Title of Invention	2-THIO-SUBSTITUTED IMIDAZOLE DERIVATIVES
Abstract	The invention relates to 2-thio-substituted imidazole derivatives of formula I, wherein the groups R¿1?, R¿2?, R¿3? and R¿4? are defined as per the description. The inventive compounds have an immunomodulating action and/or an inhibitive action on the release of cytokine and are therefore suitable for treating diseases, which are related to the dysfunction of the immune system.

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2-Thio-substituted imidazole derivatives and their use in pharmacy The present invention relates to 2-thio-substituted imidazole derivatives having immunomodulating and cytokine-release-inhibiting action, to pharmaceutical compositions comprising these compounds and to their use in pharmacy. Pharmacologically active imidazole compounds with antiinflammatory activity are already known. Thus, inter alia, compounds having 4,5-di(hetero)arylimidazole moieties have been examined more closely, and various pharmaceutical actions thereof have been described. Also known are compounds which are substituted in the 2-position. US patent 4,585,771 discloses 4,5-diphenylimidazole derivatives which are substituted in the 2-position by a pyrrolyl, indolyl, imidazoly! orthiazolyl radical and which have antiinflammatory and antiallergic activity. US patents 4,528,298 and 4,402,960 describe 4,5-di(hetero)arylimidazole derivatives which are substituted in the 2-position via a thio, sulfinyl or sulfonyl group by a phenyl, pyridyl, N-oxypyridyl, pyrimidyl. thiazolyl orthienyl radical and which have antiinflammatory and antiallergic activity. US patents 4,461,770 and 4,584,310 describe 4-{5-aryl)-5-(4-heteroaryi)imidazole derivatives which are substituted in the 2-position via a thio, sulfinyl or sulfonyl group by a substituted or unsubstituted aliphatic hydrocarbon and which, inter alia, have antiinflammatory action. DE 198 42 833 relates to 4-heteroaryi-5-phenylimidazole derivatives which are substituted in the 2-position by a phenylalkylthio group. These compounds act as antiinflammatories and inhibitors of cytokine release. WO 99/03837 and WO 93/14081 describe 2-substituted imidazoles which inhibit the synthesis of a number of inflammatory cytokines. The compounds described in WO 93/14081 have in the 2-position. attached via a sulfur atom, a phosphorus-containing substituent or an aryl or heteroaryl substituent. WO 91/10662 describes imidazole derivatives which inhibit the acyl-CoA: cholesterol 0-acyl transferase and binding of thromboxane TxA2. WO 95/00501 describes imidazole derivatives which can be used as cyclooxygenase inhibitors. The imidazole derivatives described in DE 28 23 197 A have antiinflammatory, antiallergic and immunostimulating action, J. Med. Chem. 1996, 39, 3927-37 describes compounds having 5-Iipoxygenase- and cyclooxygenase-inhibiting action, 2-(4-methylsulfinylphenyl)-4-{4-fluorophenyl-5-{pyrid-4-yl)imidazole also having cytokine-inhibiting action. It has been found that the known compounds are unstable and difficult to process, or that their efficacy is low. In spite of the fact that numerous compounds are known, there is therefore still a need for compounds having antiinflammatory action which inhibit cytokine release. It is an object of the invention to provide such compounds. Surprisingly, it has now been found that certain 2-substituted imidazole derivatives provide stable compounds which are readily processible and which have high immunomodulating and/or cytokine-release-inhibiting activity. Accordingly, the present invention provides 2-thio-substituted imidazole derivatives of the formula I aminoaryi. where the amino group is unsubstituted or substituted by one or two C1-C4-alkyl groups, aryl-C1-C4-alkyl or an aromatic or nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, which heterocyclic radical is unsubstituted or substituted by 1, 2, 3 or 4 C1-C4-alkyl groups, an aryl or aryl-C1-C4-alkyl group, R2 is selected from the group consisting of: H; C1-C6-aikyl. phenyl-C1-C4-alkyl, where the phenyl group may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, halogen, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl and C1-C4-alkylsulfonyl, C2-C5-alkenyl, C2-C6-alkenyl which is substituted by one or two halogen atoms and/or phenyl groups, where the phenyl group may independently be substituted by one or two C1-C4-alkyl or halogen atoms, C2-C6-alkynyl, C2-C6-alkynyl which is substituted by a phenyl group which may be unsubstituted or substituted by one or two C1-C4-alkyl or halogen atoms, C1-C6-alkyl which is substituted by a nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl or C1-C4-alkylsulfonyl, phenyl or phenyl which has one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, halogen, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl and C1-C4-alkylsulfonyl, or R1 and R2 together are -CH2CH2- or -CH2CH2CH2-, one of the radicals R1 and R2 is C1-C6-alkyl or an aromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, where the aromatic heterocyclic radical may have 1 or 2 substituents independently of one another selected from the group consisting of C1-C6-alkyI, amino, C1-C4-aikylamino, di-C1-C4-alkylamino, phenyl-C1-C4-alkylamino and R5CONR6-, where R5 is C1-C4-alkyl. phenyl, which may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, C1-C4-alkoxy and halogen, or C3-C3-cycloalkyJ and R6 is H, C1-C4-alkyl or benzyl, and the second of the radicals R3 and R4 is C1-C6-aikyI or aryl which is unsubstituted or substituted by a halogen atom, where only one of the radicals R3 and R4 may be C1-C6-alkyi. with the proviso that, if R1 represents aryl-C1-C5-alkyI or amino-C1-C6-alkyl. R2 represents alkylsulfonyl- or alkylsulfinylaryl-C1-C5-aikyl, their optical isomers and physiologically acceptable salts. Preference is given to compounds of the formula I in which R^ is C1-C6-alkyl which is unsubstituted or substituted by one or two hydroxyl groups or a nonaromatic heterocyclic radical. C2-C6-alkenyl, C5-C6-cycloalkyI, aryl which is unsubstituted or substituted by one or more halogen atoms or a C1-C4-alkylsulfanyl group, amino-C1-C4-alkyl, where the amino group is unsubstituted or substituted by one or two C1-C4-alkyl groups, aminoaryl, where the amino group is unsubstituted or substituted by one or two C1-C4-alkyl groups, aryl-C1-C4-alkyl or an aromatic or nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, which heterocyclic radical is unsubstituted or substituted by 1, 2, 3 or 4 C1-C4-alkyl groups, an aryl or aryl-C1-C4-alkyl group, R2 is H, C1-C6-alkyI, phenyl-C1-C5alkyl, where the phenyl group may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl. halogen, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl and C1-C4-alkylsulfonyl, C2-C6-alkenyl, C2-C6-alkenyl which is substituted by one or two halogen atoms and/or phenyl groups, where the phenyl group may independently be substituted by one or two C1-C4-alkyl or halogen atoms, C2-C6-alkynyl, C2-C6-alkynyl which is substituted by a phenyl group which may be unsubstituted or substituted by one or two C1-C4-alkyl or halogen atoms, C1-C6-alkyI which is substituted by a nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, one of the radicals R3 and R4 is C1-C6-alkyI or an aromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, where the aromatic heterocyclic radical may have 1 or 2 substituents independently of one another selected from the group consisting of d-Ce-alkyi, amino, C1-C4-a!kylamino, di-C1-C4-alkylamino. phenyl-C1-C4-alkylamino. R5CONR6-, where R6 is C1-C4-alkyl, phenyl which may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, C1-C4-alkoxy and halogen, or C3-C6-cycloalkyI, and R^ is H, C1-C4-alkyl or benzyl, and the second of the radicals R^ and R'* is C1-C6-alkyI or aryl which is unsubstituted or substituted by a halogen atom, where only one of the radicals R^ and R^ may be d-Ce-alkyl. If the compounds according to the invention have centers of asymmetry, the scope of the invention includes both racemates and optical isomers (enantiomers, diastereomers). The term "alkyl" (also in combination with other groups, such as phenylalkyi, alkylsulfonyl, etc.) embraces straight-chain and branched alkyl groups having preferably 1 to 6 or 1 to 4 carbon atoms, such as methyl, ethyl, n- and i-propyl, n-, i-and t-buty[, sec-butyl, n-pentyl and n-hexyl. The term "aryl" embraces aromatic ring systems, such as phenyl or naphthyl. The term "halogen" represents a fluorine, chlorine, bromine or iodine atom, in particular a fluorine or chlorine atom. C3-C6-CycloalkyI groups are cyclopropyl. cyclobutyl and, in particular, cyclopentyl and cyclohexyl. Nonaromatic heterocyclic radicals can be saturated or unsaturated. Preference is given to piperidinyl, piperazinyl, pyranyl, morpholinyl or pyrrolidinyl, where the piperidinyl radical may be substituted by 1, 2, 3 or 4 C1-C4-alkyl groups, in particular methyl groups. Preferred aromatic heterocyclic radicals are pyridyl, in particular 3- or 4-pyridyl, pyrimidinyl, pyrrolyl, imidazolyl, oxazolyl. isoxazolyl, furyl, thienyl orthiazolyl. The heterocyclic radical, in particular the pyridyl radical, may be substituted as mentioned above. The pyridyl radical is substituted in particular in the 2-position. Phenyl-C1-C4-alkyl is in particular benzyl or phenylethyl. Preference is given to compounds of the formula I in which one of the radicals R3 and RR4 is C1-C4-alkyl or a halogen-substituted phenyl and the second of the radicals R3 and R4 is C1-C4-alkyl or pyridyl or substituted pyridyl, with the proviso, that the two radicals are not both C1-C4-alky!. Preference is furthermore given to compounds of the formula I where R3 is halogen-substituted, in particular 4-substituted, phenyl and R4 is unsubstituted or substituted pyridyl. in particular 4-pyridyl or substituted 4-pyridyl. According to a particularly prefen"ed embodiment, the radical R3 in the formula I is 4-fluorophenyl and R4 is 4-pyridyl or substituted pyridyl. If R1 is C1-C6-alkyI which is substituted by a nonaromatic heterocyclic radical, this radical preferably contains at least one nitrogen atom, and the attachment to the alkyl group is preferably via the nitrogen atom. If R'1 is an aromatic or nonaromatic heterocyclic radical, this is preferably attached to the imidazole group via a carbon atom. R^ is preferably Ci-Ca-alkyI, C3-C6-cycloalkyI, in particular cyclopropyl, or a saturated heterocyclic radical having one or two nitrogen atoms, in particular piperidinyl or 2.2,6.6-tetramethylpiperidinyl. With particular preference, the piperidinyl or 2,2,6,6-tetramethylpiperidinyl radical is attached in the 4-position to the nitrogen atom of the imidazole. Two process variants are available for preparing the imidazole-2-thione. The two variants are illustrated in an exemplary manner using compounds in which R3 is 4-fIuorophenyl and R4 is 4-pyridyl. Compounds having other radicals R3 and R4 can be prepared in an analogous manner. Variant 1 The synthesis of the substituted imidazole-2-thiones is carried out according to the course of the reaction of scheme 1, using ethyl isonicotinate and 4-fluorophenyl-acetonitrile as starting materials. The starting materials are converted in a condensation reaction with the aid of metallic sodium in an alcohol, for example ethanol, into 2-cyano-2-(4-fluorophenyi)-1-(4-pyridyl)ethanone (compound 1). The cyano group is then removed by hydrolysis, for example with hydrobromic acid, and decarboxylation, giving 2-(4-fuorophenyl)-1-{4-pyridyl)ethanone (compound 2). In the next step, compound 2 is nitrosated in the 2-position using, for example, nitrites, such as sodium nitrite or isoamyl nitrite. This gives the compound of the formula (3), the oxime 2-(4-fluorophenyl)-1-(4-pyridyl)-a-hydroxyiminoethane. Using this intermediate, cyclization giving an imidazole derivative of the formula (4), a substituted 5-(4-fluorophenyi)-4-(4-pyridyl)imidazole N-oxide which carries the substituent R^ at the nitrogen atom in 3-position, is carried out by reaction with an imine of the general formula H2C=NRi, which is present as a 1,3,5-trisubstJtuted hexahydro-1,3,5-triazine. in an alcoholic solvent, such as ethanol, and at elevated temperature (50-90°C). The imidazole N-oxide of the formula (4) is then reacted with 2,2.4,4-tetramethyl-3-thiocyclobutanone in a chlorinated solvent to give the corresponding 3-substituted 5-(4-fluorophenyl)-4-(4-pyridyl)imidazole-2-thione (compound 5; compound of the formula I where R2 = H). Scheme 1: Synthesis route for the thiones according to the invention (variant 1) Variant 2 Initially, the oxime compound of the formula (3), 2-(4-fluorophenyl)-1-(4-pyridyl)-a-hydroxyiminoethane, is prepared as described in variant 1 (scheme 1, steps 1 to 3). Using this starting material, the synthesis of the substituted imidazoie-2-thiones is carried out according to scheme 2. 2-(4-Fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethane is, according to scheme 2, reacted with the selected amine of the general formula NH2-R1 and formaldehyde, giving, with ring closure, a compound of the formula (6), i.e. a 1-substituted 4-(4-fluorophenyi)-5-(4-pyhdyi)imida2ol-2-one. This is reacted with an excess of phosphorus oxychloride, resulting in a compound of the formula (7), i.e. a 1-substituted 4-(4-fluorophenyl)-5-(4-pyridyi)imidazole 2-chloride being formed. From this compound, the corresponding 1-substituted 4-(4-fluorophenyl)-5-{4-pyridyl)-imidazole-2-thione (compound 5) is obtained by reaction with 4-chlorobenzylthiol in a polar aprotic solvent and at elevated temperature (lOO-ISO^C). 2) Preparation of the 2-thioimidazole compound The thione compounds (5) obtained according to variant 1 or 2 are converted by substitution of the sulfur atom in the 2-position into the compounds of the formula I according to the invention where R^ ^ H, The substitutions can be carried out in a known manner by a nucleophilic substitution reaction, as shown in an exemplary manner for some compounds in scheme 3. Here, compound 5 is reacted with R^-X in an inert polar solvent, such as an alcohol. X is a readily exchangeable group, such as Hal, in particular CI. Br. 1, methylsulfonyl, tosyl etc. 2-Thioimida2o(e compounds in which the sulfur atom [lacuna] 2-position is substituted by a vinyl radical can be obtained by nucleophilic addition of compound 5 to a triple bond. To this end, 5 is reacted with a base, for example an alkali metal alkoxide in the corresponding alcohol, and then with an excess of the compound with the triple bond. The corresponding bisaryl thioethers are prepared from the 3-substituted 2-chloro-4-(4-fluorophenyl)-5-(4-pyridyl)imidazole (compound 7 from scheme 2). The compounds (7) are reacted with two equivalents of the appropriate thiophenol in an aprotic solvent, such as dimethylformamide, giving compounds of the formula (12). The corresponding regioisomeric compounds can be prepared in accordance with scheme (5). Starting with 1-(4-fIuorophenyl)-2-(4-pyridyl)-α-hydroxyiminoethanone (obtained analogously to scheme 1), compounds of the formula 15 are obtained analogously to the process of scheme 1 by reaction with the appropriate imines. Compound (13) can be prepared by the process described in WO 93/14081. Scheme 3: Scheme 4: Bisaryl thioethers These compounds can be reacted further as described in scheme 3. The imidazolethiols which carry a C1-C4-alkyl group in the 4-position are obtained from the corresponding α-hydroxyiminoethanones (compound 17/19 in scheme 6 below), analogously to schemes 1 and 2. These compounds can be reacted further according to schemes 3 and 4. The corresponding regioisomeric compounds can be prepared analogously to scheme 5. Compounds of the formula I which carry a C1-C4-alkylsulfanyl radical can be oxidized by known processes, using a suitable oxidizing agent, such as m-chloroperbenzoic acid, hydrogen peroxide, benzoyl peroxide, etc., to give the corresponding C1-C4-alkylsulfinyl or C1-C4-alkylsulfonyl compound, see scheme 7. The preparation of the compounds in which R4 is an amino- or amido-substituted heterocyclic radical, in particular a pyridyl radical, is carried out according to scheme 8, where the preparation is illustrated using 2-substituted 4-pyridine compounds as examples (compounds in which R4 is an alkyl-substituted heterocyclic radical are prepared by the processes mentioned above using appropriately substituted starting materials): Scheme 8: The amino group of the starting material 2-amino-y-picolin (24) is protected, for example by introduction of an acetyl group using acetic anhydride. The methyl group of the compound (25) is then oxidized to the carboxyl group using, for example, potassium permanganate in an aqueous medium at from 20 to 90°C. The reaction of the resulting pyridinecarboxylic acid (26) with 4-fluorophenyl-acetonithle to give compound (27) and the subsequent removal of the nitrile group are carried out in accordance with variant 1. This also results in the removal of the acetyl group on the amino group of the pyridine compound, with the compound (28) being formed. In the next step, the amino group is again protected, for example by introducing an acetyl group using acetic anhydride. The resulting compound (29) is. in accordance with variant 1 or 2 (shown in scheme 8 using variant 1), converted into the thiono compound (32). Into this compound, the desired radical R2 is introduced as described in schemes 3. 4 and 7. To introduce the desired substituent into the pyridyl group, the acetyl group is initially removed hydrolytically, for example using aqueous acid, giving the amino compound (35). An acyl radical is introduced by acylation, in particular with the corresponding acid chloride R5COCI in an inert solvent, such as an ether, for example tetrahydrofuran or dioxane. or in a chlorinated hydrocarbon, for example methylene chloride or 1,2-dichloroethan, etc. The acylation is generally carried out in the presence of a base, for example triethylamine, in an at least equimolar amount. To prepare the substituted amine compounds, compound (35) is reacted with one or two molar equivalents of an alkyl bromide or phenylalkyi bromide in an inert solvent, such as dimethylformamide, in the presence of a base, such as sodium hydride, to give the compounds (37) or (38). Alternatively, the amide compounds (34) or (36) can be reduced with lithium aluminum hydride, for example in tetrahydrofuran, to give compound 39. In vitro and in vivo, the compounds according to the invention show immunomodulating and cytokine-release inhibiting action. Cytokines are proteins such as TNF-a and IL-p which play an important role in numerous inflammatory disorders. The compounds according to the invention are, owing to their cytokine-reiease-inhibiting action, suitable for treating disorders which are associated with a disturbance of the immune system. They are suitable, for example, for treating autoimmune disorders, cancer, rheumatoid arthritis, gout, septic shock, osteoporosis, neuropathic; pain, the spread of HIV, HIV dementia, viral myocarditis, insulin-dependent diabetes, periodontal disorders, restenosis, alopecia. T-cell depletion associated with HIV infections or AIDS, psoriasis, acute pancreatitis, rejection reactions of allogenic transplants, allergic pneumonia, arteriosclerosis, multiple sclerosis, cachexia, Alzheimer's disease, stroke, ictus, colitis ulcerosa, morbus Crohn, inflammatory bowel disease (IBD), ischemia, congestive heart failure, pulmonary fibrosis, hepatitis, glioblastoma, Guillain-Barre syndrome, systemic lupus erythematodes. adult respiratory distress syndrome (ARDS) and respiratory distress syndrome. The compounds according to the invention can be administered either as individual therapeutically active compounds or as mixtures with other therapeutically active compounds. The compounds can be administered on their own; in general, however, they are formulated and administered in the form of pharmaceutical compositions, i.e. as mixtures of the active compounds with suitable pharmaceutical carriers or diluents. The compounds or compositions can be administered orally or parenterally; preferably, they are administered in oral dosage forms. The type of pharmaceutical composition or carrier or diluent depends on the desired administration form. Oral compositions, for example, can be present as tablets or capsules and may comprise customary excipients, such as binders (for example syrup, gum arable, gelatin, sorbitol, tragacanth or polyvinylpyrrolidone), fillers (for example lactose, sugar, cornstarch, calcium phosphate, sorbitol or glycerol), glidants (for example magnesium stearate. talc, polyethylene glycol or silica), disintegrants (for example starch) or wetting agents (for example sodium lauryl sulfate). Liquid oral preparations can assume the form of aqueous or oily suspensions, solutions, emulsions, syrups, elixirs or sprays and the like. They can also be present as a dry powder which is reconstituted using water or another suitable carrier. Such liquid preparations may comprise customary additives, for example suspending agents, flavors, diluents or emulsifiers. For parenteral administration, it is possible to use solutions or suspensions with customary pharmaceutical carriers. The compounds or compositions according to the invention can be administered to mammals (man or animal) in a dose of from about 0.5 mg to 100 mg per kg of body weight per day. They may be administered in one individual dose or in a plurality of doses. The activity spectmm of the compounds as inhibitors of cytokine release was examined using the test systems below, as described by C. Donat and S. Laufer in Arch. Pharm. Pharm. Med. Chem. 333. Suppl. 1. 1-40, 2000. In vitro test with human whole blood The test substance is added to samples of human potassium-EDTA whole blood (of 400 |jl each) and the samples are preincubated in a CO2 incubator (5% CO2; 95% moisture-saturated air) at 37 for 15 min. The samples are then stimulated with 1 pg/ml of LPS {E.coli 026:B6) at 37°C in a CO2 incubator (5% CO2; 95% moisture-saturated air) for 4 hours. The reaction is stopped by placing the samples on ice, adding DPBS buffer and then centrifuging at 1 000*g for 15 min. The amount of IL-β and TNFa in the plasma supernatant is then determined by ELISA. In vitro test with PBMCs The mononuclear ceils (PBMCs) from human potassium-EDTA whole blood, diluted 1:3. are isolated by density gradient centrifugation (Histopaque®-1.077). The cells are washed twice with DPBS buffer, resuspended in macrophage SFM medium and adjusted to a cell count of 1*10^ cells/ml. The resulting PBMCs suspension (samples of in each case 390 pi) and the test substance are preincubated at 37°C in a CO2 incubator (5% CO2; 95% moisture-saturated air) for 15 min. The samples are then stimulated with in each case 1 pl/ml of LPS {E.coli 026:B6) at 37°C in a CO2 incubator (5% CO2; 95% moisture-saturated air) for 4 hours. The reaction is stopped by placing the samples on ice, adding DPBS buffer and then centrifuging at 15 880*g for 12 min. The amount of IL-lβ and TNFa in the plasma supernatant is then determined by ELISA. The results of the in vitro tests are shown in tables 1 and 2 below. V The compounds according to the invention and the processes for their preparation are now described in more detail using the examples below, without limiting the invention. Examples Example 1: 4-(4-fluorophenvlV1 -methvl-5-(4-pvridvl)-2-thioimidazole a) 2-Cyano-2-(4-fluorophenyl)-1 -(4-pyridyl)ethane 250 ml of dry ethanol were added dropwise to metallic sodium (17,3 g / 0.7 mol). Ethyl isonicotinate (75.8 g / 0.5 mol) and 4-fluorophenylacetonitriie (67,6 g / 0.5 mol) were then added dropwise, and the mixture was subsequently heated under reflux for 15 min. After cooling. 600 ml of distilled water were added to the mixture. When the mixture was acidified to pH 1 using concentrated hydrochloric acid (HCI). the desired compound 2-cyano-2-(4-fluorophenyl)-1-(4-pyridyl)ethane precipitated as a yellow precipitate. The precipitate was filtered off. washed with distilled water and dried under reduced pressure over phosphorus pentoxide (P2O5). The yield was 85.0 g (62%). b) 2-(4-Fluorophenyl)-1 -(4-pyridyl)ethanone 2-Cyano-2-(4-fluorophenyl)-1-(4-pyridyl)ethane (40.6 g / 0.15 mol) from example la was suspended in 300 ml of 48% strength hydrobromic acid (HBr). and the reaction mixture was heated under reflux for 18 h. After cooling, the mixture was adjusted to pH 9 using aqueous ammonia. The compound mentioned in the title, which precipitated during this operation, was filtered off, washed with distilled water and dried under reduced pressure over P2O5, The yield was 25.6 g (80%). c) 2-(4-Fluorophenyl)-1 -(4-pyridyl)-α-hydroxyiminoethanone 15.0 g (0.07 mol) of 2-(4-fluorophenyl)-1-(4-pyridyl)ethanone from example lb were dissolved in 70 ml of glacial acetic acid. A solution of 4.8 g (0.07 mol) of NaN02 in 11 ml of water was slowly added dropwise to the initial charge, and the reaction mixture was stirred at room temperature. After 3 h, 400 ml of distilled water were added, and the mixture was stirred at room temperature for another 3 h. The compound (3) mentioned in the title precipitated out. The compound was filtered off, washed with distilled water and dried under reduced pressure over P2O5. The yield was 15.2 g (90%). d) 4-(4-Fluorophenyl)-1-methyl-5-(4-pyridyl)imidazole N-oxide 2.0 g of 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone from example 1c above and twice the equivalent amount of 1,3,5-trimethylhexahydro-1,3.5-triazine were dissolved in 20 ml of dry ethanol and heated under reflux for 10 h. After cooling, the ethanol was removed using a rotary evaporator. The slightly oily residue solidified on addition of diethyl ether. The precipitate was filtered off and dried under reduced pressure. The yield was 82%. e)4-(4-Fluorophenyl)-1-methyl-5-(4-pyridyl)imidazole-2-thJone 0.5 g of 5-(4-fluorophenyl)-4-(4-pyridyl)-3-methylimidazole N-oxide from example 1d were dissolved in 20 ml of CHCI3, and the reaction mixture was cooled in an ice-bath. An equimolar solution of 2,2.4,4-tetramethyl-3-thionocyclobutanone in CHCI3 was slowly added dropwise to the initial charge, and the mixture was then stirred in the ice-bath for 30 min. The ice-bath was removed, and stirring was continued at room temperature for 1 h. The solvent was then removed using a rotary evaporator, and the solid residue was triturated in diethyl ether. The precipitate was filtered off and dried under reduced pressure. The yield was 98%. IR: MX (cm*^) = 1601. 1506, 1229. 1004. 843. 832 ^H NMR (d6-DMSO. ppm): 12.95 (bs. 1H). 8.69-8.66 (m, 2H). 7.45-7.42 (m. 2H). 7.27-7.12 (m.4H). 3.39 (S.3H) Example 2: 1-Ethyl-4-(4-fluorophenylV5-(4-pvridyl)-2-thioimidazole a) 1-Ethyl-4-(4-fluorophenyl)-5-(4-pyridyl)imidazol-2-one Initially, 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was prepared as described in example 1, steps (a) to (c). 4.0 g of the iminoethanone were then, together with the equimolar amount of ethylamine and the equimolar amount of formaldehyde (36% strength aqueous solution), heated under reflux for 4 h. After cooling, the reaction mixture was neutralized using aqueous ammonia and extracted three times with CH2CI2. The organic phases were combined and dried over Na2SO4. The drying agent was filtered off and the solvent was removed using a rotary evaporator. The slightly oily residue was solidified by addition of diethyl ether. The precipitate was filtered off and dried under reduced pressure. The yield was 63%. b) 2-Chloro-1 -ethyl-4-(4-fluorophenyl)-5-(4-pyridyl)imidazole 35 ml of POCI3 and a small amount of NH4CI were added to 2.0 g of 1-ethyl-4-(4-fluorophenyl)-5-(4-pyridyl)imidazol-2-one, and the reaction mixture was heated under reflux for 9 h. After cooling, most of the excess POCl3 was distilled off, and distilled water was carefully added to the residue. The mixture was neutralized using 20% strength NaOH, resulting in the precipitation of the title compound. The precipitate was filtered off and dried over P2O5 under reduced pressure. Yield: 81%. c) 1 -Ethyl-4-(4-fluorophenyl)-5-(4-pyridyl)imidazole-2-thione NaH (4.5 eq.) was suspended in 10 ml of DMF, and 4-chlorobenzylthiol (4.5 eq.) was slowly added dropwise. The reaction mixture was stirred at room temperature for 45 min. 2.0 g of the 2-chIoro-1-ethyl-4-(4-fluorophenyl)-5-(4-pyridyl)imidazole obtained in the step above were then added. The mixture was heated under reflux for 10 h. After cooling, distilled water was added to the mixture, the pH was adjusted to 1 using concentrated HCI and the mixture was washed six times with diethyl ether. Neutralization of the aqueous phase with 20% strength NaOH resulted in the precipitation of the title compound. The precipitate was filtered off and dried over P2O5 under reduced pressure. Purification was by recrystallization. The yield was 50%. IR: 1/y (cm-1) = 3059, 1587, 1498, 1220. 837, 814 1H NMR (CDCI3, ppm): 12.63 (bs. 1H), 8.74-8.72 (m, 2H), 7.27-7.17 (m, 4H), 7.0-6.90 (m, 2H), 4.08 (q, 2H, J= 7.1 Hz), 1.21 (t, 3H, J= 7.1 Hz) Example 3A: 4-(4-Fluorophenyn-1-n-propyl-5-(4-pvridyl)-2-thioimidazole The process of example 1 was employed, where step d) the 2-(4-fluorophenyl)- 1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1,3,5-tri-n-propylhexahydro-1,3,5-triazine. The yield was in the range of 60-91%. IR: MX (cm*--) = 2932, 1586, 1500, 1221. 831, 814 ^H NMR (CDCI3, ppm): 12.47 (bs, 1H), 8.76-8.73 (m, 2H), 7.26-7.13 (m, 4H), 7.0-6.96 (m. 2H), 3.98 (t, 2H, J= 7.8 Hz), 1.65 (m, 2H), 0.82 (t, 3H, J= 7.4 Hz) Example 3B: 4-(4-Fluorophenyl)-1-n-propyl-5-(4-pvridyl)-2-thioimidazole Alternatively, to prepare the title compound, the process of example 2 was employed, where step a) 2-(4-fIuorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with the equimolar amount of n-propylamine. The yield was in the range of 32-72%. Example 4: 4-(4-Fluorophenyl)-1 -isopropyl-5-(4-pvridyl)-2-thioimidazole To prepare the title compound, the process of example 2 was employed, where in step a) 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with the equimolar amount of isopropylamine. IR: 1/^1 (cm'-') = 3040. 1584.1500. 1230,841.819 ^H NMR (CDCI3, ppm): 11.73 (bs, 1H). 8.76-8.74 (m. 2H.). 7.28 (m. 2H), 7.17-7.10 (m, 2H). 7.0-6.92 (m. 2H). 4.89 (m. 1H). 1.48 (s. 3H), 1.45 (s. 3H) Example 5: 1 -Cvc!ohexyl-4-(4-fluorophenvn-5-(4-pvridyl)-2-thioimidazole To prepare the title compound, the process of example 2 was used, where in step a) 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxy!minoethanone was reacted with the equimolar amount of cyclohexylamine. IR: MX (cm-1') = 2934. 1560. 1505. 1228. 842 1H NMR(CDCl3, ppm): 11.32 (bs. 1H). 8.76-8.73 (m, 2H). 7.30-7.31 (m. 2H), 7.15- 7.08 (m,2H). 7,01-6.92 (m. 2H), 4.60-4.25 (m. 1H). 2.0-1.18 (m, 10H) Example 6: 1 -Cvclopropyl-4-(4-fluorophenvn-5-(4-pvridyl)-2-thioimidazole The same process as in example 1 was used, where in step d) the 2-(4-f]uorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1,3,5-tricyclopropylhexahydro-1,3.5-triazine. IR: 1/λ (cm-1) = 3013. 1589. 1515. 1499. 1487. 1223. 830. 685 1H NMR (CDCI3. ppm): 12.76 (bs. 1H). 8.68-8.65 (m. 2H), 7.26-7.19 (m. 4H), 7.07- 6.99 (m. 2H). 3.12-3.08 (m. 1H). 1.02-0.95 (m. 2H), 0.76-0.71 (m. 2H) Example 7: 4-(4-FluorQphenyl)-1-phenyl-5-(4-pyridyl)-2-thioimidazole To prepare the title compound, the process of example 2 was employed, where in step a) 2-(4-fluorophenyi)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with the equimolar amount of aniline, IR: 1/λ (cm-'1) = 2880. 1597. 1504. 1227. 844. 825 1H NMR (CDCI3. ppm): 11.58 (bs. 1H). 8.48-8.41 (m. 2H). 7.78-6.74 (m. 11H) Example 8: 1-Benzyl-4-(4-fluorophenyl)-5-(4-pyridyl)-2-thioimidazole To prepare the title compound, the process of example 2 was employed, where in step a) 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with the equimolar amount of benzylamine. IR: 1/?i(cm-1) = 3032. 1587. 1497, 1225. 1158,837.816 1H NMR (CDCI3. ppm): 12.88 (bs. 1H). 8.56-8.53 (m, 2H). 7.27-6.90 (m. 11H). 5.28 (s. 2H) Example 9: 1 -Dimethylaminophenyl-4-(4-fluorophenyl)'5-(4-pyridyl)-2-thioimidazole To prepare the title compound, the process of example 2 was employed, where in step a) 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with the equimolar amount of 4-dimethylaminobenzylamine. IR: 1/λ (cm*'*) = 2891. 1606. 1500. 1357. 1225. 835. 816 ^H NMR (d6-DMSO. ppm): 13.05 (bs. 1H). 8.43-8.41 (m. 2H). 7.37-7.03 (m. 8H). 6.98-6.60 (m. 2H). 2,89 (s. 6H) Example 10: 4-(4-Fluorophenyl)-1 -(3-pyridyl)-5-f4-pyridyl)-2-thioimidazole To prepare the title compound, the process of example 2 was employed, where in step a) 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with the equimolar amount of 3-pyridylamin. IR: 1/λ (cm-1) = 3035, 1597, 1478, 1433. 1433. 1224. 813. 708 1H NMR (d6-DMSO. ppm): 13.34 (s, 1H). 8.54-8.45 (m, 4H). 7.76-7.75 (m, 1H). 7.40- 7.13 (m.7H) Example 11: 1-Dimethylaminoethyl-4-(4-fluorophenyl-5-(4-Pvridvyl)-2-thioimidazole The same process as in example 1 was used, where in step d) the 2-(4-fluoro- phenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1,3,5-tri(2-dimethylaminoethyl)hexahydro-1,3,5-triazine, IR: 1/λ (cm-1_2772, 1597, 1503. 1225, 835. 815 1H NMR (CDCI3, ppm): 8.74-8.72 (m, 2H), 7.30-7.17 (m, 4H). 7.04-6.94 (m, 2H), 4.13 (t, 2H. J= 6.8 Hz), 2.56 (t, 2H, J= 6.7 Hz), 2.11 (s, 6H) Example 12: 4-(4-Fluorophenyl)-5-(4-pyridyl)-1 -(2,2,6,6-tetramethylpiperidin-4-yl)-2-thioimidazole The same process as in example 1 as employed, where in step d) the 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the molar amount of 2,2,6,6-tetramethyl-4-methyleneaminopiperidine. IR: 1/λ (cm'^) = 2964, 1587, 1498, 1352, 1234, 838, 815 Example 13: 1-Dimethylaminopropyl-4-(4-fluorophenyl)-5-(4-pyridyl)-2-thioimidazole The same process as in example 1 was employed, where in step d) the 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was [lacuna] with twice the equivalent amount of 1,3,5-tri(3-dimethylaminopropyl)hexahydro-1,3,5-triazine. Example 14: 4-(4-Fluorophenyl)-1-(3-N-morpholinopropylV-5-(4-pyridyl)-2-thioimidazo!e The same process as in example 1 was employed, where in step d) the 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1.3,5-tri(N-morpholinopropyl)hexahydro-1,3,5-triazine. IR: 1/X(cm-1) = 2847, 1502, 1233, 1114,842.817 ^H NMR (CDCI3. ppm): 12.11 (bs. 1H). 8.75-8.71 (m. 2H), 7.26-7.18 (m, 4H). 7,05- 6.95 (m, 2H). 4.15-4.07 (m. 2H), 3.61-3.57 (m. 4H). 2.32-2.23 (m. 6H).1.86-1.75 (m. 2H) Example 15: 4-(4-Fluorophenyl)-1-(4-methylsulfanylphenyl)-5-(4-pvrdyl)-2-thio-imidazole The same process as in example 1 was employed, where in step d) the 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1,3,5-tri(4-methylsulfanylphenyl)hexahydro-1,3,5-triazine. IR: 1/λ (cm-'-) = 2693, 1597, 1495, 1220, 844, 817 1H NMR (CDCI3, ppm): 12.43 (bs, 1H), 8.47-8.44 (m, 2H), 7.32-7.12 (m, 6H), 7.06-6.97 (m, 2H), 6.90-6.87 (m, 2H), 2.50 (s, 3H) Example 16: 4-(4-Fluorophenyl)-1 -N-morpholinoethyl-5-(4-pvridvn-2-thioimidazole The same process as in example 1 was employed, where in step d) the 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1,3,5-tri(N-morpholinoethylhexahydro-1,3,5-triazine. IR: 1/λ (cm-'1) = 2813, 1599, 1508, 1232, 1117, 850, 835 1H NMR (d6-DMSO): 12.91 (bs, 1H), 8.71-8.68 (m, 2H), 7.49-7.46 (m, 2H), 7.25-7.16 (m, 4H), 4.04 (t, 2H, J= Hz), 2.40 (t, 2H, J= Hz), 2.16 (t, 4H, J= 3.8 Hz) Example 17: 4-(4-Fluorophenvn-1 -(3-hydroxvpropyl)-5-(4-pyridyl)-2-thioimidazole The same process as in example 1 was employed, where in step d) the 2-(4-f]uorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1,3,5-tri(3-hydroxypropylhexahydro-1,3,5-triazine. IR: 1/λ (cm-') = 3049, 2926, 1499, 1223, 1162, 1061, 838 1H NMR (d6-DMSO, ppm): 12.98 (s, 1H), 8.71-8.68 (m, 2H), 7.47-7.44 (m, 2H), 7.29- 7.12 (m, 4H), 4.47-4.43 (bs, 1H), 3.97 (t, 2H, J= 7.4 Hz), 3.27 (t, 2H, J= 6.2 Hz), 1.68-1.54 (m,2H) Example 18:1-(1-Benzylpiperidin-4-yl)-4-(4-fluorophenyl)-5-(4-pvridvn-2-thioimidazole The same process as in example 1 was employed, where in step d) the 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the molar amount of 1-benzyl-4-methyleneaminopiperidine. IR: 1/λ (cm-1) = 2903, 1504, 1247, 1227, 853, 741 1H NMR (d6-DMSO): 12.93 (s, 1H), 8.73-8.70 (m, 2H), 7.50-7.47 (m, 2H), 7.29-7.11 (m, 9H), 3.96-4.12 (m, 1H), 3.38 (s, 2H), 3.85-3.75 (m, 2H), 2.31-2.18 (m, 2H), 1.93- 1.64 (m,4H) Example 19: 1 -Allyl-4-(4-fluorophenyl)-5-(4-pyridyl)-2-thioimidazole The same process as in example 1 was employed, where in step d) the 2-(4-fluorophenyl)-1-(4-pyridyl)-α-hydroxyiminoethanone was reacted with twice the equivalent amount of 1,3,5-tri(prop-2-en-1-yl)hexahydro-1,3,5-triazine. IR: 1/λ (cm-1) = 2695. 1700. 1600. 1506,1421. 1227, 1005. 934. 927. 841. 829, 817 1H NMR (CDCl3. ppm): 12.49 (bs. 1H). 8.72-8.65 (m. 2H). 7.29-7.22 (m. 4H). 7.04-6.96 (m. 2H). 6.00-5.81 (m. 1H), 5.25-5.19 (m. 1H). 5.02-4.93 (m, 1H), 4.66-4.64 (m, 2H) Example 20: 4-(4-Fiuorophenyl)-1 -methyl-2-methylthio-5-(4-pyridylimidazole a) The 1-substituted 4-(4-fluorophenyl)-5-(4-pyridyl)imidazole-2-thione (compound 5 from scheme 1) was prepared as described in example 1, the added imine compound being 1,3.5-trimethylhexahydro-1.3,5-tria2ine. b) To methylate the sulfur. 0.7 g of the resulting thione compound (5) was then suspended under protective gas in 20 ml of dry ethanol, and the equimolar amount of dimethyl sulfate or methyl iodide was added. A spatula tip of Na2CO3 was added, and the reaction mixture was then heated under reflux for 3 h. After cooling, the inorganic salts were filtered off and the solvent was removed using a rotary evaporator. The crude product was purified by column chromatography. The yield was 43%. IR: 1/λ (cm-1) = 1603, 1510. 1220, 1160, 850. 830, 814 1H NMR (CDCI3. ppm): 8.70-8.67 (m. 2H). 7.43-7.36 (m. 2H). 7.24-7.22 (m. 2H). 6.98-6.89 (m. 2H). 3.47 (s, 3H). 2.72 (s. 3H) Example 21: 4-(4-Fluorophenyl)-2-methylthio-1-n-propyl-5-(4-pyridyl)imidazole The title compound was prepared analogously to the process of example 20. 1.3.5-tri-n-propylhexahydro-1,3,5-triazine was used for cyclizing the imidazole compound. IR: 1/λ (cm-'1) = 2929, 1601. 1511, 1221, 849, 829, 816 1H NMR (CDCI3. ppm): 8.71- 8.68 (m. 2H). 7.41-7.34 (m. 2H), 7.26-7.23 (m. 2H). 6.96-6.87 (m. 2H), 3.79 (t. 2H, J= 7.7 Hz). 2.74 (s. 3H). 1.64-1.52 (m. 2H), 0.80 (t, 3H. J= 7.4 Hz) Example 22:1-Cvclopropyl-4-(4-fluorophenvn-2-methylthio-5-(4-pvridvnimidazole The title compound was prepared analogously to the process of example 20. 1.3,5-tricyclopropylhexahydro-1.3,5-triazine was used for cyclizing the imidazole compound. 1H NMR (CDCI3, ppm): 8.64-8.61 (m, 2H). 7.41-7.34 (m. 2H). 7.27-7.24 (m, 2H). 6.98- 6.90 (m. 2H). 3.13-3.02 (m. 1H). 2.74 (s. 3H). 0.95-0.91 (m. 2H), 0.70-0.66 (m. 2H) Example 23: 4-(4-Fluorophenyl)-2-methylthio-1 -N-morpholinoethyl-5-(4-pyridyl)-imidazole The title compound was prepared analogously to the process of example 20. 1,3,5-tri(N-morpholino)ethylhexahydro-1,3,5-triazinethanamine was used for cyclizing the imidazole compound. IR: 1/X (cm-1) = 2852, 1600, 1509,1215, 1114,871,841,813 1H NMR (CDCI3, ppm): 8.71-8.68 (m, 2H), 7.41-7.34 (m, 2H), 7.30 (m, 2H), 6.96-6.87 (m, 2H), 3.96 (t, 3H, J= 7.0 Hz). 3.60 (t, 4H, J= 4.6 Hz), 2.74 (s, 3H), 2.46 (t, 2H, J= 7.0 Hz), 2.32 (t. 4H, J= 4.7 Hz) Example 24: 4-(4-Fluorophenyl)-2-methylthio-1 -N-morpholinopropyl-5-(4-pvridvn-imidazole The title compound was prepared analogously to the process of example 20. 1,3,5-tri(3-N-morpholinopropyl)hexahydro-1,3,5-triazine was used for cyclizing the imidazole compound. IR: 1/X (cm-') = 2814, 1509, 1219,1114,842 1H NMR (CDCI3. ppm): 8.71-8.68 (m. 2H), 7.41-7.36 (m, 2H), 7.27-7.23 (m, 2H), 6.96-6.87 (m, 2H), 3.98-90 (m. 2H), 3.64-3.59 (m, 4H), 2.74 (s, 3H), 2.27-2.19 (m, 6H), 1.77-1.68 (m.2H) Example 25: 4-(4-Fluorophenyl)-2-methylthio-5-(4-pyridyl)-1 -(2.2.6.6-tetramethyl-piperidin-4-yl)imidazole The title compound was prepared analogously to the process of example 20. 2,2,6,6- tetramethyl-4-methylenaminopiperidine was used for cyclizing the imidazole compound. IR: 1/?. (cm-1) = 2968, 1600, 1509, 1343, 1229, 1033, 835, 813 1H NMR (CDCI3. ppm): 8.73-8.70 (m, 2H), 7.37-7.22 (m. 4H), 6.94-6.86 (m, 2H), 4.41-4.28 (m, 1H), 2.75 (s, 3H), 2.05-2.04 (m, 2H), 1.74-1.66 (m, 2H), 1.16, 1.04 (2s, 12H) Example 26: 1 -Benzylpiperidin-4-yl-4-(4-fluorophenyl)-2-methylthio-5-(4-pvridyl)-imidazole The title compound was prepared analogously to the process of example 20. 1-benzyl-4-methylenaminopiperidine was used for cyclizing the imidazole compound. IR: 1/λ (cm-1) = 2929, 2809, 1602, 1509, 1220, 1158, 840, 828, 814, 743, 701 1H NMR (d6-DMSO, ppm): 8.72-8.69 (m, 2H), 7.41-7.38 (m. 2H), 7,30-7.21 (m. 7H), 7.09-7.0 (m. 2H). 3.60-3.72 (m, 1H), 3.40 (s. 1H). 2.85-2.80 (m, 2H). 2.42-2.22 (m, 2H). 1.81-1.76 (m,4H) Example 27: 1-Ethyl-4-(4-fluorophenyl)-2-(4-methylsulfonvnbenzylthio-5-(4-pyridylV imidazole a) The 1-substituted 4-(4-fluorophenyl)-5-(4-pyridyl)imidazole-2-thione (compound 5 of scheme 2) was prepared as described in example 2. the added amine compound being ethylamine. b) To benzylate the sulfur. o.4 g of the resulting thione compound (5) was suspended under protective gas in 15 ml of dry ethanol, and the equimolar amount of 4-methyl-sulfonylbenzyl chloride was added. A spatula tip of Na2CO3 was added, and the reaction mixture was then heated under reflux for 5 h. After cooling, the Na2CO3 was filtered off and the solvent was removed using a rotary evaporator. The crude product of the title compound (compound 9 in scheme 3.2) was purified by column chromatography. Yield: 55% IR: 1/?. (cm-') = 1510. 1304. 1149. 841. 766 'H NMR (CDCI3. ppm): 8.71-8.69 (m. 2H). 7.91-7.87 (m. 2H), 7.62-7,58 (m. 2H), 7.41-7.34 (m. 2H). 7.26-7.21 (m. 2H). 6.98-6.91 (m. 2H). 4.52 (s. 2H). 3.73 (q. 2H. J= 7.2 Hz). 3.05 (s. 3H). 1.07 (t. 3H. J= 7.2 Hz) Example 28: 2-Benzylthio-4-(4-fluorophenyl)-1-n-propyl-5-(4-pvridyl)imidazole a) The 1-substituted 4-(4-fIuorophenyl)-5-(4-pyridyl)imidazole-2-thione (compound 5 of scheme 1) was prepared as described in example 1, the added imine compound being 1.3,5-tri-n-propylhexahydro-1,3.5-triazine. b) The sulfur was benzylated using benzyl chloride, following the process of example 27 (step b), IR: 1/?i (cm---) = 1602, 1510, 1220. 851, 833. 815. 695 1H NMR (CDCI3. ppm): 8.70-8.67 (m. 2H). 7.43-7.26 (m, 6H), 7.19-7.16 (m, 2H). 6.98-6.89 (m. 2H). 4.39 (s. 2H). 3.56 (t. 2H. J= 7.6Hz), 1. 42-1.30 (m. 2H), 0.66 (t. 3H. J= 7.4 Hz) Example 29: 2-(4-Chlorobenzyl)thio-4-(4-fluorophenyl)-1-n-propyl-5-(4-pyridyl)-imidazole The title compound was prepared as described in exannple 28, except that 4-chlorobenzyl chloride was used for the benzylation. IR: 1/λ (cm-1) = 2972. 1602. 1509. 1343, 1222, 1092, 844, 828, 816, 743, 698 1H NMR (CDCb. ppm): 8.71-8.68 (m. 2H), 7.41-7.34 (m, 2H), 7.27-7.26 (m, 4H), 7.19-7.16 (nn, 2H), 6.98-6.89 (m. 2H). 4.38 (s, 2H), 3.61 (t, 2H, J= 7.6 Hz), 1.45-1.33 (m. 2H), 0.68 (t. 3H, 7.4 Hz) Example 30: 4-(4-Fluorophenyl)-2-(4-methylbenzyl)thio-1 -n-propyl-5-(4-pvridyl)-imidazole The title compound was prepared as described in example 28, except that 4-methylbenzyl chloride was used for the benzylation. IR: 1/A. (cm-1) = 2927,1603, 1510, 1222, 849, 831, 815 1H NMR (CDCI3, ppm): 8.70-8.67 (m, 2H), 7.43-7.36 (m, 2H), 7.23-7.09 (m, 6H). 6.98-6.89 (m, 2H), 4.37 (s, 2H). 3.59 (t. 2H, J= 7.7 Hz), 2.34 (s, 3H). 1.44-1.33 (m, 2H), 0.67 (t, 3H, J= 7.4 Hz) Example 31:4-(4-Fluorophenyl)-2-(4-methylthio)benzylthio-1-n-propyl-5-(4-pyridyl)-imidazole The title compound was prepared by the process of example 27, with n-propylamine being in step (a) and 4-methylthipbenzyl chloride being used in step (b) for the benzylation. IR: 1/λ (cm-1) = 2922, 1602, 1508. 1405, 1222. 848. 814 1H NMR (CDCI3. ppm): 8.70-8.67 (m. 2H). 7.42-7.35 (m. 2H). 7.24-7.15 (m. 6H). 6.98-6.89 (m. 2H). 4.37 (s. 2H). 3.60 (t, 2H. J= 7.6 Hz). 2.48 (s. 3H). 1.44-1.33 (m. 2H), 0.68 (t, 3H. J= 7.4 Hz) Example 32: 4-(4-Fluorophenyl)-2-(4-methylsulfinyl)benzylthio-1 -n-propyl-5-(4-pyridyl)-imidazole The process of example 31 was repeated, except that in step (b) 4-methyIsulfinyl- benzyl chloride was used for the benzylation. IR: 1/λ (cm-1) = 2959. 1602, 1509, 1407, 1221, 1089, 1048. 842. 816 'H NMR (CDCI3, ppm): 8.71-8.68 (m, 2H). 7.63-7.51 (m. 4H). 7.41-7.34 (m. 2H). 7.21-7.18 (m. 2H). 6.98-6.90 (m. 2H). 4.48 (s, 2H). 3.64 (t. 2H. J= 7.6 Hz). 2.72 (s, 3H), 1.42-1.35 (m, 2H), 0.69 (t, 3H, J= 7.4 Hz) Example 33: 4-(4-Fluorophenyl)-2-(4-methylsulfonyl)benzylthio-1-n-propyl-5-(4-pyridyl)imidazoie The process of example 31 was repeated, except that in step (b) 4- methylsulfonylbenzyl chlonde was used for the benzylation. IR: 1/X(cm-1)=1509, 1306, 1219, 1150,964,844.768,744 1H NMR (CDCI3, ppm): 8.70-8.68 (m, 2H), 7.91-7.87 (m. 2H), 7.62-7.58 (m, 2H), 7.41-7.26 (m, 4H). 7.0-6.92 (m, 2H), 4.55 (s, 2H), 3.66 (t. 2H, J= 7.6 Hz), 3.05 (s, 3H). 1.48-1.37 (m, 2H). 0.71 (t, 3H, J= 7.5 Hz) Example 34: 2-(4-Chlorobenzyl)thio-4-(4-fluorophenyl)-1-isopropyl-5-(4-pyridyl)-imidazole The title compound was prepared by the process of example 27, where isopropylamine was used in step (a) and 4-chlorobenzyl chloride was used in step (b) for the benzylation. IR: 1/λ (cm*^) = 1509, 1222. 1092, 850. 815 1H NMR (CDCI3, ppm): 8.73-8.71 (m. 2H), 7.38-7.21 (m, 8H). 6.97-6.88 (m, 2H). 4.49 (s. 2H). 4.27-4.20 (m, 1H), 1.38 (s, 3H), 1.27 (s. 3H) Example 35: 4-(4-Fluorophenyl)-2-(4-methylsulfQnyl)benzylthio-1 -isopropyl-5-(4-pyridyl)-imidazol The title compound was prepared by the process from example 27, where isopropylamine was used in step (a) and 4-methylsulfonylbenzyl chloride was used in step (b) for the benzylation. IR: 1/λiorw'^)- 1510, 1306. 1219. 1149,843,766.744 'H NMR (CDCI3, ppm): 8.72-8.69 (m. 2H), 7.92-7.88 (m, 2H). im-im (m, 2H). 7.35-7.21 (m, 4H). 4.60 (s, 2H), 4.25-4.18 (m. 1H), 3.05 (s. 3H), 1,39. 1.35 (2s. 6H) Example 36:1-Cyclopropyl-4-(4-fluorophenyl)-2-(1-phenylpropvnyl)thio-5-(4-pyridyl)-imidazole The title compound was prepared by the process of example 28, where 1,3.5-tricyclopropylhexahydro-1.3,5-triazine was used in step (a) and 1-phenylprop- 1-ynyl chloride was used in step (b) for the benzylation. IR: 1/λ (cm-1) = 1603, 1509. 1388. 1221. 842, 816, 753, 688 'H NMR (CDCI3. ppm): 8.64-8.61 (m. 2H). 7.44-7.22 (m, 9H). 6.99-6.91 (m. 2H). 4.31 (s, 2H). 3.18-3.11 (m, 1H), 0.97-0.90 (m, 2H), 0.75-0.69 (m, 2H) Examples 37: 1-Cvclopropyl-4-(4-fluorophenyl)-2-(1-(4-chlorQ)phenylprQpenyl)thio-5-(4'pyridyl)imidazole The procedure of example 36 was adopted, except that in step (b) 1-(4-chloro-phenyl)prop-1-enyl chloride was used for the benzylation. 1H NMR (CDCI3, ppm): 8.64-8.61 (m. 2H), 7.42-7.35 (m, 2H), 7.29-7.26 (m, 4 H), 7.23-7.20 (m, 2H), 7.0-6.91 (m. 2H). 6.60 (d. 1H, J= 15.7 Hz), 6.48 -6.37 (m, 1H), 4.11 (d, 2H. J= 6.5 Hz). 3.12-3.0 (m, 1H), 0.94-0.90 (m, 2H). 0.68-0.64 (m, 2H) Example 38: 1-Cvclopropyl-4-phenyl-2-(1-(4-fluorophenylpropenyl)thio-5-(4-pyridyl)-imidazole The procedure of example 36 was adopted, except that in step (b) 1-phenylprop- 1-enyl chloride was used for the benzylation. IR: 1/λ (cm*') = 3025, 1599, 1509. 1384, 1219. 963, 838. 824. 815, 750. 692 1H NMR (CDCI3. ppm): 8.64-8.61 (m. 2H). 7.44-7.28 (m, 7H). 7.23-7.20(m, 2H). 7.02- 6.92 (m, 2H). 6.65 (d. 2H. J= 15.8 Hz), 6.51-6.40 (m. 1H), 4.13 (d. 2H. J= 6.7 Hz), 3.11-3.04 (m, 1H). 0.95-0.88 (m. 2H), 0.71-0.65 (m, 2H) Example 39: 1 -Cvclohexyl-4-(4-fluorophenyl)-2-(4-methylsulfonyl)benzylthio-5-(4-pyridyl)imidazole The title compound was prepared by the process of example 27 where cyclo- hexylamine was used in step (a) and 4-methylsulfonylbenzyl chloride was used in step (b) for the benzylation. IR: 1/λ (cm*') = 2930. 1599. 1509, 1304. 1149. 838. 763 1H NMR (CDCI3, ppm): 8.73-8.70 (m, 2H), 7.92-7.88 (m. 2H), 7.67-7.63 (m. 2H), 7,34-7.21 (m. 4H), 6.97-6.88 (m, 2H). 4.64 (s, 2H). 3.73-.371 (m, 1H). 2.10-1.62 (m. 10 H) Example 40: 4-f4-Fluorophenyl)-2-(4-methylsulfonyl)benzylthio-1 -phenyl-5-(4-pyridyl)imidazole The procedure of example 39 was adopted, except that the amine in step (a) was aniline. IR:1/X(cm-1)= 1598, 1510,1408, 1303. 1149, 1090,840.765.694 1H NMR (CDCI3, ppm): 8.41-8.38 (m. 2H), 7.89-7.85 (m. 2H). 7.61-7.38 (m. 7H), 7.07-6.92 (m. 6H). 4.50 (s, 2H), 3.04 (s. 3H) Example 41: 1-Benzyl-4-(4-fluorophenyl)-2-(4-methylsulfonyl)benzylthio-5-(4-pyridyl)-imidazole The procedure of example 39 was adopted, except that the imine used In step (a) was benzylamine. IR: 1/A.(cm-1) = 1600. 1509, 1304. 1220, 1147, 1090,843,767,725 1H NMR (CDCia, ppm): 8.57-8.54 (m, 2H), 7.90-7.85 (m, 2H), 7.58-7.54 (m, 2H), 7.45-7.38 (m, 2H), 7.26-7.23 (m, 3H), 7.08-6.97 (m, 4H), 6.80-6.79 (m, 2H), 4.93 (s. 2H), 4.47 (s, 2H). 3.05 (s, 3H) Example 42: 2-Benzylthio-4-(4-fluorophenyl)-1 -N-mQrpholinoethyl-5-(4-pyridyl)-imidazole The title compound was prepared by the process of example 27. where N-morpholinoethylamine was used in step (a) and benzyl chloride was used in step (b) for the benzylation. IR; 1/λ (cm-1) = 2802, 1603, 1510, 1219, 1116. 870. 836. 814. 712. 695 1H NMR (CDCb. ppm): 8.71-8.68 (m, 2H). 7.44-7.37 (m. 2H), 7.30-7.26 (m, 5H), 7.26-7.19 (m, 2H), 6.99-6.90 (m. 2H), 4.37 (s. 2H), 3.80-3.54 (m.6H). 2.24-2.17 (m, 6H) Example 43: 2'Benzylthio-4-(4-fluorophenyl)-1-N-morpholinQpropyl-5-f4-pyridyl)-imidazole Example 28 was repeated, except that the added imine compound in step (a) was 1,3,5-tri(3-N-morpholinopropyl)hexahydro-1.3,5-triazine. IR: 1/λ (cm*^) = 2814, 1602, 1509, 1460. 1218. 1114. 970, 842. 812, 696 1H NMR (CDCI3. ppm): 8.70-8.67 (m, 2H), 7.43-7.26 (m. 7H). 7.20-7.17 (m. 2H). 6.98-6.89 (m. 2H), 4.39 (s. 2H). 3.74-3.56 (m. 6H). 2.19-2.06 (m. 6H), 1.55-1.36 (m, 2H) Example 44: 4-(4-Fiuorophenyl)-2-f4-methylsulfonyl)benzylthio-1 -N-morpholinoethyl-5-(4-pyridyl)imidazole The title compound was prepared by the process of example 28, where 1.3,5-tri(3-N-morpholinopropyl)hexahydro-1.3,5-triazine was used in step (a) and 4-methyl-sulfonylbenzyl chloride was used in step (b) for the benzylation. IR: 1/X (cm-1 2924. 1600. 1510. 1302. 1147,1115.839.765 1H NMR (CDCI3, ppm): 8.71-8.68 (m, 2H). 7.91-7.87 (m, 2H). 7.59-7.55 (m. 2H). 7.40-7.33 (m, 2H), 7.22-7.19 (m. 2H). 6.99-6.90 (m. 2H), 4.49 (s, 2H). 3.77 (t, 2H. J= 5.7Hz). 3.63-3.58 (m. 4H), 3.06 (s, 3H), 2.23-2.15 (m, 6H), 1.60-1.41 (m. 2H) Example 45: 4-(4-Fluorophenyl)-2-(4-methylsulfinyl)benzylthio-1-N-morpholinoethyl-5-f4-pyridyl)imidazole The title compound was prepared by the process of example 28. where 1,3.5-tri(3-N- morpholinopropyl)hexahydro-1,3,5-triazine was used in step (a) and 4-methylsulfinyl- benzyl chloride was used in step (b) for the benzylation. IR: 1/>.(cm-1) = 2956. 1601.1509. 1406, 1220, 1115. 1047.837.815 1H NMR (CDCI3, ppm): 8.71-8.68 (m, 2H), 7.63-7.50 (m. 4H). 7.41-7.34 (m. 2H). 7.22-7.19 (m. 2H). 6.98-90 (m, 2H). 4.47 (s. 2H), 3.78 (t. 2H, J= 7.8 Hz). 3.60-3.56 (m. 4H). 2.73 (s. 3H). 2.20-2.09 (m. 6H), 1.60-1.42 (m, 2H) Example 46: 2-Benzylthio-4-(4-fluorophenyl)-1-(2,2,6,6-tetramethylpiperidin-4-yl)-imidazole The title compound was prepared by the process of example 28, where 2,2,6,6-tetrα-methyl-4-methylenaminopiperidine was used in step (a) and benzyl chloride was used in step (b) for the benzylation. IR: 1λ(cm-1) = 2739, 1602.1510. 1390. 1354, 1224. 1158.840.700 Example 47: 4-(4-Fluorophenyl)'1-methyl-2-N-morpholinoethylthio-5-(4-pyridyl)-imidazole a) The 1-substituted 4-(4-fluorophenyl)-5-(4-pyridyl)imidazole-2-thione (compound 5 of scheme 1) was prepared as described in example 1. the added imine compound being 1,3,5-trimethylhexahydro-1.3.5-triazine. b) To substitute the sulfur. 0.4 g of the resulting thione compound (5) was then suspended under protective gas in 20 ml of dry ethanol. and the equimolar amount of N-(2-chloroethyl)morpholine hydrochloride was added. A spatula tip of Na2CO3 and a spatula tip of Nal were added, and the reaction mixture was then heated under reflux for 5 h. After cooling, the salts were filtered off and the solvent was removed using a rotary evaporator. The crude product of the title compound (compound 10 of scheme 3) was purified by column chromatography. Yield: 72% IR; 1/λ(cm-1) 2930, 2806, 1602, 1508. 1218, 1131, 1113, 1072,1007,865,850, 829,814 1H NMR (CDCI3, ppm): 8.70-8,67 (m, 2H). 7.41-7.34 (m, 2H), 7.26-7.21 (m, 2H), 6.97-6.88 (m, 2H), 3.69 (t. 4H, J= 4.6 Hz), 3.50 (s, 3H), 3.39 (t, 3H, J= 6.9 Hz), 2.79 (t, 2H, J= 7.0 Hz). 2.52 (t, 4H, J= 4.6 Hz) Example 48: 1 -cis-Phenylethenylthio-4-(4-fluorophenyl)-1 -methyl-5-(4-pyridyl)-jmidazole a) The 1-substituted 4-(4-fluorophenyl)-5-(4-pyridyl)Jmidazole-2-thione (compound 5 of scheme 1) was prepared as described in example 1, the added imine compound being 1,3,5-trimethylhexahydro-1.3,5-triazine. b) Dry ethanol was then added dropwise to an initial charge of 0.1 g of metallic sodium. 1.2 g of the compound (5) from step (a) were added, and a tenfold excess of phenylacetylene was then added. The reaction mixture was heated under reflux for 6 h. After cooling, the mixture was poured onto ice and extracted three times with petroleum ether. The organic phases were combined. When the organic phase was concentrated on a rotary evaporator, the title compound (compound 11 of scheme 3) precipitated out. Yield: 27% IR: 1/X (cm-1) = 3380, 1600, 1513, 1226, 842 'H NMR (CDCI3. ppm); 8.72-8.69 (m, 2H), 7.52^7.23 (m, 9H), 6.99-6.90 (m, 3H), 6.74 (d, 1H, J= 10.6 Hz), 3.52 (s,3H) Example 49: 1 -cis-Phenylethenylthio-4'(4-fluorophenyl)-1 -n-propyl-5-(4-pyridyl)-imidazole The title compound was prepared analogously to example 48, the imine added in step (a) being 1,3,5-tri-n-propylhexahydro-1,3,5-triazine. IR: 1/A. (cm-1) = 1596, 1217, 835, 776, 682 1H NMR (CDCI3, ppm): 8.74-8.71 (m, 2H), 7.49-7.25 (m. 9H), 7.02-6.89 (m, 3H), 6.73 (d, 1H, J= 10.7 Hz), 3.86 (t. 2H, J= 7.7 Hz), 1.66-1.51 (m. 2H), 0.78 (t, 3H, J= 7.4 Hz) Example 50: 2-cis-Phenylethenylthio-1 -cvclopropyl-4-(4-fluorophenyl)-5-(4-pyridyl)-imidazole The title compound was prepared analogously to example 48, the imine added in step (a) being 1,3,5-tricyclopropylhexahydro-1,3,5-triazine. IR:1/λ(cm-1) = 1596, 1509, 1385, 1217, 832, 785, 686 1H NMR (CDCI3, ppm): 8.67-8.64 (m, 2H), 7.54-7.26 (m, 10H), 7.0-6.92 (m, 2H), 6.76 (d, 1H, J= 10.8 Hz), 3.17-3.13 (m, 1H), 1.0-0.96 (m,2H), 0.72-0.68 (m, 2H) Example 51: 2-(1,2-Dibromo-2-phenylethyl)thio-4-(4-fluorophenyl)-1-n-propyl-5-(4-pyridyl)imidazole To prepare the title compound, 0.4 g of the product of example 49 (compound 11 of scheme 3) was dissolved in CH2CI2 and the equimolar amount of bromine in 15 ml of CH2CI2 was slowly added dropwise. The reaction mixture was stirred at room temperature for 5 h and then washed repeatedly with aqueous sodium thiosulfate solution. The organic phase was dried over Na2SO4, the drying agent was filtered off and the solvent was removed using a rotary evaporator. Yield: 98% IR: 1/λ. (cm-1) = 2963. 1631, 1603, 1513, 1224. 1158.840,815.697 1H NMR (CDC!3, ppm): 8.74-8.72 (m, 2H). 7.59-7.25 (m, 9H). 6.99-6.90 (m. 2H), 6.21 (d. 1H. J= 7.2 Hz). 5.74 (d. 1H. J= 7.1 Hz). 3.89-3.85 (m. 2H). 1.55-1.51 (m, 2H). 0J7(t, 3H. J=7.3Hz) Bisaryl thioether Example 52: 4-(4-Fluorophenyl)-2-phenylthio-1-n-propyl-5-(4-pyridyl)imidazo!e 2-Chloro-1-n-propyl-4-(4-fIuorophenyl)-5-(4-pyridyl)imidazole (compound 7 of scheme 4) was prepared analogously to the process described in example 2, the amine used being, as in example 3B, n-propylamine. b) The resulting imidazole compound (7) was then converted into the bisaryl thioether. To this end. NaH (2 eq.) was suspended in 10 ml of dry DMF and thiophenol (2 eq.) was slowly added dropwise. The reaction mixture was stirred at room temperature for 45 min, and 0.3 g of (4) was then added. The mixture was heated under reflux for 5.5 h. After cooling, distilled water was added to the mixture, the pH was adjusted to 1 using concentrated HCi and the mixture was washed six times with diethyl ether. When the mixture was neutralized using 20% strength NaOH the title compound (compound 12 of scheme 4) precipitated out. The precipitate was filtered off and dried over P2O5 under reduced pressure. Yield: 70% IR: 1/λ (cm*'-1) = 1509. 1226, 847, 729. 685 1H NMR (CDCI3, ppm): 8.75-8.72 (m, 2H). 7.45-7.26 (m. 9H). 6.98-6.89 (m. 2H). 3.95-3.87 (m. 2H), 1.49-1.34 (m, 2H), 0.71 (t, 3H. J= 7.4 Hz) Example 53: 2-(4-Chlorophenyl)thio-4-(4-fluorophenyl)-1-n-propyl-5-(4-pyridyl)-imidazole The same process as in example 52 was carried out, except that in step (b) 4-chlorothiophenol was used. IR; 1/A. (cm-1) = 2958, 1601, 1511, 1473, 1226,1090, 1013, 854, 824 1H NMR (d6-DMSO, ppm): 8.74-8.71 (m, 2H), 7.49-7.32 (m. 8H), 7.14-7.05 (m, 2H), 3.92 (t. 2H, J= 7.5 Hz), 1.37-1.26 (m, 2H), 0.59 (t, 3H, J= 7.4 Hz) Example 54: 4-(4-Fluorophenyl)-2-(4-methylsulfanvnphenylsulfanyl-1 -n-propvi-5-f4-pyridyl)imidazole The same process as in example 52 was carried out, except that in step (b) 4-methylsulfanylthiophenol was used. IR: 1/λ (cm*-1) = 2961, 1602, 1510, 1478. 1226, 1103. 851, 796 1H NMR (CDCI3, ppm): 8.74-8.71 (m. 2H). 7.43-7.17 (m, 8H), 6.97-6.88 (m. 2H), 3.90 (t, 2H, J= 7.7 Hz), 2.47 (s, 3H). 1.50-1.38 (m, 2H), 0.72 (t, 3H. J= 7.4 Hz) Example 55: 4-(4-Fluorophenvi)-2-f(4-methylsulfinyl)phenyl1thio-1 -n-propyl-5-(4-pyridyl)imidazole 0.4 g of the product of example 54 was dissolved in 10 ml of CH2CI2 and 0.9 equivalent of m-chioroperbenzoic acid was added. The mixture was stirred at room temperature for 3 h. The resulting precipitate was filtered off and purified by column chromatography. Yield: 73% IR: 1/λ (cm---) = 1602, 1510, 1226. 1056. 814. 699 1H NMR (CDCI3, ppm): 8.77-8.74 (m, 2H), 7.61-7.57 (m 2H), 7.46-7.37 (m, 4H), 7.30- 7.28 (m, 2H). 6.98-6.90 (m, 2H). 3.92 (t, 2H, J= 7.7 Hz), 2,72 (s, 3H), 1.49-1.45 (m, 2H), 0.72 (t. 3H, 7.4 Hz) Example 56: 4-(4-Fluorophenyl)-2-r(4-methylsulfonvnphenyl)thio-1 -n-propyl-5-(4-pyridyl)imidazole 0.4 g of the product of example 54 was dissolved in 10 ml of CH2CI2 and 2.5 equivalents of m-chloroperbenzoic acid was added. The mixture was heated under reflux for 3 h. The resulting precipitate was filtered off and purified by column chromatography. Yield: 67% IR: 1/λ (cm-1) = 2967. 1604, 1510, 1316, 1226, 1153, 1094, 1078, 954. 815, 771 1H NMR (CDCI3. ppm): 8.79-8.76 (m, 2H), 7.88-7.83 (m, 2H), 7.45-7.27 (m, 6H), 6.99-6.90 (m, 2H), 3.92 (t, 2H, J= 7.7 Hz), 3.04 (s, 3H), 1.50-1.43 (m, 2H), 0.73 (t. 3H. 7.4 Hz) 4-Methylimidazolethiols Example 57: 1 -(4-Fluorophenyl)-4-methyl-5-(4-pyridyl)imidazole-2-thiol The title compound was prepared analogously to example 1 from the corresponding α-hydroxyiminoethanone (compound 17 of scheme 6). IR: 1/λ (cm-1) = 3039. 1591. 1516. 1372. 849, 823, 780 1H NMR (d6-DMSO. ppm): 12.76 (bs, 1H), 8.47-8.44 (m, 2H), 7.28-7.24 (m, 4H). 7.03-7.0(m, 2H), 2.19(s, 3H) Example 58: 4-(4-Fluorophenyl)-5-methyl-1-(3-pyridyl)imidazole-2-thiol The title compound was prepared analogously to example 2 from the corresponding α-hydroxyiminoethanone (compound 19 of scheme 6). IR: 1/λ (cm-1) = 3035. 1515. 1482. 1430, 1367. 1227. 844, 815. 711 1H NMR (d6-DMSO. ppm): 12.67 (bs, 1H), 8.50-8.49 (m, 1H), 8.48-8.47 (m, 1H), 7.69-7.65 (m. 1H), 7.45-7.41 (m, 1H), 7.16-7.12 (m, 4H), 2.08 (s, 3H) Reqioisomeric thiols Example 59: 5-(4-Fluorophenyl)-1 -n-propyl-4-(4-pyridyl)imidazole-2-thiol a) 1 -(4-Fluorophenyl)-2-(4-pyridyl)-α-hydroxyiminoethanone 2.2 g (0.01 mol) of 1-(4-fluorophenyl)-2-(4-pyridyl)ethanone (compound 13 of scheme 5) were dissolved in 10 ml of glacial acetic acid. A solution of 0.7 g (0.01 mol) of NaNo2 in 1 ml of water was slowly added dropwise to the initial charge, and the reaction mixture was stirred at room temperature for 2 h. 50 ml of distilled water were added and stirring was continued for 1 h. The precipitated compound (14), 1-(4-fluorophenyl)-2-(4-pyridyl)-α-hydroxyiminoethanone, was filtered off, washed with distilled water and dried over P2O5 under reduced pressure. Yield: 2.0 g (80%) b) 4-(4-Fluorophenyl)-1 -methyI-5-(4-pyridyl)imidazole-2-thione 0.5 g of compound (14) was. together with twice the equivalent amount of 1,3.5-trimethylhexahydro-1,3,5-triazine, dissolved in 20 ml of dry ethanol and heated under reflux for 24 h. After cooling, the solvent was removed using a rotary evaporator. The residue was taken up in 20 ml of CHCI3. cooled in an ice-bath, and 2,2,4,4-tetramethyl-3-thionocyclobutanone was slowly added with stirring. The ice-bath was removed and stirring was continued at room temperature for 1 h. The solvent was removed using a rotary evaporator and the resulting oily residue was solidified by addition of diethyl ether. The precipitate (15) was filtered off and purified by recrystallization. Yield: 15% IR: 1/λ (cm-1) = 2727, 1604, 1397, 1223, 833, 817 1H NMR (CDCI3. ppm): 12.03 (bs, 1H), 8.50-8.47 (m, 2H), 7.39-7.20 (m, 4H), 7,10-7.07 (m, 2H), 3.93-3.85 (m, 2H), 1.72-1.56 (m, 2H), 0.82 (t, 3H, J= 7.4 Hz) Example 60: 5-(4-Fluorophenyl)-1 -N-morpholinoethyl-4-(4-pvridvOtmidazole-2-thiol The procedure of example 59 was adopted, except that the imine in step (b) was N-methylene-(N-morpholino)ethanamine. 1R 1/λ (cm'') = 2803, 1605. 1220, 1118, 849, 833 'H NMR (d6-DMSO): 13.09 (bs. 1H). 8.44-8.41 (m, 2H), 7.63-7.56 (m, 2H), 7.47-7.38 (m, 2H), 7.14-7.11 (m, 2H), 3.93 (t. 2H, J= 6.8 Hz). 3.44 (t, 4H, J= 4.5 Hz), 2.42 (t, 2H, J= 6,8 Hz), 2.14 (t. 4H. J= 4,4 Hz) Examples 61 to 65 (The compound numbers refer to scheme 8) a) 2-Acetamido-4-methyipyridine (25) 100 mg of 4-dimethylaminopyridine are added to 200.0 g of 2-aminopicoline and 400 ml of acetic anhydride, and the mixture is refluxed for 5 h. After cooling, most of the excess acetic anhydride is distilled off. the residue is poured onto ice and the mixture is neutralized using aqueous ammonia solution. The resulting precipitate (25) is filtered off and dried under reduced pressure over P2O5, Yield: 209.0 g (75%) b) 2-Acetamidopyridine-4-C3rboxylic acid (26) With stirring, 214.0 g of (25) are introduced a little at a time into an aqueous solution (temperature 50°C) of 160 g of potassium permanganate. A further 360 g of potassium permanganate are added a little at a time over a period of one hour. Here, the temperature of the reaction mixture should not exceed 90°C. The mixture is stirred for another 1.5 h and then filtered hot, and the filtrate is adjusted to pH 3-4 using cone. HCI. The resulting white precipitate (26) is filtered off and dried under reduced pressure over P2O5. Yield:108.0g(42%) c) 2-Cyano-2-(4-fluorophenyl)-1-(2-acetamido-4-pyridyl)ethanone (27) 18.0 g of (26) are taken up in 50 ml of abs. dimethylformamide (DMF), 17.0 g of carbonyldiimidazole (CD!) are added and the mixture is stirred at room temperature for 45 min. 14.9 g of 4-fluoroacetonitrile and 14.6 g of potassium tert-butoxide are then added, and the reaction mixture is heated at 120°C for 2 h. After cooling, the mixture is stirred at room temperature overnight. Ice is then added to the solution, and the mixture is neutralized using cone. HCI. The resulting precipitate (27) is filtered off and dried under reduced pressure over P2O5. Yield: 18.1 g (65%) d) 2-(4-Fluorophenyl)-1-(2-amino-4-pyridyl)ethanone (28) 150 ml of 48% strength hydrobromic acid are added to 27.9 g of (27), and the reaction mixture is boiled gently for 30 h. After cooling, the mixture is poured onto ice and neutralized with concentrated ammonia. The resulting precipitate (28) is sucked dry, washed repeatedly with petroleum ether and cold diethyl ether and dried. Yield: 11.7g(55%) e) 2-(4-Fiuorophenyl)-1-(2-acetamido-4-pyridyl)ethanone (29) 12.0 g of the compound (28) are suspended in 100 ml of acetic anhydride, a spatula tip of 4-dimethylaminopyridine is added and the reaction mixture is heated under reflux for 5 h. Most of the excess acetic anhydride is distilled off, the residue is hydrolyzed and the mixture is adjusted to pH 7 using cone, ammonia. The resulting clear precipitate (29) is filtered off and dried under reduced pressure over P2O5. Yield: 13.5 g (94%) f) 2-(4-Fluorophenyl)-1-(2-acetamido-4-pyridyl)-α-hydroxyiminoethanone(3) 30 ml of methanol are added to 2.1 g of sodium methoxide solution (30% in methanol), and this mixture is added to a solution of 1.2 g of isoamyl nitrite in 20 ml of methanol. With stirring, 3.0 g of (29) are added a little at a time, and the mixture is then stirred at room temperature for another 2 h. The solvent is distilled off. the solid residue is taken up in water and the pH is adjusted to 7 using 10% strength HCI. The resulting clear precipitate (30) is filtered off and dried under reduced pressure over P2O5. Yield: 1.8 g (54%) g) Preparation of the compounds (31): (30) is, together with twice the amount of the appropriate triazine, dissolved in absolute ethanol and refluxed until the starting material has been completely converted. After cooling, the ethanol is removed using a rotary evaporator. The slightly oily residue solidifies on addition of diethyl ether. The precipitate of compounds 31 is filtered off and dried under reduced pressure. Yields: R1=-CH3:74% R1=-C3H7:62% R1= 2.2,6,6-tetramethylpiperidin-4-yl: 81% R1= N-morpholinopropyk 72% R1= 3-hydroxypropyl-: 56% h) Preparation of the compounds (32) Compound (31) is dissolved in CHCI3 and the reaction mixture is cooled in an ice-bath. An equimolar solution of 2,2,4,4-tetramethylcyclobutane-3-thioxobutanone in CHCI3 is slowly added dropwise to the initial charge, and the mixture is then stirred in the ice-bath for 30 min. The ice-bath is removed and stirring is continued at room temperature for 1 h. The solvent is then removed using a rotary evaporator and the solid residue is triturated in diethyl ether. The precipitate (32) is filtered off and dried under reduced pressure. Yields: R1=-CH3:96% R1=-C3H7:74% R1= 2,2,6,6-tetramethylpiperidin-4-yl: 61% R1= N-morpholinopropyk 82% R1= 3-hydroxypropyl-: 71% i) Preparation of the compounds (33) Under protective gas, compound (32) is suspended in abs. ethanol, and an equimolar amount of methyl iodide is added. A spatula tip of Na2CO3 is added and the reaction mixture is refiuxed until the starting material has been completely converted. After cooling, the inorganic salts are filtered off and the solvent is removed using a rotary evaporator. The crude product (33) is purified by column chromatography. Example 61: 4-(4-Fluorophenyl)-1-methyl-5-(2-acetamido-4-pyridyl)-2-methyl-thioimidazole R1=-CH3: Yield 63% NMR (CDCI3. ppm): 8.75 (bs, 1H), 8.26-8.24 (m, 2H), 7.46- 7.39 (m, 2H), 6.97- 6.88 (m, 3H). 3.53 (s, 3H), 2.71 (s, 3H), 2.23 (s, 3H) IR (1/cm): 1669, 1607, 1543, 1505. 1416, 1268, 1218, 843 Example 62: 4-(4-Fluorophenyl)-1 -n-propyl-5-(2-acetamido-4-pyridyl)-2-methyl-thioimidazole R1=-C3H7: Yield 28% NMR (CDCI3, ppm): 8.28- 8.25 (m, 2H), 7.44-7.37 (m, 2H), 6.96-6.88 (m, 2H), 3.85 (t, 2H. J= 7.7 Hz), 2.73 (s. 3H), 2.24 (s, 3H), 1.65-1.57 (m, 2H). 0.83 (t, 3H. J= 7.4 Hz) IR (1/cm): 3303. 1674, 1544. 1501. 1416. 1264, 1213, 845 Example 63: 4-(4-Fluorophenyl)-1-(2,2,6,6-tetramethylpiperidin-4-yl)-5-(2-acetamido-4-pyridyl)-2-methylthioimidazole R1= 2,2,6,6-tetramethylpiperidin-4-yl: Yield 23% NMR (CDCI3. ppm): 10.62 (s, 1H), 8.38-8.35 (m, 2H), 8.01 (s, 1H), 7.33-7.26 (m, 2H), 7.04-6.95 (m. 3H), 4.19-4.03 (m, 1H), 2.61 (s, 3H), 2.00 (s, 3H), 1.87-1.81 (m, 2H), 1.52-1.47 (m, 2H), 0.93 (s. 6H). 0.78 (s, 6H) IR (1/cm): 2976. 1699, 1533, 1407, 1255, 838 Example 64: 4-(4-FluorophenylV1 -[3-fN-morpholino)propvn-5-(2-acetamido-4-pyridyl)-2-methylthioimidazole R1= N-morpholinopropyl-: Yield 52% NMR (CDCI3, ppm): 8.29 (m, IN), 8.12 (s, 1H), 7.42-7.35 (m, 2H), 6.96-6.87 (m. 3H). 4.08-3.92 (m, 6H), 3.17-3.00 (m, 6H). 2.74 (s. 3H), 2.41-2.34 (m, 2H), 2.24 (s, 3H) Example 65: 4-(4-Fluorophenyl)-1-(3-hvdroxvpropyl)-5-(2-acetamido-4-pyridyl)-2-methylthioimidazole R1= 3-hydroxypropyl-: Yield 32% NMR (CDCI3, ppm): 8.69 (bs, 1H). 8.23-8.19 (m, 2H). 7.44-7.37 (m, 2H), 6.98-6.86 (m, 3H), 4.04 (t, 2H, J= 7.9 Hz). 3.70 (t, 2H. J= 7.2 Hz). 2.74 (s. 3H). 2.25 (s, 3H). 2.13-2.05 (m.2H) Example 66: 4-(4-Fluorophenyl)-1 -methyl-5-(2-amino-4-pyridyl)-2-methyl-thioimidazole The compound of example 61 is dissolved in 10% strength HCI and refluxed for 14 h. After cooling, the mixture is neutralized with 20% strength NaOH. The resulting clear precipitate is filtered off and dried under reduced pressure over P2O5. Yield: 82% NMR (CDCI3. ppm): 8.16-8.13 (m, 1H). 7.50-7.43 (m. 2H). 6.98-6.89 (m, 2H). 6.60-6.57 (m. 1H). 6.41 (s 1H), 4.60 (bs. 2H,) 3.46 (s. 3H), 2.70 (s. 3H) IR (1/cm): 1629. 1542. 1509. 1215. 837. 814 Examples 67 to 69 The compound of example 66 is dissolved in abs. tetrahydrofuran (THF). and 1.2 times the amount of triethylamine is added. The reaction mixture is cooled in an ice-bath. With stirring, 1.2 times the amount of the acid chloride is added dropwise. and stirring is continued until no more starting material is present. The reaction mixture is filtered and the filtrate is concentrated to dryness. Purification of the crude product is carried out by column chromatography. Example 67: 4-([lacuna]-Fluorophenyl)-1-methyl-5-[2-(4-methoxybenzamido)-4-pyridyl]-2-methylthioimidazole Yield: 62% NMR (CDCI3, ppm): 8.66 (s, 1H), 8.44 (s. 1H). 8.30 (s, 1H), 8.29-8.28 (m, 1H), 7.94-7.89 (m, 2H), 7.49-7.42 (m, 2H), 6.95- 6.90 (m, 4H), 3. 90 (s, 3H), 3.58 (s, 3H), 2.72 (s. 3H) IR(1/cm): 3410, 1674. 1500, 1412, 1253,1175,840,759 Example 68: 4-([lacuna]-Fluorophenyl)-1-methyI-5-(2-cyclopropylamiclo-4-pyriclyl)-2-methylthioimidazole Yield: 24% NMR (CDCI3. ppm): 8.67-8.62 (m, 1H), 7.63-7.38 (m, 3H), 6.98-6.85 (m, 3H), 3.90 (s, 3H), 2.73 (s, 3H), 2.05-1.98 (m, 1H), 1.26-1.14 (m, 2H), 1.21-1.14 (m, 2H) Example 69: 4-([lacuna]-Fluorophenyl)-1-methyl-5-(2-cyclopentylamido-4-pyridyl)-2-methylthioimidazole Yield: 53% NMR (CDCI3. ppm): 8.28-8.22 (m, 3H), 7.46-7.39 (m. 2H), 6.97-6.87 (m, 3H), 3.54 (s, 3H). 2.69 (s, 3H), 1.97-1.67 (m, 8H) Examples 70 to 72 1.2 eq. of NaH are suspended in DMF, the compound of example 66 is added slowly and the reaction mixture is stirred at room temperature for 1 h. An equimolar amount of the benzyl bromide or phenylethyl bromide is added and the mixture is refluxed until no more starting material is present. The reaction mixture is diluted with water and the resulting precipitate is filtered off. The crude product is purified by column chromatography. Example 70: 4-(4-Fluorophenyl)-1 -methyl-5-(2-benzylamino-4-pyridyl)-2-methyl-thioimidazole Yield: 13% NMR (CDCI3, ppm): 8.12-8.16 (m, 1H), 7.47- 7.26 (m, 7H), 6.95-6.86 (m, 2H), 6.53-6.50 (m, 1H), 6.24 (s, 1H), 5.30 (bs, 1H), 4.47 (d, 2H, J= 5.8 Hz), 3.32 (s, 3H), 2.68 (s, 3H) IR(1/cm): 3241, 1610, 1507, 1219, 839, 813, 737, 698 Example 71: 4-(4-Fluorophenyl)-1-methyl-5-[2-(2-phenylethyl)amino-4-pyridyl)-2-methylthioimidazole Yield: 54% NMR (CDCI3, ppm): 8.12-8.10 (m, 1H), 7.41- 7.19 (m, 7H), 6.92- 6.84 (m, 2H), 6.46-6.43 (m, 1H), 6.06 (s, 1H), 5.18 (d, 1H, J= 6.3 Hz), 4.63-4.57 (m. 1H), 3.11 (s. 3H), 2.70 (s, 3H), IR (1/cm): 1605, 1505, 1432, 1219, 839, 701 If 2.5 times the amount of benzyl bromide is added, the nitrogen (13) is disubstituted Example 72: 4-(4-Fluorophenyl)-1 -methyl-5-(2-dibenzylamino-4-pyridyl)-2-methyl-thioimidazole Yield: 81% NMR (CDCI3. ppm): 8.27-8.24 (m, 1H), 7.45-7.19 (m, 12 H), 6.95- 6.86 {m, 2H), 6.51 6.48 (m, 1H), 6.31 (s. 1H), 4.80 (s. 4H), 3.17 (s, 3H), 2.66 (s, 3H) IR (1/cm): 1598, 1496, 1427, 1219, 840, 831, 734, 702 Examples 73 to 75 The compound of examples 61, 62 or 63 is dissolved in THF and, with stirring, a 10-fold excess of LiAIH4 is added. The reaction mixture is then heated for 2 h. After cooling, water is added slowly. The mixture is extracted repeatedly with CH2CI2 and the combined organic phases are dried over Na2SO4. The drying agent is filtered off and the solvent is removed. The crude product is purified by column chromatography. Example 73: 4-(4-Fluorophenyl)-1-methyl-5-f2-ethylamino-4-pyridyl)-2-methyl-thioimidazole Yield: 70% NMR (CDCI3, ppm): 8.17-8.15 (m, 1H), 7.53-7.46 (m, 2H), 6.98-6.89 (m, 2H), 6.52- 6.49 (m, 1H), 6.27-6.26 (m, 1H), 4.59 (t, 1H, J= 6.0 Hz), 3.47 (s, 3H), 3.29-3.23 (m, 2H), 2.70 (s, 3H), 1.23 (t, 3H, J= 7.1 Hz) IR (1/cm): 3235, 1604, 1562, 1506, 1435, 1221, 844, 806 Example 74: 4-(4-Fluorophenyl)-1-n-propyl-5-(2-ethylamino-4-pyridyl)-2- methylthioimidazole Yield: 25% NMR (CDCI3, ppm): 8.17-8.14 (m, 1H), 7.51-7.43 (m, 2H), 6.98-6.87 (m, 2H;. 0.06-6.50 (m, 1H), 6.27 (s, 1H), 4.61 (t, 1H, J= 2.8 Hz), 3.79 (t, 2H. 7.7 Hz). 3.28-3.22 (m, 2H), 2.71 (s, 3H), 1.66-1.54 (m. 2H), 1.24 (t. 3H, J= 7.2 Hz), 0.83 (t, 3H, J= 7.4 Hz) IR (1/cm): 3275, 2930, 1607, 1525, 1507, 1219, 846, 813 Example 75: 4-(4-Fluorophenyl)-1 -(2.2,6,6-tetramethylpiperidin-4-yl)-5-(2-ethylamino-4-pyridyl)-2-methylthioimidazole Yield: 52% NMR (CDCI3, ppm): 8.10-8.07 (m. 2H). 7.47-7.40 (m, 2H), 7.12-7.03 (m, 2H). 6.44-6.41 (m. 1H), 6.37 (s, 1H), 4.30-4,14 (m, 1H), 3.27-3.21 (m. 2H), 2.66 (s, 3H), 2.11-1.91 (m, 2H), 1.59-1.52 (m, 2H). 1.12-1.01 (m, 9H). 0.90 (s, 6H) IR (1/cm): 3325, 2959, 1603. 1516, 1499, 1217, 1158. 849. 812 Example 76: 4-(4-Fluorophenyl)-1-(3-N-morpholinopropyl)-5-(2-acetamido-4-pyridyl)-2-(4-methylsulfinylbenzyl)thioimidazole Under protective gas, 4-(4-fiuorophenyl)-1-(3-N-morpholinopropyl)-5-(2-acetamido-4-pyridyl)imidazole-2-thione is suspended in abs. ethanol and an equimolar amount of 4-methylsulfinylbenzyl chloride is added. A spatula tip of Na2CO3 is added and the reaction mixture is then refluxed until the starting material has been converted completely. After cooling, the inorganic salts are filtered off and the solvent is removed using a rotary evaporator. The crude product is purified by column chromatograpy. Yield: 27% NMR (CDCI3, ppm): 8,67 (bs, 1H), 8.28-8.25 (m. 2H). 8.12 (s, 1H). 7.64-7.49 (m, 4H), 7.44-7.37 (m. 2H), 6.98-6.86 (m, 3H), 4,45 (s. 2H). 3.81-3.65 (m. 6H). 2.72 (s, 3H). 2.54-2.52 (m. 6H). 2.22 (s, 3H), 1.85-1.73 (m, 2H) Using the process described above, the following compounds were obtained: CLAIMS 1. A 2-thio-substituted imidazole derivative of the formula I wherein R1 is selected from the group consisting of: C1-C6-alkyl which is unsubstituted or substituted by one or two hydroxyl or C1-C4-alkoxy groups or by a nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, C2-C6alkenyl, C2-C6cycloalkyl, aryl which is unsubstituted or substituted by one or more halogen atoms or by a CrC4-alkylsulfanyl group, amino-CrC4-alkyl, where the amino group is unsubstituted or substituted by one or two CrC4-alkyl groups, aminoaryl, where the amino group is unsubstituted or substituted by one or two C1-C4-alkyl groups. aryl-CrC4-alkyl or an aromatic or nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N. O and S, which heterocyclic radical is unsubstituted or substituted by 1, 2. 3 or 4 C1-C4-alkyl groups, an aryl or aryl-C1-C4-alkyl group, R2 is selected from the group consisting of: H; C1-C6-alkyl. phenyl-C1-C4-alkyl. where the phenyl group may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl. halogen. C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl and C1-C4-alkylsulfonyl. C2-C6-alkenyl, C2-C6-alkenyl which is substituted by one or two halogen atoms and/or phenyl groups, where the phenyl group may independently be substituted by one or two C1-C4-alkyl or halogen atoms. C2-C6-alkynyl. C2-C6-alkynyl which is substituted by a phenyl group which may be unsubstituted or substituted by one or two C1-C4-alkyl or halogen atoms, C1-C6-alkyI which is substituted by a nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl or C1-C4-alkylsulfonyl. phenyl or phenyl which has one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, halogen, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl and C1-C4-alkylsulfonyl, or R1 and R2 together are -CH2CH2- or -CH2CH2CH2-, one of the radicals R1 and R4 is C1-C6-alkyl or an aromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, where the aromatic heterocyclic radical may have 1 or 2 substituents independently of one another selected from the group consisting of C1-C6-alkyI, amino, C1-C4-alkylamino. di-C1-C4-alkylamino, phenyl-C1-C4-aikylamino and R5CONR6-, where R5 is C1-C4-alkyl. phenyl, which may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, C1-C4-alkoxy and halogen, or C2-C6cycloalkyI and R6 is H, C1-C4-alkyl or benzyl, and the second of the radicals R3 and R4 is C1-C6-alkyl or aryl which is unsubstituted or substituted by a halogen atom, where only one of the radicals R3 and R4 may be C1-C6-alkyl, with the proviso that, if R1 represents aryl-C1-C5-alkyl or amino-C1-C6-alkyl, where the amino group is unsubstituted or substituted by one or two C1-C4-alkyl groups, R2 represents alkylsulfonyl- or alkylsulfinylaryl-C1-C5-alkyl, or an optical isomer or physiologically acceptable salt thereof. 2. A compound of the formula I as claimed in claim 1, wherein R1 is C1-C6-alkyI which is unsubstituted or substituted by one or two hydroxyl groups or a nonaromatic heterocyclic radical, C2-C6-alkenyl. C3-C6-cycloalkyl, aryl which is unsubstituted or substituted by one or more halogen atoms or a C1-C4-alkylsulfanyl group, amino-C1-C4-alkyl, where the amino group is unsubstituted or substituted by one or two C1-C4-alkyl groups, aminoaryl. where the amino group is unsubstituted or substituted by one or two C1-C4-alkyl groups, aryl-C1-C4-alkyl or an aromatic or nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, which heterocyclic radical is unsubstituted or substituted by 1, 2, 3 or 4 C1-C4-alkyl groups, an aryl or aryl-C1-C4-alkyl group. R2 is H, C1-C6-alkyl, phenyl-C1-C4-alkyl, where the phenyl group may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, halogen, C1-C4-alkylsulfanyl. C1-C4-alkylsulfinyl and C1-C4-alkylsulfonyl, C2-C4-alkenyl, C2-C6-aIkenyl which is substituted by one or two halogen atoms and/or phenyl groups. where the phenyl group may independently be substituted by one or two C1-C4-alkyl or halogen atoms, C2-C6alkynyl, C2-C6alkynyl which is substituted by a phenyl group which may be unsubstituted or substituted by one or two C1-C4-alkyl or halogen atoms, C1-C6-alkyl which is substituted by a nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, one of the radicals R1 and R4 is C1-C6-alkyI or an aromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, and the second of the radicals R3 and R4 is C1-C6-alkyI or aryl which is unsubstituted or substituted by a halogen atom, where only one of the radicals R3 and R4 may be C1-C6-alkyi, or an optical isomer or physiologically acceptable salt thereof. A compound of the formula I as claimed in claim 1 or 2, wherein one of the radicals R3 and R4 is halogen-substituted phenyl and the second of the radicals R3 and R4 is pyridyl which may be unsubstituted or may have 1 or 2 substituents independently of one another selected from the group consisting of C1-C6-alkyi, amino, C1-C4-alkylamino, di-C1-C4-alkylamino, phenyl-C1-C4-alkylamino and R5CONR6-, where R5 is C1-C4-alkyl, phenyl which may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, C1-C4-alkoxy and halogen, or C2-C6cycloalkyI and R6 is H, C1-C4-alkyl or benzyl. A compound of the formula I as claimed in claim 3, wherein one of the radicals R3 and R4 is 4-fluorophenyl and the second of the radicals R3 and R4 is 4-pyridyl which may be unsubstituted or have 1 or 2 substituents independently of one another selected from the group consisting of C1-C6-alkyl, amino, C1-C4-alkylamino, di-C1-C4-alkylamino, phenyl-C1-C4-alkylamino and R5CONR6-, where R5 is C1-C4-alkyl. phenyl which may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, C1-C4-alkoxy and halogen, or C3-C6-cycloalkyl and R6 is H, C1-C4-aikyl or benzyl. A compound of the formula I as claimed in any of the preceding claims, wherein R4 is pyridyl which is substituted by amino, C1-C4-alkylamino, phenyl-C1-C4-alkylamino or R5CONR6-, where R5 and R6 are as defined in claim 1. A compound as claimed in claim 5, wherein R4 is 4-pyridyl which is substituted by amino, C1-C4-alkylamino, phenyl-C1-C4-alkylamino or R5CONR6-. where R5 and R6 are as defined in claim 1. A compound as claimed in claim 8, wherein R4 is 4-pyridyl which is substituted by phenyl-C1-C4-alkylamino. A compound of the formula I as claimed in any of the preceding claims, wherein R1 is C1-C3-alkyI, C2-C6cycloalkyl or 2,2.6.6-tetramethylpiperidinyl. A compound as claimed in claim 8, wherein R1 is C1-C3-alkyl or 2,2,6.6-tetramethylpiperidinyl. A compound of the formula I as claimed in any of the preceding claims, wherein R2 is C1-C6-alkyl or phenyl-C1-C4-alkyl, where the phenyl group is substituted by C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl or C1-C4"alkylsulfonyL A compound as claimed in claim 1, i.e. 1-dimethylaminoethyl-4-(4-fluorophenyl)-5-(4-pyridyl)-2-thioimidazole, 1-dimethylaminopropyl-4-(4-fluorophenyl)-5-(4-pyridyl)-2-thioimidazole or 1 -methyl-4-(4-fIuoro-phenyl )-5-[2-(1-ethylamino)pyrid-4-y!)-2-thioimida2oIe. A compound of the formula I, whereir R1 is C1-C6-alkyl which is unsubstituted or substituted by one or two hydroxyl or C1-C4-alkoxy groups, or a nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N. O and S. C2-C6cycioalkyl or an aromatic or nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, which heterocyclic radical is unsubstituted or substituted by 1, 2, 3 or 4 C1-C4-alkyl groups, an aryi or aryl-C1-C4-alkyl group. R2 is H. C1-C6-alkyi, phenyl-C1-C4-alkyl, where the phenyl group may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl. halogen, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl and C1-C4-aIkylsulfonyl, phenyl, C1-C6-alkyI substituted by a nonaromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S. C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl or C1-C4-alkylsulfonyl, oris phenyl which has one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl, halogen, C1-C4-alkylsulfanyl, C1-C4-alkylsulfinyl and C1-C4-alkylsulfonyl, one of the radicals R3 and R4 is C1-C6-alkyI or an aromatic heterocyclic radical having 5 or 6 ring atoms and 1 or 2 heteroatoms independently of one another selected from the group consisting of N, O and S, where the aromatic heterocyclic radical has 1 or 2 substituents independently of one another selected from the group consisting of C1-C6-alkyI, amino, C1-C4-alkylamino, di-C1-C4-alkylamino, phenyl-C1-C4-alkylamino and R1CONR6-, where R5is C1-C4-alkyl, phenyl which may have one or two substituents independently of one another selected from the group consisting of C1-C4-alkyl. C1-C4-alkoxy and halogen, or C2-C6cycloalkyi and R6 is H, C1-C4-alkyl or benzyl, and the second of the radicals R3 and R4 is C1-C6-alkyl or aryl which is unsubstituted or substituted by a halogen atom, where only one of the radicals R3 and R4 may be C1-C6-alkyI, or an optical isomer or physiologically acceptable salt thereof. A compound as claimed in claim 12, wherein R1 is as defined in claim 8 or 9. A process as claimed in claim 12 and 13, wherein R2 is as defined in claim 10. A process as claimed in any of claims 12 to 14, wherein R3 and R4 are as defined in any of claims 3 to 7. A pharmaceutical composition, comprising at least one compound as claimed in any of claims 1 to 15, if appropriate together with one or more pharmaceutically acceptable carriers and/or additives. The use of at least one compound as claimed in any of claims 1 to 15 for preparing a pharmaceutical composition for treating disorders associated with a disturbed immune system. A method for treating disorders associated with a disturbed immune system, wherein an amount of a compound of the formula I as claimed in any of claims 1 to 15 sufficient to have immunomodulating action and/or to inhibit the release of cytokine is administered to a person in need of such a treatment. 19. A 2-thio-substituted imidazole derivative substantially as herein described and exemplified. 20. A pharmaceutical composition substantially as herein described and exemplified. Dated this 18 day of August 2003

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1289-chenp-2003-claims duplicate.pdf

1289-chenp-2003-claims original.pdf

1289-chenp-2003-correspondnece-others.pdf

1289-chenp-2003-correspondnece-po.pdf

1289-chenp-2003-description complete duplicate.pdf

1289-chenp-2003-description complete original.pdf

1289-chenp-2003-form 1.pdf

1289-chenp-2003-form 19.pdf

1289-chenp-2003-form 26.pdf

1289-chenp-2003-form 3.pdf

1289-chenp-2003-form 5.pdf

1289-chenp-2003-pct.pdf

abs-1289-chenp-2003.jpg