester radical, for example an alkyl group of 1 to 4 carbon atoms (eg. a methyl group). In step (b), the hydroxy intermediate (VII) is treated with a chlorinating agent (eg. thionyl chloride) to convert it to the chloro- derivative (VIII).This is in turn reacted in step (c) with the appropriate alcohol,orthiol, R2XH to give the ester (IX). Treatment ofthis with ammonia in step (c) gives the carbamoyl derivative (V) which may then be converted to the cyano compound of the invention by the method of step (d) of Scheme A.

An alternative process for preparing the amide derivatives of the invention when X=0 in formula I is a variation of the Scheme B process above. This Scheme B variation is outlined below:

oR (b) R1CONH-CHCOOR6 (VII ) EIXR2 (H2so4 (H2S04 present as catalyst) XR2 ' CO & CH \ (IX) oCOOR6

XR2 XR2. (c) RlcONHd + CONHI + NH3 R1COLC-:cll COOR6 \ CONH2 (V) dehydrating XR2 / agent R1COSHCH CN (vI)

In this modified Scheme B procedure it can be seen that one can proceed directly from the hydroxy intermediate (VII) to the ester (IX) in one step. The ester (IX) is then treated with ammonia, as in step c, to produce the carbamoyl derivative (V) which in turn is converted to the cyano compound of the invention (VI) by means of the final step (step d) of the process of Scheme A.

Scheme C

XR2 dehydrating, (c) (XIV) + dehydrating , > R1CON CH ag ent / \tT H (xII) According to Scheme C, an amide R1CONH2 is first treated with sodium hydride and the anion so generated is then reacted with an alpha bromo ester R2X-CH(Br)0O2R6 to give the ester (X). This is then reacted with ammonia to give the amide (Xl), and finally (XI) is treated with a dehydrating agent to give the nitrile (XII).

A further method for preparing compounds of the invention is outlined in SchemeD.

SchemeD

XR2 (b) (XIII) c HXR2R1C3S (b) (xiii) + HXR2 Base ;' (xii) H According to Scheme D (III) is chlorinated (eg. with SO2CI2) or brominated (eg. with Cr2) in an aprotic solvent to give the highly reactive bromo- or chloro-derivative (XIII). This is treated with the appropriate alcohol or thiol in the presence of base to give the required nitrile (XII).

The chloro- or bromo- nitriles (XIII) are too unstable to be isolated and characterised, and are used within a short time after they are prepared. The final stage (b) of the scheme may conveniently be carried out by using an excess of the alcohol orthiol, and anhydrous potassium carbonate as the base. Triethylamine or other tertiary amines may also be used as the base.

Compounds of the invention in which the group E is a thiocarbamoyl radical may be prepared according to Scheme E below:

Scheme 2 or 2 XR2 XR S R1CONCH R1CON H) H3S R1CON n Pyr id in (xIv) e/Et,N 8 IINH2 H S S The reaction is conveniently carried out by passing gaseous H2S through a solution of the nitrile in a suitable solvent such as toiuene or pyridine containing a little triethylamine as catalyst. Usually the solution is externally cooled to 0-10". If the product does not separate from the solution, it may be isolated by removal of the solvent.

The amide derivatives of formula I, and compositions containing them, are variously active against a wide range of fungal diseases, particularly, for example, against: Plasmopara viticola (downy mildew) on vines and Phytophthora infestans (late blight) on potatoes and tomatoes and other species of Phytophthora Phytophthora parasitica, Phytophthora cinnamomi, Phytophthora palmivora and Phytophthora capsici on a range of commercially important crops Pseudoperonospora cubensis on cucu rbits Peronospora tabacina on tobacco Peronospora parasitica on cabbage Peronospora destructoron onions Bremia lactuca on lettuce Pythium species on a range of commercially important crops Other downy mildews and other fungal diseases, for example:: Venturia inaequalis (scab) on apples Cercospora arachidicola on peanuts and other Cercospora species, Pyricularia on rice, Xanthiomonas on rice and Fusaria cudmaria.

A particularly valuable feature of the activity of the amide derivatives is their systemic effect, ie. their ability to move in a plant to combat an infection or infestation remote from the site of initial application. Thus a derivative, or a composition containing it, may be applied to the soil surrounding the roots of a plant or to the seed or to other plant areas, eg. leaves, and be taken up by the plant through its roots, or other areas, to combat fungi locally or elsewhere on the plants.

In another aspect, therefore, the invention provides a process for combatting fungi, especially of inhibiting the growth of fungi on plants or seeds, which comprises applying to the plants, or the locus thereof, or to seeds, a fungicidally effective amount of a compound of the formula (I) as hereinbefore defined. The amount of the compound may vary, depending upon the identity of the particular compound chosen, the fungal species whose growth is to be inhibited, and the plant or locus involved.

The skilled worker in the fungicide art will readily be able to establish appropriate application rates by standard procedures without undue experimentation.

Preferred compounds for use in the fungicidal compositions of the invention and the process for combatting fungi are those defined in detail above with reference to formula I wherein R' is optionally-substituted phenyl, or heterocyclyl, for example 2-chloro-5-pyridyl, X is O or S (X is preferably 0) and R2 is optionally substituted C-C7 alkynyl, and E is CN or CSNH2.

Preferred phenyl substitution, when R1 is phenyl, is at the 3,4 or 5 positions and is alkyl, alkoxy, methylenedioxy or halogen.

The compounds used in the process and compositions of the invention are preferably applied in the form of a composition, in which the active ingredient is mixed with a carrier comprising a solid or liquid diluent. In another aspect, therefore, the invention provides a fungicidal composition, comprising as an active ingredient a compound of the formula (I) as hereinbefore defined, in admixture with a solid or liquid diluent. Preferably the composition also comprises a surface-active agent.

The amide derivatives may be used as such for anti-fungal purposes but are more conveniently formulated into compositions for such usage.

The amide derivatives and compositions containing them can be used to combat plant fungi and treat plants or seeds in a number of ways, for example they can be applied, formulated or unformulated, directly to the foliage of a plant which is infected or likely to become infected, or they can be applied also to bushes and trees, to soil or to other medium in which plants, bushes or trees are growing or to be planted, or they can be sprayed on, dusted on or applied as a cream or paste formulation. Application can be to any part of the plant, bush or tree, for example to the foliage, stems, branches, seeds or roots, orto the soil surrounding the roots.

The terms 'combatting" and "treatment" as used herein embrace all the foregoing modes of application and the term "plant" includes seedlings, bushes and trees. Furthermore, the method of the invention includes protectant, prophylactic a nd and eradicanttreatment.

The derivatives are preferably used for agricultural and horticultural purposes in the form of compositions.

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, for example ordinary grains or "slow release" granules wherein the active ingredient is mixed with a solid diluent or carrier, for example, a natural clay including kaolin, bentonite, kieselguhr, dolomite, Fuller's earth, gypsum, Hewitt's earth, diatomaceous earth and China clay; or powdered magnesia, silica or talc.

Compositions for dressing seed may, for example, comprise an agent (for example a mineral oil) for assisting the adhesion of the composition to the seed.

The compositions may also be in the form of dispersible powders 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 dispersion of emulsions may be prepared by dissolving the active ingredient(s) in an organic solvent which may contain wetting, dispersing or emulsifying agent(s) and then adding the mixture so obtained to water which may also contain wetting, dispersing or emulsifying agent(s). Suitable organic solvents are ethylene dichloride, isopropyl alcohol, propyiene glycol, diacetone alcohol, toluene, kerosene, methylnaphthalene, xylenes and trichloroethylene.

The compositions for spraying may also be in the form of aerosols wherein the formulation is held in a propellant, eg. fluorotrichloromethane or dichlorodifluoromethane.

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

The derivatives can be used in smoke generators and also as mixtures with fertilisers (eg. nitrogen- or phosphorus containing fertilisers). Compositions comprising only granules of fertilisers incorporating, for example coated with, the derivative, are preferred.

The invention therefore also provides a fertiliser composition comprising the derivative and a fertiliser.

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 surface active agent(s), dispersing agent(s), emulsifying agent(s) or 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 dodecylbenzene-sulphonate, sodium, calcium or ammonium lignosulphonate di-isopropyl- and triisopropylnaphthalene sulphonates).

Suitable non-ionic agents are the condensation products of ethylene oxide with fatty alcohols such as oleyl alcohol on ethyl alcohol, orwith alkyl phenols such as octylphenol, nonylphenol 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 ocide, and the lecithins. Suitable suspending agents are hydrophilic colloids (for example polyvinylpyrrolidone and sodium carboxymethyicellulose), 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), the concentrate to be diluted with water before use. These concentrates often should be able to withstand storage for prolonged periods and after such form aqueous preparations which remain homogenous for a sufficient time to enable them to be applied by conventional spray equipment. The concentrates may conveniently contain 10-85%, generally 25-60%, by weight of the active ingrendient(s).

When diluted 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% or 0.01% to 10% by weight or active ingredient(s) may be used.

The compositions of this invention can comprise also other compound(s) having biological activity, eg.

compounds having similar or complementary fungicidal or plant growth regulating activity or compounds having herbicidal or insecticidal activity.

The other 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 or cercospora on a variety of crops, or other diseases such as Cercosporella herpotrichoides on cereals. These mixtures of fungicides can have a broader spectrum of activity than the compound of general formula (I) alone; further the other fungicide can have a synergistic effect of the fungicidal activity of the compound of general formula (I).

Examples of otherfungicidal compound are imazalil, benomyl, carbendazim (BCM),thiophanate-methyl, captafol, captan, folpet, sulphur, dithiocarbamates, carbathiins, dicarboximides (including iprodione, vinchlozolin, procymidone), copper oxychloride, triforine, dodemorph, tridemorph, dithianon, pyrazophos, binapacryl, "Topaz", fenarimol, quinomethionate, panoctine, furalaxyl, aluminium tris(ethylphosphate), cymoxanil, ethirimol, dimethirimol, bupirimate, metalaxyl, oxadixyl, benaboxyl, ofurace, chlorothalonil, metazanine and ergosterol-synthesis inhibiting fungicides other than those here disclosed.

Suitable insecticides are pirimor, croneton,dimethoate, metasystox, formothion, and pyrethroid compounds.

The other plant growth regulating compound can be one which controls weeds or seedhead formation, improves the level of longevity of 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 be herbicides. Examples of suitable agents 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 BAP), phenoxyacetic acids (eg. 2,4-D or MCPA), substituted benzoic acids (eg. TIBA), morphactins (eg. chlorfluorecol), maleic hydrazide, glyphosate, glyphosine, long chain fatty alcohols and acids (eg. Off Shoot O or Off Shoot T), dikegulac, Sustar, Embark, substituted quaternary ammonium and phosphonium compounds (eg. 000 or Phosfon-D), Ethrel, carbetamide, Racuza, Alar, asulam, abscissic acid, isopyrimol, RH531, hydroxybenzonitriles (eg. bromoxynil), Avenge, Suffix or Lontrel.

The invention is illustrated by the following Examples, in which unless otherwise stated all parts are by weight and temperatures in degrees Celsius. The Examples that describe chemical syntheses give details in some cases of the nuclear magnetic resonance (N MR) spectra of the compounds. The information given is the chemical shift (3) for each peak in the spectrum together with a symbol to indicate the nature of the peak, as follows: s(singlet); d(doublet); m(multiplet); q(quartet); t(triplet). The solvent used was fully deuterated dimethyl sulphoxide or deuterochloroform (CDCI3). Information is also given on infra-red (IR) spectra of the compounds. The information given is the transmission for each peak together with a symbol to indicate the size of the peak; s(strong); w(weak).

Example 1 This Example illustrates the preparation of compound no.1 of Table I by the process of Scheme A.

(a) Preparation of Cchlorobenzoylamin o(brom o)acetamide To a suspension of 4-chloro benzoylaminoacetonitrile (5g) in stirred glacial acetic acid (50ml) was added all at once bromine (5.0g). After a brief induction period, the bromine colour was discharged and the product (5.8gì precipitated from the acetic acid. The product was filtered off, washed with glacial acetic acid, and then with anhydrous ether, and dried. A sample crystallised from glacial acetic acid had m.p. 157 (dec).

(b) Preparation of4-chlorobenzoylamino (propargyloxy) acetamide

The bromoamide (10.5g) prepared according to (a) above was added in one portion to propargyl alcohol stirred at room temperature for 3 hours and then stood for 48 hours. Excess alcohol was evaporated under reduced pressure and the brown oil obtained triturated with ethyl acetate/ether to give the product as a brown solid (2.4gì mpt 123-5 C. The filtrate deposited more solid which was washed with chloroform to give a white powder, (0.9g) mpt 124-6 C.

NMR(DMSO-d6ì 63.40 (t,1 H), 4.21 (d,2H), 5.60(d,1 H), 7.45(S,2H), 7.50(d,2H), 7.90(d,2H), 9.20(d,1 H).

IR (nugol) cm~1 3470(s), 3250(b), 2125(w), 1680(b) Example 2 This example illustrates the preparation of 4-chlorobenzoylamino(propargyloxy)acetonitrile having the structural formula

Phosphorus oxychloride (1.07gì was added dropwise to dry DMF(5ml) of 000. After 15 minutes this solution was added in one portion to a stirred solution of the propargyl amide (1.50g) prepared according to Example 1 in dry DMF (15ml) at 000. The resulting brown solution was stirred at OOC for 20 minutes, then poured into water (200ml) and extracted twice with ether (50ml).The ether extracts were washed with water, dried over magnesium sulphate and evaporated to give a brown oil, (1.1g). This was purified by flash chromatography on silica gel, eluting with ethyl acetate, to give the product as pale orange crystals (0.789), mpt 84-7 C.

MNR (CDCl3)#2.56(t, 1H), 4.43(d, 2H), 6.50(d, 1H), 7.48(d, 2H), 7.90(d, 2H), 8.30(d, 1H) IR (nujol) cm-1 3290(sd), 2120(w), 1670(s) Example 3 This example illustrates the preparation of compound no 3 of table I, having the chemical name Preparation of 4-bromobenzoylamino(propargyloxy)acetamide and having the structural formula:

The coresponding bromoamide (10.09) prepared similarly to the method of Example I was suspended in propargyl alcohol and the mixture stirred for 6 hours and then stood overnight. A small amount of solid was filtered, and the filtrate evaporated under reduced pressure. The residual oil and solid was stirred for 1 hour with 10% ammonium hydroxide (50ml). The solid suspension was then filtered and dried over P205 to give a buff coloured solid (6.07g).Recrystallisation from toluene gave a buff solid (4.729) mpt 130-132"C.

NMR (DMSO-d6)63.40(t,l H), 4.20(d,2H), 5.56(d,lH), 7.40(bs,2H), 7.62(d,2H), 7.80(d,2H), 9.18(d,lH) IR (nujol) cm-l 3470(s), 3270(s), 3230(s), 2105(w), 1715(s), 1650(s) Example 4 This example illustrates the preparation of compound no 4 of table I having the chemical name Preparation of4-bromobenzoylamino (propargyloxy)acetonitrile and having the structural formula:

Phosphorus oxychloride (1.95g) was added to dry DMF (4ml) at 0 C, and the solution stirred for 10 minutes, and then added to the propargyl amide (3.119) prepared according to Example 3 in dry DMF (4ml) at 0 C. After the initial exothermic reaction the mixture was cooled to 0 C and stirred for 1 hour.It was then poured into water and the mixture extracted with ether, and the ethereal extracts dried over magnesium sulphate and evaporated to yield a brown oil which crystallised (2.969). The solid was purified by flash chromatography on silica gel, eluting with light petroleum (60:80)/ethyl acetate 6:1,to give white crystals (2.059), mpt 96-98 C.

NMR (CDCl3)#2.58(t, 1H), 4.39(d,2H), 6.44(d,lH), 7.65(m,4H) IR (nujol) cm-' 3300(s), 2110(w), 1675(s) Example 5 Preparation of2-chloro-5-pyridinecarbonylamino(propargloxy)acetonitrile and having the structural formula:

To a stirred solution of 2-chloro-5-pyridinecarbonylamino acetonitrile (1.96g) in dry ethyl acetate (25my) at 42"C, was added bromine (1.6g) dropwise. After completion of the addition the mixture was stirred for 10 minutes and then filtered. To the filtrate was added propargyl alcohol (semi) foilowed by triethylamine (2.029) in dry ethyl acetate (35 ml).The white precipitate at once formed was filtered, the filtrate washed with water, dried over MgSO4 and evaporated to give a red-brown oil.

The compound was purified by HPLC on Merck 9385 silica gel, eluting with light petroleum (60:80)/ethyl acetate 3:1, to give an oil which crystallised. Recrystallisation from ether/petrol afforded a white solid (0.21 gì mpt=110-112 C.

NMR (CDC13)82.60(t,1 H),4.39(d,2Hì, 6.39 (d, 1 H); 7.40-7.60 (m,1 H); 8.39 (d,1 h); 8.84 m,1 H).

IR (nujol) cm- 3300 (sharp), 3260 (S), 2120 (W), 1670 (S).cm-' Example 6 This example illustrates a composition according to the invention which comprises an emulsifiable concentrate. The following ingredients were thoroughly mixed to give a solution Compound No. 1 of Table I 10% Ethylene dichloride 40% Calcium dodecylbenzenesulphate 5% "Lubrol" L 10% "Aromasol" H 35% Example 7 A composition in the form of grains readily dispersible in a liquid, eg. water, was prepared by grinding together the first three ingredients in the presence of added water and then mixing in the sodium acetate. The resultant mixture was dried and passed through a British Standard mesh sieve, size 44-100, to obtain the desired size of grains.

Compound No. 2 of Table I 50% "Dispersol" T 25% Lubrol"APN5 1.5% Sodium acetate 23.5% Example 8 The following ingredients were ground together to produce a powder formulation readily dispersible in liquids.

Compound No.3 of Table I 45% "Dispersol" T 5% "Lissapol" NX 0.5% "Cellofas" B600 2% Sodium acetate 47.5% Example 9 The active ingredient was dissolved in acetone and the resultant liquid was sprayed on to the granules of china clay. The solvent was then allowed to evaporate to produce a granular composition.

Compound No 4 of Table I 5% China clay granules 95% Example 10 A composition suitable for use as a seed dressing was prepared by mixing the following three ingredients.

Compound No. 1 of Table I 50% Mineral oil 2% China clay 48% Example 11 A dusting powder was prepared by mixing the active ingredient with talc.

Compound No.2 of Table I 5% Talc 95% Example 12 A Col formulation was prepared by ball-milling the constituents set out below and then forming an aqueous suspension of the ground mixture with water.

Compound No.3 of Table I 40% "Dispersol" T 10% "Lubrol" APN5 1% Water 49% Example 13 A dispersible powder formulation was made by mixing together the ingredients set out below and then grinding the mixture until all were thoroughly mixed.

Compound No.4 of Table 1 25% "Aerosol" OT/B 2% "Dispersol" A.C. 5% China clay 28% Silica 40% Example 14 This Example illustrates the preparation of a dispersible powder formulation. The ingredients were mixed and the mixture then ground in a comminution mill.

Compound No. 1 of Table 1 25% "PERMINAL" BX 1% "Dispersol" T 5% Polyvinylpyrrolidone 10% Silica 25% China clay 34% Example 15 The ingredients set out below were formulated into a dispersible powder by mixing then grinding the ingredients.

Compound No. 2 of Table I 25% "Aerosol" OT/B 2% "Dispersol" A 5% China clay 68% In examples 5 to 14 the proportions of the ingredients are given by weight and the Examples were all repeated using, as active ingredient, the other compounds of Table I.

There now follows an explanation of the compositions or substances represented by the various Trade Marks and Trade Names mentioned above.

LUBROL L: a condensate of nonyl phenol (1 mole) with ethylene oxide (13 moles).

AROMASOL H: a solvent mixture of alkylbenzenes DISPERSOL T AND AC: a mixture of sodium sulphate and a condensate of formaldehyde with sodium naphthalene sulphonate LUBROLAPN 5: a condensate of nonyl phenol (1 mole) with ethylene oxide (5.5 moles) CELLOFAS B600: a sodium carboxymethyl cellulose thickener.

Example 16 The compounds were tested against a variety of mainly foliar fungal diseases of plants. The techniques were as follows: For all tests, plants were grown in John Innes Potting Compost (No 1 or 2) in 4cm diameter minipots. The test compounds were formulated either by bead milling with aqueous Dispersol T or as a solution in acetone or acetone/ethanol which was diluted to the required concentration immediately before use. For the foliar diseases, solutions and suspensions (100ppm ai) were sprayed on the foliage and applied to the roots of the plant via the soil. The sprays were applied to maximum retention and the root drenches to a final concentration equivalent to approximately 40ppm ai/dry soil. Tween 20, to give a final concentration of 0.05%, was added when the sprays were applied to cereals (ai means "active ingredient").

Most were protectant tests where the compound was applied to the soil and roots and to the foliage one or two days before the plant was inoculated with the pathogen. However, in the case of the test against Erysiphe graminis hordeithe treatment was eradicative and the compounds were applied one day after inoculation.

The foliar pathogens were applied by spraying spore suspensions onto the leaves of the test plants.

Cultures of the soil pathogens were mixed with vermiculite into which seed was sown prior to drenching with chemical.

After inoculation, the plants or pots with seed were placed in an appropriate environment to allow infection to proceed and then incubated until the disease was ready for assessment. The period between inoculation and assessment varied from four to fourteen days according to the disease and the environment.

Disease control was recorded using the following grading system: 4=no disease 3=trace to 5% of disease on untreated plants 2=625% of disease on untreated plants 1=26-59% of disease on untreated plants 0=60-100% of disease on untreated plants The results are shown in Table II below.

TABLE II Compound Vi Po Ca Pv Xo Fc Pu Number 1 0 0 0 0 0 0 0 2 4 0 3 4 0 0 3 3 0 0 0 0 0* 0 0 4 0 0 2 4 0* 2 1 11 0 0 0 0 3 2 0 12 0 2 0 0 0 0 0 14 0 0 0 3 0 - 19 0 0 3 3 0* 0 4 22 0 2 0 3 0 - A dash, thus "-", in the table in any column indicates that the particular compound was not tested against that particular disease * tested against Xm Vi=Venturia inaequalis Po=Pyricularia oryzae Ca=Cercospora arachidicola Pv=Plasmoparaviticola Xo=Xanthomonas oryzae Fc=Fusarium culmoru Pu=Pythium ultima Xm=Xanthomonas malvacearum

Claims (10)

1. A compound of the general formula IX

or a tautomer thereof where: R1 is an aryl or substituted aryl radical or a heterocyclyl or substituted heterocyclyl radical; R2 is an alkynyl radical or substituted alkynyl radical; R6 is C1-6 alkyl; and Xis oxygen or sulphur.

2. A compound according to Claim 1, wherein R1 is phenyl or substituted phenyl.

3. A compound according to Claim 1, wherein R1 is naphthyl or substituted naphthyl.

4. A compound according to Claim, 1, wherein R1 is an aryl or heterocyclyl radical substituted with one or more groups, which substituted group or groups may be chlorine, bromine or fluorine; C1 < alkyl; C1 < alkoxy; C1 < haloaikyl; nitro or cyano.

5. A compound according to Claim 1, wherein R' is 2-chloro-5-pyridyl.

6. A compound according to Claim 1, wherein R2 is an optionally-substituted Cy7 alkynyl group.

7. A process of preparing a compound as claimed in Claim 1, wherein an amide of general formula: R-CO-NH2, where R' is as defined in Claim 1, is condensed with a glyoxylic ester of general formula HCOCOOR6, where R6 is an alkyl group of 1 to 6 carbon atoms, to produce a hydroxy intermediate of general formula (VII):

said hydroxy intermediate is treated with a chlorinating agent to convert it to a chloro-derivative of general formula (VIII):

which is then reacted with an alcohol or thiol of general formula R2XH where R2 and X are as defined in Claim 1 to produce a compound as claimed in Claim 1.

8. A process according to Claim 7, wherein said chlorinating agent is thionyl chloride.

9. A process of preparing a compound as claimed in Claim 1 but wherein X is oxygen, wherein an amide of general formula: R1--COO-NH2, where R' is as defined in Claim 1, is condensed with a glyoxylic ester of general formula HCOCOOR6, where where R6 is an alkyl group of 1 to 6 carbon atoms, to produce a hydroxy intermediate of general formula VII:

said hydroxy intermediate is treated with an alcohol of general formula R2 OH, where R2 is as defined in Claim 1, using sulphuric acid as catalyst, to produce a compound as claimed in Claim 1.

10. A process of preparing a compound as claimed in Claim 1, wherein an amide of the general formula R1--Caa-NH2 is treated with sodium hydride and the anion so generated is then reacted with an alpha bromo ester of general formula

R2 and X are as defined in Claim 1 and R6 is an alkyl group of 1 to 6 carbon atoms, to produce a compound as claimed in Claim 1.