The present invention concerns novel aryloxazolidinone compounds, pharmaceutical compositions containing them and uses of these compounds in the manufacture of medicaments for the treatment of bacterial infections. These compounds are useful antimicrobial agents effective against a variety of human and veterinary pathogens including among others Gram-positive and Gram-negative aerobic and anaerobic bacteria and especially against resistant strains of Pseudomonas aeruginosa and Enterobacteriaceae such as Klebsiella pneumoniae. The intensive use of antibiotics has lead to a drastic increase in microorganisms with genetically based resistance mechanisms. Modern medicine and socio-economic behaviour exacerbate the problem of resistance development by creating slow growth situations for pathogenic microbes, e.g. in artificial joints, and by supporting long-term host reservoirs, e.g. in immune-compromised patients. In hospital settings, an increasing number of strains of Staphylococcus aureus, Streptococcus pneumoniae, Enterococcus spp., Enterobacteriaceae and Pseudomonas aeruginosa, major sources of infections, are becoming multidrug-resistant and therefore difficult if not impossible to treat:

- S. aureus is resistant to beta-lactams, quinolones and now even to vancomycin;

- S. pneumoniae is becoming resistant to penicillin or quinolone antibiotics and even to new macrolides;

- Enteroccocci are quinolone and vancomycin resistant and beta-lactam antibiotics are inefficacious against these strains;

- Enterobacteriacea are cephalosporin- and quinolone-resistant and carbapenems are losing their efficacy (e.g. carbapenem-resistant Klebsiella pneumoniae) ;

- P. aeruginosa is beta-lactam and quinolone resistant.

Furthermore, the incidence of multidrug-resistant Gram-negative strains such as Enterobacteriaceae and Pseudomonas aeruginosa, is steadily increasing and new emerging organisms like Acinetobacter spp. or Clostridium difficile, which have been selected during therapy with the currently used antibiotics, are becoming a real problem in hospital settings (S. L. Solomon et al., Antibiotic Resistance Threats In the United States: Stepping Back from the Brink, Academy of Family Physician, page 940 Volume 89, Number 12, June 15, 2014). Therefore, there is a high medical need for new antibacterial agents which overcome these multidrug resistances in bacteria, especially Pseudomonas aeruginosa and Enterobacteriaceae such as Klebsiella pneumoniae.

We have described ceratin aryloxazolidinone compounds and their antimicrobial properties in WO 2010/041 194 and WO 2014/108832. The present invention provides novel aryloxazolidinone S,S-stereoisomers which have advantageous pharmacological properties.

Various embodiments of the present invention are difined hereafter: 1 ) The first embodiment relates to compounds of formula I

wherein Y represents hydrogen or a group selected from Y ¹ and Y ²

Y ² or a salt thereof.

2) Another embodiment relates to the compound of embodiment 1 ), wherein Y is hydrogen.

3) Another embodiment relates to the compound of embodiment 1 ), wherein Y is Y ¹ . 4) Another embodiment relates to the compound of embodiment 1 ), wherein Y is Y ² .

The compounds according to embodiments 3) and 4) exhibit antibacterial activity in biologically relevant environment (i.e. in the presence of a phosphatase, an esterase, a sulfatase or any suitable equivalent thereof capable of removing the group Y ¹ or Y ² ). In said enviorment said compounds are typically converted to the compound of embodiment 1 ).

The compounds according to any one of embodiments 1 ) to 4) are particularly active against bacteria and bacteria-like organisms. They may therefore be particularly suitable in human and veterinary medicine for the prophylaxis and chemotherapy of local and systemic infections caused by these pathogens as well as disorders related to bacterial infections comprising pneumonia, otitis media, sinusitis, bronchitis, tonsillitis, and mastoiditis related to infection by Streptococcus pneumoniae, Moraxella catarrhalis, Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus haemolyticus, or Peptostreptococcus spp.; pharyngitis, rheumatic fever, and glomerulonephritis related to infection by Streptococcus pyogenes, Groups C and G streptococci, Corynebacterium diphtheriae, or Actinobacillus haemolyticum; respiratory tract infections related to infection by Legionella pneumophila, S. pneumonia or Chlamydia pneumoniae; blood and tissue infections, including endocarditis and osteomyelitis, caused by S. aureus, S. haemolyticus, including strains resistant to known antibacterials such as, but not limited to, beta-lactams, vancomycin, aminoglycosides, quinolones, chloramphenicol, tetracyclines and macrolides; uncomplicated skin and soft tissue infections and abscesses, and puerperal fever related to infection by S. aureus, coagulase-negative staphylococci (i.e., S. epidermidis, S. haemolyticus, etc.), S. pyogenes, Streptococcus agalactiae, Streptococcal groups C-F (minute colony streptococci), viridans streptococci, Corynebacterium minutissimum, Clostridium spp., or Bartonella henselae; uncomplicated acute urinary tract infections related to infection by S. aureus or coagulase-negative staphylococcal species; urethritis and cervicitis; sexually transmitted diseases related to infection by Chlamydia trachomatis, Haemophilus ducreyi, Treponema pallidum, Ureaplasma urealyticum, or Neiserria gonorrheae; toxin diseases related to infection by S. aureus (food poisoning and toxic shock syndrome), or Groups A, B and C streptococci; conjunctivitis, keratitis, and dacrocystitis related to infection by C. trachomatis, N. gonorrhoeae, S. aureus, S. pneumoniae, S. pyogenes or Listeria spp. The preceding lists of infections and pathogens are to be interpreted merely as examples and in no way as limiting. The compounds according to one of embodiments 1 ) to 4) may be used for the preparation of a medicament, and are suitable, for the prevention or treatment of a bacterial infection selected from the group consisting of respiratory tract infections, otitis media, meningitis, skin and soft tissue infections (whether complicated or uncomplicated), pneumonia (including hospital acquired pneumonia), bacteremia, endocarditis, intraabdominal infections, gastrointestinal infections, urinary tract infections, sexually transmitted infections, foreign body infections, osteomyelitis, Lyme disease, topical infections, or ophthalmological infections, and notably for the prevention or treatment of a bacterial infection selected from the group consisting of respiratory tract infections, otitis media, meningitis, skin and soft tissue infections (whether complicated or uncomplicated), pneumonia (including hospital acquired pneumonia) and bacteremia.

The compounds according to one of embodiments 1 ) to 4) may further be useful for the preparation of a medicament, and are suitable, for the treatment of infections that are mediated by Gram positive bacteria (such as Staphylococcus aureus, Bacillus cereus, Bacillus anthracis, Corynebacterium spp. and Propionibacterium acnes), notably by Gram positive bacteria selected from the group consisting of Bacillus cereus, Bacillus anthracis and Propionibacterium acnes. In particular, The compounds according to one of embodiments 1 ) to 4) can be used for the preparation of a medicament, and are suitable, for the treatment of a bacterial infection mediated by Staphylococcus aureus (especially quinolone-resistant Staphylococcus aureus bacteria).

The compounds according to one of embodiments 1 ) to 4) may further be useful for the preparation of a medicament, and are suitable, for the treatment of infections that are mediated by Gram negative bacteria (such as E. coli, Klebsiella pneumoniae and other Enterobacteriaceae, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, Neisseria meningitidis, Moraxella catarrhalis and Bacteroides spp), notably by Gram negative bacteria selected from the group consisting of Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, Moraxella catarrhalis and Neisseria meningitidis. In particular, the compounds of formula I according to any one of embodiments 1 ) to 4), and the pharmaceutically acceptable salts thereof, can be used for the preparation of a medicament, and are suitable, for the treatment of a bacterial infection mediated by Klebsiella pneumoniae bacteria (especially multidrug-resistant or quinolone-resistant Klebsiella pneumoniae bacteria) and Pseudomonas aeruginosa.

One aspect of this invention therefore relates to the use of the compounds according to one of embodiments 1 ) to 4) for the manufacture of a medicament for the prevention or treatment of a bacterial infection (in particular one of the previously mentioned infections mediated by Gram negative bacteria or one of the previously mentioned infections mediated by Gram positive bacteria).

Another aspect of this invention relates to the use of at least one of the compounds according to embodiments 1 ) to 4) as a medicament.

Yet a further aspect of this invention relates to a composition comprising at least one of the compounds according to embodiments 1 ) to 4) and further at least one therapeutically inert excipient.

A pharmaceutical composition according to the present invention contains at least one of the compounds according to embodiments 1 ) to 4) as active agent and optionally carriers and/or diluents and/or adjuvants, and may also contain additional known antibiotics.

The production of the pharmaceutical compositions can be effected in a manner which will be familiar to any person skilled in the art (see for example Remington, The Science and Practice of Pharmacy, 21st Edition (2005), Part 5, "Pharmaceutical Manufacturing" [published by Lippincott Williams & Wilkins]) by bringing the described compounds of formula I or their pharmaceutically acceptable salts, optionally in combination with other therapeutically valuable substances, into a galenical administration form together with suitable, non-toxic, inert, therapeutically compatible solid or liquid carrier materials and, if desired, usual pharmaceutical adjuvants. Species like pigs, ruminants, horses, dogs, cats and poultry can be treated with the compounds according to one of embodiments 1 ) to 4).

Any reference to a compound according to one of embodiments 1 ) to 4) in this text is to be understood as referring also to the salts (and especially the pharmaceutically acceptable salts) of such compounds. The compounds according to embodiments 1 ) to 4) can be used as medicaments, e.g. in the form of pharmaceutical compositions for enteral or, in particular for parenteral administration (especially intravenous application).

Another aspect of the invention concerns a method for the prevention or the treatment, preferably the treatment, of a bacterial infection in a patient, comprising the administration to said patient of a pharmaceutically active amount of a compound of formula I according to one of embodiments 1 ) to 4) or a pharmaceutically acceptable salt thereof. Accordingly, the invention provides a method for the prevention or the treatment of a bacterial infection mediated by Gram negative bacteria (in particular a bacterial infection mediated by Klebsiella pneumonia bacteria, and especially by multidrug-resistant or quinolone-resistant Klebsiella pneumonia bacteria and Pseudomonas aeruginosa bacteria) in a patient, comprising the administration to said patient of a pharmaceutically active amount of a compound of formula I according to one of embodiments 1 ) to 4) or a pharmaceutically acceptable salt thereof. The invention further provides a method for the prevention or the treatment, preferably the treatment, of a bacterial infection mediated by Gram positive bacteria (in particular a bacterial infection mediated by Staphylococcus aureus bacteria, especially by quinolone-resistant Staphylococcus aureus bacteria) in a patient, comprising the administration to said patient of a pharmaceutically active amount of a compound of formula I according to one of embodiments 1 ) to 4) or a pharmaceutically acceptable salt thereof.

The compounds of formula I according to this invention may also be used for cleaning purposes, e.g. to remove pathogenic microbes and bacteria from surgical instruments, catheters and artificial implants; to make a surface, room or an area aseptic. For such purposes, the compounds of formula I could be contained in a solution, suspension/emulssion, spray, gel and/or dry powder formulation.

The compounds according to embodiments 1 ) to 4) may also be used for veterinary applications, such as treating infections in livestock and companion animals. They may further constitute substances for preserving inorganic and organic materials in particular all types of organic materials for example polymers, lubricants, paints, fibres, leather, paper and wood.

The compounds according to any one of embodiments 1 ) to 4) are suitable for the use as active chemotherapeutic compounds in human and veterinary medicine and as substances for preserving inorganic and organic materials in particular all types of organic materials for example polymers, lubricants, paints, fibers, leather, paper and wood. The present invention also includes isotopically labelled, especially ² H (deuterium) labelled compounds of formula (I), which compounds are identical to the compounds of formula (I) except that one or more atoms have each been replaced by an atom having the same atomic number but an atomic mass different from the atomic mass usually found in nature. Isotopically labelled, especially ² H (deuterium) labelled compounds of formula (I) and salts thereof are within the scope of the present invention. Substitution of hydrogen with the heavier isotope ² H (deuterium) may lead to greater metabolic stability, resulting e.g. in increased in-vivo half-life or reduced dosage requirements, or may lead to reduced inhibition of cytochrome P450 enzymes, resulting e.g. in an improved safety profile. In one embodiment of the invention, the compounds of formula (I) are not isotopically labelled, or they are labelled only with one or more deuterium atoms. In a sub-embodiment, the compounds of formula (I) are not isotopically labelled at all. Isotopically labelled compounds of formula (I) may be prepared in analogy to the methods described hereinafter, but using the appropriate isotopic variation of suitable reagents or starting materials.

The term "pharmaceutically acceptable salts" refers to salts that retain the desired biological activity of the subject compound and exhibit minimal undesired toxicological effects. Such salts include inorganic or organic acid and/or base addition salts depending on the presence of basic and/or acidic groups in the subject compound. For reference see for example 'Handbook of Pharmaceutical Salts. Properties, Selection and Use.', P. Heinrich Stahl, Camille G. Wermuth (Eds.), Wiley-VCH, 2008, and 'Pharmaceutical Salts and Co-crystals', Johan Wouters and Luc Quere (Eds.), RSC Publishing, 2012.

The term "prevention" is to be understood as equivalent to the term "profilaxis".

Besides, the term "room temperature" as used herein refers to a temperature of 25°C. The compounds of formula I can be manufactured in accordance with the present invention using the procedures described hereafter.

PREPARATION OF COMPOUNDS OF FORMULA I

The following abbreviations are used throughout the specification and the examples:

Ac acetyl

aq. aqueous

Boc ferf-butoxycarbonyl

CHO Chinese hamster ovary

CC column chromatography

DAD diode array detection

DCM dichloromethane DME 1 ,2-dimethoxyethane

DMF N,N-dimethylformamide

DMAP 4-Dimethylaminopyridine

DMPK drug metabolism pharmacokinetics

DMSO-d6 deuterated dimethylsulfoxide

EA ethyl acetate

ELSD evaporative light scattering detector

ESI electron spray ionization

Et ethyl

ex. example

Hept heptane

HPLC high pressure liquid chromatography

HV high vacuum conditions

LC liquid chromatography

min minute(s)

sec seconds

Me methyl

MeCN acetonitrile

MeOH methanol

MS mass spectroscopy

NMR Nuclear Magnetic Resonance

org. organic

prep-HPLC preparative high pressure liquid chromatography rt room temperature

sat. saturated

TBME ferf-butyl methyl ether

TFA trifluoroacetic acid

THF tetrahydrofuran

TLC thin layer chromatography

tR retention time (liquid chromatography)

UV ultraviolet light All temperatures are stated in °C. Unless otherwise indicated, the reactions take place at rt.

ANALYTICAL METHODS USED Analytical TLC characterizations were performed with 0.2 mm plates: Merck, Silica gel 60 F254. Elution is performed with EA, Hept, DCM, MeOH or mixtures thereof. Detection was done with UV or with a solution of KMn0 ₄ (10 g), Na ₂ C0 ₃ (20 g) and H ₂ 0 (1 L) with subsequent heating.

Coloumn chromatography (CC) was performed using Brunschwig 60A silica gel (0.032- 0.63 mm) or using an ISCO CombiFlash system and prepacked S1O2 cartridges, elution being carried out with either Hept-EA or DCM-MeOH mixtures with an appropriate gradient.

¹ H-NMR (400 MHz, Bruker Avance 400 or 500 MHz, Bruker Avance 500 Cryoprobe) was used to characterized the compounds. Chemical shifts δ are given in ppm relative to the solvent used; multiplicities: s = singlet, d = doublet, t = triplet, q = quadruplet, p = pentuplet, hex = hexet, hep = heptet, m = multiplet, br. = broad; coupling constants J are given in Hz.

LC-MS was used to alternatively characterized the compounds (Thermo Finnigan MSQPIus with Agilent G4220A).The analytical LC-MS data was obtained using the following respective conditions:

• MS1 data:

o Column: Zorbax SB-Aq, 3.5 μιη, 4.6 x 50 mm;

o Injection volume: 1 μί;

o Column oven temperature: 40°C;

o Pump: Dionex HPG-3200RS;

o Makeup pump: Dionex ISO-3100SD;

o DAD: Dionex DAD-30000RS;

o MS: Thermo MSQ Plus;

o ELSD: Sedere Sedex 85;

o Detection: UV 210 nm, ELSD and MS;

o MS ionization mode: ESI+;

o Eluents: A: H ₂ 0 + 0.04% TFA; and B: MeCN; o Flow rate: 4.5 mL/min;

o Gradient: 5% B (0.00 min - 0.01 min), 5% B to 95% B (0.01 min - 1.00 min), 95% B (1.00 min - 1.45 min).

• MS2 data:

o Column: Zorbax RRHD SB-Aq, 3.0 x 50 mm, 1.8 μιτι;

o Injection volume: 0.30 μΙ_;

o Column oven temperature: 40°C;

o Pump: Agilent G4220A Binary Pump;

o Makeup pump: none;

o DAD: Agilent G4212A;

o MS: Thermo MSQ Plus;

o ELSD: Sedere Sedex 90;

o Detection: UV 210 nm, ELSD and MS;

o MS ionization mode: ESI+;

o Eluents: A: H ₂ 0 + 0.04% TFA; and B: MeCN;

o Eluent flow rate: 0.8 mL/min;

o Gradient: 5% B to 95% B (0.0 min - 1.20 min), 95% B (1.20 min - 1.90 min).

• MS3 data:

o Column: Waters BEH C18, 3.0 x 50 mm, 2.5 μιτι;

o Eluents: A: H ₂ 0/NH ₃ (c(NH ₃ ) = 13 mmol/L; and B: MeCN;

o Otherwise same parameters as for obtaining MS1 data.

The number of decimals given for the corresponding [M+H ⁺ ] peak(s) as well as the retention times (tR) of each tested compound depends upon the accuracy of the LC-MS device actually used.

BIOLOGICAL METHODS USED

Bacterial growth minimal inhibitory concentrations: Minimal inhibitory concentrations (MICs; mg/L) were determined in cation-adjusted Mueller-Hinton Broth by a microdilution method following the description given in "Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically" , Approved standard, 7 ^th ed., Clinical and Laboratory Standards Institute (CLSI) Document M7-A7, Wayne, PA, USA (2006).

Genetic toxicology testing of compounds to assess their ability to cause DNA damage was done in vitro in mammalian cell assays (CHO cells). The formation of micronuclei, small DNA-staining particles outside of the nucleus, was investigated in mononucleated and binucleated cells treated with increasing concentrations of a test compound for 24h. DNA was stained with Hoechst 33342 (Mutat Res. 630:1-13, 2007), read with a high- content screening microscope (Opera Phenix, Perkin Elmer) and scored with an optimized algorithm using Harmony. Micronucleii associated with valid cells were enumerated and induction of micronuclei formation tabulated as ratio versus untreated cells if the fraction of valid cells was≥0.2.

Cytochrome P450 inhibition: The objective of this in vitro assay was to assess potential inhibition of the human cytochrome P450 (CYP450) isoforms 3A4, 2C9 and 2D6 using human liver microsomes and isoform-specific marker reactions. These data (i.e. IC50; half maximal inhibition concentration) should allow for an estimation of the potential of a compound for drug-drug interactions with co-administered drugs being metabolized via the same cytochrome P450 isoforms. This may affect plasma levels in vivo and potentially lead to adverse drug reactions or toxicity. Technically, specific marker-substrate of P450 enzymes were incubated with human liver microsomes in the presence/absence of a test compounds. The inhibition effect of the test compound towards the marker reaction was determined in incubations containing 0-100 μΜ of the test compound. The inhibitory effect was determined by the impact of the different compound concentrations towards the metabolite formation of the marker reaction. Formation of the metabolites was determined by LC-MS analysis.

Metabolic stability: Subcellular liver fractions and primary hepatocytes from different species were used to determine the in vitro intrinsic clearance of a compound in various species. The liver microsomal and hepatocytes in vitro half-life approach can be a suitable approach to measure intrinsic clearance in vitro, which can be scaled up to the in vivo situation and used in the prediction of human clearance (Obach et al., 1997). For this approach, liver fractions were incubated for up to 45 minutes in subcellular liver fractions or 2 h in primary hepatocytes at final compound concentration of 1 μΜ. Disappearance of parent compound was determined by LC-MS analysis and intrinsic clearance calculated from the slope of compound disappearance thereof. SYNTHETIC PREPARATION

Example 1 : (S)-1-{3-[(S)-2-oxo-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-d][1, 4]oxazin-6-yl)- oxazolidin-5-yl]-propylamino}-1 ,2-dihydro-pyrrolo[3,2,1-/7|quinolin-4-one: A suspension of (SJ-l-amino-l ,2-dihydro-pyrrolo[3,2,1-/y]quinolin-4-one (3.00 g; prepared according to WO2010/041 194) and 3-[(SJ-2-oxo-3-(3-oxo-3,4-dihydro-2/-/-pyrido[3,2- 0][1 ,4]oxazin-6-yl)-oxazolidin-5-yl]-propionaldehyde (5.05 g; prepared according to WO2010/041 194) in DCM/MeOH (5-1 , 50 mL) was stirred at rt for 1 h. The mixture was cooled to 0°C, treated with NaBH(OAc) ₃ (5.05 g; commercial) and stirred at 0°C for 1 h. The reaction mixture was quenched by the addition of sat. NhUCI solution. The two phases were separated and the aq. layer was extracted with DCM/MeOH (9-1 ). The combined org. layers were dried over MgS04. The solvents were removed under reduced pressure and the residue was purified by CC (DCM/MeOH 19:1 to 9:1 ) affording the title compound (4.68 g; 63% yield). MS1 (ESI, m/z): 462.02 [M+H ⁺ ]; t _R = 0.54 min. ¹ H NMR (500 MHz, DMSO-d6) δ: 11.21 (s, 1 H), 7.92 (d, J = 9.4 Hz, 1 H), 7.55-7.60 (m, 3H), 7.43 (m, 1 H), 7.21 (m, 1 H), 6.57 (d, J = 9.4 Hz, 1 H), 4.71 (m, 2H), 4.61 (s, 2H), 4.39 (dd, J = 12.8, 8.4 Hz, 1 H), 4.21 (m, 1 H), 4.03 (dd, J = 12.8, 4.0 Hz, 1 H), 3.71 (dd, J = 10.0, 7.1 Hz, 1 H), 2.60-2.71 (m, 2H), 1.76-1.81 (m, 2H), 1.50-1.59 (m, 2H).

Example 2: ((S)-4-oxo-1,2-dihydro-4H-pyrrolo[3,2,1-y]quinolin-1-yl)-{3- [(S)-2-oxo-3- (3-oxo-3,4-dihydro-2H-pyrido[3,2-/9][1,4]oxazin-6-yl)-oxazol idin-5-yl]-propyl}- carbamic acid phosphonooxymethyl ester:

21 ((S)-4-oxo-1,2-dihydro-4H^yrrolo[3,2, 1-ij]quinolin^

dihydro-2H-py do[3, 2-b][ 1,4]oxazin-6-yl)-oxazolidin-5-yl]-propyl}-carbamic acid chloromethyl ester: To a suspension of the compound of example 1 (9 g) in DCM (80 mL) were added Λ/,Λ/,Λ/',Λ/'-tetramethyl-l ,8-naphthalenediamine (8.44 g; commercial) and chloromethyl chloroformate (1.91 mL, prepared according to US2004/015291 1 ) and the mixture was stirred at rt for 90 min. 10% citric acid was added, the phases were separated and the aq. layer was extracted with DCM. The combined org. layers were washed with water and brine and dried over MgS04. The solvents were removed under reduced pressure and the residue was purified by CC (DCM/MeOH 19:1 ) affording the title compound as a colorless solid (10.09 g; 93% yield). MS1 (ESI, m/z): 553.95 [M+H ⁺ ]; t _R = 0.79 min. 2.H. 6-((S)-5-{3-[chloromethoxycarbonyl-((S)-4-oxo-1, 2-dihydro-4H-pyrrolo[3, 2, 1-ij]quinolin- 1-yl)-amino]-propyl}-2-oxo-oxazolidin-3-yl)-3-oxo-2, 3-dihydro-pyrido[3, 2-b][ 1,4]oxazine-4- carboxylic acid tert-butyl ester:

A solution of intermediate 2.i (4.55 g) in DCM (32 mL) was treated with B0C2O (1.88 g) and DMAP (50 mg) and the mixture was stirred at rt for 90 min. The solution was diluted with DCM and water was added, the phases were separated and the aq. layer was extracted with DCM. The combined org. layers were washed with water and brine and dried over MgSCU. The solvents were removed under reduced pressure and the residue was purified by CC (DCM/MeOH 1 :0 to 9:1 ) affording the title compound as a colorless solid (4.1 g; 76% yield). MS2 (ESI, m/z): 653.91 [M+H ⁺ ]; t _R = 1.04 min.

2. Hi. 6-((S)-5-{3-[(di-tert-butoxy-phosphoryloxymethoxycarbonyl)-( (S)-4-oxo-1,2-dihydro- 4H-pyrrolo[3, 2, 1 -ijjquinolin- 1 -yl) -amino ]-propyl}-2-oxo-oxazolidin-3-yl) -3-oxo-2, 3-dihydro- pyrido[3,2-b][1,4]oxazine-4-carboxylic acid tert-butyl ester:

A solution of intermediate 2.ii (5.0 g) in DME (76 mL) and tetrabutylammonium di-ierf- butylphosphate (4.1 g; commercial) was heated at 55°C for 2 h. After cooling to rt EA and water were added and the phases were separated. The aq. layer was extracted with EA and the combined org. layers were washed with water, sat. NaHCC>3 and brine and dried over MgSC . The solvents were removed under reduced pressure and the residue was purified by CC (EA/MeOH 1 :0 to 9: 1 ) affording the title compound as a colorless solid (4.7 g; 74% yield). MS2 (ESI, m/z): 828.42 [M+H ⁺ ]; t _R = 1.09 min.

2./V. ((S)-4-oxo- 1, 2-dihydro-4H-pyrrolo[3, 2, 1-ij]quinolin-1-yl)-{3-[(S)-2-oxo-3-(3-oxo-3, 4- dihydro-2H-pyrido[3, 2-b][ 1,4]oxazin-6-yl)-oxazolidin-5-yl]-propyl}-carbamic acid phosphonooxymethyl ester:

A solution of intermediate 2.iii (414 mg) in DCM (5 mL) was cooled to 0°C and treated with TFA (0.77 mL). The mixture was stirred at 0°C for 2 h. TBME (5 mL) was added and the resulting suspension was stirred at 0°C for 15 min, filtered and dried at HV. The obtained solid was dissolved in MeCN/water (1 :1 , 12 mL) and lyophilized to afford the title compound as colourless lyophilisate (276 mg; 90% yield).

¹ H NMR (DMSO-d6) δ: 1 1.22 (s, 1 H), 7.93 (d, J = 9.4 Hz, 1 H), 7.66-7.40 (m, 4H), 7.20 (m, 1 H), 6.60 (d, J = 9.4 Hz, 1 H), 6.15-5.37 (m, 2H), 4.67-4.45 (m, 4H), 4.25-4.05 (m, 2H), 3.74-2.92 (m, 4H), 1.75-1.41 (m, 4H). MS3 (ESI, m/z): 615.92 [M+H ⁺ ]; t _R = 0.42 min. Example 3: 3-(2-phosphonooxy-phenyl)-propionic acid (((S)-4-oxo-1,2-dihydro-4H- pyrrolo[3,2,1-y]quinolin-1-yl)-{3-[(S)-2-oxo-3-(3-oxo-3,4-di hydro-2H-pyrido[3,2- £)][1,4]oxazin-6-yl)-oxazolidin-5-yl]-propyl}-carbamoyloxy) -methyl ester:

31 3-[2-(di-tert-butoxy-phosphoryloxy)-phenyl]-propionic acid methyl ester: To a solution of methyl 3-(2-hydroxyphenyl)propionate (7.5 g; commercial) in THF (250 mL) at 0°C were added tetrazole (0.45 M in MeCN, 138 mL; commercial) and di-ferf-butyl N,/V-diisopropylphosphoramidite (17.3 mL, commercial) and the solution was stirred at rt for 2 h. Additional di-ferf-butyl NJv-diisopropylphosphoramidite (6.63 mL, commercial) and tetrazole (0.45 M in MeCN, 18.5 mL; commercial) were added and the resulting mixture was stirred at rt for 3.5 h. The mixture was cooled to 0°C and 30% aq. H2O2 (41 mL) was added drop wise. The mixture was stirred at 0°C for 0.75 h. Water was added to the mixture and the aq. layer was extracted with EA. The combined org. layers were washed with water and brine and dried over MgSCv The solvents were removed under reduced pressure and the residue was purified by CC (Hept/EA 99:1 to 0:1 ) affording the title compound as a yellow liquid (9.05 g; 58% yield). MS1 (ESI, m/z): 372.96 [M+H ⁺ ]; to = 0.91 min. ¹ H NMR (500 MHz, CDCI3) δ: 1.53 (s, 18H), 2.67 (m, 2H), 3.03 (m, 2H), 3.69 (s, 3H), 7.08 (t, J = 7.5 Hz, 1 H), 7.20 (m, 2H), 7.42 (d, J = 8.2 Hz, 1 H).

3.H. 3-[2-(di-tert-butoxy-phosphoryloxy)-phenyl]-propionic acid:

To a solution of intermediate 3.i (9 g) in a mixture of THF (100 mL), MeOH (100 mL) and water (50 mL) was added lithium hydroxide monohydrate (4.1 g; commercial) and the mixture was stirred at rt for 1.5 h. The majority of the solvent was evaporated and the residual aq. layer was extracted with TBME. The aq. layer was acidified with 10% citric acid to reach pH 3 and was then extracted with EA. The combined org. layers were washed with water and brine and dried over MgSCU. The solvents were removed under reduced pressure affording the title compound as an unstable yellow solid (7.95 g; 92% yield) which was directly used in the next step. MS1 (ESI, m/z): 359.22 [M+H ⁺ ]; t _R = 0.81 min. ¹ H NMR (500 MHz, CDCI3) δ: 1.53 (s, 18H), 2.71 (m, 2H), 3.05 (m, 2H), 7.1 1 (t, J = 7.4 Hz, 1 H), 7.22 (m, 2H), 7.35 (d, J = 8.2 Hz, 1 H). 3. Hi. 3-[2-(di-tert-butoxy-phosphoryloxy)-phenyl]-propionic acid (((S)-4-oxo-1 ,2-dihydro-

4H^yrrolo[3,2, 1-ij]quinolin-1-yl)-{3-[(S)-2-oxo-3-(3-oxo-3 -dihyd

b][ 1, 4]oxazin-6-yl)-oxazolidin-5-yl]-propyl}-carbamoyloxy)-methyl ester:

To a solution of intermediate 2.i (2.49 g) in DMF (27 mL) were added intermediate 3. i i (1.77 g) and K2CO3 (1.37 g) and the resulting suspension was stirred at 40°C for 2 h. After cooling to rt, EA and sat. NaHCC>3 were added and the phases were separated. The aq. layer was extracted with EA and the combined organic layers were washed with water and brine and dried over MgSCv The solvents were removed under reduced pressure and the residue was purified by CC (DCM/MeOH 1 :0 to 19:1 ) affording the title compound as a colorless solid (2.17 g; 55% yield). MS1 (ESI, m/z): 876.54 [M+H ⁺ ]; t _R = 0.94 min.

3.iv. 3-(2-Phosphonooxy-phenyl)-propionic acid (((S)-4-oxo-1,2-dihydro-4H-pyrrolo[3,2, 1- ij]quinolin-1-yl)-{3-[(S)-2-oxo-3-(3-o^

oxazolidin-5-yl]-propyl}-carbamoyloxy)-methyl ester:

To a solution of intermediate 3.iii (2.16 g) in DCM (25 mL) was added TFA (2.83 mL) at 0°C and the solution was stirred at 0°C for 3 h. TBME (25 mL) was added at 0°C and the resulting suspension was stirred at that temperature for 10 min and was then filtered. The resulting colorless solid was then suspended in water (100 mL). Under vigorous stirring sat. NaHCC>3 was slowly added until the solid was dissolved (pH 8). The aq. solution was extracted with EA to remove organic side products. The aq. layers were cooled to 0°C and then acidified with HCI 1 M to reach pH 1. The resulting suspension was filtered and the solid was dried at HV. The obtained solid was dissolved in MeCN/water (1 :1 , 60 mL) and lyophilized to afford the title compound as colourless lyophilisate (1.58 g; 84% yield). MS1 (ESI, m/z): 764.18 [M+H ⁺ ]; t _R = 0.67 min. ¹ H NMR (DMSO-d6) δ: 7.90 (d, J = 9.4 Hz, 1 H), 7.59 (d, J = 8.7 Hz, 2H), 7.38 (m, 3H), 7.16-7.22 (m, 3H), 7.04 (t, J = 7.4 Hz, 1 H), 6.95-6.20 (m, 3H), 5.79-5.50 (m, 3H), 4.55-4.63 (m, 4H), 4.21 (m, 2H), 3.68 (m, 1 H), 3.45- 3.20 (m, 2H), 2.89 (m, 2H), 2.60 (m, 2H), 1.67 (s, 2H), 1.40-1.30 (m, 2H).

PHARMACOLOGICAL PROPERTIES

The compound of Example 1 according to the present invention (inv.) and reference compounds 4 (ref.) to 9 (ref.) were tested against several Gram-positive and Gram-negative bacteria. Staphylococcus aureus A798 is a multiply resistant strain (in particular quinolone-resistant), Klebsiella pneumoniae A-651 is a multiply resistant strain (in particular quinolone-resistant), while E. coli ATCC25922 and P. aeruginosa ATCC27853 are quinolone-sensitive strains. The corresponding antibacterial test results are given in Table 1 hereafter (MICs in mg/L).

Table 1

The compounds of Examples 2 and 3 of the present invention (inv.) were tested against wild-type E. coli A-1261 in the presence of alkaline phosphatase (from bovine intestinal mucosa: Sigma P6774-2KU; Lot: SLBB1 168) or esterase (from porcine liver: Sigma E2884-5KU; Lot: 129K7010V), and in the absence of an alkaline phosphatase and esterase. The corresponding antibacterial test results are given in Table 2 hereafter (MICs in mg/L). MIC for E. coli A-1261

Active

Example metabolite In the absence of In the presence of In the

No. Example alkaline phosphatase an alkaline presence of

No. and esterase phosphatase an esterase

(2 i.U./mL) (10 i.U./mL)

2 (inv.) 1 (inv.) > 8 0.25 > 8

3 (inv.) 1 (inv.) > 8 0.25 1

Table 2

Genetic toxicity potential of the compound of Example 1 according to the present invention (inv.) and reference compounds (ref.) was assessed and the corresponding test results are given in Table 3 hereafter.

Table 3

Metabolic stability of the compounds according to the present invention (inv.) and reference compounds (ref.) in human liver microsomes and inhibition of the human cytochrome P450 (CYP450) isoforms 3A4, 2C9 and 2D6 are given in Table 4 hereafter. Intrinsic clearance

CYP450 lowest IC50

in human liver

Reference Example, of the isoenzymes

Example No. microsomes

as Published measured

^L/min*mg (μΜ)

microsomal protein)

1 (inv.) > 50 15

ex. 189,

4 (ref.) > 50 21

WO2010/041 194

ex. 74,

5 (ref.) 23 35

WO2010/041 194

ex. 135,

6 (ref.) 29 28

WO2010/041 194

ex. 86,

7 (ref.) 28 38

WO2010/041 194

ex. 136,

8 (ref.) 22 1 15

WO2010/041 194

Table 4

Surprisingly, the compound of Example 1 according to the present invention not only shows excellent antimicrobial activity against several bacterial strains (Table 1 ), it also exhibits superior pharmacological properties (Tables 3 and 4). The compounds according to Examples 2 and 3 exhibit antimicrobial activity in biologically relevant environment via formation of the compound of Example 1 (Table 2).