Method for Using Purine Derivatives

The present invention relates to antiviral purine derivatives containing an acyclic chain in the 9-position.

U.K. Patent Specification No. 1523865 and U.S. Pat. No. 4,199,574 describe a broad class of purine derivatives containing an acyclic side chain in the 9-position. These purine derivatives have been found to have antiviral activity against various classes of DNA viruses particularly against herpes viruses such as herpes simplex.

Among these derivatives, 9-(2-hydroxyethoxymethyl)guanine (otherwise known as acyclovir) has been found to have particularly good activity against herpes viruses such as herpes simplex. However, while acyclovir has been found to be especially effective upon topical or parenteral administration, it is only moderately well absorbed upon oral administration with corresponding levels of drug in the plasma. It will be appreciated that when one is treating an internal disorder by oral administration of a drug, it is clearly desirable that the drug should be well absorbed from the gastro-intestinal tract with resulting high plasma levels.

The surprising discovery has been made that a certain narrow class of purine derivatives, falling within the scope of the compounds broadly described in U.K. Patent Specification No. 1523865 and U.S. Pat. No. 4,199,574 and characterized by the presence of a hydrogen atom in the 6-position of the purine nucleus and at least one ester function at the end(s) of the substituent attached to the 9-position, can be readily converted in vivo by the actions of the molybdo-flavo-protein enzymes xanthine oxidase/dehydrogenase or aldehyde oxidase and esterase enzymes into the corresponding 6-hydroxy purine derivatives having hydroxy at the end(s) of the substituent attached to the 9-position.

The purine derivatives of this class are considerably more soluble in water than are the corresponding guanine congeners formed from them by the action of these enzymes. This improved water-solubility enables the 6-hydrogen purine analogs of formula (I) below to be used in a greater variety of aqueous pharmaceutical formulations which require some solubilisation of the drug. The above-mentioned class of 6-hydrogen purine analogues may be represented by the formula (I) ##STR4## wherein X=O or S, Y=H or CH.sub.2 OR and the R group (s may be the same or different and each) is H or ##STR5## wherein R.degree.=H, C.sub.1-16 alkyl (preferably C.sub.1-6 alkyl), optionally substituted aralkyl or optionally substituted aryl, provided that at least one R is ##STR6## and physiologically acceptable salts thereof. The aralkyl and aryl groups may be substituted, for example by one or more halogen (e.g. chlorine or bromine) atoms or amino, nitrile or sulphamido groups, the aryl moiety of the grouping advantageously containing 6 to 10 carbon atoms.

Salts of the compounds of formula (I) which may be conveniently used in therapy include physiologically acceptable salts of organic acids such as lactic, acetic, malic or p-toluenesulphonic acid as well as physiologically acceptable salts of mineral acids such as hydrochloric or sulphuric acid.

The present invention also includes the novel compounds of formula (I) as defined above with the additional proviso that R may not be ##STR7## wherein R.degree. is phenyl when Y=H and X=O.

2-Amino-9-(2-benzoyloxyethoxymethyl)purine (i.e. the benzoate ester of the compound of formula (I) wherein X represents an oxygen atom and Y represents a hydrogen atom) is disclosed in U.S. Pat. No. 4,199,547. However, there is no indication or suggestion in the said U.S. Specification that the compound can be converted in vivo into the corresponding 6-hydroxy analogue.

When compounds of formula (I) are administered, especially orally, higher blood levels of the corresponding non-esterified, 6-hydroxy compounds are attained and maintained for substantially longer periods of time than when the latter are administered directly.

The compounds of formula (I) may be converted into the corresponding non-esterified, 6-hydroxy compounds by the action of xanthine oxidase/dehydrogenase or aldehyde oxidase and esterase enzymes in vitro (or ex vivo) as a method for synthesizing the latter compounds.

The discovery that the 6-hydrogen purines of formula (I) above can be readily converted into their corresponding 6-hydroxy analogues is surprising since in previous studies with xanthine oxidase from bovine milk (H. Lettre et al. (1967) Biochem. Pharmacol., 16, 1747-1755; T. A. Krenitsky et al. (1972) Arch. Biophys., 150, 585-599) it was shown that 9-substitution obliterates or greatly diminishes the rate at which a variety of purines are oxidized.

The high level of absorption of the compounds of formula (I) from the gastrointestinal tract renders the compounds especially useful when oral administration of the compounds is desired, e.g. in the treatment of diseases caused by various DNA viruses, such as herpes infections for example herpes simplex, varicella or zoster, cytomegalovirus as well as diseases caused by hepatitis B or Epstein-Barr virus. The compounds of formula (I) can also be used for the treatment of prophylaxis of papilloma or wart virus infections. In addition to their use in human medical therapy the compounds of formula (I) can be administered to other animals for the treatment of prophylaxis of viral diseases, e.g. in other mammals. For example, those compounds of formula (I) wherein Y represents CH.sub.2 OR are especially useful for the treatment of equine rhinopneumonitis. By administration of a compound of formula (I) or physiologically acceptable salt thereof, especially by the oral route, it is possible to achieve an advantageous effect against such disorders.

According to a further feature of the present invention there are provided the compounds of formula (I) and physiologically acceptable salts thereof for use in the treatment or prophylaxis of a viral disease in an animal, e.g. a mammal such as man.

The present invention also provides a method for the treatment or prophylaxis of a viral disease in an animal, e.g. a mammal such as man which comprises administering to the animal an effective antiviral amount of a compound of formula (I) or a physiologically acceptable salt thereof.

The compounds of formula (I) and the physiologically acceptable salts thereof (hereafter collectively referred to as the active ingredients) may be administered by any route appropriate to the condition to be treated, suitable routes including oral, rectal, nasal, topical (including buccal and sublingual), viginal and parenteral (including subcutaneous, intramuscular, intravenous, intradermal, intrathecal and epidural). It will be appreciated that the preferred route may vary with for example the condition of the recipient.

For each of the above-indicated utilities and indications the amount required of an active ingredient (as above defined) will depend upon a number of factors including the severity of the condition to be treated and the identity of the recipient and will ultimately be at the discretion of the attendant physician or veterinarian. In general however, for each of these utilities and indications, a suitable, effective dose will be in the range 0.1 to 250 mg per kilogram body weight of recipient per day, preferably in the range 1 to 100 mg per kilogram body weight per day and most preferably in the range 5 to 20 mg per kilogram body weight per day; an optimum dose is about 10 mg per kilogram body weight per day. (Unless otherwise indicated all weights of active ingredient are calculated as the parent compound of formula (I): for salts thereof the figures would be increased proportionately.) The desired dose is preferably presented as two, three, four or more sub-doses administered at appropriate intervals throughout the day. These sub-doses may be administered in unit dosage forms, for example, containing 10 to 1000 mg, preferably 20 to 500 mg and most preferably 100 to 400 mg of active ingredient per unit dosage form.

While it is possible for the active ingredients to be administered alone it is preferable to present them as pharmaceutical formulations. The formulations, both for veterinary and for human use, of the present invention comprise at least one active ingredient, as above defined, together with one or more acceptable carriers therefor and optionally other therapeutic ingredients. The carrier(s) must be "acceptable" in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.

The formulations include those suitable for oral, rectal, nasal, topical (including buccal and sublingual), viginal or parenteral (including subcutaneous, intramuscular, intravenous, intradermal, intrathecal and epidural) administration. The formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. Such methods include the step of bringing into association the active ingredient with the carrier which constitutes one or more accessory ingredients. In general the formulations are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers or both, and then, if necessary, shaping the product.

Formulations of the present invention suitable for oral administration may be presented as discrete units such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient; as a powder or granules; as a solution or a suspension in an aqueous liqud or a non-aqueous liquid; or as an oil-in-water liquid emulsion or a water-in-oil liquid emulsion. The active ingredient may also be presented as a bolus, electuary or paste.

A tablet may be made by compression or moulding, optionally with one or more accessory ingredients. Compressed tablets may be prepared by compressing in a suitable machine the active ingredient in a free-flowing form such as a powder or granules, optionally mixed with a binder, lubricant, inert diluent, preservative, surface active or dispersing agent. Moulded tablets may be made by moulding in a suitable machine a mixture of the powdered compound moistened with an inert liqud diluent. The tablets may optionally be coated or scored and may be formulated so as to provide slow or controlled release of the active ingredient therein.

For infections of the eye or other external tissues e.g. mouth and skin, the formulations are preferably applied as a topical ointment or cream containing the active ingredient in an amount of, for example, 0.075 to 20% w/w, preferably 0.2 to 15% w/w and most preferably 0.5 to 10% w/w. When formulated in an ointment, the active ingredients may be employed with either a paraffinic or a water-miscible ointment base. Alternatively, the active ingredients may be formulated in a cream with an oil-in-water cream base.

If desired, the aqueous phase of the cream base may include, for example, at least 30% w/w of a polyhydric alcohol, i.e. an alcohol having two or more hydroxyl groups such as propylene glycol, butane-1,3-diol, mannitol, sorbitol, glycerol and polyethylene glycol and mixtures thereof. The topical formulations may desirably include a compound which enhances absorption or penetration of the active ingredient through the skin or other affected areas. Examples of such dermal penetration enhancers include dimethylsulphoxide and related analogues.

The oily phase of the emulsions of this invention may be constituted from known ingredients in a known manner. While the phase may comprise merely an emulsifier (otherwise known as an emulgent), it desirably comprises a mixture of at least one emulsifier with a fat or an oil or with both a fat and an oil. Preferably, a hydrophilic emulsifier is included together with a lipophilic emulsifier which acts as a stabilizer. It is also preferred to include both an oil and a fat. Together, the emulsifier(s) with or without stabilizer(s) make up the so-called emulsifying wax, and the wax together with the oil and/or fat make up the so-called emulsifying ointment base which forms the oily dispersed phase of the cream formulations.

Emulgents and emulsion stabilizers suitable for use in the formulation of the present invention include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl mono-stearate and sodium lauryl sulphate.

The choice of suitable oils or fats for the formulation is based on achieving the desired cosmetic properties, since the solubility of the active compound in most oils likely to be used in pharmaceutical emulsion formulations is very low. Thus the cream should preferably be a non-greasy, non-staining and washable product with suitable consistency to avoid leakage from tubes or other containers. Straight or branched chain, mono- or dibasic alkyl esters such as di-isoadipate, isocetyl stearate, propylene glycol diester of coconut fatty acids, isopropyl myristate, decyl oleate, isopropyl palmitate, butyl stearate, 2-ethylhexyl palmitate or a blend of branched chain esters known as Crodamol CAP may be used, the last three being preferred esters. These may be used alone or in combination depending on the properties required. Alternatively, high melting point lipids such as white soft paraffin and/or liquid paraffin or other mineral oils can be used.

Formulations suitable for topical administration to the eye also include eye drops wherein the active ingredient is dissolved or suspended in a suitable carrier, especially an aqueous solvent for the active ingredient. The active ingredient is preferably present in such formulations in a concentration of 0.5 to 20%, advantageously 0.5 to 10% particularly about 1.5% w/w.

Formulations suitable for topical administration in the mouth include lozenges comprising the active ingredient in a flavoured basis, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert basis such as gelatin and glycerin, or sucrose and acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier.

Formulations for rectal administration may be presented as a suppository with a suitable base comprising for example cocoa butter or a salicylate.

Formulations suitable for nasal administration wherein the carrier is a solid include a coarse powder having a particle size for example in the range 20 to 500 microns which is administered in the manner in which snuff is taken, i.e. by rapid inhalation through the nasal passage from a container of the powder held close up to the nose. Suitable formulations wherein the carrier is a liquid, for administration as for example a nasal spray or as nasal drops, include aqueous or oily solutions of the active ingredient.

Formulations suitable for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or spray formulations containing in addition to the active ingredient such carriers as are known in the art to be appropriate.

Formulations suitable for parenteral administration include aqueous and non-aqueous sterile injection solution which may contain anti-oxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents. The formulations may be presented in unit-dose or multi-dose containers, for example sealed ampoules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example water for injections, immediately prior to use. Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described.

Preferred unit dosage formulations are those containing a daily dose or unit daily sub-dose, as herein above recited, or an appropriate fraction thereof, of an active ingredient.

It should be understood that in addition to the ingredients particularly mentioned above the formulations of this invention may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavouring agents.

The present invention further provides veterinary compositions comprising at least one active ingredient as above defined together with a veterinary carrier therefor.

Veterinary carriers are materials useful for the purpose of administering the composition and may be solid, liquid or gaseous materials which are otherwise inert or acceptable in the veterinary art and are compatible with the active ingredient. These veterinary compositions may be administered orally, parenterally or by any other desired route.

For oral administration the compositions can be in the form of a tablet, granule, drench, paste, cachet, capsule or feed supplement. Granules may be made by the well known techniques of wet granulation, precompression or slugging. They can be administered to animals in an inert liquid vehicle so as to form a drench, or in a suspension with water or oil base. Preferably further accessory ingredients such as a dispensing agent are included. The formulations preferably contain from 15% to 85% of the active ingredient.

A paste may be formulated by suspending the active ingredient in a liquid diluent. A stiffening or thickening agent may be included together with a wetting agent or a humectant if the liquid is water. If an emulsion paste is needed than one or more surface active agents should desirably be included. From 25 to 80% weight of these paste formulations may comprise the active ingredient.

In feed supplements the active ingredient is generally present in large amounts relative to the accessory ingredients, and the supplements may be added directly or after intermediate blending or dilution. Examples of accessory ingredients for such formulations include solid, orally ingestible carriers such as corn meal, soya flour, wheat shorts, soya grits, edible vegetable materials and fermentation residues. The active ingredient is usually incorporated in one or more of the accessory ingredients and intimately and uniformly dispersed by grinding, tumbling or stirring with conventional apparatus. Formulations containing 1 to 90% by weight of the active ingredient are suitable for adding to feeds.

For the treatment of herpes infections in horses, an oral or parenteral dose of from 0.1 to 250 mg per kg body weight per day, preferably from 2 to 100 mg per kg per day may be required. The dose may be split up into discrete units administered at regular intervals during the day, and repeated daily for up to 14 days or until the infection is cleared. For viral infections in other animals the dose may vary depending on the size and metabolism of the animal. The compositions may be administered in unit dosage form, such as a tablet a few times daily in the amount of 10 to 1000 mg per unit dose.

The compounds of formula (I) and physiologically acceptable salts thereof may be prepared in conventional manner by analogous processes for preparing compounds of similar structure, such as those methods described in U.K. Patent Specification No. 1523865.

The present invention further provides a process for the preparation of the compounds of formula (I) and physiologically acceptable salts thereof which comprises:

(a) deblocking a compound of formula (II) ##STR8## (wherein X, Y and R, are as defined above and R.sup.1 represents a blocking group) to form a compound of formula (I) or a physiologically acceptable salt thereof;

(b) converting a compound of formula (III) ##STR9## (wherein X, Y and R are as defined above, M represents a hydrogen atom or a group or atom convertible into a hydrogen atom and G represents a group or atom convertible into an amino group or (when M is other than a hydrogen atom) G may alternatively represent an amino group) or a salt thereof into a compound of formula (I) or a physiologically acceptable salt thereof;

(c) reacting a compound of formula (IV) ##STR10## (wherein Q represents a leaving atom or group) with a compound of formula (V) ##STR11## (wherein R,X and Y are as defined above and A represents a leaving group or atom);

(d) closing a ring in a precursor compound having either the pyrimidine or imidazole ring incompletely formed;

(e) reducing a compound of formula ##STR12## (wherein X and R are as defined above) or a salt thereof to form a compound of formula (I) (wherein Y represents a hydroxymethyl group) or a physiologically acceptable salt thereof; or

(f) solvolysing with an alcohol of formula ROH a compound having the formula ##STR13## (wherein X is as defined above) or a salt thereof to form a compound of formula (I) (wherein Y represents a hydroxymethyl group) or a physiologically acceptable salt thereof;

(g) esterifying a compound of formula (I) wherein X and Y are as defined and at least one R is a hydrogen atom; and optionally effecting one or more of the following conversions, in any desired sequence:

(i) where the resulting product is a base, converting the said base into a physiologically acceptable acid addition salt thereof;

(ii) where the resulting product is an acid addition salt, converting the said salt into the parent base.

In method (a) the blocking group R.sup.1 may be selected for example from acyl groups such as C.sub.1-4 alkanoyl groups e.g. acetyl, or aroyl groups, e.g. benzoyl; arylmethyl groups e.g. benzyl; or tri-C.sub.1-4 alkylsilyl e.g. trimethylsilyl. Arylmethyl blocking groups may be removed for example by hydrogenolysis, e.g. by hydrogenation in the presence of Raney nickel or palladium catalyst or by the use of sodium in liquid ammonia. Acyl blocking groups may be removed for example by hydrolysis using for example an amine such as methylamine or triethylamine, advantageously in an aqueous medium. Trialkylsilyl blocking groups may be removed for example by solvolysis e.g. with alcoholic or aqueous ammonia, or by alcoholysis.

Conversion of a compound of formula (III) into a compound of formula (I), by method (b), can be achieved by various means. For example G may represent an azide group which can be reduced to an amino group by catalytic hydrogenation using a suitable catalyst such as palladium. Alternatively, G may represent a halogen atom or an alkylthio or alkylsulphonyl group which can be converted to an amino group by aminolysis using for example ammonia. Also, M may represent a halogen atom or a mercapto group which can be converted into a hydrogen atom by reduction or dethiolation respectively, both in conventional manner.

These processes together with other conventional processes are described in Fused Pyrimidines, Part II, Purines Ed. by D. J. Brown (1971), Wiley-Interscience.

In process (c), the group Q in formula (IV) may for example represent a hydrogen atom; an acyl group, e.g. a C.sub.1-4 alkanoyl group such as an acetyl group or an aroyl group such as a benzoyl group; or a tri-C.sub.1-4 alkylsilyl group such as a trimethylsilyl group. The group A in formula (V) may for example repesent a halogen atom (e.g. chlorine) or an acyloxy group wherein the acyl moiety may be for example a C.sub.1-4 alkanoyl group such as acetyl, or an aroyl group such as benzoyl. The reaction may be conveniently effected in a strong polar solvent such as dimethylformamide or hexamethylphosphoramide, advantageously in the presence of a base such as triethylamine or potassium carbonate. Alternatively, a thermal condensation may be effected by heating the compounds of formlae (IV) and (V) in the presence of a catalytic amount of a strong acid, e.g. sulphuric acid.

Process (d) involves the ring closure of either the imidazole or pyrimidine ring to give the final product. In the case of the imidazole ring this may be achieved by reaction of an appropriate precursor with a C.sub.1 reagent, such as triethylorthoformate, under for example mildly acidic conditions, at a temperature of about 25.degree. C., for several hours. A suitable precusor is a substituted pyrimidine of formula (VIII). ##STR14##

An alternative reagent is diethoxymethyl acetate, when neutral conditions at about 100.degree. C. for about 10-15 minutes are preferred.

Reduction of a compound of formula (VI) in process (e) may be achieved for example by reaction with an appropriate aldehyde reducing agent such as sodium borohydride, sodium cyanoborohydride, tetraethylammonium borohydride or pyridine/diborane/tetrahydrofuran/trifluoroacetic acid.

In process (g), hydrolysis of the compound of formula (VII) may be effected for example under basic conditions, e.g. by treatment with an organic amine such as methylamine or triethylamine.

Process (h) is carried out under mild esterification conditions using a carboxylic acid anhydride in the presence of a catalytic amount of a pyridine catalyst such as 4-dimethylaminopyridine in a polar solvent such as dimethylformamide.

The following Examples illustrate the present invention.

A 1 liter round bottom flask equipped with a magnetic stirring bar and a CaCl.sub.2 drying tube was charged with 5.0 g (29.50 mM) 2-amino-6-chloro-purine, 6.8 g (29.50 mM) 2-(chloromethylthio)ethyl benzoate, 4.07 g (29.50 mM) potassium carbonate and 750 ml of anhydrous dimethylformamide. The reaction was stirred at room temperature for 16 hours after which time another 2.0 g (8.7 mM) of 2-(chloromethylthio)ethyl benzoate along with 1.2 g (8.7 mM) potassium carbonate were added and stirring continued for an additional 24 hours at room temperature. The reaction mixture was then filtered through a pad of Celite in a sintered glass funnel and rotary evaporated in vacuo to a viscous yellow oil. The oil was adsorbed on to 20.0 g of Merck silica gel 60 (70-230 mesh) and this preadsorbed phase applied to the top of a column of Merck silica gel 60 (230-400 mesh). Elution of the column using 6:4 ethyl acetate-benzene provided 2-amino-9-(2-benzoyloxyethylthiomethyl)-6-chloro-purine as an off-white solid as a single material by TLC on silica gel 8:2 (ethyl acetate:hexane). .sup.1 H NMR, CDCl.sub.3 8.0-7.15 .delta., 6H, multiplet; 5.1 .delta., 4H, broad singlet; 4.5 .delta., 2H, triplet 2.9 .delta., 2H triplet. This product (0.98 g 2.70 mM) was placed into a 500 ml Parr hydrogenator bottle together with 2.5 g Pd(OH).sub.2 catalyst, 50 ml Et.sub.3 N and 200 ml of methanol. This was shaken on a Parr hydrogenator under 50 p.s.i. hydrogen for 16 hours at room temperature. TLC of the hydrogenolysis product on silica gel with 8% methanol-ethyl acetate showed only partial reaction. The catalyst was removed by filtration through a pad of Celite in a sintered glass funnel, 2.0 g of fresh Pd(OH).sub.2 catalyst and 7.0 ml triethylamine were added and the reaction mixture again shaken under 50 p.s.i. hydrogen for 20 hours. At this point t.l.c. showed the reaction to be complete, the catalyst was removed as before and the methanol rotary evaporated in vacuo to give a clear glass, which was taken up into 100 ml of 1:1 methanol-water containing 20% methylamine. The resulting solution was stirred at room temperature for 4 hours and rotary evaporated in vacuo to give an amorphous solid. The solid was adsorbed on to 10.0 g of 70-230 mesh Merck silica gel 60 and this preadsorbed phase applied to the top of a column of 230-400 mesh Merck silica gel 60. Elution of the column using 10% methanol in ethyl acetate provided a solid that crystallized from ethyl acetate-hexane to give the title compound in the form of tiny needles, mp. 122.degree.-124.degree. C., t.l.c.: 1 spot on silica gel with 15% methanol:thyl acetate .sup.1 H NMR dmso-d6 8.59 .delta., 1singlet; 8.15 .delta., 1H singlet; 6.56 .delta., 2H broad singlet; 5.24 .delta., 2H singlet; 4.83 .delta., 1H triplet; 3.49 .delta., 2H multiplet; 2.69 .delta., 2H multiplet; Anal.: Theory C: 42.65 H 4.92, N: 31.09. Found C: 42.70, H: 4.94, N: 31.04.

A mixture of 7.0 g (41.2 mM) of 2-amino-6-chloropurine, 4.55 g (34.4 mM) of ammonium sulfate, and 200 ml hexamethyldisilazane were combined under nitrogen and refluxed with stirring for five hours. The mixture was flash evaporated, followed by the addition of 8.8 g (23.6 mM) of 2-O-(acetylmethyl)1-1,3-bis-(O-benzoyl)glycerol in about 10 ml benzene. The mixture was heated for 1.5 hours in an oil bath and under aspirator pressure with a distilling head hookup. Then the mixture was cooled to room temperature. Methanol was added to the mixture which was placed over a steambath for 30 minutes. Next, the mixture was washed with H.sub.2 O and extracted 3 times with ethyl acetate and the organic layer dried over anhydrous magnesium sulphate for about 30 minutes. The mixture was then filtered, the salt washed with ethyl acetate and then flash evaporated. Flash column chromatography with 6:1 CH.sub.2 Cl.sub.2 /acetone eluent yielded the title compound as an analytically pure product, a white solid with a mpt. of 130.degree.-131.degree. C.

A mixture of 3.393 g (7.04 mM) of 2-amino-9-[(2-benzoyloxy-1-(benzoyloxymethyl)ethoxy)methyl]-6-chloro-9H-pu rine, 100 ml ethanol, 100 ml tetrahydrofuran, 1.9 ml triethylamine was added to 0.6 g Pd-C catalyst in a Parr bottle. The mixture was shaken under 50 P.S.I. of H.sub.2 for 24 hours. The Pd-C was filtered through a Celite pad and 0.65 g fresh Pd-C was added to the reaction mixture and the hydrogenation was continued for 4 days. Column chromatography using 100% CH.sub.2 Cl.sub.2, 4:1 CH.sub.2 Cl.sub.2 /acetone, and 100% acetone produced the title compound, mpt. 132.degree.-133.degree. C.

A mixture of 0.844 g (1.88 mM) of 2-amino-9-[(2-benzoyloxyl-1-(benzoyloxymethyl)ethoxy)methyl]-9H-purine and 100 ml of a 40% aqueous methylamine solution was stirred at room temperature for 30 minutes. The mixture was flash evaporated to a yellow oil which was then washed with water. The aqueous layer was then extracted twice with methylene chloride. The aqueous layer containing the product was then flash evaporated to a light yellow oil. Recrystallization of the oil in hot acetonirile yielded the title compound as an analytically pure ivory solid, mpt. 148.degree.-151.degree..

A mixture of 0.82 g (3.92 mM) of 9-(2-hydroxyethoxymethyl)-2-amino-9H-purine, 48 mg (0.392 mM) of a 4-dimethylaminopyridine and 0.75 ml (7.84 mM) of acetic anhydride in 18 ml of dry dimethylformamide was stirred at room temperature for two days. The reaction mixture was evaporated in vacuo and the residue dissolved in ethyl acetate and absorbed on silica gel. The solvent was removed by flash evaporation and the residual powder added to a column prepared for flash chromatography. Elution with 5% methanol in dichloromethane gave 1.0 g of a semicrystalline oil which on recrystallization from benzene-hexane gave analytically pure 9-(2-acetoxyethoxymethyl)-2-amino-9H-purine, mpt. 115.degree.-118.degree. C. An additional crop was obtained from the mother liquor.

A mixture of 0.45 g (1.88 mM) of 2-amino-9-[(2-hydroxy-1-hydroxymethylethoxy)methyl]-9H-purine, 1.15 g (11.30 mM) of acetic anhydride and 23 mg (0.188 mM) of 4-dimethylaminopyridine in 10 ml of dry dimethylformamide is stirred at room temperature for 18 hours. The solution is evaporated in vacuo and the residue dissolved in methanol and preabsorbed on silica gel. The solvent is evaporated off in vacuo and the powder added to a column prepared for flash chromatography. Elution with 10% methanol in dichloromethane yields on evaporation the title compound. Recrystallization from ethyl acetate-hexane gives analytically pure 2-amino-9-[(2-acetoxy-1-acetoxymethylethoxy)methyl]-9H-purine.

A 100 ml flask equipped with a magnetic stirring bar and a CaCl.sub.2 drying tube was charged with 1.0 g (4.4 mM) 2-amino-9-(2-hydroxyethylthiomethyl)-9H-purine, 0.054 g (0.44 mM) 4-dimethylaminopyridine, 0.9 ml (8.8 mM) acetic anhydride, and 200 ml of dry DMF. The solution was stirred for 24 hrs at room temperature and then quenched with 5 ml of MeOH. The solution was evaporated in vacuo (bath temp 40.degree. C.) and the brown oil so obtained chromatographed using the "flash" method. Elution of the column with 1.5% methanol in ethyl acetate provided a yellow oil which crystallized on standing. The light yellow crystals were dissolved in a solution of 2% MeOH in toluene and treated with 0.05 g Darco G-60. The methanol was evaporated from the toluene solution resulting in the precipitation of light yellow crystals. The product was dried for 16 hrs at 78.degree. C. to yield the title compound, mpt. 119.degree.-120.5.degree. C. Anal. Calcd. for C.sub.10 H.sub.13 N.sub.5 O.sub.2 S: C, 44.93; H, 4.9; N, 26.20. Found: C, 44.97, H, 4.96; N, 26.17. .sup.1 H NMR in DMSO.sub. 6 8.59 (1HS), 8.15 (1Hs), 6.52 (2H broad s) 5.26 (2Hs), 4.15 (2Ht J=6.36 Hz), 2.89 (2Ht J=6.36 Hz), 1.99 (3Hs).

A 5-liter, 3-neck flask was equipped with an air-stirring motor, glass stirring rod with Teflon paddle, and provision made for evacuating and fillin the flask with either N.sub.2 or H.sub.2 gas. The flask was then charged with 7.0 g (0.019M) of 2-amino-9-(2-benzoyloxyethylthiomethyl)-6-chloro-9H-purine, 14.0 g palladium hydroxide on carbon, 12.0 ml (0.163M) triethylamine, 75.0 ml H.sub.2 O and 3.0 liters of methanol. The flask was then sealed and evacuated using a water aspirator, flooded with N.sub.2 gas, evacuated until 3 complete cycles were completed. The flask was evacuated, flooded with H.sub.2 gas, evacuated and refilled with H.sub.2 gas. The stirring motor was started and the reaction was stirred under H.sub.2 (pressure to support 6" column of H.sub.2 O) for 4 days at room temperature. The solution was filtered through a sintered glass funnel and the catalyst washed with 800 ml of methanol. The methanol solution was evaporated in vacuo to give 6.0 g of a light yellow solid. The solid was absorbed to 18.0 g of 70-230 mesh silica gel 60 and this presorbed phase applied to the top of a column of 230-400 mesh silica gel 60. Elution of the column by the "Flash" method using 5% methanol in ethyl acetate provided the title compound as a white solid which was recrystallized from ethyl acetate-hexane and dried at 78.degree. C. under 1.0 mm Hg vacuum to give white flakes, mpt. 120.degree.-121.degree. C., .sup.1 H NMR in dmso d.sub.6 .delta. 8.60 (1H, s), 8.19 (1H, s), 8.0.fwdarw.7.5 (5H, m), 6.55 (2H, s) 5.32 (2H, s), 4.52 (2H, t), 3.06 (2H, t) Anal.: Theory C: 54.69, H: 4.59, N: 21.26. Found C: 54.68; H: 4.64, N: 21.24.

2-Amino-9-(2-hydroxyethylthiomethyl)-9H-purine was obtained by continued elution of the above column.

The following Examples 8 to 12 illustrate pharmaceutical formulations according to the invention where the active compound is a compound of formula (I) or a physiologically acceptable salt thereof.

Tablets were prepared from the foregoing ingredients by wet granulation followed by compression.

The two ingredients were mixed then fed to any conventional feed stuff pelleting plant.

The non-esterified, 6-hydroxy compounds produced from the compounds at formula (I) according to the teaching of this invention may be represented by formula (IA) ##STR15## wherein X is as defined above and Y.sup.1 is hydrogen or CH.sub.2 OH.