US20030130520A1

US20030130520A1 - Method of producing pesticides

Info

Publication number: US20030130520A1
Application number: US10/226,181
Authority: US
Inventors: Peter Maienfisch
Original assignee: Individual
Current assignee: Individual
Priority date: 1997-08-18
Filing date: 2002-08-22
Publication date: 2003-07-10
Also published as: HUP0003497A2; EP1005455A1; AU738428B2; AU9342398A; ID23446A; CA2300808A1; CN1271345A; RU2202544C2; WO1999009008A1; PL338645A1; KR20010022974A; US6462043B1; UA69387C2; JP2001515065A; HUP0003497A3; IL134549A0; BR9811912A

Abstract

A method of producing a compound of formula

and, if appropriate, the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form, wherein

R₁is hydrogen or C₁-C₄-alkyl;

R₂is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl or a radical —CH₂B;

Het is an unsubstituted or substituted heterocyclic radical; and

B is phenyl, 3-pyridyl or thiazolyl, which are optionally substituted;

characterised in that a compound of formula

Q—A—Q (IIa)

wherein A is a direct bond or an organic radical; or of formula

wherein U is an organic radical; and in compounds (IIa) and (IIb)

Q signifies

and R₁, R₂and Het are as defined above for formula (I), and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form, is hydrolysed;

and a method for producing the compounds of formulae (IIa), (IIb), (IIIa) and (IIIb); are described.

Description

The present invention relates to a novel type of method of producing substituted 2-nitro-guanidine derivatives.

It is known that, in order to produce 1,3-disubstituted 2-nitroguanidines, a further substituent may be introduced into monosubstituted 2-nitroguanidines (e.g. by alkylation) (see e.g. EP patent applications 0.375.907, 0.376.279 and 0.383.091). Owing to the presence of three reactive hydrogen atoms in the monosubstituted 2-nitroguanidines used as the starting material in these reactions, the previously proposed substitution reactions of this kind are often non-selective and lead to undesired substitution products. The mentioned EP patent applications describe the production of 1,3-disubstituted 2-nitroguanidines by reacting monosubstituted nitroisothioureas with primary amines whilst cleaving mercaptan. However, these nitroisothiourea compounds, containing alkylthio leaving groups, which are proposed as starting compounds in the known processes, can only be obtained with difficulty. In addition, in EP-A-0483.062, a method of producing the compounds of formula (I) by hydrolysis of hexahydro-triazines is described.

It has now been shown that the above-described methods of producing compounds of formula (I) do not satisfy the requirements in respect of purity and yield, for which reason there is therefore a need to provide improved methods of producing these compounds from readily available starting compounds. It has now surprisingly been found that the method according to the invention is able to satisfy these requirements to a large extent.

Accordingly, it is the aim of the present invention to provide an improved method of producing 1-monosubstituted and 1,3-disubstituted 2-nitroguanidines from readily obtainable starting compounds, which allows specific 1,3-disubstitution without obtaining major amounts of undesired by-products.

The object of the invention is

a) a method of producing a compound of formula

R ₁is hydrogen or C₁-C₄-alkyl;

R ₂is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl or a radical —CH₂B;

Het is an aromatic or non-aromatic, monocyclic or bicyclic heterocyclic radical which is unsubstituted or—depending on the substitution possibilities of the ring system—mono- to penta- substituted by substituents selected from the group comprising halogen, C ₁-C₃-alkyl, C₁-C₃-alkoxy, halogen-C₁-C₃-alkyl, C₁-C₃-halogenalkoxy, cyclopropyl, halogencyclopropyl, C₂-C₃-alkenyl, C₂-C₃-alkynyl, C₂-C₃-halogenalkenyl and C₂-C₃-halogenalkynyl, C₁-C₃-alkylthio, C₁-C₃-halogenalkylthio, allyloxy, propargyloxy, allylthio, propargylthio, halogenallyloxy, halogenallylthio, cyano and nitro; and

B is phenyl, 3-pyridyl or thiazolyl, which are optionally substituted by one to three substituents from the group comprising C ₁-C₃-alkyl, C₁-C₃-halogenalkyl, cyclopropyl, halogencyclopropyl, C₂-C₃-alkenyl, C₂-C₃-alkynyl, C₁-C₃-alkoxy, C₂-C₃-halogenalkenyl, C₂-C₃-halogenalkynyl, C₁-C₃-halogenalkoxy, C₁-C₃-alkylthio, C₁-C₃-halogenalkylthio, allyloxy, propargyloxy, allylthio, propargylthio, halogenallyloxy, halogenallylthio, halogen, cyano and nitro;

characterised by hydrolysing a compound of formula

Q—A—Q (IIa)

wherein A is a direct bond or an organic radical; or of formula

wherein U is an organic radical; and in compounds (IIa) and (IIb)

Q signifies

and R ₁, R₂and Het are as defined above for formula (I), and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form.

The compounds of formula (I) may be present as E/Z isomers, e.g. in the following two isomeric forms

Accordingly, any reference to compounds of formula (I) hereinbefore and hereinafter is understood to include also their corresponding E/Z isomers, even if the latter are not specifically mentioned in each case.

The compounds of formula (I) may be present partly in the form of tautomers, for example in the forms

Accordingly, any reference to compounds of formula (I) hereinbefore and hereinafter is understood to include also their corresponding tautomers, even if the latter are not specifically mentioned in each case.

The compounds of formula (I) and, where appropriate, the E/Z isomers and tautomers thereof, may be present as salts. Compounds of formula (I) having at least one basic centre may form e.g. acid addition salts. These are formed for example with strong inorganic acids, such as mineral acids, e.g. sulfuric acid, a phosphoric acid or a hydrohalic acid, or with strong organic carboxylic acids, such as C ₁-C₄alkanecarboxylic acids substituted where appropriate for example by halogen, e.g. acetic acid, such as optionally unsaturated dicarboxylic acids, e.g. oxalic, malonic, maleic, fumaric or phthalic acid, such as hydroxy-carboxylic acids, e.g. ascorbic, lactic, malic, tartaric or citric acid, or benzoic acid, or with organic sulfonic acids, typically C₁-C₄alkane or arylsulfonic acids substituted where appropriate for example by halogen, e.g. methane-, trifluoromethane- or p-toluene-sulfonic acid. Salts of compounds of formula (I) with acids of the said kind are preferably obtained when working up the reaction mixtures.

In a broader sense, compounds of formula (I) with at least one acid group can form salts with bases. Suitable salts with bases are for example metal salts, typically alkali or alkaline earth metal salts, e.g. sodium, potassium or magnesium salts, or salts with ammonia or an organic amine, such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower alkylamine, e.g. ethyl-, diethyl-, triethyl- or dimethylpropylamine, or a mono-, di- or trihydroxy-lower alkylamine, e.g. mono-, di- or triethanolamine. Corresponding internal salts where appropriate may also be formed. Preferred compounds within the scope of this invention are agrochemically advantageous salts. Hereinbefore and hereinafter, the free compounds of formula (I) are understood where appropriate to include also by analogy the corresponding salts, or the salts are understood to include also the free compounds of formula (I). The same applies to E/Z isomers and tautomers of compounds of formula (I) and salts thereof. The free form is preferred.

The statements made about the free compounds of formula (I) or the E/Z isomers and tautomers and salts thereof also apply by analogy to the compounds of formulae (IIa) and (IIb), as well as the compounds of formulae (IIa) and (IIIb) below.

In the definitions of the above formulae (I), (IIa), (IIb) and of the compounds of formulae (IIIa) and (IIIb) below, the individual generic terms are to be understood as follows:

The halogen atoms considered as substituents may be both fluorine and chlorine, and bromine and iodine, whereby fluorine, chlorine and bromine are preferred, especially chlorine. Halogen in this context is understood to be an independent substituent or part of a substituent, such as in halogenalkyl, halogenalkylthio, halogenalkoxy, halogencycloalkyl, halogenalkenyl, halogenalkynyl, halogenallyloxy or halogenallylthio. The alkyl, alkylthio, alkenyl, alkynyl and alkoxy radicals considered as substituents may be straight-chained or branched. Examples of such alkyls which may be mentioned are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec.-butyl or tert.-butyl. Suitable alkoxy radicals which may be mentioned are, inter alia: methoxy, ethoxy, propoxy, isopropoxy or butoxy and the isomers thereof. Alkylthio is for example methylthio, ethylthio, isopropylthio, propylthio or the isomeric butylthio. If the alkyl, alkoxy, alkenyl, alkynyl or cycloalkyl groups considered as substituents are substituted by halogen, they may be only partially halogenated or also perhalogenated. The above-mentioned definitions apply here to halogen, alkyl and alkoxy. Examples of the alkyl elements of these groups are methyl which is mono- to trisubstituted by fluorine, chlorine and/or bromine, such as CHF ₂or CF₃; ethyl which is mono- to pentasubstituted by fluorine, chlorine and/or bromine, such as CH₂CF₃, CF₂CF₃, CF₂CCl₃, CF₂CHCl₂, CF₂CHF₂, CF₂CFCl₂, CF₂CHBr₂, CF₂CHClF, CF₂CHBrF or CClFCHClF; propyl or isopropyl, mono- to heptasubstituted by fluorine, chlorine and/or bromine, such as CH₂CHBrCH₂Br, CF₂CHFCF₃, CH₂CF₂CF₃or CH(CF₃)₂; butyl or one of its isomers, mono- to nonasubstituted by fluorine, chlorine and/or bromine, such as CF(CF₃)CHFCF₃or CH₂(CF₂)₂CF₃; 2-chlorocyclopropyl or 2,2-difluorocyclopropyl; 2,2-difluorovinyl, 2,2-dichlorovinyl, 2-chloroalkyl, 2,3-dichiorovinyl or 2,3-dibromovinyl.

If the defined alkyl, alkoxy or cycloalkyl groups are substituted by other substituents, they may be mono- or repeatedly substituted by identical or different substituents from those listed. In the substituted groups, it is preferable for one or two further substituents to be present. The cycloalkyl radicals considered as substituents may be, for example, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl. Alkenyl and alkynyl groups contain an unsaturated carbon-carbon bond. Typical representatives are allyl, methallyl or propargyl, but also vinyl and ethynyl. The double or triple bonds in allyloxy, propargyloxy, allylthio or propargylthio are separated from the connection point to the hetero atom (O or S) preferably by a saturated carbon atom.

As with the above-mentioned alkyl, alkenyl and alkynyl groups, the alkylene, alkenylene and alkynylene groups defined in the following may also be straight-chained or branched. Examples are —CH ₂—CH₂—, —CH₂—CH₂—CH₂—, —CH₂—CH₂—CH₂—CH₂—, —CH₂—C(CH₃)H— and —C(CH₃)H—C(CH₃)H—. The alkylene, alkenylene, alkynylene, cycloalkylene, arylene or heterocyclyl groups listed below are, where appropriate, substituted in the same way as the above-mentioned alkyl, alkenyl and alkynyl groups.

Aryl or arylene signifies phenyl or naphthyl, or phenylene or naphthylene, especially phenyl or phenylene.

In the context of the present invention, the heteroaryl radical indicated as Het signifies preferably a 5- to 7-membered, aromatic or non-aromatic ring with one to three hetero atoms selected from the group comprising N, O and S. Preference is given to aromatic 5- and 6-rings, which have a nitrogen atom as the hetero atom and optionally one further hetero atom, preferably nitrogen, oxygen or sulphur, especially nitrogen.

It has now surprisingly been found that the method according to the invention is able to satisfy the requirements mentioned initially.

The hydrolysis process according to the invention may be carried out both in an acidic and in a basic medium. In the acidic range, pH values of 6 or less, especially 1 to 3, are preferred.

In the basic range, a pH value greater than 7 and up to 12, especially 8 to 12, in particular 8 to 10, is preferred. The reaction is carried out at normal pressure and at a temperature of 0 to 120° C., preferably 20 to 80° C.

The reaction is carried out in a solvent or diluent that is inert towards the reaction components. Suitable solvents are, in particular, alcohols such as methanol, ethanol, propanol and isopropanol, as well as especially water. Further appropriate solvents are e.g. ethers, such as tetrahydrofuran and dioxane, as well as other solvents which do not adversely affect the reaction. The solvents may also be used as mixtures. A compound of formula (II) is preferably hydrolysed in an aqueous medium or in a mixture of water with an alcohol.

Suitable acids for carrying out the process are preferably mineral acids, e.g. sulfuric acid, a phosphoric acid or a hydrohalic acid, an organic carboxylic acid, typically C ₁-C₄alkane-carboxylic acids substituted where appropriate for example by halogen, e.g. acetic acid, such as dicarboxylic acids that are unsaturated where necessary, e.g. oxalic, malonic, maleic, fumaric or phthalic acid, typically hydroxycarboxylic acids, e.g. ascorbic, lactic, malic, tartaric or citric acid, or benzoic acid, or an organic sulfonic acid, typically C₁-C₄alkane- or aryl-sulfonic acids substituted where appropriate for example by halogen, e.g. methanesulfonic or p-toluenesulfonic acid.

Suitable bases for carrying out the process are preferably hydroxides of alkali metals and alkaline earth metals, such as NaOH and KOH, carbonates such as Na ₂CO₃, NaHCO₃, K₂CO₃; phosphates such as Na₃PO₄, Na₂HPO₄, alcoholates such as sodium methanolate, sodium ethanolate and K-tert.-butanolate, organic amines such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower alkylamine, e.g. ethyl-, diethyl, triethyl- or dimethyl-propyl-amine, or a mono-, di- or trihydroxy lower alkylamine, e.g. mono-, di- or triethanol-amine, or dialkylaniline, for example N,N-dimethyl- or N,N-diethylaniline, as well as salts of organic acids, such as sodium acetate, potassium acetate or sodium benzoate, or mixtures thereof, for example acetate or phosphate buffers.

Especially advantageous reaction conditions are described in the examples.

The method according to the invention is preferably used to produce compounds of formula (I) in which the heterocyclic radical Het is unsaturated and is bonded by a carbon atom as a ring member to the fundamental substance. Especially preferred radicals Het are pyridyl, thiazolyl, tetrahydrofuranyl, dihydrofuranyl, furanyl, N-oxido-pyridinio, oxazolyl, isoxazolyl, thienyl, morpholinyl, piperidinyl, pyridinyl and pyrazinyl; particularly pyridyl, thiazolyl, tetrahydrofuranyl and N-oxido-pyridinio, most particularly 3-pyridyl, 2-halogenpyrid-5-yl, 2,3-dihalogenpyrid-5-yl, 2-halogenthiazol-5-yl, tetrahydrofuran-3-yl, 2-methyl-tetra-hydrofuran-4-yl, 1-oxopyrid-3-yl, 1 -oxo-2-halogenpyrid-5-yl and 1-oxo-2,3-dihalogenpyrid-5-yl.

Equally preferably, the heterocycles Het carry one to three substituents from the group halogen, C ₁-C₃-alkyl, C₁-C₃-halogenalkyl and C₁-C₃-halogenalkoxy each with 1 to 7 halogen atoms, and C₁-C₃-alkoxy, most preferably chlorine or methyl.

Furthermore, compounds of formula (I) are preferably produced according to the invention, in which the radical B is a phenyl, pyridyl or thiazolyl radical that is unsubstituted or may be substituted by one to two radicals from the group halogen, C ₁-C₃-alkyl, C₁-C₃-halogenalkyl and C₁-C₃-halogenalkoxy each with 1 to 7 halogen atoms, and C₁-C₃-alkoxy.

Of the compounds of formula (I) to be produced according to the invention, the notable ones are those in which

R ₁is hydrogen;

R ₂is hydrogen, C₁-C₃-alkyl or cyclopropyl; especially hydrogen, methyl, ethyl or cyclopropyl, in particular methyl; and

Het is pyridyl, 1-oxopyridyl, tetrahydrofuranyl, thiazolyl; or pyridyl, 1-oxidopyridinio, tetra-hydrofuranyl or thiazolyl, respectively substituted by one to three substituents from the group halogen, C ₁-C₃-alkyl, C₁-C₃-halogenalkyl as well as C₁-C₃-halogenalkoxy with 1 to 7 halogen atoms and C₁-C₃-alkoxy;

especially 2-chloropyrid-5-yl, tetrahydrofuran-3-yl, 2-methyl-tetrahydrofuran-4-yl or 2-chloro-thiazol-5-yl.

To carry out the process according to the invention, on the one hand preferably those compounds of formula (IIa) are used, in which A is straight-chained or branched C ₂-C₂₀-alkylene, C₂-C₂₀-alkenylene, C₂-C₂₀-alkynylene, C₃-C₁₂-cycloalkylene, arylene or hetero-cyclylene; whereby the groups C₂-C₂₀-alkylene, C₂-C₂₀-alkenylene, C₂-C₂₀-alkynylene, C₃-C₁₂-cycloalkylene, arylene and heterocyclylene are optionally substituted once or several times, independently of each other, and the groups C₂-C₂₀-alkylene, C₂-C₂₀-alkenylene and C₂-C₂₀-alkynylene are optionally interrupted once or several times, independently of each other, by O, N—H or N—C₁-C₁₂-alkyl, C₃-C₉-cycloalkylene, arylene or heterocyclylene; or a group —D₁—D₂—D₃—; wherein

D ₁and D₃, independently of each other, signify optionally substituted C₃-C₁₂-cycloalkylene or arylene and D₂signifies C₂-C₂₀-alkylene, C₂-C₂₀-alkenylene, C₂-C₂₀-alkynylene, O, N—H or N—C₁-C₁₂-alkyl.

Particularly preferred bridging members A are C ₂-C₁₂-alkylene, C₂-C₁₂-alkylene interrupted by one or two phenylene, cyclohexylene or piperazinylene radicals; cyclohexylene or phenylene; or the group —D₁—D₂—D₃—, wherein D₁and D₃are phenylene or dicyclohexylene and D₂is O or C₂-C₄-alkylene; A especially signifies C₂-C₄-alkylene.

On the other hand, in order to carry out the process according to the invention, preferably compounds of formula (IIb) are used as the starting material, wherein U is aryl, heterocyclyl, C ₃-C₁₂-cycloalkyl or a group

wherein

A ₁, A₂and A₃independently of one another, have the same significances as given above for A in formula (IIa), and

X signifies N or CH.

Heterocyclyl A and U in the compounds of formulae (IIa) and (IIb) is preferably an aromatic or non-aromatic, three- to ten-membered ring. If the rings A and U are aromatic, they are preferably the same rings as defined above for Het. If the rings A and U are non-aromatic heterocyclic rings, they are especially piperidinyl, piperazinyl, morpholinyl, pyrrolidinyl, tetrahydrofuranyl and dioxolanyl. The radicals A ₁, A₂and A₃independently of one another are most preferably C₂-C₄-alkylene, especially ethylene.

A further object of the invention is

b) a method of producing a compound of formula (IIa) and (IIb), in which a compound of formula

T—A—T (IIa)

or of formula

wherein A and U have the same significance as defined above for formulae (IIa) and (IIb);

and R ₂has the same significance as defined above for formula (I); and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form, is reacted when producing a compound of formula (IIIa) with two equivalents or when producing a compound of formula (IIIb) with three equivalents of a compound of formula

which is known or may be produced analogously to methods known per se, wherein R. and Het are defined as given above for formula (I) and Y is a leaving group, preferably in the presence of a base.

The following may be considered as the leaving group Y in the context of the described method of operation: halogen, preferably chlorine, bromine or iodine, especially chlorine, or sulfonic acid radicals, such as alkylsulfonic acid radicals, mesylate or tosylate.

The process step according to b) may be carried out preferably at normal or at a slightly raised pressure and in the presence of preferably aprotic solvents or diluents. Suitable solvents or diluents are e.g. ethers and ether-type compounds, such as diethyl ether, dipropyl ether, dibutyl ether, dioxane, dimethoxyethane and tetrahydrofuran; aliphatic, aromatic and halogenated hydrocarbons, especially benzene, toluene, xylene, chloroform, methylene chloride, carbon tetrachloride and chlorobenzene; nitriles such as acetonitrile or propionitrile; dimethyl sulfoxide or dimethyl formamide, as well as mixtures of these solvents. This process step is generally carried out at a temperature of −20° C. to +140° C., preferably between 0° C. and +120° C., preferably in the presence of a base. Suitable bases are e.g. carbonates, such as sodium and potassium carbonate. Hydrides may also be used as bases, for example sodium hydride, potassium hydride and calcium hydride. If required, the reaction can also be carried out in the presence of a catalyst, e.g. cesium chloride.

A further object of the invention is

c) a method of producing the compounds of formula (IIIa) and (IIIb), in which a compound of formula

H₂N—A—NH₂ (Va)

or

and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form, wherein A and U have the same significance as defined above for the compounds of formulae (IIa) and (IIb), and which are known or may be produced analogously to methods known per se, is reacted when producing a compound of formula (IIIa) either with two equivalents, or when producing a compound of formula (IIIb) with three equivalents of a compound of formula

which is known or may be produced analogously to methods known per se, and wherein R ₂has the same significance as defined for formula (I), in the presence of an excess of formaldehyde or paraformaldehyde.

The process according to c) for the preparation of the compounds of formula (III) is advantageously carried out at normal pressure, but also optionally at a raised pressure in the presence of an inert solvent and at temperatures of between 0° C. and +140° C., preferably between +20° C. and +120° C. Suitable solvents are, in particular, alcohols such as methanol, ethanol, and propanol, as well as water. Further suitable solvents are eg. aromatic hydrocarbons, such as benzene, toluene and xylene; ethers such as tetrahydrofuran, dioxane and diethyl ether, halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride and chlorobenzene, as well as other solvents which to not impair the reaction. The solvents may also be used as mixtures. The process is optionally effected adding an acidic catalyst, such as HCl, H ₂SO₄or a sulfonic acid, such as p-toluene-sulfonic acid. The resulting reaction water may be removed, if desired, using a water separator or by adding a molecular sieve.

A further object of the invention is

d) a method of producing a compound of formula (I), in which a compound of formula (Va) or (Vb) is converted into a compound of formula (IIIa) or (IIIb) by reacting it with a compound of

c) a method of producing the compounds of formula (IIa) and (IIIb), in which a compound of formula

H₂N—A—NH₂ (Va)

or

The process according to c) for the preparation of the compounds of formula (III) is advantageously carried out at normal pressure, but also optionally at a raised pressure in the presence of an inert solvent and at temperatures of between 0° C. and +140° C., preferably between +20° C. and +120° C. Suitable solvents are, in particular, alcohols such as methanol, ethanol, and propanol, as well as water. Further suitable solvents are e.g. aromatic hydrocarbons, such as benzene, toluene and xylene; ethers such as tetrahydrofuran, dioxane and diethyl ether, halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride and chlorobenzene, as well as other solvents which to not impair the reaction. The solvents may also be used as mixtures. The process is optionally effected adding an acidic catalyst, such as HCl, H ₂SO₄or a sulfonic acid, such as p-toluene-sulfonic acid. The resulting reaction water may be removed, if desired, using a water separator or by adding a molecular sieve.

A further object of the invention is

d) a method of producing a compound of formula (I), in which a compound of formula (Va) or (Vb) is converted into a compound of formula (IIIa) or (IIIb) by reacting it with a compound of formula (VI) and formaldehyde or paraformaldehyde; this compound of formula (IIIa) or (IIIb) is converted by a compound of formula (IV) into a compound of formula (IIa) or (IIb) and this compound of formula (IIa) or (IIb) is hydrolysed.

Further objects of the invention are the compounds of formulae (IIa), (IIb), (IIIa) and (IIIb), and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form.

Especially preferred embodiments of the method according to variants b) to d) may be taken from the examples.

The compounds of formula (I) produced according to the invention are known. They are valuable active ingredients in pest control, that are well tolerated by warm-blooded animals, fish and plants. The compounds of formula (I) are especially suitable for the control of insects and arachnids, which appear on crops and ornamentals in agriculture, especially in cotton, vegetable and fruit plantations, in forestry, in the protection of stock and material, as well as in the hygiene sector, especially on domestic animals and productive livestock. The compounds are especially effective against plant-damaging sucking insects, especially against aphids and plant and leaf hoppers.

EXAMPLE P1.1

Preparation of the Compound of Formula

[0079]
A mixture of 3.0 g of 1-methyl-2-nitroguanidine, 0.85 g of 1,2-diaminoethane, 15 ml of dioxane and 5.7 ml of a 37% solution of formaldehyde in water at room temperature is heated to 50° C. and stirred at this temperature for 4 hours. The mixture is then evaporated to dryness under vacuum, the residue stirred with diethyl ether and the title compound isolated by filtration. M.p. 222-223° C. (compound 1.1). [0080]

EXAMPLE P1.2

Preparation of the Compound of Formula

[0081]
A mixture of 1.8 g of 1-methyl-2-nitroguanidine, 1.35 g of paraformaldehyde and 0.78 g of 1,5-diamino-3-oxa-pentane in 20 ml of toluene and 20 ml of dioxane is mixed at room temperature with two drops of a 37% solution of HCl in water, then heated to reflux temperature and stirred at this temperature for 6 hours. The mixture is then evaporated to dryness under vacuum, the residue stirred with diethyl ether and the title compound isolated by filtration (compound 1.15). [0082]

EXAMPLE P1.3

Preparation of the Compound of Formula

[0083]
A mixture of 8.0 g of 1-methyl-2-nitroguanidine and 3.0 g of 1,4-diaminobutane in 25 ml of ethanol is mixed at room temperature with 25 ml of a 37% solution of formaldehyde in water, heated to 50° C. and stirred at this temperature for 16 hours. Then, the mixture is evaporated to dryness under vacuum, and the residue is stirred with ethanol. The title compound is obtained with a melting point of 232-234° C. (compound 1.4). [0084]

EXAMPLE P1.4

[0085]
A mixture of 6.0 g of 1-methyl-2-nitroguanidine and 5.4 g of 4,9-dioxa-1,12-diaminododecane in 25 ml of ethanol is mixed at room temperature with 19 ml of a 37% solution of formaldehyde in water, heated to 50° C. and stirred at this temperature for 16 hours. Then, the mixture is cooled to 5° C., filtered and the residue washed with a little ethanol. The title compound is obtained with a melting point of 140-143° C. (compound 1.14). [0086]

EXAMPLE P1.5

The following compounds listed in Table I can also be obtained analogously to the above methods of examples P1.1 to P1.4.

TABLE 1


Compounds of formula

No.	A	phys. data

1.1	—(CH₂)₂—	m.p. 222-
		223° C.
1.2	—CH(CH₃)—CH₂—
1.3	—(CH₂)₃—
1.4	—(CH₂)₄—	m.p. 232-
		234° C.
1.5	—(CH₂)₅—
1.6	—(CH₂)₆—
1.7	—(CH₂)₇—
1.8	—(CH₂)₈—
1.9	—(CH₂)₉—
1.10	—(CH₂)₁₀—
1.11	—(CH₂)₁₂—
1.12	—CH₂—C(CH₃)₂—CH₂—
1.13	—CH₂—CH(OH)—CH₂—
1.14	—(CH₂)₃—O—(CH₂)₄—O—(CH₂)₃—	m.p. 140-
		143° C.
1.15	—CH₂—CH₂—O—CH₂—CH₂—
1.16	—CH₂—CH(CH₃)—(CH₂)₃—
1.17	—(CH₂)₂—O—(CH₂)₂—O—(CH₂)₂—
1.18	—(CH₂)₃—O—(CH₂)₂—O—(CH₂)₂—O—(CH₂)₃—
1.19	—(CH₂)₃—N(CH₃)—(CH₂)₃—

1.20

1.21

1.22

1.23

1.24

1.25

1.26

1.27

1.28

1.29

1.30

EXAMPLE P2.1

Preparation of the Compound of Formula

[0088]
A mixture of 2.4 g of 1-methyl-2-nitroguanidine and 1.0 g of tris(2-aminoethyl)amine in 50 ml of ethanol is mixed at room temperature with 30 ml of a 37% solution of formaldehyde in water, heated to 50° C. and stirred at this temperature for 16 hours. The mixture is then evaporated to dryness under vacuum, the residue stirred with diethyl ether/ethyl acetate (1:1) and the title compound isolated by filtration (compound 2.1). [0089]

EXAMPLE P2.2

The following compounds listed in Table 2 can also be obtained analogously to the above method of example P2.1. [0090]

TABLE 2

Compounds of formula

No. A₁ A₂ A₃ X phys. data

2.1. —(CH₂)₂— —(CH₂)₂— —(CH₂)₂— N

2.2. —(CH₂)₃ —CH₂— —(CH₂)₄ CH

EXAMPLE P3.1

Preparation of the Compound of Formula

[0091]
A mixture of 2.0 g of the product obtainable according to example P1.1, 1.6 g of 2-chloro-5-chloromethylpyridine and 2.8 g of potassium carbonate in 20 ml of dimethylformamide is stirred for 9 hours at 90° C. Then, the reaction mixture is filtered, the filtrate concentrated by evaporation under vacuum, and the residue taken up in 100 ml of dichloromethane. The organic phase is washed with 50 ml of water and 50 ml of saturated sodium chloride solution, dried over MgSO[0092] ₄and evaporated to dryness. The residue is stirred with diethyl ether and the title compound isolated by filtration (compound 10.B.1).

EXAMPLE P3.2

Preparation of the Compound of Formula

[0093]
A mixture of 3.7 g of the compound obtainable according to example P1.3, 3.2 g of 2-chloro-5-chloromethylpyridine and 5.5 g of potassium carbonate in 20 ml of dimethylformamide is stirred for 16 hours at 55° C. Then, the reaction mixture is filtered, the filtrate is concentrated by evaporation under vacuum, the residue is stirred in methanol and filtration carried out. This yields the title compound with a melting point of 178-180° C. (compound 10.B.4). [0094]

EXAMPLE P3.3

[0095]
A mixture of 4.9 g of the compound obtainable according to example P1.4, 3.24 g of 2-chloro-5-chloromethylpyridine and 5.5 g of potassium carbonate in 20 ml of dimethylformamide is stirred for 16 hours at 55° C. Then, the reaction mixture is filtered, the filtrate concentrated by evaporation under vacuum, and the residue purified on silica gel with ethyl acetate/methanol (2:1) as eluant. This yields the title compound with a melting point of 70-72° C. (compound 10.B.14). [0096]

EXAMPLE P3.4

Compound of Formula

[0097]
A mixture of 2.0 g of the compound obtainable according to example P1.1, 1.95 g of 2-chloro-5-chloromethylthiazole, 4.0 g of potassium carbonate and 1.53 g of 18-Crown-6 (1,5,7,10,13,16-hexaoxacyclooctadecane) in 20 ml of tetrahydrofuran is stirred for 24 hours at 50° C. Then, the reaction mixture is filtered, the filtrate concentrated by evaporation under vacuum, and the residue purified on silica gel with dichloromethane/methanol (9:1) as eluant. This yields the title compound with a melting point of 175-178 ° C. (compound 3.B.1). [0098]

EXAMPLE P3.5

The following compounds listed in Tables 3 to 26 can also be obtained analogously to the above methods of examples P3.1 to P3.4.

TABLE B


Compounds of formula

	(IIc)

	No.	A

	B.1	—(CH₂)₂—
	B.2	—CH(CH₃)—CH₂—
	B.3	—(CH₂)₃—
	B.4	—(CH₂)₄—
	B.5	—(CH₂)₅—
	B.6	—(CH₂)₆—
	B.7	—(CH₂)₇—
	B.8	—(CH₂)₈—
	B.9	—(CH₂)₉—
	B.10	—(CH₂)₁₀—
	B.11	—(CH₂)₁₂—
	B.12	—CH₂—C(CH₃)₂—CH₂—
	B.13	—CH₂—CH(OH)—CH₂—
	B.14	—(CH₂)₃—O—(CH₂)₄—O—(CH₂)₃—
	B.15	—CH₂—CH₂—O—CH₂—CH₂—
	B.16	—CH₂—CH(CH₃)—(CH₂)₃—
	B.17	—(CH₂)₂—O—(CH₂)₂—O—(CH₂)₂—
	B.18	—(CH₂)₃—O—(CH₂)₂—O—(CH₂)₂—O—(CH₂)₃—
	B.19	—(CH₂)₃—N(CH₃)—(CH₂)₃—

	B.20

	B.21

	B.22

	B.23

	B.24

	B.25

	B.26

	B.27

	B.28

	B.29

	B.30

[0100]

TABLE 3
[0101]

TABLE 4
[0102]

TABLE 5
[0103]

TABLE 6
[0104]

TABLE 7
[0105]

TABLE 8
[0106]

TABLE 9
[0107]

TABLE 10
[0108]

TABLE 11
[0109]

TABLE 12
[0110]

TABLE 13
[0111]

TABLE 14
[0112]

TABLE C

Compounds of formula

(IId)

No. A₁ A₂ A₃ X

C.1 —(CH₂)₂— —(CH₂)₂— —(CH₂)₂— N

C.2 —(CH₂)₃ —CH₂— —(CH₂)₄ CH
[0113]

TABLE 15
[0114]

TABLE 16
[0115]

TABLE 17
[0116]

TABLE 18
[0117]

TABLE 19
[0118]

TABLE 20
[0119]

TABLE 21
[0120]

TABLE 22
[0121]

TABLE 23
[0122]

TABLE 24
[0123]

TABLE 25
[0124]

TABLE 26
[0125]
1.2 g of the compound obtainable according to example P3.1 are stirred for 16 hours at room temperature together with 10 ml of methanol and 10 ml of 1 n hydrochloric acid. The reaction mixture is concentrated to dryness by evaporation and the residue purified on silica gel with dichloromethane/methanol (95:5) as the eluant. This yields the title product with a melting point of 147-149° C. (compound 27.6). [0126]

EXAMPLE 4.2

Preparation of the Compound of Formula

[0127]
1.2 g of the compound obtainable according to example P3.4 are stirred for 40 hours at 50° C. together with 3.3 ml of methanol and 3.3 ml of 1 n hydrochloric acid. The reaction mixture is evaporated to dryness and the residue recrystallised from methanol. This yields the title product with a melting point of 170-172° C. (compound 27.1). [0128]

EXAMPLE P4.3

The following compounds listed in Table 27 can also be obtained analogously to the above methods of examples 4.1 and 4.2.

TABLE 27


Compounds of the general formula

	(I)

No.	Het	phys. data


27.1		m.p. 170-172° C.

27.2

27.3

27.4		m.p. 166-168° C.

27.5

27.6		147-149° C.

27.7

27.8		m.p. 173-174° C.

27.9

27.10

27.11

27.12

Claims

What is claimed is:

1. Method of producing a compound of formula

R₁is hydrogen or C₁-C₄-alkyl;

R₂is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl or a radical —CH₂B;

Het is an aromatic or non-aromatic, monocyclic or bicyclic heterocyclic radical which is unsubstituted or—depending on the substitution possibilities of the ring system—mono- to penta-substituted by substituents selected from the group comprising halogen, C₁-C₃-alkyl, C₁-C₃-alkoxy, halogen-C₁-C₃-alkyl, C₁-C₃-halogenalkoxy, cyclopropyl, halogencyclopropyl, C₂-C₃-alkenyl, C₂-C₃-alkynyl, C₂-C₃-halogenalkenyl and C₂-C₃-halogenalkynyl, C₁-C₃-alkylthio, C₁-C₃-halogenalkylthio, allyloxy, propargyloxy, allylthio, propargylthio, halogenallyloxy, halogenallylthio, cyano and nitro; and

B is phenyl, 3-pyridyl or thiazolyl, which are optionally substituted by one to three substituents from the group comprising C₁-C₃-alkyl, C₁-C₃-halogenalkyl, cyclopropyl, halogencyclopropyl, C₂-C₃-alkenyl, C₂-C₃-alkynyl, C₁-C₃-alkoxy, C₂-C₃-halogenalkenyl, C₂-C₃-halogenalkynyl, C₁-C₃-halogenalkoxy, C₁-C₃-alkylthio, C₁-C₃-halogenalkylthio, allyloxy, propargyloxy, allylthio, propargylthio, halogenallyloxy, halogenallylthio, halogen, cyano and nitro;

characterised by hydrolysing a compound of formula

Q—A—Q (IIa)

wherein A is a direct bond or an organic radical, or of formula

wherein U is an organic radical; and in compounds (IIa) and (Ib)

Q signifies

wherein R₁, R₂and Het are as defined above for formula (I), and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form.

2. Method according to claim 1 of producing a compound of formula (I) in free form.

3. Method according to claim 1 or 2 of producing a compound of formula (I) wherein R. is hydrogen.

4. Method according to one of claims 1 to 3 of producing a compound of formula (I), wherein

R₂is hydrogen, C₁-C₃-alkyl or cyclopropyl.

5. Method according to one of claims 1 to 4 of producing a compound of formula (I) from a compound of formula (IIa), wherein

A is straight-chained or branched C₂-C₂₀-alkylene, C₂-C₂₀-alkenylene, C₂-C₂₀-alkynylene,

C₃-C₁₂-cycloalkylene, arylene or heterocyclylene; whereby the groups C₂-C₂₀-alkylene,

C₂-C₂₀-alkenylene, C₂-C₂₀-alkynylene, C₃-C₁₂-cycloalkylene, arylene and heterocyclylene are optionally substituted once or several times, independently of each other, and the groups

C₂-C₂₀-alkylene, C₂-C₂₀-alkenylene and C₂-C₂₀-alkynylene are optionally interrupted once or several times, independently of each other, by O, N—H or N—C₁-C₁₂-alkyl, C₃-C₉-cycloalkylene, arylene or heterocyclylene; or a group —D₁-D₂-D₃—; wherein

D₁and D₃, independently of each other, signify optionally substituted C₃-C₁₂-cycloalkylene or arylene and D₂signifies C₂-C₂₀-alkylene, C₂-C₂₀-alkenylene, C₂-C₂₀-alkynylene, O, N—H or N—C₁-Cl₂-alkyl.

6. Method according to one of claims 1 to 4 of producing a compound of formula (I) from a compound of formula (IIb), wherein

U is aryl, heterocyclyl, C₃-C₁₂-cycloalkyl or a group

wherein

A₁, A₂and A₃independently of one another, have the same significances as given in claim 5 for A in formula (IIa), and

X signifies N or CH.

7. Method according to one of claims 1 to 6 of producing a compound of formula (I) wherein Het signifies 2-chloropyrid-5-yl, tetrahydrofuran-3-yl, 5-methyl-tetrahydrofuran-3-yl or 2-chlorothiazol-5-yl.

8. Method according to one of claims 1 to 7 of producing a compound of formula (I), characterised in that the pH value is less than 6.

9. Method according to one of claims 1 to 8 of producing a compound of formula (I), characterised in that it is effected in water, an alcohol or a mixture of water with an alcohol.

10. Method of producing a compound of formula

Q—A—Q (IIa)

wherein A is a direct bond or an organic radical; or of formula

wherein U is an organic radical; and in compounds (IIa) and (IIb)

Q signifies

wherein R₁, R₂and Het are as defined in claim 1 for formula (I), and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form. characterised in that a compound of formula

T—A—T (IIIa)

or of formula

wherein A and U have the same significance as defined for formulae (IIa) and (IIb);

T signifies

and R₂has the same significance as defined in claim 1 for formula (I); and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form, is reacted when producing a compound of formula (IIa) either with two equivalents, or when producing a compound of formula (IIIb) with three equivalents of a compound of formula

wherein R₁and Het are defined as in claim 1 for formula (I), and Y is a leaving group.

11. Method of producing a compound of formula (IIa) or (IIIb), as defined in claim 10, characterised in that either a compound of formula

H₂N—A—NH₂ (Va)

or

and optionally the E/Z isomers, E/Z isomeric mixtures and/or tautomers thereof, each in free form or in salt form, wherein A and U have the same significance as defined in claim 1 for the compounds of formulae (IIa) and (IIb), is reacted when producing a compound of formula (IIIa) either with two equivalents, or when producing a compound of formula (IIIb) with three equivalents of a compound of formula

wherein R₂has the same significance as defined for formula (I), in the presence of an excess of formaldehyde or paraformaldehyde.