MCP-1 is a member of the chemokine family of pro-inflammatory cytokines which mediate leukocyte chemotaxis and activation. MCP-1 is a C-C chemokine which is one of the most potent and selective T-cell and monocyte chemoattractant and activating agents known.

MCP-1 has been implicated in the pathophysiology of a large number of inflammatory diseases including rheumatoid arthritis, glomerular nephritides, lung fibrosis, restenosis (International Patent Application WO 94/09128), alveolitis (Jones et al., 1992, J. Immunol., 149,2147) and asthma. Other disease areas where MCP-1 is thought to play a part in their pathology are atherosclerosis (e. g. Koch et al., 1992, J. Clin. Invest., 90,772-779), psoriasis (Deleuran et al., 1996, J. Dermatological Science, 13,. 228-236), delayed-type hypersensitivity reactions of the skin, inflammatory bowel disease (Grimm et al., 1996, J. Leukocyte Biol., 59,. 804-812), multiple sclerosis and brain trauma (Berman et al, 1996, J. Immunol., 156,. 3017-3023). An MCP-1 inhibitor may also be useful to treat stroke, reperfusion injury, ischemia, myocardial infarction and transplant rejection.

MCP-1 acts through the MCP-1 receptor (also known as the CCR2 receptor). MCP-2 and MCP-3 may also act, at least in part, through the MCP-1 receptor. Therefore in this specification, when reference is made to"inhibition or antagonism of MCP-1"or"MCP-1 mediated effects"this includes inhibition or antagonism of MCP-2 and/or MCP-3 mediated effects when MCP-2 and/or MCP-3 are acting through the MCP-1 receptor.

Copending International Patent Application Nos. PCT/GB98/02340 and PCT/GB98/02341 describe and claim groups of compounds based upon the indole ring structure which are inhibitors of MCP-1 and therefore have applications in therapy.

The use of certain indole derivatives as NMDA antagonists is described is USP5051442, W09312780, EP-483881. Other indoles and their use as inhibitors of leukotriene biosynthesis is described in for example, EP-A-275-667.

The applicants have found a particular substitution on the indole ring produces advantageous results when used therapeutically as inhibitors of MCP-1.

According to the present invention there is provided a compound of formula (I)

X is CH2 or SO2 R'is an optionally substituted aryl or heteroaryl ring; R2 is carboxy, cyano,-C (O) CH2OH,-CONHR',-SO2NHR', tetrazol-5-yl, S03H, or a group of formula (VI)

where R8 is selected from hydrogen, alkyl, aryl, cyano, hydroxy,-SO2R'2 where R'2 is alkyl, aryl, heteroaryl, or haloalkyl, or R8 is a group- (CHR"),.-COOH where r is an integer of 1-3 and each R'3 group is independently selected from hydrogen or alkyl; R9 is hydrogen, alkyl, optionally substituted aryl such as optionally substituted phenyl or optionally subtituted heteroaryl such as 5 or 6 membered heteroaryl groups, or a group COR"where R'a is alkyl, aryl, heteroaryl or haloalkyl; R° and R"are independently selected from hydrogen or alkyl, particularly C, 4 alkyl;

R3 is hydrogen, a functional group, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heterocyclyl, optionally substituted alkoxy, optionally substituted aralkyl, optionally substituted aralkyloxy, optionally substituted cycloalkyl; R4 is a group NHCOR", NHSO2R''or OCONR'6R"where R's is optionally substituted alkyl, optionally substituted aryl or optionally substituted heteroaryl and R'G and R"are independently selected from hydrogen, optionally substituted alkyl, optionally substituted aryl and optionally substituted heteroaryl, with the proviso that at least one of Rl6 or R"is other than hydrogen, or Rl6 and R'7 together with the nitrogen atom to which they are attached form an optionally substituted heterocyclic ring which optionally contains further heteroatoms; and R5, R6 and R'are independently selected from hydrogen, a functional group or an optionally substituted hydrocarbyl groups or optionally substituted heterocyclic groups.

Suitably, where R4 is a group NHCoR'5, Rl5 is substituted alkyl, optionally substituted aryl or optionally substituted heteroaryl.

Compounds of formula (I) are inhibitors of monocyte chemoattractant protein-1. In addition, they appear to inhibit RANTES (Regulated upon Activation, Normal T-cell Expressed and Secreted), induced chemotaxis. RANTES is another chemokine from the same family as MCP-1, with a similar biological profile, but acting though the CCR1 receptor. As a result, these compounds can be used to treat disease mediated by these agents, in particular inflammatory disease.

In this specification the term'alkyl'when used either alone or as a suffix includes straight chained, branched structures. These groups may contain up to 10, preferably up to 6 and more preferably up to 4 carbon atoms. Similarly the terms"alkenyl"and"alkynyl"refer to unsaturated straight or branched structures containing for example from 2 to 10, preferably from 2 to 6 carbon atoms. Cyclic moieties such as cycloalkyl, cycloalkenyl and cycloalkynyl are similar in nature but have at least 3 carbon atoms. Terms such as"alkoxy"comprise alkyl groups as is understood in the art.

The term"halo"includes fluoro, chloro, bromo and iodo. References to aryl groups include aromatic carbocylic groups such as phenyl and naphthyl. The term"heterocyclyl" <BR> <BR> <BR> includes aromatic or non-aromatic rings, for example containing from 4 to 20, suitably from 5 to 8 ring atoms, at least one of which is a heteroatom such as oxygen, sulphur or nitrogen.

Examples of such groups include furyl. thienyl, pyrrolyl, pyrrolidinyl, imidazolyl. triazolyl, thiazolyl, tetrazolyl, oxazolyl, isoxazolyl, pyrazolyl, pyridyl, pyrimidinyl. pyrazinyl, pyridazinyl, triazinyl, quinolinyl, isoquinolinyl, quinoxalinyl, benzothiazolyl, benzoxazolyl, benzothienyl or benzofuryl.

"Heteroaryl"refers to those groups described above which have an aromatic character.

The term"aralkyl"refers to aryl substituted alkyl groups such as benzyl.

Other expressions used in the specification include"hydrocarbyl"which refers to any structure comprising carbon and hydrogen atoms. For example, these may be alkyl, alkenyl, alkynyl, aryl, heterocyclyl, alkoxy, aralkyl, cycloalkyl, cycloalkenyl or cycloalkynyl.

The term"functional group"refers to reactive substituents. They may comprise electron-donating or electron-withdrawing. Examples of such groups include halo. cyano, nitro, C (0),, R18, OR18, S (O)11R18, NR19R20, C (O) NR19R20,OC(0)NR19R20.-NR19C(O)11,R18.- NR"CONR",-N=CR"R'°, S (O),, nNR'9R20 or-NR'9S (o),"R'8 where R", R'9 and R'° are independently selected from hydrogen or optionally substituted hydrocarbyl, or R'9 and R20 together form an optionally substituted ring which optionally contains further heteroatoms such as S (0),,,, oxygen and nitrogen, n is an integer of 1 or 2, m is 1 or 2.

Suitable optional substituents for hydrocarbyl groups R", R'9 and R20 include halo, perhaloalkyl such as trifluoromethyl, mercapto, hydroxy, carboxy, alkoxy, heteroaryl, heteroaryloxy, alkenyloxy, alkynyloxy, alkoxyalkoxy, aryloxy (where the aryl group may be substituted by halo, nitro, or hydroxy), cyano, nitro, amino, mono-or di-alkyl amino, oximino or S (O),, where n is as defined above and Rx is alkyl such as C, 4 alkyl.

Suitable substituents for these hydrocarbyl or heterocylic groups include those listed above for R'8, R'9 and R'O.

Suitably R'is an optionally substituted phenyl, pyridyl, naphthyl. furyl or thienyl ring, and in particular is a substituted phenyl or pyridyl ring.

Suitable optional substitutents for R'in formula (I) include alkyl, alkenyl, alkynyl, halo, haloalkyl including perhaloalkyl such as trifluoromethyl, mercapto. alkoxy, haloalkoxy. alkenyloxy, alkynyloxy, hydroxyalkoxy, alkoxyalkoxy, alkanoyl, alkanoyloxy, cyano. nitro, amino, mono-or di-alkyl amino, oximino, sulphonamido, carbamoyl, mono or dialkylcarbamoyl or S (O)", R2'where m is as defined above and R 21 is hydrocarbyl.

Particular examples of substituents R5, R"and R', and where appropriate also R4 include hydrogen, hydroxy. halo, optionally substituted alkyl such as aralkyl, carboxyalkyl or the amide derivative thereof ; alkoxy; aryloxy; aralkyloxy ; or an amino group which is optionally substituted with alkyl, aryl or aralkyl. A specific functional group which is suitable for R', R5, R'and/or R'is a group of sub-formula (IV).

Particular examples of groups R5, R6 and R'are hydrogen, hydroxy, halo or alkoxy.

In particular R6 and R7 are hydrogen. R5 may be hydrogen but in addition is suitably a small subsitutent such as hydroxy, halo or methoxy.

Particular substituents for R'include trifluoromethyl, C, 4alkyl, halo, trifluoromethoxy, C, 4alkoxy, C, 4alkanoyl, C, 4alkanoyloxy, nitro, carbamoyl, C, 4alkoxycarbonyl, C, 4alkylsulphanyl, C, 4alkylsulphinyl, C, 4alkylsulphonyl, sulphonamido, <BR> <BR> carbamoylC, 4alkyl, N-(C, 4alkyl) carbamoylC, 4alkyl, N-(C, 4alkyl) 2carbamoyl-C, 4alkyl,<BR> <BR> hydroxyC, 4alkyl or C, 4alkoxyC, 4alkyl.

Additionally or alternatively, two such substituents together may form a divalent radical of the formula-O (CH2), 4O-attached to adjacent carbon atoms on the R'ring.

Preferred substitutents for R'are one or more non-polar substituents such as halo.

In particular, R'is substituted by one or more halo groups, in particular chlorine. A particular example of an R'group is 3,4-dichlorophenyl, 3-fluoro-4-chlorophenyl, 3-chloro-4- fluorophenyl or 2,3-dichloropyrid-5-yl.

Examples of groups R2 include carboxy; cyano ; tetrazol-5-yl ; SO1H ;-CONHR8 where R8 is selected from cyano, hydroxy,-SO.) R where R is alkyl such as C, 4alkyl, aryl such as phenyl, heteroaryl or trifluoromethyl, or R8 is a group- (CHR'°),-COOH where r is an integer of <BR> <BR> 1-3 and each R'° group is independently selected from hydrogen or alkyl such as C, 4 alkyl ; or R2 is a group-SO2NHR9 where R9'is an optionally substituted phenyl or an optionally <BR> substituted 5 or 6 membered heteroaryl group, or a group COR'4 where R'4 is alkyl such as<BR> <BR> C, 4 alkyl, aryl such as phenyl, heteroaryl or trifluoromethyl, or R2 is a group of formula (VI)

where R'°and R"are independently selected from hydrogen or alkyl, particularly C, 4 alkyl.

Preferably R 2is carboxy or a pharmaceutically acceptable salt or ester thereof.

Suitable groups R3 include hydrogen, fluoro, chloro, bromo, iodo, methyl, cyano, trifluoromethyl, hydroxymethyl, alkoxyalkyl such as C, 4alkoxymethyl, methoxy, benzyloxy, carboxyalkoxy such as carboxymethoxy, methylsulphanyl, methylsulphinyl, methylsulphonyl or carboxyC36cycloalkyl,- (CHR22) r-NR23R24 (where r is 0-2, each R22 is independently hydrogen or alkyl, in particular C, 4 alkyl, R and R24 are independently selected from H and C, 4alkyl or R23 and R24 together with the nitrogen to which they are attached form a 5 or 6 membered ring optionally containing one further heteroatom selected from O, N, S, S (O) or SO2. Suitably R23 and R24 together form a heterocylic ring such as morpholino or piperazinyl.

Other such groups R3 include optionally substituted aryl groups, such as optionally substituted phenyl or naphthyl group. Suitable substituents for phenyl groups R3 include one or more groups selected from chlorine, fluorine, methyl, trifluoromethyl, trifluoromethoxy, amino, formyl, phenyl, methoxy, phenoxy or phenyl.

R3 may comprise a range of substituents as listed above, in particular, hydrogen or a small substituent group such as C, 4alkyl in particular methyl, or trifluoromethyl, and is preferably hydrogen.

Suitable optional substitutents for the group R 15, R 16 and R 17 as they appear in the definition of R4, include functional groups as hereinbefore defined, as well as aryl or heterocyclyl groups, either of which may themselves be substituted by one or more functional groups or further aryl or heterocyclyl groups.

Particular examples of substituents for groups R 15, R 16 and R 17 include one or more groups selected from halo such as chloro; hydroxy; cyano; amino ; mono-or di-alkylamino; Cul 4 alkoxy; carboxy; sulphonamido; CONH; alkylamido where the alkyl moiety is optionally substituted for example with a functional groups such as carboxy; morpholino;

pyridyl; pyrimidinyl; phenyl optionally substituted by halo such as chloro, hydroxy, alkoxy such as methoxy, carbamoyl, acyl such as acetyl, or hydroxyalkyl where the alkyl group suitably includes at least two carbon atoms, such as hydroxyethyl. Other examples of subsitutents for phenyl groups R'5 is alkanoylamino group such as methoylamino.

Where Rl5, Rl6 and/or R is a heterocyclyl group, or where Ruz 6 and R17 together form an optionally substituted heterocyclic ring, these may be substituted by functional groups such as halo or hydroxy, or by alkyl groups such as methyl or ethyl, or alkenyl or alkynyl groups any of which may be subsituted, for example with hydroxy, as well as with further heteroaryl groups such as pyridyl. Particular examples of heterocyclic groups Rlsv Rl6 and/or Rl 7 are optionally substituted thiophenyl, optionally substituted imidazolyl, optionally subtituted pyridyl.

Thus thiophenyl groups R'5, Rl6 and/or R"may comprise pyridyl-thiophenyl, whilst an example of a substituted imidazolyl group for R'5, R'6 and/or R"is methylimidazolyl and halopyridyl in particular chloropyridyl is an example of a substituted pyridyl moiety for these groups.

Particular examples of Rl S include alkyl in particular methyl optionally substituted by a functional groups or, in particular, a heterocyclyl group where the heterocyclyl group may be optionally substituted by a functional group such as halo or hydroxy or by an alkyl group such as methyl. Preferably, R 15 is a substituted alkyl group. Where the substitutent is a functional group, it is preferably a group of formula NR'9R20 where R'9 and R20 are as defined above. Thus examples of substituted alkyl groups R 15 include morpholinomethyl or alkyl such as methyl substituted with a substituted alkyl amino group wherein the substitutents include carboxy, alkanoyl, phenyl or alkyl sulphonyl.

Other examples of R 15 are heterocylcyl groups which are optionally subsitituted for example by alkyl such as methyl, functional groups such as chloro or heterocycyl groups such as pyridyl.

Particular examples of Rl6 and Rl7 are alkyl such as methyl.

X is CH2 or SO and is preferably CH,.

Suitable pharmaceutically acceptable salts of compounds of formula (I) include acid addition salts such as methanesulfonate, fumarate, hydrochloride, hydrobromide, citrate, maleate and salts formed with phosphoric and sulphuric acid. In another aspect suitable salts are base salts such as an alkali metal salt for example sodium, an alkaline earth metal salt for

example calcium or magnesium. an organic amine salt for example triethylamine, morpholine, N-methylpiperidine, N-ethylpiperidine, procaine, dibenzylamine, N, N-dibenzylethylamine or amino acids for example lysine. There may be more than one cation or anion depending on the number of charged functions and the valency of the cations or anions. A preferred pharmaceutically acceptable salt is a sodium salt.

An in vivo hydrolysable ester of a compound of the formula (I) containing carboxy or hydroxy group is, for example, a pharmaceutically acceptable ester which is hydrolysed in the human or animal body to produce the parent acid or alcohol.

Suitable pharmaceutically acceptable esters for carboxy include alkyl esters, such as C,-6 alkyl esters for example, ethyl esters, C,, alkoxymethyl esters for example methoxymethyl, C, 6alkanoyloxymethyl esters for example pivaloyloxymethyl, phthalidyl esters, C38cycloalkoxy-carbonyloxyC, 6alkyl esters for example 1-cyclohexylcarbonyloxyethyl; 1,3-dioxolen-2-onylmethyl esters for example 5-methyl-1,3-dioxolen-2-onylmethyl; and Cl 6alkoxycarbonyloxyethyl esters for example l-methoxycarbonyloxyethyl and may be formed at any carboxy group in the compounds of this invention.

Suitable pharmaceutically acceptable esters of compounds of formula (I) are in vivo hydrolysable ester of a compound of the formula (I) containing a hydroxy group includes inorganic esters such as phosphate esters and a-acyloxyalkyl ethers and related compounds which as a result of the in vivo hydrolysis of the ester breakdown to give the parent hydroxy group. Examples of a-acyloxyalkyl ethers include acetoxymethoxy and 2,2-dimethylpropionyloxymethoxy. A selection of in vivo hydrolysable ester forming groups for hydroxy include alkanoyl, benzoyl, phenylacetyl and substituted benzoyl and phenylacetyl, alkoxycarbonyl (to give alkyl carbonate esters), dialkylcarbamoyl and N-(dialkylaminoethyl)-N-alkylcarbamoyl(dialkylaminoethyl)-N- alkylcarbamoyl (to give carbamates), dialkylaminoacetyl and carboxyacetyl.

Esters which are not in vivo hydrolysable are useful as intermediates in the production of the compounds of formula (I) and therefore these form a further aspect of the invention.

Thus examples of compounds of formula (I) include the following: Table 1

C l, n R3 R4 Rs R6 Ra Rb No. 1 H N//H H H H s s H * 2 H 0 H H Cl Cl i! f 0 . 3 HN H H Cl Cl 1* 4 H H H H Cl Cl 0 N s 0 OH J D 11 11 Cl Cl N S nu 5PIo"/ ; F=\HH C! C! o! J NH 6 H o H H Cl Cl HN J4 NX N un * 7 H N = H H Cl CI 0 ; \ N- /NH S H NHC (O) CH, NHCH2COOH H H Cl Cl 9 H N C'H H Cl Cl , AJ / . NH NH 10 H OC (O) N (CH3) 2 H H Cl Cl 11 H CH, H H Cl Cl o i (o>z o H \ J-'N OU 12Ho \° oHH Cl Cl "J Oh 13 H H H Cl Cl 0 N-v N"'OH 14 H NHC (O) CH2N (CH3) CHCOOH H H Cl Cl 15 H H H Cl Cl 0 N NpH where * indicates the point of attachment of the group to the indole ring.

Compounds of formula (I) are suitably prepared by methods such as those described in International Patent Application Nos. PCT/GB98/02340 and PCT/GB98/02341.

In particular compounds of formula (I) where R4 is NHCOR''or NHSO2R''can be prepared by reacting a compound of formula (VII)

where X, R R3, R5, R6 and R7 are as defined in relation to formula (I), R2 is a group R2 as defined in relation to formula (I) or a protected form thereof, with a compound of formula (VIII) Z-R22 (VIII) where Z is a leaving group and R22 is a group COR'S'or SO2R'S'where R'S'is group R'5 as defined in relation to formula (I) or a precursor thereof ; and thereafter if desired or necessary: (i) converting a precursor group Rl5'to a group R and/or converting a group R15 to a different such group; (ii) deprotecting a group R2'to a group R2.

Suitable leaving groups Z include halo such as chloro.

The reaction is suitably effected in an organic solvent such as dichloromethane or tetrahydrofuran in the presence of a base such as triethylamine or pyridine. Moderate temperatures, for example from 0° to 50°C and conveniently ambient temperature, are employed in the reaction.

Compounds of formula (I) where R4 is a group OCONR"'R"may be prepared by a broadly similar method by reacting a compound of formula (VIIA)

where X, R2', Rl, R3, R5, R6 and R7 are as defined in relation to formula (I), R2 is a group R2 as defined in relation to formula (I) or a protected form thereof, with a compound of formula (VIIIA) Z-CoNR'6RI7 (VIIIA) where Z, Rl6 and Rl7 are as defined above.

Compounds of formula (VIIA) can be prepared by reacting a compound of formula (IX) where R3, R5, R'and R'are as defined in relation to formula (1) and R) is as defined in relation to formula (VII) and R' () is a protecting group ; with compound of formula (X) R'-X-Z (X) where R'and X are as defined in relation to formula (1) and Zl is a leaving group, and thereafter, removing the protecting group R40.

Suitable leaving groups for Z include halide such as chloride, bromide or iodide, as well as mesylate or tosylate. The reaction is suitably effected in an organic solvent such as dimethylformamide (DMF) tetrahydrofuran (THF) or DCM in the presence of a base such as sodium hydride, sodium hydroxide, potassium carbonate. Optionally the reaction is effected in the presence of a suitable phase transfer catalyst. The choice of base and solvent is interdependent to a certain extent in that certain solvents are compatible with some bases only as is understood in the art. For example, sodium hydride may preferably be used with dimethylformamide or tetrahydrofuran and sodium hydroxide is preferably used with dichloromethane and a phase transfer catalyst.

The reaction can be carried out at moderate temperatures, for example from 0 to 50°C and conveniently at about ambient temperature.

Preferably, R is an ester group in the compound of formula IX and this may be subsequently converted to an acid or to another ester or salt, by conventional methods later in the process. For example, when X is a group SO, and R ? is a methyl ester of carboxy, it may be converted to the corresponding carboxylic acid by reaction with lithium iodide in dry pyridine or DMF.

Suitable protecting groups R40 include acetyl or benzyl. The reaction conditions employed will be variable depending upon the nature of the protecting group R40 and would be apparent to a skilled person. Acetyl groups may be removed by reaction with a strong base such as sodium methoxide, whereas benzyl groups may be removed by hydrogenation for example in the presence of a catalyst such as a palladium catalyst.

Compounds of formula (IX) may be prepared by cyclisation of a compound of formula (XII)

where R5, R6, R7 and R40 are as defined above and R12 and R13 represent a combination of moieties which can cyclise to form an appropriately substituted pyrrole ring. For example, one of R42 and R43 can be a group of formula-CH=C (R44) N3 where R44 is a group R2 as defined above, or a protected form thereof, and the other may be hydrogen. Cyclisation to form a compound of formula (XII) may then be effected by heating for example under reflux in an organic solvent, in particular a high boiling aprotic solvent such as xylene or toluene.

Alternatively, one of R42 and R43 may be nitro and the other may be a group of formula-CH2C (O) R2 where R2 is as defined above in relation to formula (VII). These compounds will cyclise in the presence of a catalyst such as palladium on carbon in the presence of hydrogen. The reaction may be effected at moderate temperatures for example of from 0 to 80°C, conveniently at about ambient temperature.

Thus examples of compounds of formula (XII) include compounds of formula (XIII) and (XIV)

Compounds of formula (XIII) where R3 is hydrogen may be prepared for example by reacting a compound of formula (XV)

with a compound of formula (XVI) N3CH2R2' (XVI) where R5, R6, R', and R2 are as defined hereinbefore. The reaction may be effected in an organic solvent such as ethanol at low temperatures of from-20 to 0°C, suitably at about 0°C.

The reaction is suitably effected in the presence of a base such as an alkoxide, in particular an ethoxide, for example potassium ethoxide.

Compounds of formula (XVI) are suitably prepared by reacting a compound of formula (XVII) R47CH2R2 (XVII) where R2 is defined above and R41 is a leaving group such as halide and in particular bromide, with an azide salt, such as an alkali metal azide salt in particular sodium azide.

Compounds of formula (XIV) may be prepared by reacting a compound of formula (XVIII)

where R5, R6, R', R', R40 and R2 are as defined above, with a compound of formula (XIX)

where R2 is as defined above and R48 leaving group such as hydroxy. Examples of compounds of formula (XVI) are oxalates such as diethyloxalate. The reaction is suitably effected in the presence of a base such as sodium hydride in an organic solvent such as THF.

Moderate temperatures of from 0° to 40°C and conveniently ambient temperature is employed.

Compounds of formula (VII) are suitably prepared using a reaction analogous to that between compounds (IX) and (X), where in place of the compound of formula (IX), a compound of formula (IXA) is employed

where R2', R3, R5, R6 and R7 are as defined above. Such compounds may be obtained by reduction of the corresponding nitro compound of formula (XX)

where R2', R3, R5, R6 and R7 are as defined above.

Compounds of formula (X), (XVI), (XV), (XVII), (XVIII), (XIX) and (XX) are either known compounds or they may be prepared from known compounds by conventional literature methods.

According to a further aspect of the invention there is provided a compound of the formula (I) as defined herein, or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof, for use in a method of treatment of the human or animal body by therapy. In particular, the compounds are used in methods of treatment of inflammatory disease.

According to a further aspect of the present invention there is provided a method for antagonising an MCP-1 mediated effect in a warm blooded animal, such as man, in need of such treatment, which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, or an in vivo hydrolysable ester thereof.

The invention also provides a pharmaceutical composition comprising a compound of formula (I) as defined herein, or a pharmaceutically acceptable salt, or an in vivo hydrolysable ester thereof, in combination with a pharmaceutically acceptable diluent or carrier.

The compositions of the invention may be in a form suitable for oral use (for example as tablets, lozenges, hard or soft capsules, aqueous or oily suspensions, emulsions, dispersible powders or granules, syrups or elixirs), for topical use (for example as creams, ointments, gels, or aqueous or oily solutions or suspensions), for administration by inhalation (for example as a finely divided powder or a liquid aerosol), for administration by insufflation (for example as a finely divided powder) or for parenteral administration (for example as a sterile aqueous or oily solution for intravenous, subcutaneous, intramuscular or intramuscular dosing or as a suppository for rectal dosing).

The compositions of the invention may be obtained by conventional procedures using conventional pharmaceutical excipients, well known in the art. Thus, compositions intended

for oral use may contain, for example, one or more colouring, sweetening, flavouring and/or preservative agents.

Suitable pharmaceutically acceptable excipients for a tablet formulation include, for example, inert diluents such as lactose, sodium carbonate, calcium phosphate or calcium carbonate, granulating and disintegrating agents such as corn starch or algenic acid; binding agents such as starch; lubricating agents such as magnesium stearate, stearic acid or talc; preservative agents such as ethyl or propyl p-hydroxybenzoate, and anti-oxidants, such as ascorbic acid. Tablet formulations may be uncoated or coated either to modify their disintegration and the subsequent absorption of the active ingredient within the gastrointestinal track, or to improve their stability and/or appearance, in either case, using conventional coating agents and procedures well known in the art.

Compositions for oral use may be in the form of hard gelatin capsules in which the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules in which the active ingredient is mixed with water or an oil such as peanut oil, liquid paraffin, or olive oil.

Aqueous suspensions generally contain the active ingredient in finely powdered form together with one or more suspending agents, such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinyl-pyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents such as lecithin or condensation products of an alkylene oxide with fatty acids (for example polyoxyethylene stearate), or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives (such as ethyl or propyl p-hydroxybenzoate, anti-oxidants (such as ascorbic acid), colouring agents, flavouring agents, and/or sweetening agents (such as sucrose, saccharine or aspartame).

Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil (such as arachis oil, olive oil, sesame oil or coconut oil) or in a mineral oil (such as liquid paraffin). The oily suspensions may also contain a thickening agent such as beeswax, hard paraffin or cetyl alcohol. Sweetening agents such as those set out above, and flavouring agents may be added to provide a palatable oral preparation. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.

Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water generally contain the active ingredient together with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients such as sweetening, flavouring and colouring agents, may also be present.

The pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil, such as olive oil or arachis oil, or a mineral oil, such as for example liquid paraffin or a mixture of any of these. Suitable emulsifying agents may be, for example, naturally-occurring gums such as gum acacia or gum tragacanth, naturally-occurring phosphatides such as soya bean, lecithin, an esters or partial esters derived from fatty acids and hexitol anhydrides (for example sorbitan monooleate) and condensation products of the said partial esters with ethylene oxide such as polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening, flavouring and preservative agents.

Syrups and elixirs may be formulated with sweetening agents such as glycerol, propylene glycol, sorbitol, aspartame or sucrose, and may also contain a demulcent, preservative, flavouring and/or colouring agent.

The pharmaceutical compositions may also be in the form of a sterile injectable aqueous or oily suspension, which may be formulated according to known procedures using one or more of the appropriate dispersing or wetting agents and suspending agents, which have been mentioned above. A sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example a solution in 1,3-butanediol.

Suppository formulations may be prepared by mixing the active ingredient with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal

temperature and will therefore melt in the rectum to release the drug. Suitable excipients include, for example, cocoa butter and polyethylene glycols.

Topical formulations, such as creams, ointments, gels and aqueous or oily solutions or suspensions, may generally be obtained by formulating an active ingredient with a conventional, topically acceptable, vehicle or diluent using conventional procedure well known in the art.

Compositions for administration by insufflation may be in the form of a finely divided powder containing particles of average diameter of, for example, 3011 or much less, the powder itself comprising either active ingredient alone or diluted with one or more physiologically acceptable carriers such as lactose. The powder for insufflation is then conveniently retained in a capsule containing, for example, 1 to 50mg of active ingredient for use with a turbo-inhaler device, such as is used for insufflation of the known agent sodium cromoglycate.

Compositions for administration by inhalation may be in the form of a conventional pressurised aerosol arranged to dispense the active ingredient either as an aerosol containing finely divided solid or liquid droplets. Conventional aerosol propellants such as volatile fluorinated hydrocarbons or hydrocarbons may be used and the aerosol device is conveniently arranged to dispense a metered quantity of active ingredient.

For further information on Formulation the reader is referred to Chapter 25.2 in Volume 5 of Comprehensive Medicinal Chemistry (Corwin Hansch; Chairman of Editorial Board), Pergamon Press 1990.

The amount of active ingredient that is combined with one or more excipients to produce a single dosage form will necessarily vary depending upon the host treated and the particular route of administration. For example, a formulation intended for oral administration to humans will generally contain, for example, from 0.5 mg to 2 g of active agent compounded with an appropriate and convenient amount of excipients which may vary from about 5 to about 98 percent by weight of the total composition. Dosage unit forms will generally contain about 1 mg to about 500 mg of an active ingredient. For further information on Routes of Administration and Dosage Regimes the reader is referred to Chapter 25. 3 in Volume 5 of Comprehensive Medicinal Chemistry (Corwin Hansch; Chairman of Editorial Board), Pergamon Press 1990.

The size of the dose for therapeutic or prophylactic purposes of a compound of the Formula I will naturally vary according to the nature and severity of the conditions, the age and sex of the animal or patient and the route of administration, according to well known principles of medicine. As mentioned above, compounds of the Formula I are useful in treating diseases or medical conditions which are due alone or in part to the effects of farnesylation of rats.

In using a compound of the Formula I for therapeutic or prophylactic purposes it will generally be administered so that a daily dose in the range, for example, 0.5 mg to 75 mg per kg body weight is received, given if required in divided doses. In general lower doses will be administered when a parenteral route is employed. Thus, for example, for intravenous administration, a dose in the range, for example, 0.5 mg to 30 mg per kg body weight will generally be used. Similarly, for administration by inhalation, a dose in the range, for example, 0.5 mg to 25 mg per kg body weight will be used. Oral administration is however preferred.

A further aspect of the invention comprises the use of a compound of formula (I) as defined above in the preparation of a medicament for the treatment of inflammatory disease.

The invention is further illustrated, but not limited by the following Examples in which the following general procedures were used unless stated otherwise.

Preparation 1 Ethyl N-(3, 4-dichlorobenzyl)-4-nitroindole-2-carboxylate Ethyl 4-nitroindole-2-carboxylate (26 g) [prepared according to S. M. Parmerter et. al.

J. Amer. Chem. Soc., 1958,80,4621], 3,4-dichlorobenzyl chloride (16 ml), potassium carbonate (17 g) and potassium iodide (2 g) in DMF (250 ml) were stirred at 60°C for 2 hours.

The reaction was concentrated in vacuo and the residue partitioned between water and dichloromethane. Iso-hexane was added to the combined organic extracts resulting in crystallisation of the product as yellow needles (39 g, 89%) NMR d (CD3SOCD3) 1.30 (t, 3H), 4.32 (q, 2H), 5.93 (s, 2H), 6.88 (dd, 1H), 7.18 (d, 1H), 7.52 (d, 1H), 7.56 (dd, 1H), 7.78 (s, 1H), 8.17 (m, 2H); M/z (+) 395 (MH), 393.

Preparation 2 Ethvl N-benzvl-4-aminoindole-2-carboxylate A mixture of ethyl 4-nitroindole-2-carboxylate (8.2 g), anhydrous potassium carbonate (6.0 g) and benzyl bromide (4.3 ml) in DMF (100 ml) was stirred at 50-60°C for 2 hours. The solvent was evaporated in vacuo and the residue partitioned between dichloromethane and water (250 ml each); the organic layer was separated, dried (MgSO4) and evaporated to give a yellow solid (12 g), which was dissolved in a mixture of tetrahydrofuran/ethanol (200 ml, 1: 1) and stirred while adding a solution of sodium dithionite (26 g) in water (50 ml). The mixture was stirred for I hour at 25°C and partitioned between dichloromethane and water (200 ml each), the organic layer was washed with water (100 ml) and dried (MgSO4).

Combined organic extracts were concentrated in vacuo and the residue purified by column chromatography using dichloromethane as eluent to give a the product as a brown solid (1.4 g 14%); NMR d (CD3SOCD3) 1.28 (t, 3H), 4.27 (q, 2H), 5.57 (s, 2H), 5.73 (s, 2H), 6.22 (d, IH), 6.62 (d, 1H), 6.95-7.05 (m, 3H), 7.15-7.30 (m, 3H), 7.60 (s, 1H).

Preparation 3 Ethyl N (3, 4-dichlorobenzvl)-4-nitroindole-2-carboxylate Sodium hydroxide (3M, 20 ml) was added to a vigorously stirred solution of ethyl 4- nitroindole-2-carboxylate (4 g), 3,4-dichlorobenzyl chloride (4.73 ml) and tetra-n-butylammonium hydrogensulphate (0.2 g) in dichloromethane (60 ml). The reaction was stirred for 48 hours then partitioned between 2M HCl and dichloromethane. Combined organic extracts were dried (MgSO4) and concentrated in vacuo and the residue purified by column chromatography using iso-hexane: 20% ethyl acetate as eluent to give the product as <BR> <BR> <BR> a yellow crystalline solid (5.26 g, 78%); NMR 6 (CD3SOCD3) 1.3 (t, 3H), 4.3 (q, 2H), 5.95 (s, 2H), 6.9 (m, 1H), 7.6 (m, 4H), 8.2 (t, 2H); Mlz (+) 393.3 (Af).

Ethyl N- (3, 4-dichlorobenzyl)-4-aminoindole-2-carboxylate A solution of ethyl N- (3, 4-dichlorobenzyl)-4-nitroindole-2-carboxylate (2.41 g) in tetrahydrofuran (100 ml) was stirred in the presence of titanium trichloride (15% aqueous solution, 50 ml) at room temperature overnight. The reaction was treated with 40% sodium hydroxide solution and extracted with 5% methanol in dichloromethane. Combined organic extracts were dried (MgS04) and concentrated in vacuo to give the product as a brown solid

(1.98 g, 89%); NMR d (CD3SOCD3) 1. 3 (t, 3H), 4.2 (q, 2H), 5.7 (s, 4H), 6.2 (d, 1H), 6.6 (d, 1H), 7.0 (m, 2H), 7.25 (m, 1H), 7.5 (d, IH), 7.6 (m, IH): M/z (+) 363. 3 (MH+).

Preparation 4 Ethyl 4-chloroacetamido-N- (3, 4-dichlorobenzvl) indole-2-carboxylate Ethyl 4-amino-N- (3, 4-dichlorobenzyl) indole-2-carboxylate (2.03 g), chloroacetyl chloride (0.5 ml) and triethylamine (4.0 ml) were stirred in dichloromethane (50 ml) for 16 hours. The reaction was washed with water, dried (MgSO4) and concentrated in vacuo. The residue was triturated with toluene to give the product as a pale grey solid (1.61 g, 65%); NMR d (CD3SOCD3) 1.28 (t, 3H), 4.30 (q, 2H), 4.40 (s, 2H), 5.81 (s, 2H), 6.88 (dd, 1H), 7.30 (m, 3H), 7.50 (d, IH), 7.76 (s, 1H), 7.78 (d, IH), 10.19 (brs, 1H) ; Ad/z (-) 439 (M'), 437.

Example1 Compound 2 Ethyl 4-chloroacetamido-N- (3, 4-dichlorobenzyl) indole-2-carboxylate (0.15 g) and morpholine (2.0 ml) were dissolved in methoxyethanol (5.0 ml) and the reaction stirred for 72 hours. The reaction was then poured into water (100 ml) and the resulting solid filtered and dried in vacuo. The solid was dissolved in THF (2.5 ml) and methanol (2.5 ml), and to this was added NaOH (3M, 2.0 ml). The reaction was stirred for 16 hours, then concentrated. The residue was dissolved in water, and precipitated by dropwise addition of acetic acid. The resulting solid was filtered and dried in vacuo to give the title compound as a white solid (0.1 g, 63%, 2 steps); NMR d (CD3SOCD3) 2.58 (t, 4H), 3.29 (s, 2H), 3.65 (t, 4H), 5.82 (s, 2H), 6.90 (dd, 1H), 7.30 (m, 3H), 7.52 (m, 2H), 7.72 (d, 1H), 9.80 (s, 1H); M/z (-) 462 (M+), 460, 418.

Example 2 The procedure described in Example 1 above was repeated using the appropriate amines. Thus were obtained the compounds described below.

Compound 3 49% yield, 2 steps; NMR d (CD3SOCD3) 2.27 (s, 3H), 2.54 (t, 4H), 2.62 (t, 4H), 3.22 (s, 2H), 5.84 (s, 2H), 6.95 (dd, 1H), 7.22 (m, 2H), 7.33 (s, 1H), 7.41 (s, 1H), 7.50 (d, 1H), 7.72 (d, 1H), 9.75 (s, 1H); M/z (-) 475 (M+), 473,429,109.

Compound 6 14% yield, 2 steps; Mlz (-) 510 (M-), 508,464.

Example 3 Di-ester of Compound 8 Ethyl 4-chloroacetamido-N- (3, 4-dichlorobenzyl) indole-2-carboxylate (0.4 g), glycine methyl ester hydrochloride (0.57 g) and triethylamine (1.25 ml) were dissolved in methoxyethanol (4.0 ml) and the reaction heated at 100°C for 6 hours. The reaction was cooled and partitioned between water and ethyl acetate. Combined organic extracts were dried (MgSO4) and concentrated and the residue purified by chromatography using toluene : ethyl acetate (1: 1) as eluent to give the product, ethyl 4-[(N-(methoxycarbonylmethyl)- glycyl) amino]-N- (3, 4-dichlorobenzyl) indole-2-carboxylate, as a pale yellow solid (0.17 g, 38%); NMR d (CD3SOCD3) 1.28 (t, 3H), 3.44 (s, 2H), 3.50 (s, 2H), 3.63 (s, 3H), 4.28 (q, 2H), 5.82 (s, 2H), 6.88 (dd, 1H), 7.10-7.30 (m, 4H), 7.50 (d, 1H), 7.69 (s, IH), 7.80 (dd, 1H), 10.00 (brs, 1H); Mlz (+) 494,492 (M+).

Example 4 Di-ester of Compound 11 Methanesulphonyl chloride (0.1 ml) was added to stirred solution of ethyl 4- [ (N- (methoxycarbonylmethyl) glycyl) amino]-N- (3, 4-dichlorobenzyl) lndole-2-carboxylate (0.33 g) and triethylamine (0.47 ml) in dichloromethane (4.0 ml) and the reaction stirred for 3 hours.

The reaction was poured into water and extracted with ethyl acetate. Combined organic extracts were dried (MgS04) and concentrated and the residue triturated with ether, filtered and dried in vacuo to give the product as a white solid (0.24 g, 63%); NMR d (CD3SOCD3)

1.27 (t, 3H), 3.10 (s, 3H), 3.67 (s, 3H), 4.20 (s, 2H), 4.28 (q+s, 2H+2H), 5.82 (s, 2H), 6.87 (dd, 1H), 7.28 (m, 3H), 7.50 (d, 1H), 7.80 (m, 2H), 10.00 (brs, I H); AILIZ (+) 572,570 (M4).

Example 5 The procedure described in the Example 4 above was repeated using the appropriate acid chloride. Thus was obtained the compound described below.

Di-ester of Compound 12 64% yield; Mlz (-) 534 (Mt), 532.

Example 6 Di-ester of Compound 14 Sarcosine ethyl ester hydrochloride (1.23 g) and potassium carbonate (1.11 g) were added to a solution of ethyl 4-chloroacetamido-N- (3, 4-dichlorobenzyl) indole-2-carboxylate (700 mg) in acetone (25 ml), stirred and heated at 65°C overnight. The reaction was partitioned between water (50 ml) and ethyl acetate (50 ml), extracted with ethyl acetate (2 x 50 ml), and dried (MgSO4). The combined organic extracts were concentrated in vacuo, and the residue purified by column chromatography using 30% ethyl acetate: toluene as eluent, to afford the product as a yellow solid (768 mg, 92%); NMR d (CD3SOCD3) 1.21 (t, 3H), 1.28 (t, 3H), 2.45 (s, 3H), 3.42 (s, 2H), 3.53 (s, 2H), 4.16 (q, 2H), 4.30 (q, 2H), 5.81 (s, 2H), 6.88 (d, IH), 7.27 (m, 2H), 7.52 (d, 1H), 7.67 (s, 1H), 7.84 (d, 1H), 9.95 (s, IH), M/z (+) 520.3 (MH+) Example 7 The procedure described in Example 6 above was repeated using the appropriate amine. Thus was obtained the compound described below.

Diester of Compound 13 93% yield; NMR d (CD3SOCD3) 1.15 (t, 3H), 1.28 (t, 3H), 3.52 (s, 3H), 3.57 (s, 3H), 3.87 (s, 2H), 4.10 (q, 2H), 4.31 (q, 2H), 5.83 (s, 2H), 6.90 (d, IH), 7.15-7.44 (m, 8H), 7.53 (d, IH), 7.67 (s, 1H), 7.83 (d, 1H); M/z (+) 596.5 (MH+).

Example 8 Di-ester of Compound 15 A solution of methyl iodide (0.026 ml) in DMF (2 ml) was added to a solution of sodium hydride (15 mg, 60% in mineral oil) and ethyl 4- [ (N-benzyl-N- ethoxycarbonylmethyl) glycyl] amino-N- (3, 4-dichlorobenzyl) indole-2-carboxylate (the diester of Compound 13) (200 mg) in DMF (4 ml), and stirred under an atmosphere of argon at ambient temperature for 4 hours. The reaction was quenched with water (50 ml) and extracted with ethyl acetate (3 x 50 ml), and the combined organic extracts were dried (MgSO4), and concentrated in vacuo to afford the product as a pale brown oil (93 mg, 45%); NMR d (CD3SOCD3) 1.05 (t, 3H), 1.30 (t, 3H), 3.21 (s, 2H), 3.28 (s, 3H), 3.41 (s, 2H), 3.70 (s, 2H), 3.93 (q, 2H), 4.30 (q, 2H), 5.84 (s, 2H), 6.90 (d, 1H), 7.01 (d, 1H), 7.07-7.40 (m, 8H), 7.48- 7.64 (m, 2H); M/z (+) 610.5 (MH+).

Example 9 Compound 8 Ethyl 4-[(N-(methoxycarbonylmethyl) glycyl) amino]-N-(3, 4-dichlorobenzyl) indole-2- carboxylate (0.15 g) was dissolved in THF/methanol (1: 1) (10 ml) and sodium hydroxide (2M, 2.5 ml) was added and the reaction stirred for 16 hours. The reaction was then concentrated in vacuo and the residue dissolved in water. The solution was acidified by dropwise addition of acetic acid, resulting in the precipitation of a white solid which was filtered, washed with water and dried in vacuo to give the desired end product as a white solid (108 mg, 79%); NMR d (CD3SOCD3) 3.40 (s, 2H), 3.64 (s, 2H), 5.82 (s, 2H), 6.92 (dd. I H), 7.20-7.38 (m, 3H), 7.50 (d, IH), 7.62 (s, IH), 7.78 (d, IH), 10.15 (brs, 1H).

Example 10 The procedure described in Example 9 above was repeated using the appropriate ester. Thus were obtained the compounds described below.

Compound 11 79% yield; NMR d (CD3SOCD3) 3. 10 (s, 3H), 4.02 (s, 2H), 4.20 (s, 2H), 5.83 (s, 2H), 6.88 (dd, 1H), 7.25 (m, 3H), 7.50 (d, 1H), 7.75 (s, 1H), 7.80 (d, I H), 10.49 (brs, 1H); M/z (-) 528 (M+), 526,360,358,289,253,217.

Compound 12 78% yield; NMR d (CD3SOCD3) 2.00 (d, 3H), 4.03 (s, 1H), 4.20 (s,lH), 4.23 (s, 1H), 4.40 (s, IH), 5.82 (s, 2H), 6.88 (m, 1H), 7.25 (m, 3H), 7.52 (dd, 1H), 7.76 (m, 2H), 10.13 (brs, IH); M/z (-) 492 (M+), 490,324,253,224.

Compound 14 60% yield; NMR d (CD3SOCD3) 2.46 (s, 3H), 3.38 (s, 2H), 3.42 (s, 2H), 5.88 (s, 2H), 6.92 (d, 1H), 7.20 (m, 2H), 7.31 (s, 1H), 7.50 (m, 2H), 7.82 (d, IH) ! Mlz (-) 462.2 (M-H+).

Compound 15 15% yield; NMR d (CD3SOCD3) 3.21 (s, 2H), 3.31 (s, 3H), 3.40 (s, 2H), 3.69 (s, 2H), 5.83 (s, 2H), 6.90 (d, 2H), 6.98 (d, 2H), 7.15 (m, 6H), 7.27 (t, lH), 7.39 (s, lH), 7.53 (m, 2H); M/z (-) 554.3 (M-tI+) Compound 13 25% yield; NMR d (CD3SOCD3) 3.44 (s, 2H), 3.46 (s, 2H), 3.85 (s, 2H), 5.91 (s, 2H), 6.87 (m, 1H), (m, 6H), 7.40 (m, 2H), 7.53 (m, 2H), 7.78 (d, lH), Mlz (-) 538.2 (M-H'), 253.2.

Example 11 N Benzvl-4 (2- (pyrid-2-vl) thiophene-5-sulphonvl)) aminoindole-2-carboxvlic acid (Compound1) To a solution of ethyl N-benzyl-4-aminoindole-2-carboxylate (140 mg) and pyridine (0.08 ml) in dichloromethane (10 ml) at 20°C was added 2- (pyrid-2-yl) thiophene-5-sulphonyl chloride (140 mg) and the reaction stirred for 2 hours. The mixture was washed with HCI (2M, 10 ml), the organic layer was concentrated in vacato and the residue purified by

chromatography on silica using ethyl acetate as eluent, to give a yellow solid which was dissolved in ethanol (50 ml) at 60°C and treated with NaOH (2M, 4.0 ml) with stirring for 2 hours. The solvent was evaporated in vacuo, the residue dissolved in water (50 ml) and filtered. The clear yellow filtrate was acidified with 2N HCl and extracted with dichloromethane/methanol (9: 1,100 ml). The organic layer was dried (MgS04) and evaporated to give a pale brown solid, which was triturated with ether to give the product as an off white powder (150 mg, 63%, 2 steps); NMR d (CD3SOCD3) 5.87 (s, 2H), 6.9-7.1 (m, 9H), 7.30 (dd, 2H), 7.43 (d, IH), 7.63 (d, lH), 7.81 (dd, 1H), 7.96 (d, 1H), 8.50 (d, 1H); M/z (-) 488 (M-H).

Example 12 The procedure described in Example 11 above was repeated using the appropriate aminoindole and sulphonyl chloride. Thus were obtained the compounds described below. <BR> <BR> <P>4- (4-Acetvlaminobenzenesulphonvl) amino-N-(3, 4-dichlorobenzv) indole-2-carboxvlic<BR> acid (Compound 4) 66% yield (2 steps); NMR d (CD3SOCD3) 2.00 (s, 3H), 5.75 (s, 2H), 6.80 (dd, 1H), 6.92 (d, 1H), 7.12 (dd, 1H), 7.22 (m, 2H), 7.48 (d, 1H), 7.56 (s, lH,), 7.66 (s, 4H), 10.24 (brs, lH), 10.45 (brs, 1H); Mlz (-) 532 (M-H+), 530. <BR> <BR> <P>N-3, 4-Dichlorobenzyl)-4-,pvrid-2-y) thiophene-5-sulphonvl)) aminoindole-2-<BR> carboxvlic acid (Compound 5) 69% yield (2 steps); NMR d (CD3SOCD3) 5.80 (s, 2H), 6.80 (dd, 1H), 7.0-7.5 (m, 8H), 7.68 (d, lH), 7.83 (dd, lH), 7.92 (d, lH), 8.48 (dd, 1H); Mlz (-) 558 (M-Ht), 556.

N-3, 4-Dichlorobenzy)-4- (1-methylimidazole-4-sulphonyl) aminoindole-2-carboxvlic acid (Compound7) 66% yield (2 steps); NMR d (CD3SOCD3) 3.60 (s, 3H), 5.78 (s, 2H), 6.86 (dd, lH), 7.04 (1H, d), 7.15 (dd, 1H), 7.20 (d, lH), 7.30 (d, 1H), 7.50 (d, 1H), 7.68 (m, 2H), 7.75 (s, 1H), 10.20 (brs, 1H); Mlz (-) 479 (M-H+), 477.

N- !-4-(2-chloropvridvl-5-sulphonvlAaminoindole-2-carboxylic acid (Compound 9) 30% yield (2 steps); NMR d (CD3SOCD3) 5.85 (s, 2H), 6.83 (d, I H), 6.93 (dd, I H), 7.03 (dd, 1H), 7.15 (d, 1H), 7.20 (s, 1H), 7.26 (s, 1H), 7.46 (d, 1H), 7.60 (d, IH), 8.05 (dd, I H), 8.62 (d, 1H); Mlz (-) 512 (M-H+), 510,508.

Example 13 Methyl N-(3, 4-dichlorobenzyl)-4- (dimethylcarbamyloxv) indole-2-carboxylate (Methyl ester of Compound 10) Dimethylcarbamyl chloride (83 mg) was added to a stirred solution of methyl N- (3,4- dichlorobenzyl)-4-hydroxyindole-2-carboxylate (150 mg), triethylamine (65 mg) and DMAP (5 mg) in dichloromethane. The reaction was stirred for 16 hours at room temperature under an atmosphere of nitrogen. The reaction was washed with hydrochloric acid (2M, 70 ml), saturated aqueous sodium hydrogencarbonate solution, water and saturated sodium chloride solution. Combined organic extracts were dried (MgSO4), concentrated in vacuo and the residue purified by column chromatography using 60% ethyl acetate: iso-hexane as eluent to give the product as a colourless gum (132 mg, 74%); NMR d (CD3SOCD3) 2.94 (s, 3H), 3.12 (s, 3H), 3.81 (s, 3H), 5.82 (s, 2H), 6.91 (m, 2H), 7.21 (s, 1H), 7.27-7.36 (m, 2H), 7.46 (d, 1H), 7.52 (d, 1H); Mlz (+) 421 (MH+).

Example 14 N- (3, 4-Dichlorobenzyl)-4- (dimethylearbamyloxy) indole-2-carboxvlic acid (Compound Desesterifiation of the compound of Example 13 using the method described in Example 9 above yielded Compound 10.

93% yield; NMR d (CD3SOCD3) 2.94 (s, 3H), 3.11 (s, 3H), 5.91 (s, 2H), 6.82 (d, 1H), 6.94- 7.03 (m, 2H), 7.18 (t, 1H), 7.29-7.39 (m, 2H), 7.50 (d, 1H); M/z (-) 405 (M-H+).

Example 15 Biological Assays for hMCP-1 Antasonists The following biological test methods, data and Examples serve to illustrate the present invention.

Abbreviations: ATCC American Type Culture Collection, Rockville, USA.

BCA Bicinchroninic acid, (used, with copper sulphate, to assay protein) BSA Bovine Serum Albumin DMEM Dulbecco's modified Eagle's medium EGTA Ethylenebis (oxyethylenenitrilo) tetraacetic acid FCS Foetal calf serum HEPES (N- [2-Hydroxyethyl] piperazine-N'- [2-ethanesulphonic acid]) HBSS Hank's Balanced Salt Solution hMCP-1 Human Monocyte Chemoattractant Protein-1 PBS Phosphate buffered saline PCR Polymerase chain reaction AMPLITAQTM, available from Perkin-Elmer Cetus, is used as the source of thermostable DNA polymerase.

Binding Buffer is 50 mM HEPES, 1 mM CaCI2,5 mM MgCl2,0.5% foetal calf serum, adjusted to pH 7.2 with 1 M NaOH.

Non-Essential Amino Acids (1OOX concentrate) is: L-Alanine, 890 mg/1; L-Asparagine, 1320 mg/l; L-Aspartic acid, 1330 mg/l; L,-Glutamic acid, 1470 mg/l; Glvcine, 750 mg/l; L-Proline, 1150 mg/1 and; L-Serine, 1050 mg/l.

Hypoxanthine and Thymidine Supplement (50x concentrate) is: hypoxanthine, 680 mg/l and; thymidine, 194 mg/1.

Penicillin-Streptomycin is: Penicillin G (sodium salt); 5000 units/ml; Streptomycin sulphate, 5000 pg/ml.

Human monocytic cell line THP-1 cells are available from ATCC, accession number ATCC TIB-202.

Hank's Balanced Salt Solution (HBSS) was obtained from Gibco; see Proc. Soc. Exp.

Biol. Med., 1949,71,196.

Synthetic cell culture medium, RPMI 1640 was obtained from Gibco; it contains inorganic salts [Ca (NO3) 2. 4H2O 100 mg/l ; KCI 400 mg/l; MgSO4.7H2O 100 mg/l; NaCI 6000

mg/l; NaHCO3 2000 mg/1 & Na2HP04 (anhyd) 800 mg/1], D-Glucose 2000 mg/l, reduced glutathione 1 mg/1, amino acids and vitamins.

FURA-2/AM is 1- [2- (5-carboxyoxazol-2-yl)-6-aminobenzofuran-5-oxy]-2- (2'-amino-5'-methylphenoxy)-ethane-N, N, N', N'-tetraacetic acid pentaacetoxymethyl ester and was obtained from Molecular Probes, Eugene, Oregon, USA.

Blood Sedimentation Buffer contains 8.5g/1 NaCl and l Og/1 hydroxyethyl cellulose.

Lysis Buffer is 0.15M NH4Cl-, 1 OmM KHCO3, lmM EDTA Whole Cell Binding Buffer is 50 mM HEPES, 1 mM CaCl2,5 mM MgCl2, 0.5% BSA, 0.01% NaNl, adjusted to pH 7.2 with 1M NaOH.

Wash buffer is 50mM HEPES. lmM CaCl2, 5mM MgCl2,0.5% heat inactivated FCS, 0.5MNaCl adjusted to pH7.2 with 1M NaOH.

General molecular biology procedures can be followed from any of the methods described in"Molecular Cloning-A Laboratory Manual"Second Edition, Sambrook, Fritsch and Maniatis (Cold Spring Harbor Laboratory, 1989). i) Cloning and expression of hMCP-1 receptor The MCP-1 receptor B (CCR2B) cDNA was cloned by PCR from THP-1 cell RNA using suitable oligonucleotide primers based on the published MCP-1 receptor sequences (Charo et al., 1994, Proc. Natl. Acad. Sci. USA, 91,2752). The resulting PCR products were cloned into vector PCR-IITM (InVitrogen, San Diego, CA.). Error free CCR2B cDNA was subcloned as a Hind III-Not I fragment into the eukaryotic expression vector pCDNA3 (InVitrogen) to generate pCDNA3/CC-CKR2A and pCDNA3/CCR2B respectively.

Linearised pCDNA3/CCR2B DNA was transfected into CHO-K1 cells by calcium phosphate precipitation (Wigler et al., 1979, Cell, 16,777). Transfected cells were selected by the addition of Geneticin Sulphate (G418, Gibco BRL) at lmg/ml, 24 hours after the cells had been transfected. Preparation of RNA and Northern blotting were carried out as described previously (Needham et al., 1995, Prot. Express. Purifie., 6,134). CHO-K1 clone 7 (CHO-CCR2B) was identified as the highest MCP-1 receptor B expressor. iil Preparation of membrane fragments CHO-CCR2B cells were grown in DMEM supplemented with 10% foetal calf serum, 2 mM glutamine, I x Non-Essential Amino Acids, 1 x Hypoxanthine and Thymidine Supplement and Penicillin-Streptomycin (at 50 llg streptomycin/ml, Gibco BRL). Membrane fragments were prepared using cell lysis/differential centrifugation methods as described

previously (Siciliano et al., 1990, J. Biol. Chem., 265,19658). Protein concentration was estimated by BCA protein assay (Pierce, Rockford, Illinois) according to the manufacturer's instructions. iii) Assa '25I MCP-1 was prepared using Bolton and Hunter conjugation (Bolton et al., 1973, Biochem. J., 133,529; Amersham International plc]. Equilibrium binding assays were carried out using the method of Ernst et al., 1994, J. Immzmol., 152,3541. Briefly, varying amounts of'25I-labeled MCP-1 were added to 7ig of purified CHO-CCR2B cell membranes in 100 Ill of Binding Buffer. After 1 hour incubation at room temperature the binding reaction mixtures were filtered and washed 5 times through a plate washer (Brandel MLR-96T Cell Harvester) using ice cold Binding Buffer. Filter mats (Brandel GF/B) were pre-soaked for 60 minutes in 0.3% polyethylenimine prior to use. Following filtration individual filters were separated into 3.5ml tubes (Sarstedt No. 55.484) and bound'25I-labeled MCP-1 was determined (LKB 1277 Gammamaster). Cold competition studies were performed as above using 100 pM'25I-labeled MCP-1 in the presence of varying concentrations of unlabelled MCP-1. Non-specific binding was determined by the inclusion of a 200-fold molar excess of unlabelled MCP-1 in the reaction.

Ligand binding studies with membrane fragments prepared from CHO-CCR2B cells showed that the CCR2B receptor was present at a concentration of 0.2 pmoles/mg of membrane protein and bound MCP-1 selectively and with high affinity (IC50 = 110 pM, Kd =120 pM). Binding to these membranes was completely reversible and reached equilibrium after 45 minutes at room temperature, and there was a linear relationship between MCP-1 binding and CHO-CCR2B cell membrane concentration when using MCP-1 at concentrations between 100 pM and 500 pM.

Test compounds dissolved in DMSO (51) were tested in competition with 100 pM labelled MCP-1 over a concentration range (0.01-501lM) in duplicate using eight point dose-response curves and IC50 concentrations were calculated.

Compounds tested of the present invention had IC50 values of 50pM or less in the hMCP-1 receptor binding assay described herein. For example Compound 2 in Table 1 showed IC50 of 1. 17pM in hMCP-l. b) MCP-1 mediated calcium flux in THP-1 cells

The human monocytic cell line THP-1 was grown in a synthetic cell culture medium RPMI 1640 supplemented with 10 % foetal calf serum, 6mM glutamine and Penicillin-Streptomycin (at 50 llg streptomycin/ml, Gibco BRL). THP-1 cells were washed in HBSS (lacking Ca2+ and Mg2+) + 1 mg/ml BSA and resuspended in the same buffer at a density of 3 x 106 cells/ml. The cells were then loaded with 1 mM FURA-2/AM for 30 min at 37°C, washed twice in HBSS, and resuspended at IXIO'cells/ml. THP-1 cell suspension (0.9 ml) was added to a 5 ml disposable cuvette containing a magnetic stirrer bar and 2.1 ml of prewarmed (37°C) HBSS containing 1 mg/ml BSA, 1 mM MgCl2 and 2 mM CaCl,. The cuvette was placed in a fluorescence spectrophotometer (Perkin Elmer. Norwalk, CT) and preincubated for 4 min at 37°C with stirring. Fluorescence was recorded over 70 sec and cells were stimulated by addition ofhMCP-1 to the cuvette after 10 sec. [Ca9+] i was measured by excitation at 340 nm and 380 nm alternately and subsequent measurement of the intensity of the fluorescence emission at 510 nm. The ratio of the intensities of the emitted fluorescent light following excitation at 340 nm and 380 nm, (R), was calculated and displayed to give and estimate of cytoplasmic [Ca'i] according to the equation:- [Ca2+] i =K (, (R-Rmin ! (Sf2/Sb2) (Rmax-R) <BR> <BR> <BR> <BR> where the Kd for FURA-2 Ca2+ complex at 37 ° C was taken to be 224nm. RXnaX is the maximal fluorescence ratio determined after addition of 10 mM Ionomycin, R,,,;, is the minimal ratio determined by the subsequent addition of a Ca2t iree solution containing 5 mM EGTA, and Sf2/Sb2 is the ratio of fluorescence values at 380 nm excitation determined at R and respectively.

Stimulation of THP-1 cells with hMCP-1 induced a rapid, transient rise in [Ca2+] i in a specific and dose dependent manner. Dose response curves indicated an approximate EC50 of 2 nm. Test compounds dissolved in DMSO (10u. were assayed for inhibition of calcium release by adding them to the cell suspension 10 sec prior to ligand addition and measuring the reduction in the transient rise in [Ca'] i. Test compounds were also checked for lack of agonist activity by addition in place of hMCP-1. c) hMCP-1 and RANTES mediated chemotaxis.

In vitro chemotaxis assays were performed using the human monocytic cell line THP-1. Cell migration through polycarbonate membranes was measured by enumerating those passing through either directly by Coulter counting or indirectly by use of a

colourimetric viability assay measuring the cleavage of a tetrazolium salt by the mitochondrial respiratory chain (Scudiero D. A. et al. 1988, Cancer Res, 48,4827-4833).

Chemoattractants were introduced into a 96-well microtitre plate which forms the lower well of a chemotaxis chamber fitted with a PVP-free 5 llm poresize polycarbonate adhesive framed filter membrane (NeuroProbe MB series, Cabin John, MD 20818, USA) according to the manufacturer's instructions. The chemoattractant was diluted as appropriate in synthetic cell culture medium, RPMI 1640 (Gibco) or supplemented with 2 mM glutamine and 0.5% BSA, or alternatively with HBSS with Ca and Mg2+ without Phenol Red (Gibco) plus 0.1% BSA. Each dilution was degassed under vacuum for 30 min and was placed (400 , in the lower wells of the chamber and THP-1 cells (5xl 05 ill 100 pI RPMI 1640 + 0.5% BSA) were incubated in each well of the upper chamber. For the inhibition of chemotaxis the chemoattractant was kept at a constant submaximal concentration determined previously (InM MCP-1) and added to the lower well together with the test compounds dissolved in DMSO (final DMSO concentration < 0.05% v/v) at varying concentrations. The chamber was incubated for 2 h at 37°C under 5 % CO2. The medium was removed from the upper wells which were then washed out with 200 pl physiological saline before opening the chamber, wiping dry the membrane surface and centrifuging the 96-well plate at 600 g for 5 min to harvest the cells. Supernatant (150 ul) was aspirated and 10 ul of cell proliferation reagent, WST-1, {4- [3- (4-iodophenyl)-2- (4-nitrophenyl)-2H-5-tetrazolio]-1,3-phenyl disulfonate} plus an electron coupling reagent (Boehringer Mannheim, Cat. no. 1644 807) was added back to the wells. The plate was incubated at 37°C for 3 h and the absorbance of the soluble formazan product was read on a microtitre plate reader at 450 nm. The data was input into a spreadsheet, corrected for any random migration in the absence of chemoattractant and the average absorbance values, standard error of the mean, and significance tests were calculated. hMCP-1 induced concentration dependent cell migration with a characteristic biphasic response, maximal 0.5-1. 0 nm.

In an alternative form of the above assay, fluorescently tagged cells can be used in order to assist in end point detection. In this case, the THP-1 cells used are fluorescently tagged by incubation in the presence of 5mM Calcein AM (Glycine, N, N'- [ [3', 6'- bis (acetyloxy)-3-oxospiro [isobenzofuran-I (3H), 9'- [9H] xanthene]-2'. 7'-diyl] bis (methylene)] bis [N- [2- [(acetyloxy) methoxy]-2-oxoethyl]]-bis [(acetyloxy) methyl] ester: Molecular Probes) for 45 minutes in the dark. Cells are harvested by centrifugation and resuspended in HBSS

(without Phenol Red) with Ca'-T, Mg'--'and 0.1% BSA. zip (2x105 cells) ofthe cell suspension are placed on the filter above each well and, as above, the unit is incubated at 37°C for 2 hours under 5% CO,. At the end of the incubation, cells are washed off the upper face of the filter with phosphate buffered saline, the filter removed from the plate and the number of cells attracted to either the underside of the filter or the lower well estimated by reading fluorescence at 485nm excitation, 538nm emission wavelengths (fmax, Molecular Devices).

The data was input into a spreadsheet, corrected for any random migration in the absence of chemoattractant and the average fluorescence values, standard error of the mean, percentage inhibition and IC, of compounds under test and significance tests can be calculated. In addition to MCP-1 induced chemotaxis, this alternative form of the assay was also used to measure inhibition of RANTES (2nM) induced chemotaxis. d) Binding to human peripheral blood mononuclear cells (PBMCs) i) Preparation of human PBMCs Fresh human blood (200ml) was obtained from volunteer donors, collected into sodium citrate anticoagulant to give a final concentration of 0.38%. The blood was mixed with Sedimentation Buffer and incubated at 37°C for 20 minutes. The supernatant was collected and centrifuged at 1700rpm for 5 minutes (Sorvall RT6000D). The pellet obtained was resuspended in 20 ml RPMI/BSA (Img/ml) and 4 x 5mls of cells were carefully layered over 4 x 5mls of Lymphoprepa (Nycomed) in 15ml centrifuge tubes. Tubes were spun at 1700rpm for 30 minutes (Sorvall RT6000D) and the resultant layer of cells was removed and transferred to 50ml Falcon tubes. The cells were washed twice in Lysis Buffer to remove any remaining red blood cells followed by 2 washes in RPMI/BSA. Cells were resuspended in 5mls of Binding Buffer. Cell number was measured on a Coulter counter and additional binding buffer was added to give a final concentration of 1.25x107 PBMCs/ml. <BR> <BR> <BR> <BR> ii) Assay<BR> <BR> <BR> <BR> <BR> I1211] MCP-I was prepared using Bolton and Hunter conjugation (Bolton et al., 1973, Biochem. J., 133,529; Amersham International plc]. Equilibrium binding assays were carried out using the method of Ernst et al., 1994, J. Imrw1unol., 152,3541. Briefly, 501 of'25I-labeled MCP-1 (final concentration 1 OOpM) was added to 40Vil (5x 105 cells) of cell suspension in a 96 well plate. Compounds, diluted in Whole Cell Binding Buffer from a stock solution of I OmM in DMSO were added in a final volume of5ul to maintain a constant DMSO concentration in the assay of 5%. Total binding was determined in the absence of compound. Non-specific

binding was defined by the addition of 5p1 cold MCP-1 to give a final assay concentration of 100nM. Assay wells were made up to a final volume of 100p1 with Whole Cell Binding Buffer and the plates sealed. Following incubation at 37°C for 60 minutes the binding reaction mixtures were filtered and washed for 10 seconds using ice cold Wash Buffer using a plate washer (Brandel MLR-96T Cell Harvester). Filter mats (Brandel GF/B) were pre-soaked for 60 minutes in 0.3% polyethylenimine plus 0.2% BSA prior to use. Following filtration individual filters were separated into 3.5ml tubes (Sarstedt No. 55.484) and bound'~5I-labeled MCP-1 was determined (LKB 1277 Gammamaster).

Test compound potency was determined by assay in duplicate using six point dose-response curves and ICso concentrations were determined.

Compound No. 13 in Table I showed 94% inhibition at 201lu.

No physiologically unacceptable toxicity was observed at the effective dose for compounds tested of the present invention.

Example 16 Pharmaceutical Compositions The following Example illustrates, but is not intended to limit, pharmaceutical dosage forms of the invention as defined herein (the active ingredient being termed"Compound X"), for therapeutic or prophylactic use in humans: (a) Tablet I mg/tablet Compound X. 100 Lactose Ph. Eur 182.75 Croscarmellose sodium 12.0 Maize starch paste (5% w/v paste) 2.25 Magnesium stearate 3.0 (b) Tablet II mg/tablet Compound X 50 Lactose Ph. Eur 223.75 Croscarmellose sodium 6.0 Maize starch 15.0 Polyvinylpyrrolidone (5% w/v paste) 2.25 Magnesium stearate 3.0 (c) TabletIII mg/tablet CompoundX 1.0 Lactose Ph. Eur 93.25 Croscarmellosesodium 4.0 Maize starch paste (5% w/v paste) 0.75 Magnesiumstearate 1.0 (d)

(e) Injection I (50 mg/ml) Compound X 5.0% w/v 1M Sodium hydroxide solution 15.0% v/v 0.1M Hydrochloric acid to adjust pH to 7.6 Polyethylene glycol 400 4.5% w/v Water for injection to 100% (f) Injection I1 (10 m/ml) Compound X 1.0% w/v Sodium phosphate BP 3.6% w/v 0.1 M Sodium hydroxide solution 15.0% v/v Water for injection to 100% (g) Injection III (lmg/ml. buffered to pH6) Compound X 0. 1 % w/v 2. 26% w/v Sodium phosphate Bd Citric acid 0.38% w/v Polyethylene glycol 400 3.5% w/v Water for injection to 100% 5 (h) AerosolI mg/ml CompoundX 10.0 Sorbitantrioleate 13.5 Trichlorofluoromethane 910.0 Dichlorodifluoromethane 490.0 (i) AerosolII! CompoundX 0.2 Sorbitantrioleate 0.27 Trichlorofluoromethane 70.0 Dichlorodifluoromethane 280.0 Dichlorotetrafluoroethane 1094. 0 10 (j) Aerosol III mg/ml Compound X 2.5 Sorbitan trioleate 3.38 Trichlorofluoromethane 67. 5 Dichlorodifluoromethane 1086.0 Dichlorotetrafluoroethane 191.6 (k) AerosolIV mg/ml CompoundX 2.5 Soyalecithin 2.7 Trichlorofluoromethane 67.5 Dichlorodifluoromethane 1086. 0 Dichlorotetrafluoroethane 191.6 (1) Ointment ml Compound X 40 mg Ethanol 300 Ill Water 300, ul 1-Dodecylazacycloheptan-2-one 50, ul Propylene glycol to 1 ml

Note: Compound X in the above formulation may comprise a compound illustrated in Examples. The above formulations may be obtained by conventional procedures well known in the pharmaceutical art. The tablets (a)- (c) may be enteric coated by conventional means, for example to provide a coating of cellulose acetate phthalate. The aerosol formulations (h)- (k) may be used in conjunction with standard, metered dose aerosol dispensers, and the suspending agents sorbitan trioleate and soya lecithin may be replaced by an alternative suspending agent such as sorbitan monooleate, sorbitan sesquioleate, polysorbate 80, polyglycerol oleate or oleic acid.