The invention is concerned especially with compounds of formula I and pharmaceutically acceptable salts and esters thereof wherein Rl is aryl or heteroaryl; R2 is hydrogen, alkyl or cycloalkyl ; R3 is hydrogen, alkyl or cycloalkyl ; R4 is hydrogen, alkyl or cycloalkyl ; R5 is alkyl, cycloalkyl, aryl, heteroaryl; R6 is hydrogen, alkyl or cycloalkyl ; A is-C (O)-;-S (0) 2-;-N (R6)-C (O)-or-O-C (O)-; nis2to6 ; and m is zero to 2.

The compounds of formula I and their pharmaceutically acceptable salts and esters are novel and have valuable pharmacological properties. They are neuropeptide ligands, for example neuropeptide receptor antagonists and in particular, they are selective neuropeptides Y Y5 receptor antagonists.

Neuropetide Y is a 36 amino acid peptide that is widely distributed in the central and peripheral nervous systems. This peptide mediates a number of physiological effects through its various receptor subtypes. Studies in animals have shown that neuropeptide Y is a powerful stimulus of food intake, and it has been demonstrated that activation of neuropeptide Y Y5 receptors results in hyperphagia and decreased thermogenesis.

Therefore compounds that antagonise neuropetide Y at the Y5 receptor subtype represent an approach to the treatment of eating disorders such as obesity and hyperphagia.

The current approach is aiming at medical intervention to induce weight loss or prevention of weight gain. This is achieved by interfering with appetite control, which is mediated by the Hypothalamus, an important brain region proven to control food intake.

Herein, neuropeptide Y (NPY) has been proven to be one of the strongest central mediators of food intake in several animal species. Increased NPY levels result in profound food intake. Various receptors of neuropeptide Y (NPY) have been described to play a role in appetite control and weight gain. Interference with these receptors is likely to reduce appetite and consequently weight gain. Reduction and long-term maintenance of body weight can also have beneficial consequences on con associated risk factors such as arthritis, cardiovascular diseases, diabetes and renal failure.

Accordingly, the compounds of formula I, their salts and esters can be used in the prophylaxis or treatment of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity.

Objects of the present invention are the compounds of formula I and their aforementioned salts and esters per se and their use as therapeutically active substances, a process for the manufacture of the said compounds, intermediates, pharmaceutical compositions, medicaments comprising the said compounds, their pharmaceutically acceptable salts and esters, the use of the said compounds, salts and esters for the prophylaxis and/or therapy of illnesses, especially in the treatment or prophylaxis of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders such as hyperphagia and particularly obesity, and the use of the said compounds, salts and esters for the production of medicaments for the treatment or prophylaxis of arthritis,

cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity.

In the present description the term"alkyl", alone or in combination, signifies a straight-chain or branched-chain alkyl group with 1 to 8 carbon atoms, preferably a straight or branched-chain alkyl group with 1 to 6 carbon atoms and particularly preferred a straight or branched-chain alkyl group with 1 to 4 carbon atoms Examples of straight- chain and branched Cl-C8 alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert. -butyl, the isomeric pentyls, the isomeric hexyls, the isomeric heptyls and the isomeric octyls, preferably methyl and ethyl and most preferred methyl.

The term"cycloalkyl", alone or in combination, signifies a cycloalkyl ring with 3 to 8 carbon atoms and preferably a cycloalkyl ring with 3 to 6 carbon atoms. Examples of C3-C8 cycloalkyl are cyclopropyl, methyl-cyclopropyl, dimethylcyclopropyl, cyclobutyl, methyl- cyclobutyl, cyclopentyl, methyl-cyclopentyl, cyclohexyl, methyl-cyclohexyl, dimethyl- cyclohexyl, cycloheptyl and cyclooctyl, preferably cyclopropyl and cyclopentyl.

The term"alkoxy", alone or in combination, signifies a group of the formula alkyl- 0-in which the term"alkyl"has the previously given significance, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec. butoxy and tert. butoxy, 2- hydroxyethoxy, 2-methoxyethoxy, preferably methoxy and ethoxy and most preferred methoxy.

The term"aryl", alone or in combination, signifies a phenyl or naphthyl group, preferably a phenyl group which optionally carries one or more, preferably one to three substituents each independently selected from halogen, haloalkyl, amino, alkyl, alkoxy, aryloxy, alkylcarbonyl, cyano, carbamoyl, alkoxycarbamoyl, methylendioxy, carboxy, alkoxycarbonyl, aminocarbonyl, alkyaminocarbonyl, dialkylaminocarbonyl, hydroxy, nitro, haloalkoxy and the like. Preferred substituents of aryl, preferably phenyl are independently selected from halogen, trifluoromethyl, alkyl, alkoxy and haloalkoxy.

The term"aralkyl", alone or in combination, signifies an alkyl or cycloalkyl group as previously defined, preferably an alkyl group in which one hydrogen atom has been replaced by an aryl group as previously defined. Preferred are benzyl, benzyl substituted with hydroxy, alkoxy or halogen, preferably fluorine.

The term"heteroaryl", alone or in combination, signifies an aromatic 5-or 6- membered ring comprising 1 to 3 atoms independently selected from nitrogen, oxygen or sulfur. Optionally, the heteroaryl ring can be substituted on one or more carbon atoms

with halogen, alkyl, alkoxy and cyano. Examples of heteroaryl rings include furyl, pyridyl, 1,2-, 1, 3- and 1,4-diazinyl or pyrazinyl, thienyl, isoxazolyl, oxazolyl, thiazolyl and pyrrolyl.

Preferred heteroaryl rings are pyridinyl, thiophenyl and pyrazinyl which are optionally substituted with alkyl.

The term"amino", alone or in combination, signifies a primary, secondary or tertiary amino group bonded via the nitrogen atom, with the secondary amino group carrying an alkyl or cycloalkyl substituent and the tertiary amino group carrying two similar or different alkyl or cycloalkyl substituents or the two nitrogen substitutents together forming a ring, such as, for example,-NH2, methylamino, ethylamino, dimethylamino, diethylamino, methyl-ethylamino, pyrrolidin-1-yl or piperidino etc., preferably amino, dimethylamino and diethylamino and particularly preferred primary amino.

The term"halogen", alone or in combination, signifies fluorine, chlorine, bromine or iodine and preferably fluorine, chlorine or bromine and particularly chlorine.

The term"haloalkyl", alone or in combination, signifies an alkyl group as previously defined, wherein one or several hydrogen atoms, preferably one to three hydrogen atoms have/has been replaced by halogen. Examples of haloalkyl groups are trifluoromethyl, pentafluoroethyl and trichloromethyl. Preferred examples are trifluoromethyl and difluoromethyl. Most preferred is trifluoromethyl.

The term"haloalkoxy", alone or in combination, signifies an alkoxy group as previously defined, wherein one or several hydrogen atoms, preferably one to three hydrogen atoms have/has been replaced by halogen. A preferred example is trifluoromethoxy.

The term"cyano", alone or in combination, signifies a-CN group.

The term"nitro", alone or in combination, signifies a-NO2 group.

The term-C (O)- means a carbonyl group.

The term-S (O) 2- means the following group: The term-N (R6)-C (O)- means the following group: The term-O-C (O)- means the following group:

Examples of pharmaceutically acceptable salts of the compounds of formula I are salts with physiologically compatible mineral acids such hydrochloric acid, sulfuric acid or phosphoric acid; or with organic acids such as methanesulfonic acid, formic acid, acetic acid, trifluoroacetic acid, citric acid, fumaric acid, maleic acid, tartaric acid, succinic acid or salicylic acid. Preferred is oxalic acid. The compounds of formula I with free carboxy groups can also form salts with physiologically compatible bases. Examples of such salts are alkali metal, alkali earth metal, ammonium and alkylammonium salts such as the Na, K, Ca or tertramethylammonium salt. The compound of formula I can also be present in the form of zwitterions.

The compounds of formula I can also be solvated, e. g. hydrated. The solvation can be effected in the course of the manufacturing process or can take place e. g. as a consequence of hygroscopic properties of an initially anhydrous compound of formula I (hydration). The term pharmaceutically acceptable salts also includes pharmaceutically acceptable solvates.

The term pharmaceutically acceptable esters of the compounds of formula I means that compounds of general formula (I) may be derivatised at functional groups to provide derivatives which are capable of conversion back to the parent compounds in vivo.

Examples of such compounds include physiologically acceptable and metabolically labile ester derivatives, such as methoxymethyl esters, methylthiomethyl esters and pivaloyloxymethyl esters. Additionally, any physiologically acceptable equivalents of the compounds of general formula (I), similar to the metabolically labile esters, which are capable of producing the parent compounds of general formula (I) in vivo, are within the scope of this invention.

In more detail, for example, the COOH groups of compounds according to formula I can be esterified. The alkyl and aralkyl esters are examples of suitable esters. The methyl, ethyl, propyl, butyl and benzyl esters are preferred esters. The methyl and ethyl esters are especially preferred. Further examples of pharmaceutically usable esters are compounds of formula I, wherein the hydroxy groups can be esterified. Examples of such esters are formate, acetate, propionate, butyrate, isobutyrate, valerate, 2-methylbutyrate, isovalerate and N, N-dimethylaminoacetate. Preferred esters are acetate and N, N- dimethylaminoacetate.

The term"lipase inhibitor"refers to compounds which are capable of inhibiting the action of lipases, for example gastric and pancreatic lipases. For example orlistat and lipstatin as described in U. S. Patent No. 4,598, 089 are potent inhibitor of lipases. Lipstatin is a natural product of microbial origin, and orlistat is the result of a hydrogenation of lipstatin. Other lipase inhibitors include a class of compound commonly referred to as panclicins. Panclicins are analogues of orlistat (Mutoh et al, 1994). The term"lipase inhibitor"refers also to polymer bound lipase inhibitors for example described in International Patent Application W099/34786 (Geltex Pharmaceuticals Inc. ). These polymers are characterized in that they have been substituted with one or more groups that inhibit lipases. The term"lipase inhibitor"also comprises pharmaceutically acceptable salts of these compounds. The term"lipase inhibitor"preferably refers to orlistat.

Orlistat is a known compound useful for the control or prevention of obesity and hyperlipidemia. See, U. S. Patent No. 4,598, 089, issued July 1,1986, which also discloses processes for making orlistat and U. S. Patent No. 6,004, 996, which discloses appropriate pharmaceutical compositions. Further suitable pharmaceutical compositions are described for example in International Patent Applications WO 00/09122 and WO 00/09123.

Additional processes for the preparation of orlistat are disclosed in European Patent Applications Publication Nos. 185,359, 189,577, 443,449, and 524,495.

Orlistat is preferably orally administered from 60 to 720 mg per day in divided doses two to three times per day. Preferred is wherein from 180 to 360 mg, most preferably 360 mg per day of a lipase inhibitor is administered to a subject, preferably in divided doses two or, particularly, three times per day. The subject is preferably an obese or overweight human, i. e. a human with a body mass index of 25 or greater. Generally, it is preferred that the lipase inhibitor be administered within about one or two hours of ingestion of a meal containing fat. Generally, for administering a lipase inhibitor as defined above it is

preferred that treatment be administered to a human who has a strong family history of obesity and has obtained a body mass index of 25 or greater.

Orlistat can be administered to humans in conventional oral compositions, such as, tablets, coated tablets, hard and soft gelatin capsules, emulsions or suspensions.

Examples of carriers which can be used for tablets, coated tablets, dragees and hard gelatin capsules are lactose, other sugars and sugar alcohols like sorbitol, mannitol, maltodextrin, or other fillers; surfactants like sodium lauryle sulfate, Brij 96, or Tween 80; disintegrants like sodium starch glycolate, maize starch or derivatives thereof; polymers like povidone, crospovidone; talc; stearic acid or its salts and the like. Suitable carriers for soft gelatin capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like. Moreover, the pharmaceutical preparations can contain preserving agents, solubilizers, stabilizing agents, wetting agents, emulsifying agents, sweetening agents, coloring agents, flavoring agents, salts for varying the osmotic pressure, buffers, coating agents and antioxidants. They can also contain still other therapeutically valuable substances. The formulations may conveniently be presented in unit dosage form and may be prepared by any methods known in the pharmaceutical art. Preferably, orlistat is administered according to the formulation shown in the Examples and in U. S. Patent No.

6,004, 996, respectively.

The compounds of formula I can contain several asymmetric centers and can be present in the form of optically pure enantiomers, mixtures of enantiomers such as, for example, racemates, optically pure diastereioisomers, mixtures of diastereoisomers, diastereoisomeric racemates or mixtures of diastereoisomeric racemates.

In the nomenclature used in the present application the ring atoms of the thiazole ring are numbered as follows: wherein Rl to R5, m, n and A are defined as before. In a preferred embodiment of the present invention kis attached to the 5-position and the substituent-C (O)-Rl is attached to the 4-position of the thiazole ring. Particularly preferred are the compounds of formula

I, wherein the substituent-C (O)-Rl is attached to the 5-position and R2 is attached to the 4-position of the thiazole ring.

Preferred are compounds of formula I, wherein R2 is hydrogen or alkyl. Particularly preferred are compounds of formula I, wherein R2 is hydrogen or methyl. Most preferred are compounds according to formula I, wherein R2 is hydogen.

A further preferred object of the present invention are compounds of formula I, wherein R3 is hydrogen or alkyl. Particularly preferred are those compounds of formula I, wherein R3 is hydrogen.

Also a preferred object of the present invention are compounds of formula I, wherein R4 is hydrogen or alkyl. Particularly preferred are compounds according to formula I, wherein R4 is hydrogen.

Another preferred object of the present invention are compounds of formula I, wherein R5 is alkyl, cycloalkyl, phenyl, phenyl substituted with one to three substituents independently selected from halogen, alkyl, alkoxy and haloalkyl, or R5 is thiophenyl or thiophenyl substituted with alkyl, or R5 is pyridinyl or pyridinyl substituted with alkyl or R is pyrazinyl or pyrazinyl substituted with alkyl. Particularly preferred are compounds according to formula I, wherein R5 is n-butyl, tert. butyl, cyclohexyl, thiophenyl, phenyl or phenyl substituted with one to three substituents independently selected from methyl, ethyl, methoxy, fluoro, chloro and trifluoromethyl. Further particularly preferred are compounds according to formula I, wherein R5 is thiophenyl or phenyl optionally substituted with one to three substituents independently selected from alkyl, alkoxy, halogen and haloalkyl.

Preferred are compounds according to formula I, wherein R5 is thiophenyl or phenyl both optionally substituted with one to three substituents independently selected from alkyl, alkoxy, halogen, haloalkyl, haloalkoxy and nitro.

A further preferred object of the present invention are compounds according to formula I, wherein R6 is hydrogen.

Also preferred are compounds of formula I, wherein Rl is pyridinyl or pyridinyl substituted with alkyl, or Rl is thiophenyl or thiophenyl substituted with alkyl or Rl is phenyl or phenyl substituted with one to three substituents independently selected from alkyl, halogen, haloalkyl or R'is pyrazinyl or pyrazinyl substituted with alkyl. Particularly preferred are compound according to formula I, wherein Rl is pyridinyl, phenyl or phenyl

substituted with one to three substituents independently selected from alkyl, alkoxy, halogen and haloalkyl. Very preferred are compounds of formula I, wherein Rl is pyridinyl or phenyl substituted with one to three substituents independently selected from alkyl, alkoxy, halogen and haloalkyl.

A further particularly preferred object of the present invention are compounds according to formula I, wherein A is-S (O) 2-.

Another preferred emodiment of the present invention are compounds of formula I, wherein A is-C (O)-.

Further preferred are compounds of formula I, wherein A is-N (R6)-C (O)-.

Also preferred are compounds of formula I, wherein A is-O-C (O) -.

Likewise preferred are compounds of formula I, wherein n is 3 to 5. Particularly preferred are compounds of formula I, wherein n is 3. Further particularly preferred are compounds of formula I, wherein n is 5.

Preferred compounds of formula I are those, wherein m is zero or 1. Particularly preferred are those compounds of formula I, wherein m is zero. A further very preferred embodiment of this invention are compounds of formula I, wherein A is-S (O) 2- and m is zero.

Examples of preferred compounds of formula I are: 1. 2-Fluoro-N- {3- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 2. 2-Methoxy-5-methyl-N- {3- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-propyl}-benz enesulfonamide 3. 2-Methoxy-5-methyl-N- {3- [5-(pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}-benz enesulfonamide 4. 2-Methoxy-5-methyl-N- {3- [5- (pyridine-4-carbonyl)-thiazol-2-ylamino]-propyl}-benz enesulfonamide 5. 2-Fluoro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide

6. 4-Methoxy-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 7. Thiophene-2-sulfoiiic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide 8. 2-Methoxy-5-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzene sulfonamide 9. 4-Fluoro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 10. 2-Methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 11. 3-Fluoro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 12. 2-Chloro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-5-trifluoromet hyl- benzenesulfonamide 13. N- {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzenesulfona mide 14. 3-Methoxy-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 15. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-2-fluoro- benzenesulfonamide 16. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-4-methoxy- benzenesulfonamide 17. Thiophene-2-sulfonic acid {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}- amide 18. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-2-methoxy-5-me thyl- benzene sulfonamide 19. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-4-fluoro- benzenesulfonamide 20. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-2-methyl- benzenesulfonamide

21. N-{3- [5-(2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3-fluoro- benzenesulfonamide 22. 2-Chloro-N-{3-[5-(2-chloro-benzoyl)-thiazol-2-ylamino]-propy l]-5-trifluoromethyl - benzenesulfonamide 23. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-benzenesulfona mide 24. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3-methoxy- benzenesulfonamide 25. {3- [5-(2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester 26. {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester 27. {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester 28. {3- [5- (2-Trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}-carba mic acid tert- butyl ester 29. Cyclohexanecarboxylic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide 30. Cyclohexanecarboxylic acid {3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide 31. Pentanoic acid [3- (5-benzoyl-thiazol-2-ylamino)-propyl]-amide 32. Pentanoic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide 33. Pentanoic acid {3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide 34. Pentanoic acid {3- [5- (2-fluoro-benzoyl)-thiazol-2-ylamino]-propyl}-amide 35. Pentanoic acid {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-amide 36. N- [3- (5-Benzoyl-thiazol-2-ylamino) -propyl]-2- (4-chloro-phenyl)-acetamide 37.2- (4-Chloro-phenyl)-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- acetamide 38.2- (4-Chloro-phenyl)-N- {3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}- acetamide

39. Thiophene-2-carboxylic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide 40. Thiophene-2-carboxylic acid {3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide 41. Thiophene-2-carboxylic acid {3- [5- (2-fluoro-benzoyl)-thiazol-2-ylamino]-propyl}- amide 42. Thiophene-2-carboxylic acid {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}- amide 43. N- {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-2-fluoro-benzam ide 44. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-2-fluoro-benza mide 45. 3-Fluoro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 46. N- {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-3-fluoro-benzam ide 47. 3-Fluoro-N-{3-[5-(2-fluoro-benzoyl)-thiazol-2-ylamino]-propy l}-benzamide 48. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3-fluoro-benza mide 49. 4-Fluoro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 50. N-{3-[5-(2-Ethyl-benzoyl )-thiazol-2-ylamino]-propyl}-4-fluoro-benzamide 51. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-4-fluoro-benza mide 52. N- {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 53. N- {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 54. N- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 55. N-{3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-4-methoxy-benza mide 56. N- [3- (5-Benzoyl-thiazol-2-ylamino)-propyl]-2-methoxy-benzamide 57. N- {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-2-methoxy-benza mide 58. 4-Chloro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 59. 4-Chloro-N- {3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide

60. Cyclohexanecarboxylic acid {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]- propyl}-amide 61. Cyclohexanecarboxylic acid {3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2- ylamino]-propyl}-amide 62. Pentanoic acid {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide 63. Pentanoic acid {3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}- amide 64. Pentanoic acid {3- [5- (2-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}- amide 65. Pentanoic acid {3- [5- (3-methyl-thiophene-2-carbonyl)-thiazol-2-ylamino]-propyl}- amide 66. 2-(4-Chloro-phenyl)-N-{3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]- propyl}-acetamide 67.2- (4-Chloro-phenyl)-N-{3- [5- (3-methyl-pyridine-2-carbonyl)-thiazol-2-ylamino]- propyl}-acetamide 68.2- (4-Chloro-phenyl)-N- {3- [5- (3-methyl-pyrazine-2-carbonyl)-thiazol-2-ylamino]- propyl}-acetamide 69. Thiophene-2-carboxylic acid {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]- propyl}-amide 70. Thiophene-2-carboxylic acid {3- [5- (3-methyl-pyridine-2-carbonyl)-thiazol-2- ylamino]-propyl}-amide 71. 2-Fluoro-N- {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}-benza mide 72. 2-Fluoro-N- {3- [5- (3-methyl-pyrazine-2-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 73. 3-Fluoro-N- {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}-benza mide 74. 3-Fluoro-N- {3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 75. 3-Fluoro-N- {3- [5- (3-methyl-pyridine-2-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide

76. 3-Fluoro-N- {3- [5- (3-methyl-pyrazine-2-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 77. 4-Fluoro-N- {3- [5-(2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}-be nzamide 78. 4-Fluoro-N- {3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 79. 4-Fluoro-N- {3- [5- (3-methyl-pyridine-2-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 80. 4-Fluoro-N- {3- [5- (3-methyl-thiophene-2-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 81. N- {3- [5- (2-Trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}-benza mide 82. N- {3- [5- (4-Methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}-be nzamide 83. 4-Methoxy-N- {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzamide 84. 4-Methoxy-N- {3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 85. 2-Methoxy-N- {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzamide 86. 4-Chloro-N- {3- [5- (2-trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzamide 87. 4-Chloro-N- {3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 88. 4-Chloro-N- {3- [5- (2-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}- benzamide 89. 1- [3- (5-Benzoyl-thiazol-2-ylamino)-propyl]-3-cyclohexyl-urea 90. 1-Cyclohexyl-3- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 91. 1-Cyclohexyl-3- {3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 92. 1- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3-cyclohexyl-u rea

93. 1- [3- (5-Benzoyl-thiazol-2-ylamino)-propyl]-3-butyl-urea 94. 1-Butyl-3- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 95. 1-Butyl-3-{3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 96. 1-Butyl-3- {3- [5- (2-fluoro-benzoyl)-thiazol-2-ylamino]-propyl}-urea 97. 1-Butyl-3- {3- [5-(2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-urea 98. 1- (2-Methoxy-phenyl)-3-13- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyll-urea 99. 1- {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-3- (2-methoxy-phenyl)-urea 100. 1- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3- (2-methoxy-phenyl) - urea 101. 1- (2-Fluoro-phenyl)-3- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 102. 1-{3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-3-(2-fluoro-phe nyl)-urea 103. 1- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3- (2-fluoro-phenyl)-urea 104. 1-(3-Fluoro-phenyl)-3-{3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 105. 1- {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-3- (3-fluoro-phenyl)-urea 106. 1- (4-Fluoro-phenyl)-3- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 107. 1-{3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-3- (4-fluoro-phenyl)-urea 108. 1- [3- (5-Benzoyl-thiazol-2-ylamino)-propyl]-3- (2-chloro-benzyl)-urea 109. 1- (2-Chloro-benzyl)-3- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 110. 1- (2-Chloro-benzyl)-3- {3- [5- (2-ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 111. 1-{3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3- (2-chloro-benzyl) -urea 112. 1- {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-3-phenyl-urea 113. 1- {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-3-phenyl-urea 114. 1- {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-3-phenyl-urea 115. 1-Butyl-3-{3-[5-(4-methyl-pyridine-3-carbonyl)-thiazol-2-yla mino]-propyl}-urea

116. 1- {3- [5- (4-Methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl}-3- phenyl-urea 117. 1-Cyclohexyld-3-{3- [5- (3-methyl-pyrazine-2-carbonyl)-thiazol-2-ylamino]-propyl}- urea 118. 1-Cyclohexyl-3-{3- [5- (3-methyl-thiophene-2-carbonyl)-thiazol-2-ylamino]- propyl}-urea 119. 4-Fluoro-N-{3- [5-(4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]-propyl} - benze nesulfonamide 120. 4-Fluoro-N- {3- [5- (3-methyl-thiophene-2-carbonyl)-thiazol-2-ylamino]-propyl}- benz enesulfonamide -121. 2-Methoxy-5-methyl-N- {3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]- propyl}-benzenesulfonamide 122. 2-Methoxy-5-methyl-N- {3- [5- (3-methyl-pyrazine-2-carbonyl)-thiazol-2-ylamino]- propyl}-benzenesulfonamide 123. 2-Methoxy-5-methyl-N- {3- [5- (3-methyl-thiophene-2-carbonyl)-thiazol-2- ylamino]-pr opyl}-benzenesulfonamide 124. 1-(4-Methoxy-phenyl)-3-{3- [5- (4-methyl-pyridine-3-carbonyl)-thiazol-2-ylamino]- propyl}-urea 125. {3- [4- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester 126. N-{3- [4-(2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 127. 2-Fluoro-N- {3- [4-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 128. 3, 5-Dimethoxy-N- {3- [4-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzamide 129. Pentanoic acid {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide 130. 1- {3- [4-(2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-3-thiophen- 2-yl-urea 131. 1-(2-Fluoro-phenyl)-3-{3- [4-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea 132. 2-Methyl-N- {3- [4-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide

133. 4-Fluoro-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 134. 3-Methoxy-N-13- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyll- benzenesulfonamide 135. 4-Methoxy-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 136. N- {3- [4- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzenesulfona mide 137. 2-Chloro-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-5- trifluoromethyl-benzenesulfonamide 138. Thiophene-2-sulfonic acid {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide 139. 3-Fluoro-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 140. 2-Methoxy-5-methyl-N-{3- [4-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzene sulfonamide 141.2, 5-Dimethoxy-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfo namide 142. 2-Fluoro-N- {5- [5-(pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 143. 4-Methoxy-N- {5- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}- benzenesulfon amide 144. Thiophene-2-sulfonic acid {5- [5-(pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}- amide 145. 2-Methoxy-5-methyl-N- {5- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}- benz enesulfonamide 146. 4-Fluoro-N- {5- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}- benzenesulfona mide 147. 2-Methyl-N- {5- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}- benzenesulfona mide

148. 3-Fluoro-N- {5- [5- (pyridme-2-carbonyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 149. 2-Chloro-N- {5- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}-5-trifluoro met hyl-benzenesulfonamide 150. N-{5- [5-(Pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}-benzenes ulfonamide 151. 3-Methoxy-N-{5- [5-(pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}- benzenesulfon amide 152. 2-Fluoro-N- {5- [5- (pyridine-4-carbonyl)-thiazol-2-ylamino]-pentyl}- benzenesulfona mide 153. 2-Methoxy-5-methyl-N- {5- [5- (pyridine-4-carbonyl)-thiazol-2-ylamino]-pentyl}- benz enesulfonamide 154. 2-Fluoro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 155. 4-Methoxy-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 156. Thiophene-2-sulfonic acid {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- amide 157. 2-Methoxy-5-methyl-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzene sulfonamide 158. 4-Fluoro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 159. 2-Methyl-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 160. 3-Fluoro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 161. 2-Chloro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-5- trifluoromethyl-benzenesulfonamide 162. N-15- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-pentyll-benzenesulfona mide

163. 3-Methoxy-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 164. N- {5- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-fluoro- benzenesulfonamide 165. N-{5- [5-(2-Chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-4-methoxy- benzenesulfonamide 166. Thiophene-2-sulfonic acid {5- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}- amide 167. N- {5- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-methoxy-5-me thyl- benzene sulfonamide 168. N- {5- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-4-fluoro- benzenesulfonamide 169. N- {5- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-methyl- benzenesulfonamide 170. N- {5- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-3-fluoro- benzenesulfonamide 171. 2-Chloro-N-{5- [5-(2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-5-trifluoro methyl -benzenesulfonamide 172. N- {5- [4-Methyl-5-(2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 173. 2-Methyl-N-{5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenes ulfonamide 174. 2-Fluoro-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenes ulfonamide 175. 3-Fluoro-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenes ulfonamide 176. 4-Fluoro-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenes ulfonamide

177. 2-Methoxy-5-methyl-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]- pentyl}-benzenesulfonamide 178. 3-Methoxy-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzene sulfonamide 179. 4-Methoxy-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzene sulfonamide 180. Thiophene-2-sulfonic acid {2- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-ethyl}- amide 181.2, 5-Dimethoxy-N-{3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 182. Thiophene-3-sulfonic acid {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- amide 183.2, 5-Dimethoxy-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 184. Thiophene-3-sulfonic acid {2- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-ethyl}- amide 185.2, 5-Dimethyl-N- {3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 186. 5-Chloro-2-methoxy-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 187. 2-Methyl-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 188. 5-Fluoro-2-methyl-N- {4- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 189. 2-Chloro-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}-5-trifluorometh yl- benzenesulfonamide 190.2, 5-Dimethyl-N- {5- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide

191. N- {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-4-trifluoromet hoxy- benzenesulfonamide 192. 4-Fluoro-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyll- benzenesulfonamide 193.2, 4-Difluoro-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 194. N- {5- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-pentyI}-4-tnRuorometho xy- benzenesulfonamide 195. 2-Chloro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-4- trifluoromethyl-benzenesulfonamide 196. 2-Fluoro-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 197. 5-Chloro-thiophene-2-sulfonic acid {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]- butyl}-amide 198. 2-Chloro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-4- trifluoromethyl-benzenesulfonamide 199. Thiophene-3-sulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide 200. 5-Fluoro-2-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 201. 3-Fluoro-N- {4- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 202. 2-Methoxy-S-methyl-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 203. Thiophene-3-sulfonic acid {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- amide 204. 5-Fluoro-2-methyl-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide

205. 5-Chloro-2-methoxy-N- {2- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-ethyl}- benzenesulfonamide 206.2, 4-Difluoro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 207.2, 5-Dimethyl-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 208.2, 5-Dimethoxy-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 209.2, 4-Difluoro-N- { 5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide 210. 5-Chloro-thiophene-2-sulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]- propyl}-amide 211. 4-Methoxy-N-{4- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 212. 5-Chloro-2-methoxy-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 213. 5-Chloro-thiophene-2-sulfonic acid {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]- pentyl}-amide 214. Thiophene-2-sulfonic acid {4- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- amide 215. 3-Methoxy-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide 216. N-{4- [5-(2-Methyl-benzoyl)-thiazol-2-ylamino]-butyl}-4-trifluorom ethoxy- benzenesulfonamide 217. Thiophene-2-sulfonic acid methyl- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]- propyl}-amide 218. 3-Methoxy-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide

219. 2-Chloro-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-4- trifluoromethyl-benzenesulfonamide 220.2, N-Dimethyl-N-{3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 221.5-Fluoro-2, N-dimethyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 222. 2-Chloro-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-5- trifluoromethyl-benzenesulfonamide 223. 4-Fluoro-N-methyl-N-13- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyll- benzenesulfonamide 224.2, 4-Diffuoro-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 225. 2-Fluoro-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazoI-2-yIamino]-propyl}- benzenesulfonamide 226. 5-Chloro-thiophene-2-sulfonic acid methyl- {3- [5- (2-methyl-benzoyl)-thiazol-2- ylamino]-propyl}-amide 227. 3-Fluoro-N-methyl-N-{3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 228. 2-Methoxy-5, N-dimethyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 229. 4-Chloro-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 230.2, 5, N-Trimethyl-N-{3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide 231. N-Methyl-N-{3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-4-nitro- benzenesulfonamide 232. 4-Methoxy-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide

233. 5-Chloro-2-methoxy-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]- propyl}-benzenesulfonamide Examples of particularly preferred compounds of formula I are: Thiophene-2-sulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide ; 2-methoxy-5-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzene sulfonamide ; 2-chloro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-5-trifluoromet hyl- benzenesulfonamide; thiophene-2-sulfonic acid {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-amide ; N- {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-2-methoxy-5-me thyl-benzene sulfonamide ; 2-chloro-N-{3- [5-(2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-5-trifluoro methyl- benzenesulfonamide ; 2-chloro-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-5-trifluoromet hyl- benzenesulfonamide; 2-methoxy-5-methyl-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzene sulfonamide ; 2-methoxy-5-methyl-N- {5- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}-benz enesulfonamide ; 4-methoxy-N-{5- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzenesulf onamide ; 2-methoxy-5-methyl-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzene sulfonamide ; 2-methyl-N-{5- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzenesulf onamide ; 3-fluoro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzenesulfona mide ; 2-chloro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-5-trifluoromet hyl- benzenesulfonamide;

N- {5- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-fluoro-benze nesulfonamide ; <BR> <BR> <BR> <BR> <BR> <BR> N-{5- [5-(2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-methoxy-5 -methyl-benzene sulfonamide ; <BR> <BR> <BR> <BR> <BR> <BR> N- {5- [5-(2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-methyl-be nzenesulfonamide ; 2-methoxy-5-methyl-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide ; 2-chloro-N-{3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-4-trifluoro methyl- benzenesulfonamide; 5-fluoro-2-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide ; 2, 5-dimethoxy-N- {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}- benzenesulfonamide ; 5-chloro-thiophene-2-sulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]- propyl}-amide ; thiophene-2-sulfonic acid {4- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-butyl}-amide ; <BR> <BR> <BR> <BR> <BR> <BR> thiophene-2-sulfonic acid methyl- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide; 2, N-dimethyl-N- { 3- [5- (2-methyl-benzoyl)-thiazol-2-ylaminoJ-propyl}- benzenesulfonamide ; 5-chloro-thiophene-2-sulfonic acid methyl- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]- propyl}-amide ; 4-chloro-N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- benzenesulfonamide and N-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-4-nitro- benzenesulfonamide.

Examples of particularly preferred compounds of formula I are: Thiophene-2-sulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide ;

2-methoxy-5-methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzene sulfonamide ; 2-chloro-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-5-trifluoromet hyl- benzenesulfonamide; thiophene-2-sulfonic acid {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-amide ; N- {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-2-methoxy-5-me thyl-benzene sulfonamide ; 2-chloro-N- {3- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-propyl}-5-trifluoromet hyl- benzenesulfonamide ; 2-chloro-N- {3- [4-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-5-trifluoro methyl- benzenesulfonamide ; 2-methoxy-5-methyl-N- {3- [4- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzene sulfonamide ; 2-methoxy-5-methyl-N- {5- [5- (pyridine-2-carbonyl)-thiazol-2-ylamino]-pentyl}-benz enesulfonamide; 4-methoxy-N-{5- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzenesulf onamide ; <BR> <BR> <BR> <BR> <BR> <BR> 2-methoxy-5-methyl-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzene sulfonamide ; 2-methyl-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzenesulfona mide ; 3-fluoro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzenesulfona mide ; 2-chloro-N- {5- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-5-trifluoromet hyl- benzenesulfonamide ; N- {5- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-fluoro-benze nesulfonamide ; <BR> <BR> <BR> <BR> <BR> <BR> N- {5- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-methoxy-5-me thyl-benzene sulfonamide ; N- {5- [5- (2-chloro-benzoyl)-thiazol-2-ylamino]-pentyl}-2-methyl-benze nesulfonamide ; and

2-methoxy-5-methyl-N- {5- [4-methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}- benzenesulfonamide.

Processes for the manufacture of compounds of formula I are an object of the invention.

The preparation of compounds of formula I of the present invention may be carried out in sequential or convergent synthetic routes. Syntheses of the invention are shown in the following Schemes. The skills required for carrying out the reaction and purification of the resulting products are known to those in the art. The substituents and indices used in the following description of the processes have the significance given above unless indicated to the contrary.

Compounds of general formula IH (R means hydrogen) can be prepared according to scheme 1 as follows: a) Bis amino derivatives IA, either commercially available or prepared from commercially available precursors by methods taught in the art, are mono-protected with a suitable protecting group (PG i. e. Boc, Fmoc, and the like), provided that PG has no adverse effect on the reaction or on the reagents involved in the synthetic route, by reaction of IA with preferably BoczO, preferably in the presence or the absence of a base such as triethylamine, diisopropylethylamine, and the like, preferably in the presence of a solvent. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, or dioxane, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice.

(literature: J. Med. Chem. , 32 (2), 391-6; 1989). b) Thioureas can be prepared from suitable starting materials according to methods known in the art. The elaboration of the thiourea-moiety in ID starting from an amino functionality, like in IB can be affected by methods described in literature. For example mono-protected derivatives IB are condensed with benzoyl isothiocyanate in a solvent.

There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can

dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, or dioxane, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield the protected urea derivatives IC. (literature: Organic Letters, 2 (20), 3237-3240 ; 2000).

The urea derivatives IC are subjected to basic cleavage conditions such as. K2CO3 aq. , and the like, in a solvent such as methanol, and the like, to liberate the urea functionality and access ureas ID. (for reaction conditions described in literature affecting such a reaction see for example: J. Med. Chem. , 32 (8), 1963-70; 1989). c) The conversion of the liberated ureas ID to Dimethylaminomethylene-thioureido derivatives IE (R2 means hydrogen) was affected by reaction of derivatives ID with N, N-Dimethylformamide dimethyl acetal either neat or in a solvent. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, or dioxane, DMF and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield the protected urea derivatives IC. For reaction conditions described in literature affecting such a reaction see for example: Heterocycles, 11"313-18 ; 1978. d) Dimethylaminomethylene-thioureido derivatives IE can be converted to thiazole derivatives IF (R2 means hydrogen) by reaction of IE with 0-bromoketones (a known compound or compound prepared by known methods. The source for 0- Bromoketones employed is indicated as appropriate) in a solvent such as ethanol, and the like, in the presence or the absence of a base. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, or dioxane, methanol, ethanol and the like. There is no particular restriction on the nature of the base used in this stage, and any base commonly used in this type of reaction may equally be employed here. Examples of such bases include triethylamine

and diisopropylethylamine, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention.

We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield the protected thiazole derivatives IF. For reaction conditions described in literature affecting such a reaction see for example: J. Heterocycl. Chem. , 16 (7), 1377-83; 1979. The resulting compound of formula IF is a compound of the present invention and may be the desired product; alternatively it may be subjected to consecutive reactions. e) Cleavage of the protecting group PG such as Boc, Fmoc, and the like from thiazole derivatives IF to access free amines IG or various salts thereof, IF is in the case PG means Boc subjected to suitable reaction conditions like acidic cleavage. There is no particular restriction on the nature of the acid used in this stage, and any acid commonly used in this type of reaction may equally be employed here. Examples of such acids include: HC1, TFA, and the like in a solvent. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dioxane, water, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield thiazole derivatives IG. For conditions described in literature affecting the cleavage of a protecting group see for example: Protecting Groups, Kocienski, P. Thieme Verlag New York 1994. f) Sulfonamides, amides, carbamates and ureas can be prepared from suitable starting materials according to methods known in the art. The conversion of the amino-moiety in IG to access sulfonamides, amides, carbamates and can be affected by methods described in literature. For example the conversion of the amine derivatives IG or their respective salts to access compounds of the general formula IH is affected by reaction of IG with suitable acid chlorides, sulfonyl chlorides, isocyanates, chloroformates, or carbonate esters (compounds known or compound prepared by known methods) respectively in a solvent like dichloromethane and in the presence or the absence of a base. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that

it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: chloroform, or dioxane, THF, and the like. There is no particular restriction on the nature of the base used in this stage, and any base commonly used in this type of reaction may equally be employed here. Examples of such bases include triethylamine and diisopropylethylamine, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield thiazole derivatives IH. For reaction conditions described in literature affecting such reactions see for example: Comprehensive Organic Transformations: A Guide to Functional Group Preparations, 2nd Edition, Richard C. Larock. John Wiley & Sons, New York, NY. 1999. Schema 1 Scheme J-CH. J nah ra rus In S'O', H\i CH2 Jr ; NH'PGN ['_CH2 Jr ; NHPh 4 Rs Ra Rs IA IC g N . A v R R/4 3 IVE NID ruz S PGI ''CHZ J'NN Ra R IF 0. 's-r ! IF R R IF 0 R 0 R N'CH2 =N- L n N . ln N Ra R3 OH IG

Compounds of general formula IIE (R2 means alkyl or cycloalkyl) can be prepared according to scheme 2 as follows: a) Thioisocyanates can be prepared from suitable starting materials according to methods known in the art. The elaboration of the thioisocyanate-moiety in IIA (R3 means hydrogen) starting from an amino functionality, can be affected by methods described in literature. For example compounds of the general formula IB (PG for example Boc, Fmoc, and such like) are condensed with carbondisulfide, neat or in a solvent. There is no particular restriction on the nature of the solvent to be employed, provided that it

has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, or dioxane, THF and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield an intermediate which is reacted with cyanamide in one-pot or after isolation of the intermediate. Elaboration of the thioisocanate derivatives IIA (R3 means hydrogen) is affected by addition of a base such as pyridine, or the like. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, or dioxane, THF and the like. There is no particular restriction on the nature of the base used in this stage, and any base commonly used in this type of reaction may equally be employed here. Examples of such bases include pyridine, triethylamine and diisopropylethylamine, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield the thioisocyanate derivatives IIA. For reaction conditions described in literature affecting such a reaction see for example: Journal of Organic Chemistry, 65 (19), 6069-6072; 2000. b) Thioureido derivatives can be prepared from suitable starting materials according to methods known in the art. The elaboration of the thioisocyanate-moiety in IIA (R3 means hydrogen) to a thioureido-moiety can be affected by methods described in literature. For example compounds of the general formula IIA are condensed with an amidine or their salts (R2 means alkyl, cycloakly), a known compound or compound prepared by known methods, in a solvent such as THF, or the like, and a base, such as NaOH, or the like. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, dioxane, THF and the like.

There is no particular restriction on the nature of the base used in this stage, and any base commonly used in this type of reaction may equally be employed here. Examples

of such bases include NaOHaq. , KOHaq, NEt3, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction from 0°C to heating to reflux temperature of the solvent. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield the thioureido derivatives IIB. For reaction conditions described in literature affecting such a reaction see for example: C. R. Seances Acad. Sci. , Ser. 2, 294 (19), 1183-6; 1982. c) Dimethylaminomethylene-thioureido derivatives IIB can be converted to thiazole derivatives IIC (R2 means alkyl, cycloalkyl) by reaction of IIB with 0-bromoketones (a known compound or compound prepared by known methods) in a solvent such as ethanol, and the like, in the presence or the absence of a base. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, DMF, dioxane, methanol, ethanol and the like. There is no particular restriction on the nature of the base used in this stage, and any base commonly used in this type of reaction may equally be employed here. Examples of such bases include triethylamine and diisopropylethylamine, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield the protected thiazole derivatives IIC (R3 means H). For reaction conditions described in literature affecting such a reaction see for example: Org. Chem. , 65 (21), 7244-7247; 2000. The resulting compound of formula IIC (R3 means H) is a compound of the present invention and may be the desired product; alternatively it may be subjected to consecutive reactions. Introduction of R3 means alkyl or cycloalky can be affected by reductive amination of IIC with the respective aldehyde under reducing conditions in a solvent. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, dioxane, THF, and the like. There is no particular restriction on the nature of the reducing agent used in this stage, and any reducing agent commonly used in this type of reaction may equally be employed here.

Examples of such reducing agents include NaBH4, NaCNBH3, and the like. The

reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield the protected thiazole derivatives IIC (R3 means alkyl or cycloalkyl). For reaction conditions described in literature affecting a reductive amination see for example: Reductive amination in: A Guide to Functional Group Preparations, 2nd Edition, Richard C. Larock. John Wiley & Sons, New York, NY.

1999. The resulting compound of formula IIC (R3 means alkyl or cycloalkyl) is a compound of the present invention and may be the desired product; alternatively it may be subjected to consecutive reactions. d) Cleavage of the protecting group such as Boc and Fmoc, and the like from thiazole derivatives IIC to access free amines IID or various salts thereof, IIC is subjected to suitable reaction conditions like for example acidic cleavage for the cleavage of the Boc-protecting group. There is no particular restriction on the nature of the acid used in this stage, and any acid commonly used in this type of reaction may equally be employed here. Examples of such acids include : HC1, TFA, and the like in a solvent.

There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dioxane, water, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield thiazole derivatives IID.

For conditions described in literature affecting the cleavage of a protecting group see for example: Protecting Groups, Kocienski, P. Thieme Verlag New York 1994. e) Sulfonamides, amides, carbamates and ureas can be prepared from suitable starting materials according to methods known in the art. The conversion of the amino-moiety in IID to access sulfonamides, amides, carbamates and ureas can be affected by methods described in literature. For example the conversion of the amine derivatives IID or their respective salts to access compounds of the general formula IIE is affected by reaction of IID with suitable acid chlorides, sulfonyl chlorides, isocyanates, chloroformates, or carbonate esters (compounds known or compound prepared by known methods) respectively in a solvent like dichloromethane and in the presence or

the absence of a base. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: chloroform, dioxane, THF, and the like. There is no particular restriction on the nature of the base used in this stage, and any base commonly used in this type of reaction may equally be employed here. Examples of such bases include triethylamine and diisopropylethylamine, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield thiazole derivatives IIE. For reaction conditions described in literature affecting such reactions see for example: Comprehensive Organic Transformations: A Guide to Functional Group Preparations, 2nd Edition, Richard C. Larock. John Wiley & Sons, New York, NY. 1999. Scheme 2 N N ,--1 14 non HE Y 14 L s W R R N-N N R4 R H R IIB 0 R 0 R Pu R PG CH2 L CHJm NT JN IID IIC Ra R3 IID IIC R R Rus : ° R1 Ra R3 IIE

Compounds of general formula IIID can be prepared according to scheme 3 as follows: a) Aminothiazoles can be prepared from suitable starting materials according to methods known in the art. The conversion of a thiourea-moiety like in derivatives of the general formula ID can be affected by methods described in literature. For example thiourea derivatives of he general formula ID are reacted with a-bromo-diketones of the general formula IIIA (compounds known or compounds prepared by known methods) in a solvent such as methanol, or the like, in the presence or the absence of a base, such as triethylamine, or the like. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, dioxane, ethanol, THF, and the like. There is no particular restriction on the nature of the base used in this stage,

and any base commonly used in this type of reaction may equally be employed here.

Examples of such bases include triethylamine and diisopropylethylamine, and the like.

The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield thiazole derivatives IIIB. For reaction conditions described in literature affecting such reactions see for example: J. Heterocycl. Chem., 16 (7), 1377-83; 1979. b) Cleavage of the protecting group such as Boc and Fmoc, and the like from thiazole derivatives IIIB to access free amines IIIC or various salts thereof, IIIB is subjected to suitable reaction conditions like for example acidic cleavage for the cleavage of the Boc-protecting group. There is no particular restriction on the nature of the acid used in this stage, and any acid commonly used in this type of reaction may equally be employed here. Examples of such acids include: HC1, TFA, and the like in a solvent.

There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dioxane, water, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield thiazole derivatives IIIC. For conditions described in literature affecting the cleavage of a protecting group see for example: Protecting Groups, Kocienski, P. Thieme Verlag New York 1994. c) Sulfonamides, amides, carbamates and ureas can be prepared from suitable starting materials according to methods known in the art. The conversion of the amino-moiety in IIIC to access sulfonamides, amides, carbamates and ureas can be affected by methods described in literature. For example the conversion of the amine derivatives IIIC or their respective salts to access compounds of the general formula IIID is affected by reaction of IIIC with suitable acid chlorides, sulfonyl chlorides, isocyanates, chloroformates, or carbonate esters (compounds known or compound prepared by known methods) respectively in a solvent, such as dioxane and methanol, and such like, and in the presence or the absence of a base, such as triethylamine, or the like.

There is no particular restriction on the nature of the solvent to be employed, provided

that it has no adverse effect on the reaction or the reagents involved and that it can dissolve the reagents, at least to some extent. Examples for suitable solvents include: dichloromethane, chloroform, dioxane, THF, and the like. There is no particular restriction on the nature of the base used in this stage, and any base commonly used in this type of reaction may equally be employed here. Examples of such bases include triethylamine and diisopropylethylamine, and the like. The reaction can take place over a wide range of temperatures, and the precise reaction temperature is not critical to the invention. We find it convenient to carry out the reaction with heating from ambient temperature to reflux. The time required for the reaction may also vary widely, depending on many factors, notably the reaction temperature and the nature of the reagents. However, a period of from 0.5 h to several days will usually suffice to yield thiazole derivatives IIID. For reaction conditions described in literature affecting such reactions see for example: Comprehensive Organic Transformations: A Guide to Functional Group Preparations, 2nd Edition, Richard C. Larock. John Wiley & Sons, New York, NY. 1999.

Scheme 3

The conversion of a compound of formula I into a pharmaceutically acceptable salt can be carried out by treatment of such a compound with an inorganic acid, for example a hydrohalic acid, such as, for example, hydrochloric acid or hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid etc. , or with an organic acid, such as, for example, acetic acid, citric acid, maleic acid, fumaric acid, tartaric acid, methanesulfonic acid or p- toluenesulfonic acid.

The conversion of compounds of formula I into pharmaceutically usable esters or amides can be carried out e. g. by treatment of suited amino or hydroxyl groups present in the molecules with an carboxylic acid such as acetic acid, with a condensating reagent such

as benzotriazol-1-yloxytris (dimethylamino) phosphonium hexafluorophosphate (BOP) or N, N-dicylohexylcarbodiimide (DCC) to produce the carboxylic ester or carboxylic amide.

Preferred intermediates are: Example H [2- (3-Amino-propylamino)-thiazol-5-yl]-phenyl-methanone ; hydrochloride Example I [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl-methanone ; hydrochloride Example J [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-ethyl-phenyl)-methanone ; hydrochloride Example K [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-fluoro-phenyl) -methanone; hydrochloride Example L [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-chloro-phenyl)-methanone ; hydrochloride Example M [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-trifluoromethyl-phenyl)-methanone ; hydrochloride Example N [2- (3-Amino-propylamino)-thiazol-5-yl]- (4-methyl-pyridin-3-yl)-methanone ; hydrochloride Example O 2- (3-Amino-propylamino)-thiazol-5-yl]- (3-methyl-pyridin-2-yl)-methanone ; hydrochloride Example P

[2- (3-Amino-propylamino)-thiazol-5-yl]- (2-methyl-pyridin-3-yl)-methanone ; hydrochloride Example Q [2- (3-Amino-propylamino)-thiazol-5-yl]- (3-methyl-pyrazin-2-yl)-methanone ; hydrochloride Example R [2- (3-Amino-propylamino)-thiazol-5-yl]- (3-methyl-thiophen-2-yl) -methanone; hydrochloride Example S [2- (5-Amino-pentylamino)-thiazol-5-yl]-o-tolyl-methanone ; hydrochloride Example T [2- (5-Amino-pentylamino)-thiazol-5-yl]-pyridin-2-yl-methanone ; hydrochloride Example U [2- (5-Amino-pentylamino)-thiazol-5-yl]-pyridin-4-yl-methanone ; hydrochloride Example V [2- (5-Amino-pentylamino)-thiazol-5-yl]- (2-chloro-phenyl)-methanone ; hydrochloride Example Y {3- [4-(2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester Example Z [2- (3-Amino-propylamino)-thiazol-4-yl]-o-tolyl-methanone ; hydrochloride Example AC {5- [4-Methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-carbamic acid tert-butyl ester Example AD

[2- (5-Amino-pentylamino)-4-methyl-thiazol-5-yl]-o-tolyl-methano ne hydrochloride Also an object of the invention are compounds described above for the production of medicaments for the prophylaxis and therapy of illnesses which are caused by disorders associated with the NPY receptor, particularly for the production of medicaments for the prophylaxis and therapy of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity.

Likewise an object of the invention are pharmaceutical compositions containing a compound of formula I described above and a therapeutically inert carrier.

An object of the invention is also the use of the compounds described above for the production of medicaments, particularly for the treatment and prophylaxis of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity.

A preferred object of the invention is the use of compounds as described before for the production of medicaments for the treatment of obesity.

A further object of the invention comprises compounds which are manufactured according to one of the described processes.

A further object of the invention is a method for the treatment and prophylaxis of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity whereby an effective amount of a compound described above is administered.

Particularly preferred is a method for the treatment of obesity whereby an effective amount of a compound as mentioned above is administered.

According to a further aspect of the invention there is provided a method of treatment of obesity in a human in need of such treatment which comprises administration to the human a therapeutically effective amount of a compound according to formula I and a therapeutically effective amount of a lipase inhibitor, particularly preferred, wherein the lipase inhibitor is orlistat. Also subject of the present invention is the mentioned method, wherein the administration is simultaneous, separate or sequential.

A further preferred embodiment of the present invention is the use of a compound of the formula I in the manufacture of a medicament for the treatment and prevention of obesity in a patient who is also receiving treatment with a lipase inhibitor, particularly preferred, wherein the lipase inhibitor is orlistat.

A preferred process for the preparation of a compound of formula I comprises the reaction of a compound of formula (II)

in the presence of a compound of formula (III) wherein Rl to R5, A, m and n are defined as before and, wherein X means e. g. chloro or bromo.

The compounds of formula I described above for use as therapeutically active substances are a further object of the invention.

Also an object of the invention are compounds described above for the production of medicaments for the prophylaxis and therapy of illnesses which are caused by disorders associated with the NPY receptor, particularly for the production of medicaments for the prophylaxis and therapy of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity.

Likewise an object of the invention is a pharmaceutical composition comprising a compound of formula I described above and a therapeutically inert carrier. Preferred is this composition comprising further a therapeutically effective amount of a lipase inhibitor. Particularly preferred is the above composition, wherein the lipase inhibitor is orlistat.

An object of the invention is also the use of the compounds described above for the production of medicaments, particularly for the treatment and prophylaxis of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity.

A further object of the invention comprises compounds which are manufactured according to one of the described processes.

A further object of the invention is a method for the treatment and prophylaxis of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity whereby an effective amount of a compound described above is administered.

According to a further aspect of the invention there is provided a method of treatment of obesity in a human in need of such treatment which comprises administration to the human a therapeutically effective amount of a compound according to formula I and a therapeutically effective amount of a lipase inhibitor, particularly preferred, wherein the lipase inhibitor is orlistat. Also subject of the present invention is the mentioned method, wherein the administration is simultaneous, separate or sequential.

A further preferred embodiment of the present invention is the use of a compound of the formula I in the manufacture of a medicament for the treatment and prevention of obesity in a patient who is also receiving treatment with a lipase inhibitor, particularly preferred, wherein the lipase inhibitor is orlistat.

Assay Procedures Cloning of mouse NPY5 receptor cDNAs : The full-length cDNA encoding the mouse NPY5 (mNPY5) receptor was amplified from mouse brain cDNA using specific primers, designed based on the published sequence, and Pfu DNA-Polymerase. The amplification product was subcloned into the mammalian expression vector pcDNA3 using Eco RI and XhoI restriction sites. Positive clones were sequenced and one clone, encoding the published sequence was selected for generation of stable cell clones.

Stable transfection: Human embryonic kidney 293 (HEK293) cells were transfected with 10 u. g mNPY5 DNA using the lipofectamine reagent (Gibco BRL) according to the manufacturer's

instruction. Two days after transfection, geneticin selection (1 mg/ml) was initiated and several stable clones were isolated. One clone was further used for pharmacological characterization.

Radioligand competition binding : Human embryonic kidney 293 cells (HEK293), expressing recombinant mouse NPY5-receptor (mNPY5) were broken by three freeze/thawing cycles in hypotonic Tris buffer (5 mM, pH 7.4, 1 mM MgCl2), homogenized and centrifuged at 72,000 x g for 15 min. The pellet was washed twice with 75 mM Tris buffer, pH 7. 4, containing 25 mM MgCl2 and 250 mM sucrose, 0.1 mM phenylmethylsulfonylfluoride and 0.1 mM 1,10- pheneanthrolin, resuspended in the same buffer and stored in aliquots at-80°C. Protein was determined according to the method of Lowry using bovine serum albumine (BSA) as a standard.

Radioligand competition binding assays were performed in 250 ut 25 mM Hepes buffer (pH 7.4, 2.5 mM CaCl2, 1 mM MgCl2, 1 % bovine serum albumine, and 0.01 % NaN3 containing 5 pLg protein, 100 pM [I] labelled peptide YY (PYY) and 10 gel DMSO containing increasing amounts of unlabelled test compounds. After incubation for 1 h at 22°C, bound and free ligand are separated by filtration over glass fibre filters. Non specific binding is assessed in the presence of 1, uM unlabelled PYY. Specific binding is defined as the difference between total binding and non specific binding. ICso values are defined as the concentration of antagonist that displaces 50 % of the binding of (125Ilabelled neuropeptide Y. It is determined by linear regression analysis after logit/log transformation of the binding data.

Results obtained in the foregoing test using representative compounds of the invention as the test compounds are shown in the following table: Compound ICso Example No. 1 2-Fluoro-N- {3- [5- (pyridine-2-carbonyl)-thiazol-2- 5. 4nM ylamino]-propyl}-benzenesulfonamide Example No. 140 2-Methoxy-5-methyl-N- {3- [4- (2-methyl-benzoyl)- 6nM thiazol-2-ylamino]-propyl}-benzene sulfonamide

Compounds as described above have ICso values below 1000 nM; more preferred compounds have IC50 values below 100 nM. Most preferred compounds have ICso values below 10 nM. These results have been obtained by using the foregoing test.

The compounds of formula I and their pharmaceutically usable salts, solvates and esters can be used as medicaments (e. g. in the form of pharmaceutical preparations). The pharmaceutical preparations can be administered internally, such as orally (e. g. in the form of tablets, coated tablets, dragees, hard and soft gelatin capsules, solutions, emulsions or suspensions), nasally (e. g. in the form of nasal sprays) or rectally (e. g. in the form of suppositories). However, the administration can also be effected parentally, such as intramuscularly or intravenously (e. g. in the form of injection solutions).

The compounds of formula I and their pharmaceutically usable salts, solvates and esters can be processed with pharmaceutically inert, inorganic or organic adjuvants for the production of tablets, coated tablets, dragees and hard gelatin capsules. Lactose, corn starch or derivatives thereof, talc, stearic acid or its salts etc. can be used, for example, as such adjuvants for tablets, dragees and hard gelatin capsules.

Suitable adjuvants for soft gelatin capsules, are, for example, vegetable oils, waxes, fats, semi-solid substances and liquid polyols, etc.

Suitable adjuvants for the production of solutions and syrups are, for example, water, polyols, saccharose, invert sugar, glucose, etc.

Suitable adjuvants for injection solutions are, for example, water, alcohols, polyols, glycerol, vegetable oils, etc.

Suitable adjuvants for suppositories are, for example, natural or hardened oils, waxes, fats, semi-solid or liquid polyols, etc.

Moreover, the pharmaceutical preparations can contain preservatives, solubilizers, viscosity-increasing substances, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They can also contain still other therapeutically valuable substances.

In accordance with the invention the compounds of formula I and their pharmaceutically usable salts, solvates and esters can be used for the prophylaxis and treatment of arthritis, cardiovascular diseases, diabetes, renal failure and particularly eating disorders and obesity. The dosage can vary in wide limits and will, of course, be fitted to the individual requirements in each particular case. In general, in the case of oral administration a daily dosage of about 0.1 mg to 20 mg per kg body weight, preferably about 0.5 mg to 4 mg per kg body weight (e. g. about 300 mg per person), divided into preferably 1-3 individual doses, which can consist, for example, of the same amounts, should be appropriate. It will, however, be clear that the upper limit given above can be exceeded when this is shown to be indicated.

The invention is illustrated hereinafter by the examples, which have no limiting character.

Examples Example A (3-Thioureido-propyl) -carbamic acid tert-butyl ester

A solution of 2 g (11.47 mmol) (3-Amino-propyl)-carbamic acid tert-butyl ester in 20 ml THF was treated with 1.62 ml (11.47 mmol) Benzoyl isothiocyanate and stirred for 1 h at room temperature. After removal of the volatiles the residue was suspended in 50 ml methanol and 4.8 g (34.4 mmol) K2CO3 in 50 ml water was added. The mixture was stirred at room temperature for 16 h, concentrated, and extracted with ethyl acetate. The combined organic layers were washed with NaHCO3 sat. , brine, dried with MgS04 and evaporated under reduced pressure. The residue was purified by flash column chromatography on silica eluting with ethyl acetate/heptane. The combined product fractions were evaporated under reduced pressure to yield 1.48 g (74%) of the title compound.

1-H-NMR (300 MHz, DMSO-d6) 8= 7.57 (s, br, 2H, NH2), 6.93 (s, br, 1H, NH), 6.80 (s, br, 1H, NH), 3.33 (m, 2H, CH2), 2.93 (m, 2H, CH2), 1.54 (m, 2H, CH2), 1.37 (s, 9H, CH3).

MS (m/e): 234.3 (MH+, 100%) Example B (5-Thioureido-pentyl)-carbamic acid tert-butyl ester

The title compound was synthesised from (5-Amino-pentyl) -carbamic acid tert-butyl ester according to the procedure described for Example A (MS (m/e): 262.4 (MH+, 100%).

Example C [3- (3-Dimethylaminomethylene-thioureido)-propyl]-carbamic acid tert-butyl ester

A mixture of 1.48 g (6.35 mmol) (3-Thioureido-propyl)-carbamic acid tert-butyl ester and 15 ml Dimethylformamide dimethyl acetal was heated to 100°C for 16 h. The mixture was concentrated and the residue was purified by flash column chromatography on silica eluting with ethyl acetate/n-hexane 1/1 to yield 1.65 g (90%) of the title compound.

1-H-NMR (300 MHz, DMSO-d6) 8= 8. 68 (s, 1H, CH), 8.63 (s, br, 1H, NH), 6.77 (s, br, 1H, NH), 3.44 (m, 2H, CH2), 3.11 (s, 3H, CH3), 2.97 (s, 3H, CH3), 2.87 (m, 2H, CH2), 1.57 (t, J = 5. 1Hz, 2H, CH2), 1. 37 (s, 9H, CH3).

MS (m/e): 289.3 (MH+, 100%) Example D [5- (3-Dimethylaminomethylene-thioureido)-pentyl]-carbamic acid tert-butyl ester The title compound was synthesised from (5-Thioureido-pentyl) -carbamic acid tert-butyl ester and Dimethylformamide dimethyl acetal according to the procedure described for Example C in 54% yield.

1-H-NMR (300 MHz, DMSO-d6) 8= 8.68 (s, 1H, CH), 8.66 (s, br, 1H, NH), 6.75 (s, br, 1H, NH), 3.45 (m, 2H, CH2), 3.11 (s, 3H, CH3), 2.97 (s, 3H, CH3), 2.90 (m, 2H, CH2), 1.50 (m, 2H, CH2), 1.20 (m, 2H, CH2), 1.36 (s, 9H, CH3).

MS (m/e): 317.4 (MH+, 100%) Example E 2-Bromo-1- (3-methyl-pyrazin-2-yl) -ethanone dihydrobromide

A solution of 5.4 g (40 mmol) 1-Pyrazin-2yl-ethanone in 21 ml HBr (33%) and 7 ml methanol was treated with 2.05 ml (40 mmol) bromine and heated to 60°C for 7 h. The precipitate was filtered off, washed with ethyl acetate/diethyl ether 1/1 and dried to obtain 8. 3 g (55%) of the title compound as grey solid.

1-H-NMR (400 MHz, DMSO-d6) 8= 8.78 (d, J = 2 Hz, 1H, H-5), 8.66 ( (d, J = 2 Hz, 1H, H-6), 5.01 (s, 2H, CH2), 2.75 (s, 3H, CH3).

MS (m/e): 215.0 (M+H, 100%).

Example F 2-Bromo-1- (4-methyl-pyridin-3-yl)-ethanone hydrobromide The title compound was synthesised according to Example E 1- (4-methyl-pyridin-3-yl)- ethanone and HBr/bromine in 85% yield as grey solid. MS (m/e): 214.0 (M+H, 100%).

Example G 2-Bromo-l- (2-ethyl-phenyl)-ethanone To a solution of 15.2 g (88 mmol) dibromethane in 120 ml THF at-75°C was added 44 ml (88 mmol) of a 2M solution of LDA in THF and subsequently 6.57 g (40 mmol) ethyl- benzoic acid methyl ester in 80 ml THF. 37.5 ml of a 1.6 M n-butyl lithium solution in n- hexane was added and after 30 min the mixture was treated carefully below-65°C with 35 ml HC1 (37%). The mixture was washed with water and NaHC03 aq. and the organic phase was dried with MgS04, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica eluting with ethyl acetate/

hexane 1: 9 twice to afford 3. 8 g (41%) of the title compound as yellow oil. MS (m/e) : 227.1 (M+H, 100%).

Example 25 {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester A mixture of 613 mg (2.9 mmol) 2-methyl phenacylbromide (literature: W09907666), 691 mg (2.4 mmol) [3- (3-Dimethylaminomethylene-thioureido)-propyl]-carbamic acid tert- butyl ester and 1 ml (7.2 mmol) NEt3 in 20 ml ethanol was heated to 100°C for 16 h. The mixture was concentrated and purified by flash column chromatography on silica eluting with ethyl acetate/n-hexane 1/1. The combined product fractions were evaporated and 693 mg (77% %) of the title compound (MS (m/e): 375.9 (MH+, 100%) ) were obtained.

Example 26 {3- [5- (2-Chloro-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl] -carbamic acid tert-butyl ester and 2-chloro phenacylbromide (commercially available) according to the procedure described for Example 25. MS (m/e): 395.8 (MH+, 100%).

Example 27 {3- [5- (2-Ethyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-ethyl phenacylbromide according to the procedure described for Example 25. MS (m/e): 389.9 (MH+, 100%).

Example 28 {3- [5- (2-Trifluoromethyl-benzoyl)-thiazol-2-ylamino]-propyl}-carba mic acid tert-butyl ester

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-trifluoromethyl phenacylbromide (literature: EP 432040) according to the procedure described for Example 25. MS (m/e) : 429.9 (MH+, 100%).

Example H [2- (3-Amino-propylamino)-thiazol-5-yl]-phenyl-methanone ; hydrochloride

A mixture of 0.5 g (1.73 mmol) [3- (3-Dimethylaminomethylene-thioureido)-propyl]- carbamic acid tert-butyl ester, 0.448 g (2.25 mmol) phenacyl bromide (commercially available) and 0.723 ml (5.2 mmol) NEt3 in 20 ml EtOH was heated to 100°C for 16 h.

After cooling to room temperature 3 ml of a 4N HC1 solution in dioxane was added and

the mixture was stirred for 2 h at 60°C. The mixture was concentrated, the precipitate was filtered off, washed with diethyl ether and dried to yield 0.505 g (81%) of the title compound.

1-H-NMR (300 MHz, DMSO-d6) 8= 9.13 (s, br, 1H, NH), 8.04 (s, br, 2H, NH2), 7.60 (m, 6H, Ph/thiazole), 3.43 (m, 2H, CH2), 2.85 (m, 2H, CH2), 1.85 (m, 2H, CH2).

MS (m/e): 262.2 (MH+, 100%) Example I [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl-methanone ; hydrochloride

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-methyl phenacyl bromide (literature: W09907666) according to the procedure described for Example H. MS (m/e) : 276.3 (MH+, 100%).

Example J [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-ethyl-phenyl) -methanone; hydrochloride

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-ethyl phenacyl bromide according to the procedure described for Example H. MS (m/e) : 290. 3 (MH+, 100%).

Example K [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-fluoro-phenyl)-methanone ; hydrochloride

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester 2-Fluoro-phenacyl bromide (commercially available) according to the procedure described for Example H. MS (m/e): 280.3 (MH+, 100%).

Example L [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-chloro-phenyl)-methanone ; hydrochloride

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester 2-Chloro-phenacyl bromide (commercially available) according to the procedure described for Example H. MS (m/e): 296.4 (MH+, 100%).

Example M [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-trifluoromethyl-phenyl)-methanone ; hydrochloride The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester 2-Trifluoromethyl-phenacyl bromide (literature: EP432040) according to the procedure described for Example H. MS (m/e): 330.4 (MH+, 100%).

Example N [2- (3-Amino-propylamino)-thiazol-5-yl]- (4-methyl-pyridin-3-yl)-methanone ; hydrochloride The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl] -carbamic acid tert-butyl ester and 2-Bromo-l- (4-methyl-pyridin-3-yl)-ethanone according to the procedure described for Example H. MS (m/e): 277.3 (MH+, 100%).

Example O 2- (3-Amino-propylamino)-thiazol-5-yl]- (3-methyl-pyridin-2-yl)-methanone ; hydrochloride The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-Bromo-l- (3-methyl-pyridin-2-yl)-ethanone (literature: W09935130) according to the procedure described for Example H. MS (m/e): 277.3 (MH+, 100%).

Example P [2- (3-Amino-propylamino)-thiazol-5-yl]- (2-methyl-pyridin-3-yl)-methanone ; hydrochloride

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-Bromo-1-(2-methyl-pyridin-3-yl)-ethanone (Literature: J. Heterocycl. Chem. 1978,15, 217) according to the procedure described for Example H. MS (m/e): 277.3 (MH+, 100%).

Example Q [2- (3-Amino-propylamino)-thiazol-5-yl]- (3-methyl-pyrazin-2-yl)-methanone ; hydrochloride The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-Bromo-1- (3-methyl-pyrazin-2-yl)-ethanone according to the procedure described for Example H. MS (m/e): 278.3 (MH+, 100%).

Example R [2- (3-Amino-propylamino)-thiazol-5-yl]- (3-methyl-thiophen-2-yl)-methanone ; hydrochloride

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2-Bromo-l- (3-methyl-thiophen-2-yl)-ethanone (Literature: EP432040) according to the procedure described for Example H. MS (m/e): 282.2 (MH+, 100%).

Example S [2- (3-Amino-propylamino)-thiazol-5-yl]-pyridin-2-yl-methanone ; hydrochloride The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 2- (bromoacetyl) pyridine hydrobromide (commercially available) according to the procedure described for Example H. MS (m/e): 263.2 (MH+, 100%).

Example Z [2- (3-Amino-propylamino)-thiazol-5-yl]-pyridin-3-yl-methanone ; hydrochloride The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl]-carbamic acid tert-butyl ester and 3- (bromoacetyl) pyridine hydrobromide (commercially available) according to the procedure described for Example H. MS (m/e): 263.2 (MH+, 100%).

Example U [2- (3-Amino-propylamino)-thiazol-5-yl]-pyridin-4-yl-methanone ; hydrochloride

The title compound was synthesised from [3- (3-Dimethylaminomethylene-thioureido)- propyl] -carbamic acid tert-butyl ester and 2-bromo-1- (4-pyridinyl)-1-ethanone hydrobromide (commercially available) according to the procedure described for Example H. MS (m/e): 263.2 (MH+, 100%).

Example V [2- (5-Amino-pentylamino)-thiazol-5-yl]-o-tolyl-methanone ; hydrochloride

A mixture of 396 mg (1.25 mmol) [5- (3-Dimethylaminomethylene-thioureido)-pentyl]- carbamic acid tert-butyl ester, 388 mg (1.82 mmol) 2-methyl phenacylbromide (Literature: W09907666) and 0.7 ml NEt3 in 8 ml ethanol was heated to 100°C for 16h. After evaporation to dryness the residue was taken up in 6 ml dioxane and treated with 3ml of a 4N HC1 in dioxane and stirred for 16 h at room temperature. After concentration the residue taken up in diethyl ether, the precipitate was filtered of and dried to yield 320 mg (75%) of the title compound. MS (m/e): 304.5 (MH+, 100%) Example W [2- (5-Amino-pentylamino)-thiazol-5-yl]-pyridin-2-yl-methanone ; hydrochloride The title compound was synthesised from [5- (3-Dimethylaminomethylene-thioureido)- pentyl]-carbamic acid tert-butyl ester and 2-Bromo-1-pyridin-2-yl-ethanone (commercially available) according to the procedure described for Example V. MS (m/e): 291.4 (MH+, 100%).

Example X [2- (5-Amino-pentylamino)-thiazol-5-yl]-pyridin-4-yl-methanone ; hydrochloride The title compound was synthesised from [5- (3-Dimethylaminomethylene-thioureido)- pentyl]-carbamic acid tert-butyl ester and 2-Bromo-1-pyridin-4-yl-ethanone (commercially available) according to the procedure described for Example V. MS (m/e): 291.3 (MH+, 100%).

Example Y [2- (5-Amino-pentylamino)-thiazol-5-yl]- (2-chloro-phenyl)-methanone ; hydrochloride The title compound was synthesised from [5- (3-Dimethylaminomethylene-thioureido)- pentyl]-carbamic acid tert-butyl ester and 2-Bromo-l- (2-chloro-phenyl)-ethanone

(commercially available) according to the procedure described for Example V. MS (m/e): 324.2 (MH+, 100%).

Example 7 Thiophene-2-sulfonic acid {3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide A mixture of 31.1 mg (0.1 mmol) [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone hydrochloride in 1 ml methanol, 18. 2 mg (0.1 mmol) Thiophene-2-sulfonyl chloride in 1 ml DCM and 0.15 ml NEt3 was stirred for 16 h at 50°C. After evaporation to dryness the residue was taken up in 1.5 ml MeOH/formic acid 1/1 and subjected to preparative HPLC separation on reversed phase eluting with an acetonitrile/water gradient. Evaporation of product fractions yielded 11.4 mg (27%) of the title compound.

MS (m/e): 386.3 ( (M-H), 100%).

According to the procedure described for the synthesis of Example 7 further sulfonamides have been synthesised from [2- (3-Amino-propylamino)-thiazolyl- or [2- (5-Amino- pentylamino)-thiazolyl derivatives and sulfonyl chlorides. The results are shown in table 1 and comprise Example 1 to Example 24, Example 119 to Example 123 and Example 142 to Example 171, and Examples 180 to Example 233.

Example 31 Pentanoic acid [3- (5-benzoyl-thiazol-2-ylamino)-propyl]-amide

A mixture of 11.9 mg (0.04 mmol) [2- (3-Amino-propylamino)-thiazol-5-yl]-phenyl- methanone hydrochloride, 5.8 mg (0.048 mmol) pentanoyl chloride and 39 ul (0.28 mmol) NEt3 in 1 ml methanol and 0.5 ml DCM was stirred at room temperature for 16 h. After evaporation to dryness the residue was taken up in 1.5 ml MeOHlformic acid 1/1 and subjected to preparative HPLC separation on reversed phase eluting with an acetonitrile/ water gradient. Evaporation of product fractions yielded 6 mg (43%) of the title compound.

MS (m/e) : 345.5 (MH+, 100%).

According to the procedure described for the synthesis of Example 31 further amides have been synthesised from [2- (3-Amino-propylamino)-thiazolyl derivatives and acid chlorides. The results are shown in table 1 and comprise Example 29 to Example 88.

Example 98 1-(2-Methoxy-phenyl)-3-{3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-urea A mixture of 12.5 mg (0.04 mmol) [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone hydrochloride, 7.6 mg (0.05 mmol) 2-Methoxyphenyl isocyanate and 39 ul NEt3 in 1 ml methanol was stirred for 16 h at roomtemperature. After evaporation to dryness the residue was taken up in 1.5 ml MeOH/formic acid 1/1 and subjected to preparative HPLC separation on reversed phase eluting with an acetonitrile/water gradient. Evaporation of product fractions yielded 7.9 mg (47%) of the title compound.

MS (m/e): 424.3 (M+, 100%) According to the procedure described for the synthesis of Example 98 further ureas have been synthesised from [2- (3-Amino-propylamino)-thiazolyl derivatives and isocyanates.

The results are shown in table 1 and comprise Example 89 to Example 118.

Example Z 1-o-Tolyl-propane-1,2-dione

A mixture of 7 g (47.23 mmol) 1-o-Tolyl-propan-2-one, 30.5 g (0.141 mol) pyridinium chlorochromate and 11.2 g (0.141 mol) pyridine in 200 ml DCM was heated to reflux for 16 h. The mixture was filtered through a pad of silica and the filtrate was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica eluting with ethyl acetate/n-hexane 1: 4. The product fractions were evaporated to yield 1.178 g (15%) of the title compound.

1-H-NMR (300 MHz, DMSO-d6) 8= 7.64 d, J = 6 Hz, 1H, phenyl), 7.52 (d, J = 6 Hz, 1H, phenyl), 7.38 (d, J = 6 Hz, 2H, phenyl), 2.52 (s, 3H, CH3), 2.49 (s, 3H, CH3).

MS (m/e) : 162 (M+, 100%) Example AA 3-Bromo-1-o-tolyl-propane-1, 2-dione A mixture of 3 g (18.49 mmol) 1-o-Tolyl-propane-1, 2-dione and 1.05 ml (20.34 mmol) bromine in 30 ml CHC13 and 0.53 ml acetic acid was heated to 70°C for 16 h. The mixture was evaporated under reduced pressure to yield 4. 35 g (98%) of the title compound.

1-H-NMR (300 MHz, DMSO-d6) 5= 7. 60 (m, 4H, phenyl), 2.52 (s, 2H, CH2), 2.51 (s, 3H, CH3).

MS (m/e) : 234.3 (MH+, 100%) Example AB {3- [4- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester

A mixture of 2.55 g (10.6 mmol) 3-Bromo-1-o-tolyl-propane-1, 2-dione, 1.9 g (8.1 mmol) (3-thioureido-propyl) -carbamic acid tert-butyl ester and 5.66 ml (40.6 mmol) NEt3 in 100 ml methanol was heated to 80°C for 2 h. The reaction mixture was evaporated under reduced pressure and the residue was purifier by flash column chromatography on silica eluting with a gradient of heptane and ethyl acetate. Evaporation of the product fractions yielded 2.17 g (71%) of the title compound as dark red oil.

1-H-NMR (300 MHz, DMSO-d6) 8= 7.82 (s, br, 1H, NH), 7.38-7. 27 (m, 5H, phenyl/ thiazole), 6.84 (s, br, 1H, NH), 3.19 (m, 2H, CH2), 2.97 (m, 2H, CH2), 2.25 (s, 3H, CH3), 1.65 (m, 2H, CH2), 1.37 (s, 9H, CH3).

MS (m/e) : 376.5 (MH+, 100%) Example AC [2- (3-Amino-propylamino)-thiazol-4-yl]-o-tolyl-methanone ; hydrochloride A mixture of 2. 17 g (5.8 mmol) {3- [4- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}- carbamic acid tert-butyl ester and 30 ml 4N HC1 in dioxane and 20 ml ethanol was stirred at room temperature for 16 h. The mixture was concentrated to yield 1.8 g (quant. ) of the title compound.

1-H-NMR (300 MHz, DMSO-d6) o= 8. 23 (s, br, 2H, NH2), 7.45-7. 35 (m, 5H, phenyl/ thiazole), 6.0 (s, br, 1H, NH), 3.39 (m, 2H, CH2), 2.86 (m, 2H, CH2), 2.29 (s, 3H, CH3), 1.91 (t, J = 6 Hz, 2H, CH2).

MS (m/e) : 276.3 (MH+, 100%) Example 138 <BR> <BR> <BR> Thiophene-2-sulfonic acid {3- [4-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide

A solution of 15.6 mg (0.5 mmol) [2- (3-Amino-propylamino)-thiazol-4-yl]-o-tolyl- methanone hydrochloride in 1 ml methanol was treated with 11.9 mg (0.65 mmol) thiophene-2-sulfonyl chloride in 0.13 ml dioxane and 34.7 ul NEt3. The mixture was stirred at 60°C for 16 h and after addition of 0.5 ml formic acid subjected to preparative HPLC separation on reversed phase eluting with an acetonitrile/water gradient.

Evaporation of the product fractions yielded 6.2 mg (29%) of the title compound.

MS (m/e): 422.3 (MH+, 100%) According to the procedure described for the synthesis of Example 138 further sulfonamides have been synthesised from thiazole derivatives and sulfonylchlorides. The results are shown in table 1 and comprise Example 132 to Example 141.

According to the procedure described for the synthesis of Example 138 amides have been synthesised with the temperature adjustment to room temperature from thiazole derivatives and acid chlorides. The results are shown in table 1 and comprise Example 126 to Example 129.

According to the procedure described for the synthesis of Example 138 ureas have been synthesised with the temperature adjustment to room temperature from thiazole derivatives and isocyanates. The results are shown in table 1 and comprise Example 130 and Example 131.

Example AD (5-Isothiocyanato-pentyl) -carbamic acid tert-butyl ester To a solution of 2 g (9.9 mmol) (5-Amino-pentyl)-carbamic acid tert-butyl ester in 40 ml THF at 0°C was added 896 pl (14.83 mmol) CS2 and allowed to srirr at room temperature for 14 h. 623 mg (14.83 mmol) cyanamide and 4 drops NEt3 was added and the mixture was heated to 4°C for 3 h. The mixture was extracted with diethyl ether and the combined organic layers were dried with MgS04. After filtration and removal of the volatiles the residue was purified by flash column chromatography on silica eluting with ethyl acetate/

cyclohexane 1: 1. The evaporation of the product fractions yielded 2.24 g (93%) of the title compound.

1-H-NMR (250 MHz, CDC13) 8= 4.58 (s, br, 1H, NH), 3.52 (t, J = 6.5Hz, 2H, NCH2), 3. 13 (dd, Jl = 6.5 Hz, J2 = 4 Hz, 2H, NHCH2), 1.74 (m, 2H, CH2), 1.50 (m, 4H, CH2), 1.44 (s, 9H, CH3).

MS (m/e): 262.3 (M+NH4,100%) Example AE {5- [3- (1-Amino-ethylidene)-thioureido]-pentyl}-carbamic acid tert-butyl ester

A solution of 245 mg (1 mmol) (5-Isothiocyanato-pentyl)-carbamic acid tert-butyl ester in 1 ml IN NaOH at 0°C was treated with 94.5 mg (1 mmol) acetidine hydrochloride in 2 ml THF and allowed to stirr for 5 h at 0°C. The mixture was extracted three times with 15 ml diethyl ether, the combined organic layers were dried with MgS04 and after filtration evaporated under reduced pressure to yield 297 mg (98%) of the title compound.

MS (m/e): 303.4 (M+H, 100%) Example AF {5- [4-Methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-carbamic acid tert-butyl ester

To a solution of 290 mg (0.96 mmol) {5- [3- (1-Amino-ethylidene)-thioureido]-pentyl}- carbamic acid tert-butyl ester in 5 ml ethanol was added 213 mg (1 mmol) o- Methylphenacyl bromide and 139, ut NEt3 and allowed to strirr for 5 h at room temperature. Afterwards the mixture was directly applied to preparative HPLC on reversed phase eluting with an acetonitrile/water gradient. The evaporation of the product fractions yielded 180 mg (45%) of the title compound.

MS (m/e) : 418.3 (M+H, 100%) Example AG [2- (5-Amino-pentylamino)-4-methyl-thiazol-5-yl]-o-tolyl-methano ne hydrochloride

A solution of 170 mg (0.4 mmol) {5- [4-Methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]- pentyl}-carbamic acid tert-butyl ester in 2 ml dioxane was treated with 1 ml 4N HC1 in dioxane and allowed to react for 5 h at room temperature. The mixture was evaporated under reduced pressure to afford 143 mg (99%) of the title compound.

1-H-NMR (300 MHz, CDC13) 8= 8.72 (s, br, 1H, NH), 7.75 (m, 2H, H-3/H-6), 7.30 (m, 2H, H-4/H-5), 4.80 (s, br, 2H, NH2), 3.68 (t, J = 6.4 Hz, 1H, NCH2), 3.23 (m, 1H, NCH2), 2.74 (m, 2H, NCH2), 2.21 (s, 3H, CH3), 1. 91 (s, 3H, CH3), 1.54 (m, 4H, CH2), 1.37 (m, 2H, CH2).

MS (m/e): 318.4 (M+H, 100%) Example 172 <BR> <BR> <BR> N- {5- [4-Methyl-5- (2-methyl-benzoyl)-thiazol-2-ylamino]-pentyl}-benzenesulfona mide A solution of 18 mg (0.05 mmol) [2- (5-Amino-pentylamino)-4-methyl-thiazol-5-yl]-o- tolyl-methanone hydrochloride in 1 ml ethanol was treated with 10.6 mg (0.06 mmol) benzenesulfonylchloride and 21 ml NEt3. The mixture was allowed to stirr for 15 h at room temperature and afterwards subjected to preparative HPLC seperation on reversed phase eluting with an acetonitrile/water gradient. Evaporation of the product fractions yielded 12.6 mg (55%) of the title compound.

MS (m/e): 458. 3 (M+H, 100%) AH (2-Thioureido-ethyl)-carbamic acid tert-butyl ester

The title compound was synthesised from (2-Amino-ethyl) -carbamic acid tert-butyl ester.

The compound is described in literature: W00121623A1 Example AI [2- (3-Dimethylaminomethylene-thioureido)-ethyl]-carbamic acid tert-butyl ester

The title compound was synthesised from (2-Thioureido-ethyl) -carbamic acid tert-butyl esterand Dimethylformamide dimethyl acetal according to the procedure described for Example C in 51% yield. MS (m/e): 275.4 (MH+, 100%) Example AJ {2- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-ethyl}-carbamic acid tert-butyl ester The title compound was synthesised from [2- (3-Dimethylaminomethylene-thioureido)- ethyl]-carbamic acid tert-butyl ester and 2-methyl phenacylbromide (Literature:

W09907666) according to the procedure described for Example 25 in 75% yield. MS (m/e): 362.1 (MH+, 100%).

Example AK [2- (2-Amino-ethylamino)-thiazol-5-yl]-o-tolyl-methanone ; hydrochloride

The title compound was synthesised from {2- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]- ethyl}-carbamic acid tert-butyl ester according to the procedure described for Example AC in quantitative yield. MS (m/e): 261.7 (MH+, 100%).

Example AL (4-Thioureido-butyl) -carbamic acid tert-butyl ester

The title compound was synthesised from (4-Amino-butyl) -carbamic acid tert-butyl ester.

The compound is described in literature: W00102379A1 Example AM [4- (3-Dimethylaminomethylene-thioureido)-butyl]-carbamic acid tert-butyl ester

The title compound was synthesised from (4-Thioureido-butyl) -carbamic acid tert-butyl ester and Dimethylformamide dimethyl acetal according to the procedure described for Example C in 76% yield. MS (m/e): 303.3 (MH+, 100%) Example AN {4- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-butyl}-carbamic acid tert-butyl ester

The title compound was synthesised from [4- (3-Dimethylaminomethylene-thioureido)- butyl]-carbamic acid tert-butyl ester and 2-methyl phenacylbromide (Literature: W09907666) according to the procedure described for Example 25 in 69% yield. MS (m/e): 390.2 (MH+, 100%).

Example AO [2- (4-Amino-butylamino)-thiazol-5-yl]-o-tolyl-methanone ; hydrochloride

The title compound was synthesised from {4- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]- butyl}-carbamic acid tert-butyl ester according to the procedure described for Example AC in quantitative yield. MS (m/e): 289. 7 (MH+, 100%).

Example AP Methyl- (4-thioureido-propyl)-carbamic acid tert-butyl ester

The title compound was synthesised from (3-Amino-propyl)-methyl-carbamic acid tert- butyl ester according to the procedure described for Example A (MS (m/e): 234.3 (MH+, 100%).

Example AQ [4- (3-Dimethylaminomethylene-thioureido)-propyl]-methyl-carbami c acid tert-butyl ester The title compound was synthesised from Methyl- (4-thioureido-butyl)-carbamic acid tert- butyl ester and Dimethylformamide dimethyl acetal according to the procedure described for Example C in 39% yield. MS (m/e): 328.9 (MH+, 100%) Example AR Methyl- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamicacidte rt-butyl ester The title compound was synthesised from [4- (3-Dimethylaminomethylene-thioureido)- butyl]-methyl-carbamic acid tert-butyl ester and 2-methyl phenacylbromide (Literature: W09907666) according to the procedure described for Example 25 in 78% yield. MS (m/e): 390.3 (MH+, 100%).

Example AS [2- (3-Methylamino-propylamino)-thiazol-5-yl]-o-tolyl-methanone ; hydrochloride

The title compound was synthesised from Methyl- {3- [5- (2-methyl-benzoyl)-thiazol-2- ylamino]-propyl}-carbamic acid tert-butyl ester according to the procedure described for Example AC in quantitative yield. MS (m/e): 289.1 (MH+, 100%).

Example AT [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl-methanone

339mg {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester was added to a solution of 25% aqueous hydrochloric acid in dioxane. The mixture was stirred lh at room temperature and maintained overnight in the refrigerator. The mixture was poured into saturated aqueous sodium bicarbonate solution (50ml). The organics were extracted with dichloromethane (3x50ml), dried over magnesium sulfate and evaporated under reduced pressure to afford the title compound as yellow foam (254mg) which was used without further purification.

Example AU N-{3- [5-(2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-N'-(l, l-dimethylethyl)- sulfamide

900mg {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-carbamic acid tert-butyl ester was dissolved in diethyl ether and hydrogen chloride in ether added dropwise with stirring. The mixture was stirred overnight at room temperature and poured into saturated aqueous sodium bicarbonate solution. The organics were extracted with dichloromethane (3x25ml), dried over magnesium sulfate and evaporated under reduced pressure to afford [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl-methanone as a yellow gum (579mg, 88%). A solution of 0. 22ml tert-butanol in hexane (2ml) was cautiously added to a stirred solution of 0. 2ml chlorosulfonyl isocyanate in hexane (5ml). The resulting white precipitate was stirred until it had dissolved (1.5h) and the mixture cooled to-78°C before the slow addition of a solution of [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone and 0. 4ml triethylamine in dichloromethane. The cooling bath was removed and the yellow mixture allowed to reach room temperature and stirred 2h at room temperature. The mixture was poured into water and the organics extracted with ethyl acetate (2x25ml). The combined organics were washed with brine, dried over magnesium sulfate and evaporated. The resulting oil was purified by column chromatography on silica gel (150g, 2: 1 ethyl acetate/hexane) to afford the title compound (241mg, 24%) as a pale yellow oil. MS (m/e): 409.3 (M-H, 100%) Example AV N- {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-acetamide

25% Aqueous hydrochloric acid was added dropwise to a solution of R04386677-000 in 2- propanol. The mixture was stirred lh at room temperature and kept in the refrigerator over the week-end. The solvent was evaporated under reduced pressure and the residue triturated with diethyl ether. Ethyl acetate (40ml) was added and the hydrochloride quenched by the addition of saturated aqueous sodium bicarbonate solution (50ml). The aqueous phase was extracted with dichloromethane (5x75ml). The combined organic phases were dried over sodium sulfate and evaporated. The residue was purified by column chromatography on silica gel. The only product isolated was the title compound, as a yellow oil which solidified on standing. Recrystallisation from a mixture of ethyl acetate, dichloromethane and hexane afforded the pure product as a light yellow solid (275mg, 13%). MS (m/e): 318. 3 (M+H, 100%) Example AW <BR> <BR> <BR> 4-Methyl-N- {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-benzenesulfona mide

[2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl-methanone was dissolved in dichloromethane and triethylamine and toluene-4-sulfonyl chloride added. The mixture

was stirred overnight at room temperature, poured into 1M pH4 phosphate buffer (5ml) and extracted with dichloromethane (3xlOml). The combined organic phases were dried over magnesium sulfate and evaporated. The oily residue was purified by column chromatography on silica gel (13: 7 hexane/acetone eluant), using a small amount of dichloromethane to apply the mixture to the column. The title compound was isolated as an off-white solid. MS (m/e) : 428.3 (M-H, 100%) Example AX Ethanesulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide The title compound was produced from [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone and ethanesulfonyl chloride according to the procedure described for Example AW. The product was isolated as an off-white solid. MS (m/e): 468.3 (M+H, 100%) Example AY 2,2, 2-Trifluoro-ethanesulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}- amide

The title compound was produced from [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone and 2,2, 2-trifluoroethanesulfonyl chloride according to the procedure described for Example AW. The product was isolated as an orange gum. MS (m/e): 422.3 (M+H, 100%) Example AZ Methanesulfonic acid {3- [5- (2-Methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide

The title compound was produced from [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone and methanesulfonyl chloride according to the procedure described for Example AW. The product was isolated as an orange gum. MS (m/e): 352.2 (M-H, 100%) Example BA Propane-2-sulfonic acid {3- [5- (2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide

The title compound was produced from [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone and 2-propanesulfonyl chloride according to the procedure described for Example AW. The product was isolated as an orange gum. MS (m/e): 380.2 (M-H, 100%)

Example BB Naphthalene-1-sulfonic acid {3- [5-(2-methyl-benzoyl)-thiazol-2-ylamino]-propyl}-amide

The title compound was produced from [2- (3-Amino-propylamino)-thiazol-5-yl]-o-tolyl- methanone and 1-naphthalenesulfonyl chloride according to the procedure described for Example AW. The product was isolated as an off-white gum. MS (m/e): 464.1 (M-H, 100%) Example BC 1,1-dimethylethyl { {3- [5-(2-Methyl-benzoyl)-thiazol-2-ylamino]-propylamino} sulfonyl]- carbamate

To a solution of 43mg [2-(3-Amino-propylamino)-thiazol-5-yl]-o-tolyl-methanone in dichloromethane was added 49mg 4-(dimethylamino)-1-[[[(1,1- dimethylethoxy) carbonyl] amino] sulfonyl]-pyridinium (Organic Letters, 2001,3, 2241). The mixture was stirred overnight at room temperature. The solvent was evaporated under reduced pressure and the solid residue purified by column chromatography on silica gel (15g, 7: 3 ethyl acetate/hexane eluant), using a small amount of dichloromethane to apply the mixture to the column. The product was isolated as an off-white solid (28mg, 40%).

MS (m/e): 453.2 (M-H, 100%) Example BD {3- [3- (1-Amino-ethylidene)-thioureido]-propyl}-carbamic acid tert-butyl ester The title compound was prepared from (3-isothiocyanatopropyl) -carbamic acid tert-butyl ester and acetamidine hydrochloride as a colourless gum (quantitative yield) according to the procedure described for Example AE. MS (m/e): 275.2 (M+H, 100%) Example BE {3- [5- (2-Ethyl-benzoyl)-4-methyl-thiazol-2-ylamino]-propyl}-carbam ic acid tert-butyl ester

A mixture of 0. 60g {3- [3- (l-Amino-ethyIidene)-thioureido]-propyl}-carbamic acid tert- butyl ester and 0.54g 2-bromo-l- (2-ethyl-phenyl)-ethanone (Example G) were dissolved in N, N-dimethylformamide and stirred overnight at room temperature. 0. 33ml Triethylamine were added and the mixture stirred 72h at room temperature. The mixture was diluted with dichloromethane, washed twice with water and once with brine, dried over magnesium sulfate, filtered and evaporated to afford the title compound (435mg) as a pale yellow solid (49%). MS (m/e): 404.5 (M+H, 100%) Example BF Naphthalene-1-sulfonic acid {3- [5- (2-ethyl-benzoyl)-4-methyl-thiazol-2-ylamino]- propyl}-amide

88mg {3- [5- (2-Ethyl-benzoyl)-4-methyl-thiazol-2-ylamino]-propyl}-carbam ic acid tert- butyl ester was dissolved in dioxane and 0. 15ml 25% aqueous hydrochloric acid added dropwise. The mixture was stirred 4h at room temperature and evaporated to dryness.

Toluene was added and the mixture evaporated to dryness and dried overnight in vacuo.

The residue was taken up in dichloromethane and 50mg naphthalene-1-sulfonyl chloride and 0. 14ml triethylamine added. The mixture was stirred overnight at room temperature and partitioned between water and dichloromethane. The organic phase was dried over magnesium sulfate and evaporated to afford the title compound (77mg, 71%) as a yellow oil. MS (m/e): 492.2 (M+H, 100%) Example BG Thiophene-2-sulfonic acid {3- [5- (2-ethyl-benzoyl)-4-methyl-thiazol-2-ylamino]-propyl}- amide

The title compound was prepared from {3- [5- (2-Ethyl-benzoyI)-4-methyl-thiazol-2- ylamino]-propyl}-carbamic acid tert-butyl ester and thiophene-2-sulfonyl chloride according to example BF. Off-white oil, 55%. MS (m/e): 448.1 (M+H, 100%) Example BH N- {3- [5- (2-Ethyl-benzoyl)-4-methyl-thiazol-2-ylamino]-propyl}-2-meth oxy-5-methyl- benzenesulfonamide

The title compound was prepared from {3- [5- (2-Ethyl-benzoyl)-4-methyl-thiazol-2- ylamino]-propyl}-carbamic acid tert-butyl ester and 6-methoxy-m-toluenesulfonyl chloride according to example XX. Light yellow oil, 67%. MS (m/e): 486. 3 (M+H, 100%)

According to Example 172 further sulfonamide derivatives have been synthesised from the corresponding aminothiazole derivative and a sulfonylchloride. The results are compiled in the table and comprise Examples 172-179. Ex. Educts Name Mass analysis 1. [2- (3-Amino-propylamino)- 2-Fluoro-N- {3- [5- 419. 2 (M-Ht)- thiazol-5-yl]-pyridin-2-yl- (pyridine-2-carbonyl) - methanone; hydrochloride and 2-thiazol-2-ylamino]- Fluorophenylsulfonyl chloride propyl}- benzenesulfonamide 2. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-445. 3 (M-H+)- thiazol-5-yl]-pyridin-2-yl- {3- [5- (pyridine-2- methanone; hydrochloride and 2-carbonyl)-thiazol-2- methoxy-5-methylphenylsulfonyl ylamino]-propyl}-benz chloride enesulfonamide 3. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-445. 3 (M-Ht)- thiazol-5-yl]-pyridin-3-yl- {3- [5- (pyridine-3- methanone; hydrochloride and 2-carbonyl)-thiazol-2- methoxy-5-methylphenylsulfonyl ylamino]-propyl}-benz chloride enesulfonamide 4. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-445. 3 (M-H+)- thiazol-5-yl]-pyridin-4-yl- {3- [5- (pyridine-4- methanone; hydrochloride and 2-carbonyl)-thiazol-2- methoxy-5-methylphenylsulfonyl ylamino]-propyl}-benz chloride enesulfonamide 5. [2- (3-Amino-propylamino)- 2-Fluoro-N- {3- [5- (2- 432. 3 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl)-thiazol- hydrochloride and 2-2-ylamino]-propyl}- Fluorophenylsulfonyl chloride benzenesulfonamide 6. [2- (3-Amino-propylamino)- 4-Methoxy-N- {3- [5- (2- 444. 3 (M-H+)- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and and 4-2-ylamino]-propyl}- methoxyphenylsulfonyl chloride benzenesulfonamide Ex. Educts Name Mass analysis 7. [2- (3-Amino-propylamino)- Thiophene-2-sulfonic 420.2 (M-H+)- thiazol-5-yl]-o-tolyl-methanone ; acid {3- (5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenylsulfonyl chloride ylamino]-propyl}-amide 8. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-458. 3 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; {3- [5- (2-methyl- hydrochloride and 2-methoxy-5-benzoyl)-thiazol-2- methylphenylsulfonyl chloride ylamino]-propyl}- benzene sulfonamide 9. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (2- 432. 3 (M-H+)- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 4-2-ylamino]-propyl}- fluorophenylsulfonyl chloride benzenesulfonamide 10. [2- (3-Amino-propylamino)- 2-Methyl-N- {3- [5- (2- 428. 4 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2-2-ylamino]-propyl}- methylphenylsulfonyl chloride benzenesulfonamide 11. [2- (3-Amino-propylamino)- 3-Fluoro-N- {3- [5- (2- 432. 4 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 3-2-ylamino]-propyl}- fluorophenylsulfonyl chloride benzenesulfonamide 12. [2- (3-Amino-propylamino)- 2-Chloro-N- {3- [5- (2- 516. 1 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and and 2-chloro-2-ylamino]-propyl}-5- 5- (trifluoromethyl) phenylsulfonyl trifluoromethyl- chloride benzenesulfonamide 13. [2- (3-Amino-propylamino)- N- {3- [5- (2-Methyl- 415. 5 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; benzoyl) -thiazol-2- hydrochloride and phenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide Ex. Educts Name Mass analysis 14. [2- (3-Amino-propylamino)- 3-Methoxy-N- {3- [5- (2- 444. 3 (M-Ht)' thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 3-2-ylamino]-propyl}- methoxyphenylsulfonyl chloride benzenesulfonamide 15. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 452. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-2- fluorophenylsulfonyl chloride fluoro- benzenesulfonamide 16. [2- (3-Amino-propylamino)- N-{3-[5-(2-Chloro- 464. 2 (M-H+)- thiazol-5-yl]-(2-chloro-phenyl)-benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-propyl}-4- methoxyphenylsulfonyl chloride methoxy- benzenesulfonamide 17. [2- (3-Amino-propylamino)- Thiophene-2-sulfonic 440.2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- acid {3- [5- (2-chloro- methanone; hydrochloride and 2-benzoyl)-thiazol-2- thiophenylsulfonyl chloride ylamino]-propyl}-amide 18. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 478. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-2- methoxy-5-methylphenylsulfonyl methoxy-5-methyl- chloride benzene sulfonamide 19. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 452. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-propyl}-4- fluorophenylsulfonyl chloride fluoro- benzenesulfonamide Ex. Educts Name Mass analysis 20. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 448. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-2- methylphenylsulfonyl chloride methyl- benzenesulfonamide 21. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 452. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 3-ylamino]-propyl}-3- fluorophenylsulfonyl chloride fluoro- benzenesulfonamide 22. [2- (3-Amino-propylamino)- 2-Chloro-N- {3- [5- (2- 536. 1 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- chloro-benzoyl)-thiazol- methanone; hydrochloride and 2-2-ylamino]-propyl}-5- chloro-5-trifluoromethyl- (trifluoromethyl) phenylsulfonyl benzenesulfonamide chloride 23. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 434. 3 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}- phenylsulfonyl chloride benzenesulfonamide 24. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 464. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 3-ylamino]-propyl}-3- methoxyphenylsulfonyl chloride methoxy- benzenesulfonamide 25. 2-methylphenacylbromideand {3- [5- (2-Methyl- 375. 9 MH+ [3- (3-dimethylaminomethylene- benzoyl)-thiazol-2- thioureido) -propyl]-carbamic ylamino]-propyl}- acid tert-butyl ester carbamic acid tert-butyl ester Ex. Educts Name Mass analysis 26. [3- (3-dimethylaminomethylene- {3- [5- (2-Chloro- 395. 8 MH+ thioureido)-propyl]-carbamic benzoyl) -thiazol-2- acid tert-butyl ester and 2-chloro ylamino]-propyl}- phenacylbromide carbamic acid tert-butyl ester 27. [3- (3-dimethylaminomethylene- {3- [5- (2-Ethyl-benzoyl)- 389. 9 MH+ thioureido)-propyl]-carbamic thiazol-2-ylamino]- acid tert-butyl ester and 2-ethyl propyl}-carbamic acid phenacylbromide tert-butyl ester 28. [3- (3-dimethylaminomethylene- {3- [5- (2- 429. 9 MH+ thioureido) -propyl] -carbamic Trifluoromethyl- acid tert-butyl ester and 2-benzoyl)-thiazol-2- trifluoromethyl phenacylbromide ylamino]-propyl}- carbamic acid tert-butyl ester 29. [2- (3-Amino-propylamino)- Cyclohexanecarboxylic 386.4 MH+ thiazol-5-ylj-o-tolyl-methanone ; acid {3- [5- (2-methyl- hydrochloride and benzoyl)-thiazol-2- cyclohexanecarbonyl chloride ylamino]-propyl}-amide 30. [2- (3-Amino-propylamino)- Cyclohexanecarboxylic 400.5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- acid {3- [5- (2-ethyl- methanone; hydrochloride and benzoyl)-thiazol-2- cyclohexanecarbonyl chloride ylamino]-propyl}-amide 31. [2- (3-Amino-propylamino)- Pentanoic acid [3- (5- 345. 5 MH+ thiazol-5-yl] -phenyl-methanone; benzoyl-thiazol-2- hydrochloride and pentanoyl ylamino)-propyl]-amide chloride Ex. Educts Name Mass analysis 32. [2- (3-Amino-propylamino)- Pentanoicacid {3- [5- (2- 360. 4 MH+ thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and pentanoyl 2-ylamino]-propyl}- chloride amide 33. [2- (3-Amino-propylamino)- Pentanoic acid 13- [5- (2- 374. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- ethyl-benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}-amide pentanoyl chloride 34. [2- (3-Amino-propylamino)- Pentanoicacid {3- [5- (2- 364. 3 MH+ thiazol-5-yl]- (2-fluoro-phenyl)- fluoro-benzoyl)-thiazol- methanone; hydrochloride and 2-ylamino]-propyl}- pentanoyl chloride amide 35. [2- (3-Amino-propylamino)- Pentanoicacid {3- [5- (2- 380. 4 MH+ thiazol-5-yl] - (2-chloro-phenyl)- chloro-benzoyl)-thiazol- methanone; hydrochloride and 2-ylamino]-propyl}- pentanoyl chloride amide 36. [2- (3-Amino-propylamino)- N- [3- (5-Benzoyl-thiazol- 414. 35 MH+ thiazol-5-yl]-phenyl-methanone ; 2-ylamino) -propyl] -2- (4- hydrochloride and 4-chloro-phenyl)- Chlorophenylacetyl chloride acetamide 37. [2- (3-Amino-propylamino)- 2- (4-Chloro-phenyl)-N- 428. 5 MH+ thiazol-5-yl] -o-tolyl-methanone; {3- [5- (2-methyl- hydrochloride and 4-benzoyl)-thiazol-2- Chlorophenylacetyl chloride ylamino]-propyl}- acetamide 38. [2- (3-Amino-propylamino)- 2- (4-Chloro-phenyl)-N- 442. 4 MH+ thiazol-5-yl]- (2-ethyl-phenyl) - {3- [5- (2-ethyl-benzoyl)- methanone; hydrochloride and 4-thiazol-2-ylamino]- Chlorophenylacetyl chloride propyl}-acetamide Ex. Educts Name Mass analysis 39. [2- (3-Amino-propylamino)- Thiophene-2-carboxylic 386. 3 MH+ thiazol-5-yl]-o-tolyl-methanone ; acid {3- [5- (2-methyl- hydrochloride and thiophene-2-benzoyl)-thiazol-2- carbonyl chloride ylamino]-propyl}-amide 40. [2- (3-Amino-propylamino)- Thiophene-2-carboxylic 400.5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- acid {3- [5- (2-ethyl- methanone; hydrochloride and benzoyl)-thiazol-2- thiophene-2-carbonyl chloride ylamino]-propyl}-amide 41. [2- (3-Amino-propylamino)- Thiophene-2-carboxylic 390.2MH+ thiazol-5-yl]- (2-fluoro-phenyl)- acid {3- [5- (2-fluoro- methanone; hydrochloride and benzoyl)-thiazol-2- thiophene-2-carbonyl chloride ylamino]-propyl}-amide 42. [2- (3-Amino-propylamino)- Thiophene-2-carboxylic 406.4 MH+ thiazol-5-yl]-(2-chloro-phenyl)-acid {3- [5- (2-chloro- methanone; hydrochloride and benzoyl)-thiazol-2- thiophene-2-carbonyl chloride ylamino]-propyl}-amide 43. [2- (3-Amino-propylamino)- N- {3- [5- (2-Ethyl- 412. 4 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-2- Fluorobenzoyl chloride fluoro-benzamide 44. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 418. 3 MH+ thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-2- Fluorobenzoyl chloride fluoro-benzamide 45. [2-(3-Amino-propylamino)-3-Fluoro-N- {3- [5- (2- 398. 4 MH+ thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 3-2-ylamino]-propyl}- Fluorobenzoyl chloride benzamide Ex. Educts Name Mass analysis 46. [2- (3-Amino-propylamino)- N- {3- [5- (2-Ethyl- 412. 4 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 3-ylamino]-propyl}-3- Fluorobenzoyl chloride fluoro-benzamide 47. [2- (3-Amino-propylamino)- 3-Fluoro-N- {3- [5- (2- 402. 5 MH+ thiazol-5-yl]-(2-fluoro-phenyl)-fluoro-benzoyl)-thiazol- methanone; hydrochloride and 3-2-ylamino]-propyl}- Fluorobenzoyl chloride benzamide 48. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 418. 3 MH+ thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 3-ylamino]-propyl}-3- Fluorobenzoyl chloride fluoro-benzamide 49. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (2- 398. 4 MH+ thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 4-2-ylamino]-propyl}- Fluorobenzoyl chloride benzamide 50. [2- (3-Amino-propylamino)- N- {3- [5- (2-Ethyl- 412. 4 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-propyl}-4- Fluorobenzoyl chloride fluoro-benzamide 51. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 418. 3 MH+ thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-propyl}-4- Fluorobenzoyl chloride fluoro-benzamide 52. [2- (3-Amino-propylamino)- N- {3- [5- (2-Methyl- 380. 4 MH+ thiazol-5-yl]-o-tolyl-methanone ; benzoyl)-thiazol-2- hydrochloride and benzoyl ylamino]-propyl}- chloride benzamide Ex. Educts Name Mass analysis 53. [2- (3-Amino-propylamino)- N- {3- [5- (2-Ethyl- 394. 4 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}- benzoyl chloride benzamide 54. [2- (3-Amino-propylamino)- N- {3- [5- (2-Chloro- 400. 4 MH+ thiazol-5-yl] - (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}- benzoyl chloride benzamide 55. [2- (3-Amino-propylamino)- N- {3- [5- (2-Ethyl- 424. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-propyl}-4- methoxybenzoyl chloride methoxy-benzamide 56. [2- (3-Amino-propylamino)- N- [3- (5-Benzoyl-thiazol- 396. 3 MH+ thiazol-5-yl] -phenyl-methanone; 2-ylamino)-propyl]-2- hydrochloride and 2-methoxy-benzamide methoxybenzoyl chloride 57. [2- (3-Amino-propylamino)- N- {3- [5- (2-Ethyl- 424. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-2- methoxybenzoyl chloride methoxy-benzamide 58. [2- (3-Amino-propylamino)- 4-Chloro-N- {3- [5- (2- 414. 3 MH+ thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 4-2-ylamino]-propyl}- chlorobenzoyl chloride benzamide 59. [2- (3-Amino-propylamino)- 4-Chloro-N- {3- [5- (2- 428. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- ethyl-benzoyl)-thiazol-2- methanone; hydrochloride 4-ylamino]-propyl}- chlorobenzoyl chloride benzamide Ex. Educts Name Mass analysis 60. [2- (3-Amino-propylamino)- Cyclohexanecarboxylic 440.5 MH+ thiazol-5-yl]- (2-trifluoromethyl- acid {3- [5- (2- phenyl) -methanone; trifluoromethyl- hydrochloride and benzoyl)-thiazol-2- cydohexyanecarbonyl chloride ylamino]-propyl}-amide 61. [2- (3-Amino-propylamino)- Cyclohexanecarboxylic 387.4 MH+ thiazol-5-yl]- (4-methyl-pyridin- acid f3- [5- (4-methyl- 3-yl)-methanone ; hydrochloride pyridine-3-carbonyl)- and cyclohexyanecarbonyl thiazol-2-ylamino]- chloride propyl}-amide 62. [2- (3-Amino-propylamino)- Pentanoic acid {3- [5- (2- 414. 4 MH+ thiazol-5-yl] - (2-trifluoromethyl- trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and pentanoyl ylamino]-propyl}-amide chloride 63. [2- (3-Amino-propylamino)- Pentanoicacid {3- [5- (4- 361. 3 MH+ thiazol-5-yl]- (4-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and pentanoyl chloride ylamino]-propyl}-amide 64. [2- (3-Amino-propylamino)- Pentanoic acid {3- [5- (2- 361. 3 MH+ thiazol-5-yl]- (2-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and pentanoyl chloride ylamino]-propyl}-amide 65. [2- (3-Amino-propylamino)- Pentanoic acid {3- [5- (3- 366. 3 MH+ thiazol-5-yl]- (3-methyl-thiophen- methyl-thiophene-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and pentanoyl chloride ylamino]-propyl}-amide Ex. Educts Name Mass analysis 66. [2- (3-Amino-propylamino)- 2- (4-Chloro-phenyl)-N- 482. 3 MH+ thiazol-5-yl]-(2-trifluoromethyl- {3- [5-(2-trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and4-ylamino]-propyl}- Chlorophenylacetyl chloride acetamide 67.2- (3-Amino-propylamino)- 2- (4-Chloro-phenyl)-N- 429. 5 MH+ thiazol-5-yl]- (3-methyl-pyridin- {3- [5- (3-methyl- 2-yl)-methanone ; hydrochloride pyridine-2-carbonyl)- and 4-Chlorophenylacetyl thiazol-2-ylamino] - chloride propyl}-acetamide 68. [2- (3-Amino-propylamino)- 2- (4-Chloro-phenyl)-N- 430. 5 MH+ thiazol-5-yl]- (3-methyl-pyrazin- {3- [5- (3-methyl- 2-yl) -methanone; hydrochloride pyrazine-2-carbonyl)- and 4-Chlorophenylacetyl thiazol-2-ylamino] - chloride propyl}-acetamide 69. [2- (3-Amino-propylamino)- Thiophene-2-carboxylic 440.4 MH+ thiazol-5-yl]-(2-trifluoromethyl-acid {3- [5- (2- phenyl) -methanone; trifluoromethyl- hydrochloride and thiophene-2-benzoyl)-thiazol-2- carbonyl chloride ylamino]-propyl}-amide 70. 2- (3-Amino-propylamino)- Thiophene-2-carboxylic 387.3 MH+ thiazol-5-yl] - (3-methyl-pyridin- acid {3- [5- (3-methyl- 2-yl) -methanone; hydrochloride pyridine-2-carbonyl)- and thiophene-2-carbonyl thiazol-2-ylamino]- chloride propyl}-amide 71. [2- (3-Amino-propylamino)-2-Fluoro-N-{3- [5-(2-452. 4 MH+ thiazol-5-yl]-(2-trifluoromethyl-trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and 2-ylamino]-propyl}- Fluorobenzoyl chloride benzamide Ex. Educts Name Mass analysis 72. [2- (3-Amino-propylamino)- 2-Fluoro-N- {3- [5- (3- 400. 4 MH+ thiazol-5-yl]- (3-methyl-pyrazin- methyl-pyrazine-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 2-Fluorobenzoyl chloride ylamino]-propyl}- benzamide 73. [2- (3-Amino-propylamino)- 3-Fluoro-N- {3- [5- (2- 452. 4 MH+ thiazol-5-yll-(2-trifluoromethyl-trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and 3-ylamino]-propyl}- Fluorobenzoyl chloride benzamide 74. [2- (3-Amino-propylamino)- 3-Fluoro-N- {3- [5- (4- 399. 4 MH+ thiazol-5-yl]- (4-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 3-Fluorobenzoyl chloride ylamino]-propyl}- benzamide 75.2- (3-Amino-propylamino)- 3-Fluoro-N- {3- [5- (3- 399. 4 MH+ thiazol-5-yl] - (3-methyl-pyridin-methyl-pyridine-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 3-Fluorobenzoyl chloride ylamino]-propyl}- benzamide 76. [2- (3-Amino-propylamino)-3-Fluoro-N-{3- [5-(3-400. 4 MH+ thiazol-5-yl]- (3-methyl-pyrazin- methyl-pyrazine-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 3-Fluorobenzoyl chloride ylamino]-propyl}- benzamide 77. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (2- 452. 4 MH+ thiazol-5-yl]- (2-trifluoromethyl- trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and 4-ylamino]-propyl}- Fluorobenzoyl chloride benzamide Ex. Educts Name Mass analysis 78. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (4- 399. 4 MH+ thiazol-5-yl] - (4-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 4-Fluorobenzoyl chloride ylamino]-propyl}- benzamide 79.2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (3- 399. 4 MH+ thiazol-5-yl]- (3-methyl-pyridin- methyl-pyridine-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 4-Fluorobenzoyl chloride ylamino]-propyl}- benzamide 80. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (3- 404. 4 MH+ thiazol-5-yl]- (3-methyl-thiophen- methyl-thiophene-2- 2-yl)-methanone ; hydrochloride carbonyl)-thiazol-2- 3-methyl-2-thiophenecarbonyl ylamino]-propyl}- chloride benzamide 81. [2- (3-Amino-propylamino)- N- {3- [5- (2- 434. 5 MH+ thiazol-5-yl] - (2-trifluoromethyl-Trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and benzoyl ylamino]-propyl}- chloride benzamide 82. [2- (3-Amino-propylamino)- N- {3- [5- (4-Methyl- 381. 4 MH+ thiazol-5-yl]- (4-methyl-pyridin- pyridine-3-carbonyl)- 3-yl) -methanone; hydrochloride thiazol-2-ylamino]- and benzoyl chloride propyl}-benzamide 83. [2- (3-Amino-propylamino)- 4-Methoxy-N- {3- [5- (2-464. 3 MH+ thiazol-5-yl] - (2-trifluoromethyl-trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and 4-ylamino]-propyl}- Methoxybenzoyl chloride benzamide Ex. Educts Name Mass analysis 84. [2-(3-Amino-propylamino)- 4-Methoxy-N-{3-[5-(4- 411. 4 MH+ thiazol-5-yl]- (4-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 4-Methoxybenzoyl chloride ylamino]-propyl}- benzamide 85. [2- (3-Amino-propylamino)- 2-Methoxy-N- {3- [5- (2- 464. 3 MH+ thiazol-5-yl]- (2-trifluoromethyl- trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and 2-ylamino]-propyl}- Methoxybenzoyl chloride benzamide 86. [2- (3-Amino-propylamino)-4-Chloro-N- {3- [5-(2-468. 2 MH+ thiazol-5-yl] - (2-trifluoromethyl- trifluoromethyl- phenyl) -methanone; benzoyl) -thiazol-2- hydrochloride and 4-ylamino]-propyl}- Chlorobenzoyl chloride benzamide 87. (2- (3-Amino-propylamino)- 4-Chloro-N- {3- [5- (4- 415. 3 MH+ thiazol-5-yl] - (4-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 4-Chlorobenzoyl chloride ylamino]-propyl}- benzamide 88. [2- (3-Amino-propylamino)- 4-Chloro-N-13- [5- (2- 415. 3 MH+ thiazol-5-yl] - (2-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 4-Chlorobenzoyl chloride ylamino]-propyl}- benzamide 89. [2- (3-Amino-propylamino)- 1- [3- (5-Benzoyl-thiazol- 386. 5 MH+ thiazol-5-yl] -phenyl-methanone; 2-ylamino)-propyl]-3- hydrochloride and cyclohexyl cyclohexyl-urea isocyanate Ex. Educts Name Mass analysis 90. [2- (3-Amino-propylamino)- l-Cyclohexyl-3- {3- [5- (2- 400. 5 MH+ thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and cyclohexyl 2-ylamino]-propyl}-urea isocyanate 91. [2-(3-Amino-propylamino)-1-Cyclohexyl-3-{3- [5-(2-414. 5 MH+ thiazol-5-yl] - (2-ethyl-phenyl)- ethyl-benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}-urea cyclohexyl isocyanate 92. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Chloro- 420. 9 MH+ thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}-3- cyclohexyl isocyanate cyclohexyl-urea 93. [2- (3-Amino-propylamino)- l- [3- (5-Benzoyl-thiazol- 360. 4 MH+ thiazol-5-yl]-phenyl-methanone ; 2-ylamino)-propyl]-3- hydrochloride and n-butyl butyl-urea isocyanante 94. [2-(3-Amino-propylamino)-1-Butyl-3- {3- [5-(2-374. 5 MH+ thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and n-butyl 2-ylamino]-propyl}-urea isocyanante 95. [2- (3-Amino-propylamino)- 1-Butyl-3- {3- [5- (2-ethyl-388. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone ; hydrochloride and n-ylamino]-propyl}-urea butyl isocyanante 96. [2- (3-Amino-propylamino)- l-Butyl-3- {3- [5- (2- 378. 4 MH+ thiazol-5-yl] - (2-fluoro-phenyl)- fluoro-benzoyl)-thiazol- methanone ; hydrochloride and n-2-ylamino]-propyl}-urea butyl isocyanante Ex. Educts Name Mass analysis 97. [2-(3-Amino-propylamino)- 1-Butyl-3-{3-[5-(2- 394. 9 MH+ thiazol-5-yl]- (2-chloro-phenyl)- chloro-benzoyl)-thiazol- methanone; hydrochloride and n-2-ylamino]-propyl}-urea butyl isocyanante 98. [2- (3-Amino-propylamino)- 1- (2-Methoxy-phenyl)-3- 424. 5 MH+ thiazol-5-yl] -o-tolyl-methanone; {3- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- Methoxyphenyl isocyanate ylamino]-propyl}-urea 99. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Ethyl- 438. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-3- (2- Methoxyphenyl isocyanate methoxy-phenyl)-urea 100. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Chloro- 444. 9 MH+ thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-3- (2- Methoxyphenyl isocyanate methoxy-phenyl)-urea 101. [2- (3-Amino-propylamino)- 1- (2-Fluoro-phenyl)-3- 412. 4 MH+ thiazol-5-yl] -o-tolyl-methanone; {3- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- Fluorophenyl isocyanate ylamino]-propyl}-urea 102. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Ethyl- 426. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-3- (2- Fluorophenyl isocyanate fluoro-phenyl)-urea 103. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Chloro- 432. 9 MH+ thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-propyl}-3- (2- Fluorophenyl isocyanate fluoro-phenyl)-urea Ex. Educts Name Mass analysis 104. [2- (3-Amino-propylamino)- 1- (3-Fluoro-phenyl)-3- 412. 4 MH+ thiazol-5-yl]-o-tolyl-methanone ; {3- [5- (2-methyl- hydrochloride and 3-benzoyl)-thiazol-2- Fluorophenyl isocyanate ylamino]-propyl}-urea 105. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Ethyl- 426. 5 MH+ thiazol-5-yl] - (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 3-ylamino]-propyl}-3- (3- Fluorophenyl isocyanate fluoro-phenyl)-urea 106. [2- (3-Amino-propylamino)- 1- (4-Fluoro-phenyl)-3- 412. 4 MH+ thiazol-5-yl]-o-tolyl-methanone ; {3- [5- (2-methyl- hydrochloride and 4-benzoyl)-thiazol-2- Fluorophenyl isocyanate ylamino]-propyl}-urea 107. [2-(3-Amino-propylamino)- 1-{3-[5-(2-Ethyl- 426. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-propyl}-3- (4- Fluorophenyl isocyanate fluoro-phenyl)-urea 108. [2- (3-Amino-propylamino)- 1- [3- (5-Benzoyl-thiazol- 428. 9 MH+ thiazol-5-yl]-phenyl-methanone ; 2-ylamino) -propyl]-3- (2- hydrochloride and 4-chloro-benzyl)-urea Chlorobenzyl isocyanate (WO0107436) 109. [2- (3-Amino-propylamino)- 1- (2-Chloro-benzyl)-3- 442. 9 MH+ thiazol-5-yl] -o-tolyl-methanone; {3- [5- (2-methyl- hydrochloride and 4-benzoyl)-thiazol-2- Chlorobenzyl isocyanate ylamino]-propyl}-urea (WO0107436) 110. [2- (3-Amino-propylamino)- 1- (2-Chloro-benzyl)-3- 457. 0 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- {3- [5- (2-ethyl-benzoyl)- methanone; hydrochloride and 4-thiazol-2-ylamino]- Chlorobenzyl isocyanate propyl}-urea (WO0107436) Ex. Educts Name Mass analysis 111. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Chloro- 463. 3 MH+ thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-propyl}-3-(2- Chlorobenzyl isocyanate chloro-benzyl)-urea (WO0107436) 112. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Methyl- 394. 5 MH+ thiazol-5-yl] -o-tolyl-methanone; benzoyl) -thiazol-2- hydrochloride and phenyl ylamino]-propyl}-3- isocyanate phenyl-urea 113. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Ethyl- 408. 5 MH+ thiazol-5-yl]- (2-ethyl-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}-3- phenyl isocyanate phenyl-urea 114. [2- (3-Amino-propylamino)- 1- {3- [5- (2-Chloro- 414. 9 MH+ thiazol-5-yl] - (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and ylamino]-propyl}-3- phenyl isocyanate phenyl-urea 115. [2- (3-Amino-propylamino)- l-Butyl-3- {3- [5- (4- 375. 5 MH+ thiazol-5-yl] - (4-methyl-pyridin-methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and n-butyl isocyanate ylamino]-propyl}-urea 116. [2- (3-Amino-propylamino)- 1- {3- [5- (4-Methyl- 395. 5 MH+ thiazol-5-yl]- (4-methyl-pyridin- pyridine-3-carbonyl)- 3-yl) -methanone; hydrochloride thiazol-2-ylamino]- and phenyl isocyanate propyl}-3-phenyl-urea 117. [2-(3-Amino-propylamino)- 1-Cyclohexyl-3-{3-[5-(3- 402. 5 MH+ thiazol-5-yl]- (3-methyl-pyrazin- methyl-pyrazine-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and cyclohexyl isocyanate ylamino]-propyl}-urea Ex. Educts Name Mass analysis 118. [2- (3-Amino-propylamino)- l-Cyclohexyl-3- {3- [5- (3- 406. 6 MH+ thiazol-5-yl]- (3-methyl-thiophen- methyl-thiophene-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and cyclohexyl isocyanate ylamino]-propyl}-urea 119. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (4- 434. 5 MH+ thiazol-5-yl] - (4-methyl-pyridin- methyl-pyridine-3- 3-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 4-Fluorophenylsulfonyl ylamino]-propyl}-benze chloride nesulfonamide 120. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [5- (3- 439. 6 MH+ thiazol-5-yl] - (3-methyl-thiophen-methyl-thiophene-2- 2-yl) -methanone; hydrochloride carbonyl)-thiazol-2- and 4-Fluorophenylsulfonyl ylamino]-propyl}-benz chloride enesulfonamide 121. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-460. 6 MH+ thiazol-5-yl]- (4-methyl-pyridin- {3- [5- (4-methyl- 3-yl) -methanone; hydrochloride pyridine-3-carbonyl)- and 2-Methoxy-5-thiazol-2-ylamino]- methylphenylsulfonyl chloride propyl}- benzenesulfonamide 122. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-461. 6 MH+ thiazol-5-yl]- (3-methyl-pyrazin- {3- [5- (3-methyl- 2-yl) -methanone; hydrochloride pyrazine-2-carbonyl)- and 2-Methoxy-5-thiazol-2-ylamino]- methylphenylsulfonyl chloride propyl}- benzenesulfonamide 123. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-465. 6 MH+ thiazol-5-yl]- (3-methyl-thiophen- {3- [5- (3-methyl- 2-yl) -methanone; hydrochloride thiophene-2-carbonyl)- and 2-Methoxy-5-thiazol-2-ylamino]-pr methylphenylsulfonyl chloride opyl}- benzenesulfonamide Ex. Educts Name Mass analysis 124. [2- (3-Amino-propylamino)- 1- (4-Methoxy-phenyl)-3- 425. 5 MH+ thiazol-5-yl]- (4-methyl-pyridin- {3- [5- (4-methyl- 3-yl) -methanone; hydrochloride pyridine-3-carbonyl)- and 4-Methoxyphenylsulfonyl thiazol-2-ylamino]- chloride propyl}-urea 125. 3-Bromo-l-o-tolyl-propane-1, 2- {3- [4- (2-Methyl- 376. 5 MH+ dione and (3-thioureido-propyl) benzoyl)-thiazol-2- carbamic acid tert-butyl ester ylamino]-propyl}- carbamic acid tert-butyl ester 126. [2- (3-Amino-propylamino)- N- {3- [4- (2-Methyl- 380. 4 MH+ thiazol-4-yl] -o-tolyl-methanone; benzoyl) -thiazol-2- hydrochloride and benzoyl ylamino]-propyl}- chloride benzamide 127. [2- (3-Amino-propylamino)- 2-Fluoro-N- {3- [4- (2- 398. 4 MH+ thiazol-4-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 2-2-ylamino]-propyl}- Fluorobenzoyl chloride benzamide 128. [2- (3-Amino-propylamino)- 3, 5-Dimethoxy-N- {3- [4-440. 5 MH+ thiazol-4-yl]-o-tolyl-methanone ; (2-methyl-benzoyl)- hydrochloride and 3, 5- thiazol-2-ylamino]- dimethoxybenzoyl chloride propyl}-benzamide 129. [2- (3-Amino-propylamino)- Pentanoic acid {3- [4- (2- 360. 3 MH+ thiazol-4-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and pentanoyl 2-ylamino]-propyl}- chloride amide 130. [2-(3-Amino-propylamino)-1-{3- [4-(2-Methyl-401. 5 MH+ thiazol-4-yl] -o-tolyl-methanone; benzoyl) -thiazol-2- hydrochloride and 2-thiophene ylamino]-propyl}-3- isocyanate thiophen-2-yl-urea Ex. Educts Name Mass analysis 131. [2- (3-Amino-propylamino)- 1- (2-Fluoro-phenyl)-3- 413. 3 MH+ thiazol-4-yl] -o-tolyl-methanone; {3- [4- (2-methyl- hydrochloride and 2-fluorophenyl benzoyl) -thiazol-2- isocyanate ylamino]-propyl}-urea 132. [2-(3-Amino-propylamino)-2-Methyl-N- {3- [4- (2- 430. 5 MH+ thiazol-4-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 2-2-ylamino]-propyl}- methylbenzenesulfonyl chloride benzenesulfonamide 133. [2- (3-Amino-propylamino)- 4-Fluoro-N- {3- [4- (2- 434. 4 MH+ thiazol-4-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 4-2-ylamino]-propyl}- fluorobenzenesulfonyl chloride benzenesulfonamide 134. [2- (3-Amino-propylamino)- 3-Methoxy-N- {3- [4- (2- 446. 3 MH+ thiazol-4-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and and 3-2-ylamino]-propyl}- methoxybenzenesulfonyl chloride benzenesulfonamide 135. [2- (3-Amino-propylamino)- 4-Methoxy-N- {3- [4- (2- 446. 3 MH+ thiazol-4-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 3-2-ylamino]-propyl}- methoxybenzenesulfonyl chloride benzenesulfonamide 136. [2- (3-Amino-propylamino)- N- {3- [4- (2-Methyl- 416. 3 MH+ thiazol-4-yl] -o-tolyl-methanone; benzoyl) -thiazol-2- hydrochloride and ylamino]-propyl}- benzenesulfonyl chloride benzenesulfonamide 137. [2- (3-Amino-propylamino)- 2-Chloro-N- {3- [4- (2- 518. 1 MH+ thiazol-4-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2-chloro-5-2-ylamino]-propyl}-5- (trifluormethyl) benzenesulfonyl trifluoromethyl- chloride benzenesulfonamide Ex. Educts Name Mass analysis 138. [2- (3-Amino-propylamino)- Thiophene-2-sulfonic 422. 3 MH+ thiazol-4-yl] -o-tolyl-methanone; acid {3- [4- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenesulfonyl chloride ylamino]-propyl}-amide 139. [2- (3-Amino-propylamino)- 3-Fluoro-N- {3- [4- (2- 434. 4 MH+ thiazol-4-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 3-2-ylamino]-propyl}- fluorobenzenesulfonyl chloride benzenesulfonamide 140. [2- (3-Amino-propylamino)- 2-Methoxy-5-methyl-N-460. 5 MH+ thiazol-4-yl] -o-tolyl-methanone; {3- [4- (2-methyl- hydrochloride and and 6-benzoyl)-thiazol-2- methoxy-m-toluenesulfonyl ylamino]-propyl}- chloride benzene sulfonamide 141. [2- (3-Amino-propylamino)- 2, 5-Dimethoxy-N- {3- [4- 476. 2 MH+ thiazol-4-yl]-o-tolyl-methanone ; (2-methyl-benzoyl)- hydrochloride and 2, 5- thiazol-2-ylamino]- dimethoxybenzenesulfonyl propyl}-benzenesulfo chloride namide 142. [2- (5-Amino-pentylamino)- 2-Fluoro-N- {5- [5- 447. 2 (M-H+)- thiazol-5-yl] -pyridin-2-yl- (pyridine-2-carbonyl)- methanone; hydrochloride and 2-thiazol-2-ylamino]- fluorobenzenesulfonyl chloride pentyl}- benzenesulfonamide 143. [2- (5-Amino-pentylamino)- 4-Methoxy-N- {5- [5- 459. 3 (M-H+)- thiazol-5-yl]-pyridin-2-yl- (pyridine-2-carbonyl) - methanone; hydrochloride and thiazol-2-ylamino]- benzenesulfonyl chloride pentyl}-benzenesulfon amide Ex. Educts Name Mass analysis 144. [2- (5-Amino-pentylamino)- Thiophene-2-sulfonic 435.3 (M-H+)- thiazol-5-yl]-pyridin-2-yl-acid {5- [5- (pyridine-2- methanone; hydrochloride and 2-carbonyl)-thiazol-2- thiophenesulfonyl chloride ylamino]-pentyl}-amide 145. [2- (5-Amino-pentylamino)- 2-Methoxy-5-methyl-N-473. 2 (M-H+)- thiazol-5-yl]-pyridin-2-yl- {5- [5- (pyridine-2- methanone; hydrochloride and 6-carbonyl)-thiazol-2- methoxy-m-toluenesulfonyl ylamino]-pentyl}-benz chloride enesulfonamide 146. [2- (5-Amino-pentylamino)- 4-Fluoro-N- {5- [5- 447. 3 (M-H+)- thiazol-5-yl] -pyridin-2-yl- (pyridine-2-carbonyl)- methanone; hydrochloride and 4-thiazol-2-ylamino]- fluorobenzenesulfonyl chloride pentyl}-benzenesulfona mide 147. [2- (5-Amino-pentylamino)- 2-Methyl-N- {5- [5- 443. 3 (M-H+)- thiazol-5-yl]-pyridin-2-yl- (pyridine-2-carbonyl) - methanone; hydrochloride and 2-thiazol-2-ylamino]- methyl benzenesulfonyl chloride pentyl}-benzenesulfona mide 148. [2- (5-Amino-pentylamino)- 3-Fluoro-N- {5- [5- 447. 2 (M-H+)- thiazol-5-yl] -pyridin-2-yl- (pyridine-2-carbonyl)- methanone; hydrochloride and 3-thiazol-2-ylamino]- fluoro benzenesulfonyl chloride pentyl}- benzenesulfonamide Ex. Educts Name Mass analysis 149. [2- (5-Amino-pentylamino)- 2-Chloro-N- {5- [5- 531. 1 (M-H+)- thiazol-5-yl] -pyridin-2-yl- (pyridine-2-carbonyl)- methanone; hydrochloride and 2-thiazol-2-ylamino]- chloro-5-pentyl}-5-trifluoromet (trifluoromethyl) benzenesulfonyl hyl-benzenesulfonamide chloride 150. [2- (5-Amino-pentylamino)- N- {5- [5- (Pyridine-2- 429. 4 (M-H+)- thiazol-5-yl]-pyridin-2-yl-carbonyl)-thiazol-2- methanone; hydrochloride and ylamino]-pentyl}- benzenesulfonyl chloride benzenesulfonamide 151. [2- (5-Amino-pentylamino)- 3-Methoxy-N- {5- [5- 459. 3 (M-H+)- thiazol-5-yl]-pyridin-2-yl- (pyridine-2-carbonyl)- methanone; hydrochloride and 3-thiazol-2-ylamino]- methoxy benzenesulfonyl chloride pentyl}-benzenesulfon amide 152. [2- (5-Amino-pentylamino)- 2-Fluoro-N- {5- [5- 447. 2 (M-H+)- thiazol-5-yl]-pyridin-4-yl- (pyridine-4-carbonyl) - methanone; hydrochloride and 2-thiazol-2-ylamino]- fluoro benzenesulfonyl chloride pentyl}-benzenesulfona mide 153. [2- (5-Amino-pentylamino)- 2-Methoxy-5-methyl-N-473. 1 (M-H+)- thiazol-5-yl]-pyridin-4-yl- {5- [5-(pyridine-4- methanone; hydrochloride and 6-carbonyl)-thiazol-2- methoxy-m-toluenesulfonyl ylamino]-pentyl}-benz chloride enesulfonamide 154. [2- (5-Amino-pentylamino)- 2-Fluoro-N- {5- [5- (2- 460. 4 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2-fluoro 2-ylamino]-pentyl}- benzenesulfonyl chloride benzenesulfonamide Ex. Educts Name Mass analysis 155. [2- (5-Amino-pentylamino)- 4-Methoxy-N- {5- [5- (2- 472. 1 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 4-methoxy 2-ylamino]-pentyl}- benzenesulfonyl chloride benzenesulfonamide 156. [2- (5-Amino-pentylamino)- Thiophene-2-sulfonic 448.2 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; acid {5- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenesulfonyl chloride ylamino]-pentyl}-amide 157. [2- (5-Amino-pentylamino)- 2-Methoxy-5-methyl-N-486. 3 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; {5- [5- (2-methyl- hydrochloride and 6-methoxy-m-benzoyl)-thiazol-2- toluenesulfonyl chloride ylamino]-pentyl}- benzene sulfonamide 158. [2- (5-Amino-pentylamino)- 4-Fluoro-N- {5- [5- (2- 460. 4 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 4-fluoro 2-ylamino]-pentyl}- benzenesulfonyl chloride benzenesulfonamide 159. [2- (5-Amino-pentylamino)- 2-Methyl-N-15- [5- (2- 456. 4 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2-methyl 2-ylamino]-pentyl}- benzenesulfonyl chloride benzenesulfonamide 160. [2- (5-Amino-pentylamino)- 3-Fluoro-N- {5- [5- (2- 460. 3 (M-H+)- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 3-2-ylamino]-pentyl}- fluorobenzenesulfonyl chloride benzenesulfonamide 161. [2- (5-Amino-pentylamino)- 2-Chloro-N- {5- [5- (2- 544. 1 (M-H+)- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 2-chloro-5-2-ylamino]-pentyl}-5- (trifluoromethyl) benzenesulfonyl trifluoromethyl- chloride benzenesulfonamide Ex. Educts Name Mass analysis 162. [2- (5-Amino-pentylamino)- N- {5- [5- (2-Methyl- 442. 3 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; benzoyl) -thiazol-2- hydrochloride and ylamino]-pentyl}- benzenesulfonyl chloride benzenesulfonamide 163. [2- (5-Amino-pentylamino)- 3-Methoxy-N- {5- [5- (2- 472. 1 (M-H+)- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl)-thiazol- hydrochloride and 3-2-ylamino]-pentyl}- methoxybenzenesulfonyl chloride benzenesulfonamide 164. [2- (5-Amino-pentylamino)- N- {5- [5- (2-Chloro- 480. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-pentyl}-2- fluorobenzenesulfonyl chloride fluoro- benzenesulfonamide 165. [2- (5-Amino-pentylamino)- N- {5- [5- (2-Chloro- 492. 2 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-pentyl}-4- methoxybenzenesulfonyl chloride methoxy- benzenesulfonamide 166. [2- (5-Amino-pentylamino)- Thiophene-2-sulfonic 468.1 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- acid {5- [5- (2-chloro- methanone; hydrochloride and 2 benzoyl)-thiazol-2- thiophenesulfonyl chloride ylamino]-pentyl}-amide 167. [2- (5-Amino-pentylamino)- N- {5- [5- (2-Chloro- 506. 2 (M-H+)- thiazol-5-yl] - (2-chloro-phenyl)-benzoyl)-thiazol-2- methanone; hydrochloride and 6-ylamino]-pentyl}-2- methoxy-m-toluenesulfonyl methoxy-5-methyl- chloride benzene sulfonamide Ex. Educts Name Mass analysis 168. [2- (5-Amino-pentylamino)- N-15- [5- (2-Chloro- 480. 3 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 4-ylamino]-pentyl}-4- fluorobenzenesulphonyl chloride fluoro- benzenesulfonamide 169. [2- (5-Amino-pentylamino)- N- {5- [5- (2-Chloro- 476. 2 (M-H+)- thiazol-5-yl] - (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 2-ylamino]-pentyl}-2- methylbenzenesulphonyl chloride methyl- benzenesulfonamide 170. [2- (5-Amino-pentylamino)- N- {5- [5- (2-Chloro- 480. 3 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- benzoyl)-thiazol-2- methanone; hydrochloride and 3-ylamino]-pentyl}-3- fluorobenzenesulphonyl chloride fluoro- benzenesulfonamide 171. [2- (5-Amino-pentylamino)- 2-Chloro-N- {5- [5- (2- 564. 0 (M-H+)- thiazol-5-yl]- (2-chloro-phenyl)- chloro-benzoyl)-thiazol- methanone; hydrochloride and 2-2-ylamino]-pentyl}-5- chloro-5-trifluoromethyl- (trifluoromethyl) benzenesulfonyl benzenesulfonamide chloride 172. [2- (5-Amino-pentylamino)-4- N- {5- [4-Methyl-5- (2- 458. 1 MH+ methyl-thiazol-5-yl]-o-tolyl-methyl-benzoyl)-thiazol- methanone hydrochloride and 2-ylamino]-pentyl}- benzenelsulphonyl chloride benzenesulfonamide 173. [2-(5-Amino-pentylamino)-4-2-Methyl-N- {5- [4-472. 3 MH+ methyl-thiazol-5-yl]-o-tolyl-methyl-5- (2-methyl- methanone hydrochloride and 2-benzoyl)-thiazol-2- methybenzenelsulphonyl chloride ylamino]-pentyl}- benzenes ulfonamide Ex. Educts Name Mass analysis 174. [2- (5-Amino-pentylamino)-4- 2-Fluoro-N- {5- [4- 476. 3 MH+ methyl-thiazol-5-yl]-o-tolyl-methyl-5- (2-methyl- methanone hydrochloride and 2-benzoyl)-thiazol-2- fluorobenzenesulphonyl chloride ylamino]-pentyl}- benzenes ulfonamide 175.. [2- (5-Amino-pentylamino)-4- 3-Fluoro-N- {5- [4- 476. 2 MH+ methyl-thiazol-5-yl]-o-tolyl-methyl-5- (2-methyl- methanone hydrochloride and 3-benzoyl)-thiazol-2- fluorobenzenesulphonyl chloride ylamino]-pentyl}- benzenes ulfonamide 176. [2- (5-Amino-pentylamino)-4- 4-Fluoro-N- {5- [4- 476. 2 MH+ methyl-thiazol-5-yl]-o-tolyl-methyl-5- (2-methyl- methanone hydrochloride and 4-benzoyl)-thiazol-2- fluorobenzenesulphonyl chloride ylamino]-pentyl}- benzenes ulfonamide 177. [2- (5-Amino-pentylamino)-4- 2-Methoxy-5-methyl-N-502. 3 MH+ methyl-thiazol-5-yl]-o-tolyl- {5- [4-methyl-5- (2- methanone hydrochloride and 6-methyl-benzoyl)-thiazol- methoxy-m-toluenesulfonyl 2-ylamino]-pentyl}- chloride benzenesulfonamide 178. [2- (5-Amino-pentylamino)-4- 3-Methoxy-N- {5- [4- 488. 3 MH+ methyl-thiazol-5-yl]-o-tolyl-methyl-5- (2-methyl- methanone hydrochloride and 3-benzoyl)-thiazol-2- methoxybenzenesulfonyl chloride ylamino]-pentyl}- benzene sulfonamide 179. [2- (5-Amino-pentylamino)-4- 4-Methoxy-N- {5- [4- 488. 3 MH+ methyl-thiazol-5-yl]-o-tolyl-methyl-5- (2-methyl- methanone hydrochloride and 4-benzoyl)-thiazol-2- methoxybenzenesulfonyl chloride ylamino]-pentyl}- benzene sulfonamide Ex. Educts Name Mass analysis 180. [2- (2-Amino-ethylamino)- Thiophene-2-sulfonic 406.2 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; acid {2- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenylsulfonyl chloride ylamino]-ethyl}-amide 181. [2- (2-Amino-propylamino)- 2, 5-Dimethoxy-N- {3- [5- 474. 1 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; (2-methyl-benzoyl)- hydrochloride and 2, 5- thiazol-2-ylamino]- dimethoxyphenylsulfonyl chloride propyl}- benzenesulfonamide 182. [2- (2-Amino-butylamino)- Thiophene-3-sulfonic 434.2 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; acid {4- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenylsulfonyl chloride ylamino]-butyl}-amide 183. [2- (5-Amino-pentylamino)- 2, 5-Dimethoxy-N- {5- [5-502. 0 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; (2-methyl-benzoyl)- hydrochloride and 2, 5- thiazol-2-ylamino]- dimethoxyphenylsulfonyl chloride pentyl}- benzenesulfonamide 184. [2- (2-Amino-ethylamino)- Thiophene-3-sulfonic 406.2 [M-H]- thiazol-5-yl] -o-tolyl-methanone; acid {2- [5- (2-methyl- hydrochloride and 3-benzoyl)-thiazol-2- thiophenylsulfonyl chloride ylamino]-ethyl}-amide 185. [2- (2-Amino-propylamino)- 2, 5-Dimethyl-N- {3- [5- 442. 2 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; (2-methyl-benzoyl)- hydrochloride and 2, 5- thiazol-2-ylamino]- dimethylphenylsulfonyl chloride propyl}- benzenesulfonamide Ex. Educts Name Mass analysis 186. [2- (2-Amino-propylamino)- 5-Chloro-2-methoxy-N-478. 0 [M-H]- thiazol-5-yl] -o-tolyl-methanone; {3- [5- (2-methyl- hydrochloride and 2-chloro-5-benzoyl)-thiazol-2- methoxyphenylsulfonyl chloride ylamino]-propyl}- benzenesulfonamide 187. [2- (2-Amino-butylamino)- 2-Methyl-N- {4- [5- (2- 442. 2 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 2-2-ylamino]-butyl}- methylbenzenesulfonyl chloride benzenesulfonamide 188. [2- (2-Amino-butylamino)- 5-Fluoro-2-methyl-N- {4- 460. 2 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; [5- (2-methyl-benzoyl)- hydrochloride and 2-methyl-5-thiazol-2-ylamino]- fluoro-benzenesulfonyl chloride butyl}- benzenesulfonamide 189. [2- (2-Amino-butylamino)- 2-Chloro-N- {4- [5- (2- 530. 0 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 2-chloro-5-2-ylamino]-butyl}-5- trifluoromethyl-benzenesulfonyl trifluoromethyl- chloride benzenesulfonamide 190. [2- (2-Amino-pentylamino)- 2, 5-Dimethyl-N- {5- [5- 470. 2 [M-H]- thiazol-5-yl] -o-tolyl-methanone; (2-methyl-benzoyl) - hydrochloride and 2, 5- thiazol-2-ylamino]- dimethylphenylsulfonyl chloride pentyl}- benzenesulfonamide 191. [2- (2-Amino-propylamino)- N- {3- [5- (2-Methyl- 498. 0 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; benzoyl)-thiazol-2- hydrochloride and 4-ylamino]-propyl}-4- trifluoromethyloxyphenylsulfonyl trifluoromethoxy- chloride benzenesulfonamide Ex. Educts Name Mass analysis 192. [2- (2-Amino-butylamino)- 4-Fluoro-N- {4- [5- (2- 446. 2 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 4-2-ylamino]-butyl}- fluorophenylsulfonyl chloride benzenesulfonamide 193. [2- (2-Amino-butylamino)- 2, 4-Difluoro-N- {4- [5- (2- 464. 1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2, 4- 2-ylamino]-butyl}- difluorophenylsulfonyl chloride benzenesulfonamide 194. [2- (2-Amino-pentylamino)- N- {5- [5- (2-Methyl- 525. 9 [M-H]- thiazol-5-yl] -o-tolyl-methanone; benzoyl) -thiazol-2- hydrochloride and 4-ylamino]-pentyl}-4- trifluoromethyloxyphenylsulfonyl trifluoromethoxy- chloride benzenesulfonamide 195. [2- (2-Amino-propyIamino)- 2-Chloro-N- {3- [5- (2- 516. 0 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2-chloro-5-2-ylamino]-propyl}-4- trifluoromethyl-benzenesulfonyl trifluoromethyl- chloride benzenesulfonamide 196. [2- (2-Amino-butylamino)- 2-Fluoro-N- {4- [5- (2- 446. 1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2-2-ylamino]-butyl}- fluorophenylsulfonyl chloride benzenesulfonamide 197. [2- (2-Amino-butylamino)- 5-Chloro-thiophene-2-468. 0 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; sulfonic acid {4- [5- (2- hydrochloride and 5-methyl-benzoyl)-thiazol- chlorothiophenyl-2-2-ylamino]-butyl}-amide sulfonylchloride Ex. Educts Name Mass analysis 198. [2- (2-Amino-pentylamino)- 2-Chloro-N- {5- [5- (2- 544. 0 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 2-chloro-5-2-ylamino]-pentyl}-4- trifluoromethyl-benzenesulfonyl trifluoromethyl- chloride benzenesulfonamide 199. [2- (2-Amino-propylamino)- Thiophene-3-sulfonic 420.1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; acid {3- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenesulfonylchloride ylamino]-propyl}-amide 200. [2- (2-Amino-propylamino)- 5-Fluoro-2-methyl-N-f3-446. 2 [M-H]- thiazol-5-yl] -o-tolyl-methanone; [5- (2-methyl-benzoyl)- hydrochloride and 2-methyl-5-thiazol-2-ylamino]- fluorobenzenesulfonylchloride propyl}- benzenesulfonamide 201. [2- (2-Amino-butylamino)- 3-Fluoro-N- {4- [5- (2- 446. 1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 3-2-ylamino]-butyl}- fluorophenylsulfonyl chloride benzenesulfonamide 202. [2- (2-Amino-butylamino)- 2-Methoxy-5-methyl-N-475. 1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; {4- [5- (2-methyl- hydrochloride and 2-methoxy-5-benzoyl)-thiazol-2- methylphenylsulfonyl chloride ylamino]-butyl}- benzenesulfonamide 203. [2- (2-Amino-pentylamino)- Thiophene-3-sulfonic 448.1 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; acid {5- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenesulfonylchloride ylamino]-pentyl}-amide Ex. Educts Name Mass analysis 204. [2- (2-Amino-pentylamino)- 5-Fluoro-2-methyl-N- {5- 474. 1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; [5- (2-methyl-benzoyl)- hydrochloride and 2-methyl-5-thiazol-2-ylamino]- fluorophenylsulfonyl chloride pentyl}- benzenesulfonamide 205. [2-(2-Amino-ethylamino)-5-Chloro-2-methoxy-N-464. 0 [M-H]- thiazol-5-yl] -o-tolyl-methanone; {2- [5- (2-methyl- hydrochloride and 2-methoxy-5-benzoyl)-thiazol-2- chlorophenylsulfonyl chloride ylamino]-ethyl}- benzenesulfonamide 206. [2- (2-Amino-propylamino)- 2, 4-Difluoro-N- {3- [5- (2- 450. 2 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2, 4-2-ylamino]-propyl}- difluorophenylsulfonyl chloride benzenesulfonamide 207. [2- (2-Amino-butylamino)-2, 5-Dimethyl-N- {4- [5-456. 3 [M-H]- thiazol-5-yl] -o-tolyl-methanone; (2-methyl-benzoyl) - hydrochloride and 2, 5- thiazol-2-ylamino]- dimethylphenylsulfonyl chloride butyl}- benzenesulfonamide 208. [2- (2-Amino-butylamino)- 2, 5-Dimethoxy-N- {4- [5- 488. 1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; (2-methyl-benzoyl) - hydrochloride and 2, 5- thiazol-2-ylamino]- dimethoxyphenylsulfonyl chloride butyl}- benzenesulfonamide 209. [2- (2-Amino-pentylamino)- 2, 4-Difluoro-N- {5- [5- (2- 478. 1 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 2, 4- 2-ylamino]-pentyl}- difluorophenylsulfonylchloride benzenesulfonamide Ex. Educts Name Mass analysis 210. [2- (2-Amino-propylamino)- 5-Chloro-thiophene-2-454. 2 [M-H)- thiazol-5-yl] -o-tolyl-methanone; sulfonic acid {3- [5- (2- hydrochloride and 5-methyl-benzoyl)-thiazol- chlorothiophenyl-2-2-ylamino]-propyl}- sulfonylchloride amide 211. [2- (2-Amino-butylamino)- 4-Methoxy-N- {4- [5- (2- 458. 2 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; methyl-benzoyl)-thiazol- hydrochloride and 4-2-ylamino]-butyl}- methoxyphenylsulfonylchloride benzenesulfonamide 212. [2- (2-Amino-butylamino)- 5-Chloro-2-methoxy-N-492. 0 [M-H]- thiazol-5-yl] -o-tolyl-methanone; {4- [5- (2-methyl- hydrochloride and 2-methoxy-5-benzoyl)-thiazol-2- chlorophenylsulfonylchloride ylamino]-butyl}- benzenesulfonamide 213. [2- (2-Amino-pentylamino)- 5-Chloro-thiophene-2-482. 1 [M-H]- thiazol-5-yl]-o-tolyl-methanone ; sulfonic acid {5- [5- (2- hydrochloride and 5-methyl-benzoyl)-thiazol- chlorothiophenyl-2-2-ylamino]-pentyl}- sulfonylchloride amide 214. [2- (2-Amino-butylamino)- Thiophene-2-sulfonic 434.2 [M-H] - thiazol-5-yl] -o-tolyl-methanone; acid {4- [5- (2-methyl- hydrochloride and 2-benzoyl)-thiazol-2- thiophenylsulfonyl chloride ylamino]-butyl}-amide 215. [2- (2-Amino-butylamino)- 3-Methoxy-N- {4- [5- (2- 458. 2 [M-H]- thiazol-5-yl] -o-tolyl-methanone; methyl-benzoyl) -thiazol- hydrochloride and 3-methoxy-2-ylamino]-butyl}- phenylsulfonylchloride benzenesulfonamide Ex. Educts Name Mass analysis 216. [2- (2-Amino-butylamino)- N- {4- [5- (2-Methyl- 512. 1 [M-H]- thiazol-5-yl]-o-tolyl=methanone ; benzoyl)-thiazol-2- hydrochloride and 4-ylamino]-butyl}-4- trifluoromethyloxy-trifluoromethoxy- phenylsulfonylchloride benzenesulfonamide 217.. [2- (3-Methylamino- Thiophene-2-sulfonic 434.2 [M-H]- propylamino) -thiazol-5-yl]-o-acid methyl- {3- [5- (2- tolyl-methanone ; hydrochloride methyl-benzoyl)-thiazol- and 2-thiophenylsulfonyl chloride 2-ylamino]-propyl}- amide 218. [2- (3-Methylamino- 3-Methoxy-N-methyl-N-458. 2 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 3-methoxyphenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide 219. [2- (3-Methylamino- 2-Chloro-N-methyl-N-530. 0 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 2-chloro-4-ylamino]-propyl}-4- trifluoromethylphenylsulfonyl trifluoromethyl- chloride benzenesulfonamide 220. [2- (3-Methylamino- 2, N-Dimethyl-N- {3- [5- 442. 2 [M-H]- propylamino) -thiazol-5-yl] -o- (2-methyl-benzoyl)- tolyl-methanone ; hydrochloride thiazol-2-ylamino]- and 2-methylphenylsulfonyl propyl}- chloride benzenesulfonamide 221. [2- (3-Methylamino- 5-Fluoro-2, N-dimethyl- 460. 2 [M-H]- propylamino)-thiazol-5-yl]-o-N- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 2-methyl-5-ylamino]-propyl}- fluorophenylsulfonyl chloride benzenesulfonamide Ex. Educts Name Mass analysis 222. [2- (3-Methylamino- 2-Chloro-N-methyl-N-530. 0 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 2-chloro-5-ylamino]-propyl}-5- trifluoromethylphenylsulfonyl trifluoromethyl- chloride benzenesulfonamide 223. [2- (3-Methylamino- 4-Fluoro-N-methyl-N-446. 1 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 4-fluorophenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide 224. [2- (3-Methylamino- 2, 4-Difluoro-N-methyl- 464. 3 [M-H]- propylamino)-thiazol-5-yl]-o-N- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 2, 4-difluorophenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide 225. [2- (3-Methylamino- 2-Fluoro-N-methyl-N-446. 1 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 2-fluorophenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide 226. [2- (3-Methylamino- 5-Chloro-thiophene-2-468. 0 [M-H]- propylamino)-thiazol-5-yl]-o-sulfonic acid methyl- {3- tolyl-methanone; hydrochloride [5- (2-methyl-benzoyl)- and 5-chlorothiophenyl-2-thiazol-2-ylamino]- sulfonylchloride propyl}-amide 227. [2- (3-Methylamino- 3-Fluoro-N-methyl-N-446. 1 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone ; hydrochloride benzoyl)-thiazol-2- and 3-fluorophenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide Ex. Educts Name Mass analysis 228. [2- (3-Methylamino- 2-Methoxy-5, N- 472. 1 [M-H]- propylamino)-thiazol-5-yl]-o-dimethyl-N- {3- [5- (2- tolyl-methanone; hydrochloride methyl-benzoyl)-thiazol- and 2-methoxy-5-2-ylamino]-propyl}- methylphenylsulfonyl chloride benzenesulfonamide 229. [2- (3-Methylamino- 4-Chloro-N-methyl-N-462. 1 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 4-chlorophenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide 230. [2- (3-Methylamino- 2, 5, N-Trimethyl-N- {3- 456. 3 [M-H]- propylamino) -thiazol-5-yl] -o- [5- (2-methyl-benzoyl)- tolyl-methanone; hydrochloride thiazol-2-ylamino]- and 2,5-methylphenylsulfonyl propyl}- chloride benzenesulfonamide 231. [2- (3-Methylamino- N-Methyl-N- {3- [5- (2- 472. 9 [M-H]- propylamino)-thiazol-5-yl]-o-methyl-benzoyl)-thiazol- tolyl-methanone; hydrochloride 2-ylamino]-propyl}-4- and 4-nitrophenylsulfonyl nitro- chloride benzenesulfonamide 232. [2- (3-Methylamino- 4-Methoxy-N-methyl-N-458. 2 [M-H]- propylamino)-thiazol-5-yl]-o- {3- [5- (2-methyl- tolyl-methanone; hydrochloride benzoyl)-thiazol-2- and 4-methoxyphenylsulfonyl ylamino]-propyl}- chloride benzenesulfonamide 233. [2- (3-Methylamino- 5-Chloro-2-methoxy-N-492. 1 [M-H]- propylamino)-thiazol-5-yl]-o-methyl-N- {3- [5- (2- tolyl-methanone; hydrochloride methyl-benzoyl)-thiazol- and 2-methoxy-5-2-ylamino)-propyl}- chlorophenylsulfonyl chloride benzenesulfonamide

Example A A compound of formula I can be used in a manner known per se as the active ingredient for the production of tablets of the following composition: Per tablet Active ingredient 200 mg Microcrystalline cellulose 155 mg Corn starch 25 mg Talc 25 mg Hydroxypropylmethylcellulose 20 mg 425 mg Example B A compound of formula I can be used in a manner known per se as the active ingredient for the production of capsules of the following composition: Per capsule Active ingredient 100.0 mg Corn starch 20.0 mg Lactose 95.0 mg Talc 4.5 mg Magnesium stearate 0.5 mg 220.0 mg

Example C Tablets containing the following ingredients can be manufactured in a conventional manner: Ingredients Per tablet Compound of formula I 10.0-100. 0 mg Lactose 125.0 mg Maize starch 75.0 mg Talc 4.0 mg Magnesium stearate 1.0 mg

Example D Capsules containing the following ingredients can be manufactured in a conventional manner: Ingredients Per capsule Compound of formula I 25.0 mg Lactose 150.0 mg Maize starch 20.0 mg Talc 5.0 mg

Example E Injection solutions can have the following composition: Compound of formula I 3.0 mg Gelatine 150.0 mg Phenol 4.7 mg Water for injection solutions ad 1.0 ml