WO2002018371A1

WO2002018371A1 - Nucleoside metabolism inhibitors

Info

Publication number: WO2002018371A1
Application number: PCT/NZ2001/000174
Authority: WO
Inventors: Richard Hubert Furneaux; Peter Charles Tyler; Vern L. Schramm
Original assignee: Industrial Research Ltd; Albert Einstein College of Medicine
Current assignee: Callaghan Innovation Research Ltd; Albert Einstein College of Medicine
Priority date: 2000-08-29
Filing date: 2001-08-24
Publication date: 2002-03-07
Anticipated expiration: 2003-02-28
Also published as: JP2004507534A; US20040053944A1; US7109331B2; US20070015772A1; AU2001284564A1

Abstract

The present invention provides a compound of formula (I), wherein: A is selected from N, CH and CR, where R is selected from halogen, optionally substituted alkyl, aralkyl and aryl, OH, NH2, NHR?1, NR1R2 and SR3¿, where R?1, R2 and R3¿ are each optionally substituted alkyl, aralkyl or aryl groups; B is selected from OH, NH¿2, NHR?4, H and halogen, where R4 is an optionally substituted alkyl, aralkyl or aryl group; D is selected from OH, NH¿2, NHR?5, H, halogen and SCH¿3?, where R?5¿ is an optionally substituted alkyl, aralkyl or aryl group; X and Y are independently selected from H, OH and halogen, with the proviso that when one of X and Y is hydroxy or halogen, the other is hydrogen; Z is OH, or, when X is hydroxy, Z is selected from hydrogen, halogen, hydroxy, SQ and OQ, where Q is an optionally substituted alkyl, aralkyl or aryl group; and W is OH or H, with the proviso that when W is OH, then A is CR where R is as defined above; or a tautomer thereof; or a pharmaceutically acceptable salt thereof; or an ester thereof; or a prodrug thereof. The invention also provides a pharmaceutical composition comprising a compound of formula (I), as well as methods of treatment using a compound of formula (I). The invention further provides methods of preparing compounds of formula (I).

Description

NUCLEOSIDE METABOLISM INHIBITORS

TECHNICAL FIELD

This invention relates to certain nucleoside analogues, pharmaceutical compositions containing the compounds and processes for preparing the compounds.

BACKGROUND OP THE INVENTION

Purine nucleoside phϋsphorylasfci (PNP) c talyst.-) the phttβphttHJIytlb blefc.vdye' of ribd- ahd deiϋ yHbdhϋolθosldfes, fo. example, thθltø ttt gUtiHine e Htl hypd dhthlhe t« glVfei the ϋdH-θ&μbndiHø nugEiM-phobt-tlte aHd dϋaHIHβ. hvjjbλdnt ihβi ϊt btHbt^* PUHHB bdsfes.

Humans deficient in purine nucleoside phosphorylase (PNP) suffer a specific T-cell immunodeficiency due to an accumulation of dGTP and its toxicity to stimulated T lymphocytes. Because of this, inhibitors against PNP are immunosuppressive, and are active against T-cell malignancies. Clinical trials are now in progress using 9-(3-pyridylmethyl)-9-deazaguanine in topical form against psoriasis and in oral form for T-cell lymphoma and immunosuppression (BioCryst Pharmaceuticals, Inc). The compound has an ICεo of 35 nM for the enzyme. In animal studies, a 50 mg/kg oral dose is required for activity in a contact sensitivity ear swelling assay in mice. For human doses, this would mean approximately 3.5 grams for a 70 kg human. With this inhibitor, PNP is difficult to inhibit due to the relatively high activity of the enzyme in blood and mammalian tissues. Nucleoside and deoxynucleoside hydrolases catalyse the hydrolysis of nucleosides and deoxynucleosides. These enzymes are not found in mammals but are required for nucleoside salvage in some protozoan parasites. Purine phosphoribosyltransferases (PPRT) catalyze the transfer of purine bases to 5-phospho-α-D-ribose-1 -pyrophosphate to form purine nucleotide 5'-phosphates. Protozoan and other parasites contain PPRT which are involved in essential purine salvage pathways. Malignant tissues also contain PPRT. Some protozoan parasites contain purine nucleoside phosphorylases which also function in purine salvage pathways. Inhibitors of nucleoside hydrolases, purine nucleoside phosphorylases and PPRT can be expected to interfere with the metabolism of parasites and therefore be usefully employed against protozoan parasites. Inhibitors of PNP and PPRT can be expected to interfere with purine metabolism in malignant tissues and therefore be usefully employed against malignant tissues.

The applicants' PCT International Patent publication WO 99/19338 describes compounds which are potent inhibitors of PNP, PPRT and/or nucleoside hydrolases.

It is an object of the present invention to provide further compounds which are effective inhibitors of PNP, PPRT and/or nucleoside hydrolases, or at least to provide the public with a useful choice.

SUMMARY OF THE INVENTION

Accordingly, in a first aspect, the present invention provides a compound of the formula:

W X

(I) wherein:

A is selected from N, CH and CR, where R is selected from halogen, optionally substituted alkyl, aralkyl and aryl, OH, NH₂, NHR¹, NR¹R² and SR³, where R¹, R² and R³ are each optionally substituted alkyl, aralkyl or aryl groups;

B is selected from OH, NH₂, NHR⁴, H and halogen, where R⁴ is an optionally substituted alkyl, aralkyl or aryl group;

D is selected from OH, NHz, NHR⁵, H, halogen and SCHs, where R⁵ is an optionally substituted alkyl, aralkyl or aryl group;

X and Y are independently selected from H, OH and halogen, with the proviso that when one of X and Y is hydroxy or halogen, the other is hydrogen;

Z is OH, or, when X is hydroxy, Z is selected from hydrogen, halogen, hydroxy, SQ and OQ, where Q is an optionally substituted alkyl, aralkyl or aryl group; and W is OH or H, with the proviso that when W is OH, then A is CR where R is as defined above;

or a tautomer thereof; or a pharmaceutically acceptable salt thereof; or an ester thereof; or a prodrug thereof.

Preferably when B is NHR⁴ and/or D is NHR⁵, then R⁴ and/or R⁵ are C¹-C⁴ alkyl.

Preferably when one or more halogens are present they are chosen from chlorine and fluorine.

Preferably when Z is SQ or OQ, Q is C1-C5 alkyl or phenyl.

Preferably D is H, or when D is other than H, B is OH.

More preferably, B is OH, D is H, OH or NH₂, X is OH or H, Y is H, most preferably with Z as OH, H, or methylthio, especially OH.

In certain preferred embodiments W is OH, Y is H, X is OH, and A is CR where R is methyl or halogen, preferably fluorine.

In other preferred embodiments, W is H, Y is H, X is OH and A is CH.

It will be appreciated that the representation of a compound of formula (I) wherein B and/or D is a hydroxy group used herein is of the enol-type tautomeric form of a corresponding amide, and this will largely exist in the amide form. The use of the enol-type tautomeric representation is simply to allow fewer structural formulae to represent the compounds of the invention. According to another aspect of the invention, there is provided a pharmaceutical composition comprising a pharmaceutically effective amount of a compound of the formula (I) as defined above.

In another aspect, the invention provides methods for treatment of diseases or conditions in which it is desirable to decrease the level of T lymphocyte activity, the method comprising administering to a mammal in need of such treatment a pharmaceutically effective amount of a compound as defined above.

In a further aspect, the invention provides methods for treatment and/or prophylaxis of parasitic infections, particularly those caused by protozoan parasites, the method comprising administering to a mammal in need of such treatment a pharmaceutically effective amount of a compound as defined above.

In further aspects, the invention provides methods of preparing compounds of formula (I) as defined above.

While the invention is broadly as defined above, it is not limited thereto and also includes embodiments of which the following description provides examples.

DESCRIPTION OF THE INVENTION

This invention provides novel compounds of the formula (I) as defined above, which are potent inhibitors of purine nucleoside phosphorylase, nucleoside hydrolases and/or phosphoribosyltransferases.

The compounds of the invention are therefore expected to have clinical utility in treating conditions in which it is desirable to decrease the level of T lymphocyte activity, such as T-cell malignancies and autoimmune diseases, including arthritis and -lupus. The invention also contemplates use of the compounds for immunosuppression for organ transplantation and for inflammatory disorders. The compounds of the invention are also expected to have utility in methods of treatment and/or prophylaxis of parasitic infections, particularly those caused by protozoan parasites, such as Giardia, Trichomonas, Leishmania, Trypanosoma, Crithidia, Herpetomonas, Leptomonas, Histomonas, Eimeria, Isopora and Plasmodium.

The compounds of formula (I) of the invention may be prepared by the methods described below:

Method A

This method may be used to prepare compounds of the formula (I) in which A is CR, where R is as defined above; ie compounds which are substituted at

C-8 of the 9-deazapurine moiety.

The method comprises reacting a compound of formula (II)

(ID

wherein R⁹ is an alkoxycarbonyl or aralkyloxycarbonyl group, Z' is a hydrogen or halogen atom, a group of formula SQ or OQ, or a trialkylsilyloxy, alkyldiarylsilyloxy or optionally substituted triarylmethoxy group and Q is an optionally substituted alkyl, aralkyl or aryl group, and R⁶ is an N-protecting group, B' and D' are independently selected from H, OR⁷ and N(R⁸)₂, and R⁷ and R⁸ are 0- and N- protecting groups respectively;

(i) with a strong base capable of deprotonation at C-8 of the 9- deazapurine moiety; then (ii) with an electrophile; and

(iii) O- and N-deprotecting the product by acid-, alkali- or fluoride ion- catalyzed hydrolysis or alcoholysis or catalytic hydrogenolysis as required for the O- and N-protecting groups in use.

Suitable strong bases are butyllithium and tert-butyllithium. Suitable electrophiles are N-fluorosulfomidobenzeme, alkyl halides such as methyl iodide, aldehydes such as acetaldehyde, or formylating agents such as dimethylformamide.

A compound of formula (II) can be prepared as described in the applicants' PCT International patent application PCT/NZ00/00048 entitled "Processes for preparing inhibitors of nucleoside metabolism" and filed on 7 April 2000, by N-protection of the product obtained by the coupling of a 1 ,N-dehydro-

1 ,4-dideoxy-1 ,4-imino-D ribitol derivative with a protected 7-halogeno- deazapurine derivative (therein described as pyrrolopyrimidine derivatives).

More specifically, a compound of the formula (II) can be prepared by the following process:

(a) reacting a compound of the formula (IV)

(IV)

wherein Z' is a hydrogen or halogen atom, a group of formula SQ or OQ, or a trialkylsilyloxy, alkyldiarylsilyloxy or optionally substituted triarylmethoxy group and Q is an optionally substituted alkyl, aralkyl or aryl group, sequentially with a halogenating agent and a sterically hindered base to form an imine;

(b) condensing the imine thus prepared with an anion produced by abstraction of the bromine or iodine atom from a compound of formula (XIX): wherein R⁵ is a bromine or iodine atom, R⁶ is an N-protecting group, B' and

D' are independently selected from H, OR⁷ and N(R⁸)₂, and R⁷ and R⁸ are O- and N- protecting groups respectively, to produce a 1 -C-(pyrrolo[3,2- c/]pyrimidin-7-yl)-1 ,4-dideoxy-1 ,4-imino-2,3-0-isopropylidene-D-ribitol derivative of formula (II) as defined above, but in which R⁹ is a hydrogen atom; and

(c) converting the compound to a compound of formula (II) in which R⁹ is alkoxycarbonyl or aralkoxycarbonyl.

The compounds of formula (II) where R⁹ is a hydrogen atom can be converted into compounds of formula (II) where R⁹ is an alkoxycarbonyl or aralkoxycarbonyl group by N-protecting with an appropriate compound containing the desired alkoxycarbonyl or aralkoxycarbonyl moiety. A suitable

N-protecting group is the terf-butoxycarbonyl group, which can be introduced by the use of ferf-butyl dicarbonate, for example in methylene chloride followed by chromatography.

The halogenating agent used in step (a) above may conveniently be N- chlorosuccinimide; and the hindered base used in step (a) may conveniently be lithium tetramethyl piperidide.

In step (b) above the bromide or iodine atom may conveniently be abstracted from the compound of formula (XIX) using butyllithium or magnesium.

The N-protecting group R⁶ in the compound of formula (XIX) may conveniently be an alkoxymethyl group (such as benzyloxymethyl), a silyl group (such as tert-butyldimethylsilyl) or an arylmethyl group (such as benzyl). The O-protecting group R⁷ may conveniently be an alkyl or arylmethyl group (such as methyl, fe/ -butyl or benzyl), and each N- protecting group R⁸ may conveniently be independently an arylmethyl group (such as benzyl or 4-methoxylbenzyl), or the two R⁸ groups together may form the 2,4-hexadien-2,5-yl group.

The compounds of formula (XIX) defined above may be prepared by known methods. Compounds of the formula (IV) defined above may also be prepared by known methods, for example as described in WO 99/1 9338 and the references cited therein.

Method B

This method may be used to prepare compounds of the formula (I) in which W is H (ie 3'deoxy compounds of formula (I)).

This method comprises reacting a compound of formula (III)

(III)

wherein R⁹ is an alkoxycarbonyl or aralkyloxycarbonyl group, Z' is a hydrogen or halogen atom, a group of formula SQ or OQ, or a trialkylsilyloxy, alkyldiarylsilyloxy or optionally substituted triarylmethoxy group and Q is an optionally substituted alkyl, aralkyl or aryl group, and R⁶ is an N-protecting group, B' and D' are independently selected from H, OR⁷ and N(R⁸)₂, R⁷ and R⁸ are 0- and N-protecting groups, respectively, and R¹⁰ is an O-protecting group;

1) with a thiocarbonylating agent; then i) with a radical reducing agent; and (iii) O- and N-deprotecting the product by acid-, alkali- or fluoride ion- catalyzed hydrolysis or alcoholysis or catalytic hydrogenolysis as required for the 0- and N-protecting groups in use.

Together, steps (i) and (ii) are known as the Barton deoxygenation sequence. Suitable thiocarbonylating agents are thiocarbonyl diimidazole, phenoxythiocarbonyl chloride, or the combination of a base, carbon disulfide and methyl iodide. Suitable radical reducing agents are tributyltin hydride and lauroyl peroxide.

A compound of formula (III) can be prepared from a compound of formula (II) above by:

(i) removal of the 2,3-O-isopropylidene group by acid-catalyzed hydrolysis;

(ii) N-protection;

(iii) selective reprotection of the 5'-hydroxy-group if necessary; and

(iv) selective reprotection of the 2'-hydroxy-group.

Step (i) can conveniently be conducted by treatment with trifluoroacetic acid in an aqueous organic solvent under reflux. Certain 5'-0-protecting groups, such as a ferf-butyldimethyl silyl group, may simultaneously be removed under these conditions, necessitating reprotection in step (iii). Reprotection can conveniently be achieved by treatment with a reagent capable of effecting selective protection of a primary hydroxy group in the presence of a secondary hydroxy group, such as trityl chloride and base.

A suitable N-protecting group is the fert-butoxycarbonyl group, which can be introduced by the use of ferf-butyl dicarbonate in step (ii).

Selective protection of the 2'-hydroxy-group can be effected by activation of the 2',3'-diol as a stannylidene acetal, e.g. by reaction with dibutyltin oxide, and fluoride ion catalyzed reaction with a reagent capable of delivering an O- protecting group, such as 4-methoxybenzyl chloride and base.

Three preferred compounds of the present invention are:

(1 S)-1 -(9-deaza-8-fluorohypoxanthin-9-yl-1 ,4-dideoxy-1 ,4-imino-D- ribitol;

(1 S)-1 -(9-deaza-8-methylhypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4-imino-D- ribitol; and (1 S)-1 -(9-deazahypoxanthin-9-yl)-1 ,3,4-trideoxy-1 ,4-imino-D-ribitol.

These compounds may conveniently be prepared as their hydrochloride salts.

The compounds of the invention are useful both in free base form and in the form of salts. The term "pharmaceutically acceptable salts" is intended to apply to non-toxic salts derived from inorganic or organic acids, including for example salts derived from the following acids - hydrochloric, sulfuric, phosphonic, acetic, lactic, fumaric, succinic, tartaric, gluconic, citric, methanesulphonic and p-toluenesulphonic acids.

The dosage of the compound to be administered can vary widely according to the nature of the patient and the disorder being treated. However, typically the dosage for an adult human will be in the range of 0.1 -1000 mg. The compounds can be administered in combination with one or more conventional pharmaceutical carriers or excipients and may be administered orally, by injection or topically.

The invention will be described in more detail with reference to the following non-limiting examples. EXAMPLES

Example 1

Preparation of B-0"fe^butyldimβthylsllyl-1_>Λ ^t ehy ι-0'1 >4-didet»xy''1_>4-i l_ιθ''

2,3-O-isoprόpylldehe-D-ribitol.

5-0-tert-Butyldimethylsilyl-1 ₎4''dideoxy-1 )4-imiho-2)3ⁱ-Oⁱ'lsDpropylidehe-'D-¹ ribitol wa& treated With Nβθ arid then lithium tetfamethyløiperidlde' as described previously (Evans, G.B.; Furnead*. R.H.j eaihSford* G.d„. έchrarnim V.I . J Ty!er> P_(5. T fihMr ή 200tij B&_> 305$). The tsetid reaction mixture as partitioned between petroleum ether ana watef and prαoeassea nsrinaiiy. C3hromatά^.aphy ϋf the residue (EtOΑ yPS dlέiJiti B^frirϊⁱBϋ yidlhiB hylSllyl'ⁱ

yield which WeiB usfe directly,

Example 2

Preparation of 7-_V-benzyloxymethyl-9-bromo-9-deaza-6-0-ethylhypoxanthine.

Sodium hydride (1 .88 g, 60 % dispersion, 47 mmol) was added to a stirred suspension of 6-chloro-9-deazapurine (K. Imai, Chem. Pharm. Bull. 1964, 12, 1030) (5.19 g, 33.8 mmol) in THF (80 mL) and the resulting mixture was stirred in an ice bath while benzyl chloromethyl ether (6 mL, 43 mmol) was added slowly. The mixture was then stirred at room temperature for 1 h. Methanol (20 mL) and sodium hydride (1 .6g, 60 %, 40 mmol) were added carefully and then after 1 h NBS was added portion-wise until t.l.c. analysis indicated the initial material was replaced by a less polar product. The solution was washed with water (x2), and processed normally.

Chromatography afforded 7-N-benzyloxymethyl-9-bromo-9-deaza-6-0- methylhypoxanthine (6.83 g, 19.6 mmol) as a solid. Recrystallized from ethanol it had m.p. 98-99 °C; ¹H NMR δ 8.60 (s. 1 H), 7.44 (s, 1 H), 7.35- 7.21 (m, 5H), 5.71 (s, 2H), 4.48 (s, 2H), 4.1 1 (s, 3H); ¹³C NMR δ 1 56.8 (C), 1 51 .4 (CH), 148.8, 136.9 (C), 131 .9, 1 28.9, 1 28.5, 128.0 (CH), 1 1 6.0, 92.8 (C), 77.6, 70.8 (CHa), 54.2 (CHs). Anal. calc. for Ci₅Hi₄BrN₃02: C, 51 .74; H, 4.05; Br, 22.95; N, 12.07. Found: C, 51 .97; H, 3.91 ; Br, 23.19;

N, 1 2.28.

Example 3

Preparation of 7-ΛΛbenzyloxymethyl-9-bromo-6-0-fe_?-butyf-9- deazahypoxanthine.

Sodium hydride (60 % dispersion, " 1 .5 g) was added slowly to a stirred suspension of 6-chloro-9-deazapurine (5.0 g) and chloromethyl benzyl ether (6 mL) in dry THF (100 mL) in an ice bath until effervescence had ceased.

Then terf-butyl alcohol (20 mL), DMF (20 mL) and more sodium hydride (60 %, 1 .5 g) were added, the cooling bath was removed and the mixture was stirred at rt for 24 h. Chloroform (200 mL) was added and the mixture was washed with water (x2) and processed normally. A solution of the crude residue in chloroform (50 mL) was stirred in an ice bath while NBS ( ^" 5 g] was added portion-wise until TLC indicated the reaction was complete. Chromatography then afforded 7-Λ/-benzyloxymethyl-9-bromo-6-0-ferf-butyl- 9-deazahypoxanthine as a pale yellow solid (5.8 g). ¹H NMR (CDCU) δ 8.55 (1 H, s), 7.41 (1 H, s), 7.34-7.20 (5H, m), 5.73 (2H, s), 4.48 (2H, s), 1 .69 (9H, s); ¹³C NMR (CDCla) δ 1 56.3 (C), 151 .1 (CH), 148.7, 137.1 (C), 131 .4,

1 28.9, 1 28.4, 1 27.8 (CH), 1 17.0, 92.6, 84.0 (C), 77.6, 70.5 (CH2), 29.0 (CHs). Example 4

Preparation of 1 «(S)-(7- \ »benEyloxymethyl^tO-(!)-te/'f*butyl-i9-' deazahypoxanthin-Q-yl)*Λ -fβ^butoxycarbόnyl-δ-0"te^butyldimethylsilyl-l ;4- dideoxy-1 ,4^iminό'-2>3-0-isopropylidene*D-ribitόl.

A solution of the product from example 3 (2.7 g) in anisole (20 mL) and ether (40 L) Was cooled to - 60 °C and butyl lithium (2.9 L, 2.4 M in hexanes) wa added; Then a solution of the product from example 1 (1 ;6 g) in ether (5 mL) Was added. The solution was allowed to warm slowly tb 10

°C and then ashed with water, dried and concentrated to dryhesa. Chromatόgraphy afforded the product mixed With the denomi ated deazahypoKanthine derivative. This mixture a§ issolved ih

isopfόpylldene-b^ibitoi (ΪΪ a).

Example 5

Preparation of 1 -(5)-(7-/V-benzyloxymethyl-9-deaza-6-0-methylhypoxanthin-9- yl)-_A/-ferf-butoxycarbonyl-5-0-ferf-butyldimethyisilyl-1,4-dideoxy-1,4-imino-

2,3-O-isopropylidene-D-ribitol.

A solution of the product from example 2 (16.0 g, 46 mmol) in anisole (1 20 mL) and ether (200 mL) was treated with butyl lithium at - 35 ° C and then the product from example 1 as described above in example 4. The crude product in methylene chloride (100 mL) was treated with di-ferf-butyl dicarbonate (8.0 g, 36 mmol) and the solution was stirred for 1 h, then concentrated to dryness. Chromatography of the residue afforded 1 -(S)-(7- Λ/-benzyloxymethyl-9-deaza-6-0-methylhypoxanthin-9-yl)-Λ -ferf- butOxyoal-bortyl-δ-O-ferf-butyldimethylsiiyi-l

Isoprbpylldθhb-D'ribitol (18.8 g, B.J mmol) £& & ayrup. ¹H N R (d_D. at 70 °C) δ 8.67 (1 H, s), 7.48 (1 H, br s), 7.09 (5H, m), 5.78 (1 H, br s), 5.67 (1 H, s), 5.44 (1 H, br s), 5.25 (2H, s), 4.54 (1 H, br s), 4.23 (2H, s), 4.09 (1 H, t, J = 9.7 Hz), 3.97 (1 H, br s), 3.77 (3H, s), 1.57 (3H, s), 1 .42 (9H, s), 1 .33

(3H, s), 0.97 (9H, s), 0.1 1 (6H, s); ¹³C NMR (CeDe at 70 °C) δ 1 56.7, 1 54.8 (C), 150.4 (CH), 149.4, 13,7.9, 133.8, 1 16.4, 1 1 1.9 (C), 84₍.6, 84.0 (CH), 79.6 (C), 77.3, 70.4 (CH2), 67.7 (CH), 63.4 (CH₂), 61 .9 (CH), 53.0 (CHs), 28.7, 27.9, 26.3, 25.8 (CHs), 18.6 (C), -4.9, -5.0 (CHs). Some aromatic signals were obscured by the solvent. HRMS (MH⁺) calc. for C3 HδiN 07Si:

655.3527. Found: 655.3553.

Example 6

Preparation of (1S)-1-(9-deaza-8-fluorohypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4- imino-D-ribitol hydrochloride.

A solution of the product from example 4 (1 .25 g) in THF (30 mL) was cooled to - 70 °C and butyl lithium (1 .5 mL, 2.4 M in hexanes) was added slowly. After 10 mins /V-fluorobenzenesulfonimide (1 .42 g) was added to the red/brown solution. After 20 mins the solution was partitioned between water and chloroform. The organic phase was processed normally and chromatography afforded 1 -(_S)-(7-Λ/-benzyloxymethyl-6-0-ferf-butyl-9-deaza- 8-fluorohypoxanthin-9-yl)-Λ/-ferf-butoxycarbonyl-5-0-ferf-butyldimethylsilyl- 1 ,4-dideoxy-1 ,4-imino-2,3-0-isopropylidene-D-ribitol (0.67 g). A solution of

0.2 g of this material in THF (5 mL) and methanol (5 mL) was stirred with tetrabutylammonium fluoride (5 mL, 1 M in THF) for 18 h. The solution was concentrated and a solution of the residue in toluene (15 mL) was washed with water (x2), dried and concentrated to dryness. The residue in ethanol (10 mL) was stirred under hydrogen in the presence of 10 % Pd/C (0.2 g) for

18 h. The solids and solvent were removed and chromatography afforded two products, one with and one without the 6-O-ferf-butyl residue on the hypoxanthine moiety. These were combined in methanol (4 mL) and 2M aq HCI (4 mL) was added. After 2 h the solution was concentrated to dryness and the residue was recrystallised from aq acetone to give (1 S)-1 -(9-deaza-8- fluorohypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4-imino-D-ribitol hydrochloride (0.043 g). ¹H NMR (D2O) δ 8.04 (1 H, s), 4.97-4.88 (2H, m), 4.48 (1 H, t, J = 4.1

Hz), 3.93 (2H, m), 3.89 (1 H, dd, J = 4.6, 9.0 Hz). Anal. calc. for CnH CIFN4θ4: requires C, 41.20; H, 4.40; Cl, 1 1 .05; N, 17.47. Found: C, 41 .01 ; H, 4.37; Cl, 1 1.1 1 ; N, 1 7.17.

Example 7

Preparation of (1S)-1-(9-deaza-8-methylhypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4- imino-D-ribitol hydrochloride.

A solution of the product from example 5 (0.29 g) in THF (7 mL) was cooled to - 70 °C and butyl lithium (0.4 mL, 2.4 M in hexanes) was added slowly. After 10 mins methyl iodide (0.25 mL) was added and 10 mins later the solution was partitioned between chloroform and water and the organic layer was processed normally followed by chromatography affording the 8-C- methyl product (0.164 g). This material in ethanol (5 mL) was stirred under hydrogen with 10 % Pd/C (0.1 g) for 3 days. Removal of the solids and solvent and chromatography afforded 1 -(S)-(9-deaza-6-0-methylhypoxanthin- 9-yl)-/V-ferf-butoxycarbonyl-1 ,4-dideoxy-1 ,4-imino-2,3-0-isopropylidene-D- ribitol (0.089 g). A solution of this material in methanol (3 mL) and cone aq HCI (3 mL) was heated under reflux for 2 h and then concentrated to dryness to give (1 S)-1 -(9-deaza-8-methylhypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4-imino-D- ribitol hydrochloride (0.061 g) as a white solid. ¹H NMR (DaO) δ 8.46 (1 H, s), 4.96 (1 H, dd, J = 9.4, 4.6 Hz), 4.89 (1 H, d, J = 9.5 Hz), 4.51 (1 H, m), 4.07 (2H, m), 3.96 (1 H, m,), 2.54 (3H, s). Anal. calc. for C.₂Hι₇CI ₄θ : C, 45.50; H, 5.41 ; Cl, 1 1 .19; N, 1 7.69. Found: C, 45.38; H, 5.41 ; Cl, 1 1 .50;

N, 1 7.80. Example 8

Preparation of 1 -(S)-(7-/V-benzyloxymethyl-9-deaza-6-0-methylhypoxanthin-9- yl)-1 ,4-dideoxy-1 ,4-imino-2,3-0-isopropylidene-D-ribitol.

A solution of the product from example 2 (4.4 g, 12.6 mmol) in anisole (60 mL) and ether (100 mL) was treated with butyl lithium and then the product from example 1 (2.4 g, 8.4 mmol) as described above in example 4, except that it was not treated with di ferf-butyl-dicarbonate. Tetrabutylammonium fluoride (1 5 mL, 1 M in THF) was added to a solution of the crude product in

THF (20 mL) and after 1 h toluene (100 mL) was added and the solution was washed with water (x2) and then processed normally. Chromatography afforded syrupy 1 -(S)-(7-/V-benzyloxymethyl-9-deaza-6-0-methylhypoxanthin- 9-yl)-1 ,4-dideoxy-1 ,4-imino-2,3~0-isopropylidene-D-ribitol (2.27 g, 5.1 6 mmol). ¹H NMR (CDCh) δ 8.51 (s, 1 H), 7.38 (s, 1 H), 7.35-7.22 (m, 5H),

5.73 (d, J = 10.6 Hz, 1 H), 5.65 (d, J = 10.6 Hz, 1 H), 4.89 (t, J = 5.7 Hz, 1 H), 4.77 (dd, J = 6.0, 2.1 Hz, 1 H), 4.50 (d, J = 5.5 Hz, 1 H), 4.48 (s, 2H), 4.09 (s, 3H), 3.74 (s, 1 H), 3.73 (s, 1 H), 3.64 (dd, J = 5.3, 2.9 Hz, 1 H), 1 .61 (s, 3H), 1 .36 (s, 3H); ¹³C NMR δ 1 56.8 (C), 150.1 (CH), 149.2, 137.3 (C), 130.9, 1 28.8, 128.4, 128.0 (CH), 1 18.3, 1 17.1 , 1 13.1 (C),

86.1 , 83.9 (CH), 77.3, 70.6 (CHa), 64.7, 64.6 (CH and CHa), 62.5 (CH), 54.0, 28.2, 25.8 (CH_). HRMS (MH ⁺ ) calc. for C23H29N4O5: 441 .2138. Found: 441 .21 1 5.

Example 9

Preparation of ( 1 S)- 1 -(9-deazahypoxanthin-9-yl)- 1 ,3,4-trideoxy- 1 ,4-imino-D- ribitol hydrochloride.

A solution of the product from example 8 (2.27 g) in THF (30 mL), water

(1 2.5 mL) and trifluoroacetic acid (2.5 mL) was heated under reflux for 1 .5 h and then concentrated to dryness. The residue in methanol. (10 mL) was treated with triethylamine (1 .5 mL) and di ferf-butyl-dicarbonate (1 .67 g). After 1 h the solution was concentrated to dryness and chromatography afforded 1 -(S)-(7-Λ/-benzyloxymethyl-9-deaza-6-0-methylhypoxanthin-9-yl)-Λ/- ferf-butoxycarbonyl-1 ,4-dideoxy-1 ,4-imino-D-ribitol (2.28 g). To a solution of 1 .74 g of this material in dichloromethane (20 mL) was added diisopropylethylamine (2.4 mL), trityl chloride (1 .17 g) and 4- dimethylaminopyridine (0.13 g). After 16 h at room temperature more trityl chloride (1 .0 g) was added and after a further 8 h the solution was processed normally followed by chromatography to give 1 -(S)-(7-Λ/- benzyloxymethyl-9-deaza-6-0-methylhypoxanthin-9-yl)-Λ/-ferf- butoxycarbonyl-1 ,4-dideoxy-1 ,4-imino-5-0-triphenylmethyl-D-ribitol (2.27 g). Dibutyltin oxide (0.17 g) was added to a solution of 0.5 g of this material in benzene (15 mL) and the mixture was heated under reflux under a Dean Stark apparatus for 1 h. Then tetrabutylammonium bromide (0.217 g) and 4- methoxybenzyl chloride (0.1 83 mL) were added and the solution was heated under reflux for 16 h. After concentrating to dryness chromatography of the residue afforded 1 -(S)-(7-Λ/-benzyloxymethyl-9-deaza-6-0-methylhypoxanthin- 9-yl)-N-fert-butoxycarbonyl-1 ,4-dideoxy-1 ,4-imino-2-0-(4-methoxybenzyl)-5- O-triphenylmethyl-D-ribitol (0.377 g) as the major product. A solution of this material in toluene (5 mL) containing thiocarbonyl diimidazole (0.148 g) was heated under reflux for 1 h. Tributyltin hydride (1 mL) was added and the solution was refluxed for a further 0.5 h. After concentrating to dryness the residue in acetonitrile was washed (x2) with petroleum ether and concentrated to dryness. Chromatography of the residue then afforded 1 - (S)-(7-N-benzyloxymethyl-9-deaza-6-0-methylhypoxanthin-9-yl)-Λ/-ferf- butoxycarbonyl-1 ,4-imino-2-0-(4-methoxybenzyl)-1 ,3,4-trideoxy-5-0- triphenyimethyl-D-ribitol (0.204 g). This material was suspended in cone. aq. HCI (5 mL) and the mixture was heated under reflux for 1 h, cooled and concentrated to dryness. Water (10 mL) was added to the residue and the mixture was extracted (x2) with chloroform. The aqueous phase was concentrated to dryness and chromatography of the residue afforded a white solid which was treated with aq. HCI and lyophilised to give (1 S)-1 -(9- deazahypoxanthin-9-yl)-1 ,3,4-trideoxy-1 ,4-imino-D-ribitol hydrochloride (0.06 g) as a white solid. ¹H NMR (D2O) δ 7.95 (1 H, s), 7.68 (1 H, s), 4.95-4.84 (2H, m), 4.21 (1 H, m), 3.97 (1 H, dd, J = 3.8, 1 2.6 Hz), 3.83 (1 H, dd, J = 6.7, 12.6 Hz), 2.46 (1 H, m), 2.30 (1 H, m); ¹³C NMR δ 1 57.5, 146.0 (C), 145.3, 131 .4 (CH), 1 20.4, 1 10.8 (C), 76.2, 63.8 (CH), 63.1 (CH2), 62.7 (CH), 36.6 (CH2). HRMS (MH) calc. for C11H15N4O3: 251 .1 144. Found: 251 .1 133.

Determination of inhibition constants for bovine purine nucleoside phosphorylase

The inhibition constants for the compounds (1 S)-1-(9-deaza-8- fluorohypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4-imino-D-ribitol hydrochloride, (1 S)-1 - (9-deaza-8-methylhypoxanthin-9-yi)-1 ,4-dideoxy-1 ,4-imino-D-ribitol hydrochloride and (1 S)-1 -(9-deazahypoxanthin-9-yl)-1 ,3,4-trideoxyl-1 ,4- dideoxy-1 ,4-imino~D-ribitol hydrochloride were determined as described in Miles et al (Biochemistry 37, 8615 (1998)) using bovine purine nucleoside phosphorylase (Sigma). Ki* is the equilibrium dissociation constant for the PNP»inhibitor complex following slow-onset inhibition. It governs the biological properties of PNP inhibition. Not all inhibitors exhibit slow-onset binding, and others have not been experimentally examined for slow-onset inhibition. Where known, slow-onset properties are indicated. Ki and Ki* values determined are shown below.

2/3 partial inhibition only

no slow onset

Although the invention has been described with reference to specific embodiments, those persons skilled in the art will appreciate that variations and modifications can be made without departing from the scope of the invention.

INDUSTRIAL APPLICABILITY

The compounds of the present invention are potent inhibitors of purine nucleoside phosphorylase, nucleoside hydrolases and/or phosphoribosyl transferases. The compounds are therefore expected to have utility in treating conditions such as T-cell malignancies and autoimmune diseases. The compounds may also be useful in immunosuppression for organ transplant and inflammatory diseases.

In addition, the compounds of the invention are expected to be useful in the treatment and/or prophylaxis of parasitic infections, particularly those caused by protozoan parasites.

Claims

A compound of the formula:

W X

(I) wherein:

A is selected from N, CH and CR, where R is selected from halogen, optionally substituted alkyl, aralkyl and aryl, OH, NHa, NHR¹, NR¹R² and SR³, where R\ R² and R³ are each optionally substituted alkyl, aralkyl or aryl groups;

B is selected from OH, NH2, NHR⁴, H and halogen, where R⁴ is an optionally substituted alkyl, aralkyl or aryl group;

D is selected from OH, NH2, NHR⁵, H, halogen and SCH3, where R⁵ is an optionally substituted alkyl, aralkyl or aryl group;

Z is OH, or, when X is hydroxy, Z is selected from hydrogen, halogen, hydroxy,

SQ and OQ, where Q is an optionally substituted alkyl, aralkyl or aryl group; and W is OH or H, with the proviso that when W is OH, then A is CR where R is as defined above;

2. A compound as claimed in claim 1 wherein B is NHR⁴ and/or D is NHR⁵, and R⁴ and/or R⁵ are Cι-C₄ alkyl.

3. A compound as claimed in claim 1 or claim 2 wherein when one or more halogens are present, they are chosen from chlorine or fluorine.

4. A compound as claimed in any one of claims 1 -3 wherein when Z is SQ or OQ, Q is C1-C5 alkyl or phenyl.

5. A compound as claimed in claim 1 wherein either D is H, or B is OH, or both.

6. A compound as claimed in claim 1 wherein B is OH, D is H, OH or NH₂, X is OH or H and Y is H.

7. A compound as claimed in any one of claims 1 -3 wherein Z is OH, H or methylthio.

8. A compound as claimed in any one of claims 1 -7 wherein W is OH, Y is H,

X is OH, and A is CR where R is methyl or halogen.

9. A compound as claimed in any one of claims 1 -7 wherein W is H, Y is H, X is OH and A is CH.

10. A compound as claimed in claim 1 selected from

(1 S)-1 -(9-deaza-8-fluorohypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4-imino-D-ribitol; (1 S)-1 -(9-deaza-8-methylhypoxanthin-9-yl)-1 ,4-dideoxy-1 ,4-imino-D-ribitol; or

(1 S)-1 -(9-deazahypoxanthin-9-yl)-1 ,3,4-trideoxy-1 ,4-imino-D-ribitol; or a tautomer thereof; or a pharmaceutically acceptable salt thereof.

1 1 . A pharmaceutical composition comprising a pharmaceutically effective amount of a compound of the formula (I) as claimed in any one of claims 1 -10, and a pharmaceutically acceptable carrier or diluent.

1 2. A method for treatment of a disease or condition in which it is desirable to decrease the level of T lymphocyte activity, the method comprising administering to a mammal in need of such treatment a pharmaceutically effective amount of a compound as claimed in any one of claims 1 -10.

13. A method for treatment and/or prophylaxis of a parasitic infection, the method comprising administering to a mammal in need of such treatment a pharmaceutically effective amount of a compound as claimed in any one of claims 1 -10.

14. A method as claimed in claim 13 wherein the parasitic infection is caused by protozoan parasites.

15. A method for preparing a compound of the formula (I) as defined in claim 1 , wherein A is CR and R is as defined in claim 1 , the method comprising reacting

(ID a compound of formula (II)

wherein R⁹ is an alkoxycarbonyl or aralkyloxycarbonyl group, Z' is a hydrogen or halogen atom, a group of formula SQ or OQ, or a trialkylsilyloxy, alkyldiarylsilyloxy or optionally substituted triarylmethoxy group and Q is an optionally substituted alkyl, aralkyl or aryl group, and R⁶ is an N-protecting group, B' and D' are independently selected from H, OR⁷ and N(R⁸)₂, and R⁷ and R⁸ are O- and N- protecting groups respectively;

(i) with a strong base capable of deprotonation at C-8 of the 9-deazapurine moiety; then

(ii) with an electrophile; and

(iii) O- and N-deprotecting the product by acid-, alkali- or fluoride ion-catalyzed hydrolysis or alcoholysis or catalytic hydrogenolysis as required for the O- and N- protecting groups in use.

16. A method as claimed in claim 15 wherein the strong base comprises butyllithium.

17. A method for preparing a compound of the formula (I) as defined in claim

1 , wherein W is H, the method comprising reacting a compound of formula (III)

(III)

wherein R⁹ is an alkoxycarbonyl or aralkyloxycarbonyl group, Z' is a hydrogen or halogen atom, a group of formula SQ or OQ, or a trialkylsilyloxy, alkyldiarylsilyloxy or optionally substituted triarylmethoxy group and Q is an optionally substituted alkyl, aralkyl or aryl group, and R⁶ is an N-protecting group, B' and D' are independently selected from H, OR⁷ and N(R⁸ , R⁷ and R⁸ are 0- and N-protecting groups, respectively, and R¹⁰ is an O-protecting group;

(i) with a thiocarbonylating agent; then

(ii) with a radical reducing agent; and

(iii) 0- and N-deprotecting the product by acid-, alkali- or fluoride ion-catalyzed hydrolysis or alcoholysis or catalytic hydrogenolysis as required for the O- and N- protecting groups in use.

18. A method as claimed in claim 17 wherein the thiocarbonylating agent is thiocarbonyl diimidazole.

19. A method as claimed in claim 17 or claim 18 wherein the radical reducing agent comprises tributyltin hydride.