The present invention relates to therapeutically active hydroxamic acid and carboxylic acid derivatives, to processes for their preparation, to pharmaceutical compositions containing them, and to the use of such compounds in medicine. In particular, the compounds are inhibitors of metalloproteinases involved in tissue degradation.

Background to the Invention

Metalloproteinase Inhibitors Compounds which have the property of inhibiting the action of metalloproteinases involved in connective tissue breakdown such as collagenase, stromelysiπ and gelatinase (known as "matrix metalloproteinases", and herein referred to as MMPs) are thought to be potentially useful for the treatment or prophylaxis of conditions involving such tissue breakdown, for example rheumatoid arthritis, osteoarthritis, osteopenias such as osteoporosis, periodontitis, gingivitis, corneal epidermal or gastric ulceration, and tumour metastasis, invasion and growth. MMP inhibitors are also of potential value in the treatment of neuroinflammatory disorders, including those involving myelin degradation, for example multiple sclerosis, as well as in the management of angiogenesis dependent diseases, which include arthritic conditions and solid tumour growth as well as psoriasis, proliferative retinopathies, neovascular glaucoma, ocular tumours, angiofibromas and hemangiomas.

Metalloproteinases are characterised by the presence in the structure of a zinc(ll) ion at the active site. It is now known that there exists a range of metalloproteinase enzymes that includes fibroblast collagenase (Type 1 ), PMN-collagenase, 72 kDa- gelatinase, 92 kDa-gelatinase, stromelysin, stromelysin-2 and PUMP-1 (L.M. Matrisian, Trends in Genetics, 1990, 6, 121 -125).

Many known MMP inhibitors are peptide derivatives, based on naturally occurring amino acids, and are analogues of the cleavage site in the collagen molecule. A recent paper by Chapman et al (J. Med. Chem. 1993, 36, 4293-4301 ) reports some

general structure/activity findings in a series c N-carboxyalkyl peptides. Other known MMP inhibitors are less peptidic in structure, and may more properly be viewed as pseudopeptides or peptide mimetics. Such compounds usually have a functional group capable of binding to the zinc (II) site in the MMP, and known classes include those in which the zinc binding ^roup is a hydroxamic acid, carboxylic acid, sulphydryl, and oxygenated phosphorus (eg phosphinic acid and phosphonic acid) groups.

Two known classes of pseudopeptide or peptide mimetic MMP inhibitors have a hydroxamic acid group and a carboxylic group respectively as their zinc binding groups. With a few exceptions, such known MMPs may be represented by the structural formula (IA)

in which X is the zinc binding hydroxamic acid (-CONHOH) or carboxylic acid (-COOH) group and the groups R-j to R ₅ are variable in accordance with the specific prior art disclosures of such compounds. The following patent publications disclose hydroxamic acid-based and/or carboxylic acid-based MMP inhibitors:

US 4599361 (Searle) EP-A-2321081 (ICI) EP-A-0236872 (Roche) EP-A-0274453 (Bellon) WO 90/05716 (British Bio-technology) WO 90/05719 (British Bio-technology) WO 91/02716 (British Bio-technology) WO 92/09563 (Glycomed) US 5183900 (Glycomed) US 5270326 (Glycomed) WO 92/17460 (SmithKline Beecham)

EP-A-0489577 (Celltech) EP-A-0489579 (Celltech) EP-A-04971 92 (Roche) US 5256657 (Sterling Winthrop) WO 92/13831 (British Bio-technology) WO 92/22523 (Research Corporation Technologies) WO 93/09090 (Yamanouchi) WO 93/090_97 (Sankyo) WO 93/20047 (British Bio-technology) WO 93/24449 (Celltech) WO 93/24475 (Celltech) EP-A-0574758 (Roche) WO 94/02447 (British Biotech) WO 94/02446 (British Biotech)

Brief Description of the Invention

The present invention makes available a new class of MMP inhibitors, related to those of.general formula (I) known from the patent publications listed above in that they also have hydroxamic acid or carboxylic acid zinc binding groups, but incorporating a major structural change in the "backbone". In the compounds of this invention the portion of the "backbone" corresponding to the bracketed portion of general formula (I) may be represented by partial formula (IIA):

where Y is a carbonyl (-C(=0)-) or sulphonyl (-S(=0) ₂ -) group.

A further advantage of compounds of the present invention is that they inhibit the production of the pro-inflammatory cytokine TNF.

Related Patent Publication

EP-A-0606046 (Ciba-Geigy), published 13th July 1994 discloses compounds also having the partial structure (IIA) where Y is a sulphonyl group.

Detailed Description of the Invention

The present invention provides a compound of general formula (II)

R-) ,_ _.

N ^ ^' \

(II)

A, wherein

X represents a -C0 ₂ H or -CONHOH group;

R-j represents:

(i) the characterising side chain of a natural or non-natural alpha amino acid, in which any functional group present may be protected;

R ₂ represents a group Z1-Q-W- where Z* represents hydrogen or an optionally substituted aryl, heteroaryl, non-aromatic heterocyclyl, cycloalkyl, or cycloalkeπyi group, and

(i) -Q-W- taken together represent a bond or

(ii) Q represents -O- or -S- and W represents a divalent C ₁ -C ₂₀ straight or branched alkyl or C2-C ₂₀ alkenyl group which

(a) may be interrupted by one or more non-adjacent ether or thioether linkages or -N(R _X )- groups wherein R _x is hydrogen, or C ₁ -C ₆ alkyl, and/or

(b) may carry one or more substituents selected from -OH, -SH,

-O(Alk), -S(Alk), halogen, -NH ₂ , -NH(Alk), -N(Alk) ₂ , -C0 ₂ H, - C0 ₂ (Alk), -CO(Alk), -CHO, -CONH ₂ , -CONH(Alk), -CON(Alk) ₂ , - (Alk)OH, -(Alk)SH, and -NHCO(Alk) where Alk represents C C ₆ alkyl, or

(iii) Q represents a bond and W represents a divalent C ₉ -C ₂₀ straight or branched alkyl or C ₂ -C ₂₀ alkenyl group which

(a) may be interrupted by one or more non-adjacent ether or thioether linkages or -N(R _X )- groups wherein R _x is hydrogen, or

CrC _θ alkyl, and/or

(b) may carry one or more substitueπts selected from -OH, -SH, -O(Alk), -S(Alk), halogen, -NH ₂ , -NH(Alk), -N(Alk) ₂ , -C0 ₂ H, - C0 ₂ (Alk), -CO(Alk), -CHO, -CONH ₂ , -CONH(Alk), -CON(Alk) ₂ , - (Alk)OH, -(Alk)SH, and -NHCO(Alk) where Alk represents d- Cβ alkyl, or

(iv) Q represents a bond and W represents a divalent C-j-Cs straight or branched alkyl group which

(a) carries one or more substituents selected from -SH, -C0 ₂ H, -C0 ₂ (Alk), -CHO, -CONH2, -CONH(Alk), -CON(Alk) ₂ , and - (Alk)SH, where Alk represents C C ₆ alkyl, and

(b) (in the case where W is C ₂ -C ₈ ) may be interrupted by one or more non-adjacent ether or thioether linkages or -N(R _X )- groups wherein R _x is hydrogen, or C--C- ₆ alkyl;

Y represents a sulphonyl (-(SO2)-) group; and

Z represents an optionally substituted aryl, or heteroaryl group;

or a salt, hydrate or solvate thereof.

A particular sub-set of the compound- ^" f the present invention are those of formula (II) above wherein R ₂ represents

(ι, a group Ar-Q-W- in which Ar represents optionally substituted aryl or heteroaryl, _Q represents -O- or -S-, and W represents a divalent C ₁ -C2 ₀ straight or branched chain alkyl moiety which may carry one or more substituents selected from OH, OMe, halogen, NH ₂ , NMeH, NMe _2> C0 ₂ H, C0 ₂ Me, COMe, CHO, CONH ₂ , CONHMe. CONMe ₂ , CH ₂ OH, NHCOMe; or

(ii) a group Ar-Q-W- in which Ar represents optionally substituted aryl or heteroaryl, Q represents a bond, and W represents a divalent C ₉ -C ₂₀ straight or branched chain alkyl moiety may carry one or more substituents selected from OH, OMe, halogen, NH ₂ , NMeH, NMe ₂ , C0 ₂ H, C0 ₂ Me, COMe, CHO, CONH ₂ , CONHMe, CONMe ₂ , CH ₂ OH, NHCOMe; or

(iii) a group Ar-Q-W- in which Ar represents optionally st .ituted aryl or heteroaryl, Q represents a bond, and W represents a divalent C-j-Cs straight or branched chain alkyl moiety which carries one or more substituents selected from -C0 ₂ H, -C0 ₂ Me, -CHO, -CONH ₂ , -CONHMe, and -CONMe ₂ ; or

(v) a cycloalkenyl(CrC ₆ )alkyl group; or

(vi) a linear saturated C ₉ -C ₂₀ or unsaturated C ₂ -C ₂ o hydrocarbon chain, which chain

(a) may be interrupted by one or more non-adjacent -O- or -S- atoms or -N(R _X )- groups wherein R _x is hydrogen, methyl or ethyl, and/or

(b) may be substituted with one or more groups selected from (C*ι- C ₆ )alkyl, OH, Oiw.e, halogen, NH ₂ , NMeH, NMe ₂ , C0 ₂ H, C0 Me,

COMe, CHO, CONH ₂ , CONHMe, CONMe ₂ , CH ₂ OH, NHCOMe,

provided that the maximum length of the chain is no more than 28 C, 0, S and N atoms; or

(vii) a linear saturated C ₂ -C ₈ hydrocarbon chain, which chain

(a) is substituted with one or more groups selected from -C0 ₂ H, - C0 ₂ Me, -CHO, -CONH2, -CONHMe, and -CONMe ₂ , and

(b) may be interrupted by one or more non-adjacent -0- or -S- atoms or -N(R _x )- groups wherein R _x is hydrogen, methyl or ethyl,

provided that the maximum length of the chain is no more than 28 C, 0, S and N atoms.

A further particular sub-set of the compounds of the present invention are those of formula (II) above wherein R ₂ represents

(i) a cycloalkenyl(CrC ₆ )alkyl group, or

(ii) a linear saturated C ₂ -C ₈ hydrocarbon chain, which chain

(a) may be interrupted by one or more non-adjacent -O- or -S- atoms or -N(R _X )- groups wherein R _x is hydrogen, methyl or ethyl, and

(b) is substituted with one or more groups selected from -CO ₂ H, - C0 ₂ Me, -CHO, -CONH ₂ , -CONHMe, and -CONMe ₂ , or

(iii) a linear saturated Cg-C ₂ o or unsaturated C ₂ -C ₂ o hydrocarbon chain, which chain

(a) may be interrupted by one or more non-adjacent -O- or -S- atoms

or -N(Rχ)- groups wherein R _x is hydrogen, methyl or ethyl, and/or

(b) may be substituted with one or more groups selected from (C*ι- C ₆ )alkyl, OH, OMe, halogen, NH ₂ , NMeH, NMe ₂ , C0 ₂ H, C0 ₂ Me, COMe, CHO, CONH ₂ , CONHMe, CONMe ₂ , CH ₂ OH, NHCOMe,

provided that the maximum length of the chain is no more than 28 C, 0, S and N atoms,

As used herein, the term "side chain of a natural or non-natural alpha amino acid" means the group R in a natural or non-natural amino acid of formula H ₂ N-CH(R)- COOH.

Examples of side chains of natural alpha amino acids include those of alanine, arginine, asparagine, aspartic acid, cysteine, cystine, glutamic acid, glycine, histidine, 5-hydroxylysine, 4-hydroxyproline, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine, α-aminoadipic acid, α-amino-n-butyric acid, 3,4-dihydroxyphenylalanine, homoserine, α-methylserine, ornithine, pipecolic acid, and thyroxine.

Examples of side chains of non-natural alpha amino acids include:

(a) a hydrocarbon group -CR ₉ R1 ₀ R _{1 1} in which each of Rg, R ₁₀ and R-π is independently hydrogen, (Ci-CβJalkyl, (C- ₂ -C ₆ )alkenyl, (C-2-C ₆ )alkynyl, phenyl(C C ₆ )alkyl; or R ₉ and R ₁₀ together with the carbon atom to which they are attached form a 3 to 8 membered cycloalkyl or a 5- to 6-membered heterocyclic ring; or Rg, R ₁₀ and Rn together with the carbon atom to which they are attached form a tricyclic ring (for example adamantyl);

or (b) a group -CR ₁₂ R ₁₃ R ₁₄ in which each of R ₁₂ and R ₁₃ is independently (C _r C ₆ )alkyl, (C ₂ -C ₆ )alkenyl, (C ₂ -C ₆ )alkyπyl, phenyl(Cι-C ₆ )alkyl, 0(C _r C ₆ ) alkyl, S(C C ₆ ) alkyl, OH, SH, OPh, OCH ₂ Ph, SPh, SCH ₂ Ph, halogen, CN,

C0 ₂ H, (Cι-C ₄ )perfluoroalkyl, CH ₂ OH, C0 ₂ (C C ₆ )alkyl, or a group phenyl or heteroaryl which is optionally substituted by one or more substituents independently selected from hydrogen, hydroxyl, halogen, CN, C0 ₂ H, C0 ₂ (CrC ₆ )alkyl, CONH ₂ , CONH(C C ₆ )alkyl, CONH(C C ₆ alkyl) ₂ , CHO, CH ₂ OH, (C C ₄ )perfluoroalkyl, 0(C C ₆ )alkyl, S(C C ₆ )alkyl, SO(C C ₆ )alkyl, S0 ₂ (CrC ₆ )alkyl, N0 ₂ , NH ₂ , NH(C C ₆ )alkyl, N((C C ₆ )alkyl) ₂ , NHCO(C _r C ₆ )alkyl, (C C ₆ )alkyl, (C ₂ -C ₆ )alkenyl, (C ₂ -C ₆ )alkynyl, (C ₃ -C ₈ )cycloalkyl, C ₄ - CsJcycloalkenyl, phenyl or benzyl; and R ₁₄ is hydrogen, OH, SH, OPh, OCH ₂ Ph, SPh, SCH ₂ Ph, halogen, CN, C0 ₂ H, (C _r C ₄ )perfluoroalkyl, CH ₂ OH, Cθ ₂ (C C ₆ )alkyl, or a group phenyl or heteroaryl which is optionally substituted by one or more substituents independently selected from hydrogen, hydroxyl, halogen, CN, C0 ₂ H, C0 ₂ (CrC ₆ )alkyl, CONH ₂ , CONH(C C ₆ )alkyl, CONH(C C ₆ alkyl) ₂ , CHO, CH ₂ OH, (C C ₄ )perfluoroalkyl, 0(C C ₆ )alkyl, S(C C ₆ )alkyl, SO(C _r C ₆ )aikyl, S0 ₂ (C _r C ₆ )alkyl, N0 ₂ , NH ₂ , NH(C ₁ -C ₆ )alkyl, N((Cι-C ₆ )alkyl) ₂ , NHCO(CrC ₆ )alkyl, (CrC ₆ )alkyl, (C ₂ -C ₆ )alkenyl, (C ₂ -C ₆ )alkynyl, (C ₃ -C ₈ )cycloalkyl, C ₄ - Ca)cycloalkenyl, phenyl or benzyl; or R ₁₂ and R ₁₃ together with the carbon atom to which they are attached form a 3 to 8 membered cycloalkyl or a 5- to 6-membered heterocyclic ring,

Functional groups in the amino acid side chains may be protected; for example carboxyl groups may be esterified (for example as a CrCe alkyl ester), amino groups may be converted to amides (for example as a COC C ₆ alkyl amide) or carbamates (for example as a C(=0)OCrC ₆ alkyl or C(=0)OCH ₂ Ph carbamate), hydroxyl groups may be converted to ethers (for example a C C _δ alkyl or a (Ci-C _δ alkyl)phenyl ether) or esters (for example a C(=0)C _r C ₆ alkyl ester) and thiol groups may be converted to thioethers (for example a C Cε alkyl thioether) or thioesters (for example a C(=0)C C ₆ alkyl thioester).

As used herein the term "cycloalkyl" means a saturated alicyclic moiety having from 3-8 carbon atoms and includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl.

The term "cycloalkenyl" means an unsaturated alicyclic moiety having from 3-8 carbon atoms and includes, for example, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl and cyclooctenyl. In the case of cycloalkenyl rings of from 5-8 carbon atoms, the ring may contain more than one double bond.

The unqualified term "heterocyclyl" or "heterocyclic" refers to a 5-8 membered heterocyclic ring containing one or more heteroatoms selected from S, N and 0, and optionally fused to a benzene ring, including for example, pyrrolyl, furyl, thienyl, imidazolyl, oxazolyl. thiazolyl, thiadiazolyl, pyrazolyl, pyridiπyl, pyrrolidinyl, pyrimidinyl, morpholinyl, piperiziπyl, iπdolyl, benzimidazole, maleimido, succinimido, phthalimido, 1 ,2-dimethyl-3,5-dioxo-1 ,2,4-triazolidin-4-yl, 3-methyl- 2,5-dioxo-1 -imidazolidinyl and 3,4,4-trimethyl-2,5-dioxo-1 -imidazolidinyl, naphththalimido (ie 1 ,3-dihydro-1 ,3-dioxo-2H-beπz[f]isoindol-2-yl), 1 ,3-dihydro-1 - oxo-2H-benz[f]isoindol-2-yl, 1 ,3-dihydro-1 ,3-dioxo-2H-pyrrolo[3,4-b]quinolin-2-yl, and 2,3.-dihydro-1 ,3-dioxo-1 H-benz[d,ejisoquinolin-2-yl

The term "aryl" refers to a mono-, bi- or tri-cyclic, substituted or unsubstituted, carbocyclic aromatic group, and to groups consisting of two covalently linked substituted or unsubstituted monocyclic carbocyclic aromatic groups. Illustrative of such groups are phenyl, bipheπyl and napthyl.

The term "heteroaryl" refers to a 5- or 6- membered substituted or unsubstituted aromatic ring containing one or more heteroatoms, and optionally fused to a benzyl or pyridyl ring; and to groups consisting of two covalently linked 5- or 6- membered substituted or unsubstituted aromatic rings each containing one or more heteroatoms; and to groups consisting of a substituted or unsubstituted monocyclic carbocyclic aromatic group covalently linked to a substituted or unsubstituted 5- or 6- membered aromatic rings containing one or more heteroatoms;. Illustrative of such groups are thienyl, furyl, pyrrolyl, imidazolyl, benzimidazolyl, thiazolyl, pyrazolyl, isoxazolyl, isothiazolyl, triazolyl, thiadiazolyl, oxadiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, 4-([l ,2,3]-thiadiazoly-4-yl)phenyl and 5- isoxazol-3-ylthienyl.

Unless otherwise specified in the context in which it occurs, the term "substituted" as applied to any moiety herein means substituted with up to four substituents, each of which independently may be (C-j-C ₆ )alkoxy, phenoxy, hydroxy, mercapto, (CrC ₆ )alkylthio, amino, halo (including fluoro, chloro, bromo and iodo), trifluoromethyl, nitro, -COOH, -CONH _2, -COORA, -NHCORA, -CONHRA, -NHRA, - NRARB, or -CONRARB wherein RA and RB are independently a (C-j-C _δ Jalkyl group.

Salts of the compounds of the invention include physiologically acceptable acid addition salts for example hydrochlorides, hydrobromides, sulphates, methane sulphonates, p-toluenesulphonates, phosphates, acetates, citrates, succinates, lactates, tartrates, fumarates and maleates. Salts may also be formed with bases, for example sodium, potassium, magnesium, and calcium salts.

There is at least one potential chiral centre in the compounds according to the invention because of the presence of potentially asymmetric carbon atoms. The presence of several asymmetric carbon atoms gives rise to a number of diastereomers with R or S stereochemistry at each chiral centre. General formula (II), and (unless specified otherwise) all other formulae in this specification are to be understood to include all such stereoisomers and mixtures (for example racemic mixtures) thereof.

In the compounds of the invention, the preferred stereochemistry is in general as follows:

C atom carrying the Ri and X group = R, but mixtures in which the above configuration predominates are also contemplated.

In the compounds of the invention:

R-j may be for example hydrogen; a (C-j-C ₆ )alkyl, (C ₂ -C ₆ )alkenyl, phenyl, substituted phenyl, phenyl(C C ₆ )alkyl, substituted phenyl(CrC ₆ )alkyl, heterocyclyl, substituted heterocyclyl, heterocyclyl(C*ι-C ₆ )alkyl, or substituted heterocyclyl(Cι-C ₆ )alkyl group; a group BSO _n A- wherein n is 0, 1 or 2 and B

is hydrogen or a (C _r C ₆ )alkyl, phenyl, substituted phenyl, heterocyclyl, substituted heterocyclyl, (C C ₆ )acyl, phenacyl or substituted phenacyl group, and A represents (C-i-CβJalkyl; an aryl(CrC ₆ )alkyl group; an amino(CrC ₆ )alkyl; hydroxy(d-C ₆ )alkyl, mercapto(Cι-C ₆ )alkyl or carboxy(CrC ₆ )alkyl wherein the amino-, hydroxy-, mercapto- or carboxyl- group are optionally protected or the carboxyl- group amidated; or a (C*ι- Cβjalkyl group substituted by maleimido, succinimido, naphthalimido, 2,3- dihydro-1 ,3-dioxo-1 H-benz[d,e]isoquinol-2-yl, carbamoyl, mono(lower alkyl)carbamoyl, di(lower alkyl)carbamoyl, di(lower alkyl)amino, carboxy- lower alkanoylamino, pyrrolidino or morpholino. Specific examples of R-i groups include hydrogen, methyl, ethyl, propyl, iso-propyl, butyl, isobutyl, tert-butyl, 2,2-dimethylpropyl, cyclohexyl, phenyl, hydroxymethyl, 2- methoxyethyl, 2-methylthioethyl, 2-methylsulphonylethyl, 4-(N,N- dimethylamino)butyl, 4-(N,N-dimethylglycylamino)butyl, allyl, methoxymethyl, phenylmethyl, phthalimidomethyl, 2-phthalimidoethyl, 4- morpholinoethyl, 4-thiomorpholinoethyl, 2-methylthiazol-4-ylmethyl, tetrazol- 5-ylmethyl, 6-chloropiperonyl, 1 -pyrazolylmethyl, pyrid-3-ylmethyl, 1-methyl- 4-imidazolylmethyl, N-methylpyrid-4-yl, 2-(pyrid-3-yloxy)ethyl, methylthiomethyl, benzylthiomethyl or thienylsulphanylmethyl. Presently preferred are compounds in which Ri is hydrogen, methyl or phenylmethyl.

R ₂ may for example be hydrogen, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n- hexadecyl, n-tridecyl, π-tetradecyl, n-pentadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl, n-eicosyl, n-heneicosyl, n-docosyl, n-tricosyl, n-tetracosyl, cyclohexyl, 3-methoxycarbonylpropyl, 3-carboxypropyl, 4- methoxycarbonylbutyl, 5-methoxycarbonylpentyl, 5-carboxypentyl, 4-(4- methoxybenzyl)benzyl, 4-phenoxy-2-chlorobenzyl , 4-([1 ,2,3]-thiadiazol-4- yl)benzyl, 2-phenyl-1 -carboxy-ethyl, propyloxymethyl, propylsulphanyl, 2-(2- methoxyethoxy)ethyl, 2-(2-methoxyethoxy(2-ethoxy))ethyl, 3-(2- methoxyethoxy)propyl, 2-phenoxy-ethyl, 2-(4-methoxy-phenoxy)-ethyl, 2- carboxyethyl, 3-carboxypropyl, 4-carboxybutyl, 6-carboxyhexyl, 7- carboxyheptyl, or 8-carboxyoctyl. Presently preferred are compounds in which R is hydrogen, n-nonyl, n-decyl, n-dodecyl, n-hexadecyl, 4-phenoxy-

2-chlorobenzyl, 4-([1 ,2,3]-thiadiazoly-4-yl)benzyl, 3-methoxycarbonylpropyl, 5-methoxycarbonylpentyl, 3-carboxypropyl, 5-carboxypentyl, 2-(2- methoxyethoxy(2-ethoxy))ethyl, 3-methoxypropyl, 2-phenoxyethyl, or 2-(4- methoxy-phenoxy)ethyl. Presently most preferred are compounds in which R ₂ is hydrogen, n-nonyl, n-decyl, n-dodecyl, 5-methoxycarbonylpentyl, 5- carboxypentyl, 3-methoxypropyl, 3-carboxypropyl, 2-phenoxyethyl, 2-(4- methoxy-phenoxy)ethyl, and 2-(2-methoxyethoxy(2-ethoxy))ethyl.

Z may for example be phenyl, 4-methylphenyl, 4-tert-butylphenyl, 3- methylphenyl, 4-chlorophenyl, 4-bromophenyl, 4-fluorophenyl, 4- trifluoromethylphenyl, 4-aminophenyl, 4-N,N-dimethylaminophenyl, 2,4,6- trimethylphenyl, 2,4,6-isopropylphenyl, 4-methoxyphenyl, 2,6- dimethoxyphenyl, 3,4-dimethoxyphenyl, 4-ethoxyphenyl, 4-n- hexyloxyphenyl, 4-n-butyloxypheπyl, 4-(2-methylbutyloxyphenyl, 4-n- heptyloxyphenyl, 4-benzyloxyoxyphenyl, 4-isopropyloxyphenyl, 4- ethoxyethoxyphenyl, 2.3-dihydrobenzofuran-5-yl, 1 -πapthyl, 2-napthyl, 2- thienyl, 2-acetamido-4-methyl-thiazol-5-yl, 4-acetamidophenyl, 3,5- dimethylisoxazol-5-yl, 2,4-dimethylisoxazol-5-yl, or 2-(isoxazol-5-yl)thien-5- yl. Presently preferred are such compounds in which Z is 4-methylphenyl, 4- methoxypheπyl, 2-acetamido-4-methyl-thiazol-5-yl, 4-acetamidophenyl, or 2- (isoxazol-5-yl)thien-5-yl.

Specific compounds of the invention include those prepared according to the preparative examples below, in particular the following:

N-Hydroxy-2-[[2-(4-methoxy-phenoxy)-ethyl]-(toluene-4-sul fonyl)-amino]- acetamide,

N-Hydroxy-2-[(4-phenoxy-ethyl)-(tolueπe-4-sulfonyl)-amin o]-acetamide,

N-Hydroxy-2-[(4-methoxy-beπzenesulfonyl)-nonyl-amino]-ac etamide,

2-[-Decyl-(toluene-4-sulfonyl)-amiπo]-N-hydroxyacetamide ,

and salts, solvates or hydrates thereof.

Compounds according to the present invention in which X is a hydroxamic acid group (-CONHOH) may be prepared from compounds of the invention in which X is a carboxylic acid group (-COOH). That process, which forms another aspect of the invention, comprises: (a) causing an acid of general formula (IV)

or an activated derivative thereof to react with hydroxylamine, O-protected hydroxylamine, N,0-diprotected hydroxylamine, or a salt thereof, Rι , R ₂ , Y and Z being as defined in general formula (II) except that any substituents in R-i , R ₂ , Y and Z which are potentially reactive with hydroxylamine, 0- protected hydroxylamine, N.O-diprotected hydroxylamine or their salts may themselves be protected from such reaction, then removing any protecting groups from the resultant hydroxamic acid moiety and from any protected substituents in R- , R ₂ , Y and Z; or

(b) deprotecting a diprotected hydroxamic acid derivative of formula (IVa)

in which R- , R ₂ , Yand Z are as defined in general formula (ll),Ri4 is an amino protecting group and R ₁₅ is a hydroxyl protecting group.

or method (a) conversion of (IV) to an activated intermediate such as the

pentafluorophenyl, hydroxysuccinyl, or hydroxybenzotriazolyl ester may be effected by reaction with the appropriate alcohol in the presence of a dehydrating agent such as dicyclohexyl dicarbodiimide (DCC), N,N-dimethylaminopropyl-N'-ethyl carbodiimide (EDC), or 2-ethoxy-1 -ethoxycarbonyl-1 ,2-dihydroquinoline (EEDQ).

Protecting groups as referred to above are well known per se, for example from the techniques of peptide chemistry. Amino groups are often protectable by benzyloxycarboπyL t-butoxycarbonyl or acetyl groups, or in the form of a phthalimido group. Hydroxy groups are often protectable as readily cleavable ethers such as the t-butyl or benzyl ether, or as readily cleavable esters such as the acetate. Carboxy groups are often protectable as readily cleavable esters, such as the t-butyl or benzyl ester.

Examples of O-protected hydroxylamines for use in method (a) above include O- benzylhydroxylamine, O-4-methoxybenzylhydroxylamine, O- trimethylsilylhydroxylamine, and 0-tert-butoxycarbonylhydroxylamine.

Examples of O.N-diprotected hydroxylamines for use in method (a) above include

N,0-bis(benzyl)hydroxylamine, N,0-bis(4-methoxybenzyl)hydroxylamine, N-tert- butoxycarbonyl-O-tert-butyldimethylsilylhydroxylamine, N-tert-butoxycarboπyl-O- tetrahydropyranylhydroxylamine, and N,0 -bis(tert-butoxycarbonyl)hydroxylamine.

For method (b) suitable protecting groups R ₁ and R ₁₅ are benzyl and substituted benzyl (eg 4-methoxybenzyl). Such protecting groups may be removed by hydrogenolysis, while the 4-methoxybenzyl group may also be removed- by acid hydrolysis.

Compounds according to the present invention in which X is a carboxylic acid group -COOH may be prepared by a process comprising hydrolysis of a compound of formula (V):

(V)

wherein R-j R ₂ , Y and Z are as defined in general formula (II), and R ₅ is a carboxy protecting group. Protected carboxy groups include readily cleavable esters, such as the tert-butyl or benzyl ester.

Compounds of formula (V) may be prepared by alkylation of the amino nitrogen of a sulfonamide of formula (VI) with an amine alkylating agent of formula (VII):

R ₂ NHS0 ₂ Z_ (VI) L-CH(R ₁ )COOR ₁₅ (VII)

wherein R* R ₂ , and Z are as defined in general formula (II) except that any substituents in R _Ϊ R ₂ , and Z, which are potentially reactive in the alkylation reaction may themselves be protected from such reaction, R ₁₅ is as defined for formula (V), and L is a leaving group. Leaving groups L for the alkylation of (VI) by (VII) are well known in the art and include halogen atoms (such as bromine) and triflate.

Sulfonamides of formula (VI) may be prepared by standard methods, including the reaction of an amine of formula (VIII) with an activated sulfonic acid of formula (IX):

R ₂ NH ₂ (VIII) HOS0 ₂ Z (IX)

wherein R ₂ , and Z are as defined in general formula (II). Suitable acivated derivatives of (IX) for condensation with (VIII) include the sulfonyl chloride.

As mentioned above, compounds of formula (II) are useful in human or veterinary medicine since they are active as inhibitors of MMPs.

Accordingly in another aspect, this invention concerns: (i) a method of management (by which is meant treatment or prophylaxis) of diseases or conditions mediated by MMPs in mammals, in particular in humans, which method comprises administering to the mammal an effective amount of a compound as defined with respect to formula (II) above; and

(ii) a compound as defined with respect to formula (II) for use in human or

veterinary medicine, particularly in the management (by which is meant treatment or prophylaxis) of diseases or conditions mediated by MMPs; and

(iii) the use of a compound as defined with respect to formula (II) in the preparation of an agent for the management (by which is meant treatment or prophylaxis) of diseases or conditions mediated by MMPs.

Diseases or conditions mediated by MMPs include those involving tissue breakdown such as bone resorption, inflammatory diseases, dermatological conditions and tumour invasion by secondary metastases, in particular rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration and tumour invasion by secondary metastases, tumour growth, tumour angiogenisis, multiple sclerosis, psoriasis, proliferative retinopathy, neovascular glaucoma, ocular tumour, angiofibroma and hemangioma.

In a further aspect of the invention there is provided a pharmaceutical or veterinary composition comprising a compound of formula (II) together with a pharmaceutically or veterinarily acceptable excipient or carrier.

One or more compounds of general formula (II) may be present in the composition together with one or more excipient or carrier.

The compounds with which the invention is concerned may be prepared for administration by any route consistent with their pharmacokinetic properties. The orally administrable compositions may be in the form of tablets, capsules, powders, granules, lozenges, liquid or gel preparations, such as oral, topical, or sterile parenteral solutions or suspensions. Tablets and capsules for oral administration may be in unit dose presentation form, and may contain conventional excipients such as binding agents, for example syrup, acacia, gelatin, sorbitol, tragacanth, or polyvinyl-pyrrolidoπe; fillers for example lactose, sugar, maize-starch, calcium phosphate, sorbitol or glycine; tabletting lubricant, for example magnesium stearate, talc, polyethylene glycol or silica; disintegrants for example potato starch, or acceptable wetting agents such as sodium lauryl sulphate. The tablets may be coated according to methods well known in normal pharmaceutical practice. Oral

liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for reconstitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents, for example sorbitol, syrup, methyl cellulose, glucose syrup, gelatin hydrogenated edible fats; emulsifying agents, for example lecithin, sorbitan monooleate, or acacia; non-aqueous vehicles (which may include edible oils), for example almond oil, fractionated coconut oil, oily esters such as glycerine, propylene glycol, or ethyl alcohol; preservatives, for example methyl or propyl p- hydroxybenzoate or sorbic acid, and if desired conventional flavouring or colouring agents.

The dosage unit involved in oral administration may contain from about 1 to 250mg, preferably from about 25 to 250mg of a compound of the invention. A suitable daily dose for a mammal may vary widely depending on the condition of the patient. However, a dose of a compound of general formula I of about 0.1 to 300mg/kg body weight, particularly from about 1 to 100mg/kg body weight may be appropriate.

For topical application to the skin, the drug may be made up into a cream, lotion or ointment. Cream or ointment formulations which may be used for the drug are conventional formulations well known in the art, for example as described in standard textbooks of pharmaceutics such as the British Pharmacopoeia.

For topical application to the eye, the drug may be made up into a solution or suspension in a suitable sterile aqueous or non aqueous vehicle. Additives, for instance buffers such as sodium metabisulphite or disodium edeate; preservatives including bactericidal and fungicidal agents such as phenyl mercuric acetate or nitrate, benzalkonium chloride or chlorhexidine, and thickening agents such as hypromellose may also be included.

The dosage for topical administration will of course depend on the size of the area being treated. For the eyes, each dose may typically be in the range from 10 to 100mg of the drug.

The active ingredient may also be administered parenterally in a sterile medium. Depending on the vehicle and concentration used, the drug can either be suspended or dissolved in the vehicle. Advantageously, adjuvants such as a local anaesthetic, preservative and buffering agents can be dissolved in the vehicle.

For use in the treatment of rheumatoid arthritis, the drug can be administered by the oral route or by injection intra-articularly into the affected joint. The daily dosage for a 70kg mammal may be in the range 10mgs to 1 gram.

The Preparative Example which follows describes the preparation of a compound which is not part of the invention, but the process conditions and preparative techniques employed are equally applicable to the preparation of the compounds of the invention having similar structures.

Examples 1 to 17 which follow illustrate embodiments of the invention but are not intended to limit the scope in any way. The amino acids used in the examples were commercially available or were prepared according to literature procedures.

The following abbreviations have been used throughout:

DIPE Diisopropyl ether

DMF N,N-Dimethylformamide

DMSO Dimethylsulfoxide

EDC N-Ethyl-N'-(3-dimethylaminopropyl)carbodiimide hydrochloride

HOBt 1 -Hydroxybenzotriazole

LDA Lithium N,N-diisopropylamide

LHMDS Lithium hexamethyidisilazide (lithium N,N-bis(trimethylsilyl)amide)

NMM N-Methylmorpholine

THF Tetrahydrofuran

TFA Trifluoroacetic acid

TLC Thin layer chromatography

1H and ¹³ C NMR spectra were recorded using a Bruker AC 250E spectrometer at

250.1 and 62.9 MHz, respectively. Elemental microanalyses were performed by CHN Analysis Ltd., Alpha House, Countesthorpe Road, South Wigston, Leicester LE8 2PJ, UK or by MEDAC Ltd, Department of Chemistry, Brunei University, Uxbridge, Middlesex UB8 3PH.

Preparative Example

N-Hydroxy-2-[octyl-(toluene-4-sulfonyl)amino]-acetamide

STEP A:

N-octyl-toluene-4-sulfonamide

A solution of toluene-4-sulfonyl chloride (5.0 g, 0.026 mol) in dry dichloromethane (150 ml) was cooled to 0°C during the dropwise addition of n-octylamine (9.6 ml, 0.058 mol) with stirring over 4 minutes. The reaction mixture was then allowed to stir for 30 minutes before being diluted with dichloromethane (200 ml) and water (200 ml). The organic layer was separated and washed consecutively with 1 M HCI, 0.5 M Na ₂ Cθ ₃ and brine before being dried over anhydrous Na2S0 ₄ . The solution was filtered and concentrated in vacuo to a crude solid which was purified by flash chromatography (silica gel, 11 % ethyl acetate in hexane) to give the title compound as a white solid (7.0 g, 94%). This material was then used immediately in the next step.

STEP B:

[Octyl-(toluene-4-sulfonyl)amino]-acetic acid terf-buty! ester

N-Octyl-toluene-4-sulfoπamide (7.0 g, 0.025 mol) was dissolved in dry THF (200

ml) and cooled to -78°C. A 1 M solution of LHMDS in THF (27.2 ml, 0.028 mol) was then added over 10 minutes. The reaction mixture was allowed to warm to -40°C with stirring over 30 minutes. Neat te/ -butyl bromoacetate (4.8 ml, 0.03 mol) was added over 5 minutes and the reaction mixture was allowed to warm to ambient temperature overnight. The reaction mixture was diluted with saturated aqueous NH ₄ CI (200 ml) and ethyl acetate (200 ml). The organic layer was separated and washed consecutively with 1 M HCI, 0.5M Na ₂ C0 ₃ and brine, dried over Na ₂ S0 ₄ , filtered and concentrated in vacuo. The resulting crude oil was purified by flash chromatography (silica gel, 6% ethyl acetate in hexane) to give the title compound as a white solid (5.2 g, 53%). ¹ H NMR: δ (CDCI ₃ ), 7.72 (2H, d, J = 8.3 Hz), 7.27 (2H, d, J = 8.4 Hz), 3.94 (2H, s), 3.23 (2H, dd, J = 7.5, 7.6 Hz), 2.42 (3H, s), 1.60 - 1.42 (2H, m), 1.39 (9H, s), 1.34 - 1.17 (1 OH, m), 0.88 (3H, t, J = 6.9 Hz).

STEP C:

[Octyl-(tolueπe-4-sulfonyl)amino]-acetic acid

An ice-cooled solution of [octyl-(toluene-4-sulfonyl)amino]-acetic acid terf-butyl ester (5.2 g, 0.013 mol) in dichloromethane (50 ml) was further diluted by the addition of 25% TFA in dichloromethane (200 ml). The reaction mixture was stored at 4°C overnight. Solvents were removed under reduced pressure and the residue was azeotroped with toluene. The resulting crude oil was purified by flash chromatography (silica gel, 10% methanol in dichloromethane) to give the title compound as a white solid (4.4 g, 99%). 1 H NMR: δ (CDCI ₃ ), 9.77 (1 H, br s), 7.71

2H, d, J = 8.3 Hz), 7.25 (2H, d, J = 8.2 Hz), 4.00 (2H, br s), 3.19 (2H, dd, J = 7.4, 7.7 Hz), 2.38 (3H, s), 1.50 - 1.30 (2H, m), 1.30 - 1.05 (1 OH, m) and 0.85 (3H, t, J = 6.6 Hz).

STEP D:

N-Benzyloxy-2-[octyl-(toluene-4-sulfonyl)amino]-acetamide

[Octyl-(toluene-4-sulfonyl)amino]-acetic acid (4.0 g, 0.012 mol) was taken up in

DMF (150 ml) and treated at room temperature with NMM (1.55 ml, 0..014 mol) followed by EDC (2.92 g, 0.015 mol). The reaction mixture was allowed to stir for 15 minutes at room temperature before the addition of HOBt (2.1 g, 0.016 mol). The reaction mixture was left to stir for a further 20 minutes before a mixture of O- benzylhydroxylamine hydrochloride (1.87 g, 0.012 mol) and NMM (2.6 ml, 0.024 mol) in DMF (50 ml) was added. The reaction mixture was allowed to stir at room temperature for a further 48 h. The DMF was removed under reduced pressure and the resulting crude oil was dissolved in ethyl acetate (200 ml). The solution was washed consecutively with 1 M HCI, 0.5M Na ₂ C0 ₃ and brine, dried over anhydrous Na ₂ S0 ₄ , filtered and concentrated under reduced pressure. The resulting crude oil was purified by flash chromatography (silica gel, 10% methanol in dichloromethane) to give an oil which was further purified by flash chromatography (silica gel, 20% ethyl acetate in hexane) to give the title compound as a white solid (1.91 g, 37%). 1 H NMR: δ (CDCI ₃ ), 9.39 (1 H, br s), 7.65 (2H, d, J =

8.2 Hz), 7.45 - 7.20 (7H, m), 4.91 (2H, s), 3.67 (2H, br s), 3.07 (2H, dd, J = 7.5, 7.9 Hz), 2.40 (3H, s), 1.50 - 1 .33 (2H, m), 1.31 - 1.10 (1 OH, m) and 0.86 (3H, t, J = 6.5 Hz).

STEP E:

N-Hydroxy-2-[octyl-(toluene-4-sulfonyl)aminoj-acetamide

N-Benzyloxy-2-[octyl-(toluene-4-sulfonyl)amino]-acetamide (1.91 g, 0.0043 mol) was taken up in ethanol (150 ml), and 10% palladium on charcoal (800 mg) was added. Hydrogen gas was bubbled through the mixture for 2 hours at room temperature. The catalyst was removed by filtration and the solvent was removed under reduced pressure to give a crude solid which was purified by recrystallization from ethyl acetate/hexane (940 mg, 61 %). m.p. 89 °C; 1H-NMR; δ (CDCI ₃ ), 7.69 (2H, d, J = 8.2 Hz), 7.32 (2H, d, J = 8.2 Hz), 3.76 (2H, s), 3.15 (1 H, d, J = 7.6 Hz), 3.12 (1 H, d, J = 7.9 Hz), 2.43 (3H, s), 1.58 - 1.41 (2H, m), 1.35 - 1.15 (10H, m) and 0.86 (3H, t, J = 6.4 Hz). 13C-NMR; δ (CDCI ₃ ), 166.6, 144.2, 134.6, 129.9, 127.4, 50.7, 49.9, 31.6, 29.1 , 29.0, 27.9, 26.6, 22.6, 21.5 and 14.0; IR (CDCI ₃ ), v _rnax 3413, 2929, 2858, 1682, 1467, 1401 , 1346, 1162 and 1091 crrH.

Found: C 57.27, H 7.87, N 7.95%; C ₁₇ H ₂₈ N ₂ 0 ₄ S requires C 57.28, H 7.92, N 7.86%.

The compounds of the following Examples 1 to 15 were prepared according to methods described in the above Preparative Example.

EXAMPLE 1

4-[Hydroxycarbamoylmethyl-(toluene-4-sulfoπyl)-amino]-bu tyric acid methyl ester

White solid, m.p. 90 - 91 °C. 1H-NMR; δ (CD ₃ OD), .7.63 (2H, d, J = 8.3 Hz), 7.28 (2H, d, J = 8.3 Hz), 3.67 (2H, s), 3.54 (3H, s), 3.12 (3H, t, J = 7.1 Hz), 2.32 (3H, s), 2.32 - 2.25 (2H, m) and 1.77 - 1.68 (2H, m). ¹ 3C-NMR; δ (CD ₃ OD), 175.2, 167.8,

145.2, 137.2, 130.8, 128.6, 52.0, 49.9, 31.4, 24.1 and 21.4. IR (KBr) v _max 3231 , 2948, 1738, 1651 , 1334 and 1159 crrH . Found C 48.61 , H 5.83, N 7.93%; Cι ₄ H ₂₀ N ₂ O ₆ S requires C 48.83, H 5.85, N 8.13%.

EXAMPLE 2

6-[Hydroxycarbamoylmethyl-(toluene-4-sulfonyl)-amino]-hex anoic acid methyl ester

Off-white solid, m.p. 77 - 78°C. 1 H-NMR; δ (CD ₃ OD), 7.63 (2H, d, J = 8.3 Hz), 7.28 (2H, d, J = 8.3 Hz), 3.67 (2H, s), 3.54 (3H, s), 3.06 (2H, t, J = 7.4 Hz), 2.32 (3H, s), 2.17 (2H, t, J = 7.4 ^" Hz), 1.52 - 1.39 (4H, m) and 1.22 - 1.10 (2H, m). 13C-NMR; δ (CD ₃ OD), 175.7, 167.8, 145.1 , 137.3, 130.8, 128.5, 51.9, 50.3, 34.5, 28.4, 27.0, 25.4 and 21.4. IR (KBr) v _max 3250, 2945, 1731 , 1649, 1332, 1 156, 657 and 558 cm-1. Found C 51.28, H 6.49, N 7.45%; C ₁₆ H24N ₂ θ ₆ S requires C 51.60, H 6.50, N 7.52%.

EXAMPLE 3

2-[Hydroxycarbamoylmethyl-(toluene-4-sulfonyl)-amino]-3-p henyl-propionic acid

Pale orange foam. 1H-NMR; δ (CDCI ₃ ), 7.46 (2H, d, J = 8.4 Hz), 7.32 - 7.26 (7H. m), 7.23 - 7.15 (1 H, m), 5.10 - 5.04 (1 H, m), 4.59 - 4.52 (1 H, d, J = 19.1 Hz), 3.87 3.80 (1 H, d, J = 19.1 Hz), 3.30 - 3.17 (2H, m) and 2.41 (3H, s). 13C-NMR; δ (CDCI3), 145.0, 134.7, 133.7, 130.2, 129.8, 128.9, 128.8, 128.6, 127.5, 127.0, 126.7, 59.3, 44.9, 36.4 and 21.4.

EXAMPLE 4

[Hexadecyl-(4-methoxy-beπzenesulfonyl)-aminoj-acetic acid

White solid, m.p. ^" 109 - 111°C. *H-NMR; δ (CDCI ₃ ), 7.83 - 7.76 (2H, m), 7.03 - 6.96 (2H, m), 4.03 (2H, s), 3.88 (3H, s), 3.21 (2H, dd, J =7.2 Hz), 1.60 - 1.44 (2H, m), 1.38 -1.19(26H, m)and0.89(3H,t,J = 6.6Hz). 13Q-NMR; δ (CDCI ₃ ), 174.2, 163.0, 131.0, 129.5, 114.1,55.6,48.6, 47.8,31.9,29.7,29.5,29.4,29.2,27.8, 26.5,22.7 and14.1. IR(KBr) v _max 2917, 2849.1714, 1257 and 1155 cm- ¹ * Found C 63.58 H 9.28 N 3.03%; C ₂₅ H ₄₃ N0 ₅ S .0.1 H ₂ 0 requires C 63.69, H 9.24, N 2.97%.

EXAMPLE 5

2-[Hexadecyl-(4-methoxy-benzenesulfonyl)-amino]-N-hydroxy -acetamide

White crystalline solid, m.p.115 - 118°C. 1H-NMR; δ ((CD ₃ ) ₂ SO), 8.74 (1H, s), 7.60 (2H, d, J = 8.8 Hz), 6.93 (2H, d, J = 8.8 Hz), 3.69 (3H, s), 2.89 (2H, dd, J = 7.2, 7.2 Hz), 1.37 - 0.91 (30H, m) and 0.70 (3H, t, J = 6.4 Hz). 13C-NMR; δ ((CD ₃ ) ₂ SO), 163.2, 161.1, 129.7, 127.9, 112.9,54.3,46.9, 45.9,30.0,27.8,27.4,27.3,25.9, 24.7, 20.8 and 12.6. IR (KBr) v _max 3189, 3072, 2918, 2851 , 1633 and 1599cm-ι. Found C 61.89, H 9.25, N 5.77%; C ₂₅ H ₄ N ₂ 0 ₅ S requires C 61.95%, H 9.15%, N 5.78%.

EXAMPLE 6

N-Hydroxy-2-[[2-(4-methoxy-phenoxy)-ethylj-(toluene-4-sul fonyl)-amino]- acetamide

White solid, m.p. 77 - 78 °C. ^ H-NMR; δ (CDCI ₃ ), 7.69 (2H, d, J = 8.3 Hz), 7.28 (2H, d, J = 8.4 Hz), 6.80 (4H, s), 4.1 1 (2H, t, J = 5.0 Hz), 3.91 (2H, s), 3.75 (3H, s), 3.52 (2H, t, J = 5.1 Hz) and 2.40 (3H, s). 13C-NMR; δ (CDCI ₃ ), 166.2, 154.4, 151.7, 144.4, 134.3, 130.0, 127.4, 1 15.5, 1 14.7, 67.0, 55.6, 51.7, 50.3 and 21.5. IR (KBr) ma 3377, 2927, 1670, 1500, 1333, 1228, 1 160 and 1034 cm-1. Found C 54.53, H 5.71 , N 6.92%; C ₁₈ H ₂₂ N ₂ 0 ₆ S requires C 54.81 , H 5.62, N 7.10%.

EXAMPLE 7

N-Hydroxy-2-[(4-phenoxy-ethyl)-(toluene-4-sulfonyl)-amino ]-acetamide

White solid, m.p. 84 - 86°C. 1 H-NMR; δ (CDCI ₃ /CD ₃ OD), 7.59 (2H, d, J = 8.3 Hz), 7.22 - 7.02 (4H, m), 6.80 (1 H, t, J = 7.3 Hz), 6.69 (2H, d, J = 7.9 Hz), 4.00 (2H, t, J = 5.4 Hz), 3.81 (2H, s), 3.46 (2H, t, J = 5.4 Hz) and 2.27 (3H, s). 13C-NMR; δ (CDCI3/CD3OD), 165.9, 157.5, 143.9, 134.6, 129.5, 129.0, 126.9, 120.8, 113.9,

65.8, 50.1 , 48.7 and 20.7. IR (CDCI ₃ ) v _max 3343, 2927, 1681 , 1599, 1497, 1350 and 1164 cm-1. Found C 53.43, H 5.39, N 7.37%; C ₁₇ H ₂ oN2θ ₅ . 0.9 H ₂ 0 requires C 53.64, H 5.77, N 7.36%.

EXAMPLE 8

2-[Decyl-(2-acetamido-4-methyl-thiazole-5-sulfonyl)-amino ]-acetamide

NHCOMe

White solid. ¹ H NMR; (CDCI ₃ ), δ 3.83 (2H, m), 3.05 (2H, m), 2.52 (3H, s), 2.35 (3H, s), 1.69 (2H, m), 1.25 - 1.15 (14H, m), 0.87 (3H, t, J = 7.2 Hz).

EXAMPLE 9

N-Hydroxy-2-(toluene-4-sulfonylamino)-acetamide

Off white solid. 1 H-NMR; δ (CD ₃ OD), 7.63 (2H, d, J = 8.3 Hz), 7.27 (2H, d, J = 8.2 Hz), 3.36 (2H, s) and 2.32 (3H, s).

EXAMPLE 10

N-Hydroxy-2-((4-methoxy-benzenesulfoπyl)-2-{2-[2-(2-meth oxy-ethoxy)-ethoxy]- ethyl}-amino)-acetamide

Pale yellow wax. 1H-NMR; δ (CD ₃ OD), 7.70 (2H, m), 6.96 (2H, m), 3.77 (5H, s), 3.59 - 3.37 (10H, br m), and 3.25 (5H, m).

EXAMPLE 11

N-Hydroxy-2-[(4-methoxy-benzenesulfonyl)-nonyl-amino]-ace tamide

White solid. 1H-NMR; δ (CD ₃ OD), 7.70 (2H, d, J = 1.9 Hz), 7.68 (2H, d, J = 1.9 Hz), 3.77 (3H, s), 3.68 - 3.54 (2H, br m), 3.04 (2H, m), 1.40 (2H, m), 1.15 (1 OH, m) and 0.79 (3H, m).

EXAMPLE 12

N-Hydroxy-2-[(5-isoxazol-3-yl-thiophene-2-sulfonyl)-nonyl -amino]-acetamide

Pale yellow soiid. 1H-NMR; δ (CD ₃ OD), 8.31 (2H, d, J = 1.9 Hz), 7.37 (2H, d, J = 3.8

Hz), 7.32 (2H, d, J_ = 3.9 Hz), 6.59 (2H, d, J = 1.9 Hz), 3.94 - 3.66 (2H, br m), 2.90 (2H, m), 1.60 (2H, m), 1.18 (10H, m) and 0.79 (3H, m).

EXAMPLE 13

2-[(Acetamidophenyl-4-sulfonyl)-decyl-amino]-N-hydroxyace tamide

Tan solid. 1H-NMR; δ (CD ₃ OD), 0.79 (3H, t), 1.12 - 1.35 (~16H, m), 2.05 (3H, s), 3.62 (2H, s), 3.92 (2H, t), 7.24 (2H, d), 7.68 (2H, d), 8.43 (1 H, s) and 8.91 (1 H, s).

EXAMPLE 14

2-[-Decyl-(toluene-4-sulfonyl)-amino]-N-hydroxyacetamide

Yellow wax. 1H-NMR; δ (CDCI ₃ ), 0.86 (3H, t), 1.24 (14H, brm), 1.62 (2H, m), 2.32 (3H, s), 3.62 (2H, s), 4.02 (2H, brt), 7.13 (2H, d), 7.67 (2H, d), 7.81 (1 H, s), 8.62 (1 H, s). 13C-NMR; δ (CDCI ₃ ), 14.1 , 21.3, 22.6, 26.2, 28.7, 29.0, 29.2, 29.3, 31.8, 48.4, 125.7, 129.0, 140.6, 141.1.

EXAMPLE 15

N-Hydroxy-2-[Decyl-4-methoxyphenylsulfonyl-amino]-acetami de

Off-white solid. 1 H-NMR; δ (CDCI ₃ ), 0.83 (3H, t), 1.14-1.42 (-16H, m), 3.80 (3H, s),

3.85 (2H, s), 3.92 (2H, t), 6.88 (2H, d) 7.68 (2H, d). 13C-NMR; δ (CDCI ₃ ), 14.9, 26.2, 29.3-30.3 (several lines), 31 .8, 55.2, 66.2, 1 13.2, 127.3, 159.6.

EXAMPLE 16

4-[Hydroxycarbamoylmethyl-(toluene-4-sulfonyl)-amino]-but yric acid (dilithium salt)

4-[Hydroxycarbamoylmethyl-(toluene-4-sulfonyl)-amino]-but yric acid methyl ester (Example 2) (294 mg, 0.86 mmol) was dissolved in methanol (5 ml) and the solution was cooled to 0°C and stirred during the addition of LiOH (76 mg, 1.80

mmol) in water (5 ml). The solution was stirred for 1 h at 0°C then at room temperature. Further portions of LiOH were added after 6h (18 mg) and 18h (18 mg). Hydrolysis was shown by TLC analysis to be complete after a further 24 h. The solvent was removed under reduced pressure to leave the title compound as a white solid (440 mg, including excess LiOH). ¹ H-NMR; δ (D ₂ 0), 7.39 (2H, d, J = 8.3 Hz), 7.10 (2H, d, J = 8.4 Hz), 3.45 (2H, s), 2.89 - 2.78 (2H, m), 2.07 (3H, s), 1.82 - 1.75 (2H, m) and 1.30 - 1.47 (2H, m). 13C-NMR; δ (D ₂ 0), 181.5, 180.3, 166.6, 145.0, 137.3, 130.7, 128.6, 50.4, 36.0, 25.9, 24.2 and 21.4. IR (KBr) v _max 3404, 1580, 1423, 1335, 1 157, 660 and 548 cm-1.

The following additional compound was prepared according to the method described in Example 19:

EXAMPLE 17

6-[Hydroxycarbamoylmethyl-(toluene-4-sulfonyl)-amino]-hex anoic acid (dilithium salt)

LiO C

Pale yellow solid. 1H-NMR; δ (D ₂ 0), 7.41 (2H, d, J = 8.3 Hz), 7.11 (2H, d, J = 8.4 Hz), 3.38 (2H, s), 2.82 (2H, m), 2.08 (3H, s), 1.74 (2H, t, J = 7.4 Hz), 1.16 - 1.03 (4H, m) and 0.87 - 0.75 (2H, m). 13C-NMR; δ (D ₂ 0), 186.3, 165.1 , 147.6, 136.6, 132.5, 129.6, 51.5, 51.4, 39.9, 29.1 , 28.3, 27.6 and 23.2. IR (KBr) v _max 3240, 2937, 1615, 1580, 1420, 1336, 1157 and 1035 crrH.