OGA INHIBITOR COMPOUNDS

FIELD OF THE INVENTION

The present invention relates to O-GlcNAc hydrolase (OGA) inhibitors, having the structure shown in Formula (I)

wherein the radicals are as defined in the specification. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes for preparing such compounds and compositions, and to the use of such compounds and

compositions for the prevention and treatment of disorders in which inhibition of OGA is beneficial, such as tauopathies, in particular Alzheimer’s disease or progressive supranuclear palsy; and neurodegenerative diseases accompanied by a tau pathology, in particular amyotrophic lateral sclerosis or frontotemporal lobe dementia caused by C90RF72 mutations.

BACKGROUND OF THE INVENTION

O-GlcNAcylation is a reversible modification of proteins where N-acetyl-D- glucosamine residues are transferred to the hydroxyl groups of serine- and threonine residues yield O-GlcNAcylated proteins. More than 1000 of such target proteins have been identified both in the cytosol and nucleus of eukaryotes. The modification is thought to regulate a huge spectrum of cellular processes including transcription, cytoskeletal processes, cell cycle, proteasomal degradation, and receptor signalling.

O-GlcNAc transferase (OGT) and O-GlcNAc hydrolase (OGA) are the only two proteins described that add (OGT) or remove (OGA) O-GlcNAc from target proteins. OGA was initially purified in 1994 from spleen preparation and 1998 identified as antigen expressed by meningiomas and termed MGEA5, consists of 916 amino

(102915 Dalton) as a monomer in the cytosolic compartment of cells. It is to be distinguished from ER- and Golgi-related glycosylation processes that are important for trafficking and secretion of proteins and different to OGA have an acidic pH optimum, whereas OGA display highest activity at neutral pH. The OGA catalytic domain with its double aspartate catalytic center resides in the N- terminal part of the enzyme which is flanked by two flexible domains. The C-terminal part consists of a putative HAT (histone acetyl transferase domain) preceded by a stalk domain. It has yet still to be proven that the HAT-domain is catalytically active.

O-GlcNAcylated proteins as well as OGT and OGA themselves are particularly abundant in the brain and neurons suggesting this modification plays an important role in the central nervous system. Indeed, studies confirmed that O-GlcNAcylation represents a key regulatory mechanism contributing to neuronal communication, memory formation and neurodegenerative disease. Moreover, it has been shown that OGT is essential for embryogenesis in several animal models and ogt null mice are embryonic lethal. OGA is also indispensible for mammalian development. Two independent studies have shown that OGA homozygous null mice do not survive beyond 24-48 hours after birth. Oga deletion has led to defects in glycogen

mobilization in pups and it caused genomic instability linked cell cycle arrest in MEFs derived from homozygous knockout embryos. The heterozygous animals survived to adulthood however they exhibited alterations in both transcription and metabolism. It is known that perturbations in O-GlcNAc cycling impact chronic metabolic diseases such as diabetes, as well as cancer. Oga heterozygosity suppressed intestinal tumorigenesis in an Apc-/+ mouse cancer model and the Oga gene ( MGEA5 ) is a documented human diabetes susceptibility locus. In addition, O-GlcNAc-modifications have been identified on several proteins that are involved in the development and progression of neurodegenerative diseases and a correlation between variations of O-GlcNAc levels on the formation of neurofibrillary tangle (NFT) protein by Tau in Alzheimer’s disease has been suggested. In addition, O-GlcNAcylation of alpha-synuclein in Parkinson’s disease has been described.

In the central nervous system six splice variants of tau have been described. Tau is encoded on chromosome 17 and consists in its longest splice variant expressed in the central nervous system of 441 amino acids. These isoforms differ by two N-terminal inserts (exon 2 and 3) and exon 10 which lie within the microtubule binding domain. Exon 10 is of considerable interest in tauopathies as it harbours multiple mutations that render tau prone to aggregation as described below. Tau protein binds to and stabilizes the neuronal microtubule cytoskeleton which is important for regulation of the intracellular transport of organelles along the axonal compartments. Thus, tau plays an important role in the formation of axons and maintenance of their integrity. In addition, a role in the physiology of dendritic spines has been suggested as well. Tau aggregation is either one of the underlying causes for a variety of so called tauopathies like PSP (progressive supranuclear palsy), Down’s syndrome (DS), FTLD (frontotemporal lobe dementia), FTDP-17 (frontotemporal dementia with

Parkinsonism- 17), Pick’s disease (PD), CBD (corticobasal degeneration), agryophilic grain disease (AGD), and AD (Alzheimer’s disease). In addition, tau pathology accompanies additional neurodegenerative diseases like amyotrophic lateral sclerosis (ALS) or FTLD cause by C90RF72 mutations. In these diseases, tau is post- translationally modified by excessive phosphorylation which is thought to detach tau from microtubules and makes it prone to aggregation. O-GlcNAcylation of tau regulates the extent of phosphorylation as serine or threonine residues carrying O- GlcNAc-residues are not amenable to phosphorylation. This effectively renders tau less prone to detaching from microtubules and reduces aggregation into neurotoxic tangles which ultimately lead to neurotoxicity and neuronal cell death. This mechanism may also reduce the cell-to-cell spreading of tau-aggregates released by neurons via along interconnected circuits in the brain which has recently been discussed to accelerate pathology in tau-related dementias. Indeed, hyperphosphorylated tau isolated from brains of AD-patients showed significantly reduced O-GlcNAcylation levels.

An OGA inhibitor administered to INPL3 tau transgenic mice successfully reduced NFT formation and neuronal loss without apparent adverse effects. This observation has been confirmed in another rodent model of tauopathy where the expression of mutant tau found in FTD can be induced (tg45l0). Dosing of a small molecule inhibitor of OGA was efficacious in reducing the formation of tau-aggregation and attenuated the cortical atrophy and ventricle enlargement. Moreover, the O-GlcNAcylation of the amyloid precursor protein (APP) favours processing via the non-amyloidogenic route to produce soluble APP fragment and avoid cleavage that results in the AD associated amyloid-beta (Ab) formation.

Maintaining O-GlcNAcylation of tau by inhibition of OGA represents a potential approach to decrease tau-phosphorylation and tau-aggregation in neurodegenerative diseases mentioned above thereby attenuating or stopping the progression of neurodegenerative tauopathy-diseases. WO2012/117219 (Summit Corp. plc., published 7 September 2012) describes N-[[5- (hydroxymethyl)pyrrolidin-2-yl]methyl]alkylamide and N-alkyl-2-[5- (hydroxymethyl)pyrrolidin-2-yl]acetamide derivatives as OGA inhibitors.

WO2014/159234 (Merck Patent GMBH, published 2 October 2014) discloses mainly

4-phenyl or benzyl-piperidine and piperazine compounds substituted at the 1 -position with an acetamido-thiazolylmethyl or acetamidoxazolylmethyl substituent and the compound N-[5-[(3-phenyl- 1 -piperidyl)methyl]thiazol-2-yl]acetamide;

W02016/0300443 (Asceneuron S.A., published 3 March 2016), WO2017/144633 and WO2017/0114639 (Asceneuron S.A., published 31 August 2017) disclose 1,4- disubstituted piperidines or piperazines as OGA inhibitors;

WO2017/144637 (Asceneuron S.A, published 31 August 2017) discloses more particular 4-substituted l-[l-(l,3-benzodioxol-5-yl)ethyl]-piperazine; l-[l-(2,3- dihydrobenzofuran-5-yl)ethyl]-; l-[l-(2,3-dihydrobenzofuran-6-yl)ethyl]-; and l-[l- (2, 3-dihydro- l,4-benzodioxin-6-yl)ethyl] -piperazine derivatives as OGA inhibitors;

WO2017/106254 (Merck Sharp & Dohme Corp.) describes substituted N-[5-[(4- methylene-l-piperidyl)methyl]thiazol-2-yl]acetamide compounds as OGA inhibitors.

There is still a need for OGA inhibitor compounds with an advantageous balance of properties, for example with improved potency, good bioavailability, pharmacokinetics, and brain penetration, and/or better toxicity profile. It is accordingly an object of the present invention to provide compounds that overcome at least some of these problems.

SUMMARY OF THE INVENTION

The present invention is directed to compounds of Formula (I)

and the tautomers and the stereoisomeric forms thereof, wherein

R ^A is a heteroaryl radical selected from the group consisting of pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, pyridazin-3-yl, pyrimidin-4-yl, pyrimidin-5-yl, and pyrazin-2-yl, each of which may be optionally substituted with 1, 2 or 3 substituents each independently selected from the group consisting of halo; cyano; Ci- ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents;

-C(0)NR ^a R ^aa ; NR ^a R ^aa ; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents; wherein R ^a and R ^aa are each independently selected from the group consisting of hydrogen and Ci- ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents;

L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, -OCH2-, -CH2O-, -NH-, -N(CH ₃ )-, -NHCH2- and -CH2NH-;

x represents 0 or 1 ;

R is H or CH ₃ ; and

R ^B is an aromatic heterobicyclic radical selected from the group consisting of (b-l) to -12)

(b-9) (b-lO) (b-l l) 0-12)

wherein

X ^la and X ^lb each independently represents CH or N; and Y ¹ represents O or S, with the proviso that at least one of X ^la and X ^lb is CH, and when Y ¹ is S, X ^la or X ^lb is N;

X ² represents CH or N; and Y ² represents O or S;

X ³ and X ⁴ are each independently selected from N and CF; with the proviso that when X ³ is N, X ⁴ is CF and when X ³ is CF, X ⁴ is N; one or two of Y ³ -Y ⁵ is a heteroatom each independently selected from the group consisting of =N-, >NH, >N(Ci- ₄ alkyl), S and O, with the proviso that up to one of Y ³ -Y ⁵ may be O or S when present; and the remaining Y ³ -Y ⁵ are each independently selected from the group consisting of CH and C(Ci_ ₄ alkyl);

X ⁵ represents CH or N;

one of Y ⁶ or Y ⁷ is =N- and the other is >NH or >NCH ₃ ;

X ⁶ , X ⁷ and X ⁸ each independently represent CH or N, with the proviso that up to one of them can be N and with the proviso that X ⁷ is C when b is the point of attachment to CHR;

Y ⁸ and Y ⁹ are each independently selected from the group consisting of O, S, NH and NCH ₃ ;

X ⁹ and X ¹⁰ each independently represent CH or N, with the proviso that at least one of them is CH;

a and b, when present, represent the point of attachment of the aromatic heterobicyclic radical R ^B to CHR;

R ¹ , R ² , and R ³ are each selected from Ci_ ₄ alkyl;

R ⁴ and R ⁵ are each selected from the group consisting of H and Ci_ ₄ alkyl;

Y ¹⁰ represents O or S;

n represents 1 or 2;

R ^c is selected from the group consisting of fluoro, methyl, hydroxy, methoxy, trifluoromethyl, and difluoromethyl;

R ^D is selected from the group consisting of hydrogen, fluoro, methyl, hydroxy, methoxy, trifluoromethyl, and difluoromethyl; and

y represents 0, 1 or 2;

with the provisos that

a) R ^c is not hydroxy or methoxy when present at the carbon atom adjacent to the nitrogen atom of the piperidinediyl or pyrrolidinediyl ring;

b) R ^c or R ^D cannot be selected simultaneously from hydroxy or methoxy when R ^c is present at the carbon atom adjacent to C-R°;

c) R ^D is not hydroxy or methoxy when L ^A is -O-, -OCH2-, -CH2O-, -NH-,

-N(CH )-, -NH(CH ₂ )- or -(CH ₂ )NH-; and the pharmaceutically acceptable salts and the solvates thereof.

Illustrative of the invention is a pharmaceutical composition comprising a

pharmaceutically acceptable carrier and any of the compounds described above. An illustration of the invention is a pharmaceutical composition made by mixing any of the compounds described above and a pharmaceutically acceptable carrier. Illustrating the invention is a process for making a pharmaceutical composition comprising mixing any of the compounds described above and a pharmaceutically acceptable carrier.

Exemplifying the invention are methods of preventing or treating a disorder mediated by the inhibition of O-GlcNAc hydrolase (OGA), comprising administering to a subject in need thereof a therapeutically effective amount of any of the compounds or pharmaceutical compositions described above.

Further exemplifying the invention are methods of inhibiting OGA, comprising administering to a subject in need thereof a prophylactically or a therapeutically effective amount of any of the compounds or pharmaceutical compositions described above.

An example of the invention is a method of preventing or treating a disorder selected from a tauopathy, in particular a tauopathy selected from the group consisting of Alzheimer’s disease, progressive supranuclear palsy, Down’s syndrome,

frontotemporal lobe dementia, frontotemporal dementia with Parkinsonism- 17, Pick’s disease, corticobasal degeneration, and agryophilic grain disease; or a

neurodegenerative disease accompanied by a tau pathology, in particular a

neurodegenerative disease selected from amyotrophic lateral sclerosis or

frontotemporal lobe dementia caused by C90RF72 mutations, comprising

administering to a subject in need thereof, a prophylactically or a therapeutically effective amount of any of the compounds or pharmaceutical compositions described above.

Another example of the invention is any of the compounds described above for use in preventing or treating a tauopathy, in particular a tauopathy selected from the group consisting of Alzheimer’s disease, progressive supranuclear palsy, Down’s syndrome, frontotemporal lobe dementia, frontotemporal dementia with Parkinsonism- 17, Pick’s disease, corticobasal degeneration, and agryophilic grain disease; or a

neurodegenerative disease accompanied by a tau pathology, in particular a

neurodegenerative disease selected from amyotrophic lateral sclerosis or frontotemporal lobe dementia caused by C90RF72 mutations, in a subject in need thereof.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is directed to compounds of Formula (I), as defined herein before, and pharmaceutically acceptable addition salts and solvates thereof. The compounds of Formula (I) are inhibitors of O-GlcNAc hydrolase (OGA) and may be useful in the prevention or treatment of tauopathies, in particular a tauopathy selected from the group consisting of Alzheimer’s disease, progressive supranuclear palsy, Down’s syndrome, frontotemporal lobe dementia, frontotemporal dementia with Parkinsonism- 17, Pick’s disease, corticobasal degeneration, and agryophilic grain disease; or maybe useful in the prevention or treatment of neurodegenerative diseases accompanied by a tau pathology, in particular a neurodegenerative disease selected from amyotrophic lateral sclerosis or frontotemporal lobe dementia caused by

C90RF72 mutations.

In a particular embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^A is a heteroaryl radical selected from the group consisting of pyridin-2-yl, pyridin-4- yl, and pyrimidin-4-yl, each of which may be optionally substituted with 1 , 2 or 3 substituents each independently selected from the group consisting of halo; cyano, Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents; -C(0)NR ^a R ^aa ; NR ^a R ^aa ; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents; wherein R ^a and R ^aa are each independently selected from the group consisting of hydrogen and Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents;

and the pharmaceutically acceptable salts and the solvates thereof.

In a further embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^A is a heteroaryl radical selected from the group consisting of pyridin-4-yl, and pyrimidin-4-yl, each of which may be optionally substituted with 1 , 2 or 3 substituents each independently selected from the group consisting of halo; cyano, Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents;

-C(0)NR ^a R ^aa ; NR ^a R ^aa ; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents; wherein R ^a and R ^aa are each independently selected from the group consisting of hydrogen and Ci- ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents;

and the pharmaceutically acceptable salts and the solvates thereof.

In a further embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^A is a heteroaryl radical selected from the group consisting of pyridin-2-yl, pyridin-4- yl, and pyrimidin-4-yl, each of which may be optionally substituted with 1, 2 or 3 substituents each independently selected from the group consisting of halo; Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents; and the pharmaceutically acceptable salts and the solvates thereof

In a further embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^A is a heteroaryl radical selected from the group consisting of pyridin-2-yl and pyridin-4-yl, in particular pyridin-4-yl, each of which may be optionally substituted with 1, 2 or 3 substituents each independently selected from the group consisting of halo; Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents;

and the pharmaceutically acceptable salts and the solvates thereof. In a further embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^A is a heteroaryl radical selected from the group consisting of pyridin-4-yl, and pyrimidin-4-yl, each of which may be optionally substituted with 1 or 2 substituents each independently selected from the group consisting of Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents;

and the pharmaceutically acceptable salts and the solvates thereof. In an additional embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein L ^A is selected from the group consisting of -CH ₂ -, -0-, -OCH ₂ -, -CH ₂ O-, -NH-, -N(0¾)-, -NHCH ₂ - and -CH ₂ NH-.

In a further, embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, -OCH ₂ - -CH ₂ O-, -NH-, -NHCH ₂ - and -CH ₂ NH-.

In an additional embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, -OCH ₂ - and -NHCH2-.

In a further embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, -OCH ₂ -, and -CH ₂ O-.

In a further embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, and -OCH ₂ -. In an additional embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein L ^A is selected from the group consisting of -CH ₂ -, -0-, -OCH ₂ - and -NHCH ₂ -.

In a further embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein L ^A is selected from the group consisting of -CH ₂ -, -0-, and -OCH ₂ -.

In another embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein y is

0.

In another embodiment, the invention is directed to compounds of Formula (I) as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R° is H.

In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of (b-l), (b-2), (b-3), (b-4), (b-5), (b-6), (b-8), (b-9) and (b-lO).

In another embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of (b-l), (b-2), (b-3), (b-4), (b-5), and (b-9).

In another embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of (b-l), (b-2), (b-5), and (b-9).

In a further embodiment, the invention is directed to compounds of Formula (I), and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of (b-5), (b-9) and (b-l2), in particular (b-5) and (b-9). In another embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein

R ^A is a heteroaryl radical selected from the group consisting of pyridin-2-yl, pyridin-4- yl and pyrimidin-4-yl, each of which may be optionally substituted with 1 , 2 or 3 substituents each independently selected from the group consisting of halo; Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents;

L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, -OCH2-, -CH2O-, -NH-, -NHCH2- and -CH2NH-;

x represents 0 or 1 ;

R is H or CFb; and

R ^B is selected from the group consisting of (b-l), (b-2), (b-3), (b-4), (b-5), (b-6), (b-8), (b-9) and (b-lO); wherein

X ^la and X ^lb each independently represents CH or N; and Y ¹ represents O or S, with the proviso that at least one of X ^la and X ^lb is CH, and when Y ¹ is S, X ^la or X ^lb is N;

X ² represents CH or N; and Y ² represents O or S;

X ³ is N and X ⁴ CF; one or two of Y ³ -Y ⁵ each independently represent =N-, >NH, or S, with the proviso that up to one of Y ³ -Y ⁵ may be S when present; and the remaining Y ³ -Y ⁵ are each independently selected from the group consisting of CH and C(Ci_ ₄ alkyl);

X ⁵ represents CH or N;

one of Y ⁶ or Y ⁷ is =N- and the other is >NH or >NCH ₃ ;

X ⁶ , X ⁷ and X ⁸ each independently represent CH or N, with the proviso that up to one of them can be N and with the proviso that X ⁷ is C when b is the point of attachment to CHR;

Y ⁸ and Y ⁹ are each O or S;

n is 1;

R ^D is H; and

y is 0;

and the pharmaceutically acceptable salts and the solvates thereof In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein

R ^A is a heteroaryl radical selected from the group consisting of pyridin-4-yl and pyrimidin-4-yl, each of which may be optionally substituted with 1 , 2 or 3 substituents each independently selected from the group consisting of halo; Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents;

L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, -OCH2-, and - CH2O-;

x represents 0 or 1 ;

R is H or CH ₃ ; and

R ^B is selected from the group consisting of (b-l), (b-2), (b-3), (b-4), (b-5), (b-6), (b-8), (b-9) and (b-lO); wherein

X ^la and X ^lb each independently represents CH or N; and Y ¹ represents O or S, with the proviso that at least one of X ^la and X ^lb is CH, and when Y ¹ is S, X ^la or X ^lb is N;

X ² represents CH or N; and Y ² represents O or S;

X ³ is N and X ⁴ CF; one or two of Y ³ -Y ⁵ each independently represent =N- or S, with the proviso that up to one of Y ³ -Y ⁵ may be S when present; and the remaining Y ³ -Y ⁵ are each independently selected from the group consisting of CH and C(Ci_ ₄ alkyl);

X ⁵ represents CH or N;

one of Y ⁶ or Y ⁷ is =N- and the other is >NH or >NCH ₃ ;

X ⁶ , X ⁷ and X ⁸ each independently represent CH or N, with the proviso that up to one of them can be N and with the proviso that X ⁷ is C when b is the point of attachment to CHR;

Y ⁸ and Y ⁹ are each O;

n is 1;

R ^D is H; and

y is 0;

and the pharmaceutically acceptable salts and the solvates thereof In another embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein

R ^A is a heteroaryl radical selected from the group consisting of pyridin-4-yl and pyrimidin-4-yl, each of which may be optionally substituted with 1 , 2 or 3 substituents each independently selected from the group consisting of halo; Ci_ ₄ alkyl optionally substituted with 1, 2, or 3 independently selected halo substituents; and Ci_ ₄ alkyloxy optionally substituted with 1, 2, or 3 independently selected halo substituents;

L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, and -OCH2-; x represents 0 or 1 ;

R is H or CFF; and

R ^B is selected from the group consisting of (b-l), (b-2), (b-3), (b-4), (b-5), (b-6), (b-8), (b-9) and (b-lO); wherein

X ^la and X ^lb each independently represents CH or N; and Y ¹ represents O or S, with the proviso that at least one of X ^la and X ^lb is CH, and when Y ¹ is S, X ^la or X ^lb is N;

X ² represents CH or N; and Y ² represents O or S;

X ³ is N and X ⁴ CF; one or two of Y ³ -Y ⁵ each independently represent =N- or S, with the proviso that up to one of Y ³ -Y ⁵ may be S when present; and the remaining Y ³ -Y ⁵ are each independently selected from the group consisting of CH and C(Ci_ ₄ alkyl);

X ⁵ represents CH or N;

one of Y ⁶ or Y ⁷ is =N- and the other is >NH or >NCH ₃ ;

X ⁶ , X ⁷ and X ⁸ each independently represent CH or N, with the proviso that up to one of them can be N and with the proviso that X ⁷ is C when b is the point of attachment to CHR;

Y ⁸ and Y ⁹ are each O;

n is 1;

R ^D is H; and

y is 0;

and the pharmaceutically acceptable salts and the solvates thereof In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of

In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of

, and

In yet another embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of

In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of

In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of

In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein R ^B is selected from the group consisting of

In a further embodiment, the invention is directed to compounds of Formula (I), as referred to herein, and the tautomers and the stereoisomeric forms thereof, wherein

R ^A is pyridin-4-yl substituted with 1 or 2 substituents each independently selected from Ci_ ₄ alkyl; L ^A is selected from the group consisting of a covalent bond, -CH ₂ -, -0-, -OCH2-, and - CH2O-, in particular selected from -CH2-, -0-, -OCH2-, and -CH2O-;

x represents 0 or 1 ;

R is CH ₃ ; and

R ^B is ;

and the pharmaceutically acceptable salts and the solvates thereof

DEFINITIONS

“Halo” shall denote fluoro, chloro and bromo;“Ci- ₄ alkyl” shall denote a straight or branched saturated alkyl group having 1, 2, 3 or 4 carbon atoms, respectively e.g.

methyl, ethyl, 1 -propyl, 2-propyl, butyl, 1 -methyl-propyl, 2-methyl- 1 -propyl, l,l-dimethylethyl, and the like;“Ci- ₄ alkyloxy” shall denote an ether radical wherein Ci_ ₄ alkyl is as defined before. When reference is made to L ^A , the definition is to be read from left to right, with the left part of the linker bound to R ^A and the right part of the linker bound to the pyrrolidinediyl or piperidinediyl ring. Thus, when L ^A is, for example, -O-CH2-, then R ^A -L ^A - is R ^A -0-CH ₂ -. When R ^c is present more than once, where possible, it may be bound at the same carbon atom of the pyrrolidinediyl or piperidinediyl ring, and each instance may be different.

In general, whenever the term“substituted” is used in the present invention, it is meant, unless otherwise indicated or is clear from the context, to indicate that one or more hydrogens, in particular 1 to 3 hydrogens, preferably 1 or 2 hydrogens, more preferably 1 hydrogen, on the atom or radical indicated in the expression using“substituted” are replaced with a selection of substituents from the indicated group, provided that the normal valency is not exceeded, and that the substitution results in a chemically stable compound, i.e. a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into a therapeutic agent.

The term "subject" as used herein, refers to an animal, preferably a mammal, most preferably a human, who is or has been the object of treatment, observation or experiment. As used herein, the term“subject” therefore encompasses patients, as well as asymptomatic or presymptomatic individuals at risk of developing a disease or condition as defined herein. The term "therapeutically effective amount" as used herein, means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated. The term "prophylactically effective amount" as used herein, means that amount of active compound or pharmaceutical agent that substantially reduces the potential for onset of the disease or disorder being prevented.

As used herein, the term "composition" is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combinations of the specified ingredients in the specified amounts.

Hereinbefore and hereinafter, the term“compound of Formula (I)” is meant to include the addition salts, the solvates and the stereoisomers thereof.

The terms“stereoisomers” or“stereochemically isomeric forms” hereinbefore or hereinafter are used interchangeably.

The invention includes all stereoisomers of the compound of Formula (I) either as a pure stereoisomer or as a mixture of two or more stereoisomers.

Enantiomers are stereoisomers that are non-superimposable mirror images of each other. A 1 : 1 mixture of a pair of enantiomers is a racemate or racemic mixture.

Diastereomers (or diastereoisomers) are stereoisomers that are not enantiomers, i.e. they are not related as mirror images. If a compound contains a double bond, the substituents may be in the E or the Z configuration. If a compound contains a disubstituted cycloalkyl group, the substituents may be in the cis or trans configuration. Therefore, the invention includes enantiomers, diastereomers, racemates, E isomers, Z isomers, cis isomers, trans isomers and mixtures thereof.

The absolute configuration is specified according to the Cahn-Ingold-Prelog system. The configuration at an asymmetric atom is specified by either R or S. Resolved compounds whose absolute configuration is not known can be designated by (+) or (-) depending on the direction in which they rotate plane polarized light.

When a specific stereoisomer is identified, this means that said stereoisomer is substantially free, i.e. associated with less than 50%, preferably less than 20%, more preferably less than 10%, even more preferably less than 5%, in particular less than 2% and most preferably less than 1%, of the other isomers. Thus, when a compound of formula (I) is for instance specified as (R), this means that the compound is substantially free of the (S) isomer; when a compound of formula (I) is for instance specified as E, this means that the compound is substantially free of the Z isomer; when a compound of formula (I) is for instance specified as cis, this means that the compound is substantially free of the trans isomer.

For use in medicine, the addition salts of the compounds of this invention refer to non toxic "pharmaceutically acceptable addition salts". Other salts may, however, be useful in the preparation of compounds according to this invention or of their

pharmaceutically acceptable addition salts. Suitable pharmaceutically acceptable addition salts of the compounds include acid addition salts which may, for example, be formed by mixing a solution of the compound with a solution of a pharmaceutically acceptable acid such as hydrochloric acid, sulfuric acid, fumaric acid, maleic acid, succinic acid, acetic acid, benzoic acid, citric acid, tartaric acid, carbonic acid or phosphoric acid. Furthermore, where the compounds of the invention carry an acidic moiety, suitable pharmaceutically acceptable addition salts thereof may include alkali metal salts, e.g., sodium or potassium salts; alkaline earth metal salts, e.g., calcium or magnesium salts; and salts formed with suitable organic ligands, e.g., quaternary ammonium salts.

Representative acids which may be used in the preparation of pharmaceutically acceptable addition salts include, but are not limited to, the following: acetic acid, 2,2-dichloroactic acid, acylated amino acids, adipic acid, alginic acid, ascorbic acid, F-aspartic acid, benzenesulfonic acid, benzoic acid, 4- acetamidobenzoic acid, (+)-camphoric acid, camphorsulfonic acid, capric acid, caproic acid, caprylic acid, cinnamic acid, citric acid, cyclamic acid, ethane- 1 ,2-disulfonic acid, ethanesulfonic acid, 2-hydroxy-ethanesulfonic acid, formic acid, fumaric acid, galactaric acid, gentisic acid, glucoheptonic acid, D-gluconic acid, D-glucoronic acid, F-glutamic acid, beta- oxo-glutaric acid, glycolic acid, hippuric acid, hydrobromic acid, hydrochloric acid, (+)-F-lactic acid, (±)-DF-lactic acid, lactobionic acid, maleic acid, (-)-F-malic acid, malonic acid, (±)-DF-mandelic acid, methanesulfonic acid, naphthalene-2-sulfonic acid, naphthalene- 1,5- disulfonic acid, l-hydroxy-2-naphthoic acid, nicotinic acid, nitric acid, oleic acid, orotic acid, oxalic acid, palmitic acid, pamoic acid, phosphoric acid, F- pyroglutamic acid, salicylic acid, 4-amino -salicylic acid, sebacic acid, stearic acid, succinic acid, sulfuric acid, tannic acid, (+)-F-tartaric acid, thiocyanic acid, p-toluenesulfonic acid, trifluoromethylsulfonic acid, and undecylenic acid.

Representative bases which may be used in the preparation of pharmaceutically acceptable addition salts include, but are not limited to, the following: ammonia, L-arginine, benethamine, benzathine, calcium hydroxide, choline, dimethylethanol- amine, diethanolamine, diethylamine, 2-(diethylamino)-ethanol, ethanolamine, ethylene-diamine, /V-mcthyl-glucaminc, hydrabamine, 1 //-imidazole, L-lysine, magnesium hydroxide, 4-(2-hydroxyethyl)-morpholine, piperazine, potassium hydroxide, l-(2-hydroxyethyl)-pyrrolidine, secondary amine, sodium hydroxide, triethanolamine, tromethamine and zinc hydroxide.

The names of compounds were generated according to the nomenclature rules agreed upon by the Chemical Abstracts Service (CAS) or according to the nomenclature rules agreed upon by the International Union of Pure and Applied Chemistry (IUPAC).

PREPARATION OF THE FINAL COMPOUNDS

The compounds according to the invention can generally be prepared by a succession of steps, each of which is known to the skilled person. In particular, the compounds can be prepared according to the following synthesis methods. The compounds of Formula (I) may be synthesized in the form of racemic mixtures of enantiomers which can be separated from one another following art-known resolution procedures. The racemic compounds of Formula (I) may be converted into the corresponding diastereomeric salt forms by reaction with a suitable chiral acid.

Said diastereomeric salt forms are subsequently separated, for example, by selective or fractional crystallization and the enantiomers are liberated therefrom by alkali. An alternative manner of separating the enantiomeric forms of the compounds of Formula (I) involves liquid chromatography using a chiral stationary phase. Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecifically.

EXPERIMENTAL PROCEDURE 1

The final compounds of Formulae (I-a), (I-b) or (I-c) can be prepared cleaving a protecting group in intermediate compounds of Formulae (Ha), (lib) or (He) according to reaction scheme (1). In reaction scheme (1) all variables are defined as in Formula (I), and PG is a suitable protecting group of the nitrogen function such as, for example,

2-(trimethylsilyl)ethoxymethyl (SEM), /e/t-butoxycarbonyl (Boc), ethoxycarbonyl, benzyl, benzyloxycarbonyl (Cbz). Suitable methods for removing such protecting groups are widely known to the person skilled in the art and comprise but are not limited to: SEM deprotection: treatment with a protic acid, such as, for example, trifluoroacetic acid, in a reaction inert solvent, such as, for example, dichloromethane; Boc deprotection: treatment with a protic acid , such as, for example, trifluoroacetic acid, in a reaction inert solvent, such as, for example, dichloromethane; ethoxycarbonyl deprotection: treatment with a strong base, such as, for example, sodium hydroxide, in a reaction inert solvent such as for example wet tetrahydrofuran; benzyl deprotection: catalytic hydrogenation in the presence of a suitable catalyst, such as, for example, palladium on carbon, in a reaction inert solvent, such as, for example, ethanol;

benzyloxycarbonyl deprotection: catalytic hydrogenation in the presence of a suitable catalyst, such as, for example, palladium on carbon, in a reaction inert solvent, such as, for example, ethanol. In reaction scheme (1) all variables are defined as in Formula (I). For simplicity only one of the two possible N-substitutcd regiosiomers on the imidazo ring is shown.

Reaction scheme 1

EXPERIMENTAL PROCEDURE 2 The final compounds of Formula (I-d) can be prepared by reacting an intermediate compound of Formula (III) with a compound of Formula (IV) according to reaction scheme (2). The reaction is performed in a suitable reaction- inert solvent, such as, for example, dichloromethane or l,2-dichloroethane, a metal hydride, such as, for example sodium triacetoxyborohydride, sodium cyanoborohydride or sodium borohydride and may require the presence of a suitable base, such as, for example, triethylamine or diisopropylethylamine, and/or a Lewis acid, such as, for example titanium

tetraisopropoxide or titanium tetrachloride, under thermal conditions, such as, 0 °C to 140 °C, more in particular at 0 °C, or at room temperature, or at 140 °C, for example for 1 hour or 24 hours. In reaction scheme (2) all variables are defined as in Formula (I).

(l-d)

Reaction scheme 2

EXPERIMENTAL PROCEDURE 3

Additionally, final compounds of Formula (I-d) can be prepared by reacting an intermediate compound of Formula (III) with a compound of Formula (V) followed by reaction of the formed imine derivative with and intermediate compound of Formula (VI) according to reaction scheme (3). The reaction is performed in a suitable reaction- inert solvent, such as, for example, anhydrous dichloromethane, a Lewis acid, such as, for example titanium tetraisopropoxide or titanium tetrachloride, under thermal conditions, such as, 0 °C to room temperature, for example for 1 hour or 24 hours. In reaction scheme (3) all variables are defined as in Formula (I), and wherein halo is chloro, bromo or iodo.

Reaction scheme 3 EXPERIMENTAL PROCEDURE 4

Additionally, final compounds of Formula (I-d) can be prepared by reacting an intermediate compound of Formula (III) with a compound of Formula (VII) according to reaction scheme (4). The reaction is performed in a suitable reaction- inert solvent, such as, for example, acetonitrile, a suitable base, such as, for example, triethylamine or diisopropylethylamine, under thermal conditions, such as, 0 °C to 75 °C, in particular, at 0 °C, or at room temperature, or at 75 °C, for example for 1 hour or 24 hours. In reaction scheme (4) all variables are defined as in Formula (I), and wherein halo is chloro, bromo or iodo.

Reaction scheme 4

EXPERIMENTAL PROCEDURE 5

Additionally, final compounds of Formula (I), wherein L ^A is -NH-CEE-, herein referred to as (I-e), can be prepared by reacting an intermediate compound of Formula (VUI-a) with a compound of Formula (IX-a) according to reaction scheme (5). The reaction is performed in the presence of a palladium catalyst, such as, for example

tris(dibenzylideneacetone)dipalladium(0), a ligand, such as, for example 2- dicyclohcxylphosphino-2'-(N,N-dimcthylamino)bi phenyl, a base, such as, for example sodium /e/ -butoxidc, a suitable reaction-inert solvent, such as, for example, anhydrous l,4-dioxane, under thermal conditions, such as, at about 100 °C, for example for 4 hour or 24 hours. In reaction scheme (5a) all variables are defined as in Formula (I), and wherein halo is chloro, bromo or iodo.

(Vlll-a) (l-e)

Reaction scheme 5 a Final compounds of Formula (I), wherein L ^A is -O-CH2-, herein referred to as (I-f) can be prepared by“Mitsunobu reaction” of a hydroxy compound of Formula (VUI-b) and a hydroxy derivative of Formula (IX-b) according to reaction scheme (5b). The reaction is performed in a suitable reaction-inert solvent, such as, for example, toluene, a phosphine, such as, triphenylphosphine, a suitable coupling agent, such as, for example DIAD (CAS: 2446-83-5), under thermal conditions, such as, for example, at about 70 °C, for example for 17 hours. In reaction scheme (5b) all variables are defined as in Formula (I).

Reaction Scheme 5b

EXPERIMENTAL PROCEDURE 6

Intermediate compounds of Formulae (Ha), (lib) or (He) can be prepared by reacting an intermediate compound of Formula (III) with a compound of Formulae (Xa), (Xb) or (Xc) followed by reaction of the formed imine derivative with and intermediate compound of Formula (VI) according to reaction scheme (6). The reaction is performed in a suitable reaction-inert solvent, such as, for example, anhydrous dichloromethane, a Lewis acid, such as, for example titanium tetraisopropoxide or titanium tetrachloride, under thermal conditions, such as, 0 °C to room temperature, for example for 1 hour or 24 hours. In reaction scheme (6) all variables are defined as in Formula (I), and wherein halo is chloro, bromo or iodo. For simplicity only one of the two possible V-substitutcd regiosiomers on the imidazo ring is shown.

Reaction scheme 6

EXPERIMENTAL PROCEDURE 7

Intermediate compounds of Formula (III) can be prepared by cleaving a protecting group in an intermediate compound of Formula (XI) according to reaction scheme (7). In reaction scheme (7) all variables are defined as in Formula (I), and PG is a suitable protecting group of the nitrogen function such as, for example, fc/ -butoxycarbonyl (Boc), ethoxycarbonyl, benzyl, benzyloxycarbonyl (Cbz). Suitable methods for removing such protecting groups are widely known to the person skilled in the art and comprise but are not limited to: Boc deprotection: treatment with a protic acid, such as, for example, trifluoroacetic acid, in a reaction inert solvent, such as, for example, dichloromethane or with an acidic resin, such as for example, Amberlist ® 15 hydrogen form in a reaction inert solvent such as methanol; ethoxycarbonyl deprotection: treatment with a strong base, such as, for example, sodium hydroxide, in a reaction inert solvent such as for example wet tetrahydrofuran; benzyl deprotection: catalytic hydrogenation in the presence of a suitable catalyst, such as, for example, palladium on carbon, in a reaction inert solvent, such as, for example, ethanol; benzyloxycarbonyl deprotection: catalytic hydrogenation in the presence of a suitable catalyst, such as, for example, palladium on carbon, in a reaction inert solvent, such as, for example, ethanol.

Reaction scheme 7

EXPERIMENTAL PROCEDURE 8

Intermediate compounds of Formula (XI) can be prepared by“Negishi coupling” reaction of a halo compound of Formula (IX) with an organozinc compound of

Formula (CII-a) according to reaction scheme (8). The reaction is performed in a suitable reaction-inert solvent, such as, for example, tetrahydrofuran, and a suitable catalyst, such as, for example, Pd(OAc) ₂ , a suitable ligand for the transition metal, such as, for example, 2-dicyclohcxylphosphino-2',6'-diisopropoxybi phenyl [CAS: 787618- 22-8], under thermal conditions, such as, for example, room temperature, for example for 1 hour. In reaction scheme (8) all variables are defined as in Formula (I), L ^A is a bond or CH ₂ and halo is preferably bromo or iodo. PG is defined as in Formula (XI).

Znl

Negishi coupling’

(Xll-a)

Reaction scheme 8

EXPERIMENTAL PROCEDURE 9

Intermediate compounds of Formula (XII) can be prepared by reaction of a halo compound of Formula (XIII) with zinc according to reaction scheme (9). The reaction is performed in a suitable reaction-inert solvent, such as, for example, tetrahydrofuran, and a suitable salt, such as, for example, lithium chloride, under thermal conditions, such as, for example, 40 °C, for example in a continuous- flow reactor. In reaction scheme (9) all variables are defined as in Formula (I), L ^A is a bond or CH ₂ and halo is preferably iodo. PG is defined as in Formula (XI).

(XIII) (XII)

Reaction scheme 9

EXPERIMENTAL PROCEDURE 10

Intermediate compounds of Formula (CI-a) can be prepared by hydrogenation reaction of an alkene compound of Formula (XIV) according to reaction scheme (10). The reaction is performed in a suitable reaction-inert solvent, such as, for example, methanol, and a suitable catalyst, such as, for example, palladium on carbon, and hydrogen, under thermal conditions, such as, for example, room temperature, for example for 3 hours. In reaction scheme (10) all variables are defined as in Formula (I) and PG is defined as in Formula (XI).

(XIV) (XI -a)

Reaction scheme 10

EXPERIMENTAL PROCEDURE 11

Intermediate compounds of Formula (XIV) can be prepared by“Suzuki coupling” reaction of an alkene compound of Formula (XV) and a halo derivative of Formula (IX) according to reaction scheme (11). The reaction is performed in a suitable reaction- inert solvent, such as, for example, l,4-dioxane, and a suitable catalyst, such as, for example, tetrakis(triphenylphosphine)palladium(0), a suitable base, such as, for example, NaHCOs (aq. sat. soltn.), under thermal conditions, such as, for example, 130 °C, for example for 30 min under microwave irradiation. In reaction scheme (11) all variables are defined as in Formula (I), halo is preferably bromo or iodo, L ^A is a bond, and PG is defined as in Formula (XI).

(XV) (XIV)

Reaction scheme 11

EXPERIMENTAL PROCEDURE 12

Intermediate compounds of Formula (XI -b) can be prepared by reaction of a hydroxy compound of Formula (XVI) and a halo derivative of Formula (IX) according to reaction scheme (12). The reaction is performed in a suitable reaction- inert solvent, such as, for example, dimethylformamide or dimethylsulfoxide, and a suitable base, such as, sodium hydride or potassium tert-butoxide, under thermal conditions, such as, for example, 50 °C, for example for 48 hours. In reaction scheme (12) all variables are defined as in Formula (I), L ^A is a bond or CEE and halo is preferably chloro, bromo or fluoro. PG is defined as in Formula (XI).

_A Aalo

^

Reaction scheme 12

EXPERIMENTAL PROCEDURE 13

Alternatively, intermediate compounds of Formula (XI-c) can be prepared by “Mitsunobu reaction” of a hydroxy compound of Formula (XVI) and a hydroxy derivative of Formula (IX-a) according to reaction scheme (13). The reaction is performed in a suitable reaction-inert solvent, such as, for example, toluene, a phosphine, such as, triphenylphosphine, a suitable coupling agent, such as, for example DIAD (CAS: 2446-83-5), under thermal conditions, such as, for example, 70 °C, for example for 17 hours. In reaction scheme (13) all variables are defined as in Formula (I), L ^A is a bond or CH ₂ and halo is preferably chloro, bromo or fluoro. PG is defined as in Formula (XI).

(XVI) (IX-b)

Reaction scheme 13

EXPERIMENTAL PROCEDURE 14

Intermediate compounds of Formula (VUI-b) can be prepared by deprotecting the alcohol group in an intermediate compound of Formula (XVII) according to reaction scheme (14). The reaction is performed in the presence of a fluoride source, such as, for example tetrabutylammonium fluoride, in a suitable reaction-inert solvent, such as, for example, dry tetrahydrofuran, under thermal conditions, such as, for example, room temperature, for example for 16 hours. In reaction scheme (14) all variables are defined as in Formula (I) and PG ¹ is selected from the group consisting of trimethylsilyl, tert- butyldimethylsilyl, triisopropylsilyl or /e/t-butyldiphcnylsilyl.

(XVII) (Vlll-b)

Reaction scheme 14 Intermediates of Formulae (IV), (V), (VI), (VII), (VUI-a), (VUI-b), (IX), (IX-a), (Xa), (Xb), (Xc), (XV), (XVI) and (XVII) are commercially available or can be prepared by known procedures to those skilled in the art. PHARMACOLOGY

The compounds of the present invention and the pharmaceutically acceptable compositions thereof inhibit O-GlcNAc hydrolase (OGA) and therefore may be useful in the treatment or prevention of diseases involving tau pathology, also known as tauopathies, and diseases with tau inclusions. Such diseases include, but are not limited to Alzheimer’s disease, amyotrophic lateral sclerosis and parkinsonism-dementia complex, argyrophilic grain disease, chronic traumatic encephalopathy, corticobasal degeneration, diffuse neurofibrillary tangles with calcification, Down’s syndrome, Familial British dementia, Familial Danish dementia, Frontotemporal dementia and parkinsonism linked to chromosome 17 (caused by MAPT mutations), Frontotemporal lobar degeneration (some cases caused by C90RF72 mutations), Gerstmann-Straussler- Scheinker disease, Guadeloupean parkinsonism, myotonic dystrophy,

neurodegeneration with brain iron accumulation, Niemann-Pick disease, type C, non- Guamanian motor neuron disease with neurofibrillary tangles, Pick’s disease, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, progressive supranuclear palsy, SLC9A6-related mental retardation, subacute sclerosing panencephalitis, tangle-only dementia, and white matter tauopathy with globular glial inclusions.

As used herein, the term“treatment” is intended to refer to all processes, wherein there may be a slowing, interrupting, arresting or stopping of the progression of a disease or an alleviation of symptoms, but does not necessarily indicate a total elimination of all symptoms. As used herein, the term“prevention” is intended to refer to all processes, wherein there may be a slowing, interrupting, arresting or stopping of the onset of a disease.

The invention also relates to a compound according to the general Formula (I), a stereoisomeric form thereof or a pharmaceutically acceptable acid or base addition salt thereof, for use in the treatment or prevention of diseases or conditions selected from the group consisting of Alzheimer’s disease, amyotrophic lateral sclerosis and parkinsonism-dementia complex, argyrophilic grain disease, chronic traumatic encephalopathy, corticobasal degeneration, diffuse neurofibrillary tangles with calcification, Down’s syndrome, Familial British dementia, Familial Danish dementia, Frontotemporal dementia and parkinsonism linked to chromosome 17 (caused by MAPT mutations), Frontotemporal lobar degeneration (some cases caused by

C90RF72 mutations), Gerstmann-Straussler-Scheinker disease, Guadeloupean parkinsonism, myotonic dystrophy, neurodegeneration with brain iron accumulation, Niemann-Pick disease, type C, non-Guamanian motor neuron disease with

neurofibrillary tangles, Pick’s disease, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, progressive supranuclear palsy, SLC9A6-related mental retardation, subacute sclerosing panencephalitis, tangle- only dementia, and white matter tauopathy with globular glial inclusions.

The invention also relates to a compound according to the general Formula (I), a stereoisomeric form thereof or a pharmaceutically acceptable acid or base addition salt thereof, for use in the treatment, prevention, amelioration, control or reduction of the risk of diseases or conditions selected from the group consisting of Alzheimer’s disease, amyotrophic lateral sclerosis and parkinsonism-dementia complex,

argyrophilic grain disease, chronic traumatic encephalopathy, corticobasal

degeneration, diffuse neurofibrillary tangles with calcification, Down’s syndrome, Familial British dementia, Familial Danish dementia, Frontotemporal dementia and parkinsonism linked to chromosome 17 (caused by MAPT mutations), Frontotemporal lobar degeneration (some cases caused by C90RF72 mutations), Gerstmann-Straussler- Scheinker disease, Guadeloupean parkinsonism, myotonic dystrophy,

neurodegeneration with brain iron accumulation, Niemann-Pick disease, type C, non- Guamanian motor neuron disease with neurofibrillary tangles, Pick’s disease, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, progressive supranuclear palsy, SLC9A6-related mental retardation, subacute sclerosing panencephalitis, tangle-only dementia, and white matter tauopathy with globular glial inclusions.

In particular, the diseases or conditions may in particular be selected from a tauopathy, more in particular a tauopathy selected from the group consisting of Alzheimer’s disease, progressive supranuclear palsy, Down’s syndrome, frontotemporal lobe dementia, frontotemporal dementia with Parkinsonism- 17, Pick’s disease, corticobasal degeneration, and agryophilic grain disease; or the diseases or conditions may in particular be neurodegenerative diseases accompanied by a tau pathology, more in particular a neurodegenerative disease selected from amyotrophic lateral sclerosis or frontotemporal lobe dementia caused by C90RF72 mutations.

Preclinical states in Alzheimer’s and tauopathy diseases:

In recent years the United States (US) National Institute for Aging and the International Working Group have proposed guidelines to better define the preclinical (asymptomatic) stages of AD (Dubois B, et al. Lancet Neurol. 2014;13:614-629;

Sperling, RA, et al. Alzheimers Dement. 2011;7:280-292). Hypothetical models postulate that Ab accumulation and tau-aggregation begins many years before the onset of overt clinical impairment. The key risk factors for elevated amyloid accumulation, tau-aggregation and development of AD are age (ie, 65 years or older), APOE genotype, and family history. Approximately one third of clinically normal older individuals over 75 years of age demonstrate evidence of Ab or tau accumulation on PET amyloid and tau imaging studies, the latter being less advanced currently. In addition, reduced Abeta-levels in CSF measurements are observed, whereas levels of non-modified as well as phosphorylated tau are elevated in CSF. Similar findings are seen in large autopsy studies and it has been shown that tau aggregates are detected in the brain as early as 20 years of age and younger. Amyloid-positive (Ab+) clinically normal individuals consistently demonstrate evidence of an“AD-like endophenotype” on other biomarkers, including disrupted functional network activity in both functional magnetic resonance imaging (MRI) and resting state connectivity,

fluorodeoxyglucose ¹⁸ F (FDG) hypometabolism, cortical thinning, and accelerated rates of atrophy. Accumulating longitudinal data also strongly suggests that Ab+ clinically normal individuals are at increased risk for cognitive decline and progression to mild cognitive impairment (MCI) and AD dementia. The Alzheimer’s scientific community is of the consensus that these Ab+ clinically normal individuals represent an early stage in the continuum of AD pathology. Thus, it has been argued that intervention with a therapeutic agent that decreases Ab production or the aggregation of tau is likely to be more effective if started at a disease stage before widespread neurodegeneration has occurred. A number of pharmaceutical companies are currently testing BACE inhibition in prodromal AD.

Thanks to evolving biomarker research, it is now possible to identify

Alzheimer’s disease at a preclinical stage before the occurrence of the first symptoms. All the different issues relating to preclinical Alzheimer’s disease such as, definitions and lexicon, the limits, the natural history, the markers of progression and the ethical consequences of detecting the disease at the asymptomatic stage, are reviewed in Alzheimer’s & Dementia 12 (2016) 292-323.

Two categories of individuals may be recognized in preclinical Alzheimer’s disease or tauopathies. Cognitively normal individuals with amyloid beta or tau aggregation evident on PET scans, or changes in CSF Abeta, tau and phospho-tau are defined as being in an“asymptomatic at risk state for Alzheimer’s disease (AR-AD)” or in a“asymptomatic state of tauopathy”. Individuals with a fully penetrant dominant autosomal mutation for familial Alzheimer’s disease are said to have“presymptomatic Alzheimer’s disease”. Dominant autosomal mutations within the tau-protein have been described for multiple forms of tauopathies as well.

Thus, in an embodiment, the invention also relates to a compound according to the general Formula (I), a stereoisomeric form thereof or a pharmaceutically acceptable acid or base addition salt thereof, for use in control or reduction of the risk of preclinical Alzheimer’s disease, prodromal Alzheimer’s disease, or tau-related neurodegeneration as observed in different forms of tauopathies.

As already mentioned hereinabove, the term“treatment” does not necessarily indicate a total elimination of all symptoms, but may also refer to symptomatic treatment in any of the disorders mentioned above. In view of the utility of the compound of Formula (I), there is provided a method of treating subjects such as warm-blooded animals, including humans, suffering from or a method of preventing subjects such as warm blooded animals, including humans, suffering from any one of the diseases mentioned hereinbefore.

Said methods comprise the administration, i.e. the systemic or topical administration, preferably oral administration, of a prophylactically or a therapeutically effective amount of a compound of Formula (I), a stereoisomeric form thereof, a

pharmaceutically acceptable addition salt or solvate thereof, to a subject such as a warm-blooded animal, including a human.

Therefore, the invention also relates to a method for the prevention and/or treatment of any of the diseases mentioned hereinbefore comprising administering a

prophylactically or a therapeutically effective amount of a compound according to the invention to a subject in need thereof.

The invention also relates to a method for modulating O-GlcNAc hydrolase (OGA) activity, comprising administering to a subject in need thereof, a prophylactically or a therapeutically effective amount of a compound according to the invention and as defined in the claims or a pharmaceutical composition according to the invention and as defined in the claims.

A method of treatment may also include administering the active ingredient on a regimen of between one and four intakes per day. In these methods of treatment the compounds according to the invention are preferably formulated prior to

administration. As described herein below, suitable pharmaceutical formulations are prepared by known procedures using well known and readily available ingredients. The compounds of the present invention, that can be suitable to treat or prevent any of the disorders mentioned above or the symptoms thereof, may be administered alone or in combination with one or more additional therapeutic agents. Combination therapy includes administration of a single pharmaceutical dosage formulation which contains a compound of Formula (I) and one or more additional therapeutic agents, as well as administration of the compound of Formula (I) and each additional therapeutic agent in its own separate pharmaceutical dosage formulation. For example, a compound of Formula (I) and a therapeutic agent may be administered to the patient together in a single oral dosage composition such as a tablet or capsule, or each agent may be administered in separate oral dosage formulations.

A skilled person will be familiar with alternative nomenclatures, nosologies, and classification systems for the diseases or conditions referred to herein. For example, the fifth edition of the Diagnostic & Statistical Manual of Mental Disorders (DSM-5™) of the American Psychiatric Association utilizes terms such as neurocognitive disorders (NCDs) (both major and mild), in particular, neurocognitive disorders due to

Alzheimer’s disease. Such terms may be used as an alternative nomenclature for some of the diseases or conditions referred to herein by the skilled person.

PHARMACEUTICAL COMPOSITIONS

The present invention also provides compositions for preventing or treating diseases in which inhibition of O-GlcNAc hydrolase (OGA) is beneficial, such as Alzheimer’s disease, progressive supranuclear palsy, Down’s syndrome, frontotemporal lobe dementia, frontotemporal dementia with Parkinsonism- 17, Pick’s disease, corticobasal degeneration, agryophilic grain disease, amyotrophic lateral sclerosis or frontotemporal lobe dementia caused by C90RF72 mutations, said compositions comprising a therapeutically effective amount of a compound according to formula (I) and a pharmaceutically acceptable carrier or diluent.

While it is possible for the active ingredient to be administered alone, it is preferable to present it as a pharmaceutical composition. Accordingly, the present invention further provides a pharmaceutical composition comprising a compound according to the present invention, together with a pharmaceutically acceptable carrier or diluent. The carrier or diluent must be“acceptable” in the sense of being compatible with the other ingredients of the composition and not deleterious to the recipients thereof.

The pharmaceutical compositions of this invention may be prepared by any methods well known in the art of pharmacy. A therapeutically effective amount of the particular compound, in base form or addition salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier, which may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirably in unitary dosage form suitable, preferably, for systemic administration such as oral, percutaneous or parenteral administration; or topical administration such as via inhalation, a nose spray, eye drops or via a cream, gel, shampoo or the like. For example, in preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed, such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit form, in which case solid

pharmaceutical carriers are obviously employed. For parenteral compositions, the carrier will usually comprise sterile water, at least in large part, though other ingredients, for example, to aid solubility, may be included. Injectable solutions, for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed. In the compositions suitable for percutaneous administration, the carrier optionally comprises a penetration enhancing agent and/or a suitable wettable agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not cause any significant deleterious effects on the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions. These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on or as an ointment.

It is especially advantageous to formulate the aforementioned pharmaceutical compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used in the specification and claims herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. Examples of such dosage unit forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, injectable solutions or suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof. The exact dosage and frequency of administration depends on the particular compound of Formula (I) used, the particular condition being treated, the severity of the condition being treated, the age, weight, sex, extent of disorder and general physical condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art. Furthermore, it is evident that said effective daily amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention.

Depending on the mode of administration, the pharmaceutical composition will comprise from 0.05 to 99% by weight, preferably from 0.1 to 70% by weight, more preferably from 0.1 to 50% by weight of the active ingredient, and, from 1 to 99.95% by weight, preferably from 30 to 99.9% by weight, more preferably from 50 to 99.9% by weight of a pharmaceutically acceptable carrier, all percentages being based on the total weight of the composition.

The present compounds can be used for systemic administration such as oral, percutaneous or parenteral administration; or topical administration such as via inhalation, a nose spray, eye drops or via a cream, gel, shampoo or the like. The compounds are preferably orally administered. The exact dosage and frequency of administration depends on the particular compound according to Formula (I) used, the particular condition being treated, the severity of the condition being treated, the age, weight, sex, extent of disorder and general physical condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art. Furthermore, it is evident that said effective daily amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention.

The amount of a compound of Formula (I) that can be combined with a carrier material to produce a single dosage form will vary depending upon the disease treated, the mammalian species, and the particular mode of administration. However, as a general guide, suitable unit doses for the compounds of the present invention can, for example, preferably contain between 0.1 mg to about 1000 mg of the active compound. A preferred unit dose is between 1 mg to about 500 mg. A more preferred unit dose is between 1 mg to about 300 mg. Even more preferred unit dose is between 1 mg to about 100 mg. Such unit doses can be administered more than once a day, for example, 2, 3, 4, 5 or 6 times a day, but preferably 1 or 2 times per day, so that the total dosage for a 70 kg adult is in the range of 0.001 to about 15 mg per kg weight of subject per administration. A preferred dosage is 0.01 to about 1.5 mg per kg weight of subject per administration, and such therapy can extend for a number of weeks or months, and in some cases, years. It will be understood, however, that the specific dose level for any particular patient will depend on a variety of factors including the activity of the specific compound employed; the age, body weight, general health, sex and diet of the individual being treated; the time and route of administration; the rate of excretion; other drugs that have previously been administered; and the severity of the particular disease undergoing therapy, as is well understood by those of skill in the area.

A typical dosage can be one 1 mg to about 100 mg tablet or 1 mg to about 300 mg taken once a day, or, multiple times per day, or one time-release capsule or tablet taken once a day and containing a proportionally higher content of active ingredient. The time-release effect can be obtained by capsule materials that dissolve at different pH values, by capsules that release slowly by osmotic pressure, or by any other known means of controlled release.

It can be necessary to use dosages outside these ranges in some cases as will be apparent to those skilled in the art. Further, it is noted that the clinician or treating physician will know how and when to start, interrupt, adjust, or terminate therapy in conjunction with individual patient response.

The invention also provides a kit comprising a compound according to the invention, prescribing information also known as“leaflet”, a blister package or bottle, and a container. Furthermore, the invention provides a kit comprising a pharmaceutical composition according to the invention, prescribing information also known as “leaflet”, a blister package or bottle, and a container. The prescribing information preferably includes advice or instructions to a patient regarding the administration of the compound or the pharmaceutical composition according to the invention. In particular, the prescribing information includes advice or instruction to a patient regarding the administration of said compound or pharmaceutical composition according to the invention, on how the compound or the pharmaceutical composition according to the invention is to be used, for the prevention and/or treatment of a tauopathy in a subject in need thereof. Thus, in an embodiment, the invention provides a kit of parts comprising a compound of Formula (I) or a stereoisomeric for thereof, or a pharmaceutically acceptable salt or a solvate thereof, or a pharmaceutical

composition comprising said compound, and instructions for preventing or treating a tauopathy. The kit referred to herein can be, in particular, a pharmaceutical package suitable for commercial sale.

For the compositions, methods and kits provided above, one of skill in the art will understand that preferred compounds for use in each are those compounds that are noted as preferred above. Still further preferred compounds for the compositions, methods and kits are those compounds provided in the non-limiting Examples below.

EXPERIMENTAL PART

Hereinafter, the term“m.p.” means melting point,“min” means minutes,“ACN”, “MeCN” or“CH3CN” mean acetonitrile,“aq.” means aqueous,“DMF” means dimethylformamide, “r.t.” or“rt” means room temperature,“rac” or“RS” means racemic,“sat.” means saturated,“SFC” means supercritical fluid chromatography, “SFC-MS” means supercritical fluid chromatography/mass spectrometry,“LC-MS” means liquid chromatography/mass spectrometry,“HPLC” means high-performance liquid chromatography,“iPrOH” means isopropyl alcohol,“RP” means reversed phase, “ _t ” means retention time (in minutes),“[M+H] ⁺ ” means the protonated mass of the free base of the compound,“wt” means weight,“THF” means tetrahydrofuran,“EtOAc” means ethyl acetate,“DCM” means dichloromethane,“DIPEA” means N,N- diisopropylethylamine,“MeOH” means methanol,“sat” means saturated,“soltn” or “sol.” means solution,“EtOH” means ethanol, , and“NMP” means N- methylpyrrolidone,“Pd(PPh3) ₄ ” means tetrakis(triphenylphosphine)palladium(0), “Pd(PPh3)2Cl ₂ ” means bis(triphenylphosphine)palladium(II) dichloride,“Pd -B Pfr” means bis(di-/er/-butylphosphine)palladium(0),“PdCl2(dppf)” means [I,G- bis(diphenylphosphino)ferrocene]dichloropalladium(II),“Dav ePhos” means 2- dicyclohexylphosphino-2’-(N,N-dimethylamino)biphenyl,“/B uXPhos” means 2-di- /er/-butylphosphino-2',4',6'-triisopropylbi phenyl and“Pd2(dba)3” means

tris(dibenzylideneaeetone)dipalladium(0).

Whenever the notation“RS” is indicated herein, it denotes that the compound is a racemic mixture at the indicated centre, unless otherwise indicated. The stereochemical configuration for centres in some compounds has been designated“i?” or“X’ when the mixture(s) was separated; for some compounds, the stereochemical configuration at indicated centers has been designated as“i?*” or“S*” when the absolute

stereochemistry is undetermined although the compound itself has been isolated as a single stereoisomer and is enantiomerically/diastereomerically pure. The enantiomeric excess of compounds reported herein was determined by analysis of the racemic mixture by supercritical fluid chromatography (SFC) followed by SFC comparison of the separated enantiomer(s).

Flow chemistry reactions were performed in a Vapourtec R2+R4 unit using standard reactors provided by the vendor. Microwave assisted reactions were performed in a single-mode reactor: InitiatorTM Sixty EXP microwave reactor (Biotage AB), or in a multimode reactor: MicroSYNTH Labstation (Milestone, Inc.).

Thin layer chromatography (TLC) was carried out on silica gel 60 F254 plates (Merck) using reagent grade solvents. Open column chromatography was performed on silica gel, particle size 60 A, mesh = 230-400 (Merck) using standard techniques.

Automated flash column chromatography was performed using ready-to-connect cartridges, on irregular silica gel, particle size 15-40 pm (normal phase disposable flash columns) on different flash systems: either a SPOT or LAFLASH systems from Armen Instrument, or PuriFlash _® 430evo systems from Interchim, or 971-FP systems from Agilent, or Isolera 1SV systems from Biotage.

PREPARATION OF INTERMEDIATES I- la, lb, lc, ld and le

A mixture of 4-chloro-2,6-dimethylpyridine (CAS: 3512-75-2; 2 g, 14.1 mmol), tert- butyl-3-(4,4,5 ,5-tetramethyl- 1 ,3 ,2-dioxaborolan-2-yl)-5 ,6-dihydropyridine- 1 (2/7)- carboxylate (CAS: 1251537-34-4; 4.8 g, 15.5 mmol) and Pd(PPh ₃ ) ₄ (CAS: 14221-01-3; 0.98 g, 0.85 mmol) in a deoxygenated mixture of a saturated solution of NaHC0 ₃ (3 mL) and l,4-dioxane (24 mL) was stirred in a sealed tube at 130 °C for 30 min under N ₂ . Then, the mixture was treated with water and extracted with DCM. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in heptane 0/100 to 100/0). The desired fractions were collected and concentrated in vacuo to afford intermediate la as a colorless oil (3.8 g, 93%).

Intermediate lb was prepared following an analogous procedure to the one described for the synthesis of intermediate la using 4-bromo-2-methoxy-6-methylpyridine (CAS: 1083169-00-9) as starting material.

/nmv-Bis(dicyclohcxylaminc)palladium(II) acetate (DAPcy, CAS: 628339-96-8; 0.114 g, 0.20 mmol) was added to a stirred mixture of 2-chloro-4-iodo-6- trifluoromethylpyridine (CAS: 205444-22-0; 3 g, 9.76 mmol), /er/-butyl-3-(4, 4,5,5- tetramethyl- 1 ,3 ,2-dioxaborolan-2-yl)-5 ,6-dihydropyridine- 1 (2/7)-carboxylatc (CAS : 1251537-34-4; 3.62 g, 11.71 mmol) and K3PO4 (6.21 g, 29.27 mmol) in EtOH (24 mL) under N ₂ . The mixture was stirred at rt for 18 h and then filtered through Celite ®. The Celite ® pad was washed with EtOAc and the filtrate evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in heptane, gradient from 0/100 to 20/80). The desired fractions were collected and concentrated in vacuo to afford intermediate lc as a colorless oil (3.8 g, 93%).

Pd(OAc) ₂ (CAS: 3375-31-3; 0.105 g, 0.47 mmol) and tricyclohexylphosphonium tetrafluoroborate (CAS: 58656-04-5; 0.345 g, 0.94 mmol) were added to a stirred mixture of intermediate lc (3.4 g, 9.37 mmol), trimethylboroxine (CAS: 823-96-1; 2.36 mL, 16.87 mmol) and K ₂ CO ₃ (2.59 g, 18.74 mmol) in deoxygenated l,4-dioxane (35 mL) under N ₂ . The mixture was stirred at 100 °C for 2 h. After cooling to rt, the mixture was washed with LEO and extracted with DCM. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in heptane, gradient from 0/100 to 15/85). The desired fractions were collected and concentrated in vacuo to yield intermediate ld as a pale-yellow oil that crystallized upon standing (2.8 g, 87%).

A 25% solution of sodium methoxide in MeOH (2.14 mL, 9.37 mmol) was added to a stirred solution of intermediate lc (3.4 g, 9.37 mmol) in MeOH (50 mL). The mixture was stirred at rt for 16 h. Then water was added and the desired product was extracted with DCM. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column

chromatography (silica; DCM in heptane, gradient from 20/80 to 100/0). The desired fractions were collected and concentrated in vacuo to yield intermediate le as a colorless oil (3.1 g, 92%).

PREPARATION OF INTERMEDIATES I-2a, 2aR, 2aS, 2b, 2c and 2d

A solution of intermediate la (3.8 g, 13.18 mmol) in EtOH (250 mL) was hydrogenated in a H-cube (Pd/C 10%, rt, full H ₂ , 1 ml/min). The solvent was evaporated in vacuo to yield intermediate 2a as a colorless oil that was used in the next step without further purification (2.7 g, 71 %) .

Pd/C (10% purity, 1.18 g, 1.11 mmol) was added to a stirred solution of intermediate la (3.20 g, 11.1 mmol) in EtOH (64.1 mL). The reaction mixture was hydrogenated (atmospheric pressure) at room temperature for 16 h. The mixture was filtered through a pad of Celite® and washed with MeOH. The filtrate was concentrated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 100:0 to 20:80) to afford intermediate 2a (3.10 g, 96%). A second purification was performed via chiral SFC (stationary phase: CHIRALPAK IC 5 pm 250*30mm, mobile phase: 65% C0 ₂ , 35% z-PrOH (0.3% z-PrNH ₂ ) to afford intermediate 2aR (1.3 g, 40%) and intermediate 2aS (1.44 g, 45%).

Intermediate 2b was prepared following an analogous procedure to the one described for the synthesis of intermediate 2a using intermediate lb as starting material.

Intermediate 2c was prepared following an analogous procedure to the one described for the synthesis of intermediate 2a using intermediate ld as starting material.

Intermediate 2d was prepared following an analogous procedure to the one described for the synthesis of intermediate 2a using intermediate le as starting material.

PREPARATION OF INTERMEDIATES I-3a, I-3aR, 3b, 3c and 3d

Amberlyst® 15 hydrogen form, strongly acidic, cation exchanger resin (CAS: 39389- 20-3; 4 meq/g, 9.3 g) was added to a solution of intermediate 2a (2.7 g, 9.30 mmol) in MeOH (47 mL). The mixture was shaken in a solid phase reactor at rt for 16 h. The resin was washed with MeOH (filtrate discarded) and then with a 7N solution of N¾ in MeOH. The filtrate was concentrated in vacuo to yield intermediate 3a as an orange oil

A solution of intermediate 2aR (1.30 g, 4.48 mmol) in MeOH (34.4 mL) was added to a closed reactor containing Amberlyst® 15 hydrogen form (CAS: 39389-20-3; 4.76 g, 22.4 mmol). The reaction mixture was shaken in a solid phase reactor at room temperature for 16 h. The resin was washed with MeOH (the fraction was discarded). NFL (7N in MeOH) (34 mL) was added and the mixture was shaken in the solid phase reactor for 2 h. The resin was filtered and was washed with NFL (7N in MeOH) (3 x 34 mL; 30 min shaken). The filtrates were concentrated in vacuo to afford intermediate 3aR (820 mg, 96%).

Intermediate 3b was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 2b as starting material.

Intermediate 3b was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20% CH ₃ CN to 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN).

Intermediate 3 c was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 2c as starting material. Intermediate 3c was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20% CH ₃ CN to 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN).

Intermediate 3d was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 2d as starting material.

Intermediate 3b was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20% CH ₃ CN to 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN).

PREPARATION OF INTERMEDIATES I-4a, 4b, 4c, 4d and 4e

Sodium hydride (CAS: 7646-69-7; 60% dispersion in mineral oil, 0.30 g, 7.45 mmol) was added to a stirred solution of l-Boc-3-hydroxypiperidine (CAS: 85275-45-2; 1.5 g, 7.45 mmol) in DMF (6 mL) at 0 °C and the mixture was stirred for 30 min. The mixture was allowed to warm to rt and a solution of 2,6-dimethyl-4-chloropyridine (CAS: 3512- 75-2; 0.95 mL g, 7.45 mmol) in DMF (1 mL) was added dropwise. The mixture was stirred at rt for 16 h and then at 60 °C for 6 h. After cooling to rt, water was added and the mixture was extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica; EtOAc in heptane, gradient from 0/100 to 30/70). The desired fractions were collected and concentrated in vacuo to yield intermediate 4a as a colorless oil (0.42 g, 18%).

Sodium hydride (CAS: 7646-69-7; 60% dispersion in mineral oil, 0.50 g, 12.42 mmol) was added to a stirred solution of l-Boc-3-hydroxypiperidine (CAS: 85275-45-2; 2.5 g, 12.42 mmol) in DMF (14 mL) at -40 °C. The mixture was stirred at -40 °C for 30 min and then a solution of 2-chloro-4-iodo-6-trifluoromethylpyridine (CAS: 205444-22-0; 3.82 g, 12.42 mmol) in DMF (4 mL) was added dropwise. The mixture was allowed to warm to rt and then was stirred for 16 h. Then the mixture was diluted with EtOAc and washed with water and brine. The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica; EtOAc in heptane, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 4d as a light-yellow oil (2.8 g, 59%).

Intermediate 4c was prepared following an analogous procedure to the one described for the synthesis of intermediate ld using intermediate 4b as starting material.

Sodium hydride (CAS: 7646-69-7; 60% dispersion in mineral oil, 0.32 g, 8.01 mmol) was added to a stirred solution of (37?)-l-(Boc)-3-hydroxypyrrolidine (CAS: 109431- 87-0; 1.5 g, 8.01 mmol) in DMF (6.4 mL) at 0 °C and the mixture was stirred for 30 min. Then the mixture was allowed to warm to rt and a solution of 4-bromo-2- methoxy-6-methylpyridine (CAS: 1083169-00-9; 1.48 mL, 8.01 mmol) was added dropwise. The mixture was stirred at 60 °C for 16 h. After cooling to rt, water was added and the mixture was extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica; EtOAc in heptane, gradient from 0/100 to 30/70). The desired fractions were collected and concentrated in vacuo to yield intermediate 4d as a colorless oil (1.67 g, 67%).

Intermediate 4c was prepared following an analogous procedure to the one described for the synthesis of intermediate 4a using 4-bromo-2-methoxy-6-methylpyridine (CAS: 1083169-00-9) as starting material. PREPARATION OF INTERMEDIATES I-5a, 5b, 5c and 5d

Intermediate 5 a was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 4a as starting material.

Intermediate 5b was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 4c as starting material.

Intermediate 5 c was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 4d as starting material.

Intermediate 5d was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 4e as starting material. PREPARATION OF INTERMEDIATES I-6a, 6b and 6c

A solution of (3S)-l-Boc-3-iodomethylpiperidine (CAS: 384829-99-6; 35 g, 107.6 mmol) in a 0.5 M solution of LiCl in THF (192.5 mL, 96.3 mmol) was pumped through a column containing activated Zn (9.35 g, 143.0 mmol) at 40 °C with flow of 1 mL/min. The outcome solution was collected under N ₂ atmosphere to yield

intermediate 6a as a clear light-brown solution that was used without any further manipulation.

For the above reaction Zn was activated as follows: A solution of TMSC1 (2.5 mL) and l-bromo-2-choroethane (0.3 mL) in THF (10 mL) was passed through the column containing Zn at a flow of 1 mL/min.

A solution of (37?)-l-Boc-3-iodomethylpyrrolidine (CAS: 1187932-69-9; 10.1 g, 32.4 mmol) in THF (65 mL) was pumped through a column containing activated Zn (30 g, 458.8 mmol) at 40 °C with a flow of 1 mL/min. The outcome solution was collected under N ₂ atmosphere to yield intermediate 6b as a clear solution that was used without any further manipulation.

For the above reaction Zn was activated as follows: A solution of TMSC1 (2 mL) and l-bromo-2-choroethane (1.2 mL) in THF (20 mL) was passed through the column containing Zn at a flow of 1 mL/min.

Intermediate 6c was prepared following an analogous procedure to the one described for the synthesis of intermediate 6b using (35)-l-Boc-3-iodomethylpyrrolidine (CAS: 224168-68-7) as starting material. PREPARATION OF INTERMEDIATES I-7a, 7b, 7c, 7d, 7e, 7f, 7g, 7h, 7i, 7j and 7k

N, A, A’ , /V’ -Tct ramcth y 1 cth y 1 c n cd i am i n c (CAS: 110-18-9; 11.97 mL, 79.8 mmol), 4- bromo-2,6-dimethylpyridine (CAS: 5093-70-9; 13.50 g, 72.55 mmol) and

Pd(PPh ₃ )2Cl ₂ (1.02 g, 1.45 mmol) were added to a stirred 0.38 M solution of intermediate 6a in THF (210 mL, 79.8 mmol) in a 400 mL EasyMax® reactor equipped with an overhead stirrer and a temperature probe at rt. The mixture was degassed with N ₂ and then stirred at 65 °C (internal temperature) for l6h. After cooling to 20 °C, a mixture of a 32% solution of NH ₃ (50 mL) and a saturated solution of NH ₄ Cl (50 mL) were added. The mixture was diluted with water (100 mL) and EtOAc (200 mL) and filtered through a Celite® pad. The organic layer was separated, washed with brine, dried (MgS04), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica, EtOAc in heptane, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 7a as an orange oil (18.5 g, 84% yield).

A 0.36 M solution of intermediate 6a in THF (42 mL, 15.12 mmol) was added to a stirred mixture of 4-bromo-2-methoxy-6-methylpyridine (CAS: 1083169-00-9; 2.98 g, 14.75 mmol) and Pd(/-Bu ₃ P) ₂ (0.22 g, 0.31 mmol) at rt under N ₂ . The mixture was stirred at reflux for 16 h. After cooling to rt a (1 : 1) mixture of a 32% solution of NFl·,

(50 mL) and a saturated solution of NELCl (50 mL) was added. The mixture was extracted with EtOAc (200 mL). The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (silica, EtOAc in heptane, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 7b as a colorless oil (4.34 g, 91%).

Intermediate 7c was prepared following an analogous procedure to the one described for the synthesis of intermediate 7b using 2-chloro-4-iodo-6-trifluoromethylpyridine (CAS: 205444-22-0) as starting material and stirring the reaction mixture at rt for lh.

Intermediate 7d was prepared following an analogous procedure to the one described for the synthesis of intermediate 7b using 2-chloro-4-iodo-6-trifluoromethoxypyridine (CAS: 1221171-96-5; prepared according to Eur. J. Org. Chem. 2010, 6043-6066) as starting material and stirring the reaction mixture at 65 °C for 3h.

Intermediate 7e was prepared following an analogous procedure to the one described for the synthesis of intermediate ld using intermediate 7c as starting material.

Intermediate 7f was prepared following an analogous procedure to the one described for the synthesis of intermediate ld using intermediate 7d as starting material.

A 0.32 M solution of intermediate 6b (34 mL, 10.88 mmol), /V,/V,/V ^, ,/V’- tetramethylethylenediamine (CAS: 110-18-9; 1.63 mL, 10.88 mmol) and Pd(PPh3) ₂ Cl ₂ (0.42 g, 0.59 mmol) were added to stirred 4-bromo-2,6-dimethylpyridine (CAS: 5093- 70-9; 1.84 g, 9.89 mmol) at rt under N ₂ . The mixture was stirred at 60 °C for lh. After cooling to rt, a 1 : 1 mixture of a 32% solution of NEE and a saturated solution of NH ₄ Cl was added. The mixture was extracted with EtOAc. The organic layer was separated, washed with brine, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (silica, EtOAc in heptane, gradient from 30/70 to 80/20). The desired fractions were collected and concentrated in vacuo to yield intermediate 7g as an oil (2.5 g, 87% yield).

A, A, A’ , A’ -Tct ramcth y 1 cth y 1 c n cd i am i n c (CAS: 110-18-9; 4.40 mL, 29.3 mmol), 4- bromo-2,6-dimethylpyrimidine (CAS: 5093-70-9; 4.20 g, 26.4 mmol) and Pd(PPh ₃ ) ₂ Cl ₂ (0.45 g, 0.64 mmol) were added to a stirred 0.35 M solution of intermediate 6c in THF (83 mL, 29.4 mmol) at rt under N ₂ . The mixture was stirred at reflux for 16 h. After cooling to rt, a 1 : 1 mixture of a 32% solution of NEE and a saturated solution of NEECl was added. The mixture was extracted with EtOAc. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (silica, EtOAc in heptane, gradient from 0/100 to 100/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 7h as an orange oil (9.07 g, 92% yield).

Intermediate 7i was prepared following an analogous procedure to the one described for the synthesis of intermediate 7h using intermediate 6c and 4-bromo-2-methoxy-6- methylpyridine (CAS: 1083169-00-9) as starting materials.

A 0.42 M solution of intermediate 6b (34 mL, 14.3 mmol) was added to a stirred mixture of 2-chloro-4-iodo-6-trifluoromethylpyridine (CAS: 205444-22-0; 4.0 g, 13.01 mmol) and Pd(/-Bu ₃ P)2 (0.33 g, 0.65 mmol) at rt under N ₂ . The mixture was stirred at rt for 1 h and then a 1 :l mixture of a 32% solution of NFT and a saturated solution of NH ₄ Cl was added. The mixture was extracted with EtOAc. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (silica, EtOAc in heptane, gradient from 0/100 to 20/80). The desired fractions were collected and concentrated in vacuo to yield intermediate 7j as a pale-yellow oil (2.50 g, 39%).

Intermediate 7k was prepared following an analogous procedure to the one described for the synthesis of intermediate ld using intermediate 7j as starting material.

PREPARATION OF INTERMEDIATES I-8a, 8b, 8c, 8d, 8e, 8f, 8g AND 8h

A 4M HC1 solution in l,4-dioxane (CAS: 7647-01-0; 148.4 mL, 593.71 mmol) was added to a stirred solution of intermediate 7a in 2-methyltetrahydrofuran (180.7 mL) at 0 °C under N ₂ . The mixture was stirred at 0 °C for 30 min and then allowed to warm to 20 °C. After lh at 20 °C, the mixture was warmed to 50 °C and stirred for a further 2 h. The solid formed was filtered off, washed with 2-methyltetrahydrofuran and dried under vacuum at 50 ⁰ C for 16 h to yield intermediate 8a*2HCl as a light-yellow solid (15.8, 96%).

HC1 (4M in l,4-dioxane, 5.5 mL, 22.0 mmol) was added to intermediate 7a (670 mg, 2.20 mmol) at 0 °C and the reaction mixture was warmed to room temperature. The reaction mixture was stirred for 3 days and concentrated to dryness in vacuo. The residue was purified by ion exchange chromatography (ISOLUTE SCX-2, MeOH and then 7N solution of NEL in MeOH) to afford intermediate 8a (425 mg, 99%).

Intermediate 8a was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 7b as starting material.

Intermediate 8a was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 7d as starting material.

Intermediate 8d was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 7f as starting material.

Intermediate 8e was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 7g as starting material.

Intermediate 8f was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 7h as starting material.

Intermediate 8g was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 7i as starting material.

Intermediate 8h was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 7k as starting material.

PREPARATION OF INTERMEDIATES I-9a, 9b, 9c, 9d, 9e and 9f

Sodium hydride (CAS: 7646-69-7; 60% dispersion in mineral oil, 0.46 g, 11.61 mmol) was added to a stirred solution of (3S)- 1 -Boc-3-hydroxymcthylpipcridinc (CAS:

140695-84-7; 2.5 g, 11.61 mmol) in DMF (10.3 mL) at 0 °C. The mixture was stirred at 0 °C for 30 min and then a solution of 4-chloro-2,6-dimethylpyridine (CAS: 3512-75-2;

1.48 mL, 11.61 mmol) in DMF (1.3 mL) was added dropwise. The mixture was stirred at 60 °C for 16 h and then the solvent was evaporated. The residue was diluted with water and extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 30/70). The desired fractions were collected and concentrated in vacuo to yield intermediate 9a as a colorless oil (2.37 g, 64%).

Intermediate 9b was prepared following an analogous procedure to the one described for the synthesis of intermediate 9a using (3/?)- l-Boc-3-hydroxymcthyl piperidine (CAS: 116574-71-1) as starting material.

Intermediate 9c was prepared following an analogous procedure to the one described for the synthesis of intermediate 9a using 4-chloro-2, 6-pyrimidine (CAS: 4472-45-1) as starting material.

Sodium hydride (CAS: 7646-69-7; 60% dispersion in mineral oil, 0.24 g, 9.96 mmol) was added to a stirred solution of (3/?)- l-Boc-3-hydroxymcthyl pyrrolidine (CAS: 138108-72-2; 1.0 g, 4.97 mmol) in DMF (10 mL) at 0 °C under N ₂ . The mixture was stirred at 0 °C for 30 min and then 4-chloro-2,6-dimethylpyridine (CAS: 3512-75-2; 0.70 mL, 5.46 mmol) was added dropwise. The mixture was stirred at 0 °C for 1 h and then at 80 °C for 20 h. After cooling to rt, a saturated solution of NH ₄ Cl was added and the mixture was extracted with EtOAc. The organic layer was separated, dried

(MgS0 ₄ ), filtered and evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 50/50 to 100/0). The desired fractions were collected and concentrated in vacuo to yield intermediate 9d as an oil

(1.4 g, 92%).

Intermediate 9 e was prepared following an analogous procedure to the one described for the synthesis of intermediate 9d using (35)-l-Boc-3-hydroxymethylpyrrolidine (CAS: 199174-24-8) as starting material.

Intermediate 9f was prepared following an analogous procedure to the one described for the synthesis of intermediate 9a using 4-bromo-2-methoxy-6-methylpyridine (CAS: 1083169-00-9) as starting material.

PREPARATION OF INTERMEDIATES I-lOa, lOb, lOc, lOd, lOe and lOf

Intermediate lOa was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 9a as starting material.

Intermediate lOb was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 9b as starting material.

Intermediate lOc was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 9c as starting material.

Intermediate lOd was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 9d as starting material.

Intermediate lOe was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 9e as starting material.

Intermediate lOf was prepared following an analogous procedure to the one described for the synthesis of intermediate 3a using intermediate 9f as starting material.

PREPARATION OF INTERMEDIATE 31

A solution of intermediate 6c (0.1M solution in THF, 66 mL,6.6 mmol) was added to a solution of 4-bromo-2-methoxy-6-methylpyridine (CAS: 1083169-00-9; 1.21 g, 6.00 mmol) and Pd(/-Bu ₃ P)2 (140 mg, 0.27 mmol). The reaction mixture was stirred at room temperature for 16 h. The mixture was treated with NH ₄ Cl (sat., aq.) and extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and the solvent was evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2,

EtOAc in heptane, gradient from 100:0 to 80:20) to afford intermediate 31 (1 g, 54%). PREPARATION OF INTEREMDIATE 32

Amberlyst® 15 hydrogen form (CAS: 39389-20-3; 4.11 mmol/g) was added to a solution of intermediate 31 (1.00 g, 3.26 mmol) in MeOH (16.6 mL). The reaction mixture was shaken for 18 h. The solvent was removed. The resin was washed few times with MeOH, then NFT (7N in MeOH) was added to the resin and shaken for 1 h. The solvent was removed and the resin was washed few times with NFT (7N in

MeOH). The solvent was evaporated in vacuo to afford intermediate 32 (600 mg, 89%). PREPARATION OF INTERMEDIATE 33

Pd(PPh3) ₄ (1.04 g, 0.90 mmol) was added to a stirred solution of 4-chloro-2,6- dimethylpyrimidine (CAS: 4472-45-1; 2.14 g, 14.9 mmol) and 5-(4,4,5,5-tetramethyl- [1, 3, 2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester (CAS: 885693-20-9; 5.09 g, 16.5 mmol) in l,4-dioxane (10 mL) in a sealed tube and under N ₂ atmosphere. The reaction mixture was stirred at 130 °C for 30 min under microwave irradiation. The mixture was treated with water and extracted with EtOAc. The combined organic extracts were dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 100/0 to 0/100) to afford intermediate 33 (4.12 g, 95%). PREPARATION OF INTERMEDIATE 34

Pd/C (10% purity, 1.51 g, 1.42 mmol) was added to a stirred solution of intermediate 33 (4.1 g, 14.2 mmol) in EtOH (82 mL) under N ₂ atmosphere. The reaction mixture was hydrogenated (atmospheric pressure) at room temperature for 16 h. The mixture was filtered through a pad of Celite® and washed with MeOH. The filtrate was concentrated in vacuo to afford intermediate 34 (3.98 g, 96%).

PREPARATION OF INTERMEDIATE 35

A solution of intermediate 34 (3.96 g, 13.6 mmol) in MeOH (105 mL) was added to a closed reactor containing Amberlyst®l5 hydrogen form (CAS: 39389-20-3; 14.5 g, 67.9 mmol). The reaction mixture was shaken in a solid phase reactor at room temperature for 16 h. The resin was washed with MeOH (the fraction was discarded). N¾ (7N in MeOH) (39 mL) was added and the mixture was shaken in the solid phase reactor for 2 h. The resin was filtered off and washed twice with N¾ (7N in MeOH) (3 x 39 mL; 30 min shaken). The filtrates were combined and concentrated in vacuo to afford intermediate 35 (2.3 g, 88%). PREPARATION OF INTERMEDIATE 36

1-36

Intermediate 36 was prepared following an analogous procedure to the one described for the synthesis of intermediate 33 using 4-chloro-2,6-dimethylpyridin-3-amine (CAS: 37652-11-2) and 5-(4,4,5,5-tetramethyl-[l,3,2]dioxaborolan-2-yl)-3,6-dihydro -2H- pyridine-l -carboxylic acid tert- butyl ester (CAS: 885693-20-9) as starting materials. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in DCM, gradient from 0/100 to 50/50) to afford intermediate 36 (2.38 g, 95%) as an oil.

PREPARATION OF INTERMEDIATE 37

Intermediate 37 was prepared following an analogous procedure to the one described for the synthesis of intermediate 34 using intermediate 36 as starting material.

PREPARATION OF INTERMEDIATE 38

Nitrosyl tetrafluoroborate (2.29 g, 19.6 mmol) was added portion wise to a solution of intermediate 37 (2.00 g, 6.55 mmol) in anhydrous DCM (20 mL). The reaction mixture was stirred at room temperature for 18 h. The reaction was filtered. The filtrate was discarded, while the precipitate was dissolved in MeOH and passed thorough an Iso lute SCX2 cartridge. The cartridge was washed with MeOH and the product was eluted with NFT in MeOH. The desired fractions were collected, and the solvents were concentrated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ , MeOH in DCM, gradient from 0/100 to 20/80). A second purification was performed by RP HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/MeCN, gradient from 95/5 to 70/30) to afford intermediate 38 (310 mg, 23%). PREPARATION OF INTERMEDIATE 39 Boc

Intermediate 6c (0.38M in THF, 11 mL, 4.18 mmol), followed by TMEDA (0.63 mL) and Pd(PPli ₃ ) ₂ Cl ₂ (68 mg, 96.9 mhioΐ) were added to 2-bromo-3,5-difluoropyridine [660425-16-1] (0.76 g, 3.92 mmol) in a sealed tube and under N2 atmosphere. The reaction mixture was stirred at 65 °C for 16 h. The reaction was quenched with a 1 : 1 solution of NH ₄ CI (sat.) and NEE (26% aq.) and extracted with EtOAc. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvent was evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, EtOAc in heptane, gradient from 0/100 to 30/70) to afford intermediate 39 (715 mg, 61%).

PREPARATION OF INTERMEDIATE 40

A solution of intermediate 38 (1.17 g, 3.91 mmol) in MeOH (19.6 mL) was added dropwise to Amberlyst®l5 hydrogen form (CAS:39389-20-3; 3.93 g, 18.5 mmol) in a solid phase reaction. Once the evolution of CO2 stopped, the reaction mixture was shaken at room temperature for 2 days. The resin was washed with MeOH (fraction was discarded) and NH3 (7N in MeOH). The filtrate was concentrated in vacuo to afford intermediate 40 (0.698 g, 90%).

PREPARATION OF INTERMEDIATE 41 Boc

Intermediate 41 was prepared following an analogous procedure to the one described for intermediate 39 starting from 4-chloro-2,6-dimethylpyrimidine (CAS: 4472-45-1). PREPARATION OF INTERMEDIATE 42

Intermediate 42 was prepared following an analogous procedure to the one described for intermediate 40 starting from intermediate 41.

PREPARATION OF INTERMEDIATE 43

(R)-tert- Butyl 3-hydroxypyrrolidine-l-carboxylate (CAS: 109431-87-0; 1.50 g, 8.01 mmol) was stirred in DMF (3.2 mL) at room temperature. NaH (60% dispersion in mineral oil, 320 mg, 8.01 mmol) was added. A solution of 4-chloro-2,6-lutidine (CAS: 3512-75-2; 1.02 mL, 8.01 mmol) in DMF (3.22 mL) was added dropwise. The reaction mixture was stirred overnight at 60 °C. The mixture was evaporated in vacuo. The residue was diluted with water and extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 0/100 to 90/10) to afford intermediate 43 (1.20 g, 51%).

PREPARATION OF INTERMEDIATE 44

A solution of intermediate 43 (1.20 g, 4.10 mmol) in MeOH (31.6 mL) was added to a closed reactor containing Amberlyst®l5 hydrogen form (CAS:39389-20-3; 4.37 g, 20.5 mmol). The reaction mixture was shaken in a solid phase reactor at room temperature for 16 h. The resin was washed with MeOH (the fraction was discarded). NFT (7N in MeOH) (31.7 mL) was added and the mixture was shaken in the solid phase reactor for 2 h. The resin was filtered off and was washed with NFT (7N in MeOH) (2 x 31 mL; 30 min shaken). The filtrates were combined and concentrated in vacuo to afford intermediate 44 (710 mg, 90%).

PREPARATION OF INTERMEDIATE 45

1-45 Boc

NaH (60% dispersion in mineral oil, 221 mg, 5.51 mmol) was added to a stirred solution of (5)-l-boc-3-hydroxypiperidine (CAS: 143900-44-1; 1.01 g, 5.01 mmol) in DMF (31 mL) at room temperature. The mixture was stirred for 15 min and 2,6- dimethyl-pyridin-4-ylmethyl chloride (CAS: 120739-87-9; 1.00 g, 5.01 mmol, 78% purity) was added. The reaction mixture was stirred at room temperature for 16 h. NH ₄ Cl (sat., aq.) was added and the mixture was extracted with EtOAc. The organic layer was washed with brine (twice), dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, EtOAc in heptane, gradient from 0/100 to 100/0) to afford intermediate 45 (1.19 g, 74%).

PREPARATION OF INTERMEDIATE 46

Intermediate 46 was prepared following an analogous procedure to the one described for the synthesis of intermediate 44 using intermediate 46 as starting material.

PREPARATION OF INTERMEDIATE 47

1-47 Boc Intermediate 47 was prepared following an analogous procedure to the one described for intermediate 45 using (R)- 1 -boc-3-hydroxypipcridinc (CAS: 143900-43-0) and 2,6- dimethyl-pyridin-4-ylmethyl chloride (CAS: 120739-87-9) as starting materials. PREPARATION OF INTERMEDIATE 48

Intermediate 48 was prepared following an analogous procedure to the one described for the synthesis of intermediate 44 using intermediate 47 as starting material. PREPARATION OF INTERMEDIATE 49

Boc

1-49

Intermediate 49 was prepared following an analogous procedure to the one described for intermediate 45 using (R)- 1 -boc-3-hydroxypyrrolidinc (CAS: 109431-87-0) and 2,6-dimethyl-pyridin-4-ylmethyl chloride (CAS: 120739-87-9) as starting materials.

PREPARATION OF INTERMEDIATE 50

Intermediate 50 was prepared following an analogous procedure to the one described for the synthesis of intermediate 44 using intermediate 49 as starting material. PREPARATION OF INTERMEDIATE 51

1-51 Boc

NaH (60% dispersion in mineral oil, 238 mg, 5.96 mmol) was added to a solution of (7?)-3 -hydroxymethyl-pyrrolidine- 1 -carboxylic acid tert- butyl ester (CAS: 138108-72- 2; 1.00 g, 4.97 mmol) in DMF (10 mL) at 0 °C under N ₂ atmosphere. The mixture was stirred at 0 °C for 15 min, and 4-bromo-2-methoxy-6-methylpyridine (CAS: 1083169- 00-9; 1.15 g, 5.47 mmol) added dropwise. The reaction mixture was stirred at 0 °C for 1 h and then at 70 °C for 20 h. The reaction was quenched with NH ₄ Cl (sat., aq.) and extracted with heptane. The organic layer was dried (MgS0 ₄ ), filtered and evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 0/100 to 50/50) to afford intermediate 51 (970 mg, 61%).

PREPARATION OF INTERMEDIATE 52

Intermediate 52 was prepared following an analogous procedure to the one described for the synthesis of intermediate 44 using intermediate 51 as starting material.

PREPARATION OF INTERMEDIATE 53

Pd ₂ dba3 (187 mg, 0.20 mmol), DavePhos (166 mg, 0.41 mmol) and NaO/-Bu (1.57 g, 16.3 mmol) were added under N ₂ atmosphere to a solution of 4-bromo-2,6- dimethylpyridine (CAS: 5093-70-9; 1.52 g, 8.17 mmol) in anhydrous l,4-dioxane (40 mL) in a sealed tube tert- Butyl 3-(aminomethyl)piperidine-l-carboxylate (CAS:

162167-97-7; 2.10 g, 9.80 mmol) was added at room temperature and the reaction mixture was stirred at 100 °C for 16 h. The mixture was diluted with EtOAc and NH ₄ Cl (aq., sat., 0.5 mL). The mixture was filtered over a pad of Celite® and the filtrate was concentrated in vacuo. The crude mixture was purified by flash column

chromatography (S1O2, MeOH in DCM, gradient from 0/100 to 50/50) to afford intermediate 53 (2.26 g, 82%).

PREPARATION OF INTERMEDIATE 54

HC1 (4M inl,4-dioxane, 25.6 mL, 103 mmol) was added dropwise to a stirred solution of intermediate 53 (2.23 g, 6.84 mmol) in MeOH (15.8 mL) at 0 °C. The reaction mixture was stirred at room temperature for 16 h and the solvent was evaporated in vacuo. The crude mixture was purified by phase reverse ([25mM

NH ₄ HC0 ₃ ]/[MeCN/Me0H (1/1), gradient from 95/5 to 63/37). The desired fractions were collected and concentrated in vacuo. MeCN (3 x 10 mL) was added and the solvent was concentrated in vacuo to afford intermediate 53 (1.3 g, 87%).

PREPARATION OF INTERMEDIATE 55

OMe Boc

NaO/-Bu (119 mg, 1.24 mmol) was added to a stirred suspension of Pd ₂ dba3 (22.7 mg, 24.7 nmol) and /BuXPhos (31.5 mg, 74.2 pmol) in l,4-dioxane (15 mL) in a sealed tube and under N ₂ atmosphere at room temperature. The reaction mixture was stirred at 95 °C for 5 min, then a mixture of (S)-(+)-3-amino- 1 -boc-pipcrdinc [625471-18-3] (129 mg, 0.64 mmol) and 4-bromo-2-methoxy-6-methylpyridine [1083169-00-9] (100 mg, 0.49 mmol) in l,4-dioxane (5 mL) was added under N ₂ atmosphere at 95 °C. The reaction mixture was stirred at 100 °C for 30 min. The mixture was diluted with NaHCCh (sat., aq.) and extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 5/95 to 100/0) to afford intermediate 55 (130 mg, 82%).

PREPARATION OF INTERMEDIATE 56

HC1 (4M in l,4-dioxane, 0.50 mL, 2.00 mmol) was added dropwise to intermediate 55 (130 mg, 0.40 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 16 h and the solvent was evaporated in vacuo. The residue was dissolved in MeOH (1 mL) and Amberlyst®A26 hydroxide form (CAS: 39339-85-0; 505 mg, 1.62 mmol) was added. The mixture was stirred at room temperature until pH was 7. The resin was removed by filtration and the solvents were evaporated in vacuo to afford intermediate 56 (85 mg, 95%).

PREPARATION OF INTERMEDIATE 57

(S)-(+)-3-Amino-l-boc-piperidine (CAS: 625471-18-3; 117 mg, 0.58 mmol) and 2- methoxy-6-methylpyridine-4-carbaldehyde (CAS: 951795-43-0; 100 mg, 0.58 mmol) were dissolved in ACN (3 mL). The reaction mixture was stirred at room temperature for 30 min, and sodium triacetoxyborohydride (371 mg, 1.75 mmol) was added. The resulting mixture was stirred at room temperature for 16 h. The mixture was diluted with NaHC0 ₃ (sat., aq.) and DCM. The aqueous layer was extracted with DCM

(twice). The combined organic layers were dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column

chromatography (S1O2, EtOAc in heptane, gradient from 0/100 to 50/50) to afford intermediate 57 (161 mg, 77%).

PREPARATION OF INTERMEDIATE 58

TFA (0.5 mL, 3.23 mmol) was added dropwise to a stirred mixture of intermediate 57 (1.00 g, 2.81 mmol) and DIPEA (0.64 mL, 3.65 mmol) in DCM (13 mL) under N ₂ atmosphere at room temperature. The reaction mixture was stirred for 16 h. The reaction was quenched with HC1 (1M) and extracted with DCM. The organic layer was washed with NaHC0 ₃ (sat., aq.) and brine, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column

chromatography (Si0 ₂ , EtOAc in heptane, gradient from 0/100 to 30/70) to afford intermediate 58 (1.1 g, 87%).

PREPARATION OF INTERMEDIATE 59

Intermediate 58 (900 mg, 1.99 mmol) and methylboronic acid [13061-96-6] (304 mg, 4.98 mmol) were added to a stirred solution of Na ₂ C0 ₃ (633 mg, 5.98 mmol) in 1,4- dioxane (4.98 mL) and H ₂ 0 (1.25 mL) under N ₂ atmosphere. PdCl ₂ (dppf)*DCM (81.3 mg, 99.6 qrnol) was added and the reaction mixture was stirred at 105 °C for 16 h. Additional amount of methylboronic acid (1.25 eq), PdCl ₂ (dppf)*DCM (0.025 eq) and Na ₂ C0 ₃ (1.5 eq) were added under N ₂ atmosphere. The reaction mixture was stirred at 105 °C for 16 h. The mixture was diluted with NaHC0 ₃ and extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, EtOAc in heptane, gradient from 0/100 to 20/80) to afford intermediate 59 (690 mg, 80%).

PREPARATION OF INTERMEDIATE 60

HC1 (4M in l,4-dioxane, 2.00 mL, 8.00 mmol) was added dropwise to intermediate 59 (690 mg, 1.60 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 16 h and the solvent was evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , MeOEPNEb in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to afford intermediate 60 (317 mg, 59%).

PREPARATION OF INTERMEDIATE 61

(S)-(+)-3-Amino-l-boc-piperidine (CAS: 625471-18-3; 449 mg, 2.24 mmol) and 2,6- dimethyl-4-pyridine carboxaldehyde (CAS: 18206-06-9; 303 mg, 2.24 mmol) were dissolved in DCM (10 mL). The reaction mixture was stirred at room temperature for 30 min and sodium triacetoxyborohydride (1.43 g, 6.73 mmol) was added. The resulting mixture was stirred at room temperature for 16 h. NaHC0 ₃ (sat., aq.) and DCM were added. The aqueous layer was extracted with DCM (twice). The combined organic extracts were dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 0/100 to 50/50) to afford intermediate 61 (577 mg, 79%). PREPARATION OF INTERMEDIATE 62

HC1 (4M in l,4-dioxane, 2.26 mL, 9.03 mmol) was added dropwise to intermediate 61 (577 mg, 1.81 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 16 h and the solvent was removed in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , MeOEENEb in DCM, gradient from 0/100 to 10/90) to afford intermediate 62 (320 mg, 80%).

PREPARATION OF INTERMEDIATES 1-1 la, 1 lb and 1 lc

-l la

Sodium hydride (CAS: 7646-69-7; 60% dispersion in mineral oil, 3.80 g, 94.97 mmol) was added portionwise to a stirred solution of 6-bromo-2-mcthyl- 17/-imidazo[4,5- hjpyridine (CAS: 42869-47-6; 10.0 g, 47.16 mmol) in DMF (100 mL) at 0 °C. The mixture was stirred at 0 °C for 30 min and then 2-(trimethylsilyl)ethoxymethylchloride (CAS: 76513-69-4; 19.20 mL, 108.47 mmol) was added dropwise. The mixture was stirred at rt for 16 h and then it was diluted with a saturated NH ₄ Cl solution and extracted with EtOAc. The organic layer was separated, washed with brine, dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 100/0). The desired fractions were collected and concentrated in vacuo to yield intermediate 1 la as a pale- brown solid (8.07 g, 50%).

l lb

Intermediate l lb was prepared following an analogous procedure to the one described for the synthesis of intermediate la using intermediate 5-chloro-2-mcthyl-3/7- imidazo[4,5-6] pyridine (CAS: 40851-92-1) as starting material. Intermediate l lb was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 5/95).

K2CO3 (3.05 g, 433.1 mmol) and methyl iodide (CAS: 74-88-4; 0.5 mL, 8.03 mmol) were added to a stirred solution of 6-bromo-2mcthyl- 1 //-imidazo[4,5-6]pyridinc (CAS: 42869-47-6, 1.35 g, 6.37 mmol) in acetone (32 mL). The mixture was stirred at rt for

16 h and then water and EtOAc were added. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield intermediate 1 lc as a brown solid (0.835 g, 58%).

PREPARATION OF INTERMEDIATES I-l2a and l2b

Pd(PPh3) ₄ (CAS: 14221-01-3; 1.36 g, 1.18 mmol) was added to a stirred mixture of intermediate l la (8.07 g, 23.57 mmol) and 4,4,5,5-tetramethyl-2-vinyl-l,3,2- dioxaborolane (CAS: 75927-49-0; 6.00 mL, 35.36 mmol) in a mixture of a saturated solution of K ₂ C0 ₃ (36.3 mL) and l,4-dioxane (36.3 mL) at rt under N ₂ . The mixture was stirred at 95 °C for 16 h. Then a saturated solution of K ₂ C0 ₃ was added and the mixture was extracted with EtOAc. The organic layer was separated, washed with brine, dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 4/96). The desired fractions were collected and concentrated in vacuo to yield intermediate l2a as an orange oil that solidified upon standing (2.07 g, 28%).

Tributyl(vinyl)tin (CAS: 123-91-1; 0.82 mL, 2.83 mmol), 2,4-di-/er/-butyl-4- methylphenol (CAS: 128-37-0; 0.24 g, 1.10 mmol) and Pd(PPh ₃ ) ₄ (CAS: 14221-01-3; 0.14 g, 0.12 mmol) were added to a stirred mixture of intermediate 1 lb (0.36 g, 1.20 mmol) in l,4-dioxane (3.8 mL) in a sealed tube under N ₂ . The mixture was stirred at 100 °C for 16 h. After cooling to rt, the mixture was filtered off and the solid washed with EtOAc. The filtrate was evaporated in vacuo and the crude product was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 5/95) The desired fractions were collected and concentrated in vacuo to yield intermediate l2b (0.25 g, 72%).

PREPARATION OF INTERMEDIATE I-l3a

LiAlEE (CAS: 16853-85-3; 1M in THF, 2.8 mL, 2.77 mmol) was added dropwise to a stirred solution of 5-ethoxycarbonyl-2-methylbenzimidazole (CAS: 717-37-3; prepared according to Eur. J. Med. Chem. 2009, 1500-1508, 0.47 g, 2.31 mmol) in THF (14 mL) at 0 °C under N ₂ . The mixture was stirred at 0 °C for 5 min and then at rt for 2 h. Then the mixture was cooled down to 0 °C and more LiAlH ₄ (1.4 mL, 1.39 mmol) was added. The mixture was stirred at 0 °C for 5 min and at rt for another 2 h. Then a saturated solution of Rochelle’s salt in ice was added and the mixture was extracted with EtOAc. The organic layer was separated, washed with brine, dried (MgS0 ₄ ), filtered and the solvents were removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NIL in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield intermediate l3a as a white solid (0.80 g, 21%).

PREPARATION OF INTERMEDIATES I-l4a, l4b, l4c and l4d

Sudan III (CAS: 85-86-9; trace amount) was added to a stirred solution of intermediate l2a (4.3 g, 7.86 mmol) in a mixture of ACN (195.5 mL) and water (9.8 mL). The solution was cooled to 0 °C and a mixture of 0 ₃ /0 ₂ was passed through the flask until the red color dissipated. The reaction was purged with N ₂ for 10 min. Then, the reaction was diluted with a saturated solution of sodium thiosulfate and extracted with EtOAc. The organic layer was separated, washed with brine, dried (Na ₂ S0 ₄ ), filtered and the solvents were removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 60/40). The desired fractions were collected and concentrated in vacuo to yield intermediate l4a as white solid (2.39 g, 55%).

Sodium periodate (CAS: 7790-28-5; 1.12 g, 5.25 mmol), osmium tetroxide (2.5% in /BuOH CAS: 20816-12-0; 0.18 mL, 0.013 mmol) and 2,6-dimethylpyridine (CAS: 108- 48-5; 0.27 mL, 2.30 mmol) were added to a stirred solution of intermediate l2b (4.3 g, 7.86 mmol) in a mixture of 1 ,4-dioxane (8.0 mL) and water (2.66 mL) in a sealed tube under N ₂ . The mixture was stirred at rt for 17 h. Then, the reaction was diluted with water and extracted with EtOAc. The organic layer was separated, washed with brine, dried (MgS0 ₄ ), filtered and the solvents were removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFT in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield intermediate l4b as a yellow oil (0.13 g, 52%).

Mn0 ₂ (0.50 g, 4.90 mmol) was added to a stirred suspension of intermediate l3a (0.080 g, 0.49 mmol) in l,4-dioxane (3 mL) in a sealed tube under N ₂ . The mixture was stirred at 80° C for 16 h. After cooling to rt, the mixture was filtered through a Celite® pad and the pad was washed with DCM. The filtrate was concentrated in vacuo to yield intermediate l4c as a white solid (0.047 g, 59%).

Tributyl(l-ethoxyvinyl)tin (CAS: 97674-02-7; 0.74 mL, 2.19 mmol) and Pd(PPli3) ₂ Cl ₂ (0.14 g, 0.19 mmol) were added to a stirred mixture of intermediate 1 lc (0.46 g, 2.03 mmol) in toluene (10 mL) in a sealed tube under N ₂ . The mixture was stirred at 80 °C for 16 h. After cooling to rt, a 1M HC1 solution (4 mL) was added and the mixture was stirred at 80 °C for a further 5 h. After cooling to rt, the mixture was poured onto a stirred mixture of a saturated NaHCCh solution and ice and extracted with DCM. The organic layer was separated, washed with brine, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFT in MeOH in DCM, gradient from 0/100 to 5/95). The desired fractions were collected and concentrated in vacuo to yield intermediate l4d as a pale-orange solid (0.24 g, 63%).

PREPARATION OF INTERMEDIATES I-l5a,l5b and l5c

6-Chloro-l//-pyrazolo[4,3-b]pyridine (CAS: 63725-51-9; 0.35 g, 2.25 mmol) was added to a stirred solution of trimethyloxoniumtetrafluoroborate (CAS: 420-37-1; 1.35 g, 9.13 mmol)and DIPEA (1.93 mL, 11.23 mmol) in DCM (13.8 mL). The mixture was stirred at rt for 72 h and quenched with a saturated solution of NaHC0 ₃ and extracted with DCM. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvent was evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 20/80 to 100/0). The desired fractions were collected and concentrated in vacuo to yield intermediate 15a as a white solid (0.27 g, 65%).

Intermediate l5b was prepared following an analogous procedure to the one described for the synthesis of intermediate l5a using 6-chloro- 1 //-pyrazolo[4,3-c]pyridinc (CAS: 1206979-33-0) as starting material.

HATU (CAS: 148893-10-1; 2.70 g, 7.10 mmol), A,O-dimethylhydroxylamine hydrochloride (CAS: 6638-79-5, 067 g, 6.87 mmol) and Et ₃ N (2.50 mL, 17.99 mmol) were added to a stirred suspension of 2-methylindazole-6-carboxylic acid (CAS:

103141-74-8; 1 g, 5.68 mmol) in DMF (28 mL) at rt under N ₂ . The mixture was stirred at rt for 16 h and then water was added. The mixture was extracted with EtOAc and the organic layer was separated, washed with brine, dried (Na ₂ S0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column

chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield intermediate 15c as an orange oil which solidified upon standing (0.405 g, 33%).

PREPARATION OF INTERMEDIATES I-l6a, l6b, !6c,l6d and l6e

Pd(PPth) ₄ (0.183 g, 0.16 mmol) was added to a stirred suspension of tributyl(l- ethoxyvinyl)tin (CAS: 97674-02-7; 0.80 mL , 2.37 mmol) and intermediate l5a (0.27 g, 1.58 mmol) in toluene (8.2 mL) in a sealed tube under N ₂ . The mixture was stirred at

100 °C for 16 h. After cooling to rt, a 2M HC1 solution (2.37 mL) was added and the mixture was stirred at 80 °C for 1 h. After cooling to rt, the mixture was neutralized with a saturated NaHC0 ₃ solution addition and extracted with a 4: 1 mixture of DCM and /PrOH. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of ME in MeOH in DCM, gradient from 0/100 to 5/95). The desired fractions were collected and concentrated in vacuo to yield intermediate l6a as a brown oil (0.097 g, 28%).

Intermediate l6b was prepared following an analogous procedure to the one described for the synthesis of intermediate l6a using intermediate 15b as starting material

Intermediate l6c was prepared following an analogous procedure to the one described for the synthesis of intermediate l6a using 6-bromo-2-mcthyl-2/7-pyrazolo[4,3- hjpyridine (CAS: 1897500-19-4) as starting material.

Intermediate l6d was prepared following an analogous procedure to the one described for the synthesis of intermediate l6a using 5-bromo-2-mcthy 1-2/7- indazolc (CAS: 465529-56-0) as starting material.

Diisobutylaluminium hydride (1M solution in THF, 2.5 mL, 2.5 mmol) was added dropwise to a stirred solution of intermediate l5c (0.4 g, 1.82 mmol) in 2- methyltetrahydrofurane (9.5 mL) at -78 °C under N ₂ . The mixture was stirred at -78 °C for 3 h and then diluted with EtOAc. Then sodium sulfate decahydrate was added and the mixture was stirred for 30 min. The mixture was filtered through a Celite® pad and the pad was washed with EtOAc. The filtrate was dried (Na ₂ S0 ₄ ) and the solvent was evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 100/0). The desired fractions were collected and concentrated in vacuo to yield intermediate l6e as a yellow solid (0.181 g, 62%).

PREPARATION OF INTERMEDIATES I-l7a, l7b and l7c

Triethyl orthoacetate (CAS: 78-39-7; 4.82 mL, 26.48 mmol) was added to a stirred mixture of 2-amino-6-bromopyridin-3-ol (CAS: 934758-27-7; 4.17 g, 22.06 mmol) and /;-tolucncsulfonic acid monohydrate (CAS: 104-15-4; 0.21 g, 1.10 mmol) in toluene (24.2 mL). The mixture was stirred at 130 °C for 1 h and then the solvent evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate l7a as a yellow solid (0.27 g, 65%). Intermediate l7b was prepared following an analogous procedure to the one described for the synthesis of intermediate l7a using triethyl orthoisobutyrate (CAS: 52698-46-1) as starting material.

Intermediate l7c was prepared following an analogous procedure to the one described for the synthesis of intermediate l7a using 2-amino-4-bromo-5-fluorobenzene(CAS: 1016234-89-1) as starting material.

PREPARATION OF INTERMEDIATES I-l8a, l8b, l8c, l8d and l8e

Pd(PPh3) ₄ (0.86 g, 0.75 mmol) was added to a stirred mixture of intermediate l7a (3.18 g, 14.93 mmol) and 4,4,5,5-tetramethyl-2-vinyl-l,3,2-dioxaborolane (CAS: 75927-49- 0; 3.80 mL, 22.39 mmol) in a mixture of a saturated solution of K2CO3 (17.86 mL) and l,4-dioxane (17.86 mL) at rt under N ₂ . The mixture was stirred at 95 °C for 16 h. Then water was added and the mixture was extracted with EtOAc. The organic layer was separated, washed with brine, dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in DCM, 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo and the residue was purified again by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 18a as a light-yellow solid (1.39 g, 58%).

Intermediate 18b was prepared following an analogous procedure to the one described for the synthesis of intermediate l8a using intermediate l7b as starting material.

Intermediate l8c was prepared following an analogous procedure to the one described for the synthesis of intermediate l8a using intermediate l7c as starting material.

Tributyl(vinyl)tin (CAS: 123-91-1; 1.0 mL, 3.42 mmol), 2,4-di-/er/-butyl-4- methylphenol (CAS: 128-37-0; 0.054 g, 0.25 mmol) and Pd(PPh3) ₄ (0.138 g, 0.12 mmol) was added to a stirred mixture of 6-bromo-2-mcthyloxazolo [5, 4-/;] pyridine (0.54 g, 2.54 mmol) in l,4-dioxane (13 mL) in a sealed tube under N ₂ . The mixture was stirred at 100 °C for 18 h. After cooling to rt, the mixture was filtered through a Celite® pad and the pad was washed with EtOAc. The filtrate was evaporated in vacuo and the crude product was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 100/0). The desired fractions were collected and concentrated in vacuo to yield intermediate 18d (0.405 g, 99%).

Intermediate l8e was prepared following an analogous procedure to the one described for the synthesis of intermediate 18d using 6-bromo-2-mcthyloxazolo[4, 5-/ ] pyridine (CAS: 494747-09-0) as starting material.

PREPARATION OF INTERMEDIATES I-l9a, l9b, l9c, l9d and l9e

Sudan III (CAS: 85-86-9; trace amount) was added to a stirred solution of intermediate l8a (1.39 g, 8.68 mmol) in a mixture of ACN (114.2 mL) and water (5.7 mL). The solution was cooled to 0°C and a mixture of O ₃ /O ₂ was passed through the flask until the red color dissipated. The reaction was purged with N ₂ for 10 min. Then, the reaction was diluted with a mixture of EtOAc and THF and extracted with a saturated solution of Na ₂ C0 ₃ . The organic layer was separated, washed with brine, dried

(Na ₂ S0 ₄ ), filtered and the solvents were removed in vacuo to yield intermediate l9a as beige solid (1.0 g, 71%). Intermediate l9b was prepared following an analogous procedure to the one described for the synthesis of intermediate l9a using intermediate 18b as starting material.

Intermediate l9c was prepared following an analogous procedure to the one described for the synthesis of intermediate l9a using intermediate l8c as starting material.

Intermediate l9c was purified by flash column chromatography (Si0 ₂ ; EtOAc in DCM, gradient from 0/100 to 20/80).

Sodium periodate (CAS: 7790-28-5; 1.19 g, 5.58 mmol) and osmium tetroxide (CAS: 20816-12-0; 2.5% in /BuOH, 0.18 mL, 0.013 mmol) were added to a stirred solution of intermediate 18d (0.40 g, 2.48 mmol) in a mixture of 1 ,4-dioxane (17.5 mL) and water (7.5 mL) under N ₂ . The mixture was stirred at rt for 2 h and then a saturated Na ₂ S ₂ 0 ₃ solution was added. The mixture was extracted with EtOAc and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 100/0). The desired fractions were collected and concentrated in vacuo to yield intermediate l9d as a white solid (0.30 g, 75%).

Intermediate l9e was prepared following an analogous procedure to the one described for the synthesis of intermediate 19b using intermediate le as starting material.

PREPARATION OF INTERMEDIATE I-20a

Tributyl(l-ethoxyvinyl)tin (CAS: 97674-02-7; 1.8 mL, 5.33 mmol) and PdCl ₂ (PPli3) ₂ (0.34 g, 0.49 mmol) were added to a stirred mixture of 6-bromofuro[3, 2-6] pyridine (CAS: 935330-61-7, 0.96 g, 4.87 mmol) in toluene (25 mL) in a sealed tube under N ₂ . The mixture was stirred at 80 °C for 16 h. After cooling to rt, a 1M HC1 solution (9.5 mL) was added and the mixture was stirred at 80 °C for a further 5 h. After cooling to rt, the mixture was poured onto a stirred mixture of a saturated NaHCCh solution and ice and extracted with DCM. The organic layer was separated, washed with brine, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in DCM, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 20a as a pale-orange solid (0.24 g, 63%).

PREPARATION OF INTERMEDIATES 1-2 la and 2 lb

Acetic anhydride (CAS: 108-24-7; 13.2 g, 129.8 mmol) was added to a stirred mixture of methyl 6-amino-5-bromopyridine-2-carboxylate (CAS: 178876-82-9; 30 g, 129.8 mmol) in toluene (600 mL) under N ₂ . The mixture was stirred at 100 °C for 36 h and then the solvent evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in petroleum ether, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 2la as a white solid (14.0 g, 40%).

Intermediate 2 lb was prepared following an analogous procedure to the one described for the synthesis of intermediate 20a using 2-amino-3-bromo-5-fluoropyridine as starting material. PREPARATION OF INTERMEDIATE I-22a Phosphorus pentasulfide (CAS: 1314-80-3; 13.7 g, 61.5 mmol) was added to a suspension of intermediate 2la (14.0 g, 51.3 mmol) in THF (200 mL) under N ₂ . The mixture was stirred at 25 °C for 16 h and then at 70 °C for 48 h. Then the solvent was evaporated in vacuo and the residue purified by flash column chromatography (Si0 ₂ ; EtOAc in petroleum ether, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 22a as a yellow solid (7.5 g, 69%).

PREPARATION OF INTERMEDIATE I-23a

NaBEE (6.81 mL, 180.0 mmol) was added to a stirred suspension of intermediate 22a (7.55 g, 36.0 mmol) in THF (60 mL). The mixture was stirred at 25 °C for 5 h and then a saturated NH ₄ Cl solution (100 mL) was added. The mixture was extracted with DCM and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo to yield intermediate 23a as a yellow solid (3.1 g, 51%).

PREPARATION OF INTERMEDIATE I-24a

Phosphorus pentasulfide (1.70 g, 7.67 mmol) was added to a suspension of intermediate 2lb (1.38 g, 5.90 mmol) in THF (32.2 mL). The mixture was stirred at rt for 16 h and an additional amount of phosphorus pentasulfide (0.39 g, 1.77 mmol) was added. The mixture was stirred at rt for another 16 h and then Cs ₂ C0 ₃ (3.08 g, 9.44 mmol) was added. The mixture was stirred at 70 °C for 16 h and then additional quantity of Cs ₂ C0 ₃ (3.08 g, 9.44 mmol) was added. The mixture was stirred at 70 °C for a further 16 h and then water was added. The mixture was extracted with EtOAc and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 60/40). The desired fractions were collected and concentrated in vacuo to yield intermediate 24a as a pale-orange solid (0.78 g, 78%). PREPARATION OF INTERMEDIATE I-25a

m-Chloroperbenzoic acid (CAS: 937-14-4; 1.13 g, 6.42 mmol) was added to a mixture of intermediate 24a (0.72 g, 4.28 mmol) in DCM (24 mL). The mixture was stirred at rt for 16 h and then more m-chloroperbenzoic acid (1.13 g, 6.42 mmol) was added. The mixture was stirred at rt for a further 3d and then water was added and the mixture extracted with DCM. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was taken up into DCM and the solid formed was filtered off and discarded. The filtrate was evaporated in vacuo and the residue purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield intermediate 25a as a white solid (0.51 g, 65%).

PREPARATION OF INTERMEDIATE I-26a

Trimethylsilyl cyanide (CAS: 7677-24-9; 0.54 mL, 4.34 mmol) was added to a mixture of intermediate 25a (0.40 g, 2.17 mmol) in ACN (5.9 mL). The mixture was stirred at 90 °C for l6h. After cooling to rt water was added and the mixture extracted with EtOAc. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; DCM). The desired fractions were collected and concentrated in vacuo to yield intermediate 26a as a white solid (0.22 g, 51%).

PREPARATION OF INTERMEDIATE I-27a

HATU (CAS: 148893-10-1; 2.36 g, 6.20 mmol) and DIPEA (2.88 mL, 16.53 mmol) and A,O-dimethylhydroxylamine hydrochloride (CAS: 6638-79-5; 0.613 g, 6.29 mmol) were added to a stirred solution of 2-methyl- l,3-benzothiazole-6-carboxylic acid (CAS: 6941-28-2; 1 g, 5.18 mmol) in DMF (25.9 mL). The mixture was stirred at rt for 16 h and then brine was added. The mixture was extracted with EtOAc and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 27a as a colorless oil which solidified upon standing (1.3 g, 96%). PREPARATION OF INTERMEDIATES I-28a, 28b and 28c

Mn0 ₂ (CAS: 1313-13-9; 7.48 g, 86.0 mmol) was added to a stirred suspension of intermediate 23a (7.55 g, 36.0 mmol) in l,4-dioxane (50 mL). The mixture was stirred at 80 °C for 16 h and then filtered through a Celite® pad. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in petroleum ether, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 28a as a yellow solid (2.0 g, 65%).

Methyl magnesium bromide (1.4M in THF/toluene, 0.85 mL, 1.19 mmol) was added to a mixture of intermediate 26a (0.12 g, 0.60 mmol) in toluene (5 mL). The mixture was stirred at rt for 16 h and then a saturated NEECl solution was added. The mixture was extracted with EtOAc and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 2/98). The desired fractions were collected and concentrated in vacuo to yield intermediate 28b as a yellow solid (0.020 g, 16%). Diisobutylaluminium hydride (1M in DCM, 2.86 mL, 2.86 mmol) was added dropwise to a stirred solution of intermediate 27a (0.5 g, 1.90 mmol) in DCM (1.2 mL) at -30 °C under N ₂ . The mixture was stirred at -30 °C for 2 h and then sodium sulfate decahydrate was added and the mixture was stirred for 30 min. The mixture was filtered through a Celite® pad and the pad was washed with DCM. The filtrate was evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 28c as a pale-yellow solid (0.24 g, 71%). PREPARATION OF INTERMEDIATE I-29a

Tributyl(l-ethoxyvinyl)tin (CAS: 97674-02-7; 1.8 mL, 5.33 mmol) and Pd(PPli3) ₂ Cl ₂ (; 0.34 g, 0.49 mmol) were added to a stirred mixture of 6-bromofuro[3, 2-6] pyridine (CAS: 935330-61-7, 0.96 g, 4.87 mmol) in toluene (25 mL) in a sealed tube under N ₂ . The mixture was stirred at 80 °C for 16 h. After cooling to rt, a 1M HC1 solution (9.5 mL) was added and the mixture was stirred at 80 °C for a further 5h. After cooling to rt, the mixture was poured onto a stirred mixture of a saturated NaHC0 ₃ solution and ice and extracted with DCM. The organic layer was separated, washed with brine, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in DCM, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 29a as a pale-orange solid (0.24 g, 63%).

PREPARATION OF INTERMEDIATE 63

Methylmagnesium bromide (1 4M in THF/toluene, 3.6 mL, 5.04 mmol) was added dropwise to a stirred solution of intermediate 27a (991 mg, 4.19 mmol) in 2-MeTHF (20 mL) at 0 °C in a round-bottom flask and under N ₂ atmosphere. The reaction mixture was stirred at 0 °C for 5 min and at room temperature for 2 h. The mixture was treated with NH ₄ Cl (sat., aq.) and extracted with EtOAc. The organic layer was dried

(MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 0/100 to 100/0) to afford intermediate 63 (672 mg, 84%).

PREPARATION OF INTERMEDIATES 64 AND 1 la

NaH (60% dispersion in mineral oil, 1.14 g, 28.5 mmol) was added portionwise to a solution of 6-bromo-2-methyl-lH-imidazolo[4,5-b]pyridine [42869-47-6] (3.00 g, 14.1 mmol) in DMF (30 mL) at 0 °C. The mixture was stirred at room temperature for 30 min and 2-(trimethylsilyl)ethoxymethyl chloride (CAS :76513-69-4; 4.51 mL, 25.5 mmol) was added at 0 °C. The reaction mixture was stirred at room temperature for 16 h. The reaction was diluted with NH ₄ Cl and extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, NFT (7N in MeOH) in DCM, gradient from 0/100 to 2/98) to afford intermediate 64 (873.3 mg, 18%) and intermediate 1 la (219 mg, 4%) as well as a mixture of the 2 products (2.11 g).

PREPARATION OF INTERMEDIATE 65

Tributyl(l-ethoxyvinyl)tin (CAS: 97674-02-7; 0.43 mL, 1.26 mmol) followed by PdCl ₂ (PPli3) ₂ (76.3 mg, 0.11 mmol) were added to a stirred deoxygenated solution of intermediate 64 (412 mg, 1.20 mmol) in toluene (5 mL) in a sealed tube and under N ₂ atmosphere. The reaction mixture was stirred at 80 °C for 16 h. Then HC1 (1M solution, 2.4 mL) was added and the mixture was stirred at 80 °C for 6 h. The mixture was added to a stirred solution of NaHC0 ₃ (sat., aq.) and ice and extracted with EtOAc. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, 7N solution of NEb in MeOH in DCM, gradient from 0/100 to 10/90) to afford intermediate 65 (56.7 mg, 27%).

PREPARATION OF INTERMEDIATE 66

NaBEE (270 mg, 7.14 mmol) was added to a solution of intermediate I-28b (375 mg, 1.78 mmol) in EtOH (8.3 mL) at 0 °C. The reaction mixture was stirred at room temperature for 10 min. Water was added and the mixture was extracted with DCM. The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford intermediate 66 (335 mg) which was used in the next step.

PREPARATION OF INTERMEDIATE 67

SOCl ₂ (0.46 mL, 6.31 mmol) was added to a solution of intermediate 66 (335 mg, crude) in DCM (11 mL) at 0 °C. The reaction mixture was stirred at room temperature for 12 h. Water was added and the mixture was extracted with DCM. The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The residue was co-evaporated with toluene (twice) and dried under vacuum to afford intermediate 67 (356 mg) which was used as such in the next step.

PREPARATION OF INTERMEDIATE 68 Acetic anhydride (0.35 mL, 3.72 mmol) was added to a solution of 2,5-dibromo-4- fluoroaniline (CAS: 172377-05-8; 1.00 g, 3.72 mmol) in toluene (5.6 mL). The reaction mixture was stirred at 100 °C for 2 days. The mixture was cooled down and the solid was filtered off and washed with Et ₂ 0 to afford intermediate 68 (0.97 g, 84%).

PREPARATION OF INTERMEDIATE 69

1-69

P ₂ S ₅ (0.90 g, 4.06 mmol) was added to a suspension of intermediate 68 (0.97 g, 3.12 mmol) in THF (17 mL). The reaction mixture was stirred at room temperature for 16 h and CS ₂ CO ₃ (1.63 g, 4.99 mmol) was added. The mixture was stirred at 70 °C for 16 h. Water and NaOH (2N, aq.) were added and the mixture was extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O ₂ , EtOAc in heptane, gradient from 0/100 to 80/20) to afford intermediate 69 (620 mg, 61%).

PREPARATION OF INTERMEDIATE 70

Intermediate 69 (620 mg, 1.90 mmol) was added to a suspension of NaH (60% dispersion in mineral oil, 91.0 mg, 2.28 mmol) in toluene (8.5 mL). The reaction mixture was stirred at room temperature for 2 h and DMF (1.7 mL) was added. The reaction mixture was stirred at 110 °C for 16 h. Brine was added and the mixture was extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo to afford intermediate 70 (430 mg, 92%). PREPARATION OF INTERMEDIATE 71 Tributyl(l-ethoxyvinyl)tin (CAS: 97674-02-7; 0.68 mL, 2.00 mmol) followed by Pd(PPh ₃ ) ₂ Cl ₂ (117 mg, 0.17 mmol) were added to a stirred solution of intermediate 70 (410 mg, 1.67 mmol) in toluene (8.2 mL) in a sealed tube and under N ₂ atmosphere. The reaction mixture was stirred at 80 °C for 16 h and HC1 (1N) was added. The mixture was stirred at 70 °C for 1 h. NaHCCh (sat., aq.) was added and the mixture was extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in DCM, gradient from 0/100 to 30/70) to afford intermediate 71 (326 mg, 94%).

PREPARATION OF INTERMEDIATE 72

NaBEL (163 mg, 4.30 mmol) was added to a solution of intermediate 71 (225 mg, 1.08 mmol) in EtOH (5.0 mL) at 0 °C. The reaction mixture was stirred at room temperature for 10 min. The mixture was diluted with water and extracted with DCM (3 x x80 mL). The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford intermediate 72 (160 mg, 70%).

PREPARATION OF INTERMEDIATE 73

1-73

SOCl ₂ (0.19 mL, 2.65 mmol) was added to a solution of intermediate 72 (140 mg, 0.66 mmol) in DCM (4.45 mL) at 0 °C. The reaction mixture was stirred at room

temperature for 12 h. The mixture was diluted with water (10 mL) and extracted with DCM (3 x 10 mL). The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo to afford intermediate 73 (170 mg) which was used as such in the next step. PREPARATION OF INTERMEDIATE 74

Tributyl(l-ethoxyvinyl)tin (CAS: 97674-02-7; 0.89 mL, 2.62 mmol) and Pd(PPh ₃ ) ₂ Cl ₂ (153 mg, 0.22 mmol) were added to a stirred solution of 6-bromo-2- methylthiazolo[5,4-b]pyridine (CAS: 886372-92-5; 500 mg, 2.18 mmol) in toluene (10.7 mL) in a sealed tube and under N ₂ atmosphere. The reaction mixture was stirred at 80 °C for 16 h. HC1 (1N) was added and the mixture was stirred at 70 °C for another 2 h. NaHC0 ₃ (sat., aq.) was added and the mixture was extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in DCM, gradient from 0/100 to 30/70) to afford intermediate 74 (230 mg, 55%).

PREPARATION OF INTERMEDIATE 75

1-75

Bromine (0.51 mL, 9.92 mmol) was added to a solution of 6-fluoro-2-methyl-3H- imidazo[4,5-b]pyridine (CAS: 954218-00-9; 1.00 g, 6.62 mmol) and sodium acetate (1.36 g, 16.5 mmol) in acetic acid (10 mL). The reaction mixture was stirred at room temperature for 16 h and at 50 °C for 4 h. Additional amount of bromine (0.85 mL, 16.5 mmol) and sodium acetate (1.35 g, 16.5 mmol) were added and the reaction mixture was stirred at room temperature for 16 h and at 50 °C for 4 h. Additional quantity of bromine (0.51 mL, 9.92 mmol) was added and the reaction mixture was stirred at room temperature for another 16 h. Na ₂ S ₂ 0 ₃ was added and the mixture was extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The crude mixture was combined with another fraction (0.33 mmol) and purified by flash column chromatography (Si0 ₂ , MeOH in DCM, gradient from 0/100 to 6/94) to afford intermediate 75 (0.52 g, 33%). PREPARATION OF INTERMEDIATE 76

Boc

To a suspension of intermediate 75 (346 mg, 1.50 mmol) and DMAP (36.8 mg, 0.30 mmol) in THF (5.77 mL) was added dropwise bis(/er/-butyl)dicarbonatc (CAS: 24424- 58-3; 657 mg, 3.00 mmol). The reaction mixture was stirred at room temperature for 16 h. NH ₄ Cl (sat., aq.) was added and the mixture was extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and concentrated in vacuo to afford intermediate 76 (516 mg, 89%, 86% purity) which was used as such in the next step. PREPARATION OF INTERMEDIATE 77

Tributyl(l-ethoxyvinyl)tin (CAS: 97674-02-7; 0.48 mL, 1.41 mmol) and Pd(PPh ₃ ) ₂ Cl ₂ (82.3 mg, 0.12 mmol) were added to a stirred solution of intermediate 76 (450 mg, 1.17 mmol) in toluene (9.0 mL) in a sealed tube and under N ₂ atmosphere. The reaction mixture was stirred at 80 °C for 48 h. HC1 (1M in H ₂ 0, 7.5 mL, 7.5 mmol) was added and the mixture was stirred at room temperature for 16 h. NaHC0 ₃ (sat., aq.) was added and the mixture was extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , MeOH in DCM, gradient from 0/100 to 10/90) to afford intermediate 77 (190 mg, 84%).

PREPARATION OF INTERMEDIATE 78

To a suspension of intermediate 77 (122 mg, 0.63 mmol) and DMAP (15.4 mg, 0.13 mmol) in THF (2.4 mL) was added dropwise bis(/er/-butyl)di carbon ate (275 mg, 1.26 mmol). The reaction mixture was stirred at room temperature for 16 h. NH ₄ Cl (sat., aq.) was added and the mixture was extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 0/100 to 40/60) to afford intermediate 78 (176 mg, 95%).

PREPARATION OF INTERMEDIATE 79

Boc

Sodium methoxide (2.84 pL, 12.4 pmol) was added to a stirred suspension of intermediate 78 (150 mg, 0.51 mmol) in MeOH (2.0 mL) at 0 °C under N ₂ atmosphere. NaBEE (19.3 mg, 0.51 mmol) was added portionwise at this temperature. The mixture was stirred for 45 min. Water was added and the mixture was extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and concentrated in vacuo. The residue was dissolved in THF (2 mL), and Et ₃ N (70 pL, 0.5 mmol) and bis (tert- butyl)dicarbonate (CAS: 24424-58-3; 120 mg, 0.55 mmol) were added at 0 °C. The reaction mixture was stirred at room temperature for 16 h and quenched with water. The mixture was extracted with DCM. The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo to afford intermediate 79 (140 mg, 93%). PREPARATION OF INTERMEDIATE 80

SOCl ₂ (84 pL, 1.15 mmol) was added dropwise to a mixture of intermediate 79 (85.0 mg, 0.29 mmol) and Et ₃ N (0.32 mL, 2.30 mmol) in DCM (1.9 mL) at 0 °C. The reaction mixture was stirred at room temperature for 12 h. The reaction was cooled to 0 °C and water was carefully added. The mixture was extracted with DCM. The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo to afford intermediate 80 which was used as such in the next step. PREPARATION OF INTERMEDIATE 85

Methylmagnesium bromide (1.4M in THF and toluene, 1.31 mL, 1.83 mmol) was added over a solution of intermediate 28a (200 mg, 1.12 mmol) in anhydrous THF (11.2 mL) at 0 °C and under N ₂ atmosphere. The reaction mixture was stirred from 0 °C to room temperature for 2 h, diluted with NH ₄ Cl (sat., aq.) and extracted with Et ₂ 0.

The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 20/80 to 100/0) to afford intermediate 85 (176 mg, 81%) as a yellow solid.

PREPARATION OF INTERMEDIATE 86

SOCl ₂ (88.6 uL, 1.18 mmol) was added to a stirred solution of intermediate 85 in anhydrous DCM (9.1 mL) at 0 °C. The reaction mixture was stirred from 0 °C to room temperature for 2 h and the solvent was evaporated in vacuo to yield intermediate 86 which was used as such in the next step.

PREPARATION OF INTERMEDIATE 87

Intermediate I-28a (376 mg, 2.11 mmol) and Ti(0/-Pr) ₄ (CAS: 546-68-9;l.87 mL, 6.33 mmol) were added to a solution of 3-((/er/-butyldimethylsiloxyl)methyl)piperidine [876147-50-1] (508 mg, 2.22 mmol) in anhydrous THF (5.41 mL) at room temperature. The reaction mixture was stirred at room temperature for 18 h. The mixture was distilled and dried in vacuo. Anhydrous THF (5.41 mL) was added and the reaction was cooled to 0 °C. Methylmagnesium bromide (1.4M in THF, 7.53 mL, 10.6 mmol) was added dropwise. The reaction mixture was stirred at 0 °C for 15 min and at room temperature for 15 h. NH ₄ Cl (sat., aq.) was added and the mixture was extracted with DCM (3 times). The combined organics extracts were dried (MgS0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column

chromatography (Si0 ₂ , heptane/EtOAc, 95:5 to 0:100) to afford intermediate 87 (635 mg, 74%).

PREPARATION OF INTERMEDIATE 88

TBAF (875 mg, 3.13 mmol) was added to a stirred solution of intermediate 1-87 (635 mg, 1.57 mmol) in THF (25 mL) at room temperature. The reaction mixture was stirred at room temperature for 3 h. The solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , DCM:MeOH (l0:l)/DCM, gradient from 0:100 to 10:90) to afford intermediate 88 (312 mg, 68%). PREPARATION OF INTERMEDIATE 89

A solution of intermediate 1-88 (312 mg, 1.07 mmol), phtalimide (173 mg, 1.18 mmol) and triphenylphosphine (421 mg, 1.61 mmol) in anhydrous THF (12.7 mL) was stirred under N ₂ atmosphere. DIAD (318 mg, 1.61 mmol) was added and the reaction mixture was stirred at room temperature overnight. The mixture was diluted with water and extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, heptane/EtOAc, gradient from 100:0 to 0:100) to afford intermediate 89 (434 mg, 96%).

PREPARATION OF INTERMEDIATE 90

Hydrazine monohydrate (75.3 pL, 1.55 mmol) was added to a stirred solution of intermediate 1-89 (434 mg, 1.03 mmol) in EtOH (12 mL). The reaction mixture was stirred at 80 °C for 2 h and room temperature for 15 h. The solvent was evaporated in vacuo. The crude mixture was dissolved in DCM and filtered. The filtrate was evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , MeOH:NH3 in DCM, gradient from 0:100 to 10:90) to afford intermediate 90 (137 mg, 46%).

PREPARATION OF INTERMEDIATES I-30a, 30b, 30c, 30d, 30e, 30f, 30g, 30h and 30i

Titanium (IV) isopropoxide (CAS: 546-68-9; 0.23 mL, 0.79 mmol) was added to a stirred solution of intermediate 3a (0.1 g, 0.53 mmol) and intermediate l4a in DCM (1.81 mL) at rt under N ₂ . The mixture was stirred at rt for 16 h. Then mixture was cooled down to 0 °C and methylmagnesium bromide (1.4M in THF/toluene, 1.88 mL, 2.63 mmol) was added. The mixture was stirred at 0 °C for 15 min and then allowed to warm up to rt and stirred for a further 2 h. Then a saturated NH ₄ Cl solution and DCM were added and the mixture was filtered through a Celite® pad. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; EtOAc in DCM, gradient from 0/100 to 50/50). The desired fractions were collected and concentrated in vacuo to yield intermediate 30a as pale-yellow oil (0.214 g, 68%).

Intermediate 30b was prepared following an analogous procedure to the one described for the synthesis of intermediate 30a using intermediates 3b and l4a as starting materials.

Intermediate 30c was prepared following an analogous procedure to the one described for the synthesis of intermediate 30a using intermediates 3c and l4a as starting materials.

-30d

Intermediate 30d was prepared following an analogous procedure to the one described for the synthesis of intermediate 30a using intermediates 3d and l4a as starting materials.

Titanium (IV) isopropoxide (CAS: 546-68-9; 0.205 mL, 0.69 mmol) was added to a stirred solution of intermediate 5b (0.12 g, 0.46 mmol) and intermediate l4a in DCM (1.81 mL) at rt under N ₂ . The mixture was stirred at 80 °C for 16 h. Then mixture was cooled down to rt and methylmagnesium bromide (1.4M in THF/toluene, 1.65 mL, 2.31 mmol) was added. The mixture was stirred at rt for 16 h and then a saturated NaHCCh solution was added. The mixture was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFL in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield intermediate 30e as a colorless oil (0.132 g, 52%).

-30f

Intermediate 3 Of was prepared following an analogous procedure to the one described for the synthesis of intermediate 30a using intermediates 8a and l4a as starting materials.

Intermediate 30g was prepared following an analogous procedure to the one described for the synthesis of intermediate 30a using intermediates 8e and l4a as starting materials.

Titanium (IV) isopropoxide (CAS: 546-68-9; 0.205 mL, 0.69 mmol) and intermediate l4b (0.135 g, 0.47 mmol) were added to a stirred solution of intermediate 8a (0.063 g, 0.31 mmol) in DCM (1 mL) at rt under N ₂ . The mixture was stirred at rt for 16 h. Then the solvent was evaporated in vacuo and the residue was dissolved in DCM (1 mL). The mixture was cooled down to 0 °C and methylmagnesium bromide (1 4M in

THF/toluene, 1.11 mL, 1.55 mmol) was added. The mixture was stirred at 0 °C for 15 min and at rt for 1.5 h and then a saturated NH ₄ Cl solution was added and the mixture was extracted with DCM. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column

chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 5/95). The desired fractions were collected and concentrated in vacuo to yield intermediate 3 Oh as a yellow oil (0.132 g, 52%).

PREPARATION OF INTERMEDIATE 91

Intermediate l4a (109 mg, 0.37 mmol) and Ti(0/-Pr) ₄ (151 pL, 0.51 mmol) were added to a stirred solution of intermediate 32 (70.0 mg, 0.34 mmol) in DCM (2 mL) under N ₂ atmosphere. The reaction mixture was stirred at room temperature for 16 h. The mixture was cooled to 0 °C and THF (1 mL) was added, followed by MeMgBr (1.4 M in THF/toluene, 1.2 mL, 1.70 mmol) dropwise. The reaction mixture was stirred at this temperature for 25 min and at room temperature for 2 h. The mixture was treated with NH ₄ Cl (sat., aq.) and water and extracted with DCM. The organic layer was dried (Na ₂ S0 ₄ ), filtered and the solvent was evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , amino functionalized, MeOH in DCM, gradient from 0/100 to 4/96). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ACN, gradient from 47/53 to 30/70) to afford intermediate 91 (84 mg, 50%).

PREPARATION OF INTERMEDIATE 92

Intermediate 92 was prepared following an analogous procedure to the one described for intermediate 91 using intermediate l4a and intermediate 8f as starting materials. The crude mixture was purified by flash column chromatography (S1O2, NH ₃ (7M in MeOH)/DCM, gradient from 0/100 to 10/90) to afford intermediate 92 (170 mg, 67%)

PREPARATION OF INTERMEDIATE 93

Intermediate l4a (80 mg, 0.33 mmol), intermediate 8h (105 mg, 0.36 mmol) and Ti(0- /Pr) ₄ (145 liL, 0.49 mmol) were dissolved in DCM (1.13 mL) at room temperature and under N ₂ atmosphere. The reaction mixture was stirred at this temperature for 16 h. Then it was cooled to 0 °C and MeMgBr (1 4M in THF/toluene, 1.17 mL, 1.64 mmol) was added dropwise. The mixture was stirred at this temperature for 15 min and at room temperature for 1 h. The mixture was treated with NH ₄ Cl (sat., aq.) and diluted with DCM. The mixture was filtered through a pad of diatomaceus earth. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, EtOAc/MeOH, gradient from 100:0 to 90:10) to 10/90) afford intermediate 93 (110 mg, 63%). PREPARATION OF INTERMEDIATE 94

Intermediate 86 (112 mg, 0.53 mmol) was added to a solution of intermediate 60 (146 mg, 0.44 mmol) in ACN (5 mL) at room temperature. The reaction mixture was stirred at 75 °C for 48 h. The solvent was removed in vacuo and the crude mixture was purified by flash column chromatography (Si0 ₂ , EtOAc in heptane, gradient from 20/80 to 100/0) to afford intermediate 94 (54.7 mg, 24%) as a yellow oil.

PREPARATION OF INTERMEDIATE 95

2,4-Dibromo-thiazole ([CAS 4175-77-3], 50 g, 205.83 mmol), N-[(2,4- dimethoxyphenyl)methyl] -2,4-dimethoxy-benzenemethanamine ([CAS 20781-23-1], 65.33 g, 205, 83 mmol) and Na ₂ C0 ₃ (65.51 g, 618 mmol) in CH3CN (500 mL) was heated for 36 hours. The mixture was concentrated and dissolved in EtOAc (lOOOmL). The mixture was washed with water (50 mL) and brine, dried over MgS0 ₄ , and concentrated to give crude product, which was purified by column chromatography on silica gel (petroleum ether/EtOAc, from 100/0 to 70/30) to give intermediate 95 (70 g, 70%) as a yellow solid. PREPARATION OF INTERMEDIATE 96

To a solution of intermediate 95 (15 g, 31.29 mmol) in anhydrous THF (20 mL) was added dropwise LDA (34.42 mL, 34.42 mmol) at a rate so the temperature did not exceed -70 °C. The resulting solution was stirred at -78 °C for 30 min. Then DMF (2.52 g, 34.42 mmol) was added dropwise as a solution in THF (20 mL) and the mixture was allowed to warm up to room temperature. The reaction was quenched with saturated NH ₄ Cl (30 mL). The mixture was extracted with EtOAc (2 x 50 mL). The combined organic layers were washed with brine, dried over MgS0 ₄ , and concentrated. The crude was purified by flash chromatography on silica gel (petroleum ether/EtOAc, from 100/0 to 80/20) to yield intermediate 96 (8 g, 45%) as a light yellow solid.

PREPARATION OF INTERMEDIATE 97

Intermediate 96 (2006.23 mg, 3.95 mmol) was added to intermediate (37?)-34 from W02018/109202 (729 mg, 3.57 mmol) at RT. After 30 min, sodium

triacetoxyborohydride (1512.43 mg, 7.14 mmol) was added to the mixture at RT and the RM was stirred for 48 h at RT. The crude was quenched with NH3/H2O and extracted with EtOAc. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvent was evaporated in vacuo. The residue was purified by automated flash chromatography (silica, 10% MeOH in DCM 0/100 to 5/95). Desired fractions were collected, concentrated under vacuo to yield intermediate 97 (1.1 g, 44%) as a sticky solid. PREPARATION OF INTERMEDIATE 98

A mixture of intermediate 97 (1050 mg, 1.51 mmol) in TFA (26.25 mL) was stirred at RT under a nitrogen atmosphere for 1.5 h. The solvent was evaporated and the mixture was taken in water, basified with K2CO3 and extracted with DCM. The organic layer was dried over MgS0 ₄ and concentrated. The residue was purified on a column with silica gel, eluent DCM/MeOH (100/0 to 90/10). The pure fractions were evaporated, yielding intermediate 98 (521 mg, 87%) as a white solid.

PREPARATION OF INTERMEDIATE 99

Acetic anhydride (7.75 mg, 0.076 mmol) was added dropwise to a solution of intermediate 98 (20 mg, 0.051 mmol) in l,4-dioxane (15 mL) while stirring. After the addition was complete, the reaction was heated at 60°C for 2 h, then at 1 l0°C for 4 h. The RM was evaporated, taken up in water/0.5 g NaHCOEDCM. The organic layer was separated, dried over MgS0 ₄ and concentrated. The residue was purified on a column with silica gel, eluent: DCM/MeOH (100/0 to 95/5). The pure fractions were concentrated, yielding intermediate 99 (135 mg, 41%) as a pale yellow foam. P

Compound 28 from W02018/109202 was labelled with [ ³ H] as follows:

Intermediate 99 (4.10 mg, 9.38 pmol) and Palladium supported on Carbon (10%, 14.4 mg) were suspended in DMF (0.2 mL) and DIPEA (12 pL, 70.6 pmol) was added. The suspension was degassed three times and stirred under an atmosphere of Tritium gas (4.2 Ci, 525 mbar initial pressure) for 2 h 47 min at RT (end pressure was 311 mbar, no more consumption of gas was observed). The solvent was removed in vacuo, and labile tritium was exchanged by adding MeOH (0.3 mL), stirring the solution, and removing the solvent again under vacuo. This process was repeated twice. Finally, the well dried solid was extracted with EtOH (5 mL) and the suspension was filtered through a 0.2 pm nylon membrane (Macherey-Nagel Polyamide syringe filter

CHROMAFIL®Xtra PA-20/25), obtaining a clear solution.

The radiochemical purity (RCP) of the crude material was determined to be 56% using the following HPLC system: Waters Atlantis T3, 5 pm, 4.6 x 250 mm; solvents A: water + 0.05% TFA, B: acetonitrile + 0.05% TFA; 0 min 0% B; 10 min 30% B; 10.2- 14.5 min 95% B; 15 min 0% B; 254 nm; 1.0 mL/min; 30 °C.

The crude was purified by HPLC: Waters Atlantis T3, 5 pm, 10 x 250 mm; solvents A: water + 0.1% TFA; B: acetonitrile + 0.1% TFA; 0 min 0% B, 15 min 45% B; 4.7 mL/min; 25 °C. The target compound eluted at 9.5 min, and isolated from the HPLC solvent mixture by solid phase extraction. Therefore, the HPLC solution was neutralized with an aqueous solution of NaHC0 ₃ and the volume of the fractions were partially reduced at the rotary evaporator. Then the product was extracted with a Phenomenex StrataX cartridge (33 pm Polymeric Reversed Phase, 100 mg, 3 mL; 8B- S100-EB) which was eluted with EtOH (5 mL). The extracted product showed an RCP of >99% and the specific activity (SA) was determined to be 10.7 Ci/mmol (396 GBq/mmol, determined by MS). Two batches 250 pCi (9.25 MBq) in 0.25 mL EtOH (lmCi/mL) and 38.8 mCi in 5 mL EtOH of [ ³ H] -ligand were isolated. PREPARATION OF THE FINAL COMPOUNDS

PREPARATION OF FINAL COMPOUND 1

Trifluoroacetic acid (0.49 mL, 6.42 mmol) was added to a stirred solution of intermediate 30a (0.214 g, 0.36 mmol) in DCM. The mixture was stirred at rt for 16 h and then evaporated in vacuo. The residue was diluted with a saturated Na ₂ C0 ₃ solution and extracted with EtOAc. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase:

gradient from 80% NH4HCO3 0.25% solution in water, 20% CH3CN to 60% NH4HCO3 0.25% solution in water, 40% CH3CN). The desired fractions were collected and extracted with EtOAc. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was dissolved in MeOH and purified by ion exchange chromatography (ISOLUTE® SCX2 cartridge; MeOH and 7N solution of NH3 in MeOH). The desired fractions were collected and evaporated in vacuo to yield compound 1 as a syrup which crystallized upon standing as a white solid (0.080 g, 64%).

PREPARATION OF FINAL COMPOUND 2

Compound 2 was prepared following an analogous procedure to the one described for the synthesis of compound 1 using intermediate 30b as starting material (0.065 g, 0.13 mmol). Compound 2 was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20% CH3CN to 0% NH4HCO3 0.25% solution in water, 100% CH3CN) to yield compound 2 as a white solid (0.024 g, 50%).

PREPARATION OF FINAL COMPOUND 3

Compound 3 was prepared following an analogous procedure to the one described for the synthesis of compound 1 using intermediate 30c as starting material (0.055 g, 0.10 mmol). Compound 2 was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20% CH ₃ CN to 0% NH ₄ HCO ₃ 0.25% solution in water, 100% CH ₃ CN) to yield compound 3 as a white solid (0.012 g, 29%).

PREPARATION OF FINAL COMPOUNDS 4a and 4b

Compounds 4a and 4b were prepared following an analogous procedure to the one described for the synthesis of compound 1 using intermediate 30d as starting material (0.060 g, 0.11 mmol). The mixture containing compounds 4a and 4b was separated by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20% CH ₃ CN to 0% NH ₄ HCO ₃ 0.25% solution in water, 100% CH ₃ CN) to yield compound 4a as (0.009 g, 20%) and compound 4b as white solids (0.012 g, 26%).

PREPARATION OF FINAL COMPOUND 5

Compound 5 was prepared following an analogous procedure to the one described for the synthesis of compound 1 using intermediate 30e as starting material (0.132 g, 0.24 mmol). Compound 5 was purified by flash column chromatography (S1O2; MeOH in DCM, gradient from 0/100 to 10/90) to yield compound 5 as a colorless oil (0.075 g, 74%).

PREPARATION OF FINAL COMPOUNDS 6a and 6b

Compounds 6a and 6b were prepared following an analogous procedure to the one described for the synthesis of compound 1 using intermediate 3 Of as starting material (0.77 g, 0.11 mmol). The mixture of compounds 6a and 6b was purified by ion exchange chromatography (ISOLUTE® SCX2 cartridge; MeOH and 7N solution of NH3 in MeOH). Compounds 6a and 6b were obtained by chiral SFC (stationary phase: Chiralpak IC 5 pm 250 x 21.2 mm, mobile phase: 60% CO2, 40% (/PrOH/DCM 80/20 (0.3% iPrNH ₂ )). The fractions containing compound 6a were evaporated in vacuo and further purified by reverse phase HPLC (stationary phase: C18 XBridge 50 x 100 mm 5 pm, mobile phase: gradient from 84% NH4HCO3 0.25% solution in water, 16%

CH ₃ CN to 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN) to yield 6a as a white solid (0.073 g, 13%). The fractions containing compound 6b were evaporated in vacuo and further purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 50 x 100 mm 5 pm, mobile phase: gradient from 84% NH ₄ HCO ₃ 0.25% solution in water, 16% CH ₃ CN to 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN) to yield 6b as a pale-yellow sticky solid (0.062 g, 11%).

PREPARATION OF FINAL COMPOUND 7

Compound 7 was prepared following an analogous procedure to the one described for the synthesis of compound 1 using intermediate 30g as starting material (0.181 g, 0.25 mmol). Compound 7 was purified by flash column chromatography (S1O ₂ ; 7N solution of NH ₃ in MeOH in DCM, gradient from 0/100 to 6/94) and by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20% CH ₃ CN to 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN) to yield compound 7 as a pale-yellow foam (0.058 g, 67%).

PREPARATION OF FINAL COMPOUND 8

Compound 8 was prepared following an analogous procedure to the one described for the synthesis of compound 1 using intermediate 30h as starting material (0.095 g, 0.19 mmol). Compound 8 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM, gradient from 0/100 to 5/95), by reverse phase HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH4HCO3 0.25% solution in water, 20% CH3CN to 60% NH4HCO3 0.25% solution in water, 40% CH3CN) and triturated with DIPE to yield compound 8 as a beige sticky solid (0.037 g, 52%). PREPARATION OF FINAL COMPOUND 9

Intermediate l4a (0.079 g, 0.27 mmol) was added to a stirred solution of intermediate 8a (0.085 g, 0.31 mmol) and Et ₃ N (0.17 mL, 1.23 mmol) in DCM (2 mL). The mixture was stirred at rt for 30 min and then sodium triacetoxyborohydride (CAS: 56553-60-7, 0.179 g, 0.85 mmol) was added. The mixture was stirred at rt for l6h and then a saturated NaHC0 ₃ solution was added. The mixture was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH ₃ in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield compound 9 as a yellow oil (0.111 g,

85%).

PREPARATION OF FINAL COMPOUND 10

A solution of intermediate 8a (0.070 g, 0.26 mmol) and Et ₃ N (0.145 mL, 1.04 mmol) in DCM (1.3 mL) was added to intermediate l4c (0.085 g, 0.31 mmol) in a sealed tube under N ₂ . The mixture was stirred at rt for 30 min and then sodium

triacetoxyborohydride (CAS: 56553-60-7, 0.179 g, 0.85 mmol) was added. The mixture was stirred at rt for 16 h and then a saturated NaHC0 ₃ solution was added. The mixture was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 5/95). The desired fractions were collected and concentrated in vacuo to yield compound 10 as a pale- yellow solid (0.062 g, 70%). PREPARATION OF FINAL COMPOUND 11

Et ₃ N (0.125 mL, 0.90 mmol), intermediate l4d (0.075 g, 0.40 mmol), titanium (IV) isopropoxide (CAS: 546-68-9; 0.110 mL, 0.37 mmol) and sodium cyanoborohydride (CAS: 25895-60-7; 0.050 g, 0.80 mmol) were added to a solution of intermediate 8a (0.110 g, 0.40 mmol) in 1 ,2-dichloroethane (1.5 mL) in a sealed tube under N ₂ . The mixture was stirred at 80 °C for 2d and then a saturated NaHC0 ₃ solution was added. The mixture was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column chromatography (amino functionalized Si0 ₂ ; EtOAc in heptane, gradient from 0/100 to 100/0), by flash column chromatography (Si0 ₂ ; 7N solution of NH ₃ in MeOH in DCM, gradient from 0/100 to 5/95) and by reverse phase HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HC0 ₃ 0.25% solution in water, 20% CH ₃ CN to 60% NH ₄ HC0 ₃ 0.25% solution in water, 40% CH ₃ CN). The desired fractions were collected and extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. to yield compound 11 as a colorless oil (0.016 g, 11%).

PREPARATION OF FINAL COMPOUND l2a, l2b and l2c

DIPEA (0.226 mL, 1.31 mmol) was added to a stirred suspension of intermediate l6a (0.097 g, 0.44 mmol) and intermediate 8a (0.158 g, 0.57 mmol) in DCM (1.34 mL).

The mixture was stirred at rt for 5 min and then titanium (IV) isopropoxide (CAS: 546- 68-9; 0.311 g, 1.09 mmol) and sodium cyanoborohydride (CAS: 25895-60-7; 0.068 g,

1.09 mmol) were added. The mixture was stirred at 80 °C for a further 1 5h and then the solvent was evaporated in vacuo. The residue was purified by flash column

chromatography (Si0 ₂ ; 7N solution of NFT in MeOH in DCM, 0/100 to 10/90) and by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH4HCO3 0.25% solution in water, 20% CH3CN to 60% NH4HCO3 0.25% solution in water, 40% CH3CN) to yield compound l2a as a yellow oil (0.036 g, 23%). A 0.03 g sample of compound l2ab was further purified by achiral SFC

(stationary phase: Chiralcel OD-H 5 pm 250 x 21.2 mm, mobile phase: 85% CO2, 15% (EtOH (0.3% iPrNTE)). Desired fractions were collected and evaporated in vacuo to yield compound l2a (0.006 g, 4%) and compound l2b (0.015 g, 9%). PREPARATION OF FINAL COMPOUND 13

Compound 13 was prepared following an analogous procedure to the one described for the synthesis of compound l2a using intermediate 16b as starting material (0.089 g, 0.51 mmol). Compound 13 was purified by flash column chromatography (Si0 ₂ ; 7N solution of N¾ in MeOH in DCM, gradient from 0/100 to 10/90), by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH4HCO3 0.25% solution in water, 20% CH3CN to 60% NH4HCO3 0.25% solution in water, 40% CH3CN) and by ion exchange chromatography (ISOLUTE® SCX2 cartridge; MeOH and 7N solution of NH3 in MeOH) to yield compound 13 as a white solid (0.037 g, 52%).

PREPARATION OF FINAL COMPOUND 14

Compound 14 was prepared following an analogous procedure to the one described for the synthesis of compound l2a using intermediate l6c as starting material (0.089 g,

0.51 mmol) and Et ₃ N (0.150 mL, 1.08 mmol) instead of DIPEA. Compound 14 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM, 0/100 to 10/90), by reverse phase HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH4HCO3 0.25% solution in water, 20% CH3CN to 60% NH4HCO3 0.25% solution in water, 40% CH3CN). The desired fractions were collected and evaporated in vacuo and the residue was dissolved in MeOH (1 mL) and a 4M solution of HC1 in l,4-dioxane was added (0.5 mL, 2.0 mmol). The mixture was stirred at rt for 5 min and then the solvents were evaporated in vacuo to yield compound 14 as a white solid (0.065 g, 41%). PREPARATION OF FINAL COMPOUND 15

Compound 15 was prepared following an analogous procedure to the one described for the synthesis of compound l2a using intermediate 16d as starting material (0.089 g, 0.51 mmol) and Et ₃ N (0.150 mL, 1.08 mmol) instead of DIPEA. Compound 15 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFL in MeOH in

DCM, 0/100 to 10/90) and by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH ₄ HCO ₃ 0.25% solution in water, 25% CH ₃ CN to 57% NH ₄ HCO ₃ 0.25% solution in water, 43% CFLCN) to yield compound 15 as a pale-yellow oil (0.027 g, 23%).

PREPARATION OF FINAL COMPOUND 16

Compound 16 was prepared following an analogous procedure to the one described for the synthesis of compound l2a using 2-acctyl-2-mcthyl-2/7-indazolc as starting material (CAS: 1159511-29-1; 0.125 g, 0.72 mmol) and Et ₃ N (0.30 mL, 2.16 mmol) instead of DIPEA. Compound 16 was purified by flash column chromatography (Si0 ₂ ;

0.7N solution of NFL in MeOH in DCM, gradient from 0/100 to 100/0), by reverse phase HPLC (stationary phase: Cl 8 XBridge 50 x 100 mm 5 pm, mobile phase:

gradient from 90% NH4HCO3 0.25% solution in water, 10% CH3CN to 66% NH4HCO3 0.25% solution in water, 34% CH3CN). The desired fractions were collected and evaporated in vacuo and the residue was dissolved in MeOH (4 mL) and a 4M solution of HC1 in l,4-dioxane was added (0.2 mL, 2.39 mmol) in a sealed tube. The mixture was stirred at rt for 1 h and then the solvents were evaporated in vacuo to yield compound 16 as a yellow solid (0.030 g, 10%). PREPARATION OF FINAL COMPOUND 17

Intermediate l6e (0.085 g, 0.53 mmol) was added to a stirred solution of intermediate 8a (0.147 g, 0.53 mmol) and Et ₃ N (0.226 mL, 1.62 mmol) in anhydrous MeOH (1.75 mL). The mixture was stirred at rt for 16 h and the sodium triacetoxyborohydride (CAS: 56553-60-7; 0.168 g, 0.80 mmol) and the mixture was stirred at rt for a further ld. Then the solvent was evaporated in vacuo and the residue purified by flash column chromatography (Si0 ₂ ; 0.7N solution of NFT in MeOH in DCM, gradient from 0/100 to 100/0) and by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% 10 mM NH ₄ HCO ₃ pH 9 solution in water, 20% CH ₃ CN to 0% 10 mM NH ₄ HCO ₃ pH 9 solution in water, 100% CH ₃ CN). The desired fractions were collected and evaporated in vacuo to yield the free base of compound 17 (0.092 g, 50%). A sample of the free base of compound 17 (0.078 g, 0.22 mmol) was dissolved in MeOH (1.09 mL) and a 37% solution of HC1 was added (0.056 mL, 0.67 mmol) in a sealed tube. The mixture was stirred at rt for 1 h and then the solvents were evaporated in vacuo to yield compound 17 as a light-yellow solid (0.093 g, 99%).

PREPARATION OF FINAL COMPOUND 18

Intermediate l9a (0.094 g, 0.58 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.213 mL, 0.73 mmol) were added to a stirred solution of intermediate 3b (0.10 g, 0.48 mmol) in DCM (2 mL) at rt under N ₂ . The mixture was stirred at rt for 16 h, cooled down to 0 °C and then methylmagnesium bromide (1 4M in THF/toluene, 1.73 mL, 2.42 mmol) was added. The mixture was stirred at 0 °C for lh and then a saturated NH4CI solution and DCM were added. The mixture was filtered through a Celite® pad. The filtrate was diluted with DCM and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; MeOH in EtOAc, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo and the residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 47% NH4HCO3 0.25% solution in water, 53% CH3CN to 30% NH4HCO3 0.25% solution in water, 70% CH3CN). The desired fractions were collected and evaporated in vacuo and the residue was dissolved in EtOAc and extracted with water. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents evaporated in vacuo to yield compound 18 as a colorless film (0.074 g, 42%).

PREPARATION OF FINAL COMPOUND 19

Compound 19 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 3c as starting material (0.080 g, 0.49 mmol). Compound 19 was purified by flash column chromatography (Si0 ₂ ; MeOH in EtOAc, gradient from 0/100 to 10/90) and by reverse phase HPLC (stationary phase:

Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 47% NH4HCO3 0.25% solution in water, 53% CH3CN to 30% NH4HCO3 0.25% solution in water, 70%

CH ₃ CN). The desired fractions were collected and evaporated in vacuo to yield compound 19 as a colorless oil (0.090 g, 54%). PREPARATION OF FINAL COMPOUND 20

Compound 20 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 3d as starting material (0.075 g, 0.46 mmol). Compound 19 was purified by flash column chromatography (Si0 ₂ ; MeOH in EtOAc, gradient from 0/100 to 10/90) and by reverse phase HPLC (stationary phase:

Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 60% NH4HCO3 0.25% solution in water, 40% CH3CN to 43% NH4HCO3 0.25% solution in water, 57% CH3CN). The desired fractions were collected and the organic solvent evaporated in vacuo. EtOAc was added and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents evaporated in vacuo to yield compound 20 as a colorless film (0.073 g, 45%).

PREPARATION OF FINAL COMPOUNDS 2 lab and 2la

2lab 2la

Intermediate l9a (0.082 g, 0.50 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.213 mL, 0.73 mmol) were added to a stirred solution of intermediate 3b (0.10 g, 0.48 mmol) in DCM (1.5 mL) at rt under N ₂ . The mixture was stirred at rt for 16 h, cooled down to 0 °C and then methylmagnesium bromide (1.4M in THF/toluene, 1.72 mL, 2.40 mmol) was added. The mixture was stirred at 0 °C for 5 min and at rt for 2 h. Then a saturated NH ₄ CI solution was added and the mixture extracted with DCM. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH ₃ in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo and the residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH ₄ HCO ₃ 0.25% solution in water, 25% CH ₃ CN to 57% NH ₄ HCO ₃ 0.25% solution in water, 43% CH ₃ CN). The desired fractions were collected and evaporated in vacuo and the residues were dissolved in EtOAc and extracted with a saturated

NaHCCE solution. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo to yield compound 2 lab (mixture 38/62 of diasterosisomers, 0.020 g, 11%) and compound 2la (0.01 g, 6%) as brown oils.

PREPARATION OF FINAL COMPOUND 22

Compound 22 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 8a as starting material (0.090 g, 0.44 mmol). Compound 22 was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 5/95) to yield compound 22 as a colorless film (0.072 g, 45%).

PREPARATION OF FINAL COMPOUND 23a and 23b

Compounds 23 a and 23b were prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 8b as starting material (0.10 g, 0.45 mmol). The mixture of compounds 23a and 23b was purified by flash column chromatography (Si0 ₂ ; 7N solution of NEE in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. Compounds 23a and 23b were separated by reverse phase HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN to 43% NH ₄ HCO ₃ 0.25% solution in water, 57% CH ₃ CN). The desired fractions were collected and the solvents were evaporated in vacuo to yield compound 23a after drying under vacuum at 50 °C for l6h (0.039 g, 22%), and compound 23b (0.008 g, 5%) as colorless oils.

PREPARATION OF FINAL COMPOUND 24ab, 24a and 24b

Compounds 24ab, 24a and 24b were prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 8c as starting material (0.10 g, 0.45 mmol). Compound 24ab was purified by flash column chromatography (S1O2; 7N solution of NH3 in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 60% NH4HCO3 0.25% solution in water, 40% CH3CN to 43% NH4HCO3 0.25% solution in water, 57% CH3CN). The desired fractions were collected and the solvents evaporated in vacuo to yield compound 23ab (mixture 40/60 of diastereoisomers, 0.029 g, 18%), compound 24a (0.010 g, 6%), and compound 24b (0.035 g, 22%) as colorless oils. PREPARATION OF FINAL COMPOUNDS 25ab and 25a

25 ab 25a

Compounds 25 ab and 25 a were prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 8d as starting material (0.10 g, 0.45 mmol). Compound 24ab was purified by flash column chromatography (Si0 ₂ ; 7N solution of N¾ in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 54% NH4HCO3 0.25% solution in water, 46% CH3CN to 36% NH4HCO3 0.25% solution in water, 63% CH3CN). The desired fractions were collected and the solvents were evaporated in vacuo to yield compound 25 ab (0.022 g, 14%) and compound 25a (0.013 g, 8%) as yellow oils.

PREPARATION OF FINAL COMPOUND 26

Intermediate l9a (0.170 g, 1.051 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.467 mL, 1.58 mmol) were added to a stirred solution of intermediate 8e (0.10 g, 0.48 mmol) in DCM (4 mL) at rt under N ₂ . The mixture was stirred at rt for l6h, cooled down to 0 °C and then methylmagnesium bromide (1.4M in THF/toluene 1.72 mL, 2.40 mmol) was added. The mixture was stirred at 0 °C for lh. Then a saturated NaHC0 ₃ solution and DCM was added and the mixture was filtered through a Celite ® pad. The filtrate was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo and the residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH ₄ HCO ₃ 0.25% solution in water, 20%

CH ₃ CN to 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN). The desired fractions were collected and evaporated in vacuo and the residue was purified by flash column chromatography (S1O ₂ ; MeOH in DCM, gradient from 0/100 to 8/95). The desired fractions were collected and evaporated in vacuo to yield compound 26 as a colorless oil (0.022 g, 6%).

PREPARATION OF FINAL COMPOUNDS 27a and 27b

Compounds 27a and 27a were prepared following an analogous procedure to the one described for the synthesis of compound 26 using intermediate 8g as starting material (0.469 g, 2.47 mmol). The mixture of compounds 27a and 27b was purified by flash column chromatography (Si0 ₂ ; MeOH in EtOAc, gradient from 20/80 to 0/100) and the desired fractions were collected and evaporated in vacuo. The residue was purified by preparative LC (irregular bare silica; 0.8% NH ₄ OH and 8% MeOH in 92% DCM) and the desired fractions were collected and evaporated in vacuo. Compounds 27a and 27b were separated by chiral SFC (stationary phase: Chiralpak IC 5 pm 250 x 30 mm, mobile phase: 60% C0 ₂ , 40% (EtOH (0.3% ,PrNH ₂ )). The desired fractions were collected and the solvents evaporated in vacuo to yield compound 27a (0.048 g, 6%) and compound 27b (0.051 g, 6%) as yellow films. PREPARATION OF FINAL COMPOUNDS 28

Compound 28 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 8f as starting material (0.275 g, 1.33 mmol). Compound 28 was purified by flash column chromatography (Si0 ₂ ; 7N solution of N¾ in MeOH in DCM in DCM, gradient from 0/100 to 5/95) and the desired fractions were collected and evaporated in vacuo. The desired fractions were collected and concentrated in vacuo and the residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH4HCO3 0.25% solution in water, 25% CH3CN to 57% NH4HCO3 0.25% solution in water, 43% CH3CN). The desired fractions were collected and evaporated in vacuo and the residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM in DCM, gradient from 0/100 to 2/98). The desired fractions were collected and evaporated in vacuo to yield compound 28 as a colorless oil (0.60 g, 15%)

PREPARATION OF FINAL COMPOUND 29

Compound 29 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediate 8h as starting material (0.10 g, 0.41 mmol). Compound 29 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 67% NH ₄ HCO ₃ 0.25% solution in water, 33% CH ₃ CN to 50% NH ₄ HCO ₃ 0.25% solution in water, 50% CH ₃ CN). The desired fractions were collected and the solvents evaporated in vacuo to yield compound 29 as a white solid (0.050 g, 30%).

PREPARATION OF FINAL COMPOUND 30

Compound 30 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediates 8a (0.09 g, 0.44 mmol) and l9a (0.10 g, 0.62 mmol) as starting materials. Compound 30 was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM in DCM, gradient from 0/100 to 5/95) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 90% NH4HCO3 0.25% solution in water, 10% CH3CN to 65% NH4HCO3 0.25% solution in water, 45% CH3CN). The desired fractions were collected and the solvents were evaporated in vacuo to yield compound 30 as a colorless sticky solid (0.091 g, 56%).

PREPARATION OF FINAL COMPOUND 31

Compound 31 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediates 8e (0.10 g, 0.53 mmol) and l9b (0.120 g, 0.63 mmol) as starting materials. Compound 31 was purified by flash column chromatography (S1O2; MeOH in DCM in DCM, gradient from 0/100 to 30/70) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 67% NH ₄ HCO ₃ 0.25% solution in water, 33% CH ₃ CN to 50% NH ₄ HCO ₃ 0.25% solution in water, 50% CH ₃ CN). The desired fractions were collected and the solvents evaporated in vacuo to yield compound 31 as a yellow oil (0.080 g, 40%).

PREPARATION OF FINAL COMPOUND 32

Compound 32 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediates 3a (0.10 g, 0.53 mmol) and l9c (0.123 g, 0.63 mmol) as starting materials. Compound 32 was purified by flash column chromatography (S1O ₂ ; 7N solution of NH ₃ in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH ₄ HCO ₃ 0.25% solution in water, 25% CH ₃ CN to 57% NH ₄ HCO ₃ 0.25% solution in water, 43% CH ₃ CN). The desired fractions were collected and the solvents were evaporated in vacuo to yield compound 32 as a colorless oil (0.030 g, 16%).

PREPARATION OF FINAL COMPOUND 33ab, 33a and 33b

Compounds 33ab, 33a and 33b were prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediates 8e (0.067 g, 0.35 mmol) and l9c (0.060 g, 0.33 mmol) as starting materials. Compound 33ab was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFU in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. Compounds 33a and 33b were separated by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 60% NH ₄ HCO ₃ 0.25% solution in water, 40% CH ₃ CN to 43% NH ₄ HCO ₃ 0.25% solution in water, 57% CH ₃ CN). The desired fractions were collected and the solvents evaporated in vacuo and the residues were dissolved in EtOAc and washed with a saturated NaHC0 ₃ solution. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo to yield compounds 33a (0.032 g, 26%) and compound 33b (0.014 g, 22%) as colorless oils. PREPARATION OF FINAL COMPOUND 34

Compound 34 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediates lOa (0.10 g, 0.45 mmol) and l9c (0.085 g, 0.48mmol) as starting materials. Compound 34 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFU in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo to yield compound 34 as a colorless oil (0.055 g, 30%). PREPARATION OF FINAL COMPOUND 35

Compound 34 was prepared following an analogous procedure to the one described for the synthesis of compound 18 using intermediates 10b (0.10 g, 0.45 mmol) and l9c (0.085 g, 0.48mmol) as starting materials. Compound 35 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFU in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo to yield compound 35 as a colorless oil (0.083 g, 46%). PREPARATION OF FINAL COMPOUND 36

Intermediate l9d (0.085 g, 0.53 mmol) and sodium triacetoxyborohydride (CAS:

56553-60-7, 0.168 g, 0.79 mmol) were added to a stirred mixture of intermediate 8a (0.090 g, 0.44 mmol) in DCM (9.4 mL). The mixture was stirred at rt for l6h and then a saturated NaHC0 ₃ solution was added. The organic layer was separated, dried

(MgS0 ₄ ), filtered and the solvents were removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo to yield compound 36 as a colorless oil (0.48 g, 31%).

PREPARATION OF FINAL COMPOUND 37

Intermediate l9e (0.041 g, 0.26 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.108 mL, 0.365 mmol) were added to a stirred solution of intermediate 8a (0.05 g, 0.24 mmol) in DCM (0.79 mL). The mixture was stirred at rt for 16 h and then sodium cyanoborohydride (CAS: 25895-60-7; 0.018 g, 0.29 mmol) was added. The mixture was stirred at rt for a further 16 h and then a 10% NH ₄ Cl solution was added. The mixture was extracted with DCM and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase:

gradient from 54% lOmM NH ₄ HC0 ₃ /NH ₄ 0H pH = 9 solution in water, 46% CH3CN to 36% lOmM NH ₄ HC0 ₃ /NH ₄ 0H pH = 9 solution in water, 64% CH3CN). The desired fractions were collected and evaporated in vacuo, and the residue was partitioned between a saturated NaHCCL solution and DCM. The organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo to yield compound 37 as a white solid (0.018 g, 21%). PREPARATION OF FINAL COMPOUND 38

Titanium (IV) isopropoxide (CAS: 546-68-9; 0.170 mL, 0.57 mmol) and then sodium cyanoborohydride (CAS: 25895-60-7; 0.059 g, 0.94 mmol) were added to a stirred solution of intermediate 8a (0.139 g, 0.68 mmol) and intermediate 20a (0.104 g, 0.65 mmol) in 1 ,2-dichloroethane (2.2 mL) in a sealed tube under N ₂ . The mixture was stirred at 80 °C for 2lh and after cooling to rt a saturated NaHC0 ₃ solution and DCM were added and the mixture was filtered through a Celite ® pad. The filtrate was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFT in MeOH in DCM, gradient from 0/100 to 5/95). The desired fractions were collected and concentrated in vacuo and the residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 67% NH4HCO3 0.25% solution in water, 33%

CH3CN to 50% NH4HCO3 0.25% solution in water, 50% CH3CN). The desired fractions were collected and extracted with EtOAc and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. and the residue was washed with a saturated NaHC0 ₃ solution to yield compounds 38 as a yellow oil (0.036 g, 14%).

PREPARATION OF FINAL COMPOUND 39

Intermediate 28a (0.121 g, 0.63 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.231 mL, 0.79 mmol) were added to a stirred solution of intermediate 3a (0.10 g, 0.53 mmol) in DCM (2.2 mL) at rt under N ₂ . The mixture was stirred at rt for 20 h, cooled down to 0 °C and then methylmagnesium bromide (1 4M in THF/toluene, 1.73 mL, 2.42 mmol) was added. The mixture was stirred at 0 °C for 2h and then a saturated NH ₄ Cl solution and DCM were added. The organic layer was separated, dried

(MgS0 ₄ ), filtered and the solvents evaporated in vacuo. The residue was purified by flash column chromatography (S1O ₂ ; 7N solution of NH ₃ in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo and the residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH ₄ HCO ₃ 0.25% solution in water, 25% CH ₃ CN to 57% NH ₄ HCO ₃ 0.25% solution in water, 43% CH ₃ CN). The desired fractions were collected and a saturated NaHCCL solution was added and the mixture extracted with DCM. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo to yield compound 39 as a white solid (0.040 g, 21%).

PREPARATION OF FINAL COMPOUND 40

Compound 40 was prepared following an analogous procedure to the one described for the synthesis of compound 39 using intermediates 5a (0.100 g, 0.48 mmol) and 28a

(0.103 g, 0.58 mmol) as starting materials. Compound 40 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH4HCO3 0.25% solution in water, 25% CH3CN to 57% NH4HCO3 0.25% solution in water, 43% CH3CN). The desired fractions were collected and the solvents evaporated in vacuo to yield compound 40 as a colorless oil (0.009 g, 5%). PREPARATION OF FINAL COMPOUND 41

Compound 41 was prepared following an analogous procedure to the one described for the synthesis of compound 39 using intermediates 5d (0.100 g, 0.45 mmol) and 28a (0.84 g, 0.47 mmol) as starting materials. Compound 40 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFU in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo to compound 41 as a light-brown oil (0.124 g, 69%).

PREPARATION OF FINAL COMPOUND 42a and 42b

Compounds 42a and 42b were prepared following an analogous procedure to the one described for the synthesis of compound 39 using intermediates 8a (0.068 g, 0.33 mmol) and 28a (0.060 g, 0.33 mmol) as starting materials. The mixture of compounds 42a and 42b was purified by flash column chromatography (Si0 ₂ ; MeOH in DCM, gradient from 0/100 to 6/94) and the desired fractions were collected and evaporated in vacuo. Compounds 4la and 4 lb were separated by chiral SFC (stationary phase:

Chiralpak IC 5 pm 250 x 30 mm, mobile phase: 60% C0 ₂ , 40% (EtOH (0.3% ,PrNH ₂ )). The desired fractions were collected and the solvents evaporated in vacuo to yield compound 42a (0.013 g, 10%) and compound 42b (0.010 g, 8%) as yellow films. PREPARATION OF FINAL COMPOUND 43

Intermediate 28a (0.178 g, 0.53 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.233 mL, 0.79 mmol) were added to a stirred solution of intermediate 8e (0.10 g, 0.53 mmol) in DCM (2 mL) at rt under N ₂ . The mixture was stirred at rt for 16 h, cooled down to 0 °C and then methylmagnesium bromide (1 4M in THF/toluene, 1.72 mL, 2.40 mmol) was added. The mixture was stirred at 0 °C for 1 h. Then a saturated NaHC0 ₃ solution and DCM were added and the mixture was filtered through a Celite ® pad. The filtrate was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFL in MeOH in DCM, gradient from 0/100 to 10/90). The desired fractions were collected and concentrated in vacuo and the residue was purified by reverse phase HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 80% NH4HCO3 0.25% solution in water, 20% CH3CN to 60% NH4HCO3 0.25% solution in water, 40% CH3CN). The desired fractions were collected and evaporated in vacuo to yield compound 43 as a colorless oil (0.035 g, 18%).

PREPARATION OF FINAL COMPOUND 44

Compound 44 was prepared following an analogous procedure to the one described for the synthesis of compound 43 using intermediates 8g (0.139 g, 0.67 mmol) and 28a (0.100 g, 0.56 mmol) as starting materials. Compound 43 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM in DCM, gradient from 0/100 to 5/95) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 67% NH4HCO3 0.25% solution in water, 33% CH ₃ CN to 67% NH ₄ HCO ₃ 0.25% solution in water, 33% CH ₃ CN). The desired fractions were collected and the solvents evaporated in vacuo yield compound 44 as an oil (0.140 g, 63%).

PREPARATION OF FINAL COMPOUNDS 45ab and 45a

Compounds 45 ab and 45 a were prepared following an analogous procedure to the one described for the synthesis of compound 39 using intermediate lOb as starting material (0.10 g, 0.45 mmol). Compound 45ab was purified by flash column chromatography (S1O2; 7N solution of NH3 in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 67% NH4HCO3 0.25% solution in water, 33% CH3CN to 50% NH4HCO3 0.25% solution in water, 50% CH3CN). The desired fractions were collected and the solvents evaporated in vacuo to yield compound 45ab (0.034 g, 19%) and compound 45a (0.029 g, 16%) as yellow oils.

PREPARATION OF FINAL COMPOUNDS 46ab and 46a

46ab

46a Compounds 46ab and 46a were prepared following an analogous procedure to the one described for the synthesis of compound 39 using intermediate lOa as starting material (0.10 g, 0.45 mmol). Compound 46ab was purified by flash column chromatography (Si0 ₂ ; 7N solution of N¾ in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 67% NH ₄ HCO ₃ 0.25% solution in water, 33% CH ₃ CN to 50% NH ₄ HCO ₃ 0.25% solution in water, 50% CH ₃ CN). The desired fractions were collected and the solvents evaporated in vacuo. The residue was dissolved in EtOAc and washed with a saturated NaHCCb solution. The organic layers were separated, dried (Na ₂ S04), filtered and the solvents evaporated in vacuo to yield compound 46ab (0.035 g, 20%) and compound 46a (0.043 g, 24%) as yellow oils.

PREPARATION OF FINAL COMPOUND 47

Intermediate 28a (0.118 g, 0.66 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.294 mL, 0.99 mmol) were added to a stirred solution of intermediate lOd (0.150 g, 0.72 mmol) in DCM (2 mL) at rt under N ₂ . The mixture was stirred at rt for l6h, cooled down to 0 °C and then methylmagnesium bromide (1 4M in THF/toluene, 1.72 mL,

2.40 mmol) was added. The mixture was stirred at 0 °C for 1 h. Then MeOH and DCM were added and the mixture was filtered through a Celite ® pad. The filtrate was treated with a saturated NH4CI solution and extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH3 in MeOH in DCM, gradient from 0/100 to 08/92). The desired fractions were collected and concentrated in vacuo to yield compound 47 as an oil (0.160 g, 63%). PREPARATION OF FINAL COMPOUND 48

Compound 48 was prepared following an analogous procedure to the one described for the synthesis of compound 46 using intermediates lOe (0.150 g, 0.73 mmol) and intermediate 28a (0.117 g, 0.66 mol) as starting materials. Compound 48 was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFU in MeOH in DCM in DCM, gradient from 0/100 to 08/92) and the desired fractions were collected and evaporated in vacuo to yield compound 48 (0.155 g, 61%) as an oil.

PREPARATION OF FINAL COMPOUNDS 49ab, 49a and 49b

Compounds 49ab, 49a and 49b were prepared following an analogous procedure to the one described for the synthesis of compound 39 using intermediates lOc (0.150 g, 0.68 mmol) and 28a (0.127 g, 0.71 mmol) as starting materials. Compound 40ab was purified by flash column chromatography (Si0 ₂ ; 7N solution of NFU in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH ₄ HCO ₃ 0.25% solution in water, 25% CH ₃ CN to 57% NH ₄ HCO ₃ 0.25% solution in water, 43% CH ₃ CN). The desired fractions were collected and the solvents evaporated in vacuo and the residues were dissolved in EtOAc and extracted with a saturated solution of NaHC0 ₃ . The organic layers were separated, dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo to yield compound 49ab as a yellow oil (0.008 g, 3%), compound 49a as a grey oil (0.016 g, 6%) and compound 49b as a yellow oil (0.017, 6%). PREPARATION OF FINAL COMPOUND 50

Intermediate 28b (0.015 g, 0.071 mmol) and titanium (IV) isopropoxide (CAS: 546-68- 9; 0.030 mL, 0.11 mmol) were added to a stirred solution of intermediate 8e (0.013 g, 0.068 mmol) in THF (0.50 mL) at rt under N ₂ . The mixture was stirred at 70 °C for 16 h and then sodium cyanoborohydride (CAS: 25895-60-7; 0.018 g, 0.29 mmol) was added. The mixture was stirred at rt for a further 16 h and then water was added. The mixture was extracted with EtOAc and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase:

gradient from 75% NH4HCO3 0.25% solution in water, 25% CH3CN to 57% NH4HCO3 0.25% solution in water, 43% CH3CN). The desired fractions were collected and evaporated in vacuo to yield compound 50 as a colorless oil (0.010 g, 38%).

PREPARATION OF FINAL COMPOUND 51

Sodium cyanoborohydride (CAS: 25895-60-7; 0.054 g, 0.87 mmol) was added to a stirred mixture of intermediate 8a (0.200 g, 0.72 mmol), intermediate 28c (0.138 g, 0.72 mmol), titanium (IV) isopropoxide (CAS: 546-68-9; 0.214 mL, 0.72 mmol) and Et3N (0.300 mL, 2.16 mmol) in DCM (2.37 mL) at rt. The mixture was stirred at 80 °C for 16 h and then water was added. The mixture was extracted with DCM and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 54% NH ₄ HCO ₃ 0.25% solution in water, 46% CH ₃ CN to 46% NH ₄ HCO ₃ 0.25% solution in water, 54% CH3CN). The desired fractions were collected and evaporated in vacuo and the residue dissolved in MeOH and treated with a 6M solution of HC1 in /PrOH. The mixture was stirred at rt for 2 h and then the solvents were evaporated in vacuo to yield compound 51 as a white solid (0.105 g, 32%).

PREPARATION OF FINAL COMPOUND 52

Et ₃ N (0.062 mL, 0.45 mmol) was added to a stirred solution of intermediate 8a (0.031 g, 0.11 mmol) in DCM (1.7 mL). The mixture was stirred at rt for 10 min and then intermediate 28a (0.020 g, 0.11 mmol) and sodium triacetoxyborohydride (CAS:

56553-60-7, 0.071 g, 0.34 mmol) were added. The mixture was stirred at rt for 18h and then a saturated NaHC0 ₃ solution was added. The mixture was extracted with DCM and the organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were removed in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH ₄ HC0 ₃ 0.25% solution in water, 25% CH ₃ CN to 57% NH ₄ HC0 ₃ 0.25% solution in water, 43% CH ₃ CN). The desired fractions were collected and concentrated in vacuo to yield compound 52 as a colorless oil (0.015 g, 36%).

PREPARATION OF FINAL COMPOUND 53

Sodium triacetoxyborohydride (CAS: 56553-60-7, 0.2151 g, 1.02 mmol) was added to a stirred solution of intermediate 8a (0.187 g, 0.68 mmol), intermediate 28c (0.120 g, 0.68 mmol) and Et ₃ N (0.282 mL, 2.03 mmol) in MeOH (2.19 mL). The mixture was stirred at rt for l6h and then water was added. The mixture was extracted with EtOAc and the organic layer was separated, dried (Na ₂ S0 ₄ ), filtered and the solvents removed in vacuo. The residue was purified by flash column chromatography (Si0 ₂ ; 7N solution of NH ₃ in MeOH in DCM in DCM, gradient from 0/100 to 05/95) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase:

gradient from 60% lOmM NH ₄ HCO ₃ /NH ₄ OH pH 7.9 solution in water, 40% CH ₃ CN to 43% lOmM NH ₄ HCO ₃ /NH ₄ OH pH 7.9 solution in water, 57% CH ₃ CN). The desired fractions were collected and concentrated in vacuo and the residue dissolved in MeOH and treated with a 6M solution of HC1 in z ^' PrOH. The mixture was stirred at rt for 2 h and then the solvents were evaporated in vacuo to yield compound 53 as a blue solid (0.055 g, 19%).

PREPARATION OF FINAL COMPOUND 54

Compound 54 was prepared following an analogous procedure to the one described for the synthesis of compound 39 using intermediate lOf as starting material (0.10 g, 0.42 mmol). Compound 54 was purified by flash column chromatography (S1O2; 7N solution of NH3 in MeOH in DCM in DCM, gradient from 0/100 to 10/90) and the desired fractions were collected and evaporated in vacuo. The residue was purified by reverse phase HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm, mobile phase: gradient from 75% NH ₄ HCO ₃ 0.25% solution in water, 25% CH ₃ CN to 57% NH ₄ HCO ₃ 0.25% solution in water, 43% CH ₃ CN). The desired fractions were collected and the solvents evaporated in vacuo. The residue was dissolved in DCM and washed with a saturated NaHC0 ₃ solution. The organic layers were separated, dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo to yield compound 54 as a colorless oil (0.050 g, 29%). PREPARATION OF COMPOUND 55

Sodium triacetoxyborohydride (CAS: 56553-60-7; 181 mg, 0.86 mmol) was added to a stirred mixture of intermediate I-8f»2HCl (150 mg, 0.57 mmol), intermediate I-28c (101 mg, 0.57 mmol) and Et ₃ N (0.24 mL. 1.71 mmol) in MeOH (1.85 mL) at room temperature. The reaction mixture was stirred for 16 h and concentrated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, NFT (7M in MeOH) in DCM, gradient from 0:100 to 10:90). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 um), mobile phase: lOmM NH4CO3H pH 7.9 solution in water/ ACN, gradient from 60:40 to 43:57). The product was stirred in MeOH and treated with HC1 (12M solution, 0.5 mL, 6.0 mmol) at room temperature for 10 min. The mixture was concentrated in vacuo and the product was dried under vacuum at 50 °C for 16 h to afford compound 55 (106 mg, 44%). PREPARATION OF COMPOUNDS 56 AND 57

Ti(0/-Pr) ₄ (CAS: 546-68-9; 281 pL, 0.95 mmol) and sodium cyanoborohydride (CAS: 25895-60-7; 71.6 mg, 1.14 mmol) were added sequentially to a mixture of intermediate I-8F*2HCl (250 mg, 0.95 mmol), intermediate 1-63 (182 mg, 0.95 mmol) and Et ₃ N (0.40 mL, 2.85 mL) in DCM (3.12 mL) at room temperature. The reaction mixture was stirred at 80 °C for 16 h in a sealed tube. The reaction was quenched with water and extracted with DCM (3 times). The combined organic layers were dried (MgS0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, (10% 7N NH ₃ in MeOH in DCM) in DCM, gradient from 0:100 to 50:50). The residue was purified again by RP HPLC (stationary phase: XBridge Cl 8 50 x 100 mm, 5 Dm), mobile phase: NH ₄ HC0 ₃ (0.25% solution in water)/ ACN, gradient from 80:20 to 0:100) to afford fraction A (28 mg) and fraction B (100 mg). HC1 (37% in H ₂ 0, 91 m L, 1.09 mmol) was added to a stirred mixture of fraction B (100 mg, 0.27 mmol) in MeOH (0.67 mL) in a sealed tube. The reaction mixture was stirred at room temperature for 1 h and concentrated in vacuo to afford compound 56 (118 mg).

Product 56 was prepared following an analogous procedure using fraction A (28 mg) as starting material.

PREPARATION OF COMPOUND 58

A solution of intermediate I-8a (75 mg, 0.37 mmol) in MeOH (2 mL) followed by

Ti(0/-Pr) ₄ (CAS: 546-68-9; 180 pL, 0.61 mmol) and sodium cyanoborohydride (CAS: 25895-60-7 (44 mg, 0.7 mmol) were added to intermediate 1-65 (57 mg, 0.33 mmol) in a sealed tube and under N ₂ atmosphere. The reaction mixture was stirred at 80 °C for 60 h. The solvent was evaporated in vacuo and the crude mixture was purified by flash column chromatography (Si0 ₂ , 7N solution of NFT in MeOH in DCM, gradient from 0: 100 to 10:90). Another purification was performed by RP HPLC (stationary phase:

Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ACN, gradient from 80:20 to 60:40). The product was treated with water and extracted with DCM. The organic layer was dried (MgS0 ₄ ), filtered and the solvents evaporated in vacuo to afford compound 58 (22 mg, 19%).

PREPARATION OF COMPOUNDS 59 AND 60

Sodium cyanoborohydride (CAS: 25895-60-7 (34.3 mg, 0.55 mmol) was added to a stirred mixture of intermediate 1-71 (100 mg, 0.48 mmol), intermediate I-8e (86.6 mg, 0.46 mmol) and Ti(0/-Pr) ₄ (CAS: 546-68-9; 200 mE, 0.68 mmol) in THF (3.35 mF) at room temperature and under N ₂ atmosphere. The reaction mixture was stirred at 70 °C for 16 h and diluted with water. The mixture was extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , MeOH in DCM, gradient from 0: 100 to 30:70). A second purification was performed by flash column

chromatography (Si0 ₂ , NFT (7N in MeOH) in DCM, gradient from 0:100 to 5:95). The desired fractions were combined and concentrated in vacuo. The residue was purified by RP HPFC (stationary phase: XBridge C18 50 x 100 mm, 5 pm), mobile phase: NH ₄ HC0 ₃ (0.25% solution in water)/ ACN, gradient from 60:40 to 43:57) to afford fraction A (38 mg) and fraction B (38 mg).

A solution of citric acid (37.1 mg, 0.19 mmol) in l,4-dioxane (0.62 mF) was added to a solution of fraction B (37 mg, 96.5 pmol) in Et ₂ 0 (1.83 mF). The mixture was stirred at room temperature for 3 h. The precipitate was filtered off and washed with Et ₂ 0. The solid was dissolved in MeOH, Et ₂ 0 was added and the mixture was concentrated in vacuo. The solid was dried in a desiccator at 50 °C for 16 h to afford compound60 (47 mg) as a white solid.

Compound 59 was prepared following the same procedure using fraction A as starting material. PREPARATION OF COMPOUNDS 61 AND 62

Compounds 61 and 62 were prepared following an analogous procedure to the one described for the synthesis of compounds 59 and 60 using intermediate 1-74 and intermediate I-8e as starting materials.

The crude mixture was purified by flash column chromatography (S1O2, DCM/MeOH, gradient from 100:0 to 70:30). A second purification was performed by flash column chromatography (Si0 ₂ , DCM/NTb (7N in MeOH), gradient from 100:0 to 95:5). The desired fractions were concentrated in vacuo. The residue was purified by RP HPLC (stationary phase: XBridge C18 50 x 100 mm, 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 69:31 to 52:48) to afford fraction A (42 mg) and fraction B (102 mg).

A solution of citric acid (41.9 mg, 0.22 mmol) in l,4-dioxane (0.70 mL) was added to a solution of fraction A (40.0 mg, 0.11 mmol) in Et ₂ 0 (2.07 mL). The mixture was stirred at room temperature for 3 h. The precipitate was filtered off and washed with Et ₂ 0. The solid was dissolved in MeOH, Et ₂ 0 was added and the mixture was concentrated in vacuo. The product was dried in a desiccator at 50 °C for 4 days to afford compound 61 (56 mg) as a white solid.

Compound 62 was prepared following an analogous procedure using fraction B as starting material.

PREPARATION OF COMPOUND 63

To a solution of intermediate I-8h (100 mg, 0.53 mmol) in DCM (31.5 mL) were added intermediate I-l9a (93.7 mg, 0.58 mmol) and Ti(0/-Pr) ₄ (CAS: 546-68-9; 0.23 mL, 0.79 mmol). The reaction mixture was stirred at room temperature overnight. Then the reaction was cooled to 0 °C and methylmagnesium bromide (3M, 0.88 mL, 2.63 mmol) was added dropwise. The reaction mixture was stirred at 0 °C for 5 min and at room temperature for 1 h. NH ₄ Cl (sat., aq.) was added and the mixture was extracted with DCM. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , NFT (7M in MeOH)/DCM, gradient from 0:100 to 3:97). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NFF ₄ FFC0 ₃ (0.25% solution in water)/ACN, gradient from 67:33 to 50:50) to afford compound 63 (21 mg, 11%).

PREPARATION OF COMPOUND 64

Compound 64 was prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-l9a and intermediate 1-32 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , NFT (7M in MeOH)/DCM, gradient from 0:100 to 3:97). The residue was purified by ion exchange chromatography using an Iso lute SCX2 cartridge and eluting with MeOH, and then with NFT (7M in MeOFF). The desired fractions were collected and concentrated in vacuo. The red oil was purified by RP FFPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NFF ₄ FFC0 ₃ (0.25% solution in water)/ACN, gradient from 67:33 to 50:50). The desired fractions were collected and the solvents partially concentrated in vacuo. The aqueous phase was extracted with EtOAc. The organic phase was dried (Na ₂ S0 ₄ ), filtered and the solvent was evaporated in vacuo to afford compound 64 (40 mg, 32%). PREPARATION OF COMPOUND 65

Compound 65 was prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-44 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , NFT (7N in MeOH)/DCM, gradient from 0;l00 to 10:90). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 Dm), mobile phase: (lOmM

NH ₄ HCO ₃ /NH ₄ OH pH=9 solution in water)/ ACN, gradient from 80:20 to 60:40). The product was dissolved in DCM and washed with NaHC0 ₃ (sat., aq.). The organic layer was dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo to afford compound 65 (124 mg, 43%).

PREPARATION OF COMPOUNDS 66 AND 67

Compounds 66 and 67 were prepared following an analogous to that described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-46 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , NH ₃ (7N in MeOH)/DCM, gradient from 0;l00 to 10:90). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH ₄ HCO ₃ (0.25% solution in water)/ ACN, gradient from 80:20 to 0:100). The residue was dissolved in EtOAc and washed with NaHC0 ₃ (sat., aq.). The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford compound 67 (26.2 mg, 15%) and compound 66 (26.7 mg, 15%). PREPARATION OF COMPOUNDS 68 AND 69

Compounds 68 and 69 were prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-48 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , NFT (7N in MeOH)/DCM, gradient from 0;l00 to 10:90). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 80:20 to 0:100). The residue was dissolved in EtOAc and washed with NaHC0 ₃ (sat., aq.). The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford compound 69 (12 mg, 7%) and compound 68 (10 mg, 6%).

PREPARATION OF COMPOUNDS 70 AND 71

Compounds 70 and 71 were prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-35 as starting materials.

The crude product was purified by flash column chromatography (Si0 ₂ , NH3 (7N in MeOH)/DCM, gradient from 0:100 to 10:90). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 67:33 to 50:50) to afford compound 70 and compound 71. The compounds were separately dissolved in EtO Ac and washed with NaHCCh (sat., aq.). The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford compound 70 (65 mg, 34%) and compound 71 (18 mg, 9%). PREPARATION OF COMPOUND 72

Compound 72 was prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-42 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , NEE (7N in MeOH)/DCM, gradient from 0:100 to 10:90) to afford compound 72 (105 mg, 55%).

PREPARATION OF COMPOUNDS 73 AND 74

Compounds 73 and 74 were prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-44 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , NEE (7N in MeOH)/DCM, gradient from 0:100 to 10:90). A second purification was performed by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 Dm), mobile phase: (lOmM

NH4HCO3/NH4OH pH=9 solution in water)/ ACN, gradient from 80:20 to 60:40). The product was dissolved in DCM and washed with NaHCO;, (sat., aq.). The organic layer was dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo to give a mixture of

diastereoisomers (112 mg). A purification was performed via chiral SFC (stationary phase: Chiralpak IG 5 pm 250*20mm, mobile phase: 55% C0 ₂ , 45% MeOH (0.3% i- PrNH ₂ )) and delivered fraction A and fraction B.

Fraction A was taken up in diethyl ether and treated with HC1 (6N solution in i-PrOH). The solvents were evaporated in vacuo to afford compound 73 (53 mg, 15%) as a white solid.

Fraction B was submitted to the same treatment to afford compound 74 (35 mg, 10%).

PREPARATION OF COMPOUNDS 75 AND 76

Compounds 75 and 76 were prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-3 a as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , DCM/MeOH, gradient from 100:0 to 90:10). A second purification was performed by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 75:25 to 57:43%). NaHC0 ₃ (sat., aq.) was added and the product extracted with DCM. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo to afford compound 75 (43.8 mg, 6%) and compound 76 (51.8 mg, 7%) as white solids.

PREPARATION OF COMPOUNDS 77 AND 78

Compounds 77 and 78 were prepared following an analogous procedure to the one described for the synthesis of compound 63 using intermediate I-28a and intermediate 1-38 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , DCM/MeOH, gradient from 100:0 to 90: 10). A second purification was performed by RP HPLC

(stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 90:10 to 60:40) to afford compound 77 (62 mg, 34%) and compound 78 (70 mg, 38%) as white solids. PREPARATION OF COMPOUND 79

Intermediate 1-40 (96.1 mg, 0.49 mmol), intermediate I-l9a (94.3 mg, 0.58 mmol) and Ti(0/-Pr) ₄ (CAS: 546-68-9; 0.21 mL, 0.73 mmol) were dissolved in DCM (2.0 mL) at room temperature and under N ₂ atmosphere. The reaction mixture was stirred for 16 h, cooled to 0 °C and methylmagnesium bromide (1 4M in THF, 1.73 mL, 2.42 mmol) was added dropwise. The reaction mixture was stirred at this temperature for 15 min and at room temperature for 1 h. The mixture was treated with NH ₄ Cl (sat., aq.), diluted with DCM and the mixture was filtered through a pad of diatomaceus earth. The organic layer was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ ,

EtOAc/MeOH, gradient from 100:0 to 90:10). The residue was purified by RP HPFC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 75:25 to 57:43) to afford compound 79 (74 mg, 43%). PREPARATION OF COMPOUND 80

Intermediate I-28a (123 mg, 0.69 mmol) and Ti(0/-Pr) ₄ (CAS: 546-68-9; 280 pL, 0.95 mmol) were added to a solution of intermediate 1-50 (130 mg, 0.63 mmol) in DCM (2.5 mL). The reaction mixture was stirred at room temperature for 16 h. The reaction was cooled to 0 °C and methylmagnesium bromide (1.4M, 2.25 mL, 3.15 mmol) was added and the reaction mixture was stirred for 2 h. The reaction was quenched with MeOH and diluted with DCM and water. The emulsion was filtered through a pad of Celite®. The filtrate was treated with NH ₄ Cl (sat., aq.) and extracted with DCM. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, NFT (7M in

MeOH)/DCM, gradient from 0:100 to 5:95). A second purification was performed by RP HPLC (stationary phase: C18 XBridge 30 x 100 mm 5 pm), mobile phase:

NH ₄ HC0 ₃ (0.25% solution in water)/ ACN, gradient from 80:20 to 60:40) to afford compound 80 (110 mg, 46%).

PREPARATION OF COMPOUND 81

Intermediate I-28a (132 mg, 0.74 mmol) and Ti(0/-Pr) ₄ (CAS: 546-68-9; 300 pL, 1.01 mmol) were added to a solution of intermediate 1-52 (150 mg, 0.68 mmol) in DCM (2.7 mL). The reaction mixture was stirred at 40 °C for 16 h. The reaction was cooled to 0 °C and methylmagnesium bromide (1.4M solution, 2.40 mL, 3.37 mmol) was added and the reaction mixture was stirred for 2 h. The reaction was quenched with MeOH and diluted with DCM and water. The emulsion was filtered through a pad of Celite®. The filtrate was treated with NH ₄ Cl (sat., aq.) and extracted with DCM. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , NFT (7M in MeOH)/DCM, gradient from 0:100 to 5:95). A second purification was performed by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase:

NH4HCO3 (0.25% solution in water)/ ACN, gradient from 67:33 to 50:50) to afford compound 81 (120 mg, 45%).

PREPARATION OF COMPOUND 82

Intermediate I-3aR (50 mg, 0.26 mmol) was dissolved in ACN (2.1 mL). Intermediate 1-80 (103 mg, 0.33 mmol) and K2CO3 (109 mg, 0.79 mmol) were added. The reaction mixture was stirred at 80 °C for 16 h. The solvent was evaporated in vacuo. The crude mixture was purified by RP HPLC (stationary phase: XBridge C18 50 x 100 mm, 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ACN, gradient from 90:10 to 65:35). The residue was purified using an Isolute® SCX-2 cartridge which was washed with MeOH, and the product was eluted with NH3 (7N in MeOH). The fraction was evaporated in vacuo and the residue was dried at 50 °C in a desiccator to afford compound 82 (20 mg, 21%) as a light yellow solid

PREPARATION OF COMPOUND 83

Compound 83 was prepared following an analogous procedure to the one described for the synthesis of compound 82 using intermediate 1-56 and intermediate 1-86 as starting materials. The crude mixture was purified reverse phase ([65mM NH ₄ OAc/ACN

(90:lO)]/[ACN/MeOH (1 :1)], gradient from 91 :19 to 45:55 to afford compound 83 (45 mg, 28%) as a white solid. PREPARATION OF COMPOUND 84

Compound 84 was prepared following an analogous procedure to the one described for the synthesis of compound 82 using intermediate 1-86 and intermediate 1-62 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , DCM/MeOH, gradient from 100:0 to 96:4). The residue was triturated in Et ₂ 0 to afford a yellow oil (100 mg).

The residue was taken into DCM and treated with HC1 (4N in l,4-dioxane, leq). The solvents were evaporated in vacuo and the product was triturated in DIPE to afford compound 84 (93 mg, 38%) as a slightly pink solid.

PREPARATION OF COMPOUNDS 85, 86 AND 87

K ₂ C0 ₃ (545 mg, 3.94 mmol) was added to a solution of intermediate 1-67 (33 mg, 1.45 mmol) and intermediate I-3aR (250 mg, 1.31 mmol) in ACN (8 mL). The reaction mixture was stirred for 20 h at 70 °C. The reaction was diluted with EtOAc, filtered through Celite®, washed with EtOAc and the filtrate was concentrated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , N¾ (7N in MeOH)/DCM, gradient from 0:100 to 5:95). A second purification was performed by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase:

NH4HCO3 (0.25% solution in water)/ ACN, gradient from 80:20 to 0:100) to afford compound 85 (95 mg, 19%). A purification via chiral SFC (stationary phase: Chiralcel OD-H 5pm 250x21.2mm, mobile phase: 75% CO2, 25% z-PrOH (0.3% /-PrNFE)) delivered fraction A (35 mg) and fraction B (36 mg, 7%).

Fraction A (35 mg) was dissolved in tert-butyl methyl ether (2 mL) and HC1 (2M, 0.14 mL, 0.27 mmol) was added under stirring. The resulting precipitate was filtered and dried at 50 °C under vacuum to afford compound 86 (38 mg) as a dihydrochloride salt. Fraction B (saalonso_3593) was subjected to an analogous treatment than the one reported for fraction A to afford product 87.

PREPARATION OF COMPOUND 88

Compound 88 was prepared following an analogous procedure to the one described for the synthesis of compounds 85, 86 and 87 using intermediate 1-73 and intermediate I- 44 as starting materials.

The crude mixture was purified by flash column chromatography (S1O2, DCM/NFb (7N in MeOH), gradient from 100:0 to 98:2). A second purification was performed by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase:

NH4HCO3 (0.25% solution in water)/ ACN, gradient from 67:33 to 50:50). The aqueous phase was extracted with EtOAc. The combined organic extracts were dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford compound 88 (114 mg, 38%) as a yellow oil. PREPARATION OF COMPOUND 89

Intermediate I-3a (45.6 mg, 0.24 mmol) and K ₂ CO ₃ (90.3 mg, 0.65 mmol) were added to a stirred solution of intermediate 1-73 (50.0 mg, 0.22 mmol) in ACN (1.74 mL). The reaction mixture was stirred overnight at 80 °C. Water was added and the mixture was extracted with DCM. The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, NH ₃ (7M in MeOH)/DCM, gradient from 0:100 to 10/90) to afford compound 89 (27 mg, 32%) as a light yellow oil.

PREPARATION OF COMPOUND 90

HC1 (6M in z-PrOH, 0.16 mL, 1.0 mmol) was added to a stirred solution of compound 89 (14.0 mg, 36.5 pmol) in Et ₂ 0 (0.1 mL). The reaction mixture was stirred at room temperature for 4 h. The solvent was concentrated in vacuo. A/t-butyl methyl ether was added and the mixture was sonicated for 5 min. The solvent was evaporated in vacuo. The process was repeated until the obtention of a solid which was dried under vacuum to afford compound 90 (16.4 mg, 98%) as a yellow solid. PREPARATION OF COMPOUND 91

Compound 91 was prepared following an analogous procedure to the one described for the synthesis of compound 89 using intermediate 1-67 and intermediate I-lOa as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , DCM/MeOH, gradient from 100:0 to 95:5). A second purification was performed via RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 67:33 to 50:50).

The residue (65 mg) was dissolved in Et ₂ 0 (0.3 mL) and HC1 (7N in z-PrOH) (0.3 mL) was added. The mixture was stirred at room temperature for 16 h. The solvent was concentrated in vacuo. Te/ -butyl methyl ether was added and the mixture was sonicated for 10 min. The solvent was removed in vacuo. The process was repeated until the obtention of a solid, which was dried under vacuum at 50 °C. The residue was dissolved in MeOH (1 mL) and the mixture was concentrated in vacuo. Tert- butylmethylether was added and the mixture was sonicated for 10 min. The solvent was evaporated in vacuo and the solid was dried at 50 °C in a desiccator to afford compound 91 (45 mg, 30%) as a white solid

PREPARATION OF COMPOUND 92

Compound 92 was prepared following an analogous procedure to the one described for the synthesis of compound 89 using intermediate 1-44 and intermediate 1-67 as starting materials. The crude mixture was purified by flash column chromatography (S1O2, DCM/NH3 (7N in MeOH), gradient from 100:0 to 95:5). A second purification was performed via RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase:

NH4HCO3 (0.25% solution in water)/ ACN, gradient from 75:25 to 57:43) to afford an oil (65 mg).

The residue (56 mg) was dissolved in /erf-butyl methyl ether (2 mL) and HC1 (2M in Et ₂ 0, 0.29 mL, 0.58 mmol) was added under stirring. The precipitate was filtered off and the product was dried in the oven at 50 °C under vacuum to afford compound 92 (65 mg) as a white solid.

PREPARATION OF COMPOUNDS 93 AND 94

Compound 50 was purified via chiral SFC (stationary phase: CHIRACEL OJ-H 5pm 250*30mm, mobile phase: 82% C0 ₂ , 18% /-PrOH (0.3% /-PrNH ₂ )) to afford fraction A (44 mg) and fraction B (42 mg).

Fraction A (44 mg, 0.11 mmol) was dissolved in Et ₂ 0 (2.38 mL) and HC1 (2N in Et ₂ 0, 0.17 mL, 0.34 mmol) was added. The precipitated was filtered to give compound 93 (38.4 mg, 73%) as a white solid.

Product 94 (39.2 mg, 79%) was obtained following an analogous procedure to the one described for the synthesis of product 93 using fraction B as starting material.

PREPARATION OF COMPOUNDS 95 AND 96

Compound 43 (364 mg) was purified via chiral SFC (stationary phase: CHIRALPAK AD-H 5 pm 250*30mm, mobile phase: 80% C0 ₂ , 20% EtOH (0.3% z-PrNEh)) to afford fraction A (141 mg) and fraction B (149 mg).

Fraction A (130 mg, 0.36 mmol) was dissolved in fc/ -butyl methyl ether (2 mL) and HC1 (2M in Et20, 2 mL, 4 mmol) was added under stirring. The precipitate was filtered and the compound was dried in the oven at 50 °C under vacuum. The crude product was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ACN, gradient from 80:20 to 0:100). The desired fractions were collected and concentrated in vacuo. The resulting product was dissolved in tert-butyl methyl ether (2 mL) and HC1 (2M in Et ₂ 0, 2 mL, 4 mmol) was added under stirring. The resulting precipitate was filtered and dried at 50 °C under vacuum to afford compound 95 (95 mg, 61%).

Fraction B (120 mg, 0.33 mmol) was dissolved in tert- butyl methyl ether (2 mL) and HC1 (2M in Et ₂ 0, 2 mL, 4 mmol) was added under stirring. The precipitate was filtered and the compound was dried in the oven at 50 °C under vacuum to afford compound 96 (90 mg, 63%).

PREPARATION OF COMPOUND 97

Compound 44 (140 mg) was purified via chiral SFC (stationary phase: CHIRALPAK AD-H 5pm 250*30mm, mobile phase: 80% C0 ₂ , 20% MeOH (0.3% z-PrNH ₂ )) to afford fraction A (54 mg) and fraction B (49 mg).

Fraction B (49 mg, 0.13 mmol) was dissolved in tert- butyl methyl ether (2 mL) and citric acid (49.2 mg, 0.26 mmol) was added under stirring. The resulting precipitate was filtered and dried at 50 °C under vacuum for 48 h to afford compound 97 (55 mg, 56%). PREPARATION OF COMPOUND 98

2 HCI

Intermediate 1-73 (65.0 mg, 0.27 mmol) was dissolved in ACN (2.2 mL) and intermediate I-l0a (65.8 mg, 0.30 mmol) and K ₂ CO ₃ (113 mg, 0.82 mmol) were added. The reaction mixture was stirred for 16 h at 80 °C . The mixture was diluted with water and extracted with DCM. The organic was dried (Na ₂ S0 ₄ ), filtered and evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O ₂ , NH3 (7N in MeOH)/DCM, gradient from 0:100 to 10:90). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ACN, gradient from 53:46 to 36:64). The residue was dissolved in EtOAc and washed with a NaHC0 ₃ (sat., aq.). The organic layer was dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo.

The residue (25 mg) was dissolved in Et ₂ 0 (0.1 mL) and HC1 (7N in z-PrOH) (0.1 mL) was added. The mixture was stirred at room temperature for 16 h and the solvent was evaporated in vacuo. Te/t-butyl methyl ether was added and the mixture was sonicated for 10 min. The solvent was concentrated in vacuo. The process was repeated until the obtention of a solid which was dried under vacuum to afford compound 98 (35 mg, 26%) as a cream solid.

PREPARATION OF COMPOUNDS 99, 100 AND 101

Compounds 99, 100 and 101 were prepared following an analogous procedure to the one reported for the synthesis of compound 98 using intermediate 1-73 and intermediate 1-46 as starting materials.

The crude mixture was purified by flash column chromatography (Si0 ₂ , NFT (7N in MeOH)/DCM, gradient from 0: 100 to 10:90). The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in water)/ ACN, gradient from 80:20 to 0:100). The residue was dissolved in EtOAc, washed with NaHCCh (sat., aq.), dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford compound 99 (92.6 mg, 38%) as a white solid.

A purification was performed via chiral SFC (stationary phase: CHIRALPAK AD-H 5pm 250*30mm, mobile phase: 80% C0 ₂ , 20% z-PrOH (0.3% /-PrNH ₂ )) to afford fraction A (37 mg) and fraction B (37 mg).

The products were separately dissolved in Et ₂ 0 (0.2 mL) and HC1 (7N in z-PrOH) (0.2 mL) was added. The mixtures were stirred at room temperature for 16 h. The solvents were evaporated in vacuo and /e/t-butyl methyl ether was added. The mixtures were sonicated for 10 min and the solvents were removed in vacuo. The process was repeated until the obtention of solids which were dried under vacuum at 50 °C for 5 h to afford compound 100 (42.3 mg, 15%) and compound 101 (44.3 mg, 15%) as solids. PREPARATION OF COMPOUND 102

To a solution of intermediate 92 (123 mg, 0.26 mmol) in DCM (1 mL) was added TFA (0.35 mL, 4.62 mmol). The reaction mixture was stirred at room temperature for 18 h. The reaction was concentrated to dryness in vacuo. The residue was purified by ion exchange chromatography using an Iso lute SCX2 cartridge and eluting with MeOH, and then with NEE (7M in MeOH). Fractions were collected and the solvents were evaporated in vacuo. The residue was purified by RP HPLC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH4HCO3 (0.25% solution in

water)/ACN, gradient from 80:20 to 60:40). The desired fractions were collected and Na ₂ C0 ₃ (sat., aq.) was added. The product extracted with DCM. The solvents were evaporated in vacuo to afford compound 102 (30 mg, 33%).

PREPARATION OF COMPOUND 103

TFA (0.24 mF, 3.18 mmol) was added to a solution of intermediate 91 (84.0 mg, 0.17 mmol) in DCM (1.3 mF) and the reaction mixture was stirred at room temperature for 18 h. The reaction was concentrated in vacuo. The crude mixture was purified by RP HPFC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH ₄ HCO ₃ (0.25% solution in water)/ACN, gradient from 80:20 to 60:40). The residue was washed with water and NaHC0 ₃ (sat., aq.) and extracted with EtOAc. The organic layer was dried (Na ₂ S0 ₄ ), filtered and the solvent was evaporated in vacuo to afford compound 103 (40 mg, 65%). PREPARATION OF COMPOUND 104

TFA (0.78 mF, 10.2 mmol) was added to a stirred solution of intermediate 93 (150 mg, 0.28 mmol) in DCM (1.55 mF). The reaction mixture was stirred at room temperature for 3 days. The solvent was evaporated in vacuo and the residue dissolved in TFA neat (1 mF). The mixture was stirred at room temperature for 16 h. The solvent was evaporated in vacuo. The residue was dissolved in DCM and washed with Na ₂ C0 ₃ (sat., aq.). The organic layer was dried (Na ₂ S0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by RP HPFC (stationary phase: Cl 8 XBridge 30 x 100 mm 5 pm), mobile phase: NH ₄ HC0 ₃ (0.25% solution in water)/ACN, gradient from 80:20 to 60:40). The desired fractions were collected and concentrated in vacuo. The aqueous phase was extracted with EtOAc (3 times). The combined organic layers were dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo to afford compound 104 (58 mg, 51%).

PREPARATION OF COMPOUNDS 105 and 106

105 (Trans) 106 (C/s)

Intermediate I-28a (120 mg, 0.67 mmol) and Ti(Oz-Pr) ₄ (CAS: 546-68-9; 0.70 mL, 2.36 mmol) were added to a solution of intermediate 1-54 (155 mg, 0.71 mmol) in anhydrous THF (2.22 mL) at room temperature. The reaction mixture was stirred for 18 h. The mixture was distillated and dried in vacuo. Anhydrous THF (2.22 mL) was added and the mixture was cooled to 0 °C. Methylmagnesium bromide (1.4M in THF, 2.41 mL, 3.37 mmol) was added dropwise and the reaction mixture was stirred at 0 °C for 15 min, and at room temperature for 15 h. NH ₄ Cl (sat., aq., 2 mL) was added and the mixture was extracted with DCM and MeOH (9: 1) (3 times). The combined organics layers were dried (MgS0 ₄ ), filtered and concentrated in vacuo. The crude mixture was purified by flash column chromatography (Si0 ₂ , NLL, (7N in MeOH)/DCM, gradient from 0: 100 to 10:90) to afford a mixture compounds (60 mg, 23%). The mixture (170 mg, 0.43 mmol) was purified by reverse phase ([65mM NH ₄ OAc/ACN

(90: lO)]/[ACN/MeOH (1 :1)], gradient from 95:5 to 63:37). The desired fractions were collected and concentrated in vacuo. Another purification was performed by reverse phase ([H ₂ 0 (25mM NH ₄ HC0 ₃ )/[MeCN/Me0H (1 : 1)], gradient from 81 : 19 to 45:55) to afford fraction A(52 mg, 87%) and fraction B (30 mg, 50%).

The products were separately taken into DCM and treated with HC1 (4N in 1 ,4-dioxane, 2 eq). The solvents were evaporated in vacuo and the products were triturated in Et ₂ 0 to afford compound 106 (51 mg) and compound 105 (27 mg) as white solids. PREPARATION OF COMPOUND 107

K2CO3 (44.7 mg, 0.32 mmol) was added to a stirred solution of intermediate 94 (54.7 mg, 0.11 mmol) in MeOH (0.29 mL) and H ₂ 0 (0.11 mL) at room temperature. The reaction mixture was stirred at 60 °C for 16 h and the organic solvent was evaporated in vacuo. The mixture was extracted with EtOAc. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, DCM/MeOH, gradient from 100:0 to 90:10). to afford compound 107 (33.2 mg, 74%) as a yellow oil. The residue (33.2 mg) was taken into DCM and treated with HC1 (4N in l,4-dioxane, 1 eq). The solvents were evaporated in vacuo and the product was triturated in Et ₂ 0 to afford compound 107 (14 mg, 29%) as a white solid.

PREPARATION OF COMPOUND 108

DIPEA (0.11 mL, 0.64 mmol) was added to a stirred solution of 4-chloro-2,6- dimethylpyrimidine [4472-45-1] (61.1 mg, 0.43 mmol), intermediate 90 (137 mg, 0.47 mmol) in 1 -butanol (5 mL). The reaction mixture was stirred at 80 °C for 20 h and at 110 °C for 2 h. The mixture was diluted with DCM and NaHC0 ₃ (sat., aq.) was added. The organic phase was separated, dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by flash column chromatography (S1O2, DCM:MeOH (l0:l)/DCM, gradient from 0:100 to 80:20). The residue (97 mg) was dissolved in DCM (5 mL) and HC1 (4M in l,4-dioxane, 60.5 uL, 0.24 mmol) was added. The solvents were concentrated in vacuo and the product was triturated in Et ₂ 0 The solid was collected by filtration and dried to afford compound 108 (90 mg, 48%) as a white solid.

PREPARATION OF COMPOUND 109

NaO/-Bu (31.0 mg, 0.32 mmol) was added to a stirred suspension of Pd ₂ dba ₃ (5.91 mg, 6.46 pmol) and /-BuXPhos (8.22 mg, 19.4 umol) in l,4-dioxane (15 mL) in a sealed tube and under N ₂ atmosphere at room temperature. The reaction mixture was stirred at 95 °C for 5 min, then a mixture of intermediate 1-90 (45.0 mg, 0.16 mmol) and 4- bromo-2-methoxy-6-methylpyridine (CAS: 1083169-00-9; 26.1 mg, 0.13 mmol) in l,4dioxane (5 mL) was added to the reaction mixture under N ₂ atmosphere at 95 °C. The reaction mixture was stirred at 100 °C for 1.5 h. The mixture was diluted with NaHC0 ₃ (sat., aq.) and extracted with DCM. The organic layer was dried (MgS0 ₄ ), filtered and the solvents were evaporated in vacuo. The crude mixture was purified by reverse phase ([65mM NEEOAc/ACN (90:lO)]/[ACN:MeOH (1 :1)], gradient from 90:10 to 54:46). The residue (18 mg) was taken into DCM and treated with HC1 (4N in l,4-dioxane, 1 eq). The solvents were evaporated in vacuo to afford compound 109 (16 mg, 26%) as a white solid.

The following compounds were prepared following the methods exemplified in the Experimental Part. In case no salt form is indicated, the compound was obtained as a free base. TABLE 1

The values of salt stoichiometr or ac con in the compounds as provided herein, are those obtained experimentally. The content of hydrochloric acid reported herein was determined by ¹ H NMR integration and/or elemental analysis. ANALYTICAL PART

MELTING POINTS

Values are peak values, and are obtained with experimental uncertainties that are commonly associated with this analytical method.

DSC823e (A): For a number of compounds, melting points were determined with a DSC823e (Mettler-Toledo) apparatus. Melting points were measured with a temperature gradient of 10 °C/minute. Maximum temperature was 300 °C. Values are peak values (A). LCMS

GENERAL PROCEDURE

The High Performance Liquid Chromatography (HPLC) measurement was performed using a LC pump, a diode-array (DAD) or a UV detector and a column as specified in the respective methods. If necessary, additional detectors were included (see table of methods below).

Flow from the column was brought to the Mass Spectrometer (MS) which was configured with an atmospheric pressure ion source. It is within the knowledge of the skilled person to set the tune parameters (e.g. scanning range, dwell time...) in order to obtain ions allowing the identification of the compound’s nominal mono isotopic molecular weight (MW) and/or exact mass monoisotopic molecular weight. Data acquisition was performed with appropriate software.

Compounds are described by their experimental retention times (R _t ) and ions. If not specified differently in the table of data, the reported molecular ion corresponds to the [M+H] ⁺ (protonated molecule) and/or [M-H] (deprotonated molecule). In case the compound was not directly ionizable the type of adduct is specified (i.e. [M+NH ₄ ] ⁺ , [M+HCOO] , [M+CH ₃ COO] etc...). For molecules with multiple isotopic patterns (Br, Cl..), the reported value is the one obtained for the lowest isotope mass. All results were obtained with experimental uncertainties that are commonly associated with the method used.

Hereinafter,“SQD” Single Quadrupole Detector,“MSD” Mass Selective Detector, “QTOF” Quadrupole-Time of Flight,“rt” room temperature,“BEH” bridged ethylsiloxane/silica hybrid, HSS” High Strength Silica,“CSH” charged surface hybrid, “UPLC” Ultra Performance Liquid Chromatography,“DAD” Diode Array Detector.

TABLE 2. LC-MS Methods (Llow expressed in mL/min; column temperature (T) in

°C; Run time in min).

TABLE 3. Analytical data - melting point (M.p.) and LCMS: [M+H] ⁺ means the protonated mass of the free base of the compound, [M-H] means the deprotonated mass of the free base of the compound or the type of adduct specified [M+CFLCOO] ). R _t means retention time (in min). For some compounds, exact mass was determined.

n.d. means not determined.

OPTICAL ROTATIONS

Optical rotations were measured on a Perkin-Elmer 341 polarimeter with a sodium lamp and reported as follows: [a]° (l, c g/lOOml, solvent, T °C).

[a] _l ^T = (100a) / (l x c): where / is the path length in dm and c is the concentration in g/lOO ml for a sample at a temperature T (°C) and a wavelength l (in nm). If the wavelength of light used is 589 nm (the sodium D line), then the symbol D might be used instead. The sign of the rotation (+ or -) should always be given. When using this equation, the concentration and solvent are always provided in parentheses after the rotation. The rotation is reported using degrees and no units of concentration are given (it is assumed to be g/lOO mL).

TABLE 4. Optical Rotation data.

SFCMS-METHODS

GENERAL PROCEDURE FOR SFC-MS METHODS

The SFC measurement was performed using an Analytical Supercritical fluid chromatography (SFC) system composed by a binary pump for delivering carbon dioxide (C0 ₂ ) and modifier, an autosampler, a column oven, a diode array detector equipped with a high-pressure flow cell standing up to 400 bars. If configured with a Mass Spectrometer (MS) the flow from the column was brought to the (MS). It is within the knowledge of the skilled person to set the tune parameters (e.g. scanning range, dwell time...) in order to obtain ions allowing the identification of the compound’s nominal monoisotopic molecular weight (MW). Data acquisition was performed with appropriate software.

TABFE 5. Analytical SFC-MS Methods (Flow expressed in mF/min; column temperature (T) in °C; Run time in minutes, Backpressure (BPR) in bars).

TABLE 6. Analytical SFC data - R _t means retention time (in minutes), [M+H] ⁺ means the protonated mass of the compound, method refers to the method used for (SFC)MS

NMR

For a number of compounds, ¹ H NMR spectra were recorded on a Bruker DPX-400 spectrometer operating at 400 MHz, on a Bruker Avance I operating at 500MHz, using CHFOROFORM- _ti (deuterated chloroform, CDCh) or DMSO-t/ _f , (deuterated DMSO, dimethyl-d6 sulfoxide) as solvent. Chemical shifts (d) are reported in parts per million (ppm) relative to tetramethylsilane (TMS), which was used as internal standard.

TABLE 7. 'H NMR results

PHARMACOLOGICAL EXAMPLES

1) OGA - BIOCHEMICAL ASSAY

The assay is based on the inhibition of the hydrolysis of fluorescein mono-B-D-N- Acetyl-Glucosamine (FM-GlcNAc) (Mariappa et al. 2015, Biochem J 470:255) by the recombinant human Meningioma Expressed Antigen 5 (MGEA5), also referred to as O-GlcNAcase (OGA). The hydrolysis FM-GlcNAc (Marker Gene technologies, cat # Ml 485) results in the formation of B-D-N-glucosamineacetate and fluorescein. The fluorescence of the latter can be measured at excitation wavelength 485 nm and emission wavelength 538nm. An increase in enzyme activity results in an increase in fluorescence signal. Full length OGA enzyme was purchased at OriGene (cat #

TP322411). The enzyme was stored in 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol at -20 °C. Thiamet G and GlcNAcStatin were tested as reference compounds (Yuzwa et al. 2008 Nature Chemical Biology 4:483; Yuzwa et al. 2012 Nature

Chemical Biology 8:393). The assay was performed in 200mM Citrate/phosphate buffer supplemented with 0.005% Tween-20. 35.6 g Na ₂ HP0 ₄ 2 H ₂ 0 (Sigma, # C0759) were dissolved in 1 L water to obtain a 200 mM solution. 19.2 g citric acid (Merck, # 1.06580) was dissolved in 1 L water to obtain a 100 mM solution. pH of the sodiumphosphate solution was adjusted with the citric acid solution to 7.2. The buffer to stop the reaction consists of a 500 mM Carbonate buffer, pH 11.0. 734 mg

FM-GlcNAc were dissolved in 5.48 mL DMSO to obtain a 250 mM solution and was stored at -20 °C. OGA was used at a 2nM concentration and FM-GlcNAc at a lOOuM final concentration. Dilutions were prepared in assay buffer. 50 nl of a compound dissolved in DMSO was dispensed on Black Proxiplate TM 384 Plus Assay plates (Perkin Elmer, #6008269) and 3 mΐ fl-OGA enzyme mix added subsequently. Plates were pre-incubated for 60 min at room temperature and then 2 mΐ FM-GlcNAc substrate mix added. Final DMSO concentrations did not exceed 1%. Plates were briefly centrifuged for 1 min at 1000 rpm and incubate at room temperature for 6 h. To stop the reaction 5 mΐ STOP buffer were added and plates centrifuge again 1 min at lOOOrpm. Fluorescence was quantified in the Thermo Scientific Fluoroskan Ascent or the PerkinElmer EnVision with excitation wavelength 485 nm and emission wavelength 538 nm.

For analysis a best-fit curve is fitted by a minimum sum of squares method. From this an IC50 value and Hill coefficient was obtained. High control (no inhibitor) and low control (saturating concentrations of standard inhibitor) were used to define the minimum and maximum values.

2) OGA - CELLULAR ASSAY

HEK293 cells inducible for P301F mutant human Tau (iso form 2N4R) were established at Janssen. Thiamet-G was used for both plate validation (high control) and as reference compound (reference EC50 assay validation). OGA inhibition is evaluated through the immunocytochemical (ICC) detection of O-GlcNAcylated proteins by the use of a monoclonal antibody (CTD110.6; Cell Signaling, #9875) detecting O-

GlcNAcylated residues as previously described (Dorfmueller et al. 2010 Chemistry & biology, 17:1250). Inhibition of OGA will result in an increase of O- GlcNAcylated protein levels resulting in an increased signal in the experiment. Cell nuclei are stained with Hoechst to give a cell culture quality control and a rough estimate of immediate compounds toxicity, if any. ICC pictures are imaged with a Perkin Elmer Opera Phenix plate microscope and quantified with the provided software Perkin Elmer Harmony 4.1.

Cells were propagated in DMEM high Glucose (Sigma, #D5796) following standard procedures. 2 days before the cell assay cells are split, counted and seeded in Poly-D- Lysine (PDL) coated 96-wells (Greiner, #655946) plate at a cell density of 12,000 cells per cm ² (4,000 cells per well) in IOOmI of Assay Medium (Low Glucose medium is used to reduce basal levels of GlcNAcylation) (Park et al. 2014 The Journal of biological chemistry 289: 13519). At the day of compound test medium from assay plates was removed and replenished with 90m1 of fresh Assay Medium. 10m1 of compounds at a lOfold final concentration were added to the wells. Plates were centrifuged shortly before incubation in the cell incubator for 6 hours. DMSO concentration was set to 0.2%. Medium is discarded by applying vacuum. For staining of cells medium was removed and cells washed once with 100 mΐ D-PBS (Sigma, #D8537). From next step onwards unless other stated assay volume was always 50m1 and incubation was performed without agitation and at room temperature. Cells were fixed in 50m1 of a 4% paraformaldehyde (PFA, Alpha aesar, # 043368) PBS solution for 15 minutes at room temperature. The PFA PBS solution was then discarded and cells washed once in lOmM Tris Buffer (LifeTechnologies, # 15567-027), l50mM NaCl (LifeTechnologies, #24740-0110, 0.1% Triton X (Alpha aesar, # A16046), pH 7.5 (ICC buffer) before being permeabilized in same buffer for 10 minutes. Samples are subsequently blocked in ICC containing 5% goat serum (Sigma, #G9023) for 45-60 minutes at room temperature. Samples were then incubated with primary antibody (1/1000 from commercial provider, see above) at 4°C overnight and subsequently washed 3 times for 5 minutes in ICC buffer. Samples were incubated with secondary fluorescent antibody (1/500 dilution, Lifetechnologies, # A-21042) and nuclei stained with Hoechst 33342 at a final concentration of lpg/ml in ICC (Lifetechnologies, # H3570) for 1 hour. Before analysis samples were washed 2 times manually for 5 minutes in ICC base buffer.

Imaging is performed using Perkin Elmer Phenix Opera using a water 20x objective and recording 9 fields per well. Intensity readout at 488nm is used as a measure of O-GlcNAcylation level of total proteins in wells. To assess potential toxicity of compounds nuclei were counted using the Hoechst staining. I Cso- values are calculated using parametric non-linear regression model fitting. As a maximum inhibition Thiamet G at a 200uM concentration is present on each plate. In addition, a concentration response of Thiamet G is calculated on each plate.

TABLE 8. Results in the biochemical and cellular assays.

EX VIVO OGA OCCUPANCY ASSAY USING [ ³ H] -LIGAND

DRUG TREATMENT AND TISSUE PREPARATION

Male NMRI or C57Bl6j mice were treated by oral (p.o.) administration of vehicle or compound. Animals were sacrificed 24 hours after administration. Brains were immediately removed from the skull, hemispheres were separated and the right hemisphere, for ex vivo OGA occupancy assay, was rapidly frozen in dry-ice cooled 2- methylbutane (-40°C). Twenty Dm-thick sagittal sections were cut using a Leica CM 3050 cryostat-microtome (Leica, Belgium), thaw-mounted on microscope slides (SuperFrost Plus Slides, Thermo Fisher Scientific) and stored at -20°C until use. After thawing, sections were dried under a cold stream of air. The sections were not washed prior to incubation. The 10 minutes incubation with 3 nM [ ³ H]-ligand was rigorously controlled. All brain sections (from compound-treated and vehicle-treated animals) were incubated in parallel. After incubation, the excess of [ ³ H]-ligand was washed off in ice-cold buffer (PBS IX and 1% BSA) 2 times 10 minutes, followed by a quick dip in distilled water. The sections were then dried under a stream of cold air.

QUANTITATIVE AUTORADIOGRAPHY AND DATA ANALYSIS

Radioactivity in the forebrain area of brain slices was measured using a b-imager with M3 vision analysis software (Biospace Lab, Paris). Specific binding was calculated as the difference between total binding and non-specific binding measured in Thiamet-G (10 mM) treated sections. Specific binding in sections from drug treated animals was normalised to binding in sections from vehicle treated mice to calculate percentage of OGA occupancy by the drug.