Title of Invention	"A THIENOPYRIMIDINDIONE COMPOUND OF FORMULA (1)"
Abstract	The invention relates to thienopyrimidindiones of formula (1): wherein: R1, R2, Q are as defined in the specification, and Ar and Ar2 are selected from certain aromatic ring systems which may be optionally substituted, as defined in the specification. Processes for the preparation of compounds of formula (I), pharmaceutical compositions containing them and their use in therapy is also described and claimed.

Title of Invention

"A THIENOPYRIMIDINDIONE COMPOUND OF FORMULA (1)"

Abstract

The invention relates to thienopyrimidindiones of formula (1): wherein: R1, R2, Q are as defined in the specification, and Ar and Ar2 are selected from certain aromatic ring systems which may be optionally substituted, as defined in the specification. Processes for the preparation of compounds of formula (I), pharmaceutical compositions containing them and their use in therapy is also described and claimed.

Full Text	The present invention relates to a thienopyrimidindione compound. The present invention relates to thienopyridazinones, processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The invention also relates to their use in the modulation of autoimmune disease. T-cells play an important role in the immune response, however in auto-immune disease T-cells are inappropriately activated against particular tissues and proliferates eg causing the inflammation associated with rheumatoid arthritis. Inhibition of the proliferation of T-cells is beneficial in the modulation of autoimmune disease. The present invention relates to compounds which are beneficial in the modulation of autoimmune disease. In accordance with the present invention, there is provided a compound of formula (1): (Formula Removed) wherein: R! and R2 each independently represent C1-6alkyl, C3-6alkenyl, C3-5cycloalkylC1-3alkyl or C3-6cycloalkyl, each of which may be optionally substituted by 1 to 3 halogen atoms; Q is CR4R5 where R4 is hydrogen, fluorine or C1-6 alkyl and R5 is hydrogen, fluorine or hydroxy; Axis a 5- to 1 0-membered aromatic ring system wherein up to 4 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substituents independently selected from C1-4alky! (optionally substituted by 1, 2 or 3 hydroxy groups), C1-4alkoxy, halogen, haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) C1-4alkoxyC1-4alkyl, C1-4alkylthio, C1-4alkoxycarbonyl, C2-4alkanoyl, oxo, thioxo, nitro, cyano, -N(R6)R7 and -(CH2)pN(R8)R9, hydroxy, C1-4alkylsulphonyl C1-4alkylsulphinyl, carbarnoyl, , haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) Cj^alkoxyCj^alkyl, Ci^alkylthio, C\^alkoxycarbonyl, Cj^alkanoyl, oxo, thioxo, nitro, cyano, -J^R^R7 and - CMalkylcarbamoyl, dHCMalkyOcarbamoyl, carboxy, S02N(R8)R9; Ar2 is a 5 or 6 membered aromatic ring containing up to 4 hetero atoms independently selected from nitrogen, sulphur or oxygen, and which may be optionally substituted by one or more groups independently selected from Chalky! (optionally substituted by 1,2 or 3 hydroxy groups), C^alkoxy, halogen, haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) CMalkoxyd^alkyl, Ci-4alkylthio, CmaUcoxycarbonyl, Ci^alkanoyl, oxo, thioxo, nitro, cyano, -N^R7 and -^(CHaJpNCR^R9, hydroxy, CMalkylsulphonyl, CMalkylsulphinyl, carbamoyl, C\. 4alkylcarbamoyl, di-(Cj.4alkyl)carbamoyl, carboxy, SO;zN(R)R9; p is 1 to 4; R6 and R7 each independently represent a hydrogen atom, CMalkanoyl or Chalky! group, or together with the nitrogen atom to which they are attached form a 5- to 7-ntembered saturated heterocyclic ring optionally containing a further 0, S, NH or Nalkyl group; R8 and R9 each independently represent a hydrogen atom, Cmalkanoyl or Chalky! group, or together with the nitrogen atom to which they are attached form a S- to 7-ntembered saturated heterocyclic ring optionally containing a further 0, S, NH or Nalkyl group; and phannaceutically acceptable salts and solvates thereof, provided that the compound is other than 5-[(45)-4-Hydroxyisoxa2a>lidin-2-ylcarbonyl]-l-(isobutyl)-3-methyl-6-[5" l-l#-pyrazoM-ylraetty^ -phenyl-l#-pyr^ ylcarbonyl]-! -isobutyl-3"methylthieno[2,3-)pyriniidine-2,4(lH,3J-f)-dione or • 6[3,5-Dimemyl-l-phenyl-lH-pyrazol^ytoethyl]-5-[(45)-4-hydroxyisoxazoUdm^ ylcarbonyI]-3-memyl-l-propylthieno[2,3- Suitably R1 is CMS alkyl or €3.5 cycloalkyl, and in particular C^ alkyl. More preferably RJ is ethyl, propyl, butyl or cyclopropyl. Most preferably R1 is ethyl, isobutyl, isopropyl or cyclopropyl. More preferably R1 is CM alkyl such as isobutyl or isopropyl. Preferably R2 is C5,6alkyl such as ethyl or methyl, more preferably methyl. Suitably Q is CR^R* where R5 is hydrogen, CH alkyl and R6 is hydrogen. Preferably Q is CRR5 where R4 and R5 are both hydrogen. Examples of 5-10 membered mono- or bi-cyclic aromatic ring systems for Ar include thienyl, ruranyl, pyrrolyl, pyrrolopyridino, imidazolyl, pyridyl, pyrazinyl, pyrimidyl, pyridazinyl, triazinyl, oxazolyl, thiazolyl, isoxazolyl, pyrazolyl, oxadiazolyl, thiadiazolyl,triazolyl,tetrazolylandquiijolyl. ... Examples of 5- to 7-rnembered saturated heterocyclic rings formed by R6 and R7 and R8 and R9 include morpholine, piperidine, N-alkyl piperidine, pierazine, pyrrolidine and the like. Preferably Ar is a 5 or 6-membered aromatic ring system wherein up to 2 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substttuents independently selected from Chalky!, CMalkoxy, halogen, haloCi^alkyl, dihaloCMalkyl, tri haHoC]4alkyl, oxo, thioxo, cyano, or Cj^alkylsulphonyl. More preferably Ar is 5-membered aromatic ring containing two nitrogen atoms and substituted as above. A particular example of Ar is an optionally substituted pyrazole ring. Preferably Ar is a substituted pyrazole ring. Most preferably Ar is a pyrazole ring di-substiruted by Chalky!, especially methyl. . For instance, Ar is suitably a group of sub-formula (i) (Figure Remove) where R10 and R11 are independently selected from H, Cj-galkyl, dihaloCi-4alkyl, or trihaloCMalkyl, and Ar2 is as defined above. In R10 and R11 are selected from H or Cj^alkyl, such as methyl. In particular, both R10 and R1 ' is Chalky! such as methyl. Ar2 is suitably a 5 or 6-membered aromatic ring system "wherein up to 3 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substituents independently selected from Cj^alkyl, Cj^alkoxy, halogen, dihaloalkyl, trihaloalkyl, oxo, thioxo, cyano, Cualkylsulphonyl. Preferably Ar2 is other than pbenyl. In particular Ar2 includes at least one heteroatom. Examples of haloalky] groups are haloCMalkyl groups which include halomethyl groups such as fluoroethyl groups. Examples of dihaloalkyl groups are dihaloCualkyl groups including difluoromethyl and dichloromethyl. Examples of trihaloalkyl groups are trihaloCMalkyl groups such as trifluoromethyl. In ft preferred embodiment, Ar1 is 5-membered aromatic ring containing a nitrogen and sulphur atom and substituted as above. Most preferably Ar2 is a thiazole ring substituted by halogen, especially fluoro. In an alternative embodiment of the invention, Ar2 is pyridine or pyrimidine. The rings cany at least one subatituent, but are preferably unsubstituted. Preferably Ar2 is pyridinyl or pyrimidinyl. Preferred compounds of formula (I) include: 6-[t3,5-dimemyl-l-(2-pyrM^ isoxazolidinyl3carbonyl3-3-mefliyl-l-(l-methylethyl)thieno[2,3-fifJpyrimidine- 2,4(l#,3/0-dione, and 6-[[3,5-dimethyM-(2-pyridinyl)-l^-pyrazol-4-yl]methyl]-5-[[(4S)-4-hydroxy-2- isoxazolidinyl]carbonyl]-3-methyl-l-(l-methylethy])thieno[2,3-]pyrimidine- and pharmaceutically acceptable salts thereof. Other preferred compounds of formula (I) include (iS)-2-[[6-[[3,5-Dimethyl-l-(2-tWazolyl)-l#-pyrazol^yl]mernyl]-l^ dioxothieno[23-^pyrimidin-5-yl]carbonyl]-4-isoxazolidinol and pharmaceutically acceptable salts thereof. Alkyl groups, whether alone or as part of another group, can be straight chained or branched. Unless otherwise stated, they may contain from 1 to 6, and preferably from 1 to 4 carbon atoms. It will be understood that a compound of the fonnula (I) or a salt thereof may exhibit the phenomenon of tautomerism and that the drawings within this specification represent only one of the possible tautomeric forms. It is to be understood mat the invention encompasses any tautomeric form. Certain compounds of formula (1) are capable of existing in stereoisomeric forms. It wll be understood that the invention encompasses all geometric and optical isomers of the compounds of formula (1) and mixtures thereof including raceraates. These also form an aspect of the present invention. Salts for use in pharmaceutical compositions will be pharmaceutically acceptable salts, but other salts may be useful in the production of the compounds of formula I and their pharmaceutically acceptable salts. Pharmaceutically acceptable salts of the invention may, for example, include acid addition salts of the compounds of fonnula I as hereinbefore defined which are sufficiently basic to form such salts...Such acid addition salts include for example salts with inorganic or organic acids affording pharmaceutically acceptable anions such as with hydrogen halides (especially hydrochloric or hydrobromic acid of which hydrochloric acid is particularly preferred) or with sulphuric or phosphoric acid, or with trifluoroacetic, citric or maleic acid. Suitable salts include hydrocnlorides, hydrobromides, phosphates, sulphates, hydrogen sulphates, alkylsulphonates, arylsulphonates, acetates, benzoates, citrates, maleates, fumarates, succinates, lactates and tartrates. In addition where the compounds of formula I are sufficiently acidic, pharmaceutically acceptable salts may be formed with an inorganic or organic base which affords a pharmaceutically acceptable cation. Such salts with inorganic or organic bases include for example an alkali metal salt, such as a sodium or potassium salt, an alkaline earth metal salt such as a calcium or magnesium salt, an ammonium salt or for example a salt with methylamine, dimethylamine, trinaethylamine, piperidine, morpholine or tris-(2-hydroxyethyl)amine. Preferred salts include an acid addition salt such as a hydrochloride, hydrobromide, phosphate, acetate, fumarate, maleate, tartrate, citrate, oxalate, methanesulfonate or /?-toluenesulfonate, or an alkali metal salt such as a sodium or potassium salt. In a further aspect the invention provides a process for the preparation of a compound of formula (I) which comprises: (a) reaction of a compound of formula (II): (Figure Remove) in which R] and R2 are as defined in formula (I) or are protected derivatives thereof, and X and Y are selected from Ci^alkyl (optionally substituted by 1,2 or 3 hydroxy groups), , haloalkyl, dihaioalkyl, trihaloalkyl, with a compound of formula (III): ^-01-02 (IH) where Ar2 is as defined in formula (I) or are protected derivatives thereof and Gl is NH, G2isNH2,SHorOH,or (b) reacting a compound of formula (IV): (Figure Remove) (IV) in which R1, R2, Ar and Ar2 are as defined in formula (I) or are protected derivatives thereof, with a compound of formula (V) (Figure Remove) in which P is a protecting group, or (c) for compounds of formula (I) where Ar has an NH group, reacting a compound of formula (VI): (Figure Remove) (VI) in which R1 and R2 and as defined in formula (I) and Ar is as defined in formula (I) provided Ar has an NH group, or are protected derivatives thereof, with a compound of foimula (VII): Ar2-!, (VII) in which Ar2 is as defined in formula (I) or is a protected derivative thereof and L is a leaving group, and optionally thereafter process (a), (b) or (c) in any order removing any protecting groups • forming a pharmaceutically acceptable salt. Reaction of compounds (II) and (III) is suitably carried out in an inert solvent eg ethanol, at a temperature of from 0°C to 100°C, preferably 10°C to 50°C, optionally in the presence of a catalytic quantity of an acid eg trifluoroacetic acid. Reaction of compounds (IV) and (V) is carried out by conversion of the carboxylic acid function to an activated form by reaction with a coupling agent eg EDCI and 1 -hydroxybenzotriazole, in an inert solvent eg dichloromethane, in the presence of a base, preferably triethylamine or ethyldiisopropylamine, at a temperature of from 0°C to 100°C, preferably 10°C to 50°C, in the presence of compound (V). Reaction of compounds (VI) and (VII) is carried out either by heating in an inert solvent such as NMP in the presence of a base, for example a metal carbonate, under microwave irradiation; or by use of catalytic (or stoicheiometric) Buchwald conditionsusing a Cu(I) salt with a diamine ligand in a solvent such as dioxan at a temperature of about 100°C. The group L is any suitable leaving group, preferably L is halogen. Compounds of formula (II) can be prepared by reacting a compound of formula (VIII): (Figure Remove) in which R1, R2 and P are as defined above and L is a leaving group with a nucleophilic fiagment of a the group Ar such as a zinc salt of a beta-diketone. L is preferably a halogen such as bromo. Compounds of formula (VIII) can be prepared from compounds of formula (IX): (Figure Remove) (IX) in which R1, R2 and P are as defined above by, for example, bromination using N-bromosuccinamide in an inert solvent such as chloroform under a light source at a temperature of from 15°C to 80°C, preferably at 50°C to 70°C. Compounds of fonnula (IX) can be prepared by protection of the corresponding alcohols of formula (X): (Figure Remove) in which R1, R2 and P are as defined above by, for example, reacting with a trialkylsilyl halide in an inert solvent such as dichloromethane at a temperature of from 0°C to 60°C, preferably 10°C to 30°C, in the presence of a base such as imidazole. Compounds of formula (X) can be prepared from acids of formula (XI): (Figure Remove) (XT) in which R1, R2 and P are as defined above by forming an acid chloride by treating with a reagent such as oxalyl chloride in an inert solvent such as dichloromethane at a temperature of from 0°C to 60°C, preferably 10°C to 30°C, followed by treatment of the resulting acid chloride with thehydroxyisooxazolidine in a solvent such as dichloromethane at a temperature of from 0°C to 60°C, preferably 10°C to 30°C in the presence of a base such as triethylamine. Compounds of formula (XI) are prepared from the corresponding esters using standard conditions. Compounds of formula (TV) can be prepared from compounds of formula (XII): (Figure Remove) in which R1, R2 and Ar are as defined above, provided that Ar contains an NH group, and R20is an ester forming group by, for example, reacting with a compound of formula (XIII) Ar-halogen (XIII) in which Ar2 is as defined above or by reaction with a compound Ar2 where Ar is as defined above provided that Ar contains a nitrogen centre. Reaction of compounds (XII) and (XIII) can be carried out in an inert solvent such as. dioxan at a temperature of 10°C to 120°C in the presence of a copper (I) salt and an alikylenc diamine. The group R20 is an ester forming group such as alkyl, especially methyl. Reaction of compounds (XII) and Ar2 can be carried out in a solvent such as dimethyl acetamide at a temperature of 10°C to 200°C in the presence of a base such as potassium carbonate optionally with microwave irradiation. A compound of formula (XII) can be prepared from a compound of formula (XV): (Figure Remove) (XV) in which R1, R2 and R20 are as defined above by reaction with a strong base such as lithium diisopropylamide in a solvent such as THF at -78°C to 0°C followed by the addition of a compound of formula (XVI): Ar-CHO (XVI) Compounds of formula (IV) are prepared from compounds of formula (XVII): (Figure Remove) which R1, R , R20, AT and Ar2 are as defined above, either by deoxygenation using a strong acid such as TFA in the presence of a hydride source such as triethylsilane, optionally in a solvent such as dichloromethane at a temperature of 10°C to 40°C,.or by activation of the hydroxyl group by esterificatioh with ana ctivated carboxylic acid such as trifluoroacetic anhydride or methane sulphonyl chloride in an inert solvent such as ethyl acetate followed by hydrogenolysis, for example using palladium on carbon at 1 to 5baratlO°Cto80°C. Compounds of formula (XVII) are prepared from compounds of formula (XV) as defined above by reacxting with compounds (XVIII): Ar2-Ar-CHO (XVIII) in which Ar and Ar2 are as ddefmed above using conditions analogous to those above for the reaction of compounds (XV) and (XVI). Compounds of formula (VI) may be made from compounds of formula (XII) by hydrolysis of the ester function (using an alkali metal or alkaline earth hydroxide in a solvent containg water eg aqueous ethanol or aqueous methanol) at a temperature of from 0°C to 100°C, or using aqueous mineral acid in an inert solvent at a temperature of from 20°C to 100°C, and then coupling the acid residue with a compound of formula (V) in the presence of a condensing agent eg PyBiOP in an inert solvent eg THF in the presence of a base such as triethylamine at a temperature of from 0°C to 30°C. Starting materials as defined above are available commercially or can be prepared using routine chemistry known in the art. The compounds of the invention are useful because they possess pharmacological activity in human and non-human animals. They are indicated as pharmaceuticals for use in the (prophylactic) treatment of autoimmune, inflammatory, proliferative and hyperproliferative diseases and immunologically mediated diseases including rejection of transplanted organs or tissues and Acquired Immunodeficiency Syndrome (AIDS). Examples of these conditions are: (1) (the respiratory tract) airways diseases including chronic obstructive pulmonary disease (COPD); asthma, such as bronchial, allergic, intrinsic, extrinsic and dust asthma, particularly chronic or inveterate asthma (e.g. late asthma and airways . hyper-responsiveness); bronchitis; acute, allergic, atrophic rhinitis and chronic rhinitis including rhinitis caseosa, hypertrophic rhinitis, rhinitis purulenta,' rhinitis sicca and rhinitis medicamentosa; membranous rhinitis including croupous, fibrinous and pseudomembranous rhinitis and scrofoulous rhinitis; seasonal rhinitis-including rhinitis nervosa (hay fever) and vasomotor rhinitis; sarcoidosis, farmer's lung and related diseases, fibroid lung and idiopathic interstitial pneumonia; (2) (bone and joints) rheumatoid arthritis, seronegative spondyloarthropathies (including ankylosing spondylitis, psoriatic arthritis and Reiter's disease), Behcet's disease, Sjogren's syndrome and systemic sclerosis; (3) (skin) psoriasis, atopical dermatitis, contact dermatitis and other eczmatous dermitides, seborrhoetic dermatitis, Lichen planus, Pemphigus, bullous Pemphigus, Epidermolysis bullosa, urticaria, angiodermas, vasculitides, erythemas, cutaneous eosinophilias, uveitis, Alopecia areata and vernal conjunctivitis; (4) (gastrointestinal tract) Coeliac disease, proctitis, eosinopilic gastro-enteritis, mastocytosis, Crohn's disease, ulcerative colitis, food-related allergies which have effects remote from the gut, e.g., migraine, rhinitis and eczema; (5) (other tissues and systemic disease) multiple sclerosis, atherosclerosis, Acquired Immunodeiiciency Syndrome (AIDS), lupus erythematosus, systemic lupus, erythematosus, Hashimoto's thyroiditis, myasthenia gravis, type I diabetes, nephrotic syndrome, eosinophilia fascitis, hyper IgE syndrome, lepromatous leprosy, sezary syndrome and idiopathic thrombocytopenia pupura; (6) (allograft rejection) acute and chronic following, for example, transplantation of kidney, heart, liver, lung, bone marrow, skin and cornea; and chronic graft versus host disease; and (7) cancer. Accordingly, the present invention provides a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined for use in therapy. In another aspect, the invention provides the use of a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined in the manufacture of a medicament for use in therapy. In the context of the present specification, the terra "therapy" also includes "prophylaxis'1 unless there are specific indications to the contrary. The terms "therapeutic" and "therapeutically" should be construed accordingly. Prophylaxis is expected to be particularly relevant to the treatment of persons who have suffered a previous episode of, or are otherwise considered to be at increased risk of, the disease or condition in question. Persons at risk of developing a particular disease or condition generally include those having a family history of the disease or condition, or those who have been identified by genetic testing or screening to be particularly susceptible to developing the disease or condition. The invention further provides a method of effecting immunosuppression (e.g. in the treatment of allograft rejection) which comprises administering to a patient a therapeutically effective amount of a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined. The invention still further provides a method of treating, or reducing the risk of, an airways disease (e.g. asthma or COPD) in a patient suffering from, or at risk of, said disease, which comprises administering to the patient a therapeutically effective amount of a compound of formula (1) or a pharxnaceutically-acceptable salt thereof as hereinbefore defined. For the above-mentioned therapeutic uses the dosage administered will, of course, vary with the compound employed, the mode of administration, the treatment desired and the disorder indicated. However, in general, for effecting immunosuppression, the daily dosage pf the compound of formula (1) will be in the range from 0.1 mg/kg, preferably from 0.3 mg/kg, more preferably from 0.5 mg/kg and still more preferably from Img/kg up to and including 30 mg/kg. For the treatment of airways diseases, the daily dosage of the compound of formula (1) will typically be in the range from 0.001 mg/kg to 30 mg/kg. The compounds of formula (1) and pharmaceutically-acceptable salts thereof may be used on their own but will generally be administered in the form of a pharmaceutical composition in which the formula (1) compoundVsalt/solvate (active ingredient) is in association with apharmaceutically-acceptable adjuvant, diluent or carrier. Depending on the mode of administration, the pharmaceutical composition will preferably comprise fiom 0.05 to 99 %w (per cent by weight), more preferably less than 80 %w,' e.g. from 0.10 to 70 %w, and even more preferably less than 50 %w, of active ingredient, all percentages by weight being based on total composition. Thus, the present invention also provides a pharmaceutical composition comprising a compound of formula (1) or apharmaceutically acceptable salt thereof as hereinbefore defined, in association with a pharmaceutically acceptable adjuvant, diluent or carrier. The invention further provides a process for the preparation of a pharmaceutical composition of the invention which comprises mixing a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined, with a pharmaceutically acceptable adjuvant, diluent or carrier. The pharmaceutical composition of the invention may be administered topically (e.g. to the lung and/or airways or to the skin) in the form of solutions, suspensions, heptafluoroalkane aerosols and dry powder formulations; or systemically, e.g. by oral administration in the form of tablets, capsules, syrups, powders or granules, or by parenteral administration in the form of solutions or suspensions, or by subcutaneous administration or by rectal administration in the form of suppositories or transdermally. The ability of compounds which can inhibit PMA/ionomycin-stimulated peripheral blood mononuclear cell proliferation can be assessed, for example using the procedure set out below. The invention will now be illustrated in the following Examples in which, unless otherwise stated: (i) evaporations were carried out by rotary evaporation in vscuo and work-up procedures were carried out after removal of residual solids such as drying agents by filtration; (ii) operations were carried out at ambient temperature, that is in the range 18-25 °C and under an atmosphere of an inert gas such as argon or nitrogen; (iii) yields are given for illustration only and are not necessarily the maximum attainable; (iv) the structures of the end-products of the formula I were confirmed by nuclear (generally proton) magnetic resonance (NMR) and mass spectral techniques; proton . magnetic resonance chemical shift values were measured on the delta scale and peak multiplicities are shown as follows: s, singlet; d, doublet; t, triplet; m, multiple!; br, broad; q, quartet, quin, quintet; (v) intermediates were not generally fully characterised and purity was assessed by thin layer chromatography (TLC), high-performance liquid chromatography (HPLC), mass spectrometry (MS), infra-red (IR) or NMR analysis; Abbreviations 2,3-Dichloro-5,6-dicyano-l,4-benzoquinone DDQ Dimethylformamide DMF Tetrahydrofuran THF The following examples illustrate the invention. Example 1 6-r[3.S-dimethvl-l-(2-pvrimidlnvlVlJy-Pvra2ol-4-vnmethvn-5-nr4St-4-hvdroxv-2- ioxazolldinyllcrbonn-3-mehI-l-a-methvIethl)thienof23- a) pthvlroethvl 2-methvl-5-Q^.N-methvlemvlaminoVthiophene-3.4-dicarbpxylate Ethoxycarbonylmethylene triphenyl phosphorane (33.8 g) in dry THF (200 ml) was treated with isopropyl isothiocyanate (10.1 g) at 65°C for 16 h under nitrogen. The mixture was cooled to -78°C and methyl 3-bromo-2-oxo-butanoate was added. Tlie reaction was allowed to warm slowly to room temperature. After 24h at room temperature more methyl 3-bromo-2-oxo-butanoate (2.8 g) was added and the mixture was warmed to 60°C for 16 h. The cooled reaction was poured into water (1.5L) and extracted into ether. Drying and evaporation gave an oil which was chromatographed (SiOj/lO:! isohexane-ethyl acetate then 5:1 isohexane-ethyl acetate) to afford the subtitle compound (23.5 g). 8 'HCDCB 1-23-1.35(9H, m), 2.26(3H,s), 3.46(1H, m), 3.82(3H, s), 4.2(2H, q), 7.42(1H, br.s) b>Memvn.23.4-tetrahvdro-3.6-drfflethvl-l-ri-metfavlethvn-2.4-dioxo-thieno[2.3-f/]pvrimidme-S-carboxvlate Silver cyanate (13.5 g) suspended in anhydrous toluene (90 ml) under nitrogen was treated dropwise with acetyl chloride (5.34 ml) and stirred vigorously for 30 min. The product of step a) (23 g) dissolved in anhydrous toluene (15 ml) was added and the mixture was stirred for 72 h. Ether (360 ml) was added and the insoluble material was filtered off and washed with a small volume of ether. The combined organic solutions were washed with saturated sodium bicarbonate solution, dried and evaporated. The residue was treated with a solution of sodium methoxide in methanol (25wt%, 64 ml) at room temperature for 72 h. The reaction was cooled in ice and treated with trimethylsilyl chloride (50.8 ml) and stirred at room temperature overnight. All volatiles were removed in vacua and the residue partitioned between water and ethyl acetate. Drying and evaporation of the organic solution left a residue, which was daromatographed (SiOa/2:l isohexane-ethyl acetate then 3:2 isohexane-ethyl acetate) to isolate the major component (12.2 g). This was taken in dry DMF (ISO ml) with potassium carbonate (6.95 g) and methyl iodide (7.1 g) for 72 h at room temperature. The mixture was poured into water (2L), acidified and extracted into ether. Washing with brine, drying and evaporation gave a solid which was boiled in isohexane (200 ml) containing ethyl acetate (3 ml). On cooling the precipitated pale yellow solid was collected and dried, to afford the sub-title compound (10.5 g). MS(APCI)[M+Hf297 5 'HCDCB 1 -6(6H, d), 2.44(3H,s), 3.37(3H, s), 3.95(3H, s), 4.66(1H, br) c) 1.23.4-Tetrahvdro-3.6-dimethvl-l -(I -methvlethvl)-2.4-dioxo-thienor2.3-i^pvrimidine-5-carboxvlic acid To a solution of the product of step b) (3.81 g) in THF (50 ml) and methanol (5 ml) was added IN NaOH (25.7 ml) and the mixture stirred under nitrogen for 18 hr. It was acidified with 2.5N HC1 and extracted with DCM, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pisessure to give the sub-title compound as a solid (3.40 g) MS(ESI)283[M+Hf mpthvlethvl)thicaio[2.3- To a suspension of the product of part c) (3.40 g) in DCM (50 ml) was added oxalyl chloride (1 . 1 6 ml) and DMF (10 p,l) and the mixture stirred under nitrogen for 2 hr. The add chloride solution was added to a suspension of (iS)-4-isoxazolidinol hydrochloride (1 ,51 g) and triethylamine (3.52 ml) in DCM (20 ml) at 0°C under nitrogen and the mixture stirred at room temperature for 3 hr. It was washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with ethyl acetate to give the sub-title compound as a solid (2.52 g). MS (ESI) 354 [M+Hf 6 'HDMSO 1.50-1.52 (6H, m), 2.30-2.34 (3H, m), 3.18-3.19 (3H, m), 3.42-4.08 (4H, m), 4.59-4.74 (2H, m), 5.49-5.50 (1H, m) e)5-rf(4S)-4-rr(l.l-DimethvlethvI)dimetfavl8ilvnoxv1-2-isoxazolidinvncarbonvl1-3.6- dimethvl-l-(l-n^thvlethvl)thienor2.3-«/)pvrimidine-2.4fl^r.3^)-dione To a solution of the product of part d) (2.52 g) in DCM (30 ml) was added imidazole (0.53 g) and tert-butyldimethylsilyl chloride (1.18 g) and the mixture stirred under nitrogen for 24 hr. It was acidified with IN HC1 and extracted with DCM, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with i-hexane/ethyl acetate (3:1) followed by i- hexane/ethyl acetate (1 : 1) to give the sub-title compound (2.42 g). 8 ]HDMSO 0.09 (6H, d), 0.86 (9H, s), 1.50 (6H, d), 2.31-2.34 (3H, m), 3.18-3.19 (3H, m), 3.44-4.15 (4H, m), 4.50-4.97 (2H, m) f) 6-Bromomethvl-5-rrf4SV4-rrn . 1 -dimethvletfavndimeihvlsilvl')oxv1-2-JsoKazlidinvlcabonvl--methvl-l-fl-neftvleJhvnthieno2.3- . to a solution of the product of part e) (2.42 g) in chloroform (100 ml) was added N-bromosuccinimide (1.01 g) and the mixture heated under reflux whilst being irradiated with a 300W tungsten lamp for 2 hr. It was cooled, washed with IN NaOH solution, washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure to give the sub-title compound (2.83 g) MS (ESI) 546 and 548 [M+Hf -AceWl-3-oxobutvlV5-f [Y4SV4-f f fl .1 -dimemvleftvlMimethvlsilvnoxvl-2- 2.4n#.3#)-dione A solution of the product of part f) (2.83 g) and zinc acetylacetonate hydrate (1 .47 g) in chloroform (50 ml) was heated under refhix for 1 hr. It was cooled, washed with sodium bicarbonate solution, filtered through celite, washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure to give the sub-title compound (2.93 g) MS (ESI) 566 [M+Hf h\|)5-[fr4S)-4-rrd.l-Dimethvlernvndimefo^ -\rimi me^hvl6Jhvl)thieno[2.3-ff]pvrimidiri6-2.4(lJ?.3H)-dione To a solution of the product of part g) (0.73 g) in chloroform (25 ml) was added pyrimidin-2-ylhydrazine (0.27 g) and the mixture stirred for 48 hr. It was washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with i-hexane/ethyl acetate (1:1) followed by i-hexane/ethyl acetate (1 :4) to give the sub-title compound (0.43 g). MS (ESI) 640 i>6-[[3.S-Dmtethvl-l-(2-pvrimidinvlVlH-pvrazol-4-vnmethvn-S-r('(4SV4-hvdroxv-2- is^xazolidinvl1c^bonyl]-3'methyl-i-n-methylethvl)tfaieno[23-^pvriniidine- 2f4 A solution of the product of part h) (0.43 g) and trifluoroacetic acid (0.5 ml) in DCM (10 ml) was stirred for 72 hr. It was concentrated in vacuo, diluted with sodium bicarbonate solution, and extracted with ethyl acetate, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with ethyl acetate then ethyl acetate/methanol (9:1) to give the title compound (30 rag). MS (APCI) 526 [M+Hf 8 'HDMSO 1.44-1.46 (6H, m), 2.16-2.19 (3H, m), 2.53-2.55 (3H, m), 3.17-3.19 (3H, m), 3.48-4.14 (6H, m), 4.38 (1H, s, br), 4.60-4.80 (1H, m), 5.48-5.52 (1H, m), 7.46 (1H, dt), 8.87 (2H, t) Example 2 6-^3^-dimethvl-l-f2-pyridinyn-lfl-pvrazol-4-vl1methyn-5-fK4S'>-4-hvdroxv-2- isxazoltdinvncarbonvn-3-methl-l-fl-methvIethlHhieno2vrtmidine- (Figure Remove) rra.S-dimethvl-l-f2-T)vridinvlVlH-ovrazol-4-vnmethvn-3-methvl-l-n-m^thvlethvnthienof23-^]pvrlmidine-2.4('l/jr.3/:^-dione To a solution of the product of example 1 part g) (0.73 g) in chloroform (25 ml) was added pyridin-2-ylhydrazine (0.28 g) and the mixture stirred for 48 hr. It was washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, elating with i-hexane followed by i-hexane/ethyl acetate (1:1) to give the sub-title compound (0.28 g). M$ (ESI) 639 [M+Hf isotazolidinlcarbonvl--methvl-(l-methvlethvnihieno2J- A solution of the product of part a) (0.28 g) and trifluoroacetic acid (0.5 ml) in DCM (10 ml) was stirred for 72 hr. It was concentrated in vacuo, diluted with sodium bicarbonate solution, and extracted with ethyl acetate, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with ethyl acetate then ethyl acetate/methanol (49:1) to give the title compound (88 mg). MS (APCI) 525 [M+HJ 6 'HDMSO 1.44-1.47 (6H, m), 2.17-2.19 (3H, m), 2.56-2.58 (3H, m), 3.47-4.14 (6H, m), 4.38 (1H, s, br), 4.60-4.80 (1H, m), 5.51-5.52 (1H, m), 7.30-7.34 (1H, m), 7.80 (1H, d), 7.95 (lH,dt), 8.45-8.47 (lH,m) Example 3 (5)-2-[(6-[[3,5-Dimethyl-l-(2-thiazolyl)'lJH-pyrazol-4-yllmethyl]-l,2,3,4-tetrahydro-3-jnethyl-l-(l-methylethyl>2,4-dioxothieno[23- (Figure Remove) Amixtureof(5)-2-[[6-[(3,5-dimethyl-l/f-pyrazol-4-yl)methyl]-l,2,3,4-tetrahydro-3-methyl-1 -(1 -methylethyl)-2,4-dioxothiejio[2,3- MS (APCI -fve) M+H » 531.1 5 IHj3MS0.120°C 1.47 (6H, d), 2.17 (3H, s), 2.60 (3H, s), 3.20 (3H, s), 3.46 (1H, d), 3.75 (1H, d), 3,89-3.95 (2H, m), 3.89 (2H, s), 4.46 (1H, sep), 4.70 (1H, s), 5.08 (1H, s), 7.38 (!H,d),7.56(lH,d). Pharmacological Data Inhibition of PM A/ionomycin-stimulated peripheral blood mononuclear cell proliferation The assay for PMA/ionomytin-stimulated PBMC proliferation was performed in 96-wetl flat-bottomed microtitre plates. Compounds were prepared as lOmM stock solutions in dimethyl sulfbxide. A 50-fold dilution of this was prepared in RPMI and serial dilutions were prepared from this solution. 1 Oul of the 50-fold diluted stock, or dilutions of it, were added to the well to .give concentrations in the assay starting at 9.5p.M and going down. Into each well was placed 1 x 105 PBMC, prepared from human peripheral blood from a single donor, in RPMI1640 medium supplemented with 10% human serum, 2mM glutamtne and penicillin/streptomycin. Phorbol myristate acetate (PMA) (0.5ng/ml final concentration) and ionomycin (500ng/ml final concentration) were added to these cells in supplemented RPMI1640 medium (as above) so that the final volume of the assay was 0.2ml. The cells were incubated at 37°C in a humidified atmosphere at 5% carbon dioxide for 72 hours. 3H-Thymidine (O.SuCi) was added for the final 6 hours of the incubation. The level of radioactivity, incorporated by the cells was then determined and this is a measure of proliferation. The compounds of the Examples were found to exhibit an IAso value of less than 1 x 10** M in the above test. Of the specific examples, examples 1 had aPIAsoof 8.3 and Example 3 had a P1A50 of 9.07 in the above test. We Claims: 1. A thienopyrimidindione compound of formula (1): (Formula Removed) wherein: R1 and R2 each independently represent C1-6alkyl, C3-6alkenyl, C3-5cycloalkylC1-3alkyl or C3-6cycloalkyl, each of which may be optionally substituted by 1 to 3 halogen atoms; Q is CR4R5 where R4 is hydrogen, fluorine or C1-6 alkyl and R5 is hydrogen, fluorine or hydroxy; Ar is a 5- to 10-membered aromatic ring system wherein up to 4 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substituents independently selected from C1-4alkyl (optionally substituted by 1, 2 or 3 hydroxy groups), C1-4alkoxy, halogen, haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) C1-4alkoxyC1-4alkyl, C1-4alkylthio, C1-4alkoxycarbonyl, C2-4alkanoyl, oxo, thioxo, nitro, cyano, -N(R6)R7 and -(CH2)pN(R8)R9, hydroxy, C1-4alkylsulphonyl, C1-4alkylsulphinyl, carbamoyl, C1-4alkylcarbamoyl, di-(C1-4alkyl)carbamoyl, carboxy, SO2N(R8)R9; Ar2 is a 5 or 6 membered aromatic ring containing up to 4 hetero atoms independently selected from nitrogen, sulphur or oxygen, wherein the 6. A compound as claimed in claim 5 wherein Ar is a group of sub-formula (i) (Formula Removed) where R10 and R11 are independently selected from H, C1-6alkyl, or haloC1-6alkyl and Ar2 is as defined above. 7. A compound as claimed in any one of claims 1 to 6 wherein Ar2 is a 5 or 6- membered aromatic ring system wherein up to 3 ring atoms of the aromatic ring system may be heteroatoms independently selected from nitrogen, oxygen and sulphur, wherein the ring system includes at least one heteroatom, and which ring system is optionally substituted by one or more substituents independently selected from C1-4alkyl, C1-4alkoxy, halogen, dihaloalkyl, trihaloalkyl, oxo, thioxo, cyano and C1-4- alkylsulphonyl. 8. A compound as claimed in claim 7 wherein Ar2 is pyridinyl or pyrimidinyl. 9. A compound as claimed in claim 7 wherein Ar2 is thiazolyl. 10. A thienopyrimidindione compound of formula (I) as claimed in claim 1 wherein: 3,5-dimethyl-l-(2-pyrimidinyl)-lH-pyrazol-4-yl]methyl]-5-[[(4S)-4- hydroxy-2-isoxazolidinyl]carbonyl]-3-methyl-l-(l-methylethyl)thieno[2,3- d]pyrimidine-2,4(lH,3H)-dione, 6-[[3,5-dimethyl-l-(2-pyridinyl)-lH-pyrazol-4-yl]methyl]-5-[[(4S)-4-hydroxy-2-isoxazolidinyl]carbonyl]-3-methyl-l-(l-methylethyl)thieno[2,3-d]pyrimidine-2,4(lH,3H)-dione, or (S)-2-[[6-[[3,5-Dimethyl-l-(2-thiazolyl)-lH-pyrazol-4-yl]methyl]-l ,2,3,4- tetrahydro-3-methyl-l-(l-methylethyl)-2,4-dioxothieno[2,3-d]pyrimidin- 5-yl]carbonyl]-4-isoxazolidinol or pharmaceutically acceptable salts thereof. 11. A pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof as claimed in any one of claims 1 to 10 in association with a pharmaceutical carrier, which composition comprises from 0.05 to 99 w% of active ingredient and the remaining being pharmaceutical carrier, all percentages by weight being based on total composition. 12. A process for the preparation of a compound of formula (I) as claimed in claim 1 which comprises: (a) reaction of a compound of formula (II): (Formula Removed) in which R1 and R2 are as claimed in claim 1 for formula (I) or are protected derivatives thereof, and X and Y are selected from C1-4alkyl (optionally substituted by 1,2 or 3 hydroxy groups), C1-4alkoxy, haloalkyl, dihaloalkyl, trihaloalkyl, C1-4alkoxyC1-4alkyl, C1-4alkoxycarbonyl,-(CH2)pN(R8)R9, with a compound of formula (III): Ar2-Gl-G2 (III) where Ar2 is as claimed in claim 1 for formula (I) or are protected derivatives thereof and Gl is NH, G2 is NH2, SH or OH, which reaction is carried out in an inert solvent, at a temperature of from 0°C to 100°C preferably 10°C to 50°C and optionally in the presence of a catalytic quantity of an acid, and optionally thereafter process (a) in any order • removing any protecting groups • forming a pharmaceutically acceptable salt.

Full Text

The present invention relates to a thienopyrimidindione compound.
The present invention relates to thienopyridazinones, processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The invention also relates to their use in the modulation of autoimmune disease.
T-cells play an important role in the immune response, however in auto-immune disease T-cells are inappropriately activated against particular tissues and proliferates eg causing the inflammation associated with rheumatoid arthritis. Inhibition of the proliferation of T-cells is beneficial in the modulation of autoimmune disease. The present invention relates to compounds which are beneficial in the modulation of autoimmune disease.
In accordance with the present invention, there is provided a compound of formula (1):
(Formula Removed)
wherein:
R! and R2 each independently represent C1-6alkyl, C3-6alkenyl, C3-5cycloalkylC1-3alkyl or C3-6cycloalkyl, each of which may be optionally substituted by 1 to 3 halogen atoms;
Q is CR4R5 where R4 is hydrogen, fluorine or C1-6 alkyl and R5 is hydrogen, fluorine or hydroxy;
Axis a 5- to 1 0-membered aromatic ring system wherein up to 4 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substituents independently selected from C1-4alky! (optionally substituted by 1, 2 or 3 hydroxy groups), C1-4alkoxy, halogen, haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) C1-4alkoxyC1-4alkyl, C1-4alkylthio, C1-4alkoxycarbonyl, C2-4alkanoyl, oxo, thioxo, nitro, cyano, -N(R6)R7 and -(CH2)pN(R8)R9, hydroxy, C1-4alkylsulphonyl C1-4alkylsulphinyl, carbarnoyl,
, haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) Cj^alkoxyCj^alkyl, Ci^alkylthio, C\^alkoxycarbonyl, Cj^alkanoyl, oxo, thioxo, nitro, cyano, -J^R^R7 and - CMalkylcarbamoyl, dHCMalkyOcarbamoyl, carboxy, S02N(R8)R9;
Ar2 is a 5 or 6 membered aromatic ring containing up to 4 hetero atoms independently selected from nitrogen, sulphur or oxygen, and which may be optionally substituted by one or more groups independently selected from Chalky! (optionally substituted by 1,2 or 3 hydroxy groups), C^alkoxy, halogen, haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) CMalkoxyd^alkyl, Ci-4alkylthio, CmaUcoxycarbonyl, Ci^alkanoyl, oxo, thioxo, nitro, cyano, -N^R7 and -^(CHaJpNCR^R9, hydroxy, CMalkylsulphonyl, CMalkylsulphinyl, carbamoyl, C\. 4alkylcarbamoyl, di-(Cj.4alkyl)carbamoyl, carboxy, SO;zN(R*)R9;
p is 1 to 4;
R6 and R7 each independently represent a hydrogen atom, CMalkanoyl or Chalky! group, or together with the nitrogen atom to which they are attached form a 5- to 7-ntembered saturated heterocyclic ring optionally containing a further 0, S, NH or Nalkyl group;
R8 and R9 each independently represent a hydrogen atom, Cmalkanoyl or Chalky! group, or together with the nitrogen atom to which they are attached form a S- to 7-ntembered saturated heterocyclic ring optionally containing a further 0, S, NH or Nalkyl group;
and phannaceutically acceptable salts and solvates thereof, provided that the compound is other than 5-[(45)-4-Hydroxyisoxa2a>lidin-2-ylcarbonyl]-l-(isobutyl)-3-methyl-6-[5" l-l#-pyrazoM-ylraetty^
-phenyl-l#-pyr^
ylcarbonyl]-! -isobutyl-3"methylthieno[2,3-)pyriniidine-2,4(lH,3J-f)-dione or • 6*[3,5-Dimemyl-l-phenyl-lH-pyrazol^ytoethyl]-5-[(45)-4-hydroxyisoxazoUdm^ ylcarbonyI]-3-memyl-l-propylthieno[2,3- Suitably R1 is CMS alkyl or €3.5 cycloalkyl, and in particular C^ alkyl. More preferably RJ is ethyl, propyl, butyl or cyclopropyl. Most preferably R1 is ethyl, isobutyl, isopropyl or cyclopropyl.
More preferably R1 is CM alkyl such as isobutyl or isopropyl.
Preferably R2 is C5,6alkyl such as ethyl or methyl, more preferably methyl.
Suitably Q is CR^R* where R5 is hydrogen, CH alkyl and R6 is hydrogen. Preferably Q is CR*R5 where R4 and R5 are both hydrogen.
Examples of 5-10 membered mono- or bi-cyclic aromatic ring systems for Ar include thienyl, ruranyl, pyrrolyl, pyrrolopyridino, imidazolyl, pyridyl, pyrazinyl, pyrimidyl, pyridazinyl, triazinyl, oxazolyl, thiazolyl, isoxazolyl, pyrazolyl, oxadiazolyl, thiadiazolyl,triazolyl,tetrazolylandquiijolyl. ...
Examples of 5- to 7-rnembered saturated heterocyclic rings formed by R6 and R7 and R8 and R9 include morpholine, piperidine, N-alkyl piperidine, pierazine, pyrrolidine and the like. Preferably Ar is a 5 or 6-membered aromatic ring system wherein up to 2 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substttuents independently selected from Chalky!, CMalkoxy, halogen, haloCi^alkyl, dihaloCMalkyl, tri haHoC]4alkyl, oxo, thioxo, cyano, or Cj^alkylsulphonyl.
More preferably Ar is 5-membered aromatic ring containing two nitrogen atoms and substituted as above.
A particular example of Ar is an optionally substituted pyrazole ring. Preferably Ar is a substituted pyrazole ring.
Most preferably Ar is a pyrazole ring di-substiruted by Chalky!, especially methyl. . For instance, Ar is suitably a group of sub-formula (i)
(Figure Remove)
where R10 and R11 are independently selected from H, Cj-galkyl, dihaloCi-4alkyl, or trihaloCMalkyl, and Ar2 is as defined above.
In R10 and R11 are selected from H or Cj^alkyl, such as methyl. In particular, both R10 and R1 ' is Chalky! such as methyl.
Ar2 is suitably a 5 or 6-membered aromatic ring system "wherein up to 3 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substituents independently selected from Cj^alkyl, Cj^alkoxy, halogen, dihaloalkyl, trihaloalkyl, oxo, thioxo, cyano, Cualkylsulphonyl.
Preferably Ar2 is other than pbenyl. In particular Ar2 includes at least one heteroatom.
Examples of haloalky] groups are haloCMalkyl groups which include halomethyl groups such as fluoroethyl groups. Examples of dihaloalkyl groups are dihaloCualkyl groups including difluoromethyl and dichloromethyl. Examples of trihaloalkyl groups are trihaloCMalkyl groups such as trifluoromethyl.
In ft preferred embodiment, Ar1 is 5-membered aromatic ring containing a nitrogen and sulphur atom and substituted as above. Most preferably Ar2 is a thiazole ring substituted by halogen, especially fluoro.
In an alternative embodiment of the invention, Ar2 is pyridine or pyrimidine. The rings cany at least one subatituent, but are preferably unsubstituted.
Preferably Ar2 is pyridinyl or pyrimidinyl.
Preferred compounds of formula (I) include:
6-[t3,5-dimemyl-l-(2-pyrM^ isoxazolidinyl3carbonyl3-3-mefliyl-l-(l-methylethyl)thieno[2,3-fifJpyrimidine-
2,4(l#,3/0-dione, and 6-[[3,5-dimethyM-(2-pyridinyl)-l^-pyrazol-4-yl]methyl]-5-[[(4S)-4-hydroxy-2-
isoxazolidinyl]carbonyl]-3-methyl-l-(l-methylethy])thieno[2,3-]pyrimidine-
and pharmaceutically acceptable salts thereof.
Other preferred compounds of formula (I) include (iS)-2-[[6-[[3,5-Dimethyl-l-(2-tWazolyl)-l#-pyrazol^yl]mernyl]-l^ dioxothieno[23-^pyrimidin-5-yl]carbonyl]-4-isoxazolidinol and pharmaceutically acceptable salts thereof.
Alkyl groups, whether alone or as part of another group, can be straight chained or branched. Unless otherwise stated, they may contain from 1 to 6, and preferably from 1 to 4 carbon atoms.
It will be understood that a compound of the fonnula (I) or a salt thereof may exhibit the phenomenon of tautomerism and that the drawings within this specification represent only one of the possible tautomeric forms. It is to be understood mat the invention encompasses any tautomeric form.
Certain compounds of formula (1) are capable of existing in stereoisomeric forms. It wll be understood that the invention encompasses all geometric and optical isomers of the compounds of formula (1) and mixtures thereof including raceraates. These also form an aspect of the present invention.
Salts for use in pharmaceutical compositions will be pharmaceutically acceptable salts, but other salts may be useful in the production of the compounds of formula I and their pharmaceutically acceptable salts. Pharmaceutically acceptable salts of the invention may, for example, include acid addition salts of the compounds of fonnula I as hereinbefore defined which are sufficiently basic to form such salts...Such acid addition salts include for example salts with inorganic or organic acids affording pharmaceutically acceptable anions such as with hydrogen halides (especially hydrochloric or hydrobromic acid of which hydrochloric acid is particularly preferred) or with sulphuric or phosphoric acid, or with trifluoroacetic, citric or maleic acid. Suitable salts include hydrocnlorides, hydrobromides, phosphates, sulphates, hydrogen sulphates, alkylsulphonates, arylsulphonates, acetates, benzoates, citrates, maleates, fumarates, succinates, lactates and tartrates. In addition where the compounds of formula I are sufficiently acidic, pharmaceutically acceptable salts may be formed with an inorganic or organic base which affords a pharmaceutically acceptable cation. Such salts with inorganic or organic bases include for example an alkali metal salt, such as a sodium or potassium salt, an alkaline earth metal salt such as a calcium or magnesium salt, an ammonium salt or for example a salt with methylamine, dimethylamine, trinaethylamine, piperidine, morpholine or tris-(2-hydroxyethyl)amine.
Preferred salts include an acid addition salt such as a hydrochloride, hydrobromide, phosphate, acetate, fumarate, maleate, tartrate, citrate, oxalate, methanesulfonate or /?-toluenesulfonate, or an alkali metal salt such as a sodium or potassium salt.
In a further aspect the invention provides a process for the preparation of a compound of formula (I) which comprises:
(a) reaction of a compound of formula (II):
(Figure Remove)
in which R] and R2 are as defined in formula (I) or are protected derivatives thereof, and X and Y are selected from Ci^alkyl (optionally substituted by 1,2 or 3 hydroxy groups), , haloalkyl, dihaioalkyl, trihaloalkyl,
with a compound of formula (III): ^-01-02 (IH)
where Ar2 is as defined in formula (I) or are protected derivatives thereof and Gl is NH, G2isNH2,SHorOH,or

(b) reacting a compound of formula (IV):

(Figure Remove)

(IV)
in which R1, R2, Ar and Ar2 are as defined in formula (I) or are protected derivatives
thereof, with a compound of formula (V)
(Figure Remove)
in which P is a protecting group, or
(c) for compounds of formula (I) where Ar has an NH group, reacting a compound of formula (VI):
(Figure Remove)
(VI)
in which R1 and R2 and as defined in formula (I) and Ar is as defined in formula (I) provided Ar has an NH group, or are protected derivatives thereof, with a compound of foimula (VII):
Ar2-!, (VII)
in which Ar2 is as defined in formula (I) or is a protected derivative thereof and L is a leaving group,
and optionally thereafter process (a), (b) or (c) in any order
* removing any protecting groups
• forming a pharmaceutically acceptable salt.
Reaction of compounds (II) and (III) is suitably carried out in an inert solvent eg ethanol, at a temperature of from 0°C to 100°C, preferably 10°C to 50°C, optionally in the presence of a catalytic quantity of an acid eg trifluoroacetic acid.
Reaction of compounds (IV) and (V) is carried out by conversion of the carboxylic acid function to an activated form by reaction with a coupling agent eg EDCI and 1 -hydroxybenzotriazole, in an inert solvent eg dichloromethane, in the presence of a base, preferably triethylamine or ethyldiisopropylamine, at a temperature of from 0°C to 100°C, preferably 10°C to 50°C, in the presence of compound (V).
Reaction of compounds (VI) and (VII) is carried out either by heating in an inert solvent such as NMP in the presence of a base, for example a metal carbonate, under microwave irradiation; or by use of catalytic (or stoicheiometric) Buchwald conditionsusing a Cu(I) salt with a diamine ligand in a solvent such as dioxan at a temperature of about 100°C. The group L is any suitable leaving group, preferably L is halogen.
Compounds of formula (II) can be prepared by reacting a compound of formula (VIII):
(Figure Remove)

in which R1, R2 and P are as defined above and L is a leaving group with a nucleophilic fiagment of a the group Ar such as a zinc salt of a beta-diketone. L is preferably a halogen such as bromo.
Compounds of formula (VIII) can be prepared from compounds of formula (IX):

(Figure Remove)

(IX)
in which R1, R2 and P are as defined above by, for example, bromination using N-bromosuccinamide in an inert solvent such as chloroform under a light source at a temperature of from 15°C to 80°C, preferably at 50°C to 70°C.
Compounds of fonnula (IX) can be prepared by protection of the corresponding alcohols of formula (X):
(Figure Remove)
in which R1, R2 and P are as defined above by, for example, reacting with a trialkylsilyl halide in an inert solvent such as dichloromethane at a temperature of from 0°C to 60°C, preferably 10°C to 30°C, in the presence of a base such as imidazole.

Compounds of formula (X) can be prepared from acids of formula (XI):

(Figure Remove)

(XT)
in which R1, R2 and P are as defined above by forming an acid chloride by treating with a reagent such as oxalyl chloride in an inert solvent such as dichloromethane at a temperature of from 0°C to 60°C, preferably 10°C to 30°C, followed by treatment of the resulting acid chloride with thehydroxyisooxazolidine in a solvent such as dichloromethane at a temperature of from 0°C to 60°C, preferably 10°C to 30°C in the presence of a base such as triethylamine.
Compounds of formula (XI) are prepared from the corresponding esters using standard conditions.
Compounds of formula (TV) can be prepared from compounds of formula (XII):

(Figure Remove)

in which R1, R2 and Ar are as defined above, provided that Ar contains an NH group, and R20is an ester forming group by, for example, reacting with a compound of formula (XIII)
Ar*-halogen (XIII)

in which Ar2 is as defined above or by reaction with a compound Ar2 where Ar is as defined above provided that Ar contains a nitrogen centre.
Reaction of compounds (XII) and (XIII) can be carried out in an inert solvent such as. dioxan at a temperature of 10°C to 120°C in the presence of a copper (I) salt and an alikylenc diamine. The group R20 is an ester forming group such as alkyl, especially methyl.
Reaction of compounds (XII) and Ar2 can be carried out in a solvent such as dimethyl acetamide at a temperature of 10°C to 200°C in the presence of a base such as potassium carbonate optionally with microwave irradiation.
A compound of formula (XII) can be prepared from a compound of formula (XV):
(Figure Remove)
(XV)
in which R1, R2 and R20 are as defined above by reaction with a strong base such as lithium diisopropylamide in a solvent such as THF at -78°C to 0°C followed by the addition of a compound of formula (XVI):
Ar-CHO (XVI)
Compounds of formula (IV) are prepared from compounds of formula (XVII):
(Figure Remove)
which R1, R , R20, AT and Ar2 are as defined above, either by deoxygenation using a strong acid such as TFA in the presence of a hydride source such as triethylsilane, optionally in a solvent such as dichloromethane at a temperature of 10°C to 40°C,.or by activation of the hydroxyl group by esterificatioh with ana ctivated carboxylic acid such as trifluoroacetic anhydride or methane sulphonyl chloride in an inert solvent such as ethyl acetate followed by hydrogenolysis, for example using palladium on carbon at 1 to 5baratlO°Cto80°C.
Compounds of formula (XVII) are prepared from compounds of formula (XV) as defined above by reacxting with compounds (XVIII):
Ar2-Ar-CHO (XVIII)
in which Ar and Ar2 are as ddefmed above using conditions analogous to those above for the reaction of compounds (XV) and (XVI).
Compounds of formula (VI) may be made from compounds of formula (XII) by hydrolysis of the ester function (using an alkali metal or alkaline earth hydroxide in a solvent containg water eg aqueous ethanol or aqueous methanol) at a temperature of from 0°C to 100°C, or using aqueous mineral acid in an inert solvent at a temperature of from 20°C to 100°C, and then coupling the acid residue with a compound of formula (V) in the presence of a condensing agent eg PyBiOP in an inert solvent eg THF in the presence of a base such as triethylamine at a temperature of from 0°C to 30°C.
Starting materials as defined above are available commercially or can be prepared using routine chemistry known in the art.
The compounds of the invention are useful because they possess pharmacological activity in human and non-human animals. They are indicated as pharmaceuticals for use in the (prophylactic) treatment of autoimmune, inflammatory, proliferative and hyperproliferative diseases and immunologically mediated diseases including rejection of transplanted organs or tissues and Acquired Immunodeficiency Syndrome (AIDS).
Examples of these conditions are:
(1) (the respiratory tract) airways diseases including chronic obstructive pulmonary disease (COPD); asthma, such as bronchial, allergic, intrinsic, extrinsic and dust
asthma, particularly chronic or inveterate asthma (e.g. late asthma and airways . hyper-responsiveness); bronchitis; acute, allergic, atrophic rhinitis and chronic rhinitis including rhinitis caseosa, hypertrophic rhinitis, rhinitis purulenta,' rhinitis sicca and rhinitis medicamentosa; membranous rhinitis including croupous, fibrinous and pseudomembranous rhinitis and scrofoulous rhinitis; seasonal rhinitis-including rhinitis nervosa (hay fever) and vasomotor rhinitis; sarcoidosis, farmer's lung and related diseases, fibroid lung and idiopathic interstitial pneumonia;
(2) (bone and joints) rheumatoid arthritis, seronegative spondyloarthropathies
(including ankylosing spondylitis, psoriatic arthritis and Reiter's disease), Behcet's
disease, Sjogren's syndrome and systemic sclerosis;
(3) (skin) psoriasis, atopical dermatitis, contact dermatitis and other eczmatous
dermitides, seborrhoetic dermatitis, Lichen planus, Pemphigus, bullous Pemphigus,
Epidermolysis bullosa, urticaria, angiodermas, vasculitides, erythemas, cutaneous
eosinophilias, uveitis, Alopecia areata and vernal conjunctivitis;

(4) (gastrointestinal tract) Coeliac disease, proctitis, eosinopilic gastro-enteritis,
mastocytosis, Crohn's disease, ulcerative colitis, food-related allergies which have
effects remote from the gut, e.g., migraine, rhinitis and eczema;
(5) (other tissues and systemic disease) multiple sclerosis, atherosclerosis, Acquired
Immunodeiiciency Syndrome (AIDS), lupus erythematosus, systemic lupus,
erythematosus, Hashimoto's thyroiditis, myasthenia gravis, type I diabetes,
nephrotic syndrome, eosinophilia fascitis, hyper IgE syndrome, lepromatous
leprosy, sezary syndrome and idiopathic thrombocytopenia pupura;
(6) (allograft rejection) acute and chronic following, for example, transplantation of
kidney, heart, liver, lung, bone marrow, skin and cornea; and chronic graft versus
host disease; and
(7) cancer.
Accordingly, the present invention provides a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined for use in therapy.
In another aspect, the invention provides the use of a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined in the manufacture of a medicament for use in therapy.
In the context of the present specification, the terra "therapy" also includes "prophylaxis'1 unless there are specific indications to the contrary. The terms "therapeutic" and "therapeutically" should be construed accordingly.
Prophylaxis is expected to be particularly relevant to the treatment of persons who have suffered a previous episode of, or are otherwise considered to be at increased risk of, the disease or condition in question. Persons at risk of developing a particular disease or condition generally include those having a family history of the disease or condition, or those who have been identified by genetic testing or screening to be particularly susceptible to developing the disease or condition.
The invention further provides a method of effecting immunosuppression (e.g. in the treatment of allograft rejection) which comprises administering to a patient a therapeutically effective amount of a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined.
The invention still further provides a method of treating, or reducing the risk of, an airways disease (e.g. asthma or COPD) in a patient suffering from, or at risk of, said disease, which comprises administering to the patient a therapeutically effective amount of a compound of formula (1) or a pharxnaceutically-acceptable salt thereof as hereinbefore defined.
For the above-mentioned therapeutic uses the dosage administered will, of course, vary with the compound employed, the mode of administration, the treatment desired and the disorder indicated. However, in general, for effecting immunosuppression, the daily dosage pf the compound of formula (1) will be in the range from 0.1 mg/kg, preferably from 0.3 mg/kg, more preferably from 0.5 mg/kg and still more preferably from Img/kg up to and including 30 mg/kg. For the treatment of airways diseases, the daily dosage of the compound of formula (1) will typically be in the range from 0.001 mg/kg to 30 mg/kg.
The compounds of formula (1) and pharmaceutically-acceptable salts thereof may be used on their own but will generally be administered in the form of a pharmaceutical
composition in which the formula (1) compoundVsalt/solvate (active ingredient) is in association with apharmaceutically-acceptable adjuvant, diluent or carrier. Depending on the mode of administration, the pharmaceutical composition will preferably comprise fiom 0.05 to 99 %w (per cent by weight), more preferably less than 80 %w,' e.g. from 0.10 to 70 %w, and even more preferably less than 50 %w, of active ingredient, all percentages by weight being based on total composition.
Thus, the present invention also provides a pharmaceutical composition comprising a compound of formula (1) or apharmaceutically acceptable salt thereof as hereinbefore defined, in association with a pharmaceutically acceptable adjuvant, diluent or carrier.
The invention further provides a process for the preparation of a pharmaceutical composition of the invention which comprises mixing a compound of formula (1) or a pharmaceutically acceptable salt thereof as hereinbefore defined, with a pharmaceutically acceptable adjuvant, diluent or carrier.
The pharmaceutical composition of the invention may be administered topically (e.g. to the lung and/or airways or to the skin) in the form of solutions, suspensions, heptafluoroalkane aerosols and dry powder formulations; or systemically, e.g. by oral administration in the form of tablets, capsules, syrups, powders or granules, or by parenteral administration in the form of solutions or suspensions, or by subcutaneous administration or by rectal administration in the form of suppositories or transdermally.
The ability of compounds which can inhibit PMA/ionomycin-stimulated peripheral blood mononuclear cell proliferation can be assessed, for example using the procedure set out below.
The invention will now be illustrated in the following Examples in which, unless otherwise stated:
(i) evaporations were carried out by rotary evaporation in vscuo and work-up procedures were carried out after removal of residual solids such as drying agents by filtration;
(ii) operations were carried out at ambient temperature, that is in the range 18-25 °C and under an atmosphere of an inert gas such as argon or nitrogen;
(iii) yields are given for illustration only and are not necessarily the maximum attainable;
(iv) the structures of the end-products of the formula I were confirmed by nuclear (generally proton) magnetic resonance (NMR) and mass spectral techniques; proton . magnetic resonance chemical shift values were measured on the delta scale and peak multiplicities are shown as follows: s, singlet; d, doublet; t, triplet; m, multiple!; br, broad; q, quartet, quin, quintet;
(v) intermediates were not generally fully characterised and purity was assessed by thin layer chromatography (TLC), high-performance liquid chromatography (HPLC), mass spectrometry (MS), infra-red (IR) or NMR analysis;
Abbreviations
2,3-Dichloro-5,6-dicyano-l,4-benzoquinone DDQ
Dimethylformamide DMF
Tetrahydrofuran THF
The following examples illustrate the invention.
Example 1
6-r[3.S-dimethvl-l-(2-pvrimidlnvlVlJy-Pvra2ol-4-vnmethvn-5-nr4St-4-hvdroxv-2-
ioxazolldinyllcrbonn-3-mehI-l-a-methvIethl)thienof23- a) pthvlroethvl 2-methvl-5-Q^.N-methvlemvlaminoVthiophene-3.4-dicarbpxylate Ethoxycarbonylmethylene triphenyl phosphorane (33.8 g) in dry THF (200 ml) was treated with isopropyl isothiocyanate (10.1 g) at 65°C for 16 h under nitrogen. The mixture was cooled to -78°C and methyl 3-bromo-2-oxo-butanoate was added. Tlie reaction was allowed to warm slowly to room temperature. After 24h at room

temperature more methyl 3-bromo-2-oxo-butanoate (2.8 g) was added and the mixture was warmed to 60°C for 16 h. The cooled reaction was poured into water (1.5L) and extracted into ether. Drying and evaporation gave an oil which was chromatographed (SiOj/lO:! isohexane-ethyl acetate then 5:1 isohexane-ethyl acetate) to afford the subtitle compound (23.5 g).
8 'HCDCB 1-23-1.35(9H, m), 2.26(3H,s), 3.46(1H, m), 3.82(3H, s), 4.2(2H, q), 7.42(1H, br.s)
b>Memvn.23.4-tetrahvdro-3.6-drfflethvl-l-ri-metfavlethvn-2.4-dioxo-thieno[2.3-f/]pvrimidme-S-carboxvlate
Silver cyanate (13.5 g) suspended in anhydrous toluene (90 ml) under nitrogen was treated dropwise with acetyl chloride (5.34 ml) and stirred vigorously for 30 min. The product of step a) (23 g) dissolved in anhydrous toluene (15 ml) was added and the mixture was stirred for 72 h. Ether (360 ml) was added and the insoluble material was filtered off and washed with a small volume of ether. The combined organic solutions were washed with saturated sodium bicarbonate solution, dried and evaporated. The residue was treated with a solution of sodium methoxide in methanol (25wt%, 64 ml) at room temperature for 72 h. The reaction was cooled in ice and treated with trimethylsilyl chloride (50.8 ml) and stirred at room temperature overnight. All volatiles were removed in vacua and the residue partitioned between water and ethyl acetate. Drying and evaporation of the organic solution left a residue, which was daromatographed (SiOa/2:l isohexane-ethyl acetate then 3:2 isohexane-ethyl acetate) to isolate the major component (12.2 g). This was taken in dry DMF (ISO ml) with potassium carbonate (6.95 g) and methyl iodide (7.1 g) for 72 h at room temperature. The mixture was poured into water (2L), acidified and extracted into ether. Washing with brine, drying and evaporation gave a solid which was boiled in isohexane (200 ml) containing ethyl acetate (3 ml). On cooling the precipitated pale yellow solid was collected and dried, to afford the sub-title compound (10.5 g). MS(APCI)[M+Hf297 5 'HCDCB 1 -6(6H, d), 2.44(3H,s), 3.37(3H, s), 3.95(3H, s), 4.66(1H, br)
c) 1.23.4-Tetrahvdro-3.6-dimethvl-l -(I -methvlethvl)-2.4-dioxo-thienor2.3-i^pvrimidine-5-carboxvlic acid
To a solution of the product of step b) (3.81 g) in THF (50 ml) and methanol (5 ml) was added IN NaOH (25.7 ml) and the mixture stirred under nitrogen for 18 hr. It was acidified with 2.5N HC1 and extracted with DCM, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pisessure to give the sub-title compound as a solid (3.40 g) MS(ESI)283[M+Hf

mpthvlethvl)thicaio[2.3- To a suspension of the product of part c) (3.40 g) in DCM (50 ml) was added oxalyl chloride (1 . 1 6 ml) and DMF (10 p,l) and the mixture stirred under nitrogen for 2 hr. The add chloride solution was added to a suspension of (iS)-4-isoxazolidinol hydrochloride (1 ,51 g) and triethylamine (3.52 ml) in DCM (20 ml) at 0°C under nitrogen and the mixture stirred at room temperature for 3 hr. It was washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with ethyl acetate to give the sub-title compound as a solid (2.52 g). MS (ESI) 354 [M+Hf
6 'HDMSO 1.50-1.52 (6H, m), 2.30-2.34 (3H, m), 3.18-3.19 (3H, m), 3.42-4.08 (4H, m), 4.59-4.74 (2H, m), 5.49-5.50 (1H, m)
e)5-rf(4S)-4-rr(l.l-DimethvlethvI)dimetfavl8ilvnoxv1-2-isoxazolidinvncarbonvl1-3.6-
dimethvl-l-(l-n^thvlethvl)thienor2.3-«/)pvrimidine-2.4fl^r.3^)-dione
To a solution of the product of part d) (2.52 g) in DCM (30 ml) was added imidazole
(0.53 g) and tert-butyldimethylsilyl chloride (1.18 g) and the mixture stirred under
nitrogen for 24 hr. It was acidified with IN HC1 and extracted with DCM, the organic
extracts washed with water, dried over anhydrous magnesium sulfate, filtered and
evaporated under reduced pressure. The residue was purified by column
chromatography over silica, eluting with i-hexane/ethyl acetate (3:1) followed by i-
hexane/ethyl acetate (1 : 1) to give the sub-title compound (2.42 g).
8 ]HDMSO 0.09 (6H, d), 0.86 (9H, s), 1.50 (6H, d), 2.31-2.34 (3H, m), 3.18-3.19 (3H, m),
3.44-4.15 (4H, m), 4.50-4.97 (2H, m)
f) 6-Bromomethvl-5-rrf4SV4-rrn . 1 -dimethvletfavndimeihvlsilvl')oxv1-2-JsoKazlidinvlcabonvl--methvl-l-fl-neftvleJhvnthieno2.3- . to a solution of the product of part e) (2.42 g) in chloroform (100 ml) was added N-bromosuccinimide (1.01 g) and the mixture heated under reflux whilst being irradiated with a 300W tungsten lamp for 2 hr. It was cooled, washed with IN NaOH solution, washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure to give the sub-title compound (2.83 g) MS (ESI) 546 and 548 [M+Hf
-AceWl-3-oxobutvlV5-f [Y4SV4-f f fl .1 -dimemvleftvlMimethvlsilvnoxvl-2-
2.4n#.3#)-dione

A solution of the product of part f) (2.83 g) and zinc acetylacetonate hydrate (1 .47 g) in chloroform (50 ml) was heated under refhix for 1 hr. It was cooled, washed with sodium bicarbonate solution, filtered through celite, washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure to give the sub-title compound (2.93 g) MS (ESI) 566 [M+Hf
h|)5-[fr4S)-4-rrd.l-Dimethvlernvndimefo^ -\rimi
me^hvl6Jhvl)thieno[2.3-ff]pvrimidiri6-2.4(lJ?.3H)-dione To a solution of the product of part g) (0.73 g) in chloroform (25 ml) was added pyrimidin-2-ylhydrazine (0.27 g) and the mixture stirred for 48 hr. It was washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with i-hexane/ethyl acetate (1:1) followed by i-hexane/ethyl acetate (1 :4) to give the sub-title compound (0.43 g). MS (ESI) 640
i>6-[[3.S-Dmtethvl-l-(2-pvrimidinvlVlH-pvrazol-4-vnmethvn-S-r('(4SV4-hvdroxv-2-
is^xazolidinvl1c^bonyl]-3'methyl-i-n-methylethvl)tfaieno[23-^pvriniidine-
2f4 A solution of the product of part h) (0.43 g) and trifluoroacetic acid (0.5 ml) in DCM (10
ml) was stirred for 72 hr. It was concentrated in vacuo, diluted with sodium bicarbonate
solution, and extracted with ethyl acetate, the organic extracts washed with water, dried
over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The
residue was purified by column chromatography over silica, eluting with ethyl acetate
then ethyl acetate/methanol (9:1) to give the title compound (30 rag).
MS (APCI) 526 [M+Hf
8 'HDMSO 1.44-1.46 (6H, m), 2.16-2.19 (3H, m), 2.53-2.55 (3H, m), 3.17-3.19 (3H, m),
3.48-4.14 (6H, m), 4.38 (1H, s, br), 4.60-4.80 (1H, m), 5.48-5.52 (1H, m), 7.46 (1H, dt),
8.87 (2H, t)

Example 2
6-^3^-dimethvl-l-f2-pyridinyn-lfl-pvrazol-4-vl1methyn-5-fK4S'>-4-hvdroxv-2-
isxazoltdinvncarbonvn-3-methl-l-fl-methvIethlHhieno2vrtmidine-
(Figure Remove)
rra.S-dimethvl-l-f2-T)vridinvlVlH-ovrazol-4-vnmethvn-3-methvl-l-n-m^thvlethvnthienof23-^]pvrlmidine-2.4('l/jr.3/:^-dione
To a solution of the product of example 1 part g) (0.73 g) in chloroform (25 ml) was added pyridin-2-ylhydrazine (0.28 g) and the mixture stirred for 48 hr. It was washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, elating with i-hexane followed by i-hexane/ethyl acetate (1:1) to give the sub-title compound (0.28 g). M$ (ESI) 639 [M+Hf
isotazolidinlcarbonvl--methvl-(l-methvlethvnihieno2J- A solution of the product of part a) (0.28 g) and trifluoroacetic acid (0.5 ml) in DCM (10 ml) was stirred for 72 hr. It was concentrated in vacuo, diluted with sodium bicarbonate solution, and extracted with ethyl acetate, the organic extracts washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with ethyl acetate then ethyl acetate/methanol (49:1) to give the title compound (88 mg). MS (APCI) 525 [M+HJ*
6 'HDMSO 1.44-1.47 (6H, m), 2.17-2.19 (3H, m), 2.56-2.58 (3H, m), 3.47-4.14 (6H, m), 4.38 (1H, s, br), 4.60-4.80 (1H, m), 5.51-5.52 (1H, m), 7.30-7.34 (1H, m), 7.80 (1H, d), 7.95 (lH,dt), 8.45-8.47 (lH,m)
Example 3
(5)-2-[(6-[[3,5-Dimethyl-l-(2-thiazolyl)'lJH-pyrazol-4-yllmethyl]-l,2,3,4-tetrahydro-3-jnethyl-l-(l-methylethyl>2,4-dioxothieno[23- (Figure Remove)
Amixtureof(5)-2-[[6-[(3,5-dimethyl-l/f-pyrazol-4-yl)methyl]-l,2,3,4-tetrahydro-3-methyl-1 -(1 -methylethyl)-2,4-dioxothiejio[2,3- MS (APCI -fve) M+H » 531.1
5 IHj3MS0.120°C 1.47 (6H, d), 2.17 (3H, s), 2.60 (3H, s), 3.20 (3H, s), 3.46 (1H, d), 3.75
(1H, d), 3,89-3.95 (2H, m), 3.89 (2H, s), 4.46 (1H, sep), 4.70 (1H, s), 5.08 (1H, s), 7.38
(!H,d),7.56(lH,d).
Pharmacological Data
Inhibition of PM A/ionomycin-stimulated peripheral blood mononuclear cell proliferation
The assay for PMA/ionomytin-stimulated PBMC proliferation was performed in 96-wetl
flat-bottomed microtitre plates. Compounds were prepared as lOmM stock solutions in dimethyl sulfbxide. A 50-fold dilution of this was prepared in RPMI and serial dilutions were prepared from this solution. 1 Oul of the 50-fold diluted stock, or dilutions of it, were added to the well to .give concentrations in the assay starting at 9.5p.M and going down. Into each well was placed 1 x 105 PBMC, prepared from human peripheral blood from a single donor, in RPMI1640 medium supplemented with 10% human serum, 2mM glutamtne and penicillin/streptomycin. Phorbol myristate acetate (PMA) (0.5ng/ml final concentration) and ionomycin (500ng/ml final concentration) were added to these cells in supplemented RPMI1640 medium (as above) so that the final volume of the assay was 0.2ml. The cells were incubated at 37°C in a humidified atmosphere at 5% carbon dioxide for 72 hours. 3H-Thymidine (O.SuCi) was added for the final 6 hours of the incubation. The level of radioactivity, incorporated by the cells was then determined and this is a measure of proliferation.
The compounds of the Examples were found to exhibit an IAso value of less than 1 x 10** M in the above test. Of the specific examples, examples 1 had aPIAsoof 8.3 and Example 3 had a P1A50 of 9.07 in the above test.

We Claims:
1. A thienopyrimidindione compound of formula (1):
(Formula Removed)
wherein:
R1 and R2 each independently represent C1-6alkyl, C3-6alkenyl, C3-5cycloalkylC1-3alkyl or C3-6cycloalkyl, each of which may be optionally substituted by 1 to 3 halogen atoms;
Q is CR4R5 where R4 is hydrogen, fluorine or C1-6 alkyl and R5 is hydrogen, fluorine or hydroxy;
Ar is a 5- to 10-membered aromatic ring system wherein up to 4 ring atoms may be heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by one or more substituents independently selected from C1-4alkyl (optionally substituted by 1, 2 or 3 hydroxy groups), C1-4alkoxy, halogen, haloalkyl, dihaloalkyl, or trihaloalkyl, (wherein alkyl groups suitably contain from 1 to 4 carbon atoms) C1-4alkoxyC1-4alkyl, C1-4alkylthio, C1-4alkoxycarbonyl, C2-4alkanoyl, oxo, thioxo, nitro, cyano, -N(R6)R7 and
-(CH2)pN(R8)R9, hydroxy, C1-4alkylsulphonyl, C1-4alkylsulphinyl, carbamoyl, C1-4alkylcarbamoyl, di-(C1-4alkyl)carbamoyl, carboxy, SO2N(R8)R9;
Ar2 is a 5 or 6 membered aromatic ring containing up to 4 hetero atoms independently selected from nitrogen, sulphur or oxygen, wherein the

6. A compound as claimed in claim 5 wherein Ar is a group of sub-formula (i)
(Formula Removed)
where R10 and R11 are independently selected from H, C1-6alkyl, or haloC1-6alkyl and Ar2 is as defined above.
7. A compound as claimed in any one of claims 1 to 6 wherein Ar2 is a 5 or
6- membered aromatic ring system wherein up to 3 ring atoms of the
aromatic ring system may be heteroatoms independently selected from
nitrogen, oxygen and sulphur, wherein the ring system includes at least
one heteroatom, and which ring system is optionally substituted by one
or more substituents independently selected from C1-4alkyl, C1-4alkoxy,
halogen, dihaloalkyl, trihaloalkyl, oxo, thioxo, cyano and C1-4-
alkylsulphonyl.
8. A compound as claimed in claim 7 wherein Ar2 is pyridinyl or
pyrimidinyl.
9. A compound as claimed in claim 7 wherein Ar2 is thiazolyl.
10. A thienopyrimidindione compound of formula (I) as claimed in claim 1
wherein:
3,5-dimethyl-l-(2-pyrimidinyl)-lH-pyrazol-4-yl]methyl]-5-[[(4S)-4-
hydroxy-2-isoxazolidinyl]carbonyl]-3-methyl-l-(l-methylethyl)thieno[2,3-
d]pyrimidine-2,4(lH,3H)-dione,

6-[[3,5-dimethyl-l-(2-pyridinyl)-lH-pyrazol-4-yl]methyl]-5-[[(4S)-4-hydroxy-2-isoxazolidinyl]carbonyl]-3-methyl-l-(l-methylethyl)thieno[2,3-d]pyrimidine-2,4(lH,3H)-dione, or
(S)-2-[[6-[[3,5-Dimethyl-l-(2-thiazolyl)-lH-pyrazol-4-yl]methyl]-l ,2,3,4-
tetrahydro-3-methyl-l-(l-methylethyl)-2,4-dioxothieno[2,3-d]pyrimidin-
5-yl]carbonyl]-4-isoxazolidinol
or pharmaceutically acceptable salts thereof.
11. A pharmaceutical composition comprising a compound of formula (I) or a
pharmaceutically acceptable salt thereof as claimed in any one of claims
1 to 10 in association with a pharmaceutical carrier, which composition
comprises from 0.05 to 99 w% of active ingredient and the remaining
being pharmaceutical carrier, all percentages by weight being based on
total composition.
12. A process for the preparation of a compound of formula (I) as
claimed in claim 1 which comprises:
(a) reaction of a compound of formula (II):
(Formula Removed)
in which R1 and R2 are as claimed in claim 1 for formula (I) or are protected derivatives thereof, and X and Y are selected from C1-4alkyl (optionally substituted by 1,2 or 3 hydroxy groups),
C1-4alkoxy, haloalkyl, dihaloalkyl, trihaloalkyl, C1-4alkoxyC1-4alkyl,

C1-4alkoxycarbonyl,-(CH2)pN(R8)R9, with a compound of formula (III): Ar2-Gl-G2 (III)
where Ar2 is as claimed in claim 1 for formula (I) or are protected derivatives thereof and Gl is NH, G2 is NH2, SH or OH,
which reaction is carried out in an inert solvent, at a temperature of from 0°C to 100°C preferably 10°C to 50°C and optionally in the presence of a catalytic quantity of an acid,
and optionally thereafter process (a) in any order
• removing any protecting groups
• forming a pharmaceutically acceptable salt.

Documents:

2945-DELNP-2005-Abstract-(31-12-2007).pdf

2945-DELNP-2005-Abstract-05-05-2008.pdf

2945-delnp-2005-abstract.pdf

2945-DELNP-2005-Claims-(31-12-2007).pdf

2945-DELNP-2005-Claims-05-05-2008.pdf

2945-delnp-2005-claims.pdf

2945-DELNP-2005-Correspondence-Others-(31-12-2007).pdf

2945-DELNP-2005-Correspondence-Others-05-05-2008.pdf

2945-delnp-2005-correspondence-others.pdf

2945-DELNP-2005-Description (Complete)-(31-12-2007).pdf

2945-DELNP-2005-Description (Complete)-05-05-2008.pdf

2945-delnp-2005-description (complete).pdf

2945-DELNP-2005-Form-1-(31-12-2007).pdf

2945-DELNP-2005-Form-1-05-05-2008.pdf

2945-delnp-2005-form-1.pdf

2945-delnp-2005-form-18.pdf

2945-DELNP-2005-Form-2-(31-12-2007).pdf

2945-DELNP-2005-Form-2-05-05-2008.pdf

2945-delnp-2005-form-2.pdf

2945-DELNP-2005-Form-3-(31-12-2007).pdf

2945-delnp-2005-form-3.pdf

2945-delnp-2005-form-5.pdf

2945-DELNP-2005-GPA-(31-12-2007).pdf

2945-delnp-2005-gpa.pdf

2945-DELNP-2005-Others-Document-(31-12-2007).pdf

2945-delnp-2005-pct-304.pdf

2945-delnp-2005-pct-409.pdf

2945-delnp-2005-pct-search report.pdf

2945-DELNP-2005-Petition-137-(31-12-2007).pdf

2945-DELNP-2005-Petition-138-(31-12-2007).pdf

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Patent Number

220218

Indian Patent Application Number

2945/DELNP/2005

PG Journal Number

30/2008

Publication Date

25-Jul-2008

Grant Date

19-May-2008

Date of Filing

01-Jul-2005

Name of Patentee

ASTRAZENECA AB

Applicant Address

Inventors:

#	Inventor's Name	Inventor's Address
1	ANTHONY HOWARD INGALL
2	SIMON DAVID GUILE

PCT International Classification Number

C07D 513/04

PCT International Application Number

PCT/SE2004/000053

PCT International Filing date

2004-01-15

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	0300117-9	2003-01-17	Sweden
2	0300118-7	2003-01-17	Sweden