Introduction

The present invention relates to 2-oxo-1-pyrrolidinyl imidazothiadiazole derivatives, processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals.

WO201 1/047860 discloses 2-oxo-1-pyrrolidinyl imidazothiadiazole derivatives compounds of the following formula A:

wherein:

R ¹ is a C-| _4 alkyl containing at least one halogen substituent;

R2 is either a halogen or a C-1.4 alkyl containing at least one halogen substituent; and

R3 is a C-| _4 alkyl containing at least one hydroxy or alkoxy substituent. A persistent problem in seizure control arises with those patients who do not at all or only insufficiently respond to currently available treatments. Those patients are viewed as being refractory to treatment and represent a considerable challenge for the medical community. It is estimated that about 30% of epilepsy patients are to be classified as being refractory. Hence, there is a need to develop new medications that specifically target this population of patients. The compounds of that invention are for use as a medicament, in the treatment of epilepsy, epileptogenesis, seizure disorders, convulsions, in particular for refractory seizures.

Summary of the invention This invention provides new 2-oxo-1 -pyrrolidinyl imidazothiadiazole derivatives having the formula (I), their geometrical isomers, enantiomers, diastereoisomers, isotopes and mixtures, or a pharmaceutically acceptable salt thereof,

Further aspects of the invention will become apparent from the detailed description. Detailed description of the invention

The present invention relates to 2-oxo-1 -pyrrolidinyl imidazothiadiazole derivatives according to formula (I),

wherein

R ¹ is a C-| _4 alkyl optionally substituted by one or more halogen substituents; R2 is a C-| _4 alkyl containing at least one hydroxy or alkoxy substituent; R3 is a methyl (including -CD ₃ )

The term“C1.4 alkyl” as used herein refers to alkyl groups having 1 to 4 carbon atoms. This term is exemplified by groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, ferf-butyl.“C1.4 alkyl” groups may be substituted by one or more substituents selected from halogen, hydroxy or alkoxy.

The term“Hydroxy” as used herein represents a group of formula -OH.

The term“Alkoxy” as used herein refers to a group -O-R where R includes“C- _| _4 alkyl” as defined here above.

The term“Halogen” as used herein refers to fluoro, chloro, bromo and iodo atoms, preferably fluoro and chloro.

The present invention includes within its scope tautomers, geometrical isomers, enantiomers, diastereomers, isotopes, and mixtures, and a pharmaceutically acceptable salt of compounds of formula (I). For example, any moiety indicated as“H” in formula (I) may be a hydrogen, or its isotopes, deuterium or tritium. Generally, R^ is a C1.4 alkyl optionally substituted by one or more halogen substituents.

In one embodiment, R^ is an unsubstituted C1.4 alkyl. In a first aspect of this embodiment, R1 is n-propyl. In a second aspect of this embodiment, R1 is i-butyl.

In another embodiment, R^ is a C1.4 alkyl substituted by one or more halogen. In a first aspect of this embodiment, R^ is 2,2-difluoropropyl. In a second aspect of this embodiment, R^ is 2-chloro-2,2-difluoroethyl. In a third aspect of this embodiment, R^ is 2,2-difluoroethyl. In a fourth aspect of this embodiment, R^ is 2,2,2-trifluoroethyl. In a fifth aspect of this embodiment, R^ is 2-fluoroethyl.

In a specific embodiment, R^ is i-butyl, a n-propyl, 2,2-difluoropropyl, 2-chloro-2,2- difluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, or 2-fluoroethyl. In another specific embodiment, R^ is i-butyl, n-propyl, 2-chloro-2,2-difluoroethyl, 2,2- difluoropropyl or 2,2,2-trifluoroethyl.

In a preferred embodiment, R^ is n-propyl, 2-chloro-2,2-difluoroethyl, 2,2-difluoropropyl or 2,2,2-trifluoroethyl..

Generally, R^ is a C1.4 alkyl containing at least one hydroxy or alkoxy substituent. In one embodiment, is a C-1.4 alkyl containing at least one hydroxy substituent. In one aspect of this embodiment, is a hydroxymethyl.

In another embodiment, R^ is a C-1.4 alkyl containing at least one methoxy substituent. In a first aspect of this embodiment, R^ is methoxymethyl. In a second aspect of this embodiment, R^ is CD3O-CH2-. In a third aspect of this embodiment, R^ is CH3O-CD2-. In a fourth aspect of this embodiment, R^ is CD3O-CD2-.

In a further specific embodiment, R^ is a hydroxymethyl, a methoxymethyl, CD ₃ O-CH2-, CH3O-CD2- or CD3O-CD2-.

In a preferred embodiment, R^ is methoxymethyl, CD3O-CH2-, CH3O-CD2- or CD3O- CD2-.

In a particular embodiment, R^ is methoxymethyl.

R ³ generally represents methyl. In one aspect, R ³ represents -CH3. In another aspect, R ³ represents -CD ₃ .

In a further specific embodiment, compounds of formula (I) are those wherein:

• R ¹ is a n-propyl, 2-chloro-2,2-difluoroethyl, a 2,2-difluoropropyl or a 2,2,2- trifluoroethyl moiety;

• R2 is a hydroxymethyl, methoxymethyl, CD ₃ O-CH ₂ -, CH ₃ O-CD ₂ - or CD ₃ O-CD ₂ -; and

• R3 is -CH3 or -CD ₃ .

In a further preferred specific embodiment, compounds of formula (I) are those wherein: • R ¹ isn-propyl, 2-chloro-2,2-difluoroethyl, 2,2-difluoropropyl or 2,2, 2-trifluoroethyl ;

• R2 ismethoxymethyl, CD ₃ O-CH ₂ -, CH ₃ O-CD ₂ - or CD ₃ O-CD ₂ -; and

• R3 is CH3 or CD ₃ .

Specific compounds of the present invention are those selected from the group consisting of: · (4R)-4-(2-chloro-2,2-difluoro-ethyl)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 - b][1 ,3,4]thiadiazol-5-yl]methyl]pyrrolidin-2-one;

• (4S)-4-(2-chloro-2,2-difluoro-ethyl)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 - b][1 ,3,4]thiadiazol-5-yl]methyl]pyrrolidin-2-one; (4S)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]- 4-propyl-pyrrolidin-2-one;

• (4R)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 -b][1 ,3,4]thiadiazol-5-yl]methyl]- 4-propyl-pyrrolidin-2-one; · (4R)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]-

4-(2,2,2-trifluoroethyl)pyrrolidin-2-one;

• (4S)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]- 4-(2,2,2-trifluoroethyl)pyrrolidin-2-one;

• (4R)-4-(2-chloro-2,2-difluoro-ethyl)-1-[[2-(methoxymethyl)-6 -(trideuteriomethyl) imidazo[2, 1 -b][1 ,3,4]thiadiazol-5-yl]methyl]pyrrolidin-2-one;

• (4R)-(2,2-difluoropropyl)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 -b][1 ,3,4]- thiadiazol-5-yl]methyl]pyrrolidin-2-one ; and

• (4S)-(2,2-difluoropropyl)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 -b][1 ,3,4]- thiadiazol-5-yl]methyl]pyrrolidin-2-one The compounds of the present invention are beneficial for the treatment of epilepsy, epileptogenesis, seizure disorders, convulsions, in particular, for the treatment of refractory seizures.

The following paragraphs provide definitions of the various chemical moieties that make up the compounds according to the invention and are intended to apply uniformly throughout the specification and claims unless an otherwise expressly set out definition provides a broader definition.

The“pharmaceutically acceptable salts” according to the invention include therapeutic- cally active, non-toxic acid or base salt forms which the compounds of formula (I) are able to form. The acid addition salt form of a compound of formula (I) that occurs in its free form as a base can be obtained by treating the free base with an appropriate acid such as an inorganic acid, for example, a hydrohalic such as hydrochloric or hydrobromic, sulfuric, nitric, phosphoric and the like; or an organic acid, such as, for example, acetic, trifluoroacetic, hydroxyacetic, propanoic, lactic, pyruvic, malonic, succinic, maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p- toluenesulfonic, cyclamic, salicylic, p-aminosalicylic, pamoic and the like. The compounds of formula (I) containing acidic protons may be converted into their therapeutically active, non-toxic base addition salt forms, e.g. metal or amine salts, by treatment with appropriate organic and inorganic bases. Appropriate base salt forms include, for example, ammonium salts, alkali and earth alkaline metal salts, e.g. lithium, sodium, potassium, magnesium, calcium salts and the like, salts with organic bases, e.g. N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids such as, for example, arginine, lysine and the like.

Conversely said salt forms can be converted into the free forms by treatment with an appropriate base or acid. Compounds of the formula (I) and their salts can be in the form of a solvate, which is included within the scope of the present invention. Such solvates include for example hydrates, alcoholates and the like.

Compounds of formula (I) and/or their intermediates may have at least one stereogenic center in their structure. This stereogenic center may be present in a R or a S configuration, said R and S notation is used in correspondence with the rules described in Pure Appl. Chem., 45 (1976) 1 1-30. The invention thus also relates to all stereoisomeric forms such as enantiomeric and diastereo iso meric forms of the compounds of formula (I) or mixtures thereof (including all possible mixtures of stereoisomers). With respect to the present invention reference to a compound or compounds is intended to encompass that compound in each of its possible isomeric forms and mixtures thereof, unless the particular isomeric form is referred to specifically. The expression “enantiomerically pure” as used herein refers to compounds which have enantiomeric excess (ee) greater than 95%.

Compounds according to the present invention may exist in different polymorphic forms. Although not explicitly indicated in the above formula, such forms are intended to be included within the scope of the present invention.

The compounds of formula (I) according to the invention can be prepared analogously to conventional methods as understood by the person skilled in the art of synthetic organic chemistry. According to one embodiment, compounds having the general formula (I) may be prepared by reaction of a compound of formula (II) with an pyrrolidone of formula (III) according to the following scheme,

wherein R1 and R^ have the same definitions as defined above for compounds of formula (I).

This reaction may be performed using an acid such as p-toluenesulfonic acid in an aprotic solvent such as sulfolane at high temperature.

Compounds of formula (II) may be prepared by hydroxymethylation of a compound of formula (IV) according to the the following scheme,

wherein R^ and R^ have the same definition as defined above for compounds of formula (I).

This reaction may be performed using a formylating agent such as paraformaldehyde under acidic conditions in a polar solvent such as dioxane at 100°C, or according to any other method known to the person skilled in the art.

Compounds of formula (IV) may be synthesized by reaction of a compound of formula (V) with a bromo derivative of formula (VI) according to the following scheme,

wherein R^ and R^ have the same definition as described above for compounds of formula (I).

This reaction can be performed using procedures described in the literature or known to the person skilled in the art. According to another embodiment, compounds of formula (I) may be synthesized by a Friedel-Crafts-type reaction of a compound of formula (IV) with a pyrrolidone of formula (VII) according to the following scheme,

wherein R^ and R3 have the same definitions as defined above for compounds of formula (I).

This reaction can be performed with pyrrolidones of formula (VII) bearing a leaving group (Y) such as a chlorine atom or a p-toluenesulfonyl group, in the presence of a Lewis acid such as zinc chloride or ferric chloride in a polar solvent such as sulfolane or dioxane at temperatures ranging from 100-120°C, or according to any procedure described in the literature or known to the person skilled in the art.

Compounds of formula (VII) may be prepared from the corresponding pyrrolidones of formula (VIII) according to the methods described in PCT patent application W02006/ 128693 or according to any other method known to the person skilled in the art.

The synthesis of compounds of formula (VIII) can be performed using procedures described in the literature or known to the person skilled in the art. Compounds of formula (V) and of formula (VI) are either commercially available or may be synthesized according to any method known to the person skilled in the art.

The compounds of the present invention are beneficial for the treatment of epilepsy, epileptogenesis, seizure disorders, convulsions, in particular, of refractory seizures. Hence, in another embodiment, the present invention provides a compound of formula (I) as defined above, or a pharmaceutically acceptable salt thereof, for use as a medicament.

In one aspect of that embodiment, the present invention also provides a compound of formula (I) as defined above, or a pharmaceutically acceptable salt thereof, for use in the treatment and/or prevention of epilepsy, epileptogenesis, seizure disorders, convulsions, in particular, of refractory seizures.

In a further embodiment, the present invention provides the use of a compound of formula (I) as defined above, or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for the treatment and/or prevention of epilepsy, epileptogenesis, seizure disorders, convulsions, in particular, for the treatment of refractory seizures.

Seizures can be classified as refractory when a patient fails to achieve seizure freedom for 12 months or more of state of the art treatment with two or more anti-epileptic drugs at maximal tolerated doses. The International League Against Epilepsy (ILAE) has defined drug resistant epilepsy as “failure of adequate trials of two tolerated and appropriately chosen and used AED schedules (whether as monotherapies or in combination) to achieve sustained seizure freedom”.

The methods of the invention comprise administration to a mammal (preferably a human) suffering from above mentioned conditions or disorders, of a compound according to the invention in an amount sufficient to alleviate or prevent the disorder or condition.

The present invention therefore also includes within its scope a method for the treatment and/or prevention of of epilepsy, epileptogenesis, seizure disorders, convulsions, in particular of refractory seizures, which comprises administering to a patient in need of such treatment an effective amount of a compound of formula (I) as defined above, or a pharmaceutically acceptable salt thereof.

The compound is conveniently administered in any suitable unit dosage form, including but not limited to one containing 1 to 2000 mg, preferably 1 to 1000 mg, more preferably 1 to 500 mg of active ingredient per unit dosage form.

The term “treatment” as used herein includes curative treatment and prophylactic treatment. By“curative” is meant efficacy in treating a current symptomatic episode of a disorder or condition.

By“prophylactic” is meant prevention of the occurrence or recurrence of a disorder or condition. The term “epilepsy” as used herein refers to a chronic neurologic condition characterised by unprovoked, recurrent epileptic seizures. An epileptic seizure is the manisfestation of an abnormal and excessive synchronised discharge of a set of cerebral neurons; its clinical manifestations are sudden and transient. The term “epilepsy” as used herein can also refer to a disorder of brain function characterised by the periodic occurrence of seizures. Seizures can be“nonepileptic” when evoked in a normal brain by conditions such as high fever or exposure to toxins or“epileptic” when evoked without evident provocation.

The term“seizure” as used herein refers to a transient alteration of behaviour due to the disordered, synchronous, and rhythmic firing of populations of brain neurones. A further aspect of the present invention relates to a pharmaceutical composition comprising an effective amount of a compound of formula (I) in combination with a pharmaceutically acceptable diluent or carrier.

Activity in any of the above-mentioned indications can of course be determined by carrying out suitable clinical trials in a manner known to a person skilled in the relevant art for the particular indication and/or in the design of clinical trials in general.

For treating diseases, compounds of formula (I) or their pharmaceutically acceptable salts may be employed at an effective daily dosage and administered in the form of a pharmaceutical composition.

Therefore, another embodiment of the present invention concerns a pharmaceutical composition comprising an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof in combination with a pharmaceutically acceptable diluent or carrier.

To prepare a pharmaceutical composition according to the invention, one or more of the compounds of formula (I) or a pharmaceutically acceptable salt thereof is intimately admixed with a pharmaceutical diluent or carrier according to conventional pharmaceutical compounding techniques known to the skilled practitioner. Suitable diluents and carriers may take a wide variety of forms depending on the desired route of administration, e.g., oral, rectal, parenteral or intranasal.

Pharmaceutical compositions comprising compounds according to the invention can, for example, be administered orally, parenterally, i.e., intravenously, intramuscularly or subcutaneously, intrathecally, transdermally (patch), by inhalation or intranasally.

Pharmaceutical compositions suitable for oral administration can be solids or liquids and can, for example, be in the form of tablets, pills, dragees, gelatin capsules, solutions, syrups, chewing-gums and the like.

To this end the active ingredient may be mixed with an inert diluent or a non-toxic pharmaceutically acceptable carrier such as starch or lactose. Optionally, these pharmaceutical compositions can also contain a binder such as microcrystalline cellulose, gum tragacanth or gelatine, a disintegrant such as alginic acid, a lubricant such as magnesium stearate, a glidant such as colloidal silicon dioxide, a sweetener such as sucrose or saccharin, or colouring agents or a flavouring agent such as peppermint or methyl salicylate.

The invention also contemplates compositions which can release the active substance in a controlled manner.

Pharmaceutical compositions which can be used for parenteral administration are in conventional form such as aqueous or oily solutions or suspensions generally contained in ampoules, disposable syringes, glass or plastics vials or infusion containers.

In addition to the active ingredient, these solutions or suspensions can optionally also contain a sterile diluent such as water for injection, a physiological saline solution, oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents, antibacterial agents such as benzyl alcohol, antioxidants such as ascorbic acid or sodium bisulphite, chelating agents such as ethylene diamine-tetra-acetic acid, buffers such as acetates, citrates or phosphates and agents for adjusting the osmolarity, such as sodium chloride or dextrose.

These pharmaceutical forms are prepared using methods which are routinely used by pharmacists.

The amount of active ingredient in the pharmaceutical compositions can fall within a wide range of concentrations and depends on a variety of factors such as the patient’s sex, age, weight and medical condition, as well as on the method of administration. Thus the quantity of compound of formula (I) in compositions for oral administration is at least 0.5% by weight and can be up to 80% by weight with respect to the total weight of the composition. In accordance with the invention it has also been found that the compounds of formula (I) or the pharmaceutically acceptable salts thereof can be administered alone or in combination with other pharmaceutically active ingredients. Non-limiting examples of such additional compounds which can be cited for use in combination with the compounds according to the invention are antivirals, antispastics (e.g. baclofen), antiemetics, antimanic mood stabilizing agents, analgesics (e.g. aspirin, ibuprofen, paracetamol), narcotic analgesics, topical anesthetics, opioid analgesics, lithium salts, antidepressants (e.g. mianserin, fluoxetine, trazodone), tricyclic antidepressants (e.g. imipramine, desipramine), anticonvulsants (e.g. valproic acid, carbamazepine, phenytoin), antipsychotics (e.g. risperidone, haloperidol), neuroleptics, benzodiazepines (e.g. diazepam, clonazepam), phenothiazines (e.g. chlorpromazine), calcium channel blockers, amphetamine, clonidine, lidocaine, mexiletine, capsaicin, caffeine, quetiapine, serotonin antagonists, b-blockers, antiarrhythmics, triptans, ergot derivatives and amantadine.

For oral compositions, the daily dosage is in the range 1 mg to 2000 mg of compounds of formula (I). Preferably in the range 1 mg to 1000 mg of compounds of formula (I), most preferably 1 mg to 500 mg.

In compositions for parenteral administration, the quantity of compound of formula (I) present is at least 0.5% by weight and can be up to 33% by weight with respect to the total weight of the composition. For the preferred parenteral compositions, the dosage unit is in the range 1 mg to 2000 mg of compounds of formula (I).

The daily dose can fall within a wide range of dosage units of compound of formula (I) and is generally in the range 1 to 2000 mg, preferably 1 to 1000 mg. However, it should be understood that the specific doses can be adapted to particular cases depending on the individual requirements, at the physician’s discretion. The SV2 proteins binding compounds provided by this invention and labeled derivatives thereof may be useful as standards and reagents in determining the ability of tested compounds (e.g., a potential pharmaceutical) to bind to the SV2 proteins. Labeled derivatives of SV2 proteins’ ligands provided by this invention may also be useful as radiotracers for positron emission tomography (PET) imaging or for single photon emission computerized tomography (SPECT).

The present invention therefore further provides labelled ligands as tools to screen chemical libraries for the discovery of potential pharmaceutical agents, in particular for treatment and prevention of the conditions set forth herein, on the basis of more potent binding to SV2 proteins, for localizing SV2 proteins in tissues, and for characterizing purified SV2 proteins. SV2 proteins include SV2A, SV2B, and SV2C whereby SV2A is the binding site for the anti-seizure drug levetiracetam and its analogs. The SV2 isoforms SV2A, SV2B, or SV2C can be derived from tissues, especially brain, from any mammal species, including human, rat or mice. Alternately the isoforms may be cloned versions of any mammalian species, including human, rat, and mice, heterologously expressed and used for assays. The screening method comprises exposing brain membranes, such as mammalian or human brain membranes, or cell lines expressing SV2 proteins or fragments thereof, especially SV2A and SV2C, but including SV2B, to a putative agent and incubating the membranes or proteins or fragments and the agent with labelled compound of formula (I). The method further comprises determining if the binding of the compound of formula (I) to the protein is inhibited by the putative agent, thereby identifying binding partners for the protein. Thus, the screening assays enable the identification of new drugs or compounds that interact with SV2 proteins. The present invention also provides photoactivable ligands of SV2 proteins.

The labelled-ligands can also be used as tools to assess the conformation state of SV2 proteins after solubilization, purification and chromatography. The labelled-ligands may be directly or indirectly labeled. Examples of suitable labels include a radiolabel, such as 3H , a fluorescent label, an enzyme, europium, biotin and other conventional labels for assays of this type.

Labelled compounds of formula (I) are useful in the methods as probes in assays to screen for new compounds or agents that bind to the SV2 proteins (SV2A, SV2B and SV2C). In such assay embodiments, ligands can be used without modification or can be modified in a variety of ways; for example, by labelling, such as covalently or non- covalently joining a moiety which directly or indirectly provides a detectable signal. In any of these assays, the materials can be labelled either directly or indirectly. Possibilities for direct labelling include label groups such as: radiolabels including, but not limited to, |] enzymes such as peroxidase and alkaline phosphatase, and fluorescent labels capable of monitoring the change in fluorescence intensity, wavelength shift, or fluorescence polarization, including, but not limited to, fluorescein or rhodamine. Possibilities for indirect labelling include biotinylation of one constituent followed by binding to avidin coupled to one of the above label groups or the use of anti-ligand antibodies. The compounds may also include spacers or linkers in cases where the compounds are to be attached to a solid support. To identify agents or compounds which compete or interact with labelled ligands according to the invention for binding to the SV2 proteins (especially SV2A and SV2C), intact cells, cellular or membrane fragments containing SV2A or SV2C or the entire SV2 protein or a fragment thereof can be used. The agent or compound may be incubated with the cells, membranes, SV2 protein or fragment prior to, at the same time as, or after incubation with labelled levetiracetam or an analog or derivative thereof. Assays may be modified or prepared in any available format, including high-throughput screening (HTS) assays that monitor the binding of levetiracetam or the binding of derivatives or analogs thereof to SV2 proteins or fragments thereof. In many drug screening programs which test libraries of compounds, high throughput assays are desirable in order to maximize the number of compounds surveyed in a given period of time. Such screening assays may use intact cells, cellular or membrane fragments containing SV2 as well as cell-free or membrane-free systems, such as may be derived with purified or semi-purified proteins. The advantage of the assay with membrane fragment containing SV2 or purified SV2 proteins and peptides is that the effects of cellular toxicity and/or bioavailability of the test compound can be generally ignored, the assay instead being focused primarily on the effect of the drug on the molecular target as may be manifest in an inhibition of, for instance, binding between two molecules. The assay can be formulated to detect the ability of a test agent or compound to inhibit binding of labeled ligand according to the invention to SV2 or a fragment of SV2 or of labelled levetiracetam, or derivatives or analogs thereof, to SV2 or a fragment of SV2 protein. The inhibition of complex formation may be detected by a variety of techniques such as filtration assays, Flashplates (Perkin Elmer), scintillation proximity assays (SPA, GE). For high-throughput screenings (HTS), scintillation proximity assay which uses microspheres coated with biological membranes or flashplates coated with biological membranes arepowerful methods that do not require separation or washing steps.

A problem which can be faced when developing compounds for use in therapy is the capacity of certain compounds (perpetrator drugs), which could be co-administered together with the compounds of the present invention (victim drugs), to induce CYP450 enzymes, in particular CYP3A4/5. The induction of such enzymes by the perpetrator drugs may impact the exposure of the victim drug, when mainly metabolized by CYP450 enzymes and CYP3A4/5 in particular, thereby potentially altering their efficacy profile. It is therefore desirable to develop compounds with limited potential for metabolization by CYP3A4/5 enzymes.

The CYP3A4/5 contribution to the total metabolism of compounds according to the present invention has been evaluated by calculating the ratio between human hepatocytes clearances in absence and presence of a selective CYP3A4/5 inhibitor such as azamulin.

When tested in this assay according to the protocol described in the present patent application, compounds according to the present invention exhibit a fraction metabolized by CYP3A4/5 (F _m,CYP 3 _A 4 _/ 5) typically lower than 40%, therefore minimizing the risk for drug-drug interactions when coadministered with CYP450 inducers.

In addition, it may be beneficial that the compounds according to the present invention demonstrate low intrinsic clearances.

EXPERIMENTAL SECTION Abbreviations/recurrent reagents

Ac: acetyl

ACN: Acetonitrile

Brine: Saturated aqueous sodium chloride solution

nBu: n-butyl

fBu: fert-butyl

Bz: benzoyl

CV: column volumes

DCM: Dichloromethane

DMF: A/,A/-Dimethylformamide

DMSO: Dimethylsulfoxide

Et: Ethyl

EtOH : Ethanol

Et ₂ 0: Diethyl ether

EtOAc: Ethyl acetate

h: Hour

HPLC: High Pressure Liquid Chromatography

LC: Liquid Chromatography

LCMS: Liquid Chromatography Mass Spectrometry

MeOH: Methanol

min.: minutes MTBE: methyl tert-butyl ether

NMR: Nuclear magnetic resonance

PrOH: isopropanol

PTSA: p-toluenesulfonic acid

RT: room temperature

SFC: Supercritical Fluid Chromatography

THF: Tetrahydrofuran

TLC: Thin Layer Chromatography Analytical methods

All reactions involving air or moisture-sensitive reagents were performed under a nitrogen or argon atmosphere using dried solvents and glassware. Experiments requiring microwave irradiation are performed on a Biotage Initiator Sixty microwave oven upgraded with version 2.0 of the operating software. Experiments are run to reach the required temperature as quickly as possible (maximum irradiation power: 400 W, no external cooling). Commercial solvents and reagents were generally used without further purification, including anhydrous solvents when appropriate (generally Sure-Seal™ products from Aldrich Chemical Company or AcroSeal™ from ACROS Organics). In general reactions were followed by thin layer chromatography, HPLC or mass spectrometry analyses.

HPLC analyses are performed using an Agilent 1 100 series HPLC system mounted with a Waters XBridge MS C18, 5 pm, 150 X 4. 6 mm column. The gradient runs from 100% solvent A (water/ACN/ammonium formate solution 85/5/10 (v/v/v)) to 100% solvent B (water/ACN/ammonium formate solution 5/85/10 (v/v/v) in 6 min. with a hold at 100% B of 5 minutes. The flow rate is set at 8 mL/min during 6 min. then increased at 3 mL/min during 2 min. with a hold at 3 mL/min during 3 minutes. A split of 1/25 is used just before API source. The chromatography is carried out at 45°C. The ammonium formate solution (pH~8.5) is prepared by dissolution of ammonium formate (630 mg) in water (1 L) and addition of ammonium hydroxide 30% (500 pL).

It will be apparent to the one skilled in the art that different retention times may be obtained for LC data if different analytical conditions are used.

Mass spectrometric measurements in LCMS mode are performed as follows:

For basic elution, analyses are performed using:

A QDA Waters simple quadrupole mass spectrometer is used for LCMS analysis. This spectrometer is equipped with an ESI source and an UPLC Acquity Hclass with diode array detector (200 to 400 nm). Data are acquired in a full MS scan from m/z 70 to 800 in positive mode with an basic elution. The reverse phase separation is carried out at 45°C on a Waters Acquity UPLC BEHC18 1.7 pm (2.1 x 50 mm) column for basic elution. Gradient elution is done with water/ACN/ammonium formate (95/5/63 mg/L) (solvent A) and ACN/water/ammonium formate (95/5/63 mg/L) (solvent B). Injection volume: 1 pL. Full flow in MS.

Basic program“4 min”

Basic program“10 min

- For acidic elution, analyses are performed using:

A QDA Waters simple quadrupole mass spectrometer is used for LCMS analysis. This spectrometer is equipped with an ESI source and an UPLC Acquity Hclass with diode array detector (200 to 400 nm). Data are acquired in a full MS scan from m/z 70 to 800 in positive mode with an acidic elution. The reverse phase separation is carried out at 45°C on a Waters Acquity UPLC HSS T3 1.8 pm (2.1 x 50 mm) column for acidic elution. Gradient elution is done with water/ACN/TFA (95/5/0.5 mL/L) (solvent A) and ACN (solvent B). Injection volume: 1 pL. Full flow in MS. Acidic program“4 min

Acidic program“10 min

Crude materials could be purified by normal phase chromatography, (acidic or basic) reverse phase chromatography, chiral separation or recrystallization.

Normal reverse phase chromatography are performed using silica gel columns (100:200 mesh silica gel or Puriflash ^® -50SIHC-JP columns from Interchim).

Preparative reverse phase chromatography are performed as follows:

- LCMS purification (Basic mode, LCMS prep) using a SQD or QM Waters triple quadrupole mass spectrometer is used for LCMS purification. This spectrometer is equipped with an ESI source and a Prep LC controller Waters quaternary pump with diode array detector (210 to 400 nm).

MS parameters : ESI capillary voltage 3 kV. Cone and Extractor voltage 10. Source block temperature 120°C. Desolvation temperature 300°C. Cone gaz flow 30 L/h (Nitrogen), Desolvation Gas flow 650 L/h.Data are acquired in a full MS scan from m/z 100 to 700 in positive mode with an acidic or a basic elution.

LC parameters : The reverse phase separation is carried out at rt on a XBridge prep OBD C18 column (5 pm, 30 x 50 mm) (basic elution). Gradient elution is done with Water (solvent A), ACN (solvent B), Ammonium bicarbonate in water 8 g/L + 500 pL/L NH ₄ OH 30% (solvent C) (pH~8.5). HPLC flow rate: 35 mL/min to 60 mL/min, injection volume: 1 ml_. The splitting ratio is set at +/- 1/6000 to MS.

Preparative Chiral Chromatographic separations are performed on using liquid phase chromatography or supercritical fluid chromatography (SFC) instruments with various mixtures of lower alcohols and C ₅ to Cs linear, branched or cyclic alkanes at 360 mL/min. Solvent mixtures as well as columns are described in individual procedures.

Products were generally dried under vacuum before final analyses and submission to biological testing.

NMR spectra are recorded on a BRUKER AVANCEIII 400 MHz-Ultrashield NMR Spectrometer fitted with a Windows 7 Professional workstation running Topspin 3.2 software and a 5 mm Double Resonance Broadband Probe (PABBI 1 H/19F-BB Z-GRD Z82021/0075) or a 1 mm Triple Resonance Probe (PATXI 1 H / D-13C/15N Z-GRD Z868301/004). The compounds were studied in DMSO-ak, or CDCI ₃ solution at a probe temperature of 300 K and at a concentration of 10 mg/mL. The instrument is locked on the deuterium signal of DMSO-c/ ₆ , or CDCI ₃ . Chemical shifts are given in ppm downfield from TMS (tetramethylsilane) taken as internal standard. Optical rotations ([OI]D) were measured on a PERKIN-ELMER polarimeter 341 in a cuvette dm) at a 10 mg/ml_ concentration, at a temperature mentioned in the specific examples, at 589 nm (sodium lamp).

The following examples illustrate how the compounds covered by formula (I) may be synthesized. They are provided for illustrative purposes only and are not intended, nor should they be construed, as limiting the invention in any manner. Those skilled in the art will appreciate that routine variations and modifications of the following examples can be made without exceeding the spirit or scope of the invention.

Example 1. Synthesis of (4R)-4-(2-chloro-2.2-difluoro-ethyl)-1-IT2-(methoxymethyl)- 6-methyl-imidazor2.1-biri .3.4lthiadiazol-5-vHmethyllpyrrc>lidin-2-one 1A

II

1.1 Synthesis of 2-(methoxymethyl)-6-methyl-imidazo[2, 1 -b][1 ,3,4]thiadiazole II

To a solution of 5-(methoxymethyl)-1 ,3,4-thiadiazol-2-amine I (CAS: 15884-86-3, WO201 1/047860, 1.0 eq., 7.0 g, 48.2 mmol) in DMF (95 ml_), at 100 °C, was added dropwise a solution of bromoacetone (1.0 eq., 4.2 ml_, 46.2 mmol, 97% purity) in DMF (5 mL). The reaction mixture was stirred at 100 °C for 3 h. The reaction mixture was cooled to room temperature (RT) and the solvent was evaporated until dryness under high vacuum to give a brown oil. The crude was purified by flash chromatography Biotage Isolera Four (100 g KP-SNAP silica gel column in a gradient of 0% to 10% methanol in dichloromethane over 14CV) and the pure fractions were evaporated to dryness to give 2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazole II (5.0 g, 25.1 1 mmol) as a yellow/orange solid.

Yield: 52%

LC/MS: [M+H] ⁺ = 184.0 ¹ H NMR (400 MHz, DMSO -cfe): d 8.53 (m, 1 H), 4.76 (s, 2H), 3.40 (s, 3H), 2.25 (d, J = 1 .0 Hz, 3H).

1.2 Synthesis of [2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5- yl]methanol III

In a sealed tube, 2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazole II (1.0 eq., 5.0 g, 25.1 mmol), paraformaldehyde (6.0 eq., 4.50 g, 150 mmol) and an aqueous solution of hydrochloric acid (4N) (2 equiv., 12.55 ml_, 50.2 mmol) were mixed in 1 ,4- dioxane (12.5 ml_). The mixture was stirred at 100 °C for 18 h, then the crude mixture was warmed to RT and an aqueous saturated solution of NaHCC> ₃ was added until pH=6-7. The aqueous layer was extracted with ethyl acetate (3 times) and the combined organic layers were washed with brine, dried over MgSCU, filtered and evaporated to dryness. The crude was purified by flash chromatography Biotage Isolera Four (100 g KP-SNAP silica gel column in a gradient of 0% to 5% methanol in dichloromethane over 12CV). The purest fractions were evaporated to dryness to give [2-(methoxymethyl)-6- methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methanol III (4.0 g, 18.57 mmol) as a white solid.

Yield: 74%

LC/MS: [M+H] ⁺ = 214.0 ¹ H NMR (400 MHz, DMSO -cfe): d 5.10 (t, J = 5.4 Hz, 1 H), 4.79 (s, 2H), 4.63 (d, J = 5.4 Hz, 2H), 3.41 (s, 3H), 2.26 (s, 3H).

1.3 Synthesis of (4R)-4-(2-chloro-2,2-difluoro-ethyl)-1-[[2-(methoxymethyl)-6 -methyl- imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]pyrrolidin-2-one 1A

To a mixture of [2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5- yl]methanol III (1.0 eq., 3.65 g, 17.1 mmol) and (4R)-4-(2-chloro-2,2-difluoro- ethyl)pyrrolidin-2-one IV (CAS: 1294000-89-7, WO201 1/047860, 1.2 eq., 4.14 g, 20.5 mmol) in sulfolane (86 ml_), was added p-toluenesulfonic acid monohydrate (1.0 eq., 3.3 g, 17.1 mmol) and the mixture was stirred at 1 10 °C for 16 h. The mixture was cooled to room temperature then water was added and the aqueous layer was extracted with MTBE (4 times). The combined organic layer were washed with brine (4 times), dried over MgS0 ₄ , filtered and evaporated to dryness. The obtained crude was purified by achiral SFC (Phenomenex S1O2 Beta 10pm, D=5 cm L=34 cm, 300 g / C0 ₂ /MeOH co- solvant gradient from 1 % to 40% / 150 bars / 360 mL/min) to give (4R)-4-(2-chloro-2,2- difluoro-ethyl)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1-b ][1 ,3,4]thiadiazol-5- yl]methyl]pyrrolidin-2-one (2.32 g, 6.12 mmol) as a brown oil.

Yield: 36% LC/MS: [M+H] ⁺ = 379.1

¹ H NMR (400 MHz, DMSO -cfe): d 4.77 (s, 2H), 4.60 (s, 2H), 3.40 (s, 4H), 3.05 (dd, J = 9.4, 7.5 Hz, 1 H), 2.72-2.56 (m, 3H), 2.42 (dd, J=16.4, 8.2 Hz, 1 H), 2.26 (s, 3H), 2.17 (dd, J= 16.4, 8.6 Hz, 1 H).

(4S)-4-(2-chloro-2,2-difluoro-ethyl)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 - b][1 ,3,4]thiadiazol-5-yl]methyl]pyrrolidin-2-one 1 B was prepared according to the same procedure starting from [2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5- yl]methanol III (1.0 eq., 700 mg, 3.3 mmol) and racemic 4-(2-chloro-2,2-difluoro- ethyl)pyrrolidin-2-one IV-rac (CAS: 1294000-88-6, WO201 1/047860, 720 mg, 3.9 mmol).

The obtained crude mixture was purified by reverse phase flash chromatography Biotage Isolera Four (SNAP 60 g / Cie column in a gradient of 5% to 95% of acetonitrile in water over 15CV). The purest fractions were evaporated to dryness to give of a yellow oil (650 mg) which was repurified by achiral SFC (DIOL 5pm D=5 cm L=25 cm 300 g, co-solvent methanol 5%) to give of a clear yellow oil (220 mg). The mixture of enantiomers was then purified by chiral reverse phase chromatography (AS 50x265, 5pm, 300g, EtOH/Heptane 50/50, 100 mL/min., 35°C) to give (4S)-4-(2-chloro-2,2- difluoro-ethyl)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1-b ][1 ,3,4]thiadiazol-5- yl]methyl]pyrrolidin-2-one 1B (second eluted peak, retention time = 18 min., 83 mg, 0,217 mmol) as a clear oil.

Yield: 6.6 % LC/MS: [M+H] ⁺ = 379

¹ H NMR (400 MHz, DMSO -d ₆ ) d 4.77 (s, 2H), 4.60 (s, 2H), 3.44 (dd, J = 9.5, 7.7 Hz, 1 H), 3.40 (s, 3H), 3.05 (dd, J = 9.4, 7.5 Hz, 1 H), 2.63 (ttd, J = 13.7, 8.2, 4.4 Hz, 3H), 2.42 (dd, J = 16.4, 8.2 Hz, 1 H), 2.26 (s, 3H), 2.17 (dd, J = 16.4, 8.7 Hz, 1 H). Chiral HPLC (AS, EtOH/heptane 50/50, 30°C, 1.5 mL/min.): 1A : 2.01 min. ; 1 B: 3.02 min.

Example 2. Synthesis of -1-IT2-(methoxymethyl)-6-methyl-imidazor2.1-

biri .3.41thiadiazol-5-yllmethyll-4-propyl-pyrrolidin-2-one 2A and -1-IT2-

(methoxymethyl)-6-methyl-imidazor2.1-biri .3.4lthiadiazol-5-yllmethyll-4-propyl- pyrrolidin-2-one 2B

2.1 Synthesis of (4S)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol 5-yl]methyl]-4-propyl-pyrrolidin-2-one 2A and (4R)-1-[[2-(methoxymethyl)-6-methyl- imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]-4-propyl-pyrrolidin-2-one 2B.To a mixture of [2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methanol III (1.0 eq., 200 mg, 0.94 mmol) and 4-propylpyrrolidin-2-one V (CAS: 89895-19-2, 1.8 eq., 214 mg,

1.68 mmol) in sulfolane (4.7 ml_), was added p-toluenesulfonic acid monohydrate (1.0 eq., 178 mg, 0.94 mmol) and the mixture was stirred at 1 10 °C for 16 h. The mixture was cooled to room temperature and was directly purified by reverse phase preparative HPLC (basic conditions) to give a beige solid (130 mg) which was purified a second time by achiral SFC (Princeton 2-ethylpyridine 5 pm S1O2 5 cm-200g / C0 ₂ /MeOH co-solvant, gradient from 1 % to 40% / 150 bars / 360 mL/min) to give the expected compound as a brown oil (93 mg). The two enantiomers were separated by chiral SFC (AD 50x279 mm, C0 ₂ /MeOH co-solvent 10% / 360 mL/min, 30 °C) to give (4S)-1-[[2-(methoxymethyl)-6- methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]-4-propyl-pyrrolidin-2-one 2A (31 mg, 0.096 mmol) and (4R)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1 -b][1 ,3,4]thiadiazol-5- yl]methyl]-4-propyl-pyrrolidin-2-one 2B (26 mg, 0.081 mmol) as brown oils. The absolute stereochemistry of 2A and 2B has been unambiguously assessed by alpha-D comparison with an authentic sample of 2B synthesized according to the same procedure starting from (4R)-4-propylpyrrolidone (CAS: 930123-37-8; W02007031263).

Estimated Yields: 10 and 9%

LC/MS: [M+H] ⁺ = 323.1 Ή NMR (400 MHz, DMSO -d ₆ ) d 4.78 (s, 2H), 4.58 (s, 2H), 3.45-3.32 (m, 4H), 2.85 (dd, J = 9.3, 6.9 Hz, 1 H), 2.37 (dd, J=16.4, 8.7 Hz, 1 H), 2.25 (s, 3H), 1.92 (dd, J=16.3, 7.5 Hz, 1 H), 1.35-1.1 1 (m, 5H), 0.82 (t, J=7.1 Hz, 3H).

Alpha-D (2B, MeOH, 10 mg/mL, 29°C) = +13.8

Example 3. Synthesis of (4R)-1-rr2-(methoxymethyl)-6-methyl-imidazor2.1- biri .3.41thiadiazol-5-vnmethyll-4-(2.2.2-trifluoroethyl)pyrrc> ;lidin-2-one 3A

3.1 Synthesis of (4R)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 -b][1 ,3,4]thiadiazol- 5-yl]methyl]-4-(2,2,2-trifluoroethyl)pyrrolidin-2-one 3A

To a mixture of [2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5- yl]methanol III (1.0 eq., 100 mg, 0.47 mmol) and (4R)-4-(2,2,2-trifluoroethyl)pyrrolidin-2- one VI (CAS: 1294001-34-5, WO201 1/47860, 1.8 eq., 141 mg, 0.84 mmol) in sulfolane (2.3 ml_), was added p-toluenesulfonic acid monohydrate (1.0 eq., 90 mg, 0.47 mmol) and the mixture was stirred at 1 10 °C for 3.5 h. The mixture was cooled to room temperature and was directly purified by reverse phase preparative HPLC (basic conditions) to give a beige solid (125 mg) which was purified a second time by reverse phase preparative HPLC (KROMASIL-Eternity XT Cie 10pm, ACN/H2O/NH4OH gradient from 30/70/0.1 to 60/40/0.1 ). The purest fractions were evaporated to dryness to give (4R)-1 -[[2-(methoxymethyl)-6-methyl-imidazo[2, 1 -b][1 ,3,4]thiadiazol-5-yl]methyl]-4- (2,2,2-trifluoroethyl)pyrrolidin-2-one 3A (69 mg, 0.19 mmol) as a brown oil. Yield: 41 %

LC/MS: [M+H] ⁺ = 363.1

¹ H NMR (400 MHz, DMSO -d ₆ ) d 4.78 (s, 2H), 4.61 (s, 2H), 3.41 (m, 4H), 3.03 (dd, J = 9.4, 7.6 Hz, 1 H), 2.47-2.36 (m, 3H), 2.27 (s, 3H), 2.15 (dd, J=16.3, 8.8 Hz, 1 H).

(4S)-1-[[2-(methoxymethyl)-6-methyl-imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]-4- (2,2,2-trifluoroethyl)pyrrolidin-2-one 3B is prepared according to the same procedure starting from (4S)-4-(2,2,2-trifluoroethyl)pyrrolidin-2-one VII. Yield: 32%

Example 4. (4R)-4-(2-chloro-2.2-difluoro-ethyl)-1-IT2-(methoxymethyl)-6

(trideuteriomethyl) imidazor2.1-biri .3.4lthiadiazol-5-yllmethvHpyrrc>lidin-2-one 4

Synthesis of 1-bromo-1 ,1 ,3,3,3-pentadeuterio-propan-2-one VIII

To a mixture of 1 ,1 ,1 ,3,3,3-hexadeuteriopropan-2-one (1.0 eq., 1.5 g, 23.0 mmol) in methanol (25 ml_) at 0 °C was added dropwise bromine (1.0 eq., 1 .2 ml_, 23.0 mmol) and the mixture was stirred at 0 °C for 3 h. Water (10 ml_) was added and the reaction mixture was stirred overnight at RT. The aqueous layer was extracted with diethyl ether (3 times) and the combined organic layers were dried over MgSCU, filtered and evaporated to dryness (at 20°C) to give 1-bromo-1 ,1 ,3,3,3-pentadeuterio-propan-2-one (2.16 g, 15.25 mmol, 65% Yield) as a pale yellow oil which was used as such in the next step without further analysis and purification. 4.2 B. Synthesis of 2-(methoxymethyl)-6-(trideuteriomethyl)imidazo[2,1- b][1 ,3,4]thiadiazole IX.

To a solution of 5-(methoxymethyl)-1 ,3,4-thiadiazol-2-amine | (1.0 eq., 8.0 g, 55.1 mmol) in DMF (100 ml_), at 100 °C, was added dropwise a solution of 1-bromo- 1 ,1 ,3,3,3-pentadeuterio-propan-2-one VIII (1.05 eq., 8.22 g, 57.9 mmol) in DMF (20 ml_). The reaction mixture was stirred at 1 10 °C for 2 h 30. The mixture was then cooled to RT, a saturated solution of NaHCC> ₃ was added and the solvent was evaporated until dryness. The obtained crude was then diluted in EtOAc, filtered and the filtrate was evaporated until dryness to give a brown oil (9.5 g). The crude was purified by flash chromatography Biotage Isolera Four (100 g KP-SNAP silica gel column in a gradient of 0% to 10% methanol in dichloromethane over 14CV) and the pure fractions were evaporated to dryness to give 2-(methoxymethyl)-6-(trideuteriomethyl)imidazo[2,1- b][1 ,3,4]thiadiazole IX (3.05 g, 15.6 mmol) as a yellow solid.

Yield: 28%

LC/MS: [M+H] ⁺ = 187.2 ¹ H NMR (400 MHz, DMSO-d6) d 7.45 (s, 1 H), 4.70 (s, 2H), 3.48 (s, 3H)

4.3 (4R)-4-(2-chloro-2,2-difluoro-ethyl)-1-[[2-(methoxymethyl)-6 -(trideuteriomethyl) imidazo[2,1-b][1 ,3,4]thiadiazol-5-yl]methyl]pyrrolidin-2-one 4 To a mixture of (4R)-4-(2-chloro-2,2-difluoro-ethyl)-1-(hydroxymethyl)pyrrol idin-2-one X (CAS: 1294000-97-7, WO201 1/047860, 1.0 eq., 150 mg, 0.70 mmol) in dichloromethane (3 mL) at 0°C was added dropwise thionyl chloride (3 eq., 0.317 ml_, 2.16 mmol) and the reaction mixture was stirred at RT for 2 h. The mixture was then evaporated to dryness to give an orange oil, mostly (4R)-4-(2-chloro-2,2-difluoro-ethyl)-1- (chloromethyl)pyrrolidin-2-one XI (CAS: 1294001-06-1 , WO201 1/047860, 160 mg, 0.69 mmol, 98.2% Yield), which was directly used in the next step without any purification.

To a solution of the obtained compound (4R)-4-(2-chloro-2,2-difluoro-ethyl)-1- (chloromethyl)pyrrolidin-2-one XI (1 eq., 160 mg, 0.69 mmol), in 1 ,4-dioxane (3 mL) at RT was added and 2-(methoxymethyl)-6-(trideuteriomethyl)imidazo[2, 1- b][1 ,3,4]thiadiazole IX (1.0 eq., 130 mg, 0.69 mmol) and zinc chloride (0.1 eq, 10 mg,

0.07 mmol). The reaction mixture was stirred at 1 10 °C for 18 h, then cooled, filtered and evaporated until dryness to give a dark oil which was purified by flash chromatography Biotage Isolera Four (10 g KP-SNAP silica gel column in a gradient of 0% to 10% methanol in dichloromethane over 12CV). The purest fractions were evaporated to dryness and purified by reverse phase preparative HPLC (KROMASIL-Eternity XT Cis 10pm, ACN/H ₂ O/NH ₄ OH gradient from 30/70/0.1 to 60/40/0.1 ) to give (4R)-4-(2-chloro- 2,2-difluoro-ethyl)-1-[[2-(methoxymethyl)-6-(trideuteriometh yl)imidazo[2,1 - b][1 ,3,4]thiadiazol-5-yl]methyl]pyrrolidin-2-one 4 (71 mg, 0.18 mmol) as a yellow oil.

Yield: 26%

LC/MS: [M+H] ⁺ = 382.8

¹ H NMR (400 MHz, DMSO -cfe): d 4.77 (s, 2H), 4.60 (s, 2H), 3.44 (dd, J = 9.5, 7.6 Hz, 1 H), 3.40 (s, 3H), 3.05 (dd, J = 9.5, 7.4 Hz, 1 H), 2.72 - 2.53 (m, 3H), 2.42 (dd, J = 16.4, 8.1 Hz, 1 H), 2.17 (dd, J = 16.4, 8.6 Hz, 1 H).

Example 5. 4-(2.2-difluoropropyl)-1-IT2-(methoxymethyl)-6-methyl-imidaz or2.1- biri .3.41-thiadiazol-5-vnmethyllpyrrolidin-2-one 5A and 5B

enantiomer B 5B

5.1 Synthesis of 4-(2,2-difluoropropyl)-1-[[2-(methoxymethyl)-6-methyl-imidaz o[2,1- b][1 ,3,4]-thiadiazol-5-yl]methyl]pyrrolidin-2-one 5A and 5B

To a mixture of 4-(2,2-difluoropropyl)-1-(hydroxymethyl)pyrrolidin-2-one XII (CAS: 1294000-92-2, WO201 1/047860, 1.0 eq., 250 mg, 1.3 mmol) in dichloromethane (5 ml) at 0°C was added thionyl chloride (3.0 eq., 260 pi, 3.6 mmol) and the reaction was stirred at room temperature for 3h. The crude mixture was concentrated to dryness. To the obtained yellow oil was added a solution of 2-(methoxymethyl)-6-methyl-imidazo[2,1- b][1 ,3,4]thiadiazole II (0.9 eq, 210 mg, 1.1 mmol) in 1 ,4-dioxane (7 ml) and zinc chloride (0.1 eq., 14 mg, 0.13 mmol). The mixture was stirred at 100°C for 22 h. Water was then added to the mixture and the aqueous layer was extracted with ethyl acetate (three times). The combined organic layers were washed with brine, dried over MgSCU, filtered and evaporated to dryness to give a yellow oil.

The yellow oil was purified by reverse phase LC/MS in basic mode to give a clear oil which was repurified by achiral SFC (Phenomenex S1O2 Beta 10pm D=5 cm L=34 cm 300 gr, co-solvent MeOH 10%) to give pure 5 as a racemic mixture. The mixture of enantiomers was separated by chiral SFC (Luxcell4 ^* MeOH 25%, 360 ml_/min., 35°C) to give 4-(2,2-difluoropropyl)-1-[[2-(methoxymethyl)-6-methyl- imidazo[2,1-b][1 ,3,4]-thiadiazol-5-yl]methyl]pyrrolidin-2-one 5A (first eluted, 6.28 min., 7 mg, 0.02 mmol, 1.6% Yield) and 5B (second eluted, 8.63 min., 8 mg, 0.02 mmol, 1.8% Yield). Yield: 3.3% (1.8% + 1.6%)

LC/MS: [M+H] ⁺ = 359.1

Ή NMR (400 MHz, DMSO -d ₆ ) d 4.77 (s, 2H), 4.58 (d, J = 2.5 Hz, 2H), 3.39 (s, 3H), 2.96 (dd, J = 9.5, 7.7 Hz, 1 H), 2.45 - 2.35 (m, 3H), 2.25 (s, 3H), 1.54 (t, J = 19.1 Hz, 3H).

Chiral HPLC (SFC, LuxCelH, 3 pm, 3 mL/min., 30°C, 20% MeOH): 5A: 2.24 min ; 5B: 3.09 min.

Table (I) indicates the IUPAC name (or the name generated from Accelerys Draw 4.0) of the compound, the ion peak observed in mass spectroscopy and the ¹ H NMR description.

Table I: Physical Characterization of Example Compounds.

Example 5. Binding Assays to SV2A and SV2C.

Human SV2A and SV2C proteins were expressed in human embryonic kidney (HEK) cells. HEK SV2A and HEK SV2C membrane preparations were prepared as described in Gillard et al (Eur. J. Pharmacol. 2006, 536, 102-108). To measure affinity of non- labelled compounds, competition experiments were performed as follow: Membranes expressing SV2 proteins (5 to 15 pg proteins per assay) were incubated for 60 min at 37°C with either [ ³ H]-2-[4-(3-azidophenyl)-2-oxo-1-pyrrolidinyl] butanamide (5 nM) and/or [ ³ H]-4R-(2-chloro-2,2-difluoroethyl)-1-{[2-(methoxymethy l)-6-(trifluoromethyl)imidazo[2,1- b][1 ,3,4]thiadiazol-5-yl]methyl}pyrrolidin-2-one (25 nM) in 0.2 ml of a 50 mM Tris-HCI buffer (pH 7.4) containing 2 mM MgCh, 0.1 % dimethylsulfoxide and ten increasing concentrations of non-labelled test compound (0.1 nM to 10 pM). At the end of the incubation period, the membrane-bound radioligand was recovered by rapid filtration through GF/C glass fiber filters pre-soaked in 0.1 % polyethyleneimine. Membranes were washed with at least 4 times the assay volume of ice-cold 50 mM Tris HCI buffer (pH 7.4). The filters were dried and the radioactivity determined by liquid scintillation. The entire filtration step did not exceed 10 sec. Measured affinity pICso values were corrected to pKi according to Cheng and Prusoff (Biochem. Pharmacol. 1973, 22(23), 3099-3108).

Compounds of formula (I) according to the invention typically show pKi SV2A values of at least 6.5. and pKi SV2C values of at least 6.0.

Example 6. Seizure models.

Male NMRI mice (Charles River, Germany) weighing 22-32 g are used in all experiments. The animals are kept on a 12/12-h light/dark cycle with lights on at 6:00 am and are housed at a temperature maintained at 20-21 °C and at humidity of about 40%. The mice are housed in groups of 10 per cage (Type III). All animals have free access to standard pellet food and water before random assignment to experimental groups consisting of 10 mice each. All animal experiments are done according to the National Rules on Animal Experiments and conducted in accordance with the guidelines of the European Community Council directive 2010/63/EU. A local ethical committee approved the experimental protocols.

6.1 6 Hz seizure model

The 6 Hz model is carried out according to a previously described protocol (Kaminski et al., Epilepsia (2004), 45, 864-867). Briefly, corneal stimulation (44 mA, 0.2 ms-duration monopolar rectangular pulses at 6 Hz for 3 s) is delivered by a constant-current device (ECT Unit 57800; Ugo Basile, Comerio, Italy). A drop of 0.4% oxybuprocaine hydrochloride (Unicaine, Thea, France) is placed on the eyes before electrical stimulation. During the stimulation, mice are manually restrained and released into the observation cage (38 x 26 x 14 cm) immediately after the current application. The seizures are often preceded by a brief period (~2-3 s) of intense locomotor agitation (wild running and jumping). The animals then exhibit a“stunned” posture associated with rearing, forelimb automatic movements and clonus, twitching of the vibrissae, and Strub-tail. At the end of the seizure, animals resume their normal exploratory behavior. The experimental endpoint is protection against the seizure. The animal is considered to be protected if it resumes its normal exploratory behavior within 7 s from the stimulation. In vivo activities determined for test compounds are typically comprised between 0.05 mg/kg and 10 mg/kg after single IP dosing. 6.2 Pentylenetetrazol (PTZ) seizure model

Pentylenetetrazol is used at the previously established CD ₉₇ dose of 89 mg/kg; a convulsive dose inducing clonic convulsions of all four extremities in 97% of mice (Klitgaard et al. , Eur. J. Pharmacol. (1998), 353, 191-206). Immediately following pentylenetetrazol injection the mice are placed individually in Perspex cages and observed for the presence of clonic convulsions in all four extremities and tonic hindlimb extension during 60 min period.

In vivo activities determined for test compounds are typically comprised between 0.5 mg/kg and 30 mg/kg after single IP dosing. Example 7. Azamulin assay

Cryopreserved human hepatocytes (pool of 20 donors, BSU batch from Celsis/IVT/Bioreclamation) were thawed accordingly the provider’s information. Viability (trypan blue exclusion) was higher than 75%. Pre-incubations (250 pL of hepatocytes suspension at 2x10 ⁶ hepatocytes/mL) were carried out with William’s medium, containing 2 mM of glutamine and 15 mM of Hepes, in 48-well plates at +37°C, in an incubator (5% CO2), under gentle agitation (vibrating agitator, Titramax 100, ca 300 rpm) during 30 min. After the pre-incubation, the incubation was initiated by adding to hepatocytes, 250 pl_ of culture medium (see composition above) containing UCB compound (1 mM) or midazolam (positive control) with or without azamulin (6 mM - specific CYP3A4/5 inhibitor). Final concentrations of UCB compound and azamulin in the incubates are 0.5 pM and 3 mM, respectively. The cell suspensions was rapidly rehomogenized by 2 in-out pipetting. After 0, 30, 60, 120, 180 and 240 minutes of incubation, reactions were stopped by transferring 50 pi of incubates into the appropriate well from 96-well plate containing 50 mI_ of ice cold acetonitrile with ketoconazole 1 mM as internal standard. Before each sampling, cell incubates are re-homogenized by 2 in out pipetting.

Once the incubation is finished, 96-well plates are centrifuged at ca 3700 rpm, +4°C, for 15 minutes. 50 pL of supernatants are transferred into the wells of other deep well plates to which 150 pl_ of H2O Millipore were added. These samples were are analyzed by micro UPLC/HR-MS for parent disappearance and monitoring of metabolite formation. The CYP3A4/5 contribution known as fraction metabolized by CYP3A4/5 (f _m ,cYP3A4/5) was calculated for each compound from the ratio between CLint (based on parent parent drug disappearance) in absence and in presence of azamulin, by using the following equation :

The fraction metabolized by CYP3A4/5 (f _m, c _YP 3 _A 4 _/ 5) of test compounds are typically comprised between 0 and 40%.