AU2020267321B2

AU2020267321B2 - Furanone compounds and lactam analogues thereof

Info

Publication number: AU2020267321B2
Application number: AU2020267321A
Authority: AU
Inventors: George Iskander; Naresh Kumar
Original assignee: Unilever Global IP Ltd
Current assignee: Unilever Global IP Ltd
Priority date: 2006-10-06
Filing date: 2020-11-13
Publication date: 2022-01-06
Anticipated expiration: 2027-10-08
Also published as: AU2019202284A1; AU2017232092A1; AU2015201005A1; AU2020267321A1

Abstract

C:\Interwo n\NRPortbl\DCC\RBR\18663453_i.docx-2/04/2019 ABSTRACT The present invention provides a compound of formula I and a compound of formula II, methods of use and formulations thereof. R1 R6 R3 R4 R'18 X) X X 0 ex R

Description

DCC-13/1[/2020

FURANONE COMPOUNDS AND LACTAM ANALOGUES THEREOF

This is a divisional application of Australian Patent Application No. 2019202284, the entire contents of which are incorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to furanone and lactam derivatives which have antibacterial properties, methods for their synthesis and their uses.

BACKGROUND OF THE INVENTION

Certain furanone compounds and lactam analogues of furanone compounds have been shown to have antibacterial properties and are described, for instance, in WO 99/54323 and WO 2004/016588.

The present inventors have found new synthetic approaches which allow them to access novel classes of furanone compounds and lactam analogues thereof. These compounds have antibacterial properties and have been shown to have efficacy in the inhibition of biofilms and expression of virulence.

SUMMARY OF THE INVENTION

Accordingly, in a first aspect, the present invention provides a compound of formula I R1

R3 R

X 0) X R2

I wherein: X is selected from -0- or -N(Rs)-; wherein R 5 is selected from H, alkyl, aryl and arylalkyl; R1 is selected from H, halo, alkyl, aryl and heteroaryl;

R2 and R4 are each independently selected from hydrogen, aryl and heteroaryl with the proviso that both R2 and R4 cannot be hydrogen; and

R3 is selected from H, alkyl, heteroaryl and aryl.

In a second aspect, the present invention provides a compound of formula II

R6

R8 R7

0 Xx R9

II

wherein:

X is selected from -O- or -N(Rio)-;

wherein Rio is selected from H, alkyl, aryl and arylalkyl;

R 6 is selected from H, halo, alkyl, aryl and heteroaryl;

R 7 is selected from H, halo, alkyl, arylalkyl, aryl and heteroaryl;

R 8 is selected from H, halo and alkyl; and

R 9 is selected from H, halo, alkyl, arylalkyl, aryl and heteroaryl.

In a third aspect, the present provides a method of treating or preventing a microbial infection in a subject, the method comprising administering a compound of formula I or a compound of formula II to the subject.

In a fourth aspect, the present invention provides a method of preventing or inhibiting microbial contamination of a surface, the method comprising administering to the surface a compound of formula I or a compound of formula II.

In a fifth aspect, the present invention provides a formulation comprising a compound of formula I or a compound of formula I.

DETAILED DESCRIPTION OF THE INVENTION

In a first aspect, the present invention provides compound of formula I

R1

R3 RR

0 X2

wherein:

X is selected from -O- or -N(R)-;

wherein R 5 is selected from H, alkyl, aryl and arylalkyl;

R, is selected from H, halo, alkyl, aryl and heteroaryl;

R2 and R4 are each independently selected from hydrogen, aryl and heteroaryl with the proviso that both R2 and R 4 cannot be hydrogen; and

R 3 is selected from H, alkyl, heteroaryl and aryl.

Preferably, R 4 is H.

Preferably R 3 is H.

In a preferred embodiment R2 is aryl. Preferably aryl is an optionally substituted phenyl group and even more preferably the optionally substituted phenyl group is substituted with one or more substituents selected from the group consisting of CF 3 , OCF 3 , cyano (CN), halo and alkoxyl. It is preferred that halo is F. It is also preferred that alkoxyl is methoxyl.

In another preferred embodiment R2 is heteroaryl. Preferably heteroaryl is a five membered heteroaromatic ring containing one or more heteroatoms selected from 0, N and S. Even more preferably the five-membered heteroaromatic ring is a thiophene.

In yet another preferred embodiment, R 1 is aryl. Preferably aryl is an optionally substituted phenyl group, even more preferably the optionally substituted phenyl group is substituted with one or more substituents selected from the group consisting of CF3 , OCF 3

, cyano (CN) and halo. It is preferred that halo is F.

In still another preferred embodiment R, is heteroaryl. Preferably heteroaryl is a five membered heteroaromatic ring containing one or more heteroatoms selected from 0, N and S. Even more preferably the five-membered heteroaromatic ring is a thiophene.

In yet another preferred embodiment R 1 is halo, preferably halo is Br.

In another preferred embodiment, each of R, and R 2 are the same substituent selected from aryl and heteroaryl. Preferably, aryl.

In a preferred embodiment, the present invention provides a compound selected from compounds 13, 17, 19, 20, 21, 22, 23, 24, 25, 26, 30, 31, 32, 33, 34 and 35 as defined in the Examples.

In a second aspect, the present invention provides a compound of formula II

R6

R8 R7

0 X R9

II

wherein:

X is selected from -O- or -N(Rio)-;

wherein RIO is selected from H, alkyl, aryl and arylalkyl;

R 6 is selected from H, halo, alkyl, aryl and heteroaryl;

R 7 is selected from H, halo, alkyl, arylalkyl, aryl and heteroaryl;

R 8 is selected from H, halo and alkyl; and

R9 is selected from H, halo, alkyl, arylalkyl, aryl and heteroaryl.

Preferably R 8is H or halo. Preferably halo is Br.

In a preferred embodiment, each of R 7 and R9 is H.

In still another preferred embodiment R 7 and R8 are each independently selected from H and alkyl.

In another preferred embodiment R 6 is aryl. Preferably aryl is an optionally substituted phenyl group. It is preferred that the optionally substituted phenyl group is substituted with one or more substituents selected from the group consisting of CF3 , OCF3 , cyano (CN) and halo. Preferably halo is F or Br.

In still another preferred embodiment R6 is heteroaryl. Preferably heteroaryl is a five membered heteroaromatic ring containing one or more heteroatoms selected from 0, N and S. Even more preferably the five-membered heteroaromatic ring is selected from the group consisting of thiophene, isoxazole, furan and pyrazole. The five-membered heteroaromatic ring may be substituted with one or more alkyl groups. Preferably the one or more alkyl groups are methyl.

In yet another preferred embodiment R 6 is halo, preferably halo is Br.

In a preferred embodiment, the present invention provides a compound selected from compounds 1, 2, 3 ,4, 5, 6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 18, 27, 28 and 29 as defined in the Examples.

The microbial infection may be a bacterial, protozoal or fungal infection. Preferably, the infection is a bacterial infection.

The compounds of the present invention can act as quorum sensing inhibitors. In particular, the compounds have been shown to inhibit quorum sensing in Pseudomonassp. The compounds therefore find use in any application where the inhibition of quorum sensing is desired. For example, the compounds of the present invention may have use in preventing the establishment of biofilms and expression of virulence by microorganisms through the inhibition of quorum sensing systems and/or other extracellular systems (eg see, International publication No WO 2002/047681, the disclosure of which is incorporated herein in its entirety).

The compounds of the present invention have been shown to inhibit the formation of Pseudomonas sp. and E coli biofilms. The formation of biofilims is one instance of quorum sensing. The presence of the quorum sensing pathways (such as those involving homoserine lactones) in a wide range of bacteria indicates that the compounds of the present invention can be used to effectively treat not only Pseudomonas sp. and E coli biofilms but also biofilms composed of other bacteria.

The following is a non-exhaustive list of groups of Gram-Negative bacteria that have members which use homoserine lactones for cell-cell communication: anaerobic Gram Negative Straight, Curved and Helical Rods; Bacteroidaceae; The Rickettsias and Chlamydias; Dissimilatory Sulfate--or Sulfur-Reducing Bacteria; the Mycoplasmas; The mycobacteria; Budding and/or Appendaged Bacteria; Sheathed Bacteria; Nocardioforms; and Actinomycetes, for example. See Bergey's Manual of Systematic Bacteriology, First Ed., John G. Holt, Editor in Chief (1984), incorporated herein by reference.

Further microbial infections that may be treated by the compounds of the present invention include bacterial infections caused by Staph. aureus, Staph epidermis, Serratia spp., Vibrio spp., and Strep. pneumonia and other organisms including the A12 system; protozoal infections caused by Acanthamoeba; and fungal infections caused by Fusarium spp.

Preferably, the method of the third aspect may be used to treat or prevent a microbial infection in a subject that is characterised by biofilm formation.

The present invention is suitable for biofilms originating from a single type of organism and for mixed biofilms. By "mixed biofilms" is meant biofilms created by more than one type of microorganism. It is envisioned that mixed biofilms could be created by at least two organisms from the group consisting of bacteria, algae, fungi, and protozoa.

Non-limiting examples of human infections involving biofilms include dental caries, periodontitis, otitis media, muscular skeletal infections, necrotising fascitis, biliary tract infection, urinary tract infection, respiratory tract infection, osteomyelitis, bacterial prostatitis, native valve endocarditis, cystic fibrosis pneumonia, meloidosis, and nosocomial infections such as ICU pneumonia, urinary catheter cystitis, peritoneal dialysis (CAPD) peritonitis, and biliary stent blockage. Biofilm formation can affect sutures, exit sites, arteriovenous sites, scleral buckles, contact lenses, IUDs, endotracheal tubes, Hickman catheters, central venous catheters, mechanical heart valves, vascular grafts, orthopedic devices, penile prostheses. Further applications are described in Costerton J et al, (1999) Vol. 284, Science pp1318-1322 and Costerton J and Steward, (2001) Battling Biofilms, Scientific American pp 75-81, the disclosures of which are incorporated herein by reference.

Other locations in which biofilms may form include dental plaque which may lead to gum disease and cavities, contact lenses which may lead to eye infections, ears which may lead to chronic infection and lungs which may lead to pneumonia.

The infection may be of a cystic fibrosis sufferer. The infection may be that resulting from a skin infection, burn infection and/or wound infection. The method and composition of the invention may be particularly suitable for the treatment of infection in immuno compromised individuals.

The compounds of the present invention have been shown to be particularly effective in preventing bacterial contamination of surfaces, in particular by preventing the formation of biofilms.

Accordingly, in a fourth aspect, the present invention provides a method of preventing or inhibiting microbial contamination of a surface, the method comprising administering to the surface a compound of formula I or a compound of formula II.

The microbial contamination may be protozoal, fungal or bacterial contamination.

In a preferred form, the microbial contamination is a bacterial contamination. In a more preferred form, the bacterial contamination is a biofilm.

The surface may be any natural or artificial surface. The term "artificial surface" means that the surface is not naturally occurring. In one embodiment, the surface is not an external surface (eg skin) or an internal surface of a human being or animal. In another embodiment, the surface is an external surface or an internal surface of a human being or animal.

Suitable surfaces include the surfaces of articles for which it is desirable to prevent bacterial contamination. These include: medical devices, for example, implantable biomedical devices such as urinary catheters, percutaneous access catheters, stents, orthopaedic implants, bone and dental ceramics and polymers as well as non-implantable devices such as contact lenses, contact lens storage cases, and the like.

The material from which the article is formed can be a metal, a ceramic, a solid synthetic polymer, or a solid natural polymer, for example a solid biopolymer. Examples of useful materials for this invention are titanium, hydroxyapatite, polyethylene (which are useful materials for orthopaedic implants), polyurethanes, organosiloxane polymers, perfluorinated polymers (which are useful materials for instance for catheters, soft tissue augmentation, and blood contacting devices such as heart valves), acrylic hydrogel polymers, HEMA/GMA polymers and silicon/siloxane hydrogel polymers (for instance for contact lens and intraocular lens applications), and the like, and any combination thereof. Further included are resin composites, compomers and resin-modified glass ionomers used in oral care. The surfaces of these materials can be chemically inert or contain reactive functional groups.

Further examples of articles include archival documents, antiques and art, rare and valuable seeds intended for storage (e. g. seed banks of conservation groups), etc in which case the substrate may be paper, material or other natural or synthetic material.

The article may be a shell fish or aquaculture apparatus, for example, that described in WO 1999/005227, the disclosure of which is incorporated herein by reference.

The surface of the article may be any hard surface such as metal, organic and inorganic polymer surface, natural and synthetic elastomers, board, glass, wood, paper, concrete, rock, marble, gypsum and ceramic materials which optionally are coated, eg with paint, enamel etc; or any soft surface such as fibres of any kind (yams, textiles, vegetable fibres, rock wool, hair etc.); or porous surfaces; skin (human or animal); keratinous materials (nails etc.). The hard surface can be present in process equipment or components of oil and gas infrastructure, deaeraters, a water treatment plant, cooling equipment, a cooling tower, a water treatment plant, a dairy, a food processing plant, a chemical or pharmaceutical process plant. The porous surface can be present in a filter, eg. a membrane filter.

Particular examples of articles whose surfaces may be treated in accordance with the invention include, but are not limited to, toilet bowls, bathtubs, drains, highchairs, counter tops, vegetables, meat processing rooms, butcher shops, food preparation areas, air ducts, air-conditioners, carpets, paper or woven product treatment, nappies (diapers), personal hygiene products (eg sanitary napkins) and washing machines. The compounds may be formulated in the form of a toilet drop-in or spray-on devices for prevention and removal of soil and under rim cleaner for toilets. The compounds of the present invention also have applications in cleaning of Industrial surfaces such as floors, benches, walls and the like and these and other surfaces in medical establishments such as hospitals (eg surfaces in operating theatres), veterinary hospitals, and in mortuaries and funeral parlours.

Further examples of surfaces which may be treated include hard, rigid surfaces such as tanks and tubing, pipes, glazed ceramic, porcelain, glass, metal, wood, chrome, plastic, vinyl and formica or soft flexible surfaces such as shower curtains, upholstery, laundry and carpeting. It is also envisioned that both woven and non woven and porous and non-porous surfaces would be suitable.

The compound may be administered by any suitable means. For instance, the compound may be attached to the surface using the techniques and surfaces described in WO 2004/016588. Examples include providing the compounds of the present invention as part of an oligomer or polymer by, for instance, co-polymerising the compound with other monomers or attaching the compound to the polymer backbone by techniques well known to those in the art.

Methods for the covalent immobilization of organic molecules onto solid surfaces are well known to those skilled in the art. Interfacial reactions leading to the formation of covalent interfacial bonds are derived from well known organic-synthetic reactions. The choice of immobilization reaction depends on both the nature of the substrate material and the chemical composition of the compound of the present invention that is desired for a particular application.

For example, a compound that contains a hydroxyl group in a side chain distal to the ring system, can be linked covalently onto surfaces using epoxide chemistry analogous to the reaction pathway described for the immobilization of polysaccharides onto epoxidated surfaces in Li et al., Surface Modification of Polymeric Biomaterials (BD Ratner and DG Castner, Eds), Plenum Press, NY, 1996 pages 165-173 (the disclosure of which is incorporated herein in its entirety), through isocyanate groups attached to the surface to produce stable urethane linkages through thermal processes, or through carboxylic acid groups or their equivalents, such as acid chlorides, on the surface to produce ester linkages. A compound that contains an aldehyde group can be linked onto surface amine groups using a reductive animation reaction. A compound that contains a carboxylic acid group can be linked onto surface amine groups using carbodiimide chemistry.

Interfacial coupling reactions must of course be selected not only for their ability to achieve the desired covalent linkage but also for avoidance of adverse effects on the furanone compound or furanone compounds to be attached. Particularly, the furanone ring system tends to be labile to alkaline conditions. Such limitations are well known to those skilled in the art. Among the many possible interfacial coupling reactions known in the art, there is sufficient scope for selection of reactions that proceed in a suitable pH range and with furanones substituted with various functional groups in various positions.

Some solid substrate materials possess reactive surface chemical groups that can undergo chemical reactions with a partner group on a compound and thereby form a covalent interfacial linkage directly.

Alternatively, in situ covalent linkage can be made directly through the addition of a doubly functionalised linker molecule to the active surface in the presence of an appropriate compound, or stepwise by sequential addition of doubly functionalised linker molecules and then an appropriate compound. It is not always possible to immobilize furanone compounds directly onto solid substrate materials; in these cases, surface activation or one or more interfacial bonding layers is used to effect covalent immobilization of the compounds.

Surface activation of solid substrate materials can be achieved in a number of ways. Examples are corona discharge treatment or low pressure plasma treatment of polymers. These methods are well known to introduce a variety of functional groups onto polymeric surfaces.

An alternative approach is to provide an interfacial bonding layer interspersed between the solid substrate material or medical device and the compound layer. The application of a thin interfacial bonding layer can be done using methods such as dip coating, spin coating, or plasma polymerization. The chemistry of the bonding layer is selected such that appropriate reactive chemical groups are provided on the surface of this layer, groups that then are accessible for reaction with compound of the invention.

Particularly versatile is the subsequent application of multiple thin interfacial bonding layers; this method can provide a very wide range of desired chemical groups on the surface for the immobilization of a wide range of functionalized furanones and enables usage of compounds optimized for their biological efficacy.

By providing a thin, surface-coated layer of compounds, the optical quality of antibacterial devices of this invention is not reduced, which makes the invention applicable to transparent ophthalmic devices such as contact lenses and intraocular lenses.

The present invention provides thin surface coatings that provide antimicrobial properties and/or antifungal properties to solid materials onto which the coatings have been applied. More particularly, the coatings may be designed to reduce or prevent colonization of biomedical devices by bacteria that cause adverse effects on the health of human users of biomedical devices when such devices are colonized by bacteria.

Alternatively, the compound may be administered in the form of a formulation.

Accordingly, the present invention further provides a formulation comprising a compound of Formula I or a compound of Formula II and a carrier.

Examples of the types of carrier that may be used with the compounds of Formula I and the compounds of Formula II are disclosed in WO 2004/016588.

The formulations may be in any suitable form. The formulation may include a carrier or diluent. The carrier may be liquid or solid. For example, the compositions may be in the form of a solution or suspension of at least one of the compounds in a liquid. The liquid may be an aqueous solvent or a non-aqueous solvent. The liquid may consist of or comprise a one or more organic solvents. The liquid may be an ionic liquid. Particular examples of carrier or diluents include, but are not limited to, water, polyethylene glycol, propylene glycol, cyclodextrin and derivatives thereof.

The composition may be formulated for delivery in an aerosol or powder form.

The composition may include organic or inorganic polymeric substances. For example, the compound of the invention may be admixed with a polymer or bound to, or adsorbed on to, a polymer.

When the composition is to be formulated as a disinfectant or cleaning formulation, the composition may include conventional additives used in such formulations. Non-limiting examples of the physical form of the formulations include powders, solutions, suspensions, dispersions, emulsions and gels.

A compound of the invention may be incorporated into epidermal bandages and lotions. Alternatively, the compounds of the invention may be incorporated into cosmetic formulations, for example, aftershave lotions, skin creams, deodorants and anti-dandruff shampoos.

Compositions of the present invention may be in the form of an aqueous solution or suspension containing a cleaning-effective amount of the active compound described above. The cleaning composition may be in the form of a spray, a dispensable liquid, or a toilet tank drop-in, under-rim product for prevention, removal and cleaning of toilets and other wet or intermittently wet surfaces in domestic or industrial environments.

The compositions of the present invention may additionally comprise a surfactant selected from the group consisting of anionic, non-ionic, amphoteric, biological surfactants and mixtures thereof. Most preferably, the surfactant is sodium dodecyl sulfate.

One or more adjuvant compounds may be added to the cleaning solution of the present invention. They may be selected from one or more of biocides, fungicides, antibiotics, and mixtures thereof to affect planktonics. pH regulators, perfumes, dyes or colorants may also be added. In addition, the adjuvant could be a cell permeabilisation agent such as EDTA or FDS.

By "cleaning-effective" amount of active compound, it is meant an amount of the compound which is necessary to remove at least 10% of bacteria from a biofilm as determined by a reduction in numbers of bacteria within the biofilm when compared with a biofilm not exposed to the active compound.

Preferably, the formulation is a pharmaceutical formulation.

Formulations for pharmaceutical uses may incorporate pharmaceutically acceptable carriers, diluents and excipients known to those skilled in the art. The formulations make be formulated for parenteral or non-parenteral administration. The formulations may be formulated for methods of introduction including, but not limited to, topical, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, ophthalmic, and oral routes. They may be formulated for administration by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and may be administered together with other biologically active agents. Administration may be localized or systemic. The formulation may be formulated for intraventricular and intrathecal injection.

Pulmonary administration can also be employed, e.g., by use of an inhaler or nebulizer, and formulation with an aerosolizing agent.

In certain preferred embodiments the formulation further comprises other active agents such as antibiotics and cleaning agents.

In other embodiments of the present invention, the formulation may be formulated as a dentifrice, a mouthwash or a composition for the treatment of dental caries. The composition may be formulated for acne treatment or cleaning and disinfecting contact lenses (eg as a saline solution).

The term "alkyl" is taken to mean both straight chain and branched alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tertiary butyl, and the like. Preferably the alkyl group is a lower alkyl of 1 to 10 carbon atoms, more preferably 1 to 6 carbon atoms.

In certain embodiments, the carbon chain of the alkyl group is interrupted with one or more heteroatoms. For instance, a polyethylene glycol group of the form -(H2 C H20),H is to be understood to be an alkyl group of such an embodiment.

The term "cycloalkyl" as used herein refers to cyclic hydrocarbon groups. Suitable cycloalkyl groups include but are not limited to cyclopropyl and cyclohexyl.

The term "alkoxy" denotes straight chain or branched alkyloxy, preferably C 11.0 alkoxy. Examples include methoxy, ethoxy, n-propoxy, isopropoxy and the different butoxy isomers.

The term "alkenyl" includes groups formed from straight chain, branched or mono- or polycyclic alkenes and polyenes. Substituents include mono- or poly-unsaturated alkyl or cycloalkyl groups as previously defined, preferably C 2 jo alkenyl. Examples of alkenyl include vinyl, allyl, 1-methylvinyl, butenyl, iso-butenyl, 3-methyl-2-butenyl, 1-pentenyl, cyclopentenyl, 1-methyl-cyclopentenyl, 1-hexenyl, 3-hexenyl, cyclohexenyl, 1-heptenyl, 3-heptenyl, 1-octenyl, cyclooctenyl, 1-nonenyl, 2-nonenyl, 3-nonenyl, 1-decenyl, 3 decenyl, 1,3-butadienyl, 1,4-pentadienyl, 1,3-cyclopentadienyl, 1,3-hexadienyl, 1,4 hexadienyl, 1,3-cyclohexadienyl, 1,4-cyclohexadienyl, 1,3-cycloheptadienyl, 1,3,5 cycloheptatrienyl, or 1,3,5,7-cyclooctatetraenyl.

The term "alkynyl" as used herein, refers to straight chain or branched hydrocarbon groups containing one or more triple bonds. Suitable alkynyl groups include, but are not limited to ethynyl, propynyl, butynyl, pentynyl and hexenyl.

The term "halogen" includes fluorine, chlorine, bromine or iodine, preferably bromine or fluorine.

The term "heteroatoms" denotes 0, N, S or Si.

The term "acyl" used either alone or in compound words such as "acyloxy", "acylthio", "acylamino" or diacylamino" denotes an alkanoyl, aroyl, heteroyl, carbamoyl, alkoxycarbonyl, alkanesulfonyl, arysulfonyl, and is preferably a C1 .10 alkanoyl. Examples of acyl include carbamoyl; straight chain or branched alkanoyl, such as formyl, acetyl, propanoyl, butanoyl, 2-methylpropanoyl, pentanoyl, 2,2-dimethylpropanoyl, hexanoyl, heptanoyl, octanoyl, nonanoyl, decanoyl; alkoxycarbonyl, such as methoxycarbonyl, ethoxycarbonyl, t-butoxycarbonyl, t-pentyloxycarbonyl or heptyloxycarbonyl; cycloalkanecarbonyl such as cyclopropanecarbonyl cyclobutanecarbonyl, cyclopentanecarbonyl or cyclohexanecarbonyl; alkanesulfonyl, such as methanesulfonyl or ethanesulfonyl; alkoxysulfonyl, such as methoxysulfonyl or ethoxysulfonyl; heterocycloalkanecarbonyl; heterocycloalkanoyl, such as pyrrolidinylacetyl, pyrrolidinylpropanoyl, pyrrolinylacetyl, pyrrolylacetyl, pyrrolidinylbutanoyl, pyrrolidinylpentanoyl, pyrrolidinylhexanoyl or thiazolidinylacetyl; heterocyclylalkenoyl, such as heterocyclylpropenoyl, heterocyclylbutenoyl, heterocyclylpentenoyl or heterocyclylhexenoyl; or heterocyclylglyoxyloyl, such as, thiazolidinylglyoxyloyl or pyrrolidinylglyoxyloyl.

The term "aryl" refers to aryl groups having 6 through 10 carbon atoms and includes, for example, phenyl, naphthyl, indenyl. Preferably, the aryl group is phenyl or naphthyl.

The term "arylalkyl" includes groups such as benzyl and phenethyl groups which comprise an alkyl chain with an aryl substituent.

The term "heterocyclyl" includes monocyclic, polycyclic, fused or conjugated hydrocarbon residues, preferably C 3 . 6, wherein one or more carbon atoms (and where appropriate, hydrogen atoms attached thereto) are replaced by a heteroatom so as to provide a non aromatic residue. Suitable heteroatoms include 0, N, and S. When two or more carbon atoms are replaced, this may be by two or more of the same heteroatom or by different heteroatoms. Suitable examples of heterocyclic groups include pyrollodinyl, piperidyl, piperazinyl, morpholino, quinolinyl, isoquinolinyl, thiomorpholino, dioxanyl, tetrahydrofuranyl,tetrahydropyranyl,andtetrahydropyrrolyl.

The term "heteroaryl" includes a 5- or 6-membered heteroaromatic ring containing one or more heteroatoms selected from 0, N and S. Suitable examples of heteroaryl groups include tetrazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, imidazolyl, pyrazolyl, pyridinyl, pyrimidinyl, oxazolyl, and oxadiazolyl.

Each alkyl, cycloalkyl, alkoxy, oxoalkyl, alkenyl, heterocyclyl, heteroaryl, aryl, and arylalkyl group may optionally be substituted by one or more groups selected from alkyl, cycloalkyl, alkenyl, alkynyl, aryl, arylalkyl, heterocyclyl, heteroaryl, cyano, halo, carboxyl, haloalkyl, haloalkynyl, hydroxy, substituted or unsubstituted alkoxy, alkenyloxy, haloalkoxy, haloalkenyloxy, nitro, amino, nitroalkyl, nitroalkenyl, nitroalkynyl, nitroheterocyclyl, alkylamino, dialkylamino, alkenylamine, alkynylamino, acyl, alkenoyl, alkynoyl, acylamino, diacylamino, acyloxy, alkylsulfonyloxy, heterocyclyl, heterocycloxy, heterocyclamino, haloheterocyclyl, alkylsulfenyl, alkylcarbonyloxy, alkylthio, acylthio, phosphorus-containing groups such as phosphono and phosphinyl.

In order that the nature of the present invention may be more clearly understood, preferred forms thereof will now be described with reference to the following non-limiting examples.

GENERALPROCEDURES

Mono-coupling palladium-catalysed cross-coupling reaction.

Procedure utilising Potassium Fluoride as base and Toluene/Water solvent mixture at reflux:

A mixture containing 4-bromo-5(H)furanone (1 mmol), phenylboronic acid (1.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.05 mmol), tetrabutylammonium iodide (0.05 mmol) and potassium fluoride (6 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 12-24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine

(3x50 mL), dried over anhydrous magnesium 'sulfate and evaporated to dryness under reduced pressure. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum, 50:50 dichloromethane/light petroleum or 100% dichloromethane) giving the desired product 4-phenyl-5(H)furanone.

Procedure utilising Potassium Fluoride as base and Tetrahydrofuran/Water solvent mixture at reflux:

A mixture containing 4-bromo-5(H)furanone (1 mmol), phenylboronic acid (1.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.05 mmol), tetrabutylammonium iodide (0.05 mmol) and aqueous potassium fluoride (2M, 6 mmol) in tetrahydrofuran (15 mL) was refluxed for 12-24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x50 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum, 50:50 dichloromethane/light petroleum or 100% dichloromethane) giving the desired product - 4-phenyl-5(H)furanone.

Procedure utilising Potassium Fluoride as base and Tetrahydrofuran/Water solvent mixture at room temperature:

A mixture containing 4-bromo-5(H)furanone (1 mmol), phenylboronic acid (1.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.05 mmol), tetrabutylammonium iodide (0.05 mmol) and aqueous potassium fluoride (2M, 6 mmol) in tetrahydrofuran (15 mL) was stirred at room temperature for 24-48 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x50 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum, 50:50 dichloromethane/light petroleum or 100% dichloromethane) giving the desired product - 4-phenyl-5(H)furanone.

Procedure utilising Cesium Fluoride as base and Toluene/Water solvent mixture at room temperature:

A mixture containing 4-bromo-5(H)furanone (1 mmol), phenylboronic acid (1.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.05 mmol), tetrabutylammonium iodide (0.05 mmol) and cesium fluoride (3 mmol) in toluene (10 mL) and water (10 mL) were stirred for 48-72 h under nitrogen at room temperature. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x50 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum, 50:50 dichloromethane/light petroleum or 100% dichloromethane) giving the desired product - 4-phenyl-5(H)furanone.

Procedure utilising Cesium Fluoride as base and Toluene/Water solvent mixture at reflux:

A mixture containing 4-bromo-5(H)furanone (1 mmol), phenylboronic acid (1.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.05 mmol), tetrabutylammonium iodide (0.05 mmol) and cesium fluoride (3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 12-24 h under nitrogen. After cooling brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x50 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum, 50:50 dichloromethane/light petroleum or 100% dichloromethane) giving the desired product - 4-phenyl-5(H)furanone.

Di-coupling palladium-catalysed cross-coupling reaction.

A mixture containing 4-bromo-5-bromomethylene-2(5H)-furanone (1 mmol), phenylboronic acid (2.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.05 mmol), tetrabutylammonium iodide (0.05 mmol) and cesium fluoride (3 mmol) in toluene (10 mL) and water (10 mL) were stirred for 48-72 h under nitrogen at room temperature.

Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x50 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum, 50:50 dichloromethane/light petroleum or 100% dichloromethane) giving the desired product 4-phenyl-5-bromomethylene-2-(5H)-furanone.

EXAMPLES

1. COMPOUNDS

Example 1

4-(2',4'-Difluorophenyl)furan-2(5H)-one1.

F -- F

0

1

A mixture containing 4-bromo-5(H)furanone (0.211 g, 1.295 mmol), pinacolate(2,4 difluorophenylboronic) ester (0.402 g, 1.675 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.047 g, 6.696x10-2 mol), tetrabutylammonium iodide (0.028 g, 7.580x10-2 mmol) and potassium fluoride (0.325 g, 5.594 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(2',4'-dfluoropheny)furan 2(5H)-one 1 (0.162 g, 64%) as a pale yellow powder, dec. 135-136°C (ref. PDS-1-59). UV-Vis m. (MeOH) 242(429) nm; H NMR (CDCl 3, 300 MHz) 8 7.48 (ddd, 2H, J= 6.0

Hz, J= 8.3 Hz, J= 14.3 Hz, H6'), 7.05-6.93 (m, 2H, H3', H5'), 6.48 (t, 1H, J= 1.5 Hz, H3), 5.24 (t, 2H, J= 1.9 Hz, H5); "C NMR (CDC13, 75 MHz) 8 173.4 (C2), 166.4 (d, J= 13.0 Hz, C4'), 163.1 (dd, J= 12.3 Hz, J= 15.2 Hz, C4), 159.8 (d, J= 12.3 Hz, C2'), 157.3 (d, J= 2.9 Hz, C1'), 129.4 (dd, J= 5.1 Hz, J= 10.1 Hz, C6'), 115.8 (dd, J= 2.2 Hz, J= 8.7 Hz, C33), 112.9 (dd, J= 3.6 Hz, J= 21.7 Hz, C5'), 105.4 (t, J= 25.3 Hz, C3'), 71.7 (d, J= 7.2 Hz, C5); '9F NMR (CDCl 3, 282 MHz) 8 -103.27 (d, IF, J= 10.32 Hz, C2'-F), -105.56 (d, IF, J= 10.32 Hz, C4'-F); IR (KBr) 3118, 3076, 3059, 1799, 1739, 1619, 1586, 1509, 1456,1433,1358,1332,1267,1167,1149,1107,1051,997,961,898,889,874,811,735, 619, 584, 528, 453 cm~1.

Example 2

4-(4'-Fluorophenyl)furan-2(5H)-one2.

F

0

2

A mixture containing 4-bromo-5(H)furanone (0.249 g, 1.528 mmol), 4 fluorophenylboronic acid (0.280 g, 2.001 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.056 g, 7.978x10-2 mmol), tetrabutylammonium iodide (0.032 g, 8.663x10-2 mmol) and potassium fluoride (0.369 g, 6.351 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(4'-fluoropheny)furan-2(5H) one 2 (0.208 g, 76%) as a pale yellow powder, dec. 151-153C (ref. PDS-1-61). UV-Vis km. (MeOH) 245(790) nm; IH NMR (CDC 3) 8 7.52 (dddd, 2H, J= 3.0 Hz, J= 5.3 Hz, J = 8.3 Hz, J= 10.2 Hz, H2', H6'), 7.17 (dddd, 2H, J= 3.0 Hz, J= 5.3 Hz, J= 8.3 Hz, J= 9.8 Hz, H3', H5'), 6.33 (t, 1H, J= 1.9 Hz, H3), 5.21 (d, 2H, J= 1.5 Hz, H5); 1 3 C NMR (CDC 3, 75 MHz) 173.6 (C2), 166.2 (C4), 162.6 (C4'), 128.6 (d, J= 8.7 Hz, C2', C6'), 125.9 (d, J= 3.6 Hz, Cl'), 116.5 (d, J= 22.4 Hz, C3', C5'), 112.7 (d, J= 2.2 Hz, C3), 70.8 (C5); "F NMR (CDC 3, 282 MHz) 8 -106.98 (s, IF, C4'-F); IR (KBr) 3116, 3072, 2962, 2943, 1786, 1736, 1623, 1598, 1510, 1474, 1451, 1419, 1352, 1322, 1306, 1279, 1224, 1161, 1101, 1047, 991, 891, 872, 860, 840, 817, 807, 706, 587, 549, 542, 475 cm1

. Example 3

4-(4'-Trifluoromethylphenyl)furan-2(5H)-one3.

CF 3

0

3

Utilization of potassium fluoride as base; A mixture containing 4-bromo-5(H)furanone (0.250 g, 1.534 mmol), pinacolato(4-trifluoromethylphenylboronic) ester (0.504 g, 1.852 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.054 g, 7.694x10- mmol), tetrabutylammonium iodide (0.029 g, 7.851x10 mmol) and potassium fluoride (0.362 g, 6.231 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(4'-trifluoromethylphenyl)furan 2(5H)-one 3 (0.206 g, 59%) as a pale yellow powder, dec. 157-158C (ref. PDS-1-63). Utilisation of cesium fluoride as base; A mixture containing 4-bromo-5(H)furanone (1.010 g, 6.198 mmol), 4-trifluoromethylphenylboronic acid (1.432 g, 7.540 mmol), trans- dichlorobis(triphenylphosphine)palladium (II) (0.216 g, 3.077x10-1 mmol), tetrabutylammonium iodide (0.119 g, 3.222x10' mmol) and cesium fluoride (4.681 g, 30.811 mmol) in toluene (30 mL) and water (30 mL) were gently refluxed for 24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x50 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) to give 4-(4'-trifluoromethylphenyl)furan-2(5H)-one6 (1.211 g, 86%) as a pale yellow powder, (ref. PDS-2-97). UV-Vis .a (MeOH) 209(16722), 260(20923) nm; 'H NMR (CDC 3) 5 7.75 (d, 2H, J= 8.3 Hz, H3', H5'), 7.63 (d, 2H, J= 8.3 Hz, H2', H6'),6.48

(t, IH, J= 1.9 Hz, H3), 5.21 (d, 2H, J= 1.9 Hz, H5); 3 C NMR (CDCl 3, 75 MHz) 8 173.0 (C2), 162.0 (C4), 133.27 (q, J= 33.0 Hz, C4'), 132.95 (Cl'), 126.8 (C2', C6'), 126.3 (q, J= 3.6 Hz, C3', C5'), 123.4 (q, J = 270.8 Hz, C4'-CF 3), 115.5 (C3), 70.8 (C5); 19F NMR (CDC 3, 282 MHz) 8 -63.54 (s, 3F, C4'-CF3); IR (KBr) 3094, 2941, 1794, 1759, 1626, 1615, 1577, 1439, 1418, 1325, 1247, 1160, 1113, 1070, 1049, 1016, 994, 891, 872, 844, 772, 748, 708, 692, 679, 601, 521, 438, 422 cm- .

Example 4

4-(4'-Cyanophenyl)furan-2(5H)-one4.

CN

0

4

A mixture containing 4-bromo-5(H)furanone (0.251 g, 1.540 mmol), 4 cyanophenylboronic acid (0.283 g, 1.887 nunol), trans dichlorobis(triphenylphosphine)palladium (II) (0.056 g, 7.978x10-2 mmol), tetrabutylammonium iodide (0.026 g, 7.040x10-2 mmol) and potassium fluoride (0.358 g,

6.162 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(4'-cyanopheny)furan-2(5H) one 4 (0.223 g, 78%) as a pale yellow powder, dec. 227-228°C (ref. PDS-1-65). UV-Vis Xmax(MeOH) 246(1330) nm; 'H NMR (CDCl 3) 67.78 (dd, 2H, J= 1.9 Hz, J= 6.4 Hz, H2', H6'), 7.61 (dd, 2H, J= 2.2 Hz, J= 6.4 Hz, H3', H5'), 6.51 (t, 1H, J= 1.9 Hz, H3), 5.23 (d, 2H, J= 1.9 Hz, H5); "C NMR (CDCI3) 8 172.6 (C2), 161.3 (C4), 133.7 (C'), 133.0 (C3', C5'), 127.0 (C2', C6'), 117.7 (C4'-CN), 116.4 (C3),115.2 (C4'), 70.7 (C5); IR (KBr) 3098, 2933, 2227, 1790, 1747, 1622, 1605, 1558, 1505, 1450, 1418, 1328, 1279, 1166, 1047, 993, 895, 868, 832, 706, 561, 518 cm-.

Example 5

4-(4'-Trifluoromethoxyphenyl)furan-2(5H)-one5.

OCF 3

0/0

5

A mixture containing 4-bromo-5(H)furanone (0.274 g, 1.681 mmol), 4 trifluoromethoxyphenylboronic acid (0.417 g, 2.025 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.060 g, 8.548x10-2 mmol), tetrabutylammonium iodide (0.032 g, 8.663x10-2 mmol) and potassium fluoride (0.401 g, 6.902 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 100% dichloromethane) to give 4 (4'-trifluoromethoxyphenyl)furan-2(5H)-one 5 (0.354 g, 86%) as a pale yellow powder, m.p. 122-123 0C (ref. PDS-1-115). UV-Vis max (MeOH) 211(22865), 269(28180) nm; 1H NMR (CDCl) 8 7.56 (dt, 2H, J= 2.6 Hz, J= 9.4 Hz, H2', H6'), 7.32 (d, 2H, J= 7.9 Hz, H3', H5'), 6.38 (t, 1H, J= 1.9 Hz, H3), 5.21 (d, 2H, J= 1.9 Hz, H5); 3 C NMR (CDC 3)6 173.3 (C2), 162.2 (C4'), 151.4 (C4), 128.20 (Cl'), 128.17 (C3), 121.4 (C2', C6'), 120.3 (q, J= 257.0 Hz, C4'-OCF 3 ), 113.9 (C3', CS'), 70.8 (C5); "F NMR (CDC 3 , 282 MHz) 8 58.19 (s, 3F, C4'-OCF3); IR (KBr) 3109, 3073, 3011, 2936, 1790, 1747, 1624, 1588, 1513, 1443, 1422, 1252, 1159, 1046, 1018, 989, 921, 893, 847, 804, 742, 705, 611, 556, 471 cm-.

Example 6

4-(Thiophen-2'-yl)furan-2(5H)-one 6.

SN.

0 o

6

A mixture containing 4-bromo-5(H)furanone (0.271 g, 1.663 mmol), 2-thiopheneboronic acid (0.265 g, 2.071 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.060 g, 8.548x10 2 mmol), tetrabutylammonium iodide (0.030 g, 8.122x102 mmol) and potassium fluoride (0.386 g, 6.644 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 12 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(thiophen 2'-yl)furan-2(5H)-one 6 (0.245 g, 89%) as a pale yellow powder, m.p. 94-96.5°C (ref.

PDS-2-3). UV-Vis Xma (MeOH) 246(1870), 349(909) nm; 'H NMR (CDCl3) 8 7.50 (d, 1H, J= 4.9 Hz, H3'), 7.26 (d, 1H, J= 3.4 Hz, H5'), 7.06 (t, IH, J= 4.5 Hz, H4'), 6.03 (s, 1H, H3), 5.07 (d, 2H, J= 1.5 Hz, H5); 3 C NMR (CDC1 3 , 75 MHz) 8 173.2 (C2), 157.1 (C4), 132.3 (C2'), 130.3 (C5'), 128.4 (C4'), 128.2 (C3'), 110.6 (C3), 70.6 (C5); IR (KBr) 3097, 3084, 2934, 1788, 1735, 1616, 1450, 1421, 1354, 1322, 1244, 1204, 1157, 1090, 1033, 892, 872, 858, 840, 822, 730, 704, 638 cm-;

Example 7

4-(3',5'-Dimethylisoxazol-4'-yl)furan-2(5H)-one7.

0,

0 0

7

A mixture containing 4-bromo-5(H)furanone (0.288 g, 1.767 mmol), 4-(3,5 dimethylisoxazoleboronic acid (0.299 g, 2.122 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.063 g, 8.976x10-2 mmol), tetrabutylammonium iodide (0.031 g, 8.392x10-2 mmol) and potassium fluoride (0.338 g, 5.818 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 12 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(3',5'-dimethyisoxazol-4' yl)furan-2(5H)-one 7 (0.229 g, 72%) as a pale yellow powder, m.p. 101-103 0 C (ref. PDS 2-5). UV-Vis mX. (MeOH) 246(489) nm; 'H NMR (CDCl,3 300 MHz) 8 6.13 (t, IH, J= 1.5 Hz, H3), 5.13 (d J=. 1.9 Hz, H4), 2.55 (s, 3H, C3'-CH3), 2.38 (s, 3H, C5'-CH3); "C NMR (CDC 3, 75 MHz) 8 173.1 (C2), 169.3 (C5'), 158.2 (C4), 154.4 (C3'), 113.2 (C3), 108.0 (C4'), 71.3 (C5), 13.3 (C3'-CH3), 12.0 (C5'-CH3); IR (KBr) 3114, 2974, 2938, 1799,

1763, 1635, 1620, 1591, 1496, 1448, 1425, 1415, 1392, 1352, 1270, 1238, 1160, 1063, 1016, 980, 895, 847, 759, 739, 706, 583, 511 cm1

. Example 8

4-(3'-Trifluoromethylphenyl)furan-2(5H)-one8.

CF 3

0

8

A mixture containing 4-bromo-5(H)furanone (0.280 g, 1.712 mmol), 3 trifluoromethylphenylboronic acid (0.406 g, 2.138 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.061 g, 8.691xl0- mmol), tetrabutylammonium iodide (0.032 g, 8.663x10- mmol) and potassium fluoride (0.427 g, 7.349 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 12 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(3'-trfluoromethylphenyl)furan 2(5H)-one 8 (0.377 g, 96%) as a pale yellow powder, m.p. 124-125°C (ref. PDS-2-7). UV Vis Xma (MeOH) 211(17625), 262(17835) nm; 'H NMR (CDCl 3, 300 MHz) 8 7.76-7.70 (m, 3H, H2', H4', H6'), 7.64 (q, 1H, J= 7.5 Hz, H5'), 6.46 (t, J= 1.9 Hz, H3), 5.24 (d, 2H, 3 J= 1.9 Hz, H5); C NMR (CDCl3, 75 MHz) 8 173.0 (C2), 162.1 (C4), 131.9 (q, J= 33.2 Hz, C3'), 130.5 (Cl'), 130.0 (C6'), 129.6 (C'), 128.1 (q, J= 4.3 Hz, C4'), 123.4 (t, J= 270.8 Hz, C3'-CF 3), 123.1 (q, J= 3.6 Hz, C2'), 114.8 (C3), 70.8 (C5); 1 9F NMR (CDCl 3 ,

282 MHz) 8 -63.40 (s, 3F, C3'-CF3); IR (KBr) 3102, 3077, 2939, 2875, 1943, 1783, 1743, 1627, 1498, 1455, 1437, 1366, 1339, 1317, 1269, 1236, 1160, 1121, 1097, 1077, 1054, 997, 888, 865, 819, 780, 694, 679, 646, 545, 437, 413 cm 1 .

Example 9

4-(2'-Trifluoromethylphenyl)furan-2(5H)-one9.

- CF 3 0 0

9

A mixture containing 4-bromo-5(H)furanone (0.267 g, 1.638 mmol), 2 trifluoromethylphenylboronic acid (0.382 g, 2.011 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.059 g, 8.406x10-2 mmol), tetrabutylammonium iodide (0.041 g, 1.110x10I 1 mmol) and potassium fluoride (0.380 g, 6.540 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 12 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(2'-trifluoromethylphenyl)furan 2(5H)-one 9 (0.210 g, 56%) as a pale yellow powder, m.p. 49-50C (ref. PDS-2-9). UV Vis m. (MeOH) 208(29654) nm; IH NMR (CDC 3, 300 MHz) 5 7.81 (dd, 1H, J= 1.1 Hz, J= 7.1 Hz, H3'), 7.68-7.57 (m, 2H, H5', H6'),7.38 (d, 1H, J= 7.2 Hz, H4'), 6.24 (t, 1H, J= 1.9 Hz, H3), 5.07 (d, 2H, J= 2.3 Hz, H5); 3C NMR (CDCl 3 , 75 MHz) 6 ; ' 9F NMR (CDC 3, 282 MHz) 8 -58.64 (s, 3F, C2'-CF3); IR (KBr) 3109, 2940, 1786, 1751, 1638, 1602,1580,1498,1447,1317,1295,1269,1237,1163,1126,1069,1047,1036,996,887, 872, 775, 756, 731, 707, 669, 641, 595, 548, 522, 496 cm-1 .

Example 10

4-(Furan-3'-yl)furan-2(5H)-one10.

0

0 0

10

A mixture containing 4-bromo-5(H)furanone (0.261 g, 1.602 mmol), pinacolate(3 furanboronic) ester (0.392 g, 2.020 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.058 g, 8.263x10-2 mmol), tetrabutylammonium iodide (0.062 g, 1.678x10-l mmol) and potassium fluoride (0.393 g, 6.764 mmol) in toluene (10 mL) and water (10 mL) were gently refluxed for 12 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(3'-furan)furan-2(3H)-one 10 (0.043 g, 18%) as brown needles, m.p. 101-1020 C (ref. PDS-2-1 1). UV-Vis kmax (MeOH) 244(1724) nm; IH NMR (CDC 3, 300 MHz) 57.73 (s, 1H, H2'), 7.53 (t, 1H, J= 1.5 Hz, H5'), 6.60 (t, 1H, J= 1.1 Hz, H3), 6.11 (t, 1H, J= 1.5 Hz, H4'), 5.06 (d, 2H, J= 1.9 Hz, 3 H5); C NMR (CDCl3, 75 MHz) 8 173.7 (C2), 156.2 (C4), 145.0 (C4'), 141.9 (C1'), 117.5 (C2'), 112.4 (C3), 108.2 (C3'), 70.8 (C5); IR (KBr) 3141, 3114, 3051, 1790, 1736, 1673, 1519, 1470, 1447, 1405, 1355, 1322, 1275, 1236, 1158, 1019, 894, 871, 852, 828, 752, 702, 644, 596, 547, 527, 501 cm t .

Example 11

4-Bromofuran-2(5H)-one 11.

Br

11

Under and inert atmosphere of anhydrous nitrogen, a solution of oxalyl bromide (10.5 mL, 111.888 mmol) in anhydrous dichloromethane (20 mL) was added dropwise over a 1 h period to a cold (-20°C) solution of tetronic acid (10.013 g, 100.060 mmol) in a solvent mixture of anhydrous dimethylformamide (10 mL) and anhydrous dichloromethane (200 mL) resulting in the formation of a yellow precipitate. The resulting yellow mixture was allowed to warm slowly over 1 h to0°C before the ice bath was removed and the resulting yellow mixture allowed to stir for a further 4 h at room temperature, which during this time the yellow precipitate darkened and turned green. Water (100 mL) was added and the product extracted with diethyl ether (3x200 mL). The organic fractions were combined, washed with water (2x100 mL), saturated sodium bicarbonate (2x200 mL), brine (2x200 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a pale brown coloured solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) to give 4-bromofuran-2(5H)-one 11 (12.578 g, 77%) as a yellow solid. Recrystallisation from diethyl ether gave 4-bromo 5(H)furanone 11 as colourless needles, m.p. 72-74C (ref. PDS-2-51). UV-Vis kma (MeOH) 221(13428) nm; H NMR (CDC 3 , 300 MHz) 8 6.36 (t, 1H, J= 1.9 Hz, H3), 4.87 (t, 1H, J= 1.9 Hz, H5); 3C NMR (CDC 3, 75 MHz) 8 170.8 (C2),146.1 (C4), 121.8 (C3), 74.9 (C5); IR (Nujol) 3096, 2923, 2853, 1777, 1742, 1598, 1439, 1411, 1341, 1263, 1152, 1056, 1013, 884, 867, 845, 699 cm-.

Example 12

4-(N-Methylpyrazol-4'-yl)furan-2(5H)-one 12.

N

0 N

12

A mixture containing 4-bromo-5(H)furanone (0.247 g, 1.516 mmol), 4-(N methylpyrazole)boronic acid (0.391 g, 1.879 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.057 g, 8.12lxI0-2 mmol), tetrabutylammonium iodide (0.027 g, 7.31Ox10-2 mmol) and aqueous potassium fluoride (2M, 3 mL, 6.000 mmol) in tetrahydrofuran (17 mL) was refluxed for 12 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(N-methylpyrazol-4'-yl)furan-2(5H)-one 12 (0.207 g, 83%) as a pale yellow powder, m.p. 181-182C (ref. PDS-2-59). UV-Vis kma (MeOH) 209(2725), 272(4536) nm; H NMR (CDC 3, 300 MHz) 8 7.69 (s, 1H, H3'), 765 (s, 1H, H5'),6.03 (t, 1H, J= 1.5 Hz, H3), 5.05 (d, 2H, J= 1.9 Hz, H5), 3.96 (s, 3H, Ni' 3 CH); C NMR (CDCl3, 75 MHz) 3 174.2 (C2), 156.5 (C4), 138.1 (C3'), 129.1 (C5'), 113.2 (C4'), 109.8 (C3), 70.9 (C5), 39.4 (N'-CH3); IR (KBr) 3450, 3174, 3110, 3093, 2949, 1788, 1728, 1636, 1542, 1485, 1441, 1409, 1383, 1347, 1299, 1269, 1261, 1210, 1160, 1065, 1024, 997, 980, 962, 894, 859, 843, 722, 704, 664, 624, 544, 507 cm- .

Example 13

(Z)-4-Phenyl-5-(3'-trifluoromethyl)benzylidene)furan-2(5H)-one13.

0

CF 3

13

A mixture containing (Z)-5-(bromomethylene)-4-phenylfuran-2(5H)-one (0.295 g, 1.175 mmol), 3-trifluoromethylphenylboronic acid (0.278 g, 1.464 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.043 g, 6.126x10-2 mmol), tetrabutylammonium iodide (0.023 g, 6.227x10-2 mmol) and aqueous potassium fluoride (2M, 3 mL, 6.000 mmol) in tetrahydrofuran (17 mL) was refluxed for 24 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 20:80 dichloromethane/light petroleum) to give (Z)-4-phenyl-5-(3'-trifluoromethyl)benzylidene)furan-2(5H)-one13 (0.337 g, 91%) as a pale yellow powder, m.p. 108-110°C (ref. PDS-2-65). UV-Vis amax (MeOH) 242(1350), 356(4085) nm; 'H NMR (CDC 3, 300 MHz) 68.11 (d, 1H, J= 7.5 Hz, H4'), 7.91 (s, 1H, H2'), 7.60-7.49 (m, 7H, H2", H3, H4", H5", H5', H6", H6'),6.27 (s, 1H, H3), 6.19 (s, 1H, HI"'); 3 C NMR (CDCl3, 75 MHz) 8 ; 9' F NMR (CDCl 3, 282 MHz) 6 -63.25 (s, 3F,C3' CF3); IR (KBr) 3067, 1822, 1759, 1650, 1611, 1588, 1573, 1489, 1446, 1350, 1326, 1211, 1188,1169,1118, 1072, 1000,920,903,863,846,824,796,769,756,700,691,679,665, 634, 552, 508, 470 cm-1.

Example 14

4-(Thiophen-3'-yl)furan-2(5H)-one14.

S

02

14

Utilization of potassium fluoride as base in THF; A mixture containing 4-bromo 5(H)furanone (0.252 g, 1.546 mmol), 3-thiopheneboronic acid (0.249 g, 1.946 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.060 g, 8.548x10-2 mmol), tetrabutylammonium iodide (0.033 g, 8.934x10-2 mmol) and aqueous potassium fluoride (2M, 4 mL, 8.000 mmol) in tetrahydrofuran (16 mL) was stirred at room temperature for 24 h under nitrogen before brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a light brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum followed by 100% dichloromethane) to give 4-(thiophen-3'-yl)furan-2(5H)-one 14 (0.245 g, 95%) as a pale yellow powder. Recrystallisation from dichloromethane/light petroleum furnished colourless needles, m.p. 130.5-132C (ref. PDS-2-77). Utilization of cesium fluoride as base in toluene; A mixture containing 4-bromo-5(H)furanone (0.500 g, 3.068 mmol), 3 thiopheneboronic acid (0.710 g, 3.738 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.105 g, 1.496x10~" mmol), tetrabutylammonium iodide (0.068 g, 1.841x10-1 mmol) and cesium fluoride (1.951 g, 12.842 mmol) in toluene (10 mL) and water (10 mL) was stirred at reflux for 12 h under nitrogen. The reaction mixture was allowed to cool before brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give an orange solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) to give 4 (thiophen-3'-y)furan-2(5H)-one 18 (0.490 g, 96%) as a yellow powder. Recrystallisation from dichloromethane/light petroleum furnished colourless needles, (ref. PDS-2-113). UV-Vis kmx (MeOH) 225(28729), 276(51973) un; 'H NMR (CDCl, 300 MHz) 6 7.58 (dd, 1H, J= 1.5 Hz, J= 3.0 Hz, H5'), 7.44 (dd, 1H, J= 3.0 Hz, J= 5.3 Hz, H4'), 7.28 (dd, lH, J= 1.1 Hz, J= 4.9 Hz, H2'), 6.16 (t, 1H, J= 1.5 Hz, H3), 5.14 (d, 1H, J= 1.9 Hz, H5); "C NMR (CDCl3, 75 MHz) 6 174.0 (C2), 158.5 (C4), 131.8 (C3'), 127.6 (C4'), 126.2 (C5'), 125.5 (C3), 111.9 (C2'), 71.0 (C5); IR (KBr) 3119, 3091, 1937, 1793, 1731, 1621, 1506, 1473, 1446, 1423, 1347, 1301, 1199, 1163, 1041, 1003, 928, 894, 870, 842, 798, 791, 714, 700, 634, 619, 545, 488 cm-.

Example 15

4-(2',4'-Bis(trifluoromethyl)phenyl)furan-2(5H)-one15.

CF 3

- CF 3 0 0

15

A mixture containing 4-bromo-5(H)furanone (0.331 g, 2.031 mmol), (2,4' bis(trifluoromethyl)phenyl)boronic acid (0.641 g, 2.485 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.075 g, 1.069x10' mmol), tetrabutylammonium iodide (0.037 g, 1.002x0 mmol) and aqueous potassium fluoride (2M, 5 mL, 10.000 mmol) in tetrahydrofuran (15 mL) was refluxed for 48 h under nitrogen before the reaction mixture was allowed to cool to room temperature. Brine (50 mL) was added and the product extracted with dichloromethane (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) to give 4-(2',4'-bis(trifluoromethyl)phenyl)furan-2(5H)-one15 (0.169 g, 28%) as a pale yellow powder. Recrystallisation from dichloromethane/light petroleum furnished colourless needles, m.p. 116-117°C (ref. PDS-2-81). UV-Vis max (MeOH) 204(47498) nm;'HNMR(CDCl 3,300 MHz) 8 8.05 (s, 1H,H3'), 7.93 (d, 1H,J= 7.9 Hz,H5'),7.56(d, 3 1H, J= 7.9 Hz, H6'), 6.30 (t, IH, J= 1.9 Hz, H3), 5.09 (d, 1H, J= 2.3 Hz, H5); C NMR (CDC 3, 75 MHz) 8 171.9 (C2), 161.4 (C4), 133.7 (C1'), 132.6 (q, J= 33.9 Hz, C4'-CF 3), 130.3 (C3), 129.2 (q, J= 32.5 Hz, C2'-CF3 ), 129.1 (d, J= 2.9 Hz, C'), 124.6 (d, J= 2.2 Hz, C4'), 124.0 (ddd, J= 4.3 Hz, J= 7.9 Hz, J= 9.4 Hz, C6'), 121.4 (d, J= 2.2 Hz, C3'), 121.0 (d, J= 2.9 Hz, C2'), 73.3 (d, J= 2.2 Hz, C5); '9 F NMR (CDCl 3, 470 MHz) 6 -59.04 (s, 3F, C2'-CF3), -63.66 (s, 3F, C4'-CF3 ); IR (KBr) 3138, 3104, 3057, 2938, 1792, 1742, 1649, 1624, 1584, 1510, 1466, 1438, 1353, 1315, 1281, 1269, 1205, 1168, 1144, 1128, 1087, 1068, 1042, 994, 918,896, 882, 871, 859, 825, 762, 751, 733, 708,687, 673, 661, 617, 583, 552, 479, 465 cm-1.

Example 16

3-Bromo-4-(4'-(trifluoromethyl)phenyl)furan-2-(5H)-one16.

CF 3

Br

0 0

16

A mixture containing 3,4-dibromofuran-2(5H)-one (0.518 g, 2.142 mmol), 4 trifluoromethylphenylboronic acid (0.509 g, 2.680 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.069 g, 9.83lx102 mmol), tetrabutylammonium iodide (0.038 g, 1.029x10' mmol) and cesium fluoride (0.872 g, 5.740 mmol) in toluene (10 mL) and water (10 mL) was stirred at room temperature for 72 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x50 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give an orange solid. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum) to give 3-bromo-4-(4'-(trifluoromethyl)phenyl)furan-2-

(5H)-one 16 (0.312 g, 47%) as a pale yellow powder. Further purification by recrystallisation from dichloromethane/light petroleum furnished colourless needles, (ref. PDS-2-115); 'H NMR (CDCl, 300 MHz) 8 7.94 (d, 2H, J= 8.3 Hz, H3', H5'), 7.78 (d, 2H, J= 8.3 Hz, H2, H6'), 5.21 (s, 2H, H5).

Example 17

(Z)-4-(4'-(trifluoromethyl)phenyl)-5-(4"-(trifluoromethyl)benzylidene)furan-2(5H)-one17.

CF 3

0 0

CF 3

17

A mixture containing (Z)-5-(bromomethylene)-4-bromofuran-2(5H)-one (0.505 g, 1.989 mmol), 4-trifluoromethylphenylboronic acid (0.961 g, 5.059 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.070 g, 9.973x10-2 mmol), tetrabutylammonium iodide (0.037 g, 1.001x10' mmol) and cesium fluoride (1.592 g, 10.479 mmol) in toluene (16 mL) and water (16 mL) was stirred at room temperature for 96 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x20 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give an orange solid. The resulting solid was chromatographed (silica gel: eluent 25:75 dichloromethane/light petroleum) to give (Z)-4-(4'-(trifluoromethyl)phenyl)-5-(4" (trifluoromethyl)benzylidene)furan-2(5H)-one17 (0.581 g, 76%) as a pale yellow powder, m.p. 127.5-129°C (ref.PDS-2-105). 'H NMR (CDC 3, 300 MHz) 67.90 (d, 2H, J= 8.30 Hz, C3', C5'), 7.82 (d, 2H, J= 8.30 Hz, C3", C5"), 7.65 (d, 2H, J= 8.30 Hz, C2', C6'), 7.64 (d, 2H, J= 8.30 Hz, C2", C6"), 6.35 (s, H, C3), 6.12 (s, 1H, Cl').

Example 18

(Z)-4-(Thiophen-3-yl)-5-(thiophen-3-ylmethylene)furan-2(5H)-one 18.

S

0 0

18

A mixture containing (Z)-4-bromo-5-(bromomethylene)furan-2(5H)-one (0.502 g, 1.977 mmol), 3-thiopheneboronic acid (0.553 g, 4.322 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.068 g, 9.688x10-2 mmol), tetrabutylammonium iodide (0.037 g, 1.137x10-l mmol) and cesium fluoride (1.221 g, 8.038 mmol) in toluene (10 mL) and water (10 mL) was stirred at room temperature for 72 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was subjected to recrystallization to give (Z) 4-(thiophen-3-yl)-5-(thiophen-3-ylmethylene)furan-2(5H)-one18.

Example 19

(Z)-4-(Thiophen-2-yl)-5-(thiophen-2-ylmethylene)furan-2(5H)-one19.

O

0 0 'S

A mixture containing (Z)-4-bromo-5-(bromomethylene)furan-2(5H)-one (0.503 g, 1.981 mmol), 2-thiopheneboronic acid (0.560 g, 4.377 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.072 g, 1.026x10~1 mmol), tetrabutylammonium iodide (0.072 g, 1.002x10 mmol) and cesium fluoride (1.257 g, 8.275 mmol) in toluene (10 mL) and water (10 mL) was stirred at room temperature for 72 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was subjected to recrystallization to give (Z) 4-(thiophen-2-yl)-5-(thiophen-2-ylmethylene)furan-2(5H)-one19.

Example 20

(Z)-4-(4'-Fluorophenyl)-5-(4"-fluorobenzylidene)furan-2(5H)-one20.

F F

20

A mixture containing (Z)-4-bromo-5-(bromomethylene)furan-2(5H)-one (0.500 g, 1.969 mmol), 4-fluorophenylboronic acid (0.610 g, 4.360 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.069 g, 9.831xi1-2 mmol), tetrabutylammonium iodide (0.038 g, 1.029x10' mmol) and cesium fluoride (1.211 g, 7.972 mmol) in toluene (10 mL) and water (10 mL) was stirred at room temperature for 72 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was subjected to recrystallization to give (Z) 4-(4'-fluorophenyl)-5-(4"-fluorobenzylidene)furan-2(5H)-one20.

Example 21

(Z)-4-(4'-(Trifluoromethoxy)phenyl)-5-(4"-(trifluoromethoxy)benzylidene)furan-2(5H)-one 21.

OCF 3

0 0

OCF 3

21

A mixture containing (Z)-4-bromo-5-(bromomethylene)furan-2(5H)-one (0.5026 g, 1.980 mmol), 4-(trifluoromethoxy)phenylboronic acid (0.8983 g, 4.362 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.0711 g, 1.013x10- mmol), tetrabutylammonium iodide (0.0381 g, 1.031x101 mmol) and cesium fluoride (1.3094 g, 8.620 mmol) in toluene (10 mL) and water (10 mL) was stirred at room temperature for 72 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was subjected to recrystallization to give (Z) 4-(4'-(trifluoromethoxy)phenyl)-5-(4"-(trifluoromethoxy)benzylidene)furan-2(5H)-one21.

Example 22

(Z)-4-(4'-Cyanophenyl)-5-(4'"-cyanobenzylidene)furan-2(5H)-one22.

CN

0 \

CN

22

A mixture containing (Z)-4-bromo-5-(bromomethylene)furan-2(5H)-one (0.5315 g, 2.094 mmol), 4-cyanophenylboronic acid (0.6583 g, 4.390 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.0688 g, 9.802x10-2 mmol), tetrabutylammonium iodide (0.0366 g, 9.908x10-2 mmol) and cesium fluoride (1.2432 g, 8.184 mmol) in toluene (10 mL) and water (10 mL) was stirred at room temperature for 72 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was subjected to recrystallization to give (Z) 4-(4'-cyanophenyl)-5-(4"-cyanobenzylidene)furan-2(5H)-one22.

Example 23

(Z)-4-(3'-(Trifluoromethyl)phenyl)-5-(3"-(trifluoromethyl)benzylidene)furan-2(5H)-one23.

CF 3

0 0

F3C

23

A mixture containing (Z)-4-bromo-5-(bromomethylene)furan-2(5H)-one (0.5038 g, 1.984 mmol), 3-(trifluoromethyl)phenylboronic acid (0.8330 g, 4.386 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.0746 g, 1.063x10' mmol), tetrabutylammonium iodide (0.0477 g, 1.291x101 mmol) and cesium fluoride (1.5039 g, 9.901 mmol) in toluene (10 mL) and water (10 mL) was stirred at room temperature for 72 h under nitrogen. Brine (50 mL) was added and the product extracted with ethyl acetate (3x50 mL). The organic fractions were combined, washed with brine (3x20 mL), dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give a dark brown solid. The resulting solid was subjected to recrystallization to give (Z) 4-(3'-(trifluoromethyl)phenyl)-5-(3"-(trifluoromethyl)benzylidene)furan-2(5H)-one23.

Examples 24 to 26

In addition, the following compounds were prepared by similar methodologies to those described above:

Br Br

S -

24 25

F H

26

Example 27

5-methyl-4-phenyl-2(5H)furanone 27.

O H

27

A solution of 5-methylene-4-phenyl-2(5H)furanone (2.63 mmol) in ethanol (50 mL) containing Pd-C (25 mgs; 5%) was hydrogenated under an atmosphere of hydrogen at room temperature for 24 hr. The catalyst was filtered off using a pad of Celite and the solvent evaporated in vacuo, leaving a colourless semi-solid, which upon flash chromatography using (EtOAc, CH2 C12 ; 1:5) as the eluent gave 5-methyl-4-phenyl 2(5H)furanone 27 as a semi-solid in 90% yield. 'H NMR: S(CDCl 3) 3.33 (d, J 4Hz, 3H, C5-Me), 5.56 (q, J 4 Hz, lH, C5-H), 6.26 (s, 1H, C3-H) and 7.47 (s, 5H, Ar H's). 3 C NMR: 19.71, 65.85, 66.39, 113.67, 127.11, 129.14,129.87,131.20 168.79,172.54.

Example 28

(Z)-5-(4-fluorobenzylidene)furan-2(5H)-one28.

20 200

F

A mixture containing 5-bromomethylene-2(5H)furanone (0.175 g, 1 mmol), 4 fluorophenylboronic acid (0.168 g, 1.2 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL x 3). The organic fractions were combined, washed with brine (50 mL x 3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 28 as a white powder. Yield 0.164 g (86%), m.p. 140 - 142°C, UV-Vis Xmax(MeOH) 225(22535),330(56424)nm.

'H NMR (CDC 3) 8 7.81-7.74 (m, 2H, H2' and H6'), 7.48 (d, J= 5.3 Hz, 1H, H4), 7.11 7.04 (m. 2H, 13' and H5'), 6.20 (d, J= 5.3 Hz, 1H, H3), 5.99 (s,1H, 116). IR (Nujol) 1738, 1600, 1547, 1505, 1462, 1419, 1377, 1304, 1291, 1234, 1185, 1166, 1113, 1094, 1071, 1019, 948, 930, 887, 852, 836, 822, 781, 764 cm- 1 .

Example 29

(Z)-5-(4-(trifluoromethyl)benzylidene)furan-2(5H)-one29.

W0

CF 3

29

A mixture containing 5-bromomethylene-2(5H)furanone (0.175 g, 1 mmol), 4 trifluoromethylphenylboronic acid (0.228 g, 1.2 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL x 3). The organic fractions were combined, washed with brine (50 mL x 3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 29 as a light yellow powder. Yield 0.133 g (55%), m.p. 92 - 94°C, UV Vis Xm (MeOH) 223 (15948), 237 (10856), 323(35739) nim. 'H NMR (CDCl 3) 8 7.87 (d, J= 8.3 Hz, 2H, H2' and H6'), 7.63 (d, J= 8.3 Hz, 2H, H3' and H 5'), 7.52 (d, J= 5.7 Hz, 1H, H4),, 6.28 (d, J= 4.9 Hz,1H, H3), 6.04 (s,1H,116).

3C NMR (CDCl, 75 MHz) 6 169.5 (C), 149.6 (C), 145.0 (CH), 136.1 (C), 130.6 (CH), 130.5 (q, J= 32.7 Hz, C), 125.6 (q, J= 3.9 Hz, CH), 123.8 (q, J= 272.0 Hz, CF3 ), 119.3 (CH), 112.0 (CH). IR (Nujol) 1784, 1759, 1462, 1376, 1326, 1160, 1111, 1069, 884 cm1.

Example 30

(Z)-5-(3-(trifluoromethyl)benzylidene)furan-2(5H)-one30.

0 0

. CF 3

30

A mixture containing 5-bromomethylene-2(5H)firanone (0.175 g, 1 mmol), 3 trifluoromethylphenylboronic acid (0.228 g, 1.2 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL x 3). The organic fractions were combined, washed with brine (50 mL x 3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 30 as a light brown powder. Yield 0.180 g (75%), m.p. 69 - 71°C, UV Vis Xma (MeOH) 223 (15166), 323 (31738) nm.

H NMR (CDC 3) 8 8.01 (d, J= 7.5 Hz,1H, H6'), 7.92 (s, 1H, H2'), 7.57-7.47 (m, 2H, H4' and H5'), 7.51 (d, J= 5.2 Hz, 1H, H4), 6.27-6.25 (m, 1H, H3), 6.03 (s, 1H, H6).

3C NMR (CDC 3, 75 MHz) 6 169.5 (C), 149.3 (C), 145.0 (CH), 133.5 (C), 133.4 (CH), 131.2 (q, J= 32.4 Hz, C), 129.3 (CH), 127.0 (q, J= 3.9 Hz, CH), 125.4 (q, J= 3.9 Hz, CH), 123.7 (q, J= 272,5 Hz, CF3 ), 119.1 (CH), 112.0 (CH). IR (Nujol) 1758, 1463, 1326, 1299, 1220, 1165, 1132, 1108, 1097, 1079, 942, 899, 871, 860, 811, 799, 765, 651 cm1

. Example 31

(Z)-5-(Thiophen-3-methylene)furan-2(5H)-one31.

0`

SI

31

A mixture containing 5-bromomethylene-2(5H)furanone (0.175 g, 1 mmol), 3 thiopheneboronic acid (0.154 g, 1.2 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL x 3). The organic fractions were combined, washed with brine (50 mL x 3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 31 as a light yellow powder. Yield 0.131 g (74%), m.p. 65 - 67°C, UV

Vis Xma (MeOH) 208 (11976), 239 (8483), 340 (27730) nm. 'H NMR (CDCl 3) 6 7.76 7.45 (m. 1H, H), 7.54-7.52 (m, IH, H), 7.46 (d, J= 5.3 Hz, 1H, H), 7.36-7.33 (m, IH, ArH), 6.19-6.17 (m, 1H, H), 6.11 (s, 1H, H6). 3C NMR (CDC13 , 75 MHz) 6 169.9 (C), 147.4 (C), 144.6 (CH), 134.2 (C), 128.8 (CH), 128.6 (CH), 126.1 (CH), 117.9 (CH), 108.1

(CH). IR (Nujol) 1743, 1645, 1546, 1506, 1463, 1377, 1328, 1243, 1178, 1111, 1074, 964, 934, 890, 879, 793, 766, 708, 646 cm-

. Example 32

(Z)-5-(Thiophen-2-ylmethylene)furan-2-(5H)-one32.

0

-S

32

A mixture containing 5-bromomethylene-2(5H)furanone (0.175 g, 1 mmol), 2 thiopheneboronic acid (0.154 g, 1.2 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL x 3). The organic fractions were combined, washed with brine (50 mL x 3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 32 as a yellow powder. Yield 0.170 g (95%), m.p. 100 - 102°C. 'H NMR (CDC 3 ) 8 7.50 (d, J= 4.9 Hz, 1H, H3'), 7.46 (d, J= 5.3 Hz, 1H, H4), 7.38 (d, J= 3.4 Hz, 1H, H5'), 7.08-7.05(m, 1H, H4'), 6.31 (s, 1H, H6), 6.17 (d, J= 5.3 Hz, 1H, H3). 3 C NMR (CDC 3 , 75 MHz) 8 169.5 (C), 146.6 (C), 143.8 (CH), 136.0 (C), 131.3 (CH), 130.7 (CH), 127.7 (CH), 118.0 (CH), 107.5 (CH). IR (Nujol) 1777, 1738, 1459, 1417, 1376, 1107, 935, 886, 731 cm^1.

Example 33

(Z)-5-(4-Methoxybenzylidene)furan-2-(5H)-one33.

0 0

OMe

33

A mixture containing 5-bromomethylene-2(5H)furanone (0.175 g, 1 mmol), 4 methoxyphenylboronic acid (0.182 g, 1.2 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL x 3). The organic fractions were combined, washed with brine (50 mL x 3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 33 as a yellow powder. Yield 0.163 g (80%), m.p. 118 - 120°C, 'H NMR (CDC 3 ) 8 7.76-7.71 (m, 2H, H3' and H5'), 7.45 (d, J= 5.2 Hz, 1H, H4), 6.93- 6.88 (m, 2H, H2' and H6'), 6.14-6.12 (m, 1H, H3), 5.97 (bs, 1H, H6), 3.83 (s, 3H). 1 3 C NMR (CDC 3 , 75 MHz) 6 170.5 (C), 160.5 (C), 147.0 (C), 145.0 (C), 132.4 (CH), 125.6 (CH), 116.8 (CH), 114.3 (CH), 114.2 (CH), 55.3 CH 3 ). IR (Nujol) 1789,1737,1604,1551, 1509, 1458, 1376, 1302, 1258, 1175, 1119, 1025, 931, 893, 813 cm-.

Example 34

4-Aryl-IH-pyrrol-2(5H)-ones

Initially a mixture of acetophenone (0.052 mol) and ethylbromoacetate (0.055 mol) was prepared in dry hexane-toluene mixture (50 mls,1:1; v:v), 10 mL of this solution was added drop wise to pre-heated (ca 40-50°C) zinc dust (0.055 mol) and the reaction mixture was stirred. After the reaction has commenced, the rest of the solution was added at such a rate so as to maintain a gentle reflux (ca 0.5 hr). After addition, the mixture was heated at reflux for further 2hr. The mixture was cooled, and sulfuric acid (40 mL; 2.5M) was added to decompose the organo-zinc complex. The organic phase was separated, washed with brine (ca 25 mL), dried (Na 2SO 4) and the solvent removed in vacuo leaving ethyl-3-aryl-3 hydroxybutanoate as an oil (ca 80-100%), which was used without further purification.

This product was dehydrated by refluxing it with P2 0 5 (0.052 mol) for 1 hr in toluene (100 mL). The mixture was cooled and passed through a plug'of Celite/silica. The solvent was removed, and the residue flash-chromatographed using dichloromethane as eluent giving ethyl-3-aryl-2-butenoate in 80-98% yield. The unsaturated ester, N-bromosuccinimide (1.1 mol/mol) in carbon tetrachloride (100-140 mL) and a few crystals of perbenzoic acid, were heated at reflux for 48 hrs, while shining a 100 watt lamp over the reaction mixture. The mixture was cooled, filtered through a Celite/silica plug, and the solvent evaporated in vacuo leaving ethyl-4-bromo-3-aryl-2-butenoate (60-100%) as a solid/semi-solid. The later product was dissolved in diethylether (ca 40-50 mL) and cooled in a bath of dry ice/acetone. Gaseous ammonia was passed through the mixture till the total volume in the flask reached 100 mL. The mixture was left to warm up to room temperature (4-24 hrs) and the precipitated product was filtered, washed with water, cold ether and dried to yield 4-aryl-1H-pyrrol-2(5H)-one in 30-55% yield.

Example 35

4-(4'-Bromophenyl)-pyrrol-2(5H)-one35.

Br

O N H

4-(4'-Bromophenyl)-pyrrol-2(5H)-one 35 (46%); colourless needles from ethanol, m.p. 233-235°C (decomp). kma 218(p 15,571), 225(14,597) and 278 (26,113) nm. 'H N.M.R. 6 (DMSO-d) 4.33 (2H, s, C5- CH2 ), 6.53 (1H, s, C3-H) and 7.59-7.61 (4H. Ar H's). 3 C

N.M.R. 8 (DMSO-d 6): 22.12, 47.85, 60.62, 72.62, 121.55, 124.38, 123.60, 131.70, 156.18 and 173.80.

Example 36

4-(4'-Fluorophenyl)-1H-pyrrol-2(5H)one36.

F N H

36

4-(4'-Fluorophenyl)-1H-pyrro-2(5H)one 36, (40%), pale brown needles (ethanol), m.p. 190 0C km. 205(F 15,539) and 269 (19,650) nm. 'H NMR: 8 (CD3 OD) 4.47 (2H, s, C5 CH2); 6.41 (s, 1H, C4-H), 7.13-7.19 (t, 2H, Ar H's) and 7.65-7.69 (m, 2H, Ar H's). 1 3 C NMR: 48.34, 65.38, 115.34, 123.58, 125.23, 125.32, 128.02, 157.88, 165.48 and 175.72.

2. ANTIBACTERIAL ASSAYS

Example 1

N-acylated homoserine lactone (AHL) quorum sensing assay

The present applicant has demonstrated that certain furanones and furanone analogues can inhibit AHL-mediated quorum sensing in bacteria. Compounds of the present invention were compared to compounds of the prior art in order using an AHL-quorum sensing assay which utilises a reporter strain that expresses Green Fluorescent Protein (GFP) in the presence of AHL signals. The assay is performed by measuring GFP output in the presence of the compound to be measured and comparing the output to a control. By using multiple samples at varying concentrations of compound and AHL, an inhibition index of compound activity can be generated. The inhibition index used in the present example is the relative amount of compound required to reduce GFP expression to 40% of the control. The inhibition index is termed AIC40. Lower values of AIC40 represent better inhibitors of the AHL quorum sensing system.

The reporter strain of bacterium used in this assay is E coli into which the V fischeri luxRI system has been engineered. A gfp gene is fused to the QS controlled luxI promoter as is described in (Andersen et al., 2001, and Andersen et al, 1998).

Measurement ofAIC40 (ID40 at 3 nM OHHL)

Determination of the activity of compounds using the E. coli based luxRI construct was performed as follows.

Inhibition kinetics

In a 15 mL plastic tube, mix 3 mL of o.n. culture of the lux reporter strain with 12 mL fresh medium, incubate at 37°C. Label six tubes, 10, 20, two 50 and two 100. To each of the tubes, add OHHL (3-oxohexanoyl homoserine lactone) to a final concentration of 10, 20, 50, or 100 nM respectively in the AB medium (add enough medium to distribute across the appropriate number of wells). To the first row of the microplate (row A), add 200 ul of the OHHL/AB mixture. To the remaining rows (B-H) add 100 ul of the OHHL/AB mixture. To the first row (A) add compounds to be tested to the 200 ul mixture of OHHL/AB. Make a dilution series in the first 7 rows by transferring 100 tL from wells in row 1 to wells in row 2 and so on. Discard the remaining 100 pL from row 7. Add 100 pL diluted lux monitor to each well. Incubate the plate 2 hours at 37C and measure green fluorescence using the "Victor" plate reader.

Data treatment

Calculate ID 40 for each column. To do this, calculate the relative activity in each well. Each column is calculated separately, the well that does not contain furanone is set to 100% activity (the wells in row 8). Make a plot for each concentration of OHHL vs. the range of compound concentrations used. Calculate the amount of compound needed to lower the relative activity to 40%, this is termed inhibiting dose 40%, ID40. For each compound an inhibition index, AIC 4 0 , is found as follows: plot ID 40 against its respective AHL concentration; AIC 4 0is the slope of the best straight line through the plotted points and origin.

Compound measurements

The results of compound measurements using the AHL-quorum sensing assay are shown in Table I below.

Example 2

LasR assay

Compounds of the present invention were also assayed using a LasR assay. The LasR assay provides a measurement of quorum sensing inhibition activity. The higher the percentage inhibition, the more effective the compound. In the LasR assay, an unstable gfp has been fused to the elastase promoter, so that the amount of Gfp is regulated by the QS system. The plasmid is put into Pseudomonas aeruginosawhich makes its own AHL signals. The assay is performed by adding the compounds to be tested to the system at the beginning of the experiment, at different concentrations. Gfp expression is measured at different times during growth, ending at the 24 h time point. The percentage fluorescence was determined at the time point when the fluorescence reached its maximum in the control, usually around 11-12 h after inoculation.

The results of the compound measurements using the LasR assay are shown in Table 1 below.

Table 1: Results of N-acylated homoserine lactone (AHL) quorum sensing assay and LasR assay

Compound AIC40 LasR (% inhibition at 25 ug/mI (ID40 at 3 nM compound) OHHL) 2 14.39 (39.4) Not tested F

00

1 7.6(17.83) Not tested F

- F

3 0.77(4.37) 22% CF 3

5 5.9(11.37) 19.3 % (43.2% at 50 pg/ml) OCF 3

Compound AIC40 LasR (% inhibition at 25 ug/ml (ID40 at 3 nM compound) OHHL)

8 Not tested 22% (42.2% at 50 pg/ml)

CF 3

6 24.6(58.7) 10%

0

14 4.9 (60 iM) 15% S

0

12 Not tested (22.9% at 50 pg/ml) yle

ON

Not tested 20% (78% at 100Ipg/ml) Br

0

26 Not tested 30% (76% at 100 pg/ml) Br

O

Compound AIC40 LasR (% inhibition at 25 ug/ml (ID40 at 3 nM compound) OHHL)

27 Not tested 9% (57% at 100 tg/ml)

00?

28 Not tested 13% (53 at 100 pg/ml)

O N H H

29 Not tested 15.8% 38.4% at 100 pg/ml) F

O O H

23 4.64(22.1) 23% (46.4 % at 100 tg/ml) CN

/ \ CN

24 Not tested 19% (35% at 100 pg/ml)

CF 3

0

CF 3

Compound AIC40 LasR (% inhibition at 25 ug/ml (ID40 at 3 nM compound) OHHL)

21 4.4(148) 14.7% (47% at 100 ptg/ml) F

0 \

F

Example 3

Inhibition of bioflm formation

Compounds were run in a Petri dish model-where the cells of E. coli or Pseudomonas aeruginosa were exposed to the compound for 48 h. The amount of biofilm was determined by combining image data of the XY (surface cover in one plane) and XZ (depth). The controls gave good biofilm cover and some structure formation.

E. coli

Compound % biofilm

6 (40 pg/mL) 97%

6 (25 pg/mL) 87.7%

Pseudomonas aeruginosa

Compound % biofilm

6 (10 pg/mL) 77%

Throughout this specification the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.

All publications mentioned in this specification are herein incorporated by reference. Any discussion of documents, acts, materials, devices, articles or the like which has been included in the present specification is solely for the purpose of providing a context for the present invention. It is not to be taken as an admission that any or all of these matters form part of the prior art base or were common general knowledge in the field relevant to the present invention as it existed before the priority date of each claim of this application.

It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.

REFERENCES

ANDERSEN, J. B., HEYDORN, A., HENTZER, M., EBERL, L., GEISENBERGER, 0., CHRISTENSEN, B., BAK, MOLIN, S. & GIVSKOV, M. (2001) Gfp-based n-acyl homoserine lactone sensor systems for detection of bacterial communication. Apple. Environ. Microbiol., 67,575-585.

ANDERSEN, J. B., STERNBERG, C., POULSEN, L. K., BJORN, S. P., GIVSKOV, M. & MOLIN, S. (1998) New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. AppL. Environ. Microbiol., 64, 2240-2246.

Claims

DCC-8/12/2021 57 THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:

1. A compound of formula II

R6

R8

X R9 0)R

II

wherein:

X is selected from -0- or -N(Rio)-;

wherein Rio is selected from H, alkyl, aryl and arylalkyl;

R 6 is phenyl substituted with one or more substituents selected from the group consisting of

CF 3 , OCF 3 , cyano (CN), halo, F and Br;

R 7 and R9 are H; and

R8 is H;

provided that the compound is not selected from:

4-(4-bromophenyl)-1,5-dihydro-1-phenyl-2H-pyrrol-2-one;

4-[3-(trifluoromethyl)phenyl]-2(5H)-furanone;

4-(4-chlorophenyl)-2(5H)-furanone;

4-(4-fluorophenyl)-2(5H)-furanone;

4-(4-chlorophenyl)-1,5-dihydro-1-(1-methylethyl)-2H-pyrrol-2-one;

4-(4-bromophenyl)-2(5H)-furanone;

3,4-dibromo-2(5H)-furanone; 4-(3-chlorophenyl)-2(5H)-furanone;

4-(2-chlorophenyl)-2(5H)-furanone;

4-(3,4-dichlorophenyl)-2(5H)-furanone;

4-(2-bromophenyl)-2(5H)-furanone;

4-(4-fluorophenyl)-1,5-dihydro-1-(4-methoxyphenyl)-2H-pyrrol-2-one;

4-(4-chlorophenyl)-1,5-dihydro-2H-pyrrol-2-one;

1,5-dihydro-4-[4-(trifluoromethyl)phenyl]-2H-pyrrol-2-one;

1,5-dihydro-1-(phenylmethyl)-4-[4-(trifluoromethyl)phenyl]-2H-pyrrol-2-one; and

4-(4-cyanophenyl)-2(5H)-furanone.

2. A compound of formula II

R6

R8

X R9 0)R

II

wherein:

X is -N(Rio)-;

wherein Rio is selected from H, methyl, ethyl and arylalkyl;

R 6 is phenyl, wherein the phenyl is substituted with one or more substituents selected from the

group consisting of OCF 3 , cyano (CN), F and Br;

R 7 and R9 are H; and

R8 is H.

3. A compound according to claim 1 selected from the group consisting of:

F CF 3 OCF 3 CF 3

- F - -- CF 3 - CF 3 0 0 0 0 0 0

F Br

o/ \

0 H N ;and H

4. A method of treating or preventing a Gram-negative bacterial infection in a subject by administering to said subject a compound according to any one of claims I to 3.

5. A method of preventing or inhibiting Gram-negative bacterial contamination of a surface, the method comprising administering to the surface a compound according to any one of claims I to 3.

6. A formulation comprising a compound according to any one of claims I to 3.