EP1644353A1 - Amide-substituted 1,2,4-triazin-5(2h)-ones for the treatment of chronically inflammatory diseases - Google Patents

Abstract

The invention relates to amide-substituted 1,2,4-triazin-5(2H)-ones, to methods for the production thereof, and to the use of the same for producing medicaments for the treatment and/or prophylaxis of diseases, especially chronically inflammatory diseases such as rheumatoid diseases, and cardiovascular diseases such as dyslipidemia, arteriosclerosis and coronary heart diseases Formula (I).

Description

AMID SUBSTITUTED 1, 2, 4-TRIAZINE-5 (2H) -ONE FOR THE TREATMENT OF CHRONICALLY INFLAMMATORY DISEASES

The invention relates to id-substituted 1,2,4-triazin-5 (2H) -ones and processes for their preparation and their use for the manufacture of medicaments for the treatment and / or prophylaxis of diseases, in particular chronic inflammatory diseases, such as e.g. Diseases of the rheumatoid type, and cardiovascular diseases, such as Dyslipidemia, arteriosclerosis and coronary heart disease.

The synthesis of amide-substituted 1,2,4-triazine-5 (2H) -ones is described in G. Hornyak, et al., Acta Chimica Academiae Scientiarum Hungaricae, 1969, 61 (2), 181-196.

WO 03/41712 relates inter alia to triazinones as Lp-PLA2 inhibitors for the treatment of arteriosclerosis. ^"

The inflammatory component in the pathophysiology of arteriosclerosis is widely recognized today. The inflammatory vascular changes result from the reaction of immigrating monocytes with pathogenic lipoproteins in the artery wall. Especially the formation of foam cells from the monocytes by immigrant Aufαahme of oxidized ^'lipids plays a central role in a plaque development and stability. In order to be recognized by monocytes, native lipoproteins must be modified to an atherogenic form. The enzyme 'platelet-activating factor acetylhydrolase' (PAF-AH) plays a key role in this by forming the inflammation mediators lysophosphatidylcholine and oxidized fatty acids from oxidized LDL (low-density lipoprotein). Plasma PAF-AH is a calcium-independent member of the phospholipase A2 family secreted by monocytes and macrophages. The substrates of the PAF-AH are the platelet-activating factor (PAF) and oxidized phospholipids in the oxidized. LDL (oxLDL). By splitting off an acyl residue in the sn-2 position, oxidized fatty acids and lysophosphatidylcholine (LysoPC) are formed. The pro-inflammatory mediator LysoPC is responsible for the accumulation of cholesterol ester-loaded monocytes (foam cells) in the arteries (Quinn, et al., Proc. Natl. Acad. Sei. USA 1988, 85, 2805-2809). This leads to the formation of the so-called 'fatty streaks', which is the first visible arteriosclerotic vascular change. An inhibitor of PAF-AH would stop the formation of these macrophage-enriched lesions and would therefore be useful for the treatment of arteriosclerosis. The increased LysoPC content of oxLDL also appears to be responsible for the endothelial dysfunction that is observed in patients with arteriosclerosis. PAF-AH inhibitors are therefore also suitable for the treatment of this phenomenon. Furthermore, their use would make sense in all diseases that are based on endothelial dysfunction, such as diabetes, high blood pressure and angina pectoris.

In addition, PAF-AH inhibitors could be used in any disease that has activated monocytes, macrophages or lymphocytes, since all of these cells express the enzyme.

It is therefore an object of the present invention to provide new PAF-AH inhibitors for the treatment of chronic inflammatory diseases and cardiovascular diseases in humans and animals.

Surprisingly, it was found that the amide-substituted 1,2,4-triazin-5 (2H) -one inhibitors described in the present invention are PAF-AH inhibitors.

The invention relates to compounds of the formula

in which

Y represents an oxygen atom or a sulfur atom,

m represents a number 1, 2 or 3,

n stands for a number 1, 2, 3 or 4,

R ^{1 stands} for CC ₆ alkyl or C ₃ -C ₇ cycloalkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano, oxo, phenyl, hydroxycarbonyl, Alkoxycarbonyl, A inocarbonyl and alkylaminocarbonyl,

R ^{2 represents} 5- to 10-membered heteroaryl, where heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxyl, arnino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylthio, aryl, aryloxy, hydroxycarbonyl, alkoxycarbonyl , Aminocarbonyl, alkylaminocarbonyl, alkylcarbonyl and alkylcarbonylamino,

R ^{3 represents} hydrogen or C, -C ₆ alkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxyl, amino, halogen, alkoxy, alkylamino, hydroxyalkylamino, alkylthio , Heterocyclyl, heteroaryl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl and alkylcarbonylamino,. ... , in which heterocyclyl and heteroaryl can in turn be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxyl, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylthio, Hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl and alkylcarbonylamino,

or

R ^{3 represents} a 3- to 8-membered heterocyclyl having 1 to 2 nitrogen atoms, where heterocyclyl can be substituted by 1 to 2 substituents, the substituents being selected independently of one another from the group consisting of, optionally with hydroxyl, amino or Alkoxy substituted alkyl,

R ^{4 stands} for aryl or heteroaryl, where aryl and heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino , Alkylthio, alkylsulfonyl, aryl, aryloxy, heteroaryl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl, alkylcarbonylamino, alkylaminosulfonyl and alkylsulfonylamino, in which alkyl, alkoxy, alkylthio and alkylsulfonyl can be substituted with 1 to 3 substituents halogen, and in which aryl and heteroaryl can in turn be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylthio, alkylsulfonyl, hydroxycarbonyl , Alkoxycarbonyl, ^• aminocarbonyl, alkylammocarbonyl, alkylcarbonyl, alkylcarbonylamino, alkylaminosulfonyl and alkylsulfonylamino, in which alkyl, alkoxy, alkylthio and alkylsulfonyl can in turn be substituted with 1 to 3 substituents halogen, and their salts, their solvates and the solvates of their salts.

Compounds according to the invention are the compounds of the formula (I) and their salts, solvates and solvates of the salts, and also the compounds encompassed by the formula (I) hereinafter referred to as exemplary embodiment (e) and their salts, solvates and solvates of the salts, to the extent the compounds mentioned below of formula (I) are not already salts, solvates or solvates of the salts.

Depending on their structure, the compounds according to the invention can exist in stereoisomeric forms (enantiomers, diastereomers). The invention therefore relates to the enantiomers or diastereomers and their respective mixtures. The stereoisomerically uniform constituents can be isolated in a known manner from such mixtures of enantiomers and / or diastereomers.

Provided that compounds of the invention may exist in tautomeric forms, the ^'present invention includes all tautomeric forms.

In the context of the present invention, preferred salts are physiologically acceptable salts of the compounds according to the invention. Also included, however, are salts which are themselves unsuitable for pharmaceutical applications but can be used, for example, for the isolation or purification of the compounds according to the invention.

Physiologically acceptable salts of the compounds according to the invention include acid addition salts of mineral acids, carboxylic acids and sulfonic acids, for example salts of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, toluenesulfonic acid, benzenesulfonic acid, naphthalenedisulfonic acid, acetic acid, trifluoroacetic acid acid, propionic acid, lactic acid, tartaric acid, malic acid, citric acid, fumaric acid, maleic acid and benzoic acid. ^"

Physiologically acceptable salts of the compounds of the invention also include salts of conventional bases such as for example and preferably alkali metal salts (eg sodium and potassium 5 salts), alkaline earth metal salts (such as ^"., Calcium and magnesium salts) and ammonium salts derived from ammonia or organic amines of 1 up to 16 carbon atoms, such as, for example and preferably, ethylamine, diethylamine, triethylamine, ethyldiisopropylamine, monoethanolamine, diethanolamine, triethanolamine, dicyclohexylamine, dimethylaminoethanol, procaine, dibenzylamine, N-methylmorpholine, arginine, lysine, ethylenediamine and ethylenediamine. 0 Solvates in the context of the invention are those forms of the compounds of the invention - -. Denotes that ^"in solid or liquid state by coordination with Lnmrs <s- agent molecules forming a complex Hydrates are a specific form of solvates where the coordination is with water he follows.

The free base of the salts of the compounds according to the invention can be obtained, for example, by adding an aqueous base, for example dilute sodium hydroxide solution, and subsequent extraction with a solvent by methods known to the person skilled in the art.

In the context of the present invention, unless otherwise specified, the substituents have the following meaning:

Alkyl per se and "alk" and "alkyl" in alkoxy. Alkylthio. Alkylamino, alkylsulfonyl, alkoxy-0 carbonyl, alkylammocarbonyl. Alkylcarbonyl. Alkylcarbonylamino, alkylaminosulfonyl and alkylsulfonylamino represent a linear or branched alkyl radical with generally 1 to 6, preferably 1 to 4, particularly preferably 1 to 3 carbon atoms, by way of example and preferably methyl, ethyl, n-propyl, isopropyl, n-butyl, tert-butyl, n-pentyl and n-hexyl.

Alkoxy exemplifies and preferably methoxy, ethoxy, n-propoxy, isopropoxy, tert-5 butoxy, n-pentoxy and n-hexoxy.

Alkylthio is exemplary and preferably methylthio, ethylthio, n-propylthio, isopropylthio, tert-butylthio, n-pentylthio and n-hexylthio.

Alkylamino stands for an alkylamino radical with one or two (independently selected) alkyl substituents, for example and preferably for methylarnino, ethylamino, n-0 propylamino, isopropylamino, tert-butylamino, n-pentylamino, ^' n-hexylamino, NN-dimethylamino, NN -Diethylamino, N-ethyl-N-methylamino, N-methyl-Nn-propylamino, N-isopropyl-Nn- propylamino, N-tert-butyl-N-methylamino, N-ethyl-Nn-pentylamino and Nn-hexyl-N-methylamino.

C ₁ -C ₃ alkylamino is, for example, a monoalkylamino radical having 1 to 3 carbon atoms or a dialkylamino radical each having 1 to 3 carbon atoms per alkyl substituent.

Alkylsulfonyl is exemplified and preferably methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, isopropylsulfonyl, tert-butylsulfonyl, n-pentylsulfonyl ^' and n-hexylsulfonyl.

Alkoxycarbonyl exemplifies and preferably represents methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl, tert-butoxycarbonyl, n-pentoxycarbonyl and n-hexoxycarbonyl.

Alkylammocarbonyl stands for an alkylaminocarbonyl radical with one or two (independently selected) alkyl substituents, the alkyl substituents independently of one another generally having 1 to 6, preferably 1 to 4, particularly preferably 1 to 3 carbon atoms, by way of example and preferably methylaminocarbonyl, ethylaminocarbonyl, n-propylamino-carbonyl, isopropylaminocarbonyl, tert.-butylaminocarbonyl, n-pentylarninocarbonyl, n-hexylaminocarbonyl, NN-dimethylamrnocarbonyl, NN-diethylaminocarbonyl, N-ethyl-N-methyl-arninocarbonyl, N-methyl-Nn-propyl N-isopropyl-Nn-propylarninocarbonyl, N-tert-butyl-N-methylaminocarbonyl, N-emyl-Nn-pentylamino-carbonyl and Nn-hexyl-N-methylamino-carbonyl.

C ₁ -C ₃ alkylaminocarbonyl represents, for example, a monoalkylaminocarbonyl radical having 1 to 3 carbon atoms or a dialkylaminocarbonyl radical each having 1 to 3 carbon atoms per alkyl substituent.

Alkylcarbonyl is an example and preferably methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, isopropylcarbonyl, tert-butylcarbonyl, n-pentylcarbonyl and n-hexylcarbonyl.

Alkylcarbonylamino is exemplary and preferably methylcarbonylamino, ethylcarbonylamino, n-propylcarbonylamino, isopropylcarbonylamino, tert-butylcarbonylamino, n-pentylcarbonylamino and n-hexylcarbonylamino.

Allc laminosulfonyl represents an alkylaminosulfonyl radical with one or two (independently selected) alkyl substituents, the alkyl substituents independently of one another generally having 1 to 6, preferably 1 to 4, particularly preferably 1 to 3 carbon atoms, for example and preferably methylaminosulfonyl, ethylaminosulfonyl, n-propylaminosulfonyl, isopropylaminosulfonyl, tert-butylaminosulfonyl, n-pentylaminosulfonyl, n-hexylamino sulfonyl, NN-dimethylaminosulfonyl, NN-diethylaminosulfonyl, N-ethyl-N-methylaminosulfonyl, N-methyl-Nn-propylaminosulfonyl, N-isopropyl-Nn-propylaminosulfonyl, N-tert-butyl-N-methylaminosulfonyl, N-ethyl -Nn-pentylaminosulfonyl and Nn-hexyl-N-memylaminosulfonyl.

C ₁ -C ₃ alkylaminosulfonyl is, for example, a monoalkylaminosulfonyl radical having 1 to 3 carbon atoms or a dialkylaminosulfonyl radical each having 1 to 3 carbon atoms per alkyl substituent.

Alkylsulfonylamino is exemplary and preferably methylsulfonylamino, ethylsulfonylamino, n-propylsulfonylamino, isopropylsulfonylamino, tert-butylsulfonylamino, n-pentylsulfonylamino and n-hexylsulfonylamino.

Cycloalkyl stands for a cycloalkyl group with usually 3 to 8, preferably 5 to 7 carbon atoms, examples and preferably for cycloalkyl are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl.

Aryl stands for a mono- to tricyclic aromatic radical with generally 6 to 14, preferably 6 to 10 carbon atoms, examples and preferably for aryl are phenyl, antaphthyl and phenanthrenyl.

Aryloxy stands for a mono- to tricyclic aromatic radical with generally 6 to 14, preferably 6 to 10 carbon atoms, which is bonded via an oxygen atom, for example and preferably for aryloxy, phenoxy, Νaphthyloxy and phenanthrenyloxy are mentioned.

Heteroaryl stands for an aromatic, mono- or bicyclic radical with generally 5 to 10, preferably 5 to 6 ring atoms and up to 5, preferably up to 4 heteroatoms from the series S, O and Ν, a nitrogen atom also being a Ν- Can form oxide, by way of example and preferably for thienyl, furyl, pyrrolyl, thiazolyl, oxazolyl, oxadiazolyl, pyrazolyl, imidazolyl, pyridyl, pyrimidyl, pyridazinyl, pyrazinyl,. Indolyl, indazolyl, benzofuranyl, benzothiophenyl, quinolinyl, isoquinolinyl, benzoxazolyl, benzimidazolyl.

Heterocyclyl stands for a mono- or bicyclic, heterocyclic radical with generally 4 to 10, preferably 5 to 8 ring atoms and up to 3, preferably up to 2 heteroatoms and / or hetero groups from the series Ν, O, S, SO, S0 ₂ , whereby a nitrogen atom can also form a Ν-oxide. The heterocyclyl residues can be saturated or partially unsaturated. 5- to 8-membered, monocyclic saturated heterocyclyl radicals having up to two heteroatoms from the O, Ν and S series are preferred, for example and preferably for oxetan-3-yl, pyrrolidin-2-yl, pyrrolidin-3-yl, pyrrolinyl, Tetrahydrofuranyl, tetrahydrothienyl, pyranyl, piperidin-1-yl, piperidin-2-yl, Piperidin-3-yl, piperidin-4-yl, thiopyranyl, morpholin-1-yl, morpholin-2-yl, morpholin-3-yl, perhydroazepinyl, piperazin-1-yl, piperazin-2-yl.

Halogen represents fluorine, chlorine, bromine and iodine, preferably fluorine and chlorine.

A symbol * on a bond means the point of attachment in the molecule. If radicals in the compounds according to the invention are substituted, the radicals, unless otherwise specified, can be substituted one or more times in the same or different manner. A substitution with up to three identical or different substituents is preferred. Substitution with a substituent is very particularly preferred.

Preferred compounds of the formula (I) are those in which Y represents an oxygen atom or a sulfur atom, m represents a number 1 or 2, n represents a number 1, 2 or 3,

R ^{1 represents} C ₁ -C ₆ -alkyl or C ₃ -C ₆ -cycloalkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano, oxo, Phenyl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl and alkylammocarbonyl,

R ^{2 stands} for 5- to 10-membered heteroaryl, where heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy , Alkylamino, alkylthio, aryl, aryloxy, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl and alkylcarbonylamino,

, R ^{3 stands} for hydrogen or CC ₆ alkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, alkoxy, alkylamino and hydroxyalkylamino, or R ^{3 represents} a 5- to 7-membered heterocyclyl having 1 to 2 nitrogen atoms, it being possible for heterocyclyl to be substituted with 1 to 2 substituents, the substituents being selected independently of one another from the group consisting of optionally substituted with hydroxyl, amino or alkoxy alkyl,

R ^{4 represents} aryl or heteroaryl, where aryl and heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, aryl, aryloxy , Heteroaryl, alkylammocarbonyl and alkylcarbonylamino, in which ΛlkylTrrϊd alkoxy can be substituted with 1 to 3 substituents halogen, and in which aryl and heteroaryl can in turn be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano , Trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylammocarbonyl and alkylcarbonylamino, in which alkyl and alkoxy can in turn be substituted with 1 to 3 halogen substituents,

and their salts, their solvates and the solvates of their salts.

Preferred compounds of the formula (I) are also those which

Y represents a sulfur atom,

m represents the number 1,

n stands for the number 1,

R ^{1 stands} for C ¹ -C ₄ -alkyl, cyclopentyl or cyclohexyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of fluorine, cyano, oxo, phenyl, alkoxycarbonyl, aminocarbonyl and Alkylammocarbonyl, R ^{2 stands} for pyridyl, thienyl, furyl, thiazolyl, oxadiazolyl, benzimidazolyl or benzoxazolyl, it being possible for pyridyl, thienyl, furyl, thiazolyl, oxadiazolyl, benzimidazolyl and benzoxazolyl to be substituted with 1 to 3 substituents, the substituents being selected independently from one another Group consisting of halogen, trifluoromethyl, trifluoromethoxy and methyl,

R ^{3 represents} hydrogen or -CC alkyl, where alkyl can be substituted with a substituent, the substituent being selected from the group consisting of amino and C 1 -C ₄ -alkylamino,

or"

R ^{3 represents} piperidinyl or pyrrolidinyl, it being possible for piperidinyl and pyrrolidinyl to be substituted by a C ₄ alkyl substituent,

R ⁴ represents phenyl, where phenyl may be substituted with a substituent, whereby the substituent is selected from the group consisting of trifluoromethyl, trifluoromethoxy, Cι-C ₄ - alkyl, Cι-C ₄ -alkoxy and phenyl, which phenyl in turn be substituted can with a substituent, the substituent being selected from the group consisting of halogen, trifluoromethyl, trifluoromethoxy, C _r C ₃ alkyl and CC ₃ alkoxy,

and their salts, their solvates and the solvates of their salts.

Preferred compounds of the formula (I) are also those in which

Y represents a sulfur atom,

m represents the number 1,

n stands for the number 1,

R ^{1 represents} -Gralkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of fluorine, cyano, oxo, phenyl and alkoxycarbonyl,

R ^{2 represents} pyridyl, thienyl, furyl or thiazolyl, where pyridyl, thienyl, furyl and thiazolyl can be substituted by 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, trifluoromethyl, trifluoromethoxy and methyl,

R ^{3 represents} hydrogen or C _r C ₄ alkyl, where alkyl can be substituted with a substituent, the substituent being selected from the group consisting of amino and C ₄ alkylamino,

or

R ^{3 represents} piperidinyl or pyrrolidinyl, where piperidinyl and pyrrolidinyl can be substituted by a substituent C1-C-alkyl,

R ⁴ stands for phenyl, where phenyl can be substituted with a substituent, the substituent being selected from the group consisting of CC ₄ alkyl, C 1 -C ₄ alkoxy and phenyl, in which phenyl can in turn be substituted with a substituent, the substituent being selected from the group consisting of halogen, trifluoromethyl, C1-C ₃ -alkyl and Cι-C ₃ -alkoxy,

and their salts, their solvates and the solvates of their salts.

Preferred compounds of the formula (I) are also those in which

Y represents an oxygen atom or a sulfur atom,

m represents a number 1, 2 or 3,

n stands for a number 1, 2, 3 or 4,

R ^{1 represents} C _r C ₆ ~ alkyl or C ₃ -C ₇ cycloalkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, oxo, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl and alkylammocarbonyl,

R represents 5- to 10-membered heteroaryl, where heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxyl, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, Alkylamino, alkylthio, aryl, aryloxy, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl and alkylcarbonylamino,

R ^{J represents} hydrogen or CC ₆ alkyl, where alkyl can be substituted with 1 to 3 substituents, where the substituents. are independently selected from the group consisting of hydroxy, amino, halogen, alkoxy, alkylamino, hydroxyalkylamino, alkylthio, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl and alkylcarbonylamino,

R ^{4 stands} for aryl or heteroaryl, where aryl and heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxyl, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino , Alkylthio, alkylsulfonyl, aryl, aryloxy, heteroaryl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl, alkylcarbonylamino, alkylaminosulfonyl and alkylsulfonylamino, in which aryl and heteroaryl can in turn be substituted with 1 to 3 substituents, the substituents being selected independently of one another, the substituents being selected independently of one another, the substituents being selected independently of one another Group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylthio, alkylsulfonyl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl, alkylcarbonylamino, alkylaminosulfonyl and alkylsulfonylamino,

and their salts, their solvates and the solvates of their salts.

Preferred compounds of the formula (I) are those in which Y represents an oxygen atom or a sulfur atom,

m represents a number 1 or 2,

n stands for a number - 1, 2 or 3,

R ^{1 represents} C-Cβ-alkyl or C ₃ -C ₆ cycloalkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, oxo, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl and alkylammocarbonyl,

R ^{2 stands} for 5- to 10-membered heteroaryl, where heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy , Alkylamino, alkylthio, aryl, aryloxy, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, alkylcarbonyl and alkylcarbonylamino,

R ^{3 represents} hydrogen or -CC ₆ -alkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, alkoxy, alkylamino and hydroxyalkylamino,

R ^{4 represents} aryl or heteroaryl, where aryl and heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, aryl, aryloxy , Heteroaryl, alkylammocarbonyl and alkylcarbonylamino, in which aryl and heteroaryl may in turn be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylammocarbonyl and alkylcarbonylamino .

and their salts, their solvates and the solvates of their salts.

Preferred compounds of the formula (I) are also those in which Y represents a sulfur atom,

m represents the number 1,

n ^'stands for the number 1,

R ^{1 stands} for C _r C ₄ alkyl or cyclohexyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of fluorine, oxo and alkoxycarbonyl,

R ^{2 represents} pyridyl, thienyl, furyl or benzoxazolyl, where pyridyl, thienyl, furyl and benzoxazolyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, trifluoromethyl and trifluoromethoxy,

R ^{3 represents} hydrogen or diethylaminoethyl,

R ^{4 represents} phenyl, where phenyl can be substituted with a phenyl, in which phenyl can in turn be substituted with a substituent, the substituent being selected from the group consisting of halogen, trifluoromethyl, trifluoromethoxy, CC ₃ alkyl and CC ₃ alkoxy , -

and their salts, their solvates and the solvates of their salts.

Preferred compounds of the formula (I) are those in which Y represents a sulfur atom.

Preference is also given to those compounds of the formula (I) in which m represents the number 1.

Those compounds of the formula (I) in which n represents the number 1 are also preferred.

Preference is also given to those compounds of the formula (I) in which R ^{1 represents} ethyl, ethoxycarbonylethyl, 3-oxobut-l-yl, trifluoromethyl or cyclohexyl.

Preference is also given to those compounds of the formula (ϊ) in which R ^{2 represents} pyridyl, thienyl, furyl or benzoxazolyl. Preferred compounds of the formula (I) are those in which R ^{3 represents} hydrogen or diethylaminoethyl.

Preferred compounds of the formula (I) are those in which R ^{4 is} a substituent of the formula

stands for R ^{5 stands} for hydrogen, halogen, trifluoromethyl or trifluoromethoxy.

The invention further relates to a process for the preparation of the compounds of the formula (I), wherein compounds of the formula

in which

Y, m, n, R ¹ and R ^{2 have} the meaning given above,

with compounds of the formula

3 /, FT R (m),

in which

R ³ and R ^{4 have} the meaning given above,

be implemented. The reaction is generally carried out in inert solvents, in the presence of dehydrating reagents, if appropriate in the presence of a base, preferably in a temperature range from 0 ° C. to room temperature at atmospheric pressure.

■ Suitable dehydration reagents are, for example, carbodiimides such as N, N-diethyl, NN'-dipropyl, NN'-diisopropyl, NN'-dicyclohexylcarbodiimide, N- (3-dimethylaminoisopropyl) -N'-ethylcarbodiimide hydrochloride (EDC) (optionally in the presence of penta- fluorophenol (PFP)), N-cyclohexylcarbodiimide-N'-propyloxymethyl-polystyrene (PS-carbodiimide) or carbonyl compounds such as carbonyldiimidazole, or 1,2-oxazolium compounds such as 2-ethyl-5-phenyl-lj2-oxazolium-3-sulfate or 2 -tert.-butyl-5-methyl-isoxazolium perchlorate, or acylamino compounds such as 2-ethoxy-l-ethoxycarbonyl-l, 2-dihydroquinoline, or propanephos-

- Phonic acid anhydride, or isobutyl chloroformate, or bis (2-oxo-3-oxazolidinyl) phosphoryl chloride or benzohiazolyloxy-tri (dimethylamino) phosphbnM ^: hhexafluorophosphate, or 0- (benzotriazol-l-yl) -N, N, N ' , N'-tetτa-methyluronium hexafluorophosphate (HBTU), 2- (2-oxo-l- (2H) -pyridyl) - 1,1,3,3-tetramethyluronium tetrafluoroborate (TPTU) or 0- (7-azabenzotriazole-l -yl) -N, N, N ', N'-tetramethyl uronium hexafluorophosphate (HATU), or 1-hydroxybenzetriazole (HOBt), or benzotriazol-l-yloxytris (dimethylamino) phosphonium hexafluorophosphate (BOP), or mixtures thereof bases. The condensation is preferably carried out using HOBt and EDC.

Bases are, for example, alkali carbonates, e.g. Sodium or potassium carbonate, or hydrogen bicarbonate, or organic bases such as trialkylamines, e.g. Triethylamine, N-methylmorpholine, N-methylpiperidine, 4-dimethylaminopyridine or diisopropylethylamine. The condensation is preferably carried out with diisopropylethylamine.

Inert solvents are, for example, halogenated hydrocarbons such as dichloromethane or trichloromethane, hydrocarbons such as benzene, nitromethane, dioxane, dimethylformamide, acetonitrile or hexamethylphosphoric triamide. It is also possible to use mixtures of the solvents. Dichloromethane or dimethylformamide is particularly preferred.

The compounds of the formula (JE) are known or can be synthesized from the corresponding starting materials by known processes.

The compounds of the formula (H) are known or can be prepared by compounds of the formula

in which

Y, m, n, R ¹ and R ^{2 have} the meaning given above, and

R ⁶ ÜR alkyl, preferably methyl, ethyl or _{tert-butyl,,,,.}

with bases (methyl, ethyl) or with acids (tert-butyl).

The reaction is generally carried out in inert solvents, preferably in a temperature range from 0 ° C. to room temperature at normal pressure.

In the case of reaction with bases are, ^"for example, alkali metal hydroxides as bases such as sodium, lithium or potassium hydroxide, or alkali metal carbonates such as cesium carbonate, sodium or Kahumcarbonat, is preferably sodium hydroxide. Examples of solvents are halogenated hydrocarbons such as methylene chloride, trichloromethane, tetrachloromethane, trichloroethane, tetrachloromethane - Chloroethane, 1,2-dichloroethane or trichlorethylene, ethers such as diethyl ether, methyl tert-butyl ether, 1, 2-dimethoxyethane, dioxane or tetrahydrofuran, alcohols such as methanol, ethanol, n-propanol or iso-propanol, or other solvents such as Dimethylformamide, dimethylacetamide, dimethyl sulfoxide, acetonitrile or pyridine, or mixtures of solvents, preferred solvents are tetrahydrofuran and / or methanol or dioxane.

In the case of reaction with acids, suitable acids are, for example, hydrogen chloride or trifluoroacetic acid. Solvents are, for example, halogenated hydrocarbons such as dichloromethane or trichloromethane, or ethers such as diethyl ether, tetrahydrofuran or dioxane, or other solvents such as dimethylformamide or acetonitrile. It is also possible to use mixtures of the solvents. The use of hydrogen chloride in dioxane or trifluoroacetic acid in dichloromethane is particularly preferred.

The compounds of formula (JE) are known or can be prepared by compounds of formula

in which

Y, m, R ¹ and R ^{2 have} the meaning given above,

with compounds of the formula

in which

n and R ^{6 have} the meaning given above, and

X ^{1 represents} halogen, preferably iodine or bromine,

be implemented.

The reaction is generally carried out in inert solvents, in the presence of a base, preferably in a temperature range from 0 ° C. to 40 ° C. at normal pressure.

Inert solvents are, for example, halogenated hydrocarbons such as methylene chloride, trichloromethane or 1,2-dichloroethane, ethers such as dioxane, tetrahydrofuran or 1,2-dimethoxyethane, or other solvents such as acetone, dimethylformamide, dimethylacetamide, 2-butanone or acetonitrile, tetrahydrofuran or methylene chloride is preferred.

Bases are, for example, alkali carbonates such as cesium carbonate, sodium or potassium carbonate, or sodium or potassium methoxide, or sodium or potassium ethanol or potassium tert-butoxide, or amides such as sodium amide, lithium bis (trimethylsilyl) amide or lithium diisopropyl amide, or other bases such as sodium hydride, DBU, triethylamine or diisopropylethylamine, diisopropylethylamine is preferred. The compounds of the formula (V) are known or can be synthesized from the corresponding starting materials by known processes.

The compounds of the formula (IV) are known or can be prepared by compounding the formula

in which

Y and R ^{1 have} the meaning given above, with compounds of the formula - (CH ₂ ) - x ² (vπ), in which m and R ^{2 have} the meaning given above, and

_, X ^{2 represents} halogen, preferably iodine or bromine.

The reaction is generally carried out in a solvent, in the presence of a base, preferably in a temperature range from 0 ° C. to 40 ° C. at normal pressure.

Solvents are, for example, halogenated hydrocarbons such as methylene chloride, trichloromethane or 1,2-dichloroethane, ethers such as dioxane, tetrahydrofuran or 1,2-dimethoxyethane, or other solvents such as acetone, dimethylformamide, dimethylacetamide, 2-butanone or acetonitrile, or water or mixtures of the solvents with Water, water is preferred. Bases are, for example, alkali carbonates such as cesium carbonate, sodium or potassium carbonate, or sodium or potassium methoxide, or sodium or potassium ethanol or potassium tert-butoxide, or amides such as sodium amide, lithium bis (trimethylsilyl) amide or lithium diisopropyl amide, or others Bases such as sodium hydride, DBU, triethylamine or diisopropylethylamine, preference is given to potassium carbonate. One equivalent of the compounds of the formula (VE) is used, based on the compounds of the formula (VI).

The compounds of the formulas (VI) and (VII) are known or can be synthesized from the corresponding starting materials by known processes.

The preparation of the compounds according to the invention can be illustrated by the following synthesis scheme.

Scheme 1:

The compounds according to the invention show an unforeseeable, valuable pharmacological spectrum of action.

They are therefore suitable for use as medicaments for the treatment and / or prophylaxis of diseases in humans and animals.

The pharmaceutical activity of the compounds according to the invention can be explained by their action as PAF-AH inhibitors. The present invention furthermore relates to the use of the compounds according to the invention for the treatment and / or prophylaxis of diseases, preferably cardiovascular diseases, in particular arteriosclerosis.

The compounds according to the invention can be used in the prevention and treatment of cardiovascular diseases, such as e.g. Atherosclerosis, reperfusion tissue damage after stroke, heart attack or peripheral arterial and venous vascular diseases and essential or pregnancy-induced high blood pressure.

Furthermore, the compounds according to the invention can be used in all types of diseases which include lipid oxidation, inflammation and increased enzyme activity, such as, for example, arthritis, rheumatoid arthritis, diabetes mellitus, kidney inflammation, osteoporosis, Crohn's disease, chronic inflammatory lung diseases such as adult respiratory distress syndromes (AJRDS), inflammatory diseases of the brain such as Alzheimer's disease, sepsis, and acute and chronic inflammation, restenosis after ^'PTCA, transplant rejection, inflammatory fibrotic organ changes such as liver fibrosis, or generalized autoimmune disease systemic lupus erythematosus or other forms of lupus erythematosus or dermal inflammatory diseases like psoriasis.

Because of their pharmacological properties, the compounds according to the invention can be used alone and, if necessary, in combination with other active ingredients, in particular with anti-hyperlipidemic, anti-arteriosclerotic, anti-diabetic, anti-inflammatory or anti-hypertensive active ingredients. Examples of these are cholesterol synthesis inhibitors such as e.g. Statins, antioxidants such as Probucol, PPAR activators, irisulin sensitizers, calcium channel antagonists, and non-steroidal anti-inflammatory drugs.

The present invention further relates to the use of the compounds ¹ of the invention for the treatment and / or prophylaxis of diseases, especially of the aforementioned diseases.

The present invention furthermore relates to the use of the compounds according to the invention for the manufacture of a medicament for the treatment and / or prophylaxis of diseases, in particular the aforementioned diseases.

The present invention furthermore relates to a method for the treatment and / or prophylaxis of diseases, in particular the aforementioned diseases, using a therapeutically effective amount of the compounds according to the invention. The compounds according to the invention can act systemically and / or locally. For this purpose, they can be applied in a suitable manner, such as, for example, orally, parenterally, pulmonally, nasally, sublingually, lingually, buccally, rectally, dermally, transdermally, conjunctivally, otically or as an implant or stent.

For these administration routes, the compounds according to the invention can be administered in suitable administration forms.

For oral administration, state-of-the-art, fast and / or modified application forms which release the compounds according to the invention and contain the compounds according to the invention in crystalline and / or amorphized and / or dissolved form, such as e.g. Tablets (non-coated or coated tablets, for example • with gastric juice-resistant or delayed dissolving or insoluble coatings, control the release of the compound according to the invention), tablets or films / wafers which disintegrate rapidly in the oral cavity, films / lyophilisates, capsules (for example Hard or soft gelatin capsules), dragees, granules, pellets, powders, emulsions, suspensions, aerosols. or solutions.

Parenteral administration can be done by bypassing an absorption step (e.g. intravenous, intraarterial, intracardiac, intraspinal or intralumbal) or by switching on absorption (e.g. intramuscular, subcutaneous, intracutaneous, percutaneous or intraperitoneal). Suitable forms of application for parenteral administration include: Injection and irifusion preparations in the form of solutions, suspensions, emulsions, lyophilisates or sterile powders.

Oral application is preferred.

For the other application routes, e.g. Inhalation medication forms (including powder inhalers, nebulizers), nasal drops, solutions, sprays; tablets, films / wafers or capsules to be applied lingually, sublingually or buccally, suppositories, ear or eye preparations, vaginal capsules, aqueous suspensions (lotions, shaking mixes), lipophilic suspensions, ointments, creams, transdermal therapeutic systems (such as plasters), Milk, pastes, foams, scattering powder, implants or stents.

The compounds according to the invention can be converted into the administration forms mentioned. This can be done in a manner known per se by mixing with inert, non-toxic, pharmaceutically suitable auxiliaries. These auxiliaries include, inter alia, carriers (for example microcrystalline cellulose, lactose, mannitol), solvents (for example liquid polymer ethylene glycols), emulsifiers and dispersing or wetting agents (for example sodium dodecyl sulfate, polyoxysorbitanoleate), binders (for example polyvinylpyrrolidone), synthetic and natural polymers (for example albumin), stabilizers (for example antioxidants such as ascorbic acid), dyes (for example inorganic pigments such as iron oxides ) and taste and / or smell.

The present invention further relates to medicaments which contain at least one compound according to the invention, usually together with one or more inert, non-toxic, pharmaceutically suitable auxiliaries, and to their use for the purposes mentioned above.

In general, it has proven to be advantageous to administer amounts of approximately * 5- ™ is- 250 mg / kg body weight per 24 hours for parenteral administration in order to achieve effective results. When administered orally, the amount is about 5 to 100 mg / kg body weight per 24 hours.

Nevertheless, it may be necessary to deviate from the amounts mentioned, depending on body weight, route of administration, individual behavior towards the active ingredient, type of preparation and time or interval at which the application is carried out. In some cases it may be sufficient to make do with less than the aforementioned minimum quantity, while in other cases the above upper limit must be exceeded. In the case of application of larger quantities, it may be advisable to distribute them in several single doses over the day.

The percentages in the following tests and examples are, unless stated otherwise, percentages by weight; Parts are parts by weight. Solvent ratios, dilution ratios and concentration details of liquid / liquid solutions each relate to the volume. "W / v" means "weight / volume". For example, "10% w / v" means: 100 ml of solution or suspension contain 10 g of substance. A examples

Abbreviations:

Absolute

Boc tert-butoxycarbonyl

CDClj Deuterochlorofbrm

C0 ₂ carbon dioxide

TLC thin layer chromatography

DIEA NN-diisopropylethylamine

DMSO Dimethylsulfoxid d..Th. of theory

EDC - N '- (3-dimethylaminopropyl) -N-e.thylcarbodiimide eq. equivalent to

ESI electrospray ionization (for MS)

Total saturated h hour

HOBt 1 -hydroxy-1H-benzotriazole

HPLC high pressure, high performance liquid chromatography conc. concentrated

LC-MS liquid chromatography-coupled mass spectroscopy

Min minutes ^"

MS mass spectroscopy

MW ^■ molecular weight [g / mol]

NMR nuclear magnetic resonance spectroscopy

Rf retention index (at DC)

RP-HPLC reverse phase HPLC

RT room temperature

Rt retention time (with HPLC)

TFA trifluoroacetic acid

THF tetrahydrofuran

HPLC and LC-MS methods:

Method 1 (LC-MS): Instrument: Micromass Quattro LCZ, with HPLC Agilent Series 1100; Column: Grom-SIL120 ODS-4 HE, 50 mm x 2.0 mm, 3 μm; Eluent A: 1 1 water + 1 ml 50% formic acid, eluent B: 1 1 acetonitrile + 1 ml 50% formic acid; Gradient: 0.0 min 100% A - »0.2 min 100% A -» 2.9 min 30% A -> 3.1 min 10% A -> 4.5 min 10% A; Oven: 55 ° C; Flow: 0.8 ml / min; UV detection: 208-400 nm.

Method 2 (LC-MS): Device type MS: Micromass ZQ; Device type HPLC: HP 1100 Series; UV DAD; Column: Phenomenex Synergi 2μ Hydro-RP Mercury 20mm x 4mm; Eluent A: 1 1 water + 5 0.5 ml 50% formic acid, eluent B: 1 1 acetonitrile + 0.5 ml 50% formic acid; Gradient: 0.0 min 90% A - 2.5 min 30% A -> 3.0 min 5% A - 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 min / 4.5 min 2 ml / min; Oven: 50 ° C; UV detection: 210 nm.

Method 3 (LC-MS): Device type MS: Micromass ZQ; Device type HPLC: Waters Alliance 2795; Column: Phenomenex Synergi 2μ Hydro-RP Mercury 20mm x 4mm; Eluent A: 1 1 water + 0.5 ml 10 50% formic acid, eluent B: 1 1 acetonitrile + 0.5 ml 50% formic acid; Gradient: 0.0 min - -. 90% A- ^ -3.§'EHn_30% A - 3.0 min 5% A - 4.5 min- 5% A ;. Flow: 0.0 min l ^" ml / min, 2.5 rnra / 3.Q min / 4.5 min 2 ml / min; oven: 50 ° C; UV detection: 210 nm.

Method 4 (HPLC): Instrument: HP 1100 with DAD detection; Column: Kromasil RP-18, 60 mm x 2 mm, 3.5 μm; Eluent A: 5 ml HCIO ₄ / I water, eluent B: acetonitrile; Gradient: 0 min 2% B, 0.5

15 min 2% B, 4.5 min 90% B, 6.5 min 90% B; Flow: 0.75 ml / min; Oven: 30 ° C; UV detection: 210 nm.

Method 5 (LC-MS): Instrument: Micromass Quattro LCZ with HPLC Agilent Series 1100; Column: Phenomenex Synergi 2μ Hydro-RP Mercury 20mm x 4mm; Eluent A: 1 1 water + 0.5 ml 50% formic acid, eluent B: 1 1 acetonitrile + 0.5 ml 50% formic acid; Gradient: 0.0 min 90% A ^■ > 2.5 min 30% A - 3.0 min 5% A - 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 20 min 4.5 min 2 ml / min; Oven: 50 ° C; UV detection: 208-400 nm.

Method 6 (HPLC): Instrument: Hewlett Packard Series 1050; Column: Symmetry TM C18 3.9 mm x 150 mm; Eluent A: water, eluent B: acetonitrile; Gradient: 0.0 min 10% B -> 0.6 min 10% B -> 3.8 min 100% B ^■ 5.0 min 100% B - 5.5 min 10% B; Running time: 6.0 min; Flow: 1.5 ml / min; Injection volume: 10 μl; UV detection: 214 nm and 254 nm.

25 Method 7 (GC-MS): Instrument: Micromass GCT, GC6890; Column: Restek RTX-35MS, 30 mx 250 μm x 0.25 μm; constant flow with helium: 0.88 ml / min; Oven: 60 ° C; Inlet: 250 ° C; Gradient: 60 ° C (hold 0.30 min), 50 ° C / min -> 120 ° C, 16 ° C / min -> 250 ° C, 30 ° C / min -> 300 ° C (hold 1.7 min).

Method 8 (preparative HPLC): column: GromSil C18, 250 mm x 30 mm; Flow: 40 ml / min; 30 running time: 40 min; Detection: 210 nm; Eluent A: water with 0.05% formic acid, eluent B: acetonitrile, gradient: 5 min 10% B - »35 min 95% B - 37 min 95% B -> 40.01 min 10% B. Starting compounds: Example 1A

(2Z) -2 - [(aminocarbonothioyl) hydrazono] butanoate

- »5.95 g- (4545 - rarnol ^ 2-Qxobutanoic acid ethyl ester are dissolved in 30 ml ethanol and - mixed with 4.14 g (45.45 mrnoi) thiosemicarbazide. After adding 0.23 ml concentrated hydrochloric acid, the reaction mixture is allowed to stir at RT overnight. The precipitate obtained is filtered off, washed with ethanol and the filtrate is concentrated, and the solid which precipitates is filtered off, giving a total of 9.71 g (quant) of crude product which is not further purified.

LC-MS (method 1): R _t = 2.08 min and 2.56 min (isomeric products)

MS (ES ⁺ ): m / z = 203 (M) ⁺

Example 2A

6-ethyl-3-thioxo-3,4-dihydro-l, 2 _J 4-triazin-5 (2iy) -one

2.05 g (10.1 mmol) of ethyl 2- [2- (aminocarbonothioyl) hydrazino] butanoate are suspended in 11 ml of ethanol. 1.13 g (20.2 mmol) of potassium hydroxide, dissolved in 11 ml of water, are added. The mixture is stirred under reflux for 2 hours, then it is concentrated on a rotary evaporator and acidified with a few drops of concentrated hydrochloric acid. The mixture is then cooled in an ice bath and the solid obtained is filtered off. 1.75 g (quant) of crude product, which is not further purified, are obtained. HPLC (method 4): R _t = 2.04 min

MS (EI): m / z = 157 (M) ⁺

Example 3A

Of potassium 6- (3-ethoxy-3-oxopropyl) -5-oxo-2,5-dihydro-l, 2,4-triazin-3-thiolate

5 g (24.7 mmol) of diethyl 2-üxoglutarate are dissolved in 13 ml of ethanol, 2.25 g (24.7 mmol) of thiosemicarbazide and 0.12 ml of concentrated hydrochloric acid are added and the mixture is stirred at RT overnight. The precipitate is filtered off, washed with ethanol and dried in vacuo. The solid obtained is suspended in 25 ml of ethanol, treated with 1.03.g of potassium hydroxide dissolved in 25 ml of ethanol and heated with stirring for 2 hours at reflux ^'. Then part of the solvent is evaporated. When cooling in an ice bath, a solid precipitates, which is filtered off and, after washing with diethyl ether, dried in vacuo. 5.55 g (79% of theory) of crude product, which is not further purified, are obtained.

Example 4A 6-Ethyl-3 - [(pyridin-2-ylmethyl) thio] -l, 2,4-triazin-5 (2H) -one

To a solution of 100 mg (0.64 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one and 175.8 mg (1.27 mmol) potassium carbonate in 10 ml water 162.5 mg (0.64 mmol) of 2- (bromomethyl) pyridine hydrobromide are added. After 14 h at room temperature, the pH is adjusted to 1 with 1 N hydrochloric acid and the reaction solution is purified by preparative HPLC. ^" The product fractions are combined, concentrated in vacuo and dried in a high vacuum. 99 mg (44% of theory) of the title compound are obtained, which is reacted further without additional purification.

HPLC (method 4): R _t = 2.83 min.

MS (EI): m / z = 249 (M + H) ⁺ .

Example 5A

6-ethyl-3 - [(pyridin-4-ylmethyl) thio] -l, 2,4-triazin-5 (2H) -one

To a solution of 100 mg (0.64 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one and 175.8 mg (1.27 mmol) potassium carbonate in 10 ml water 162.5 mg (0.64 mmol) of 4- (bromomethyl) pyridine hydrobromide are added. After 14 h at room temperature, the pH is adjusted to 1 with 1 N hydrochloric acid and the reaction solution is purified by preparative HPLC. The product fractions are combined, concentrated in vacuo and dried in a high vacuum. 73 mg (44% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 2.67 min.

MS (EI): m / z = 249 (M + H) ⁺ .

Example 6A

6-ethyl-3 - ({[6- (tτifluormethyl) pyridin-3-yl] methyl} thio) -l, 2,4-triazin-5 -one (2H)

x HCI To a solution of 160 mg (1.02 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one and 140.7 mg (1.02 mmol) potassium carbonate in 15 ml water 246.8 mg (1.03 mmol) of 5- (brorrrmethyl) -2- (trifluoromethyl) pyridine are added. After 14 h at room temperature, the pH is adjusted to 1 with 1 ml of 1 N hydrochloric acid, the resulting precipitate is filtered off with suction, washed with water and dried in a high vacuum. 213 mg (66% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 3.75 min. ,

MS (EI): m / z. = 317 (M + H) ⁺ .

Example 7A

3 - {[(5-Chloro-2-thienyl) methyl] thio} -6-ethyl-1, 2,4-triazin-5 (2H) -one

To a solution of 160 mg (1.02 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one and 140.7 mg (1.02 mmol) potassium carbonate in 15 ml water 171.7 mg (1.03 mmol) of 2-chloro-5- (chloromethyl) thiophene are added. After 14 h at room temperature the precipitate formed is isolated and the mother liquor is adjusted to pH 1 with 1 N hydrochloric acid. The resulting precipitate is filtered off, washed with water and dried in a high vacuum. Combining the solids gives 69.1 mg (21% of theory) of the title compound.

HPLC (method 4): R _t = 4.05 min.

MS (EI): mz = 288 (M + H) ⁺ . Example 8A

3 - [(l, 3-benzoxazol-2-ylmethyl) thio] -6-ethyl-l, 2,4-triazin-5 (2H) -one

To a solution of 200 mg (1.27 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one and 175.8 mg (1.27 mmol) potassium carbonate in 15 ml water 215.4 mg (1.29 mmol) of 2- (chloromethyl) -1, 3-benzoxazole are added. After 18 h at room temperature, the reaction mixture is extracted with dichloromethane. The aqueous phase is adjusted to pH 1 with 2N hydrochloric acid and extracted three times with dichloromethane. The combined organic phases are dried over sodium sulfate, concentrated in vacuo and dried in a high vacuum. 187 mg (46% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 3.61 min.

MS (EI): m / z = 289 (M + H) ⁺ .

Example 9A

[6-Ethyl-5-oxo-3 - [(pyridin-2-ylmethyl) thio] -l _J 2,4-triazin-2 (5H) -yl] ethyl acetate

A solution of 79 mg (0.32 mmol) 6-ethyl-3 - [(pyridm-2-ylmethyl) thio] -l, 2,4-triazin-5 (2H) -one and 66.5 μl (0.38 mmol) N, N -Diisopropylamine in 1.0 ml dichloromethane is added at-0 ° C with 39.5 μl (0.33 mmol) ethyl iodoacetate. After 18 h at room temperature, 3 ml of water are added to the reaction mixture. After evaporating the dichloromethane on a rotary evaporator, the remaining volume is purified by means of preparative HPLC. The product fractions are combined, concentrated in vacuo and dried in a high vacuum. 53 mg (50% of theory) of the title compound are obtained.

LC-MS (Method 2): R _t = 1.70 min,

MS (ESI): m / z = 335 (M + H) ⁺ .

Example 10A

[6-Ethyl-5-oxo-3 - ({[6- (trifluoromethyl) pyridin-3-ylmethyl} thio) -1, 2,4-triazin-2 (5H) -yl] ethyl acetate

A solution of 104 mg (0.29 mmol) 6-ethyl-3 - ({[6- (trifluoromethyl) pyridin-3-ylmethyl} thio) - l, 2,4-triazin-5 (2H) -one and 128.4 μl ( 0.74 mmol) of NN-diisopropylamine in 1.0 ml of dichloromethane is mixed with 36.6 μl (0.31 mmol) of ethyl iodoacetate at 0 ° C. After 18 h at room temperature, a further 36.6 μl (0.31 mmol) of ethyl iodoacetate are added, and the mixture is stirred for a further 18 h. After acidification with 1 N hydrochloric acid, the reaction mixture is purified by means of preparative HPLC. The product fractions are combined, concentrated in vacuo and dried in a high vacuum. 95 mg (77% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.35 min. +

MS (EI): m / z = 403 (M + H) Example 11A

[6-ethyl-5-oxo-3 - ({[6- (trifluoromethyl) pyridin-3-yl] methyl} thio) -l, 2,4-triazin-2 (5H) -yl] acetic acid

A solution of 40 mg (0.10 mmol) of [6-ethyl-5-oxo-3 - ({[6- (trifluoromethyl) pyridin-3-yl] methyl} - thio) -l, 2,4-triazin-2 ( 5H) -yl] acetic acid ethyl ester in ^' 1. ^' 5 ^" ml of dioxane is mixed with 298 μl (0.15 mmol) of 1 N sodium hydroxide solution at room temperature. After 35 min the reaction mixture is purified by preparative HPLC. The product fractions are combined, concentrated in vacuo and Dried under high vacuum, 19 mg (51% of theory) of the title compound are obtained.

LC-MS (method 3): R _t = 1.46 min,

MS (ESI): mz = 375 (M + H) ⁺ .

Example 12A

[3 - {[(5-Chloro-2-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-tτiazin-2 (5H) -yl] acetic acid tert-butyl ester

To a solution of 50 mg (0.17 mmol) 3 - {[(5-chloro-2-thienyl) methyl] thio} -6-ethyl-l, 2 ₃ 4-triazine 5 (2H) -one and 36.3 μl ( 0.21 mmol) N, N-diisopropylethylamine in 0.5 ml dichloromethane, 26.9 μl (0.18 mmol) tert-butyl bromoacetate are added at 0 ° C. After 18 h at room temperature, the reaction mixture is mixed with 3 ml of water and concentrated in vacuo to about 3 ml. The residue is purified by means of preparative HPLC. The product fractions are combined, concentrated in vacuo and dried in a high vacuum. 49 mg (50% of theory) of the title compound are obtained, which is used without further purification.

- LC-MS (method 2): R _t = 2.79 min,

MS (ESI): mz = 402 (M + H) ⁺ .

Example 13A

[3 - [(1,3-Benzoxazol-2-ylmethyl) thio] -6-ethyl-5-oxo-1,2,4-triazin-2 (5H) -yl] acetic acid tert-butyl ester.

To a solution of 100 mg (0.35 mmol) of 3 - [(l, 3-benzoxazol-2-ylmethyl) thio] -6-ethyl-l, 2,4-triazin-5 (2H) -one and 72.5 μl (0.42 mmol) of N, N-diisopropylethylamine in 1.0 ml of dichloromethane, 53.8 μl (0.18 mmol) of tert-butyl bromoacetate are added at 0 ° C. After 18 h at room temperature, the reaction mixture is mixed with 3 ml of water and concentrated in vacuo to about 3 ml. The residue is purified by preparative HPLC. The product fractions are combined, concentrated in vacuo and dried in a high vacuum. 104 mg (75% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.57 min.

MS (EI): m / z = 403 (M + H) ⁺ . Example 14A

4 '- (trifluoromethyl) biphenyl-4-carbaldehyde

1.0 g (4.44 mmol) of l-bromo-4- (trifluoromethyl) benzene, 1.13 g (7.56 mmol) of 4-formylphenylboronic acid and 0.94 g (8.89 mmol) of sodium carbonate are placed in 7.5 ml of water and 20.0 ml of dimethoxyethane. Argon is passed through the mixture for 1 h. Then 0.26 g (0.22 mmol) of tetrakis (triphenylphosphine) palladium (0) (Pd (PPh ₃ ) ₄ ) are added and the mixture is stirred at reflux for 18 h. The reaction mixture is taken up in 25 ml of ethyl acetate, filtered through kieselguhr, once with 20 ml of 1N hydrochloric acid and sat. Washed sodium chloride solution, dried over sodium sulfate and concentrated in vacuo. After chromatography on silica gel (cyclohexane / ethyl acetate: 10/1 -> 3/1), the product fractions are concentrated and dried in a high vacuum. 1.01 g (91% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.99 min.

MS (EI): m / z = 285 (M + N ₂ H ₇ ) ⁺ .

Example 15A

N, N-diethyl-N '- {[4' - (tτifluormethyl) biphenyl-4-yl] methyl} ethane-l _J 2-diamine

500 mg of molecular sieve 4 Ä (powder, <5 micron) are added to a solution of 500 mg (2.00 mmol) of 4 '- (trifluoromethyl) biphenyl-4-carbaldehyde and 280.8 μl (2.00 mmol) of l-amino-2-diethylaminoethane. After 18 h at room temperature, the reaction mixture is filtered, washed with dichloromethane and concentrated in vacuo. The raw material is abs in 5 ml. Dissolved ethanol and mixed with 90.7 mg (2.40 mmol) sodium borohydride at 0 ° C. After 1 h at room temperature, the reaction mixture is mixed with water and extracted with dichloromethane. The combined organic phases are dried over sodium sulfate and concentrated in vacuo. After chromatography on silica gel (cyclohexane / ethyl acetate: 3/1), the product fractions are ions combined, concentrated in vacuo and dried in a high vacuum. 585 mg (75% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.10 min.

MS (EI): mz = 351 (M + H) ⁺ .

Example 16A

N '- (4-butoxybenzyl) -N, N-diethylethane-1,2-diamine

1.58 ml (11.2 mmol) of l-amino-2-diethylaminoethane and 3.5 g of molecular sieve 4 Ä (powder, <5 micron) are added to a solution of 2 g (11.2 mmol) of 4-butoxybenzaldehyde in 70 ml of dichloromethane. After 18 h at room temperature, the reaction mixture is filtered, washed with dichloromethane and concentrated in vacuo. The raw material is abs in 40 ml. Dissolved ethanol and mixed with 509 mg (13.5 mmol) sodium borohydride at 0 ° C. After 2 h at room temperature, the reaction mixture is mixed with 50 ml of water and extracted three times with 100 ml of dichloromethane each time. The combined organic phases are dried over sodium sulfate and concentrated in vacuo. After chromatography on silica gel (cyclohexane / ethyl acetate: 1/1 -> 3 / l -> toluene / ethanol / triethylamine 95/4/1), the product fractions are combined, concentrated in vacuo and dried in a high vacuum. 1.64 g (51% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 3.82 min. ^' .

MS (EI): mz = 279 (M + H) ⁺

Example 17A

NN-Diethyl-N '- (4-isopropylbenzyl) ethane-l, 2-diamine

1.9 ml (13.5 mmol) of l-amino-2-diethylaminoethane and 3.5 g of molecular sieve 4 Ä (powder, <5 micron) are added to a solution of 2 g (13.5 mmol) of 4-isopropylbenzaldehyde in 70 ml of dichloromethane. After 18 h at room temperature, the reaction mixture is filtered, washed with dichloromethane and concentrated in vacuo. The raw material is abs in 40 ml. Dissolved ethanol and mixed with 613 mg (16.2 mmol) sodium borohydride at 0 ° C. After 2 h at room temperature, the reaction mixture is mixed with 50 ml of water and extracted three times with 100 ml of dichloromethane each time. , The combined organic phases are dried over sodium sulfate and concentrated in vacuo. After chromatography on silica gel (cyclohexane / ethyl acetate. 1/1 -> 3/1 -> toluene / ethanol / triethylamine 95/4/1), the product fractions are combined, concentrated in vacuo and dried in a high vacuum. 2.07 g (60% of theory) of the title compound are obtained.

HPLC (method 4): R _t "- = 3.65 min. ^•

MS (EI): m / z = 249 (M + H) ⁺

Example 18A

6-Cyclopentyl-3-thioxo-3,4,4-dihydro-1,2,4-triazin-5 (2H) -one

3.00 g (17.6 mmol) of 2-cyclopentyl-2-oxoacetic acid ethyl ester (can be prepared, for example, according to Y. Akiyama et al., Chem. Pharm. Bull., 1984, 32 (5), 1800-1807) in 20 ml of ethanol are 1.61 g (17.6 mmol) thiosemicarbazide and 88 μl concentrated hydrochloric acid. The mixture is stirred at room temperature overnight. The reaction is terminated by adding 50 ml of water. After extraction three times with ethyl acetate (50 ml each), the organic phases are dried over magnesium sulfate and the solvent is removed under reduced pressure. The residue is taken up in 11 ml of ethanol and 11 ml of water, and 1.15 g (20.6 mmol) of potassium hydroxide are added. After heating under reflux for 2 h, the mixture is adjusted to pH 1 with concentrated hydrochloric acid. The mixture is cooled and the solid which has precipitated is filtered off with suction. 2.01 g of product (99% of theory) are obtained.

MS (ESI): m / z = 198 (M + H) ⁺ 'H-NMR (200 MHz, DMSO-d ₆ ): δ = 1.52-1.74 (m, 6H), 1.75-1.96 (m, 2H), 3.04-3.23 (m, IH), 12.96-13.27 (br. S , 2H).

Example 19A

6- (2-phenylethyl) -3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one ^•

0.44 g (4.9 mmol) of thiosemicarbazide and 24 μl of concentrated hydrochloric acid are added to 1.00 g (4.85 mmol) of ethyl benzylpyruvate in 6 ml of ethanol. After stirring overnight at room temperature, the precipitated solid is filtered off with suction. The mother liquor is freed from the solvent under reduced pressure. The residue and the extracted solid are taken up in 4 ml of water and 4 ml of ethanol. 402 mg (7.16 mmol) of potassium hydroxide are added and the mixture is heated under reflux for 2 h. The pH is adjusted to 1 using concentrated hydrochloric acid. The mixture is cooled and the solid which has precipitated is filtered off with suction. 678 mg of product (81% of theory) are obtained.

MS (ESI): m / z = 234 (M + H) ⁺

^! H-NMR (200 MHz, DMSO-d ₆ ): δ = 2.72-2.94 (m, 4H), 7.14-7.34 (, 5H), 13.10 (s, IH), 13.34 (s, IH).

Example 20A

3- (5-oxo-3-thioxo-2,3,4,5-tetrahydro-l, 2,4-triazin-6-yl) propionic acid

123 μl hydrochloric acid are added to a solution of 2.25 g (24.69 mmol) thiosemicarbazide and 4.99 g (24.69 mmol) diethyl 2-oxoglutarate in 13 ml ethanol. After 18 h at room temperature, the precipitated solid is filtered off, washed with ethanol and dried. The intermediate is taken up in 40 ml of ethanol / water 1/1, mixed with 2.77 g (49.38 mmol) of potassium hydroxide and stirred at reflux for 2 h. The pH is adjusted to pH 1 using hydrochloric acid. The resulting solid is filtered off and dried under high vacuum. 2.4 g (48% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 1.29 min.

MS (EI): m / z = 202 (M + H) ⁺

Example 21A

3- (5-oxo-3-thioxo-2,3,4,5-tetrahydro-l, 2,4-triazin-6-yl) propionic acid ethyl ester

1.70 g (8.45 mmol) of 3- (5-oxo-3-thioxo-2,3,4,5-tetrahydro-l, 2,4-triazin-6-yl) propionic acid are dissolved in 17 ml of ethanol, with 740 μl (10.14 ^' mmol) _. Thionyl chloride was added and the mixture was stirred at reflux overnight. The reaction mixture is concentrated and dried in a high vacuum. 1.8 g (93% of theory) of the title compound are obtained. ^"

LC-MS (method 3): R _t = 1.07 min.

MS (ESIpos): m / z = 230 (M + H) ⁺

Example 22A

3 - {[(5-chloro-3-thienyl) methyl] thio) -6-ethyl-1, 2,4-triazin-5 (2H) -one

To a solution of 200 mg (1.27 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one and 175.8 mg (1.27 mmol) potassium carbonate in 15 ml water 214.7 mg (1.29 mmol) of 2-chloro-4-

(Chloromethyl) thiophene added. After 14 h at room temperature, the temperature is increased to 80 ° C for 18 h heated. After cooling, it is adjusted to pH 1 with 2 N hydrochloric acid, concentrated to about 5 ml in vacuo and purified by means of preparative HPLC. The product fractions are combined, concentrated in vacuo and dried in a high vacuum. 155 mg (42% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.02 min. ^'

MS (EI): m / z = 288 (M + H) ⁺

Example 23A

3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-l, 2,4-triazin-5 (2H) -one

To a solution of 300 mg (1.52 mmol) of 6-cyclopentyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) - one, 254 mg (1.52 mmol) of 2-chloro-4 - (Chloromethyl) thiophene and 397 μl (2.28 mmol) NN-diisopropylethylamine added. After 2 h at room temperature, the reaction mixture is purified by means of preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 202 mg (40% of theory) of the title compound are obtained,

LC-MS (Method 5): R _t = 2.39 min.

MS (ESIpos): mz = 328 (M + H) ⁺

Example 24A

3 - {[(5-chloro-3-thienyl) methyl] thio} -6- (2-phenylethyl) -l, 2,4-triazin-5 -one (2H)

215 mg (1.29 mmol) 2 are added to a solution of 300 mg (1.29 mmol) of 6- (2-phenylethyl) -3-thioxo-3 _J 4-dihydro-l ₃ 2,4-triazine 5 (2H) -one -Chlor-4- (chloromethyl) thiophene and 340 μl (1.93 mmol) of NN-diisopropylethylamine were added. After 2 h at room temperature, the reaction mixture is purified by means of preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 174 mg (37% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 2.29 min.

MS (ESIpos): m / z = 364 (M + H) ⁺

Example 25A

3- (3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-2,5-dihydro-l, 2,4-triazin-6-yl) propionic acid ethyl ester

To a solution of 300 mg (1.31 mmol) of 3- (5-oxo-3-thioxo-2,3,4,5-tetrahydro-l, 2,4-tτiazin-6-yl) propionate, 219 mg (1.31 mmol ) 2-Chloro-4- (chloromethyl) thiophene and 570 μl (3.27 mmol) NN-diisopropylethylamine added. After 2 h at room temperature, the reaction mixture is purified by means of preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 185 mg (39% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.22 min.

MS (EI): m / z = 377 (M + NH ₄ ) ⁺

Example 26A

[3 - {[(5-Chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid tert-butyl ester

To a solution of 500 mg (1.74 mmol) of 3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-l, 2,4-triazin-5 (2H) -one in 7.2 ml of dichloromethane 0.26 ml (1.74 mmol) tert-butyl bromoacetic acid and 0.45 ml (2.61 mmol) NN-diisopropylethylamine are added. After 18 h at room temperature, the reaction mixture is concentrated and the residue is purified by preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 495 mg (71% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 5.08 min.

MS (EI): m / z = 402 (M + H) ⁺

Example 27A

[6-Efhyl-3 - {[(5 -methyl-1,3,4-oxadiazol-2-yl) methyl] thio} -5-oxo- 1, 2,4-triazin-2 (5H) -yl] tert-butyl acetate

A solution of 150 mg (0.95 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one, 126.5 mg (0.95 mmol) 2- (chloromethyl) - 5-methyl-l, 3,4-oxadiazole and 249.3 μl (1.43 mmol) of NN-diisopropylethylamine are stirred at room temperature for 2 h. 140 μl (0.95 mmol) tert-butyl bromoacetate and a further 249.3 μl (1.43 mmol) NN-diisopropylethylamine are added. together. After 18 h at room temperature, the flask contents are cleaned using preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 105 mg (30% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.10 min.

MS (EI): mz = 368 (M + H) ⁺

Example 28A

[6-ethyl-3 - {[(2-methyl-l, 3-thiazol-4-yl) methyl] thio} -5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid, ethyl tert-butyl ester

A solution of 200 mg (1.27 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one, 234.2 mg (1.27 mmol) 4- (chloromethyl) - 2-methyl-l, 3-thiazole and 1.33 ml (7.63 mmol) of NN-diisopropylethylamine are stirred at room temperature for 2 h. 187 μl (1.27 mmol) tert-butyl bromoacetic acid are added. After 18 h at room temperature, the flask contents are cleaned using preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 140 mg (29% of theory) of the title compound are obtained.

LC-MS (Method 5): R _t = 2.24 min.

MS. (ESIpos): mz = 383 (M + H) ⁺ Example 29A

[3 - [(1H-Benzimidazol-2-ylmethyl) thio] -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid tert-butyl ester

A solution of 200 mg (1.27 mmol) 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one, 212 mg (1.27 mmol) 2- (chloromethyl) - 1H-benzimidazole and 665 μl (3.82 mmol) of NN-diisopropylethylamine are stirred at room temperature for 2 h. 187 μl (1.27 mmol) tert-butyl bromoacetic acid are added. After 18 h at room temperature, the flask contents are cleaned using preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 210 mg (41% of theory) of the title compound are obtained.

LC-MS (Method 5): R _t = 1.83 mm.

MS (ESIpos): m / z = 402 (M + H) ⁺

Example 30A

3 - {[(5-Chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid tert-butyl ester

To a solution of 190 mg (0.58 mmol) 3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-l, 2,4-triazin-5 (2H) -one in 3 ml dichloromethane 135.6 mg (0.70 mmol) tert-butyl bromoacetate and 151.4 μl (0.87 mmol) NN-diisopropylethylamine are added. After 18 h at room temperature, the reaction mixture is concentrated and the residue is purified by preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 170 mg (66% of theory) of the title compound are obtained.

LC-MS (method 2): R _t = 3.07 min.

MS (ESIpos): m / z - 442 (M + H) ⁺

Example 31A

[3 - {[(5-Chloro-3-thienyl) methyiIthio} -5-oxo-6- (2-phenylethyl) -l, 2,4-tτiazin-2 (5H) -yl] acetic acid, tert-butyl ester

To a solution of 174 mg (0.48 mmol) of 3 - {[(5-chloro-3-thienyl) methyl] thio} -6- (2-phenylethyl) - 1,2,4-triazin-5 (2H) -one 74.1 μl (0.50 mmol) tert-butyl bromoacetate and 124.9 μl (0.72 mmol) NN-diisopropylethylamine are added in 3 ml dichloromethane. After 18 h at room temperature, the reaction mixture is concentrated and the residue is purified by preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 94 mg (41% of theory) of the title compound are obtained.

LC-MS (method 3): R _t = 3.0? minute

MS (ESIpos): m / z = 478 (M + H) ⁺ Example 32A

3- (2- (2-tert-butoxy-2-oxoethyl) -3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-2,5-dihydro-l, 2, 4-triazin-6-yl) ethyl propionate -

To a solution of 90 mg (0.25 mmol) of 3- (3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-2,5-dihydro-l, 2,4-triazine-6 -yl) ethyl propionate in 2 ml dichloromethane, 51.2 mg (0.26 mmol) bromoacetic acid tert-butyl ester and 70 μl (0.38 mmol) NN-diisopropylethylamine are added. After 18 h at room temperature, the reaction mixture is concentrated and the residue is purified by means of preparative HPLC. The product fractions are combined, concentrated and dried in a high vacuum. 90 mg (76% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 5.04 min.

MS (EI): m / z = 474 (M + H) ⁺

Example 33A

[3 - {[(5-Chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-1, 2,4-triazin-2 (5H) -yl] acetic acid

360 mg (0.90 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid Tert-butyl ester are reacted in a mixture of 8 ml dichloromethane / TFA (1/1). After 18 h at room temperature, the reaction mixture is concentrated, taken up in a little DMSO and purified by means of preparative HPLC. The product fractions are concentrated and dried in a high vacuum. 225 mg (73% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.10 min.

MS (EI): m / z = 346 (M + H) ⁺

Example 34A

[6-ethyl-3 - {[(5-methyl-l, 3 _J 4-oxadiazol-2-yl) methyl] thio} -5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid

97 mg (0.26 mmol) 6-ethyl-3 - {[(5-methyl-l ₎ 3,4-oxadiazol-2-yl) methyl] thio} -5-oxo-l, 2,4-triazine-2 ( 5H) -yl] acetic acid tert-butyl ester are reacted in a mixture of 1.2 ml dichloromethane / TFA (5/1). After 18 h at room temperature, the reaction mixture is concentrated, taken up in a little DMSO and purified by means of preparative HPLC. The product fractions are concentrated and dried in a high vacuum. 95 mg of a crude substance are obtained, which is not further purified.

LC-MS (Method 2): R _t = 0.75 min.

MS (ESIpos): m / z = 312 (M + H) ⁺

Example 35A

[6-ethyl-3 - {[(2-methyl-l, 3-thiazol-4-yl) methyl] thio} -5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid

140 mg (0:37 mmol) of [6-ethyl-3 - {[(2-methyl-l, 3-thiazol-4-yl) methyl] thio} -5-oxo-l, 2 _J 4-triazin-2 (5H ) -yl] tert-butyl acetate are dissolved in 2 ml of dichloromethane. After adding 282 μl (3.66 mmol) of TFA, the mixture is stirred at room temperature for 18 h. It is taken up in acetonitrile / water, adjusted to pH 4-5 with 10% sodium hydrogen carbonate solution and by means of

^'' preparative HPLC cleaned. 236 mg of a raw substance are obtained, which are no further

- is cleaned. LC-MS (Method 3): R _t = 1.09 min.

MS (ESIpos): m / z = 327 (M + H) ⁺

Example 36A

[3 - [(lH-benzimidazol-2-ylmethyl) thio] -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid

210 mg (0.52 mmol) [3 - [(1H-benzimidazol-2-ylmethyl) thio] -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid tert. -butyl ester are dissolved in 2 ml dichloromethane. After adding 403 μl (5.23 mmol) of TFA, the mixture is stirred at room temperature for 18 h. It is taken up in acetonitrile / water, adjusted with 10% _{hydrochloric>} sodium bicarbonate solution to pH 4-5 and using preparative HPLC purified. 250 mg of a raw substance are obtained, which is not further purified.

LC-MS (Method 2): R _t = 1.21 min.

MS (ESIpos): m / z = 346 (M + H) ⁺

Example 37A

[3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-1, 2,4-triazin-2 (5H) -yl] acetic acid

140 _. mg (0.31 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-l ₎ 2,4-triazine-2 (5H) -yl] acetic acid tert .-Butyl esters are reacted in a mixture of 2 ml dichloromethane / TFA (3/1). After 18 h at room temperature, the reaction mixture is concentrated, taken up in a little DMSO and purified by means of preparative HPLC. The product fractions are concentrated and dried in a high vacuum. This gives 125 ^'mg of the title compound, which is not purified further.

LC-MS (method 3): R _t = 2.04 min.

MS (ESIpos): m / z = 386 (M + H) ⁺

Example 38A

[3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-phenylethyl) -l, 2,4-triazin-2 (5H) -yl] acetic acid

94 mg (0.20 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-phenylethyl) -l, 2,4-triazm-2 (5H) - yl] tert-butyl acetate are reacted in a mixture of 4 ml dichloromethane / TFA (1/1). After 18 h at room temperature, the reaction mixture is concentrated, taken up in a little DMSO and purified by means of preparative HPLC. The product fractions are concentrated and dried in a high vacuum. 82 mg (99% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 2.13 min.

MS (ESIpos): m / z = 422 (M + H) ⁺

Example 39A

[3 - {[(5-chloro-3-thienyl) methyl] thio} -6- (3-ethoxy-3-oxopropyl) -5-oxo-l, 2,4-triazin-2 (5H) - yl] acetic acid

90 mg (0.19 mmol) 3- (2- (2-tert-butoxy-2-oxoethyl) -3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo- 2,5- dihydro-l, 2,4-triazin-6-yl) propionic acid ethyl ester are reacted in a mixture of 3 ml dichloromethane and 0.146 ml TFA. After 18 h at room temperature, the reaction mixture is concentrated, taken up in a little DMSO and purified by means of preparative HPLC. The pro- Duct fractions are concentrated and dried in a high vacuum. 90 mg of a raw substance are obtained, which is not further purified.

HPLC (method 4): R _t = 4.16 min.

MS (EI): m / z = 418 (M + H) ⁺ Example 40A

(2,5-dichloro-3-thienyl) methanol

Under argon, 13.9 ml (13.9 mmol) presented a lM solution of lithium aluminum hydride in THF added dropwise and dissolved at room temperature 5.0 g (23.2 mmol) of 2,5-dichlorothiophene-3-carbonyl chloride in ^'50 ml of THF. You stir 30. min and drops in 1N hydrochloric acid to the reaction mixture until the precipitated solid dissolves again. It is diluted with water and ethyl acetate, • the organic phase is separated off and washed with water, dried over magnesium sulfate and concentrated in vacuo. 3.58 g (84% of theory) of product are obtained.

TLC: R _r value: 0.29 (dichloromethane) HPLC (method 6): R _t = 4.20 min.

MS (ESIpos): m / z = 182, 184 (M) ⁺

Η NMR (300 MHz, CDC1 ₃ ): δ = 6.88 (s, IH), 4.57 ^" (s, 2H), 1.60 (s, broad, OH).

Example 41A

3- (bromomethyl) -2,5-dichlorothiophene

A solution of 500 mg (2.73 mmol) (2,5-dichloro-3-thienyl) methanol in 10 ml dichloromethane is cooled to -5 ° C. and 0.1 ml (1.09 mmol) phosphorus tribromide are slowly added dropwise. The mixture is allowed to come to room temperature, stirred for 15 min and the reaction is ended by adding Water. The organic phase is separated off, dried over magnesium sulfate and concentrated in vacuo. 570 mg (85% of theory) of product are obtained, which is reacted in the subsequent step without further purification.

DC: R _r value: 0.86 (dichloromethane)

GC-MS (Method 7): R _t = 6.52 min.

MS (CIpos): m / z = 246 (M) ⁺

* H-NMR (300 MHz, CDCh): δ = 6.83 (s, IH), 4.35 (s, 2H).

Example 42A

3 - {[(2,5-dichloro-3-thienyl) methyl] thio} -6-ethyl-l, 2,4-triazin-5 (2H) -one

To a solution of 354 mg (2.25 mmol) 6-ethyl-3-thioxo-3,4-dihydro-1,2 _; 4-triazin-5 (2H) -one and 312 mg (2.25 mmol) potassium carbonate in 30 ml water are added 560 mg (2.28 mmol) 3- (bromomethyl) - 2,5-dichlorothiophene and stirred overnight at room temperature. The precipitated crystals are filtered off and washed several times with water. The aqueous phase is extracted several times with dichloromethane. The combined organic phases are dried over magnesium sulfate and concentrated in vacuo. The residue obtained is purified together with the precipitated crystals over silica gel (mobile phase: cyclohexane / ethyl acetate 3: 1). 270 mg (37% of theory) of product are obtained.

TLC: R _r value: 0.48 (cyclohexane / ethyl acetate 1: 1)

LC-MS (method 2): R _t = 2.25 min

MS (ESIpos): m / z = 322, 324 (M + H) ⁺

Η NMR (300 MHz, CDC1 ₃ ): δ = 10.72 (s, broad, IH), 6.88 (s, IH), 4.37 (s, 2H), 2.72 (q, 2H), 1.21 (t, 3H). Example 43A

[3 - {[(2,5-dichloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazine-2 (5H) -yl] acetic acid tert-butyl ester

Under argon, a solution of 250 mg (0.78 mmol) of 3 - {[(2,5-dichloro-3-thienyl) methyl] thio} - 6-ethyl-l _J-triazine 2,4-5 -one (2H) submitted in 10 ml dichloromethane. Then 0.18 ml (1.0 mmol) of diisopropylethylamine and 0.14 ml (0.93 mmol) of tert-butyl bromoacetic acid are added and the mixture is stirred at 40 ° C. overnight. The reaction solution is washed with water, the organic phase is separated off, dried over magnesium sulfate and concentrated in vacuo. The resulting residue is purified over silica gel (eluent: cyclohexane / Essigsäureethyle ^'most 3: 1). 163 mg (48% of theory) of product are obtained.

TLC: R _r value: 0.68 (cyclohexane / ethyl acetate 1: 1)

MS (ESIpos): m / z = 436, 438 (M + H) ⁺

Η NMR (300 MHz, CDC1 ₃ ): δ = 6.90 (s, IH), 4.60 (s, 2H), 4.40 (s, 2H), 2.72 (q, 2H), 1.47 (s, 9H), 1.21 ( t, 3H).

Example 44 A

[3 - {[(2,5-dichloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid

A solution of 140 mg (0.32 mmol) of tert-butyl- [3 - {[(2,5-dichloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazine -2 (5H) -yl] acetate in 2 ml dichloromethane is cooled to 0 ° C. and 1 ml (13 mmol) trifluoroacetic acid is slowly added dropwise. The mixture is stirred overnight at room temperature and the reaction is ended by adding water. , The organic phase is washed with water, dried over magnesium sulfate and concentrated in vacuo. You get! 16 mg (95% of theory) of product, which is reacted in the subsequent step without further purification.

HPLC (method 6): R _t = 4.71 min.

LC-MS (method 2): R = 2.19 min.

MS (ESIpos): mz = 380, 382 (M + H) ⁺

Example 45A

6-ethyl-3 - [(4-methoxybenzyl) thio] - 1, 2,4-triazin-5 (2H) -one

To a solution of 5.00 g (31.8 mmol) of 6-ethyl-3-thioxo-3,4-dihydro-l, 2,4-triazin-5 (2H) -one and 4.39 g (31.8 mmol) of potassium carbonate in 250 ml of water 5.03 g (32.1 mmol) of 4-methoxybenzyl chloride are added and the mixture is stirred at room temperature overnight. The precipitated crystals are filtered off, washed with a little water and dried at 40 ° C. in a high vacuum. 5.56 g (63% of theory) of product are obtained. After adding ^" IN hydrochloric acid", a further 2.63 g (30% of theory) of product can be isolated from the aqueous phase.

HPLC (method 6): R _t = 3.74 min.

LC-MS (Method 3): R _t = 1.81 min.

MS (ESLieg): m / z = 276 (MH) ⁺

'H NMR (300 MHz, CDC1 ₃ ): δ = 7.28 (d, 2H), 6.83 (d, 2H), 4.42 (s, 2H), 3.78 (s, 3H), 2.70 (q, 2H), 1.19 (t, 3H). Example 46A

[6-Ethyl-3 - [(4-methoxybenzyl) thio] -5-oxo- 1, 2,4-triazin-2 (5H) -yl] methyl acetate

A solution of 5.0 g (18 mmol) of 6-ethyl-3 - [(4-methoxybenzyl) thio] -1.2 _^ 4-triazin-5 (2H) -one in 170 ml of dichloromethane is introduced under argon. Then 4.7 ml (27 mmol) diisopropylethylamine ^' and 2.05 ml (21.6 mmol) methyl bromoacetate are added and the mixture is stirred overnight at room temperature. Water is added to the reaction solution and the organic phase is separated off. The organic phase is washed with water and pH 7 buffer, dried over magnesium sulfate and concentrated in vacuo. The residue obtained is purified on silica gel (mobile phase: dichloromethane / ethyl acetate 20: 1). 4.02 g (64% of theory) of product are obtained.

TLC: R _r value: 0.33 (dichloromethane / ethyl acetate 10: 1)

HPLC (method 6): R _t = 4.17 min.

LC-MS (Method 5): R _t = 2.22 min.

MS (ESIpos): m / z = 350 (M + H) ⁺

MS (DCI, NH ₃ ): m / z = 350 (M + H) ⁺ , 367 (M + NH ₄ ) ⁺

Η NMR (300 MHz, CDC1 ₃ ): δ = 7.89 (d, 2H), 6.84 (d, 2H), 4.74 (s, 2H), 4.46 (s, 2H), 3.79 (s, 6H), 2.72 ( q, 2H), 1.16 (t, 3H). Example 47A

[6-ethyl-3 - [(4-methoxybenzyl) thio] -5-oxo-l, 2,4-triazin-2 (5H) -yl] acetic acid

A solution of 4.00 g (11.5 mmol) of methyl [6-ethyl-3 - [(4-methoxybenzyl) thio] -5-oxo-l, 2,4-trιazin-2 (5H) -yl] acetate in 100 ml An IM solution of 0.5 g (12.6 mmol) of sodium hydroxide in water is added to the dioxane and the mixture is stirred at room temperature for 5 h. The mixture is acidified with 1N hydrochloric acid and extracted several times with 1: 1 dichloromethane / ethyl acetate. The combined organic phases are dried over magnesium sulfate and concentrated in vacuo. 3.04 g (79% of theory) of product are obtained.

HPLC (method 6): R _t = 3.86 min.

LC-MS (Method 5): R _t = 1.70 min.

MS (ESIpos): m / z = 336 (M + H) ⁺

'H-NMR (300 MHz, DMSO-d ₆ ): δ = 13.5 (s, broad, IH), 7.35 (d, 2H), 6.88 (d, 2H), 4.80 (s, 2H), 4.40 (s, 2H), 3.74 (s, 3H), 2.56 (q, 2H), 1.12 (t, 3H).

Example 48 A

N- [2- (Diethylamino) ethyl] -2- [6-ethyl-3 - [(4-methoxybenzyl) thio] -5-oxo-l, 2 ₎ 4-triazin-2 (5H) -yl] -N - {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide

To a solution of 3.0 g (8.95 mmol) of [6-ethyl-3 - [(4-me oxybenzyl) thio] -5-oxo-l, 2,4-tτiazin- 2 (5H) -yl] acetic acid and 3.45 g (9.84 mmol) NN-diethyl-N '- {[4' - (trifluoromethyl) biphenyl-4-yl] - methyl} ethane-1,2-diamine in 30 ml DMF become 3.9 ml (22.4 mmol) DIEA and 2.0 ml (11.6 mmol) (benzotriazol-l-yloxy) bisdimethylaminomethylium fluoroborate and the mixture was stirred at 40 ° C. overnight. After adding water, the reaction mixture is extracted with dichloromethane. The combined organic phases are dried over magnesium sulfate and concentrated in vacuo. The residue obtained is purified on silica gel (eluent: dichloromethane / methanol 50: 1). 3.48 g (58% of theory) of product are obtained.

LC-MS (Method 2): R _t = 2.22 min.

MS (ESIpos): m / z = 668 (M + H) ⁺

Example 49A

N- [2- (Diethylamino) ethyl] -2- (6-ethyl-5-oxo-3-thio o-4,5-dihydro-l, 2,4-triazin-2 (3H) -yl) -N - {[4 ^, - (tτifluoromethyl) biphenyl-4-yl] methyl} acetamide trifluoroacetate

To a solution of 3.4 g (5! Mmol) of N- [2- (diethylamino) ethyl] -2- [6-ethyl-3 - [(4-methoxybenzyl) thio] -5-oxo-l, 2, 4-triazin-2 (5H) -yl] -N - {[4 '- (1xifluoromemyl) biphenyl-4-yl] methyl} -acetarnide in 150 ml dichloromethane, 20 ml trifluoroacetic acid are added and the mixture is stirred for 2 hours at room temperature , The mixture is concentrated in vacuo and the residue is purified on silica gel (eluent: dichloromethane / methanol 100: 1 to 40: 1). 2.5 g (75% of theory) of product are obtained.

HPLC (method 6): R _t = 3.33 min.

LC-MS (Method 3): Rt = 2.13 min. ■

MS (ESIpos): m / z = 548 (M + H) ⁺

¹ H- MR ^" (400 MHz, CDC1 ₃ ): δ = 13.35 (s, broad, IH), 9.50 (s, broad) and 9.20 (s, broad, together IH), 7.95-7.72 (m, 6H), 7.54 (d) and 7.44 (d, together 2H), 5.37 (s) and 5.31 (s, together 2H), 4.77 (s) and 4.66 (s, together 2H), 3.73 (t) and 3.58 (t, together 2H) ), 3.23-3.10 (m, 6H), 2.56 (q, 2H), 1.22-1.06 (m, 9H).

Example 50A

(5-fluoro-2-thienyl) methanol

1.8 ml (1.8 mmol) of a solution of lithium aluminum hydride in THF are introduced and 250 mg (1.7 mmol) of 5-fluorothiophene-2-carboxylic acid in 15 ml of THF are added dropwise. It is stirred for 1 h at room temperature and 1N hydrochloric acid is added dropwise to the reaction mixture until the precipitated solid dissolves again. It is extracted several times with dichloromethane, the organic phase is dried over magnesium sulfate and concentrated in vacuo. 204 mg (90% of theory) of product are obtained, which is reacted in the subsequent step without further purification.

HPLC (method 6): R _t = 3.25 min.

Η NMR (400 MHz, CDC1 ₃ ): δ = 6.60 (t, IH), 6.32 (dd, IH), 4.68 (d, 2H), 1.70 (s, broad, IH).

Example 51A

1-Methyl-N- {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} piperidin-4-amine

A solution of 1.5 g (5.97 mmol) ^^ '- (trifluoromethyl ^ biphenyl ^ -yljmethanamin and 0.76 g (6.57 mmol) 1-methyl-4-piperidone in a mixture of 15 ml methanol and 1 ml acetic acid is mixed with 0.45 g ( After 18 h at room temperature, the reaction mixture is mixed with 30 ml of 1N sodium hydroxide solution, the methanol is largely removed on a rotary evaporator and the residue is extracted several times with dichloromethane, the combined organic phases are dried over sodium sulfate and concentrated in vacuo is dissolved in methanol and purified by preparative HPLC, giving 1.64 g (78% of theory) of the title compound.

HPLC (method 4): R _t = 4.08 min.

MS (EI): mz = 349 (M + H) ⁺ .

Example 52A 1-Ethyl-N - {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} piperidin-4-amine

The production is carried out analogously to the production of Example 51A.

- HPLC (method 4): R _t = 4.19 min. MS (El): m / z = 363 (M + H) ⁺ .

Execution examples:

Examples 1 to 3 in the following table are prepared analogously to Example 4.

Example 4

N- [2- (Diethylamino) ethyl] -2- [6-ethyl-5-oxo-3 - ({[6- (trifluoromethyl) pyridin-3-yl] methyl} thio) - 1, 2,4-triazine -2 (5H) -yl] -N- {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide ^•

To a solution of 19 mg (0.05 mmol) [6-ethyl-5-oxo-3 - ({[6- (trifluoromethyl) pyridin-3-yl] - methyl} thio) -l, 2,4-triazin-2 (5H) -yl] acetic acid in 1 ml dichloromethane, 21 mg (0.06 mmol) NN-diethyl-N '- {[4' - (trifluoromethyl) biphenyl-4-yl] methyl} ethane-1,2-diamine _J 0.7 mg (0.01 mmol) HOBt and 11 mg (0.06 mmol) EDC. The mixture is stirred for 18 h, 2 ml of water are added to the reaction mixture and the mixture is concentrated in vacuo. The residue is purified by preparative HPLC. 17 mg (48% of theory) of product are obtained.

HPLC (method 6): R _t = 3.44 min.

LC-MS (method 3): R _t = 2.02 min. ^''

MS (ESIpos): m / z = 707 (M + H) ⁺ . ^'

'H-ΝMR (300 MHz, DMSO-d ₆ ): δ = 9.12 (s, IH), 8.64 (d, IH), 8.16 (d, IH), 7.83 (dd, 6H), 7.56 (d, 2H) , 5.45 (s, 2H), 4.97 (s, 2H), 4.79 (s, 2H), 4.19 (t, 2H), 3.54 (t, 2H), 3.43 (q, 4H), 2.77 (q, 2H), 1.38 (t, 6H), 1.22 (t, 3H).

Examples 5 to 7 in the following table are prepared analogously to Example 4.

Example 8

2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-1 _; 2,4-triazin-2 (5H) -yl] -N- [2- (diethylamino) ethyl] -N- {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide

To a solution of 140 mg (0.40 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxol, 2,4-triazine-2 (5H) - yl] acetic acid and 141.9 mg (0.40 mmol) NN-diethyl-N ^J - {[4 '- (trifluoromethyl) - biphenyl-4-yl] methyl} ethane-1,2-diamine in 4 ml dichloromethane become 85.4 mg at room temperature (0.45 mmol) EDC and 5.5 mg (0.04 mmol) HOBt added. After 18 h at Raum¬

^{■ The} temperature of the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 240 mg (87% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 2.49 min.

MS (ESIpos): m / z = 678 (M + H) ⁺ 0 ^""" Η-NMR (400 MHz, DCOOD): δ = 7.88-7.76 (m, 6H), 7.53 (, 2H), 7.27 (m , IH), 7.01 (m, IH), 5.43 (s, 2H), 4.96 (s, 2H), 4.49 (s, 2H), 4.11 (m, 2H), 3.55 (m, 2H), 3.43 (q, 4H), 2.80 (q, 2H), 1.38 (tr, 6H), 1.25 (tr, 3H).

Examples 9 to 15 in the following table are prepared analogously to Example 4.

Example 16

3- {3 - {[(5-chloro-3-thienyl) methyl] thio} -2- [2 - ([2- (diethylamino) ethyl] {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} anιino) -2-oxoethyl] -5-oxo-2,5-dihydro-l, 2,4-triazin-6-yl} ethyl propionate

To a solution of 90 mg (0.14 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6- (3-ethoxy-3-oxopropyl) -5-oxo-l, 2.4 -triazin-2 (5H) -yl] acetic acid in 2 ml of DMF, 49.8 mg (0.14 mmol) of NN-diethyl-N '- {[4' - (trifluoromethyl) biphenyl-4-yl] methyl} ethane-1,2 diamine, 27.3 mg (0.10 mmol) EDC and 1.9 mg (0.01 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 23 mg (22% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.94 min.

MS (EI): m / z = 750 (M + H) ⁺ Examples 17 to 24 in the following table are prepared analogously to Example 4.

Example 25

N- (4-Butoxybenzyl) -2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) - yl] - N- [2- (diethylamino) ethyl3acetamide

To a solution of 85 mg (0.25 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazine-2 (5H) - yl] acetic acid in 2 ml DMF 68.4 mg (0.25 mmol) N '- (4-butoxybenzyl) -NNr diethylethan-l, 2-diamine, 47.1 mg (0.25 mmol) EDC and 3.3 mg (0.02 mmol) HOBt are added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 27 mg (18% of theory) of the title compound are obtained. LC-MS (Method 2): R _t = 1.97 min.

MS (ESIpos): mz = 606 (M + H) ⁺

Example 26

2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] -N- [2- (diethylamino) ethyl] -N- (4-isopropylbenzyl) acetamide

To a solution of 85 mg (0.25 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-triazm-2 (5H) - yl] acetic acid in 2 ml DMF, 61.1 mg (0.25 mmol) N, N-diethyl-N '- (4-isopropylbenzyl) ethane-1,2-diamine, 47.1 mg (0.25 mmol) EDC and 3.3 mg (0.02 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentration of the product fractions and drying in a high vacuum, 41 mg (29% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 1.97 min.

MS (ESIpos): m / z = 576 (M + H) ⁺

Example 27

N- [2- (diethylamino) ethyl] -2- [6-ethyl-3 - {[(5-methyl-l, 3 _J 4-oxadiazol-2-yl) methyl] thio} -5-oxo-l, 2,4-triazin-2 (5H) -yl] -N - {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetaιnid

To a solution of 40 mg (0.13 mmol) [6-ethyl-3 - {[(5-methyl-l, 3,4-oxadiazol-2-yl) methyl] - thio} -5-oxo-l, 2, 4-tτiazin-2 (5H) -yl] acetic acid and 45.0 mg (0.13 mmol) of NN-diethyl-N '- {[4'- (trifluoromethyl) biphenyl-4-yl] methyl} ethane-1,2-diamine in 1 ml DMF 27.1 mg (0.14 mmol) EDC and 1.7 mg (0.01 mmol) HOBt are added at room temperature. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 33 mg (40%) d. Th.) Of the title compound.

HPLC (method 4): R _t = 4.50 min.

MS (EI): m / z = 644 (M + H) ⁺

Example 28

N- (4-butoxybenzyl) -N- [2- (diethylamino) ethyl] -2- [6-ethyl-3 - {[(5-methyl-l, 3,4-oxadiazol-2-yl) methyl] thio} -5-oxo-l, 2,4-triazin-2 (5H) -yl] acetamide

To a solution of 54 mg (0.17 mmol) [6-ethyl-3 - {[(5-methyl-l, 3,4-oxadiazol-2-yl) methylJ-thio} -5-oxo-l, 2,4 -triazin-2 (5Η) -yl] acetic acid and 48.3 mg (0.13 mmol) N '- (4-butoxybenzyι) -NN- diethylethane-1,2-diamine in 1 ml DMF are 36.6 mg (0.19 mmol) EDC at room temperature and 2.3 mg (0.02 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 43 mg (43% of theory) of the title compound are obtained.

HPLC (method 4): R _t = 4.30 min.

MS (EI): m / z = 572 (M + H) ⁺

Example 29

N- [2- (diethylamino) ethyl] -2- [6-ethyl-3 - {[(2-methyl-l, 3-thiazol-4-yl) methyl] thio} -5-oxo-l, 2, 4-triazm-2 (5H) -yl] -N - {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide

To a solution of 50 mg (0.15 mmol) [6-ethyl-3 - {[(2-methyl-l, 3-thiazol-4-yl) methyl] thio} -5-oxo-l, 2,4-triazine -2 (5H) -yl] acetic acid in 2 ml dichloromethane / DMF 1: 1, 53.7 mg (0.15 mmol) N, N-diethyl-N '- {[4' - (trifluoromethyl) biphenyl-4-yl] methyl} ethane-l, 2-diamine, 29.4 mg (0.15 mmol) EDC and 2! mg (0.02 mmol) HOBt. added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 34 mg (34% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 1.97 min.

MS (ESIpos): m / z = 659 (M + H) ⁺

'H NMR (400 MHz, CF ₃ COOD): δ = 7.87 (s, IH), 7.64 (m, 2H), 7.48 (m, 4H), 7.30 (m, 2H), 5.38 (s, 2H), 4.75 (s, 2H), 4.63 (s, 2H), 3.89 (m, 2H), 3.29 (m, 2H), 3.21 (q, 4H), 2.92 (s, 3H), 2.76 (q, 2H), 1.21 (tr, 6H), 1.18 (tr, 3H). Example 30

2- [3 - [(lH-Benzinndazol-2-ylmethyl) thio] -6-ethyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] -N- [2- (diethyl- amino) ethyl] -N- {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide

To a solution of 50 mg (0.14 mmol) of [3 - [(1H-benzimidazol-2-ylmethyl) thio] -6-ethyl-5-oxol, 2,4-triazin-2 (5H) -yl] acetic acid in 2 ml dichloromethane / DMF 1: 1 50.7 mg (0.14 mmol) NN-diethyl-N '- {[4' - (trifluoromethyl) biphenyl-4-yl] methyl} ethane-1,2-diamine, 27.8 mg ( 0.14 mmol) EDC and 2.0 mg (0.01 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying under high vacuum 28 mg (29% Th. D.) To obtain ^'the title compound.

LC-MS (method 3): R _t = 1.80 min.

MS (ESIpos): m / z = 678 (M + H) ⁺

Example 31

2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-l, 2, 4-triazin-2 (5H) -yl] -N- [2- (diethylamino) ethyl] -N - {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide

To a solution of 42 mg (0.11 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-l, 2,4-triazine-2 (5H) - yl] acetic acid in ml DMF, 38.1 mg (0.11 mmol) NN-diethyl-N'- {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} ethane-1,2-diamine, 20.9 mg (0.11 mmol) EDC and 1.5 mg (0.01 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 29 mg (37% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 2-40 min.

MS (ESIpos): mz = 718 (M + H) ⁺

Example 32

N- (4-butoxybenzyl) -2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-1, 2,4-triazine-2 (5H) - yl] -N- [2- (diethylamino) ethyl] acetamide

To a solution of 42 mg (0.11 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-l, 2,4-triazine-2 (5H) - yl] acetic acid in 2 ml of DMF, 30.3 mg (0.11 mmol) of N '- (4-butoxybenzyl) -NN-diethylethane-1,2-diamine, 20.9 mg (0.11 mmol) of EDC and 1.5 mg (0.01 mmol) of HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 20 mg (28% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 2.31 min.

MS (ESIpos): m / z = 646 (M + H) ⁺

Example 33

2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclopentyl-5-oxo-l, 2,4-triazin-2 (5H) -yl] -N- [2- (diethylamino) ethyl] -N- (4-isopropylbenzyl) acetamide

To a solution of 42 mg (0.11 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-cyclophtyl-5-oxo-1, 2,4-triazine-2 (5H) - yl] acetic acid in 2 ml of DMF, 27.0 mg (0.11 mmol) of NN-diethyl-N'- (4-isopropylbenzyl) ethane-1,2-diamine, 20.9 mg (0.11 mmol) of EDC and 1.5 mg (0.01 mmol) of HOBt are added , After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 9 mg (13% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 2.25 min.

MS (ESIpos): mz = 616 (M + H) ⁺

Example 34

2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-phenylethyl) -l _J 2,4-triazin-2 (5H) -yl] -N - [2- (diethylamino) ethyl] -N- {[4 '- (1xifluoromethyl) biphenyl-4-yl] methyl} acetamide

To a solution of 41 mg (0.10 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-phenylethyl) -l, 2,4-triazine -2 (5H) -yl] acetic acid in 2 ml DMF will be 34! mg (0.10 mmol) NN-diethyl-N '- {[4' - (tτifluoromethyl) biphenyl-4-yl] methyl} ethane-1,2-diamine, 18.6 mg (0.10 mmol) EDC and 1.3 mg (0.01 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 44 mg (60% of theory) of the title compound are obtained.

LC-MS (Method 3): R _t = 2.39 min.

MS (ESIpos): mz = 754 (M + H) ⁺

'H NMR (400 MHz, CF ₃ COOD): δ = 7.78 (m, 4H), 7.72 (m, 2H), 7.44 (m, 2H), 7.30 (m, 2H), 7.24 (m, 3H), 7.19 (s, IH, partly HD exchange), 6.89 (s, IH), 5.50 (s, 2H), 4.91 (s, 2H), 4.60 (s, 2H), 4! 1 (m, 2H), 3.55 (, 2H), 3.41 (q, 4H), 3.30 (, 2H), 3.15 (m, 2H), 1.42 (tr, 6H). Example 35

N- (4-butoxybenzyl) -2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-ρhenylethyl) -l, 2,4-tτiazine-2 (5H) -yl], N- [2- (diethylamino) ethyl] acetamide

To a solution of 41 mg (0.10 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-phenylethyl) -l, 2,4-triazine -2 (5H) -yl] acetic acid in 2 ml DMF, add 34.1 mg (0.10 mmol) N '- (4-butoxybenzyl) -NN-diethylethane-1,2-diamine, 18.6 mg (0.10 mmol) EDC and 1.3 mg (0.01 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 34 mg (51% of theory) of the title compound are obtained.

LC-MS (Method 2): R _t = 2.16 min.

MS (ESIpos): mz = 682 (M + H) ⁺

Example 36

2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-phenylethyl) -l, 2,4-triazin-2 (5H) -yl] -N - [2- (diethylamino) ethyl] -N- (4-isopropylbenzyl) acetamide

To a solution of 35 mg (0.08 mmol) [3 - {[(5-chloro-3-thienyl) methyl] thio} -5-oxo-6- (2-phenylethyl) -l, 2,4-triazine -2 (5H) -yl] acetic acid in 2 ml DMF, 20.6 mg (0.08 mmol) NN-diethyl-N '- (4-isopropylbenzyl) ethane-1,2-diamine, 15.9 mg (0.08 mmol) EDC and 1! mg (0.01 mmol) HOBt added. After 18 h at room temperature, the reaction mixture is purified by means of preparative HPLC. After concentrating the product fractions and drying in a high vacuum, 25 mg (46% of theory) of the title compound are obtained.

LC-MS (Method 2): R _t = 2.09 min.

MS (ESIpos): m / z = 652 (M + H) ⁺

Example 37

2- [3 - {[(2,5-dichloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-1, 2,4-triazin-2 (5H) -yl] -N- [ 2- (diethylamino) ethyl] -N - {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide

To a solution of 100 mg (0.26 mmol) [3 - {[(2,5-dichloro-3-thienyl) methyl] thio} -6-ethyl-5-oxol, 2,4-triazine-2 (5H ) -yl] acetic acid and 92 mg (0.26 mmoi) N, N-diethyl-N '- {[4' - (trifluoromethyl) - biphenyl-4-yl] methyl} ethane-1,2-diamine in dichloromethane become 4 mg (0.03 mmol) HOBt and 55 mg (0.29 mmol) EDC hydrochloride were added and the mixture was stirred at room temperature overnight. After adding water, the organic phase is separated off, washed with saturated sodium hydrogen carbonate solution and water, dried over magnesium sulfate and concentrated in vacuo. The residue obtained is over. Silica gel cleaned (eluent: dichloromethane / methanol 40: 1). Product 66 mg (35% d. Th.) Is obtained. ^'

HPLC (method 6): R _t = 3.75 min.

LC-MS (Method 3): R _t = 2.39 min.

MS (ESIpos): m / z = 712, 714 (M + H) ⁺

Η NMR (400 MHz, CDC1 ₃ ): δ = 7.73 - 7.58 (m, 4H), 7.61 (d) and 7.54 (d, together 2H), 7.35 (d, 2H), 6.93 (s) and 6.89 (s , together IH), 5.17 (s) and 4.81 (s, together 2H), 4.70 (s „2H), 4.43 (s) and 4.38 (s, together 2H), 3.55 (t) and 3.29 (t, together 2H) , 2.78 -2.48 (m, 8H), 1.28 - 1.16 (m, 3H), 1.04 - 0.98 (m, 6H). Example 38

N- [2- (diethylamino) ethyl] -2- [6-ethyl-3 - {[(5-fluoro-2-thienyl) methyl] thio} -5-oxo-l, 2 ₎ 4-triazine 2 ( 5H) -yl] -N- {[4 '- (tifluoromethyl) biρhenyl-4-yl] methyl} acetamide

41 mg (0.15 mmol) of phosphorus tribromide are added dropwise to a solution of 50 mg (0.38 mmol) of (5-fluoro-2-thienyl) methanol cooled to -10 ° C. in 1 ml of dichloromethane and the mixture is stirred at room temperature for 15 min. Water is added, the phases are separated, the organic phase is dried over magnesium sulfate and concentrated in vacuo. The residue is taken up in 1 ml of DMF, 80 mg (0.13 mmol) of N- [2- (diethylamino) ethyl] -2- (6-ethyl-5-oxo-3-thioxo-4,5-dihydro-1,2) , 4-friazin-2 (3H) -yl) -N - {[4 '- (rrifluoromethyl) biphenyl-4-yl] methyl} -acetamide trifluoroacetate and 64 mg (0.2 mmol) of cesium carbonate were added and the mixture was added at room temperature stirred overnight. Water is added to the reaction mixture, extracted several times with diethyl ether, the organic phase is dried over magnesium sulfate and concentrated in vacuo. The residue is purified by preparative HPLC. 24 mg (27% of theory) of product are obtained.

HPLC (method 6): R _t = 3.53 min.

LC-MS (method 3): R _t = 2! 8 min.

MS (ESIpos): mz = 662 (M + H) ⁺

'H NMR (300 MHz, DMSO-d ₆ ): δ = 7.92-7.74 (m, 5H), 7.68 (d, IH), 7.47-7.35 (m, 2H), 6.85-6.77 (m, IH), 6.55-6.50 (m, IH), 5.33 (s) and 5.02 (s, together 2H), 4.74 (s) and 4.63 (s, together 2H), 4.60-4.53 (m, 2H), 3.39-3.30 (m, 2H), 2.64-2.60 (m, 8H), 1.14-1-07 (m, 3H), 0.98-0.87 (m, 6H). Example 39

2- [3 - {[(5-chloro-3-thienyl) methyl] thio} -6-ethyl-5-oxo-l, 2,4-tτiazin-2 (5H) -yl] -N- (l- methylpiperidin-4-yl) -N - {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide formate salt

The preparation is carried out starting from Example 33 A and Example 51A analogously to the procedure of Example 4, using TBTU as coupling reagent. The purification via HPLC is carried out in the presence of formic acid in the eluent A. The product is isolated as a formate salt.

HPLC (method 4): R _t = 4.87 min.

MS (ESIpos): m z = 676 (M + H)

'H-ΝMR (400 MHz, TFA-d: δ = 8.2 (s, IH), 7.8-6.8 (m, 10H), 5.4 (s, 2H), 4.9 (m, 3H), 4.6 (s, 2H) , 3.8 (m, 2H), 3.3 (m, 2H), 3! (S, 3H), 3.0 (q, 2H), 2.5 (m, 2H), 2.3 (m, 2H), 1.4 (t, 3H) Rotamers of the amide bond occur, the signals of the predominant rotamer are described.

Example 40

2- [3 - {[(5-chloro-3-tMenyl) methyl] 1mo} -6-yl-5-oxo-l, 2,4-1riazm-2 (5H) -yl] -N- (l -ethylpiperidin-4-yl) -N- {[4 '- (trifluoromethyl) biphenyl-4-yl] methyl} acetamide formate salt

The preparation takes place starting from example 33A and example 52A analogously to the instruction of example 4 using TBTU as coupling reagent. The purification via HPLC is carried out in the presence of formic acid in the eluent A. The product is isolated as a formate salt.

HPLC (method 4): R _t = 4.90 min.

MS (ESIpos): m / z = 690 (M + H)

'H-ΝMR (400 MHz, TFA-d,): δ = 8.2 (s, IH), 7.8-6.8 (m, 10H), 5.4 (s, 2H), 4.9 (m, 3H), 4.6 (s, 2H), 3.9 (m, 2H), 3.4 (m, 2H), 3.3 (m, 2H), 3.0 (q, 2H), 2.5 (m, 2H), 2.3 (m, 2H), 1.5 (t, 3H) ), 1.4 (t, 3H). Rotamers of the amide bond occur, the signals of the predominant rotamer are described.

B) Assessment of physiological effectiveness

The suitability of the compounds according to the invention for the treatment of cardiovascular diseases can be shown in the following assay systems:

In vitro assay of the PAF-AH

Purification of the PAF-AH from human plasma

PAF-AH activity is isolated from the LDL fraction of human plasma. This is done according to a protocol by Stafforini et al. (J. Biol. Chem. 1987, 262: 4223-4230). After isolation of the LDL fraction via a potassium bromide density gradient, solubilization is carried out with 0.1% Tween-20 (buffer: 20 mM K ₂ HP0 ₄ fK. ₂ P0 ₄ , pH 6.8). Then fractionation on a DEAE-Sepharose column (buffer: 20 mM K ₂ HPO ₄ / KH ₂ PO ₄ , pH 6.8, 0.1% Tween-20, gradient: 0-300 mM KCl). The fractions with PAF-AH activity are pooled, dialyzed (50 mM Tris pH 7.5; 0.1% Tween-20) and then purified on a MonoQ column (buffer: 50 mM Tris pH 7.5; 0.1% Tween-20, gradient: 0 -600mM KCl).

Thio-PAF Assay

2-Thio-PAF (Cayman Chemicals, Ann Arbor, MI, USA) is used as a substrate for the PAF-AH. BODIPY FL L-cysteine (Molecular Probes, Eugene, OR, USA) serves as an indicator of the free thiol group of the resulting product. The reaction is carried out in a buffer of 100 mM Tris-HC1, pH 8.2, 1 mM EGTA, 150 mM NaCl, 50 mM MgCl ₂ with the addition of 25 μM substrate, 10 μM indicator and 0! μg / ml PAF-AH incubated at 37 ° C and the fluorescence (excitation 485 nm / emission 515 nm) measured in the fluorescence reader Spectra Fluor (Tecan, Crailsheim, Germany). The results are shown in Table A:

Table A:

In vivo assay of the PAF-AH

To determine the anti-atherosclerotic effect of PAF-AH inhibitors, the LDL-, receptor-deficient. Watanabe rabbit (Buja, L.M., ärteriosclerosis .1983, 3, 87-101) was used. Either in short-term examinations (1-2 months) the anti- atherosclerotic effect is determined indirectly by a change in gene expression, of relevant marker genes in tissue susceptible to atherosclerosis, or. Long-term studies (3-6 months) directly determined the formation of atherosclerotic plaques using histological techniques.

C) Examples of pharmaceutical compositions

The substances according to the invention can be converted into pharmaceutical preparations as follows:

Tablet:

Composition: 100 mg of the compound of Example 1, 50 mg lactose (monohydrate), 50 mg corn starch, 10 mg polyvinylpyrolidone (PVP 25) (from BASF, Germany) and 2 mg magnesium stearate.

Tablet weight 212 mg. Diameter 8 mm, radius of curvature 12 mm.

production:

The mixture of the compound of Example 1, lactose and starch is granulated with a 5% solution (m / m) of the PVP in water. The granules are dried with the magnesium stearate for 5 min. mixed. This mixture is compressed with a conventional tablet press (tablet format see above). Oral suspension:

Composition:

1000 mg of the compound of Example 1, 1000 mg of ethanol (96%), 400 mg of Rhodigel (Xanfhan gum) (from FMC, USA) and 99 g of water.

A single dose of 100 mg of the compound according to the invention corresponds to 10 ml of oral suspension.

production:

The Rhodigel is suspended in ethanol, the compound of Example 1 is added to the suspension. The water is added with stirring. The mixture is stirred for about 6 hours until the swelling of the Rhodigel is complete.

Solution that can be administered intravenously:

Composition:

1 mg of the compound of Example 1, 15 g of polyethylene glycol 400 and 250 g of water for injections. ,

production:

The compound of Example 1 is dissolved together with polyethylene glycol 400 in the water with stirring. The solution is sterile filtered (pore diameter 0.22 μm) and filled into heat-sterilized infusion bottles under aseptic conditions. These are closed with infusion stoppers and crimp caps.

Claims

Patent claims

1. Compound of the formula

r. - -. , ^, . -in which ^' •

5 Y represents an oxygen atom or a sulfur atom, m represents a number 1, 2 or 3, n represents a number 1, 2, 3 or 4,

R ^{1 represents} Ci-Cβ-alkyl or C ₃ -C ₇ cycloalkyl, where alkyl can be substituted with 1 to 3 substituents, the sub-10 substituents being selected independently of one another from the group consisting of halogen, cyano, oxo, Phenyl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl and alkylammocarbonyl,

R ^{2 represents} 5- to 10-membered heteroaryl, where heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxyl, amino, halogen, cyano, trifluoromethyl, trifluorine ethoxy, Alkyl, alkoxy, alkylamino, alkylthio, aryl, aryloxy, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylammocarbonyl, alkylcarbonyl and alkylcarbonylamino, ^'

20 R ^{3 represents} hydrogen or CC ₆ alkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of from hydroxy, amino, halogen, alkoxy, alkylamino, hydroxyalkylamino, alkylthio, heterocyclyl, heteroaryl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, alkylcarbonyl and alkylcarbonylamino, in which heterocyclyl and heteroaryl can in turn be substituted by 1 to 3 substituents independently of one another, where the substituents can be substituted independently of one another are selected from the group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylthio, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, alkylcarbonyl and alkylcarbonylamino,

or

R ^{3 represents} a 3- to 8-membered heterocyclyl having 1 to 2 nitrogen atoms, it being possible for heterocyclyl to be substituted with 1 to 2 substituents, the substituents being selected independently of one another from the group consisting of optionally substituted with hydroxyl, amino or alkoxy alkyl,

R ^{4 stands} for aryl or heteroaryl, where aryl and heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino , Alkylthio, alkylsulfonyl, aryl, aryloxy, heteroaryl, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, alkylcarbonyl, alkylcarbonylamino, alkylaminosulfonyl and alkylsulfonylamino, in which alkyl, alkoxy, alkylthio and alkylsulfonyl may be substituted with 1 to 3 aryl substituents and halogen, 1 and 3 aryl substituents, halogen, and halo can in turn be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxyl, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylthio, alkylsulfonyl, hydroxycarbonyl, alkoxycarbonyl, Aminocarbonyl, alkylaminocarbonyl, alkylcarbon yl, alkylcarbonylamino, alkylaminosulfonyl and alkylsulfonylamino, wherein alkyl, alkoxy, alkylthio and alkylsulfonyl can in turn be substituted with 1 to 3 halogen substituents, or one of their salts, their solvates or the solvates of their salts.

2. Compound according to claim 1, characterized in that Y stands for an oxygen atom or a sulfur atom, m stands for a number 1 or 2, n stands for a number 1, 2 or 3,

R ^{1 represents} Ci-Cβ-alkyl or C ₃ -C ₅ -cycloalkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano, oxo, phenyl , Hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl and alkylammocarbonyl,

R ^{2 stands} for 5- to 10-membered heteroaryl, where heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of hydroxy, amino, halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy , Alkylamino, alkylthio, aryl, aryloxy, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, alkylcarbonyl and alkylcarbonylamino, R ^{3 represents} hydrogen or C ₁ -C ₆ -alkyl, where alkyl can be substituted by 1 to 3 substituents, the substituents being independent of one another are selected from the group consisting of hydroxy, amino, alkoxy, alkylamino and hydroxyallcylamino, or R ^{3 represents} a 5- to 7-membered heterocyclyl having 1 to 2 nitrogen atoms, where heterocyclyl can be substituted by 1 to 2 substituents, the substituents are independently selected from the group consisting of, optionally with hydroxy, amino or alkoxy s substituted alkyl, R ^{4 represents} aryl or heteroaryl, where aryl and heteroaryl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen, cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, aryl, aryloxy , Heteroaryl, alkylaminocarbonyl and alkylcarbonylamino, in which alkyl and alkoxy can be substituted with 1 to 3 substituents halogen, and in which aryl and "heteroaryl in turn can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of halogen , Cyano, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, alkylamino, alkylaminocarbonyl and alkylcarbonylamino, in which alkyl and alkoxy in turn can be substituted with 1 to 3 halogen substituents.

3. Connection according to one of claims 1 or 2, characterized in that

Y stands for a sulfur atom, m stands for the number 1, n stands for the number 1,

R ^{1 stands} for CC ₄ alkyl, where alkyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another from the group consisting of fluorine, cyano, oxo, phenyl and alkoxycarbonyl, R ² for pyridyl, thienyl, furyl or thiazolyl, where pyridyl, thienyl, furyl and thiazolyl can be substituted with 1 to 3 substituents, the substituents being selected independently of one another are selected from the group consisting of halogen, trifluoromethyl, trifluoromethoxy and methyl,

R ^{3 represents} hydrogen or CC ₄ -alkyl, where alkyl can be substituted by a substituent, the substituent being selected from the group consisting of amino and C ₁ -C ₄ -alkylamino, or

R ^{3 represents} piperidinyl or pyrrolidinyl, it being possible for piperidinyl and pyrrolidinyl to be substituted by a substituent CC ₄ -alkyl, R ⁴ . represents phenyl, where phenyl can be substituted by a substituent, the substituent being selected from the group consisting of CC ₄ -alkyl, C1-C ₄ -alkoxy and phenyl, in which phenyl can in turn be substituted by a substituent, the substituent is selected from the group consisting of halogen, trifluoromethyl, C ₁ -C 3 alkyl and C ₁ -C ₃ alkoxy.

4. A process for the preparation of a compound of formula (I) according to claim 1, characterized in that a compound of formula

in which

Y, m, n, R ¹ and R ^{2 have} the meaning given in claim 1, with a compound of the formula in which

R ³ and R ^{4 have} the meaning given in claim 1 is implemented.

5. A compound according to any one of claims 1 to 3 for the treatment and / or prophylaxis of diseases.

6.. Medicament containing at least one compound according to one of claims 1 to 3 in combination with - at least iron - pharmaceutically acceptable, pharmaceutically acceptable carriers or other excipients.

7. Use of a compound according to any one of claims 1 to 3 for the manufacture of a medicament.

8. Medicament according to claim 6 for the treatment and / or prophylaxis of chronic inflammatory diseases or cardiovascular diseases.

9. A method for combating arteriosclerosis in humans and animals by administering an effective amount of at least one compound according to one of claims I to 3.