Non-natural nucleotides and dinucleotides

[0001] This invention relates to a series of non-natural nucleotides and dinucleotides, to compositions containing them, to processes for their preparation and to their use in medicine.

[0002] Extracellular nucleotides such as adenosine triphosphate (ATP), uridine triphosphate (UTP) and uridine diphosphate (UDP) play a fundamental role in mediating a number of physiological functions including, for example a general role in the control of secretions such as the clearance of retained mucus secretions and stimulation of ciliary beat frequency and particularly a central role in the coordination of mucociliary clearance mechanisms in the lung. Molecular biological techniques have allowed the discovery of several families of membrane bound receptors for these highly charged molecules. Thus, the P2X receptors are ligand-gated ion channels that are implicated in various neuromodulatory processes. The P2Y family of receptors are 7-transmembrane G-protein coupled receptors that bind both purine and pyrimidine nucleotides (Williams and Bhagwat, Ann. Rep. Med. Chem. 1996, 31, 21-30).

[0003] The P2Y receptors have been further subdivided into 9 subtypes known as P2Y1 to P2Y8 and P2Y11 (Fisher, B., Exp. Opin. Ther. Patents, 1999, 9, 385-399; Yerxa, B. R. and Johnson, F. L., Drugs of the Future, 1999, 24, 759-769). P2Y2 receptors have been implicated in the pathology of several disease states including lung diseases such as chronic obstructive pulmonary disease (which includes amongst others cystic fibrosis, chronic bronchitis and emphysema) and tear secretion, thrombosis, pain, cancer, sepsis and ischaemia-reperfusion injury.

[0004] P2Y2 receptors are found on the apical surface of airway epithelia and are believed to be the major coordinators of mucociliary clearance mechanisms in the lung. The continuous, cephalad movement of lower respiratory material is necessary for the clearance of inhaled pathogenic organisms or injurious particles and is essential to maintain airways necessary for efficient gas exchange. The movement of airway secretions, along with accompanying lumenal cells and free foreign particles is accomplished by the actions of several cell types within the respiratory tract. Mucous is secreted by goblet cells and submucosal glands and forms a gel-like protective sheet within the lumen of the respiratory tract. The layer of mucus is propelled by the rhythmical, coordinated beat of the ciliated epithelial cells lining the airways from the terminal bronchi to the oropharynx and lining of the nose. The viscous mucous sheet would be immovable except that it floats on a much less viscous layer of fluid above the beating cilia. This periciliary fluid layer is maintained by the transport of ions (chloride and sodium) across the epithelium into the lumen of the airways followed by passive diffusion of water. Activation of P2Y2 by its presumed endogenous agonist, UTP, as well as by other nucleoside phosphates leads to increased mucociliary clearance presumably by increased chloride and water transport across the luminal surface (Mason, S. et al Br. J. Pharmacol., 1991, 103, 1649-1656), increased cilia beat frequency (Drutz, D. et al, Drug Dev. Res. 1996, 37, 185), increased mucin release (Lethem, M. et al, Am. J. Respir. Cell Mol. Biol., 1993, 9, 315-322) and increased surfactant release (Gobran, L. et al, Am. J. Physiol., 1994, 272, L187-196).

[0005] It has recently been discovered that the P2Y6 receptor, which selectively recognizes UDP as a potent ligand, also exists in airway tissue (International Patent Specification WO 99/09998). P2Y6 activation is also associated with chloride ion secretion and may play a role in coordination of mucociliary clearance mechanisms.

[0006] Cystic fibrosis (CF) is the most lethal genetic disease in Caucasians in the U.S.A., affecting approximately 1 in 2000 individuals (Fiel, S. B. et al, Semin. Respir. Crit. Care Med., 1994, 15, 349-355), with median survival age being 30 years. CF occurs due to mutations in the gene that codes for the CF Transmembrane Conductance Regulator (CFTR) protein (Rommens, J. M. et al, Science, 1989, 245, 1059-1080). These mutations account for the abnormalities in sodium, chloride and water transport across epithelial cells resulting in dehydration and thickening of the mucus layer above the affected cells. The inability of CF patients to clear this thickened mucus and potential pathogens leads to chronic lung infection, progressive lung disease and impaired lung function, with lung infection accounting for 90% of deaths from CF.

[0007] New therapeutic approaches to the treatment of CF are required and one approach is the provision of agents that correct the underlying ion transport defects via physiological mechanisms that do not rely on the CFTR in order to normalize airway secretions, leading to improved mucociliary clearance and prevention of lung infections and damage. In this regard P2Y2 and P2Y6 receptor agonists may enhance mucociliary clearance by the mechanisms just mentioned. UTP, UDP and ATP have been demonstrated to activate chloride channel function, leading to hydration of lung mucin secretions (U.S. Pat. No. 5,292,498 and International Patent Specification WO99/09998) and increased ciliary beat frequency (Boucher, R. et al, Adenosine and Adenine Nucleotides: From Molecular Biology to Integrative Physiology, 525-532, Belardinelli, L. and Pelleg, A., Eds, Alumwer Academic Publishers, Boston, 1995) in the lung epithelial cells of CF patients. A combination of aerosolised UTP and amiloride has also been reported to improve mucociliary clearance from the peripheral airways of the lungs of CF patients to near normal levels (Bennett, W. D. et al, AM. J. Res. Critical Care Med. 1996, 153, 1796-1802).

[0008] Additionally a series of dinucleotides have also been disclosed as useful in the treatment of airway diseases including CF (U.S. Pat. No. 5,635,160), chronic brochitis (International Patent Specifications WO 98/34942 and WO 99/61012) and sinusitis (U.S. Pat. No. 5,972,904).

[0009] Abnormal tear secretion can lead to dry eye disease, a general term for indications produced by abnormalities of the precorneal tear film characterised by a decrease in tear production or an increase in tear film evaporation, in combination with the resulting ocular surface disease. Current treatment of dry eye disease is limited to the use of artificial tears which is a short lived solution. Tear secretion may be stimulated from lacrimal accessory tissues via P2Y2 and/or P2Y4 purinergic receptor mediated mechanisms similar to those that hydrate airway epithelia, and agonists of these receptors may be useful in the treatment of dry eye disease.

[0010] P2Y2 and P2Y4 receptors also play a role in the control of glucose uptake into mammalian cardiac mycocytes (see International Patent Specification WO 99/43326). Use of agonists of these receptors to enhance glucose uptake may be used to minimize ischemic cardiac damage, such as that attributable to angina, myocardial infarction, cardiac arrhythmia, coronary artery disease, diabetes mellitus and cardiac ischemia attributable to shock, stress or exertion.

[0011] Since UTP, UDP and related dinucleotides are subject to rapid degradation in vivo their actions are likely to be short lived. Consequently there is a need for alternative long acting P2Y agonists. We have now found such a group of compounds which are potent long acting P2Y agonists, particularly P2Y2, P2Y4 and/or P2Y6 agonists. The compounds are of use in medicine, for example in the treatment of diseases and disorders involving abnormal secretory mechanisms such as inadequate functioning of the mucociliary clearance mechanisms or abnormal tear secretion or in the treatment of diseases involving inappropriate cellular glucose uptake.

[0012] Thus according to one aspect of the invention we provide a compound of formula (1):

[0013] wherein:

[0014] G is a hydrogen atom or an optionally substituted aliphatic, heteroaliphatic, cycloaliphatic, polycycloaliphatic, aromatic or heteroaromatic group or a group of formula:

[0015] in which Y and Z is each independently a hydrogen or halogen atom or a hydroxyl (—OH), alkoxy, azido (—N3), amino (—NH2), alkylamino or dialkylamino group, b represents the point of attachment to the remainder of the compound of formula (1) and B is an optionally substituted nitrogen containing heterocyclic group of formula:

[0016] in which c represents the point of attachment of B to the nucleoside of formula (1a), dashed lines indicate optional bonds, J is an oxygen or sulphur atom, one of D and E is a carbon or nitrogen atom and the other is a carbon atom and M, Q, R, U, V, W and X is each a carbon, nitrogen, oxygen or sulphur atom, provided that:

[0017] (1) when one of M, Q and R is an oxygen or sulphur atom at least one of the remaining atoms M, Q and R is a carbon atom; and

[0018] (2) when at least one of U, V, W and X is an oxygen or sulphur atom at least one bond in the ring in which it occurs is saturated; and

[0019] (3) no more than two of U, V, W and X may be an oxygen or sulphur atom; and

[0020] (4) when two of U, V, W and X is an oxygen or sulphur atom these are not directly bonded together; and

[0021] (5) no more than three of U, V, W and X may be a nitrogen atom; and

[0022] (6) no more than a total of three of U, V, W and X may be a nitrogen, oxygen and/or sulphur atom;

[0023] G′ is a group of formula:

[0024] in which B′ is a heterocyclic group as previously defined for B, Z′ and Y′ is each an atom or group as previously defined for Z and b is as previously defined;

[0025] n is zero, or the integer 1 or 2;

[0026] m is zero or the integer 1 or 2;

[0027] and the salts, solvates, hydrates and N-oxides thereof for use in modulating P2Y receptor activity.

[0028] The compounds of formula (1) are potent long acting agonists of P2Y receptors, particularly P2Y2, P2Y6 and/or P2Y4 receptors. The ability of the compounds to act in this way may be simply determined by employing tests such as those described hereinafter.

[0029] The compounds according to the invention are generally of use in modulating secretory processes and in particular are of use in the prophylaxis and treatment of lung diseases or disorders such as those involving inadequate functioning of the mucociliary clearance mechanisms such as chronic obstructive pulmonary disease and the invention extends to such a use and to the use of the compounds for the manufacture of a medicament for treating such diseases or disorders.

[0030] Diseases or disorders of this type include chronic bronchitis, Primary Ciliary Dyskinesia and cystic fibrosis. Additionally compounds according to the invention may be used in the prevention of pneumonia due to immobility. Furthermore, due to their general ability to increase hydration, clear retained mucus secretions and stimulate ciliary beat frequency, the compounds according to the invention are also useful in the treatment of sinusitis, otitis media, post-operative mucous retention, nasolacrimal duct obstructions, female infertility or irritation caused by vaginal dryness and nasolacrimal duct obstructions. In addition the compounds according to the present invention are useful for treating dry eye and retinal detachment. The compounds may also be of use in the control of glucose uptake in mammalian cardiac mycocytes.

[0031] For the prophylaxis or treatment of disease the compounds according to the invention may be administered as pharmaceutical compositions, and according to a further aspect of the invention we provide a pharmaceutical composition which comprises a compound of formula (1) together with one or more pharmaceutically acceptable carriers, excipients or diluents.

[0032] Pharmaceutical compositions according to the invention may take a form suitable for oral, buccal, parenteral, nasal, topical, vaginal or rectal administration, or a form suitable for administration by inhalation or insufflation.

[0033] For oral administration, the pharmaceutical compositions may take the form of, for example, tablets, lozenges or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g. pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g. lactose, microcrystalline cellulose or calcium hydrogen phosphate); lubricants (e.g. magnesium stearate, talc or silica); disintegrants (e.g. potato starch or sodium glycollate); or wetting agents (e.g. sodium lauryl sulphate). The tablets may be coated by methods well known in the art. Liquid preparations for oral administration may take the form of, for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents, emulsifying agents, non-aqueous vehicles and preservatives. The preparations may also contain buffer salts, flavouring, colouring and sweetening agents as appropriate.

[0034] Preparations for oral administration may be suitably formulated to give controlled release of the active compound.

[0035] For buccal administration the compositions may take the form of tablets or lozenges formulated in conventional manner.

[0036] The compounds for formula (1) may be formulated for parenteral administration by injection e.g. by bolus injection or infusion. Formulations for injection may be presented in unit dosage form, e.g. in glass ampoule or multi dose containers, e.g. glass vials. The compositions for injection may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising, preserving and/or dispersing agents. Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. sterile pyrogen-free water, before use. For particle mediated administration the compounds of formula (1) may be coated on particles such as microscopic gold particles.

[0037] In addition to the formulations described above, the compounds of formula (1) may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation or by intramuscular injection.

[0038] For nasal administration or administration by inhalation, the compounds for use according to the present invention are conveniently delivered in the form of an aerosol spray presentation for pressurised packs or a nebuliser, with the use of suitable propellant, e.g. dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas or mixture of gases.

[0039] For topical administration the compounds of formula (1) may be delivered in the form of a liquid or gel suspension in the form of drops, spray or gel. These formulations may be prepared by mixing the active ingredient with a suitable physiologically compatible vehicle. Such vehicles include for example saline solution, water soluble polyethers such as polyethylene glycol, polyvinyls such as polyvinyl alcohol, cellulose derivatives such as methylcellulose, petroleum derivatives such as mineral oil and white petroleum, animal fats such as lanolin, polymers of acrylic acid such as carboxypolymethylene gel, vegetable fats such as peanut oil and polysaccharides such as dextrans.

[0040] For vaginal or rectal administration the compounds of formula (1) may be formulated as a suppository. These formulations may be prepared by mixing the active ingredient with a suitable non-irritating excipient which is a solid at room temperature but liquid at the body temperature. Such materials include for example cocoa butter and polyethylene glycols.

[0041] The compositions may, if desired, be presented in a pack or dispenser device which may contain one or more unit dosage forms containing the active ingredient. The pack or dispensing device may be accompanied by instructions for administration.

[0042] The quantity of a compound of the invention required for the prophylaxis or treatment of a particular condition will vary depending on the compound chosen, and the condition of the patient to be treated. In general, however, daily dosages may range from around 100 ng/kg to 100 mg/kg e.g. around 0.01 mg/kg to 40 mg/kg body weight for oral or buccal administration, from around 10 ng/kg to 50 mg/kg body weight for parenteral administration and around 0.05 mg to around 1000 mg e.g. around 0.5 mg to around 1000 mg for nasal administration or administration by inhalation or insufflation.

[0043] Particular compounds of formula (1) form a further aspect of the invention and in a further aspect we therefore provide a compound of formula (1e):

[0044] wherein:

[0045] G is a hydrogen atom or an optionally substituted aliphatic, heteroaliphatic, cycloaliphatic, polycycloaliphatic, aromatic or heteroaromatic group or a group of formula:

[0046] in which Y and Z is each independently a hydrogen or halogen atom or a hydroxyl (—OH), alkoxy, azido (—N3), amino (—NH2), alkylamino or dialkylamino group, b represents the point of attachment to the remainder of the compound of formula (1) and B is an optionally substituted nitrogen containing heterocyclic group of formula:

[0047] in which c represents the point of attachment of B to the nucleoside of formula (1a), dashed lines indicate optional bonds, J is an oxygen or sulphur atom, one of D and E is a carbon or nitrogen atom and the other is a carbon atom and M, Q, R, U, V, W and X is each a carbon, nitrogen, oxygen or sulphur atom, provided that:

[0048] (1) when one of M, Q and R is an oxygen or sulphur atom at least one of the remaining atoms M, Q and R is a carbon atom; and

[0049] (2) when at least one of U, V, W and X is an oxygen or sulphur atom at least one bond in the ring in which it occurs is saturated; and

[0050] (3) no more than two of U, V, W and X may be an oxygen or sulphur atom; and

[0051] (4) when two of U, V, W and X is an oxygen or sulphur atom these are not directly bonded together; and

[0052] (5) no more than three of U, V, W and X may be a nitrogen atom; and

[0053] (6) no more than a total of three of U, V, W and X may be a nitrogen, oxygen and/or sulphur atom;

[0054] G′ is a group of formula:

[0055] in which B′ is a heterocyclic group as previously defined for B, Z′ and Y′ is each an atom or group as previously defined for Z and b is as previously defined;

[0056] n is zero, or the integer 1 or 2;

[0057] m is zero or the integer 1 or 2;

[0058] provided that when G is a hydrogen atom, n is zero and m is the integer 1, G′ is not a group of formula (1d) in which Y′ is a hydroxyl (—OH) group, Z′ is a hydrogen atom and B′ is a 1 (2H)-isoquinolinone, 6-methyl-1 (2H)-isoquinolinone, 8-methyl-1 (2H)-isoquinolinone or 4-(1-propynyl)-1 (2H)-isoquinolinone group;

[0059] and the salts, solvates, hydrates and N-oxides thereof.

[0060] For the purposes of this application non-natural nucleotides include those nucleotides of formula (1) whilst natural nucleotides include those nucleotides containing a purine or pyrimidine base.

[0061] It will be appreciated that compound of formulae (1), (1a), (1b), (1c), (1d) and (1e) may have one or more chiral centres, and exist as enantiomers or diastereomers (for example as indicated by wiggly lines in formula (1a)). The invention is understood to extend to all such enantiomers, diastereomers and mixtures thereof, including racemates. In addition, compounds of formula (1), (1a), (1b), (1c), (1d) and (1e) may exist as tautomers, for example keto (CH2C═O)-enol (CH═CHOH) tautomers. Formulae (1), (1a), (1b), (1c), (1d) and (1e) and the formulae hereinafter are intended to represent all individual isomers, tautomers and mixtures thereof unless stated or shown otherwise.

[0062] The following general terms as used herein have the stated meaning unless specifically described otherwise.

[0063] As used herein the term “alkyl” whether present as a group or part of a group includes straight or branched C1-6alkyl groups, for example C1-4alkyl groups such as methyl, ethyl, n-propyl, i-propyl or t-butyl groups. Similarly, the terms “alkenyl” or “alkynyl” are intended to mean straight or branched C2-6alkenyl or C2-6alkynyl groups such as C2-4alkenyl or C2-4alkynyl groups. Optional substituents which may be present on these groups include those optional substituents mentioned hereinafter in relation to G when G is an optionally substituted aliphatic group.

[0064] The term halogen is intended to include fluorine, chlorine, bromine or iodine atoms.

[0065] The term “haloalkyl” is intended to include those alkyl groups just mentioned sustituted by one, two or three of the halogen atoms just described. Particular examples of such groups include —CF3, —CCl3, —CHF2, —CHCl2, —CH2F and —CH2Cl groups.

[0066] The term “alkoxy” as used herein is intended to include straight or branched C1-6alkoxy e.g. C1-4alkoxy such as methoxy, ethoxy, n-propoxy, i-propoxy and t-butoxy. “Haloalkoxy” as used herein includes any of these alkoxy groups substituted by one, two or three halogen atoms as described above. Particular examples include —OCF3, —OCCl3, —OCHF2, —OCHCl2, —OCH2F and —OCH2Cl groups.

[0067] As used herein the term “alkylthio” is intended to include straight or branched C1-6alkylthio, e.g. C1-4alkylthio such as methylthio or ethylthio.

[0068] As used herein the term “alkylamino or dialkylamino” is intended to include the groups —NHR1 and —N(R1)2 [where R1 is an optionally substituted straight or branched alkyl group]. Where two R1 groups are present these may be the same or different.

[0069] When the group G is present in compounds of formula (1) as an optionally substituted aliphatic group it may be an optionally substituted C1-10aliphatic chain. Particular examples include optionally substituted straight or branched chain C1-6alkylene, C2-6alkenylene, or C2-6alkynylene chains.

[0070] Particular examples of aliphatic groups represented by G include optionally substituted —CH3, —CH2CH3, —CH(CH3)CH3, —(CH2)2CH3, —(CH2)3CH3, —CH(CH3)(CH2)2CH3, —CH2C H(CH3)CH3, —C(CH3)2CH3, —CH2C(CH3)2CH3, —(CH2)2CH(CH3)CH3, —CH(CH3)CH2CH3, —CH(CH3)CH2CH(CH3)2, —CH2CH (CH3)CH2CH3, —(CH2)2C(CH3)3, —(CH2)4CH3, —(CH2)5CH3, —CHCH2, —CHCHCH3, —CH2CHCH2, —CHCHCH2CH3, —CH2CHCHCH3, —(CH2)2CHCH2, —CCH, —CCCH3, —CH2CCH, —CCCH2CH3, —CH2CCCH3 or —(CH2)2CCH2 groups.

[0071] Heteroaliphatic groups represented by the group G in the compounds of formula (1) include the aliphatic groups just described but with each additionally containing one, two, three or four L1 atoms or groups where L1 is an oxygen or sulphur atom or NH or N(R1) group. Each L1 atom or group may interrupt the aliphatic group, or may be positioned at its terminal carbon atom to connect the group to an adjoining atom or group. Particular examples include optionally substituted -L1CH3, —CH2L1CH3, -L1CH2CH3, —CH2L1CH2CH3, —(CH2)2L1CH3, —(CH2)3L1CH3, -L1(CH2)3, -L1CH2CHCH2 and —(CH2)2L1CH2CH3 groups.

[0072] The optional substituents which may be present on aliphatic or heteroaliphatic groups represented by G include one, two, three or more substituents where each substituent may be the same or different and is selected from halogen atoms, e.g. fluorine, chlorine, bromine or iodine atoms, or hydroxyl (—OH), C1-6alkoxy, e.g. methoxy or ethoxy, C1-6haloalkoxy, e.g. trifluoromethoxy or difluoromethoxy, thiol (—SH), C1-6alkylthio e.g. methylthio or ethylthio or optionally substituted cycloaliphatic, heterocycloaliphatic, aromatic or heteroaromatic groups.

[0073] Optionally substituted cycloaliphatic and heterocycloaliphatic groups when present as optional substituents on aliphatic or heteroaliphatic groups represented by G include optionally substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentenyl, tetrahydrofuranyl, dihydrofuranyl, 1,3-dioxanyl and tetrahydropyranyl groups. The optional substituents that may be present on such groups include those optional substituents as described in relation to G when G is an optionally substituted aliphatic group.

[0074] Optionally substituted aromatic and heteroaromatic groups when present as optional substituents on aliphatic or heteroaliphatic groups represented by G include those optionally substituted aromatic and heteroaromatic groups described hereinafter in relation to G, especially optionally substituted phenyl, thienyl, furanyl, pyridyl and pyrimidinyl groups.

[0075] Optionally substituted cycloaliphatic groups represented by the group G in compounds of the invention include optionally substituted C3-10cycloaliphatic groups. Particular examples include optionally substituted C3-10cycloalkyl, e.g. C3-7cycloalkyl or C3-10cycloalkenyl, e.g C3-7cycloalkenyl groups.

[0076] Optionally substituted polycycloaliphatic groups represented by the group G include optionally substituted C7-10bi-or tricycloalkyl or C7-10bi- or tricycloalkenyl groups.

[0077] Particular examples of cycloaliphatic and polycycloaliphatic groups represented by the group G include optionally substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, 2-cyclobuten-1-yl, 2-cyclopenten-1-yl, 3-cyclopenten-1-yl, adamantyl, norbornyl, and norbornenyl, groups.

[0078] The optional substituents which may be present on the cycloaliphatic and polycycloaliphatic groups represented by the group G include one, two, three or more substituents selected from halogen atoms, or C1-6alkyl, e.g. methyl or ethyl, haloC1-6alkyl, e.g. halomethyl or haloethyl such as difluoromethyl or trifluoromethyl, optionally substituted by hydroxyl, e.g.—C(OH)(CF3)2, hydroxyl (—OH), C1-6alkoxy, e.g. methoxy or ethoxy, haloC1-6alkoxy, eg. halomethoxy or haloethoxy such as difluoromethoxy or trifluoromethoxy, thiol (—SH), C1-6alkylthiol, e.g. methylthiol or ethylthiol or optionally substituted cycloalphatic, heterocycloaliphatic, aromatic or heteroaromatic groups.

[0079] Optionally substituted cycloaliphatic, heterocycloaliphatic, aromatic or heteroaromatic groups when present as optional substituents on the cycloaliphatic and polycycloaliphatic groups represented by the group G include those optionally substituted cycloaliphatic, heterocycloaliphatic, aromatic or heteroaromatic groups as described hereinbefore in relation to optional substituents on aliphatic or heteroaliphatic groups represented by G.

[0080] Optionally substituted aromatic groups represented by the group G include for example monocyclic or bicyclic fused ring C6-12aromatic groups, such as phenyl, 1- or 2-napthyl, 1- or 2-tetrahydronapthyl, indanyl or indenyl groups.

[0081] Heteroaromatic groups represented by the group G include for example C1-9heteroaromatic groups containing for example one, two, three or four heteroatoms selected from oxygen, sulphur or nitrogen atoms. In general, the heteroaromatic groups may be for example monocyclic or bicyclic fused ring heteroaromatic groups. Monocyclic heteroaromatic groups include for example five- or six-membered heteroaromatic groups containing one, two, three or four heteroatoms selected from oxygen, sulphur or nitrogen atoms. Bicyclic heteroaromatic groups include for example eight- to thirteen-membered fused ring heteroaromatic groups containing one, two or more heteroatoms selected from oxygen, sulphur or nitrogen atoms.

[0082] Particular examples of heteroaromatic groups of these types include pyrrolyl, furyl, imidazolyl, N—C1-6alkylimidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,3-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,3,5-triazinyl, 1,2,4-triazinyl, 1,2,3-triazinyl, benzofuryl, [2,3-dihydro]benzofuryl, benzothienyl, [2,3-dihydro]benzothienyl, benzotriazolyl, indolyl, indolinyl, indazolinyl, benzimidazolyl, imidazo[1,2-a]pyridyl, benzothiazolyl, benzoxazolyl, benzisoxazolyl, benzopyranyl, [3,4-dihydro]benzopyranyl, quinazolinyl, quinoxalinyl, naphthyridinyl, pyrido[3,4-b]pyridyl, pyrido[3,2-b]pyridyl, pyrido[4,3-b]pyridyl, quinolinyl, isoquinolinyl, phthalazinyl, tetrazolyl, 5,6,7,8-tetrahydroquinolinyl, 5,6,7,8-tetrahydroisoquinolinyl, imidyl, e.g. succinimidyl, phthalimidyl or naphthalimidyl such as 1,8-naphthalimidyl, pyrazolo[4,3-d]pyrimidinyl, furo[3,2-d]pyrimidinyl, thieno[3,2-d]pyrimidinyl, pyrrolo[3,2-d]pyrimidinyl, pyrazolo[3,2-b]pyridinyl, furo[3,2-b]pyridinyl, thieno[3,2-b]pyridinyl, pyrrolo[3,2-b]pyridinyl, thiazolo[3,2-a]pyyridinyl, pyrido[1,2-a]pyrimidinyl, tetrahydroimidazo[1,2-a]pyrimidinyl and dihydroimidazo[1,2-a]pyrimidinyl groups.

[0083] Optional substituents which may be present on aromatic or heteroaromatic groups represented by the group G include one, two, three or more substituents, selected from halogen atoms, for example fluorine, chlorine, bromine or iodine atoms or nitro, cyano, hydroxyl (—OH), C1-6alkyl, e.g. methyl, ethyl or i-propyl, haloC1-6alkyl, e.g. trifluoromethyl or difluoromethyl, C1-6alkoxy, e.g. methoxy, ethoxy or i-propoxy, haloC1-6alkoxy, e.g. trifluoromethyloxy or difluoromethyloxy, carboxyl (—CO2H), esterified carboxyl, —CONHR11 [where R11 is a hydrogen atom or a straight or branched alkyl group], —CONR11R12 [where R12 is as just defined for R11] or —CONHet1 [where —NHet1 is an optionally substituted C5-7cyclicamino group optionally containing one or more other —O— or —S— atoms or —N(R12)—, —C(O)— or —C(S)— groups]groups

[0084] When aromatic or heteroaromatic groups represented by G are substituted with an esterified carboxyl group it may be for example a group of formula —CO2Alk4 wherein Alk4 is a straight or branched, optionally substituted C1-8alkyl group such as a methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl or t-butyl group or a C6-12arylC1-8alkyl group such as an optionally substituted benzyl, phenylethyl, phenylpropyl, 1-naphthylmethyl or 2-naphthylmethyl group. Optional substituents present on the Alk4 group include those optional substituents as described hereinbefore in relation to G when G is an aliphatic group.

[0085] When —NHet1 forms part of an optional substituent on aromatic or heteroaromatic groups represented by G it may be for example an optionally substituted pyrrolidinyl, pyrazolidinyl, piperazinyl, morpholinyl, thiomorpholinyl, piperidinyl or thiazolidinyl group. Optional substituents which may be present on —NHet1 include those substituents as described hereinbefore in relation to G when G is an aliphatic group.

[0086] Particular non-limiting examples of optionally substituted nitrogen containing heterocyclic groups of formula (1b) represented by B or B′ include optionally substituted:

[0087] where J and c are as previously defined and A represents an O, S or N atom or NH group.

[0088] Particular non-limiting examples of optionally substituted nitrogen containing heterocyclic groups of formula (1c) represented by B or B′ include optionally substituted:

[0089] where J and c are as previously defined and A represents an O or S atom or NH group.

[0090] The heterocyclic group represented by B and/or B′ may be optionally substituted on any available carbon or nitrogen atom. One, two, three or more of the same or different substituents (R13) may be present and each substituent may be selected from an atom or group -L4(Alk5)tL5(R14)u in which L4 and L5 which may be the same or different is each a covalent bond or a linker atom or group, t is zero or the integer 1, u is an integer 1, 2 or 3, Alk5 is a straight or branched C1-6alkylene, C2-6alkenylene or C2-6alkynylene chain, optionally interrupted by one, two or three —O— or —S— atoms or —S(O)n— [where n is an integer 1 or 2] or —N(R12)— groups and R14 is a hydrogen or halogen atom or a group selected from alkyl, —OR15 [where R15 is a hydrogen atom or an optionally substituted alkyl group], —SR15, —NR15R16 [where R16 is as just defined for R15 and may be the same or different], —NO2, —N3, —CN, —CO2R15, —SO3H, —SOR15, —SO2R15, —SO3R15, —OCO2R15, —CONR15R16, —OCONR15R16, —CSNR15R16, —COR15, —OCOR15, —N(R15)COR16, —N(R15)CSR16, —SO2N(R15)(R16), —N(R15)SO2R16, —N(R15)CON(R16)(R17) [where R17 is as just defined for R15], —N(R15)CSN(R16)(R17), —N(R15)SO2N(R16)(R17), aryl or a heteroaryl group.

[0091] When in the group -L4(Alk5)tL5(R14)u L5 is a covalent bond, t is the integer 1 and u is an integer 1, 2 or 3, it is to be understood that the substituent or substituents R14 may be present on any suitable carbon atom in -Alk5. Where more than one R14 substituent is present these may be the same or different and may be present on the same or different atom in -Alk5. Clearly, when L4 and L5 is each a covalent bond, u is zero and no substituent R14 is present the alkylene, alkenylene or alkynylene chain represented by Alk5 (t is the integer 1) becomes an alkyl, alkenyl or alkynyl group.

[0092] When L4 and/or L5 is present in these substituents as a linker atom or group it may be any divalent linking atom or group. Particular examples include —O— or —S— atoms or —C(O)—, —C(O)O—, —OC(O)—, —C(S)—, —S(O)—, —S(O)2—, —N(R2)— [where R2 is a hydrogen atom or a straight or branched alkyl group], —N(R2)O—, —N(R2)N—, —CON(R2)—, —OC(O)N(R2)—, —CSN(R2)—, —N(R2)CO—, —N(R2)C(O)O—, —N(R2)CS—, —S(O)2N(R2)—, —N(R2)S(O)2—, —N(R2)CON(R2)—, —N(R2)CSN(R2)— or —N(R2)SO2N(R2)— groups. Where L4 and/or L5 contains two R2 groups these may be the same or different.

[0093] When R14, R15, R16 and/or R17 is present as an optionally substituted alkyl group it may be an optionally substituted straight or branched C1-6alkyl group as previously generally and particularly defined or an optionally substituted C3-7cycloalkyl group as an optionally substituted cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl group. Optional substituents which may be present on such groups include those optional substituents as previously described.

[0094] Additionally when the groups R15 and R16 or R16 and R17 are both alkyl groups these groups may be joined, together with the N atom to which they are attached, to form a heterocyclic ring. Such heterocyclic rings may be optionally interrupted by a further heteroatom or heteroatom containing group selected from —O—, —S—, —N(R15)—, —C(O)— or —C(S)— groups. Particular examples of such heterocyclic rings include piperidinyl, pyrazolidinyl, morpholinyl, thiomorpholinyl, pyrrolidinyl, imidazolidinyl and piperazinyl rings.

[0095] When Alk5 is present in or as a substituent it may be for example a methylene, ethylene, n-propylene, i-propylene, n-butylene, i-butylene, s-butylene, t-butylene, ethenylene, 1-propenylene, 2-propenylene, 1-butenylene, 2-butenylene, 3-butenylene, ethynylene, 1-propynylene, 2-propynylene, 1-butynylene, 2-butynylene or 3-butynylene chain, optionally interrupted by one, two, or three —O— or —S—, atoms or —S(O)—, —S(O)2— or —N(R15)— groups.

[0096] Aryl and heteroaryl groups represented by R14 include those aromatic and heteroaromatic groups as previously described in relation to the group G. Optional substituents which may be present on these groups include those optional substituents described hereinbefore when G is an aromatic or heteroaromatic group.

[0097] Examples of the substituents represented by -L4(Alk5)tL5(R14)u when present as R13 substituents on heterocycles represented by the group B in compounds of the invention include atoms or groups -L4Alk5L5R14, -L4Alk5R14, -Alk5L5R14, -L4R14 and -Alk5R14 wherein L4, Alk5, L5 and R14 are as defined above. Particular examples of such substituents include -L4CH2L5R14, -L4CH(CH3)L5R14, —L4CH(CH2)2L5R14, -L4CH2R14, -L4CH(CH3)R14, -L4(CH2)2R14, —CH2R14, —CH(CH3)R14, —(CH2)2R14, —CHCHR14, —CH2CHCHR14, —CCR14, —CH2CCR14 and —R14 groups.

[0098] Thus R13 substituents on heterocycles of formula represented by the group B in compounds of the invention may include for example one, two, three or more halogen atoms, e.g. fluorine, chlorine, bromine or iodine atoms, and/or C1-6alkyl, e.g. methyl, ethyl, n-propyl, i-propyl, n-butyl or t-butyl, C2-6alkenyl, e.g. —CHCH2, —CHCHCH3, —CH2CHCH2 or —CH2CHCHCH3, C2-6alkynyl, e.g. —CCH, —CCCH3, —CH2CCH or —CH2CCCH3, C3-7cycloalkyl, e.g. cyclobutyl, cyclopentyl, optionally substituted aryl, e.g. optionally substituted phenyl, optionally substituted heteroaryl, e.g. optionally substituted pyridyl, pyrimidinyl, pyrrolyl, furyl, thiazolyl, or thienyl, optionally substituted arylC1-6alkyl or heteroarylC1-6alkyl, e.g. optionally substituted benzyl, pyridylmethylenyl, thiazolmethylenyl, optionally substituted aryloxy, e.g. phenoxy, optionally substituted heteroaryloxy, e.g. optionally substituted pyridyloxy, thiazolyoxy, optionally substituted arylthio or heteroarylthio, e.g. optionally substituted phenylthio or pyridylthio, optionally substituted arylC1-6alkyloxy or heteroarylC1-6alkyloxy, e.g. optionally substituted benzyloxy, pyridylmethoxy, thiazolylmethoxy, optionally substituted arylC1-6alkylamino or heteroarylC1-6alkylamino, e.g. optionally substituted benzylamino, pyridylmethylamino, thiazolylmethylamino, optionally substituted arylC1-6alkylthio or heteroarylC1-6alkylthio, e.g. benzothio, pyridylmethylthio or thiazolylmethylthio C1-6hydroxyalkyl, e.g. hydroxymethyl, hydroxyethyl or —C(OH)(CF3)2, carboxyC1-6alkyl, e.g. carboxyethyl, C1-6alkylthio e.g. methylthio or ethylthio, carboxyC1-6alkylthio, e.g. carboxymethylthio, 2-carboxyethylthio or 3-carboxypropylthio, C1-6alkoxy, e.g. methoxy or ethoxy, hydroxyC1-6alkoxy, e.g. 2-hydroxyethoxy, haloC1-6alkyl, e.g. —CF3, —CHF2, CH2F, haloC1-6alkoxy, e.g. —OCF3, —OCHF2, —OCH2F, C1-6alkylamino, e.g. methylamino or ethylamino, amino (—NH2), aminoC1-6alkyl, e.g. aminomethyl or aminoethyl, C1-6dialkylamino, e.g. dimethylamino or diethylamino, C1-6alkylaminoC1-6alkyl, e.g. ethylaminoethyl, C1-6 dialkylaminoC1-6alkyl, e.g. diethylaminoethyl, aminoC1-6alkoxy, e.g. aminoethoxy, C1-6alkylaminoC1-6alkoxy, e.g. methylaminoethoxy, C1-6dialkylaminoC1-6alkoxy, e.g. dimethylaminoethoxy, diethylaminoethoxy, diisopropylaminoethoxy, or dimethylaminopropoxy, nitro, azido, cyano, amidino, hydroxyl (—OH), formyl [HC(O)—], carboxyl (—CO2H), —CO2Alk6 [where Alk6 is as defined above for Alk4], C1-6 alkanoyl e.g. acetyl, thiol (—SH), thioC1-6alkyl, e.g. thiomethyl or thioethyl, sulphonyl (—SO3H), C1-6alkylsulphonyl, e.g. methylsulphonyl, aminosulphonyl (—SO2NH2), C1-6 alkylaminosulphonyl, e.g. methylaminosulphonyl or ethylaminosulphonyl, C1-6dialkylaminosulphonyl, e.g. dimethylaminosulphonyl or diethylaminosulphonyl, phenylaminosulphonyl, carboxamido (—CONH2), C1-6alkylaminocarbonyl, e.g. methylaminocarbonyl or ethylaminocarbonyl, C1-6dialkylaminocarbonyl, e.g. dimethylaminocarbonyl or diethylaminocarbonyl, aminoC1-6alkylaminocarbonyl, e.g. aminoethylaminocarbonyl, C1-6dialkylaminoC1-6alkylaminocarbonyl, e.g. diethylaminoethylaminocarbonyl, aminocarbonylamino, C1-6alkylaminocarbonylamino, e.g. methylaminocarbonylamino or ethylaminocarbonylamino, C1-6dialkylaminocarbonylamino, e.g. dimethylaminocarbonylamino or diethylaminocarbonylamino, C1-6alkylaminocabonylC1-6alkylamino, e.g. methylaminocarbonylmethylamino, aminothiocarbonylamino, C1-6alkylaminothiocarbonylamino, e.g. methylaminothiocarbonylamino or ethylaminothiocarbonylamino, C1-6dialkylaminothiocarbonylamino, e.g. dimethylaminothiocarbonylamino or diethylaminothiocarbonylamino, C1-6alkylaminothiocarbonylC1-6alkylamino, e.g. ethylaminothiocarbonylmethylamino, C1-6alkylsulphonylamino, e.g. methylsulphonylamino or ethylsulphonylamino, C1-6dialkylsulphonylamino, e.g. dimethylsulphonylamino or diethylsulphonylamino, aminosulphonylamino (—NHSO2NH2), C1-6alkylamino-sulphonylamino, e.g. methylaminosulphonylamino or ethylaminosulphonylamino, C1-6dialkylaminosulphonylamino, e.g. dimethylaminosulphonylamino or diethylaminosulphonylamino, C1-6alkanoylamino, e.g. acetylamino, aminoC1-6alkanoylamino e.g. aminoacetylamino, C1-6dialkylamino-C1-6alkanoylamino, e.g. dimethylaminoacetylamino, C1-6alkanoylaminoC1-6alkyl, e.g. acetylaminomethyl, C1-6alkanoylaminoC1-6alkylamino, e.g. acetamidoethylamino, C1-6alkoxycarbonylamino, e.g. methoxycarbonylamino, ethoxycarbonylamino or t-butoxycarbonylamino groups.

[0099] Where desired, two R13 substituents may be linked together to form a cyclic group such as a cyclic ether, e.g. a C1-6alkylenedioxy group such as methylenedioxy or ethylenedioxy.

[0100] The presence of certain substituents in the compounds of formula (1) may enable salts of the compounds to be formed. Suitable salts include pharmaceutically acceptable salts, for example acid addition salts derived from inorganic or organic acids, and salts derived from inorganic and organic bases.

[0101] Acid addition salts include hydrochlorides, hydrobromides, hydroiodides, alkylsulphonates, e.g. methanesulphonates, ethanesulphonates, or isothionates, arylsulphonates, e.g. p-toluenesulphonates, besylates or napsylates, phosphates, sulphates, hydrogen sulphates, acetates, trifluoroacetates, propionates, citrates, maleates, fumarates, malonates, succinates, lactates, oxalates, tartrates and benzoates.

[0102] Salts derived from inorganic or organic bases include alkali metal salts such as sodium, lithium or potassium salts, alkaline earth metal salts such as magnesium or calcium salts, and organic amine salts such as ammonia, morpholine, piperidine, dimethylamine, trimethylamine, diethylamine, triethylamine, cyclohexylamine or tris(hydroxymethyl)aminomethane salts.

[0103] Particularly useful salts of compounds according to the invention include pharmaceutically acceptable salts, especially base addition pharmaceutically acceptable salts.

[0104] One particular class of compounds of formulae (1) and (1e) is that wherein the group G′ has the formula (1d) in which the furanose sugar is preferably in the β-configuration, preferably the β-D-configuration, most preferably the β-D-ribofuranose configuration.

[0105] In general in compounds of formula (1) and (1e) E, Q, R, V, W and X when present is each preferably a carbon atom.

[0106] In general in compounds of formula (1) and (1e) Y′ and Z′ is each preferably a hydroxyl (—OH), amino (—NH2) or azido (—N3) group, most preferably a hydroxyl (—OH) group.

[0107] A particularly useful group of compounds according to the invention has the formula (2a):

[0108] wherein h is zero or the integer 1, 2, 3 or 4;

[0109] Z′ is a hydroxyl (—OH), amino (—NH2) or azido (—N3) group;

[0110] G, J, D and U are as previously defined for compounds of formula (1);

[0111] R13 is an optional substituent as previously defined which may be on any available carbon or nitrogen atom of the heterocyclic ring B′;

[0112] and the salts, solvates, hydrates and N-oxides thereof.

[0113] Another particularly useful group of compounds according to the invention has the formula (2a′):

[0114] wherein Z′ is a hydroxyl (—OH), amino (—NH2) or azido (—N3) group;

[0115] G, J, D and U are as previously defined for compounds of formula (1);

[0116] R13 is a substituent as previously defined;

[0117] and the salts, solvates, hydrates and N-oxides thereof.

[0118] Another particularly useful class of compounds include those of formula (2a″):

[0119] wherein Z′ is a hydroxyl (—OH), amino (—NH2) or azido (—N3) group;

[0120] G, J, D and U are as previously defined for compounds of formula (1);

[0121] R13 is a substituent as previously defined, R13a is a substituent as previously defined for R13 which may be on any available carbon or nitrogen atom of the heterocyclic ring B′; k is an integer 1, 2 or 3;

[0122] and the salts, solvates, hydrates and N-oxides thereof.

[0123] Yet another useful class of compounds according to the invention has the formula (2a′″):

[0124] wherein Z′ is a hydroxyl (—OH), amino (—NH2) or azido (—N3) group;

[0125] G, J, D and U are as previously defined for compounds of formula (1);

[0126] R13 is a substituent as previously defined, R13a is a substituent as previously defined for R13;

[0127] and the salts, solvates, hydrates and N-oxides thereof.

[0128] A further particularly useful group of compounds according to the invention has the formula (2b):

[0129] wherein h is zero or the integer 1, 2, 3 or 4;

[0130] J, G, M and Z′ are as previously defined for compounds of formula (1);

[0131] the ribose sugar is of natural β-D configuration as shown;

[0132] R13 is an optional substituent as previously defined which may be on any available carbon or nitrogen atom of the heterocyclic ring B′;

[0133] and the salts, solvates, hydrates and N-oxides thereof.

[0134] In compounds of formula (2b) Z′ is preferably a hydroxyl (—OH), amino (—NH2) or azido (—N3) group.

[0135] In compounds of formula (1), (1e), (2a), (2a′), (2a″), (2a′″) and (2b) Z′ is most preferably a hydroxyl (—OH) group.

[0136] Particularly useful R13 substituents when present in compounds of formulae (1), (1e), (2a), (2a′), (2a″), (2a′″) and (2b) include halogen atoms, especially fluorine or chlorine atoms, or straight or branched C1-6alkyl groups, especially methyl, ethyl, propyl or isopropyl groups, C2-6alkenyl, especially —CHCH2 and —CHCHCH3, C1-6alkynyl, especially —CCH and —CCCH3, C3-8cycloalkyl groups, especially cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl groups, haloC1-6alkyl groups, especially halomethyl groups, especially —CF3 and —CHF2 groups, C1-6alkoxy groups, especially methoxy or ethoxy groups, haloC1-6alkoxy groups, especially halomethoxy groups, most especially —OCF3 or —OCHF2 groups, C1-6alkylthiol groups, especially methylthiol or ethylthiol groups, —CN, —CO2Alk6, especially —CO2CH3 and —CO2C(CH3)3, —NO2, amino (—NH2), substituted amino (—NR15R16), especially —NHCH3 and —N(CH3)2, —N(R15)COR16, especially —NHCOCH3, COR15, especially —COCH3, groups, C6-12aromatic groups, especially optionally substituted phenyl or five- or six-membered monocyclic heteroaromatic groups containing one, two, three or four heteroatoms selected from oxygen, sulphur or nitrogen atoms, especially optionally substituted furyl, thienyl, pyridyl or pyrimidinyl, most especially optionally substituted pyridyl groups.

[0137] Optional substituents which may be present on R13 aromatic or heteroaromatic groups include halogen atoms, especially fluorine and chlorine atoms and —CN, C1-6alkylthiol groups, especially methylthiol or ethylthiol groups, C1-6alkoxy groups, especially methoxy or ethoxy groups, and substituted amino (—NR15R16), especially —NHCH3 and —N(CH3)2 groups.

[0138] Particularly preferred R13 substituents are halogen atoms, especially fluorine and chlorine atoms and —CN groups.

[0139] Particularly preferred R13a substituents include C1-6alkylthiol groups, especially methylthiol or ethylthiol groups, C1-6alkoxy groups, especially methoxy or ethoxy groups, and substituted amino (—NR15R16), especially —NHCH3 and —N(CH3)2.

[0140] In general in compounds of formula (1), (1e), (2a), (2a′), (2a″) and (2a′″) D and U is each preferably a carbon or nitrogen atom.

[0141] In one preferred class of compounds of formulae (1), (1e), (2a), (2a′), (2a″) and (2a′″) D and U is each a carbon atom.

[0142] In another preferred class of compounds of formulae (1), (1e), (2a), (2a′), (2a″) and (2a′″) D and U is each a nitrogen atom.

[0143] In another preferred class of compounds of formulae (1), (1e), (2a), (2a′), (2a″) and (2a′″) D is a carbon atom and U is a nitrogen atom.

[0144] In another preferred class of compounds of formulae (1), (1e), (2a), (2a′), (2a″) and (2a′″) D is a nitrogen atom and U is each a carbon atom.

[0145] In one preferred class of compounds of formulae (1), (1e) and (2b) M is an oxygen or sulphur atom.

[0146] In another preferred class of compounds of formulae (1), (1e), (2a), (2a′), (2a″), (2a′″) and (2b) G is a hydrogen atom. In this class of compounds m is preferably the integer 1 and n is preferably zero.

[0147] In another preferred class of compounds of formulae (1), (1 e), (2a), (2a′), (2a″), (2a′″) and (2b) G is a nucleoside of formula (1a) in which the furanose sugar is preferably in the β-configuration, preferably the β-D-configuration, most preferably the β-D-ribofuranose configuration as shown in formula (2c):

[0148] where the letter b indicates the point of attachment to the remainder of the compound of formula (1), (1e), (2a), (2a′), (2a″), (2a′″) or (2b). In this class of compounds m and n is each preferably the integer 1. In one preferred group of compounds of this class the heterocycle B is a group of formula (2d):

[0149] wherein h, c and J are as previously defined and D, U and R13 are as previously generally defined and particularly defined in relation to compounds of formula (2a). In another preferred group of compounds of this class the heterocycle B is a group of formula (2e):

[0150] wherein h, c and J are as previously defined and M and R13 are as previously generally defined and particularly defined in relation to compounds of formula (2b). A most preferred group of compounds of this class is that where the optionally substituted heterocycles B and B′ are identical and each is a group of formula (2d) or (2e). A further most preferred group of compounds of this class is that where B is an optionally substituted heterocycle of formula (2d) and B′ is an optionally substituted heterocycle of formula (2e).

[0151] In another preferred group of compounds of formulae (1), (2a), (2a′), (2a″), (2a′″) and (2b) G is a C1-6alkyl group, especially a methyl, ethyl, propyl, isopropyl or t-butyl group, a haloC1-6alkyl group, especially a trifluoromethyl or difluoromethyl group, a C1-6heteroalkyl group, especially ethyloxymethyl, propyloxymethyl or butyloxymethyl group, an optionally substituted C3-7heterocycloalkylC1-6alkyl group, especially an optionally substituted tetrahydrofuranylmethyl or dihydrofuranylmethyl group, an optionally substituted C6-10arylC1-6alkyl group, especially an optionally substituted benzyl or phenylethyl group, an optionally substituted C1-9heteroarylC1-6alkyl group, especially an optionally substituted pyridylmethyl, thienylmethyl, furanylmethyl or pyrimidinylmethyl group, an optionally substituted C3-7cycloalkylC1-6alkyl group, especially an optionally substituted cyclopropylmethyl, cyclopentylmethyl or cyclohexylmethyl group, an optionally substituted C3-7heterocycloalkyl group, especially an optionally substituted morpholinyl, thiomorpholinyl, piperidinyl, piperazinyl or pyrrolidinyl group, an optionally substituted C6-10aromatic group, especially an optionally substituted phenyl group or an optionally substituted C1-9heteroaromatic group, especially an optionally substituted pyridyl, pyrimidinyl, thienyl or furanyl group.

[0152] One particular compound is:

[0153] (2R,3S,4R,5R)-3,4-dihydroxy-5-(1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl triphosphate tris-ammonium salt;

[0154] and the free acid, other pharmaceutically acceptable salts, solvates, hydrates and N-oxides thereof.

[0155] A particular group of compounds includes:

[0156] (2R,3S,4R,5R)-5-(7-chloro-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl triphosphate tris-ammonium salt;

[0157] (2R,3S,4R,5R)-5-(7-cyano-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl triphosphate tris-ammonium salt;

[0158] (2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxo-4H-thieno[3,2]pyridin-5-yl)-tetrahydro-furan-2-ylmethyl triphosphate tris-ammonium salt;

[0159] (2R,3S,4R,5R)-3,4-dihydroxy-5-(1-thioxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl triphosphate tris-ammonium salt;

[0160] (2R,3S,4R,5R)-5-(7-chloro-1-thioxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl triphosphate tris-ammonium salt;

[0161] and the free acid, other pharmaceutically acceptable salts, solvates, hydrates and N-oxides thereof.

[0162] Another particular group of compounds includes:

[0163] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl triphosphate tris-ammonium salt;

[0164] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-fluoro-1-thioxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl triphosphate tris-ammonium salt;

[0165] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-methylsulfanyl-7-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl triphosphate tris-ammonium salt;

[0166] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-dimethylamino-7-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl triphosphate tris-ammonium salt;

[0167] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-fluoro-6-methoxy-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl triphosphate tris-ammonium salt;

[0168] and the free acid, other pharmaceutically acceptable salts, solvates, hydrates and N-oxides thereof.

[0169] The compounds of the invention may be prepared by a number of processes as generally described below and more specifically in the Examples hereinafter. In the following process description, the symbols G, G′, B, B′, m and n when used in the formulae depicted are to be understood to represent those groups described above in relation to formula (1) unless otherwise indicated. In the reactions described below, it may be necessary to protect reactive functional groups, for example hydroxy, amino, thio, phosphate or carboxy groups, where these are desired in the final product, to avoid their unwanted participation in the reactions. Conventional protecting groups may be used in accordance with standard practice [see, for example, Green, T. W. in “Protective Groups in Organic Synthesis”, John Wiley and Sons, 1999 and the Examples hereinafter]. In some instances, deprotection may be the final step in the synthesis of a compound of formula (1) and the processes according to the invention described hereinafter are to be understood to extend to such removal of protecting groups. For convenience the processes described below all refer to a preparation of a compound of formula (1) but clearly the description applies equally to the preparation of compounds of formulae (1e), (2a), (2a′), (2a″), (2a′″) or (2b).

[0170] Thus according to a further aspect of the invention a triphosphate of formula (1) [in which G is a hydrogen atom, n is zero and m is the integer 1] may be prepared by reaction of a compound of formula (3):

[0171] with a bis(tri-alkylammonium) pyrophosphate, for example bis(tri-n-butylammonium) pyrophosphate in the presence of an organic base such as a trialkylamine, e.g. tributylamine in an anhydrous solvent e.g. an amide such as dimethylformamide or a sulfoxide such as dimethyl sulfoxide at a temperature from around 0 to 80° C., optionally followed by purification of the product (1) by for example ion exchange chromatography using a Luna C18 column eluting with an ammonium acetate buffer or an anion exchange resin such as DEAE-A25 sephadex or Q-sepharose HP eluting with for example an ammonium salt buffer such as triethylammonium bicarbonate or ammonium bicarbonate. Such methods of preparing compounds of formula (1) are well known and may be found in for example Kovacs, T., Tetrahedron Letters 1988, 29, 4525; Burgess, K. and Cook, D., Chem. Rev., 2000, 100, 2047.

[0172] Compounds of formula (1) in the ammonium ion salt form may be readily converted to other salt forms, for example the sodium salt form, by treatment with a cation exchange resin such as DOWEX®-50 in its Na+ form.

[0173] Intermediates of formula (3) may be obtained by the reaction of a compound of formula (1d) [where b now represents an —OH group] with a phosphorylating agent, for example phosphorous oxychloride in the presence of a weakly nucleophilic strong organic base such as Proton Sponge® in an anhydrous organic solvent, e.g. a phosphate such as trimethylphosphate or triethylphosphate at a low temperature, e.g. around 0° C. Such methods of preparing intermediates of formula (3) are well known and may be found in for example Yoshikawa, M. et al, Bull. Chem. Soc. Jpn. 1969, 42, 3505.

[0174] In a further procedure compounds of formula (1) in which G is other than a hydrogen atom and n and m is each the integer 1 may be prepared by reaction of the tri-n-butylammonium salt of a compound of formula (1) in which G is a hydrogen atom, n is zero and m is the integer 1 with an activating agent such as carbonyldiimidazole or a dialkyl carbodiimide, e.g. dicyclohexyl carbodiimide in the presence of an ammonium salt e.g. tri-n-butylammonium salt of a monophosphate of formula (4);

[0175] in a polar aprotic organic solvent such as a formamide e.g. dimethylformamide, a sulfoxide e.g. dimethylsulfoxide, a pyrrolidine e.g. N-methylpyrrolidine, a phosphate e.g. triethylphosphate, a cyclic ether e.g. dioxane or an amine e.g. pyridine at a temperature from 0 to about 60° C.

[0176] Purification of the resulting compounds of formula (1) may be achieved by any of the previously mentioned ion exchange procedures or by high performance liquid chromatography.

[0177] Methods of preparing monophosphates of formula (4) are well known in the art and may be found in for example Slotin, L. A., Synthesis, 1977, 737; Yoshikawa, M., et al, Bull. Chem. Soc. Jpn., 1969, 42, 3505.

[0178] In an alternative procedure for the preparation of compounds of formula (1) in which G is a group of formula (1a), G′ is a group of formula (1d), n and m is each the integer 1 and the heterocyclic groups B and B′ are the same a diphosphate of formula (1f) [G is a hydrogen atom and n and m is each zero];

[0179] may be condensed with a further diphosphate of formula (1f) using any of the above mentioned activating agents.

[0180] Diphosphates of formula (1f) may be obtained from intermediate salts of formula (5):

[0181] by reaction with a trialkylammonium phosphate salt e.g. bis(tri-n-butylammonium) orthophosphate in an anhydrous organic solvent such as anhydrous pyridine at around ambient temperature or in a phosphate solvent such as triethylphosphate at an elevated temperature e.g around 50° C., as described by Moffatt, J. G. et al, J. Am. Chem. Soc. 1961, 83, 649-658 and Can. J. Chem. 1964, 42, 599-604.

[0182] Intermediates of formula (5) may be obtained by reaction of a salt of formula (6):

[0183] [or the free acid of a compound of formula (6)] with an activating agent such as a dialkyl carbodimide e.g dicyclohexyl carbodimide or a carbonylimidazole, in the presence of an organic amine such as a cyclic amine e.g. morpholine in a solvent e.g. an alcohol such as t-butanol, i-propanol, ethanol or methanol in the presence of added water at a temperature from ambient to the reflux temperature.

[0184] In a further procedure for the preparation of compounds of formula (1) intermediates of formula (5) may be converted to triphosphates of formula (1) [in which G is a hydrogen atom, n is zero and m is the integer 1] by reaction with pyrophosphate (preferably as its tri-n-butylammonium salt) in an anhydrous polar aprotic solvent, for example dimethyl sulfoxide at for example ambient temperature.

[0185] Intermediate compounds of formula (1a) and (1d) [where b now represents an —OH group] may be prepared by the methods described hereinafter or by such well known methods as those of Niedballa, U. and Vorbruggen, H. J. Org. Chem., 1974, 39, 3654-59, 3660-63 and 3668-71; Mao, D. T. et al, J. Med. Chem. 1984, 27, 160-4; Ogawa, A. K. et al, J. Am. Chem. Soc., 2000, 122, 3274-87 and Berger, M. et al, Angew Chem Int Ed, 2000, 39, 2940-42.

[0186] Where in the general processes described above intermediates such as those of formulae (1a), (1d), (3), (4), (5) and (6) are not commercially available or known in the literature they may be readily obtained from simpler known compounds by one or more standard synthetic methods employing substitution, oxidation, reduction or cleavage reactions. Particular substitution approaches include conventional alkylation, arylation, heteroarylation, acylation, thioacylation, halogenation, sulphonylation, nitration, formylation and coupling procedures. It will be appreciated that these methods may also be used to obtain or modify other compounds of formulae (1), (1e), (2a), (2a′), (2a″), (2a′″) and (2b) and also to further functionalize intermediates of formulae (1a), (1d), (3), (4), (5) and (6) where appropriate functional groups exist in these compounds.

[0187] Thus intermediates of formulae (1a), (1d), (3), (4), (5) and (6) and any other intermediates described herein required to obtain compounds of formula (1) may be prepared by methods known to those skilled in the art following procedures set forth in references such as Rodd's Chemistry of Carbon Compounds, Volumes 1-15 and Supplementals (Elsevier Science Publishers, 1989), Fieser and Fieser's Reagents for Organic Synthesis, Volumes 1-19 (John Wiley and Sons, 1999), Comprehensive Heterocyclic Chemistry, Ed. Katritzky et al, Volumes 1-8, 1984 and Volumes 1-11, 1994 (Pergamon), Comprehensive Organic Functional Group Transformations, Ed. Katritzky et al, Volumes 1-7, 1995 (Pergamon), Comprehensive Organic Synthesis, Ed. Trost and Flemming, Volumes 1-9, (Pergamon, 1991), Encyclopedia of Reagents for Organic Synthesis Ed. Paquette, Volumes 1-8 (John Wiley and Sons, 1995), Larock's Comprehensive Organic Transformations (VCH Publishers Inc., 1989) and March's Advanced Organic Chemistry (John Wiley and Sons, 1992)

[0188] Compounds of the invention and intermediates thereto may be prepared by alkylation, arylation or heteroarylation. For example, compounds containing a -L3H or -L4H group (where L3 and L4 is each a linker atom or group) may be treated with an alkylating agent R9(Alk2)qZ1 or (R14)uL5(Alk5)tZ1 respectively in which Z1 is a leaving atom or group such as a halogen atom, e.g. a fluorine, bromine, iodine or chlorine atom or a sulphonyloxy group such as an alkylsulphonyloxy, e.g. trifluoromethylsulphonyloxy or arylsulphonyloxy, e.g. p-toluenesulphonyloxy group.

[0189] The reaction may be carried out in the presence of a base such as a carbonate, e.g. caesium or potassium carbonate, an alkoxide, e.g. potassium t-butoxide, or a hydride, e.g. sodium hydride, in a dipolar aprotic solvent such as an amide, e.g. a substituted amide such as dimethylformamide or an ether, e.g. a cyclic ether such as tetrahydrofuran.

[0190] In another example, compounds containing a -L3H or -L4H or group as defined above may be functionalised by acylation or thioacylation, for example by reaction with one of the alkylating agents just described but in which Z1 is replaced by a —C(O)Z2, C(S)Z2, —N(R2)COZ2 or —N(R2)C(S)Z2 group in which Z2 is a leaving atom or group as described for Z1. The reaction may be performed in the presence of a base, such as a hydride, e.g. sodium hydride or an amine, e.g. triethylamine or N-methylmorpholine, in a solvent such as a halogenated hydrocarbon, e.g. dichloromethane or carbon tetrachloride or an amide, e.g. dimethyl-formamide, at for example ambient temperature. Alternatively, the acylation may be carried out under the same conditions with an acid (for example one of the alkylating agents described above in which Z1 is replaced by a —CO2H group) in the presence of a condensing agent, for example a diimide such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide or N,N′-dicyclohexylcarbodiimide, or a benzotriazole such as [O-(7-azabenzo-triazol-1-yl)-1,1,3,3-tetramethyluronium]hexafluorophosphate advantageously in the presence of a catalyst such as a N-hydroxy compound e.g. a N-hydroxytriazole such as 1-hydroxybenzotriazole. Alternatively the acid may be reacted with a chloroformate, for example ethylchloroformate, prior to the desired acylation reaction.

[0191] In a further example compounds may be obtained by sulphonylation of a compound containing an —OH group by reaction with one of the above alkylating agents but in which Z1 is replaced by a —S(O)Hal or —SO2Hal group [in which Hal is a halogen atom such as chlorine atom] in the presence of a base, for example an inorganic base such as sodium hydride in a solvent such as an amide, e.g. a substituted amide such as dimethylformamide at for example ambient temperature.

[0192] In another example, compounds containing a -L3H or -L4H group as defined above may be coupled with one of the alkylation agents just described but in which Z1 is replaced by an —OH group in a solvent such as tetrahydrofuran in the presence of a phosphine, e.g. triphenylphosphine and an activator such as diethyl, diisopropyl- or dimethylazodicarboxylate.

[0193] In a further example, ester groups —CO2R6, —CO2Alk4, —CO2Alk6 or —CO2R15 in the compounds may be converted to the corresponding acid [—CO2H] by acid- or base-catalysed hydrolysis depending on the nature of the groups R6, Alk4, Alk6 or R15. Acid- or base-catalysed hydrolysis may be achieved for example by treatment with an organic or inorganic acid, e.g. trifluoroacetic acid in an aqueous solvent or a mineral acid such as hydrochloric acid in a solvent such as dioxan or an alkali metal hydroxide, e.g. lithium hydroxide in an aqueous alcohol, e.g. aqueous methanol.

[0194] In a further example, —OR6 or —OR11 groups [where R6 or R11 each represents an alkyl group such as methyl group] in compounds of formula (1) may be cleaved to the corresponding alcohol —OH by reaction with boron tribromide in a solvent such as a halogenated hydrocarbon, e.g. dichloromethane at a low temperature, e.g. around −78° C.

[0195] Alcohol [—OH] groups may also be obtained by hydrogenation of a corresponding —OCH2R30 group (where R30 is an aryl group) using a metal catalyst, for example palladium on a support such as carbon in a solvent such as ethanol in the presence of ammonium formate, cyclohexadiene or hydrogen, from around ambient to the reflux temperature. In another example, —OH groups may be generated from the corresponding ester [e.g. CO2Alk2 or CO2R6] or aldehyde [—CHO] by reduction, using for example a complex metal hydride such as lithium aluminium hydride or sodium borohydride in a solvent such as methanol.

[0196] In another example, alcohol —OH groups in the compounds may be converted to a corresponding —OR6 or —OR11 group by coupling with a reagent R6OH or R11OH in a solvent such as tetrahydrofuran in the presence of a phosphine, e.g. triphenylphosphine and an activator such as diethyl-, diisopropyl-, or dimethylazodicarboxylate.

[0197] Aminosulphonylamino [—NHSO2NHR7] groups in the compounds may be obtained, in another example, by reaction of a corresponding amine [—NH2] with a sulphamide R7NHSO2NH2 in the presence of an organic base such as pyridine at an elevated temperature, e.g. the reflux temperature.

[0198] In another example compounds containing a —NHCSR11 or —CSNHR16, may be prepared by treating a corresponding compound containing a —NHCOR11 or —CONHR16 group with a thiation reagent, such as Lawesson's Reagent or P2S5, in an anhydrous solvent, for example a cyclic ether such as tetrahydrofuran, at an elevated temperature such as the reflux temperature.

[0199] In a further example amine (—NH2) groups may be alkylated using a reductive alkylation process employing an aldehyde and a borohydride, for example sodium triacetoxyborohyride or sodium cyanoborohydride, in a solvent such as a halogenated hydrocarbon, e.g. dichloromethane, a ketone such as acetone, or an alcohol, e.g. ethanol, where necessary in the presence of an acid such as acetic acid at around ambient temperature.

[0200] In a further example, amine [—NH2] groups in compounds of formula (1) may be obtained by hydrolysis from a corresponding imide by reaction with hydrazine in a solvent such as an alcohol, e.g. ethanol at ambient temperature.

[0201] In another example, a nitro [—NO2] group may be reduced to an amine [—NH2], for example by catalytic hydrogenation using for example hydrogen in the presence of a metal catalyst, for example palladium on a support such as carbon in a solvent such as an ether, e.g. tetrahydrofuran or an alcohol e.g. methanol, or by chemical reduction using for example a metal, e.g. tin or iron, in the presence of an acid such as hydrochloric acid.

[0202] In a further example amine (—CH2NH2) groups in compounds of formula (1) and intermediates thereto may be obtained by reduction of nitriles (—CN), for example by catalytic hydrogenation using for example hydrogen in the presence of a metal catalyst, for example palladium on a support such as carbon, or Raney® nickel, in a solvent such as an ether e.g. a cyclic ether such as tetrahydrofuran or an alcohol e.g. methanol or ethanol, optionally in the presence of ammonia solution at a temperature from ambient to the reflux temperature, or by chemical reduction using for example a metal hydride e.g. lithium aluminium hydride, in a solvent such as an ether e.g. a cyclic ether such as tetrahydrofuran, at a temperature from 0° C. to the reflux temperature.

[0203] Aromatic halogen substituents in the compounds may be subjected to halogen-metal exchange with a base, for example a lithium base such as n-butyl or t-butyl lithium, optionally at a low temperature, e.g. around −78° C., in a solvent such as tetrahydrofuran and then quenched with an electrophile to introduce a desired substituent. Thus, for example, a formyl group may be introduced by using dimethylformamide as the electrophile; a thiomethyl group may be introduced by using dimethyldisulphide as the electrophile. Aromatic acids may be generated by quenching aromatic Grignard reagents with carbon dioxide.

[0204] In another example, sulphur atoms in the compounds, for example when present in a linker group L3 or L4 may be oxidised to the corresponding sulphoxide or sulphone using an oxidising agent such as a peroxy acid, e.g. 3-chloroperoxybenzoic acid, in an inert solvent such as a halogenated hydrocarbon, e.g. dichloromethane, at around ambient temperature.

[0205] N-oxides of compounds of formula (1) may be prepared for example by oxidation of the corresponding nitrogen base using an oxidising agent such as hydrogen peroxide in the presence of an acid such as acetic acid, at an elevated temperature, for example around 70° C. to 80° C., or alternatively by reaction with a peracid such as peracetic acid in a solvent, e.g. dichloromethane, at ambient temperature.

[0206] Salts of compounds of formula (1) may be prepared by reaction of a compound of formula (1) with an appropriate base in a suitable solvent or mixture of solvents e.g. an organic solvent such as an ether e.g. diethylether, or an alcohol, e.g. ethanol or an aqueous solvent using conventional procedures. Salts of compounds of formula (1) may be exchanged for other salts by use of conventional ion-exchange chromatography procedures.

[0207] Where it is desired to obtain a particular enantiomer of a compound of formula (1) this may be produced from a corresponding mixture of enantiomers using any suitable conventional procedure for resolving enantiomers.

[0208] Thus for example diastereomeric derivatives, e.g. salts, may be produced by reaction of a mixture of enantiomers of formula (1) e.g. a racemate, and an appropriate chiral compound, e.g. a chiral base. The diastereomers may then be separated by any convenient means, for example by crystallisation and the desired enantiomer recovered, e.g. by treatment with an acid in the instance where the diastereomer is a salt.

[0209] In another resolution process a racemate of formula (1) may be separated using chiral High Performance Liquid Chromatography. Alternatively, if desired a particular enantiomer may be obtained by using an appropriate chiral intermediate in one of the processes described above.

[0210] Chromatography, recrystallisation and other conventional separation procedures may also be used with intermediates or final products where it is desired to obtain a particular geometric isomer of the invention.

[0211] The following Examples illustrate the invention. All temperatures are in ° C. The following abbreviations are used:

1NMM—N-methylmorpholine;EtOAc—ethyl acetate;MeOH—methanol;BOC—butoxycarbonyl;DCM—dichloromethane;AcOH—acetic acid;DIPEA—diisopropylethylamine;EtOH—ethanol;Pyr—pyridine;DMF—N,N-dimethylformamide;DMSO—dimethylsulphoxide;iPr—isopropyl;Et2O—diethylether;Me—methyl;THF—tetrahydrofuran;RT—room temperatureLCMS—liquid chromatography -mass spectroscopy

[0212] NMR's were obtained at the indicated frequency (quoted as δH or δ31P values) The compounds were named with the aid of Beilstein Autonom. In certain instances an alternative name is also quoted.

[0213] LCMS was performed on a Hewlett Packard 1100 LC/MSD instrument using a Phenomenex Luna 3 μ C18(2) 50×4.6 mm column and electrospray ionisation in +ve mode. Compounds were eluted with a mobile phase formed from solution A (0.1% aqueous formic acid) and solution B (0.1% formic acid in acetonitrile) with the following gradient and column conditions. Initial=5% B, 2 min=95% B, 3 min=95% B, 5 min=5% B; column temp 40°; flow rate 0.9 ml min−1; detection UV DAD 210-450 nM.

[0214] Intermediate 1

[0215] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one Tribenzoate

[0216] (Alternatively: 2-β-D-Ribofuranosyl-1 (2H)-isoquinolinone-2′,3′,5′-tribenzoate)

[0217] To a suspension of 2H-isoquinolin-1-one (1.04 g, 7.2 mmol) in dry acetonitrile (50 mL) under nitrogen was added dropwise (N,O)-bis-trimethylsilylacetamide (1.79 mL, 7.2 mmol). The resultant solution was stirred at RT for 30 min before addition of β-D-ribofuranose-1-acetate-2,3,5-tribenzoate (3.03g, 6.0 mmol). The solution was cooled to 0° and SnCl4 (1.76 mL, 15.0 mmol) added dropwise under a nitrogen flush. The golden yellow solution was stirred at 0° for 30 min before warming to RT and stirring for 5 h. The reaction was diluted with EtOAc (100 mL) and poured into saturated aqueous sodium bicarbonate solution (200 mL). The aqueous phase was extracted with EtOAc (2×150 mL), and the combined organic extracts washed with brine (1×200 mL), dried (MgSO4) and the solvents removed in vacuo to give a colourless syrup. The crude product was purified by column chromatography (SiO2, 4:1 hexanes/EtOAc) to give the title compound as a white glassy solid (2.75 g, 78%). δH (400 MHz, CDCl3) 8.40 (1H, d, J 7.6 Hz), 8.15 (2H, m), 7.97 (4H, m), 7.65-7.45 (8H, m), 7.47 (4H, m), 7.29 (1H, d, J 7.6 Hz), 6.80 (1H, d, J 5.1 Hz), 6.41 (1H, d, J 7.6 Hz), 6.00 (1H, t, J 5.6 Hz), 5.90 (1H, t, J 5.6 Hz), 4.89 (1H, dd, J 12.1, 2.9 Hz), 4.78 (1H, m), 4.71 (1H, dd, J 12.1, 3.9 Hz); LCMS m/z (ES+, 70 eV) 590 (M+H)+, 612 (M+Na)+; RT 5.07 min.

[0218] Intermediate 2

[0219] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one

[0220] (Alternatively: 2-β-D-Ribofuranosyl-1(2H)-isoquinolinone)

[0221] To a solution of Intermediate 1 (2.75 g, 4.67 mmol), in dry MeOH (50 mL) at 0°, was added sodium methoxide (1.01 g, 18.7 mmol) portionwise. The reaction was allowed to warm to RT and stirred for 30 min. Ammonium chloride (2.00 g, 37.4 mmol) was added and the mixture allowed to stir for 10 min. The solvents were removed in vacuo and the crude residue purified by column chromatography (SiO2; 9:1 DCM/MeOH) to give the title compound as a white powder (1.00 g, 78%). δH (400 MHz, MeOD) 8.33 (1H, d, J 8.1 Hz), 7.79 (1H, d, J 7.6 Hz), 7.72 (1H, t, J 7.2 Hz), 7.63 (1H, d, J 7.8 Hz), 7.53 (1H, t, J 8.2 Hz), 6.71 (1H, d, J 7.6 Hz), 6.36 (1H, d, J 3.8 Hz), 4.24 (2H, m), 4.11 (1H, m), 3.94 (1H, dd, J 12.3, 2.7 Hz), 3.82 (1H, dd, J 12.2, 3.4 Hz); LCMS m/z (ES+, 70 eV) 300 (M+Na)+; RT 2.43 min.

[0222] Intermediate 3

[0223] 3-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3H-pyrido[2,3-d]pyrimidin-4-one Tribenzoate

[0224] (Alternatively: 3-β-D-Ribofuranosyl Pyrido[2,3-d]pyrimidin-4(3H)-one-2′,3′,5′-tribenzoate)

[0225] To a suspension of 3H-pyrido[2,3-d]pyrimidin-4-one (327 mg, 2.22 mmol) in dry acetonitrile (15 mL) under nitrogen was added dropwise (N,O)bis-trimethylsilylacetamide (540 μL, 2.22 mmol). The resultant solution was stirred at RT for 30 min before addition of β-D-ribofuranose-1-acetate-2,3,5-tribenzoate (1.02 g, 2.02 mmol). The solution was cooled to 0° and trimethylsilyltriflate (548 μL, 3.03 mmol) added dropwise under a nitrogen flush. The golden yellow solution was stirred at 0° for 10 min before warming to RT and stirring for 18 h. The reaction was diluted with DCM (200 mL) and poured into ice cold saturated aqueous sodium bicarbonate solution (300 mL). The aqueous phase was extracted with DCM (2×200 mL), and the combined organic extracts washed with brine (2×200 mL), dried (MgSO4) and the solvents removed in vacuo to give 1.37 g of a crude off white solid. The crude product was purified by column chromatography (SiO2; 3:2 EtOAc/hexanes) to give the title compound as a white crystalline solid (490 mg, 37%). δH (400 MHz, CDCl3) 8.71 (1H, s), 8.67 (1H, m), 8.63 (1H, dd, J 7.9, 2.0 Hz), 8.04 (2H, m), 7.97 (2H, m), 7.91 (2H, m), 7.60-7.51 (3H, m), 7.50-7.30 (7H, m), 6.49 (1H, d, J 3.5 Hz), 6.21 (1H, m), 6.17 (1H, t, J 6.4 Hz), 4.87 (2H, m), 4.74 (1H, m); LCMS m/z (ES+, 70 eV) 592 (M+H)+, RT 4.80 min.

[0226] Intermediate 4

[0227] 3-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3H-pyrido[2,3-d]pyrimidin-4-one

[0228] (Alternatively: 3-β-D-Ribofuranosyl Pyrido[2,3-d]pyrimidin-4(3H)-one)

[0229] To a solution of Intermediate 3 (490 mg, 0.83 mmol), in dry MeOH (15 mL) at 0° was added sodium methoxide (180 mg, 3.33 mmol) portionwise. The reaction was allowed to warm to RT and stirred for 40 minutes. Ammonium chloride (355 mg, 6.64 mmol) was added and the mixture allowed to stir for 10 minutes. The solvents were removed in vacuo and the crude residue purified by column chromatography (SiO2; 9:1 DCM/MeOH) to give the title compound as an off white powder (174 mg, 76%); δH (400 MHz, MeOD) 9.17 (1H, s), 8.77 (1H, dd, J 4.7, 1.9 Hz), 8.47 (1H, dd, J 8.0, 1.9 Hz), 7.52 (1H, dd, J 7.9, 4.7 Hz), 6.54 (1H, d, J 3.0 Hz), 4.30 (1H, m), 4.25 (1H, m), 4.08 (1H, m), 3.90 (1H, dd, J 12.3, 2.5 Hz), 3.73 (1H, dd, J 9.6, 2.5 Hz); LCMS m/z (ES+, 70 eV): 581 (2M+Na)+; RT 0.76 min.

[0230] Intermediate 5

[0231] 1-Oxy-6H-[1,6]naphthyridin-5-one

[0232] 6H-[1,6]-Naphthyridin-5-one (1 g) was taken up in dichloromethane (15 ml) and peracetic acid (2 ml, 36%) added. The reaction was stirred at rt overnight. The precipitated solid was removed by filtration and washed with diethyl ether (3×15 ml) to yield on drying the title compound as a green solid (0.88 g, 73%). TLC Rf 0.08 (5% methanol-dichloromethane).

[0233] The following compounds were prepared following the procedure for Intermediate 1:

[0234] Intermediate 6

[0235] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-4-methyl-2H-isoquinolin-1-one Tribenzoate

[0236] From 4-methyl-2H-isoquinolin-1-one (0.875 g), with purification by flash chromatography (25% ethyl acetate-hexane) to give the title compound as a white foam (2.02 g, 60%). TLC Rf 0.30 (30% ethyl acetate-hexane)

[0237] Intermediate 7

[0238] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2H-isoquinolin-1-one Tribenzoate

[0239] From 5-methyl-2H-isoquinolin-1-one (0.283 g), with purification by flash chromatography (30% ethyl acetate-hexane to give the title compound as a white foam (0.589, 65%). TLC Rf 0.43 (30% ethyl acetate-hexane)

[0240] Intermediate 8

[0241] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6-methyl-2H-isoquinolin-1-one Tribenzoate

[0242] From 6-methyl-2H-isoquinolin-1-one (0.3 g), with purification by flash chromatography (10% ethyl acetate-hexane followed by 40% ethyl acetate-hexane) to give the title compound as a glass (4.8 g, 80%). TLC Rf 0.40 (30% ethyl acetate-hexane)

[0243] Intermediate 9

[0244] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-methyl-2H-isoquinolin-1-one Tribenzoate

[0245] From 7-methyl-2H-isoquinolin-1-one (0.5 g) with purification by flash chromatography (70% hexane-ethyl acetate) to give the title compound as a white solid (1.45 g, 77%). TLC Rf 0.34 (60% hexane-ethyl acetate)

[0246] Intermediate 10

[0247] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-8-methyl-2H-isoquinolin-1-one Tribenzoate

[0248] From 8-methyl-2H-isoquinolin-1-one (0.5 g), with purification by flash chromatography (1% ethyl acetate-dichloromethane) to give the title compound as a cream foam (0.583 g, 37%). TLC Rf 0.45 (30% ethyl acetate-hexane)

[0249] Intermediate 11

[0250] 4-Chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one Tribenzoate

[0251] From 4-chloro-2H-isoquinolin-1-one (0.3 g), with purification by flash chromatography (20% ethyl acetate-hexane) to give the title compound as a cream foam (0.78 g, 80%). TLC Rf 0.44 (30% ethyl acetate-hexane)

[0252] Intermediate 12

[0253] 6-Chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one Tribenzoate

[0254] From 6-chloro-2H-isoquinolin-1-one (0.368 g), with purification by flash chromatography (70% hexane-ethyl acetate) to give the title compound as a white solid (1.03 g, 83%). TLC Rf 0.6 (6:4 hexane-ethyl acetate)

[0255] Intermediate 13

[0256] 7-Chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one Tribenzoate

[0257] From 7-chloro-2H-isoquinolin-1-one (0.4 g), with purification by flash chromatography (15% ethyl acetate-hexane) to give the title compound as a white solid (0.45 g, 33%). TLC Rf 0.27 (15% ethyl acetate-hexane)

[0258] Intermediate 14

[0259] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-methoxy-2H-isoquinolin-1-one Tribenzoate

[0260] From a 1:1 mixture of 7-methoxy-2H-isoquinolin-1-one and 1-(2-isocyanato-vinyl)-4-methoxy-benzene (581 mg) with purification by flash chromatography (3:1 heptane-ethyl acetate) to give the title compound as a white foam (411 mg, 40%). TLC Rf 0.26 (3:1 heptane-ethyl acetate)

Intermediate 15

[0261] 7-Bromo-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one Tribenzoate

[0262] From 7-bromo-2H-isoquinolin-1-one (1.75 g) with purification by flash chromatography (3:1 heptane-ethyl acetate) to give the title compound as a white foam (3.75 g, 71%). TLC Rf 0.23 (3:1 heptane-ethyl acetate)

[0263] Intermediate 16

[0264] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5H-thieno[3,2-c]pyridin-4-one Tribenzoate

[0265] From 5H-thieno[3,2-c]pyridin-4-one (250 mg) with purification by flash chromatography (20% ethyl acetate-hexane followed by 40% ethyl acetate-hexane) to give the title compound as an off white solid (0.70 g, 83%). TLC Rf 0.35 (30% ethyl acetate in hexane)

[0266] Intermediate 17

[0267] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3-methyl-5H-isoxazolo[4,5-c]pyridin-4-one Tribenzoate

[0268] From 3-methyl-5H-isoxazolo[4,5-c]pyridin-4-one (240 mg) with purification by column chromatography (1:2:7 tetrahydrofuran-ethyl acetate-hexane followed by 1:5:4 tetrahydrofuran-ethyl acetate-hexane) to give the title compound as a white solid (650 mg, 68%). TLC Rf 0.38 (30% ethyl acetate in hexane)

[0269] Intermediate 18

[0270] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-1-methyl-1,5-dihydro-pyrrolo[3,2-c]pyridin-4-one Tribenzoate

[0271] From 1-methyl-1,5-dihydro-pyrrolo[3,2-c]pyridin-4-one (300 mg) with purification by column chromatography (10% ethyl acetate-hexane followed by 50% ethyl acetate-hexane) to give the title compound as a pale yellow gum (0.31 g, 23%). TLC Rf 0.7 (ethyl acetate)

[0272] Intermediate 19

[0273] 6-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-1-hydroxy-6H-[1,6]naphthyridin-5-one Tribenzoate

[0274] From 1-oxy-6H-[1,6]naphthyridin-5-one (0.55 g), with purification by flash chromatography (5% methanol-dichloromethane) to give the title compound as a white solid (0.57 g, 28%). TLC Rf 0.45 (5% methanol-dichloromethane).

[0275] Intermediate 20

[0276] 6-[(2R,3R,4S,5 R)-(3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-6H-furo[2,3-c]pyridin-7-one Tribenzoate

[0277] From 6H-furo[2,3-c]pyridin-7-one (0.5 g), with purification by flash chromatography (30% ethyl acetate-hexane followed by 50% ethyl acetate-hexane) to give the title compound as a white solid (0.45 g, 21%). TLC Rf 0.16 (30% ethyl acetate/hexane).

[0278] Intermediate 21

[0279] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5,6,7,8-tetrahydro-2H-isoquinolin-1-one Tribenzoate

[0280] To a suspension of a 1.1:1 mixture of 5,6,7,8-tetrahydro-2H-isoquinolin-1-one and octahydro-isoquinolin-1-one (760 mg) and β-D-ribofuranose 1-acetate 2,3,5-tribenzoate (1.24 g) in acetonitrile (20 ml) under an atmosphere of nitrogen was added N,O-bis(trimethylsilyl)acetamide (0.78 ml). The reaction was heated with stirring at 70° C. for 25 min then trimethylsilyl trifluoromethane sulfonate (0.67 ml) was added and heating continued for a further 1 h 45 min. The reaction was left to cool then diluted with ethyl acetate (30 ml) and washed with saturated sodium bicarbonate solution (50 ml). The aqueous was extracted with ethyl acetate (20 ml) and the combined organics washed with brine (20 ml) then dried over anhydrous MgSO4. The solvent was removed under reduced pressure and the residue purified by flash chromatography (SiO2, 30% ethyl acetate-hexane) to give the title compound as a white solid (1.32 g, 82%). TLC Rf 0.73 (40% hexane in ethyl acetate)

[0281] Intermediate 22

[0282] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-cyano-2H-isoquinolin-1-one Tribenzoate

[0283] A mixture of 7-bromo-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one tribenzoate (1.0 g) and copper(I) cyanide (2.0 g) in N,N-dimethylformamide (10 ml) was heated to reflux overnight. After cooling to room temperature the mixture was partitioned between ethyl acetate (100 ml) and water (100 ml). The organics were washed with water (2×100 ml), dried over anhydrous MgSO4 and evaporated under reduced pressure. The residue was purified by flash chromatography (2:1 heptane-ethyl acetate followed by 1:1 heptane-ethyl acetate) to give the title compound as a white foam (605 mg, 66%). TLC Rf 0.62 (1:1 heptane-ethyl acetate)

[0284] Intermediate 23

[0285] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-pyridin-3-yl-2H-isoquinolin-1-one Tribenzoate

[0286] A mixture of 7-bromo-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one tribenzoate (500 mg), pyridine-3-boronic acid 1,3-propanediol cyclic ester (119 mg) and potassium phosphate buffer (1M, 2 ml) in ethylene glycol dimethyl ether (10 ml) was degassed three times. Tetrakis(triphenylphosphine)palladium(0) (421 mg) was added and the reaction degassed once more before heating to reflux for three hours. The reaction mixture was adsorbed onto silica and purified by flash chromatography (ethyl acetate) to give the title compound as a yellow solid (200 mg, 40%). TLC Rf 0.5 (ethyl acetate)

[0287] Intermediate 24

[0288] '6-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6H-[1,6]naphthyridin-5-one Tribenzoate

[0289] 6-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-1-hydroxy-6H-[1,6]naphthyridin-5-one tribenzoate (0.93 g) and triphenylphoshine (0.4 g) were combined in tetrahydrofuran (20 ml) and heated at reflux for 5 days. On cooling the reaction was adsorbed onto silica and purified by flash chromatography (30% ethyl acetate-hexane followed by 50% ethyl acetate-hexane) to yield the title compound as a white solid (0.55 g, 62%). TLC Rf 0.28 (50% ethyl acetate-hexane).

[0290] Intermediate 25

[0291] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3,4-dihydro-2H-isoquinolin-1-one

[0292] 2-[(2S,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-ylmethyl]-2H-isoquinolin-1-one (0.25 g) and palladium (10% on carbon, 120 mg), were taken up in a mixture of ethanol (10 ml), tetrahydrofuran (10 ml) and acetic acid (2 ml), and stirred under hydrogen (1 atmos) for 8 h. The reaction was filtered and the filtrate evaporated in vacuo to yield the title compound as a white solid (0.24 g). Mass spectrum m/z 280 (M+1, 100%)

[0293] Intermediate 26

[0294] 2-[(2R,3R,4S,5R)-(3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione Tribenzoate

[0295] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one (1.38 g) was heated at relux with Lawessons reagent (2.279) in chlorobenzene (30 ml) for 4 hours. The reaction was allowed to cool before being diluted with dichloromethane (15 ml) and filtered. The filtrate was adsorbed onto silica and purified by flash chromatography (25% hexane-dichloromethane followed by dichloromethane) to yield the title compound as a glass (0.819, 57%). TLC Rf 0.43 (30% ethyl acetate-hexane).

[0296] The following compound was prepared in the same manner as intermediate 26:

[0297] Intermediate 27

[0298] 7-Chloro-2-[(2R,3R,4S,5R)-(3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione Tribenzoate

[0299] From 7-chloro-2-[(2R,3R,4S,5 R)-(3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one (1.29), with purification by flash chromatography (2:1 hexane-ethyl acetate), to yield the title compound as a yellow solid (0.18g, 15%). TLC Rf 0.48 (eluent 2:1 hexane-ethyl acetate).

[0300] The following compounds were prepared following the procedure for Intermediate 2:

[0301] Intermediate 28

[0302] 2-[(2R,3R,4S,5 R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-4-methyl-2H-isoquinolin-1-one

[0303] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-4-methyl-2H-isoquinolin-1-one tribenzoate (1.8 g), with purification by flash chromatography (20% ethyl acetate in hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (0.67 g, 77%). TLC Rf 0.25 (ethyl acetate)

Intermediate 29

[0304] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2H-isoquinolin-1-one

[0305] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2H-isoquinolin-1-one tribenzoate (0.587 g), with purification by flash chromatography (30% ethyl acetate in hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (0.23 g, 80%). TLC Rf 0.62 (10% methanol in ethyl acetate)

[0306] Intermediate 30

[0307] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6-methyl-2H-isoquinolin-1-one

[0308] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6-methyl-2H-isoquinolin-1-one tribenzoate (4.9 g), with purification by flash chromatography (20% ethyl acetate in hexane followed by 20% methanol in ethyl acetate) to give the title compound as a white solid (1.7 g, 80%). TLC Rf 0.55 (10% methanol in ethyl acetate)

[0309] Intermediate 31

[0310] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-methyl-2H-isoquinolin-1-one

[0311] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-methyl-2H-isoquinolin-1-one tribenzoate (1.45 g), with purification by flash chromatography (30% ethyl acetate in hexane followed by 10% methanol in dichloromethane) to give the title compound as a white solid (0.56 g, 82%). TLC Rf 0.5 (10% methanol in dichloromethane)

[0312] Intermediate 32

[0313] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-8-methyl-2H-isoquinolin-1-one

[0314] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-8-methyl-2H-isoquinolin-1-one tribenzoate (0.39 g), with purification by flash chromatography (30% ethyl acetate in hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white foam (0.14 g, 72%). TLC Rf 0.73 (10% methanol in ethyl acetate)

[0315] Intermediate 33

[0316] 4-Chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one

[0317] From 4-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one tribenzoate (0.78 g), with purification by flash chromatography (1:1 hexane-ethyl acetate hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (0.33 g, 88%). TLC Rf 0.46 (10% methanol in ethyl acetate)

[0318] Intermediate 34

[0319] 6-Chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one

[0320] From 6-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one tribenzoate (0.53 g), with purification by flash chromatography (6% methanol in dichloromethane) to give the title compound as a white solid (0.16 g, 61%). TLC Rf 0.29 (6% methanol in dichloromethane)

[0321] Intermediate 35

[0322] 7-Chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one

[0323] From 7-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one tribenzoate (0.45 g), with purification by flash chromatography (1:1 hexane-ethyl acetate hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (0.14 g, 61%). TLC Rf 0.58 (ethyl acetate)

[0324] Intermediate 36

[0325] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-methoxy-2H-isoquinolin-1-one

[0326] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-methoxy-2H-isoquinolin-1-one tribenzoate (411 mg) with purification by flash chromatography (3:1 heptane-ethyl acetate followed by 10% methanol in ethyl acetate) to give the title compound as a colourless glass (157 mg, 77%). TLC Rf 0.26 (ethyl acetate)

[0327] Intermediate 37

[0328] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-cyano-2H-isoquinolin-1-one

[0329] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-cyano-2H-isoquinolin-1-one tribenzoate (250 mg) with purification by flash chromatography (ethyl acetate followed by 5% methanol in ethyl acetate) to give the title compound as a white solid (68 mg, 55%). TLC Rf 0.32 (ethyl acetate)

[0330] Intermediate 38

[0331] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-pyridin-3-yl-2H-isoquinolin-1-one

[0332] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-pyridin-3-yl-2H-isoquinolin-1-one tribenzoate (200 mg) with purification by flash chromatography (10% methanol in dichloromethane) to give the title compound as an off white solid (100 mg, 94%). TLC Rf 0.42 (10% methanol in dichloromethane)

[0333] Intermediate 39

[0334] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5H-thieno[3,2-c]pyridin-4-one

[0335] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5H-thieno [3,2-c]pyridin-4-one tribenzoate (0.34 g) with purification by flash chromatography (20% ethyl acetate in hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (175 mg, quantitative). TLC Rf 0.15 (ethyl acetate)

[0336] Intermediate 40

[0337] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3-methyl-5H-isoxazolo[4,5-c]pyridin-4-one

[0338] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3-methyl-5H-isoxazolo[4,5-c]pyridin-4-one tribenzoate (345 mg) with purification by flash chromatography (20% ethyl acetate in hexane followed by 20% methanol in ethyl acetate) to give the title compound as a white solid (143 mg, 87%). TLC Rf 0.55 (10% methanol in ethyl acetate)

[0339] Intermediate 41

[0340] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-1-methyl-1,5-dihydro-pyrrolo[3,2-c]pyridin-4-one

[0341] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-1-methyl-1,5-dihydro-pyrrolo[3,2-c]pyridin-4-one tribenzoate (0.26 g) with purification by flash chromatography (20% ethyl acetate in hexane followed by 20% methanol in ethyl acetate) to give the title compound as a pale yellow glass (69 mg, 56%). TLC Rf 0.35 (10% methanol in ethyl acetate)

[0342] Intermediate 42

[0343] '6-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6H-[1,6]naphthyridin-5-one

[0344] From '6-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6H-[1,6]naphthyridin-5-one tribenzoate (0.55 g), with purification by flash chromatography (5% methanol in ethyl acetate followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (0.22 g, 83%). TLC Rf 0.42 (10% methanol in ethyl acetate).

[0345] Intermediate 43

[0346] 6-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6H-furo[2,3-c]pyridin-7-one

[0347] From 6-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6H-furo[2,3-c]pyridin-7-one tribenzoate (0.4 g), with purification by flash chromatography (10% methanol in ethyl acetate) to give the title compound as a white solid (0.12 g, 71%). TLC Rf 0.39 (10% methanol in ethyl acetate).

[0348] Intermediate 44

[0349] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5,6,7,8-tetrahydro-2H-isoquinolin-1-one

[0350] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-dihydroxymethyl-tetrahydro-furan-2-yl]-5,6,7,8-tetrahydro-2H-isoquinolin-1-one tribenzoate (1.0 g) with purification by flash chromatography (30% ethyl acetate in hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (400 mg, 85%). TLC Rf 0.52 (10% methanol in ethyl acetate)

[0351] Intermediate 45

[0352] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione

[0353] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione tribenzoate (0.8 g), with purification by flash chromatography (5% methanol in ethyl acetate followed by 10% methanol in ethyl acetate) to give the title compound as a yellow solid (0.29 g, 77%). TLC Rf 0.69 (10% methanol in ethyl acetate).

[0354] Intermediate 46

[0355] 7-Chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione

[0356] From 7-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione tribenzoate (0.18 g), with purification by flash chromatography (5% methanol in ethyl acetate) to give the title compound as a yellow solid (0.05 g, 55%). TLC Rf 0.17 (5% methanol in ethyl acetate).

[0357] Intermediate 47

[0358] (E)-3-(4-Methylsulfanylphenyl)acrylic Acid

[0359] A solution of 4-(methylsulfanyl)benzaldehyde (9.53 g), malonic acid (15 g) and piperidine (0.6 ml) in pyridine (25 ml) was heated at 110° C. under nitrogen for 5 h, and allowed to cool. The mixture was concentrated in vacuo, adding toluene to assist removal of pyridine, and the resulting solid was filtered, washed with toluene then diethyl ether-hexane (1:4) to give the title compound as a pale yellow solid (10.9 g, 90%); TLC Rf 0.8 (EtOAc).

[0360] Intermediate 48

[0361] 7-Methylsulfanyl-2H-isoquinolin-1-one

[0362] Triethylamine (9.1 ml) was added to a stirred solution/suspension of 4-(E)-3-(4-methylsulfanylphenyl)acrylic acid (6.5 g) in acetone (70 ml) in an ice-water bath. Ethyl chloroformate (4.81 ml) was added to the resulting clear solution, while maintaining the reaction mixture below 25° C. The mixture was stirred for 1 h in the ice-water-bath, and a solution of sodium azide (3.64 g) in water (20 ml) was added dropwise. The mixture was stirred for a further 1.5 h, poured into water (150 ml), and extracted with toluene (150 ml). The extract was dried (MgSO4), and the acetone removed under reduced pressure. The resulting toluene solution (˜120 ml) was added dropwise to a solution of tributylamine (9 ml) in diphenylmethane (45 ml) at 180° C. The temperature was kept between 185 and 200° C. during the addition, and toluene was distilled out of the reaction mixture. The mixture was heated for a further 1 h at 220-230° C., and allowed to cool. The resulting crystalline material was filtered and washed with hexane to give the title compound as a pale yellow solid (2.62 g, 41%); TLC Rf 0.15 (50% EtOAc in hexane).

[0363] The following intermediates were prepared following the procedure for intermediate 48:

[0364] Intermediate 49

[0365] 6-Fluoro-2H-isoquinolin-1-one

[0366] From 4-fluorocinnamic acid (9.73 g), to give the title compound as a pale yellow solid (0.353 g, 3.7%); TLC Rf 0.35 (6% MeOH in DCM).

[0367] Intermediate 50

[0368] 7-Fluoro-2H-isoquinolin-1-one

[0369] From 3-fluorocinnamic acid (10.25 g) to give the title compound as a pale yellow solid (4.42 g, 44%). TLC Rf 0.62 (ethyl acetate)

[0370] Intermediate 51

[0371] 6,7-Difluoro-2H-isoquinolin-1-one

[0372] From (E)-3-(3,4-difluorophenyl)acrylic acid (10.3 g), to give the title compound as a pale yellow solid (2.13 g, 21%); TLC Rf 0.7 (EtOAc).

[0373] Intermediate 52

[0374] (3,4-Dichlorobenzylidene)(2,2-dimethoxyethyl)amine

[0375] 3,4-Dichlorobenzaldehyde (23.9 g) and aminoacetaldehyde dimethyl acetal (14.4 g) were heated in toluene (250 ml) under nitrogen with a Dean-Stark trap at reflux for 30 minutes. The mixture was concentrated to give the title compound as an orange-brown oil (˜36 g, quantitative); δ 1H (300 MHz, CDCl3) 8.22 (1H, s), 7.88 (1H, dd), 7.56 (1H, dd), 7.48 (1H, d), 4.68 (1H, t), 3.78 (2H, d) and 3.44 (6H, s).

[0376] The following intermediates were prepared following the procedure for intermediate 52:

[0377] Intermediate 53

[0378] (2,3-Dichlorobenzylidene)(2,2-dimethoxyethyl)amine

[0379] From 2,3-dichlorobenzaldehyde (30 g) and aminoacetaldehyde dimethyl acetal (18 g), to give the title compound as a pale orange-brown oil (˜45 g, quantitative); δ 1H (300 MHz, CDCl3) 8.74 (1H, s), 7.96 (1H, dd), 7.54 (1H, dd), 7.24 (1H, t), 4.72 (1H, t), 3.84 (2H, d) and 3.44 (6H, s).

[0380] Intermediate 54

[0381] (2-Fluorobenzylidene)(2,2-dimethoxyethyl)amine

[0382] From 2-fluorobenzaldehyde (20.8 g) and aminoacetaldehyde dimethyl acetal (17.6 g), to give the title compound as a pale orange-brown oil (˜35 g, quantitative); δ 1H (300 MHz, CDCl3) 8.60 (1H, s), 8.00 (1H, t), 7.40 (1H, q), 7.18 (1H, t), 7.08 (1H, t), 4.70 (1H, t), 3.82 (2H, d) and 3.42 (6H, s).

[0383] Intermediate 55

[0384] 6,7-Dichloroisoquinoline

[0385] (3,4-Dichlorobenzylidene)(2,2-dimethoxyethyl)amine (38.4 g) and cold concentrated sulfuric acid (60 ml) were added separately, dropwise, over a period of 20 minutes to concentrated sulfuric acid (180 ml) at 140° C. The mixture was stirred at 130-140° C. for 30 minutes, allowed to cool, and carefully poured onto ice (1 kg). Solid material was removed by filtration, and the mixture extracted with dichloromethane (2×200 ml). The mixture was cautiously basified with 10M sodium hydroxide, and, after allowing to cool, extracted with diethyl ether (2×300 ml). These extracts were combined, dried and concentrated to give a mixture of the title compound and isomeric 5,6-dichloroisoquinoline as a beige solid (5.58 g, 21%). Chromatography (20% to 50% EtOAc in hexane) followed by recrystallisation from heptane-ethyl acetate (9:1) gave the title compound as a beige solid (1.3 g, 5%); TLC Rf 0.55 (EtOAc).

[0386] The following intermediates were prepared following the procedure for intermediate 55:

[0387] Intermediate 56

[0388] 7,8-Dichloroisoquinoline

[0389] From (2,3-Dichlorobenzylidene)(2,2-dimethoxyethyl)amine (45 g), to give the title compound as a brown solid (12.5 g, 49%); TLC Rf 0.6 (EtOAc).

[0390] Intermediate 57

[0391] 8-Fluoroisoguinoline

[0392] From (2-Fluorobenzylidene)(2,2-dimethoxyethyl)amine (35 g), to give the title compound as a pale yellow solid (0.79, 3%); TLC Rf 0.45 (50% EtOAc in hexane).

[0393] Intermediate 58

[0394] 6,7-Dichloroisoquinoline 2-oxide

[0395] 3-Chloroperoxybenzoic acid (57-86%, 0.716 g) was added to a solution of 6,7-dichloroisoquinoline (0.343 g) in dichloromethane (10 ml) at rt, and the mixture stirred for 2 h. The mixture was diluted with dichloromethane (50 ml) and methanol (5 ml), and washed with sodium hydroxide solution (2M, 60 ml). The aqueous phase was extracted with dichloromethane (2×20 ml), and the combined organic phases dried (MgSO4) and concentrated. The residue was chromatographed (graded eluent, 5-10% MeOH in EtOAc) to give the title compound as a white solid (0.323 g, 87%); TLC Rf 0.26 (5% MeOH in EtOAc).

[0396] The following intermediates were prepared following the procedure for intermediate 58:

[0397] Intermediate 59

[0398] 7,8-Dichloroisoquinoline 2-oxide

[0399] From 7,8-dichloroisoquinoline (2.0 g) and 3-chloroperoxybenzoic acid (57-86%, 4.18 g), without chromatography, to give the title compound as a white solid (1.81 g, 84%); TLC Rf 0.19 (5% MeOH in EtOAc).

[0400] Intermediate 60

[0401] 8-Fluoroisoquinoline 2-oxide

[0402] From 8-fluoroisoquinoline (0.69 g) and 3-chloroperoxybenzoic acid (57-86%, 1.62 g), without chromatography, to give the title compound as a pale beige solid (0.73 g, 95%); TLC Rf 0.05 (EtOAc).

[0403] Intermediate 61

[0404] 6,7-Dichloro-2H-isoquinolin-1-one

[0405] 6,7-Dichloroisoquinoline 2-oxide (0.3239) was dissolved in acetic anhydride (5 ml), and the mixture heated under reflux for 3 h. The mixture was concentrated under reduced pressure, and the residue heated in aqueous sodium hydroxide (2M, 10 ml) for 1 h. The mixture was acidified to pH 6 with citric acid (5% in water), and extracted with dichloromethane (2×20 ml). The combined organic phases were dried (MgSO4) and concentrated to give the title compound as a pale brown solid (0.299 g, 92%); TLC Rf 0.5 (EtOAc).

[0406] The following intermediates were prepared following the procedure for intermediate 61:

[0407] Intermediate 62

[0408] 7,8-dichloro-2H-isoquinolin-1-one

[0409] From 7,8-dichloroisoquinoline 2-oxide (0.914 g), to give the title compound as a pale brown solid (0.713 g, 78%); TLC Rf 0.63 (5% MeOH in EtOAc).

[0410] Intermediate 63

[0411] 8-fluoro-2H-isoquinolin-1-one

[0412] From 8-fluoroisoquinoline 2-oxide (0.72 g), via chromatography (graded eluent, from 40% EtOAc in hexane to 5% MeOH in EtOAc) of the residue obtained, to give the title compound as a pale beige solid (0.287 g, 40%); TLC Rf 0.7 (EtOAc).

[0413] The following intermediates were prepared following the procedure for intermediate 1:

[0414] Intermediate 64

[0415] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-bromo-2H-isoquinolin-1-one Tribenzoate

[0416] From 6-bromo-2H-isoquinolin-1-one (1.5 g) to give the title compound as a white solid (3.14 g, 69%); TLC Rf 0.38 (2:1 ethyl acetate-hexane).

[0417] Intermediate 65

[0418] 5-(2R,3R,4S,5R)-(3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-5H-furo[3,2-C]pyridin-4-one Tribenzoate

[0419] From 5H-furo[3,2-c]pyridin-4-one (0.50 g) to give the title compound as a brown solid (1.426 g, 80%); TLC Rf 0.59 (40% EtOAc in hexane).

[0420] Intermediate 66

[0421] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3,5-dihydro-2H-furo[3,2-c]pyridin-4-one Tribenzoate

[0422] From 3,5-dihydro-2H-furo[3,2-c]pyridin-4-one (0.26 g) with purification by flash chromatography (1:1 ethyl acetate-hexane) to give the title compound as a white solid (0.73 g, 67%). TLC Rf 0.30 (1:1 ethyl acetate-hexane)

[0423] Intermediate 67

[0424] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methylsulfanyl-2H-isoquinolin-1-one Tribenzoate

[0425] From 7-methylsulfanyl-2H-isoquinolin-1-one (0.828 g) to give the title compound as a yellow solid (1.30 g, 47%); TLC Rf 0.35 (30% EtOAc in hexane).

[0426] Intermediate 68

[0427] 2-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-6-fluoro-2H-isoquinolin-1-one Tribenzoate

[0428] From 7-fluoro-2H-isoquinolin-1-one (0.212 g) to give the title compound as a white solid (0.291 g, 49%); TLC Rf 0.25 (20% EtOAc in hexane).

[0429] Intermediate 69

[0430] 2-((1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl)-7-fluoro-2H-isoquinolin-1-one Tribenzoate

[0431] From 7-fluoro-2H-isoquinolin-1-one (0.5 g) with purification by flash chromatography (7:3 ethyl acetate-hexane) to give the title compound as a white solid (0.67 g, 45%). TLC Rf 0.37 (3:7 ethyl acetate-hexane)

[0432] Intermediate 70

[0433] 2-((1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl)-6,7-difluoro-2H-isoquinolin-1-one Tribenzoate

[0434] From 6,7-difluoro-2H-isoquinolin-1-one (2.07 g) with purification by flash chromatography (7:3 ethyl acetate-hexane) to give the title compound as a white solid (2.29 g, 38%). TLC Rf 0.48 (3:7 ethyl acetate-hexane)

[0435] Intermediate 71

[0436] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6,7-dichloro-2H-isoquinolin-1-one Tribenzoate

[0437] From 6,7-dichloro-2H-isoquinolin-1-one (0.299 g) to give the title compound as a pale brown solid (0.447 g, 49%); TLC Rf 0.36 (30% EtOAc in hexane).

[0438] Intermediate 72

[0439] 2-[(2 R,3R,4S,5 R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7,8-dichloro-2H-isoquinolin-1-one Tribenzoate

[0440] From 7,8-dichloro-2H-isoquinolin-1-one (0.350 g) to give the title compound as a pale brown solid (0.292 g, 27%); TLC Rf 0.4 (dichloromethane).

[0441] Intermediate 73

[0442] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-8-fluoro-2H-isoquinolin-1-one Tribenzoate

[0443] From 8-fluoro-2H-isoquinolin-1-one (0.275 g) to give the title compound as a white solid (0.75 g, 74%); TLC Rf 0.2 (30% EtOAc in hexane).

[0444] Intermediate 74

[0445] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methanesulfonyl-2H-isoquinolin-1-one Tribenzoate

[0446] 3-Chloroperoxybenzoic acid (57-86%, 0.526 g) was added to a solution of 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methylsulfanyl-2H-isoquinolin-1-one tribenzoate (0.442 g) in dichloromethane (5 ml) cooled in an ice-water bath, and the mixture stirred for 2 h at that temperature. The mixture was concentrated, and the residue chromatographed (20% EtOAc in hexane) to give the title compound as a white solid (0.266 g, 57%); TLC Rf 0.25 (50% EtOAc in hexane).

[0447] The following intermediate was prepared following the procedure for intermediate 22:

[0448] Intermediate 75

[0449] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-cyano-2H-isoquinolin-1-one Tribenzoate

[0450] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-bromo-2H-isoquinolin-1-one tribenzoate (1.13 g) and copper (I) cyanide (1.5 g) in DMF (10 ml), to give the title compound as a white solid (0.368 g, 36%); TLC Rf 0.59 (50% heptane in EtOAc)

[0451] The following intermediate was prepared following the procedure for intermediate 26:

[0452] Intermediate 76

[0453] 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-2H-isoquinoline-1-thione Tribenzoate

[0454] From 2-((1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl)-7-fluoro-2H-isoquinolin-1-one tribenzoate (1.4 g) and Lawesson's reagent (2.24 g) in chlorobenzene (25 ml), with purification by flash chromatography (graded eluent, from 0% to 20% EtOAc in hexane), to give the title compound as a yellow solid (0.984 g, 69%); TLC Rf 0.71 (DCM).

[0455] The following intermediates were prepared following the procedure for intermediate 2:

[0456] Intermediate 77

[0457] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-cyano-2H-isoquinolin-1-one

[0458] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-cyano-2H-isoquinolin-1-one tribenzoate (0.33 g) and sodium methoxide (0.12 g), with purification by flash chromatography (graded eluent, from 5% to 10% MeOH in DCM), to give the title compound as a white solid (0.103 g, 63%);

[0459] TLC Rf 0.26 (5% MeOH/DCM).

[0460] Intermediate 78

[0461] 5-(2R,3R,4S,5R)-(3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-5H-furo[3,2-c]pyridin-4-one

[0462] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-5H-furo[3,2-c]pyridin-4-one tribenzoate (0.40 g) and sodium methoxide (0.17 g), with purification by flash chromatography (graded eluent, from 20% EtOAc in hexane to 10% MeOH in EtOAc), to give the title compound as a white solid (0.150 g, 79%); TLC Rf 0.39 (10% MeOH/EtOAc).

[0463] Intermediate 79

[0464] 5-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3,5-dihydro-2H-furo[3,2-c]pyridin-4-one

[0465] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3,5-dihydro-2H-furo[3,2-c]pyridin-4-one tribenzoate (0.66 g) with purification by flash chromatography (5% methanol-dichloromethane followed by 10% methanol-dichloromethane) to give the title compound as a white foam (0.27 g, 87%). TLC Rf 0.27 (10% methanol-dichloromethane)

[0466] Intermediate 80

[0467] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methylsulfanyl-2H-isoquinolin-1-one

[0468] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methylsulfanyl-2H-isoquinolin-1-one tribenzoate (0.49 g) and sodium methoxide (0.17 g), with purification by flash chromatography (graded eluent, from 20% EtOAc in hexane to 10% MeOH in EtOAc), to give the title compound as a white solid (0.186 g, 75%); TLC Rf 0.3 (EtOAc).

[0469] Intermediate 81

[0470] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methanesulfonyl-2H-isoquinolin-1-one

[0471] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methanesulfonyl-2H-isoquinolin-1-one tribenzoate (0.25 g) and sodium methoxide (0.08 g), with purification by flash chromatography (graded eluent, from 20% EtOAc in hexane to 10% MeOH in EtOAc), to give the title compound as a white solid (0.119 g, 89%); TLC Rf 0.5 (10% MeOH in EtOAc).

[0472] Intermediate 82

[0473] 2-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-6-fluoro-2H-isoquinolin-1-one

[0474] From 2-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-6-fluoro-2H-isoquinolin-1-one tribenzoate (0.391 g) and sodium methoxide (0.139), with purification by flash chromatography (graded eluent, from 40% EtOAc in hexane to 6% MeOH in DCM), to give the title compound as a white solid (0.132 g, 70%)

[0475] Intermediate 83

[0476] 2-(1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl)-7-fluoro-2H-isoquinolin-1-one

[0477] From 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-2H isoquinolin-1-one tribenzoate (0.40 g) with purification by flash chromatography (30% ethyl acetate in hexane followed by 10% methanol in ethyl acetate) to give the title compound as a white solid (0.14 g, 74%). TLC Rf 0.68 (10% methanol-ethyl acetate)

[0478] Intermediate 84

[0479] 2-[(1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-2H-isoquinoline-1-thione

[0480] From 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-2H-isoquinoline-1-thione tribenzoate (0.639) with purification by flash chromatography (30% ethyl acetate in hexane followed by 10% methanol in ethyl acetate) to give the title compound as a yellow solid (0.30 g, 96%). TLC Rf 0.50 (ethyl acetate)

[0481] Intermediate 85

[0482] 2-((1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl)-6,7-difluoro-2H-isoquinolin-1-one

[0483] From 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-6,7-difluoro-2H-isoquinolin-1-one tribenzoate (2.29 g) with purification by flash chromatography (30% ethyl acetate-hexane followed by 10% methanol-ethyl acetate) to give the title compound as a white solid (0.95 g, 83%). TLC Rf 0.67 (10% methanol-ethyl acetate)

[0484] Intermediate 86

[0485] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6,7-dichloro-2H-isoquinolin-1-one

[0486] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6,7-dichloro-2H-isoquinolin-1-one tribenzoate (0.447 g) and sodium methoxide (0.16 g), with purification by flash chromatography (graded eluent, from 30% EtOAc in hexane to 5% MeOH in EtOAc), to give the title compound as a white solid (0.206 g, 88%); TLC Rf 0.5 (5% MeOH in EtOAc).

[0487] Intermediate 87

[0488] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7,8-dichloro-2H-isoquinolin-1-one

[0489] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7,8-dichloro-2H-isoquinolin-1-one tribenzoate (0.365 g) and sodium methoxide (0.12 g), with purification by flash chromatography (graded eluent, from 30% EtOAc in hexane to 20% MeOH in EtOAc), to give the title compound as a white solid (0.126 g, 82%); TLC Rf 0.6 (EtOAc).

[0490] Intermediate 88

[0491] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-8-fluoro-2H-isoquinolin-1-one

[0492] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-8-fluoro-2H-isoquinolin-1-one tribenzoate (0.74 g) and sodium methoxide (0.26 g), with purification by flash chromatography (graded eluent, from 20% EtOAc in hexane to 10% MeOH in EtOAc), to give the title compound as a white solid (0.254 g, 71%); TLC Rf 0.25 (EtOAc).

[0493] Intermediate 89

[0494] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-4-fluoro-2H-isoquinolin-1-one

[0495] Selectfluor® (720 mg) was added to a suspension of 2-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-2H-isoquinolin-1-one (510 mg) in acetonitrile (10 ml) under nitrogen at rt, and the mixture stirred at rt for 3 h. The mixture was concentrated, and the residue adsorbed onto silica and chromatographed (graded eluent, 30% EtOAc in hexane to neat EtOAc, with 10% THF to aid solubility) to give a white solid (90 mg) which was dissolved) in DMSO (3 ml). Sodium methoxide (100 mg) was added and the mixture stirred for 4 days at rt under nitrogen. The mixture was chromatographed (EtOAc:THF:MeOH 90:9:1) to give the title Product as a white solid (80 mg, 80%); TLC Rf 0.55 (EtOAc).

[0496] Intermediate 90

[0497] 2-[(1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-6-methylsulfanyl-2H-isoquinolin-1-one

[0498] A mixture of 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-6,7-difluoro-2H-isoquinolin-1-one (200 mg) and sodium thiomethoxide (67 mg) in ethanol (5 ml) was heated to reflux for 1 h. After cooling to rt, the mixture was diluted with toluene (10 ml), evaporated under reduced pressure, and the residue purified by flash chromatography (SiO2, ethyl acetate followed by 10% methanol-ethyl acetate) to give the title compound as a white solid (145 mg, 66%). TLC Rf 0.67 (10% methanol-ethyl acetate)

[0499] Intermediate 91

[0500] 2-((1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl)-6-dimethylamino-7-fluoro-2H-isoquinolin-1-one

[0501] A mixture of 2[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-6,7-difluoro-2H-isoquinolin-1-one (200 mg) and dimethylamine (20 ml of 40% w/v in water) was heated to 90° C. for 2 h. The mixture was cooled to rt, evaporated under reduced pressure, and the residue purified by flash chromatography (SiO2, 20% methanol-ethyl acetate) to give the title compound as a white gum (201 mg, 93%). TLC Rf 0.54 (10% methanol-ethyl acetate)

[0502] Intermediate 92

[0503] 7-Chloro-2-((3aR,4R,6R,6aR)-6-hydroxymethyl-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-2H-isoquinolin-1-one

[0504] Pyridine hydrochloride (0.41g) and trimethylorthoformate (1.75 ml) were added to a solution of 7-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one (1.0 g) in DMF (15 ml) and the mixture stirred overnight at rt. The mixture was partitioned between water (100 ml) and ethyl acetate (100 ml). The organics were separated, washed with water (100 ml), dried (MgSO4), evaporated under reduced pressure and the residue purified by flash chromatography (SiO2, 5% methanol-dichloromethane) to give the title compound as a clear gum (0.54 g, 48%). TLC Rf 0.45 (5% methanol-dichloromethane)

[0505] Intermediate 93

[0506] Toluene-4-sulfonic Acid (3aR,4R,6R,6aR)-6-(7-chloro-1-oxo-1H-isoquinolin-2-yl)-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl Ester

[0507] 7-Chloro-2-((3aR,4R,6R,6aR)-6-hydroxymethyl-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-2H-isoquinolin-1-one (0.76 g), tosyl chloride (0.49 g) and N,N-dimethylaminopyridine (0.34 g) were combined in dichloromethane (30 ml) and stirred overnight at rt. The reaction mixture was evaporated under reduced pressure and the residue purified by flash chromatography (SiO2, 2% methanol in dichloromethane) to give the title compound as a white foam (0.95 g, 87%). TLC Rf 0.74 (5% methanol-dichloromethane)

[0508] Intermediate 94

[0509] Toluene-4-sulfonic Acid (2R,3S,4R,5R)-5-(7-chloro-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl Ester

[0510] Toluene-4-sulfonic acid (3aR,4R,6R,6aR)-6-(7-chloro-1-oxo-1H-isoquinolin-2-yl)-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester (0.95 g) was dissolved in acetonitrile (5 ml). Hydrochloric acid (3.0 ml of a 1.0M solution in water) was added, and the mixture stirred at rt for 2.5 h. The reaction mixture was evaporated under reduced pressure and the residue purified by flash chromatography (5% methanol-dichloromethane) to give the title compound as a white foam (0.65 g, 76%). TLC Rf 0.19 (5% methanol-dichloromethane)

[0511] Intermediate 95

[0512] 7-Chloro-2-(2R,3R,4S,5R-(3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-2H-isoquinolin-1-one Diphosphate Bis-ammonium Salt

[0513] Toluene-4-sulfonic acid 5-(2R,3R,4S,5R)-(7-chloro-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydrofuran-2-ylmethyl ester 4 (0.85 g) was combined with pyrophosphoric acid tetrabutylammonium salt (4 g) in acetonitrile (1.5 ml) and stirred at RT for 5 days. Purification by preparative HPLC yielded the title compound as a white solid (0.5 g, 63%); mass spectrum m/z 470 (M−1).

[0514] Intermediate 96

[0515] 2-[(1R,2S,3R,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-6-methoxy-2H-isoquinolin-1-one

[0516] A solution of sodium methoxide in methanol was prepared by stirring sodium metal (180 mg) in methanol (10 ml) at room temperature for 45 minutes. The solution was added to 2-((1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl)-6,7-difluoro-2H-isoquinolin-1-one (190 mg) and the mixture heated to reflux overnight. The reaction mixture was evaporated under reduced pressure and the residue purified by flash chromatography (10% methanol-ethyl acetate followed by 40% methanol-ethyl acetate) to give the title compound as a white solid (99 mg, 52%); TLC Rf 0.29 (ethyl acetate)

EXAMPLE 1

[0517] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0518] (Alternatively: 2-β-D-Ribofuranosyl-1(2H)-isoquinolinone-5′-triphosphate tris-ammonium Salt)

[0519] Intermediate 2 (217 mg, 0.78 mmol) and proton sponge (251 mg, 1.17 mmol) were dissolved in trimethylphosphate (3.5 mL) under nitrogen. The solution was cooled to 0° and freshly distilled POCl3 (80 μL, 0.86 mmol), added dropwise. The bright violet suspension was stirred at 0° for 4 h whereupon a solution of tributyl ammonium pyrophosphate and tributylamine (8 mL, 0.5M in dry DMF with 10% v/v tributylamine) was added in one portion. After exactly 2 min the reaction was quenched with aqueous 100 mM ammonium hydrogen carbonate solution (25 mL). The mixture was allowed to stir at RT for 15 min before being diluted with water (20 mL) and washed with Et2O (2×30 mL). The aqueous layer was concentrated in vacuo and the crude residue dissolved in water (10 mL) and freeze dried. The crude product was purified by ion exchange chromatography (Akta FPLC, 5 mL HiTrap Q-Sepharose HP anion exchange column (Pharmacia), 100 mM to 400 mM aqueous ammonium hydrogen carbonate buffer eluting at 5 mL per minute), to give after azeotroping of the isolated solid with water (10 times) and freeze drying, the title compound as a white powder (76 mg, 19%). δH (400 MHz, D2O) 8.21 (1H, d, J 8.1 Hz), 7.74 (1H, t, J 7.2 Hz), 7.65 (1H, t, J 6.6 Hz), 7.54 (1H, t, J 7.2 Hz), 6.88 (1H, d, J 7.6 Hz), 6.39 (1H, d, J 4.7 Hz), 4.40 (2H, m), 4.25 (3H, m); δ 31P (161 MHz, D2O) −4.81 (1P, m), −9.74 (1P, d, JP-P=13 Hz), −20.1 (1P, m).

EXAMPLE 2

[0520] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(4-oxo-4H-pyrido[2,3-d]-pyrimidin-3-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0521] (Alternatively: 3-β-D-Ribofuranosyl-pyrido[2,3-d]pyrimidin-4(3H)-one-5′-triphosphate tris-ammonium Salt)

[0522] Intermediate 4 (220 mg, 0.79 mmol) and proton sponge (254 mg, 1.19 mmol) were dissolved in trimethylphosphate (3.5 mL) under nitrogen. The solution was cooled to 0° and freshly distilled POCl3 (81 μL, 0.87 mmol), added dropwise. The bright inky blue suspension was stirred at 0° for 4 h whereupon a solution of tributyl ammonium pyrophosphate and tributylamine (8 mL, 0.5M in dry DMF with 10% v/v tributylamine) was added in one portion. After exactly 2 min the reaction was quenched with aqueous 100 mM ammonium hydrogen carbonate solution (25 mL). The mixture was allowed to stir at RT for 15 min before being diluted with water (20 mL) and washed with Et2O (2×30 mL). The aqueous layer was concentrated in vacuo and the bright yellow residue dissolved in water (15 mL) and freeze dried. The crude product was purified by ion exchange chromatography (Akta FPLC, 5 mL HiTrap Q-Sepharose HP anion exchange column, 100 mM to 400 mM aqueous ammonium hydrogen carbonate buffer eluting at 5 mL per minute), to give after azeotroping of the isolated solid with water (10 times) and freeze drying, the title compound as a tan solid (27 mg, 7%); δH (400 MHz, D2O) 8.96 (1H, s), 8.77 (1H, dd, J 4.9, 2.0 Hz), 8.43 (1H, dd, J 8.1, 4.0 Hz), 7.55 (1H, dd, J 8.0, 4.7 Hz), 6.52 (1H, d, J 2.2 Hz), 4.45-4.40 (1H, m), 4.30-4.10 (3H, m), 4.10-3.80 (1H, m); δ 31P (161 MHz, D2O) −4.87 (1P, m), −9.75 (1P, d, JP-P=89 Hz), −20.14 (1P, m).

EXAMPLE 3

[0523] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(4-methyl-1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0524] Trimethylphosphate (2.1 ml) was added to a mixture of 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-4-methyl-2H-isoquinolin-1-one (150 mg) and proton sponge (165.5 mg) at room temperature under nitrogen. The mixture was stirred at room temperature until all the solid had dissolved and was then cooled in an ice bath. Phosphorous oxychloride (0.053 ml) was added dropwise and the mixture stirred for 2 h before simultaneous addition of tributylamine (0.52 ml) and a 0.5M solution of tributylammonium pyrophosphate in DMF (5.2 ml). The mixture was stirred for a further 2 min then quenched by addition of aqueous ammonium bicarbonate (129 mg in 13 ml of water) and stirred for 15 min. The volatile solvents were evaporated in vacuo and the residue purified by reverse phase ion-pair chromatography on a Luna C18 column eluting with an ammonium acetate buffer. Fractions containing the desired triphosphate were extracted onto an ion exchange SPE cartidge which was eluted with 10% aqueous ammonia to give, after evaporation of the solvent in vacuo, the title compound as a white gum (15 mg). 1HNMR(400 mHz, D2O) 8.35 (H, d), 7.9-7.8 (2H, m), 7.65 (H, t), 7.55 (H, s), 6.5 (H, d), 5.55-5.45 (2H, m), 4.4-4.3 (3H, m), 3.1 (3H, s); 31PNMR(162 mHz, D2O) −7.0 (d, JP-P=19 Hz), −10.1 (d, JP-P=20 Hz), −21.1 (t, JP-P=19 Hz); Mass spectrum m/z 530 (M−1)

[0525] The following examples were prepared following the procedure for example 3:

EXAMPLE 4

[0526] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(5-methyl-1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0527] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-2H-isoquinolin-1-one (205 mg) to give the title compound as as a white solid (50 mg). 1HNMR(400 mHz, D2O) 8.15 (H, d), 7.75 (H, d), 7.65 (H, d), 7.5 (H, t), 7.1 (H, d), 6.45 (H, d), 4.55-4.45 (2H, m), 4.4-4.3 (3H, m), 2.55 (3H, s); 31 PNMR(162 mHz, D2O) −7.4 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz), −21.4 (t, JP-P=20 Hz); Mass spectrum m/z 530 (M−1)

EXAMPLE 5

[0528] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-methyl-1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0529] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6-methyl-2H-isoquinolin-1-one (119 mg) to give the title compound as a white gum (10 mg).

[0530]

1
HNMR(400 mHz, D2O) 8.1 (H, d), 7.6 (H, d), 7.4 (H, s), 7.3 (H, d), 6.8 (H, d), 6.35 (H, d), 4.35-4.3 (H, m), 4.25-4.2 (H, t), 4.2-4.05 (3H, m), 2.4 (3H, s); 31 PNMR(162 mHz, D2O) −8.8 (d, JP-P=20 Hz), −10.2 (d, JP-P=20 Hz), −22.0 (t, JP-P=20 Hz); Mass spectrum m/z 530 (M−1)

EXAMPLE 6

[0531] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-methyl-1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0532] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-methyl-2H-isoquinolin-1-one (246 mg) to give the title compound as a white gum (30 mg).

[0533]

1
HNMR(400 mHz, D2O) 8.15 (H, s), 7.7-7.6 (3H, m), 6.95 (H, d), 6.45 (H, d), 4.5 (H, m), 4.45 (H, m), 4.35-4.3 (3H, m), 2.5 (3H, S); 31PNMR(162 mHz, D2O) −5.1 (d, JP-P=20 Hz), −9.9 (d, JP-P=19 Hz), −20.8 (t, JP-P=20 Hz); Mass spectrum m/z 530 (M−1)

EXAMPLE 7

[0534] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(8-methyl-1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0535] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-8-methyl-2H-isoquinolin-1-one (138 mg) to give the title compound as a white solid (69 mg). 1HNMR(400 mHz, D2O) 7.7-7.6 (2H, m), 7.55 (H, d), 7.4 (H, d), 6.85 (H, d), 6.4 (H, d), 4.45-4.4 (2H, m), 4.3-4.25 (3H, m), (CH3 obscured); 31PNMR(162 mHz, D2O) −7.3 (d, JP-P=19 Hz), −10.2 (d, JP-P=19 Hz), −21.7 (t, JP-P=19 Hz); Mass spectrum m/z 530 (M−1)

EXAMPLE 8

[0536] (2R,3S,4R,5R)-5-(4-Chloro-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0537] From 4-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one (200 mg) to give the title compound as a white solid (20 mg). 1HNMR(400 mHz, D2O) 8.4 (H, d), 8.1 (H, d), 8.0-7.9 (2H, m), 7.7 (H, t), 6.45 (H, d), 4.5-4.4 (2H, m), 4.35-4.3 (3H, m); 31PNMR(162 mHz, D2O) −8.8 (d, JP-P=18 Hz), −10.2 (d, JP-P=19 Hz), −21.6 (t, JP-P=19 Hz); Mass spectrum m/z 550 (M−1)

EXAMPLE 9

[0538] (2R,3S,4R,5R)-5-(6-Chloro-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0539] From 6-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one (161 mg) to give the title compound as a white solid (12 mg). 1HNMR(400 mHz, D2O) 8.25 (H, d), 7.8-7.7 (2H, m), 7.55 (H, d), 6.9 (H, d), 6.4 (H, d), 4.45-4.4 (2H, m), 4.35-4.3 (3H, m); 31PNMR(162 mHz, D2O) −9.2 (d, JP-P=20 Hz), −10.1 (d, JP-P=19 Hz), −21.7 (t, JP-P=19 Hz); Mass spectrum m/z 550 (M−1)

EXAMPLE 10

[0540] (2R,3S,4R,5R)-5-(7-Chloro-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0541] From 7-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinolin-1-one (200 mg) to give the title compound as a white solid (94 mg).

[0542]

1
HNMR(400 mHz, D2O) 8.25 (H, s), 7.8-7.7 (3H, m), 6.95 (H, d), 6.45 (H, d), 4.45-4.4 (2H, m), 4.35-4.3 (H, m); 31PNMR(162 mHz, D2O) −8.7 (d, JP-P=19 Hz), −10.0 (d, JP-P=19 Hz), −21.6 (br s); Mass spectrum m/z 550 (M−1)

EXAMPLE 11

[0543] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-methoxy-1-oxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0544] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-fu ran-2-yl]-7-methoxy-2H-isoquinolin-1-one (200 mg) to give the title compound as a colourless gum (45 mg). 1HNMR(400 mHz, D2O) 7.8-7.6 (3H, m), 7.45 (H, d), 6.95 (H, d), 6.45 (H, d), 4.5-4.45 (2H, m), 4.35-4.3 (3H, m), 3.95 (3H, s); 31PNMR(162 mHz, D2O) −8.8 (d, JP-P=19 Hz), −10.0 (d, JP-P=20 Hz), −21.7 (JP-P=19 Hz); Mass spectrum m/z 546 (M−1)

EXAMPLE 12

[0545] (2R,3S,4R,5R)-5-(7-Cyano-1-oxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0546] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-cyano-2H-isoquinolin-1-one (126 mg) to give the title compound as a white solid (62 mg).

[0547]

1
HNMR(400 mHz, D2O) 8.6 (H, s), 8.0 (H, d), 7.9 (H, d), 7.8 (H, d), 6.95 (H, d), 6.45 (H, d), 7.45-7.4 (2H, m), 7.35-7.3 (3H, m); 31PNMR(162 mHz, D2O) −8.0 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz), −21.5 (t, JP-P=20 Hz); Mass spectrum m/z 541 (M−1)

EXAMPLE 13

[0548] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(1-oxo-7-pyridin-3-yl-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0549] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-7-pyridin-3-yl-2H-isoquinolin-1-one (104 mg) to give the title compound as a white solid (17 mg). 1HNMR(400 mHz, D2O) 8.9 (H, s), 8.55-8.5 (2H, m), 8.2 (H, d), 8.1 (H, d), 7.8 (H, d), 7.75 (H, d), 7.55 (H, t), 7.0 (H, d), 6.45 (H, d), 4.5-4.45 (H, m), 4.35-4.3 (3H, m); 31PNMR(162 mHz, D2O) −6.7 (d, JP-P=18 Hz), −10.0 (d, JP-P=19 Hz), −21.1 (t, JP-P=19 Hz); Mass spectrum m/z 593 (M−1)

EXAMPLE 14

[0550] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(4-oxo-4H-thieno[3,2]pyridin-5-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0551] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5H-thieno[3,2-c]pyridin-4-one (105 mg) to give the title compound as a white solid (52 mg).

[0552]

1
HNMR(400 mHz, D2O) 7.9 (H, d), 7.6-7.55 (2H, m), 7.2 (H, d), 6.45 (H, d), 4.5 (H, t), 4.4 (H, t), 4.35-4.3 (3H, m); 31PNMR(162 mHz, D2O) −8.0 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz), −21.5 (t, JP-P=19 Hz); Mass spectrum m/z 522 (M−1)

EXAMPLE 15

[0553] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(3-methyl-4-oxo-4H-isoxazolo[4,5]pyridin-5-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0554] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3-methyl-5H-isoxazolo[4,5-c]pyridin-4-one (133 mg) to give the title compound as a clear gum (20 mg). 1HNMR(400 mHz, D2O) 8.15 (H, d), 6.95 (H, d), 4.45 (H, t), 4.4 (H, t), 4.4-4.3 (3H, m), 2.55 (3H, s); 31PNMR(162 mHz, D2O) −8.5 (d, JP-P=19 Hz), −10.0 (d, JP-P=20 Hz), −21.6 (t, JP-P=20 Hz); Mass spectrum m/z 521 (M−1)

EXAMPLE 16

[0555] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(1-methyl-4-oxo-1,4-dihydro-pyrrolo[3,2]pyridin-5-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0556] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-1-methyl-1,5-dihydro-pyrrolo[3,2-c]pyridin-4-one (62 mg) to give the title compound as a white gum (6 mg). 1HNMR(400 mHz, D2O) 7.75 (H, d), 7.2 (H, d), 7.0 (H, s), 6.8 (H, d), 6.55 (H, d), 4.55-4.5 (2H, m), 4.4-4.35 (3H, m), 3.85 (3H, s); 31PNMR(162 mHz, D2O) −8.7 (d, JP-P=20 Hz), −10.0 (d, JP-P=19 Hz), −21.5 (t, JP-P=20 Hz); Mass spectrum m/z 519 (M−1)

EXAMPLE 17

[0557] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(5-oxo-5H-[1,6]naphthyridin-6-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0558] From '6-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-6H-[1,6]naphthyridin-5-one (100 mg) to give the title compound as a white gum (4.8 mg).

[0559]

1
HNMR(400 mHz, D2O) 8.95 (H, d), 8.7 (H, d), 8.0 (H, d), 7.6 (H, dd), 7.0 (H, d), 6.4 (H, d), 4.5-4.4 (2H, m), 4.35-4.3 (3H, m); 31PNMR(162 mHz, D2O) −8.6 (br s), −10.0 (d, JP-P=20 Hz), −21.5 (t, JP-P=19 Hz); Mass spectrum m/z 517 (M−1)

EXAMPLE 18

[0560] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-oxo-7H-furo[2,3]pyridin-6-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0561] From 6-[(2R,3 R,4S,5 R)-(3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-6H-furo[2,3-c]pyridin-7-one (100 mg) to give the title compound as a white solid (10 mg).

[0562]

1
HNMR(400 mHz, D2O) 7.95 (H, s), 7.8 (H, d), 7.0 (H, d), 6.9 (H, s), 6.45 (H, d), 4.5 (H, t), 4.45 (H, t), 4.35-4.3 (3H, m); 31PNMR(162 mHz, D2O) −7.0 (d, JP-P=16 Hz), −10.0 (d, JP-P=20 Hz), −21.3 (t, JP-P=20 Hz); Mass spectrum m/z 506 (M−1)

EXAMPLE 19

[0563] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(1-oxo-5.6.7.8-tetrahydro-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0564] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-5,6,7,8-tetrahydro-2H-isoquinolin-1-one (206 mg) to give the title compound as a clear gum (63 mg). 1HNMR(400 mHz, D2O) 7.8 (H, d), 6.45 (H, d), 6.3 (H, d), 4.4-4.35 (2H, m), 4.35-4.3 (3H, m), 2.65-2.6 (2H, m), 2.45-2.4 (2H, m), 1.8-1.7 (4H, m); 31PNMR(162 mHz, D2O) −8.8 (d, JP-P=20 Hz), −10.2 (d, JP-P=20 Hz), −21.8 (t, JP-P=19 Hz); Mass spectrum m/z 520 (M−1)

EXAMPLE 20

[0565] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0566] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3,4-dihydro-2H-isoquinolin-1-one (156 mg) to give the title compound as a clear gum (43 mg). 1HNMR(400 mHz, D2O) 7.95 (H, d), 7.65 (H, t), 7.5-7.4 (2H, m), 6.25 (H, d), 4.45-4.4 (2H, m), 4.25-4.15 (3H, m), 3.8-3.7 (H, m), 3.7-3.6 (H, m), 3.1-3.0 (2H, m); 31PNMR(162 mHz, D2O) −6.4 (d, JP-P=20 Hz), −9.9 (d, JP-P=20 Hz), −21.1 (t, JP-P=20 Hz); Mass spectrum m/z 518 (M−1)

EXAMPLE 21

[0567] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(1-thioxo-1H-isoquinolin-2-yl)-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0568] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione (160 mg) to give the title compound as a yellow solid (45 mg).

[0569]

1
HNMR(400 mHz, D2O) 9.0 (H, d), 8.35 (H, d), 7.85-7.8 (2H, m), 7.75-7.7 (H, m), 7.45 (H, d), 7.2 (H, s), 4.55-4.5 (2H, m), 4.45-4.4 (3H, m); 31PNMR(162 mHz, D2O) −7.0 (d, JP-P=19 Hz), −10.0 (d, JP-P=20 Hz), −21.2 (t, JP-P=20 Hz); Mass spectrum m/z 532 (M−1)

EXAMPLE 22

[0570] (2R,3S,4R,5R)-5-(7-Chloro-1-thioxo-1H-isoquinolin-2-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl Triphosphate tris-ammonium Salt

[0571] From 7-chloro-2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-2H-isoquinoline-1-thione (100 mg) to give the title compound as a yellow solid (40 mg). 1HNMR(400 mHz, D2O) 8.95 (H, s), 8.35 (H, d), 7.8 (2H, s), 7.4 (H, d), 7.15 (H, s), 4.55-4.35 (5H, m); 31PNMR(162 mHz, D2O) −7.4 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz), −21.4 (t, JP-P=20 Hz); Mass spectrum m/z 566 (M−1)

EXAMPLE 23

[0572] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-cyano-2H-isoquinolin-1-one Triphosphate tris-ammonium Salt

[0573] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-1-oxo-1,2-dihydro-isoquinoline-7-carbonitrile (126 mg) to give the title compound as a white solid (11 mg); δ 1H (400 MHz, D2O) 8.4 (H, d), 8.2 (H, s), 7.8 (H, d), 7.7 (H, d), 7.0 (H, d), 6.4 (H, d), 4.5 (H, t), 4.4 (H, t), 4.35-4.30 (3H, m); δ 31P (400 MHz, D2O) −6.8 (m), −10.0 (d, JP-P=20 Hz), −21.3 (m); mass spectrum m/z 541 (M−1)

EXAMPLE 24

[0574] 5-(2R,3R,4S,5R)-(3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-5H-furo[3,2-c]pyridin-4-one Triphosphate tris-ammonium Salt

[0575] From 5-(2R,3R,4S,5R)-(3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-5H-furo[3,2-c]pyridin-4-one (105 mg) to give the title compound as a white gum (6 mg); δ 1H (400 MHz, D2O) 8.0 (H, d), 7.70 (H, d), 7.0 (H, d), 6.95 (H, d), 6.40 (H, d), 4.55 (H, t), 4.45 (H, t) 4.25-4.35 (H, m) and 3.30 (H, m); δ 31P (161 MHz, D2O) −7.0 (m), −10.0 (d, JP-P=20 Hz) and −21.5 (t, JP-P=19 Hz); mass spectrum m/z 506 (M−1).

EXAMPLE 25

[0576] 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3,5-dihydro-2H-fluro[3,2-c]pyridin-4-one Triphosphate tris-ammonium Salt

[0577] From 5-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl]-3,5 dihydro-2H-furo[3,2-c]pyridin-4-one (120 mg) to give the title compound as a white gum (8 mg); δ 1H (400 MHz, D2O) 8.0 (H, d), 6.45 (H, d), 6.25 (H, d), 4.5 (H, t), 4.35 (H, t), 4.3-4.2 (3H, m) and 3.1 (2H, t), remaining CH2 obscured; δ 31P (161 MHz, D2O) −8.8 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz), −21.8 (t, JP-P=19 Hz); mass spectrum m/z 504 (M−1).

EXAMPLE 26

[0578] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-methylsulfanyl-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0579] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methylsulfanyl-2H-isoquinolin-1-one (105 mg) to give the title compound as a white solid (10 mg); δ 1H (400 MHz, D2O) 8.08 (H, d), 7.72-7.64 (3H, m), 6.92 (H, d), 6.46 (H, d), 4.50-4.44 (2H, m), 4.40-4.30 (3H, m) and 2.62 (3H, S); δ 31P (161 MHz, D2O) −6.5 (m), −9.9 (d, JP-P=19 Hz) and −20.8 (m); mass spectrum m/z 562 (M−1).

EXAMPLE 27

[0580] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-methanesulfonyl-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0581] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-methanesulfonyl-2H-isoquinolin-1-one (111 mg) to give the title compound as a white solid (20 mg); δ 1H (400 MHz, D2O) 8.84 (H, s), 8.22 (H, d), 8.00-7.92 (2H, m), 7.06 (H, d), 6.46 (H, d), 4.52-4.44 (2H, m), 4.42-4.28 (3H, m) and 3.36 (3H, S); δ 31P (161 MHz, D2O) −8.3 (m), −10.0 (d, JP-P=19 Hz) and −21.3 (m); mass spectrum m/z 594 (M−1).

EXAMPLE 28

[0582] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(4-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0583] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-8-fluoro-2H-isoquinolin-1-one (100 mg) to give the title compound as a white solid (8 mg); δ 1H (400 MHz, D2O) 8.36 (H, d), 7.98-7.90 (2H, m), 7.84 (H, d), 7.74 (H, ddd), 6.46 (H, d), 4.52 (H, t), 4.46 (H, t) and 4.40-4.30 (3H, m); δ 31P (161 MHz, D2O) −5.5 (d, JP-P=21 Hz), −10.0 (d, JP-P=20 Hz) and −21.1 (t, JP-P=20 Hz); mass spectrum m/z 534 (M−1).

EXAMPLE 29

[0584] 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-fluoro-2H-isoquinolin-1-one Triphosphate tris-ammonium Salt

[0585] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)]-6-fluoro-2H-isoquinolin-1-one (132 mg) to give the title compound as a white solid (8 mg); 6 1H (400 MHz, D2O) 8.39 (H, dd), 7.80 (H, d), 7.48 (H, dd), 7.39 (H, dd), 6.96 (H, d), 6.49 (H, d), 4.78 (2H, m), 4.48 (H, m), 4.30 (H, m); δ 31P (161 MHz, D2O) −6.3 (m), −10.1 (d, JP-P=20 Hz), −21.2 (t, JP-P=20 Hz); mass spectrum m/z 530 (M−1).

EXAMPLE 30

[0586] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0587] From 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-2H-isoquinolin-1-one (144 mg) to give the title compound as a white solid (7 mg); δ 1H (400 MHz, D2O) 7.85 (H, d), 7.75 (H, d), 7.55 (H, d), 6.90 (H, d), 6.45 (H, d), 4.55-4.45 (2H, m), 4.40-4.30 (3H, m) and 2.60 (3H, s); δ 31P (161 MHz, D2O) −6.0 (m), −10.0 (d, JP-P=20 Hz) and −21.0 (t, JP-P=20 Hz); mass spectrum m/z 534 (M−1).

EXAMPLE 31

[0588] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-fluoro-1-thioxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0589] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7-fluoro-2H-isoquinolin-1-thione (190 mg) to give the title compound as a yellow solid (60 mg); δ 1H (400 MHz, D2O) 8.65 (H, d), 8.35 (H, d), 7.90 (H, m), 7.65 (H, m), 7.45 (H, d), 7.15 (H, s) and 4.55-4.40 (5H, m); δ 31P (161 MHz, D2O) −6.5 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz) and −21.2 (t, JP-P=20 Hz); mass spectrum m/z 550 (M−1).

EXAMPLE 32

[0590] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(6.7-difluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0591] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6,7-difluoro-2H-isoquinolin-1-one (151 mg) to give the title compound as a white solid (24 mg); δ 1H (400 MHz, D2O) 7.85 (H, d), 7.75 (H, d), 7.55 (H, d), 6.90 (H, d), 6.45 (H, d), 4.55-4.45 (2H, m), 4.40-4.30 (3H, m) and 2.60 (3H, S); δ 31P (161 MHz, D2O) −7.6 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz) and −21.0 (t, JP-P=19 Hz); mass spectrum m/z 552 (M−1).

EXAMPLE 33

[0592] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-methylsulfanyl-7-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0593] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6-methanesulfonyl-7-fluoro-2H-isoquinolin-1-one (100 mg) to give the title compound as a white solid (39 mg); δ 1H (400 MHz, D2O) 7.85 (H, d), 7.75 (H, d), 7.55 (H, d), 6.90 (H, d), 6.45 (H, d), 4.55-4.45 (2H, m), 4.40-4.30 (3H, m) and 2.60 (3H, s); δ 31P (161 MHz, D2O) −6.0 (d, JP-P=21 Hz), −10.0 (d, JP-P=20 Hz) and −21.0 (t, JP-P=20 Hz); mass spectrum m/z 580 (M−1).

EXAMPLE 34

[0594] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-dimethylamino-7-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0595] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-y]-6-dimethylamino-7-fluoro-2H-isoquinolin-1-one (100 mg) to give the title compound as a white solid (16 mg); δ 1H (400 MHz, D2O) 7.80 (H, d), 7.60 (H, d), 7.15 (H, d), 6.80 (H, d), 6.35 (H, d), 4.45-4.35 (2H, m), 4.30-4.20 (3H, m) and 2.85 (6H, S); δ 31P (161 MHz, D2O) −6.6 (d, JP-P=20 Hz), −10.0 (d, JP-P=20 Hz) and −21.3 (t, JP-P=20 Hz); mass spectrum m/z 645 (M−1).

EXAMPLE 35

[0596] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(6,7-dichloro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0597] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-6,7-dichloro-2H-isoquinolin-1-one (206 mg) to give the title compound as a white solid (50 mg); δ 1H (400 MHz, D2O) 8.40 (H, s), 7.90 (H, s), 7.80 (H, d), 6.90 (H, d), 6.45 (H, d), 4.50 (H, t), 4.45 (H, t) and 4.40-4.30 (3H, m); δ 31P (161 MHz, D2O) −6.6 (m), −10.0 (d, JP-P=19 Hz) and −21.3 (m); mass spectrum m/z 585 (M−1).

EXAMPLE 36

[0598] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7,8-dichloro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0599] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-7,8-dichloro-2H-isoquinolin-1-one (126 mg) to give the title compound as a white solid (50 mg); δ 1H (400 MHz, D2O) 8.40 (H, s), 7.90 (H, s), 7.80 (H, d), 6.90 (H, d), 6.45 (H, d), 4.50 (H, t), 4.45 (H, t) and 4.40-4.30 (3H, m); δ 31P (161 MHz, D2O) −6.5 (m), −10.0 (d, JP-P=19 Hz) and −21.3 (m); mass spectrum m/z 584 (M−1).

EXAMPLE 37

[0600] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(8-fluoro-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0601] From 2-[(2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-8-fluoro-2H-isoquinolin-1-one (100 mg) to give the title compound as a white solid (20 mg); δ 1H (400 MHz, D2O) 7.80-7.70 (2H, m), 7.44 (H, d), 7.26 (H, dd), 6.96 (H, d), 6.42 (H, d), 4.50 (H, t), 4.44 (H, t) and 4.38-4.28 (3H, m); δ 31P (161 MHz, D2O) −5.7 (d, JP-P=20 Hz), −9.8 (d, JP-P=20 Hz) and −20.9 (t, JP-P=20 Hz); mass spectrum m/z 534 (M−1).

EXAMPLE 38

[0602] (2R,3S,4R,5R)-3,4-Dihydroxy-5-(7-fluoro-6-methoxy-1-oxo-1H-isoquinolin-2-yl)tetrahydrofuran-2-ylmethyl Triphosphate tris-ammonium Salt

[0603] From 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-hydroxymethyl-cyclopentyl]-7-fluoro-6-methoxy-2H-isoquinolin-1-one to give the title compound as a white solid (16 mg); δ 1H (400 MHz, D2O) 7.9 (H, d), 7.75 (H, d), 7.4 (H, d), 6.9 (H, d), 6.45 (H, d), 4.55 (H, t), 4.4 (H, t), 4.35-4.3 (3H, m) and 4.0 (3H, s); δ 31P (161 MHz, D2O) −6.2 (m), −10.0 (d, JP-P=20 Hz), −21.0 (t, JP-P=19 Hz); mass spectrum m/z 560 (M−1).

EXAMPLE 39

[0604] P1,P4-di[7-chloro-2-(2R,3R,4S,5R-(3,4-dihydroxy-5-hydroxy methyltetrahydrofuran-2-yl)-2H-isoquinolin-1-one]5′-tetraphosphate tris-triethylamine Salt

[0605] 7-Chloro-2-(2R,3R,4S,5R-(3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-2H-isoquinolin-1-one diphosphate bis-ammonium salt (71 mg) was taken up in water and passed through a Dowex (50×8-200) column. This collected fractions were reduced in volume, neutralised with tetrabutyl ammonium hydroxide, and the mixture freeze dried. This was then taken up in dimethylformamide (5 ml) and carbonyl diimidazole (13 mg) added. The reaction was heated to 50° C. for 2.5 hrs, before carbonyl diimidazole (13 mg) was added. After a further 2.5 hrs at 50° C. the reaction was quenched by the addition of water and purified by preparative HPLC to yield the title compound as a white solid (5 mg); δ 1H (400 MHz, D2O) 7.50 (2H, s), 7.30 (4H, m), 7.12 (2H, d), 6.38 (2H, d), 6.04 (2H, d), 4.01-4.15 (4H, m), 3.0-2.9 (18H, q), 2.71-2.82 (6H, m) and 1.0-0.9 (27H, t); δ 31P (161 MHz, D2O) −9.8 (m) and −21.5 (m); mass spectrum m/z 925 (M−1).

[0606] P2Y2 Assay

[0607] The P2Y2 clone was isolated from placental cDNA by PCR, using specific primers, inserted between the NotI and EcoR1 sites in the multi-cloning site of the pIRESpuro vector (Clontech). The vector was stably transfected into a human astrocytoma cell-line, 1321 N1, and raised under puromycin selection. The cells were maintained in Dulbecco's MEM growth medium, containing 10% fcs, 2 mM glutamine, 1% non-essential amino acids, 2 μg/ml puromycin, at 37° C. with 5% CO2 and grown to sub-confluence, before removing with trypsin and re-seeding. Prior to assay, cells were seeded at 1×104 cells/well in 100 μl of growth medium in a 96-well black walled, clear bottomed tissue culture plate and incubated at 37° C. overnight.

[0608] The culture medium was gently removed from the wells and replaced with wash buffer (Hank's Balanced Salts Solution with 0.2% BSA and 20 mM HEPES pH 7.2) containing 2 μM Fluo-4 and 0.02% pluronic acid. The plate was incubated at 37° C. for 1 hour, then gently washed twice and 100 μl wash buffer added per well.

[0609] The calcium response assay was performed in a FLIPR™ (Molecular Devices). The compound of the invention was dissolved in DMSO and then diluted in wash buffer to give a DMSO concentration of 0.3% (reduced to 0.1% when added to the assay plate in the FLIPR™). The compound was added to the assay plate after a 10 second baseline. After a further 3 minutes a UTP stimulus was added. The response of the compound was compared to that of UTP.

[0610] Human P2Y4 receptors were cloned from genomic DNA by PCR, whilst P2Y6 receptors were isolated from a human peripheral blood mononuclear cell cDNA library. These receptors were stably expressed in 1321N1 cells and assayed as described above for P2Y2 receptors.

[0611] In the above assays the preferred compound of the invention generally has EC50 values in the P2Y2, P2Y6 and/or P2Y4 assays of 10 μM and below.

Number	Date	Country
0103060.0	Feb 2001	GB
0115545.6	Jun 2001	GB
0129704.3	Dec 2001	GB

Non-natural nucleotides and dinucleotides

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