Title of Invention

IMIDAZO PYRIDINE DERIVATIVES WHICH INHIBIT GASTRIC ACID SECRETION

Abstract

A compound of the formula I I or a pharmaceutically acceptable salt thereof/wherein 'Ri is (a) H, (b) CH3, or (c) CH2OH; R2 is (a) CH3, or (b) CH2CH3; R3is (a) H, (b) C1C6 alkyl, (c) hydroxylated C1C6 alkyl, or (d) halogen; R4is (a) H, (b) C1C6 alkyl, (c) hydroxylated C1C6 alkyl, or (d) halogen; RSis (a) H, or 42 (b) halogen; R6 and R7 are independently selected substituents, comprising C, H,N, O, S, Se, P or Halogen atoms, which give compounds of Formula I a molecular weight<600, provided that at least one of R6 and R7 can not be H, C1C6. alkyl, hydroxylated C1C6 alkyl, or C1C6 alkoxy-substituted C1C6 alkyl, and Xis (a) NH, or (b)O.

Full Text

FORM 2 THE PATENTS ACT 1970 [39 OF 1970] COMPLETE SPECIFICATION [See Section 10] "IMIDAZO PYRIDINE DERIVATIVES WHICH INHIBIT GASTRIC ACID SECRETION" ASTRAZENECA AB, a Swedish company, of S-151 85 Sodertalje, SWEDEN, The following specification particularly describes the nature of the invention and the manner in which it is to be performed:- GRANTED 28-11-2005 1 TECHNICAL FIELD The present invention relates to novel compounds, and pharmaceuticaUy acceptable salts thereof, which inhibit exogenously or endogenously stimulated gastric acid secretion and thus can be used in the prevention and treatment of gastrointestinal inflammatory diseases. In further aspects, the invention relates to compounds of the invention for use in therapy; to processes for preparation of such new compounds; to pharmaceutical compositions containing at least one compound of the invention, or a pharmaceuticaUy acceptable salt thereof, as active ingredient; and to the use of the active compounds in the manufacture of medicaments for the medical use indicated above. The invention also relates to new intermediates for in the preparation of the novel compounds. The application has a co-pending application number IN/PCT/2000, 00496/MUM. BACKGROUND ART Substituted imidazo[l,2-a]pyridines, useful in the treatment of peptic ulcer diseases, are known in the art, e.g. from EP-B-0033094 and US 4,450,164 (Schering Corporation); from EP-B-0204285 and US 4,725,601 (Fujisawa Pharmaceutical Co.); and from pubhcations by J.J. Kaminski et al. in the Journal of Medical Chemistry (vol. 28,876-892,1985; vol. 30,2031-2046,1987; vol. 30, 2047-2051,1987; vol. 32,1686-1700,1989; and vol. 34,533-541,1991). For a review of the pharmacology of the gastric acid pump (the H+, K+-ATPase), see Sachs et al. (1995) Annu. Rev. Pharmacol. Toxicol. 35:277-305. DISCLOSURE OF THE INVENTION It has surprisingly been found that compounds of the Formula I, which are imidazo pyridine derivatives in which the phenyl moiety is substituted, and in which the imidazo pyridine moiety is substituted with a carboxamide group in 6-position are particularly 2 effective as inhibitors of the gastrointestinal H+t K+-ATPase and thereby as inhibitors of gastric acid secretion. The carboxamide group in 6-position is optionally selected to give compounds of Formula I a molecular weight In one aspect, the invention thus relates to compounds of the general Formula I or a pharmaceutically acceptable salt thereof, wherein Rl is (a)H, (b) CH3, or (c) CH2OH; R2 IS (a) CH3, or (b) CH2CH3; R3 is (a)H, (b)C,-C6alkyl, (c) hydroxylated C\-C& alkyl, or (d) halogen; 3 (a)H. (b)C1C6 alkyl, (c) hydroxy lated C1C6 alkyl, or (d) halogen; R5is (a)H,or (b) halogen; R6 and R7 are independently selected substituents, comprising C, H, N, O, S , Se , P and Halogen atoms, which give compounds of Formula I a molecular weight ft 1 that at least one of R and R can not be H, C1C6 alky], hydroxylated C1C6 alkyl.or C1C6 , alkoxy-substituted Cj-Cg alkyl, and X is (a) NH, or (b)0. As used herein, the term "C1C6 alkyl" denotes a straight or branched alkyl group having from 1 to 6 carbon atoms. Examples of said C1C6 alkyl include methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, t-butyl and straight- and branched-chain pentyl and hexyl. The term "halogen" includes fluoro, chloro, bromo and iodo. The substitutents R and R are defined as independently selected substituents, comprising C, H, N, O, S , Se , P or Halogen atoms, which give compounds of Formula I a molecular weight 4 Examples of substituents that fall within the scope of this definition includes, but is not limited to, (a) H. (b) C1C6 alkyl, (c) hydroxylated C1C6 alkyl, (d) C1C6 alkoxy-substituted C1C6 alkyl, (e) C2-C6 alkenyl, (f) C2-C6 alkynyl, ( g ) halogenated C1C6 alkyl, (h) C3-C8 cycloalkyl, (i) cycloalkyl-substituted C1C6i alkyl, (j) aryl, in which aryl represents phenyl, pyridyl, thienyl, imidazolyl, indolyl. naphthyl or furanyl, optionally substituted by one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino, C1C6 alkyl-NH-, (C1C6 alkyl)2-N-or CN or NH2S02. (k) aryl substituted C1C6 alkyl, in which aryl represents phenyl, pyridyl, thienyl, imidazolyl, indolyl, naphthyl or furanyl, optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino C1C6 alkyl-NH-, (C1C6 alkyl)2-N- CN or NH2S02, (1) R8-(C1C6) alkyl-, wherein R8 is NH2C=0-, C1C6 alkyl-NHC=0- (C1C6 alkyl)2NC=0-. C1C6 alkyl-OOC- NH2S02-, C1C6 alkyl-S02NH- ArS02NH-, cyano, C,-C6 alkyl-CO-NH- C,-C6 alkyl-OOCNH- C,-C6 alkyl- 0-. C7-C12 alkyl-O- CrC6 alkyl-SO-, C,-C6 alkyl-S-, C1C6 alkyl-SC^,-, C1C6 alkyl-C=0-. NH2- C1C6 alkyl-NH-, (C1C6 alkyl^N- ArCONH-, Ar(C1C6 alkyl)CONH, ArNHS02~, (Ar)7-N-S02- C1C6 alkyl-NHSCb- ArS- ArSO-, ArS02-, ArC=0- NH2CONH- C1C6 alkyl-NHCONH-, (C,-C6 alkyl)2- NCONH-, ArNHCONH- Ar-O-, Ar-NH-, Ar(C1C6 alkyl)N-, (C1C6 alkyl)2NS02-, hydroxylated C1C6 alkyl-O- or morpholinyl; wherein Ar represents phenyl, pyridyl, thienyl, imidazolyl, indolji, naphthyl or furanyl, optionally substituted with one or more substituents selected from halogen, C1C6 alkyl. C1C6 alkoxy, CF3, OH, CN, nitro, amino, C1C6 alkyl-NH-, or C1C6 alkyl^N- 5 (m) C7-C12 . (n) OH, O-C1C6 alkyl, or O-hydroxylated C1C6 alkyl, 9 IQ o) /)~~~ wherein R andR are independently H or C1C6 alkyl, p) R» L(CrC6) alkyl-COO-(C1C6 )alkyl- wherein R! > is HOOC-, C1C6 alkyl-OOC- or an amino carbonyl group with the formula wherein R12, R13 are the same or different H, or C1C6 alkyl R6 and R7, together with the nitrogen atom to which they are attached, form a saturated or unsaturated ring optionally containing one or more further heteroatoms (for example morpholine, piperazine, pyrrolidine, piperidine), optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino C1C6alkyl-NH-, (C1C6 alkyI)2-N- CN ,NH2S02, phenyl NH2CO-, C1C6alkyl-CO-, the ring can be fused with an aromatic ring (such as tetrahydroquinoline); Both the pure enantiomers, racemic mixtures and unequal mixtures of two enantiomers are within the scope of the invention. It should be understood that all the diastereomeric forms possible (pure enantiomers, racemic mixtures and unequal mixtures of two enantiomers) are within the scope of the invention. Also included in the invention are derivatives of the compounds of the Formula I which have the biological function of the compounds of the Formula I, such as prodrugs. It will also be appreciated by those skilled in the art, although derivatives of compounds of formula I may not possess pharmacological activity as such, they may be administered parenterally or orally and thereafter metabolised in the body to form compounds of the invention which are pharmacologically active. Such derivatives may therefore be described 6 as "prodrugs". All prodrugs of compounds of formula I are included within the scope of the invention. Depending on the process conditions the end products of the Formula I are obtained either in neutral or salt form. Both the free base and the salts of these end products are within the scope of the invention. Acid addition salts of the new compounds may in a manner known per se be transformed into the free base using basic agents such as alkali or by ion exchange. The free base obtained may also form salts with organic or inorganic acids. In the preparation of acid addition salts, preferably such acids are used which form suitably pharmaceutically acceptable salts. Examples of such acids are hydrohalogen acids such as hydrochloric acid, sulphuric acid, phosphoric acid, nitric acid, aliphatic, alicyclic, aromatic or heterocyclic carboxyl or sulphonic acids, such as formic acid, acetic acid, propionic acid, succinic acid, glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, ascorbic acid, maleic acid, hydroxymaleic acid, pyruvic acid, p-hydroxybensoic acid, embonic acid, methanesulphonic acid, ethanesulphonic acid, hydroxyethanesulphonic acid, halogenbensenesulphonic acid, toluenesulphonic acid or naphthalenesulphonic acid. Preferred compounds according to the invention are those of the Formula I wherein R' is CH3 or CH2OH; R2 is CH3 or CH2CH3; R3 is CH3 or CH2CH3; R4 is CH3 or CH2CH3; R5 is H, Br, Cl, or F: R6 and R7 are independently (provided that at least one of R6 and R7 can not be H, C1C6 alkyl, hydroxylated C1C66 alkyl or C1C6 alkoxy-substituted C1C6 alkyl): (a)H, (b)C1C6 alkyl, (c) hydroxylated C|-Cg alkyl, (d) C1C6 alkoxy-substituted C1C6 alkyl, (e) C2-C6 alkenyl, (f) C2-C6 alkynyl, 7 ( g) halogenated C1C6 alkyl. (h) C3-C8 cycloalkylv (i) cycloalkyl-substituted C1C6alkyl, (j) aryl, in which aryl represents phenyl, pyridyl, thienyl, imidazolyl, indolyl, naphthyl or furanyl, optionally substituted by one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino, C1C6 alkyl-NH-, (C1C6 alkyl)2-N-, or CN or NH2S02, (k) aryl substituted C1C6 alkyl, in which aryl represents phenyl, pyridyl, thienyl, imidazolyl, indolyl, naphthyl or furanyl, optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH. nitro. amino C1C6 alkyl-NH- (C,-C6 alkyDo-N-. CN or NH2S02, (l)R8-(C1C6) alkyl-, wherein R8 is NH2C=CK C,-C6 alkyl-NHC=0-, (C,-C6 alkyl)2NC=0-, q-Q alkyl-OOC-, NH2S02-, C,-C6alkyl-S02NH-, ArS02NH-, cyano, C,-C6 alkyl-CO-NH- C,-C6 alkyl-OOCNH-, CrC6 alkyl- 0-, C7-C12 alkyl-O- C^Q alkyl-SO-, C1C6alkyl-S-, C,-C6 alkyl-SO,-, C1C6 alkyl-C=0-, NH2-, C,-C6 alkyl-NH-, (C,-C6 alkyl^N- ArCONH-, Ar(C1C6 alkyl)CONH, ArNHSCb-, (Ar)2-N-S02-, C,-C6 alkyl-NHSO,-, ArS-, ArSO-, ArS02-, ArC=0-, NH2C0NH- CrC6 alkyl-NHCONH-, (C,-C6 alky\y±- NCONH-, ArNHCONH-, (C1C6 alkyl)2-N-S02-. Ar-O-, Ar-NH-, Ar(Cj-C6 alkyl)N-, (C,-C6 alkyl)2NS02-, hydroxylated C1-C6 alkyl-O- or morpholinyl; wherein Ar represents phenyl, pyridyl, thienyl, imidazolyl, indoljl. naphthyl or furanyl, optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, CN, nitro, amino, C1C6 alkyl-NH-, or (C1C6 alkyDsN-, (m) C7-C12 - (n) OH, 0-CrC6 alkyl, or O-hydroxylated C^CQ alkyl, 9 10 wherein R and R are independently H or Q-Cg alkyl, £p) R1 '-(C1C6) alkyl-COO-(C1C6) alkyl- wherein R1' is HOOC-, C1C6 alkyl-OOC- or an amino Carbonvl STOLID with the formula 8 "^ N 1.2 R'2 wherein R12, R13 are the same or different H, or C1C6 alkyl R6 and R7, together with the nitrogen atom to which they are attached, form a saturated or unsaturated ring optionally containing one or more further heteroatoms (for example morpholine, piperazine, pyrrolidine, piperidine), optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino C1C6 alkyl-NH-, (C1C6 alkyl^-N-, CN ,NH2S02, phenyl. NH2CO-, C1C6 alkyl-CO-, the ring can be fused with an aromatic ring (such as tetrahydroquinoline); More preferred compounds according to the invention are those of the Formula I wherein R' is CH3 or CH2OH: R2 is CH3, R3 is CH3 or CH2CH3; R4 is CH3 or CH2CH3; R5 is H. Br, CI, or F; R6 and R7 are independently (provided that at least one of R6 and R7 can not be H, C1C6alkyl, hydroxylated C1C6, alkyl or C1C6 alkoxy-substituted C1C6alkyl) (a)H, (b)C1C6 alkyl, (c) hydroxylated C1C6 alkyl, (d) C1C6 alkoxy-substitutedC1C6 alkyl, (e) haiogenated C1C6 alkyl, (f) aryl, in which aryl represents phenyl, pyridyl, imidazolyl, indolyl, or naphthyl, optionally substituted by one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, C1C6 alkyl-NH- (C1C6 alkyl^-N-, or CN, (g) aryl substituted Cj-C6 alkyl, in which aryl represents phenyl, pyridyl, imidazolyl, indolyl, or naphthyl, optionally substituted with one or more substituents selected from halogen, C1C6 alkyi, C1C6 alkoxy, CF3, or OH, 9 R6 and R7, together with the nitrogen atom to which they are attached, form a saturated or unsaturated ring optionally containing one or more further heteroatoms (for example morphoiine, piperazine, pyrrolidine, piperidine), optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino, CN ,NH2S02, phenyl, NH2CO-, CrC6 alkyl-CO-, the ring can be fused with an aromatic ring (such as tetrahydroquinolinc) Most preferred compounds according to the invention are; • 2,3-dimethyl-8-(2-ethyl-6-methylbenzy lamino)-6-(morpholinocarbonyl)-imidazo[ 1,2- a]pyridine • N-(4-ethoxyphenyi)-8-(2-ethyl-6-methylben2ylamino)-2,3-dirxiethylimidazo[1.2-a]pyridine-6-carboxamide • N-[2-(dimethylamine)-2-Oxoethyl]-8-(2-ethyl-6-methylbenzylamino)-N,2,3-trimethylimidazo[ 1,2-a]pyridine-6-carboxamide • (8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimidazo[ 1,2-a]pyridin-yl)(4-methylpiperazino)methanone • 1 -((8-(2-ethyl-6-methylbenzylairuno)-2,3-dimethylimidazo[ 1,2-a]pyridin -6-yl)carbonyl)-2-(s)-pyrrolidinecarboxamide • 8-(2-ethyl-6-methylbenzylamino)-N-hydroxy-2,3-dimethylimidazo[ 1,2-a]pyridine-6-carboxamide 10 • (2-ethyI-6 methyIbenzylamino)-N-(2-(2-hydroxyethoxy)ethyl)-2,3-dimethylimida2o[ 1,2-a]pyridine-6-carboxamide • (8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimidazo( 1 t2-a]pyridin-6-yI)(3-hydroxy-1 -pyrrolidinyl)methanone • N-(3,4-dihydroxyphenethyl)-8-(2-ethyl-6-methylbenzylamino)-2,3-dimcthylimidazo[ 1,2-a]pyridine-6-carboxamide • 8-(2-ethyl-6-methylbenzylamino-3-(hydroxymethyl)-2-methyl-6-(morpholinocarbonyl)-imidazo[ 1,2-a]pyridine • N-((8-(2-ethyl-6-methylbenzy l)amino)-2,3-dimethylimidazo[ 1,2-a]pyridin-6-yl)carbonyl)guanidine • 4-(2-(((8-(2-ethyl-6-methylbenzy lamino)-2,3-dimethylimidazo[ 1,2-a]pyridin-6-yl)carbonyl)amino)ethoxy)-4-oxobutanoic acid Preparation The present invention also provides the following process for the manufacture of compounds with the general Formula I. A process for manufacture of compounds with the general Formula I comprises the following steps: a) Compounds of Formula II 11 wherein R1, R2. R3, R4, R5, and X are as defined in Formula I, can be hydro lyzed uudcr .standard conditions to the corresponding carboxylic acid to the corresponding enrboxyhc acid compounds of formula III b) Compounds of the Formula III wherein R1, R2, K\ R41, K5 and X is as defined in Formula I can be rcacted with amino compounds of Formula IV NH wherein R6 and R7 arc as denned for Formula I, in the presence of a coupling reagent to the corresponding amide compounds ofthc Formula I. The reaction can be carried out in nn inert solvent'under standard conditions. The present invention also provides the following process for the manufacture ol inicrmediate compounds vviih the treneral Formula ll. A process in: manufacture of compounds with the general formula ll where:;; X :s N'l i comprises the following steps 12 a) Compounds of the general Formula V can be reacted with amino compounds of the general Formula IV IV i > wherein R6 and R7 are both hydrogen, to the corresponding amide of the Formula VI. The reaction can be carried out in standard conditions in an inert solvent. VI 5 b) Compounds of the general Formula VI can be reacted with ammonia to compounds of the general Formula VII 13 wherein R6 and R7 are both hydrogen. The reactions can be carried out under standard conditions in an inert solvent. c) Compounds of the Formula VII can be reduced e.g. by using hydrogen and a catalyst such as Pd/C to compounds of the Formula VIII VIII *> wherein R6 and R7 are both hydrogen. The reaction can be carried out under standard conditions in an inert solvent. d) The imidazo[l,2-a]pyridine compounds of the Formula X can be prepared by reacting h compounds of the general Formula VIII with compounds of the general Formula IX wherein R2 is as defined for Formula I and Z is a leaving group such as halogen, mesyl. jo tosyl and R9 represents H, CH3 or an ester group such as COOCH3, COOC2H5 etc. 14 The reaction is carried out under standard condition, in an inert solvent such a, acetone, acclouilrile. alcohol, diniethylfomiamide, etc. wilh or without a base. e) Compounds of the Formula X can be reacted with compounds of the Fomuila X.1 wherem R3, R4 and R6 are as defined for Formula I and Y is a leaving group, such as a halide, tusyl or mcsyl, to the compounds of the Formula XII. 15 wherein R2, R3, R4, and R5 are as defined for Formula I and R6 and R7 both hydrogen and R9 is H, CH3 or an ester group such as COOCH3, COOC2H5, etc. It is convenient to conduct this reaction in an inert solvent, e.g. acetone, acetonitrile, dimethoxyethane, methanol, ethanol or dimethylformamide with or without a base. The base is e.g. an alkali metal hydroxide, such as sodium hydroxide and potassium hydroxide, an alkali metal carbonate, such as potassium carbonate and sodium carbonate; or an organic amine, such as triethylamine. f) Reduction of compounds of the general Formula XII wherein R9 is an ester group e.g. by using lithium borohydride in an inert solvent, such as tetrahydrofuran or diethyl ether, to the compounds of the general Formula I wherein R1 is CH2OH and R6 and R7 are both hydrogen. Medical use In a further aspect, the invention relates to compounds of the formula I for use in therapy, in particular for use against gastrointestinal inflammatory diseases. The invention also provides the use of a compound of the formula I in the manufacture of a medicament for the inhibition of gastric acid secretion, or for the treatment of gastrointestinal inflammatory diseases. The compounds according to the invention may thus be used for prevention and treatment of gastrointestinal inflammatory diseases, and gastric acid-related diseases in mammals including man, such as gastritis, gastric ulcer, duodenal ulcer, reflux esophagitis and : Zollinger-EUison syndrome. Furthermore, the compounds may be used for treatment of other gastrointestinal disorders where gastric antisecretory effect is desirable, e.g. in patients with gastrinomas, and in patients with acute upper gastrointestinal bleeding. They may also be used in patients in intensive care situations, and pre-and postoperatively to prevent acid aspiration and stress ulceration. 16 The typical daily dose of the active substance varies within a wide range and will depend on various factors such as for example the individual requirement of each patient, the route of administration and the disease. In general, oral and parenteral dosages will be in the range of 5 to 1000 mg per day of active substance, iPharmaceutical formulations In yet a further aspect, the invention relates to pharmaceutical compositions containing at least one compound of the invention, or a pharmaceutically acceptable salt thereof, as active ingredient. The compounds of the invention can also be used in formulations together with other active ingredients, e.g. antibiotics such as amoxicillin. For clinical use, the compounds of the invention are formulated into pharmaceutical formulations for oral, rectal, parenteral or other mode of administration. The pharmaceutical formulation contains at least one compound of the invention in combination with one or more pharmaceutically acceptable ingredients. The carrier may be in the form of a solid, semi-solid or liquid diluent, or a capsule. These pharmaceutical preparations are a further object of the invention. Usually the amount of active compounds is between 0.1-95% by weight of the preparation, preferably between 0.1-20% by weight in preparations for parenteral use and preferably between 0.1 and 50% by weight in preparations for oral administration. In the preparation of pharmaceutical formulations containing a compound of the present invention in the form of dosage units for oral administration the compound selected may be mixed with solid, powdered ingredients, such as lactose, saccharose, sorbitol, mannitol, starch, amylopectin, cellulose derivatives, gelatin, or another suitable ingredient, as well as with disintegrating agents and lubricating agents such as magnesium stearate. calcium stearate, sodium stearyl fumarate and polyethylene glycol waxes. The mixture is then processed into gra'nules or pressed into tablets. 17 Soft gelatin capsules may be prepared with capsules containing a mixture of the active compound or compounds of the invention, vegetable oil, fat, or other suitable vehicle for soft gelatin capsules. Hard gelatin capsules may contain granules of the active compound, Hard gelatin capsules may also contain the active compound in combination with solid powdered ingredients such as lactose, saccharose, sorbitol, mannitol, potato starch, com starch, amylopectin. cellulose derivatives or gelatin. Dosage units for rectal administration may be prepared (i) in the form of suppositories which contain the active substance mixed with a neutral fat base; (ii) in the form of a gelatin rectal capsule which contains the active substance in a mixture with a vegetable oil, paraffin oil or other suitable vehicle for gelatin rectal capsules; (iii) in the form of a ready-made micro enema; or (iv) in the form of a dry micro enema formulation to be reconstituted in a suitable solvent just prior to administration. Liquid preparations for oral administration may be prepared in the form of syrups or suspensions, e.g. solutions or suspensions containing from 0.1% to 20% by weight of the active ingredient and the remainder consisting of sugar or sugar alcohols and a mixture of ethanol, water, glycerol, propylene glycol and polyethylene glycol. If desired, such liquid preparations may contain coloring agents, flavoring agents, saccharine and carboxymethyl cellulose or other thickening agent. Liquid preparations for oral administration may also be prepared in the form of a dry powder to be reconstituted with a suitable solvent prior to use. : Solutions for parenteral administration may be prepared as a solution of a compound of the invention in a pharmaceutically acceptable solvent, preferably in a concentration from 0.1% to 10% by weight. These solutions may also contain stabilizing ingredients and/or buffering ingredients and are dispensed into unit doses in the form of ampoules or vials. Solutions for parenteral administration may also be prepared as a dry preparation to by reconstituted with a suitable solvent extemporaneously before use. 18 The compounds according to the present invention can also be used in formulations, together or in combination for simultaneous, separate or sequential use, with other active ingredients, e.g. for the treatment or prophylaxis of conditions involving infection by Helicobacter pylori of human gastric mucosa. Such other active ingredients may be antimicrobial agents, in particular: • p-lactam antibiotics such as amoxicillin, ampicillin, cephalothin, cefaclor or cefixime; • macrolides such as erythromycin, or clarithromycin; • tetracyclines such as tetracycline or doxycycline; • aminoglycosides such as gentamycin, kanamycin or amikacin; • quinolones such as norfloxacin, ciprofloxacin or enoxacin; • others such as metronidazole, nitrofurantoin or chloramphenicol; or • preparations containing bismuth salts such as bismuth subcitrate, bismuth subsalicylate, bismuth subcarbonate, bismuth subnitrate or bismuth subgallate. The compounds according to the present invention can also be used together or in combination for simultaneous, separate or sequential use with antacids such as aluminium hydroxide, magnesium carbonate and magnesium hydroxid or alginic acid, or together or in combination for simultaneous, separate or sequential use with pharmaceuticals which inhibit acid secretion, such as, H2-blockers [e.g cimetidine, ranitidine), H /K - ATPase inhibitors {e.g. omeprazole, pantoprazole, lansoprazole or rabeprazole), or together or in combination for simultaneous, separate or sequential use with gastroprokinetics (e.g. cisapride or mosapride). Intermediates A further aspect of the invention is new intermediate compounds which are useful in the synthesis of compounds according to the invention. Thus, the invention includes 19 (a) a compound o f the fonnula XVTII XVIII wherein Rl7R2>R3,R4,R5andX are as defined for Formula I. (b) a compound of the formula VTH wherein R2-, R6 and R7 are as defined for Formula I; and R9 is H, ClP or an cslte group' such as COOCIl3, COOC2H5. etc.; 20 (c) a compound of the formula X x wlicrcin R2, R3, R4, R-\ R6 iind R7 ire as defined for Formula I, and R9 is an ester group such as COOCH3, COOC2fr5 etc.; EXAMPLES I. PREPARATION 01' COMPOUNDS OF THE INVENTION Example LI 21 Synthesis of 2,3-diinethyl-S-(2-ethiyl'-6--melhylbeii7.ylainiiio)- 6-(inorpholii\ncarbvnyl)-imidazo( 1,2-a]pyridine t) 2.3-Dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[ 1,2-a]pyridine-6-carboxylic acid (0.15 g, 0.44 mmol) and o-Benzotriazol-l~yl-N,N,N',N-Tetramediyluronium tetrafluoroborate (TBTU)(0.14 g, 0.44 mmol) were added to methylene chloride (10 ml). Morpholine (0.12 g, 1.4 mmol) was added and the reaction mixture was stirred at ambient temperature for 1.5 h. The reaction mixture was added to a column with silica gel and purification by chromatography using ethylacetate : methylene chloride (1:1) as eluent gave 0.12 g (66%) of the desired product. 'H-NMR (300 MHz, CDC13): 5 1.2 (t, 3H), 2.32 (s, 3H), 2.35 (s, 3H), 2.37 (s. 3H), 2.7 (q, 2H), 3.7 (s, 8H), 4.35 (d, 2H), 4.95 (bs, 1H), 6.15 (s, 1H), 7.0-7.2 (m, 3H), 7.4 (s, 1H) Example 1.2 15 Synthesis ofN-(4-ethoxyphenyl)-8-(2-ethyl-6-meihylbenzylamino)-2,3-dimethylimidazo{ 1.2-a]pyrid'me-6-carboxamide 2,3-Dimethyl-8-(2-ethyI-6-methylbenzylamino)-imidazo[ 1,2-a]pyridine-6-carboxylic acid (0.15 g, 0.44 mmol) and o-BenzotriazoI-l-yl-N,N,N\N'-Tetramethyluronium tetrafluoroborate (TBTU)(0.14 g, 0.44 mmol) were added to methylene chloride (10 ml). 4-ethoxyanilin(0.19 g, 1.4 mmol) was added and the reaction mixture was stirred at ambient temperature for 72 h. The solvent was evaporated under reduced pressure and the residue was added to a column with silica gel and was purified by chromatography using methylene chloride : methanol (95:5) as eluent. The residue was treated with a hot mixture 22 of hexane : ethyl acetate (2:1) and the product was filtered off and dried to obtain 0.14 g (74 %) of the desired compound as white crystals. H-NMR (300 MHz. CDC13): 5 1.2 (t, 3H), 1.4 (t,3H), 2.35 (s. 9H), 2.65 (q, 2H), 4.0 (q. 2H), 4.35 (d, 2H), 4.9 (t, 1H), 6.55 (s, 1H), 6.85 (d, 2H), 7.0-7.2 (m, 3H), 7.5 (d, 2H), 7.9 (s, IH), 8.l5(s. IH) Example 1.3 11 Synthesis of N-[2-{dimethylamine)-2-oxoethyl]-8-(2-ethyl-6-methylbenzylamino)~N,2,3-trimethylimidazo[l,2-a]pyridine-6-carboxamide 2,3-Dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[ 1,2-aJpyridine-6-carboxylic acid (0.13 g, 0.38 mmol) and o-Benzotriazol-l-yl-N,N,N\N'-Tetramethyluroniurn tetrafluoroborate (TBTU) (0.12 g, 0.38 mmol) were added to methylene chloride (10 ml). N,N.DimethyI-2-methylamino-acetamide (0.088 g, 0.38 mmol) was added and the reaction mixture was stirred at ambient temperature for 1 h. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography using methylene chloride : methanol as eluent (95:5) which gave 80 mg (48 %) of the title product. iH-NMR (500 MHz, CDC13): 5 1.2 (t, 3H), 2.3 (s„ 6H), 2.35 (s, 3H), 2.65 (q, 2H)f 2.75 ( s, 6H), 2.95 (s, 3H), 3.15 (s, 2H), 4.35 (bs, 2H), 4.85 (bs, IH), 6.25 (s, IH), 7.0-7.2 (m, 3H), 7.45 (s, IH). Example 1.4 23 Synthesis of'(8'(2-ethyl-6-methylbmzylamino)-2,3-dimethylimidazo[ 1,2-a]pyridin-yl)(4-methylpiperazino)methanone 23-dimethyl-8-(2-emyl-6-memylbenzylamino)-imidazo[l,2-a]pyridine-6-carboxylicacid (0.5 g, 1.48 mmol) and o-BenzotriazoM-yl-NJsr,N%N'-Tetramewy]uronium tetrafluoroborate (TBTU)(0.48 g, 0.1.5 mmol) were added to methylene chloride (20 ml) and the mixture was stirred for 5 rnin. N-methylpiperazine (0.16g, 1.6 mmol) was added and the reaction mixture was stirred at ambient temperature overnight. The solvent was evaporated under reduced pressure and purification of the residue by column chromatography on silica gel using methylene chloride:methanol (9:1) as eluent gave 0.46 g (74 %) of the title compound. iH-NMR (500 MHz,CDCl3): 5 1.22 (t, 3H), 2.34 (s, 3H), 2.36 (s, 3H), 2.38 (s, 3H), 2.47 (bs, 4H), 2.71 (q, 2H). 2.80 (s, 3H), 3.65 (bs, 4H), 4.36 (d, 2H), 4.94 (t, 1H), 6.19 (s, 1H), 7.04-7.18 (m, 3H), 7.42 (s, 1H) Example 1.5 Synthesis of l-((8-(2-ethyl-6-methylbenzylamino)-2,3-dimethyIimidazo(l,2-a]pyridin -6-yl)carbonyl)-2'(s)-pyrrolidinecarboxamide 24 2,3-dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[l,2-a]pyridine-6-carboxylicacid (0.15 g, 0.44 mmol) , o-Benzotriazol-l-yl-N,N>N,,N'-Tetramethyluronium tetrafluoroborate (TBTU)(0.14 g, 0.45 mmol) and triethylamine (0.05 g, 0.5 mmol) were added to methylene chloride (10 ml) and the mixture was stirred for 10 min.(S)-prolinamide (0.016 g, 0.45 mmol) was added and the reaction mixture was stirred at ambient temperature for 1 h.. The solvent was evaporated under reduced pressure and purification of the residue by column chromatography on silica gel using methylene chloride:methanol (9:1) as eluent and crystallization from diethyl ether gave 0.07 g (36 %) of the title compound. 1H-NMR (500 MHz,CDCl3): 5 1.21 (t, 3H), 2.1-2.2 (m, 4H), 2.33 (s, 3H), 2.35 (s ,3H), 2.37 (s, 3H), 2.70 (q, 2H), 3.65-3.75 (m, 2H), 4.36 (d, 2H), 4.80 (bs, 1H), 4.94 (bs (1H), 5.88 (s, 1H), 6.33 (s, 1H), 6.98 (s, 1H), 7.04-7.19 (m,3H), 7.54 (s, 1H) Example 1.6 Synthesis of 8-(2-ethyl~6-methylbenzylamino)-N-hydroxy-2,3-dimethylimidazo[ 1,2-aJpyridine-6-carboxamide 25 2,3-dimethy]-8-(2-ethyl-6-methylben2ylamino)-iniidazot 1,2-a)pyridine-6-carboxylic acid (0.15 g, 0.45 mmol), o-Ben2otriazoM-yI-N,NJsI'^'-TetramethyIuronium tetrafiuoroborate (TBTU)(0.14 g, 0.45 mmol), triethylamine (0.1 g, 0.99 mmol) and hydroxylamine hydrochloride (0.031 g, 0.46 mmol) in dimethylformamide (5 ml). The title compound were prepared according to Example 1.5 (Yield: 0.016 g, 10 %) 1H-NMR (500 MHz,CDCl3): 5 1.15 (bs, 3H), 2,25 (bs, 9H), 2.6 (bs, 2H), 4.25 (bs, 2H), 4.95 (bs, 1H), 6.45 (bs, 1H), 6.9-7.1 (m, 3H), 7.75 (bs, 1H) Example 1.7 Synthesis of(2-ethyl-6methylbenzylamino)-N'(2-(2-hydroxyethoxy)ethyl)-2,3-dimethylimidazo[l,2-a]pyridine-6-carboxamide 2,3-dimethyl-8-(2-ethyl-6-rnethylbenzy]amino)-imidazo[ 1,2-a]pyridine-6-carboxylic acid (0.3 g, 0.88 mmol), c~BeiuotriazoM-yJ-N,N,N\N'-Tetramethyluroniuiri tetrafiuoroborate 26 (TBTU)(0.29 g, 0.90 mmol) and 2-(2-aminoethoxy)ethanol (0.2 g, 1.9 mmol) in methylene chloride (10 ml). The title compound were prepared according to Example 1.5 (Yield: 0.24 g, 80 %) 1H-NMR (500 MHz,CDCl3): 5 1.25 (t, 3H), 2.25 (s, 3H), 2.3 (s, 3H), 2.35 (s, 3H), 2.75 (q, 2H), 3.4-3.45 (m, 2H), 3.55-3.7 (ra, 6H), 4.35 (d, 2H), 5.05 (t, 1H), 6.45 (s, 1H), 7.0-7.2 (m, 4H), 7.5 (s, 1H) Example 1.8 Synthesis of (8-(2-ethyl-6'methy[benzylamino)-2,3-dimethylimidazo[l,2-a]pyridin-6-yl)(3-hydroxy-l~pyrrolidinyl)methanone ii 2,3-dimemyl-8-(2-ethyl-6-memylbeiizylamino)-irnidazo[ 1,2-a]pyridine-6-carboxylic acid (0.15 g, 0.44 mmol), o-Benzotriazol-l-yl-N,N,N' ,N'-Tetramethyluronium tetrafluoroborate (TBTU)(0.14 g, 0.44 mmol) and 3-pyrrolidinol (0.12 g, 1.4 mmol) in methylene chloride (10 ml). The title compound were prepared according to Example 1.4. Crystallization from ethylacetate:hexane(2:I) (Yield: 0.24 g, 80 %) 4 1H-NMR (300 MHz,CDCl3): 5 1.23 (t, 3H), 1.93 (bs, 2H), 2.33 (s, 3H), 2.34 (s,3H), 2.41 (s, 3H), 2.70 (q, 2H), 3.51-3.89 (m, 4H), 4.35 (d, 2H), 4.38-4.55 (m, 1H), 5.04 (bs, 1H), 6.35 (s, 1H), 7.01-7.16 (m, 3H), 7.51 (s, 1H) 27 Example 1.9 Synthesis of N-(3,4-dihydroxyphenethyl)~8-(2-ethy[-6-methylbenzylamino)-2,3-. dimethylimidazo[l,2-a)pyridine-6-carboxamide 23-dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[l,2-a]pyridine-6-carboxylicacid (0.15 g, 0.44 mmol) and o-Benzotriazol-l-yl-N,N,N',N'-Tetramethyluronium tetrafluoroborate (TBTU)(0.14 g, 0.45 mmol) were added to dimethylformamide(10 ml) and the mixture was stirred for 5 min. 3,4-dihydroxyphenetylamin (0.27 g 1.4 mmol) and triethylamine (0.28 g, 1.4 mmol) were added was added and the reaction mixture was stirred at ambient temperature for 72 h.. The solvent was evaporated under reduced pressure and purification of the residue by column chromatography on silica gel using methylene chloride:methanol (9:1) as eluent and crystallization from acetonitrile gave 0.059 g (28 %) of the title compound. :o 1H-NMR (400 MHz,DMSO-d6): 5 1.15 (t, IH), 2.22 (s, 3H), 2.33 (s, 3H), 2.37 (s, 3H), 2.65-2.74 (m, 4H), 3.41 (q, 2H), 4.37 (d, 2H), 4.85 (t, IH), 6.48 (dd, IH), 6.63-6.66 (m, 2H), 6.70 (d, IH), 7.07-7.21 (m, 3H), 8.04 (d, IH), 8.49 (t, IH), 8.63 (s, IH), 8.75 (s, IH) Example 1.10 Synthesis of 8-(2-ethyl-6-methylbenzylamino-3-(hydroxymethyl)-2-methyl-6-(morpkolinocarbonyl)-imidazo[l,2-a]pyridine 28 8-(2-ethyl-6-methylbenzylamino)-3-hydroxymethyl-2-iDethyIimidazo[l,2-a]pyridine-6-carboxylic acid (0.012 g, 0.034 mmol), o-Benzotriazol-l-yl-N,N,N',N'-Tetramethyluronium tetrafluoroborate (TBTU)(0.011 g, 0.034 mmol) and morpholine (0.009 g, 0.1 mmol) in methylene chloride (1 ml) The title compound were prepared according to Example 1.1. (Yield: 0.008 g, 56 %) 1H-NMR (300 MHz,DMSO-d6): 6 1.23 (t, 3H), 2.33 (s, 3H), 2.39 (s, 3H), 2.72 (q, 2H), 3.74 (bs, 8H), 4.37 (d, 2H), 4.85 (s, 2H), 5.02 (t, IH), 6.27 (d, IH), 7.06-7.22 (m, 3H), 7.75 (d, IH) Example 1.86 Synthesis ofN-((8-(2-ethyl-6-methylbenzyl)amino)-2,3-dimethylimidazo[l,2-a]pyridin-6-yl)carbonyl)guanidine 29 2,3-dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[ 1,2-a]pyridine-6-carboxylic acid " (0.5 g, 1.5 nunoi), diisopropyethylamin (0.57 g, 1.5 mmol) and guanidine carbonate (0.53 g, 2.9 mmol) were added to dimethylformamide (10 ml). o-Benzotriazol-l-yl-N,N,N\N'-Tetramethyluronium tetrafluoroborate (TBTU)(0.48 g, 1.5 mmol) was added and the reaction mixture was stirred at 50 °C for 3 h.. The solvent was evaporated under reduced pressure and purification of the residue by column chromatography on silica gel using methylene chloride:methanol (100:15) as eluent and crystallization from diethyl ether gave 0.12 g (21 %) of the title compound. 1H-NMR (500 MHz,CDCl3): 5 1.1 (t, 3H), 2.25 (s, 3H), 2.3 (s, 3H), 2.35 (s, 3H), 2.7 (q, 2H), 4.35 (d, 2H), 4.8 (bs, 1H), 6.9 (s, 1H), 7.05-7.2 (m, 3H), 8.25 (s, 1H) Example 1.87 Synthesis of 4-(2-(((8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimidazo[l,2-a]pyridm-6-yl)carbonyl)amino)ethoxy)-4-oxobutanoic acid. ^^ 2,3 dimethyl-8-(2-ethyl-6-methylbenzylamino)-N-hydroxyethyl-imidazo[ 1,2-a]pyridine-6-carboxamide (250 mg, 0.263 mmol) and succinic anhydride (100 mg, 1.00 mmol) were added to 7 ml of acetone. The mixture was refluxed for 48 h. The presiptated product was filtered off and washed with acetone and ether to give 288 mg (91%) of the title compound. 1H-NMR (500 MHz, DMSO): 5 1.16 (t, 3H), 2.24 (s, 3H), 2.35 (s, 3H), 2.39 (s, 3H), 2.48-2.58 (m, 4H), 2.70 (q, 2H), 3.54 (q, 2H), 4.19 (t, 2H), 4.39 (d, 2H), 4.90 (t, 1H), 6.72 (s, 1H), 7.09-7.22 (m, 3H), 8.08 (s, 1H), 8.59 (t. 1H), 12.25 (s, 1H). 30 Example 11-85 was prepared by paralleJl-synthesis using the following method: Solution A: 0.149 mmol in 1 ml dimethylformamide Solution B (TBTU): 0.297 mmol in 1 ml dimethylformamide Solution C + D: Amin (C) (0.297 mmol in 1 ml dimethylformamide) + TEA (D) (0.594 mmol in 1 ml dimethylamin) To a solution A (300 ul) were added solution B (150 u.1) and solution C+D (150 ul). The reaction was stirred by shaking at room temperature overnight. The solvent was evaporated under reduced pressure. The residue was solved in dichloromethane/methanol (9/l)(600 ul) and was filtred through a plug of silca gel (100 mg) and the gel was washed with dichloromethane/methanol (9/1) (0.5-1.0 ml). The filtrate was evaporated under reduced pressure to give the desired compounds. (If needed the compounds were purified by preparative HPLC.) 31 The analyses of the examples was made by HPLC and the compounds were identified by LC-mass spectroscopy. All compounds prepared in Example 11-85 showed a mass spectrum that confirmed the proposed structure. As the starting compound A in the reactions the following compounds were used. As the starting compound C in the reaction the following amines were used. 32 33 The Examples 11-85 were prepered according to scheme 1 The primary or the secondary amino nitrogen is the nitrogen involved in the reaction. e.g. Al + C5 —> Example 27 34 An + Cn —> Example 11-85 2. PREPARATION OF INTERMEDIATES Example 2.1 Synthesis of 8~(2-ethylbenzylamino}-2,3-dimethyIimidaza[ 1,2-a]pyridine-6-carboxylic acid 8-(2-ethylbenzylamino)-2.3-dimethyIimidazo[l,2-a]pyridine-6-carboxamide (1.0 g. 0.0031 mol) and sodium hydroxide (1.2 g, 0.031 mol) were solved in ethanol (95 %)(30 ml) and 35 was refluxed overnight. The solvent was evaporated under reduced pressure and to the residue was added water. The pH was adjusted to 7 by addition of cone HC1 (2.6 ml) and the solid that precipitated was isolated by filtration, washed with water and dried to give 1.0 g (99 %) of the title compound. 1H-NMR (300 MHz,DMSO-d6): 5 1.2 (t, 3H). 2.25 (s, 3H), 2.35 (s, 3H), 2.7 (q, 2H), 4.45 (d, 2H), 6.3 (s, IH), 6.45 (t, IH), 7.05-7.25 (m, 4H), 7.95 (s, 1H) Example 2.2 Synthesis of 8-(2,6-diethylbenzylamino)-2.3-dimethyliinidazo[l,2~a]pyridine-6~carboxylic acid 8-(2,6-diethylbenzylamino)-2,3-dimethylimida2o[ 1.2-a]pyridine-6-carboxamide (1.5 g, 0.0043 mol) and sodium hydroxide (1.7 g, 0.043 mol) were solved in ethanoi (95 %) (30 ml). The title compound were prepared according to Example 1.4. (Yield: 1.5 g, 99 %) JH-NMR (400 MHz.DMSO-d6): 5 1.14 (t. 6H), 2.22 (s, 3H), 2.37 (s, 3H), 2.67 (q. 4H). 4.37 (d, 2H), 4.89 (t, IH), 6.68 (s. IH), 7.11 (d, 2H), 7.23 (t, IH), 8.09 (s, IH) Example 2.3 Synthesis of 8-(2,6'dimethyl-4-fluorobenzyiamino)-2,3~dimethylimidazo(1,2-a]pyridine-6-carboxylic acid 8-(2,6-dimethyl-4-fluorobenzylamino)-2,3-dimethylimidazo[l,2-a]pyridine-6-carboxamide mesylate (1.47 g, 0.0034 mol) and sodium hydroxide (1.7 g, 0.034 mol) were solved in ethanoi (95 %) (30 ml). The title compound were prepared according to Example 2.1. (Yield: I.I g, 95 %) 36 iH-NMR (400 MHr,DMSO-d6): 5 2.23 (s, 3H), 2.34 (s, 6H), 2.36 (s, 3H), 4.31 (d, 2H), 5.04 (bs, IH), 6.70 (s, IH), 6.90 (d, 2H), 8.02 (s, IH) Example 2,4 Synthesis of 8-(2-isopropyl-6-methylbenzylamino)-23-dimethylimidazo[l,2-a]pyridine'6-carboxylic acid 8-(2-isopropyl-6-methylbenzylamino)-2,3-dimethylimidazo[l,2'a]pyridine-6-carboxamide mesylate (1.2 g, 0.0027 mol) and sodium hydroxide (1.1 g, 0.027mol) were solved in ethanol(95 %) (25 ml). The title compound were prepared according to Example 2.1. (Yield: 1.1 g, 95 %) *H-NMR (300 MHz,DMSO-d5): 5 1.69 (d, 6H), 2.74 (s, 3H), 2.85 (s, 3H), 2.89 (s, 3H), 3.73 (m, IH),4.90 (d, 2H), 5.48 (t, IH), 7.19 (s, IH), 7.55-7.61 (m, IH), 7.70-7.76 (m, 2H),8.60(s, IH) Example 2.5 Synthesis of 8-(2-ethyl-6-methylbenzylamino)~2J-dimethylimidazo[l,2-a]pyridine-6-carboxylic acid 8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimida2o[l,2-a]pyridine-6-carboxamide mesylate (11.0 g, 0.025 mol) and sodium hydroxide (7.0 g, 0.17 mol) were solved in : s ethanol(95 %) (120 ml) and was refluxed for 20 h. The solvent was evaporated under reduced pressure and to the residue was added water (150 ml). The pH was adjusted to 5 by addition of cone HC1 and acetic acid and the solid that precipitated was isolated by filtration, washed with water and acetone, and dried to give 7.6 g (88 %) of the utle compound 37 1H-NMR (500 MHz-DMSO-dfi): 5 1.15 (t. 3H), 2.26 (s, 3H), 2.34 (s. 3H). 2.39 (s, 3H), 2.69 (q, 2H), 4.38 (d, 2H). 5-2 (bs, 1H), 6.73 (s, 1H), 7.07-7.2 (m, 3H). 8.12 (s, 1H) Example 2.6 Synthesisof8-(2-ethyl-6-methylbenzylamino)'3-hydroxymethyl-2-methylimidazo[1.2-aJpyridine-6'Carboxylic acid 8-(2-ethyl-6^methylbenzylamino)-3-hydroxymethyl-2-methylimidazo[l,2-a]pyridine-6- carboxamide (0.02 g, 0.057 m mol) and sodium hydroxide (0.02 g, 0.29 mmol) were solved in ethanol (95 %) (1 ml) and was refluxed for 20 h. The solvent was evaporated under reduced pressure and to the residue was added water (1 ml). The pH was adjusted to 5 by addition of acetic acid and the solid that precipitated was isolated by filtration, washed with water and dried to give 0.012 g (60 %) of the title compound, iH-NMR (300 MHz.DMSO-d6): 5 1.14 (t, 3H), 2.22 (s. 3H), 2.33 (s. 3H), 2.67 (q. 2H). 4.33 (d, 2H), 4.55 (bs, 1H). 4.67 (s, 2H), 6.83 (s. 1H), 7.06-7.24 (m, 3H), 8.15 (s. 1H) BIOLOGICAL TESTS /. In vitro experiments Acid secretion inhibition in isolated rabbit gastric glands Inhibiting effect on acid secretion in vitro in isolated rabbit gastric glands was measured as described by Berglindh et al. (1976) Acta Physiol. Scand. 97,401-414. Determination ofH+,K*-ATPase activity Membrane vesicles {2.5 to 5 ug) were incubaved for 15 min at +37°C in IS mM Pipes/Ttis buffer pH 7.4 containing 2 mM MgCl2. 10 mM KC1 and 2 raM ATP. The ATPase activity 38 was estimated as release of inorganic phosphate from ATP, as described by LeBel et al. (1978) Anal. Biochem. 85. 86-89. 2. In vivo experiments Inhibiting effect on acid secretion in female rats Female rats of the Sprague-Dawly strain are used. They are equipped with cannulated fistulae in the stomach (lumen) and the upper part of the duodenum, for collection of gastric secretions and administration of test substances, respectively. A recovery period of 14 days after surgery is allowed before testing commenced. Before secretory tests, the animals are deprived of food but not water for 20 h. The stomach is repeatedly washed thirough the gastric cannula with tap water (+37°C), and 6 ml Ringer- Glucose given subcutaneously. Acid secretion is stimulated with infusion during 2.5-4 h (1.2 ml/h, subcutaneously) of pentagastrin and carbachol (20 and 110 nmol/kg-h, respectively), during which time gastric secretions are collected in 30-min fractions. Test substances or vehicle are given either at 60 min after starting the stimulation (intravenous and intraduodenal dosing, 1 ml/kg), or 2 h before starting the stimulation (oral dosing, 5 ml/kg, gastric cannula closed). The time interval between dosing and stimulation may be increased in order to study the duration of action. Gastric juice samples are titrated to pH 7.0 with NaOH, 0.1 M, and acid output calculated as the product of titrant volume and concentration. Further calculations are based on group mean responses from 4-6 rats. In the case of administration during stimulation; the acid output during the periods after administration of test substance or vehicle are expressed as fractional responses, setting the acid output in the 30-min period preceding administration to 1.0. Percentage inhibition is calculated from the fractional responses elicited by test compound and vehicle. In the case of administration before stimulation; percentage inhibition is calculated directly from acid output recorded after test compound and vehicle. 39 Bioavailability in rat Adult rats of the Sprague-Dawley strain are used. One to three days prior to the experiments all rats are prepared by cannulation of the left carotid artery under anaesthesia. The rats used for intravenous experiments are also cannulated in the jugular vein (Popovic (1960) J. Appl. Physiol. 15, 727-728). The cannulas are exteriorized at the nape of me neck. Blood samples (0.1 - 0.4 g) are drawn repeatedly from the carotid artery at intervals up to 5.5 hours after given dose. The samples are frozen until analysis of the test compound. Bioavailability is assessed by calculating the quotient between the area under blood/plasma concentration (AUC) curve following (i) intraduodenal (i.d.) or oral (p.o.) administration and (ii) intravenous (i.v.) administration from the rat or the dog, respectively. The area under the blood concentration vs. time curve, AUC. is determined by the log/linear trapezoidal rule and extrapolated to infinity by dividing the last determined blood concentration by the elimination rate constant in the terminal phase. The systemic : bioavailability (F%) following intraduodenal or oral administration is calculated as F(%) = (AUC (p.o. or i.d.) / AUC (i.v.)) x 100. Inhibition of gastric acid secretion and bioavailability in the conscious dog. Labrador retriever or Harrier dogs of either sex are used. They are equipped with a duodenal fistula for the administration of test compounds or vehicle and a cannulated gastric fistula or a Heidenhaim-pouch for the collection of gastric secretion. Before secretory tests the animals are fasted for about 18 h but water is freely allowed, Gastric acid secretion is stimulated for up to 6.5 h infusion of histamine dihydrochloride (12 ml/h) at a dose producing about 80% of the individual maximal secretory response, and 40 gastric juice collected in consecutive 30-min fractions. Test substance or vehicle is given orally, i.d. or i.v., 1 or 1.5 h after starting the histamine infusion, in a volume of 0.5 ml/kg body weight. In the case of oral administration, it should be pointed out that the test compound is administered to the acid secreting main stomach of the Heidenham-pouch dog. The acidity of the gastric juice samples are determined by titration to pH 7.0, and the acid output calculated. The acid output in the collection periods after administration of test substance or vehicle are expressed as fractional responses, setting the acid output in the fraction preceding administration to 1.0. Percentage inhibition is calculated from fractional responses elicited by test compound and vehicle. Blood samples for the analysis of test compound concentration in plasma are taken at intervals up to 4 h after dosing. Plasma is separated and frozen within 30 min after collection and later analyzed. The systemic bioavailability (F%) after oral or i.d. administration is calculated as described above in the rat model. 41 WE CLAIM:- 1. A compound of the formula I I or a pharmaceutically acceptable salt thereof/wherein 'Ri is (a) H, (b) CH3, or (c) CH2OH; R2 is (a) CH3, or (b) CH2CH3; R3is (a) H, (b) C1C6 alkyl, (c) hydroxylated C1C6 alkyl, or (d) halogen; R4is (a) H, (b) C1C6 alkyl, (c) hydroxylated C1C6 alkyl, or (d) halogen; RSis (a) H, or 42 (b) halogen; R6 and R7 are independently selected substituents, comprising C, H,N, O, S, Se, P or Halogen atoms, which give compounds of Formula I a molecular weight (a) NH, or (b)O. 2. A compound as claimed in claim 1 wherein R1 is CH3 or CH2HO; R2 is CH3 or CH2CH3; R3 is CH3 or CH2CH3; R4 is CH3 or CH2CH3; R5 is H, Br, CI, or F; R6 and R7 are independently (provided that at least one of R6 and R7 can not be H, C1C6 alkyl, hydroxylated C1C6 alkyl or C1C6 alkoxy-substituted C1C6 alkyl): (a)H, (b) Ci-Ce alkyl, (c) hydroxylated C1C6 alkyl, (d) C1C6 alkoxy-substituted Ci-Ce alkyl, (e)C1C6 alkenyl, (f) C1C6 alkynyl, (g) halogenated C1C6 alkyl, (h) C3-C8 cycloalkyl, (i) cycloalkyl-substituted C1C6alkyl, (j) aryl, in which aryl represents phenyl, pyridyl, thienyl, imidazolyl, indolyl, naphthyl or furanyl, optionally substituted by one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino, C1C6 alky-NH-, (C1C6 alkyl)2-N-, or CN or NH2SO2. (k) aryl substituted Ci-Ce alkyl, in which aryl represents phenyl, pyridyl thienyl, imidazolyl, indolyl, naphthyl or furanyl, optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino Ci-C6 alkyl-NH-, (Ci-C6 alkyl)2-N-, CN or NH2SO2, 43 (m) C7-C12, (n) OH, O-Ci-Ce alkyl, or O-hydroxylated C1C6 alkyl, (o' wherein R9 and R10 are independently H or C1C6alkyl, (p) R"-( C1C6) alkyl-COO-( C1C6) alkyl- wherein R" is HOOC-, C1C6 alkyl-OOC-or an amino carbonyl group with the formula wherein R12, R13 are the same or different H, or C1C6 alkyl R6 and R7, together with the nitrogen atom to which they are attached, form a saturated or unsaturated ring optionally containing one or more further heteroatoms (for example morpholine, piperazine, pyrrolidine, piperidine), optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino C1C6 alkyl-NH-, (C1C6 alkyl)2-N-, CN, NH2SO2, phenyl, NH2CO-, C1C6 alkyl-CO-, the ring can be fused with an aromatic ring (such as tetrahydroquinoline), or a pharmaceutically acceptable salt thereof. 44 3. A compound as claimed claim 1 or 2 wherein R1 is CH3 or CH2OH: R2 is CH3, R3 is CH3 or CH2CH3; R4 is CH3 or CH2CH3; R5 is H, Br, CI, or F; R6 and R7 are independently (provided that at least one of R6 and R7 can not be H, C1C6 alkyl, hydroxylated C1C6 alkyl or C1C6 alkoxy-substituted C1C6 alkyl), (a) H, ■(b) C1C6 alkyl, (c) hydroxylated C1C6 alkyl, (d) C1C6 alkoxy-substituted Ci-Ce alkyl, (e) halogenated C1C6alkyl, (f) aryl, in which aryl represents phenyl, pyridyl, imidazolyl, indolyl, or naphthyl, optionally substituted by one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, C1C6 alkyl-NH-, (C1C6 alkyl)2-N-, or CN, (g) aryl substituted C1C6 alkyl, in which aryl represents phenyl, pyridyl, imidazolyl, indolyl, or naphthyl, optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, or OH, (h) R8-( C1C6) alkyl-, wherein Rs is NH2C=0-, C1C6 alkyl-NHC=0-, (C1C6 alkyl)2NC=0-, C1C6 alkyl-OOC-, cyano, C1C6 alkyl-CO-NH-, C1C6 alkyl- OOCNH-, C1C6 alkyl-O-, C7-C12 alkyl-O- C1C6 alkyl-SO-, Ci-Ce alkyl-S-, C1C6 alkyl-C=0-, -ArCONH-, Ar(C1C6 alkyl)CONH, ArC=0-, NH2CONH- C1C6 alkyl-NHCONH-, (C1C6 alkyl)2-NCONH-, ArNHCONH-, hydroxylated C1C6 alkyl-O- or morpholiny; wherein Ar represents phenyl, pyridyl, imidazolyl, indolyl, or naphthyl optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, Ci-Ce alkoxy, CF3, OH, CN, (i) C7-C12 alkyl, (J) OH, 45 (k) RH-(C1C6) alkyl-COO-(C1C6) alkyl- wherein R" is HOOC-, or C1C6 alkyl-OOC, R6 and R7, together with the nitrogen atom to which they are attached, form a saturated or unsaturated ring optionally containing one or more further heteroatoms (for example morpholine, piperazine, pyrrolidine, piperidine), optionally substituted with one or more substituents selected from halogen, C1C6 alkyl, C1C6 alkoxy, CF3, OH, nitro, amino, CN, NH2SO2, phenyl, NH2CO-, C1C6 alkyl-CO-, the ring can be fused with an aromatic ring (such as tetrahydroquinoline). 4. The compound as claimed in claims 1 to 3 being; 2,3 -dimethyl-8 -(2 -ethyl-6 -methylbenzylamino) -6-(morpholinocarbonyl)-imidazo[ 1,2-a]pyridine, N-(4-ethoxyphenyl)-8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimidazo[ 1,2-a]pyridme-6-carboxamide, N-[2-(diine1±iylanmie)-2-oxoethyl]~8-(2-ethyl-6-methylben2ylamino)~ N, 2,3 -trimethylimidazo[ 1,2 -a] pyridine-6 -carboxamide, (8-(2-ettiyl-6-methylberizylamino)-2,3-dimethylimidazo[ 1,2-a]pyridine-yl)(4-methylpiperazino)methanone, l-((8-(2-ethyl-6-methylben^lamino)-2,3-dimethylimidazo[ 1,2-a]pyridin-6-yl)carbonyl)-2-(s)-pyrrolidinecarboxamide. (8-(2-ethyl-6-methylben2ylamino)-N-hydroxy-2,3-dimethylimidazo[ 1,2-a]pyridine-6-carboxamide, (2 -ethyl-6 -metiiylbenzylamino) -N- (2 - (-2 -hydroxyethoxy)ethyl) -2,3 -dimethylimidazo[ 1,2-a]pyridine-6-carboxamide, (8-(2-ethyl-6-methylbenzylamino)-2,3-dimethylimidazo[l,2-a]pyridin-6-yl) (3-hydroxy-1 -pyrrolidin.yl)methanone, N-(3,4-dihydroxyphenethyl)-8-(2-ethyl-6-methylben^lainino)-2,3-dimethylimidazof 1,2-a]pyridine-6-carboxamide, 8-(2-e&yl~6-raethylbenzylamino-3-(hydroxynie1±iyl)-2-niethyl-6-(morpholinocarbonyl) -imidazo [ 1,2 -a] pyridine, 46 N- ((8 - (2 -ethyl-6-methylbenzyl) amino) -2,3 -dimethylirmdazo[ 1,2 -a]pyridin-6-yl)carbonyl)guanidine, 4-(2-(((8-(2-ethyl-6-methylberi2ylammo)-2,3-dimethylimidazo[l?2-a]pyridin-6-yl)carbonyl)aniino)ehoxy)-4-oxobutanoic acid, or a pharmaceutically acceptable salt thereof- as herein discussed. 5. A compound as claimed in any of claims 1 to 4 as a hydrochloride or mesylate salt. 6. A process for the preparation of a compound as claimed in any of claims 1 to 5, comprising (a) hydrolyzing a compound of the Formula II wherein R1, R2 R3, R4, R5, and X are as defined in claim 1, under standard conditions to the corresponding carboxylic acid compound of Formula III 47 HO MJ (b) reacting a compound of the Formula III with an amino compound of Formula IV wherein R6 and R7 are as defined for claim 1, in the presence of a coupling reagent in an inert solvent and under standard conditions to the corresponding amide compound. (d) reducing a compound of the Formula V wherein R6 and R7 are as defined in claim 1 in an inert solvent under standard conditions to a compound of the Formula VI Q VI (d) reacting a compound of the Formula VI wherein R6 and R7 are as defined in claim 1 with a compound of Formula VII 48 wherein R2 is as defined in claim 1, Z is a leaving group and R9 represent H, CH3 or an ester group, in an inert solvent with or without a base to a compound of the Formula VIII O (e) reacting a compound of the Formula VIII wherein R6, R7 and R2 axe as defined in claim 1, and R9 is H, CH3 or an ester group with a compound of Formula IX ,Y IX wherein R3, R4, and R5 are as defined in claim 1, and Y is a leaving group in an inert solvent with or without a base, to a compound of the Formula X 0 X (fj reducing a compound of Formula X wherein R9 is an ester group in an inert solvent to a compound of the Formula I wherein R1 is CH2OH and X isNH. 49 7. A process for the preparation of a compound as claimed in any one of claims 1 to 5, wherein X is NH and R1 is H or CH3, comprising (a) reacting a compound of the Formula II p II with an alcohol compound of the general formula R10-OH, wherein R10 is an alkyl group under standard conditions, to a compound of the Formula XI XI (b) reacting a compound of the Formula XI wherein R10 is an alkyl group, with ammonia in an inert solvent under standard conditions to a compound of the Formula XII XQ (c) reducing a compound of the Formula XII wherein R10 is an alkyl group in an inert solvent under standard conditions to a compound of the Formula XIII 50 xm (d) reacting a compound of the Formula XIII wherein R10 is an alkyl group with a compound of Formula XIV o wherein R2 is as defined in claimed 1, Z is a leaving group and R11 represent H or CH3, in an inert solvent with or without a base to a compound of the Formula XV XV (e) reacting a compound of the Formula XV wherein R10 is an alkyl group, R2 are as defined in claim 1 and R11 is H or CH3 with a compound of Formula IX .Y IX wherein R3, R4, and R5 are as defined in claim 1 and Y is a leaving group in an inert solvent with or without a base to a compound of the Formula XVI 51 XVI (f) reacting a compound of Formula XVI wherein R2, R3, R4 and R5 are as defined in claim 1, R10 is an alkyl group and R11 is H or CH3 with a compound of Formula III wherein R6 and R7 are as defined in claim 1, under standard conditions, to a compound of Formula I wherein R1 is H or CH3 and X is NH. 8. A process for the preparation of a compound as claimed in any one of claims 1 to 5 comprising (a) treating a compound of Formula XVII XVII 52 wherein Ri, R2, R3? R4? RS and x are as defined in claim 1 and R10 is an alkyl group, with acid or base under standard conditions to a compound of Formula XVIII 0 xvm (b) reacting a compound of Formula XVIII wherein R1, R2, R3, R4, R5 and X is defined in claim 1 with a compound of Formula III wherein R6 and R7 are as defined in claim 1, in the presence of a coupling reagent in an inert solvent under standard conditions, to a compound of Formula I. Dated this 12th day of October, 2000. 53

Documents:

in-pct-2000-00496-mum-cancelled pages(28-11-2005).pdf

in-pct-2000-00496-mum-cancelled pages(5-1-2006).pdf

in-pct-2000-00496-mum-claims(12-10-2000).pdf

in-pct-2000-00496-mum-claims(amended)-(5-1-2006).pdf

in-pct-2000-00496-mum-claims(granted)-(28-11-2005).pdf

in-pct-2000-00496-mum-claims(granted)-(8-1-2007).pdf

in-pct-2000-00496-mum-correspondence 1(16-1-2009).pdf

in-pct-2000-00496-mum-correspondence(28-11-2005).pdf

in-pct-2000-00496-mum-correspondence(5-1-2006).pdf

in-pct-2000-00496-mum-correspondence(ipo)-(20-3-2007).pdf

in-pct-2000-00496-mum-correspondence(ipo)-(8-1-2007).pdf

in-pct-2000-00496-mum-description(complete)-(12-10-2000).pdf

in-pct-2000-00496-mum-description(granted)-(8-1-2007).pdf

in-pct-2000-00496-mum-form 1(12-10-2000).pdf

in-pct-2000-00496-mum-form 13(15-1-2001).pdf

in-pct-2000-00496-mum-form 19(24-5-2004).pdf

in-pct-2000-00496-mum-form 1a(28-11-2005).pdf

in-pct-2000-00496-mum-form 2(granted)-(28-11-2005).pdf

in-pct-2000-00496-mum-form 2(granted)-(8-1-2007).pdf

in-pct-2000-00496-mum-form 2(title page)-(granted)-(8-1-2007).pdf

in-pct-2000-00496-mum-form 3(12-10-2000).pdf

in-pct-2000-00496-mum-form 4(8-12-2005).pdf

in-pct-2000-00496-mum-form 5(12-10-2000).pdf

in-pct-2000-00496-mum-form 5(28-11-2005).pdf

in-pct-2000-00496-mum-form-pct-ipea-409(28-11-2005).pdf

IN-PCT-2000-00496-MUM-POWER OF AUTHORITY(22-5-2001).pdf

in-pct-2000-00496-mum-power of authority(28-11-2005).pdf

in-pct-2000-00496-mum-power of authority(28-9-2000).pdf

in-pct-2000-00496-mum-power of authority(8-1-2007).pdf

in-pct-2000-00496-mum-specification(amended)-(15-1-2001).pdf

in-pct-2000-00496-mum-specification(amended)-(28-11-2005).pdf

in-pct-2000-00496-mum-wo international publication report(12-10-2000).pdf