CA2291994C - Derivatives and analogues of 2-deoxy-2,3-didehydro-n-acetyl neuraminic acid and their use as antiviral agents - Google Patents

Abstract

Derivatives and analogues of 2-deoxy-2,3-didehydro-N-acetyl neuraminic acid, pharmaceutical formulations thereof, methods for their preparation and their use in the treatment of viral infections, in particular influenza, are described.

Description

!"~
" DERIVATIVES AND ANALOGUES OF 2-DEOXY-2-,3-DIDEEYDRO-N-ACETYL
NEURAMINIC ACID AND THEIR USE AS ANTIVIRAL AGENTS"
This is a divisional application of Canadian patent application serial number 2,081,356 filad on April 24, 1991.
This invention relates to a new class of chemical compounds and to their use in medicine. In particular the invention concerns new 4-substituted-2-deoxy 2,3-didehydro derivatives of a-D-neuraminic acid, methods for their preparation, pharmaceutical formulations thereof and their use as antiviral agents.
Enzymes with the ability to cleave N-acetyl neuraminic acid (NANA~, also known as sialic acid, from other sugars are present in many microorganisms. These include bacteria such as Vibrio cholerae, Clostridium perfringens, Streptococcus pneumoniae, and Arthrobacter sialoohilus, and viruses such as influenza virus, parainfluenza virus, mumps virus, Newcastle disease virus, fowl plague virus, and Sendai virus. Most of these viruses are of the orthomyxovirus or paramyxovirus groups, and carry a neuraminidase activity on the surface of the virus particles.
Many of the neuraminidase-possessing organisms are major pathogens of man and/or animals, and some, such as influenza virus, Newcastle disease virus, and fowl plague virus, cause diseases of enormous economic importance.

It has long been thought that inhibitors of neuraminidase activity might prevent infection by neuraminidase-bearing viruses. Most of the known neuraminidase inhibitors are analogues of neuraminic acid, such as 2-deoxy-2,3-didehydro-N-acetylneuraminic acid (DANA) and its derivatives. See, e.g., Meindl et al., Virology 1974 58 457-63. The most active of these is 2-deoxy-2,3-dehydro-N-trifluoroacetyl-neuraminic acid (FANA~, which inhibits multi-cycle replication of influenza and parainfluenza viruses in vitro. See Palese et al., virology 1974 _59 490-498.
A number of ?-deoxy-2,3-didehydro-N-acetyl-neuram~.~,~c acid dermatmes are known in the art. See for example P. Memdl et al., Virology, 58, 457-463 c1974~; P.
Memdl and H. Tuppy, Mh. Chem, 100 (4;, 1295-1306 (1969); M.
Flashner et al., Carbohydrate Research, 103, 281-285 c1982~;
... Zbiral et al., Liebigs Ann Chem, 159-155 c1989>; T. Ogawa ,,~.. WO 91/16320 PCT/AU91/00161 and Y. Ito, Tetrahedron Letters, 28 (49), 6221-6224 (1987>;
T. Goto et al.,.Tetrahedron letters, 27 <43), 5229-5232 (1986); H. Ogura et al., Chew. Pharm. Bull, 36 (12), 4807-4813 (1988); German Offenlegungschrift P 1439249. Many of these compounds are active in vitro against neuraminidase from V. cholerae or Newcastle disease virus as well as that from influenza virus. Neuraminidase in at least some strains of influenza or parainfluenza viruses has also been reported to be inhibited in vitro by 3-aza-2,3,4-trideoxy-4-oxo-D-arabinoctonic acid b-lactone and O-~-N-acetyl-D-neuraminosyl 2--->3)-2-acetamido-2-deoxy-D-glucose. See Zakstel'skaya et al., Vop. Virol. 1972 17 223-28.
Neuraminidase from Arthrobacter sialonhilus is inhibited in vitro by the glycals 2,3-dehydro-4-epi-N-acetyl-neuraminic acid, 2,3-dehydro-2-deoxy-N-acetylneuraminic acid and 5-acetamido-2,6-anhydro-2,3,5-trideoxy-D-manno-non-2-en-4-ulosonate, and by their methyl esters. See Rumar et al., Carbohydrate Res. 1981 94 123-130; Carbohydrate Res. 1982 103 281-285. The thio analogues 2-a-azido-6-thio-neuraminic acid and 2-deoxy-2,3-didehydro-6-thioneuraminic acid, Mack &
Brossmer, Tetrahedron Letters 1987 ZB 191-194, and the fluorinated analogue N-acetyl-2,3-difluoro-a-D-neuraminic acid, Nakajima et al., Agric. Biol. Chem. 1988 52 1209-1215, were reported to inhibit neuraminidase, although the type of neuraminidase was not identified. Schmid et al., Tetrahedron Letters 1958 29 3643-3646, described the synthesis of 2 deoxy-N-acetyl-a-D-neuraminic acid, but did not report its activity or otherwise against neuraminidase.
None of the known inhibitors of neuraminidase activity in vitro has been shown to possess antiviral activity in vivo, and indeed some, such as FANA, have specifically been shown to be inactive in vivo. Thus the conventional wisdom has accordingly considered that compounds exhibiting in vitro inhibition of viral neuraminidase would not effect an in vivo blockade of virus infection.
Meindl and Tuppy, Hoppe-Seyler's Z. Physiol Chem.
1969 350 1088, described hydrogenation of the olefinic double bond of 2-deoxy-2,3-dehydro-N-acetylneuraminic acid to produce the [3-anomer of 2-deoxy-N-acetylneuraminic acid.
This (i-anomer did not inhibit Vibrio cholerae neuraminidase.
The most potent in vitro inhibitors of viral neuraminidase have thus been identified as compounds that are based on the neuraminic acid framework, and these are thought by some to be transition-state analogues. Miller et al., Biochem. Biophys. Res. Comm. 1978 83 1479. But while many of the aforementioned neuraminic acid analogues are competitive inhibitors of neuraminidases, to date, none has been reported as showing anti-viral activity in vivo. For example, although a half-planar, unsaturated 6-member ring system has been asserted to be important for inhibitory activity, see Dernick et al. in ANTIVIRAL CHEMOTHERAPY (K. K. Gauri ed.) Academic Press, 1981, at pages 327-336, some compounds characterized by such a system, notably FANA, have been reported not to possess in vivo anti-viral activity. See Palese and Schulman in CHEMOPROPHYLAXIS AND VIRUS INFECTION
OF THE UPPER RESPIRATORY TRACT, Vol. 1 (J. S. Oxford ed.) CRC
Press, 1977, at pages 189-205.
We have now found novel 4-substituted 2-deoxy-2,3-didehydro derivatives of a-D-neuraminic acid which are active in vivo.
The invention therefore provides in a first aspect compounds of formula (I) or formula (Ia) Rs A R~
R~ I ( I ) a - R i R2 Ft: A R ~
,,.
R~ (lao R R3~ 2 where in general formula (I), A is oxygen, carbon or sulphur, and in general formula (Ia), A is nitrogen or carbon;

R1 denotes COOH, P(O><OH>2, NOZ, SOOH, S03H, tetrazol, CH2CH0, CHO or CH(CHO)2, R2 denotes H, OR6, F, C1, Br, CN, NHR6, SR6 or CH2X, wherein X is NHR6, halogen or OR6 and R6 is hydrogen; an acyl group having 1 to 4 carbon atoms; a linear or cyclic alkyl group having 1 to 6 carbon atoms, or a halogen-substituted analogue thereof; an allyl group or an unsubstituted aryl group or an aryl substituted by a halogen, an OH group, an N02 group, an NH2 group or a COON group, R3 and R3~ are the same or different, and each denotes hydrogen, CN, NHR6, N3, SR6, =N-OR6, OR6, guanidine, N - R6 , NR6 , N ---i O , -NH-N-R6 I I

CHI-N ~N - or - N~
R4 denotes NHR6, SR6, OR6, COOR6, N02, C(R6)3, CH2COOR6, CH2N02 or CH2NHR6, and R5 denotes CH2YR6, CHYR6CH2YR6 or CHYR6CHYRSCH2YR6, where Y is O, S, NH or H, and successive Y moieties in an R5 group are the same or different, and pharmaceutically acceptable salts or derivatives thereof.
In both these formulae R1, R2, R3, R3~, R4, R5 and R6 are subject to the provisos that in general formula (I), (i) when R3 or R3~ is OR6 or hydrogen, and A is oxygen or sulphur, then said compound cannot have both (a) an R2 that is hydrogen and (b) an R4 that is NH-acyl, and (ii) Rs represents a covalent bond when Y is hydrogen, and that in general formula (Ia), (i) when R3 or R3~ is OR6 or hydrogen, and A is nitrogen, then said compound cannot have both (a) an R2 that is hydrogen, and (b) an R4 that is NH-acyl, and ' S (iii R6 represents a covalent bond when Y is hydrogen.
' In a preferred embodiment, the compound has general formula (III
HO OI-I
,,, 0 COO H ( I I ) ~k 1.f CH;CO.I\rH~
R' i.e. in general formula (I) above, Rl is COON, R2 is hydrogen, R4 is acetamido, and RS is -CHOH.CHOH.CH20H, and R3 is hydrogen or R3~, where R3~ denotes -N3, -CN, -CHZNH2, or -N.R8.R9;
R8 and R9 are the same or different, and each denotes hydrogen, a linear or cyclic alkyl group of 1 to 6 carbon atoms, an acyl or substitued acyl group of 1 to 6 carbon atoms, -C.(NH).NH2, -CHZ.COOH, -CHZCH2-01i or -CH2.CH. (Rl~ (R11), Rl~and R11 may be the same or different, and each . denotes oxygen or R12N=, and R12 denotes.hydrogen, -OH, -OCH3, -NHS, or (CH3)2N-.
we have found a particular subclass of compounds of ' formula (I~ which are unexpectedly more actLve than their corresponding 4-hydroxy analogues.
' 25 Thus in a particularly preferred aspect the invention provides compounds of formula <Ib~
svBST~-rv. >~ s~GS~

Q H / OzH
1-i0 I_, II ,:/c Rye ~H ' R3n wherein R3b is (alk)xNR6bR7br CN or N3 where alk is unsubstituted or substituted methylene, x is 0 or 1 R6b is hydrogen, C1_6alkyl (e. g. methyl, ethyl), aryl (e.g. phenyl), aralkyl (e.g. phenCl_4alkyl such as benzyl), amidine, NR~bR8b, or an unsaturated or saturated ring containing one or more heteroatoms (such as nitrogen, oxygen or sulphur>, Rib is hydrogen, C1_6alkyl (e.g. methyl, ethyl), or allyl, or NR6bR~b forms an optionally substituted 5 or 6 membered ring optionally containing one or more additional heteroatoms (such as nitrogen, oxygen or sulphur , R8b is hydrogen or C1_salkyl, and R4b is NHCOR9b where R9b is hydrogen, substituted or unsubstituted Cl_4alkyl or aryl, and pharmaceutically acceptable salts of the compounds of formula (Ib> and their pharmaceutically acceptable derivatives.
In the compounds of formula (Ib) the substituents (for example the groug R6 in the substituent R3~ may themselves bear substituents conventionally associated in the art of pharmaceutical chemistry with such substituents.
Preferably R3 is NRfiR~, in particular NH2 or guanidino.
Preferabl~~ R4 is NHCOR9 where R9 is methyl or halogen substituted methyl (e. g. FCH2, F2CH-, F3C).
References herein to preferred definitions of groups in compounds of formula (I) apply mutatis mutandis to the corresponding groups in formulae (Ia), (Ib) and (II).
C1_4alkyl as used herein includes both straight chain (e. g. methyl, ethyl) and branched chain (e. g.

isopropyl, t-butyl) alkyl groups.
By pharmaceutically acceptable derivative is meant any pharmaceutically acceptable ester or salt of such ester of the compounds of formula (I) or any other compound which upon administration to the recipient is capable of providing (directly or indirectly) a compound of formula (I) or an antivirally active metabolite or residue thereof.
It will be appreciated by those skilled in the art that the compounds of formula (I) may be modified to provide pharmaceutically acceptable derivatives thereof at any of the functional groups in the compounds. Of particular interest as such derivatives are compounds modified at the C-1 carboxyl function, the C-7 or C-9 hydroxyl functions, or at amino groups. Thus compounds of interest include Cl_4alkyl (such as methyl, ethyl or propyl e.g. isopropyl) or aryl (e. g. phenyl, benzoyl) esters of the compounds of formula (I), C-7 or C-9 esters of compounds of formula (I) such as acetyl esters thereof, C-7 or C-9 ethers such as phenyl ethers, benzyl ethers, p-tolyl ethers, and acylated amino derivatives such as formyl, acetamido.
It will be appreciated by those skilled in the art that the pharmaceutically acceptable derivatives of the compounds of formula (I) may be derivatised at more than one position.
Pharmaceutically acceptable salts of the compounds of formula <I> include those derived from pharmaceutically acceptable, inorganic and organic acids and bases. Examples of suitable acids include hydrochloric, hydrobromic, sulphuric, nitric, perchloric, fumaric, malefic, phosphoric, glycollic, lactic, salicylic, succinic, toluene-p-sulphonic, tartaric, acetic, citric, methanesulphonic, formic, benzoic, malonic, naphthalene-2-sulphonic and benzenesulphonic acids.
Other acids such as oxalic, while not in themselves pharmaceutically acceptable, may be useful in the preparation of salts useful as intermediates in obtaining compounds of the invention and their pharmaceutically acceptable acid addition salts.
Salts derived from appropriate bases include alkali - g metal (e. g. sodium), alkaline earth metal (e. g.
magnesium), ammonium and NRq cwhere R. is Cl-4alkyl) salts.
References hereinafter to a compound of the invention include the compounds of formula i::~) and pharmaceutically acceptable salts and derivatives thereof.
Particularly preferred compounds of the invention include :-5-Acetamido-4-amino--2,3,4,5-tetradeoxy-D-Qlycero-D-Qalacto-non-2~-enopyranosonic acid (also known as 5-(acetylamino>-4-ami..no-~,6-anhydra-3,4,5-trideoxy-D-Qlycero-D-Qalacto--non-2-enoic: acid>, salts thereof including the rhodium salt and 5-Acetam..do-4-guanicaino-'~ , ~ , 4 , 5-to tradeoxy-D-crlycero--D.-Qalacto-::ion-"?-enopy_~anosonic acid ( alsc known. as 5-(Acetylamino)-2,6-~~n:hydro-4-guar.idino-3,4,5-trideoxy-D-elycero--h-Qalacto-ruon-2-enoic acid) and salts thereof, including the ammonium salt.
Preferred ~::campounds of the present in~rention include:
sodium 5-ace~amido-~:-azido-2, ~, ~, 5-tetradeoxv-D-giycero~-i;-gal acto-non-a.-enopy:anosonate whic:~: i s also known as 4-Azido-Neu5Ac2en;
sodium 5-awetamido-=E-amino-2, 3, ~~, 5-tetradeoxy-D-glycero-L~-talo-non-2-enopyranoscnat~e which ~~s also knowr.~ as 4-epi-ami.zo-Neu4Ac2er:~;
methyl 5-acetamido-'i, 8, 9-tri-O-a=etyl-4-N-allylamino-2, 3, 4, 5-tetradeoxy-D-g,:yceno-D-galacto-nor-2-enopyranosonate wh:..ch is also known as 4--N, N-diallylami.no-NeuS, 7, g, 9Ac42en1Me;
methyl 5-a~etamido-'7, e, 9-tri-0-acetyl-4-N, D1-diallylamino-2, 3, ~, 5-tetradec;xy-D--glycer~~-D-galacto-non-2-enopyranosonate wh:i.ch is also known as 4-N-<~llylamino-Neu5, 7, 8, 9Ac4:?enlMe; and methyl 5- acetamido--', 8, 9--tri-O-acetyl-4-azido-2, 3, ~, 5-t:etradeoxy-L'--~lycero-L-ta-~.o-non-2-eropyranosonat:e which is also known as 4-epi-azidoNeu5,7,e,GAc42eniMe.

_. pa The compounds of formula (I) possess antiviral activity. In particular these compounds are inhibitors of viral neuraminidasE~ of crthomyxavir_uses and paramyxoviz-uses for example the vi=:vat neuramirlitiase of influenza A and F3, parainfluenza, mumps, and Newcastle disease, fowl plague and Sendai virus.
There is thus provided in a further aspect of the invention a compound of formula (I) or a pharmaceutically acceptable salt or derivative thereof for use as an active therapeutic agent, i.n particular as an antiviral agent, for example in the treatment of orthomyxovirus and paramyxo~.~irus infections.
In a furt:Zer cr a:Lternative aspect there is provided a method :i::c:~r the treatment of a viral ir.fectio:~, for example orthomyxovirus and paramyxovirus infections in a mammal .including mark comprisinc; the step of administering to said mammal an effs~cai.ve amount of a compound of foxznul~a ( I >
or a pharmaceutically acceptable salt or derivative thereof.
There is also provided in a further or alternative aspect use of a co;npound of the invention far the manufacture of a medicament fo:r the treatment of a viral infection.
It will be appreciated by those skilled in the art .. . .. - CA 02291994 1999-12-07 _ g _ that reference herein to treatment extends to prophylaxis as well as the treatment of established infections or symptoms.
It will be further appreciated that the amount of a compound of the invention required for use in treatment will vary not only with the particular compound selected but also with the route of administration, the nature of the condition being treated and the age and condition of the patient, and will ultimately be at the discretion of the attendant physician or veterinarian. In general however, a IO suitable dose will be in the range of from about 0.01 to 750mg/kg of bodyweight per day preferably in .the range of 0.1 to 100 mg/kg/day, most preferably in the range of 0.5 to 25 mg/kg/day.
In particular we have found that the effective doses of the compounds tested are related to their in vitro potency. Thus DANA (which has IC50 plaque reduction of 5~g/ml) has been found to be effective at doses of between 1 and lOmg/kg per treatment. The corresponding methyl ester of DANA (IC50 50-100~g/ml) is effective at proportionally higher dose.
Treatment is preferably commenced before or at the time of infection and continued until virus is no longer present in the respiratory tract. However the compounds are also effective when given post-infection, for example after the appearance of established symptoms.
Suitably treatment is given 1-4 times daily and continued for 3-7, e.g. 5 days post infection depending upon the particular compound used.
The desired dose.may be presented in a single dose or as divided doses administered at appropriate intervals, for example as two, three, four or more sub-doses per day.
The compound is conveniently administered in unit dosage from for example containing 10 to 1500mg, conveniently 20 to 1000mg, most conveniently 50 to 700mg of active ingredient per unit dosage form.
While it is possible that, for use in therapy, a compound of the invention may be administered as the raw chemical, it is preferable to present the active ingredient as a pharmaceutical formulation.
The invention thus further provides a pharmaceutical formulation comprising a compound of the , formula (I) or formula (Ia), but not subject to the proviso thereto, or a pharmaceutically acceptable salt or derivative _ thereof together with a pharmaceutically acceptable carrier therefor.
The carrier must be 'acceptable' in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
The pharmaceutical formulations may be in the form of conventional formulations for the intended mode of administration.
For intranasal administration according to the method of the invention the neuraminidase inhibitors may be administered by any of the methods and formulations employed in the art for intranasal administration.
Thus in general the compounds may be administered in the form of a solution or a suspension or as a dry powder.
Solutions and suspensions will generally be aqueous, for example prepared from water alone (for example sterile or pyrogen-free water>, or water and a physiologically acceptable co-solvent (for example ethanol, propylene glycol, and polyethylene glycols such as PEG 400).
Such solutions or suspensions may additionally contain other excipients for example preservatives (such as benzalkonium chloride), solubilising agents/surfactants such as polysorbates (e. g. Tween 80, Span 80, benzalkonium chloride), buffering agents, isotonicity-adjusting agents (for example sodium chloride), absorption enhancers and viscosity enhancers. Suspensions may additionally contain suspending agents (for example microcrystalline cellulose, , carboxymethyl cellulose sodium).
Solutions or suspensions are applied directly to _ the nasal cavity by conventional means, for example with a dropper, pipette or spray. The formulations may be provided in single or multidose form. In the latter case a means of dose metering is desirably provided. In the case of a dropper or pipette this may be achieved by the patient administering an appropriate, predetermined volume of the solution or suspension. In the case of a spray this may be achieved for example by means of a metering atomising spray pump.
Intranasal administration may also be achieved by means of an aerosol formulation in which the compound is provided in a pressurised pack with a suitable propellant such as a chlorofluorocarbon (CFC), for example dichlorodi-fluoromethane, trichlorofluoromethane or dichlorotetrafluro-roethane, carbon dioxide or other suitable gas. The aerosol may conveniently also contain a surfactant such as lecithin.
The dose of drug may be controlled by provision of a metered valve.
Alternatively the compounds may be provided in the form of a dry powder, for example a powder mix of the compound in a suitable powder base such as lactose, starch, starch derivatives such as hydroxypropylmethyl cellulose and polyvinylpyrrolidine (PVP>. Conveniently the powder carrier will form a gel in the nasal cavity. The powder composition may be presented in unit dose form, for example in capsules or cartridges of e.g. gelatin or blister packs from which the powder may be administered by means of an inhaler.
In the intranasal formulations the compound will generally have a small particle size, for example of the order of 5 microns or less. Such a particle size may be obtained by means known in the art, for example by micronisation.
When desired the formulations may be adapted to give sustained release of the active ingredient. The compounds of the invention may also be used in combination with other therapeutic agents, for example other anti-infective agents. In particular the compounds of the invention may be employed with other antiviral agents. The invention thus provides in a further aspect a combination comprising a compound of formula (I) or a pharmaceutically acceptable salt or derivative thereof together with another therapeutically active agent, in particular an antiviral agent.
The combinations referred to above may conveniently , be presented for use in the form of a pharmaceutical formulation and thus such formulations comprising a , combination as defined above together with a pharmaceutically acceptable carrier therefor comprise a further aspect of the invention.
Suitable therapeutic agents for use in such combinations include other anti-infective agents, in particular anti-bacterial and anti-viral agents such as those used to treat respiratory infections. For example, other compounds effective against influenza viruses, such as amantadine, rimantadine and ribavirin, may be included in such combinations.
The individual components of such combinations may be administered either sequentially or simultaneously in separate or combined pharmaceutical formulations.
When the compounds of the invention are used with a second therapeutic agent active against the same virus, the dose of each compound may either be the same as or differ from that employed when each compound is used alone.
Appropriate doses will be readily appreciated by those skilled in the art.
The compound of formula (I> and its pharmaceutically acceptable salts and derivatives may be prepared by any method known in the art for the preparation of compounds of analogous structure.
In one such.process (A> a compound of formula (III) n OL
(III) z wherein R2 is as defined in formula (I>, and L is a leaving group (for example a sulphonic acid residue such as tosyl, mesyl, trifluoromesyl) or a protected derivative thereof is reacted with the appropriate nucleophile, for example azide, cyanide, an appropriate carbanion, or thioacetate.
The compounds of formula (III) may be obtained from the corresponding compounds of formula (IV) p (IV) R
by inversion of the 4-OH group by methods known in the art, for example by reaction with a Lewis acid (such as BF3 etherate) followed by hydrolysis. The compounds of formula (IV) are either known in the art or may be obtained by methods analogous to those for preparing the known compounds.
In a second method (B) the compounds of formula (I) may be prepared from other compounds of formula (I) by interconversion. Thus compounds of formula (I) wherein R3 is NH2 or CH2NH2 may be prepared by reduction of the corresponding azido or cyano analogues respectively.
Compounds wherein R3 is NH alkyl or guanidino may be prepared by derivatisation of the corresponding compound wherein R3 is NH2.
Compounds of formula I where R1 is COON may be prepared by hydrolysis. of the corresponding ester under either acidic or basic conditions, for example at pH 11-12 (using a base such as sodium or ammonium hydroxide , or at pH
2-3 (using an acid such as sulphuric acid>.
As will be appreciated by those skilled in the art, it may be necessary or desirable at any stage in the above described processes to protect one or more sensitive groups in the molecule to prevent undesirable side reactions; the protecting group may be removed at any convenient subsequent stage in the reaction sequence.

WO 91/16320 PG'r/AU91/00161 The protecting groups used in the preparation of compounds of formula (I) may be used in conventional manner.
See for example 'Protective Groups in Organic Chemistry' Ed.
J. F. W. McOmie (Plenum Press 1973) or 'Protective Groups in Organic Synthesis' by Theodora W Greene (John Wiley and Sons 1981>.
Conventional amino protecting groups may include for example aralkyl groups, such as benzyl, diphenylmethyl or triphenylmethyl groups; and acyl groups such as N-benzyloxy-carbonyl or t-butoxycarbonyl. Thus, compounds of general formula tI) wherein one or both of the groups R2 and R3 represent hydrogen may be prepared by deprotection of a corresponding protected compound.
Hydroxy groups may be protected, for example, by aralkyl groups, such as benzyl, diphenylmethyl or triphenylmethyl groups, acyl groups, such as acetyl; silicon protecting groups, such as trimethylsilyl groups; or as tetrahydropyran derivatives.
Removal of any protecting groups present may be achieved by conventional procedures. Thus an aralkyl group, such as benzyl, may be cleaved by hydrogenolysis in the presence of a catalyst (e. g. palladium on charcoal>; an acyl group such as N-benzyioxycarbonyl, may be removed by hydrolysis with, for example, hydrogen bromide in acetic acid or by reduction, for example by catalytic hydrogenation;
silicon protecting groups may be removed, for example, by treatment with fluoride ion; tetrahydropyran groups may be cleaved by hydrolysis under acidic conditions.
Where it is desired to isolate a compound of the invention as a salt, for example as an acid addition salt, this may be achieved by treating the free base of general formula (I> with an appropriate acid, preferably with an equivalent amount, or with creatinine sulphate in a suitable solvent (e. g. aqueous ethanol).
The present invention is further described by the following examgles, which are for illustrative purposes only, and should not be construed as a limitation of the invention.

General Methodolocries The following general methods are appliicable to the synthesis of compounds of the invention.
Deacetylation Treatment of the acetylated material with Amberlite IRA-400 tOH-) with stirring, for a period of time, generally 2-3 h, at room temperature results in complete de-O-acetylation. The resin is filtered off and the filtrate concentrated to dryness to afford the desired de-O-acetylation material.
Those skilled in the art would recognise that other standard procedures are available for the complete de-O-acetylation of the same material, such as treatment with sodium methoxide in methanol.
Deesterification The completely de-O_-acetylated material is taken up in aqueous sodium hydroxide and stirred at room temperature for a period of time, generally 2-3 h. The mixture is then adjusted to pH 7.0-7.5 with Dowex 50w X 8 (H+) resin.
Filtration followed by freeze-drying of the filtrate affords the desired deesterified material.
Those skilled in the art would readily be able to identify several alternative options for the deesterification of the same material such as acid hydrolysis, alternative _ base hydrolyses e.g. ammonium hydroxide, potassium hydroxide.
Intermediate.compounds referred to in Examples 1 to 15 are identified as follows:

Methyl 5-acetamido-7,8,9-tri-O-acetyl-2,3,5-trideoxy-D-glycero-D-talo-non-2-enopyranosonate (4-epi-Neu5,7,8,9Ac42en1Me) Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-azido-2,3,5-trideoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-azido-Neu5,7,8,9Ac42en1Me) Methyl 5-acetamido-7,8,9-tri-0-acetyl-4-amino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-amino-Neu5,7,8,9Ac42en1Me>

Methyl 5-acetamido-7,8,9-tri-0-acetyl-4-N,N-diallylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N,N-diallylamino-Neu5,7,8,9Ac42en1Me) Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-N-allylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N-allylamino-Neu5,7,8,9Ac42en1Me) Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-amino-2,3,4,5-tetradeoxy-D-glycero-D-talo-non-2-enopyranosonate (4-epi-4-aminoNeu5,7,8,9Ac42en1Me) Methyl 7,8,9-tri-O-acetyl-2,3,5-trideoxy-4',5'-dihydro-2'-methyloxazolo L5,4-d7 D-glycero-D-talo-non-2-enopyranosonate (4-epi-4,5-oxazaloNeu7,8,9Ac32en1Me) Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-azido-2,3,4,5-tetradeoxy-D-glycero-D-talo-non-2-enopyranosonate (4-epi-azidoNeu5,7,8,9Ac42en1Me) Methyl 5-acetamido-4-azido-2,3,4,5-tetradeoxy-D-glycero-D~-talo-non-2-enopyranosonate (4-epi-azidoNeu5Ac2enlMe) Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-N-methylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N-methylamino-Neu5,7,8,9Ac42en1Me) WO 91/16320 PC1'/AU91/00161 Methyl 5-acetamido-4-N-methylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N-methylamino-Neu5Ac2enlMe) Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-N,N-dimethylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2enopyranosonate (4-N,N-dimethylamino-Neu5,7,8,9Ac42en1Me) Methyl 5-acetamido-4-N,N-dimethylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N,N-dimethylaminoNeu5Ac2enlMe>

Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-N-methoxycarbonylmethylamino-2,3,4,5-tetradeoxy-D-glycero-_D-galacto-non-2-enopyranosonate (4-N-methoxycarbonylmethylaminoNeu5,7,8,9Ac42en1Me>

Methyl 5-acetamido-4-N-methoxycarbonylmethylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N-methoxycarbonylmethylaminoNeu5Ac2enlMe>

Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-N-2/-hydroxyethylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N-2/-hydroxyethylaminoNeu5,7,8,9-Ac42en1Me) COMPOrJND 28 Methyl 5-acetamido-4-N-2/-hydroxyethylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N-2/-hydroxyethylaminoNeu5,7,8,9Ac42en1Me) Methyl 5-acetamido-7,8,9-tri-O-acetyl-4-N-2/-hydroxyethylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-N-2/-hydroxyethylaminoNeu5Ac2enlMe) 3-Deoxy-D-glycero-D-galacto-2-nonulopyranosonic acid EKDN) Methyl 3-Deoxy-D-glycero-D-galacto-2-nonulopyranosonate (KDNIMe) Methyl (4,5,7,8,9-penta-O-acetyl-2,3-dideoxy-D-glycero-(3-D-galacto-2-nonulopyranosyl chlorid)onate (KDN4,5,7,8,9Ac52~iC11Me) Methyl 4,5,7,8,9-penta-O-acetyl-2,3-dideoxy-D-glycero-D-galacto-non-2-enopyranosonate (KDN4,5,7,8,9Ac52en1Me) Methyl 2,3-dideoxy-D-glycero-D-galacto-non-2-enopyranosonate (KDN2enlMe) Hydrazinium 4,5-diamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (Hydrazinium 4,5-diaminoNeu2en~

4,5-diamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonic acid (4,5-diaminoNeu2en) Example 1 The preparation of Sodium 5-Acetamido-.4-azido-2,3,4,5-tetradeoxy-D-alvcero-D-Qalacto-non-2-enopyranosonate (4-Azido-Neu5Ac2en) (4) The overall reaction scheme is as follows:
Ac O'~ /~,c 1) BPf.&~O ',O A
HiC O H
~ C
O
s O O O MepF~F~ AO U
H
O

~---~~-2) HOA.c/8t~yi AcctaWH3C ~~rt O

Hz0 (2) O (I) O

. I) Tf~OJ~rldlo~l ~z~

2) NcN~/n-BuiN.HSO, l DMF

OH
OH O O' Na' f ) NaOMc~OH EilC
Ac p'~' ~

/ ~ O D p O
- /
.

N~ 2) OH ~~ O

N~

(4) (3) A
.. __ - ---- - CA 02291994 1999-12-07 . Preparation of (2) To an agitated solution of methyl 5-acetamido-4,7,8,9-tetra-0-acetyl-2,3,5-trideoxy-D-glycero-D-Qalacto-non-2-enopyranosonate (1) (1500 mg, 3.17 mmol) in a mixture of benzene (50 ml) and methanol (300 mg) was added dropwise BF3Et20 (12 ml) over thirty minutes under a nitrogen atmosphere at room temperature. The whole mixture was then allowed to stir at room temperature for 16 hours. The solution was diluted with ethyl acetate (250 ml), washed successively with saturated NaHC03 solution (30 ml x 3) and water (20 ml x 3), then evaporated to a small volume (about 10 ml), to which was added water (0.5 ml) and acetic acid (0.5 ml). The whole mixture was then stirred at room temperature for two days before being diluted with ethyl acetate (200 ml). The ethyl acetate solution was washed with 5~ NaHC03 solution (30 ml x 2) and water (20 ml x 3), then evaporated to dryness. The residue was chromatographed (silica gel, ethyl acetate as eluting solvent) to afford pure compound (2> (550 mg, 40~).
1H-nmr (CDC13) a (ppm); 1.95, 2.06, 2.08, 2.10, 2.35 (s, 15H, Acetyl CH3 x 5), 3.80 (s, 3H, COOCH3), 4.1-4.4 (m, 4H, H4, H5, H6, Hg), 4.82 (dd, 1H, J9~8 l.SHz, J9~9, 12.3Hz, H9), 5.27 (m, 1H, H8), 5.45 (dd, .1H, J7~8 3.5Hz, H7), 6.15 (d, 1H, J3~4 5.4Hz, H3), 6.47 (d, 1H, JNH,S 8~BHz, -CONH).
Preparation of (3) To a stirred solution of compound t2) (800 mg, 1.67 mmol) in anhydrous dichloromethane (10 ml) and dry pyridine (316 mg, 4 mmol) at -30° to -40°C, was added dropwise a solution of trifluoromethane sulphonic anhydride (Tf20) (556 mg, 2 mmol) in dichloromethane (2 ml) over 15 minutes. The reaction mixture was then stirred at -30° for 5 hours, and concentrated to dryness in vacuo. The residue was then dissolved in dry DMF (5 ml) containing a mixture of sodium azide (650 mg, 10 mmol) and tetrabutylammonium hydrogen sulphate (170 mg, 0.5 mmol>. The reaction mixture was stirred at room temperature for 16 hours, and then evaporated ''~ WO 91/16320 PGT/AU91/00161 to dryness under high vacuum. The residue was partitioned between ethyl acetate (200 ml) and water (50 ml>. The organic layer was separated and washed with water (50 ml x 2), dried over Na2S04, evaporated to leave a residue (780 mg), which was subjected to double chromatography (silica gel, the first solvent system was ethyl acetate/acetone:
8/1; the second solvent system was dichloromethane/water:
10/1) to afford a colourless oil (3) (185 mg, 24%).
MS. (FAB) 457 (M+ + 1), 414 (M+ -N3. tac720D + 19.1°
(Cl,MeOH).ir.(CHC13) cm-1 2100 (N-N3). 1748 (carbonyl). 1H-nmr (CDC13> b (ppm). 2.04, 2.05, 2.06, 2.12, (s, 12H, Acetyl CH3 x 4). 3.79 (s, 3H, COOCH3), 3.91 (ddd, 1H, JS~NH 8~4Hz, J5~4 8.8 Hz, J5~6 9.9Hz, H5), 4.17 (dd, 1H, J9.8 6.8Hz, J9.9, 12.5Hz, H8.), 4.42 (dd, 1H, J4~3 2.9Hz, J4~5 8.8Hz, H4), 4.48 (dd, 1H, J6~7 2.3Hz, J6~5 9.9Hz, H6 4.46 (dd, 1H, J9~8 2.7Hz, J9~9. 12.5Hz, H9), 5.31 (m, 1H, J8~7 5.2Hz, J8~9 2.7Hz, J8~9., 6.8Hz, H8), 5.45 (dd, 1H, J7~6 2.3Hz, J7~8 5.2Hz, H7>, 5.96 (d, 1H, J3~4 2.9H, H3), 6.13 (d, 1H, JNH,S 8.4Hz, -CONH) 13C-~r (CDC13) 6 (ppm) 20.7 (CH3-CO-O-), 23.2 (CH3C0-NH), 48.3 (C5>, 52.6 (COOCH3), 57.8 (C4), 62.1 <C9>. 67.7, 70.9 (C7, C8>, 75.9 (C6), 107.6 (C3), 145.1 (C2), 161.5 (C1), 1?0.2, 170.3, 170.7, (acetyl -C ~ 0 x 4).
Preparation of (4) Compound (3) (50 mg, 0.11 mmol> was dissolved in anhydrous methanol (5 ml) containing sodium methoxide (8 mg, 0.15 mmol). The mixture was stirred at room temperature far 2 hours and concentrated to dryness in vacuo. The residue was taken up in Water (3 ml), stirred at room temperature for 1.5 hours, ajusted to pH 6-7 with Dowex 50 x 8 (H+) resin, and then lyophilised to afford the title compound (4) (35 mg, 94~).

- . ~- CA 02291994 1999-12-07 i.r. (KBr>cm-1 3400 (br.-OH>, 2100 (-N3>, 1714 (carbonyl).
1H-nmr (D20) b (ppm>. 2.06 <5, 3H, acetyl CH3), 3.64 (dd, 1H, J9.~8 6.3Hz, J9.~9 11.8Hz, H9~), 3.65 (dd, 1H, J7~6 3.9Hz, J7.8 6.8Hz, H7), 3.88 (dd, 1H, J9~g 2.6Hz, J9~9 ' 5 11.8Hz, H9), 3.94 (m, 1H, J8~7 6.8Hz, J8~9 2.6Hz, J8~9.
6.3Hz, H8), 4.21 (dd, 1H, J5~4 10.4Hz, J5~6 8.9Hz, H5>, 4.31 ' Cdd, 1H, J4~3 2.2Hz, J4~5 2.2Hz, J4~5 10.4Hz, H4), 4.34 (dd, 1H, J6~5 8.9Hz, J6~7 3.9Hz, H6) 5.82 (d, 1H, J3~4 2.2Hz, H3).
Example 2 The preparation of Sodium 5-Acetamido-4-amino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (4-amino-Neu5Ac2en) (6) The overall reaction scheme is as follows:
oAc O'A°O~ O HsC.O HZSJpyrldirx oAc O'A'~~ O HIC,O
urr ~ o / o Ac Ny ~H~N
1 ) NaOMdMoOH OH
I~O UH O O. Nay 2) ON' ~H~ ~ O
Pre aration of (S) Into a solution of methyl 5-acetamido-7,8,9-tri-O-acetyl-4-azido-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (3) prepared as in Example 1, (95 mg, 0.208 mmol) in pyridine (6 ml) was bubbled with H2S for 16 hours at room temperature. The solution was then flushed with nitrogen for 15 minutes, and evaporated to remove pyridine ' 20 under high vacuum. The residue was chromatographed (silica gel, ethyl acetate/isopropanol/water = 5/2/1) to afford a colourless compound (5) (50 mg, 56%).

MS. (FAB) 431 (M+ + 1), 414 (M+ -NH2), ~~~20D +34.5° (C1, MeOH>. i.r. (CHC13) cm-1 3400 (br.NH2), 1740 (carbonyl).
1H-nmr (CDC13 + CD30D) E (ppm). 1.96, 2.06, 2.07, 2.10 (s, 12H acetyl CH3 x 4), 3.81 (S, 3H, -COOCH3>, 3.92 (brt, 1H, J~r~4 & J~r~6 lOHz, H5), 4.17 (dd, 1H, J9.~8 7.2H2, J9.~9 12.3Hz, H9.), 4.22 (br. dd, 2H, J4~5 & J6~5 lOHz, J4~3 & J6~7 2.lHz, H4 & H6>, 4.71 (dd, 1H, J9~8 2.6Hz, J9~9. 12.3Hz, H9), 5.31 (m, 1H, J8~7 4.9H2, J8~9 2.6Hz, J8~9. 7.2Hz, H83, 5.45 (d, 1H, J'7~6 2.lHz, J7~8 4.9Hz, H7>, 5.97 (d, 1H, J3~4 2.lHz, H3).
13C_~ (CDC13 + CD30D> 8 (ppm) 20.2, 20.3 (CH3-CO-O-), 22.3 (CH3-CO-NH), 48.2 (C5), 50.4 (C4), 52.0 (COOCH3), 52.1 (C9), 67.8, 71.2 (C7, C8), 76.5 (C6), 112.5 (C3), 143.5 (C2), 162.0 (C1>, 170.2, 170.4, 170.8, 172.2 (acetyl -C = 0 x 4).
Preparation of (6) Compound (5> (50 mg, 0.116 mmol> was dissolved in anhydrous methanol (5 ml) containing sodium methoxide (12.4 mg, 0.23 mmol). The mixture was stirred at room temperature for 1.5 hours and evaporated to dryness in vacuo at 30°C.
The residue was stirred in water (3 ml) at room temperature until TLC (silica gel, ethyl acetate/methanol/0.1 N HC1 =
5/4/1) indicated that hydrolysis was complete. The solution (pH about 10.5) was then gradually adjusted to around pH 7.5 by Dowex 50 x 8 (H+) resin. As soon as the pH of the solution reached 7.5, the suspension was quickly filtered by a press filter. The filtrate was lyophilised to afford the title compound (6) (30 mg, 83$).
1H-nmr (D20) 6 (ppm). 2.07 (S, 3H, acetyl CH3), 3.59 - 3.70 m, 2H, H7 & H9.), 3.89 (dd, 1H J9~8 2.6Hz, -J9 9.
11.8Hz, H9>, 3.95 (m, 1H, H8>, 3.99 (brd, 1H, J4~5 10.6Hz, H4), 4.21 (brt, 1H, J5~4 & J5~6 10.6Hz, H5), 4.29 (brd, 1H, J6~5 I0.6Hz, H6>, 5.66 (d, 1H J3~4 l.9Hz, H3).

Example 3 The preparation of Ammonium 5-Acetamido-4-guanidino-2,3,4,5-tetradeoxy-D-crlvcero-D-ctalacto-non-2-enopyranosonate (7) The overall reaction scheme is as follows:
OAc HO
S-CH;
A O Ill~zN-C=i~iH HU ()1~ ~t) o "- UAc c) NH ~~rl ~~,~~~ p ~ CEi3 Nib ~V_.~ O' Ac~ tlZN 2) powcz SOGV z 8, Ac~ f1N
N1~
(S) NH~OH HzN

(7) Into a solution of S-methylisourea (546 mg, 3 mmol>
in water (15 mL> at ice-bath temperature, methyl-5,7,8,9-tri-O-acetyl-4-amino-2,3,4,5-tetradeoxy-D-Qlycero-D-Qalacto-non-2-enopyranosonate (5) prepared as in Example 2 (40 mg, 0.093 mmol> was added. The reaction mixture was stirred at S°C for seven days and poured onto a column of Dowex 50w X 8 (H+) resin (35 mL>. The column was then washed with cold water (700 mL) and eluted with 1.5 M NH40H solution. The eluate (120 mL> was concentrated to dryness under high vacuum. The resulting residue was chromatographed (silica gel; solvent system 1: ethyl acetate/isopropanol/water, 1/5/1; solvent system 2: 75~ isopropanol) to provide the title compound (7) ( 8 mg, 24 . 50 .
Compound (7) gave a strong, positive Sakaguchi reaction, indicating the presence of a guanidine group. NMR
data for compound (7) are given below. 1H-nmr (D20 + CD30D) b lppm).
2.06 (s, 2H, acetyl CH3), 3.60 (br. d., 1H, J7~8 9.4Hz, H7), 3.63 (dd, 1H, J9.~8 6.2Hz, J9.~9 11.8Hz, H9.), 3.76 (br. d., ' 1H, J4~5 9.4Hz, H4), 3.87 (dd, 1H, J9~8 2.6Hz, J9~9., Il.BHz, H9), 3.93 (ddd, 1H, J8~7 9.4Hz, J8~9 2.6Hz, JB~g~ 6.2Hz, H8), ' 4.01 (dd, 1H, J5~4 9.4Hz, J5~6 10.6Hz, H5>, 4.20 (br. d., 1H
J6~5 10.6Hz, H6), 5.63 (d, 1H, J3~4 2.lHz, H3).

''"'' wo 9v~s~zo rcri~u9vooi6i ~ - 24 -Example 4 Sodium 5-Acetamido-4-N,N-diallylamino-2,3,4,5-tetradeoxy-D-alvcero-D-aalacto-non-2-enopyranosonate. (9).
The overall reaction scheme is as follows:
OAc OAc A O O ~uyi br«Na~ Ac0 ~ OAc v ~ . , " OAc O ~ CH, ~gZ~~ ' ~ ° -.: _ , ~.. ..! ~'Fi, c~
Ac HiN Ac t (5) Fi,C ~ ~ ~ X11.
«~
HO
llNaObtelMeOH HO (1~j O
N: ,, O
:OOH' Ac ~N~\
HZC CHi (9) , Into a solution of allyl bromide (60mg, O.Smmol) '~ WO 91/16320 PGT/AU91/00161 and methyl 5-acetamido-7,8,9-tri-O-acetyl-4-amino-2,3,4,5-tetradeoxy-D-crlycero-D-Qalacto-non-2-enopyranosonate (5>
(90mg, 0.209mmo1) in acetonitrile (5mL), was added silver carbonate (116mg, 0.418mmo1). The mixture was stirred and protected from light at room temperature for 16 h. The resulting suspension was filtered, and the filtrate was ' evaporated to dryness. The residue was subjected to flash-column chromotography silica gel, ethyl acetate containing 10% methanol) to afford methyl 5-acetamido-7,8,9-tri-O-acetyl-4-N,N-diallylamino-2,3,4,5-tetradeoxy-D-dlycero-D-Qalacto-non-2-enopyranosonate (8) (85mg, 80%).
1H-nmr (CDC13) 8 (ppm) 1.94, 2.05, 2.06, 2.11 <s, 12H, acetyl CH3 x 4), 2.97 (dd, 2H, JlOa,lOb & J10'a,10'b 14.3Hz, Jl0a,I1 & J10'a,ll' 7~6Hz, HlOa & H10'a)~ 3~24 (dd, 2H, Jlpb,l0a & J10'b,10'a 14.3Hz, J10b,11 & J10'b,ll' 4~9Hz, HlOb & H10'b), 3.58 (dd, 1H, J4~3 2.4Hz, J4~5 9.3Hz, H4>, 3.79 (s, 3H, COOCH3), 4.12-4.26 (m, 3H, H6, H9~, H5), 4.70 (dd, 1H, J9~8 2.6Hz, J9~9. 12.3Hz, H9), 5.09 (dd, 2H, Jl2cis,11 &
J12'cis,ll' 10.6Hz, Jl2gem & J12'gem-1~5Hz, Hl2cis &
H12'cis)~ 5.14 (dd, 2H, Jl2trans,ll & J12'trans,ll' 17.7Hz, Jl2gem & J12'gem -1~SHz, Hl2trans & H12'trans)~ 5~27-5.32 (m, 2H, H8 & -CONH->, 5.55 (dd, iH, J7~6 2.lHz, J7~8 4.7Hz, H7), 5.72 (m, 2H, H11 & H11~), 6.07 (d, 1H, J3~4 2.4Hz, H3>.
Compound (8) (80mg, 0.156mmo1> was dissolved in anhydrous methanol (lOmL) containing sodium methoxide (16.2mg, 0.30mmol).
The solution was stirred at room temperature for 2 h, then evaporated to dryness. The residue was taken up in water (5mL), and left at room temperature for 2 h. The resulting solution was neutralized with Dowex 50 x 8 (H+) and freeze-dried to afford the title compound (9) (49mg, 80%>.
1H-nmr (D20) b (ppm) 1.94 (s, 3H, Acetyl CH3), 3.24-3.44 (m, ' 35 4H, H10 x 2 & HlOr x 2>, 3.48-4.33 (m, 7H, H4, H5, H6, H7, H8, H9 & H9.), 5.24-5.29 (m, 4H, H12 x 2 & H12. x 2), 5.69 (d, 1H, J3~4 ~2Hz, H3), 5.73-5.76 (m, 2H, H11 & H11') ~ WO 91/16320 PGT/AU91/00161 Example 5 Sodium 5-Acetamido-4-N-allylamino-2,3,4,5-tetra-deoxy-D-Qlvcero-D-Qalacto-non-2-enopyranosonate (11) The overall reaction scheme was as follows:
OAc OAc A OAc p O ~uy~ x~,~d~ Ac0 7 OAc O
-,,. 0 z CH, ~sz°o~W'' ° CH
,NH ~ O~ ..~ ,N: ~ ~ O
Ac HzN Ac s f~N , (5) ~~ \L1(, i, HO (1()1 » N~oM~nt~on HO O O O
NF i nofr Ac IiN
CHz (l1) To a solution of allyl bromide (48mg, 0.40mmo1) and compound (5) (155mg, 0.36mmo1) in acetonitrile (5mL) was added silver carbonate (107mg, 0.38mmo1). The mixture was stirred, whilst protected from light, at room temperature for 16 h. The resulting suspension was filtered off, and the filtrate Was evaporated to dryness. The residue was chromatograph~d an a silica gel column (ethyl acetate/
isopropanol/water = 5:2:1). Fractions with an Rf value of 0.5 were combined and evaporated to dryness to afford compound (10) (53mg, 32%). The starting material (5) with an Rf value of 0.3 (6lmg, 39%) and N, N-diallyl derivative (8) with an Rf. value of 0.9 (20mg, 1l%) were recovered respectively.

1H-nmr (CDC13) of compound (10) is shown as follows 8 (ppm) 1.96, 2.05, 2.06, 2.11(x, 12H, Acetyl CH3 x 4), 3.25 (dd, IH, JlOa,lOb-14.1Hz, J10a,11 5~BHz, HlOa), 3~37 (dd, 1H, Jl0b,l0a-14.1Hz, J10b,11 5~9Hz, HlOb), 3.43 (dd, 1H, J4,3 ~ 5 3.lHz, J4~5 7.5Hz, H4), 3.79 (s, 3H, COOCH3), 4.09 (ddd, 1H, J5~4 7.5Hz, JS~~g.lHz, J5~6 8.lHz, H5), 4.21 (dd, 1H, Jg.~B
7.lHz, J9.~g-12.2Hz, Hg.), 4.30 (dd, 1H, J6~5 S.lHz, J6~7 4.lHz, H6), 4.63 (dd, 1H, Jg~B 3.2Hz, Jg~g.-12.2Hz, Hg), 5.09 (dd, 1H, Jl2cis,11 10.2Hz, Jl2cis,12trans-1~3Hz, Hl2cis), 5.18 (dd, 1H, Jl2trans,ll 17.1Hz, Jl2trans,l2cis-1~3Hz, Hl2trans), 5~36 (ddd, 1H, J8~7 4.2Hz, JB~g 3.2Hz, JB~g 7.lHz, H8), 5.57 (dd, 1H, J7~6 4.lHz, J~~B 4.2Hz, H~>, 5.65 (d, 1H, JNH,5 9~lHz, -CONH-), 5.83 (dddd, 1H, J11,12trans 17.1Hz, J11,12cis 10.2Hz, J11,10a 5~BHz, Jll,lOb 5~9Hz, H11), 6.09 (d, 1H, J3~4 3.lHz, H3).
Compound (10) (50mg, O.llmmol) was stirred in anhydrous methanol (5mL) containing sodium methoxide (l2mg, 0.225mmo1> at room temperature for 2 h, then evaporated to dryness. The residue was redissolved in water (5mL> and allowed to stand at room temperature for 2 h before being neutralized with Dowex 50 x 8 (H+) resin. The aqueous solution was freeze-dried to afford compound (11> (3lmg, 78~).
1H-nmr (D20) a (ppm) 2.02 (s, 3H, CH3C0), 3.42 (dd, 1H, JlOa,lOb-13.4Hz, J10a,11 6.6Hz, HlOa), 3.52 (dd, 1H, Jl0b,l0a-13.4Hz, J10b,11 6~3Hz, JlOb), 3~51-4.27 (m, 7H, H4, H5, H6, H7, H8, Hg & Hg.), 5.30 (dd, 1H, Jl2cis,12trans '"l.SHz, Jl2cis,11 10.3Hz, Hl2cis), 5~34 (dd, 1H, Jl2trans,l2cis~1~5Hz, Jl2trans,ll 17.7Hz, Hl2trans), 5~72 (d, 1H, J3~4 2.4Hz, H3), 5.89 (dddd, J11,10a 6~6Hz, Jll,lOb 6.3Hz, J11,12cis 10.3Hz, J11,12trans 17.7Hz, H11)~

Example 6 Sodium 5-Acetamido-4-amino-2,3,4,5-tetra deoxy-D-Qlycero-D-talo-non-2-enopyranosonate t14).
. The overall reaction scheme is as follows:
OAc OAc 9 r OH a Nt(, Ac OAc O O CH n rr2o~y~;2a2 Ac 7 OAc s O' i (, , CH
NH ~ U ~ ~ ---~ , NH s ~ I U ' a AC 21 NN~Duso~rWYkthYiamu~c AC 5 1) NaN~n~8u4N~HSO~duene/H20 (2) 111i2slpyndum ( 121 HyC
/ () UAc N',UAc . ~.
1 Cli ;
H() Ac0 U nmt.ednc IKA uK! ( I 11 )ao o)a No2 0 z) oIr ~ N
Ac O
()a) To a stirred solution of compound (2) (500mg, 1.04mmo1) in anhydrous dichloromethane (8mL) containing pyridine (205mg, 2.6mmo1) at -30°, was added dropwise a solution of trifluoromethanesulphonic anhydride (Tf20) (367mg, l.3mmo1) in dichloromethane (2mL) over a period of 20 minutes. The reaction mixture was then stirred at -30° for 5 ~h, and finally evaporated to dryness under reduced pressure.
The resulting residue was stirred in dry DMF containing N,N-diisopropylethylamine (194mg, l.5mmo1) at room temperature for 16 h. The reaction mixture was concentrated under high vacuum to remove DMF. The residue was then stirred in a two-phase mixture of toluene (5mL> and water (5mL) containing tetra-n-butylammonium hydrogen sulphate (950mg, 2.8mmo1) and sodium azide (137mg, 2.lmmol). The mixture was stirred at room temperature for 16 h and then evagorated to dryness. The residue was partitioned between ~.,.'~

ethyl acetate (50mL) and water (lSmL), with the organic layer washed successively with water (5mL x 2>, and then evaporated to dryness. The residue was taken up in pyridine (5mL), bubbled with H2S, and then evaporated to dryness. The residue was subjected to flash-column chromotography (silica gel, the first solvent system was ethyl acetate, the second ' solvent system was ethyl acetate/iso-propanol/H20 : 5/2/1).
The ethyl acetate eluate contained compound (13) (260mg, 53$). The fractions with a positive ninhydrin reaction, collected from the second solvent system, were combined and evaporated to dryness to afford compound (12> (32mg, 6.5$).
MS <FAB), 431 (M+ + 1), 414 (M+ - NH2).
1H-nmr (CDC13 + CD30D> 5 (ppm> 1.96, 2.06, 2.08, 2.09 (s, 12H, Acetyl CH3 x 4), 3.52 (dd, 1H, J4~3 S.SHz, J4~5 4.5Hz, H4), 3.80 (s, 3H, COOCH3), 4.16 (dd, 1H, J6~5 10.2Hz, J6~7 2.3Hz, H6), 4.17 (dd, 1H, J9.~9-12.4Hz, J9.~8 7.3Hz, H9.), 4.23 (dd, 1H, J5~6 10.2Hz, J5~4 4.5Hz, H5), 4.73 (dd, 1H, J9~9~-12.4Hz, J9~8 2.7Hz, H9), 5.34 (ddd, 1H, J8~7 4.7Hz, J8~9 2.7Hz, J8~9. 7.3Hz, H8>, 5.45 (dd, 1H, J7~6 2.3Hz, J7~8 4.7Hz, H7), 6.12 (d, 1H, J3~4 5.5Hz, H3>.
13C-~r (CDC13 + CD30D) 8 (ppm) 20.7 (CH3C(O)0-), 23.1(CH3C(O)N-), 43.8(C5), 46.2(C4), 52.4(COOCH3>, 62.3(C9), 68.3, 71.8(C7, C8), 73.0(C6), 111.5(C3>, 143.8(C2>, 162.4(C1), 170.3 & 170.8(CH3C0 x 4).
Compound (12) was stirred in anhydrous methanol (5mL> containing Amberlite IR.A-400 (OH-) resin (100mg> at room temperature for 3,h. Following filtration, the filtrate was evaporated to dryness. The residue was dissolved in water (5mL) and adjusted to pHl3 with O.1M NaOH.
The aqueous solution was stirred at room temperature for 2 hr ' and then neutralized with Dowex 50 x 8 (H+) resin. After filtration, the filtrate was lyophilized to afford compound (14) (l6mg, 70~), which was positive in the ninhydrin reaction.

1H-nmr (D20) 8 (ppm) 2.10 (s, 3H, CH3C0),,3.67-3.76 (m, 2H, H4 & H9.), 3.92 (dd, 1H, J9~8 2.8Hz, J9~9.-Il.9Hz, H9), 3.90-4.02 (m, 2H, H7 & H8), 4.37-4.44 (m, 2H, H~ & H6), 5.81 (d, 1H, J3~4 5.14Hz, H3).
Example 7 Sodium 5-acetamido-4-azido-2,3,4,5-tetradeoxy-D-glycero-D-talo-non-2-enopyranosonate (17).
OAc N
HOO COOMe Ate' f Ac ~ COOMe AcH N; ,L
Ac0 1)TfZO/pyridinc/DCM AcHN .
--~..~ Ac0 2I N.N-diisapropylethylam~ne/UMF
3> NaN ~-Bu N.HSO 1 S
3/ a a/~'olucne/H,_O
410.1 MHC1 NaC)MeJMe<)H

HO ~ -O COONa NaOH HO ~ O COOMe AcHN . ~ AcHN .
HO

To a stirring solution of compound (2) (500 mg,1.04 mmol) in anhydrous dichloromethane (8 mL) containing pyridine (205 mg, 2.6 mmol) at -30°C, a solution of trifluoromethane-sulphonic anhydride (Tf20) (367 mg, 1.3 mmol) in dichloro-methane (2 mL) was added dropwise over a period of 20 minutes. The reaction mixture was then stirrred at 3°C for 5 h, and finally evaporated to dryness under reduced pressure.
Tt-se resulting residue was stirred in dry DMF containing N,N-diisopro~ylethylamine~(194 mg, 1.5 mmol) at room temperature for 16 h. The reaction mixture was concentrated under high vacuum to remove DMF. The residue was then ' stirred in a two-phase mixture of toluene (5 mL) and water (5 mL) containing tetra-n-butylammonium hydrogen sulphate (950 mg, 2.8 mmol) and sodium azide (137 mg, 2.1 mmol). The mixture was stirred at room temperature for 16 h and then was diluted with 0.2 M HC1 (5 mL). The mixture was stirred at room temperature for 48 h. To this reaction mixture were added ethyl acetate (50 mL) and 2 M HC1 (l mL). The organic ' S layer was separated and washed with water (5 mL X 3), then evaporated to dryness. The residue was subjected to flash column-chromatography (silica gel, ethyl acetate/hexane=2/1).
The fractions with Rf value of 0.32 (ethylacetate/hexane=2/1 as developing solvent) were combined and evaporated to dryness to afford compound (15>. (40 mg, 8.4%). The column was then eluted with ethyl acetate/methanol=10/1 to recover the starting material (2) (280 mg,56%>. Compound (15) was isolated as a white foam substance.
MS (FAB) 457 (M++1>, 414 (M+-N3), i.r. (CHC13) cm-1 2108 (-N3), 1748 (carbonyl) 1H-nmr (CDC13), E (ppm)1.97, 2.04, 2.06, 2.07 (s,l2H, acetyl CH3 x 4), 3.82 (s, 3H, COOCH3), 4.12"'4.20 (m, 3H,C6, C4 &
C9), 4.51 (ddd, 1H, J5~4 4.4Hz, J5~6 10.7Hz, JS, NH, 10.1Hz, H5), 4.69 (dd, 1H, J9~8 2.6Hz, J9~9. 12.4Hz, Hg), 5.31 (m, 1H, J8~7 4.9Hz, JB~g 2.6Hz, J8~9~ ?.OHz, H8), 5.45 (dd, 1H, J7~6 2.lHz, J7~8 4.9Hz, H7>, 5.68 (d, 1H, JNH,S 10.1Hz,CONH), 6.15 (d, 1H, J3~4 5.7Hz, H3) 13C_~r (CDC13) d (ppm) 20.7, 20.8, (CH3C0-O x 3), 23.1 (O CH3 CO-NH), 44.8 (C5>, 52.6 (COOCH~), 54.8 (C4), 62.1 (C9), 67.6, 71.3 (C7, C8), 73.5 (C6), 104.5 tC3), 146.3 (C2), 161.5 (C1), 169.9, 170.2, 170.5 (acetyl, -C=O X 4) Compound (15) (40 mg, 0.088 mmol> was dissolved in anhydrous methanol (4 mL) containing sodium methoxide (6.4 mg, 0.12 mmol). The mixture was stirred at room temperature for 2 h and concentrated to dryness in vacuo to afford compound (16), Which was then dissolved in water (3 mL), stirred at room temperature for 2 h, adjusted to pH 6m7 with Dowex 50 X 8 (H+) resin, and then lyophilised to give the title compound (17) as a yellowish powder (25 mg, 83%).

/'~

i.r. (KBr) cm 1 3400 (br, -OH), 2108 (-N3), 1714 (carbonyl) 1H-nmr (D20) E (ppm) 1.97 (s, 3H, acetyl), 3.5"'4.4 (m, 7H, H4, H5, H6,H7, H8, H9, & H9'), 6.07 (d, J3~4 5.6Hz, H3) Example 8 Sodium 5-acetamido-4-N-methylamino-2,3,4.5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (20) OAc OAc Ac0 ~ O COOMe Ac0 ~ O COOMe AcHN;
MeUAg200~Ft~Q~1 AcHN .
NHZ ~. A~ NHCH3 is Naor.~rNC~i OH OH
HO ~ O CppNa NaOH HO
AcHN . ~ AcH COOMe HO
NHCHg Hi0 HO NHCH3 l9 To a solution of methyl iodide (15 mg, 0.10 mmol) and compound (5) (48 mg, 0.11 mmol) in acetonitrile (6 mL>

10 was added silver carbonate (42 mg, 0.15 mmol>. The mixture Was stirred whilst protected from light, at room temperature for 16 h. The resulting suspension was filtered off, and the filtrate was evaporated to dryness. The residue was subjected to chromatography (silica gel, ethyl acetate/isopropanol/
15 water=5/2/1). Fractions with Rf value of 0.36 were combined and concentrated in vacuum to dryness to afford compound (18) (25 mg, 51%).

.. . . -. -~ CA 02291994 1999-12-07 MS (FAB) 445 (M++1), 414 (M+ - NHCH3) 1H - nmr (CDC13) a (ppm>
1.95, 2.05, 2.06, 2.12 (s, 12H, acetyl CH3 X 4), 2.45 (s, 3H, N-CH3), 3.72 (dd, 1H, J4~3 2.3Hz, J4~5 9.2Hz, H4), 3.89 (s, 3H, COOCH3), 4.16 (dd, 1H, Jg.~B 7.2Hz, J9',9 12.3Hz, Hg'), 4.26 (ddd, 1H, J5~4 9.2Hz, JS~NH 9.lHz, J5~6 9.OHz, H5), 4.36 (dd, 1H, J6~5 9.OHz, J6~7 2.7Hz, H6), 4.64 (dd, 1H, J9~g 2.9Hz, J9~g~ I2.3Hz, H9), 5.34 (m, 1H, J8~7 4.8Hz, JB~g 2.9Hz, Jg~g~ 7.2Hz, Hg), 5.51 (dd, 1H, J~~6 2.7Hz, J~~B
4.8Hz), 6.05 (d, 1H, J3~4 2.3Hz, H3) Compound (18) (25 mg, 0.056 mmol) was stirred in anhydrous methanol (5 mL) containing sodium methoxide (5.4 mg, 0.1 mmol) at room temperature for 2 h, then evaporated to dryness to give compound (19), which was redissolved in water (5 mL) and allowed to stand at room temperature for 2 h before being neutralized with Dowex 50 x 8 (H+) resin. The filtrate was lyophilised to afford compound (20) (15 mg, 82~).
1H-nmr (D20) E (ppm) 1.94 (s, 3H, CH3C0), 2.43 (s, 3H, N-CH3), 3. 54.3 (m, 7H, H4, H5, H6, H~, H8, Hg & Hg'), 5.65 (d, 1H, J3~4 2Hz, H3) Example 9 Sodium 5-acetamido-4-N,N-dimethylamino-2,3,4,5-tetradeoxy-D-giycero-D-galacto-non-2-enopyranosonate (23>.
OAc AcO, O OAc .
COOMe AcHN; / AcOAcH O / COOMe ACO MeIlAg2O~~lQ~i3Q~t N f'~2 --. Ac0 NMe2 zi Amlx~litc IRA-400(OH7 McOH
OH OH
HO O COONa NaOH HO ~ O COOMe AcHN . / , AcH
HO
NMe2 H20 HO NMe2 z2 To a solution of methyl iodide (65 mg, 0.46 mmol) and compound (5) (100 mg, 0.23 mmol) in acetonitrile (15 mL>
was added silver carbonate (127 mg, 0.46 mmol). The mixture was stirred and protected from light at room temperature for 16 h. The resulting suspension was filtered off and the filtrate was evaporated to dryness. The residue was subjected twice to flash-column chromatography (silica gel, ethyl acetate/ isopropanol/water=5/2/1> to afford compound (21) (30 mg, 28$> as a colourless foam.
MS (FAB) 459 (M++1) 414 (M+-N(CH3)2) 1H-nmr (CDC13) b (ppm) 1.98, 2.05, 2.06, 2.12 Cs, 12H, acetyl, CH3 X 4), 2.33 (br s, 6H, N(CH3>2), 3.42 (dd, 1H, J4~3 2.8 Hz, J4~5 8.6Hz, H4), 3.79 (s, 3H, COOCH3), 4.17 (dd, 1H, J9'8 7.4Hz, J9.~9 12.3Hz, H9'), 4.18 (ddd, 1H, J5~4 8.5Hz, JS, NH 8.9Hz, J5~6 9.OHz, H5), 4.31 (dd, 1H, J6~5 9.OHz, J6~7 2.9Hz, H6), 4.68 (dd, 1H, ~
J9r8 3.OHz, J9~9. 12.3Hz, H9), 5.31 (m, 1H, J8~7 4.4Hz, J8~9 3.OHz, JB~g. 7.4Hz, H8), 5.51 (dd, 1H, J~~6 2.9Hz, J7~8 4.4Hz, H7), 5.79 (d, 1H, JNH,S 8~9Hz, CONH>, 6.09 Cd, 1H, J3~4 2.8Hz, H3) Compound (21) (30 mg, 0.066 mmol) was stirred in anhydrous methanol (4 mL) containing dry Amberlite IRA 400 (OH-) resin (90 mg) at room temperature for 3 h, then the resin filtered off. The filtrate and washings were combined and evaporated to dryness to afford compound (22> (20 mg), which was stirred in water (5 mL) at pH 12 at room temperature for 2 h, then was adjusted to pH 7.5 with Dowex 50 X 8 (H+> before filtration. The filtrate was lyophilised to afford compound (23) (15 mg, 66%) as a white powder.
1H-nmr (D20> 8 (ppm>
1.97 (s, 3H, acetyl), 2.33 (s, 6H, N(CH3)2), 3.50"4.26 (m, 7H, H4, H5, H6, H7, H8, Hg & H9.), 5.71 (d, J3~4 l.8Hz, H3) Example 10 Disodium 5-acetamido-4-N-oxycarbonylmethyl-amino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate <26).
OAc OAc Ac0 O COOMe Ac0 9 ~ O z AcHN; COOMe ACO ~ B~2~Mc/AgZCO~CH~CN ACH N . 4 NH2 -.-.. A~ 5 NHCH2COOMe 5 241 l1 NaOMe/McOH
OH OH
HO ~ O COONa NaOH HO. ~ O COOMe AcHN - ~ AcHN .
HO NHCH2COONa H20 HO NHCH2COOMe To a solution of methyl a-bromoacetate (36 mg, 0.23 mmol) and compound (5> (100 mg, 0.23 mmvl) in acetonitrile (12 mL) was added silver carbonate (64 mg, 0.23 mmol). The mixture was stirred at room temperature for 16 h whilst shielded from light, then filtered. The filtrate was ,rte evaporated to dryness. The residue was chromatographed on silica-gel column (ethyl acetate/isopropanol/water=5/2/1).
Fractions with Rf value of 0.60 were collected and evaporated to dryness to afford compound (24) (80 mg, 68.5%).
1H-nmr (CDC13) 8 (ppm) 1.97, 2.044, 2.047, 2.11 (s, 12H, acetyl CH3 x 4), 3.49 (AB, 2H, J~ 17.6Hz, H10 x 2), 3.50 <dd, 1H, J4~3 2.9Hz, J4~5 8.4Hz, H4), 3.71 (s, 3H,C1100Me), 3.79 (s, 3H,Cl00Me), 4.09 (ddd, 1H, J5~4 8.4 Hz, JS~NH 8.8Hz, J5,6 8.lHz,HS>, 4.17 (dd, 1H, J9.~8 7.4Hz, J9.~g 12.3Hz, H9.), 4.32 (dd, 1H, J6~5 B.IHz, J6~7 4.lHz, H6), 4.63 (dd, 1H, J9~8 3.lHz, J9~9.
12.3Hz, H9), 5.37 Cm, lH, J8~7 4.lHz, J8~9 3.lHz, J8~9.
7.4Hz, H8), 5.56 (t, 1H, J~~6 4.lHz, J~~B 4.lHz, H7>, 6.03 (d, 1H, JNH,S 8.8Hz, CONH), 6.04 (d, IH, J3~4 2.9Hz, H3) Compound (24) (80 mg, 0.159 mmol) was stirred in anhydrous methanol (20 mL> containing sodium methoxide (18 mg, 0.32 mmol) at room temperature for 2 h, then evaporated to dryness to give compound (26), which was redissolved in water (15 mL). The solution was allowed to stand at room temperature for 2 h before being adjusted to pH 7 by Dowex 50 x 8 (H+> resin. The filtrate was freeze-dried to afford compound (25) as a white powder (59 mg, 94.6%).
1H-nmr (D20) 8 (ppm) 2.04 <s, 3H, acetyl), 3.58 (AB, 2H, Jp~ 1?.6 Hz, H10 x 2), 3.50"'4.40 (M, 7H, H4, H5, H6, H7, H8, H9 & H9.), 5.68 (d, 1H, J3~4 2.lHz, H3) ,~w.
w ' CA 02291994 1999-12-07 Example 11 Sodium 5-acetamido-4-N-2'-hydroxyethylamino-2,3,4,5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (29>
OAC
OAC
A~ACHN~'~COOMe AC0,9 ~ ~ 6 O Z 1 ACO tirCli~CH~OWAgtCO~/CI~~CN ACHN . d / COOMe NHy ACO 5 NHCHyCH20H
~ 1(I I I
Amlxrlire (IZA-C(1(r(Uf~ ) n~~cH f .
OH OH
HO ~ ~O COONa NaC)!i HO ~ ~O COOMe ACH N~\l~ AcH N\\l H O '/ ~ H ~~'1O
NHCHpCH20H FtZU NHCH2CHpOH

ZS
To a solution of bromoethanol (158 mg, 1.26 mmol) and compound (5> <84 mg, 0.195 mmol> in acetonitrile (10 mL>
was added silver carbonate (100 mg, 0.36 mmol). The mixture was protected from light and stirred at room temperature for 7 days. Then it was filtered off, the filtrate was evaporated to dryness. The residue was chromatographed on a silica gel column (ethyl acetate/isopropanol/water=5/2/1).
Fractions with Rf value of 0.4 were combined and evaporated to dryness to afford compound (27> (40 mL, 40~).
MS (FAB> 475 (M++1), 414 (M+-NHCH2CH20H) 1H-nmr (CDC13) a (ppm) 1.96, 2.05, 2.10 (s, 12H, acetyl CH3 x 4), 2.29 (br. s, 2H, NH &0H), 2.76 (ABm, 2H, H10 X 2), 3.47 (dd, 1H, J4~3 2.9Hz, J4~5 7.5Hz, H4>, ss".62 (t, 2H, J11,10 4.9Hz, H11 x 2), 3.79 (s, 3H, COOCH3), 4.15 (ddd, 1H, J5~4 7.5Hz, J5~6 8.4Hz, JS, NH
8.3Hz, H5), 4.19 (dd, 1H, J9.~8 7.5Hz, J9.~~ 12.3Hz H9~>, 4.29 (dd, 1H, J6~5 8.4Hz, J6~7 3.8Hz, H6), 4.65 (dd, 1H, J9~8 .
2.9Hz, Jg~9. 12.3Hz, H9), 5.36 (m, 1H, J8~7 4Hz, J8~9 2.9Hz, JB~g~ 7.5Hz, H8), 5.55 (dd, 1H, J7~6 3.8Hz, J7~8 4Hz, H7), 6.08 (d, 1H, J3~4 2.9Hz, H3>, 6.09 (d, 1H, JNH,5 8.3Hz, CONH) 13C_~ (CDC13) 8 (ppm) 20.6, 20.8, (CH3-CO-O- x 3), 23.10 (CH3-Co-NH), 46.5 (C5>, 47.2 (C10), 52.3 tCH3COOCH3), 55.6 tC4), 61.1 (C11), 62.1 tC9), 68.1, 71.1 tC7,C8), 76.7 (C6), 111.6 (C3), 143.7 tC2), 162.1 (C1), 170.1, 170.3, 170.6, 171.0 (acetyl carbonyl x 4) Compound (27) (40 mg, 0.084 mmol) was stirred in anhydrous methanol (10 mL) containing dry Amberlite IRA-400 (OH-) (120 mg) at room temperature for 4 h, then filtered.
The filtrate and washings were combined and evaporated to IO dryness to give compound (28), which was redissolved in water (10 mL) and adjusted to pH 13 by adding NaOH. The aqueous solution was left at room temperature for 3 h before being adjusted to pH 6m7 with Dowex 50 x 8 (H+) resin. The solution after filtration was lyophilised to afford compound (29) as a white powder (20 mg 66~).
1H-nmr (D20) a tppm) 1.99 ts, 3H, acetyl), 2.91 tAB, 2H, H10 x 2), 3.53 ~ 4.25 (m, 9H, H4, H5, H6, H~, H8, H9, H9., H11 X 2), 5.65 (d, J3~4 2.24 Hz, H3) Example 12 Sodium 2,-3-dideoxy-D-glycero-D-galacto-non-2-enopyranosonate (35) ' ~ aH off a,..~ off off H'/McOli OH ~ _ ~ O COOCHa O
OH
OH
30 3!
CEI ,COCI
,OAc OAc OAc G
O COOMe ~OAc Ac0 ~ O COOCF~, \A~: ~ AgNO~/CIi,CN ' Ac0' OAc Ac OAc NaOMc/McOH
,OH , COOMe NaOH/FIzO ~ O COONa W ~ HO ; /
OH

Compound (30,) (332 mg, 1.24 mmol) was stirred in anhydrous methanol (40 mL) containing Dowex 50 x 8 (H+) resin (50 mg) at room temperature for 16 h before filtration. The filtrate was evaporated to dryness to give compound (31) (320 ' mg, 1.13 mmol, 91.5%), which was stirred in acetyl chloride (5 mL) at room temperature for 3 days then evaporated to dryness to afford Compound (32) (539 mg, 1.057 mmol, 93.6%).
The residue was dissolved in acetonitrile (20 mL> containing silver nitrate (500 mg, 2.94 mmol) and potassium carbonate (90 mg, 0.65 mmol) protected from light and stirred at room temperature for 16 h, then filtered. The filtrate was evaporated to small volume and partitioned between ethyl acetate (75 mL) and water (15 mL). The organic layer was washed with water (10 mL x 3) and evaporated to dryness. The residue was chromatographed on silica gel column (ethyl acetate/hexane=2/1> to afford pure compound (33) <200 mg, 0.423 mmol, 40~).
1H-nmr (CDC13) 8 (ppm) IO 2.062, 2.070, 2.073, 2.094, 2.096 (s, 15H, acetyl CH3 x 5), 3.80 (s, 3H, COOCH3), 4.19 (dd, 1H, J9~8 5.9Hz, J9.~9 12.3Hz, H9'), 4.33 (dd, 1H, J6~5 9.4Hz, J6~7 3.OHz, H6), 4.57 (dd, 1H, J9~8 l.9Hz, J9~9. 12.3Hz, H9>, 5.20 (dd, 1H, J5~4 7.OHz, J~r~6 9.4Hz, H5), 5.38 (m, 1H, J8~7 5.lHz, J8~9 l.9Hz, JB~g.
5.9Hz H8), 5.49 (dd, 1H, J7~6 3.OHz, J7~8 5.lHz, H7), 5.57 (dd, 1H, J4~3 3.lHz, J4~5 7.OHz, H4), 5.97 (d, 1H, J3~4 3.lHz, H3>
Compound (33> (100 mg, 0.211 mmol> was stirred in anhydrous methanol (10 mL) containing sodium methoxide (24 mg, 0.423 mmol) at room temperature for 3 h, then evaporated to dryness to afford compound (34) (50 mg, 90~), which was redissolved in water (5 mL) and left at room temperature for 3 h before adjusted to pH 7 with Dowex 50 x 8 (H+) resin.
The solution was freeze-dried to give compound (35) (47 mg, 91~).
1H-nmr (D20) E (ppm) 3.69 ldd, 1H, J9.8 5.6Hz, J9.9 12.0Hz, H9.), 3.76 (dd,lH, J5~4 7.8Hz, J5~6 10.5Hz H5), 3.87 - 3.99 (m, 3H, H7, H8, H9), 4.13 (d, 1H, J6~c~ 10.5Hz, H6), 4.40 (dd, 1H, J4~3 2.3Hz, J4~5 7.8Hz, H4), 5.67 (d, 1H, J3~4 2.3Hz H3) ,~~w Example 13 Sodium 4,5-Diamino-2,3,4,5-tetradeoxy-D-glycero-D-qalacto-non-2-enopyranosonate (38) , OH OH
HO O COO- HO ~ O
AcHN; ~ ~H N . COO' HO NH2NH~.HzO
NH2 ~ HO NHz Heat 1 ) Ambcrti~e IRA-40D(HCUO
2) I.S M HCOOH
3) Ambcrlite lR-4B(OH~) OH OH
HO ~ O COONa NaOH HO ~ O COOH
WH2N . I wH2N . I

~8 37 A solution of compound (6> (125 mg, 0.40 mmol> in hydrazine hydrate (5 m1a) under argon was heated at 85°C for 3 days, and the resulting mixture was vacuum evaporated to dryness. The residue was dissolved in water (15 mL) and passed through a column of Amberlite IRA-400 lHCOO-), then eluted with 1.5 M HCOOH. The eluate (200 mL) was evaporated to dryness. The residue was chromatographed on silica gel deactivated with 10% water (developing solvent:
isopropanol/water = 4/1). The fractions with Rf value of 0.1 were combined and evaporated to dryness, then freeze-dried.
The residue, compound (36), was dissolved in water (10 mL), passed through a small column of Amberlite IR-4B (OH-)(10 mL). The effluent was evaporated to dryness to give compound (37), MS (FAB) of which was 249 (M++1). Compound (37> was dissolved in water and adjusted to pH 7.5 with 0.1 M NaOH, then freeze-dried to afford compound (38) (20 mg, 20%) as a white powder.

1H-nmr (D20) a (ppm) 3.01 (dd, 1H, J5~49.7Hz, J5~6 10.2Hz, H5), 3,58 (m, 2H, H9, &
H7), 3.80m3.89 (m, 3H, H4, H8, & H9>, 4.06 (d, 1H, 36,5 10.2Hz, H6), 5.54 (d, 1H, J3~4 2.4Hz, H3) Example 14 Methyl 5-acetamido-2,3,5-trideoxy-9-(p-toluenesulphonyl)-D-glycero-D-galacto-non-2- ' enopyranosonate (39).
A solution made up of methyl 5-acetamido-2,3,5-trideoxy-D-glycero-D-galacto-non-2-enopyranosopate (1000- - mg., 3.16 mmol> in dry pyridine (85 mL) was cooled in an ice-bath.
p-Toluenesulphonyl chloride (660 mg., 3.46 mmol) was added and the pale yellow homogeneous solution left to stir overnight at 4°C.
Further p-toluenesulphonyl chloride t220 mg., 1.15 mmol) was added and the solution left to stir for an additional 4h at room temperature.
Workup was first by addition of water (1 mL) followed by rotary evaporation to afford a viscous yellow oil which was flash chromatographed (Si02, EtOAc/i-PrOH/H20, 6/2/l,v/v/v) to give as the major product 1.19 g. (80% yield) of compound (39).
i.r (KBr) ~ vmax (cm 1) 2964 (OH), 1730 (C02CH3), 1656 (NHAc), 1358, 1174 (S02), 810, 662, 550 (Ar) MS (FAB); 460 (M+H+) 1H nmr (300 MHz, CD30D/TMS>; a (ppm> = 2.03 (s, 3H, NHAc), 2.45 (s, 3H, ArCH3), 3.49 (d, 1H, J6~71.70, H6), 3.76 (s, 3H, C02CH3), 3.91 (dd, 1H, J5~6 10.80, H5>, 3.98-4.13 tm, 3H, H8, H9 and H9'), 4.28 (dd, 1H, J7~8 9.55, H7), 4.39 (dd, 1H, J4~58.64, H4), 5.92 (d, 1H, J3~4 2.49, H3), 7.74 (d, 2H, ArH), 7.79 (d, 2H, ArH) Example 15 Methyl 5-acetamido-9-azido-2,3,5,9-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (40) Methyl 5-acetamido-2,3,5-trideoxy-9-(p toluenesulphonyl)-D-glycero-D-galacto-non-2-enopyranosonate (39) (600 mg., 1.27 mmol) and lithium azide (186 mg., 3.80 mmol) were dissolved in dry DMF (20 mL) and the yellow homogenous solution heated to 80°C. After 2 h, further lithium azide (186 mg., 3.80 mmol) was added and the solution left at 80°C overnight. The solvent was removed by rotary evaporation and the remaining dark brown oil dissolved in pyridine (2 mL) and flash chromatvgraphed (Si02, 5/2/1 EtOAc/i-PrOH/H20). The major product was compound (40) (370 mg., 88~ yield) obtained as a white foam.
i.r.(KBr):vmax (cm 1) 3428 (s,OH), 2104 (s, N3), 1730 (s, C02CH3), 1656 (s, NHAc) MS (FAB) . 331 (M+H+) 1H nmr (300 MHz, D20): d (ppm> = 1.94 (s, 3H, NHAc), 3.37 (dd, 1H, H9'), 3.48 - 3.57 (m, 2H, J8~9, 5.77, H8 and J9~9' 13.16, Hg), 3.66 (s, 3H, C02CH3), 3.91 - 3.98 (m, 2H, H5 and H6), 4.15 (d, 1H, J7~8 10.86, H7), 4.38 (dd, 1H, J4~5 8.88, H4), 5.91 (d, 1H, J3~4 2.44, H3) Example 16 Methyl 5,9-diacetamido-2,3,5,9-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (41).
. Thiolacetic acid (130 mL, 1.82 mmol) was added to methyl 5-acetamido-9-azido-2,3,5,9-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (70 mg.,0.21 mmvl) to give a pale yellow solution that was left to stir overnight at room temperature.
Excess thiolacetic acid was then evaporated off under low pressure and the remaining solid repeatedly treated with water followed by evaporation (3x3 mL>. The remaining solid was dissolved in methanol (4 m1,), filtered and the WO 91!16320 PCT/AU91/0016I

filtrate applied to a preparative tlc plate (Si02, 20 cm. x 20 cm. x 2 mm. eluted with 5/2/1 EtOAc/i-PrOH/H20). The band with Rf=0.47 was worked up to give 51 mg. (70$ yield) of compound (41) as a white powder.
i.r. CKBr) ~ vmax (cm I) 3400 (s, OH), 1728 (s,C02CH3), 1656 (s, NHAc) MS (FAB) . 347 (M+H+) 1H nmr 1300 MHz, D20> . 3 (ppm) = I.96 (s, 3H, NHAc), 2.00 (s, 3H, NHAc), 3.23 (dd, 1H, H9'), 3.48 (d, 1H, H6), 3.56 (dd, 1H, J9~9' 14.17, H9), 3.75 (s, 3H, C02CH3), 3,89 (m, 1H, J8~9 2.90, J8~9. 7.40, H8), 4.02 (dd, 1H, J5~6 9.10, H5>, 4.22 (d, 1H, J7~8 10.85, H7), 4.45 (dd, 1H, J4~5 8.94, H4), 5.61 td, 1H, ,T3~4 2.47, H3);
Example 17 5,9-diacetamido-2,3,5,9-tetradeoxy-D-crlycero-D-cralacto-non-2-enopyranosonic acid (42).
The preparation of compound (42) from compound (39) is summarized below:
OH
TsO~ ~ O O H
COOMe N ~ O
Ac HO OH / LiN,IUn~BO°c 3AcHN . / COOMe HO OH

CH,COSH
OH
OH
AcHN ~ O COOH t) OEi AcHN, ~ O COOMe AcHN .
HO OH AcHN .
2) H' HO OH
4s 4!

A solution of methyl 5,9-diacetamido-2,3,5,9-tetradeoxl-D-glycero-D-galacto-non-2-enopyranosonate (41) (46 mg., 0.13 mmol) dissolved in O.1M aq. sodium hydroxide (5 mL) was stirred at room temperature for 2.5 h. The solution was then adjusted to pH 5 with Dowex 50W-X8 (H+), the resin filtered off and the filtrate lyophilized to give 40 mg.
(91~ yield) of compound (42) as a white powder.
i.r. (KHr) . vmax (cm 1) 3376 (s, OH), 1652 (s, NHAc) MS (FAB) . 333 (M+H+) 1H nmr (300 MHz, D20) . a (ppm) = 1.89 (s, 3H, NHAc), 1.93 (s, 3H, NHAc), 3.15 <dd, 1H, H9'), 3.40 (d, 1H, H6), 3.48 (dd, 1H, J9~9' 14.18, H9), 3.82 (m, 1H, J8~9 3.01, J8~9. 7.43, H8), 3.94 (dd, 1H, J5,6 10.42, H5), 4.13 (d, 1H, J~~B 10.91, H7), 4.36 (dd, 1H, J4,5 8.80, H4), 5.81 (d, 1H, J3~4 2.41, H3) Example 18 Methyl 5-acetamido-9-cyano-2,3,5,9-tetradeoxy-_D-glycero-D-galacto-non-2-enopyranosonate (43>
A solution of methyl 5-acetamido-2,3,5-trideoxy-9-(p-toluenesulphonyl)-D-glycero-D-galacto-non-2-enopyranosonate (39) (80 mg., 0.17 mmol), tert-butylammonium cyanide (2 mg) and sodium cyanide (12 mg., 0.25 mmol) in dry DMSO <1.25 mL) was stirred at room temperature for 5 days.
Workup by preparative thin layer chromatography (Si02, 20 cm. x 20 cm. x 2 mm. eluted with EtOAc/ i-PrOH/H20, 5/2/1> gave as the major component 30 mg. (61~
yield) of compound (43> as a cream coloured powder.
<Rf=0.74).
i.r.(KBR) . vex (cm-1> 3440 (s, OH), 2256 (w, CN), I726 (s, C02CH3), 1638 (s, NHAc) MS (FAB) . 315 (M+H+>
1H nmr (300mHz, D20) : 8 (ppm) - 1.92 (s, 3H, NHAc), 2.75 (dd, 1H, H9'), 2.93 (dd, 1H, Jg~g.17.22, H9), 3.55 (dd, 1H, J6~~ 1.17, H6), 3.67 (s, 3H, C02CH3), 4.02 (dd, 1H, J5~6 9.05, H5), 4.13-4.19 (m, 1H, J8~9 3.91, J8~9.6.56, H8), 4.16 (dd, 1H, J~~B 10.90, H7), 4.37 (dd, 1H,J4~5 8.95, H4), 5.90 (d, 1H, J3~4 2.42, H3) ~
Exam>ale 19 5-Acetamido-9-cyano-2,3,5,9-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonic acid (44>.
The methodology used to prepare 5-acetamido-9-cyano-2,3,5,9-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonic acid (44) is summarised below:
OH OH
TsO~ ~ O COOMe N C ~ O COOMe ACHN . ~ NaCNp_guiNQ~! ACHN .
HO OE"~ ... HO OH
DMSO/5 days l 1 aq Na01 i 2) H~ cesui OH
NC ~ O COON
AcHN .
HO CZH
Methyl 5-acetamido-9-cyano-2,3,5,9-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate (43) (80 mg., 0.25 mmol) was dissolved in O.1M aq. sodium hydroxide (10 mL) and the resultant solution stirred at room temperature for 3 h.
The pH was then adjusted to 4 with Dowex 50W-X8(H+), the resin filtered off and the filtrate lyophilized to give 75 mg (98$ yield) of compound (43) as a fluffy white powder.

i.r. (KBr) : vmax (cm 1) 3370 (s,OH), 2254 (w, CN), 1656 (s, NHAc) MS (FAB) : 301 (M+H+) 1H nmr (300MHz, D20> : 3 (ppm) = 1.98 (s, 3H, NHAc), 2.70 (dd, 1H, H9'), 2.88 (dd, 1H, J9~9. 17.27, H9), 3.48 (d, 1H, H6), 3.97 (dd, 1H, J5~6 9.84, H5), 4.09-4.24 (m, 2H, H7 and H8,J8~9 3.90,J8~9' 6.53), 4.41 (dd, 1H, J4~5 8.87, H4), 5.80 (d, 1H, J3~4 2.42, H3) Example 20 Inhibition of Influenza Virus Neuraminidase An in vitro bioassay of the above-described compounds against N2 influenza virus neuraminidase was conducted, following Warner and O'Brien, Biochemistry, 1979 18 2783-2787. For comparison, with the same assay the Ki for 2-deoxy-N-acety-a-D-neuraminic acid was determined to be 3 x 10-4 M.
Values for Ki were measured via a spectrofluorometric technique which uses the fluorogenic substrate 4-methylumbelliferyl N-acetylneuraminic acid (MUN>, as described by Meyers et al., Anal. Biochem. 1980 I01 166-174. For both enzymes, the assay mixture contained test compound at several concentrations between 0 and 2 mM, and approximately 1 mU enzyme in buffer (32.5 mM MES, 4 mM CaCl2, pH 6.5 for N2; 32.5 mM acetate, 4 mM CaCl2, pH 5.5 for V.
cholerae neuraminidase).
The reaction was started by the addition of MUN to final concentrations of 75 or 40 ~M. After 5 minutes at 37°C, 2.4 ml 0.1 M glycine-NaOH, pH 10.2 was added to 0.1 ml reaction mixture to terminate the reaction. Fluorescence was read at excitation 365 nm, emission 450 nm, and appropriate MUN blanks (containing no enzyme) were subtracted from readings. The Ki was estimated by Dixon plots (1/fluorescence versus compound concentration). Results are summarized in Table 1, and unless otherwise stated, refer to inhibition of N2 neuraminidase.

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, Example 21 Inhibition of Influenza Virus Replication _In Vitro Inhibition of influenza A/Singapore/1/57 (H2N2) and Influenza B/Victoria/102/85 replication in vitro was measured by reduction of viral plaque formation in Madin Darby canine kidney (MDCK) cells Monolayers of confluent MDCK cells, grown in six well tissue culture plates, were inoculated with 0.3 ml of virus diluted to give about 50-100 plaques/well. Virus was diluted in serum-free minimal essential medium (MEM) containing 2 ~g/ml N-tosyl-1-phenylalanine chloromethyl ketone (TPCK) treated trypsin (Worthington Enzymes), and test compound.
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Once overlaid, plates were incubated at 37°C, 5~
C02 for 3 days. Cells were then fixed with 5~
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cn Sodium 5-acetamido-4-N-allyl-N-hydroxy-2,3,4,5-tetradeoxy-D-glvcero-D-galacto-non-2-enopyranosonate (45) can readily be prepared from compound (11) described in Example 5, using oxidation methods.
Example 22 In Vivo Anti-Viral Activity The compounds of Examples 2,3 and 6 (4-amino, 4-guanidino and 4-epi-amino), as well as the compound DANA (2-deoxy-N-acetyl-ac-D-neuraminic acid), which was shown in Example 20 to have anti-neuraminidase activity in vitro, were tested for anti-viral activity in a standard in vivo assay.
When administered intranasally to mice before and during challenge with influenza A virus, these compounds reduced the titre of virus in lung tissue 1 to 3 days after infection.
Mice were infected intranasally with 50 ~1 of 103 TCID50 units/mouse of H2N2 influenza A virus (A/Sing/1/57).
The test compound was admionistered intranasally at a dose rate of either 12.5 or 25 mg/kg body weight (50 ~1 of aqueous solution/mouse) as follows: 24 hours and 3 hours before infection; 3 hours after infection then twice daily on each of days 1, 2 and 3 after infection. The structurally unrelated compounds ribavirin and amantadine were also used for comparison.
The mice were sacrificed on days 1, 2 and 3 after infection, their lungs removed and virus titres in the lungs measured. The titres were plotted graphically and expressed as the percentage area under the curves (AUC) compared to those for untreated mice. Results are summarized below.

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N ~ b C ~ 'C
~ ~

~ b o ro~ ~ w 'o N ro 7 a a o ~ ~ o U ~ ~ N ~ .a ~

t ~ N ~ c~~ O
fx C

. E
~iN
fad N

w z '-1 '.~N 111 N

All three compounds tested showed greater potency than DANA.
Example 23 The following formulations are representative of compositions according to the invention:
AQUEOUS SOLUTION

$% w/w Compound of formula (I) 10.0 Benzalkonium chloride 0.04 Phenyiethyl alcohol 0.40 Purified water to 100$ w/w AQUEOUS COSOLVENT SOLUTION

$ w/w Compound of formula (I) 10.0 Benzalkonium chloride 0.04 Polyethylene glycol 400 10.0 Propylene glycol 30.0 Purified water to 100$ w/w AEROSOL FORMULATION

~ w/w Compound of formula (I) 7,5 Lecithin 0.4 Propellant 11 25.6 Propellant 12 66.5 DRY POWDER FORMULATION
.

~ w.w .

Compound of formula (I) 40.0 Lactose 60.0 These formulations are prepared by admixture of the active ingredient and excipients by conventional pharmaceutical methods. ' It will be clearly understood that the invention in its general aspect is not limited to the specific details referred to hereinabove.

Claims (27)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. A compound of formula (I) or formula (Ia) wherein in general formula (I), A is oxygen, carbon or sulphur, and in general formula (Ia), A is nitrogen or carbon;
R1 denotes COOH, P(0) (OH)2, NO2, SOOH, SO3H, tetrazol, CH2CHO, CHO or CH(CHO)2, R2 denotes H, OR6, F, Cl, Br, CN, NHR6, SR6 or CH2X, wherein X is NHR6, halogen or OR6 and R6 is hydrogen; an acyl group having 1 to 4 carbon atoms; a linear or cyclic alkyl group having 1 to 6 carbon atoms, or a halogen-substituted analogue thereof; an allyl group or an unsubstituted aryl group or an aryl substituted by a halogen, an OH group, an NO2 group or a COOH group, R3 and R3' are the same or different, and each denotes hydrogen, CN, NHR6, N3, SR6, =N-OR6, OR6 guanidino, or R4 denotes NHR6, SR6, OR6, COOR6, NO2, C(R6)3, CH2COOR6, CH2NO2 or CH2NHR6, and R5 denotes CH2YR6, CHYR6CH2YR6 or CHYR6CHYR6CH2YR6, where Y is O, S, NH or H, and successive Y moieties in an R5 group are the same or different, and pharmaceutically acceptable salts or derivatives thereof, provided that in general formula (I) (i) when R3 or R3' is OR6 or hydrogen, and A is oxygen or sulphur, then said compound cannot have both (a) an R2 that is hydrogen and (b) an R4 that is O-acyl or NH-acyl, and (ii) R6 represents a covalent bond when Y is hydrogen, and that in general formula (Ia), (i) when R3 or R3' is OR6 or hydrogen, and A is nitrogen, then said compound cannot have both (a) an R2 that is hydrogen, and (b) an R4 that is NH-acyl, and (ii) R6 represents a covalent bond when Y is hydrogen.

2. A compound as claimed in Claim 1 wherein the compound is a compound of formula (II) wherein R3 is hydrogen or R3' and R3' is -N3, -CN, -CH2NH2, or -N.R8.R9;
R8 and R9 are the same or different, and each denotes hydrogen, a linear or cyclic alkyl group of 1 to 6 carbon atoms, an acyl or substituted acyl group of 1 to 6 carbon atoms, -C. (NH).
NH2, -CH2. COON, CH2-CH2-OH or -CH2.CH (R10)(R11), R10 and R11 may be the same or different, and each denotes oxygen or R12N=, and R12 denotes hydrogen, -OH, -OCH3, -NH2, or (CH3)2N-or a pharmaceutically acceptable salt or derivative thereof.

3. A compound as claimed in Claim 1 or Claim 2 wherein R3 is NHR6.

4. A compound as claimed in Claim 1 or 2 wherein R3 is

5. A compound as claimed in Claim 1 and selected from the group consisting of:-Sodium 5-acetamido-4-azido-2, 3, 4, 5-tetradeoxy-~-glycero-~-galacto-non-2-enopyranosonate;
Sodium 5-acetamido-4-N, N-diallylamino-2, 3, 4, 5-tetradeoxvy-~-glycero-~-galacto-non-2-enopyranosonate:
Sodium 5-acetamido-4-N-allylamino-2, 3, 4, 5-tetradeoxy-~-glycero-~-galacto-non-2-enopyranosonate:
Sodium 5-acetamido-4-amino-2, 3, 4, 5-tetradeoxy-~-glycero-~-talo-non-2-enopyranosonate;
Methyl 5-acetamido-7, 8, 9-tri-O-acetyl-4-N, N-diallylamino-2, 3, 4, 5-tetradeoxy-~-glycero-~-galacto-non-2-enapyranosonate ;

Sodium 5-acetamido-4-N, N-diallylamino-2, 3, 4, 5-tetradeoxy-~-glycero-~-galacto-non-2-enopyranosonate;
Methyl 5-acetamido-7, 8, 9-tri-0-acetyl-4-N-allylamino-2, 3, 4, 5-tetradeoxy-~-glycero-~-galacto-non-2-enopyranosonate;
Sodium 5-acetamido-4-N, N-dimethylamino-2, 3, 4, 5-tetradeoky-~-glycero-~-galacto-non-2-enopyranosonate;
Sodium 2, 3-dideoxy-~-glycero-D-galacto-non-2-enopyranosonate; and Methyl 5-acetamido-7, 8, 9-tri-0-acetyl-4-azido-2, 3. 4. 5-tetradeoxy-~-glycero-~-talo-non-2-enopyranosonate.

6. A pharmaceutical formulation comprising a compound of formula (I) or (Ia) as defined in any one of Claims 1 to 5 or a pharmaceutically acceptable salt or derivative thereof, together with a pharmaceutically acceptable carrier therefor.

7. A pharmaceutical formulation as claimed in Claim 6 wherein the formulation is adapted for intranasal administration.

8. Use of a compound of formula (I) or (Ia) as defined in Claim 1 in the manufacture of a medicament for the treatment of a viral infection.

9. Use of a compound as claimed in Claim 8 wherein the viral infection is influenza.

10. Use of a compound of formula (I) or formula (Ia) wherein in general formula (I), A is oxygen, carbon or sulphur, and in general formula (Ia), A is nitrogen or carbon;
R1 denotes COOH, P(O) (OH)2, NO2, SOOH, SO3H, tetrazol, CH2CHO, CHO or CH (CHO)2, R2 denotes H, OR6, F, Cl, Br, CN, NHR6, SR6 or CH2X, wherein X is NHR6, halogen or OR6 and R6 is hydrogen; an acyl group having 1 to 4 carbon atoms; a linear or cyclic alkyl group having 1 to 6 carbon atoms, or a hologen-substituted analogue thereof; an allyl group or an unsubstituted aryl group or an aryl substituted by a halogen, an OH group, an NO2 group, an NH2 group or a COOH group, R3 and R3' are the same or different, and each denotes hydrogen, CN, NHR6, N3, SR6, =N-OR6, OR6, guanidino, R4 denotes NHR6, SR6, OR6, COOR6, NO2, C(R6)3, CH3COOR6, CH2NO2 or CH2NHR6, and R5 denotes CH2YR6, CHYR6CH2YR6 or CHYR6CHYR6CH2YR6, where Y is O, S, NH
or H, and successive Y moieties in an R5 group are the same or different, or a pharmaceutically acceptable salt or derivative thereof, for the treatment of a mammal including man suffering from a viral infection.

11. Use of an effective amount of a compound of formula (I) or (Ia) as defined in Claim 1 for the treatment of a mammal including man suffering from a viral infection.

12. Use as claimed in Claim 11 wherein the viral infection is influenza.

13. Use as claimed in Claim 10 or 11 wherein the infection is by a respiratory virus.

14. A method for the preparation of a compound of formula (I) as defined in Claim 1 which comprises the steps of (A) reaction of a compound, of formula (III) wherein R1, R2, R4 and R5 are defined in Claim 1 and OL is a leaving group with a nucleophile;
or (B) interconversion of one compound of formula (I) to another compound of formula (I), and if necessary or desired, subjecting the resulting compound to one or two further reactions comprising:
(i) removing any protecting groups;
(ii) converting a compound of formula (I) or a salt thereof into a pharmaceutically acceptable salt thereof.

15. Use of an effective amount of a compound of formula (Ib) wherein R3b is (alk) x NR6bR7b, CN or N3;
where alk is an unsubstituted or substituted methylene;
x is O or 1;
R6b is hydrogen, C1-6alkyl, aryl, aralkyl, amidine, NR7bR8b or an unsaturated or saturated ring containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen and sulphur;
R7b is hydrogen, C1-6alkyl, or allyl;
R8h is hydrogen, C1-6alkyl; and R4b is NHCOR9b where R9b is hydrogen, substituted or unsubstituted C1-4alkyl or aryl;
or a pharmaceutically acceptable salt or derivative thereof, for the treatment of a mammal including man suffering from a viral infection.

16. Use as claimed in Claim 15 wherein said compound of the general formula (Ib) R3b is NH2 or NHC (=NH) NH2.

17. Use as claimed in Claim 15 wherein said compound is 5-acetamido-4-amino-2,3, 4, 5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonic acid and pharmaceutically acceptable salts and derivatives thereof.

18. Use as claimed in Claim 15 wherein said compound is sodium 5-acetamido-4-amino-2, 3, 4, 5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate.

19. Use as claimed in Claim 15 wherein said compound is 5-acetamido-4-guanidine-2, 3, 4, 5-tetradeoxy-D-glycero-D-galacto-non-2-enopyransosonic acid and pharmaceutically acceptable salts and derivatives thereof.

20. Use as claimed in Claim 15 wherein said compound is ammonium 5-acetamido-4-guanidino-2, 3, 4, 5-tetradeoxy-D-glycero-D-galacto-non-2-enopyranosonate.

21. Use as claimed in Claim 15 wherein a compound of the general formula (Ib) as claimed in Claim 15 is used as an active ingredient together with a pharmaceutically acceptable carrier therefor.

22. Use as claimed in Claim 15 wherein a pharmaceutical formulation suitable for intranasal administration comprising a compound as claimed in Claim 15 is used as an active ingredient together with a pharmaceutically acceptable carrier therefor.

23. Use as claimed in Claim 21 wherein the active ingredient is 5-acetamido-4-amino-2, 3, 4, 5-tetradeoxy-D-glycero-D-galacto-non-2-enopyransosonic acid or a pharmaceutically acceptable salt thereof.

24. Use as claimed in Claim 21 wherein the active ingredient is 5-acetamido-4-guanidino-2, 3, 4, 5-tetradeoxy-D-glycero-D-galacto-non-2-enopyransosonic acid or a pharmaceutically acceptable salt thereof.

25. Use as claimed in any one of Claims 15 to 24 wherein the infection is a viral respiratory infection.

26. Use as claimed in any one of Claims 15 to 24 wherein the viral infection is influenza.

27. A method for the preparation of a compound of formula (Ib) as defined in Claim 15 which comprises the steps of:
(A) reaction of a compound of formula (IIIb) wherein R4b is as defined in Claim 15 and OL is a leaving group, or a protected derivative of said compound, with a nucleophile; or (B) interconversion of one compound of formula (Ib) to another compound of formula (Ib) and if necessary subjecting the resulting compound to one or two further reactions comprising:
(i) removing any protecting groups;
(ii) converting a compound of formula (Ib) or a salt thereof into a pharmaceutically acceptable salt thereof.