4-ANILINO-QUINOLINE COMPOUNDS AS ANTI-CANCER AGENTS

FIELD OF THE INVENTION:

The invention relates to novel compounds active for the treatment of cancer. BACKGROUND OF THE INVENTION:

Cutaneous melanoma deriving from the transformation of melanocytes is one of the most lethal cancers among young adults. Its incidence has increased at a dramatic rate during the last decades. Melanoma has a high capability of invasion and rapid metastasis to other organs.

Immune-checkpoint blockades targeting cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), and more recently Programmed Death 1 (PD1) and Programmed Death-Ligand 1 (PDL-1), are recent and major breakthroughs in cancer therapy. Initially developed to treat metastatic melanomas, antibodies against those targets significantly increase overall patient survival and are now being evaluated to treat other solid cancers such as those of the kidney, prostate, colon, and lung. Although anti-PDl antibodies have shown better results than anti- CTLA-4 antibodies, the response rate remains low (10% to 57%), depending on the cancer type and the treatment combinations. The combination of anti-PDl and anti-CTLA-4 to treat melanoma has given the best complete response rate so far, 11.5%, but is associated with an almost 70% rate of grade 3 or grade 4 side effects. Few patients therefore benefit from those approaches, and no predictive factor for the response has yet been identified. Accumulating evidence suggests that interferon gamma (IFN-γ) plays a key role in the response to anti-PDl treatment (1-3). A meta-analysis of all the immune-based approaches to melanoma treatment (including anti-PDl) showed that patients with vitiligo id depigmentation have significantly better rates of progression-free survival and overall survival compared with other patients (4). Furthermore, patients with vitiligo have a threefold lesser risk of developing melanoma (5). An increasing number of data indicate that the IFN-y/CXCLlO pathway, which is involved in the vitiligoid depigmentation process, plays a key role in determining melanoma risk (6). Thus, the IFN-γ response is implicated as a key factor facilitating the checkpoint-blockade treatment approaches. Inventors of the instant application recently showed that the inhibition of the non-canonical NF-kB pathway, as well as that of the upstream NF-kB-inducing kinase (NIK), restores a senescence program in melanoma cells through decreased EZH2 transcription and significantly reduces tumor growth (7). There are increasing evidences that cellular senescence can trigger or potentiate tumor immune surveillance (8). The instant invention provides new NIK inhibitors that decrease EZH2 at the transcriptional level and induce the production of an IFN-γ response by the treated cell. These NIK inhibitors reduce the size of subcutaneous tumors without showing any specific toxicity, and when combined with anti-PDl treatment lead to a dramatic reduction in tumor size with complete regression in some cases. Those effects are associated with a marked increase in the numbers and activation of macrophages, dendritic cells, and T-cells within the treated tumors.

SUMMARY OF THE INVENTION:

The invention relates to compounds of general formula:

in which Ri, R ₂ , R ₅ , R6 and n have the meanings indicated below, and to pharmaceutical compositions containing such compounds as well as the uses thereof.

DETAILED DESCRIPTION OF THE INVENTION:

The invention relates to compounds of general formula (I)

wherein

Ri is selected from H, alkyl, Halo, OH, O-alkyl, NH ₂ , NH-alkyl, N-(alkyl) ₂ , S-alkyl, CF ₃ , OCF ₃ , OCF ₂ H and 0(CH ₂ ) _n iO(CH ₂ ) _n2 CH ₃ , m being 1 to 4 and n ₂ being 0 to 3, Halo being selected from CI, F, Br and I;

n is 1 or 2,

when n is 2, then it is also possible for Ri to form with the phenyl group at the meta and para positions a dioxolane group or a 1,4 dioxane group,

R ₂ is selected from H, Halo and NR ₃ R ₄ , Halo being defined as previously,

R ₃ is H and R ₄ is phenyl optionally substituted with one or more substituents selected from OH, O-alkyl and Halo, or R3 and R4 together form a (CH ₂ ) ₂ 0(CH ₂ ) ₂ chain, that is to say that NR ₃ R ₄ forms a morpholino group

R ₅ is selected from H, cyclic radical, O-alkyl, 0-(CH ₂ ) _n i -(cyclic radical), (CH ₂ ) _n i -(cyclic radical), ni being defined as previously, said cyclic radical being chosen

5 is selected from H and Halo,

with the proviso that when R ₂ is Halo or R^ is Halo then R5 is not H,

its pharmaceutically acceptable salts and/or optical isomers, tautomers, solvates or isotopic variations thereof.

In the above general formula (I), unless specified otherwise:

Alkyl denotes a straight chain or branched group containing 1, 2, 3, 4, 5 or 6 carbon atoms. Examples of suitable alkyl radicals are methyl, ethyl, n-propyl, cyclopropyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, cyclopentyl, isopentyl, n-hexyl, cyclohexyl, etc.

Alkyl is preferably a straight chain group comprising from 1 to 4 carbon atoms. Alkyl is preferably methyl.

The free bond on the phenyl group means that the phenyl may be substituted in the ortho, meta or para position and when n is 2, in two of the ortho, meta or para positions.

Halo means fluoro, chloro, bromo and iodo. A preferred Halo group for Ri is fluoro or chloro, and more preferably chloro.

A preferred halo group for R ₂ is chloro.

A first preferred group of compounds includes compounds of general formula (2):

wherein R _{l s} R ₅ , 5 and n are as defined above, R ₂ is NR ₃ R ₄ and R3, R4 are as defined above. A second preferred group of compounds includes compounds of general formula (3)

wherein R _{l s} R ₅ , 5 and n are as defined above, R ₂ is X, X is Halo as defined above, and R ₅ is not H. Preferably X is chloro.

According to an embodiment of the invention, Ri is selected from methyl (CH ₃ ), fluoro (F), chloro (CI), hydroxy (OH), methoxy (OCH ₃ ), CF ₃ , OCF ₃ , OCF ₂ H and 0(CH ₂ ) ₂ OCH ₃ , and when n is 2 then the substituents Ri are identical or different.

According to another embodiment of the invention, when n is 2 then the two Ri form with the phenyl group at the meta and para positions a dioxolane group or a 1,4 dioxane group.

According to an embodiment of the invention, in the compounds defined above, when R ₂ is NR ₃ R4, then R ₃ is H and R4 is a phenyl unsubstituted or substituted with one or two groups, identical or different, selected from OH, OCH ₃ and Halo, Halo being preferably chloro.

According to another embodiment of the invention, in the compounds defined above, when R ₂ is NR ₃ R4, then R ₃ and R4 together form a (CH ₂ ) ₂ 0(CH ₂ ) ₂ chain, that is to say that

NR ₃ R4 forms a morpholino

According to an advantageous embodiment of the invention, preferred compounds are those of general formula (2), wherein R ₂ is NR ₃ R4 and forms a morpholino group, said compounds being more particularly the following:

- N-(3,5-difluorophenyl)-7-morpholinoquinolin-4-amine (compound 10),

- N-(/?-tolyl) 7-morpholinoquinolin-4-amine (compound 11),

- N-(o-tolyl)-7-morpholinoquinolin-4-amine (compound 12),

- N-(4-methoxyphenyl)-7-morpholinoquinolin-4-amine (compound 13),

- N-(3-methoxyphenyl)-7-morpholinoquinolin-4-amine (compound 14) and

- N-(3-(trifluoromethyl)phenyl)-7-morpholinoquinolin-4-amine (compound 15). According to another advantageous embodiment of the invention, preferred compounds are those of general formula (2), wherein R ₂ is NR ₃ R ₄ , R ₃ being H and R ₄ a phenyl unsubstituted or substituted with one or two groups as defined above, said compounds being more particularly the following:

- N ⁴ , N ⁷ -bis(4-methoxyphenyl)quinolin-4,7-diamine (compound 16),

- N ⁴ , N ⁷ -bis(3-methoxyphenyl)quinolin-4,7-diamine (compound 17),

- N ⁴ -(3,5-difluorophenyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 18),

N ⁴ -(3,5-difluorophenyl)-N ⁷ -(3-chloro-4-hydroxyphenyl)quinolin-4,7-diamine (compound 19) (also named 2-chloro-4-((4-((3,5-difluorophenyl)amino)quinolin-7- y l)amino)pheno 1) ,

- N ⁴ -(/?-tolyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 20),

- N ⁴ -(/?-tolyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 21),

- N ⁴ -(3-(trifluoromethyl)phenyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine

(compound 22),

- N ⁴ -(o-tolyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 23),

- N ⁴ -(4-methoxyphenyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 24),

- N ⁴ -(3-methoxyphenyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 25) and

- N ⁴ -(3,5-difluorophenyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (26).

According to another advantageous embodiment of the invention, preferred compounds are those of general formula (3) which are more particularly the following:

- N-(4-methoxyphenyl)-7-chloro-2-methoxy-quinolin-4-amine (compound 27),

- N-(3,4-dimethoxyphenyl)-7-chloro-2-morpholino-quinolin-4-ami ne (compound 28), - N-(3,4-dimethoxyphenyl)-7-chloro-2-(4-methylpiperazin-l-yl)- quinolin-4-amine

(compound 29),

- N-(4-methoxyphenyl)-7-chloro-2-morpholino-quinolin-4-amine (compound 30),

N-(4-methoxyphenyl)-7-chloro-2-(4-methylpiperazin- 1 -yl)-quinolin-4-amine (compound 31),

- N-(3,4-dimethoxyphenyl)-7-chloro-2-(2-morpholinoethoxy)quino lin-4-amine

(compound 32) and

- N-(3,4-dimethoxyphenyl)-7-chloro-2-methoxy-quinolin-4-amine (compound 33). The compounds of formula (I), their pharmaceutically acceptable salts and/or derived forms, are valuable pharmaceutically active compounds suitable for the therapy and prophylaxis of various cancers.

The invention thus also pertains to compounds of formula (I) as defined above and, if appropriate, their pharmaceutically acceptable salts and/or optical isomers, tautomers, solvates or isotopic variations thereof for use in the treatment of cancer, namely solid tumor cancer, and preferably those selected from melanoma, bladder, kidney, prostate, colon, lung, breast and blood cancer. Compounds of the invention may be administered as crystalline or amorphous products.

They may be obtained, for example, as solid plugs, powders, or films by methods such as precipitation, crystallization, freeze-drying, spray drying, or evaporative drying. Microwave or radio frequency drying may be used for this purpose.

They may be administered alone or in combination with one or more other compounds of the invention or in combination with one or more other drugs (or as any combination thereof). Generally, they will be administered as a formulation in association with one or more pharmaceutically acceptable excipients. The term "excipient" is used herein to describe any ingredient other than the compound(s) of the invention. The choice of excipient will to a large extent depend on factors such as the particular mode of administration, the effect of the excipient on solubility and stability, and the nature of the dosage form. Pharmaceutical compositions suitable for the delivery of compounds of the present invention and methods for their preparation will be readily apparent to those skilled in the art. Such compositions and methods for their preparation may be found, for example, in 'Remington's Pharmaceutical Sciences', 19th Edition (Mack Publishing Company, 1995).

Another aspect of the invention is thus a pharmaceutical composition comprising a compound of general formula (I) as defined above and a pharmaceutically acceptable carrier.

The compounds of the invention may be administered by any suitable route.

Thus, a compound of the invention may be formulated as a pharmaceutical composition for oral, buccal, intranasal, parenteral (e. g. intravenous, intramuscular or subcutaneous), topical or rectal administration or in a form suitable for administration by inhalation or insufflation. For oral administration, the pharmaceutical composition may take the form of, for example, a tablet or capsule prepared by conventional means with a pharmaceutically acceptable excipient such as a binding agent (e. g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); filler (e. g., lactose, microcrystalline cellulose or calcium phosphate); lubricant (e. g., magnesium stearate, talc or silica); disintegrant (e. g., potato starch or sodium starch glycolate); or wetting agent (e. g., sodium lauryl sulphate).

The tablets may be coated by methods well known in the art. Liquid preparations for oral administration may take the form of a, for example, solution, syrup or suspension, or they may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may be prepared by conventional means with a pharmaceutically acceptable additive such as a suspending agent (e. g., sorbitol syrup, methyl cellulose or hydrogenated edible fats); emulsifying agent (e. g., lecithin or acacia); nonaqueous vehicle (e. g., almond oil, oily esters or ethyl alcohol); and preservative (e. g., methyl or propyl p-hydroxybenzoates or sorbic acid).

For buccal administration, the composition may take the form of tablets or lozenges formulated in conventional manner. A compound of the present invention may also be formulated for sustained delivery according to methods well known to those of ordinary skill in the art. Examples of such formulations can be found in United States Patents 3,538, 214, 4,060, 598,4, 173,626, 3,119, 742, and 3,492, 397, which are herein incorporated by reference in their entirety.

A compound of the invention may be formulated for parenteral administration by injection, including using conventional catheterization techniques or infusion. Formulations for injection may be presented in unit dosage form, e.g., in ampules or in multi-dose containers, with an added preservative. The compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain a formulating agent such as a suspending, stabilizing and/or dispersing agent. Alternatively, the active ingredient may be in powder form for reconstitution with a suitable vehicle, e. g., sterile pyrogen-free water, before use parenteral formulations are typically aqueous solutions which may contain excipients such as salts, carbohydrates and buffering agents (preferably to a pH of from 3 to 9), but, for some applications, they may be more suitably formulated as a sterile non-aqueous solution or as a dried form to be used in conjunction with a suitable vehicle such as sterile, pyrogen-free water. Inasmuch as it may desirable to administer a combination of active compounds, for example, for the purpose of treating a particular disease or condition, it is within the scope of the present invention that two or more pharmaceutical compositions, at least one of which contains a compound in accordance with the invention, may conveniently be combined in the form of a kit suitable for coadministration of the compositions. Thus, the kit of the invention comprises two or more separate pharmaceutical compositions, at least one of which contains a compound of formula (I) in accordance with the invention, and means for separately retaining said compositions, such as a container, divided bottle, or divided foil packet. An example of such a kit is the familiar blister pack used for the packaging of tablets, capsules and the like.

The kit of the invention is particularly suitable for administering different dosage forms, for example parenteral, for administering the separate compositions at different dosage intervals, or for titrating the separate compositions against one another. To assist compliance, the kit typically comprises directions for administration and may be provided with a so-called memory aid.

For administration to human patients, the total daily dose of the compounds of the invention is typically in the range 0.001 mg to 5000 mg depending, of course, on the mode of administration. For example, an intravenous daily dose may only require from 0.001 mg to 40 mg. The total daily dose may be administered in single or divided doses and may, at the physician's discretion, fall outside of the typical range given herein.

These dosages are based on an average human subject having a weight of about 65 kg to

70 kg. The physician will readily be able to determine doses for subjects whose weight falls outside this range, such as infants and the elderly.

For the avoidance of doubt, references herein to "treatment" include references to curative, palliative and prophylactic treatment.

According to another embodiment of the present invention, the compounds of the formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, can also be used as a combination with one or more additional therapeutic agents to be coadministered to a patient to obtain some particularly desired therapeutic end result such as the treatment of cancers solid tumor cancers such as melanoma, bladder, kidney, prostate, colon, pancreas, lung and blood cancers, such as Hodgkin disease.

Preferably, the compounds of the invention either alone or in combination are administered to patients at metastatic stage suffering from melanoma, renal cancer, colorectal cancer, lung cancer, specifically non-small lung cancer and prostate cancer. The second and more additional therapeutic agents may also be compounds of the formula (I), or a pharmaceutically acceptable salt, derived forms or compositions thereof, or one or more compounds known in the art for the treatment of the conditions listed above. More typically, the second and more therapeutic agents will be selected from a different class of therapeutic agents.

As used herein, the terms "co-administration", "co-administered" and "in combination with", referring to the compounds of formula (I) and one or more other therapeutic agents, is intended to mean, and does refer to and include the following: simultaneous administration of such combination of compound(s) of formula (I) and therapeutic agent(s) to a patient in need of treatment, when such components are formulated together into a single dosage form which releases said components at substantially the same time to said patient, substantially simultaneous administration of such combination of compound(s) of formula (I) and therapeutic agent(s) to a patient in need of treatment, when such components are formulated apart from each other into separate dosage forms which are taken at substantially the same time by said patient, whereupon said components are released at substantially the same time to said patient, sequential administration of such combination compound(s) of formula (I) and therapeutic agent(s) to a patient in need of treatment, when such components are formulated apart from each other into separate dosage forms which are taken at consecutive times by said patient with a significant time interval between each administration, whereupon said components are released at substantially different times to said patient; and sequential administration of such combination of compound(s) of formula (I) and therapeutic agent(s) to a patient in need of treatment, when such components are formulated together into a single dosage form which releases said components in a controlled manner whereupon they are concurrently, consecutively, and/or administered at the same and/or different times by said patient, where each part may be administered by either the same or different route.

Suitable examples of other therapeutic agents which may be used in combination with the compound(s) of formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, include, but are by no means limited to:

- Anti-cancer agents used for the therapy of cancers such as dacarbazine,

- Nitrosourea alkylating agents, such as fotemustine,

- BRAF inhibitors such as vemurafenib or dabrafenib,

- MEK inhibitors such as trametinib,

- Anti- CTLA4 antibodies, such as ipilimumab,

- Anti PD1 antibodies, such as nivolumab, pidizilumab, pembrolizumab and AMP-514, - Anti PD1 fusion protein such as AMP-224,

- Anti PD-Ll antibodies, such as atezolizumab, durvalumab, avelumab, utomilumab and MPDL3280A,

- Other immune checkpoint blocking agents or, in general, therapeutic agents based on immune approaches for treating cancer.

The compounds of the invention are co-administered with an antibody selected from an anti-PDl antibody, an anti-CTLA4 antibody and an anti-PD-Ll antibody and a mixture of two or more thereof.

According to a specific embodiment, the present invention relates to pharmaceutical composition comprising:

- a compound of general formula (I)

wherein

Ri is selected from H, alkyl, Halo, OH, O-alkyl, NH ₂ , NH-alkyl, N-(alkyl) ₂ , S-alkyl, CF ₃ , OCF ₃ , OCF ₂ H and 0(CH ₂ )„iO(CH ₂ ) _n2 CH ₃ , ¾ being 1 to 4 and n ₂ being 0 to 3, Halo being selected from CI, F, Br and I;

n is 1 or 2;

when n is 2, then it is also possible for Ri to form with the phenyl group at the meta and para positions a dioxolane group or a 1,4 dioxane group,

R ₂ is selected from H, Halo and NR ₃ R ₄ ; Halo being defined as previously,

R ₃ is H and R ₄ is phenyl optionally substituted with one or more substituents selected from OH, O-alkyl and Halo or R ₃ and R ₄ together form a (CH ₂ ) ₂ 0(CH ₂ ) ₂ chain,

R ₅ is selected from H, cyclic radical, O-alkyl, 0-(CH ₂ ) _n i -(cyclic radical), -(cyclic radical), ¾ being defined as previously, said cyclic radical being chosen

5 is selected from H and Halo,

its pharmaceutically acceptable salts and/or optical isomers, tautomers, solvates or isotopic variations thereof, - at least one antibody selected from an anti-PDl antibody, an anti-CTLA4 antibody, an anti-PD-Ll antibody and a mixture of two or more thereof, and

- optionally at least one pharmaceutically acceptable carrier. According to an advantageous embodiment of the invention, preferred compounds used in the above mentioned pharmaceutical composition are those of general formula (I) which are more particularly the following:

- N-(3,5-difluorophenyl)-7-chloroquinolin-4-amine (compound 1),

- N-(4-methylphenyl)-7-chloroquinolin-4-amine (compound 2),

- N-(3-trifluoromethylphenyl)-7-chloroquinolin-4-amine (compound 3),

- N-(2-methylphenyl)-7-chloroquinolin-4-amine (compound 4),

- N-(4-methoxyphenyl)-7-chloroquinolin-4-amine (compound 5),

- N-(3-methoxyphenyl)-7-chloroquinolin-4-amine (compound 6),

- N-(4-hydroxyphenyl)-7-chloroquinolin-4-amine (compound 7),

- N-(4-hydroxy-3-chlorophenyl)-7-chloroquinolin-4-amine (compound 8),

- N-(4-trifluoromethylphenyl)-7-chloroquinolin-4-amine (compound 9),

- N-(3,5-difluorophenyl)-7-morpholinoquinolin-4-amine (compound 10),

- N-(4-(difluoromethoxy)phenyl)-7-chloro-quinolin-4-amine (compound 34),

- N-(4-methoxy-3-(2-methoxyethoxy)phenyl)-7-chloro-quinolin-4- amine (compound 35),

- N-(4-trifluoromethoxyphenyl)-6-chloroquinolin-4-amine (compound 36),

- N-(2,4-dimethoxyphenyl)-6-chloroquinolin-4-amine (compound 37),

- N-(3,4-dimethoxyphenyl)-7-chloroquinolin-4-amine (compound 38),

- N-(2,4-dimethoxyphenyl)-7-chloroquinolin-4-amine (compound 39),

- N-(/?-tolyl) 7-morpholinoquinolin-4-amine (compound 11),

- N-(o-tolyl)-7-morpholinoquinolin-4-amine (compound 12),

- N-(4-methoxyphenyl)-7-morpholinoquinolin-4-amine (compound 13),

- N-(3-methoxyphenyl)-7-morpholinoquinolin-4-amine (compound 14),

- N-(3-(trifluoromethyl)phenyl)-7-morpholinoquinolin-4-amine (compound 15), - N ⁴ , N ⁷ -bis(4-methoxyphenyl)quinolin-4,7-diamine (compound 16),

- N ⁴ , N ⁷ -bis(3-methoxyphenyl)quinolin-4,7-diamine (compound 17),

- N ⁴ -(3,5-difluorophenyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 18),

N ⁴ -(3,5-difluorophenyl)-N ⁷ -(3-chloro-4-hydroxyphenyl)quinolin-4,7-diamine (compound 19), - N ⁴ -(/?-tolyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 20),

- N ⁴ -( ?-tolyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 21),

N ⁴ -(3-(trinuoromethyl)phenyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 22),

- N ⁴ -(o-tolyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 23),

- N ⁴ -(4-methoxyphenyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 24),

- N ⁴ -(3-methoxyphenyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 25),

- N ⁴ -(3,5-difluorophenyl)-N ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 26),

- N-(4-methoxyphenyl)-7-chloro-2-methoxy-quinolin-4-amine (compound 27),

- N-(3,4-dimethoxyphenyl)-7-chloro-2-morpholino-quinolin-4-ami ne (compound 28),

N-(3,4-dimethoxyphenyl)-7-chloro-2-(4-methylpiperazin-l-y l)-quinolin-4-amine (compound 29),

- N-(4-methoxyphenyl)-7-chloro-2-morpholino-quinolin-4-amine (compound 30),

N-(4-methoxyphenyl)-7-chloro-2-(4-methylpiperazin- 1 -yl)-quinolin-4-amine (compound 31),

N-(3,4-dimethoxyphenyl)-7-chloro-2-(2-morpholinoethoxy)quino lin-4-amine (compound 32),

- N-(3,4-dimethoxyphenyl)-7-chloro-2-methoxy-quinolin-4-amine (compound 33),

- 7-chloro-N-(2,3-dihydroxybenzo[¾][l ,4]dioxin-6-yl)quinolin-4-amine (40),

- 7-chloro-N-(benzo[d][l ,3]dioxol-5-yl)quinolin-4-amine (41).

The last two compounds (40) and (41) correspond respectively to compounds (I) as defined above wherein, when n is 2, then Ri form respectively with the phenyl group at the meta and para positions a 1 ,4 dioxane group (compound 40) or a dioxolane group (compound 41).

The present invention also relates to a pharmaceutical composition as defined above which additionally comprising another anti-cancer drug.

The invention more particularly relates to a pharmaceutical composition as defined above, as a combined preparation for simultaneous, separate or sequential use in the treatment of cancer, said being preferably selected from melanoma, bladder, kidney, prostate, colon, lung, breast and blood cancer.

According to another specific embodiment, the invention relates to a compound of general formula (I):

wherein

Ri is selected from H, alkyl, Halo, OH, O-alkyl, NH ₂ , NH-alkyl, N-(alkyl) ₂ , S-alkyl, CF ₃ , OCF ₃ , OCF ₂ H and 0(CH ₂ )„iO(CH ₂ ) _n2 CH ₃ , ni being 1 to 4 and n ₂ being 0 to 3, Halo being selected from CI, F, Br and I;

n is 1 or 2,

when n is 2, then it is also possible for Ri to form with the phenyl group at the meta and para positions a dioxolane group or a 1,4 dioxane group,

R ₂ is selected from H, Halo and NR ₃ R ₄ , Halo being defined as previously,

R ₃ is H and R ₄ is phenyl optionally substituted with one or more substituents selected from OH, O-alkyl and Halo,

or R ₃ and R ₄ together form a (CH ₂ ) ₂ 0(CH ₂ ) ₂ chain, that is to say that NR ₃ R ₄ forms a morpholino group

R ₅ is selected from H, cyclic radical, O-alkyl, 0-(CH ₂ ) _n i -(cyclic radical), (CH ₂ ) _n i -(cyclic radical), ¾ being defined as previously, said cyclic radical being chosen

5 is selected from H and Halo,

with the proviso that when R ₂ is F and R5 = R^ = H then Ri is not 3-Cl ; 4-Cl ; 3-F ; 4- OCH ₃ ; 4-CH ₃ ; 3-Cl and 4-F ; 3-Cl and 4-Cl ; or 4-F ;

and with the proviso that when R ₂ is CI and R5 = R^ = H then Ri is not 4-OH or 4-Cl ; its pharmaceutically acceptable salts and/or optical isomers, tautomers, solvates or isotopic variations thereof,

for use in the treatment of cancer, said cancer being preferably selected from melanoma, bladder, kidney, prostate, colon, lung, breast and blood cancer, and more preferably selected from melanoma and colon cancer.

More particularly, the compounds for use as defined above are chosen from compounds (1) to (6) and (8) to (41) as defined above. It is to be appreciated that all references herein to treatment include curative, palliative and prophylactic treatment. The description, which follows, concerns the therapeutic applications to which the compounds of formula (I) may be put.

A still further aspect of the present invention also relates to the use of the compounds of formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, for the manufacture of a drug having an anticancer activity.

In particular, the present inventions concerns the use of the compounds of formula (I), or pharmaceutically acceptable salts, derived forms or compositions thereof, for the manufacture of a drug for the treatment of a solid tumor cancer selected melanoma, colon, lung and breast cancer.

As a consequence, the present invention provides a particularly interesting method to treat a mammal, including a human being, with an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt, derived form or composition thereof.

More precisely, the present invention provides a particularly interesting method for the treatment of a cancer disease in a mammal, including a human being, in particular the diseases and/or conditions listed above, comprising administering said mammal with an effective amount of a compound of formula (I), its pharmaceutically acceptable salts and/or derived forms.

The compounds of the formula (I) may be prepared using conventional procedures such as by the following illustrative methods in which the various substituents are as previously defined for the compounds of the formula (I) unless otherwise stated.

The procedure for preparing the compounds of the invention, wherein R5 = R^ = H and R ₂ is chloro or NR ₃ R ₄ comprises the following steps:

i) Reacting 4,7-dichloroquinoline with a compound of formula 4:

to obtain a compound of formula 3

ii) If appropriate, reacting the compound of formula 3 with a compound of general formula 5: HNR ₃ R ₄ iii) Obtaining the compound of formula (2), that is subsequently isolated and purified.

Step i) is performed in the conditions of an aromatic nucleophilic substitution in an acidic medium (Journal of the American Chemical Society, 1946, vol 68, 1807-1808).

Step ii) is performed in the conditions of a Buchwald-Hartwig coupling (Angewandte Chemie, International edition,1995, vol 34,1348-1350) in the presence of a catalyst, such as palladium and a base in a suitable solvent, e.g. Toluene, DME or dioxane.

Compounds of general formula 3 wherein R5 = R^ = H and X is fluoro or bromo, can be prepared starting from the corresponding 4-chloro-7-haloquinoline, according to the previously reported procedures (see for examples: Bioorg. Med. Chem. 2013, 21 (11), 3147- 3153 ; J. Med. Chem., 2015, 58 (14), 5522-5537).

Compounds of general formula (I) wherein R ₂ = R5 = H and R ₂ is Halo can be prepared starting from the corresponding 4-chloro-6-haloquinoline, according to the procedure described above for compound of formula (3).

Compounds of general formula (I) wherein R ₅ ≠ H, R ₂ = CI and 5 = H can be prepared by the following steps:

i) Reacting 2,4,7-trichloroquinoline with a compound of formula 4:

to obtain a compound of formula

ii) If appropriate, reacting the compound of formula 6 with a compound of general formula : HNR ₃ R ₄ or O-alkyl.

Step i) is performed in the conditions of an aromatic substitution in basic medium in DMA (Tetrahedron Letters, 2013, vol 54, 6900-6904).

Step ii) is performed in the conditions of an aromatic substitution.

Pharmaceutically acceptable salts of the compounds of formula (I) include the acid addition and base salts thereof. Suitable acid addition salts are formed from acids, which form non-toxic salts.

Examples include the acetate, aspartate, benzoate, besylate, bicarbonate/carbonate, bisulphate/sulphate, borate, camsylate, citrate, edisylate, esylate, formate, fumarate, gluceptate, gluconate, glucuronate, hexafluorophosphate, hibenzate, hydrochloride/chloride, hydrobromide/bromide, hydroiodide/iodide, isethionate, lactate, malate, maleate, malonate, mesylate, methylsulphate, naphthylate, 2-napsylate, nicotinate, nitrate, orotate, oxalate, palmitate, pamoate, phosphate/hydrogen phosphate/dihydrogen phosphate, saccharate, stearate, succinate, tartrate, tosylate and trifluoroacetate and xinafoate salts.

Suitable base salts are formed from bases, which form non-toxic salts.

Examples include the aluminium, arginine, benzathine, calcium, choline, diethylamine, diolamine, glycine, lysine, magnesium, meglumine, olamine, potassium, sodium, tromethamine and zinc salts. Hemisalts of acids and bases may also be formed, for example, hemisulphate and hemicalcium salts.

For a review on suitable salts, see "Handbook of Pharmaceutical Salts: Properties, Selection, and Use" by Stahl and Wermuth (Wiley- VCH, Weinheim, Germany, 2002).

Pharmaceutically acceptable salts of compounds of formula (I) may be prepared by one or more of three methods:

(i) by reacting the compound of formula (I) with the desired acid or base;

(ii) by removing an acid- or base- labile protecting group from a suitable precursor of the compound of formula (I) or by ring-opening a suitable cyclic precursor, for example, a lactone or lactam, using the desired acid or base; or

(iii) by converting one salt of the compound of formula (I) to another by reaction with an appropriate acid or base or by means of a suitable ion exchange column.

All three reactions are typically carried out in solution. The resulting salt may precipitate out and be collected by filtration or may be recovered by evaporation of the solvent. The degree of ionization in the resulting salt may vary from completely ionized to almost non- ionized.

The compounds of the invention may exist in both unsolvated and solvated forms.

The term 'solvate' is used herein to describe a molecular complex comprising the compound of the invention and a stoichiometric amount of one or more pharmaceutically acceptable solvent molecules, for example, ethanol. The term 'hydrate' is employed when said solvent is water.

Included within the scope of the invention are complexes such as clathrates, drug-host inclusion complexes wherein, in contrast to the aforementioned solvates, the drug and host are present in stoichiometric or non-stoichiometric amounts. Also included are complexes of the drug containing two or more organic and/or inorganic components, which may be in stoichiometric or non-stoichiometric amounts. The resulting complexes may be ionised, partially ionized, or non-ionized. For a review of such complexes, see J Pharm Sci, 64 (8), 1269-1288 by Haleblian (August 1975).

Hereinafter all references to compounds of formula (I) include references to salts, solvates and complexes thereof and to solvates and complexes of salts thereof.

The compounds of the invention include compounds of formula (I) as hereinbefore defined, including all polymorphs and crystal habits thereof, prodrugs and isomers thereof (including optical, geometric and tautomeric isomers) as hereinafter defined and isotopically- labeled compounds of formula (I).

As indicated, so-called 'pro-drugs' of the compounds of formula (I) are also within the scope of the invention. Thus certain derivatives of compounds of formula (I) which may have little or no pharmacological activity themselves can, when administered into or onto the body, be converted into compounds of formula (I) having the desired activity, for example, by hydrolytic cleavage. Such derivatives are referred to as 'prodrugs'. Further information on the use of prodrugs may be found in 'Pro-drugs as Novel Delivery Systems, Vol. 14, ACS Symposium Series (T. Higuchi and W. Stella) and 'Bioreversible Carriers in Drug Design', Pergamon Press, 1987 (ed. E. B Roche, American Pharmaceutical Association).

Prodrugs in accordance with the invention can, for example, be produced by replacing appropriate functionalities present in the compounds of formula (I) with certain moieties known to those skilled in the art as 'pro -moieties' as described, for example, in "Design of Prodrugs" by H. Bundgaard (Elsevier, 1985).

Some examples of prodrugs in accordance with the invention include:

(i) where the compound of formula (I) contains a carboxylic acid functionality (COOH), an ester thereof, for example, a compound wherein the hydrogen of the carboxylic acid functionality of the compound of formula (I) is replaced by (Cl-C8)alkyl;

(ii) where the compound of formula (I) contains an alcohol functionality (-OH), an ether thereof, for example, a compound wherein the hydrogen of the alcohol functionality of the compound of formula (I) is replaced by (Cl-C6)alkanoyloxymethyl; and

(iii) where the compound of formula (I) contains a primary or secondary amino functionality, an amide thereof, for example, a compound wherein, as the case may be, one or both hydrogens of the amino functionality of the compound of formula (I) is/are replaced by (Ci-Cio)alkanoyl. Further examples of replacement groups in accordance with the foregoing examples and examples of other prodrug types may be found in the aforementioned references. Moreover, certain compounds of formula (I) may themselves act as prodrugs of other compounds of formula (I).

Also included within the scope of the invention are metabolites of compounds of formula (I), that is, compounds formed in vivo upon administration of the drug. Some examples of metabolites in accordance with the invention include:

(i) Where the compound of formula (I) contains a methyl group, an hydroxymethyl derivative thereof;

(ii) Where the compound of formula (I) contains a tertiary amino group, a secondary amino derivative thereof;

(iii) Where the compound of formula (I) contains a secondary amino group, a primary derivative thereof;

(iv) Where the compound of formula (I) contains a phenyl moiety, a phenol derivative thereof.

Compounds of formula (I) containing one or more asymmetric carbon atoms can exist as two or more stereoisomers. Included within the scope of the present invention are all stereoisomers, geometric isomers and tautomeric forms of the compounds of formula (I), including compounds exhibiting more than one type of isomerism, and mixtures of one or more thereof. Also included is acid addition or base salts wherein the counter ion is optically active, for example, d-lactate or 1-lysine, or racemic, for example, dl-tartrate or dl-arginine. Conventional techniques for the preparation/isolation of individual enantiomers include chiral synthesis from a suitable optically pure precursor or resolution of the racemate (or the racemate of a salt or derivative) using, for example, chiral high-pressure liquid chromatography (HPLC).

Alternatively, the racemate (or a racemic precursor) may be reacted with a suitable optically active compound, for example, an alcohol, or, in the case where the compound of formula (I) contains an acidic or basic moiety, an acid or base such as tartaric acid or 1- phenylethylamine. The resulting diastereomeric mixture may be separated by chromatography and/or fractional crystallization and one or both of the diastereoisomers converted to the corresponding pure enantiomer(s) by means well known to a skilled person.

Chiral compounds of the invention (and chiral precursors thereof) may be obtained in enantiomerically-enriched form using chromatography, typically HPLC (chiral columns), on an asymmetric resin with a mobile phase consisting of a hydrocarbon, typically heptane or hexane, containing from 0 to 50% by volume of isopropanol, typically from 2% to 20%, and from 0 to 5% by volume of an alkylamine, typically 0.1% diethylamine. For reverse HPLC CH ₃ CN and H ₂ 0, MeOH or iPrOH and H ₂ 0 are used as solvents. Concentration of the eluate affords the enriched mixture.

Stereoisomeric conglomerates may be separated by conventional techniques known to those skilled in the art-see, for example, "Stereochemistry of Organic Compounds" by E. L. Eliel (Wiley, New York, 1994). "Chiral Separation Techniques", by G. Subramanian. John Wiley & Sons, 2008. "Preparative Enantioselective Chromatography" by G. B. Cox. Wiley, 2005.

Pharmaceutically acceptable solvates in accordance with the invention include those wherein the solvent of crystallization may be isotopically substituted, e.g. D ₂ 0.

The following examples illustrate the preparation of the compounds of the formula (I) and their pharmacological properties.

FIGURES:

Figure 1. Compound 5 displays the same secretory phenotype and senescence- inducing capacity as the knockdown of the NF-kB non-canonical pathway in different cancer cells.

A/B. mPvNA levels of EZH2 (A) or CDKN1A and IFNG (B) in A375 cells treated for

96 h with increasing concentrations of Compound 5. C. IFN-γ measured by ELISA in different cell lines treated with Compound 5 or DMSO for 96 h.

* p<0.05 against respective controls.

Figure 2. Compound 5 potentiates the anti-PDl immune response in Balb/c mice subcutaneously injected with CT26 colon-cancer cells.

A. Tumor progression in Balb/c mice subcutaneously injected with CT26 cells (0.5 x 10 ⁶ ). After 3 days, treatment with compound 5 (10 mg/kg) or DMSO was given by intraperitoneal injection every other day starting 3 days after the first injection. Two groups of mice (with either DMSO or compound 5 treatment) were treated with anti-PDl antibody injected subcutaneously every other day. Number of mice for each treatment group = 10.

B. Percentage of Cdl lC+ (Ml macrophages) and Cdl lC- (M2 macrophages) cells detected in the tumors using flow cytometry.

C. Percentage of CD40+ DCs measured by flow cytometry. D. Density of CD8+ CD3+ T-cells in tumors from different treatments measured by flow cytometry.

* p<0.05 against respective controls; # p<0.05 for double treatment against single treatment.

Figure 3. Compound 5 treatment is effective when used alone in reducing tumor growth in vivo and potentiates the anti-PDl immune response in C57B16 mice subcutaneously injected with B16 melanoma cells. B16 cells were injected subcutaneously and the tumors were let to grow until an average volume of 100 mm ³ was reached. The mice were then sorted into four groups with similar average tumor volume and standard deviation. Treatment with compound 5 (10 mg/kg) or control (DMSO) was given by intraperitoneal injection every day. Anti-PDl antibodies (125 μg/mouse) was given every other day alone or combined with daily injection of compound 5. Number of mice for each treatment group = 8.

A. Survival curves. *** p<0.001 against respective controls.

B. Evolution of tumor growth in mm ³ for each condition. Evolution in days in the abscissa.

EXAMPLES

Example 1: Preparations of compounds of the invention

1. General procedure for the preparation of compounds of formula 3 wherein R ₅ =

Re =H and X = CI

0.5 ml of hydrochloric acid 2M, 400mg (2mmol) of 4,7-dichloroquinoline and 2mmol of the amine of formula 4 are added in 15 ml of water. The solution is stirred under reflux for two hours. The colour of the reacting medium changes quickly. After two hours of reaction, the medium is cooled to room temperature. A precipitate corresponding to the expected product appears; it is isolated by filtration and does not require further purification. It is placed in a heat chamber at 60°C to eliminate residual water.

The following compounds 1 to 9 were prepared according to the procedure above:

1.1.

(4-((3,5-difluorophenyl)amino)-7-chloroquinolinium chloride (compound 1)

Formula: C15H10CI2N2F2

Exact Mass: 326.0189

Molecular Weight: 327.1558

R = 80 % 1H NMR (200 MHz, DMSO- 6); δ 14.85 (s, 1H), 11.18 (s, 1H), 8.82 (d, J = 9.2 Hz, 1H), 8.64 (d, J = 6.9 Hz, 1H), 8.17 (d, J = 2.1 Hz, 1H), 7.93 (dd, J = 9.2, 2.1 Hz, 1H), 7.43 - 7.24 (m, 3H), 7.10 (d, J= 6.9 Hz, 1H).

¹⁹ F NMR (188 MHz, DMSO- 6); δ 107.96.

1 ³ C NMR (126 MHz, DMSO- 6), δ 163.8 (d, J = 15 Hz), 161.9 (d, J = 15 Hz), 154.3,

143.9, 140.1 (t), 139.2, 138.5, 127.7, 126.3, 119.4, 116.3, 108.8 - 108.3 (2C), 102.7 (t), 101.5.

1.2.

4-((4-methylphenyl)amino)-7-chloroquinolinium chloride (compound 2)

Formula: C16H14CI2N2

Exact Mass: 304.0534

Molecular Weight: 305.2020

R = 81 %

1H NMR (200 MHz, DMSO- 6); δ 14.46 (s, 1H), 11.03 (s, 1H), 8.79 (d, J = 9.1 Hz, 1H), 8.50 (d, J = 7.0 Hz, 1H), 8.11 (d, J = 2.1 Hz, 1H), 7.89 (dd, J = 9.1, 2.1 Hz, 1H), 7.38 (d, J = 1.5 Hz, 4H), 6.73 (d, J = 7.0 Hz, 1H), 2.39 (s, 3H).

¹³ C NMR (50 MHz, DMSO- 6); δ 155.0, 143.3, 139.1, 138.3, 137.2, 134.3, 130.4 (2C), 127.3, 126.1, 125.4 (2C), 119.2, 115.8, 100.1, 20.7.

1.3.

4-((3-trifluoromethylphenyl)amino)-7-chloroquinolinium chloride (compound 3) Formula: C16H11CI2F3N2

Exact Mass: 358.0251

Molecular Weight: 359.1732

R = 83 %

1H NMR (200 MHz, DMSO- 6); δ 14.86 (s, 1H), 11.29 (s, 1H), 8.87 (d, J = 9.1 Hz, 1H), 8.60 (d, J = 6.9 Hz, 1H), 8.19 (d, J = 2.1 Hz, 1H), 7.97 - 7.75 (m, 5H), 6.91 (d, J = 6.9 Hz, 1H).

¹⁹ F NMR (188 MHz, DMSO- 6); δ -60.61, -61.13, -61.21, -61.30, -61.32, -62.06.

1 ³ C NMR (126 MHz, DMSO- 6); δ 154.7, 144.0, 139.2, 138.6, 138.1, 131.3, 130.5 (q), 129.3, 127.7, 126.1, 123.9 (d, J = 3.6 Hz), 123,8 (q, J = 272 Hz), 122.0 (d, J = 3.8 Hz), 119.5, 116.3, 100.7.

1.4.

4-((2-methylphenyl) amino)-7-chloroquinolinium chloride (compound 4)

Formula: C16H14CI2N2

Exact Mass: 304.0534 Molecular Weight: 305.2020

R = 76 %

1H NMR (200 MHz, DMSO- 6); δ 14.71 (s, 1H), 11.08 (s, 1H), 8.89 (d, J = 9.1 Hz, 1H), 8.48 (d, J = 7.0 Hz, 1H), 8.17 (d, J = 2.1 Hz, 1H), 7.89 (dd, J = 9.1, 2.1 Hz, 1H), 7.43 (m, 4H), 6.23 (d, J = 7.0 Hz, 1H), 2.21 (s, 3H).

¹³ C NMR (50 MHz, DMSO- 6); δ 155.4, 143.4, 138.9, 138.3, 135.2, 135.1, 131.6, 128.7, 127.6, 127.4, 127.3, 125.9, 119.2, 115.4, 99.9, 40.7, 40.3, 39.9, 39.7, 39.5, 39.0, 38.6, 38.2, 17.2.

1.5.

4-((4-methoxyphenyl)amino)-7-chloroquinolinium chloride (compound 5)

Formula: C16H14CI2N2O

Exact Mass: 320.0483

Molecular Weight: 321.2010

R = 77 %

1H NMR (200 MHz, DMSO- 6); δ 14.60 (s, 1H), 11.06 (s, 1H), 8.82 (d, J = 9.2 Hz,

1H), 8.49 (d, J = 7.0 Hz, 1H), 8.14 (d, J = 2.1 Hz, 1H), 7.87 (dd, J = 9.1, 2.1 Hz, 1H), 7.40 (d, J = 8.9 Hz, 2H), 7.13 (d, 2H), 6.65 (d, J = 7.0 Hz, 1H), 3.36 (s, 3H).

¹³ C NMR (50 MHz, DMSO- 6); δ 158.4, 155.3, 143.0, 138.9, 138.2, 129.3, 127.1, 127.1, 126.0, 119.1, 115.6, 115.1, 99.9, 55.4.

1.6.

4-((3-methoxyphenyl)amino)-7-chloroquinolinium chloride (compound 6)

Formula: C16H14CI2N2O

Exact Mass: 320.0483

Molecular Weight: 321.2010

R = 64 %

1H NMR (200 MHz, DMSO- 6); δ 14.80 (s, 1H), 11.18 (s, 1H), 8.87 (d, J = 9.1 Hz, 1H), 8.52 (d, J = 7.0 Hz, 1H), 8.18 (d, J = 2.1 Hz, 1H), 7.88 (dd, J = 9.2, 2.1 Hz, 1H), 7.49 (t, J = 8.3 Hz, 1H), 7.11 - 6.97 (m, 3H), 6.84 (d, J = 7.0 Hz, 1H), 3.80 (s, 3H).

¹³ C NMR (50 MHz, DMSO- 6); δ 160.3, 154.8, 143.3, 138.9, 138.3, 138.03, 130.7, 127.3, 126.1, 119.1, 117.3, 115.9, 113.2, 111.0, 100.5, 55.4.

1.7.

4-((4-hydroxyphenyl)amino)-7-chloroquinolinium chloride (compound 7)

Formula: C15H12CI2N2O

Exact Mass: 306.0327 Molecular Weight: 307.1740

R = 77 %

1H NMR (200 MHz, DMSO- 6); δ 14.71 (s, 1H), 11.04 (s, 1H), 9.96 (s, 1H), 8.83 (d, J = 9.2 Hz, 1H), 8.45 (d, J = 7.0 Hz, 1H), 8.15 (d, J = 2.1 Hz, 1H), 7.83 (dd, J = 9.1, 2.0 Hz, 1H), 7.25 (d, J = 8.6 Hz, 2H), 6.95 (d, J = 8.9 Hz, 2H), 6.61 (d, J = 7.0 Hz).

¹³ C NMR (50 MHz, DMSO- 6); δ 156.9, 155.3, 142.8, 138.8, 138.2, 127.6, 127.1 (3C), 125.9, 118.9, 116.4 (2C), 115.5, 99.8.

1.8.

4-((4-hydroxy-3-chlorophenyl)amino)-7-chloroquinolinium chloride (compound 8) Formula: Ci ₅ HiiCl ₃ N ₂ 0

Exact Mass: 339.9937

Molecular Weight: 341.6160

R = 85 %

1H NMR (200 MHz, DMSO- 6); δ 14.59 (s, 1H), 11.03 (s, 1H), 10.75 (s, 1H), 8.79 (d, J = 9.1 Hz, 1H), 8.50 (d, J = 7.0 Hz, 1H), 8.13 (d, J = 2.1 Hz, 1H), 7.87 (dd, J = 9.1, 2.1 Hz, 1H), 7.50 (d, J = 2.4 Hz, 1H), 7.27 (dd, J = 8.7, 2.4 Hz, 1H), 7.18 (d, J = 8.6 Hz, 1H), 6.69 (d, J = 7.0 Hz, 1H).

¹³ C NMR (50 MHz, DMSO- 6); δ 155.3, 152.7, 143.1, 138.8, 138.3, 128.4, 127.3, 127.2, 126.0, 125.7, 120.2, 119.1, 117.3, 115.6, 100.2.

1.9.

4-((4-trifluoromethylphenyl)amino)-7-chloroquinolinium chloride (compound 9)

Formula: Ci ₆ HnCl ₂ F ₃ N ₂

Exact Mass: 358.0251

Molecular Weight: 359.1732

R = 84 %

1H NMR (200 MHz, DMSO- 6); δ 14.86 (s, 1H), 11.26 (s, 1H), 8.86 (d, J = 9.1 Hz, 1H), 8.62 (d, J = 6.9 Hz, 1H), 8.17 (d, J = 2.1 Hz, 1H), 8.00 - 7.87 (two overlapping d, 3H), 7.74 (d, J = 8.3 Hz, 2H), 7.05 (d, J = 7.0 Hz, 1H).

¹⁹ F NMR (188 MHz, DMSO- 6); δ -60.81.

1 ³ C NMR (50 MHz, DMSO- 6); δ 154.3, 143.8, 141.0, 139.1, 138.5, 127.6, 126.9 (4C),

126.2, 125.3 (2C), 119.3, 116.4, 101.0.

1.10

7-chloro- V-(4-(difluoromethoxy)phenyl)quinolin-4-amine (compound 34)

Chemical Formula: Ci ₆ HnClF ₂ N ₂ 0 Exact Mass: 320,05

Molecular Weight: 320,72

R = 87%

1H NMR (200 MHz, DMSO- 6) δ 11.25 (s, 1H), 8.89 (d, J = 9.2 Hz, 1H), 8.53 (d, J = 7.0 Hz, 1H), 8.18 (d, J= 2.1 Hz, 1H), 7.88 (dd, J= 9.1, 2.1 Hz, 1H), 7.71 (s, OH), 7.56 (d, J = 8.9 Hz, 2H), 7.43 - 7.32 (m, 2H), 6.98 (s, OH), 6.75 (d, J= 7.0 Hz, 1H).

¹³ C NMR (101 MHz, DMSO- 6) δ 155.2, 149.8, 143.7, 139.1, 138.7, 134.0, 127.6, 127.5, 126.2, 120.4, 119.4, 116.4 (t, J= 258.5 Hz), 116.0, 100.4.

MS: ESI (m/z): [M+H] ⁺ calcd for C _I6 H _{I I} C1F ₂ N ₂ 0 321.05 found 321.27

HPLC: Purity λ ₂₅₄ : 99.8%, tR: 3.23

1.11

7-chloro- V-(4-methoxy-3-(2-methoxyethoxy)phenyl)quinolin-4-amine (compound

35)

Chemical Formula: Ci ₉ Hi ₉ Cl ₂ 0 ₃

Exact Mass: 358,11

Molecular Weight: 358,82

R = 75%

1H NMR (500 MHz, DMSO- 6) δ 14.48 (s, 1H), 10.95 (s, 1H), 8.77 (d, J = 9.1 Hz, 1H), 8.48 (d, J= 7.0 Hz, 1H), 8.11 (d, J= 2.1 Hz, 1H), 7.86 (dd, J= 9.0, 2.1 Hz, 1H), 7.13 (d, J = 8.5 Hz, 1H), 7.09 (d, J = 2.4 Hz, 1H), 7.00 (dd, J = 8.4, 2.4 Hz, 1H), 6.73 (d, J = 7.0 Hz, 1H), 4.09 (t, J= 4.5 Hz, 2H), 3.83 (s, 3H), 3.67 (d, J= 4.7 Hz, 2H), 3.31 (s, 2H).

¹³ C NMR (50 MHz, DMSO- 6) δ 155.2, 148.6, 148.2, 142.9, 138.9, 138.2, 129.4, 127.1, 126.1, 119.0, 117.9, 115.6, 112.4, 1 10.8, 100.2, 70.2, 67.8, 58.2, 55.7, 40.7, 40.3, 39.9, 39.5, 39.0, 38.6, 38.2.

MS: ESI (m/z): [M+H] ⁺ calcd for Ci ₉ Hi ₉ ClN ₂ 0 ₃ 359,11 found 359.20

HPLC: Purity λ ₂₅₄ : 100%, tR: 3.41

1.12

7-chloro- V-(3,4-dimethoxyphenyl)quinolin-4-amine (compound 38)

Chemical Formula: Ci ₇ Hi ₅ Cl ₂ 0 ₂

Exact Mass: 314,08

Molecular Weight: 314,77

R = 59%

1H NMR (500 MHz, DMSO- 6) δ 14.52 (s, 1H), 10.96 (s, 1H), 8.78 (d, J = 9.1 Hz, 1H), 8.48 (d, J= 7.0 Hz, 1H), 8.12 (d, J= 2.2 Hz, 1H), 7.86 (dd, J= 9.1, 2.2 Hz, 1H), 7.13 (d, J = 8.6 Hz, 1H), 7.08 (d, J = 2.4 Hz, 1H), 7.00 (dd, J = 8.5, 2.4 Hz, 1H), 6.73 (d, J = 7.0 Hz, 1H), 3.82 (s, 3H), 3.78 (s, 3H).

¹³ C NMR (50 MHz, DMSO- 6) δ 155.2, 149.4, 148.1, 142.9, 138.9, 138.2, 129.5,

127.1, 126.1, 119.0, 117.7, 115.6, 112.2, 109.7, 100.2, 55.7, 40.7, 40.3, 39.9, 39.5, 39.0, 38.6, 38.2.

MS: ESI (m/z): [M+H] ⁺ calcd for Ci ₇ Hi ₅ ClN ₂ 0 ₂ 315.08 found 315.13

HPLC: Purity λ ₂₅₄ : 100%, tR: 3.37

1.13

7-chloro- V-(2,4-dimethoxyphenyl)quinolin-4-amine (compound 39)

Chemical Formula: Ci ₇ Hi ₅ ClN ₂ 0 ₂

Exact Mass: 314,08

Molecular Weight: 314,77

1H NMR (200MHz, DMSO- 6) δ: 14.70 (br, 1H), 10.87 (s, 1H), 8.86 (d, J = 9.2 Hz, 1H), 8.45 (d, J= 7.0 Hz, 1H), 8.20 (d, J= 2.1 Hz, 1H), 7.83 (dd, J= 9.0, 2.1 Hz, 1H), 7.30 (d, J = 8.6 Hz, 1H), 6.81 (d, J = 2.5 Hz, 1H), 6.68 (dd, J = 8.7, 2.6 Hz, 1H), 6.27 (d, J = 7.0 Hz, 1H), 3.84 (s, 3H), 3.77 (s, 3H).

¹³ C NMR (50MHz, DMSO- 6) δ: 160.4, 155.8, 155.3 142.7, 138.9, 138.2, 128.8,

127.2, 126.0, 119.2, 117.4, 115.4, 105.6, 100.6, 99.8, 55.9, 55.6.

MS: ESI (m/z): [M+H] ⁺ calcd for Ci ₇ Hi ₅ ClN ₂ 0 ₂ 315.08 found 315.20

HPLC: Purity λ ₂₅₄ : 99.6%, tR: 3.49

1.14

7-chloro-N-(2,3-dihydrobenzo[b] [l,4]dioxin-6-yl)quinolin-4-amine (compound 40)

Chemical Formula: Ci ₇ Hi ₃ Cl ₂ 0 ₂

Exact Mass: 312,06

Molecular Weight: 312,75

R = 32%

1H NMR (400 MHz, DMSO- 6) δ 11.02 (s, 1H), 8.83 (d, J = 9.1 Hz, 2H), 8.48 (d, J = 7.0 Hz, 2H), 8.16 (d, J= 2.2 Hz, 2H), 7.83 (dd, J= 9.1, 2.1 Hz, 2H), 7.03 (d, J= 8.6 Hz, 2H), 6.99 (d, J= 2.4 Hz, 2H), 6.92 (dd, J= 8.5, 2.5 Hz, 2H), 6.71 (d, J= 6.9 Hz, 2H), 4.30 (s, 9H).

¹³ C NMR (101 MHz, DMSO) δ 155.1, 144.0, 143.4, 142.8, 139.3, 138.2, 130.0, 127.1, 126.1, 119.4, 118.6, 118.0, 115.8, 114.5, 100.2, 64.2, 64.1, 39.5.

MS: ESI (m/z): [M+H] ⁺ calcd for Ci ₇ Hi ₃ ClN ₂ 0 ₂ 313.06 found 313.24 HPLC: Purity λ ₂₅₄ : 100%, tR: 3.09

1.15

N-(benzo[d] [l,3]dioxol-5-yl)-7-chloroquinolin-4-amine (compound 41)

Chemical Formula: Ci ₆ HnCl ₂ 0 ₂

Exact Mass: 298,05

Molecular Weight: 298,72

1H NMR (400 MHz, DMSO-d ₆ ) δ 14.78 (s, 1H), 11.09 (s, 1H), 8.84 (d, J= 9.1 Hz, 1H), 8.49 (d, J = 7.0 Hz, 1H), 8.17 (d, J = 2.1 Hz, 1H), 7.85 (dd, J = 9.1 , 2.1 Hz, 1H), 7.10 (d, J = 3.9 Hz, 1H), 7.08 (d, J= 2.2 Hz, 1H), 6.94 (dd, J= 8.2, 2.1 Hz, 1H), 6.70 (d, J= 7.0 Hz, 1H), 6.14 (s, 2H).

¹³ C NMR (101 MHz, DMSO) δ 155.4, 148.3, 146.7, 143.2, 139.0, 138.3, 130.6, 127.2, 126.1, 119.3, 119.2, 115.7, 108.9, 107.0, 101.9, 100.3, 39.5.

MS: ESI (m/z): [M+H] ⁺ calcd for C _I6 H _{I I} C1N ₂ 0 ₂ 299.05 found 299.18

HPLC: Purity λ ₂₅₄ : 99.0, tR: 3.21

2. General procedure for the preparation of compounds of formula 3 wherein R ₅ is O-alkyl, 0-(CH ₂ ) _n i-(cyclic radical), (CH ₂ )„i-(cyclic radical), ni being 1 to 4, said cyclic radical being chosen from and ¾ , Rg = H and X = CI.

To a solution of compound of formula 6 (leq) in THF was added slowly sodium methoxide (2eq) or NaH (2eq) follow by the addition of 2-morpholinoethan-l-ol (2eq). The resulting mixture was stirred at reflux until reaction completion, as monitored by TLC. After cooling to r.t, the crude mixture was adsorbed on silica and purified on a column chromatography using methanol/dichloromethane as the eluent (gradient 0/100 to 5/95, v/v).

The following compounds 27 to 33 were prepared according to the procedure above.

2.1

7-chloro-2-methoxy-N-(4-methoxyphenyl)quinolin-4-amine (compound 27)

Chemical Formula: Ci ₇ Hi ₅ Cl ₂ 0 ₂

Exact Mass: 314,08

Molecular Weight: 314,77

R = 37% 1H NMR (200 MHz, DMSO- 6) δ 8.82 (s, 1H), 8.30 (d, J = 8.9 Hz, 1H), 7.66 (d, J = 2.2 Hz, 1H), 7.40 (dd, J= 8.9, 2.3 Hz, 1H), 7.26 (d, J= 8.9 Hz, 2H), 7.01 (d, J= 8.9 Hz, 2H), 5.96 (s, 1H), 3.85 (s, 3H), 3.78 (s, 3H).

¹³ C NMR ¹³ C NMR (50 MHz, DMSO- 6) δ 164.2, 156.5, 151.3, 148.0, 134.1, 132.4, 125.8, 123.9, 122.6, 116.3, 114.6, 88.6, 55.2, 52.7.

MS: ESI (m/z): [M+H] ⁺ calcd for Ci ₇ Hi ₅ ClN ₂ 0 ₂ 315.08 found 315.20

HPLC: Purity λ ₂₅₄ : 97.7%, tR: 3.74

2.2

7-chloro-N-(3,4-dimethoxyphenyl)-2-methoxyquinolin-4-amine (compound 33) Chemical Formula: Ci ₈ Hi ₇ ClN ₂ 0 ₃

Exact Mass: 344,09

Molecular Weight: 344,80

R = 34%

1H NMR (200 MHz, DMSO- 6) δ 8.80 (s, 1H), 8.28 (d, J = 8.9 Hz, 1H), 7.64 (d, J = 2.2 Hz, 1H), 7.38 (dd, J= 8.8, 2.3 Hz, 1H), 6.99 (d, J= 8.5 Hz, 1H), 6.93 - 6.81 (m, 2H), 6.04 (s, 1H), 3.84 (s, 3H), 3.76 (s, 3H), 3.73 (s, 3H).

¹³ C NMR (50 MHz, DMSO- 6) δ 164.2, 151.1, 149.3, 148.0, 146.1, 134.1, 132.8, 125.8, 123.9, 122.6, 116.3, 116.2, 112.3, 108.9, 88.9, 55.7, 55.5, 52.7.

MS: ESI (m/z): [M+H] ⁺ calcd for Ci ₈ Hi ₇ ClN ₂ 0 ₃ 345.09 found 345.20

HPLC: Purity λ ₂₅₄ : 97.2%, tR: 3.57

2.3

7-chloro-N-(3,4-dimethoxyphenyl)-2-(2-morpholinoethoxy)quino lin-4-amine (compound 32)

Chemical Formula: C ₂₃ H ₂₆ CrN ₃ 0 ₄

Exact Mass: 443,16

Molecular Weight: 443,93

R = 37%

1H NMR (200 MHz, DMSO- 6) δ 8.83 (s, 1H), 8.29 (d, J = 9.0 Hz, 1H), 7.63 (d, J = 2.2 Hz, 1H), 7.40 (dd, J= 8.9, 2.2 Hz, 1H), 7.02 (d, J= 8.5 Hz, 1H), 6.92 (d, J= 2.3 Hz, 1H), 6.87 (dd, J= 8.3, 2.4 Hz, 1H), 5.99 (s, 1H), 4.40 (t, J= 5.8 Hz, 2H), 3.78 (s, 3H), 3.75 (s, 2H), 3.54 (t, J= 4.7 Hz, 5H), 2.63 (t, J= 5.8 Hz, 2H), 2.46 - 2.35 (m, 4H).

¹³ C NMR (50 MHz, DMSO- 6) δ 163.8, 151.4, 149.3, 147.9, 146.2, 134.2, 132.7, 125.8, 123.9, 122.6, 116.5, 116.2, 112.3, 109.2, 89.0, 66.1, 62.3, 56.9, 55.6, 55.5, 53.5.

MS: ESI (m/z): [M+H] ⁺ calcd for C ₂₃ H ₂₆ C1N ₃ 0 ₄ 444.16 found 444.0 HPLC: Purity λ ₂₅₄ : 99.5%, tR: 3.12

3. General procedure for the preparation of compounds of formula 3 wherein R ₅ is cyclic radical chosen from and ^ « , R^H and X = CI.

A solution of compound of formula 6 (leq) was stirred in morpholine (or N- methylpiperazine) 0.5 mmol/mL at 90°C until reaction completion, as monitored by TLC. After cooling to room temperature, the crude mixture is adsorbed on silica and purified on a column using methanol/dichloromethane as the eluent (gradient 0/100 to 5/95, v/v).

The following compounds 28 to 31 were prepared according to the general procedure described above.

3.1

7-chloro-N-(4-methoxyphenyl)-2-morpholinoquinolin-4-amine (compound 30)

Chemical Formula: C ₂ oH ₂ oCl ₃ 0 ₂

Exact Mass: 369,12

Molecular Weight: 369,85

1H NMR (200 MHz, DMSC /6) δ 8.60 (s, 1H), 8.16 (d, J = 8.9 Hz, 1H), 7.46 (d, J = 2.2 Hz, 1H), 7.27 (d, J= 8.9 Hz, 1H), 7.19 (dd, J= 8.8, 2.2 Hz, 1H), 7.04 - 6.95 (m, 2H), 6.24 (s, 1H), 3.77 (s, 3H), 3.64 (t, J= 4.7 Hz, 4H), 3.43 (d, J= 4.9 Hz, 4H).

¹³ C NMR (50 MHz, DMSC /6) δ 159.1, 156.0, 149.8, 149.2, 133.8, 132.9, 125.2, 125.0, 123.7, 120.6, 114.6, 114.6, 86.6, 66.0, 55.2, 44.8.

MS: ESI (m/z): [M+H] ⁺ calcd for C ₂₀ H ₂₀ CIN ₃ O ₂ 370.12 found 370.27

HPLC: Purity λ ₂₅₄ : 98.2%, tR: 3.36

3.2

7-chloro-N-(3,4-dimethoxyphenyl)-2-morpholinoquinolin-4-amin e (compound 28)

Chemical Formula: C ₂ iH ₂₂ Cl ₃ 0 ₃

Exact Mass: 399,13

Molecular Weight: 399,88

R = 56%

1H NMR (200 MHz, DMSC /6) δ 8.62 (s, 1H), 8.16 (d, J = 8.9 Hz, 1H), 7.47 (d, J = 2.2 Hz, 1H), 7.19 (dd, J = 8.8, 2.2 Hz, 1H), 7.04 - 6.93 (m, 2H), 6.86 (dd, J = 8.4, 2.3 Hz, 1H), 6.37 (s, 1H), 3.76 (s, 3H), 3.74 (s, 3H), 3.65 (t, J= 4.6 Hz, 4H), 3.45 (d, J= 4.8 Hz, 4H). ¹³ C NMR ¹³ C NMR (50 MHz, DMSO- 6) δ 159.1, 149.5, 149.3, 149.2, 145.5, 133.8, 133.3, 125.0, 123.7, 120.6, 115.2, 114.6, 112.3, 108.0, 87.1, 66.0, 55.6, 55.5, 44.8.

MS: ESI (m/z): [M+H] ⁺ calcd for C ₂₁ H ₂₂ CIN ₃ O ₃ 400.13 found 400.27

HPLC: Purity λ ₂₅₄ : 98.2%, tR: 3.36

3.3

7-chloro-N-(4-methoxyphenyl)-2-(4-methylpiperazin-l-yl)quino lin-4-amine

(compound 31)

Chemical Formula: C ₂ iH ₂₃ ClN ₄ 0

Exact Mass: 382,16

Molecular Weight: 382,89

R = 57%

1H NMR (200 MHz, DMSO- 6) δ 8.56 (s, 1H), 8.14 (d, J = 8.9 Hz, 1H), 7.44 (d, J = 2.2 Hz, 1H), 7.26 (d, J= 8.7 Hz, 2H), 7.17 (dd, J= 8.8, 2.2 Hz, 1H), 6.99 (d, J= 8.8 Hz, 2H), 6.24 (s, 1H), 3.77 (s, 3H), 3.46 (d, J= 4.7 Hz, 4H), 2.34 (d, J= 5.0 Hz, 4H), 2.17 (s, 3H).

1 ³ C NMR (50 MHz, DMSO- 6) δ 158.9, 156.0, 149.7, 149.4, 133.8, 132.9, 125.1,

124.9, 123.6, 120.4, 114.6, 114.4, 86.8, 55.2, 54.4, 45.7, 44.3.

MS: ESI (m/z): [M+H] ⁺ calcd for C ₂ iH ₂₃ ClN ₄ 0383.16 found 383.20

HPLC: Purity λ ₂₅₄ : 99.5%, tR: 2.76

3.4

7-chloro-N-(3,4-dimethoxyphenyl)-2-(4-methylpiperazin-l-yl)q uinolin-4-amine (compound 29)

Chemical Formula: C ₂₂ H ₂₅ C1N ₄ 0 ₂

Exact Mass: 412,17

Molecular Weight: 412,92

R = 58%

1H NMR (200 MHz, DMSO- 6) δ 8.58 (s, 1H), 8.14 (d, J = 8.9 Hz, 1H), 7.45 (d, J = 2.2 Hz, 1H), 7.17 (dd, J = 8.8, 2.2 Hz, 1H), 7.04 - 6.93 (m, 2H), 6.86 (dd, J = 8.4, 2.3 Hz, 1H), 6.39 (s, 1H), 3.76 (s, 3H), 3.74 (s, 3H), 3.48 (t, J= 4.7 Hz, 4H), 2.35 (d, J= 4.9 Hz, 4H), 2.17 (s, 3H).

1 ³ C NMR (50 MHz, DMSO- 6) δ 158.8, 156.1, 149.4, 149.1, 145.4, 133.8, 133.4,

124.9, 123.6, 120.4, 115.1, 114.5, 112.4, 107.9, 87.3, 55.6, 55.4, 54.4, 45.7, 44.3.

MS: ESI (m/z): [M+H] ⁺ calcd for C ₂₂ H ₂₅ C1N ₄ 0 ₂ 413.17 found 413.13

HPLC: Purity λ ₂₅₄ : 98.8%, tR: 2.71 4. General procedure for the preparation of compounds of formula 3 wherein R ₅ = R-2 ⁼ H, K(, ⁼ CI.

The following compounds were prepared using the same procedures as compound of formula (3), or alternatively by microwave irradiation at 80°C for lh of a mixture of 4,6- dichloroquinoline and amine in ethanol. Then, after cooling at r.t ethyl acetate was added and the resulting precipitate was collected, wash with ethyl acetate and diethyl ether to afford pure product without any further purifications.

The following compounds 36 to 37 were prepared according to the procedure above. 4.1

6-chloro- V-(2,4-dimethoxyphenyl)quinolin-4-amine (compound 37)

Chemical Formula: C ₁₇ H ₁₅ CI ₂ O ₂

Exact Mass: 314,08

Molecular Weight: 314,77

R = 58%

1H NMR (200MHz, CDC1 ₃ ) δ 14.90 (br, 1H), 10.47 (s, 1H), 9.19 (d, J = 2.0 Hz, 1H), 8.19 (d, J = 9.0 Hz, 1H), 7.98 (d, J = 6.9 Hz, 1H), 7.57 (dd, J = 9.0, 1.9 Hz, 1H), 7.30-7.26 (m, 1H), 6.39-6.34 (m, 2H), 6.22 (d, J= 6.9 Hz, 1H), 3.74 (s, 3H), 3.64 (s, 3H).

¹³ C NMR (50MHz, CDC1 ₃ ) δ 160.8, 155.5, 155.3, 140.4, 137.0, 133.8, 132.9, 128.7, 123.9, 122.3, 118.3, 117.7, 105.2, 100.6, 99.6, 55.7.

MS: ESI (m/z): [M+H] ⁺ calcd for Ci ₇ Hi ₅ ClN ₂ 0 ₂ 315.77 found 315.13

HPLC: Purity λ ₂₅₄ : 100%, tR: 3.52

4.2

6-chloro- V-(4-(trifluoromethoxy)phenyl)quinolin-4-amine (compound 36)

Chemical Formula: Ci ₆ Hi ₀ ClF ₃ N ₂ O

Exact Mass: 338,04

Molecular Weight: 338,71

R = 71%

1H NMR (200 MHz, DMSC /6) δ 15.22 (s, 1H), 11.33 (s, 1H), 9.13 (d, J = 2.1 Hz, 1H), 8.55 (d, J= 6.9 Hz, 1H), 8.19 (d, J= 9.0 Hz, 1H), 8.06 (dd, J= 9.1, 2.0 Hz, 1H), 7.61 (q, J= 8.9 Hz, 4H), 6.88 (d, J= 6.9 Hz, 1H).

¹³ C NMR (101 MHz, DMSC /6) δ 154.1, 146.7, 143.1, 137.0, 136.3, 134.0, 131.7, 127.2, 123.4, 122.5, 122.4, 120.0 (q, J= 256.7 Hz), 118.3, 100.5.

MS: ESI (m/z): [M+H] ⁺ calcd for C _I6 H _IO C1F ₃ N ₂ 0 339.04 found 339.27 HPLC: Purity λ ₂₅₄ : 99.8%, tR: 3.96

Example 2: Preparations of compounds of formula 2 1. General procedure for the preparation of compounds of formula 2 wherein R ₅ =

100 mg of the compound of formula 3, 1.2 equivalents of the amine of formula 5, 2% molar of [Pd(acac)(IPr*)Cl] and 3 equivalents of tBuOK are placed in a screw cap vial fitted with a septum, under an argon atmosphere before adding 1ml of degassed 1,4-dioxane. The reacting medium is heated at 110°C for 24hours. Upon return to room temperature, the crude mixture is adsorbed on silica and purified on a column using methanol/dichloromethane as the eluent (gradient 0/100 to 5/95, v/v).

The following compounds 10, 12-13, 16, 18-19, 23, 25 and 26 were prepared according to the general procedure described above.

1.1

N-(3,5-difluorophenyl)-7-morpholinoquinolin-4-amine (compound 10)

Formula: Ci ₉ Hi ₇ F ₂ N ₃ 0

Exact Mass: 341.1340

Molecular Weight: 341.3618

R = 46 %

1H NMR (200 MHz, DMSO- 6); δ 9.14 (br, 1H), 8.45 (d, J = 5.2 Hz, 1H), 8.13 (d, J = 9.3 Hz, 1H), 7.43 (dd, J = 9.3, 2.6 Hz, 1H), 7.16 (d, J = 2.5 Hz, 1H), 7.06-6.92 (m, 3H), 6.82 (tt, J = 9.3, 2.3 Hz, 1H), 3.79 (t, J = 4.5 Hz, 4H), 3.29 (t, J = 4.5 Hz, 4H).

¹³ C NMR (50 MHz, DMSO- 6); δ 165.6-165.2 (d), 160.7-160.4 (d), 151.7, 150.5, 150.4, 145.3, 122.8, 116.6, 113.9, 109.6, 102.7 (2C), 102.1, 96.9 (t, J = 26,2 Hz, 2C), 65.9 (2C), 47.9 (2C).

¹⁹ F NMR (188 MHz, DMSO- 6); δ -109.35, -109.40, -109.44.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C^H^NsC), 342.1340; found : 342.1416.

1.2.

N-(o-tolyl)-7-morpholinoquinolin-4-amine (compound 12)

Formula: C _2O H _2I N _B O

Exact Mass: 319.1685

Molecular Weight: 319.4080

R = 60 % 1H NMR (200 MHz, CDC1 ₃ ); δ 8.38 (d, J = 5.4 Hz, 1H), 7.85 (d, J = 9.2 Hz, 1H), 7.38 (d, J = 2.4 Hz, 1H), 7.36-7.19 (m, 5H), 6.47 (s, 1H), 6.33 (d, J = 5.4 Hz, 1H), 3.92 (t, J = 4.7 Hz, 4H), 3.34 (d, J = 4.9 Hz, 4H), 2.27 (s, 3H).

¹³ C NMR (50 MHz, CDC1 ₃ ); δ 152.2, 150.2 149.6, 148.9, 137.8, 133.8, 131.5, 127.3, 126.4, 125.8, 121.1, 116.9, 112.9, 110.7, 100.4, 66.8 (2C), 48.9 (2C), 17.9.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C ₂ oH ₂ 2N ₃ 0, 320.1760; found : 320.1757.

1.3.

V-(4-methoxyphenyl)-7-morpholinoquinolin-4-amine (compound 13)

Formula: C ₂ oH ₂ iN ₃ 0 ₂

Exact Mass: 335.1634

Molecular Weight: 335.4070

R = 68 %

1H NMR (200 MHz, CDC1 ₃ ); δ 8.38 (d, J = 5.6 Hz, 1H), 7.80 (d, J = 8.9 Hz, 1H), 7.34 - 7.21 (m, 4H), 6.97 (d, J = 8.6 Hz, 2H), 6.55 (d, J = 5.5 Hz, 1H), 3.92 (t, J = 4.7 Hz, 4H), 3.85 (s, 3H), 3.33 (t, J = 4.8 Hz, 4H).

¹³ C NMR (50 MHz, DMSO- 6); δ 156.1, 151.4, 150.4, 150.2, 148.6, 133.0, 125.3, 122.6, 115.8, 114.5 (2C), 112.7, 109.8 (2C), 98.6, 65.9 (2C), 55.2 (2C), 48.0.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C ₂₀ H ₂₂ N ₃ O ₂ 336.1709; found : 336,1706.

1.4.

TV ⁴ , V ⁷ -bis(4-methoxyphenyl)quinolin-4,7-diamine (compound 16)

Formula: C ₂₃ H ₂ iN ₃ 0 ₂

Exact Mass: 371.1634

Molecular Weight: 371.4400

R = 17 %

1H NMR (500 MHz, MeOD); δ 8.10 (d, J = 9.2 Hz, 1H), 8.02 (d, J = 6.2 Hz, 1H), 7.28 -

7.23 (m, 2H), 7.23-7.19 (m, 2H), 7.16 (dd, J = 9.2, 2.2 Hz, 1H), 7.11 (d, J = 2.3 Hz, lH),7.03-6.98 (m, 2H), 6.96-6.92 (m, 2H), 6.42 (d, J = 6.2 Hz, 1H), 3.83 (s, 3H), 3.80 (s, 3H).

¹³ C NMR (126 MHz, MeOD); δ 159.9, 158.1, 154.3, 151.1, 148.0, 147.2, 135.8, 133.4, 128.1 (2C), 125.1 (2C), 124.6, 118.9, 116.3 (2C), 116.2 (2C), 112.7, 103.4, 99.7, 56.1, 56.4.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C ₂₃ H ₂₂ N ₃ 0 ₂ , 372.1709 ; found : 372.1706.

1.5.

N ⁴ -(3,5-difluorophenyl)-N ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 18)

Formula: C ₂₂ Hi ₇ F ₂ N ₃ 0 Exact Mass: 377.1340

Molecular Weight: 377.3948

R = 24 %

1H NMR (200 MHz, DMSO- 6); δ 9.30 (br s, 1H), 8.41 (s, 1H), 8.37 (d, J = 5.3 Hz, 1H), 8.08 (d, J = 8.9 Hz, 1H), 7.22 (d, J = 3.2 Hz, 2H), 7.20-7.14 (m, 2H), 6.99 (d, J = 3.2 Hz, 2H), 6.96-6.90 (m, 3H), 6.82 (tt, J = 9.4, 2.3 Hz, 1H), 3.75 (s, 3H).

1 ⁹ F NMR (188 MHz, DMSO- 6); δ -109.62, -109.67, -109.72.

¹³ C NMR (50 MHz, DMSO- 6); δ 165.6, 160.7, 154.7, 150.4, 149.9, 146.72, 145.7, 134.6, 123.2, 121.9 (2C), 117.2, 114.6 (2C), 113.5, 106.3 (2C), 102.7, 102.3, 102.1, 96.8, 55.2.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C ₂₂ Hi ₈ F ₂ N30, 378.1412; found : 378.1415.

1.6.

2-chloro-4-((4-((3,5-difluorophenyl)amino)quinolin-7-yl)amin o)phenol (compound

19)

Formula: C _2I H _I4 C1F ₂ N ₃ 0

Exact Mass: 397.0793

Molecular Weight: 397.8098

R = 65 %

1H NMR (500 MHz, DMSO- 6); δ 9.90 (s, 1H), 9.09 (s, 1H), 8.39 (s, 1H), 8.37 (s, 1H), 8.07 (d, J = 9.1 Hz, 1H), 7.22 (d, J = 2.4 Hz, 1H), 7.19 (d, J = 2.6 Hz, 1H), 7.16 (dd, J = 9.2, 2.5 Hz, 1H), 7.07 (dd, J = 8.7, 2.7 Hz, 1H), 7.00 - 6.91 (m, 4H), 6.80 (tt, J = 9.6, 2.6 Hz, 1H).

¹³ C NMR (126 MHz, DMSO- 6) δ 164.1, 163.9, 162.2, 162.1, 153.1, 150.8, 148.4, 146.2, 134.3, 133.1, 123.4, 122.9, 122.9, 121.7, 120.7, 119.8, 117.4, 117.3, 115.8, 115.8, 113.9, 113.5, 107.4, 102.6, 102.5, 102.2, 97.0, 97.0, 96.8, 96.6.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C _2I H _{I 5} C1F ₂ N ₃ 0, 398.0866; found : 398.0866.

1.7.

V ⁴ -(o-tolyl)- V ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 23)

Formula: C ₂₃ H ₂ iN ₃ 0

Exact Mass: 355.1685

Molecular Weight: 355.4410

R = 88 %

1H NMR (200 MHz, CDC1 ₃ ); δ 8.35 (d, J = 5.5 Hz, 1H), 7.87 (d, J = 9.0 Hz, 1H), 7.62 (d, J = 2.4 Hz, 1H), 7.36-7.13 (m, 6H), 6.82 (ddd, J = 7.9, 2.0, 0.7 Hz, 1H), 6.77 (t, J = 2.2 Hz, 1H), 6.58 (ddd, J = 8.1, 2.3, 0.7 Hz, 1H), 6.31 (d, J = 5.4 Hz, 1H), 6.19 (s, 1H), 3.80 (s, 3H), 2.27 (s, 3H).

¹³ C NMR (126 MHz, MeOD); 162.6, 157.9, 151.94, 150.3, 149.5, 142.9, 136.3, 131.6, 124.8 (2C), 124.3, 118.9, 116.9, 116.1 (2C), 114.1, 11 1.7, 110.5, 105.7, 101.0, 56.4, 56.2.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C23H22N3O, 356.1757, found : 356.1764.

1.8.

V ⁴ -(3-methoxyphenyl)- V ⁷ -(4-methoxyphenyl)quinolin-4,7-diamine (compound 25)

Formula: C23H21N3O2

Exact Mass: 371.1634

Molecular Weight: 371.4400

R = 58 %

1H NMR (500 MHz, MeOD); δ 8.14 (d, J = 5.8 Hz, 1H), 8.09 (d, J = 9.1 Hz, 1H), 7.32 (t, J = 8.1 Hz, 1H), 7.24 - 7.20 (m, 2H), 7.19 (d, J = 2.3 Hz, 1H), 7.16 (dd, J = 9.1, 2.4 Hz, 1H), 6.96 - 6.92 (m, 3H), 6.91 (t, J = 2.2 Hz, 1H), 6.77 (ddd, J = 8.3, 2.5, 0.9 Hz, 1H), 6.75 (d, J = 5.9 Hz, 1H), 3.81 (s, 3H), 3.80 (s, 3H).

¹³ C NMR (126 MHz, MeOD); δ 162.6, 157.9, 151.9, 150.28, 149.5, 142.9, 136.3, 131.6, 124.8 (2C), 124.3, 118.9, 116.9, 116.1 (2C), 114.1, 111.7, 110.5, 105.7, 101.0, 56.4, 56.2.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C23H22N3O2, 372.17093, found : 372.17065.

1.9

V ⁴ -(3,5-difluorophenyl)- V ⁷ -(3-methoxyphenyl)quinolin-4,7-diamine (compound 26)

Formula: C22H17F2N3O

Exact Mass: 377.1340

Molecular Weight: 377.3948

R = 23 %

1H NMR (500 MHz, MeOD); δ 8.32 (d, J = 5.4 Hz, 1H), 8.05 (d, J = 9.1 Hz, 1H), 7.52

(d, J = 2.3 Hz, 1H), 7.27 (dd, J = 9.1, 2.4 Hz, 1H), 7.21 (t, J = 8.1 Hz, 1H), 6.98 (d, J = 5.5 Hz, 1H), 6.94 - 6.89 (m, 2H), 6.85 (ddd, J = 8.0, 2.1 , 0.9 Hz, 1H), 6.83 (t, J = 2.2 Hz, 1H), 6.62 (tt, J = 9.2, 2.3 Hz, 1H), 6.56 (ddd, J = 8.2, 2.5, 0.9 Hz, 1H), 3.79 (s, 3H).

¹³ C (126 MHz, MeOD): δ 165.19 (dd, J = 245, 15 Hz), 162.2, 151.4 , 151.0 , 148.9 , 147.5 , 145.5 (t, J = 13 Hz), 144.7 , 131.0 , 123.8 , 119.7, 115.6, 112.8, 109.1, 108.4, 106.0, 104.6 (dd, J = 14, 7 Hz), 103.0 , 98.8 (t, J = 26 Hz), 55.6.

HRMS-ESI (m/z) : [M+H] ⁺ calcd for C ₂ 2Hi ₈ F ₂ N ₃ 0, 378.1412; found : 378.1414.

HPLC: Purity λ ₂₅₄ : 96%, tR: 3.94 Example 3: In vitro activity of the compounds of the invention

3.1 Ability to decrease EZH2 mRNA level in A375 (determination of dose- response)

Typically, 30000-50000 cells were plated in six-well culture plates and incubated 24 h later with increasing concentration of NIK inhibitors or vehicle. Cells were incubated with the inhibitors for 4 days prior to harvesting for RNA extraction and PCR. Total RNA was isolated from cells using the RNAeasy minikit (Qiagen) according to the manufacturer's procedure. Reverse transcription was performed using the AMV reverse transcription system (Promega), and quantitative PCR was performed with Power Sybr green (Applied Biosystems, Life Technologies, Grand Island, NY) following the manufacturer's instructions. The PCR was carried out on a Step One plus Real-Time PCR system (Applied Biosystems). All analyses were done in triplicate, and a melting curve analysis was performed to control for product quality and specificity. Expression levels were calculated using the comparative method of relative quantification, with SB34 as a normalizer. The data were analyzed for statistical significance using Student's t-test. The results are presented as the mean ± SEM relative to the control. Primers were obtained from primer bank or primer depot (http://pga.mgh.harvard.edu/primerbank/, https://primerdepot.nci.nih.gov), and their specificity was verified using primer blast (http://www.ncbi.nlm.nih.gov/tools/primer-blast/).

The following results were obtained:

Here IC50 represents the concentration necessary to obtain 50% of EZH2 transcription activity.

By decreasing EZH2 transcription, NIK inhibitors restore senescence in treated cancer cells. A simple beta-galactosidase assay using increasing doses of the compounds allows assessing the potential good candidate. Then the best candidates are tested to study their capacity to decrease EZH2 transcription and concomitantly increasing the expression of CDK 1A and IFN-γ.

3.2 A375 cell proliferation assay

Cells were counted using a Malassez chamber. The average and standard deviation were calculated from triplicate experiments. Antiproliferative effects were evaluated by trypan blue exclusion assay. Briefly, cells were seeded into 12-well plate and grown in media supplemented with indicated compound at 1 or ΙΟμΜ for 48h or 96h. Cells were washed with PBS and detached by trypsinization, collected and colored by trypan blue. Dead and living cells were counted and proliferation was calculated as follow: Proliferation (%) = [(treated cell number/untreated cells number)* 100].

The following results were obtained.

Compounds Proliferation (%)

tested At ΙμΜ - At 10μΜ - At ΙμΜ - At 10μΜ - 48H 48H 96H 96H

5 91,0 67,5 77,1 58,1

19 74,7 0,4 74,9 0,0

8 81,3 82,1 74,0 67,5

7 84,6 95,2 91,1 79,4

26 54,9 0,4 9,9 0,0

38 90,8 33,5 46,9 15,7

39 88,3 18,1 34,3 13,6

35 103,7 84,7 85,3 79,9

37 84,0 80,5 87,4 53,0

36 104,70 49,70 97,74 9,89

27 98,66 67,79 85,59 21,75

28 98,4 92 87,85 82,77

29 89,6 67,2 87,57 4,80

30 88 87,2 73,16 37,01

31 106,4 37,6 83,33 3,39

32 96 100 84,46 82,20 33 106,4 101,6 97,18 95,20

34 96 77,6 98,59 37,85

These results show that the compounds of the invention are efficient to slow tumor cell proliferation.

3.3 Melanocyte and fibroblast viability assay

Cell viability effects were evaluated by trypan blue exclusion assay. Briefly, cells were seeded into 12-well plate and grown in media supplemented with indicated compound at 10μΜ for 96h. Cells were washed with PBS and detached by trypsinization, collected and colored by trypan blue. Dead and living cells were counted and cell viability was calculated as follow: Viability (%) = 100 - [(dead cell number/total cells)* 100].

The following results were obtained :

Compounds Viability (%) at 10 μΜ

tested Fibroblast Melanocyte

5 98,6 99,5

19 n.d n.d

8 98,6 98,0

7 97,7 99,1

26 n.d n.d

38 93,3 99,2

39 100,0 99,5

35 99,5 99,1

37 94,6 98,7

36 92,1 73,4

27 93,9 76,9

28 95,7 99,1

29 41,6 91,2

30 96,4 94,2

31 29,6 33,1

32 99,4 98,6 33 97,7 60,1

34 98,3 98,7 n.d: non-determined

These results show that the compounds of the invention do not present any toxicity towards normal human fibroblast and melanocyte.

The compounds of the invention, in particular compound 5, restored senescence in A375 cells with a clear, dose-dependent effect. They also decreased EZH2 transcription in a dose-dependent manner (Figure 1A for compound 5) and concomitantly increased the expression of CDK 1A and IFN-γ (Figure IB for compound 5). The secretomes of A375, CI 2.06, and A549 cells treated with compound 5 were studied. The secretomes produced by the compound 5-treated cells had a clear IFN-γ signature and were similar to those produced by NFkB2-siRNA-treated cells (Figure 1C). The effects of compound 5 with those ofNFkB2- siRNA were compared on the proliferation of A375, C12.06, and A549 cells. Compared with controls, the treatments had similar inhibitory effects on the proliferation of the cancer cells. Neither treatment had any effect on the proliferation of normal human melanocytes or fibroblasts. The A375, C12.06, and A549 cells treated with compound 5 produced significantly more IFN-γ than control cells . Finally, compound 5 decreased p52, and EZH2 at the protein level (and in some cases also RelB) in each of the cancer cell types. Compound 5 also induced an increase in STAT1 phosphorylation but did not increase cleaved PARP or activate caspase 3, LC3 or CHOP, supporting its specificity.

Example 4: In vivo activity of the compounds of the invention

In light of the promising in vitro results, the efficacy of compound 5 was tested in vivo for treating solid cancer, either alone or with immune-checkpoint blockers.

4.1 In colorectal cancer

Subcutaneous tumor development

0.5 10 ⁶ cells in 100 yL PBS were subcutaneously injected into 4-week-old female C57B1/6 mice (for the B16 experiment) or Balb/c mice (for the CT26 experiments). DZNEP is an inhibitor of the catalytic activity of EZH2 and was used as an additional control. 1 mg/kg DZNEP and 10 mg/kg compound 5 were used for the subsequent experiments. Tridimensional measurements were performed daily, and the tumor volume was expressed as mm ³ . The tumors were allowed to grow until the total burden per mouse reached 1000 mm ³ or until the mice showed > 20% weight loss, at which point the mice were sacrificed. Freshly collected tumors were dissociated and stained for immune-cell infiltrate using a flow cytometer. CD3+ T cells from spleen tissue were negatively selected using myltennyi magnetic columns and put in contact with naive CT26 cells for 24 or 48 h. The CT26 cells were subsequently stained with DAPI (0.5 μg/ml, Molecular Probes, Grand Island, NY, USA). The T-cells were stained with CD8, perforin, and granzyme B antibodies and analyzed immediately by flow cytometry using a MACS-Quant Analyzer (Miltenyi Biotec, Paris, France).

All animal experimentation was carried out in accordance with the Declaration of Helsinki and was reviewed and approved by the French Ethic Committee (Minister of Agriculture, Approval Number Protocol: PEA NCE/2013-73)

Immune cell staining and analysis

Tumors were extracted and disaggregated using 70 μΜ strainers. Then, the cells were re-suspended in ice-cold PBS (Life Technologies, 14190169) and incubated for 30 min (4°C in the dark) with one or more of the following monoclonal anti-mouse antibodies, all of which are specific for mouse epitopes, according to the manufacturer's protocol: eFluor® 450-anti- F4/80 (BM8, eBioscience), PE/FITC/APC-anti-CD3 (145-2C11, BD Pharmingen), Pacific Blue-anti-CD4 (RM4-5, BD Pharmingen), PE-Cy7-anti-CD8 (53-6.7, BD Pharmingen), APC- anti-CDl lb (Ml/70, BD Pharmingen), FITC/PE-anti-CDl lc (HL3, BD Pharmingen), APC- Cy7-anti-CD25 (PC61, BD Pharmingen), PE-anti-CD40 (3/23, BD Pharmingen), FITC-anti- CD80 (B7-1, BD Pharmingen), PE-Cy7-anti-CD86 (B7-2, BD Pharmingen), FITC/PE-anti- NK1.1 (PK136, BD Pharmingen), PE-anti-FoxP3 (MF23, BD Pharmingen), APC/PE-anti- IFN-γ (XMG1.2, BD Pharmingen), PE-anti-perforin (eBioOMAK-D, eBioscience), and PE- Cy7-anti-Granzyme B (NGZB RUO, eBioscience). FoxP3 was detected by cell intranuclear staining employing the BD Pharmingen™ Mouse Foxp3 Buffer Set according to the manufacturer's instructions. IFN-γ, perforin, and granzyme B were detected by intracellular staining using the BD Cytofix/Cytoperm™ Kit following the manufacturer's instructions. Once stained, the cells were washed twice with PBS prior to analysis by flow cytometry. Fluorescence was measured using a MACSQuant® Analyzer (Miltenyi, Paris, France).

Negative selection Spleens were extracted and disaggregated, and the cells were resuspended in PBS. T- cells were isolated by CD3 negative selection to avoid activation. For that purpose, the cells were incubated for 15 min (4°C in the dark) with the following mixture of monoclonal FITC- anti-mouse antibodies according to the manufacturer's protocol: TER-119 (TER-119, eBioscience), CD19 (6D5, BD Pharmingen), CD45R/B220 (30-F11, BD Pharmingen), CDl lb (Ml/70, BD Pharmingen), and CD49b (DX5, BD Pharmingen). Then, the cells were washed and incubated with magnetic anti-FITC MicroBeads for 15 min. The cells were then washed, centrifuged, and resuspended in 500 iiL PBS prior to passage through an LS Column (Miltenyi ) attached to a MACS® Separator (Miltenyi ) followed by 3 mL PBS. The flow- through containing the enriched fraction of CD3 cells was collected and analyzed by flow cytometry to determine the yield of the enrichment (CD3 cells constituted a minimum 70% of the total ceils collected).

Statistical analysis

The majority of the data are presented as the average ± SD of at least three independent experiments, each performed in triplicate. The statistical significance of the experiments was evaluated using an unpaired two-tailed Student ^' s t-test; * indicates a P value < 0.05; ** indicates a P value < 0.01. Representative experiments are presented as the average ± SD of the triplicate measurements of an experiment that was reproduced at least two times.

Tests for statistical significance in the animal experiments were performed using the ann Whitney Wilco on test.

In order to evaluate the new approach in different types of cancer, compound 5 was tested in colorectal cancer cells. CT26 cells were subcutaneously injected into syngeneic mice. After 3 days, the mice were treated intraperitoneally with DZNEP, compound 5, and anti-PDl as monotherapies and combined. Additional treatments in which the mice received DZNEP or compound 5 plus anti-PDl with an anti-CD8 antibody added to neutralize the T- cell response were included. The growth of the CT26 tumors was significantly reduced by each monotherapy (Figures 2A). The combination treatments had a dramatic effect on tumor size, not only reducing the tumor growth but also decreasing the tumor volume in the last days of the experiment. Signs of tumor regression and tumor-free mice were even observed. When anti-CD8 was added to the combination treatment, the growth of the tumors was markedly increased, highlighting the role of immune surveillance in controlling tumor development. The number of Ml macrophages and the percentage of Ml macrophages among the total macrophage population were increased in all the treated mice, especially in the mice that received the combination treatments (Figure 2C). Each of the treatments increased the numbers and activation of DCs and the numbers of CD 8+ and CD4+ cells infiltrating the tumors (Figure 2D). The treatments increased the number of NK cells infiltrating the tumors, and the increase was significantly greater for the combination therapies .The mice treated with compound 5 showed no clinical signs of toxicity and had similar liver weight and systemic glycemia compared to the other mice. The liver enzymes in the blood of the mice treated with compound 5 remained in the normal range. Finally, CD3+ T-cells were isolated by negative selection from the spleens of the treated mice and cocultured with naive CT26 cells. The T- cells isolated from the mice treated with DZNEP, compound 5, or the combination therapies were more effective in killing CT26 cells. The CD8+ cells from the treated mice showed higher expression levels of perforin and granzyme B.

These results show not only that compound 5 is well tolerated and effective in reducing tumor growth by itself but also that compound 5 clearly potentiates anti-PDl treatment. The immune cells that are recruited and activated at the tumor site by compound 5 are able to recirculate and then recognize and efficiently kill new tumor cells.

4.2 In melanoma

The inventors then asked whether compound 5 was able to increase the survival rate of mice with already established tumor and, if that was the case, also in this situation was able to synergize with anti-PDl treatment. They thus decided to use the model B16 melanoma cells in C57B16 mice. B16 cells were again injected subcutaneously and the tumors were let to grow until an average volume of 100 mm3 was reached. The mice were then sorted into four groups with similar average tumor volume and standard deviation and the treatments (control group, compound 5, anti-PDl and combination of compound 5 and anti-PDl) applied with the same protocol as in the CT26 experiment. The tumors were allowed to grow until the total burden per mouse reached 1000 mm3, at which point the mouse was sacrificed. The results indicate that even in this case the single treatments (median survival for compound 5 treatment was 20 days from injection while for anti-PDl was 19 days) were effective in reducing the tumor growth in comparison with the control (median survival was 13 days) (Figure 3A and 3B). The combination of treatments demonstrated a synergistic effect with 2 cases of tumor regression and a median survival of 28 days. Moreover, in this latter experiment, no death dependent from compound 5 treatment was observed. Taken globally, these last results thus show not only that compound 5 is well tolerated and effective in reducing tumor growth by itself but also that compound 5 clearly potentiates anti- PD1 treatment in particular in lung-cancer and colon-cancer.

REFERENCES:

Throughout this application, various references describe the state of the art to which this invention pertains. The disclosures of these references are hereby incorporated by reference into the present disclosure.

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