AU734992B2 - A solid-phase technology for the preparation of combinatorial libraries through amide-bond anchoring - Google Patents

Description

WO 99/26902 PCT/GB98/03523 1 A Solid-Phase Technology for the Preparation of Combinatorial Libraries Through Amide-bond Anchoring Introduction Combinatorial chemistry techniques, which are methods for the parallel preparation of many molecules compared to traditional single serial techniques, have the potential to play a pivotal role in the design and development of drug-like molecules. International Application No. WO 97/40065 describes a combinatorial library technology which has been developed as a tool to accelerate the development of inhibitors of proteolytic enzymes. A protease is screened against a large addressable library of potential protease substrates, swiftly providing an assay for proteolytic activity based upon internally quenched fluorescence. Along with the establishment of a sensitive assay, a wealth of substrate structure-activity data is gathered which may be used in the design of an inhibitor.

International Application No. WO 98/17628 describes a novel solid-phase methodology allowing flexible variation of the N and C termini of a discrete target compound, or a combinatorial approach leading to parallel preparation of many analogues of a target compound. This approach allows for great flexibility in the primary sequence assembly of many chemical classes of compound libraries.

However, a potential limitation to International Application No. WO 98/17628 may be encountered when considering a further level of complexity in library synthesis the absolute chiral integrity of all chiral centres in the target molecules. Under certain circumstances the Ca terminal amino acid of an assembled sequence can undergo epimerisation with the resulting loss of chiral integrity.

Here, a chemical method for the C-terminal activation and coupling of solid phase bound protected peptide and peptidomimetic sequences, with no Ca epimerisation, is described. The method allows the synthesis of combinatorial SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 2 libraries where full flexibility of the choice of required residues is needed for the target compounds.

It will readily be appreciated by those skilled in the art that a general solid phase combinatorial route to the desired molecule would not be restricted to the development ofpeptides but would include non-peptides and also those containing peptidomimetics. Moreover, any molecule useful for any type of interaction e.g.

receptor agonists, antagonists for which these molecules exhibit activity may be developed in a combinatorial manner. Here, a novel solid-phase methodology is described allowing the flexible variation of required residues, and allowing a combinatorial approach leading to parallel preparation of many molecules.

Background Chemistry The Current Problem Solid phase based syntheses utilise a cross-linked polymer (a resin support) which is functionalised with a chemically reactive unit (a linker). A functional group (carboxylic acid, amine, hydroxyl, sulphydryl etc) from an initial intermediate of the final desired compound is reversibly and covalently attached to the resin through the linker. Sequential chemical transformations of this now resin-bound intermediate to the final compound are then performed. At each stage, excess and spent reagents are removed from the growing resin-bound product by simple filtration and washing this being the overriding factor providing expedient synthesis compared to solution based synthesis. As a final step, the fully assembled product is released from the solid support by cleavage of the covalent bond between the linker and product functional group.

Traditional solid phase peptide synthesis utilises a linker derivatised resin support to which the Ca carboxyl of the C-terminal residue is covalently attached.

The desired sequence is sequentially assembled (using individual elements at each stage to give a single final product or using mixtures of elements at each stage to give a mixture or 'library' of final products). Then the product is released into SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 solution by cleavage of the C-terminal residue linker bond. This provides the free C-terminal carboxylic acid. To provide alternative C-terminal functionalities different linkers have been developed. However virtually all linkers described to date release a functional group (carboxylic acid, amine, primary amide, hydroxyl, sulphydryl etc) present in the final product. Thus an obvious problem arises if the desired compound is devoid of one of the above functionalities. For example peptidyl acyloxymethyl ketones, a potent class of inhibitor of the cysteinyl protease Derp I, a major allergen of the house dust mite contain no obvious functional group by which a linker can attach an intermediate to a resin. Therefore current solid phase techniques cannot prepare many types of potential drug candidates as single discrete compounds let alone defined libraries of analogues.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 4 A Novel Solid-Phase Based Solution i) Strategy The only functional element that is always required to be present in the target molecule is a single secondary amide group. Thus, the attachment of initial intermediates through the conserved secondary amide group to a resin support provides a unique route to any class of linear compounds. Following subsequent solid phase assembly of the desired compound/s, the covalent bond between the linker and now tertiary amide is cleaved to regenerate the conserved secondary amide. During the sequential chemical transformations leading to the final secondary amide product, one has two options. Coupling reactions (the addition of a new chemical moiety providing a part of the final product) may be performed using single building blocks, leading to a single final product. Alternatively, each coupling stage may be performed using chemical mixtures, providing a combinatorial library of final products in which both the N and C terminal residues have been varied. This latter route greatly expands the number and range of drug-like molecules that may be accessed in an overall drug discovery programme.

ii)Chemistrv The vast majority of solid phase syntheses described over the last decade use side-chain functional group protection which is removed by acidolytic cleavage together with Na-protection removed by base. The wide range of commercially available building blocks is thus based upon this Scheme. A popular strategy in solid phase synthesis is, as a final synthetic step, the concomitant removal of side-chain protection along with product-linker cleavage. Thus, many linkers described in the literature are cleaved from the product by acidolytic treatment. A further desirable feature of a linker is the ability to readily derivatise with a wide range of reagents.

An ideal linker should therefore encompass all of the above properties.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 There are a number of backbone amide protecting groups which generate amides upon acidolytic treatment described in the literature. Johnson, Quibell and Sheppard have described the development of a backbone amide protection system.

This system (not a linker in its own right) was designed to protect the backbone amide of a peptide (previously attached to the resin through a C-terminal residuelinker moiety) during synthesis. Following completion of peptide assembly, the group was removed as a final step along with side-chain deprotection and peptidelinker cleavage by trifluoroacetic acid (TFA). It was found that the use of a 2hydroxyl rather than a 2-methoxy group allowed the subsequent acylation to be performed with a wide range of reagents, through an acyl transfer mechanism. In contrast, the 2-methoxy derivatised system cannot undergo the acyl transfer reaction and was found to have a very limited applicability.

The group of Barany have recently described a backbone amide linker. This linker does not contain the acyl transfer option during acylation and is therefore not of general applicability.

International Application No. WO 98/17628 describes a novel solid-phase methodology which contains an acyl transfer element along with the correct chemical properties of the backbone amide linker making the system compatible with a wide body of commercially available reagents. The linker provides the necessary chemistry to achieve the general goal, being the flexible combinatorial preparation of many libraries of different classes of drug-like molecules having both N and C terminal residues variable simultaneously.

However, this linker has the limitation that under certain circumstances a Ca terminal amino acid can undergo epimerisation with the resulting loss of chiral integrity. Classically, when reactions are performed in a particular sequence where an amino acid residue is activated in the absence of urethane protection, loss of chiral integrity may occur. An example of this is the preparation of backbone cyclised peptides. Here, the C-terminal amino acid residue of a peptide sequence is activated, without urethane protection, facilitating closure to a cyclic peptide and SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 6 may give significant epimersiation of the Ca of the activated amino acid residue.

This problem severely restricts the fully flexible synthesis of cyclic peptides, with full chiral integrity, to a method of preparation which relies on the activation of a glycine (achiral), or proline (good chiral stability) respectively.

Summary of the Invention In general, the present invention provides the means to suppress epimerisation of the Ca terminal amino acid of protected peptide sequence during coupling by using the protection moiety shown in which is referred to as a "precursor linker" by virtue of having the aldehyde group.

CHO

R

OH

(1) This moiety has a number of features; the functional group R and the 2hydroxyl function lie in a para position relative to each other while the ether residue lies in a para position relative to the aldehyde residue. RI is an electron donating alkyl group.

The R group is a moiety that.may readily be interconverted between electron- SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 7 withdrawing and electron donating. This is based on the safety catch principle. The principle, that a stable bond is smoothly converted to a labile one at a convenient point during a synthesis, has been applied in peptide chemistry for the development of linkers and protecting groups. One approach has been to exploit the facile reductive conversion of a sulphoxide to sulphide. This approach when applied to the precursor linker provides the functional protection moieties which are referred to as "linker compounds".

In a preferred aspect the present invention provides a resin linked compound of the general formula: *e* oe SUBSTITUTE SHEET (RULE 26) WO "/26902 WO 9926902PCT/GB98/03523

Y-N-R'

Liker-resin Y-N-R2 Linker-resin wherein the linker moiety has the general formula (B)

Z

R1CR 2

(B)

wherein X is (CHDnR3 where R3 is an -CO- g-roup for attachment to the terminal NH group of the solid phase through a standard bond eg carboxyl amide; R I is methyl or another such suitalble alkvl known in the art; n is between 2 and 12, preferably 4; Y is H or an Na functional g-roup protective moiety such as Fmoc; R2 is a variable residue; and R2' is an intermediate form of R-1 which is subsequently chemically transformed to give the desired R2.

In a further preferred aspect the present invention provides an alternative presentation of SUBSTITUTE SHEET (RULE WO 99/26902 PCT/GB98/03523 9 the linker whereby the attachment to the solid phase via X is through the ether residue of(B), as shown in 0 0 0* 0 00 0 0 00

(C)

wherein X is (CH~R3, where R3 is an -CO- group for attachment to the terminal NH group of the solid phase through a standard bond eg carboxyl amide; R1 is methyl or another such suitable alkvi known in the art; and n is between 2 and 12, preferably 4.

In a further preferred aspect the present invention provides an intermediate group of general formula Y-N-R2' LINKER RESIN for use in a method of preparation of a compound of general formula (A) SUBSTITUTE SHEET (RULE 26) P:\WPflOCSCRVShdIeySpcc747730.Wdc-74/01 R4-C-NH-R2 wherein R4 is a variable residue; and wherein the linker moiety has the general formula or (C) S 5* 0 S* SO S

S

S

555055

S

5*5*

S

.5.5 OSOfi

S

S

55..

0 4 5

/CHZ

KOS

O

RL-0 RI S6 P:\WPDOCS\CRN\ShcleySpcle7487730.spe.doc-17;4/01 9b wherein X is (CH 2 )nR3 where R3 is an -CO- group for attachment to the terminal NH group of the solid phase through a standard bond eg carboxyl amide; R1 is methyl or another such suitable alkyl known in the art; n is between 2 and 12, preferably 4; Y is H or an Na functional group protective moiety such as Fmoc; R2 is a variable residue; and 10 R21 is an intermediate form of R2 which is subsequently chemically transformed to give the desired R2.

In another preferred aspect of the invention there is provided an intermediate compound of general formula Y-N-R2

LINKER-RESIN

wherein the linker moiety has the general formula or (C) OS OH

RI*O

A LI (B) P:\WPDOCS\CRN\ShellU"ySpc7487730.spc.doc-17/4/01 9c 0OH a1 -SO

(C)

wherein X is (CH2)nR3 where R3 is an -CO- group for attachment to the terminal NH group of the solid phase through a standard bond eg carboxyl amide; R1 is methyl or another such suitable alkyl known in the art; n is between 2 and 12, preferably 4; Y is H or an Na functional group protective moiety such as Fmoc; g R2 is a variable residue; and R2' is an intermediate form of R2 which is subsequently chemically transformed to give the desired R2.

In yet a further preferred aspect of the invention, there is provided a method which comprises the steps of Scheme 1 described herein, for making a precursor linker compound of formula 1 for use in a method of preparation of a resin bound intermediate compound.

In a further preferred aspect of the invention there is provided a method which comprises the steps of Scheme 2, described herein, for making a precursor linker compound of formula 1 for use in a method of preparation of a resin bound intermediate compound.

P:\WPDOCSCRNLShellcySpe s7487730.spe.doc-17/4/01 9d In further preferred aspects the invention provides methods which comprise the steps of Scheme 3 or Scheme 4, described herein.

In yet a further preferred aspect of the invention there is provided a method which comprises the steps of i) forming a plurality of intermediate resin linked compounds Y-N-R2' Linker-resin or .Y-N-R2 Linker-resin ii) forming from said intermediates a plurality of resin linked compounds having variable residues R4 and R2 or R4 and R2' therein; iii) Cleaving the compounds from the linkers to produce a plurality of compounds of general formula A; and iv) optionally transforming R21 to R2 either before or after cleavage; whereby the product of step (iii) or (iv) provides a combinatorial library of compounds of formula In yet a further preferred aspect of the present invention there is provided a method which comprises the steps of Scheme 5, for producing a compound of general formula Ac-X-X-X-X-AMC.

P:\WPDOCS\CRN\Shcllc)Spec\7487730.sp.doc 740 9e In a further preferred aspect of the present invention provides a resin linked compound which is the product of step of Scheme 3 or the product of step of Scheme 4 (optionally having one or both protective groups shown in said Schemes varied to be another protective group).

The compounds of the invention may be utilised for the preparation of a combinatorial library of compounds of general formula R4-CO-NH-R 2 wherein R 4 and R 2 are both variable residues.

10 Further aspects of the present invention will become apparent from the 'description provided herein after.

Definition: As used herein the term is (CH 2 )nR3" is to be understood to encompass embodiments in which (CH 2 is selected from: a linear alkyl group; WO 99/26902 PCT/GB98/03523 a branched alkyl group; and a non-aromatic ring system which may optionally be attached to a linear or branched alkyl group.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT-/GB98/03523 Example Use of the Novel Technology Preparation of an Acid Derivative Precursor Linker of General Formula (1) The compound was prepared as detailed in Scheme 1. In that reaction scheme, the preparative steps were as follows: Scheme 1 Steps CuSO 4 NiI 4 SCN H 2 S0 4 Gii Isobutvlene DCM MeTf.

(iii) NaOH Dioxane H 2 0.

(iv) DMS0.

CH

3 1 Cs 2

CO

3

MEK.

(vi) NaBH 4 L EtOH H 2 0.

(vii) Methyl bromovalerate CS 2

CO

3

MIEK.

(Viii) POC1 3 /DMIF Dichloroethane.

(ix) LiOH /EtCH H 2 0.

SUBSTITUTE SHEET (RULE WO 99/26902 WO 9926902PCT/GB98/03523 Scheme 1.

OH

M

N OH OH

OH

S-/

0 )e (2) 3

M)

SOCH

3 -K 0 (iii) '0 d/1K b (iv)

IOH

SH

(3) I (vii) C OCH3

SZH

(6) 1 1- O OH OCH3 (Ni) H OCH3 I

OCH

3 S OCH 3 (8) SUBSTITUTE SHEET (RULE WO 99/26902 PCT/GB98/03523 13 General Experimental procedures Analytical HPLC was performed using a Phenomenex Jupiter C4 reversed phase column (250 x 4.6 mm id). Solvent system used: solvent A: 0.1% aqueous TFA. Solvent B: 90% acetonitrile, 10% solvent A. Analytical gradient used solvent B, to 90% solvent B over 27 min. Mass spectra were recorded using a Fisons VG single platform spectrometer in either positive ES (electrospray) or APCI (Atmospheric Pressure Chemical lonisation) mode. 400MHz NMR were acquired at the University of Cambridge NMR service. Chemical shifts are reported in parts per million and were referenced to residual solvent peaks within deuterated solvents.

DEPT (distortionless enhancement through polarization transfer) analysis is noted by CH or CH 3 (positive) and C or CH, (negative) signals. Analytical thin-laver chromatography (TLC) was conducted on prelayered silica gel Plates. Visualisation of plates was accomplished using a 254 nm bUV light (for chromophores). Flash chromatoraphy was conducted upon Kieselgel 60, 230-400 mesh and was run under a slight positive pressure. Solvents used were either reagent or HPLC grade.

Reactions were carried out at ambient temperature under nitrogen unless otherwise noted. Solvent mixtures are expressed as volume: volume ratios. All starting materials were commercially available unless otherwise stated.

Preparation of 6-Hvdroxv-2H-1.3-benzoxathiol-2-one. i.

Resorcinol (0.lmmol, llg) and copper sulphate (0.2mmol, 31.8g) were dissolved in water (250mL) with vigorous stirring. Ammonium thiocyanate (0.4mmol, 31g) in water (50mL) was added in one portion, the solution turned from blue to black and was left to stir at room temperature for 2 hours. The resultant white suspension was filtered through celite; and washed with a further 50mL of water.

The resultant filtrate was stirred vigorously with the addition of sodium carbonate 5.3g) in water (50mL) in one portion. After 10min the precipitate formed was filtered and dissolved in concentrated HCI (140mL) and water (260mL) with careful heating for 1 hour at 100 0 C. The solution was filtered whilst hot with product precipitation occurred upon cooling to room temperature. The resulting precipitate was filtered and washed with cold water and recrystalised from boiling water. Excess water was removed in vacuo to yield a white solid m.p. 159 0

C.

'H NMR (D 6 DMSO) 5 10.01 (1H, brs, ArOH), 7.47 (1H, d, J 8.6 Hz, ArH), 6.83 1H, d, J2.2 Hz, ArH), 6.74 (1H, dd, J2.2, 6 Hz, Ari) SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 14 "C NMR (D 6 DMSO) 5 169.86 157.58 148.37 123.65 113.10 110.64 99.58 HPLC retention 10.01min.

APCI-MS (positive mode) found 169 (MIH), calculated C 7 Ha0 2 S (167.98) Preparation of 6-(tert-butoxv)-2H-1.3-benzoxathiol-2-one. (2) A suspension of 6-hydroxy-2H-1,3-benzoxathiol-2-one (12mmol, 2g), in DCM (25mL), the solution was cooled to -300C. Isobutylene was condensed into the pressure tube (5mL) followed by the addition of methyl triflate (1.9mmol, 450 L).

The sealed tubes were allowed to come to room temperature, and stirred for 3 hours at which point the suspension became colourless. The reaction was cooled to -30"C and the reaction quenched with N-methyl morpholine (12mmol, 1.1 ImL), and allowed to come to room temperature. Water (50mL) was added and the aqueous solution was extracted with ethyl acetate (2 x 50mL). The organics were washed with saturated brine (2 x 50mL), 0.5M KHSO 4 (2 x 50mL) and finally water (2 x 50mL). The organics were dried over MgSO 4 filtered and solvent removed in vacuo, yielding 2.3g (92% yield) of a pale yellow gum.

'H NMR (CDC1) 5 7.24 (1H, d, J8Hz, ArH), 6.94 (1H, d, J2Hz, ArH 6.88 (1H, dd, J2, 8.5Hz, ArH), 1.34 (9H, s, C(CH-) 3 "C NMR (CDC1:) 8 169.51 155.36 148.26 122.06 122.46 116.80 108.32 79.994, 28.72 HPLC retention 18.35min.

APCI-MS (positive mode) Preparation of 5-(tert-butoxv)-2-sulfonvl phenol 6-(tert-butoxy)-2H-1,3-benzoxathiol-2-one (llmmol, 2.49g) was dissolved in dioxane (105mmol, 9.60mL) with vigorous stirring at 5 0 C. A 2N solution of NaOH (10.56mL) was added in a dropwise manor over 10 minutes with vigorous stirring.

Cooling was maintained for 10 minutes further then the solution was allowed to warm to room temperature for 1 hour. Dioxane was removed in vacuo, the remaining slurry was taken up in water (0lmL) and washed with tert-butyl ether (20mL). The aqueous layer was carefully acidified with 1N HC1 to pH 3 and extracted with ethyl acetate (2 x 20mL). The resultant organic layer was dried over magnesium sulphate, filtered and solvent removed in vacuo to yield 1.52g, of a pale yellow solid.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 'H NivfR (D 6 DMSO) 5 7.06 (1H1, d, J 8.3Hz, ArT,64 1,d J.HAH,63 (1H, dd, J2.5, 3.3)Hz, Ar 3.30 (1H, s, OH or SH), 1.23 (9H, s, C(CH-) 3 "13 M Rv.D 6 DMSO)58153.52, 129.150, 115.19, (0)112.07, 110.69, (0) 77i.67, 28.49, HPLC retention: 15.62min.

Preparation of 5-(tert-buto-xv)-2-4 I-(tert-butoxv')-2-hvdroxvnhenvlI disulfanvI} phenol. 5-(terr-butoxy)-2-sulfonyl phenol (7.7mmol. 1 was dissolved in the minimum amount of DMSO (IlOm.L) with vigorous stirring for 15 hours. The reaction was quenched with water (200m.L) and extracted with tert-butil ether (2 x The organics were dried over MgSO 4 and solvents removed in vacuo yieldirng 1.41g of a pale yellow gum, which was stored under.Argon.

H N1vAR AD DM50) 5 7.25 (2H, d, J13.5 Hz. 2 x ArK), 6.45 (2H, d, J 2.5 Hz. 2 x .ArH), 6.41 dd.J2.5, 3.5 Hz. 2 x Ar~H 1.27 (ISHs, 2 xC(CH-)-z) 1 Cc1NMvR AD DMSO) 5 1531.52.(1), 129.150, 115.19, 112.07, 110.69. (0) 77.67, 23.49, ES-MS (positive mode): Found 395 (QVflfl: Calculated C 20

H

26 O4S 2 (394.13) Preparation of di 14-(tert-butoxv')-2-methonhenvlI disulfide. 5-(tert-butoxv)-2- {[-(tert-butoxv)-2-hvdroxyphenyl] disulfanyl) phenol. (1) (3.llmmol. 1.222). methyl iodide (9.35nimol, 3m1) and caesium carbonate (l2mmol.

3.9g) were suspended in methyl-ethyl ketone (12.5mL) and stirred under nitrogen for hours. The suspension was filtered throug-h celite, washed with ethyl acetate (2 x lOmL) and solvent removed in vacuo yielding 1.22 of a pale red oil.

'H INIR PD 6 DMSO) 8 7.37 (2H. d. J3.5 Hz. 2 x ArHl), 6.52-6.62 (4H, m, 4 x.Ar-H, 3.76 (6H, s, 2 x OCHj 3 1.30 (1ISH. s, 2 x OC(CH-0 3 3 C NNvM AD DMSO) 5 157.39,(1), 156.59, 129.75, 117.11, 115.32, 107.08, 73.57, 55.31, 23.46, HPLC retention: 25.09min.

ES-MS (positive mode); found 423, (UNfl), calculated CIIH 30

O

4

S

2 422.59.

Preparation of 4-(tert-bu toxv)-2-methoxvphenvI hvdrosulfide. SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 16 Di [4-(tert-butoxy)-2-methoxyphenvl disulfide. (2.1imol, 9 00msz) was dissolved in ethanol (4mL) and cooled to 0 0 C in a NaCI-ice bath. A solution of sodium borohydride (4mmol, 0.15g) in water (5mL) was added dropwise over minutes, allowed to come to room temperature over 1 hour and stirred at room temperature for 6 hours. Solvent was removed in vacuo; the resultant residue was redissolved in water (lOmL) and acidified to pH 5 with IN HC1. The acidified solution was washed with ethyl acetate (2 x solvent removed in vacuo yielding 800mg of a pale yellow solid.

'H N'MR AD DMISO) 6 7.20 (IH. d, J13.3Hz. ArK'). 6.56 (1K. d. 12.3Hz. AxH), 6.50 (iN. dd,12.3, S.3'Hz AxH, 3.73 (3H. s. OCH-), 1.23 (9H, s. OC(CTH-)..

NIVI AD DMISO) 5 155.18, 153.37, 123.87, 116.10, 114.06. 107.72, 78.06, 55.73, 2S.47, h'LC retention: 13.48 mini.

ES-M)vS (positive mode); found 213(v~ Calcuated C, 1

K

1 6 0j 9 S (212).

Prenaration of methyl 5-1 4-(trn-butoxvN)-2-methoxvDhenvl sulfanvll pentanoate. 4 -(tert-butoxy)-2-methoxvphenyl hydrosulfide. (2.3xnnol, 500mg), (3.6mm-ol. IniL) and caesiun carbonate (16-2mmol. 5.2g) were suspended in methyl-ethyl ketone (5rnL) and refiuxed under nitrogen at 85 0 C for 4 hours. The suspension was allowed to cool, filtered through celite and solvent removed in vacuc yielding a yellow oil.

KH NV-,I (D 6 DMSO) 6 7.13 (1K. d. J18.2 Hz, ArH) 6.54 6.57 (2H. mn. 2 x ArE), 3.76 (3H, s, 3.58 (3H, s, COOCH-,), 2.81 (2H. t. J 7.1Hz, SCH-), 2.50 (2H, m, COCK,), 1.81 (2H, dt, J 6.0, 7.1Hz. CKCH-)), 1.63 (2H, dt. J 7.1, 7.8 Hz,

CHCH

2 1.31 (9H, s, C(CH-) 3 '3C 1N1V DMSO (D 6

DMSO)

6 173.05,(1), 157.46, 154.84, 129.47, 117.58, 115.45, 107.27,( 78.16, 55.13, 51.13, 34.45, 32.21, 31.44, 27.8313, 23.

00, KPLC retention: 20.07 minutes.

ES-MS (positive mode); found 327, calculated C 17

H

26 0OIS, 326.45.

SUBSTITUTE SHEET (RULE WO 99/26902 WO 9926902PCT/GB98/03523 17 Prelmration of methyl 5-f(5-formvl-4-hvdroxv*-2-methoxvvhenvl)sufanvl ventanoate. (8) Methyl 5- 4 -(tert-butoxy)-2-methoxvphenl] sulfanyl pentanoate (7) (0.6mmol, 200mg) was dissolved in dichioroethane (l.O2inmol, 124 L) and DMvF (0.9mmol, 100 L) at 0 0 C. To this vigorously stirred solution was added POC1 3 (1.O2=nol, 124 L) in a dropwise manor over 15 minutes. After addition, the solution was maintained at 0 0 C for a further 60 minutes and room temperature for 16 hours. The reaction was quenched by the slow addition of ice (lOrnl-) over 1 hour, extraction of the aqueous solution occurred via the addition of DCM (2 x 5OniL). The organic phase was washed with saturated brine (2 x 5Om.L) and dried over M!S0 4 t, filtered and solvent removed in vacuo to yield 150 m2 (84% crude, 1:4 ratio of nonformvlated: formvlated product) of a dark yellow gum, which was purified by column chromatography. (eluant; ethyl acetate! hexane) NMR (D 6 DM',SO)569.83 s, COH), 7.13 (1K,d,.18.2 1z.ArK),6.54 6.57 (1K. m. ASH), 3.76 (3K. s, 3.58 3H. S. COOCHII), 2.93 (2K. t, 1 .1z SCH-). 2.50 (2H. m, COCH-), 1.83 (2K. dt, 1 6.0, 7.1Hz. CHCH-), 1.63 (2H. dt. J 7.1, 7.8 Hz, CH CK 2 '3C Nv.NI DMSO PD 6

DMSO)

190.01 (0)173.05,(l), 157.46, 15 1.66, 129.4I7, 117.58, 1 15.415. (0) 107.27., 78.16, 551,(0), 31445, 32.21, 31.44.(1), 27.81, KPLC retention: 16.7 minutes.

ES-M-'vS (positive mode): Found 299 Calculated CI.LH 8 0 5 ;S (298).

Preparation of 5- V5-formvl-4-bvdroxv-2-methox-phenvl) sulfanVil Dentanoic acid. (9) Methyl 5-[(5-forrnvl-4-hydroxy-2-methoxyphenyl)sulfanyl] pentanoate (8) (0.Smmol, 235mg) was dissolved in a solution of LiOH (9mmol, 2 10mg) in Methanol: water 5mL). The- solution was stirred at room temperature for hours then acidified to pK4 with IN HCl, extracted into ethyl acetate (2 x 4OmL), SUBSTiTUTE SHEET (RULE WO 99/26902 WO 9926902PCT/GB98/03523 18 dried over MgCSO0 4 The solvent was removed in vacuc yielding 200mg of a pale yellow oil.

'HN'IR MD 6 DMSO)569.84 (1H,s, COH), 7.13 (1H,d,J.8.2 Hz, Ar H)65 (1K, m, Ar) 3.76 (3H, s, OCH-), 2.93 (2H. t, .1 7.1Hz, SCH,), 2.50 (2H. in.

COCI), 1.83 (2H, dt, J 6.0, 7. 1Hz. CHICH-)), 1.63 (2H. dt, J 7.1, 7.8 -Hz, CHCH.?), '3C NMVIR DMSO (D6 DMSO) 190.01 173.05 157.46 151.66 129.47 117.58 115.45. (0 107.27 (0),78.16 (1)55.13 (0),51.13 (0),31.45 (1),31.44(l).

HPLC retention: 13 .93 minutes.

ES-MS (positive mode). Found: 235 (iTvf). Calculated CuH)60 5 S (234).

Preparation of an alternative Acid Derivative Precursor Linker of the General Formula 1 The compound was prepared as detailed in Scheme 2. In that reaction Scheme the preparative steps were as follows: Scheme 2 S tens CUS0 4

NH

4 LSCN H-0 (ii) Isobutvlene CH2Cl. MeTf (iii) NaOH Dioxane /H-0 (iv) DMSO Mv Mlethyl bromovalerate Cs 2

CO

3

MEK

(vi) NaBH 4 L ethanol /H:0 (vii) CH 3 1 CsCO 3

MEK

(viii) POC1 3 /DMNF /Dichioroethane (ix) LiOH Iethanol HI0 SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 Scheme 2 OH

OH

'N OH 0

-K

0 0 0

I

(iv)' O H s-'

OH

'N

(v) 0 I 00 C- H-0C (vi) 0 (vii) II 0

H

SCH

3 0 (viii) 0 CI 0 0H 3

SCH

3 0 OH (ix) SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 Example Libraries of compounds have been synthesised using the novel solid phase combinatorial chemistry of the present invention.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/4GB98/03523 Example 1 Scheme 3 O OH

H

0 0 0 OH

(I

(ii) (iii)

CHN'

(iv) Mv R 0 OTMAC jLI~ptfe LN Hi- Fmoc Il

OH

0 0 a O--Rs I (viii) (ix) (vi) (vii) Peptide R ci H N 0 0 OH I H 0 00 0 11

H

Peptide C F-1 I R 0 H N 0 i 0 0

N'

H H 0 yKA-f4Pe3id

-N~

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 21 Example 1 Steps for Scheme 3 Novasyn TG resin BOP HOBt NMMN DN4F (ii) H-.AA-O-CTTMA TOMF (111) NaCNBH 4 THF /AcOH H,0 Fmoc-C1 DIBA /DMIF (iv) Standard Emoc-polvamide synthesis MCPBA DCM (vi) 1%1/ TFA./ DCMN/ (vii) H-Leu-.AMC /BOP HOBt NMO (viii) I DCM' (ix) BOP HOBt DLEA DMNF TFA DMS/ NH 4

I

SUBSTITUTE SHEET (RULE WO 99/26902 PCT/GB98/03523 23 Scheme 3 General Procedures for use f the Sulfoxide Handle.

Incorporation of Handle onto NovaSvn TG amino resin. 5-[(5-formyl-4-hydroxy-2-methoxyphenyl) sulfanyl] pentanoic acid. (9) (2.8mmol, 800mg), BOP (2.8mmol, 1.06g), and HOBt (4.2mmol, 642mg) were combined and dissolved in DMF (10mL N-methyl morpholine (4.2mmol, 390IL) was added, and after 5 minutes preactivation, this solution was added to NovaSvn TG amino resin (0.24mmol 4g). The reaction was allowed to proceed for 8 hours.

The resultant resin-handle complex was washed with DMF (5 x 2 min), CH2C12 (5 x 2 min), MeOH (3 x 2 min) and TBDME 5 x 2 min). The resin was dried initially under a positive nitrogen pressure and then in vacuo.

Incorporation of first residue onto BAL-TG-resin via reductive amination.(ll).

Linker-resin complex (10) was allowed to eqilibrate in trimethylorthoformate containing H-L-Leu-CTMA (28mmol, 4.62g). The reaction is allowed to proceed in a capped syringe for 5 hours. The resultant resin-complex was washed with dry THF (5 x 2 min) and dried under a positive pressure of nitrogen. The resin was then suspended in dry THF/ acetic acid/water (90:5:5, v/v/v, 20mL) containing sodium cyanoborohydride (14mmol, 882mg) for 14 hours. The resultant resin conjugate was washed with DMF/water v/v, 20mL x MeOH (20mL x 9) and tert-butyl ether (30mL x 1) allowing the solvent to percolate through the resin bed for seconds. The resin conjugate was dried under a positive nitrogen pressure and in vacuo for 2 hours.

Oxidation of the resin bound peptide-linker coniugate.

The resin-linker-AA-OCTMA complex was initially reated with Fmoc-Cl and DIEA to protect the the secondary amine nitrogen prior to oxidation of the sulfide.

The nitrogen dried resin conjugate (500mg) was suspended in a solution of MCPBA (250mg in 25mL DCM). The reaction was allowed to proceed in a capped syringe for hours. The resultant resin-complex was washed with DCM (2 x 20mL), DMF (2 x methanol (2 x 20mL) and finally tert-butyl ether (2 x 20mL). The resin conjugate was dried under a positive nitrogen pressure and finally in a vacuum desicator ovemigsht.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 24 Acvlation of resin conjugate (11) via symmetrical anhydrides. (A general case) Fmoc-amino acid (20eq excess to resin loading) is dissolved suspended in dichloromethane (5mL mmol amino acid) with stirring and ice cooling in a Falcon tube. If the amino acid appears insoluble, then DMF (500iaL) is added to aid dissolution. Diisopropylcarbodiimide(10eq) in DCM (ImL) is added over a few minutes, and the mixture stirred at 0°C for 30 minutes. Resin conjugate (11) was added to the anhydride solution, sealed and left to react for the appropriate time. The fully acylated resin cojugate is filtered and washed with DMF (5 x 50mL), methanol x 50mL) and tert-butyl ether (2 x Solid phase peptide chemistry was carried out using standard solid phase Fmoc-AA-Opfp HOBt couplings. The C-terminal protecting group chosen was the in house developed Fmoc-AA-OCTLMA derivatives. These Fmoc amino acid derivatives are stable throughout Fmoc-polyamide peptide synthesis, and can be removed using weak solutions of TFA in conjunction with the appropriate scavengers (TFA/ TES).

0 Ph 1 FmocHN.. I

R

0 NH 2

CH

3 Fmoc-AA-OCTMA Removal of the CTMA protecting group.

Peptide-resin conjugate (100mg) was suspended in a solution of 2%TFA 1%TES in DCM (10mL) for 15 minute x 2. The resin was filtered, washed with DMF x O1mL), methanol (5 x 10mL) and tert butyl ether (5 x 10mL) and dried under a positive nitrogen pressure.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 Cvclization to gi Cycl_ (AAj-LA!:AA_-AA-A-A Peptide-resin (50mg, 0.24inmol 2, was treated with suspended in Imi of a solution of DMvf containing BOP (16mg, .O36mmol), HOBt (6mg, .O36mmol) and NlvflI (4pL, 0.03 6mmol). The resin was aggitated for 24 hours, removal of reaeents occurred via filtration, followed by washing with DN{F (2 x 2inL), methanol (2 x 2miL) and tert-butyl ether (2 x 2m.L). The resin was dried under a positive pressure of nitrogen prior to cleavage.

COUpjin!Z of H-A--AMC to resin bound peptide.

Peptide-resin (50mg, 0.24rnmol g, was treated with suspended in lml of a solution of DMFE containing BOP (16mg, 0.O36rnol), H-OBt (6mg, 0.036rrmoi) and NiVQv1 (4uL, 0.036mnmo1) and (0.03 6rnol). The resin was aggitated for 2 hours, removal of reagents occurred via filtration, followed by washing with D-'v\fl (2 x 2niL), methanol (2 x 2rnL) and tert-butyl ether (2 x 2naL). The resin was dried under a positive pressure of nitrogen prior to cleavage.

£ilaae from the sulfoxide linker-resin con jueate.

Peptide-resin conjugate (50mg, 0.24mxol substitution) was suspended in TFA TES DMS /1H20 (90/1/1/8) containing I mol of NH 4 I. The suspension was a~itated at room temperature for 2 hours. The resin was filtered, the resultant filtrate was szargzed down under a stream of nitrogzen and the peptide precipitated via the slow addition of cold tert butvl ether, spun down via cenurfftgation and air dried prior to IiPLC analysis.

Data for compounds prepared utilising resin bound sulfoxide linkage agent.

Linear peptide sequence prepared via Emoc polyamide synthesis: Compound of general formula cvclo -(AA -AA- 2

AA

3

-AA

4 A5s-AA 6 H-Leu-Tyr-Leu-Ser-Gln-Leu-OH, C 35

H

37

N

7 0 10 calculated 735.89, found 73 (Ivfii). BHPLC retention 12.78 minutes.

Cyclo (-Leu-Tyr-Leu-Ser-Gln-Leu-) calculated 717.89, found 719.8 HPLC retention 14.13 minutes Compound of the general formula X-AA ,-A.A 2

-AA

3

-AA

4

-AMC

Fmoc-Ser-Ghn-Leu-OH, C29H 36

N

4

O

8 calculated 568.68, found 569.5 590.9 HPLC retention 21.03 minutes.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9/2902PCT/4B98/03523 26 Ac-Ser-Gln-Leu-Leu-AMvC,

C

32

H

46 0 9

N

6 calculated 658.93, found 659.8 cQva{), 680.9 (TMNa). EIPLC retention 13.09 minutes.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 Examole 2 Scheme 4 O' OH 0 OH CTMAO I 11 i -k I NH OH H 0 (i H0 i) (iii)I IC 0 H H, 0, 0 0'-

H

3 CS H (iV) (v R 0_ CTMAON~~- Pectide -NH- Fncc u

OH

0 11

H

3 CS 0

H

(ix) Peptide RIc HN

N

OH

N

O,-S 0 H Q (vi) (vii)

HN

H

0 17-7)_ ,jL: Peptide KNH 2

OH

NN

\-j4

N

H

3

S

0 (x)

CH

3 nh

HN

H

R N0Ltd NH SUBSTITUTE SHEET (RULE WO 99/26902 WO 9926902PCT/GB98/03S23 28 Example 2 Steps Scheme 4 Novasvn TG resin B OP HOBt NMM~v DMNF (ii) H-A-A-C-CTvLk TONME (iii) NaCNBH 4 THE /AcOH H-0 Emoc-CI 'DIEA! DNMF (iv) Standard Fmoc-polvamide synthesis MCPBA DCM (vi) I1%o'TEAI/DCMI (vii) H-Lcu-A.MC /BOP I HOBt O (viii') 1%/TEA DCM (ix) BOP HOBt /DIBA.' D,.MF TF.A/ D.MS/N-LI SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 29 Example 3 Combinatorial libraries of peptidyl cyclic compounds which can be cyclised from linear compounds of general formula and cleaved to provide cyclic compounds of the general formula in which AAI-AA, are independently combinatorially variable.

-OH AA4 CD) CE) Okle It is a particular advantage of the use of this linker that the class of compound can utilise any available residue, be it a peptide, peptidomimetic or other, as during the synthesis the chiral integrity of the Co is protected. Therefore, the need to include specialised residues in this position, such as proline or glycine, which cannot easily be epimerised in the reaction, is eliminated.

Thus according to a further aspect of the invention there are provided libraries of compounds and individual compounds per se of the formula whether attached to the linker or in cleaved form together with libraries and individual SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 compounds per se of the formula To a person skilled in the art it will be apparent that the use of this technology will enable cyclic compounds with a variable number of residues present including but not limited to AA,-AA 4

AA,-AA

5 and AA,-AA 6 SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 31 Example 4 The present invention can be used to produce combinatorial libraries useful for designing appropriate peptide-based substrates and inhibitors for proteases (and other enzymes).

A known class of compounds having three variable amino acid residues X of general formula Ac-X-X-X-Asp-aminomethylcoumarin have been proposed for investigating protease specificities of interleukin-1 P converting enzyme (ICE) ref: Rans et al, Chem. Biol., 1997, Vol. 4, No. 2. A scissile bond between Asp and AMC can be cleaved to release the fluorogenic AMC group. The present invention allows for the production of a general library class of compounds -X-X-X-X-AMC which have four variable amino acid residues X. Such compounds are referred to hereafter as "4X-AMC". The compounds can be synthesised according to the present invention and libraries of the compounds can be used to rapidly and accurately assess enzymatic specificity. In the following description, Scheme 5 provides a generic synthetic route to 4X-AMC compounds, and Scheme 6 provides a specific example of the synthesis of the compound Ac-Tyr-Leu-Leu-Lys- AMC. It is to be noted that the precursor compound prior to step A corresponds to the product of step (ix) of scheme 2 wherein R=SMe and the product is resin bound.

Also the product of step B corresponds to the intermediate of claim 1 wherein is the variable residue precursor and Y=Fmoc.

Furthermore, those skilled in the art can readily appreciate that the compound prior to step A could be chosen to have the: -SOMe rather than the -SMe substituent.

However, due to the interconvertability of these moieties the reductive amination of step A would reduce -SOMe to -SMe followed by re-oxidation to -SOMe in step B.

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 Example 4(a) Scheme

CHO

HO

A

N SiMe

O-(CH

2 4 -C0-Solid Phas

NH-X

3

-BZHL

OH

2 B NO I 1 S M e e 0 1(CH 2 4 -C-Solid Phase Fmoc-NX 3 -BzHL

OH

2

HOC

SOMe

O-(CH

2 4 .CO-Solid Phase Fmoc-NX 3

_COOH

HO

-l NSOMe

O-(CH

2 4 -CO-Soljd Phase H N-X 3 _CON H-X 4 (Boc)-AMC

OH

2 E FO N SOMe

O-(CH

2 4 -CO-Solid Phase

G

Fmoc -NX 3

-CONH-X

4 (Soc)-AMC

OH

2 H0 ,1 11 SOMe 0-(CH 2 4 -CO-Solid Phase

E

Fmoc- X 2

NX

3

_CONHX

4 (Boc)-AMC

CH

2

HO

G

SOMe 0-(CH 2 4 -CO-Solid Phase Ac,-X' _X 2

_X

3

_X

4

_AMC

SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 Scheme for Synthesis of 4X-AIVIC A 1. NH,-X3-BzHL and 2. Reductive Amination B. 1. Fmoc-CI. DIEA. DCMN/ 2. m-chlorope-rbenzoic acid C. 1. 1 ,oTFA, DC M D. 1. NH')-X 4 (Boc)-AIMC 2. BOP, HOBt. NMM~v E. 1. Piperidine. DMF F. 1. (Fznoc-X 2 2. DCM G. 1. Solid-phase synthesis 2.Reduction of SOMe to SiMe Cleavage OCH3 0 AMC BzHL= _CM SUBSTITUTE SHEET (RULE WO 99/26902 WO 9926902PCT/GB98/03523 Example 4(b) Scheme 6

CHO

HO I

A

N' SMe

O-(CH

2 4 CO-Solid Phasi NH-Leu-BzHL

OH

2 B

HO

HO N SMe

O-(CH

2 4 00-Soid Phase oc-N-Leu-BzHL

OH

2 SOMe

O-(CH

2 4 -CO-Solid Phase Fmoc -N-Leu-OOOH Emoc N-Leu-CON H-Lys( Boc)-AMC

OH

2

OH

2 HO HO T E N SOM N SOMe

O-(CH

2 4 -CO-Soid Phase O-(CH 2 4 -CO-Soiid Phase HN-Leu-CONH-Lys(Bo0c)-AMC Fmoc-Leu -N-LeuCONH-Lys(Boc)-AMC

OH

2

OH

2 E HO F HO G N SOMe N SOMe 0-(CH 2 4 -C0-Solid Phase

O-(OH

2 4 .00-Solid Phase G Ac-Tvr-Leu-Leu-Lvs-AN1C SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 Scheme for Synthesis Ac-Tyr-Leu-Leu-Lvs-AMC A 1. NI-,-Leu-BzHL and 2. Reductive Amination B. 1. Fmoc-Cl. DIEA, DCM 2. m-chloroperbenzoic acid C. 1.1% TFA, DCMV D. 1. NH:-Lvs(Boc)-AvfC BOP. HCBt, NMMl..v E. 1. Piperidine. DMF F. 1.

DCM

G. 1. Solid-phase synthesis 2Reduction of SO~le to Si~te 3. Cleavage

OCH

3 BzHL= CH OCH3 SUBSTITUTE SHEET (RULE P:\WPDOCS\CRN\Shelicy\Spoc\7487730.spe.doc-17/4KI The reference to any prior art in this specification is not, and should not be taken as, an acknowledgement or any form of suggestion that the prior art forms part of the common general knowledge in Australia.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers or steps but not the exclusion of any other integer or group of integers or steps.

9*

Claims (10)

1. An intermediate compound of general formula S Y-N-R2' LINKER RESIN for use in a method of prenaration of a compound of general formula (A) 04CN.R wherein R4 is a variable residue; and wherein the linker moiety has the general formula or (C) lOS OR RI-0 SUBSTITUTE SHEET (RULE 26). WO 99/26902 PCT/GB98/03523 37 OH R1 SO (C) wherein X is (CH)R3 where R3 is an -CO- group for attachment to the terminal NH group of the solid phase through a standard bond eg carboxyl amide; R1 is methyl or another such suitable alkyl known in the art; n is between 2 and 12, preferably 4; Y is H or an Na functional group protective moiety such as Fmoc; R2 is a variable residue; and R2' is an intermediate form of R2 which is subsequently chemically transformed to give the desired R2. SUBSTITUTE SHEET (RULE 26) WO 99/26902 WO 9926902PCT/GB98/03523 38

2. An intermediate compound of general formula Y-N-R2 LINKER-RESIN wherein the linker moiety has the general formula or (C) XOS OH OH XO CH7 RI So (C) SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523 39 wherein X is (CHI,)R3 where R3 is an -CO- group for attachment to the terminal NH group of the solid phase through a standard bond eg carboxyl amide; R1 is methyl or another such suitable alkyl known in the art; n is between 2 and 12, preferably 4; Y is H or an Na functional group protective moiety such as Fmoc; R2 is a variable residue; and R2' is an intermediate form of R2 which is subsequently chemically transformed to give the desired R2.

3. An acyl derivative of an intermediate compound according to claim 1 or 2 having the general formula 0 R4-C-N-R2: LINKER RESIN o II R4-C-N-R2 LINKER RESIN (F) wherein R4 is an amino acid, peptide or peptidomimetic sequence which is combinatorially variable. SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523

4. A method which comprises the steps of Scheme 1, for making a precursor linker compound of formula 1 for use in a method of preparation of a resin- bound intermediate compound according to claim 1 or claim 2. A method which comprises the steps of Scheme 2, for making a precursor linker compound of formula 1 for use in a method of preparation of a resin- bound intermediate compound according to claim 1 or claim 2.

6. A method which comprises the steps of Scheme 3.

7. A method which comprises the steps of Scheme 4.

8. A method which comprises the steps of i) forming a plurality of intermediate resin linked compounds according to claim 1 or claim 2; ii) forming from said intermediates a plurality of resin linked compounds having variable residues R4 and R2 or R4 and R2 1 therein; iii) cleaving the compounds from the linkers to produce a plurality of compounds of general formula A; and iv) optionally transforming R2' to R2 either before or after cleavage; whereby the product of step (iii) or (iv) provides a combinatorial library of compounds of formula

9. A method which comprises the steps of Scheme 5, for producing a compound of general formula Ac-X-X-X-X-AMC. A method according to claim 9 which comprises forming a plurality of said compounds Ac-X-X-X-X-AMC having variable residues X, whereby the product of the method is a combinatorial library of said compounds. SUBSTITUTE SHEET (RULE 26) WO 99/26902 PCT/GB98/03523

11. A resin linked compound which is the product of step of Scheme 3 or the product of step of Scheme 4 (optionally having one or both protective groups shown in said Schemes varied to be another protective group).

12. Intermediate compounds, acyl derivatives thereof having the general formula methods, or a resin linked compound substantially as herein described with reference to the examples. DATED this 17th day of April, 2001 MEDIVIR UK LIMITED By its Patent Attorneys DAVIES COLLISON CAVE S S S S S S. S p SUBSTITUTE SHEET (RULE 26)